Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors
Autor(a) principal: | |
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Data de Publicação: | 2002 |
Outros Autores: | , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1097/00002030-200201040-00014 http://repositorio.unifesp.br/handle/11600/26730 |
Resumo: | Objective: To corroborate the validity of the recently developed sensitive/less sensitive (S/LS) dual enzyme immunoassay (EIA) strategy for the detection of recently infected individuals and to genetically analyze recently transmitted strains of HIV-1 in a US blood donor population.Design: the S/LS EIA strategy was used to identify 33 recently infected subjects among 281 enrolled HIV-1 seropositive blood donors (from a total of 410 HIV-1 infected subjects identified from 5 230 463 blood donations screened by participating US blood centers in 1995-1996)Methods: We analysed three host response and viral characteristics were associated with recent HIV-1 infection: rapidly increasing EIA optical density (OD) values, genetically homogeneous env gene quasispecies, and putative non-syncytium inducing env V3 loop sequences. the drug resistance genotypes of the recently transmitted strains were determined by DNA sequencing.Results: Increasing EIA OD values, clonal HIV-1 quasispecies and V3 loop sequences with inferred NSI phenotypes were generally detected in LS EIA non-reactive samples, Thirty-two subtype B and one CRF02_AG recombinant HIV-1 were detected. Genetic evidence for drug resistance to zidovudine (K70R) and non-nucleoside analog reverse transcriptase inhibitors (VI 081) was detected in one strain each, and three other strains showed the presence of accessory protease inhibitor resistance mutations.Conclusions: Immunologic and virologic results further substantiate the validity of the S/LS EIA strategy for the detection of recent infections and illustrate its use for targeting molecular and epidemiological investigations to incident cases identified from large cross-sectional screening programs, rather than the more costly and logistically difficult longitudinal studies. (C) 2002 Lippincott Williams Wilkins. |
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Repositório Institucional da UNIFESP |
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Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donorsacute infectionepidemiologyHIV diagnostic testsHIV sequence variabilityseroprevalencesurveillancedetuned EIAObjective: To corroborate the validity of the recently developed sensitive/less sensitive (S/LS) dual enzyme immunoassay (EIA) strategy for the detection of recently infected individuals and to genetically analyze recently transmitted strains of HIV-1 in a US blood donor population.Design: the S/LS EIA strategy was used to identify 33 recently infected subjects among 281 enrolled HIV-1 seropositive blood donors (from a total of 410 HIV-1 infected subjects identified from 5 230 463 blood donations screened by participating US blood centers in 1995-1996)Methods: We analysed three host response and viral characteristics were associated with recent HIV-1 infection: rapidly increasing EIA optical density (OD) values, genetically homogeneous env gene quasispecies, and putative non-syncytium inducing env V3 loop sequences. the drug resistance genotypes of the recently transmitted strains were determined by DNA sequencing.Results: Increasing EIA OD values, clonal HIV-1 quasispecies and V3 loop sequences with inferred NSI phenotypes were generally detected in LS EIA non-reactive samples, Thirty-two subtype B and one CRF02_AG recombinant HIV-1 were detected. Genetic evidence for drug resistance to zidovudine (K70R) and non-nucleoside analog reverse transcriptase inhibitors (VI 081) was detected in one strain each, and three other strains showed the presence of accessory protease inhibitor resistance mutations.Conclusions: Immunologic and virologic results further substantiate the validity of the S/LS EIA strategy for the detection of recent infections and illustrate its use for targeting molecular and epidemiological investigations to incident cases identified from large cross-sectional screening programs, rather than the more costly and logistically difficult longitudinal studies. (C) 2002 Lippincott Williams Wilkins.Blood Ctr Pacific, San Francisco, CA 94118 USAUniversidade Federal de São Paulo, São Paulo, BrazilUniv Calif San Francisco, Dept Med, San Francisco, CA USANatl Blood Data Resource Ctr, Bethesda, MD USACtr Dis Control & Prevent, Atlanta, GA USAUniv Calif San Francisco, Dept Lab Med, San Francisco, CA 94143 USAUniversidade Federal de São Paulo, São Paulo, BrazilWeb of ScienceLippincott Williams & WilkinsBlood Ctr PacificUniversidade Federal de São Paulo (UNIFESP)Univ Calif San FranciscoNatl Blood Data Resource CtrCtr Dis Control & PreventMachado, Daisy M. [UNIFESP}Delwart, E. L.Diaz, Ricardo Sobhie [UNIFESP]Oliveira, Carlos F. de [UNIFESP]Alves, Katia [UNIFESP]Rawal, B. D.Sullivan, M.Gwinn, M.Clark, K. A.Busch, M. P.2016-01-24T12:33:13Z2016-01-24T12:33:13Z2002-01-04info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion113-119http://dx.doi.org/10.1097/00002030-200201040-00014Aids. Philadelphia: Lippincott Williams & Wilkins, v. 16, n. 1, p. 113-119, 2002.10.1097/00002030-200201040-000140269-9370http://repositorio.unifesp.br/handle/11600/26730WOS:000173225800014engAidsinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2016-01-24T10:33:13Zoai:repositorio.unifesp.br/:11600/26730Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652016-01-24T10:33:13Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
title |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
spellingShingle |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors Machado, Daisy M. [UNIFESP} acute infection epidemiology HIV diagnostic tests HIV sequence variability seroprevalence surveillance detuned EIA |
title_short |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
title_full |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
title_fullStr |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
title_full_unstemmed |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
title_sort |
Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors |
author |
Machado, Daisy M. [UNIFESP} |
author_facet |
Machado, Daisy M. [UNIFESP} Delwart, E. L. Diaz, Ricardo Sobhie [UNIFESP] Oliveira, Carlos F. de [UNIFESP] Alves, Katia [UNIFESP] Rawal, B. D. Sullivan, M. Gwinn, M. Clark, K. A. Busch, M. P. |
author_role |
author |
author2 |
Delwart, E. L. Diaz, Ricardo Sobhie [UNIFESP] Oliveira, Carlos F. de [UNIFESP] Alves, Katia [UNIFESP] Rawal, B. D. Sullivan, M. Gwinn, M. Clark, K. A. Busch, M. P. |
author2_role |
author author author author author author author author author |
dc.contributor.none.fl_str_mv |
Blood Ctr Pacific Universidade Federal de São Paulo (UNIFESP) Univ Calif San Francisco Natl Blood Data Resource Ctr Ctr Dis Control & Prevent |
dc.contributor.author.fl_str_mv |
Machado, Daisy M. [UNIFESP} Delwart, E. L. Diaz, Ricardo Sobhie [UNIFESP] Oliveira, Carlos F. de [UNIFESP] Alves, Katia [UNIFESP] Rawal, B. D. Sullivan, M. Gwinn, M. Clark, K. A. Busch, M. P. |
dc.subject.por.fl_str_mv |
acute infection epidemiology HIV diagnostic tests HIV sequence variability seroprevalence surveillance detuned EIA |
topic |
acute infection epidemiology HIV diagnostic tests HIV sequence variability seroprevalence surveillance detuned EIA |
description |
Objective: To corroborate the validity of the recently developed sensitive/less sensitive (S/LS) dual enzyme immunoassay (EIA) strategy for the detection of recently infected individuals and to genetically analyze recently transmitted strains of HIV-1 in a US blood donor population.Design: the S/LS EIA strategy was used to identify 33 recently infected subjects among 281 enrolled HIV-1 seropositive blood donors (from a total of 410 HIV-1 infected subjects identified from 5 230 463 blood donations screened by participating US blood centers in 1995-1996)Methods: We analysed three host response and viral characteristics were associated with recent HIV-1 infection: rapidly increasing EIA optical density (OD) values, genetically homogeneous env gene quasispecies, and putative non-syncytium inducing env V3 loop sequences. the drug resistance genotypes of the recently transmitted strains were determined by DNA sequencing.Results: Increasing EIA OD values, clonal HIV-1 quasispecies and V3 loop sequences with inferred NSI phenotypes were generally detected in LS EIA non-reactive samples, Thirty-two subtype B and one CRF02_AG recombinant HIV-1 were detected. Genetic evidence for drug resistance to zidovudine (K70R) and non-nucleoside analog reverse transcriptase inhibitors (VI 081) was detected in one strain each, and three other strains showed the presence of accessory protease inhibitor resistance mutations.Conclusions: Immunologic and virologic results further substantiate the validity of the S/LS EIA strategy for the detection of recent infections and illustrate its use for targeting molecular and epidemiological investigations to incident cases identified from large cross-sectional screening programs, rather than the more costly and logistically difficult longitudinal studies. (C) 2002 Lippincott Williams Wilkins. |
publishDate |
2002 |
dc.date.none.fl_str_mv |
2002-01-04 2016-01-24T12:33:13Z 2016-01-24T12:33:13Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1097/00002030-200201040-00014 Aids. Philadelphia: Lippincott Williams & Wilkins, v. 16, n. 1, p. 113-119, 2002. 10.1097/00002030-200201040-00014 0269-9370 http://repositorio.unifesp.br/handle/11600/26730 WOS:000173225800014 |
url |
http://dx.doi.org/10.1097/00002030-200201040-00014 http://repositorio.unifesp.br/handle/11600/26730 |
identifier_str_mv |
Aids. Philadelphia: Lippincott Williams & Wilkins, v. 16, n. 1, p. 113-119, 2002. 10.1097/00002030-200201040-00014 0269-9370 WOS:000173225800014 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Aids |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
113-119 |
dc.publisher.none.fl_str_mv |
Lippincott Williams & Wilkins |
publisher.none.fl_str_mv |
Lippincott Williams & Wilkins |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268408853692416 |