Inactivation of MSMEG_0412 gene drastically affects surface related properties of Mycobacterium smegmatis. Issue 1 (December 2016)

• Record Type: Journal Article
• Authors: Zanfardino, Anna; Migliardi, Adriana; D'Alonzo, Daniele; Lombardi, Angela; Varcamonti, Mario; Cordone, Angela
• Is Part Of: BMC microbiology. Volume 16:Issue 1(2016)
• Page Start: 1
• Page End: 10
• Publication Date: 2016-12
• Subjects: Mycobacterium smegmatis -- msmeg_0412 -- GPLs -- Lipolytic -- Cell wall -- Biofilm; Microbiology -- Periodicals; 579.05
• DOI: 10.1186/s12866-016-0888-z
• Languages: English
• ISSNs: 1471-2180

Abstract

Abstract Background The outermost layer of mycobacterial cell wall is rich in lipids and glycolipids, surface molecules which differ among species.Mycobacterium smegmatis, an attractive model for the study of both pathogenic and non-pathogenic mycobacteria, presents glycopeptidolipids (GPLs). All the genes necessary for the biosynthesis of such molecules are clustered in a single region of 65 kb and among them, themsmeg_0412 gene has not been characterized yet. Here we report the isolation and subsequent analysis of a MSMEG_0412 null mutant strain. Results The inactivation of themsmeg_0412 gene had a drastic impact on bacterial surface properties which resulted in the lack of sliding motility, altered biofilm formation and enhanced drug susceptibility. The GPLs analysis showed that the observed mutant phenotype was due to GPLs deficiencies on the mycobacterial cell wall. In addition, we report that the expression of the gene is enhanced in the presence of lipidic substrates and that the encoded protein has a membrane localization. Conclusion msmeg_0412 plays a crucial role for GPLs production and translocation onM. smegmatis surface. Its deletion alters the surface properties and the antibiotic permeability of the mycobacterial cell barrier.