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Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)

A growing number of emerging HIV-1 recombinants classified as circulating recombinant forms (CRFs) have been identified in Southeast Asia in recent years, establishing a molecular diversity of increasing complexity in the region. Here, we constructed a replication-competent HIV-1 clone for CRF33_01B...

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Autores principales: Tee, Kok Keng, Kusagawa, Shigeru, Li, Xiao-Jie, Onogi, Narumi, Isogai, Maya, Hase, Saiki, Uenishi, Rie, Liao, Huanan, Kamarulzaman, Adeeba, Takebe, Yutaka
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722735/
https://www.ncbi.nlm.nih.gov/pubmed/19688091
http://dx.doi.org/10.1371/journal.pone.0006666
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author Tee, Kok Keng
Kusagawa, Shigeru
Li, Xiao-Jie
Onogi, Narumi
Isogai, Maya
Hase, Saiki
Uenishi, Rie
Liao, Huanan
Kamarulzaman, Adeeba
Takebe, Yutaka
author_facet Tee, Kok Keng
Kusagawa, Shigeru
Li, Xiao-Jie
Onogi, Narumi
Isogai, Maya
Hase, Saiki
Uenishi, Rie
Liao, Huanan
Kamarulzaman, Adeeba
Takebe, Yutaka
author_sort Tee, Kok Keng
collection PubMed
description A growing number of emerging HIV-1 recombinants classified as circulating recombinant forms (CRFs) have been identified in Southeast Asia in recent years, establishing a molecular diversity of increasing complexity in the region. Here, we constructed a replication-competent HIV-1 clone for CRF33_01B (designated p05MYKL045.1), a newly identified recombinant comprised of CRF01_AE and subtype B. p05MYKL045.1 was reconstituted by cloning of the near full-length HIV-1 sequence from a newly-diagnosed individual presumably infected heterosexually in Kuala Lumpur, Malaysia. The chimeric clone, which contains the 5′ LTR (long terminal repeat) region of p93JP-NH1 (a previously isolated CRF01_AE infectious clone), showed robust viral replication in the human peripheral blood mononuclear cells. This clone demonstrated robust viral propagation and profound syncytium formation in CD4(+), CXCR4-expressing human glioma NP-2 cells, indicating that p05MYKL045.1 is a CXCR4-using virus. Viral propagation, however, was not detected in various human T cell lines including MT-2, M8166, Sup-T1, H9, Jurkat, Molt-4 and PM1. p05MYKL045.1 appears to proliferate only in restricted host range, suggesting that unknown viral and/or cellular host factors may play a role in viral infectivity and replication in human T cell lines. Availability of a CRF33_01B molecular clone will be useful in facilitating the development of vaccine candidates that match the HIV-1 strains circulating in Southeast Asia.
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spelling pubmed-27227352009-08-18 Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B) Tee, Kok Keng Kusagawa, Shigeru Li, Xiao-Jie Onogi, Narumi Isogai, Maya Hase, Saiki Uenishi, Rie Liao, Huanan Kamarulzaman, Adeeba Takebe, Yutaka PLoS One Research Article A growing number of emerging HIV-1 recombinants classified as circulating recombinant forms (CRFs) have been identified in Southeast Asia in recent years, establishing a molecular diversity of increasing complexity in the region. Here, we constructed a replication-competent HIV-1 clone for CRF33_01B (designated p05MYKL045.1), a newly identified recombinant comprised of CRF01_AE and subtype B. p05MYKL045.1 was reconstituted by cloning of the near full-length HIV-1 sequence from a newly-diagnosed individual presumably infected heterosexually in Kuala Lumpur, Malaysia. The chimeric clone, which contains the 5′ LTR (long terminal repeat) region of p93JP-NH1 (a previously isolated CRF01_AE infectious clone), showed robust viral replication in the human peripheral blood mononuclear cells. This clone demonstrated robust viral propagation and profound syncytium formation in CD4(+), CXCR4-expressing human glioma NP-2 cells, indicating that p05MYKL045.1 is a CXCR4-using virus. Viral propagation, however, was not detected in various human T cell lines including MT-2, M8166, Sup-T1, H9, Jurkat, Molt-4 and PM1. p05MYKL045.1 appears to proliferate only in restricted host range, suggesting that unknown viral and/or cellular host factors may play a role in viral infectivity and replication in human T cell lines. Availability of a CRF33_01B molecular clone will be useful in facilitating the development of vaccine candidates that match the HIV-1 strains circulating in Southeast Asia. Public Library of Science 2009-08-18 /pmc/articles/PMC2722735/ /pubmed/19688091 http://dx.doi.org/10.1371/journal.pone.0006666 Text en Tee et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Tee, Kok Keng
Kusagawa, Shigeru
Li, Xiao-Jie
Onogi, Narumi
Isogai, Maya
Hase, Saiki
Uenishi, Rie
Liao, Huanan
Kamarulzaman, Adeeba
Takebe, Yutaka
Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title_full Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title_fullStr Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title_full_unstemmed Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title_short Isolation and Characterization of a Replication-Competent Molecular Clone of an HIV-1 Circulating Recombinant Form (CRF33_01B)
title_sort isolation and characterization of a replication-competent molecular clone of an hiv-1 circulating recombinant form (crf33_01b)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722735/
https://www.ncbi.nlm.nih.gov/pubmed/19688091
http://dx.doi.org/10.1371/journal.pone.0006666
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