Regulation of Growth, Cell Shape, Cell Division, and Gene Expression by Second Messengers (p)ppGpp and Cyclic Di-GMP in Mycobacterium smegmatis

• Published in: Journal of bacteriology 2016-05, Vol.198 (9), p.1414-1422
• Main Authors: Gupta, Kuldeepkumar Ramnaresh, Baloni, Priyanka, Indi, Shantinath S, Chatterji, Dipankar
• Format: Article
• Language: English
• Subjects: Bacteria; Bacterial proteins; Bacteriology; Biofilms; Biofilms - growth & development; Cell division; Cell Division - genetics; Cold Temperature; Cold tolerance; Cyclic GMP - analogs & derivatives; Cyclic GMP - metabolism; Detoxification; Fluorescence microscopy; Gene Expression; Gene Expression Regulation, Bacterial; Genotype & phenotype; Gram-positive bacteria; Guanosine Pentaphosphate - genetics; Guanosine Pentaphosphate - metabolism; Lipids; Mycobacterium smegmatis; Mycobacterium smegmatis - cytology; Mycobacterium smegmatis - genetics; Mycobacterium smegmatis - growth & development; Mycobacterium smegmatis - metabolism; Phenotype; Second Messenger Systems; Signal Transduction - genetics; Stress, Physiological - genetics
• ISSN: 0021-9193; 1098-5530
• DOI: 10.1128/JB.00126-16

The alarmone (p)ppGpp regulates transcription, translation, replication, virulence, lipid synthesis, antibiotic sensitivity, biofilm formation, and other functions in bacteria. Signaling nucleotide cyclic di-GMP (c-di-GMP) regulates biofilm formation, motility, virulence, the cell cycle, and other functions. In Mycobacterium smegmatis, both (p)ppGpp and c-di-GMP are synthesized and degraded by bifunctional proteins Rel(Msm) and DcpA, encoded by rel(Msm) and dcpA genes, respectively. We have previously shown that the Δrel(Msm) and ΔdcpA knockout strains are antibiotic resistant and defective in biofilm formation, show altered cell surface properties, and have reduced levels of glycopeptidolipids and polar lipids in their cell wall (K. R. Gupta, S. Kasetty, and D. Chatterji, Appl Environ Microbiol 81:2571-2578, 2015,http://dx.doi.org/10.1128/AEM.03999-14). In this work, we have explored the phenotypes that are affected by both (p)ppGpp and c-di-GMP in mycobacteria. We have shown that both (p)ppGpp and c-di-GMP are needed to maintain the proper growth rate under stress conditions such as carbon deprivation and cold shock. Scanning electron microscopy showed that low levels of these second messengers result in elongated cells, while high levels reduce the cell length and embed the cells in a biofilm-like matrix. Fluorescence microscopy revealed that the elongated Δrel(Msm) and ΔdcpA cells are multinucleate, while transmission electron microscopy showed that the elongated cells are multiseptate. Gene expression analysis also showed that genes belonging to functional categories such as virulence, detoxification, lipid metabolism, and cell-wall-related processes were differentially expressed. Our results suggests that both (p)ppGpp and c-di-GMP affect some common phenotypes in M. smegmatis, thus raising a possibility of cross talk between these two second messengers in mycobacteria. Our work has expanded the horizon of (p)ppGpp and c-di-GMP signaling in Gram-positive bacteria. We have come across a novel observation that M. smegmatis needs (p)ppGpp and c-di-GMP for cold tolerance. We had previously shown that the Δrel(Msm) and ΔdcpA strains are defective in biofilm formation. In this work, the overproduction of (p)ppGpp and c-di-GMP encased M. smegmatis in a biofilm-like matrix, which shows that both (p)ppGpp and c-di-GMP are needed for biofilm formation. The regulation of cell length and cell division by (p)ppGpp was known in mycobacteria, but our work shows tha