Abstract

BackgroundTuberculosis (TB) is the largest cause of death in human immunodeficiency virus type 1 (HIV-1) infection, having claimed an estimated one third to one half of the 30 million AIDS deaths that have occurred worldwide. Different strains of Mycobacterium tuberculosis (MTb), the causative agent of TB, are known to modify the host immune response in a strain-specific manner. However, a MTb strain-specific impact upon the regulation of HIV-1 replication has not previously been established.Methology/Principal FindingsWe isolated normal human peripheral blood mononuclear cells (PBMC) and co-infected them with HIV-1 and with either the well characterized CDC1551 or HN878 MTb clinical isolate. We show that HIV-1 co-infection with the CDC1551 MTb strain results in higher levels of virus replication relative to co-infection with the HN878 MTb strain ex vivo. Furthermore, we show that the distinct pattern of CDC1551 or HN878 induced HIV-1 replication is associated with significantly increased levels of TNF and IL-6, and of the transcription and nuclear translocation of the p65 subunit of the transcription factor NF-κB, by CDC1551 relative to HN878.Conclusions/SignificanceThese results provide a precedent for TB strain-specific effects upon HIV-1 replication and thus for TB strain-specific pathogenesis in the outcome of HIV-1/TB co-infection. MTb strain-specific factors and mechanisms involved in the regulation of HIV-1 during co-infection will be of importance in understanding the basic pathogenesis of HIV-1/TB co-infection.

Highlights

  • Mycobacterium tuberculosis (MTb), the causative agent of tuberculosis (TB) disease, is the most frequent co-infection in human immune deficiency virus type 1 (HIV-1) infected patients

  • While MTb strain variation appears to affect the course of TB, does it differentially regulate human immunodeficiency virus type 1 (HIV-1) replication? Using an ex vivo HIV-1/TB co-infection model, here we show that infection of human peripheral blood mononuclear cells (PBMC) with the CDC1551 MTb strain causes significantly higher viral replication of clinical isolates representative of HIV-1 subtypes B, C, and E, as compared to infection with HN878

  • HIV-1 replication was higher in all cultures co-infected with MTb compared to cultures infected with HIV-1 alone (Figure 1A)

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Summary

Introduction

Mycobacterium tuberculosis (MTb), the causative agent of tuberculosis (TB) disease, is the most frequent co-infection in human immune deficiency virus type 1 (HIV-1) infected patients. The progressive immune compromise associated with HIV-1 infection and AIDS results in reactivation of TB disease in latently infected individuals, and an increase in primary TB and secondary TB infection [8,9,10,11]. Tuberculosis (TB) is the largest cause of death in human immunodeficiency virus type 1 (HIV-1) infection, having claimed an estimated one third to one half of the 30 million AIDS deaths that have occurred worldwide. We show that HIV-1 coinfection with the CDC1551 MTb strain results in higher levels of virus replication relative to co-infection with the HN878 MTb strain ex vivo. We show that the distinct pattern of CDC1551 or HN878 induced HIV-1 replication is associated with significantly increased levels of TNF and IL-6, and of the transcription and nuclear translocation of the p65 subunit of the transcription factor NF-kB, by CDC1551 relative to HN878

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