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1.
J Zoo Wildl Med ; 55(1): 182-194, 2024 Mar.
Article En | MEDLINE | ID: mdl-38453501

This study examined the viral shedding kinetics of elephant endotheliotropic herpesvirus (EEHV) in African elephants (Loxodonta africana) compared to viral shedding behavior in Asian elephants (Elephas maximus). Little is known about the transmission dynamics and epidemiology of this disease in African elephants. In light of recent clinical cases and mortalities, this paper aims to identify trends in viral biology. Trunk wash samples were collected from 22 African elephants from four North American zoological institutions that had recently experienced herd viremias or translocations. Processing of these samples included DNA extraction followed by qPCR to quantitate viral DNA load. The results were then compared with available literature that chronicled similar cases in Asian and African elephants. Minimal EEHV shedding was detected in response to varied herd translocations. Increased shedding was recorded in herds in which an elephant experienced an EEHV viremia when compared to baseline shedding. These index infections were followed by subsequent viremias in other elephants, although it is not known if these were recrudescence, transient controlled viremias, and/or primary infections via transmission to other elephants. When compared to historically published data, it was observed that EEHV3 cases in African elephants and EEHV1A cases in Asian elephants had consistently higher levels of viral DNA in the blood than were shed in trunk secretions, a fact that is seemingly inconsistent with such severe cases of disease and the high mortality rates associated with those respective types. The findings produced in this study highlight the need for more routine monitoring of viral shedding in African elephant herds to elucidate possible EEHV transmission and recrudescence factors for ex situ population management.


Elephants , Herpesviridae Infections , Herpesviridae , Animals , Herpesviridae Infections/epidemiology , Herpesviridae Infections/veterinary , DNA, Viral/genetics , Viremia/veterinary , Animals, Zoo/genetics , Herpesviridae/genetics , Recurrence
2.
J Zoo Wildl Med ; 54(2): 394-400, 2023 Jul.
Article En | MEDLINE | ID: mdl-37428705

Trypanosoma cruzi is a protozoan parasite primarily transmitted by triatomine insects (Hemiptera: subfamily Reduviidae) and is the cause of Chagas disease (CD). This report describes three cases of CD in a mob of five slender-tailed meerkats (Suricata suricatta) living in an outdoor exhibit at one zoological institution in Texas. The index case was a 9.5-yr-old female that presented with ataxia, lethargy, and pleural effusion. This case was diagnosed with CD postmortem via cytology, T. cruzi PCR of whole blood and lung fluid, and histology. Blood was opportunistically collected from the remaining four meerkats 28 d after the death of the index case and tested by PCR and serology. The second case was a clinically normal 7.5-yr-old male that tested PCR and antibody positive and the third case was a clinically normal 9-yr-old female that tested PCR positive. The second animal presented depressed, with pneumonia, and with continuous shivering 53 d after blood collection, and clinically improved after treatment with antibiotics and supportive care. Fifteen days later, the animal was found minimally responsive and died shortly thereafter. Histologic examination revealed Trypanosoma sp. amastigotes in the myocardium and the tissue was positive for T. cruzi DNA. The third meerkat, which received two separate courses of benznidazole over a span of almost 2 yr, was monitored routinely by PCR and serology and appeared clinically normal until found dead on exhibit 93 d after completion of the second treatment. Myocardium was positive for T. cruzi DNA. To the authors' knowledge, this case series is the first to document Chagas disease in meerkats and features associated cytologic and histologic findings.


Chagas Disease , Herpestidae , Trypanosoma cruzi , Male , Female , Animals , Chagas Disease/diagnosis , Chagas Disease/drug therapy , Chagas Disease/veterinary , Myocardium , Herpestidae/genetics , Lung , DNA , Trypanosoma cruzi/genetics
3.
Int J Parasitol Parasites Wildl ; 20: 133-137, 2023 Apr.
Article En | MEDLINE | ID: mdl-36845224

We report a case of Spirometra infection in a Samar cobra (Naja samarensis) imported from the Philippines, belonging to a zoological collection in the southern United States. Under a poor post-surgical prognosis, the snake was euthanized, and at necropsy plerocercoids of a Diphyllobotriidea were found in its subcutaneous tissues and musculature. Molecular and phylogenetic analyses of the complete cytochrome oxidase c subunit I (cox1) gene of the mitochondrial DNA confirmed that the isolate belonged to the genus Spirometra and was closely related to Spirometra mansoni isolates from Asian countries (bootstrap support = 99.4%). Considering the origin and clinical history and handling of the animal, the snake probably arrived infected in America. We suggest the inclusion of diagnostic imaging in the investigation of sparganosis in research and disease surveillance protocols applied in the pre- and post-quarantine period to asymptomatic animals imported from endemic areas.

4.
J Vet Diagn Invest ; 32(3): 471-475, 2020 05.
Article En | MEDLINE | ID: mdl-32274981

We identified a novel herpesvirus in a captive juvenile white stork (Ciconia ciconia) that experienced progressive weight loss followed by death. Histologic findings included severe splenic and hepatic necrosis, and intranuclear inclusion bodies in hepatocytes and unidentified splenic cells. The virus was amplified, sequenced, and subsequently accessioned as Ciconiid alphaherpesvirus 1. Phylogenetic analysis was performed and revealed that this virus is more closely related to mammalian herpesviruses than those within the genus Mardivirus. Additional sequence of viruses in this area may elucidate the ancestral virus that jumped from reptilian to mammalian hosts.


Bird Diseases/virology , Birds , Herpesviridae Infections/veterinary , Herpesviridae/classification , Herpesviridae/isolation & purification , Liver Diseases/veterinary , Splenic Diseases/veterinary , Animals , Bird Diseases/pathology , Fatal Outcome , Herpesviridae Infections/pathology , Herpesviridae Infections/virology , Liver Diseases/virology , Phylogeny , Splenic Diseases/pathology , Splenic Diseases/virology
5.
J Zoo Wildl Med ; 46(4): 691-8, 2015 Dec.
Article En | MEDLINE | ID: mdl-26667524

The immune responses of 35 captive African wild dogs (Lycaon pictus) to an inactivated rabies virus vaccine were evaluated. Seventeen animals received one 1-ml dose of inactivated rabies vaccine administered intramuscularly, while 18 received two 1-ml doses given simultaneously but at different injection sites. Sera were collected from all animals prior to vaccination and intermittently from a subset of animals between 3 and 49 mo postvaccination. Rabies neutralizing serum antibody titers were measured by rapid fluorescent focus inhibition testing. Within 3 mo postvaccination, all 28 animals that were tested within that time period had seroconverted. Overall, titers were significantly higher among animals given two doses of vaccine than among those given a single dose, although this difference was no longer significant by 15 mo postvaccination. Regardless of initial dose, a single administration of inactivated rabies virus vaccine resulted in long-term elevation of titers in the African wild dogs in this study. In the two individuals followed for greater than 36 mo, both (one from each group) maintained detectable titers.


Canidae , Dose-Response Relationship, Immunologic , Rabies Vaccines/immunology , Rabies/veterinary , Animals , Animals, Zoo , Rabies/prevention & control , Rabies Vaccines/administration & dosage , Vaccines, Inactivated/administration & dosage , Vaccines, Inactivated/immunology
6.
J Am Vet Med Assoc ; 245(4): 419-24, 2014 Aug 15.
Article En | MEDLINE | ID: mdl-25075826

CASE DESCRIPTION: A 4-year-old castrated male domestic ferret (Mustela putorius furo) was examined because of a 3-week history of intermittent seizures, signs of depression, hypocalcemia, and hyperphosphatemia. CLINICAL FINDINGS: Plasma biochemical analysis confirmed hyperphosphatemia (17.7 mg/dL) and low concentrations of total (4.3 mg/dL) and ionized (0.49 mmol/L) calcium. Serum parathyroid hormone concentration (2.30 pmol/L) was low or in the low part of the reference interval. TREATMENT AND OUTCOME: Calcium gluconate was administered (2.0 mg/kg/h [0.9 mg/lb/h], IV), followed by a transition to administration of calcium carbonate (53 mg/kg [24.1 mg/lb], PO, q 12 h) and dihydrotachysterol (0.02 mg/kg/d [0.009 mg/lb/d], PO). Attitude of the ferret improved and seizures ceased as blood calcium concentrations increased. The ferret was reexamined because of seizures approximately 1 year after oral maintenance administration of dihydrotachysterol and calcium was initiated. The ferret responded well to emergency and long-term treatment but then was lost to follow-up monitoring. The ferret died approximately 2 years after the initial evaluation and treatment. Hypertrophic cardiomyopathy was diagnosed during necropsy, but the parathyroid glands could not be identified. CLINICAL RELEVANCE: To the authors' knowledge, primary hypoparathyroidism has not previously been reported in a ferret. The condition should be considered for ferrets with hypocalcemia and hyperphosphatemia without azotemia. Treatment with dihydrotachysterol and oral supplementation of calcium appeared to be a viable option for long-term management.


Calcium Carbonate/therapeutic use , Calcium Gluconate/therapeutic use , Dihydrotachysterol/therapeutic use , Ferrets , Hypoparathyroidism/veterinary , Vitamins/therapeutic use , Animals , Calcium Carbonate/administration & dosage , Calcium Gluconate/administration & dosage , Dihydrotachysterol/administration & dosage , Hypocalcemia/veterinary , Hypoparathyroidism/blood , Hypoparathyroidism/drug therapy , Male , Vitamins/administration & dosage
7.
J Zoo Wildl Med ; 44(4): 882-8, 2013 Dec.
Article En | MEDLINE | ID: mdl-24450046

A series of three doses of recombinant canary-pox-vectored canine distemper virus vaccine was administered at 1-mo intervals, orally (n = 8) or intramuscularly (n = 13), to 21 previously unvaccinated juvenile African wild dogs (Lycaon pictus) at the Wildlife Conservation Society's Bronx Zoo. Titers were measured by serum neutralization at each vaccination and at intervals over a period of 3.5-21.5 mo after the initial vaccination. All postvaccination titers were negative for orally vaccinated animals at all sampling time points. Of the animals that received intramuscular vaccinations, 100% had presumed protective titers by the end of the course of vaccination, but only 50% of those sampled at 6.5 mo postvaccination had positive titers. None of the three animals sampled at 21.5 mo postvaccination had positive titers.


Canidae , Distemper/prevention & control , Vaccination/veterinary , Viral Vaccines/immunology , Administration, Oral , Animals , Animals, Zoo , Canarypox virus , Distemper Virus, Canine/immunology , Female , Hemangioma , Male , Vaccines, Synthetic , Viral Vaccines/administration & dosage
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