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Taylor CR, Rowntree VJ. 1973. Temperature
regulation and heat balance in running cheetahs: a strategy for sprinters?
American Journal of Physiology 224(1):848-51.
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Cheetahs sprint at speeds exceeding 100 km/h. At
this speed their calculated heat production would be more than 60 times greater
than that at rest. The cheetah stores most of the heat produced while running:
70% of the heat produced during a 15-min run at 11 km/h was stored; this
increased to 90% at 18 km/h. The cheetah refused to run when rectal temperature
reached 40.5 °C, Thus, the distance at which a cheetah pursues its prey appears
to be limited by the rise in the body temperature. The resting cheetah
possesses substantial capability for dissipating heat evaporatively and can
maintain a constant body temperature of about 40 °C when air temperature is 50
°C. During running these evaporative heat-loss mechanisms are not activated. By
comparison, the goat, a non-sprinter, increased evaporation and stored much
less heat while running than the cheetah.
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Taylor_&_Rowntree_1973_Temperature_regulation_in_cheetahs.pdf
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Taylor CR, Shkolnik A, Dmi'el
R, Baharav D, Borut A. 1974. Running in cheetahs, gazelles, and goats: energy
cost and limb configuration. American Journal of Physiology 227(4):848-50.
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Functional anatomists have
argued that an animal can be built to run cheaply by lightening the distal
parts of the limbs and/or by concentrating the muscle mass of the limbs around
their pivot points. These arguments assume that much of the energy expended as
animals run at a constant speed goes into alternately accelerating and decelerating
the limbs. Gazelles, goats, and cheetahs offer a nice gradation of limb
configurations in animals of similar total mass and limb length and, therefore,
provide the opportunity to quantify the effect of limb design on the energy
cost of running. We found that, despite large differences in limb
configuration, the energetic cost was nearly identical over a wide range of
speeds. Also, the observed energetic cost of running was almost the same as
that predicted on the basis of body weight for all three species cheetahs, 0.14
ml O2 (gkm)-1 observed vs. 0.13 ml O2 (gkm)-1
predicted; gazelle, 0.16 ml O2 (gkm)-1 observed vs. 0.15
ml O2 (gkm)-1 predicted; and goat, 0.18 ml O2
(gkm)-1 observed vs. 0.14 ml O2 (gkm)-1
predicted. Thus the relationship between body weight and energetic cost of
running apparently applies to animals with very different limb configurations
and is more general than anticipated. This suggests that most of the energy
expended in running at a constant speed is not used to accelerate and
decelerate the limbs.
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Taylor_et_al_1974_Running_in_cheetahs_gazelles_and_goats.pdf
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Taylor F. 1990. Endangered
species benefit from research. News & Features:5-8.
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In 1981, O'Brien joined a team
of scientists at the National Zoological Park working to unravel the problem of
poor breeding and endangered survival of captive cheetahs. Using molecular
techniques on blood and skin sample he found that the cheetah has a profound
lack of genetic diversity, particularly at the major histocompatibility complex
(MHC), that can cause problems for disease resistance. O'Brien and his
colleagues theorized that the cheetah had gone through a severe population
bottleneck, where the number of cheetahs had dropped to just a few individuals,
and close relatives were forced to breed.
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Taylor_1990_Endangered_species_benefit_from_research.pdf
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Teer JG. A plan for cheetah conservation in Namibia.
Report,
39 p.
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The U.S. Fish and Wildlife Service requests specific information
on several conditions and operations which affect the protection and
utilization of endangered and threatened life when requests are made for
changes in a species' status. The proposed conservation plan was cooperatively developed
with Safari Club International, the Ministry of Environment and Tourism of
Namibia, and the Namibia Professional Hunters Association (NAPHA). Cheetah
numbers were estimated in the late 1980s to be 2500. Various factors
influencing the cheetahs' future in Namibia are discussed.
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Teer_
A_Plan_for_Cheetah_Conservation_in_Namibia.pdf
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Tennant MB, Craig SJ. 1977. Breeding cheetahs at the Lion Country Safari Parks: a summary. Int Zoo
Yb 17(167):169.
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A six-year study aimed at
determining the conditions under which the cheetah is most likely to reproduce.
Comprehensive behavioural notes were taken and still and cine cameras and tape
recorders were used in the collection of data. This paper summarizes the
conditions and events leading to births and attempts to evaluate the factors
involved. Main factors that have contributed to the success of the cheetah
breeding programme include a quality commercially prepared diet, a large
compound with wide field of vision and which excludes sensory awareness of
other large carnivores, females of at least three years of age, predetermined
sexual activity levels for males and the fighting, females was apparently
courted and impregnated by one male alone.
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Tennant_&_Craig_1977_Breeding_Cheetahs_at_the_Lion_Country_Safari_Parks.pdf
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Terio KA, Marker L, Overstrom
EW, Brown JL. 2003. Analysis of ovarian and adrenal activity in Namibian
cheetahs. South African Journal of Wildlife Research 33(2):71-8.
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Captive breeding of cheetahs (Acinonyx
jubatus) has had limited success because a high percentage of captive
females exhibit a lack of ovarian activity. This study examined concentrations
of ovarian and adrenal hormones in wild-caught cheetahs (n=3) housed in large
outdoor enclosures on private game ranches in Namibia. Cheetahs were monitored
for a 16-month period to investigate the effect of season on ovarian and
adrenal function. Secretory profiles of oestradiol, progestagen, and cortisol
metabolites were quantified non-invasively using faecal steroid analysis. All
three cheetahs exhibited ovarian activity; however, none cycled continuously.
Periods of anoestrus occurred during overlapping periods between August and
December 1994, but not during the same time period in 1995. Mean duration of
the oestrous cycle, oestrus period and baseline concentrations of reproductive
hormones were consistent with those observed in other captive cheetah
populations. Concentrations of faecal corticoids were lower than those from
captive cheetahs in North America. There was no correlation between adrenal
activity and ovarian function. Spontaneous ovulation was documented in one
cheetah. These findings support those of earlier studies that even under
natural and, therefore, presumably ideal environmental conditions, reproductive
activity in captive cheetahs is not continuous.
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Terio_et_al_2003_Analysis_of_ovarian_and_adrenal_activity_in_Namibian_cheetahs.pdf
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Terio KA, Marker L, Munson L. 2004. Evidence for chronic stress in captive but not free-ranging cheethas (Acinonyx
jubatus) based on adrenal morphology and function. J Wildl Dis
40(2):259-66.
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The cheetah (Acinonyx
jubatus) is highly endangered because of loss of habitat in the wild and failure
to thrive in captivity. Cheetahs in zoos reproduce poorly and have high
prevalences of unusual diseases that cause morbidity and mortality. These
diseases are rarely observed in free-ranging cheetahs but have been documented
in cheetahs that have been captured and held in captive settings either
temporarily or permanently. Because captivity may be stressful for this species
and stress is suspected as contributing to poor health and reproduction, this
study aimed to measure chronic stress by comparing baseline concentrations of
fecal corticoid metabolites and adrenal gland morphology between captive and
free-ranging cheetahs. Additionally, concentrations of estradiol and
testosterone metabolites were quantified to determine whether concentrations of
gonadal steroids correlated with corticoid concentration and to assure that
corticosteroids in the free-ranging samples were not altered by environmental
conditions. Concentrations of fecal corticoids, estradiol, and testosterone
were quantified by radioimmunoassay in 20 free-ranging and 20 captive cheetahs
from samples collected between 1994 and 1999. Concentrations of baseline fecal
corticoids were significantly higher (p=0.005) in captive cheetahs
(196.08±36.20 ng/g dry feces) than free-ranging cheetahs (71.40±14.35 ng/g dry
feces). Testosterone concentrations were lower in captive male cheetahs
(9.09±2.84 ng/g dry feces) than in free-ranging cheetahs (34.52±12.11 ng/g dry
feces), which suggests suppression by elevated corticoids in the captive males.
Evidence for similar suppression of estradiol concentrations in females was not
present. Adrenal corticomedullary ratios were determined on midsagittal
sections of adrenal glands from 13 free-ranging and 13 captive cheetahs
obtained between 1991 and 2002. The degree of vacuolation of cortical cells in
the zona fasciulata was graded for each animal. Corticomedullary ratios were
larger (p=0.05) in captive cheetahs; however, there was no difference (p=0.31)
in the degree of corticocyte vacuolation between the two populations. These
data provide both morphologic and functional evidence suggestive of chronic
stress in captive cheetahs. Further research into the role of hypercortisolemia
in the pathogenesis of the reproductive abnormalities and unusual diseases of captive
cheetahs is needed.
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Terio_et_al_2004_Chronic_stress_in_captive_cheetahs.pdf
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Terio KA, Munson L, Marker L,
Aldridge BM, Solnick JV. 2005. Comparison of Helicobacter spp. In
Cheetahs (Acinonyx jubatus) with and without gastritis. Journal of
Clinical Microbiology 43(1):229-34.
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Chronic gastritis causes
significant morbidity and mortality in captive cheetahs but is rare in wild
cheetahs despite colonization by abundant spiral bacteria. This research aimed
to identify the Helicobacter species that were associated with gastritis in
captive cheetahs but are apparently commensal in wild cheetahs. Helicobacter
species were characterized by PCR amplification and sequencing of the 16s rRNA,
urease, and cagA genes and by transmission electron microscopy of frozen
or formalin-fixed paraffin-embedded gastric samples from 33 cheetahs infected
with Helicobacter organisms (10 wild without gastritis and 23 captive with
gastritis). Samples were screened for mixed infections by denaturant gel
gradient electrophoresis of the 16s rRNA gene and by transmission electron
microscopy. There was no association between Helicobacter infection and the
presence or severity of gastritis. Eight cheetahs had 16s rRNA sequences that
were most similar (98 to 99%) to H. pylori. Twenty-five cheetahs had sequences
that were most similar (97 to 99%) to "H. heilmannii" or H. felis. No
cheetahs had mixed infections. The ultrastructural morphology of all bacteria
was most consistent with "H. heilmannii," even when 16s rRNA
sequences were H. pylori-like. The urease gene from H. pylori-like bacteria
could not be amplified with primers for either "H. heilmannii" or H.
pylori urease, suggesting that this bacteria is neither H. pylori nor "H.
heilmannii." The cagA gene was not identified in any case. These findings
question a direct role for Helicobacter infection in the pathogenesis of
gastritis and support the premise that host factors account for the differences
in disease between captive and wild cheetah populations.
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Terio_et_al_2005_Helicobacter_in_cheetahs_with_and_without_gastritis.pdf
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Thalwitzer S, Wachter B, Robert N, Wibbelt G,
Müller T, Lonzer J, Meli ML, Bay G, Hober H, Lutz H. 2010. Seroprevalences
to viral pathogens in free-ranging and captive cheetahs (Acinonyx jubatus)
on Namibian Farmland. Clinical and Vaccine Immunology 17, 232-238. |
Cheetah (Acinonyx jubatus) populations
are diminishing rapidly in their natural habitat. One reason for their decline
is thought to be a high susceptibility to (infectious) diseases because
cheetahs in zoos suffer from high disease-induced mortality. Data on the health
status of free-ranging cheetahs are scarce, and little is known about their
exposure and susceptibility to infectious diseases. We determined
seroprevalences to nine key viruses (feline herpesvirus 1, feline calicivirus,
feline parvovirus, feline coronavirus, canine distemper virus, feline
immunodeficiency virus [FIV], puma lentivirus, feline leukemia virus, and
rabies virus) in 68 free-ranging cheetahs on east-central Namibian farmland, 24
nonvaccinated Namibian captive cheetahs, and several other wild carnivore
species and conducted necropsies of cheetahs and other wild carnivores. Eight
of 11 other wild carnivores were seropositive for at least one of the viruses,
including the first record of an FIV-like infection in a wild felid west of the
Kalahari, the caracal (Felis caracal). Seroprevalences of the
free-ranging cheetahs were below 5% for all nine viruses, which is
significantly lower than seroprevalences in nonvaccinated captive cheetahs and
those for five of seven viruses in previously studied free-ranging cheetahs
from north-central Namibia (L. Munson, L. Marker, E. Dubovi, J. A. Spencer, J.
F. Evermann, and S. J. O'Brien, J. Wildl. Dis. 40:23-31, 2004). There was no
clinical or pathological evidence of infectious diseases in living or dead
cheetahs. The results suggest that while free-ranging wild carnivores may be a
source of pathogens, the distribution of seroprevalences across studies
mirrored local human population density and factors associated with human
habitation, probably reflecting contact opportunities with (nonvaccinated)
domestic and feral cats and dogs. They also suggest that Namibian cheetahs
respond effectively to viral challenges, encouraging consistent and sustainable
conservation efforts. |
Thalwitzer_et_al_2010_Seroprevalence_to_viral_pathogens_in_cheetahs_from_Namibia.pdf
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Thomas P, Balme G, Hunter L,
McCabe-Parodi J. 2005. Using scent attractants to non-invasively collect hair
samples from cheetahs, leopards and lions. Animal Keepr's Forum 7/8:342-84.
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The goal of this project was
to document the responses of free-ranging cheetahs (Acinonyx jubatus)
and other large African felids to novel scents in an attempt to refine methods
for surveying felid populations. Specifically, the purpose of the study was:
1) To ascertain whether African felids are attracted to novel scents. While
captive cats are drawn to a wide variety of fragrances, we wanted to assess the
response of free-ranging felids to novel scents where they might i) explore
scents because they are unfamiliar and interesting, or ii) avoid scents because
they might be associated with human activity.
2) Assess whether these scents would elicit rubbing responses that could be
used to facilitate the collection of hair samples from African felids. If
successful, this technique could be used as an effective tool to non-invasively
collect hair samples for genetic analyses.
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Thomas_et_al_2005_Scent_attractants_to_collect_hair_samples_from_cats.pdf
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Thompson RA, Vestal BM. 1974. Survey
of conditions associated with breeding cheetah in captivity. Report
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On the basis of a
questionnaire-survey returned by twenty zoological institutions, the following
factors appear to be significant in successful breeding of captive cheetahs:
1) No African carnivores housed in the proximity of the cheetahs.
2) A relatively large enclosure size-on the order of 1000 m2 or larger
3) In most instances, the first successful breeding occurred when the cheetahs
had been in the collection a short time. Therefore, breeding attempts should be
initiated as soon as possible after acquisition of the animals.
4) Isolation and reintroduction is not productive.
5) There appears to be a July-August, December-January pattern of seasonality
of estrus, hence reintroductions in those time periods may be more productive.
6) Facilities should be available to isolate a pregnant female or female and
young.
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Thompson_&_Vestal_1974_Survey_of_Conditions_Associated_with_Breeding_Cheetah.pdf
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Thompson SE. 1990. Bringing up
baby. Zoo Life:57-63.
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Breeding in captivity is very
difficult with cheetahs. Female cheetahs are very choosy. They won't take just
any male. Scientists discovered a connection between infertility in female
cheetahs and the exotic feline diet fed to many captive cats. Cheetahs are more
susceptible to disease than other cats - this may be one result of an ancient
genetic bottleneck. When the king cheetah was first reported in 1926, it was
believed to be a cheetah-leopard hybrid. It is distinguished by its blotchy
sports and dark broad stripes down its back.
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Thompson_1990_Bringing_Up_Baby.pdf
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Thorn M, Green M, Keith M, Marnewick K,
Bateman PW, Cameron EZ, Scott DM. 2011. Large-scale
distribution patterns of carnivores in northern South Africa: implications for
conservation and monitoring. Oryx 45, 579-586. |
Accurate assessment
of carnivore population status is frequently hindered
by insufficient distribution data. For northern
South Africa we address this deficit by mapping
new records from landscape-scale sign surveys, questionnaire
interviews, problem animal records and camera trapping.
The black-backed jackal Canis mesomelas and caracal
Caracal caracal remain common and widespread. Ranges
of the serval Leptailurus serval and brown hyaena
Hyaena brunnea were much larger than previous estimates,
reducing the risk of simultaneous extirpation across
all occupied locations. The proportion of range
area occupied was larger for several species, notably
the leopard Panthera pardus, cheetah Acinonyx jubatus
and serval. We conclude that the serval continues
to recover from historical threats and is expanding
into new areas. A larger brown hyaena range and
less fragmented pattern of occurrence probably confers
greater resilience to threats than was suggested
by previous data. Reduced extinction risk arising
from the increased area occupied by the cheetah
and leopard is tempered by probable local range
contraction. Our maps provide baseline information
for monitoring the distribution of these six species,
which is essential in managing ecological issues
that have a spatial component such as responses
to changing land use. Our results also demonstrate
the utility of detection/nondetection surveys in
rapid assessment of carnivore populations at large
spatial scales.
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Thorn_et_al_2011_Distribution_patterns_of_carnivores_in_northern_South_Africa.pdf
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Tjaronda W. 2006. New beef
label to support cheetah. New Era;11,1-2.
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Namibian farmers will export
beef under a new label in support of the conservation of the endangered animal.
Farmers who export the beef will be certified Cheetah Country Farmers and will
be monitored as practising cheetah-friendly livestock management. They will be
paid a premium for the best beef they sell. Cheetah Country Beef is but one of
the many conservation economic initiatives that CCF has embarked on to save the
life of the Cheetah in Namibia.
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Tjaronda_2006_New_Beef_Label_to_Support_Cheetah.pdf
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Tong JR. 1974. Breeding
cheetahs at the Beekse Bergen Safari Park. Int Zoo Yb 14:129-30.
|
Several interesting point about a successful breeding. The
cheetahs had lived together as a group for three years and were never seperated
from each other. Before the period during which mating took place, no female
had been observed in oestrus, so it may be assumed that the animals were ready
for breeding at approximately 3.5-4 years. The most important factor appears to
be the new external interest created for the cheetahs shortly before mating.
There were sections containing lions which were replaced by African ungulates.
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Tong_1974_Breeding_Cheetahs_at_the_Beekse_Bergen_Safari_Park.pdf
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Troyer JL, Pecon-Slattery J,
Roelke ME, Johnson W, VandeWoude S, Vazguez-Salat N, Brown M, Frank L,
Woodroffe R, Winterbach C, Winterbach H, Hemson G, Bush M, Alexander KA,
Revilla E, O'Brien SJ. 2005. Seroprevalence and genomic divirgence of
circulating strains of feline immunodeficiency virus among Felidae and
Hyaenidae species. Journal of Virology 79:8282-94.
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Feline immunodeficiency virus
(FIV) infects umerous wild and domestic feline species and is closely related
to human immunodeficiency virus (HIV) and simian immunodeficiency virus (SIV).
Species-specific strains of FIV have been described for domestic cat (Felis
catus), puma (Puma concolor), lion (Panthera leo), leopard (Panthera
pardus), and Pallas' cat (Otocolobus manul). Here, we employ a
three-antigen Western blot screening (domestic cat, puma, and lion FIV
antigens) and PCR analysis to survey worldwide prevalence, distribution, and
genomic differentiation of FIV based on 3,055 specimens from 35 Felidae and 3
Hyaenidae species. Although FIV infects a wide variety of host species, it is
confirmed to be endemic in free-ranging populations of nine Felidae and one
Hyaenidae species. These include the large African carnivores (lion, leopard,
cheetah, and spotted hyena), where FIV is widely distributed in multiple
populations; most of the South American felids (puma, jaguar, ocelot, margay,
Geoffroy's cat, and tigrina), which maintain a lower FIV-positive level
throughout their range; and two Asian species, the Pallas' cat, which has a
species-specific strain of FIV, and the leopard cat, which has a domestic cat
FIV strain in one population. Phylogenetic analysis of FIV proviral sequence
demonstrates that most species for which FIV is endemic harbor monophyletic,
genetically distinct species-specific FIV strains, suggesting that FIV transfer between cat species
has occurred in the past but is quite infrequent today.
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Troyer_et_al_2005_Strains_of_FIV_among_Felidae_and
Hyaenidae.pdf
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Truyen U, Parrish CR, Harder
TC, Kaaden O-R. 1995. There is nothing permanent except change. The emergence
of new virus diseases. Veterinary Microbiology 43:103-22.
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The sudden appearance of
apparently new viruses with pathogenic potential is of fundamental importance
in medical microbiology and a constant threat to humans and animals. The
emergence of a "new" pathogen is not an isolated event, as for
instance the frequent appearance of new influenza virus strains demonstrates.
Often the new virus strains co-circulate with the older strains in a
susceptible population, but a replacement of the older strains has been also
observed. In rare instances the new viruses can cause dramatic epidemies or
pandemics, such as those observed with the human immunodeficiency virus, canine
parvovirus, or most recently, with the agent of bovine spongiform
encephalogathy in the United Kingdom. The mechanisms of the emergence are not
always clearly understood, but an altered host range appears to be a common
event. Whether a true change in host range occurs, or whether the virus adapted
to the host and replicated more efficiently, is often unknown. This review
tries to summarize the facts that are known about a wide variety of
"new" viruses of mammals, such as the simian, human and feline
lentiviruses, the feline coronaviruses, the feline parvoviruses, the carnivore
morbilliviruses, the influenza A viruses, and the transmissible spongiform
encephalopathies. A particular emphasis will be put on the genetic mechanisms
that might have taken place and that might have been responsible for their
sudden appearance.
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Truyen_et_al_1995_Emerge_of_new_virus_diseases.pdf
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Turnbull P. 2005. Anthrax
vaccination evaluation study in cheetah. Animal Keeper's Forum 32(7/8):329.
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It has been recognized for
decades that anthrax (that disease now so notorious for its biological warfare
and bioterrorism associations) is a common natural seasonal disease among the
herbivorous species of the Etosha National Park, occasionally affecting
livestock and wildlife in other parts of Namibia. Of particular concern all
along has been the additional threat is poses to the already endangered black
rhino in Etosha, but it was only very recently realized that cheetah were dying
in substantial numbers there from this disease.
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Turnbull_2005_Anthrax_vaccination_evaluation_study_in_cheetah.pdf
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Tyler JW, Cullor JS. 1989.
Titers, tests, and truisms: rational interpretation of diagnostic serologic
testing. JAVMA 194(11):1550-8.
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The recent availability of
serologic tests has changed the practice of veterinary medicine. These assays
not only assist with the diagnosis and treatment of recognized syndromes, but
they permit identification of new, poorly defined disease entities. Assays kits
are available for FeLV, dirofilariasis, rheumatoid arthritis, enterotoxigenic
colibacillosis, and failure of passive transfere. The purpose of this report is
to discuss the theory behind diagnostic serologic testing, rebut selected
misconceptions, and suggest strategies for interpreting the results of
diagnostic serologic tests. Also, the authors have provided adaptations of
standard statistical methods, sample calculations, general references, and a
glossary of terms.
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Tyler_&_Cullor_1989_Rational_interpretation_of_diagnostic_serologic_testing.pdf
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