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Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling

Phage therapy is challenged by the frequent emergence of bacterial resistance to phages. As an interspecies signaling molecule, indole plays important roles in regulating bacterial behaviors. However, it is unclear whether indole is involved in the phage-bacterium interactions. Here, we report that...

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Autores principales: Xuan, Guanhua, Dou, Qin, Kong, Jiuna, Lin, Hong, Wang, Jingxue
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927445/
https://www.ncbi.nlm.nih.gov/pubmed/36602321
http://dx.doi.org/10.1128/spectrum.03911-22
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author Xuan, Guanhua
Dou, Qin
Kong, Jiuna
Lin, Hong
Wang, Jingxue
author_facet Xuan, Guanhua
Dou, Qin
Kong, Jiuna
Lin, Hong
Wang, Jingxue
author_sort Xuan, Guanhua
collection PubMed
description Phage therapy is challenged by the frequent emergence of bacterial resistance to phages. As an interspecies signaling molecule, indole plays important roles in regulating bacterial behaviors. However, it is unclear whether indole is involved in the phage-bacterium interactions. Here, we report that indole modulated phage resistance of Pseudomonas aeruginosa PAO1. Specifically, we found that the type IV pilus (T4P) acts as an important receptor for P. aeruginosa phages vB_Pae_S1 and vB_Pae_TR, and indole could protect P. aeruginosa against phage infection via decreasing the T4P-mediated phage adsorption. Further investigation demonstrated that indole downregulated the expression of genes pilA, pilB, and pilQ, which are essential for T4P assembly and activity. Indole inhibits phage attacks, but our data suggest that indole functions not through interfering with the AHL-based QS pathway, although las quorum sensing (QS) of P. aeruginosa PAO1 were reported to promote phage infection. Our finding confirms the important roles of indole in virus-host interactions, which will provide important enlightenment in promoting phage therapy for P. aeruginosa infections. IMPORTANCE Our finding is significant with respect to the study of the interactions between phage and host. Although the important roles of indole in bacterial physiology have been revealed, no direct examples of indole participating in phage-host interactions were reported. This study reports that indole could modulate the phage resistance of indole-nonproducing Pseudomonas aeruginosa PAO1 through inhibition of phage adsorption mechanism. Our finding will be significant for guiding phage therapy and fill some gaps in the field of phage-host interactions.
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spelling pubmed-99274452023-02-15 Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling Xuan, Guanhua Dou, Qin Kong, Jiuna Lin, Hong Wang, Jingxue Microbiol Spectr Research Article Phage therapy is challenged by the frequent emergence of bacterial resistance to phages. As an interspecies signaling molecule, indole plays important roles in regulating bacterial behaviors. However, it is unclear whether indole is involved in the phage-bacterium interactions. Here, we report that indole modulated phage resistance of Pseudomonas aeruginosa PAO1. Specifically, we found that the type IV pilus (T4P) acts as an important receptor for P. aeruginosa phages vB_Pae_S1 and vB_Pae_TR, and indole could protect P. aeruginosa against phage infection via decreasing the T4P-mediated phage adsorption. Further investigation demonstrated that indole downregulated the expression of genes pilA, pilB, and pilQ, which are essential for T4P assembly and activity. Indole inhibits phage attacks, but our data suggest that indole functions not through interfering with the AHL-based QS pathway, although las quorum sensing (QS) of P. aeruginosa PAO1 were reported to promote phage infection. Our finding confirms the important roles of indole in virus-host interactions, which will provide important enlightenment in promoting phage therapy for P. aeruginosa infections. IMPORTANCE Our finding is significant with respect to the study of the interactions between phage and host. Although the important roles of indole in bacterial physiology have been revealed, no direct examples of indole participating in phage-host interactions were reported. This study reports that indole could modulate the phage resistance of indole-nonproducing Pseudomonas aeruginosa PAO1 through inhibition of phage adsorption mechanism. Our finding will be significant for guiding phage therapy and fill some gaps in the field of phage-host interactions. American Society for Microbiology 2023-01-05 /pmc/articles/PMC9927445/ /pubmed/36602321 http://dx.doi.org/10.1128/spectrum.03911-22 Text en Copyright © 2023 Xuan et al. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Research Article
Xuan, Guanhua
Dou, Qin
Kong, Jiuna
Lin, Hong
Wang, Jingxue
Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title_full Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title_fullStr Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title_full_unstemmed Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title_short Pseudomonas aeruginosa Resists Phage Infection via Eavesdropping on Indole Signaling
title_sort pseudomonas aeruginosa resists phage infection via eavesdropping on indole signaling
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9927445/
https://www.ncbi.nlm.nih.gov/pubmed/36602321
http://dx.doi.org/10.1128/spectrum.03911-22
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