Saturday, July 07, 2012
Subject: TX Animal Health Commission Accepting Comments on Chronic Wasting
Disease Rule Proposal
Texas Animal Health Commission (TAHC) NEWS RELEASE
Texas Animal Health Commission
"Serving Texas Animal Agriculture Since 1893"
Dee Ellis, DVM, MPA ● Executive Director
P.O. Box l2966 ● Austin, Texas 78711 ● (800) 550-8242 http://www.tahc.state.tx.us
For more information contact the Communication & PR Dept. at
1-800-550-0710 or at bonnie.ramirez@tahc.state.tx.us
_____________________________________________________________________________________________
FOR IMMEDIATE RELEASE
July 6, 2012
TAHC Now Accepting Comments on Chronic Wasting Disease Rule Proposal
AUSTIN - The Texas Animal Health Commission (Commission) is currently
accepting public comments on a rule proposed at its June 5 meeting to amend
Chapter 40, entitled "Chronic Wasting Disease (CWD)". The proposed rule will
affect certain cervid species and delineates movement restriction zones and
other necessary disease management practices related to the control of CWD in
far west Texas.
CWD has been discovered in mule deer in the Hueco Mountains of southern
New Mexico, very near the Texas state line. The potential risk of animals moving
back and forth between Texas and New Mexico has raised significant concern among
wildlife and animal health officials that the disease is also present in deer
living in the Texas portion of the same mountain range. Currently CWD is not
known to exist anywhere in Texas, but has been found in 16 other states in free
ranging and/or captive cervid herds.
CWD is not known to affect people, but a number of cervid species are
susceptible. Besides mule deer, other susceptible species include white-tailed
deer, elk, red deer, sika deer and moose. The progressively fatal disease is
most commonly exhibited by chronic weight loss, and abnormal behavior such as
disorientation. Prions are the infectious agent of CWD, and can be found
throughout the body of an infected animal. The prions are present in the body
fluids of infected animals, and can be shed onto the soil where they may remain
viable and able to infect other susceptible animals for many years. For this
reason the proposed TAHC rules apply to land as well as animals within the
proposed zones.
The proposed rules are intended to define susceptible species, establish
boundaries for a High Risk Zone (HRZ) and Containment Zone (CZ), restrict
movement within the zones, establish surveillance systems within the zones, and
also address requirements for new or existing herds ability to gain CWD
monitored status designations by TAHC. Counties affected by the proposed rules
include El Paso, and portions of Hudspeth, Culberson and Reeves.
The proposed TAHC rules apply to the non-indigenous species of cervid
species of Texas under its jurisdiction including moose, red deer, elk and Sika.
The Texas Parks and Wildlife Department (TPWD) is also proposing similar rules
for the cervid species it regulates (indigenous to Texas), including
white-tailed deer and mule deer.
The TAHC rule proposals have a comment period of 30 days. They may be
commented on until 5 p.m. on Monday, August 6, 2012.
The Commission is also proposing amendments to the following:
Chapter 43, entitled "Tuberculosis" Chapter 45, entitled "Reportable
Diseases" Chapter 49, entitled "Equine, Piroplasmosis"
A detailed explanation of each rule proposal, including the CWD rule can be
found on the TAHC web site at http://www.tahc.state.tx.us/regs/proposals.html
.
Comments on the TAHC's proposed regulations must be submitted in writing
to Carol Pivonka, Texas Animal Health Commission, 2105 Kramer Lane, Austin,
Texas 78758, by fax at (512) 719-0721 or by e-mail to comments@tahc.state.tx.us
.
Founded in 1893, the Texas Animal Health Commission works to protect the
health of all Texas livestock, including: cattle, swine, poultry, sheep, goats,
equine animals, and exotic livestock.
###
Rules proposed at the June 5, 2012 Commission meeting
Chapter 40, CWD - Create CWD movement restriction zone(s) in the Trans
Pecos Region
View
Comment
comments@tahc.state.tx.us
The Texas Animal Health Commission (Commission) proposes new §40.6, CWD
Movement Restriction Zone, in Chapter 40, which is entitled “Chronic Wasting
Disease”. The new section will create Chronic Wasting Disease (CWD) movement
restriction zone(s) in the Trans Pecos Region.
There is a task force comprised of members of affected deer and exotic
livestock associations, private veterinary practitioners, and wildlife
biologists who assist the Texas Parks and Wildlife Department (TPWD) and
Commission staff in developing a response plan for CWD detected in mule deer
harvested in New Mexico within 1-2 miles of the Texas border. They recently met
and provided both agencies with recommendations on a strategy to address the
risk of exposure of CWD to susceptible species in Texas. The recommendations
follow the creation of CWD Movement Restriction Zone(s) for the area with
restrictions put in place to protect against the exposure and spread of CWD from
New Mexico. These recommendations are being taken in a coordinated effort by
both TPWD and the Commission.
It was recently disclosed that through CWD sampling efforts of New Mexico
Game and Fish personnel that CWD has been detected in mule deer in the southern
Sacramento Mountains and northern Hueco Mountains, in southern New Mexico. While
sample sizes are very small, it seems that the CWD prevalence may be quite high
in that location. Several of the animals sampled were located in close proximity
to the Texas border. This is significant for the state of Texas, considering
basic biology and movement patterns of susceptible species located there such as
mule deer and elk indicate that the animals may be moving back and forth between
Texas and New Mexico.
Prions are found ubiquitously throughout the body of an infected animal,
and can be shed onto soil, where they may remain viable and able to infect other
susceptible animals for many years. Suspected additional susceptible species
besides mule deer, white tail deer and elk, include red deer and sika deer.
There is still no evidence that humans or domestic livestock can be infected
with CWD.
Deer populations in other states where CWD prevalence exceeds 40% have
experienced significant (>45%) population declines. As the prevalence rates
increase and geographic distribution has expanded in other states, hunters are
more likely to alter hunting behaviors which may include avoiding areas with
high CWD prevalence. This could have an adverse economic impact on local
communities dependent on hunting revenue, and could affect TPWD efforts to
manage cervid populations through hunter harvest.
Considering the seemingly high CWD prevalence rate in the Sacramento and
Hueco Mountains of New Mexico, CWD may be well established in the population and
in the environment in Texas at this time. The current area of concern was
delineated as all land west of the Pecos River and IH 20, and north of IH 10 to
Ft. Hancock, and all land west and north of Ft. Hancock and the Containment Zone
(CZ) was delineated as all land west of HWY 62-180 and HWY 54, and north of IH
10 to Ft. Hancock, and all land west and north of Ft. Hancock. Data regarding
mule deer population parameters and mule deer movements, knowledge on elk
movements, and the geography and habitat types of the area were considered in
the delineation of these zones.
snip...
Considering the seemingly high CWD prevalence rate in the Sacramento and
Hueco Mountains of New Mexico, CWD may be well established in the population and
in the environment in Texas at this time. The current area of concern was
delineated as all land west of the Pecos River and IH 20, and north of IH 10 to
Ft. Hancock, and all land west and north of Ft. Hancock and the Containment Zone
(CZ) was delineated as all land west of HWY 62-180 and HWY 54, and north of IH
10 to Ft. Hancock, and all land west and north of Ft. Hancock. Data regarding
mule deer population parameters and mule deer movements, knowledge on elk
movements, and the geography and habitat types of the area were considered in
the delineation of these zones.
snip...
Greetings TAHC et al,
I would kindly, once again, like to comment on the importance of testing
for CWD. I tried to warn you in 2001, again in 2005, 2006, again later in 2011,
2012, and now as you stated here ;
There is a task force comprised of members of affected deer and exotic
livestock associations, private veterinary practitioners, and wildlife
biologists who assist the Texas Parks and Wildlife Department (TPWD) and
Commission staff in developing a response plan for CWD detected in mule deer
harvested in New Mexico within 1-2 miles of the Texas border. They recently met
and provided both agencies with recommendations on a strategy to address the
risk of exposure of CWD to susceptible species in Texas. The recommendations
follow the creation of CWD Movement Restriction Zone(s) for the area with
restrictions put in place to protect against the exposure and spread of CWD from
New Mexico. These recommendations are being taken in a coordinated effort by
both TPWD and the Commission.
It was recently disclosed that through CWD sampling efforts of New Mexico
Game and Fish personnel that CWD has been detected in mule deer in the southern
Sacramento Mountains and northern Hueco Mountains, in southern New Mexico. While
sample sizes are very small, it seems that the CWD prevalence may be quite high
in that location. Several of the animals sampled were located in close proximity
to the Texas border. This is significant for the state of Texas, considering
basic biology and movement patterns of susceptible species located there such as
mule deer and elk indicate that the animals may be moving back and forth between
Texas and New Mexico.
Considering the seemingly high CWD prevalence rate in the Sacramento and
Hueco Mountains of New Mexico, CWD may be well established in the population and
in the environment in Texas at this time. The current area of concern was
delineated as all land west of the Pecos River and IH 20, and north of IH 10 to
Ft. Hancock, and all land west and north of Ft. Hancock and the Containment Zone
(CZ) was delineated as all land west of HWY 62-180 and HWY 54, and north of IH
10 to Ft. Hancock, and all land west and north of Ft. Hancock. Data regarding
mule deer population parameters and mule deer movements, knowledge on elk
movements, and the geography and habitat types of the area were considered in
the delineation of these zones.
The fact of the matter is, CWD has been waltzing across Texas for over a
decade from the WSMR at New Mexico border, and the state of Texas, in my
opinion, knew this. in my opinion, the state of Texas purposely tested the least
amount of cervids in that area for years, why, they knew it was there, and I
warned you of this in 2001, 2005, and year after year after year. now, it’s too
late. Game farms and ranchers i.e. high fence operations here in Texas are out
of control in my opinion, with the TAHC not having a clue as to the infection
rate of CWD (if any) at these high fence operations. it has been proven in the
past, they are nothing but a petri dish for CWD infection rates, with the
highest infection rate in Wisconsin at the Buckhorn Flats Game farm toping out
at 80%. TAHC actions now on CWD, as I finally applaud them, may well be much too
late, and not near enough. I pray that I am wrong. However, because of this, I
think the movement restrictions on cervids in Texas should include every region
in the state of Texas, until a very large cwd sampling over a period of 7 to 10
years. ...
here are a few of my pleas to the TAHC about CWD waltzing into Texas for
over a decade ;
2001 - 2002
Subject: Texas Borders Reopened for Importing Black-Tailed Deer & Elk
New Entry Regulations in Effect $ CWD TESTING STATISTICS ?
Date: Fri, 6 Sep 2002 17:18:16 –0700
From: "Terry S. Singeltary Sr."
Reply-To: Bovine Spongiform Encephalopathy
To: BSE-L@uni-karlsruhe.de
######## Bovine Spongiform Encephalopathy #########
NEWS RELEASE
Texas Animal Health Commission
Box l2966 * Austin, Texas 78711 * (800) 550-8242 * FAX (512) 719-0719
Linda Logan, DVM, PhD * Executive Director
For info, contact Carla Everett, information officer, at 1-800-550-8242,
ext. 710, or ceverett@tahc.state.tx.us
snip...
TEXAS OLD STATISTICS BELOW FOR PAST CWD TESTING;
Subject: CWD testing in Texas
Date: Sun, 25 Aug 2002 19:45:14 –0500
From: Kenneth Waldrup
To: flounder@wt.net
CC: mcoats@tahc.state.tx.us
Dear Dr. Singletary,
In Fiscal Year 2001, seven deer from Texas were tested by the National
Veterinary Services Laboratory (NVSL) for CWD (5 fallow deer and 2 white-tailed
deer). In Fiscal Year 2002, seven elk from Texas were tested at NVSL (no deer).
During these two years, an additional six elk and one white-tailed deer were
tested at the Texas Veterinary Medical Diagnostic Laboratory (TVMDL). In Fiscal
Year 2002, four white-tailed deer (free-ranging clinical suspects) and at least
eight other white-tailed deer have been tested at TVMDL. One elk has been tested
at NVSL. All of these animals have been found negative for CWD. Dr. Jerry Cooke
of the Texas Parks and Wildlife Department also has records of 601 clinically
ill white-tailed deer which were necropsied at Texas A&M during the late
1960's and early 1970's, and no spongiform encepalopathies were noted.
Thank you for your consideration.
Ken Waldrup, DVM, PhD Texas Animal Health Commission
========================
TEXAS CWD STATUS
Captive Cervids
There have been no reported CWD infections of captive elk or deer in Texas.
There is currently no mandatory surveillance program for susceptible cervids
kept on game farms, although, there has been voluntary surveillance since 1999,
which requires owners of participating herds to maintain an annual herd
inventory and submit samples for all mortalities of animals over 16 months of
age.
snip...
SO, i thought i would just see where these Ecoregions were, and just how
the CWD testing was distributed. YOU would think that with the cluster of CWD
bordering TEXAS at the WPMR in NM, you would have thought this would be where
the major CWD testing samples were to have been taken? wrong! let's have a look
at the sample testing. here is map of CWD in NM WPMR bordering TEXAS;
NEW MEXICO 7 POSITIVE CWD WHITE SANDS MISSILE RANGE MAP
NEXT, let's have a look at the overall distribution of CWD in Free-Ranging
Cervids and see where the CWD cluster in NM WSMR borders TEXAS;
Current Distribution of Chronic Wasting Disease in Free-Ranging Cervids
NOW, the MAP of the Exoregion where the samples were taken to test for CWD;
CWD SURVEILLANCE SAMPLE SUBMISSIONS TEXAS
Ecoregions of TEXAS
IF you look at the area around the NM WSMR where the CWD cluster was and
where it borders TEXAS, that ecoregion is called Trans Pecos region. Seems if my
Geography and my Ciphering is correct ;-) that region only tested 55% of it's
goal. THE most important area on the MAP and they only test some 96 samples,
this in an area that has found some 7 positive animals? NOW if we look at the
only other border where these deer from NM could cross the border into TEXAS,
this area is called the High Plains ecoregion, and again, we find that the
sampling for CWD was pathetic. HERE we find that only 9% of it's goal of CWD
sampling was met, only 16 samples were tested from some 175 that were suppose to
be sampled.
AS i said before;
> SADLY, they have not tested enough from the total population to
> know if CWD is in Texas or not.
BUT now, I will go one step further and state categorically that they are
not trying to find it. just the opposite it seems, they are waiting for CWD to
find them, as with BSE/TSE in cattle, and it will eventually...
snip...end...TSS
===============================
2005
SEE MAP OF CWD ON THE BORDER OF NEW MEXICO VERY CLOSE TO TEXAS ;
NO update on CWD testing in Texas, New Mexico that i could find. I have
inquired about it though, no reply yet...
-------- Original Message --------
Subject: CWD testing to date TEXAS ?
Date: Mon, 09 May 2005 12:26:20 –0500
From: "Terry S. Singeltary Sr."
To: kristen.everett@tpwd.state.tx.us
Hello Mrs. Everett,
I am most curious about the current status on CWD testing in Texas. could
you please tell me what the current and past testing figures are to date and
what geographical locations these tests have been in. good bust on the illegal
deer trapping case. keep up the good work there.........
thank you, with kindest regards,
Terry S. Singeltary Sr. P.O. Box 42 Bacliff, Texas USA 77518
-------- Original Message --------
Subject: CWD testing in New Mexico
Date: Mon, 09 May 2005 14:39:18 –0500
From: "Terry S. Singeltary Sr."
To: ispa@state.nm.us
Greetings,
I am most curious of the current and past CWD testing in New Mexico, and
there geographical locations...
thank you,
Terry S. Singeltary SR. CJD Watch
#################### https://lists.aegee.org/bse-l.html
####################
2006
----- Original Message -----
From: "Terry S. Singeltary Sr." flounder9@VERIZON.NET
To: BSE-L@aegee.org
Sent: Saturday, December 23, 2006 1:47 PM
Subject: CWD in New Mexico 35 MILES FROM TEXAS BORDER and low testing
sampling figures -- what gives TAHC ???
Subject: CWD in New Mexico 35 MILES FROM TEXAS BORDER and low testing
sampling figures -- what gives TAHC ???
Date: December 23, 2006 at 11:25 am PST
Greetings BSE-L members,
i never know if i am going crazy or just more of the same BSe. several
years ago i brought up the fact to the TAHC that CWD was literally at the Texas
borders and that the sample size for cwd testing was no where near enough in the
location of that zone bordering NM. well, i just wrote them another letter
questioning this again on Dec. 14, 2006 (see below) and showed them two
different pdf maps, one referencing this url, which both worked just fine then.
since then, i have NOT received a letter from them answering my question, and
the url for the map i used as reference is no longer working? i had reference
this map several times from the hunter-kill cwd sampling as of 31 August 2005
pdf which NO longer works now??? but here are those figures for that zone
bordering NM, for those that were questioning the url. the testing samples
elsewhere across Texas where much much more than that figure in the zone
bordering NM where CWD has been documented bordering TEXAS, near the White Sands
Missile Range. SO, why was the Texas hunter-kill cwd sampling as of 31 August
2005 document removed from the internet??? you know, this reminds me of the
infamous TEXAS MAD COW that i documented some 7 or 8 months before USDA et al
documented it, when the TAHC accidentally started ramping up for the
announcement on there web site, then removed it (see history at bottom). i am
not screaming conspiracy here, but confusious is confused again on the ciphering
there using for geographical distribution of cwd tissue sample size survey, IF
they are serious about finding CWD in TEXAS. common sense would tell you if cwd
is 35 miles from the border, you would not run across state and have your larger
samples there, and least samples 35 miles from where is what
found..........daaa..........TSS
THEN NOTICE CWD sample along that border in TEXAS, Three Year Summary of
Hunter-Kill CWD sampling as of 31 August 2005 of only 191 samples, then compare
to the other sample locations ;
TPWD has been conducting surveys of hunter-kill animals since 2002 and has
collected more than 7300 samples (as of 31 August 2005). In total, there have
been over 9400 samples, both hunter-kill and private samples, tested in Texas to
date, and no positives have been found.
SO, out of a total of 9,400 samples taken for CWD surveillance in TEXAS
since 2002 of both hunter-kill and private kill, ONLY 191 samples have been
taken in the most likely place one would find CWD i.e. the border where CWD has
been documented at TEXAS and New Mexico
latest map NM cwd old data
CWD in New Mexico ;
What is the Department doing to prevent the spread of CWD?
Chronic wasting disease (CWD) was recently detected in a mule deer from
Unit 34. Until 2005, CWD had only been found in Unit 19. With this discovery,
the Department will increase its surveillance of deer and elk harvested in Units
29, 30 and 34.
Lymph nodes and/or brain stems from every harvested deer and brain stems
from all elk taken in Unit 34 will be sampled.
snip...
CWD SURVEILLANCE TEXAS
IMPLEMENTATION OF A GEOGRAPHICALLY FOCUSED CWD SURVEILLANCE PROGRAM FOR
FREE-RANGING CERVIDS
A geographically-focused free-ranging cervid Monitoring Program was
implemented during the fall 2002 deer-hunting season. Brain stem samples from
hunter-killed deer will be obtained from TPWD Wildlife Management Areas (WMA),
State Parks, and where otherwise available with hunter and/or landowner
permission, from deer taken on private land. Volume 1, Sixth Edition of United
States Department of Agriculture, Animal and Plant Health Inspection Service,
Veterinary Services, Regulatory Statistics (Appendix D1) indicates that 148
samples is sufficient to detect disease at two per-cent prevalence, regardless
of the population size. Therefore the goal is to acquire 148 samples from each
of the State's ten ecoregions provided adequate sampling distribution is
achieved across each ecoregion. The five year 2002 -2006, goal is to
cumulatively collect 459 samples from each of the ten ecoregions. The cumulative
sample would be used statistically to detect CWD at one per-cent prevalence
level with 99 per-cent confidence. However, funding from APHIS/USDA could
provide the necessary funds for sampling at the one per-cent prevalence level
each year. TAHC conducted a risk assessment of counties where deer and elk have
been imported and where high densities of free-ranging deer occur. The
assessment was conducted for USDA funding consideration. The risk assessment was
based on limited number of criteria. Since CWD could potentially occur anywhere
in Texas, monitoring efforts would be focused to achieve a stratified sampling
scheme across each ecoregion of the State.
Confidentiality laws restrict the type of data TPWD personnel can collect
as it relates to a specific parcel of land. Therefore, personnel will ensure
that no property specific information is collected (i.e. ranch name or exact
location) without the landowner's written permission. The following are
guidelines for data and sample collection distributed to TPWD personnel prior to
sample collection:
A Texas Veterinary Medical Diagnostic Laboratory (TVMDL) Accession Form
must be submitted with brain stem samples.
The most important items to be filled out are the TPWD employee name,
address and phone number, and "Patient/Deer ID". County of Kill can be recorded
on the bottom of the form, but DO NOT report any information that identifies the
specific parcel of land.
The "Patient/Deer ID" number MUST BE specific to the field data sheet the
employee is using to record data.
Specific CWD field data sheets will not be provided, as current field data
sheets (i.e. Age/Weight Antler Data Sheets, Hunter Check Station Data Sheets,
etc.) will be appropriate in most cases. Field staff may produce their own CWD
data sheet if necessary.
The field data sheet must contain:
Employee Name
Sample Number (same as Patient/Deer ID on TVMDL Accession Form
Sample Date
Deer Age
Deer Sex
County of Kill
Hunter Name
Hunting License Number
Ranch name or tract name/location ONLY with landowner permission. Should a
CWD positive be detected, TAHC will use hunter contact information to conduct
CWD investigation under their regulatory authority. Make sure the container
containing the brain stem sample is legibly identified with the sample number,
deer age and sex, county of kill and date. Although the sample number is all
that is needed, additional information will help resolve any problems should
batches of samples be combined.
Should a landowner retain deer heads for our sampling purposes, remind the
landowner to issue the hunters a proof of sex document as provided for in TAHC
65.10 (c). In addition, a Wildlife resource document (PWD 905) must accompany
the head until the carcass reaches a final destination and finally
processed.
Samples MAY NOT be taken from legally harvested deer without the hunter's
consent.
ACTIONS SHOULD A CWD POSITIVE BE DETECTED
Should sampling detect a CWD positive animal, TAHC and TPWD would activate
the Media Response Plan (Appendix F). TAHC and TPWD would immediately begin
review of the information at hand and determine the action to be taken within
the Response Plan (Appendix C.) The first action should be to inform landowners
adjacent to the property containing the CWD positive and hold a meeting with
advisory committees and affected landowner to discuss plans for secondary
sampling. Planning for secondary sampling, investigating movements of deer into
and away from property for further actions would then be the next step. The
secondary sampling is critical for determining distribution and prevalence of
the disease.
As distribution and prevalence is being determined, information review and
discussions with TPWD advisory committees (e.g., Private Lands Advisory Board,
Hunting Advisory Committee, White-tailed Deer Advisory Committee etc.) and
landowners would take place in order to determine the appropriate management
action to be taken.
and the discovery of several CWD positive mule deer in New Mexico,
approximately 35 miles north of the Texas border were well out of the known
boundaries of the disease.
The disease prevalence appears to be increasing in localized areas,
although it is not clear whether this is due to increased incidence, or
increased surveillance, reporting, and testing. Information from states with
direct experience in managing CWD is being used for developing Texas plans as we
learn from their experiences.
TPWD and TAHC are developing stepped up targeted and geographically-focused
surveillance plans to monitor free-ranging deer for the presence of the disease
and a rapid response plan to guide both TPWD and TAHC should CWD be detected in
the State. TPWD and TAHC are also evaluating cervid management laws, rules, and
policies for free ranging and scientific breeder permitted cervids under their
authority to identify issues and potential weaknesses related to disease
management. In these efforts, TPWD and TAHC will work with other agencies and
organizations responsible for or are concerned about cervid disease management
in an attempt to ensure comprehensive approaches to effective management of CWD
risks (see Appendix C: Importation of Susceptible Cervids).
----- Original Message -----
From: Terry S. Singeltary Sr.
To: thurmanf@tahc.state.tx.us
Sent: Thursday, December 14, 2006 9:52 PM
Subject: cwd at Texas border and low sampling figures ???
Greetings TAHC,
can someone please explain to me any reasoning at all for the very low
sampling for CWD which have been taken where CWD is literally right at the steps
of one of Texas borders, but yet across the state elsewhere, the numbers for
testing increases ???
i do not understand the low sampling for cwd size where it is at our
borders, compared to the highter numbers elsewhere???
see Texas hunter kill sample for CWD to Aug 31, 2005
see map where CWD has been documented at Texas border in free ranging deer
and elk
kind regards,
Terry
Subject: CWD 3 NEW CASES SOUTHERN NEW MEXICO
Date: July 10, 2006 at 8:51 am PST
New Mexico Department of Game and Fish
Media contact: Dan Williams, (505) 476-8004
Public contact: (505) 476-8000
dan.williams@state.nm.us
FOR IMMEDIATE RELEASE, JULY 7, 2006:
3 SOUTHERN NEW MEXICO DEER TEST POSITIVE FOR CHRONIC WASTING DISEASE
SANTA FE – Three deer in southern New Mexico have tested positive for
chronic wasting disease, bringing the total number of confirmed CWD-infected
deer in the state to 15 since the first infected deer was discovered in
2002.
The Department received test results Wednesday from the state Veterinary
Diagnostic Services laboratory in Albuquerque that two wild deer captured near
the White Sands Missile Range headquarters east of Las Cruces had tested
positive for chronic wasting disease. A third wild deer captured in the small
community of Timberon in the southern Sacramento Mountains also tested positive
for the disease.
The discoveries of the infected deer were part of the Department's ongoing
efforts to monitor the disease, which to date has been confined to the southern
Sacramento Mountains southeast of Cloudcroft and areas surrounding the Organ
Mountains near Las Cruces. Two wild elk from the southern Sacramento Mountains
tested positive for the disease in December 2005.
Chronic wasting disease is a fatal neurological illness that afflicts deer,
elk and moose. There is no evidence of CWD being transmitted to humans or
livestock. The disease causes animals to become emaciated, display abnormal
behavior and lose control of bodily functions. To date, it has been found in
captive and wild deer, elk and moose in eight states and two Canadian
provinces.
For more information about CWD in New Mexico and how hunters can assist in
research and prevention, please visit the New Mexico Department of Game and Fish
Web site, www.wildlife.state.nm.us . More information about CWD also can be
found on the Chronic Wasting Disease Alliance site at www.cwd-info.org/ .
###
SEE MAP NM
SEE SAMPLING MAP TEXAS
CWD Sampling Maps
Three Year Summary of Hunter-Kill CWD Sampling (as of August 31, 2005)
CWD Sampling Maps
Three Year Summary of Hunter-Kill CWD Sampling (as of August 31,
2005)
USDA CWD Maps
March 2006 — Current Distribution of CWD
TAHC CWD Monitoring Program Information
CWD Sample Submission and Costs
2006 Factsheet For Producers Enrolling in the Complete Herd Monitoring
Program
USDA CWD Maps
March 2006 — Current Distribution of CWD
TAHC CWD Monitoring Program Information
CWD Sample Submission and Costs
2006 Factsheet For Producers Enrolling in the Complete Herd Monitoring
Program
----- Original Message -----
From: "Terry S. Singeltary Sr."
To:
Sent: Monday, June 27, 2005 6:51 PM
Subject: CWD TWO NEW CASES NEAR WHITE SANDS MISSLE RANGE NEW MEXICO
##################### Bovine Spongiform Encephalopathy
#####################
From: TSS ()
Subject: CWD TWO NEW CASES NEAR WHITE SANDS MISSLE RANGE NEW MEXICO
Date: June 27, 2005 at 4:43 pm PST
New Mexico Department of Game and Fish
Contact: Dan Williams, (505) 476-8004
dan.williams@state.nm.us
FOR IMMEDIATE RELEASE, JUNE 24, 2005:
TWO MULE DEER TEST POSITIVE FOR CHRONIC WASTING DISEASE
ANGLER LANDS STATE RECORD BLUE CATFISH AT ELEPHANT BUTTE LAKE
TWO MULE DEER TEST POSITIVE FOR CHRONIC WASTING DISEASE
SANTA FE – Two mule deer captured in the Organ Mountains as part of an
ongoing research project near White Sands Missile Range have tested positive for
chronic wasting disease (CWD), a fatal neurological disease that attacks the
brains of infected deer and elk, the Department of Game and Fish
announced.
The number of confirmed CWD cases in New Mexico now stands at 11 since
2002, when the disease was first confirmed in a deer found near the eastern
foothills of the Organ Mountains. All 11 CWD-infected deer were found in the
same general area of southern New Mexico. The origin of the disease in New
Mexico remains unknown.
The carcasses of the infected deer will be incinerated, said Kerry Mower,
the Department’s lead wildlife disease biologist.
Chronic wasting disease causes animals to become emaciated, display
abnormal behavior, lose bodily functions and die. The disease has been found in
wild deer and elk, and in captive deer and elk, in eight states and two
Canadian provinces. There currently is no evidence of CWD being transmitted
to humans or livestock.
Mower said the most recent CWD-positive deer showed no obvious physical
signs of having the disease. They were captured in April 2005 and tested as part
of a 3-year-old research project studying deer population dynamics in southern
New Mexico. More than 140 deer have been captured alive and tested for the
study, in which researchers hope to find the cause of a 10-year decline in the
area deer population. Study participants include the Department of Game and
Fish, the U.S. Army at White Sands Missile Range and Fort Bliss, Bureau of Land
Management, U.S. Geological Survey at New Mexico State University, and San
Andres National Wildlife Refuge.
Hunters can assist the Department in its CWD research and prevention
efforts by bringing their fresh, legally
harvested deer or elk head to an area office, where officers will remove
the brain stem for testing. Participants will be eligible for drawings for an
oryx hunt on White Sands Missile Range and a trophy elk hunt on the Valle Vidal.
For more information about the drawing and chronic wasting disease, visit the
Department web site at
www.wildlife.state.nm.us.
SEE MAP ;
Greetings list members,
I am deeply concerned with these CWD mad deer so close to the Texas border.
WHAT keeps them from crossing the border to Texas ??? IF these illegal aliens
can so easily cross our borders, why not these infected deer? maybe we should
get these minute men to start watching for mad deer coming in to Texas from New
Mexico.
I mentioned my concerns several other times before;
-------- Original Message --------
Subject: Current status of CWD testing in Texas
Date: Tue, 10 May 2005 09:09:47 –0500
From: "kschwaus"
To:
Mr. Singeltary,
I was asked to provide you with the following information. If you have any
other questions regarding CWD sampling in Texas, please do not hesitate to give
me a call. My office number is below.
Below I have included a chart showing CWD samples that have been tested
since the fall of 2002 through the present at the eco-region level. The second
chart shows the totals on a given year. The unknown location samples come from
private individuals sending in samples directly to the Texas Veterinary Medical
Diagnostic Lab (TVMDL). Due to the confidentiality laws that the TVMDL operates
under, they are unable to provide TPWD with the location of those samples.
Region Population Estimate
Sampling from Fall 2002 to Present
Pineywoods
502,521
975
Gulf Prairie
90,664
441
Post Oak Savannah
291,119
1146
Black Land Prairies
54,505
153
Cross Timbers
441,031
1015
Edwards Plateau
1,608,390
1618
South Texas Plains
500,183
1253
Rolling Plains
231,358
352
High Plains
49,981
81
Trans Pecos
148,174
173
Unknown Location
1,896
Total
3,917,926
9,103
Samples Collected By
2002-03
2003-04
2004-Present
TPWD
1,722
2,955
2,540
Private (unknown location)
326
608
952
Total
2,048
3,563
3,492
Thank you,
Kevin Schwausch
Big Game Program Specialist
Texas Parks & Wildlife Department
PO Box 1394
Burnet, TX 78611
512-756-4476
===============================
I would like to thank Kevin and TPWD for there prompt reply with updated
data.
I am still concerned about the Texas, New Mexico border and New Mexico's
apparent lack of CWD testing updates. Makes one wonder about there CWD testing
program. NO report/reply back from New Mexico about there CWD testing update
yet. ...
TSS
===================
-------- Original Message --------
Subject: CWD SURVEILLANCE TEXAS UPDATE (kinda)
Date: Mon, 9 May 2005 14:52:48 –0500
From: "Terry S. Singeltary Sr."
Reply-To: Bovine Spongiform Encephalopathy
To: BSE-L@aegee.org
snip...see full text ;
Date: Thu, 28 Dec 2006 12:03:19 –0600
Reply-To: Sustainable Agriculture Network Discussion Group
Sender: Sustainable Agriculture Network Discussion Group
From: "Terry S. Singeltary Sr."
Subject: Fw: CWD in New Mexico 35 MILES FROM TEXAS BORDER and low testing
sampling figures -- what gives TAHC ???
2011 - 2012
Friday, October 28, 2011
CWD Herd Monitoring Program to be Enforced Jan. 2012 TEXAS
Greetings TAHC et al,
A kind greetings from Bacliff, Texas.
In reply to ;
Texas Animal Health Commission (TAHC) Announcement October 27, 2011
I kindly submit the following ;
Wednesday, June 13, 2012
TAHC Modifies Entry Requirements Effective Immediately for Cervids DUE TO
CWD
FOR IMMEDIATE RELEASE
Monday, March 26, 2012
Texas Prepares for Chronic Wasting Disease CWD Possibility in Far West
Texas
Monday, March 26, 2012
3 CASES OF CWD FOUND NEW MEXICO MULE DEER SEVERAL MILS FROM TEXAS BORDER
Saturday, June 09, 2012
USDA Establishes a Herd Certification Program for Chronic Wasting Disease
in the United States
Thursday, May 31, 2012
CHRONIC WASTING DISEASE CWD PRION2012 Aerosol, Inhalation transmission,
Scrapie, cats, species barrier, burial, and more
Tuesday, June 05, 2012
Captive Deer Breeding Legislation Overwhelmingly Defeated During 2012
Legislative Session
Monday, June 11, 2012
OHIO Captive deer escapees and non-reporting
CWD has been identified in free-ranging cervids in 15 US states and 2
Canadian provinces and in ≈ 100 captive herds in 15 states and provinces and in
South Korea (Figure 1, panel B).
SNIP...
Long-term effects of CWD on cervid populations and ecosystems remain
unclear as the disease continues to spread and prevalence increases. In captive
herds, CWD might persist at high levels and lead to complete herd destruction in
the absence of human culling. Epidemiologic modeling suggests the disease could
have severe effects on free-ranging deer populations, depending on hunting
policies and environmental persistence (8,9). CWD has been associated with large
decreases in free-ranging mule deer populations in an area of high CWD
prevalence (Boulder, Colorado, USA) (5).
PLEASE STUDY THIS MAP, COMPARE FARMED CWD TO WILD CWD...TSS
Saturday, February 18, 2012
Occurrence, Transmission, and Zoonotic Potential of Chronic Wasting Disease
CDC Volume 18, Number 3—March 2012
CWD has been identified in free-ranging cervids in 15 US states and 2
Canadian provinces and in ≈100 captive herds in 15 states and provinces and in
South Korea (Figure 1, panel B).
Thursday, February 09, 2012
50 GAME FARMS IN USA INFECTED WITH CHRONIC WASTING DISEASE
Tuesday, December 20, 2011
CHRONIC WASTING DISEASE CWD WISCONSIN Almond Deer (Buckhorn Flats) Farm
Update DECEMBER 2011
The CWD infection rate was nearly 80%, the highest ever in a North American
captive herd.
RECOMMENDATION: That the Board approve the purchase of 80 acres of land for
$465,000 for the Statewide Wildlife Habitat Program in Portage County and
approve the restrictions on public use of the site.
snip...see full text and much more here ;
Tuesday, December 20, 2011
CHRONIC WASTING DISEASE CWD WISCONSIN Almond Deer (Buckhorn Flats) Farm
Update DECEMBER 2011
Monday, June 25, 2012
US Department of Agriculture ends funding for chronic wasting disease
CWD
for all those game farmers that thought the USDA was the save all to the
cervid game farming and ranching with CWD, instead of the DNR. please see ;
CWD TEXAS TAHC OLD FILE HISTORY
updated from some of my old files. ...
Subject: CWD SURVEILLANCE STATISTICS TEXAS (total testing figures less
than 50 in two years)
Date: Sun, 25 Aug 2002 21:06:49 –0700
From: "Terry S. Singeltary Sr."
Reply-To: Bovine Spongiform Encephalopathy
To: BSE-L@uni-karlsruhe.de
######## Bovine Spongiform Encephalopathy #########
greetings list members,
here are some figures on CWD testing in TEXAS...TSS
Dear Dr. Singletary,
In Fiscal Year 2001, seven deer from Texas were tested by the National
Veterinary Services Laboratory (NVSL) for CWD (5 fallow deer and 2 white-tailed
deer). In Fiscal Year 2002, seven elk from Texas were tested at NVSL (no deer).
During these two years, an additional six elk and one white-tailed deer were
tested at the Texas Veterinary Medical Diagnostic Laboratory (TVMDL). In Fiscal
Year 2002, four white-tailed deer (free-ranging clinical suspects) and at least
eight other white-tailed deer have been tested at TVMDL. One elk has been tested
at NVSL. All of these animals have been found negative for CWD. Dr. Jerry Cooke
of the Texas Parks and Wildlife Department also has records of 601 clinically
ill white-tailed deer which were necropsied at Texas A&M during the late
1960's and early 1970's, and no spongiform encepalopathies were noted. Thank you
for your consideration.
xxxxxxx
Texas Animal Health Commission
(personal communication...TSS)
Austin 8 news
snip...
"There's about 4 million deer in the state of Texas, and as a resource I
think we need to be doing as much as we can to look for these diseases," said
Doug Humphreys with Texas Parks and Wildlife. "Right now Texas is clear. We
haven't found any, but that doesn't mean we don't look."
With approximately 4 million animals, Texas has the largest population of
white-tailed deer in the nation. In addition, about 19,000 white-tailed deer and
17,000 elk are being held in private facilities. To know if CWD is present in
captive herds, TPWD and Texas Animal Health Commission are working with breeders
to monitor their herds.
How is it spread?
It is not known exactly how CWD is spread. It is believed that the agent
responsible for the disease may be spread both directly (animal to animal
contact) and indirectly (soil or other surface to animal). It is thought that
the most common mode of transmission from an infected animal is via saliva,
feces, and urine.
some surveillance?
beyond the _potential_ methods of transmissions above, why, not a single
word of SRM of various TSE species in feed as a source?
it's a known fact they have been feeding the deer/elk the same stuff as
cows here in USA.
and the oral route has been documented of CWD to mule deer fawns in lab
studies.
not to say that other _potential_ transmission mechanisms are possible,
but why over look the obvious?
TSS
########### http://mailhost.rz.uni-karlsruhe.de/warc/bse-l.html
############
From: Ken Waldrup, DVM, PhD (host25-207.tahc.state.tx.us)
Subject: Re: CWD SAMPLING TEXAS (but NOT in the obvious place, the NM,
TEXAS border)
Date: December 15, 2003 at 3:43 pm PST
In Reply to: CWD SAMPLING TEXAS (but NOT in the obvious place, the NM,
TEXAS border) posted by TSS on December 12, 2003 at 2:15 pm:
Dear sirs: With regard to your comment about Texas NOT looking for CWD
along the New Mexico border, it is painfully obvious that you do not know or
understand the natural distribution of mule deer out there or the rights of the
land owners in this state. As of 15 December 2003, a total of 42 deer had been
sampled from what we call "Trans-Pecos", beyond the Pecos River. Mule deer are
very widely dispersed through this area, sometimes at densities of one animal
per 6 square miles. The Texas Parks and Wildlife Department does not have the
legal authority to trepass on private property to collect deer. Some landowners
are cooperative. Some are not. Franklin State Park is at the very tip of Texas,
and deer from the park have been tested (all negative). One of the single
largest land owners along the border is the National Park Service. Deer and elk
from the Guadalupe Peak National Park cannot be collected with federal
permission. The sampling throughout the state is based on the deer populations
by eco-region and is dictated by the availability of funds. I am concerned about
your insinuation that CWD is a human health risk. We are at a stand-off - you
have no proof that it is and I have no definitive proof that it isn't. However I
would say that the inferred evidence from Colorado, Wyoming and Wisconsin
suggests that CWD is not a human health concern (i.e. no evidence of an
increased incidence of human brain disorders within the CWD "endemic" areas of
these states). From my professional interactions with the Texas Parks and
Wildlife Department, I can definitely say that they want to do a thorough and
sound survey throughout the state, not willy-nilly "look here, look there".
There are limitations of manpower, finances and, in some places, deer
populations. I would congratulate TPWD for doing the best job with the
limitations at hand rather than trying to browbeat them when you obviously do
not understand the ecology of West Texas. Thank you for your consideration.
======================
From: TSS (216-119-139-126.ipset19.wt.net)
Subject: Re: CWD SAMPLING TEXAS (but NOT in the obvious place, the NM,
TEXAS border)
Date: December 16, 2003 at 11:03 am PST
In Reply to: Re: CWD SAMPLING TEXAS (but NOT in the obvious place, the NM,
TEXAS border) posted by Ken Waldrup, DVM, PhD on December 15, 2003 at 3:43
pm:
HEllo Dr. Waldrup,
thank you for your comments and time to come to this board.
Ken Waldrup, DVM, PhD states;
> it is painfully obvious that you do not know or understand the natural
distribution of mule deer out there or the rights of the land owners in this
state...
TSS states;
I am concerned about all deer/elk not just mule deer, and the rights of
land owners (in the case with human/animal TSEs) well i am not sure of the
correct terminology, but when the States deer/elk/cattle/sheep/humans are at
risk, there should be no rights for land owners in this case. the state should
have the right to test those animals. there are too many folks out there that
are just plain ignorant about this agent. with an agent such as this, you cannot
let landowners (and i am one) dictate human/animal health, especially when you
cannot regulate the movement of such animals...
Ken Waldrup, DVM, PhD states;
> Deer and elk from the Guadalupe Peak National Park cannot be collected
with federal permission.
TSS states;
I do not understand this? so there is no recourse of action even if every
deer/elk was contaminated with CWD in this area (hypothetical)?
Ken Waldrup, DVM, PhD states;
> I am concerned about your insinuation that CWD is a human health risk.
We are at a stand-off - you have no proof that it is and I have no definitive
proof that it isn't. However I would say that the inferred evidence from
Colorado, Wyoming and Wisconsin suggests that CWD is not a human health concern
(i.e. no evidence of an increased incidence of human brain disorders within the
CWD "endemic" areas of these states)...
TSS states;
indeed i am concerned as well with your insinuation about CWD not being a
human health risk. NO, we are not at a standoff, i just think you are wrong in
insinuating this when you have absolutely no proof, BUT, CWD does transmit to
primate, and there have never been tranmission studies done on man (that's my
proof). SO, hypothetically there is more proof that CWD has the potential to
infect man than there is proof that it cannot. this should mean something, and
in my opinion warrant some sort of public concern. BUT the only concern seems to
be with the Industries involved, not for human/animal health. and you have this
study;
The EMBO Journal, Vol. 19, No. 17 pp. 4425-4430, 2000 © European Molecular
Biology Organization
Evidence of a molecular barrier limiting susceptibility of humans, cattle
and sheep to chronic wasting disease
G.J. Raymond1, A. Bossers2, L.D. Raymond1, K.I. O?Rourke3, L.E. McHolland4,
P.K. Bryant III4, M.W. Miller5, E.S. Williams6, M. Smits2 and B.
Caughey1,7
1NIAID/NIH Rocky Mountain Laboratories, Hamilton, MT 59840, 3USDA/ARS/ADRU,
Pullman, WA 99164-7030, 4USDA/ARS/ABADRL, Laramie, WY 82071, 5Colorado Division
of Wildlife, Wildlife Research Center, Fort Collins, CO 80526-2097, 6Department
of Veterinary Sciences, University of Wyoming, Laramie, WY 82070, USA and
2ID-Lelystad, Institute for Animal Science and Health, Lelystad, The Netherlands
7Corresponding author e-mail: bcaughey@nih.gov Received June 7, 2000; revised
July 3, 2000; accepted July 5, 2000.
snip...
Clearly, it is premature to draw firm conclusions about CWD passing
naturally into humans, cattle and sheep, but the present results suggest that
CWD transmissions to humans would be as limited by PrP incompatibility as
transmissions of BSE or sheep scrapie to humans. Although there is no evidence
that sheep scrapie has affected humans, it is likely that BSE has caused variant
CJD in 74 people (definite and probable variant CJD cases to date according to
the UK CJD Surveillance Unit). Given the presumably large number of people
exposed to BSE infectivity, the susceptibility of humans may still be very low
compared with cattle, which would be consistent with the relatively inefficient
conversion of human PrP-sen by PrPBSE. Nonetheless, since humans have apparently
been infected by BSE, it would seem prudent to take reasonable measures to limit
exposure of humans (as well as sheep and cattle) to CWD infectivity as has been
recommended for other animal TSEs.
snip...
Ken Waldrup, DVM, PhD states;
> However I would say that the inferred evidence from Colorado, Wyoming
and Wisconsin suggests that CWD is not a human health concern (i.e. no evidence
of an increased incidence of human brain disorders within the CWD "endemic"
areas of these states)...
TSS states;
I disagree with this on several fronts as well. for one thing there is no
CJD surveillance to speak of, and there have been an increase of CJD in the USA
in the young. some of these unfortunate folks have consumed deer and elk and
been avid hunters. what will cwdCJD look like? could it look like sporadic CJD?
(please see below)
The active surveillance study of 1996, however, only looked at cases in
which physicians attributed the deaths to CJD. Misdiagnosed patients or patients
who never saw a neurologist were not tabulated thus CJD may be grossly
underreported. Many neurological ailments share symptoms, especially early on.
According to various studies, autopsies have found that CJD is misdiagnosed as
other ills, such as dementia or Alzheimer's disease, 5 to 13 percent of the
time. The CDC finds that around 50,000 Americans die from Alzheimer's each year
228 CHAPTER 14 (about 4 million have the disease, according to the Alzheimer's
Association). Therefore, one could argue that thousands of CJD cases are being
missed. (On the flip side, CJD could be mistakenly diagnosed as Alzheimer's
disease or dementia, but the number of CJD patients is so small that they
wouldn't dramatically skew the statistics for other neurological ills.) In part
to address the issue of misdiagnosis, CJD families have asked the CDC to place
the disease on the national list of officially notifiable illnesses, which tends
to include more contagious conditions such as AIDS, tuberculosis, hepatitis, and
viral forms of encephalitis. Currently, only some states impose this
requirement. CDC officials have discounted the utility of such an approach,
arguing that it would duplicate the mortality data, which is more accurate than
early diag- noses of CJD, anyway. Moreover, mandatory reporting of CJD cases
does not necessarily guarantee the end to missed cases.8 One clue suggests that
the passive system is undercounting CJD in the U.S.: racial difference. The
number of black CJD victims is about 38 percent that of white victims. Rather
than sporadic CJD being a one- in-a-million lottery, it's more like
one-in-2.5-million for African- Americans. Access to medical care might be one
reason. Schonberger recounted that the CDC had asked other countries with
substantial black populations to submit CJD figures for comparison but found
that the surveillance in those countries was inadequate. "We haven't been able
to find any comparable literature on this issue, so it's still up in the air,"
Schonberger said. On the other hand, Alzheimer's disease is more common among
black people than whites, with an estimated higher prevalence ranging from 14
percent to almost 100 percent, according to a February 2002 report by the
Alzheimer's Association. Are some black CJD cases being misdiagnosed as
Alzheimer's? Answering critics like Terry Singeltary, who feels that the U.S.
under- counts CJD, Schonberger conceded that the current surveillance system has
errors but stated that most of the errors will be confined to the older
population. As Schonberger pointed out, no doctor would misdiagnose a
30-year-old CJD patient as having Alzheimer's. The average age of the first 100
variant CJD victims was 29; should the epidemiology of vCJD changeif older
people start coming down with itthen there would be problems. "The adequacy of
our overall CJD surveillance would be Laying Odds 229 greatly reduced should the
proportion of older individuals affected by variant CJD substantially increase,"
Schonberger explained.9 To date, only brain autopsies can confirm CJD. To
encourage the necessary neuropathological studies, in 1997 the CDC helped
establish the National Prion Disease Pathology Surveillance Center at Case
Western Reserve University, under the directorship of Pierluigi Gambetti. But
the number of brains examined has fallen far short of the number of CJD cases in
the U.S.: Gambetti's lab, which receives brains based on referrals from local
physicians and families, looked at only 99 sporadic CJD cases in 2000 and 138 in
2001, when about 300 each year are expected. "I'm very unhappy with the
numbers," Gambetti lamented. "European countries see 100 or 90 percent of all
the cases suspected. We see 30 to 40 percent."10 Most families don't think about
having an autopsy done (which can cost upward of $1,500 if the hospitals don't
pick up the tab), and mem- bers of the support group CJD Voice have said they
were too distraught to think of shipping a loved one's brain by Federal Express
to Gambetti's lab. (For accurate analyses of brain tissue, the autopsy must be
performed within 72 hours of death, assuming the body has been kept
refrigerated.) Moreover, physicians often do not suggest an autopsy, perhaps
because of liability fears should the postmortem reveal that the original
diagnosis was wrong. Gambetti has been work- ing on establishing a network that
would enable postmortems to be done near where the deceased person lived and
without cost to the family. He is also working on advertising the existence of
his surveil- lance center, via meetings and letters to neurologists,
pathologists, and other specialists. Gambetti is also attempting to combat what
he termed "hysteria" over the potential for infection that has pathologists
irrationally shunning CJD cases while they willingly conduct arguably riskier
AIDS autopsies. "In order to make people aware, you have to keep informing them
over and over and over," he said. Money is the main reason why the U.S. lags
behind Europe in terms of surveillance. To adequately survey the 290 U.S.
million residents, "you need a lot of money," Robert Will explained. "There was
a CJD meeting of families in America in which poor old Larry {Schonberger] got
attacked fairly vigorously because there wasn't proper surveillance. You could
only do proper surveillance if you have adequate resources. 230 CHAPTER 14
That's the bottom line. We're very fortunate in the U.K.; we have very generous
resources for CJD surveillance." Moreover, the U.K. makes feline spongifbrm
encephalopathy an offi- cially notifiable disease. Domestic cats proved to be
good sentinel ani- mals because they dine on the meat not fit for human
consumption the parts more likely to harbor prion infectivity. In the U.S., FSE
isn't federally notifiable. And while the USDA says it has sent educational
material to private veterinarians and works with vet schools,21 it's not clear
just how many vets can spot FSE, which has never been reported in the U.S.
Certainly, not many cat postmortems are done.
The only active portion of the U.S. CJD surveillance system are the
follow-up investigations conducted for victims of CJD under 55 years of age. It
began in 1996, when young people in the U.K. started succumb- ing to variant
CJD. Victims under 30 years of age especially arouse interest, because such
cases could indicate an infection from the envi- ronment. Except for the variant
CJD case in Florida, the CDC has clas- sified all of these more youthful cases
of CJD as having either sporadic or familial origins. One such age cluster
involved the three venison eaters that the CDC tried unsuccessfully to link to
the deer-and-elk borne chronic wasting disease.
A second grouping occurred in 2002 in a pair of Michigan men. The twoone
26 years old, the other 28 did not know each other but lived in neighboring
counties in Michigan and went to the same hospi- tal for diagnosis.12 The CDC's
investigation turned up nothing that suggested a new form of CJD had emerged.
But the increased frequency of young CJD cases is disturbing. In the 18-year
period between 1979 and 1996, the U.S. had 12 cases in patients under 30, and
only one of them had the sporadic form of CJD. (The other cases resulted from
heredity or from transmission via contami- nated growth hormone or dura mater
grafts.13) Between 1997 and 2001, five people under 30 died of sporadic CJD: the
three venison eaters and the two Michigan patients. That represents a
substantial blip of five young cases in five years, as opposed to only one case
in 18 years. Physicians at the University of Michigan Health System who examined
the two Michigan men concluded: As a result of our findings, we feel that
sporadic CJD may be more common than previously thought, that it may occur in
younger indi- Laying Odds 231 viduals than currently perceived, and that some
cases may go undiag- nosed due to insufficient testing. . . . We recommend that
physicians everywhere begin to consider CJD in rapidly progressive neurological
decline of unknown causes in people under 30 years of age, and that brain biopsy
and autopsy with genetic and prion analysis be performed in all such cases.14
Pathologically, the recent bout of young casualties in the U.S. appears to be no
different from CJD already seen in America. Yet theoretically it may have come
from a new source of infection, based on an unex- pected result announced in
late November 2002. John Collinge of the British Medical Research Council's
Prion Unit found that not all trans- genic mice infected with BSE prions
developed the neuropathological and molecular characteristics of variant CJD;
some of the mice instead generated the molecular features of sporadic CJD.
Therefore, some CJD cases classified as sporadic may have actually been caused
by BSE prions, Collinge hypothesized.15 So far, the epidemiology of CJD in the
U.K. does not bear out that suppositionthere has been no substantial uptick in
sporadic CJD as would be expected if BSE could paint more than one pathological
picture. But the preliminary study, taken at face value, could be seen as
evidence that something infectious is happening in the cases of young, sporadic
CJD victims in the U.S. Another mouse study, reported in March 2002, fueled
concern that prion infections may be more common than previously thought.16
Stanley Prusiner's lab found that mice infected with mouse prions accu- mulated
PrPSc in their skeletal muscles, mostly in those in the hind limbs. In some
mice, each gram of muscle contained some 10 million infectious doseson par with
that in the brain in other experiments involving intracerebral inoculation. To
some CJD researchers, this find- ing suggested that muscle meat from cows might
not be safe, after all, and that the measures taken in Europe to protect the
food supply banning high-risk cow partsmay not be enough. Although this study
may seem alarming, its implications are not as sweeping as they may appear. Only
a minority of results in mouse stud- ies end up having a direct analog in
humans. The skeletal muscle discov- ery warrants further examination, but it
would be premature to alter food policies. Prions are different for each
species, and accumulation of prions varies from species to species and from
disease to disease. Furthermore, BSE cattle muscle has failed to sicken mice in
bioassay 232 CHAPTER 14 work, suggesting that little or no infectious prions
lurk there. What such findings truly reveal is that prion diseases are
complicated and still mysterious, and trying to quantify the risks for human
health is fraught with uncertainties...
snip...284 pages... The Pathological Protein: Mad Cow, Chronic Wasting, and
Other Deadly Prion Diseases, Philip Yam Philip Yam News Editor Scientific
American www.sciam.com
CJD screening may miss thousands of cases
By Steve Mitchell UPI Medical Correspondent Published 7/21/2003 3:00 PM
View printer-friendly version
WASHINGTON, July 21 (UPI) -- The federal government's monitoring system for
cases of Creutzfeldt-Jakob disease, a fatal human brain illness, could be
missing tens of thousands of victims, scientists and consumer advocates have
told United Press International.
Creutzfeldt-Jakob disease or CJD can be caused by eating beef contaminated
with mad cow disease, but the critics assert without a better tracking system it
might be impossible to determine whether any CJD cases are due to mad cow or
obtain an accurate picture of the prevalence of the disorder in the United
States.
Beginning in the late 1990s, more than 100 people contracted CJD in the
United Kingdom and several European countries after eating beef infected with
bovine spongiform encephalopathy -- the clinical name for mad cow disease.
No case of mad cow has ever been detected in U.S. cattle and the Centers
for Disease Control and Prevention's monitoring system has never detected a case
of CJD due to eating contaminated American beef. Nevertheless, critics say, the
CDC's system misses many cases of the disease, which currently is untreatable
and is always fatal.
The first symptoms of CJD typically include memory loss and difficulty
keeping balance and walking. As the disease destroys the brain, patients rapidly
progress in a matter of months to difficulty with movement, an inability to talk
and swallow and, finally, death.
Spontaneously-occurring or sporadic CJD is a rare disorder. Only about 300
cases appear nationwide each year, but several studies have suggested the
disorder might be more common than thought and as many as tens of thousands of
cases might be going unrecognized.
Clusters of CJD have been reported in various areas of the United States --
Pennsylvania in 1993, Florida in 1994, Oregon in 1996, New York in 1999-2000 and
Texas in 1996. In addition, several people in New Jersey developed CJD in recent
years, including a 56 year old woman who died on May 31, 2003. Although in some
instances, a mad cow link was suspected, all of the cases ultimately were
classified as sporadic.
People who develop CJD from eating mad-cow-contaminated beef have been
thought to develop a specific form of the disorder called variant CJD. But new
research, released last December, indicates the mad cow pathogen can cause both
sporadic CJD and the variant form.
"Now people are beginning to realize that because something looks like
sporadic CJD they can't necessarily conclude that it's not linked to (mad cow
disease)," said Laura Manuelidis, section chief of surgery in the neuropathology
department at Yale University, who conducted a 1989 study that found 13 percent
of Alzheimer's patients actually had CJD.
Several studies, including Manuelidis', have found that autopsies reveal 3
percent to 13 percent of patients diagnosed with Alzheimer's or dementia
actually suffered from CJD. Those numbers might sound low, but there are 4
million Alzheimer's cases and hundreds of thousands of dementia cases in the
United States. A small percentage of those cases could add up to 120,000 or more
CJD victims going undetected and not included in official statistics.
Experiences in England and Switzerland -- two countries that discovered mad
cow disease in their cattle -- have heightened concerns about the possibility
some cases of sporadic CJD are due to consuming mad-cow-tainted beef. Both
countries have reported increases in sporadic CJD since mad cow was first
detected in British herds in 1986.
Switzerland discovered last year its CJD rate was twice that of any other
country in the world. Switzerland had been seeing about eight to 11 cases per
year from 1997 to 2000. Then the incidence more than doubled, to 19 cases in
2001 and 18 cases in 2002.
The CDC says the annual rate of CJD in the United States is one case per
million people, but the above studies suggest the true prevalence of CJD is not
known, Manuelidis told UPI.
Diagnosing CJD or Alzheimer's is difficult because no test exists that can
identify either disease in a living patient with certainty. So physicians must
rely on the patient's symptoms to determine which illness might be present.
Sometimes, however, the symptoms of one disease can appear similar to the other
disorder. The only way to determine the disease conclusively is to perform an
autopsy on the brain after death.
Unfortunately, although autopsies once were performed on approximately half
of all corpses, the frequency has dropped to 15 percent or less in the United
States. The National Center for Health Statistics -- a branch of the CDC --
stopped collecting autopsy data in 1995.
"If we don't do autopsies and we don't look at people's brains ... we have
no idea about what is the general prevalence of these kinds of infections and
(whether) it is changing," Manuelidis said.
At the same time autopsies have been declining, the number of deaths
attributed to Alzheimer's has increased more than 50-fold since 1979, going from
857 deaths then to nearly 50,000 in 2000. Though it is unlikely the dramatic
increase in Alzheimer's is due entirely to misdiagnosed CJD cases, it "could
explain some of the increase we've seen," Manuelidis said.
"Neurodegenerative disease and Alzheimer's disease have become a
wastebasket" for mental illness in the elderly that is difficult to diagnose
conclusively, she said. "In other words, what people call Alzheimer's now is
more broad than what people used to call it, and that has the possibility of
encompassing more diseases -- including CJD."
The autopsy studies that found undiagnosed CJD cases raise the question of
whether the United States "already has an undetected epidemic here," Jeff
Nelson, director of vegsource.com, a vegetarian advocacy Web site, told
UPI.
"What's the source of that?" Nelson asked. "Could it be the same source of
encephalitis we saw in minks?"
Nelson referred to an outbreak of a mad-cow-type disorder in minks in
Wisconsin in the 1980s. The origin was traced back to the animals' diet, which
included parts of so-called downer cattle -- sick cows that are unable to stand,
which often indicates a neurological disease, including mad cow. The mink
disease raised concerns about whether U.S. cattle were carrying a mad-cow-like
pathogen even prior to the U.K. epidemic that began in 1986.
Andrew Monjan, chief of the neuropsychology of aging program at the
National Institute of Aging -- part of the National Institutes of Health in
Bethesda, Md. -- acknowledged there has been an increase in U.S. Alzheimer's
cases. However, he told UPI, this probably is due to the aging of the population
-- as people grow older, they develop a higher risk of developing
Alzheimer's.
"There's been no change in the number of CJD cases in the country and there
has been clearly a tracking of the unusual cases of CJD" that could be due to
mad cow disease, Monjan said. However, Terry Singletary, coordinator of CJD
Watch -- an organization founded to track CJD cases -- says efforts to track the
disease have been close to nonexistent. For example, only 12 states require such
reports. Therefore, many cases might be going undetected, unreported or
misdiagnosed.
If more states made CJD a reportable illness, there would be more clusters
detected across the United States, said Singletary, who became involved with CJD
advocacy after his mother died from a form of CJD known as Heidenhain variant.
In the 18-year period between 1979 and 1996, he noted, the country saw a jump
from one case of sporadic CJD in people under the age of 30 -- a warning sign
for a link to mad cow because nearly all of the U.K. victims were 30 years of
age or younger -- to five cases in five years between 1997 and 2001. "That
represents a substantial blip," he told UPI.
Singletary also said there have been increases in sporadic CJD in France,
Germany and Italy, all of which have detected mad cow disease in their
cattle.
So far, the CDC has refused to impose a national requirement that
physicians and hospitals report cases of the disease. The agency has not chosen
to make CJD a reportable disease because "making it reportable is not
necessarily directly helpful in surveillance because in some states where it's
reportable you may not get the physician to report it," said Dr. Ermias Belay,
CDC's medical epidemiologist working on CJD.
Instead, the agency relies on other methods, including death certificates
and urging physicians to send suspicious cases to the National Prion Disease
Pathology Surveillance Center at Case Western Reserve University in Cleveland,
which is funded by the CDC. However, because autopsies generally are not done,
if a CJD case is misdiagnosed as Alzheimer's or dementia, a correct diagnosis
might never be determined and therefore the cause of death listed on a death
certificate might be inaccurate.
Belay told UPI he discounted this possibility. It is unlikely to happen, he
said, because it is easy to distinguish CJD from Alzheimer's -- the two
conditions display different symptoms.
Manuelidis disagreed. It can be quite difficult to determine accurately if
a patient has CJD, as evidenced by her study, in which respected and competent
neurologists and psychiatrists at Yale originally diagnosed patients with
Alzheimer's, yet were wrong at least 13 percent of the time. Another study
conducted at the University of Pennsylvania, which found 6 percent of dementia
patients actually were suffering from CJD, supports the difficulty in
distinguishing the illnesses correctly.
The U. Penn. researchers concluded: "These results show that in patients
with a clinical diagnosis of dementia, the etiology (cause) cannot be accurately
predicted during life."
In addition, the NPDPSC sees less than half of all the CJD cases each year,
so the CDC's investigational system not only is missing many of the misdiagnosed
CJD cases, it also is not conducting autopsies on most of the detected
cases.
Belay said the CDC follows up on all cases of CJD that occur in people
under age 55, as these could be linked to variant -- mad-cow-related -- CJD. But
so far, all have turned out to be sporadic forms of the disease. About 30 cases
of the disorder occur each year in the United States in this age group, while
the remaining 270 or so are older.
The case of Carrie Mahan -- a Philadelphia woman who developed a brain
disorder that appeared to be CJD and died from it in 2000 at the age of 29 --
illustrates just how difficult it can be to diagnose the disease.
Mahan's physician, Dr. Peter Crinos of the University of Pennsylvania
Medical Center, ruled out other disorders and felt certain the young woman had
died of CJD, a concern that raised the possibility of a link to mad cow disease
because of her young age. When neuropathologist Nicholas Gonatas, who had seen
CJD before, examined Mahan's brain after her death, he, likewise, was confident
he detected the microscopic, sponge-like holes caused by the disease. But when
he sent brain samples to the NPDPSC, the results came back negative. Gonatas,
convinced the surveillance center's finding was erroneous, sent off two more
samples, only to have them both come back negative.
Subsequent research, however, has shown the test used by the surveillance
center cannot rule out CJD, said Crinos, an assistant professor of
neurology.
"There's no question that Carrie had a spongiform encephalopathy," Crinos
said, but added although it appeared to be CJD, it is difficult if not
impossible to say if it was due to mad cow disease.
Crinos told UPI until the CDC implements a better tracking system, a lot of
questions will remain about CJD and cases like Carrie Mahan's. One central
question: Why are cases of what is presumed to be a rare disease popping up in
clusters in certain areas of the country? Crinos said the clustering suggests an
environmental or food-borne cause, but so far, "No one knows the answer to
that."
Copyright © 2001-2003 United Press International
One reason for this was the _inaccuracy_ in coding of cases correctly
certified as CJD Coding is carried out by staff who are not medically qualified
and it is not surprising that coding errors occur in the processing of large
numbers of certificates. In 1982, 12,000 certificates per week were processed at
the office of population censuses and surveys bu 15 coders and 6 checkers
(Alderson et al., 1983). The occurrence of both inter- and intra-observer coding
errors has been described (Curb et al., 1983) and the _inaccuracies_ of BOTH
certification and coding discovered in this study _support_ the introduction of
a more accurate system of death certificates and a more detailed and specific
coding system...
snip...
AS implied in the Inset 25 we must not _ASSUME_ that transmission of BSE to
other species will invariably present pathology typical of a scrapie-like
disease.
snip...
Ken Waldrup, DVM, PhD states;
> and is dictated by the availability of funds.
snip...
> From my professional interactions with the Texas Parks and Wildlife
Department, I can definitely say that they want to do a thorough and sound
survey throughout the state, not willy-nilly "look here, look there". There are
limitations of manpower, finances and, in some places, deer populations. I would
congratulate TPWD for doing the best job with the limitations at hand...
TSS states;
I would concur here, and congradulate them as well. BUT, it is not enough.
we must do massive testing and thorough testing in all geographical locations.
IF the USA has 270 BILLION to rebuild Iraq, it would seem that we could find
enough money to fend off a disease that theoretically could wipe out the deer,
elk, cattle, and sheep populations if continued to be ignored, not to speak of
what it could do to humans in the long haul, through various proven routes and
sources...
Ken Waldrup, DVM, PhD states;
> rather than trying to browbeat them when you obviously do not
understand the ecology of West Texas.
TSS states;
I am not browbeating anyone, or no intention, just trying to keep the fire
lit here Sir, and this I must do. I think I know more of what I speak of than
you seem to be aware of. I am very concerned with the minimal amount of money
and time and effort being spent in TEXAS on CWD, especially with the real threat
of sub-clinical CWD/TSE infections and especially with cattle, but that's a no
no.
again, thank you for your comments, they are very much appreciated.
kind regards, Terry
=================
Tuesday, June 26, 2012
Creutzfeldt Jakob Disease Human TSE report update North America, Canada,
Mexico, and USDA PRION UNIT as of May 18, 2012
type determination pending Creutzfeldt Jakob Disease (tdpCJD), is on the
rise in Canada and the USA
SEE STEADY INCREASE OF SPORADIC CJD IN THE U.K. TO 2011, from 28 in 1990,
to 90 cases in 2011, the highest number to date in any given year, for sporadic
CJD. remember, sporadic CJD is not a single strain, but many strains of unknown,
undocumented origin, to date. ...TSS
*** Spraker suggested an interesting explanation for the occurrence of CWD.
The deer pens at the Foot Hills Campus were built some 30-40 years ago by a Dr.
Bob Davis. At or abut that time, allegedly, some scrapie work was conducted at
this site. When deer were introduced to the pens they occupied ground that had
previously been occupied by sheep.
(PLEASE NOTE SOME OF THESE OLD UK GOVERNMENT FILE URLS ARE SLOW TO OPEN,
AND SOMETIMES YOU MAY HAVE TO CLICK ON MULTIPLE TIMES, PLEASE BE PATIENT, ANY
PROBLEMS PLEASE WRITE ME PRIVATELY, AND I WILL TRY AND FIX OR SEND YOU OLD PDF
FILE...TSS)
CJD9/10022
October 1994
Mr R.N. Elmhirst Chairman British Deer Farmers Association Holly Lodge
Spencers Lane BerksWell Coventry CV7 7BZ
Dear Mr Elmhirst,
CREUTZFELDT-JAKOB DISEASE (CJD) SURVEILLANCE UNIT REPORT
Thank you for your recent letter concerning the publication of the third
annual report from the CJD Surveillance Unit. I am sorry that you are
dissatisfied with the way in which this report was published.
The Surveillance Unit is a completely independant outside body and the
Department of Health is committed to publishing their reports as soon as they
become available. In the circumstances it is not the practice to circulate the
report for comment since the findings of the report would not be amended. In
future we can ensure that the British Deer Farmers Association receives a copy
of the report in advance of publication.
The Chief Medical Officer has undertaken to keep the public fully informed
of the results of any research in respect of CJD. This report was entirely the
work of the unit and was produced completely independantly of the the
Department.
The statistical results reqarding the consumption of venison was put into
perspective in the body of the report and was not mentioned at all in the press
release. Media attention regarding this report was low key but gave a realistic
presentation of the statistical findings of the Unit. This approach to
publication was successful in that consumption of venison was highlighted only
once by the media ie. in the News at one television proqramme.
I believe that a further statement about the report, or indeed statistical
links between CJD and consumption of venison, would increase, and quite possibly
give damaging credence, to the whole issue. From the low key media reports of
which I am aware it seems unlikely that venison consumption will suffer
adversely, if at all.
http://web.archive.org/web/20030511010117/http://www.bseinquiry.gov.uk/files/yb/1994/10/00003001.pdf
PLUS, THE CDC DID NOT PUT THIS WARNING OUT FOR THE WELL BEING OF THE DEER
AND ELK ;
Thursday, May 26, 2011
Travel History, Hunting, and Venison Consumption Related to Prion Disease
Exposure, 2006-2007 FoodNet Population Survey
Journal of the American Dietetic Association Volume 111, Issue 6 , Pages
858-863, June 2011.
NOR IS THE FDA recalling this CWD positive elk meat for the well being of
the dead elk ;
Wednesday, March 18, 2009
Noah's Ark Holding, LLC, Dawson, MN RECALL Elk products contain meat
derived from an elk confirmed to have CWD NV, CA, TX, CO, NY, UT, FL, OK RECALLS
AND FIELD CORRECTIONS: FOODS CLASS II
Thursday, May 26, 2011
Travel History, Hunting, and Venison Consumption Related to Prion Disease
Exposure, 2006-2007 FoodNet Population Survey Journal of the American Dietetic
Association Volume 111, Issue 6 , Pages 858-863, June 2011.
Travel History, Hunting, and Venison Consumption Related to Prion Disease
Exposure, 2006-2007 FoodNet Population Survey
Joseph Y. Abrams, MPH, Ryan A. Maddox, MPH , Alexis R. Harvey, MPH ,
Lawrence B. Schonberger, MD , Ermias D. Belay, MD
Accepted 15 November 2010. Abstract Full Text PDF References .
Abstract
The transmission of bovine spongiform encephalopathy (BSE) to human beings
and the spread of chronic wasting disease (CWD) among cervids have prompted
concerns about zoonotic transmission of prion diseases. Travel to the United
Kingdom and other European countries, hunting for deer or elk, and venison
consumption could result in the exposure of US residents to the agents that
cause BSE and CWD. The Foodborne Diseases Active Surveillance Network 2006-2007
population survey was used to assess the prevalence of these behaviors among
residents of 10 catchment areas across the United States. Of 17,372 survey
respondents, 19.4% reported travel to the United Kingdom since 1980, and 29.5%
reported travel to any of the nine European countries considered to be
BSE-endemic since 1980. The proportion of respondents who had ever hunted deer
or elk was 18.5%, and 1.2% had hunted deer or elk in a CWD–endemic area. More
than two thirds (67.4%) reported having ever eaten deer or elk meat. Respondents
who traveled spent more time in the United Kingdom (median 14 days) than in any
other BSE-endemic country. Of the 11,635 respondents who had consumed venison,
59.8% ate venison at most one to two times during their year of highest
consumption, and 88.6% had obtained all of their meat from the wild. The survey
results were useful in determining the prevalence and frequency of behaviors
that could be important factors for foodborne prion transmission.
"These findings indicate that a high percentage of the United States
population engages in hunting and/or venison consumption. If CWD continues to
spread to more areas across the country, a substantial number of people could
potentially be exposed to the infectious agent."
Potential Venison Exposure Among FoodNet Population Survey Respondents,
2006-2007
Ryan A. Maddox1*, Joseph Y. Abrams1, Robert C. Holman1, Lawrence B.
Schonberger1, Ermias D. Belay1 Division of Viral and Rickettsial Diseases,
National Center for Zoonotic, Vector-Borne, and Enteric Diseases, Centers for
Disease Control and Prevention, Atlanta, GA *Corresponding author e-mail:
rmaddox@cdc.gov
The foodborne transmission of bovine spongiform encephalopathy to humans,
resulting in variant Creutzfeldt-Jakob disease, indicates that humans can be
susceptible to animal prion diseases. However, it is not known whether foodborne
exposure to the agent causing chronic wasting disease (CWD) in cervids can cause
human disease. The United States Foodborne Diseases Active Surveillance Network
(FoodNet) conducts surveillance for foodborne diseases through an extensive
survey administered to respondents in selected states. To describe the frequency
of deer and elk hunting and venison consumption, five questions were included in
the 2006-2007 FoodNet survey. This survey included 17,372 respondents in ten
states: California, Colorado, Connecticut, Georgia, Maryland, Minnesota, New
Mexico, New York, Oregon, and Tennessee. Of these respondents, 3,220 (18.5%)
reported ever hunting deer or elk, with 217 (1.3%) reporting hunting in a
CWD-endemic area (northeastern Colorado, southeastern Wyoming, and southwestern
Nebraska). Of the 217 CWD-endemic area hunters, 74 (34.1%) were residents of
Colorado. Respondents reporting hunting were significantly more likely to be
male than female (prevalence ratio: 3.3, 95% confidence interval: 3.1-3.6) and,
in general, older respondents were significantly more likely to report hunting
than younger respondents. Venison consumption was reported by more than half
(67.4%) of the study population, and most venison consumers (94.1%) reported
that at least half of their venison came from the wild. However, more than half
(59.1%) of the consumers reported eating venison only one to five times in their
life or only once or twice a year. These findings indicate that a high
percentage of the United States population engages in hunting and/or venison
consumption. If CWD continues to spread to more areas across the country, a
substantial number of people could potentially be exposed to the infectious
agent.
now, let’s see what the authors said about this casual link, personal
communications years ago. see where it is stated NO STRONG evidence. so, does
this mean there IS casual evidence ????
“Our conclusion stating that we found no strong evidence of CWD
transmission to humans”
From: TSS (216-119-163-189.ipset45.wt.net)
Subject: CWD aka MAD DEER/ELK TO HUMANS ???
Date: September 30, 2002 at 7:06 am PST
From: "Belay, Ermias"
To:
Cc: "Race, Richard (NIH)" ; ; "Belay, Ermias"
Sent: Monday, September 30, 2002 9:22 AM
Subject: RE: TO CDC AND NIH - PUB MED- 3 MORE DEATHS - CWD - YOUNG HUNTERS
Dear Sir/Madam,
In the Archives of Neurology you quoted (the abstract of which was attached
to your email), we did not say CWD in humans will present like variant CJD.
That assumption would be wrong. I encourage you to read the whole article
and call me if you have questions or need more clarification (phone:
404-639-3091). Also, we do not claim that "no-one has ever been infected with
prion disease from eating venison." Our conclusion stating that we found no
strong evidence of CWD transmission to humans in the article you quoted or in
any other forum is limited to the patients we investigated.
Ermias Belay, M.D. Centers for Disease Control and Prevention
-----Original Message-----
From:
Sent: Sunday, September 29, 2002 10:15 AM
To: rr26k@nih.gov; rrace@niaid.nih.gov; ebb8@CDC.GOV
Subject: TO CDC AND NIH - PUB MED- 3 MORE DEATHS - CWD - YOUNG HUNTERS
Sunday, November 10, 2002 6:26 PM ......snip........end..............TSS
Thursday, April 03, 2008
A prion disease of cervids: Chronic wasting disease
2008 1: Vet Res. 2008 Apr 3;39(4):41
A prion disease of cervids: Chronic wasting disease
Sigurdson CJ.
snip...
*** twenty-seven CJD patients who regularly consumed venison were reported
to the Surveillance Center***,
snip...
full text ;
Monday, November 14, 2011
WYOMING Creutzfeldt Jakob Disease, CWD, TSE, PRION REPORTING 2011
Wednesday, November 16, 2011
Wisconsin Creutzfeldt Jakob Disease, CWD, TSE, PRION REPORTING 2011
Sunday, November 13, 2011
COLORADO CWD CJD TSE PRION REPORTING 2011
Monday, May 23, 2011 CDC
Assesses Potential Human Exposure to Prion Diseases Travel Warning
Public release date: 23-May-2011
Contact: Francesca Costanzo adajmedia@elsevier.com 215-239-3249 Elsevier
Health Sciences
CDC assesses potential human exposure to prion diseases Study results
reported in the Journal of the American Dietetic Association Philadelphia, PA,
May 23, 2011 – Researchers from the Centers for Disease Control and Prevention
(CDC) have examined the potential for human exposure to prion diseases, looking
at hunting, venison consumption, and travel to areas in which prion diseases
have been reported in animals. Three prion diseases in particular – bovine
spongiform encephalopathy (BSE or "Mad Cow Disease"), variant Creutzfeldt-Jakob
disease (vCJD), and chronic wasting disease (CWD) – were specified in the
investigation. The results of this investigation are published in the June issue
of the Journal of the American Dietetic Association.
"While prion diseases are rare, they are generally fatal for anyone who
becomes infected. More than anything else, the results of this study support the
need for continued surveillance of prion diseases," commented lead investigator
Joseph Y. Abrams, MPH, National Center for Emerging and Zoonotic Infectious
Diseases, CDC, Atlanta."But it's also important that people know the facts about
these diseases, especially since this study shows that a good number of people
have participated in activities that may expose them to infection-causing
agents."
Although rare, human prion diseases such as CJD may be related to BSE.
Prion (proteinaceous infectious particles) diseases are a group of rare brain
diseases that affect humans and animals. When a person gets a prion disease,
brain function is impaired. This causes memory and personality changes,
dementia, and problems with movement. All of these worsen over time. These
diseases are invariably fatal. Since these diseases may take years to manifest,
knowing the extent of human exposure to possible prion diseases could become
important in the event of an outbreak.
CDC investigators evaluated the results of the 2006-2007 population survey
conducted by the Foodborne Diseases Active Surveillance Network (FoodNet). This
survey collects information on food consumption practices, health outcomes, and
demographic characteristics of residents of the participating Emerging
Infections Program sites. The survey was conducted in Connecticut, Georgia,
Maryland, Minnesota, New Mexico, Oregon, and Tennessee, as well as five counties
in the San Francisco Bay area, seven counties in the Greater Denver area, and 34
counties in western and northeastern New York.
Survey participants were asked about behaviors that could be associated
with exposure to the agents causing BSE and CWD, including travel to the nine
countries considered to be BSE-endemic (United Kingdom, Republic of Ireland,
France, Portugal, Switzerland, Italy, the Netherlands, Germany, Spain) and the
cumulative length of stay in each of those countries. Respondents were asked if
they ever had hunted for deer or elk, and if that hunting had taken place in
areas considered to be CWD-endemic (northeastern Colorado, southeastern Wyoming
or southwestern Nebraska). They were also asked if they had ever consumed
venison, the frequency of consumption, and whether the meat came from the wild.
The proportion of survey respondents who reported travel to at least one of
the nine BSE endemic countries since 1980 was 29.5%. Travel to the United
Kingdom was reported by 19.4% of respondents, higher than to any other
BSE-endemic country. Among those who traveled, the median duration of travel to
the United Kingdom (14 days) was longer than that of any other BSE-endemic
country. Travelers to the UK were more likely to have spent at least 30 days in
the country (24.9%) compared to travelers to any other BSE endemic country. The
prevalence and extent of travel to the UK indicate that health concerns in the
UK may also become issues for US residents.
The proportion of survey respondents reporting having hunted for deer or
elk was 18.5% and 1.2% reported having hunted for deer or elk in CWD-endemic
areas. Venison consumption was reported by 67.4% of FoodNet respondents, and
88.6% of those reporting venison consumption had obtained all of their meat from
the wild. These findings reinforce the importance of CWD surveillance and
control programs for wild deer and elk to reduce human exposure to the CWD
agent. Hunters in CWD-endemic areas are advised to take simple precautions such
as: avoiding consuming meat from sickly deer or elk, avoiding consuming brain or
spinal cord tissues, minimizing the handling of brain and spinal cord tissues,
and wearing gloves when field-dressing carcasses.
According to Abrams, "The 2006-2007 FoodNet population survey provides
useful information should foodborne prion infection become an increasing public
health concern in the future. The data presented describe the prevalence of
important behaviors and their associations with demographic characteristics.
Surveillance of BSE, CWD, and human prion diseases are critical aspects of
addressing the burden of these diseases in animal populations and how that may
relate to human health."
###
The article is "Travel history, hunting, and venison consumption related to
prion disease exposure, 2006-2007 FoodNet population survey" by Joseph Y.
Abrams, MPH; Ryan A. Maddox, MPH; Alexis R Harvey, MPH; Lawrence B. Schonberger,
MD; and Ermias D. Belay, MD. It appears in the Journal of the American Dietetic
Association, Volume 111, Issue 6 (June 2011) published by Elsevier.
In an accompanying podcast CDC's Joseph Y. Abrams discusses travel,
hunting, and eating venison in relation to prion diseases. It is available at http://adajournal.org/content/podcast.
Monday, October 10, 2011
EFSA Journal 2011 The European Response to BSE: A Success Story
snip...
EFSA and the European Centre for Disease Prevention and Control (ECDC)
recently delivered a scientific opinion on any possible epidemiological or
molecular association between TSEs in animals and humans (EFSA Panel on
Biological Hazards (BIOHAZ) and ECDC, 2011). This opinion confirmed Classical
BSE prions as the only TSE agents demonstrated to be zoonotic so far but the
possibility that a small proportion of human cases so far classified as
"sporadic" CJD are of zoonotic origin could not be excluded. Moreover,
transmission experiments to non-human primates suggest that some TSE agents in
addition to Classical BSE prions in cattle (namely L-type Atypical BSE,
Classical BSE in sheep, transmissible mink encephalopathy (TME) and chronic
wasting disease (CWD) agents) might have zoonotic potential.
snip...
see follow-up here about North America BSE Mad Cow TSE prion risk factors,
and the ever emerging strains of Transmissible Spongiform Encephalopathy in many
species here in the USA, including humans ;
Thursday, August 12, 2010
Seven main threats for the future linked to prions
First threat
The TSE road map defining the evolution of European policy for protection
against prion diseases is based on a certain numbers of hypotheses some of which
may turn out to be erroneous. In particular, a form of BSE (called atypical
Bovine Spongiform Encephalopathy), recently identified by systematic testing in
aged cattle without clinical signs, may be the origin of classical BSE and thus
potentially constitute a reservoir, which may be impossible to eradicate if a
sporadic origin is confirmed.
***Also, a link is suspected between atypical BSE and some apparently
sporadic cases of Creutzfeldt-Jakob disease in humans. These atypical BSE cases
constitute an unforeseen first threat that could sharply modify the European
approach to prion diseases.
Second threat
snip...
Sunday, January 22, 2012
Chronic Wasting Disease CWD cervids interspecies transmission
Thursday, January 26, 2012
The Risk of Prion Zoonoses
Science 27 January 2012: Vol. 335 no. 6067 pp. 411-413 DOI:
10.1126/science.1218167
Thursday, January 26, 2012
Facilitated Cross-Species Transmission of Prions in Extraneural Tissue
Science 27 January 2012: Vol. 335 no. 6067 pp. 472-475 DOI:
10.1126/science.1215659
Friday, June 29, 2012
Highly Efficient Prion Transmission by Blood Transfusion
layperson
Terry S. Singeltary Sr.
P.O. Box 42
Bacliff, Texas USA 77518
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