ClpV3 of the H3-Type VI Secretion System (H3-T6SS) Affects Multiple Virulence Factors in Pseudomonas aeruginosa
The type VI secretion system (T6SS) is a toxic effector delivery apparatus widely distributed in Gram-negative bacteria. The opportunistic pathogen encodes three T6SSs, namely H1-, H2-, and H3-T6SS. Each T6SS possesses its own effectors and their roles are not yet fully understood. Here, we report t...
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Published in | Frontiers in microbiology Vol. 11; p. 1096 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Switzerland
Frontiers Media S.A
29.05.2020
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Subjects | |
Online Access | Get full text |
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Summary: | The type VI secretion system (T6SS) is a toxic effector delivery apparatus widely distributed in Gram-negative bacteria. The opportunistic pathogen
encodes three T6SSs, namely H1-, H2-, and H3-T6SS. Each T6SS possesses its own effectors and their roles are not yet fully understood. Here, we report that an H3-T6SS deletion mutant PAO1(Δ
) significantly affected the virulence-related phenotypes including pyocyanin production, biofilm formation, proteolytic activity, and motilities. Most interestingly, the expression of T3SS genes was markedly affected, indicating a link between H3-T6SS and T3SS. RNA-Sequencing was performed to globally identify the genes differentially expressed when H3-T6SS was inactivated and the results obtained correlated well with the observed phenotypes. Interestingly, the expressions of T2SS, T3SS, H2-T6SS, and H3-T6SS were all significantly decreased, while H1-T6SS was increased in the PAO1(Δ
) strain. We also observed that the intracellular concentration of secondary messenger cAMP was reduced in PAO1(Δ
), and the c-di-GMP level was also decreased as indicated by the decreased
reporter activity. Finally, by using a
infection model, we show that H3-T6SS plays a key role in the pathogenicity of
. Overall, our study highlights the unique connection of H3-T6SS in
with T3SS, pyocyanin production, biofilm formation and
pathogenicity. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Giovanni Di Bonaventura, Università degli Studi Gabriele d’Annunzio Chieti e Pescara, Italy This article was submitted to Infectious Diseases, a section of the journal Frontiers in Microbiology Reviewed by: Patrick Kyle Taylor, Simon Fraser University, Canada; Gloria Soberón-Chávez, National Autonomous University of Mexico, Mexico |
ISSN: | 1664-302X 1664-302X |
DOI: | 10.3389/fmicb.2020.01096 |