High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA
Use of CCR5 antagonists requires previous viral tropism determination. The available methods have high cost, are time-consuming, or require highly trained personnel, and sophisticated equipment. We compared a flow cytometry-based tropism assay with geno2pheno method to determine HIV-1 tropism in AID...
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doaj-ef62d97d89884c6db54cf252f87df7b02020-11-25T02:56:31ZengElsevierBrazilian Journal of Infectious Diseases1413-86702015-03-01192163169S1413-86702015000200163High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNAAlex José Leite Torres0Luis Fernando de Macedo Brígido1Marcos Herculano Nunes Abrahão2Ana Luiza Dias Angelo3Gilcivaldo de Jesus Ferreira4Luana Portes Coelho5João Leandro Ferreira6Célia Regina Mayoral Pedroso Jorge7Eduardo Martins Netto8Carlos Brites9Laboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, Brazil; Corresponding author.Grupo de pesquisa para caracterização de Retrovírus em humanos do Instituto Adolfo Lutz, São Paulo, SP, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilGrupo de pesquisa para caracterização de Retrovírus em humanos do Instituto Adolfo Lutz, São Paulo, SP, BrazilGrupo de pesquisa para caracterização de Retrovírus em humanos do Instituto Adolfo Lutz, São Paulo, SP, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilLaboratório de Pesquisa em Infectologia, Hospital Universitário Professor Edgard Santos, Universidade Federal da Bahia, Salvador, BA, BrazilUse of CCR5 antagonists requires previous viral tropism determination. The available methods have high cost, are time-consuming, or require highly trained personnel, and sophisticated equipment. We compared a flow cytometry-based tropism assay with geno2pheno method to determine HIV-1 tropism in AIDS patients, in Bahia, Brazil. We tested peripheral blood mononuclear cells of 102 AIDS patients under antiretroviral therapy by using a cytometry-based tropism assay and geno2pheno assay. Cellular membrane receptors were identified by using CXCR4, CCR5 and CD4 monoclonal antibodies, while detection of cytoplasmic mRNAs for gag and pol HIV regions was achieved by using a labeled probe. Genotypic identification of X4 and R5 tropic viruses was attempted by geno2pheno algorithm. There was a high degree of concordance between cytometry-based tropism assay and geno2pheno algorithm in determination of HIV-1 tropism. Cytometry-based tropism assay demonstrated higher sensitivity and specificity in comparison to geno2pheno, which was used as a gold-standard. One sample could not be amplified by geno2pheno method, but was classified as duotropic by cytometry-based tropism assay. We did not find any association between CD4+ count or plasma HIV-1 RNA viral load and tropism results. The overall performances of cytometry-based tropism assay and geno2pheno assay were almost identical in determination of HIV-1 tropism. Keywords: HIV-1, Tropism, Flow cytometry, Geno2phenohttp://www.sciencedirect.com/science/article/pii/S1413867015000550 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Alex José Leite Torres Luis Fernando de Macedo Brígido Marcos Herculano Nunes Abrahão Ana Luiza Dias Angelo Gilcivaldo de Jesus Ferreira Luana Portes Coelho João Leandro Ferreira Célia Regina Mayoral Pedroso Jorge Eduardo Martins Netto Carlos Brites |
spellingShingle |
Alex José Leite Torres Luis Fernando de Macedo Brígido Marcos Herculano Nunes Abrahão Ana Luiza Dias Angelo Gilcivaldo de Jesus Ferreira Luana Portes Coelho João Leandro Ferreira Célia Regina Mayoral Pedroso Jorge Eduardo Martins Netto Carlos Brites High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA Brazilian Journal of Infectious Diseases |
author_facet |
Alex José Leite Torres Luis Fernando de Macedo Brígido Marcos Herculano Nunes Abrahão Ana Luiza Dias Angelo Gilcivaldo de Jesus Ferreira Luana Portes Coelho João Leandro Ferreira Célia Regina Mayoral Pedroso Jorge Eduardo Martins Netto Carlos Brites |
author_sort |
Alex José Leite Torres |
title |
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA |
title_short |
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA |
title_full |
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA |
title_fullStr |
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA |
title_full_unstemmed |
High degree of concordance between flow cytometry and geno2pheno methods for HIV-1 tropism determination in proviral DNA |
title_sort |
high degree of concordance between flow cytometry and geno2pheno methods for hiv-1 tropism determination in proviral dna |
publisher |
Elsevier |
series |
Brazilian Journal of Infectious Diseases |
issn |
1413-8670 |
publishDate |
2015-03-01 |
description |
Use of CCR5 antagonists requires previous viral tropism determination. The available methods have high cost, are time-consuming, or require highly trained personnel, and sophisticated equipment. We compared a flow cytometry-based tropism assay with geno2pheno method to determine HIV-1 tropism in AIDS patients, in Bahia, Brazil. We tested peripheral blood mononuclear cells of 102 AIDS patients under antiretroviral therapy by using a cytometry-based tropism assay and geno2pheno assay. Cellular membrane receptors were identified by using CXCR4, CCR5 and CD4 monoclonal antibodies, while detection of cytoplasmic mRNAs for gag and pol HIV regions was achieved by using a labeled probe. Genotypic identification of X4 and R5 tropic viruses was attempted by geno2pheno algorithm. There was a high degree of concordance between cytometry-based tropism assay and geno2pheno algorithm in determination of HIV-1 tropism. Cytometry-based tropism assay demonstrated higher sensitivity and specificity in comparison to geno2pheno, which was used as a gold-standard. One sample could not be amplified by geno2pheno method, but was classified as duotropic by cytometry-based tropism assay. We did not find any association between CD4+ count or plasma HIV-1 RNA viral load and tropism results. The overall performances of cytometry-based tropism assay and geno2pheno assay were almost identical in determination of HIV-1 tropism. Keywords: HIV-1, Tropism, Flow cytometry, Geno2pheno |
url |
http://www.sciencedirect.com/science/article/pii/S1413867015000550 |
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