Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.

In nature, most bacteria live in biofilms where they compete with their siblings and other species for space and nutrients. Some bacteria produce antibiotics in biofilms; however, since the diffusion of antibiotics is generally hindered in biofilms by extracellular polymeric substances, i.e., the bi...

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Main Authors: Kazuo Kobayashi, Yukako Ikemoto
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-10-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1008232
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author Kazuo Kobayashi
Yukako Ikemoto
author_facet Kazuo Kobayashi
Yukako Ikemoto
author_sort Kazuo Kobayashi
collection DOAJ
description In nature, most bacteria live in biofilms where they compete with their siblings and other species for space and nutrients. Some bacteria produce antibiotics in biofilms; however, since the diffusion of antibiotics is generally hindered in biofilms by extracellular polymeric substances, i.e., the biofilm matrix, their function remains unclear. The Bacillus subtilis yitPOM operon is a paralog of the sdpABC operon, which produces the secreted peptide toxin SDP. Unlike sdpABC, yitPOM is induced in biofilms by the DegS-DegU two-component regulatory system. High yitPOM expression leads to the production of a secreted toxin called YIT. Expression of yitQ, which lies upstream of yitPOM, confers resistance to the YIT toxin, suggesting that YitQ is an anti-toxin protein for the YIT toxin. The alternative sigma factor SigW also contributes to YIT toxin resistance. In a mutant lacking yitQ and sigW, the YIT toxin specifically inhibits biofilm formation, and the extracellular neutral protease NprB is required for this inhibition. The requirement for NprB is eliminated by Δeps and ΔbslA mutations, either of which impairs production of biofilm matrix polymers. Overexpression of biofilm matrix polymers prevents the action of the SDP toxin but not the YIT toxin. These results indicate that, unlike the SDP toxin and many conventional antibiotics, the YIT toxin can pass through layers of biofilm matrix polymers to attack cells within biofilms with assistance from NprB. When the wild-type strain and the YIT-sensitive mutant were grown together on a solid medium, the wild-type strain formed biofilms that excluded the YIT-sensitive mutant. This observation suggests that the YIT toxin protects B. subtilis biofilms against competitors. Several bacteria are known to produce antibiotics in biofilms. We propose that some bacteria including B. subtilis may have evolved specialized antibiotics that can function within biofilms.
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spelling doaj.art-42f6e6825f5b4a17941c8d6721964df32022-12-21T18:30:36ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042019-10-011510e100823210.1371/journal.pgen.1008232Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.Kazuo KobayashiYukako IkemotoIn nature, most bacteria live in biofilms where they compete with their siblings and other species for space and nutrients. Some bacteria produce antibiotics in biofilms; however, since the diffusion of antibiotics is generally hindered in biofilms by extracellular polymeric substances, i.e., the biofilm matrix, their function remains unclear. The Bacillus subtilis yitPOM operon is a paralog of the sdpABC operon, which produces the secreted peptide toxin SDP. Unlike sdpABC, yitPOM is induced in biofilms by the DegS-DegU two-component regulatory system. High yitPOM expression leads to the production of a secreted toxin called YIT. Expression of yitQ, which lies upstream of yitPOM, confers resistance to the YIT toxin, suggesting that YitQ is an anti-toxin protein for the YIT toxin. The alternative sigma factor SigW also contributes to YIT toxin resistance. In a mutant lacking yitQ and sigW, the YIT toxin specifically inhibits biofilm formation, and the extracellular neutral protease NprB is required for this inhibition. The requirement for NprB is eliminated by Δeps and ΔbslA mutations, either of which impairs production of biofilm matrix polymers. Overexpression of biofilm matrix polymers prevents the action of the SDP toxin but not the YIT toxin. These results indicate that, unlike the SDP toxin and many conventional antibiotics, the YIT toxin can pass through layers of biofilm matrix polymers to attack cells within biofilms with assistance from NprB. When the wild-type strain and the YIT-sensitive mutant were grown together on a solid medium, the wild-type strain formed biofilms that excluded the YIT-sensitive mutant. This observation suggests that the YIT toxin protects B. subtilis biofilms against competitors. Several bacteria are known to produce antibiotics in biofilms. We propose that some bacteria including B. subtilis may have evolved specialized antibiotics that can function within biofilms.https://doi.org/10.1371/journal.pgen.1008232
spellingShingle Kazuo Kobayashi
Yukako Ikemoto
Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
PLoS Genetics
title Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
title_full Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
title_fullStr Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
title_full_unstemmed Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
title_short Biofilm-associated toxin and extracellular protease cooperatively suppress competitors in Bacillus subtilis biofilms.
title_sort biofilm associated toxin and extracellular protease cooperatively suppress competitors in bacillus subtilis biofilms
url https://doi.org/10.1371/journal.pgen.1008232
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