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Ecopathology of Ranaviruses Infecting Amphibians

Overview
Journal Viruses
Publisher MDPI
Specialty Microbiology
Date 2011 Dec 14
PMID 22163349
Citations 56
Authors
Affiliations
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Abstract

Ranaviruses are capable of infecting amphibians from at least 14 families and over 70 individual species. Ranaviruses infect multiple cell types, often culminating in organ necrosis and massive hemorrhaging. Subclinical infections have been documented, although their role in ranavirus persistence and emergence remains unclear. Water is an effective transmission medium for ranaviruses, and survival outside the host may be for significant duration. In aquatic communities, amphibians, reptiles and fish may serve as reservoirs. Controlled studies have shown that susceptibility to ranavirus infection and disease varies among amphibian species and developmental stages, and likely is impacted by host-pathogen coevolution, as well as, exogenous environmental factors. Field studies have demonstrated that the likelihood of epizootics is increased in areas of cattle grazing, where aquatic vegetation is sparse and water quality is poor. Translocation of infected amphibians through commercial trade (e.g., food, fish bait, pet industry) contributes to the spread of ranaviruses. Such introductions may be of particular concern, as several studies report that ranaviruses isolated from ranaculture, aquaculture, and bait facilities have greater virulence (i.e., ability to cause disease) than wild-type isolates. Future investigations should focus on the genetic basis for pathogen virulence and host susceptibility, ecological and anthropogenic mechanisms contributing to emergence, and vaccine development for use in captive populations and species reintroduction programs.

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References
1.
Majji S, LaPatra S, Long S, Sample R, Bryan L, Sinning A . Rana catesbeiana virus Z (RCV-Z): a novel pathogenic ranavirus. Dis Aquat Organ. 2007; 73(1):1-11. DOI: 10.3354/dao073001. View

2.
Haislip N, Gray M, Hoverman J, Miller D . Development and disease: how susceptibility to an emerging pathogen changes through anuran development. PLoS One. 2011; 6(7):e22307. PMC: 3142128. DOI: 10.1371/journal.pone.0022307. View

3.
Robert J, Abramowitz L, Gantress J, Morales H . Xenopus laevis: a possible vector of Ranavirus infection?. J Wildl Dis. 2007; 43(4):645-52. DOI: 10.7589/0090-3558-43.4.645. View

4.
Bryan L, Baldwin C, Gray M, Miller D . Efficacy of select disinfectants at inactivating Ranavirus. Dis Aquat Organ. 2009; 84(2):89-94. DOI: 10.3354/dao02036. View

5.
Gray M, Miller D, Hoverman J . Ecology and pathology of amphibian ranaviruses. Dis Aquat Organ. 2010; 87(3):243-66. DOI: 10.3354/dao02138. View