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Resuscitation-Promoting Factors Are Required for Mycobacterium smegmatis Biofilm Formation
Author(s) -
Christopher Ealand,
Binayak Rimal,
James D. Chang,
Lethabo Mashigo,
Melissa D. Chengalroyen,
Lusanda Mapela,
Germar M. Beukes,
Edith E. Machowski,
Sung Joon Kim,
Bavesh D Kana
Publication year - 2018
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.00687-18
Subject(s) - peptidoglycan , mycobacterium smegmatis , biofilm , mutant , cell wall , spheroplast , biology , strain (injury) , lysozyme , microbiology and biotechnology , biochemistry , bacteria , gene , chemistry , escherichia coli , genetics , mycobacterium tuberculosis , medicine , tuberculosis , pathology , anatomy
The cell wall of pathogenic mycobacteria is composed of peptidoglycan, arabinogalactan, mycolic acids, and an outer capsule. This inherent complexity renders it resistant to many antibiotics. Consequently, its biosynthesis and remodeling during growth directly impact viability. Resuscitation-promoting factors (Rpfs), enzymes with lytic transglycosylase activity, have been associated with the revival of dormant cells and subsequent resumption of vegetative growth.Mycobacterium smegmatis , a soil saprophyte and close relative of the human pathogenMycobacterium tuberculosis , encodes four distinct Rpfs. Herein, we assessed the relationship between Rpfs and biofilm formation, which is used as a model to study drug tolerance and bacterial signaling in mycobacteria. We demonstrated that progressive deletion ofrpf genes hampered the development of biofilms and reduced drug tolerance. These effects were accompanied by a reduction in muropeptide production and altered peptidoglycan cross-linking. Collectively, these observations point to an important role for Rpfs in mycobacterial communication and drug tolerance.

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