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Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection

To understand the pathogenicity of acquired immune deficiency syndrome (AIDS), it is important to clarify where, when and how the virus replicates in the body of infected individuals. To identify the major virus replication site at the end stage of SHIV infection, we investigated the systemic tissue...

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Autores principales: Matsuyama-Murata, Megumi, Inaba, Katsuhisa, Horiuchi, Reii, Fukazawa, Yoshinori, Ibuki, Kentaro, Hayami, Masanori, Miura, Tomoyuki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717482/
https://www.ncbi.nlm.nih.gov/pubmed/23885255
http://dx.doi.org/10.3389/fmicb.2013.00204
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author Matsuyama-Murata, Megumi
Inaba, Katsuhisa
Horiuchi, Reii
Fukazawa, Yoshinori
Ibuki, Kentaro
Hayami, Masanori
Miura, Tomoyuki
author_facet Matsuyama-Murata, Megumi
Inaba, Katsuhisa
Horiuchi, Reii
Fukazawa, Yoshinori
Ibuki, Kentaro
Hayami, Masanori
Miura, Tomoyuki
author_sort Matsuyama-Murata, Megumi
collection PubMed
description To understand the pathogenicity of acquired immune deficiency syndrome (AIDS), it is important to clarify where, when and how the virus replicates in the body of infected individuals. To identify the major virus replication site at the end stage of SHIV infection, we investigated the systemic tissues of SHIV-infected monkeys that developed AIDS-like disease. We quantified proviral DNA, and compared the mutation patterns of the viruses in various systemic tissues and in peripheral blood through phylogenetic analysis of the full genome sequence. We found that the amounts of proviral DNA detected in internal tissues were higher than those in peripheral blood mononuclear cells. In the sequence and phylogenetic tree analyses, the mutation patterns of the viruses in each tissue were generally different. However, the mutation pattern of the viruses in the jejunum and mesenteric lymph node were most similar to that of plasma viral RNA among the tissues examined in all three monkeys. In two of the three monkeys, which were euthanized earlier, viruses in the jejunum and mesenteric lymph node occupied the root position of the phylogenetic tree. Furthermore, in these tissues, more than 50% of SHIV-expressing cells were identified as macrophages based on co-expression of CD68. These results suggest that macrophages of the small intestine and/or mesenteric lymph node are the major virus production site at the end stage of SHIV infection of macaques.
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spelling pubmed-37174822013-07-24 Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection Matsuyama-Murata, Megumi Inaba, Katsuhisa Horiuchi, Reii Fukazawa, Yoshinori Ibuki, Kentaro Hayami, Masanori Miura, Tomoyuki Front Microbiol Microbiology To understand the pathogenicity of acquired immune deficiency syndrome (AIDS), it is important to clarify where, when and how the virus replicates in the body of infected individuals. To identify the major virus replication site at the end stage of SHIV infection, we investigated the systemic tissues of SHIV-infected monkeys that developed AIDS-like disease. We quantified proviral DNA, and compared the mutation patterns of the viruses in various systemic tissues and in peripheral blood through phylogenetic analysis of the full genome sequence. We found that the amounts of proviral DNA detected in internal tissues were higher than those in peripheral blood mononuclear cells. In the sequence and phylogenetic tree analyses, the mutation patterns of the viruses in each tissue were generally different. However, the mutation pattern of the viruses in the jejunum and mesenteric lymph node were most similar to that of plasma viral RNA among the tissues examined in all three monkeys. In two of the three monkeys, which were euthanized earlier, viruses in the jejunum and mesenteric lymph node occupied the root position of the phylogenetic tree. Furthermore, in these tissues, more than 50% of SHIV-expressing cells were identified as macrophages based on co-expression of CD68. These results suggest that macrophages of the small intestine and/or mesenteric lymph node are the major virus production site at the end stage of SHIV infection of macaques. Frontiers Media S.A. 2013-07-22 /pmc/articles/PMC3717482/ /pubmed/23885255 http://dx.doi.org/10.3389/fmicb.2013.00204 Text en Copyright © 2013 Matsuyama-Murata, Inaba, Horiuchi, Fukazawa, Ibuki, Hayami and Miura. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc.
spellingShingle Microbiology
Matsuyama-Murata, Megumi
Inaba, Katsuhisa
Horiuchi, Reii
Fukazawa, Yoshinori
Ibuki, Kentaro
Hayami, Masanori
Miura, Tomoyuki
Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title_full Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title_fullStr Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title_full_unstemmed Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title_short Genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
title_sort genetic similarity of circulating and small intestinal virus at the end stage of acute pathogenic simian-human immunodeficiency virus infection
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3717482/
https://www.ncbi.nlm.nih.gov/pubmed/23885255
http://dx.doi.org/10.3389/fmicb.2013.00204
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