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Fluoroacetate residues in ground squirrel and coyote tissues due to primary or secondary 1080 poisoning.

Fluoroacetate residues in various tissues of 1080-poisoned ground squirrels and coyotes are listed. The tissues (excluding the stomach) of squirrels poisoned with an average of 0.8 mg 1080/kg (low dose) contained from 182 to 1309 ppb fluoroacetate. In squirrels poisoned with an average of 4.8 mg 1080/kg (high dose), the tissue residues ranged from 535 to 9754 ppb fluoroacetate. Tissues from coyotes which died after consuming 1080-poisoned ground squirrels were also analyzed for fluoroacetate residues. Residues in these coyote kidneys and livers ranged from less than 10 ppb to 95 ppb fluoroacetate. The residue findings in this research indicate that a diagnostic assay for 1080 in tissues must be reliable at 10 ppb (or less) fluoroacetate.

Animals↗

Gas chromatographic analysis of coyote and magpie tissues for residues of compound 1080 (sodium fluoroacetate).

Tissues of coyotes and magpies administered known dosages of 1080 were analyzed for residues by an analytical method specifying gas chromatography and electron capture detection. The repeatability of the method was determined for the replicate analyses of coyote muscle tissue samples aged under different storage conditions. The average coefficient of variation (CV) was 6% for quadruplicate determinations of 1080 in fresh tissues, 12-14% for samples stored at - 10 degrees C for 30-60 days, and 24% for samples aged for 7 days at ambient temperatures. The larger CV value obtained for stored samples is attributed more to greater sample variability than to less precision of the analytical method. Residues of 1080 appear to be relatively stable in tissues; there was essentially no change in the concentration of 1080 in samples stored up to 28 days at ambient temperature. Residue levels in the muscle, heart, kidney, and intestine were comparable, slightly lower in the liver, and much higher in the stomach. The concentration of 1080 in the muscle tissue was related to the administered dosages. Correlation analyses of dosages and residue levels in coyote muscle tissue showed a correlation coefficient of 0.99 for 1080 administered by gavage, and 0.88 for 1080 administered by bait. A correlation coefficient of 0.99 was observed between dosages and mean residues in the breast muscle tissues of magpies. The average CV value was 3.5% for duplicate analyses of 1 g samples of magpie tissues.

Animals↗

Serologic survey for hantavirus infection in domestic animals and coyotes from New Mexico and northeastern Arizona.

OBJECTIVE: To determine whether animals had serologic evidence of infection with Sin Nombre virus (SNV). DESIGN: Prospective serosurvey. SAMPLE POPULATION: Serum samples were obtained from 145 cats, 85 dogs, 120 horses, and 24 cattle between April 1993 and August 1994 and 54 coyotes between December 1994 and February 1995. PROCEDURE: Serum samples were analyzed by western immunoblot assays for reaction with SNV nucleocapsid antigen. Samples with reactivity to SNV nucleocapsid proteins were used to probe multiple-antigen blots containing recombinant fusion proteins derived from prototypic hantaviruses. Lung tissue or blood clots were used in nested reverse-transcriptase polymerase chain reaction assays for a 320-nucleotide portion of the SNV G1 gene. RESULTS: Sera from 4 of 145 (2.8%) cats and 4 of 85 (3.5%) dogs had trace reactivity to full-length SNV-encoded nucleocapsid proteins. All samples from horses, cattle, and coyotes were nonreactive. Sera from cats and dogs that had trace IgG-antibody reactivity to nucleocapsid proteins were then tested for IgG-antibody reactivity to nucleocapsid proteins of prototypic hantaviruses. One cat had multiple cross-reactivities with these hantaviruses, consistent with exposure to a hantavirus; however, epitope mapping studies did not support this conclusion. Reverse-transcriptase polymerase chain reaction studies of blood clots or lung tissue from 2 animals that had weak reactivity to SNV failed to amplify any hantavirus sequence. CLINICAL IMPLICATIONS: Domestic animals, particularly dogs and cats, as well as coyotes do not appear to have a major role in the maintenance and transmission of SNV.

Animals↗

A Bartonella vinsonii berkhoffii typing scheme based upon 16S-23S ITS and Pap31 sequences from dog, coyote, gray fox, and human isolates.

Since the isolation of Bartonella vinsonii subspecies berkhoffii from a dog with endocarditis in 1993, this organism has emerged as an important pathogen in dogs and as an emerging pathogen in people. Current evidence indicates that coyotes, dogs and gray foxes potentially serve as reservoir hosts. Based upon sequence differences within the 16S-23S ITS region and Pap31 gene, we propose a classification scheme that divides B. vinsonii subsp. berkhoffii isolates into four distinct types. Two conserved sequences, of 37 and 18 bp, respectively, are differentially present within the ITS region of each of the four B. vinsonii subsp. berkhoffii types. To date, B. vinsonii berkhoffii types I, II, and III have been identified in the US, type III in Europe and type IV in Canada. Based upon the proposed genotyping scheme, the geographic distribution of B. vinsonii berkhoffii types needs to be more thoroughly delineated in future molecular epidemiological studies involving Bartonella infection in coyotes, dogs, gray foxes, human beings and potentially other animals or in arthropod vectors. Strain typing may help to better define the reservoir potential, carriership patterns, modes of transmission, and geographic distribution for each B. vinsonii berkhoffii type.

Animals↗

Influence of extender, freezing rate, and thawing rate on post-thaw motility, viability and morphology of coyote (Canis latrans) spermatozoa.

The objective of this study was to examine the post-thaw effects of three cryoprotective extenders (Tris-fructose-citric acid extender, Tris-glucose-citric acid extender, and lactose extender), three linear freezing rates (-1, -6, and -20 degrees C/min), and three thawing rates (37 degrees C water bath for 120s, 60 degrees C water bath for 30s, and 70 degrees C water bath for 8s) on coyote spermatozoa. After thawing, the findings supported that cryopreservation of coyote (Canis latrans) spermatozoa frozen at a moderate freezing rate (-6 degrees C/min), in either a Tris-fructose or Tris-glucose extender, and thawed at a slow rate (37 degrees C water bath for 120s) or moderate rate (60 degrees C water bath for 30s), resulted in a more vigorous post-thaw motility (range, 57.5-44.0%) and viability (range, 64-49.6%) with the least amount of morphological and acrosomal abnormalities.

Acrosome↗

Characterizing noise in nonhuman vocalizations: Acoustic analysis and human perception of barks by coyotes and dogs.

Measuring noise as a component of mammalian vocalizations is of interest because of its potential relevance to the communicative function. However, methods for characterizing and quantifying noise are less well established than methods applicable to harmonically structured aspects of signals. Using barks of coyotes and domestic dogs, we compared six acoustic measures and studied how they are related to human perception of noisiness. Measures of harmonic-to-noise-ratio (HNR), percent voicing, and shimmer were found to be the best predictors of perceptual rating by human listeners. Both acoustics and perception indicated that noisiness was similar across coyote and dog barks, but within each species there was significant variation among the individual vocalizers. The advantages and disadvantages of the various measures are discussed.

Acoustics↗

Microencapsulation and dissolution parameters of undecenovanillylamide: a potential coyote deterrent.

The microencapsulation and dissolution of undecenovanillylamide (I), a potential coyote-aversive agent for use on sheep, were studied. While I has been shown to protect sheep, its short duration of action makes it economically unfeasible. Compound I microcapsules were prepared, and optimum conditions for encapsulation via complex coacervation were determined. Microcapsules that were hardened for 0.5, 1, and 2 hr, as well as I powder, were characterized according to their dissolution. Longer hardening times resulted in slower release, with all encapsulated I forms being released slower than the powder. The dissolution t50 for unencapsulated powder was less than 3 min; for microcapsules hardened for 30 min, the dissolution t50 was 7.3 min; for those hardened 60 min, the t50 was 17.7 min; and for those hardened 120 min, the t50 was 28 min. The encapsulated I would have a longer field life and, therefore, might be a viable economic and ecologic answer to coyote protection for sheep.

Animals↗

Electroejaculation of the coyote.

Two electroejaculators were used to collect semen from 40 adult male coyotes. The most effective apparatus used a two-ring rectal probe and an AC voltage of 18 (Vrms) at 1000 Hz. With this ejaculator, 11 of 15 coyotes produced a satisfactory semen sample, which averaged 0.9 ml in volume and 70 million spermatozoa per ml.

Journal Article↗

Spatial analysis of Yersinia pestis and Bartonella vinsonii subsp. berkhoffii seroprevalence in California coyotes (Canis latrans).

Zoonotic transmission of sylvatic plague caused by Yersinia pestis occurs in California, USA. Human infections with various Bartonella species have been reported recently. Coyotes (Canis latrans) are ubiquitous throughout California and can become infected with both bacterial agents, making the species useful for surveillance purposes. This study examined the geographic distribution of 863 coyotes tested for Y. pestis and Bartonella vinsonii subsp. berkhoffii serologic status to gain insight into the natural history of B. vinsonii subsp. berkhoffii and to characterize the spatial distribution of the two agents. We found 11.7% of specimens positive to Y. pestis and 35.5% positive to B. vinsonii subsp. berkhoffii. The two pathogens had distinct spatial clusters: Y. pestis was more prevalent in eastern portions of the state and B. vinsonii subsp. berkhoffii in coastal regions. Prevalence of Y. pestis increased with increasing elevation, whereas prevalence of B. vinsonii subsp. berkhoffii decreased with increasing elevation. There were differences in the proportions of positive animals on a yearly basis to both pathogens.

Animals↗

Coyote control and taste aversion.

Studies in which conditioned taste aversion was used as a non-lethal method to suppress coyote predation are reviewed in light of the controversy that surrounds such research. It is concluded that the negative results obtained to date may have been due to theoretical and methodological problems in the studies. Uncritical acceptance of those results has slowed progress on an effective and inexpensive method of coyote management.

Animals↗

Coyote control and taste aversion: a predation problem or a people problem?

Failures to suppress coyote predation on domestic livestock using the conditioned taste aversion paradigm may be due to such factors as poor livestock management procedures and overestimated coyote predation data, in addition to theoretical and methodological problems as indicated by Forthman Quick, Gustavson and Rusiniak.

Animals↗

Pedigree-based assignment tests for reversing coyote (Canis latrans) introgression into the wild red wolf (Canis rufus) population.

The principal threat to the persistence of the endangered red wolf (Canis rufus) in the wild is hybridization with the coyote (Canis latrans). To facilitate idengification and removal of hybrids, assignment tests are developed which use genotype data to estimate identity as coyote, 1/4, 1/2, 3/4 or full red wolf. The tests use genotypes from the red wolves that founded the surviving population and the resulting pedigree, rather than a contemporary red wolf sample. The tests are evaluated by analysing both captive red wolves at 18 microsatellite loci, and data simulated under a highly parameterized, biologically reasonable model. The accuracy of assignment rates are generally high, with over 95% of known red wolves idengified correctly. There are, however, tradeoffs between ambiguous assignments and misassignments, and between misidengifying red wolves as hybrids and hybrids as red wolves. These result in a compromise between limiting introgression and avoiding demographic losses. The management priorities and level of introgression determine the combination of test and removal strategy that best balances these tradeoffs. Ultimately, we conclude that the use of the assignment tests has the capacity to arrest and reverse introgression. To our knowledge, the presented approach is novel in that it accounts for genetic drift when the genotypes under analysis are temporally separated from the reference populations to which they are being assigned. These methods may be valuable in cases where reference databases for small populations have aged substantially, pedigree information is available or data are generated from historical samples.

Animals↗

Sarcocystis fusiformis infection in the coyote (Canis latrans).

Of 150 fecal samples from coyotes from northern Utah and southern Idaho, 21 contained coccidian sporocysts. These were found singly, contained four sporozoites and a granular residuum, and averaged 16.9 x 10.9 mum in size. None of four lambs inoculated with these sporocysts showed clinical signs of disease, and no parasites were found in their tissues. One calf inoculated with 135,000 sporocysts and another inoculated with 720,000 sporocysts eventually became unable to rise from recumbency. One was killed after 43 days; the other died at 50 days. Both calves had a mild mononuclear cell infiltration into the connective tissue adjacent to vessels in the heart, other striated muscles, kidney, and liver, and a moderate lymphoid hyperplasia in the spleen and lymph nodes. Schizonts were observed in a lymph node, and young sarcocysts were observed in skeletal and cardiac muscles. Four coyotes fed bovine heart infected with Sarcocystis passed sporulated sporocysts in their feces that were indistinguishable from those in the fecal samples from Utah and Idaho.

Animals↗

Case report of a coyote attack in Yellowstone National Park.

We report the case of an unprovoked coyote attack on a human visitor to Yellowstone National Park. Although the patient suffered only soft tissue injuries, unprovoked attacks are rarely reported in the medical literature. This case and plans on how to manage coyote attacks are discussed.

Animals↗

Dirofilariasis in Iowa coyotes.

(Dirofilaria immitis) were found in eight of 220 (3.6%) coyotes (Canis latrans) collected from fur buyers in Adams, Carroll, Cass, and Warren counties in southwestern Iowa. Infections ranged from one to 23 worms per coyote.

Animals↗

Coccidia of coyotes in eastern Colorado.

Eighty-two coyote fecal samples were collected from eastern Colorado and examined for coccidia. Sporocysts of Sarcocystis were observed in 17 of the samples and oocysts of Isospora ohioensis were observed in two samples. Ten fecal samples contained eimerian coccidia thought to be pseudoparasites of the coyote acquired while ingesting heavily infected rabbits.

Animals↗

Oral papillomatosis in coyotes (Canis latrans) and wolves (Canis lupus) of Alberta.

Twelve cases of oral papillomatosis were detected in wild carnivores of Alberta, ten in coyotes (Canis latrans) and two in wolves (Canis lupus). Lesions ranged from mild with a few small papillomas to severe with much of the surface of the lips, tongue and buccal cavity covered with papillomas. Three of five coyotes with severe papillomatosis were in obvious poor health. The gross and histologic lesions are described and the significance of this disease in wild carnivores is discussed.

Alberta↗