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Conditional toxicity and synergy drive diversity among antibacterial effectors
Bacteria in polymicrobial habitats contend with a persistent barrage of competitors, often under rapidly changing environmental conditions(1). The direct antagonism of competitor cells is thus an important bacterial survival strategy(2). Towards this end, many bacterial species employ an arsenal of...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876133/ https://www.ncbi.nlm.nih.gov/pubmed/29459733 http://dx.doi.org/10.1038/s41564-018-0113-y |
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author | LaCourse, Kaitlyn D. Peterson, S. Brook Kulasekara, Hemantha D. Radey, Matthew C. Kim, Jungyun Mougous, Joseph D. |
author_facet | LaCourse, Kaitlyn D. Peterson, S. Brook Kulasekara, Hemantha D. Radey, Matthew C. Kim, Jungyun Mougous, Joseph D. |
author_sort | LaCourse, Kaitlyn D. |
collection | PubMed |
description | Bacteria in polymicrobial habitats contend with a persistent barrage of competitors, often under rapidly changing environmental conditions(1). The direct antagonism of competitor cells is thus an important bacterial survival strategy(2). Towards this end, many bacterial species employ an arsenal of antimicrobial effectors with multiple activities; however, the benefits conferred by the simultaneous deployment of diverse toxins are unknown. Here we show that the multiple effectors delivered to competitor bacteria by the type VI secretion system (T6SS) of Pseudomonas aeruginosa display conditional efficacy and act synergistically. One of these effectors, Tse4, is most active in high salinity environments and synergizes with effectors that degrade the cell wall or inactivate intracellular electron carriers. We find Tse4 synergizes with these disparate mechanisms by forming pores that disrupt the ΔΨ component of the proton motive force. Our results provide evidence that the concomitant delivery of a cocktail of effectors serves as a bet-hedging strategy to promote bacterial competitiveness in the face of unpredictable and variable environmental conditions. |
format | Online Article Text |
id | pubmed-5876133 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-58761332018-08-19 Conditional toxicity and synergy drive diversity among antibacterial effectors LaCourse, Kaitlyn D. Peterson, S. Brook Kulasekara, Hemantha D. Radey, Matthew C. Kim, Jungyun Mougous, Joseph D. Nat Microbiol Article Bacteria in polymicrobial habitats contend with a persistent barrage of competitors, often under rapidly changing environmental conditions(1). The direct antagonism of competitor cells is thus an important bacterial survival strategy(2). Towards this end, many bacterial species employ an arsenal of antimicrobial effectors with multiple activities; however, the benefits conferred by the simultaneous deployment of diverse toxins are unknown. Here we show that the multiple effectors delivered to competitor bacteria by the type VI secretion system (T6SS) of Pseudomonas aeruginosa display conditional efficacy and act synergistically. One of these effectors, Tse4, is most active in high salinity environments and synergizes with effectors that degrade the cell wall or inactivate intracellular electron carriers. We find Tse4 synergizes with these disparate mechanisms by forming pores that disrupt the ΔΨ component of the proton motive force. Our results provide evidence that the concomitant delivery of a cocktail of effectors serves as a bet-hedging strategy to promote bacterial competitiveness in the face of unpredictable and variable environmental conditions. 2018-02-19 2018-04 /pmc/articles/PMC5876133/ /pubmed/29459733 http://dx.doi.org/10.1038/s41564-018-0113-y Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article LaCourse, Kaitlyn D. Peterson, S. Brook Kulasekara, Hemantha D. Radey, Matthew C. Kim, Jungyun Mougous, Joseph D. Conditional toxicity and synergy drive diversity among antibacterial effectors |
title | Conditional toxicity and synergy drive diversity among antibacterial effectors |
title_full | Conditional toxicity and synergy drive diversity among antibacterial effectors |
title_fullStr | Conditional toxicity and synergy drive diversity among antibacterial effectors |
title_full_unstemmed | Conditional toxicity and synergy drive diversity among antibacterial effectors |
title_short | Conditional toxicity and synergy drive diversity among antibacterial effectors |
title_sort | conditional toxicity and synergy drive diversity among antibacterial effectors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5876133/ https://www.ncbi.nlm.nih.gov/pubmed/29459733 http://dx.doi.org/10.1038/s41564-018-0113-y |
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