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GLOBAL ADVANCED RESEARCH JOURNAL OF MICROBIOLOGY (GARJM) ISSN: 2315-5116

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             Vol. 2(3) March 2013

                                   

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Global Advanced Research Journal of Microbiology (GARJM) ISSN: 2315-5116

March 2013 Vol. 2(3), pp 047-053

Copyright © 2013 Global Advanced Research Journals

 

 

Full Length Research Paper

 

Differential HIV-1 Co-Receptor Usage in Blood and the Reproductive Tract: Implications for Co-Receptor Antagonist Usage

 

*Kemebradikumo Pondei1, Mieebi Wankasi2 and Juliana Pondei3

 

1Department of Medical Microbiology and Parasitology

2Department of Medical Laboratory Sciences, Faculty of Basic Medical Sciences, College of Health Sciences, Niger Delta University, Amassoma, Wilberforce Island, Bayelsa State, Nigeria.

3Department of Biology, Federal University, Otuoke, Bayelsa State, Nigeria.

 

*Corresponding author Email: kemepondei@hotmail.com

Tel: +2348030940882

 

Accepted 11 March, 2013

 

Abstract

 

The Human immunodeficiency virus type 1 (HIV-1) is still a serious global health problem especially in Sub-Saharan Africa. HIV-1 most times uses two co-receptors (CCR5 or CXCR4) for infection of permissible cells. Without these receptors, HIV-1 cannot establish infection. The introduction of co-receptor antagonists in the treatment of HIV-1 infection has made co-receptor usage determination very important. This study sought to predict the co-receptor usage of viral sequences derived from the blood and genital tract. Using the charge rule and PSSM algorithm, the co-receptor usage of HIV-1 sequences derived from the blood and genital tract of 29 HIV-1 infected patients (10 male, 19 female) was predicted. 14 out of 29 patients had CXCR4-using viruses in at least one body compartment. 13 of these had mixtures of X4 and R5 viruses in either compartment, whilst one patient had only X4 viruses in both compartments. 15 patients had R5 viruses only in both compartments. The same co-receptor usage was predicted using the charge rule and PSSM for only the HIV-1 subtypes B sequences. The presence of CXCR4-using viruses in not easily accessible compartments like the genital tract could have serious implications in the treatment of HIV-1 infection with new drugs like maraviroc, as co-receptor usage testing done before therapy uses blood samples only. X4 viruses could be present in other compartments of the body. We suggest the testing of samples from other compartments of the body in addition to blood, to forestall outgrowth of X4 viruses where cryptic X4 viruses exist.

 

Keywords: Maraviroc, CXCR4, CCR5, Co-receptor usage

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