Loading…
Differential fadE28 expression associated with phenotypic virulence of Mycobacterium tuberculosis
Ability to persist in human macrophages is central to the virulence of Mycobacterium tuberculosis and is not invariable among various strains. Differential gene expression that is associated with phenotypic virulence may provide additional information of virulent genes involved in the pathogenesis o...
Saved in:
Published in: | Microbial pathogenesis 2008-07, Vol.45 (1), p.12-17 |
---|---|
Main Authors: | , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | Ability to persist in human macrophages is central to the virulence of
Mycobacterium tuberculosis and is not invariable among various strains. Differential gene expression that is associated with phenotypic virulence may provide additional information of virulent genes involved in the pathogenesis of
M. tuberculosis, which is not fully elucidated. Three hypervirulent strains of
M. tuberculosis isolated from patients suffering with tuberculous meningitis were shown to grow more rapidly inside human macrophages in a previous study. In the current investigation, expression of 7 mycobacterial genes (
fadE28,
mce1A,
mymA,
acr,
sigA,
sugC, and
Rv3723) of these strains during
ex vivo macrophage challenge and
in vitro acid shock was quantified by real-time PCR. Using
rrs gene as a normalisation gene,
fadE28 gene exhibited differential gene expression that is associated with phenotypic virulence, whereas the other 6 genes showed indistinguishable expression patterns. Up-regulation of
fadE28 gene in the hypervirulent strains may account for virulence by increasing the efficiency of beta-oxidation, which is important for the persistence in macrophages as
M. tuberculosis uses fatty acids preferably inside phagosome of macrophages. The
fadE28 gene, together with its adjacent genes may also be critical in the process of lipid modification that could facilitate parasitism in human macrophages. |
---|---|
ISSN: | 0882-4010 1096-1208 |
DOI: | 10.1016/j.micpath.2008.01.006 |