|
|
Sundberg, J. P., Van Ranst, M., Montali, R., Homer, B. L., Miller, W. H., Rowland, P. H., et al. (2000). Feline papillomas and papillomaviruses. Vet Pathol, 37(1), 1–10.
Abstract: Papillomaviruses (PVs) are highly species- and site-specific pathogens of stratified squamous epithelium. Although PV infections in the various Felidae are rarely reported, we identified productive infections in six cat species. PV-induced proliferative skin or mucous membrane lesions were confirmed by immunohistochemical screening for papillomavirus-specific capsid antigens. Seven monoclonal antibodies, each of which reacts with an immunodominant antigenic determinant of the bovine papillomavirus L1 gene product, revealed that feline PV capsid epitopes were conserved to various degrees. This battery of monoclonal antibodies established differential expression patterns among cutaneous and oral PVs of snow leopards and domestic cats, suggesting that they represent distinct viruses. Clinically, the lesions in all species and anatomic sites were locally extensive and frequently multiple. Histologically, the areas of epidermal hyperplasia were flat with a similarity to benign tumors induced by cutaneotropic, carcinogenic PVs in immunosuppressed human patients. Limited restriction endonuclease analyses of viral genomic DNA confirmed the variability among three viral genomes recovered from available frozen tissue. Because most previous PV isolates have been species specific, these studies suggest that at least eight different cat papillomaviruses infect the oral cavity (tentative designations: Asian lion, Panthera leo, P1PV; snow leopard, Panthera uncia, PuPV-1; bobcat, Felis rufus, FrPV; Florida panther, Felis concolor, FcPV; clouded leopard, Neofelis nebulosa, NnPV; and domestic cat, Felis domesticus, FdPV-2) or skin (domestic cat, F. domesticus, FdPV-1; and snow leopard, P. uncia, PuPV-2).
|
|
|
|
Thorel, M. F., Karoui, C., Varnerot, A., Fleury, C., & Vincent, V. (1998). Isolation of Mycobacterium bovis from baboons, leopards and a sea-lion. Vet Res, 29(2), 207–212.
Abstract: This study reports on two series of cases of Mycobacterium bovis infection in zoo animals. The first was in a captive population of baboons (Papio hamadryas) and the second in a mixed group of wild mammals, including four leopards (Panthera uncia and Panthera pardus) and a sea-lion (Otaria byrona). The isolation and identification of strains of M. bovis confirmed the presence of M. bovis infections in both zoos. The epidemiological study using genetic markers such as the IS6110-based DNA fingerprinting system made it possible to differentiate between M. bovis strains. The M. bovis strains isolated from baboons were shown to contain a single IS6110 copy, as usually do cattle isolates, whereas the M. bovis strains isolated from the other exotic animals presented multiple copies. This finding suggests that the origin of the contamination for the baboons in zoo A could be related to cattle. The origin of the contamination for the leopards and sea-lion in zoo B is more difficult to determine. In conclusion, the authors suggest some recommendations for avoiding outbreaks of tuberculosis infections in zoos.
|
|
|
|
Trepanier, L. A., Cribb, A. E., Spielberg, S. P., & Ray, K. (1998). Deficiency of cytosolic arylamine N-acetylation in the domestic cat and wild felids caused by the presence of a single NAT1-like gene. Pharmacogenetics, 8(2), 169–179.
Abstract: The purpose of this study was to determine the molecular basis for a relative deficiency in the cat of cytosolic arylamine N- acetyltransferase (NAT), an enzyme family that is important in the metabolism of xenobiotics and that normally consists of at least two related enzymes, NAT1 and NAT2. N-acetyltransferase in feline liver showed high affinity (mean Km = 2.1 microM) for p-aminobenzoic acid, an NAT1 selective substrate in humans and rabbits, but showed a very poor affinity (mean Km > 10 mM) for sulfamethazine, an NAT2 selective substrate in humans and rabbits. Immunoreactive N-acetyltransferase was detected in feline liver, bladder and colon using an NAT1-specific antipeptide antibody, but was not detected in any tissues using an NAT2- specific antibody. Southern blot analysis of genomic DNA demonstrated a single band in domestic cats using each of six restriction digests; single bands were also found on Southern blot analysis of six wild felids. The deduced amino acid sequence of the central portion of feline N-acetyltransferase, obtained by polymerase chain reaction amplification in both domestic cats and seven wild felids (lion, tiger, lynx, snow leopard, bobcat, Asian leopard cat and cheetah), contained three residues, Phe125, Arg127, and Tyr129, which determine NAT1-like substrate specificity in humans. These results support the conclusion that cytosolic arylamine N-acetylation activity is low in the cat because of the presence of a single N-acetyltransferase that has substrate specificity, immunogenicity and sequence characteristics similar to human NAT1, and that the unusual presence of only a single N- acetyltransferase gene appears to be a family wide trait shared by other felids.
|
|
|
|
Warren E.Johnson, E. E. (2006). The Late Miocene Radiation of Modern Felidae: A Genetic Assessment (Stephen J.O'Brien Emma Teeling Agostinho Antunes W. J. M. Jill Pecon-Slattery, Ed.) (Vol. 311). Washington D.C.
Abstract: Modern felid species descend from relatively recent (<11 million years ago) divergence and
speciation events that produced successful predatory carnivores worldwide but that have
confounded taxonomic classifications. A highly resolved molecular phylogeny with divergence dates
for all living cat species, derived from autosomal, X-linked, Y-linked, and mitochondrial gene
segments (22,789 base pairs) and 16 fossil calibrations define eight principal lineages produced
through at least 10 intercontinental migrations facilitated by sea-level fluctuations. A ghost lineage
analysis indicates that available felid fossils underestimate (i.e., unrepresented basal branch
length) first occurrence by an average of 76%, revealing a low representation of felid lineages
in paleontological remains. The phylogenetic performance of distinct gene classes showed that
Y-chromosome segments are appreciably more informative than mitochondrial DNA, X-linked,
or autosomal genes in resolving the rapid Felidae species radiation.
|
|
|
|
Wasser, S. (1998). Snow Leopard Genetics: New Techniques (Vol. xvi). Seattle: Islt.
|
|
|
|
Weiskopf, S. R., Kachel, S. M., McCarthy, K. P. (2016). What Are Snow Leopards Really Eating? Identifying Bias in Food-Habit Studies. Wildlife Society Bulletin, , 1–8.
Abstract: Declining prey populations are widely recognized as a primary threat to snow leopard (Panthera
uncia) populations throughout their range. Effective snow leopard conservation will depend upon reliable
knowledge of food habits. Unfortunately, past food-habit studies may be biased by inclusion of nontarget
species in fecal analysis, potentially misinforming managers about snow leopard prey requirements.
Differentiation between snow leopard and sympatric carnivore scat is now cost-effective and reliable using
genetics. We used fecal mitochondrial DNA sequencing to identify scat depositors and assessment bias in
snow leopard food-habit studies. We compared presumed, via field identification, and genetically confirmed
snow leopard scats collected during 2005 and 2012 from 4 sites in Central Asia, using standard forensic
microscopy to identify prey species. Field identification success varied across study sites, ranging from 21% to
64% genetically confirmed snow leopard scats. Our results confirm the importance of large ungulate prey for
snow leopards. Studies that fail to account for potentially commonplace misidentification of snow leopard
scat may mistakenly include a large percentage of scats originating from other carnivores and report
inaccurate dietary assessments. Relying on field identification of scats led to overestimation of percent
occurrence, biomass, and number of small mammals consumed, but underestimated values of these measures for large ungulates in snow leopard diet. This clarification suggests that the conservation value of secondary prey, such as marmots (Marmota spp.) and other small mammals, may be overstated in the literature; stable snow leopard populations are perhaps more reliant upon large ungulate prey than previously understood.
|
|
|
|
Zhang, F., Jiang, Z., Zeng, Y., & McCarthy, T. (2007). Development of primers to characterize the mitochondrial control region of the snow leopard (Uncia uncia) (Vol. 7).
Abstract: The snow leopard (Uncia uncia) is a rare carnivore living above the snow line in central Asia. Using universal primers for the mitochondrial genome control region hypervariable
region 1 (HVR1), we isolated a 411-bp fragment of HVR1 and then designed specific primers
near each end of this sequence in the conserved regions. These primers were shown to yield
good polymerase chain reaction products and to be species specific. Of the 12 snow leopards
studied, there were 11 segregating sites and six haplotypes. An identification case of snow
leopard carcass (confiscated by the police) proved the primers to be a useful tool for forensic
diagnosis in field and population genetics studies.
|
|
