Cargando…

Recombinant Viruses and Early Global HIV-1 Epidemic

Central Africa was the epicenter of the HIV type 1 (HIV-1) pandemic. Understanding the early epidemic in the Democratic Republic of the Congo, formerly Zaire, could provide insight into how HIV evolved and assist vaccine design and intervention efforts. Using enzyme immunosorbent assays, we tested 3...

Descripción completa

Detalles Bibliográficos
Autores principales: Kalish, Marcia L., Robbins, Kenneth E., Pieniazek, Danuta, Schaefer, Amanda, Nzilambi, Nzila, Quinn, Thomas C., St. Louis, Michael E., Youngpairoj, Ae S., Phillips, Jonathan, Jaffe, Harold W., Folks, Thomas M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Centers for Disease Control and Prevention 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323344/
https://www.ncbi.nlm.nih.gov/pubmed/15324542
http://dx.doi.org/10.3201/eid1007.030904
_version_ 1782229178693713920
author Kalish, Marcia L.
Robbins, Kenneth E.
Pieniazek, Danuta
Schaefer, Amanda
Nzilambi, Nzila
Quinn, Thomas C.
St. Louis, Michael E.
Youngpairoj, Ae S.
Phillips, Jonathan
Jaffe, Harold W.
Folks, Thomas M.
author_facet Kalish, Marcia L.
Robbins, Kenneth E.
Pieniazek, Danuta
Schaefer, Amanda
Nzilambi, Nzila
Quinn, Thomas C.
St. Louis, Michael E.
Youngpairoj, Ae S.
Phillips, Jonathan
Jaffe, Harold W.
Folks, Thomas M.
author_sort Kalish, Marcia L.
collection PubMed
description Central Africa was the epicenter of the HIV type 1 (HIV-1) pandemic. Understanding the early epidemic in the Democratic Republic of the Congo, formerly Zaire, could provide insight into how HIV evolved and assist vaccine design and intervention efforts. Using enzyme immunosorbent assays, we tested 3,988 serum samples collected in Kinshasa in the mid-1980s and confirmed seroreactivity by Western blot. Polymerase chain reaction of gag p17, env C2V3C3, and/or gp41; DNA sequencing; and genetic analyses were performed. Gene regions representing all the HIV-1 group M clades and unclassifiable sequences were found. From two or three short gene regions, 37% of the strains represented recombinant viruses, multiple infections, or both, which suggests that if whole genome sequences were available, most of these strains would have mosaic genomes. We propose that the HIV epidemic was well established in central Africa by the early 1980s and that some recombinant viruses most likely seeded the early global epidemic.
format Online
Article
Text
id pubmed-3323344
institution National Center for Biotechnology Information
language English
publishDate 2004
publisher Centers for Disease Control and Prevention
record_format MEDLINE/PubMed
spelling pubmed-33233442012-04-17 Recombinant Viruses and Early Global HIV-1 Epidemic Kalish, Marcia L. Robbins, Kenneth E. Pieniazek, Danuta Schaefer, Amanda Nzilambi, Nzila Quinn, Thomas C. St. Louis, Michael E. Youngpairoj, Ae S. Phillips, Jonathan Jaffe, Harold W. Folks, Thomas M. Emerg Infect Dis Research Central Africa was the epicenter of the HIV type 1 (HIV-1) pandemic. Understanding the early epidemic in the Democratic Republic of the Congo, formerly Zaire, could provide insight into how HIV evolved and assist vaccine design and intervention efforts. Using enzyme immunosorbent assays, we tested 3,988 serum samples collected in Kinshasa in the mid-1980s and confirmed seroreactivity by Western blot. Polymerase chain reaction of gag p17, env C2V3C3, and/or gp41; DNA sequencing; and genetic analyses were performed. Gene regions representing all the HIV-1 group M clades and unclassifiable sequences were found. From two or three short gene regions, 37% of the strains represented recombinant viruses, multiple infections, or both, which suggests that if whole genome sequences were available, most of these strains would have mosaic genomes. We propose that the HIV epidemic was well established in central Africa by the early 1980s and that some recombinant viruses most likely seeded the early global epidemic. Centers for Disease Control and Prevention 2004-07 /pmc/articles/PMC3323344/ /pubmed/15324542 http://dx.doi.org/10.3201/eid1007.030904 Text en https://creativecommons.org/licenses/by/4.0/This is a publication of the U.S. Government. This publication is in the public domain and is therefore without copyright. All text from this work may be reprinted freely. Use of these materials should be properly cited.
spellingShingle Research
Kalish, Marcia L.
Robbins, Kenneth E.
Pieniazek, Danuta
Schaefer, Amanda
Nzilambi, Nzila
Quinn, Thomas C.
St. Louis, Michael E.
Youngpairoj, Ae S.
Phillips, Jonathan
Jaffe, Harold W.
Folks, Thomas M.
Recombinant Viruses and Early Global HIV-1 Epidemic
title Recombinant Viruses and Early Global HIV-1 Epidemic
title_full Recombinant Viruses and Early Global HIV-1 Epidemic
title_fullStr Recombinant Viruses and Early Global HIV-1 Epidemic
title_full_unstemmed Recombinant Viruses and Early Global HIV-1 Epidemic
title_short Recombinant Viruses and Early Global HIV-1 Epidemic
title_sort recombinant viruses and early global hiv-1 epidemic
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3323344/
https://www.ncbi.nlm.nih.gov/pubmed/15324542
http://dx.doi.org/10.3201/eid1007.030904
work_keys_str_mv AT kalishmarcial recombinantvirusesandearlyglobalhiv1epidemic
AT robbinskennethe recombinantvirusesandearlyglobalhiv1epidemic
AT pieniazekdanuta recombinantvirusesandearlyglobalhiv1epidemic
AT schaeferamanda recombinantvirusesandearlyglobalhiv1epidemic
AT nzilambinzila recombinantvirusesandearlyglobalhiv1epidemic
AT quinnthomasc recombinantvirusesandearlyglobalhiv1epidemic
AT stlouismichaele recombinantvirusesandearlyglobalhiv1epidemic
AT youngpairojaes recombinantvirusesandearlyglobalhiv1epidemic
AT phillipsjonathan recombinantvirusesandearlyglobalhiv1epidemic
AT jaffeharoldw recombinantvirusesandearlyglobalhiv1epidemic
AT folksthomasm recombinantvirusesandearlyglobalhiv1epidemic