Myxobacteria produce outer membrane-enclosed tubes in unstructured environments

• Published in: Journal of bacteriology Vol. 196; no. 10; pp. 1807 - 1814
• Main Authors: Wei, Xueming, Vassallo, Christopher N, Pathak, Darshankumar T, Wall, Daniel
• Format: Journal Article
• Language: English
• Published: United States American Society for Microbiology 01.05.2014
• Subjects: Anti-Bacterial Agents - pharmacology; Bacterial Outer Membrane Proteins - physiology; Bacterial proteins; Bacteriological Techniques; Bacteriology; Cell Membrane - physiology; Environmental conditions; Gene Expression Regulation, Bacterial - physiology; Genetics; Gram-negative bacteria; Luminescent Proteins; Membranes; Microbial Interactions; Morphology; Myxobacteria; Myxococcus xanthus; Myxococcus xanthus - cytology; Myxococcus xanthus - drug effects; Myxococcus xanthus - physiology; Red Fluorescent Protein; Staining and Labeling; Transmission electron microscopy
• ISSN: 0021-9193; 1098-5530
• DOI: 10.1128/jb.00850-13

Myxobacteria are social microbes that exhibit complex multicellular behaviors. By use of fluorescent reporters, we show that Myxococcus xanthus isolates produce long narrow filaments that are enclosed by the outer membrane (OM) and contain proteins. We show that these OM tube (OMT) structures are produced at surprisingly high levels when cells are placed in liquid medium or buffer without agitation. OMTs can be long and easily exceed multiple cell lengths. When viewed by transmission electron microscopy, their morphology varies between tubes and chain-like structures. Intermediate-like structures are also found, suggesting that OMTs may transition between these two morphotypes. In support of this, video epifluorescence microscopy found that OMTs in solution dynamically twist and jiggle. On hard surfaces, myxobacteria glide, and upon cell-cell contact, they can efficiently exchange their OM proteins and lipids by a TraAB-dependent mechanism. Although the structure of OMTs hints at a possible role as conduits for exchange, evidence is presented to the contrary. For example, abundant OMT production occurs in traA or traB mutants and when cells are grown in liquid medium, yet transfer cannot occur under these conditions. Thus, genetic and environmental conditions that promote OMT production are incongruent with OM exchange.