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Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation
Receptive ano-rectal intercourse is a major cause of HIV infection in men having sex with men and in heterosexuals. Current knowledge of the mechanisms of entry and dissemination during HIV rectal transmission is scarce and does not allow the development of preventive strategies. We investigated the...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2011
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090405/ https://www.ncbi.nlm.nih.gov/pubmed/21573012 http://dx.doi.org/10.1371/journal.pone.0019493 |
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author | Ribeiro dos Santos, Patricia Rancez, Magali Prétet, Jean-Luc Michel-Salzat, Alice Messent, Valérie Bogdanova, Anna Couëdel-Courteille, Anne Souil, Evelyne Cheynier, Rémi Butor, Cécile |
author_facet | Ribeiro dos Santos, Patricia Rancez, Magali Prétet, Jean-Luc Michel-Salzat, Alice Messent, Valérie Bogdanova, Anna Couëdel-Courteille, Anne Souil, Evelyne Cheynier, Rémi Butor, Cécile |
author_sort | Ribeiro dos Santos, Patricia |
collection | PubMed |
description | Receptive ano-rectal intercourse is a major cause of HIV infection in men having sex with men and in heterosexuals. Current knowledge of the mechanisms of entry and dissemination during HIV rectal transmission is scarce and does not allow the development of preventive strategies. We investigated the early steps of rectal infection in rhesus macaques inoculated with the pathogenic isolate SIVmac251 and necropsied four hours to nine days later. All macaques were positive for SIV. Control macaques inoculated with heat-inactivated virus were consistently negative for SIV. SIV DNA was detected in the rectum as early as four hours post infection by nested PCR for gag in many laser-microdissected samples of lymphoid aggregates and lamina propria but never in follicle-associated epithelium. Scarce SIV antigen positive cells were observed by immunohistofluorescence in the rectum, among intraepithelial and lamina propria cells as well as in clusters in lymphoid aggregates, four hours post infection and onwards. These cells were T cells and non-T cells that were not epithelial cells, CD68(+) macrophages, DC-SIGN(+) cells or fascin(+) dendritic cells. DC-SIGN(+) cells carried infectious virus. Detection of Env singly spliced mRNA in the mucosa by nested RT-PCR indicated ongoing viral replication. Strikingly, four hours post infection colic lymph nodes were also infected in all macaques as either SIV DNA or infectious virus was recovered. Rapid SIV entry and dissemination is consistent with trans-epithelial transport. Virions appear to cross the follicle-associated epithelium, and also the digestive epithelium. Viral replication could however be more efficient in lymphoid aggregates. The initial sequence of events differs from both vaginal and oral infections, which implies that prevention strategies for rectal transmission will have to be specific. Microbicides will need to protect both digestive and follicle-associated epithelia. Vaccines will need to induce immunity in lymph nodes as well as in the rectum. |
format | Text |
id | pubmed-3090405 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-30904052011-05-13 Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation Ribeiro dos Santos, Patricia Rancez, Magali Prétet, Jean-Luc Michel-Salzat, Alice Messent, Valérie Bogdanova, Anna Couëdel-Courteille, Anne Souil, Evelyne Cheynier, Rémi Butor, Cécile PLoS One Research Article Receptive ano-rectal intercourse is a major cause of HIV infection in men having sex with men and in heterosexuals. Current knowledge of the mechanisms of entry and dissemination during HIV rectal transmission is scarce and does not allow the development of preventive strategies. We investigated the early steps of rectal infection in rhesus macaques inoculated with the pathogenic isolate SIVmac251 and necropsied four hours to nine days later. All macaques were positive for SIV. Control macaques inoculated with heat-inactivated virus were consistently negative for SIV. SIV DNA was detected in the rectum as early as four hours post infection by nested PCR for gag in many laser-microdissected samples of lymphoid aggregates and lamina propria but never in follicle-associated epithelium. Scarce SIV antigen positive cells were observed by immunohistofluorescence in the rectum, among intraepithelial and lamina propria cells as well as in clusters in lymphoid aggregates, four hours post infection and onwards. These cells were T cells and non-T cells that were not epithelial cells, CD68(+) macrophages, DC-SIGN(+) cells or fascin(+) dendritic cells. DC-SIGN(+) cells carried infectious virus. Detection of Env singly spliced mRNA in the mucosa by nested RT-PCR indicated ongoing viral replication. Strikingly, four hours post infection colic lymph nodes were also infected in all macaques as either SIV DNA or infectious virus was recovered. Rapid SIV entry and dissemination is consistent with trans-epithelial transport. Virions appear to cross the follicle-associated epithelium, and also the digestive epithelium. Viral replication could however be more efficient in lymphoid aggregates. The initial sequence of events differs from both vaginal and oral infections, which implies that prevention strategies for rectal transmission will have to be specific. Microbicides will need to protect both digestive and follicle-associated epithelia. Vaccines will need to induce immunity in lymph nodes as well as in the rectum. Public Library of Science 2011-05-09 /pmc/articles/PMC3090405/ /pubmed/21573012 http://dx.doi.org/10.1371/journal.pone.0019493 Text en Ribeiro dos Santos 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 Ribeiro dos Santos, Patricia Rancez, Magali Prétet, Jean-Luc Michel-Salzat, Alice Messent, Valérie Bogdanova, Anna Couëdel-Courteille, Anne Souil, Evelyne Cheynier, Rémi Butor, Cécile Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title | Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title_full | Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title_fullStr | Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title_full_unstemmed | Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title_short | Rapid Dissemination of SIV Follows Multisite Entry after Rectal Inoculation |
title_sort | rapid dissemination of siv follows multisite entry after rectal inoculation |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3090405/ https://www.ncbi.nlm.nih.gov/pubmed/21573012 http://dx.doi.org/10.1371/journal.pone.0019493 |
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