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Fluorescence Live-cell Imaging of the Complete Vegetative Cell Cycle of the Slow-growing Social Bacterium Myxococcus xanthus
Published on: June 20, 2018
Kin discrimination and outer membrane exchange in Myxococcus xanthus: Experimental analysis of a natural population
Sarah M Cossey1, Yuen-Tsu Nicco Yu1, Laura Cossu2
1Institute for Integrative Biology, Department of Environmental Systems Science, ETH Zürich, Switzerland.
Abstract:
In some species of myxobacteria, adjacent cells sufficiently similar at the adhesin protein TraA can exchange components of their outer membranes. The primary benefits of such outer membrane exchange (OME) in natural populations are unclear, but in some OME interactions, transferred OM content can include SitA toxins that kill OME participants lacking an appropriate immunity gene. Such OME-dependent toxin transfer across Myxococcus xanthus strains that differ only in their sitBAI toxin/antitoxin cassette can mediate inter-strain killing and generate colony-merger incompatibilities (CMIs)-inter-colony border phenotypes between distinct genotypes that differ from respective self-self colony interfaces. Here we ask whether OME-dependent toxin transfer is a common cause of prevalent CMIs and antagonisms between M. xanthus natural isolates identical at TraA. We disrupted traA in eleven isolates from a cm-scale soil population and assayed whether traA disruption eliminated or reduced CMIs between swarming colonies or antagonisms between strains in mixed cultures. Among 33 isolate pairs identical at traA that form clear CMIs, in no case did functional disruption of traA in one partner detectably alter CMI phenotypes. Further, traA disruption did not alleviate strong antagonisms observed during starvation-induced fruiting-body development in seven pairs of strains identical at traA. Collectively, our results suggest that most mechanisms of interference competition and inter-colony kin discrimination in natural populations of myxobacteria do not require OME. Finally, our experiments also indicate that several closely related laboratory reference strains kill some natural isolates by toxins delivered by a shared, OME-independent type VI secretion system (T6SS), suggesting that some antagonisms between sympatric natural isolates may also involve T6SS toxins.
Insights
Outer membrane exchange (OME) is not the primary driver of colony-merger incompatibilities (CMIs) or antagonism in myxobacteria. Most interactions between these bacteria do not require OME, with some antagonisms potentially involving type VI secretion systems (T6SS).
Area of Science:
- Microbiology
- Bacterial Interactions
- Myxobacteria Ecology
Background:
- Outer membrane exchange (OME) in myxobacteria allows cell-to-cell transfer of outer membrane components.
- OME can mediate toxin transfer, leading to inter-strain killing and colony-merger incompatibilities (CMIs).
- The role of OME in natural populations and its contribution to prevalent CMIs are not fully understood.
Purpose of the Study:
- To investigate if OME-dependent toxin transfer commonly causes CMIs and antagonisms between natural isolates of Myxococcus xanthus.
- To determine the necessity of the adhesin protein TraA for mediating these interactions.
Main Methods:
- Disruption of the traA gene in eleven natural isolates of M. xanthus.
- Assaying CMIs between swarming colonies of wild-type and traA-disrupted strains.
- Evaluating antagonisms between strains during starvation-induced fruiting-body development in mixed cultures.
Main Results:
- Disruption of traA did not alter or reduce CMIs in 33 isolate pairs that exhibited CMIs.
- traA disruption did not alleviate strong antagonisms observed during fruiting-body development in seven strain pairs.
- Some laboratory strains utilize an OME-independent type VI secretion system (T6SS) to deliver toxins, causing antagonism.
Conclusions:
- OME is not the primary mechanism for interference competition or kin discrimination in most natural myxobacteria populations.
- CMIs and antagonisms between M. xanthus isolates are largely independent of OME.
- Type VI secretion systems (T6SS) may play a significant role in antagonisms between sympatric natural isolates.

