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Growth inhibition of Akkermansia muciniphila by a secreted pathobiont sialidase
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AbstractAkkermansia muciniphila is considered a key constituent of a healthy gut microbiota. In inflammatory bowel disease (IBD), A. muciniphila has a reduced abundance while other, putative pathogenic, mucus colonizers bloom. We hypothesized that interbacterial competition may contribute to this observation. By screening the supernatants of a panel of enteric bacteria, we discovered that a previously uncharacterized Allobaculum species potently inhibits the growth of A. muciniphila. Mass spectrometry analysis identified a secreted Allobaculum sialidase as inhibitor of A. muciniphila growth. The sialidase targets sialic acids on casein O-glycans, thereby altering the accessibility of nutrients critical for A. muciniphila. The altered glycometabolic niche results in distorted A. muciniphila cell division and efficiently arrests its growth. The identification of a novel mechanism of A. muciniphila growth inhibition by a competing bacterial pathobiont may provide a rationale for interventions aimed at restoring and maintaining a healthy microbiota symbiosis in patients with intestinal disease.
Cold Spring Harbor Laboratory
Title: Growth inhibition of Akkermansia muciniphila by a secreted pathobiont sialidase
Description:
AbstractAkkermansia muciniphila is considered a key constituent of a healthy gut microbiota.
In inflammatory bowel disease (IBD), A.
muciniphila has a reduced abundance while other, putative pathogenic, mucus colonizers bloom.
We hypothesized that interbacterial competition may contribute to this observation.
By screening the supernatants of a panel of enteric bacteria, we discovered that a previously uncharacterized Allobaculum species potently inhibits the growth of A.
muciniphila.
Mass spectrometry analysis identified a secreted Allobaculum sialidase as inhibitor of A.
muciniphila growth.
The sialidase targets sialic acids on casein O-glycans, thereby altering the accessibility of nutrients critical for A.
muciniphila.
The altered glycometabolic niche results in distorted A.
muciniphila cell division and efficiently arrests its growth.
The identification of a novel mechanism of A.
muciniphila growth inhibition by a competing bacterial pathobiont may provide a rationale for interventions aimed at restoring and maintaining a healthy microbiota symbiosis in patients with intestinal disease.
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