The Stringent Response of Mycobacterium tuberculosis Is Required for Long-Term Survival
0301 basic medicine
2. Zero hunger
Time Factors
Genotype
Macrophages
Guanosine Pentaphosphate
Mycobacterium tuberculosis
Cell Line
Culture Media
3. Good health
Ligases
03 medical and health sciences
Phenotype
Mutagenesis
Humans
DOI:
10.1128/jb.182.17.4889-4898.2000
Publication Date:
2002-07-27T10:00:58Z
AUTHORS (6)
ABSTRACT
ABSTRACT
The stringent response utilizes hyperphosphorylated guanine [(p)ppGpp] as a signaling molecule to control bacterial gene expression involved in long-term survival under starvation conditions. In gram-negative bacteria, (p)ppGpp is produced by the activity of the related RelA and SpoT proteins.
Mycobacterium tuberculosis
contains a single homolog of these proteins (Rel
Mtb
) and responds to nutrient starvation by producing (p)ppGpp. A
rel
Mtb
knockout strain was constructed in a virulent strain of
M. tuberculosis
, H37Rv, by allelic replacement. The
rel
Mtb
mutant displayed a significantly slower aerobic growth rate than the wild type in synthetic liquid media, whether rich or minimal. The growth rate of the wild type was equivalent to that of the mutant when citrate or phospholipid was employed as the sole carbon source. These two organisms also showed identical growth rates within a human macrophage-like cell line. These results suggest that the in vivo carbon source does not represent a stressful condition for the bacilli, since it appears to be utilized in a similar Rel
Mtb
-independent manner. In vitro growth in liquid media represents a condition that benefits from Rel
Mtb
-mediated adaptation. Long-term survival of the
rel
Mtb
mutant during in vitro starvation or nutrient run out in normal media was significantly impaired compared to that in the wild type. In addition, the mutant was significantly less able to survive extended anerobic incubation than the wild-type virulent organism. Thus, the Rel
Mtb
protein is required for long-term survival of pathogenic mycobacteria under starvation conditions.
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