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Construction of a High Titer Infectious HIV-1 Subtype C Proviral Clone from South Africa

The Human Immunodeficiency Virus type 1 (HIV-1) subtype C is currently the predominant subtype worldwide. Cell culture studies of Sub-Saharan African subtype C proviral plasmids are hampered by the low replication capacity of the resulting viruses, although viral loads in subtype C infected patients...

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Detalles Bibliográficos
Autores principales: Jacobs, Graeme B., Bock, Stefanie, Schuch, Anita, Moschall, Rebecca, Schrom, Eva-Maria, Zahn, Juliane, Reuter, Christian, Preiser, Wolfgang, Rethwilm, Axel, Engelbrecht, Susan, Kerkau, Thomas, Bodem, Jochen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3499832/
https://www.ncbi.nlm.nih.gov/pubmed/23170185
http://dx.doi.org/10.3390/v4091830
Descripción
Sumario:The Human Immunodeficiency Virus type 1 (HIV-1) subtype C is currently the predominant subtype worldwide. Cell culture studies of Sub-Saharan African subtype C proviral plasmids are hampered by the low replication capacity of the resulting viruses, although viral loads in subtype C infected patients are as high as those from patients with subtype B. Here, we describe the sequencing and construction of a new HIV-1 subtype C proviral clone (pZAC), replicating more than one order of magnitude better than the previous subtype C plasmids. We identify the env-region for being the determinant for the higher viral titers and the pZAC Env to be M-tropic. This higher replication capacity does not lead to a higher cytotoxicity compared to previously described subtype C viruses. In addition, the pZAC Vpu is also shown to be able to down-regulate CD4, but fails to fully counteract CD317.