Cargando…

Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation

The human immunodeficiency virus (HIV) is primarily transmitted by heterosexual contact, and approximately equal numbers of men and women worldwide are infected with the virus. Understanding the biology of HIV acquisition and dissemination in men exposed to the virus by insertive penile intercourse...

Descripción completa

Detalles Bibliográficos
Autores principales: Ma, Zhong-Min, Dutra, Joseph, Fritts, Linda, Miller, Christopher J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810538/
https://www.ncbi.nlm.nih.gov/pubmed/26865706
http://dx.doi.org/10.1128/JVI.02947-15
_version_ 1782423832286461952
author Ma, Zhong-Min
Dutra, Joseph
Fritts, Linda
Miller, Christopher J.
author_facet Ma, Zhong-Min
Dutra, Joseph
Fritts, Linda
Miller, Christopher J.
author_sort Ma, Zhong-Min
collection PubMed
description The human immunodeficiency virus (HIV) is primarily transmitted by heterosexual contact, and approximately equal numbers of men and women worldwide are infected with the virus. Understanding the biology of HIV acquisition and dissemination in men exposed to the virus by insertive penile intercourse is likely to help with the rational design of vaccines that can limit or prevent HIV transmission. To characterize the target cells and dissemination pathways involved in establishing systemic simian immunodeficiency virus (SIV) infection, we necropsied male rhesus macaques at 1, 3, 7, and 14 days after penile SIV inoculation and quantified the levels of unspliced SIV RNA and spliced SIV RNA in tissue lysates and the number of SIV RNA-positive cells in tissue sections. We found that penile (glans, foreskin, coronal sulcus) T cells and, to a lesser extent, macrophages and dendritic cells are primary targets of infection and that SIV rapidly reaches the regional lymph nodes. At 7 days after inoculation, SIV had disseminated to the blood, systemic lymph nodes, and mucosal lymphoid tissues. Further, at 7 days postinoculation (p.i.), spliced SIV RNA levels were the highest in the genital lymph nodes, indicating that this is the site where the infection is initially amplified. By 14 days p.i., spliced SIV RNA levels were high in all tissues, but they were the highest in the gastrointestinal tract, indicating that the primary site of virus replication had shifted from the genital lymph nodes to the gut. The stepwise pattern of virus replication and dissemination described here suggests that vaccine-elicited immune responses in the genital lymph nodes could help prevent infection after penile SIV challenge. IMPORTANCE To be the most effective, vaccines should produce antiviral immune responses in the anatomic sites of virus replication. Thus, understanding the path taken by HIV from the mucosal surfaces, which are the site of virus exposure, to the deeper tissues where the virus replicates will provide insight into where AIDS vaccines should produce immunity to be the most effective. In this study, we determined that, by day 7 after penile inoculation, SIV has moved first to the inguinal lymph nodes and replicates to high levels. Although the virus is widely disseminated to other tissues by day 7, replication is largely limited to the inguinal lymph nodes. The step-by-step movement of SIV from penile mucosal surfaces to the draining lymph nodes may allow an HIV vaccine that produces immunity in these lymph nodes to block HIV from establishing an infection in an exposed person.
format Online
Article
Text
id pubmed-4810538
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher American Society for Microbiology
record_format MEDLINE/PubMed
spelling pubmed-48105382016-04-04 Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation Ma, Zhong-Min Dutra, Joseph Fritts, Linda Miller, Christopher J. J Virol Pathogenesis and Immunity The human immunodeficiency virus (HIV) is primarily transmitted by heterosexual contact, and approximately equal numbers of men and women worldwide are infected with the virus. Understanding the biology of HIV acquisition and dissemination in men exposed to the virus by insertive penile intercourse is likely to help with the rational design of vaccines that can limit or prevent HIV transmission. To characterize the target cells and dissemination pathways involved in establishing systemic simian immunodeficiency virus (SIV) infection, we necropsied male rhesus macaques at 1, 3, 7, and 14 days after penile SIV inoculation and quantified the levels of unspliced SIV RNA and spliced SIV RNA in tissue lysates and the number of SIV RNA-positive cells in tissue sections. We found that penile (glans, foreskin, coronal sulcus) T cells and, to a lesser extent, macrophages and dendritic cells are primary targets of infection and that SIV rapidly reaches the regional lymph nodes. At 7 days after inoculation, SIV had disseminated to the blood, systemic lymph nodes, and mucosal lymphoid tissues. Further, at 7 days postinoculation (p.i.), spliced SIV RNA levels were the highest in the genital lymph nodes, indicating that this is the site where the infection is initially amplified. By 14 days p.i., spliced SIV RNA levels were high in all tissues, but they were the highest in the gastrointestinal tract, indicating that the primary site of virus replication had shifted from the genital lymph nodes to the gut. The stepwise pattern of virus replication and dissemination described here suggests that vaccine-elicited immune responses in the genital lymph nodes could help prevent infection after penile SIV challenge. IMPORTANCE To be the most effective, vaccines should produce antiviral immune responses in the anatomic sites of virus replication. Thus, understanding the path taken by HIV from the mucosal surfaces, which are the site of virus exposure, to the deeper tissues where the virus replicates will provide insight into where AIDS vaccines should produce immunity to be the most effective. In this study, we determined that, by day 7 after penile inoculation, SIV has moved first to the inguinal lymph nodes and replicates to high levels. Although the virus is widely disseminated to other tissues by day 7, replication is largely limited to the inguinal lymph nodes. The step-by-step movement of SIV from penile mucosal surfaces to the draining lymph nodes may allow an HIV vaccine that produces immunity in these lymph nodes to block HIV from establishing an infection in an exposed person. American Society for Microbiology 2016-03-28 /pmc/articles/PMC4810538/ /pubmed/26865706 http://dx.doi.org/10.1128/JVI.02947-15 Text en Copyright © 2016 Ma et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Pathogenesis and Immunity
Ma, Zhong-Min
Dutra, Joseph
Fritts, Linda
Miller, Christopher J.
Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title_full Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title_fullStr Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title_full_unstemmed Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title_short Lymphatic Dissemination of Simian Immunodeficiency Virus after Penile Inoculation
title_sort lymphatic dissemination of simian immunodeficiency virus after penile inoculation
topic Pathogenesis and Immunity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4810538/
https://www.ncbi.nlm.nih.gov/pubmed/26865706
http://dx.doi.org/10.1128/JVI.02947-15
work_keys_str_mv AT mazhongmin lymphaticdisseminationofsimianimmunodeficiencyvirusafterpenileinoculation
AT dutrajoseph lymphaticdisseminationofsimianimmunodeficiencyvirusafterpenileinoculation
AT frittslinda lymphaticdisseminationofsimianimmunodeficiencyvirusafterpenileinoculation
AT millerchristopherj lymphaticdisseminationofsimianimmunodeficiencyvirusafterpenileinoculation