Use of the sensitive/less-sensitive (detuned) EIA strategy for targeting genetic analysis of HIV-1 to recently infected blood donors

Detalhes bibliográficos
Autor(a) principal: Machado, Daisy M. [UNIFESP}
Data de Publicação: 2002
Outros Autores: 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.
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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spelling 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
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