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Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan

Epidemiological studies suggest that retroviruses, including human immunodeficiency virus type 1, are associated with cardiomyopathy and myocarditis, but a causal relationship remains to be established. We encountered unusual cardiomyocyte hypertrophy and mitosis in Japanese native fowls infected wi...

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Autores principales: Nakamura, Sayuri, Ochiai, Kenji, Ochi, Akihiro, Yabushita, Hiroki, Abe, Asumi, Kishi, Sayaka, Sunden, Yuji, Umemura, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900567/
https://www.ncbi.nlm.nih.gov/pubmed/24466146
http://dx.doi.org/10.1371/journal.pone.0086546
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author Nakamura, Sayuri
Ochiai, Kenji
Ochi, Akihiro
Yabushita, Hiroki
Abe, Asumi
Kishi, Sayaka
Sunden, Yuji
Umemura, Takashi
author_facet Nakamura, Sayuri
Ochiai, Kenji
Ochi, Akihiro
Yabushita, Hiroki
Abe, Asumi
Kishi, Sayaka
Sunden, Yuji
Umemura, Takashi
author_sort Nakamura, Sayuri
collection PubMed
description Epidemiological studies suggest that retroviruses, including human immunodeficiency virus type 1, are associated with cardiomyopathy and myocarditis, but a causal relationship remains to be established. We encountered unusual cardiomyocyte hypertrophy and mitosis in Japanese native fowls infected with subgroup A of the avian leukosis viruses (ALVs-A), which belong to the genus Alpharetrovirus of the family Retroviridae and mainly induce lymphoid neoplasm in chickens. The affected hearts were evaluated by histopathology and immunohistochemistry, viral isolation, viral genome sequencing and experimental infection. There was non-suppurative myocarditis in eighteen fowls and seven of them had abnormal cardiomyocytes, which were distributed predominantly in the left ventricular wall and showed hypertrophic cytoplasm and atypical large nuclei. Nuclear chains and mitosis were frequently noted in these cardiomyocytes and immunohistochemistry for proliferating cell nuclear antigen supported the enhancement of mitotic activity. ALVs were isolated from all affected cases and phylogenic analysis of envSU genes showed that the isolates were mainly classified into two different clusters, suggesting viral genome diversity. In ovo experimental infection with two of the isolates was demonstrated to cause myocarditis and cardiomyocyte hypertrophy similar to those in the naturally occurring lesions and cardiac hamartoma (rhabdomyoma) in a shorter period of time (at 70 days of age) than expected. These results indicate that ALVs cause myocarditis as well as cardiomyocyte abnormality in chickens, implying a pathogenetic mechanism different from insertional mutagenesis and the existence of retrovirus-induced heart disorder.
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spelling pubmed-39005672014-01-24 Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan Nakamura, Sayuri Ochiai, Kenji Ochi, Akihiro Yabushita, Hiroki Abe, Asumi Kishi, Sayaka Sunden, Yuji Umemura, Takashi PLoS One Research Article Epidemiological studies suggest that retroviruses, including human immunodeficiency virus type 1, are associated with cardiomyopathy and myocarditis, but a causal relationship remains to be established. We encountered unusual cardiomyocyte hypertrophy and mitosis in Japanese native fowls infected with subgroup A of the avian leukosis viruses (ALVs-A), which belong to the genus Alpharetrovirus of the family Retroviridae and mainly induce lymphoid neoplasm in chickens. The affected hearts were evaluated by histopathology and immunohistochemistry, viral isolation, viral genome sequencing and experimental infection. There was non-suppurative myocarditis in eighteen fowls and seven of them had abnormal cardiomyocytes, which were distributed predominantly in the left ventricular wall and showed hypertrophic cytoplasm and atypical large nuclei. Nuclear chains and mitosis were frequently noted in these cardiomyocytes and immunohistochemistry for proliferating cell nuclear antigen supported the enhancement of mitotic activity. ALVs were isolated from all affected cases and phylogenic analysis of envSU genes showed that the isolates were mainly classified into two different clusters, suggesting viral genome diversity. In ovo experimental infection with two of the isolates was demonstrated to cause myocarditis and cardiomyocyte hypertrophy similar to those in the naturally occurring lesions and cardiac hamartoma (rhabdomyoma) in a shorter period of time (at 70 days of age) than expected. These results indicate that ALVs cause myocarditis as well as cardiomyocyte abnormality in chickens, implying a pathogenetic mechanism different from insertional mutagenesis and the existence of retrovirus-induced heart disorder. Public Library of Science 2014-01-23 /pmc/articles/PMC3900567/ /pubmed/24466146 http://dx.doi.org/10.1371/journal.pone.0086546 Text en © 2014 Nakamura et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Nakamura, Sayuri
Ochiai, Kenji
Ochi, Akihiro
Yabushita, Hiroki
Abe, Asumi
Kishi, Sayaka
Sunden, Yuji
Umemura, Takashi
Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title_full Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title_fullStr Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title_full_unstemmed Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title_short Cardiac Pathology and Molecular Epidemiology by Avian Leukosis Viruses in Japan
title_sort cardiac pathology and molecular epidemiology by avian leukosis viruses in japan
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3900567/
https://www.ncbi.nlm.nih.gov/pubmed/24466146
http://dx.doi.org/10.1371/journal.pone.0086546
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