Regulation of macrophage gene expression by Mycobacterium tuberculosis: down-regulation of mitochondrial cytochrome c oxidase.

S Ragno, I Estrada-Garcia, R Butler, M J Colston
Author Information
  1. S Ragno: Division of Mycobacterial Research, National Institute for Medical Research, London NW7 1AA, United Kingdom.

Abstract

We have investigated changes in gene expression in mouse peritoneal macrophages following infection with virulent Mycobacterium tuberculosis. Using differential-display reverse transcription-PCR (RT-PCR), we have identified a gene that was markedly down-regulated within 6 h of infection and remained so for the duration of the experiment (5 days). On sequencing, this gene was found to encode the murine cytochrome c oxidase subunit VIIc (COX VIIc). Down-regulation of COX VIIc during M. tuberculosis infection was confirmed by three independent techniques: limiting-dilution RT-PCR, RNase protection assay, and Northern analysis. Limiting-dilution RT-PCR and Northern analysis were also used to analyze the specificity of this regulation; heat-killed M. tuberculosis, Mycobacterium bovis BCG, and latex beads had no effect on expression of COX VIIc. Down-regulation of this enzyme was also confirmed by using adherent cells isolated from spleens of M. tuberculosis-infected mice. These ex vivo macrophages showed apoptotic features, suggesting a possible involvement of cytochrome c oxidase in the programmed cell death of the host cells.

Associated Data

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MeSH Term

Animals
Apoptosis
Base Sequence
Cells, Cultured
Disease Models, Animal
Down-Regulation
Electron Transport Complex IV
Female
Macrophages
Mice
Mice, Inbred BALB C
Mice, Nude
Mitochondria
Molecular Sequence Data
Mycobacterium tuberculosis
Nuclear Proteins
Polymerase Chain Reaction
RNA, Messenger
Spleen
Tuberculosis

Chemicals

Cox7C protein, human
Nuclear Proteins
RNA, Messenger
Electron Transport Complex IV

Word Cloud

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