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Mycobacterium tuberculosis Cells Growing in Macrophages Are Filamentous and Deficient in FtsZ Rings
Author(s) -
Ashwini Chauhan,
Murty V. V. S. Madiraju,
Marek Fol,
Lofton Hava,
Erin A. Maloney,
Robert C. Reynolds,
Malini Rajagopalan
Publication year - 2006
Publication title -
journal of bacteriology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.652
H-Index - 246
eISSN - 1067-8832
pISSN - 0021-9193
DOI - 10.1128/jb.188.5.1856-1865.2006
Subject(s) - ftsz , cell division , biology , microbiology and biotechnology , mycobacterium tuberculosis , intracellular , cell , cytoskeleton , tuberculosis , biochemistry , medicine , pathology
FtsZ, a bacterial homolog of tubulin, forms a structural element called the FtsZ ring (Z ring) at the predivisional midcell site and sets up a scaffold for the assembly of other cell division proteins. The genetic aspects of FtsZ-catalyzed cell division and its assembly dynamics inMycobacterium tuberculosis are unknown. Here, with anM. tuberculosis strain containing FtsZTB tagged with green fluorescent protein as the sole source of FtsZ, we examined FtsZ structures under various growth conditions. We found that midcell Z rings are present in approximately 11% of actively growing cells, suggesting that the low frequency of Z rings is reflective of their slow growth rate. Next, we showed that SRI-3072, a reported FtsZTB inhibitor, disrupted Z-ring assembly and inhibited cell division and growth ofM. tuberculosis . We also showed thatM. tuberculosis cells grown in macrophages are filamentous and that only a small fraction had midcell Z rings. The majority of filamentous cells contained nonring, spiral-like FtsZ structures along their entire length. The levels of FtsZ in bacteria grown in macrophages or in broth were comparable, suggesting that Z-ring formation at midcell sites was compromised during intracellular growth. Our results suggest that the intraphagosomal milieu alters the expression ofM. tuberculosis genes affecting Z-ring formation and thereby cell division.

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