Microbial Herd Protection Mediated by Antagonistic Interaction in Polymicrobial Communities
Authored by Megan J Q Wong, Xiaoye Liang, Matt Smart, Le Tang, Richard Moore, Brian Ingalls, Tao G Dong
Date Published: 2016
DOI: 10.1128/aem.02210-16
Sponsors:
Alberta Innovates
National Science and Engineering Research Council of Canada (NSERC)
Alberta Livestock and Meat Agency (ALMA)
Platforms:
Python
Model Documentation:
Other Narrative
Model Code URLs:
Model code not found
Abstract
In host and natural environments, microbes often exist in complex
multispecies communities. The molecular mechanisms through which such
communities develop and persist, despite significant antagonistic
interactions between species, are not well understood. The type VI
secretion system (T6SS) is a lethal weapon commonly employed by
Gram-negative bacteria to inhibit neighboring species through the
delivery of toxic effectors. It is well established that intraspecies
protection is conferred by immunity proteins that neutralize effector
toxicities. In contrast, the mechanisms for interspecies protection are
not clear. Here we use two T6SS-active antagonistic bacterial species, Aeromonas hydrophila and Vibrio cholerae, to demonstrate that
interspecies protection is dependent on effectors. A. hydrophila and V.
cholerae do not share conserved immunity genes but could coexist equally
in a mixture. However, mutants lacking the T6SS or effectors were
effectively eliminated by the competing wild-type strain. Time-lapse
microscopic analyses showed that mutually lethal interactions drive the
segregation of mixed species into distinct single-species clusters by
eliminating interspersed single cells. Cluster formation provides herd
protection by abolishing lethal interactions inside each cluster and
restricting the interactions to the boundary. Using an agent-based
modeling approach, we simulated the antagonistic interactions of two
hypothetical species. The resulting simulations recapitulated our
experimental observations. These results provide mechanistic insights
regarding the general role of microbial weapons in determining the
structures of complex multispecies communities.
IMPORTANCE
Investigating the warfare of microbes allows us to better understand the
ecological relationships in complex microbial communities such as the
human microbiota. Here we use the T6SS, a deadly bacterial weapon, as a
model to demonstrate the importance of lethal interactions in
determining community structures and the exchange of genetic materials.
This simplified model elucidates a mechanism of microbial herd
protection by which competing antagonistic species can coexist in the
same niche, despite their diverse mutually destructive activities. Our
results also suggest that antagonistic interactions impose strong
selection that could promote multicellular organism-like social
behaviors and contribute to the transition to multicellularity during
evolution.
Tags
Proteins
Expression
Identification
Vi secretion system
Vibrio-cholerae
Clostridium-difficile
Virulence
Effectors
Toxin
Aeromonas