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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...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Centers for Disease Control and Prevention
2004
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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 |
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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 |
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