DivIVA concentrates mycobacterial cell envelope assembly for initiation and stabilization of polar growth. Issue 12 (30th November 2018)

• Record Type: Journal Article
• Authors: Melzer, Emily S.; Sein, Caralyn E.; Chambers, James J.; Siegrist, M. Sloan
• Is Part Of: Cytoskeleton. Volume 75:Issue 12(2018)
• Page Start: 498
• Page End: 507
• Publication Date: 2018-11-30
• Subjects: DivIVA -- mycobacteria -- peptidoglycan -- shape -- Wag31; Cytoskeleton -- Periodicals; 571.65405
• DOI: 10.1002/cm.21490
• Languages: English
• ISSNs: 1949-3584

Abstract

Abstract: In many model organisms, diffuse patterning of cell wall peptidoglycan synthesis by the actin homolog MreB enables the bacteria to maintain their characteristic rod shape. In Caulobacter crescentus and Escherichia coli, MreB is also required to sculpt this morphology de novo. Mycobacteria are rod‐shaped but expand their cell wall from discrete polar or subpolar zones. In this genus, the tropomyosin‐like protein DivIVA is required for the maintenance of cell morphology. DivIVA has also been proposed to direct peptidoglycan synthesis to the tips of the mycobacterial cell. The precise nature of this regulation is unclear, as is its role in creating rod shape from scratch. We find that DivIVA localizes nascent cell wall and covalently associated mycomembrane but is dispensable for the assembly process itself. Mycobacterium smegmatis rendered spherical by peptidoglycan digestion or by DivIVA depletion are able to regain rod shape at the population level in the presence of DivIVA. At the single cell level, there is a close spatiotemporal correlation between DivIVA foci, rod extrusion and concentrated cell wall synthesis. Thus, although the precise mechanistic details differ from other organisms, M. smegmatis also establish and propagate rod shape by cytoskeleton‐controlled patterning of peptidoglycan. Our data further support the emerging notion that morphology is a hardwired trait of bacterial cells.