The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems
Burkholderia pseudomallei is a category B pathogen and the causative agent of melioidosis - a serious infectious disease that is typically acquired directly from environmental reservoirs. Nearly all B. pseudomallei strains sequenced to date ( > 85 isolates) contain gene clusters that are related...
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th-mahidol.137482018-06-11T11:53:56Z The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems Kiel Nikolakakis Saba Amber J. Scott Wilbur Elie J. Diner Stephanie K. Aoki Stephen J. Poole Apichai Tuanyok Paul S. Keim Sharon Peacock Christopher S. Hayes David A. Low University of California, Santa Barbara Northern Arizona University Translational Genomics Research Institute Mahidol University University of Arizona University of California, Berkeley ETH Zurich University of Cambridge Biochemistry, Genetics and Molecular Biology Immunology and Microbiology Burkholderia pseudomallei is a category B pathogen and the causative agent of melioidosis - a serious infectious disease that is typically acquired directly from environmental reservoirs. Nearly all B. pseudomallei strains sequenced to date ( > 85 isolates) contain gene clusters that are related to the contact-dependent growth inhibition (CDI) systems of γ-proteobacteria. CDI systems from Escherichia coli and Dickeya dadantii play significant roles in bacterial competition, suggesting these systems may also contribute to the competitive fitness of B. pseudomallei. Here, we identify 10 distinct CDI systems in B. pseudomallei based on polymorphisms within the cdiA-CT/cdiI coding regions, which are predicted to encode CdiA-CT/CdiI toxin/immunity protein pairs. Biochemical analysis of three B. pseudomallei CdiA-CTs revealed that each protein possesses a distinct tRNase activity capable of inhibiting cell growth. These toxin activities are blocked by cognate CdiI immunity proteins, which specifically bind the CdiA-CT and protect cells from growth inhibition. Using Burkholderia thailandensis E264 as a model, we show that a CDI system from B. pseudomallei 1026b mediates CDI and is capable of delivering CdiA-CT toxins derived from other B. pseudomallei strains. These results demonstrate that Burkholderia species contain functional CDI systems, which may confer a competitive advantage to these bacteria. © 2012 Blackwell Publishing Ltd. 2018-06-11T04:37:28Z 2018-06-11T04:37:28Z 2012-05-01 Article Molecular Microbiology. Vol.84, No.3 (2012), 516-529 10.1111/j.1365-2958.2012.08039.x 13652958 0950382X 2-s2.0-84859954131 https://repository.li.mahidol.ac.th/handle/123456789/13748 Mahidol University SCOPUS https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84859954131&origin=inward |
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Biochemistry, Genetics and Molecular Biology Immunology and Microbiology Kiel Nikolakakis Saba Amber J. Scott Wilbur Elie J. Diner Stephanie K. Aoki Stephen J. Poole Apichai Tuanyok Paul S. Keim Sharon Peacock Christopher S. Hayes David A. Low The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
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Burkholderia pseudomallei is a category B pathogen and the causative agent of melioidosis - a serious infectious disease that is typically acquired directly from environmental reservoirs. Nearly all B. pseudomallei strains sequenced to date ( > 85 isolates) contain gene clusters that are related to the contact-dependent growth inhibition (CDI) systems of γ-proteobacteria. CDI systems from Escherichia coli and Dickeya dadantii play significant roles in bacterial competition, suggesting these systems may also contribute to the competitive fitness of B. pseudomallei. Here, we identify 10 distinct CDI systems in B. pseudomallei based on polymorphisms within the cdiA-CT/cdiI coding regions, which are predicted to encode CdiA-CT/CdiI toxin/immunity protein pairs. Biochemical analysis of three B. pseudomallei CdiA-CTs revealed that each protein possesses a distinct tRNase activity capable of inhibiting cell growth. These toxin activities are blocked by cognate CdiI immunity proteins, which specifically bind the CdiA-CT and protect cells from growth inhibition. Using Burkholderia thailandensis E264 as a model, we show that a CDI system from B. pseudomallei 1026b mediates CDI and is capable of delivering CdiA-CT toxins derived from other B. pseudomallei strains. These results demonstrate that Burkholderia species contain functional CDI systems, which may confer a competitive advantage to these bacteria. © 2012 Blackwell Publishing Ltd. |
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University of California, Santa Barbara |
author_facet |
University of California, Santa Barbara Kiel Nikolakakis Saba Amber J. Scott Wilbur Elie J. Diner Stephanie K. Aoki Stephen J. Poole Apichai Tuanyok Paul S. Keim Sharon Peacock Christopher S. Hayes David A. Low |
format |
Article |
author |
Kiel Nikolakakis Saba Amber J. Scott Wilbur Elie J. Diner Stephanie K. Aoki Stephen J. Poole Apichai Tuanyok Paul S. Keim Sharon Peacock Christopher S. Hayes David A. Low |
author_sort |
Kiel Nikolakakis |
title |
The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
title_short |
The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
title_full |
The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
title_fullStr |
The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
title_full_unstemmed |
The toxin/immunity network of Burkholderia pseudomallei contact-dependent growth inhibition (CDI) systems |
title_sort |
toxin/immunity network of burkholderia pseudomallei contact-dependent growth inhibition (cdi) systems |
publishDate |
2018 |
url |
https://repository.li.mahidol.ac.th/handle/123456789/13748 |
_version_ |
1763497939855998976 |