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Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector

Tat and Nef are very important regulatory proteins of HIV-1. They enhance viral replication and down-regulate expression of MHC Class I molecules, respectively. The antigens are now considered to be targets for HIV vaccine development. The expression of Tat and Nef in Salmonella vaccines has not pre...

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Autores principales: Chin’ombe, Nyasha, Lebeko, Maribanyana, Kgatle, Mankgopo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The African Field Epidemiology Network 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909692/
https://www.ncbi.nlm.nih.gov/pubmed/24498468
http://dx.doi.org/10.11604/pamj.2013.16.19.2759
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author Chin’ombe, Nyasha
Lebeko, Maribanyana
Kgatle, Mankgopo
author_facet Chin’ombe, Nyasha
Lebeko, Maribanyana
Kgatle, Mankgopo
author_sort Chin’ombe, Nyasha
collection PubMed
description Tat and Nef are very important regulatory proteins of HIV-1. They enhance viral replication and down-regulate expression of MHC Class I molecules, respectively. The antigens are now considered to be targets for HIV vaccine development. The expression of Tat and Nef in Salmonella vaccines has not previously been investigated. In this study, HIV-1 Subtype C tat and nef genes were cloned into an expression plasmid and their expression investigated in Salmonella. Very high-level expression of the two HIV-1 antigens was demonstrated in the recombinant Salmonella. The antigens were also successfully purified in bulk from the bacterium.Salmonella can therefore potentially be used to overexpress HIV-1 antigens and used as a possible delivery system in HIV-1 vaccine development.
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spelling pubmed-39096922014-02-04 Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector Chin’ombe, Nyasha Lebeko, Maribanyana Kgatle, Mankgopo Pan Afr Med J Short Communication Tat and Nef are very important regulatory proteins of HIV-1. They enhance viral replication and down-regulate expression of MHC Class I molecules, respectively. The antigens are now considered to be targets for HIV vaccine development. The expression of Tat and Nef in Salmonella vaccines has not previously been investigated. In this study, HIV-1 Subtype C tat and nef genes were cloned into an expression plasmid and their expression investigated in Salmonella. Very high-level expression of the two HIV-1 antigens was demonstrated in the recombinant Salmonella. The antigens were also successfully purified in bulk from the bacterium.Salmonella can therefore potentially be used to overexpress HIV-1 antigens and used as a possible delivery system in HIV-1 vaccine development. The African Field Epidemiology Network 2013-09-17 /pmc/articles/PMC3909692/ /pubmed/24498468 http://dx.doi.org/10.11604/pamj.2013.16.19.2759 Text en © Nyasha Chin’ombe et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. 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 work is properly cited.
spellingShingle Short Communication
Chin’ombe, Nyasha
Lebeko, Maribanyana
Kgatle, Mankgopo
Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title_full Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title_fullStr Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title_full_unstemmed Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title_short Overexpression of recombinant HIV-1 Subtype C Tat and Nef in a Salmonella vaccine vector
title_sort overexpression of recombinant hiv-1 subtype c tat and nef in a salmonella vaccine vector
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3909692/
https://www.ncbi.nlm.nih.gov/pubmed/24498468
http://dx.doi.org/10.11604/pamj.2013.16.19.2759
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