Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response

ABSTRACT Competitive interactions between bacteria reveal physiological adaptations that benefit fitness. Bacillus subtilis is a Gram-positive species with several adaptive mechanisms for competition and environmental stress. Biofilm formation, sporulation, and motility are the outcomes of widesprea...

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Autores principales: Yongjin Liu, Steven Kyle, Paul D. Straight
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Publicado: American Society for Microbiology 2018
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spelling oai:doaj.org-article:894e7c9277494a01bebc685942900d8f2021-11-15T15:22:01ZAntibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response10.1128/mSphere.00586-172379-5042https://doaj.org/article/894e7c9277494a01bebc685942900d8f2018-02-01T00:00:00Zhttps://journals.asm.org/doi/10.1128/mSphere.00586-17https://doaj.org/toc/2379-5042ABSTRACT Competitive interactions between bacteria reveal physiological adaptations that benefit fitness. Bacillus subtilis is a Gram-positive species with several adaptive mechanisms for competition and environmental stress. Biofilm formation, sporulation, and motility are the outcomes of widespread changes in a population of B. subtilis. These changes emerge from complex, regulated pathways for adapting to external stresses, including competition from other species. To identify competition-specific functions, we cultured B. subtilis with multiple species of Streptomyces and observed altered patterns of growth for each organism. In particular, when plated on agar medium near Streptomyces venezuelae, B. subtilis initiates a robust and reproducible mobile response. To investigate the mechanistic basis for the interaction, we determined the type of motility used by B. subtilis and isolated inducing metabolites produced by S. venezuelae. Bacillus subtilis has three defined forms of motility: swimming, swarming, and sliding. Streptomyces venezuelae induced sliding motility specifically in our experiments. The inducing agents produced by S. venezuelae were identified as chloramphenicol and a brominated derivative at subinhibitory concentrations. Upon further characterization of the mobile response, our results demonstrated that subinhibitory concentrations of chloramphenicol, erythromycin, tetracycline, and spectinomycin all activate a sliding motility response by B. subtilis. Our data are consistent with sliding motility initiating under conditions of protein translation stress. This report underscores the importance of hormesis as an early warning system for potential bacterial competitors and antibiotic exposure. IMPORTANCE Antibiotic resistance is a major challenge for the effective treatment of infectious diseases. Identifying adaptive mechanisms that bacteria use to survive low levels of antibiotic stress is important for understanding pathways to antibiotic resistance. Furthermore, little is known about the effects of individual bacterial interactions on multispecies communities. This work demonstrates that subinhibitory amounts of some antibiotics produced by streptomycetes induce active motility in B. subtilis, which may alter species interaction dynamics among species-diverse bacterial communities in natural environments. The use of antibiotics at subinhibitory concentrations results in many changes in bacteria, including changes in biofilm formation, small-colony variants, formation of persisters, and motility. Identifying the mechanistic bases of these adaptations is crucial for understanding how bacterial communities are impacted by antibiotics.Yongjin LiuSteven KylePaul D. StraightAmerican Society for MicrobiologyarticleBacillus subtilisStreptomyces venezuelaeantibioticschloramphenicolcompetitionhormesisMicrobiologyQR1-502ENmSphere, Vol 3, Iss 1 (2018)
institution DOAJ
collection DOAJ
language EN
topic Bacillus subtilis
Streptomyces venezuelae
antibiotics
chloramphenicol
competition
hormesis
Microbiology
QR1-502
spellingShingle Bacillus subtilis
Streptomyces venezuelae
antibiotics
chloramphenicol
competition
hormesis
Microbiology
QR1-502
Yongjin Liu
Steven Kyle
Paul D. Straight
Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
description ABSTRACT Competitive interactions between bacteria reveal physiological adaptations that benefit fitness. Bacillus subtilis is a Gram-positive species with several adaptive mechanisms for competition and environmental stress. Biofilm formation, sporulation, and motility are the outcomes of widespread changes in a population of B. subtilis. These changes emerge from complex, regulated pathways for adapting to external stresses, including competition from other species. To identify competition-specific functions, we cultured B. subtilis with multiple species of Streptomyces and observed altered patterns of growth for each organism. In particular, when plated on agar medium near Streptomyces venezuelae, B. subtilis initiates a robust and reproducible mobile response. To investigate the mechanistic basis for the interaction, we determined the type of motility used by B. subtilis and isolated inducing metabolites produced by S. venezuelae. Bacillus subtilis has three defined forms of motility: swimming, swarming, and sliding. Streptomyces venezuelae induced sliding motility specifically in our experiments. The inducing agents produced by S. venezuelae were identified as chloramphenicol and a brominated derivative at subinhibitory concentrations. Upon further characterization of the mobile response, our results demonstrated that subinhibitory concentrations of chloramphenicol, erythromycin, tetracycline, and spectinomycin all activate a sliding motility response by B. subtilis. Our data are consistent with sliding motility initiating under conditions of protein translation stress. This report underscores the importance of hormesis as an early warning system for potential bacterial competitors and antibiotic exposure. IMPORTANCE Antibiotic resistance is a major challenge for the effective treatment of infectious diseases. Identifying adaptive mechanisms that bacteria use to survive low levels of antibiotic stress is important for understanding pathways to antibiotic resistance. Furthermore, little is known about the effects of individual bacterial interactions on multispecies communities. This work demonstrates that subinhibitory amounts of some antibiotics produced by streptomycetes induce active motility in B. subtilis, which may alter species interaction dynamics among species-diverse bacterial communities in natural environments. The use of antibiotics at subinhibitory concentrations results in many changes in bacteria, including changes in biofilm formation, small-colony variants, formation of persisters, and motility. Identifying the mechanistic bases of these adaptations is crucial for understanding how bacterial communities are impacted by antibiotics.
format article
author Yongjin Liu
Steven Kyle
Paul D. Straight
author_facet Yongjin Liu
Steven Kyle
Paul D. Straight
author_sort Yongjin Liu
title Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
title_short Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
title_full Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
title_fullStr Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
title_full_unstemmed Antibiotic Stimulation of a <named-content content-type="genus-species">Bacillus subtilis</named-content> Migratory Response
title_sort antibiotic stimulation of a <named-content content-type="genus-species">bacillus subtilis</named-content> migratory response
publisher American Society for Microbiology
publishDate 2018
url https://doaj.org/article/894e7c9277494a01bebc685942900d8f
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AT pauldstraight antibioticstimulationofanamedcontentcontenttypegenusspeciesbacillussubtilisnamedcontentmigratoryresponse
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