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Ranavirus infections associated with skin lesions in lizards

Ranaviral disease in amphibians has been studied intensely during the last decade, as associated mass-mortality events are considered to be a global threat to wild animal populations. Several studies have also included other susceptible ectothermic vertebrates (fish and reptiles), but only very few...

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Autores principales: Stöhr, Anke C, Blahak, Silvia, Heckers, Kim O, Wiechert, Jutta, Behncke, Helge, Mathes, Karina, Günther, Pascale, Zwart, Peer, Ball, Inna, Rüschoff, Birgit, Marschang, Rachel E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850657/
https://www.ncbi.nlm.nih.gov/pubmed/24073785
http://dx.doi.org/10.1186/1297-9716-44-84
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author Stöhr, Anke C
Blahak, Silvia
Heckers, Kim O
Wiechert, Jutta
Behncke, Helge
Mathes, Karina
Günther, Pascale
Zwart, Peer
Ball, Inna
Rüschoff, Birgit
Marschang, Rachel E
author_facet Stöhr, Anke C
Blahak, Silvia
Heckers, Kim O
Wiechert, Jutta
Behncke, Helge
Mathes, Karina
Günther, Pascale
Zwart, Peer
Ball, Inna
Rüschoff, Birgit
Marschang, Rachel E
author_sort Stöhr, Anke C
collection PubMed
description Ranaviral disease in amphibians has been studied intensely during the last decade, as associated mass-mortality events are considered to be a global threat to wild animal populations. Several studies have also included other susceptible ectothermic vertebrates (fish and reptiles), but only very few cases of ranavirus infections in lizards have been previously detected. In this study, we focused on clinically suspicious lizards and tested these animals for the presence of ranaviruses. Virological screening of samples from lizards with increased mortality and skin lesions over a course of four years led to the detection of ranaviral infections in seven different groups. Affected species were: brown anoles (Anolis sagrei), Asian glass lizards (Dopasia gracilis), green anoles (Anolis carolinensis), green iguanas (Iguana iguana), and a central bearded dragon (Pogona vitticeps). Purulent to ulcerative-necrotizing dermatitis and hyperkeratosis were diagnosed in pathological examinations. All animals tested positive for the presence of ranavirus by PCR and a part of the major capsid protein (MCP) gene of each virus was sequenced. Three different ranaviruses were isolated in cell culture. The analyzed portions of the MCP gene from each of the five different viruses detected were distinct from one another and were 98.4-100% identical to the corresponding portion of the frog virus 3 (FV3) genome. This is the first description of ranavirus infections in these five lizard species. The similarity in the pathological lesions observed in these different cases indicates that ranaviral infection may be an important differential diagnosis for skin lesions in lizards.
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spelling pubmed-38506572013-12-05 Ranavirus infections associated with skin lesions in lizards Stöhr, Anke C Blahak, Silvia Heckers, Kim O Wiechert, Jutta Behncke, Helge Mathes, Karina Günther, Pascale Zwart, Peer Ball, Inna Rüschoff, Birgit Marschang, Rachel E Vet Res Research Ranaviral disease in amphibians has been studied intensely during the last decade, as associated mass-mortality events are considered to be a global threat to wild animal populations. Several studies have also included other susceptible ectothermic vertebrates (fish and reptiles), but only very few cases of ranavirus infections in lizards have been previously detected. In this study, we focused on clinically suspicious lizards and tested these animals for the presence of ranaviruses. Virological screening of samples from lizards with increased mortality and skin lesions over a course of four years led to the detection of ranaviral infections in seven different groups. Affected species were: brown anoles (Anolis sagrei), Asian glass lizards (Dopasia gracilis), green anoles (Anolis carolinensis), green iguanas (Iguana iguana), and a central bearded dragon (Pogona vitticeps). Purulent to ulcerative-necrotizing dermatitis and hyperkeratosis were diagnosed in pathological examinations. All animals tested positive for the presence of ranavirus by PCR and a part of the major capsid protein (MCP) gene of each virus was sequenced. Three different ranaviruses were isolated in cell culture. The analyzed portions of the MCP gene from each of the five different viruses detected were distinct from one another and were 98.4-100% identical to the corresponding portion of the frog virus 3 (FV3) genome. This is the first description of ranavirus infections in these five lizard species. The similarity in the pathological lesions observed in these different cases indicates that ranaviral infection may be an important differential diagnosis for skin lesions in lizards. BioMed Central 2013 2013-09-27 /pmc/articles/PMC3850657/ /pubmed/24073785 http://dx.doi.org/10.1186/1297-9716-44-84 Text en Copyright © 2013 Stöhr et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Stöhr, Anke C
Blahak, Silvia
Heckers, Kim O
Wiechert, Jutta
Behncke, Helge
Mathes, Karina
Günther, Pascale
Zwart, Peer
Ball, Inna
Rüschoff, Birgit
Marschang, Rachel E
Ranavirus infections associated with skin lesions in lizards
title Ranavirus infections associated with skin lesions in lizards
title_full Ranavirus infections associated with skin lesions in lizards
title_fullStr Ranavirus infections associated with skin lesions in lizards
title_full_unstemmed Ranavirus infections associated with skin lesions in lizards
title_short Ranavirus infections associated with skin lesions in lizards
title_sort ranavirus infections associated with skin lesions in lizards
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3850657/
https://www.ncbi.nlm.nih.gov/pubmed/24073785
http://dx.doi.org/10.1186/1297-9716-44-84
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