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Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients

BACKGROUND: COVID-19 pneumonia has caused huge impact on the health of infected patients and associated with high morbidity and mortality. Shift in the lung microbial ecology upon such viral infection often worsens the disease and increases host susceptibility to superinfections. Bacterial superinfe...

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Autores principales: Qu, Jiuxin, Cai, Zhao, Duan, Xiangke, Zhang, Han, Cheng, Hang, Han, Shuhong, Yu, Kaiwei, Jiang, Zhaofang, Zhang, Yingdan, Liu, Yang, Bai, Fang, Liu, Yingxia, Liu, Lei, Yang, Liang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827185/
https://www.ncbi.nlm.nih.gov/pubmed/35139898
http://dx.doi.org/10.1186/s13578-022-00748-z
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author Qu, Jiuxin
Cai, Zhao
Duan, Xiangke
Zhang, Han
Cheng, Hang
Han, Shuhong
Yu, Kaiwei
Jiang, Zhaofang
Zhang, Yingdan
Liu, Yang
Bai, Fang
Liu, Yingxia
Liu, Lei
Yang, Liang
author_facet Qu, Jiuxin
Cai, Zhao
Duan, Xiangke
Zhang, Han
Cheng, Hang
Han, Shuhong
Yu, Kaiwei
Jiang, Zhaofang
Zhang, Yingdan
Liu, Yang
Bai, Fang
Liu, Yingxia
Liu, Lei
Yang, Liang
author_sort Qu, Jiuxin
collection PubMed
description BACKGROUND: COVID-19 pneumonia has caused huge impact on the health of infected patients and associated with high morbidity and mortality. Shift in the lung microbial ecology upon such viral infection often worsens the disease and increases host susceptibility to superinfections. Bacterial superinfection contributes to the aggravation of COVID-19 and poses a great challenge to clinical treatments. An in-depth investigation on superinfecting bacteria in COVID-19 patients might facilitate understanding of lung microenvironment post virus infections and superinfection mechanism. RESULTS: We analyzed the adaptation of two pairs of P. aeruginosa strains with the same MLST type isolated from two critical COVID-19 patients by combining sequencing analysis and phenotypic assays. Both P. aeruginosa strains were found to turn on alginate biosynthesis and attenuate type VI secretion system (T6SS) during short-term colonization in the COVID-19 patients, which results in excessive biofilm formation and virulence reduction-two distinct markers for chronic infections. The macrophage cytotoxicity test and intracellular reactive oxygen species measurement confirmed that the adapted P. aeruginosa strains reduced their virulence towards host cells and are better to escape from host immune clearance than their ancestors. CONCLUSION: Our study suggests that SARS-CoV-2 infection can create a lung environment that allow rapid adaptive evolution of bacterial pathogens with genetic traits suitable for chronic infections. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00748-z.
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spelling pubmed-88271852022-02-10 Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients Qu, Jiuxin Cai, Zhao Duan, Xiangke Zhang, Han Cheng, Hang Han, Shuhong Yu, Kaiwei Jiang, Zhaofang Zhang, Yingdan Liu, Yang Bai, Fang Liu, Yingxia Liu, Lei Yang, Liang Cell Biosci Research BACKGROUND: COVID-19 pneumonia has caused huge impact on the health of infected patients and associated with high morbidity and mortality. Shift in the lung microbial ecology upon such viral infection often worsens the disease and increases host susceptibility to superinfections. Bacterial superinfection contributes to the aggravation of COVID-19 and poses a great challenge to clinical treatments. An in-depth investigation on superinfecting bacteria in COVID-19 patients might facilitate understanding of lung microenvironment post virus infections and superinfection mechanism. RESULTS: We analyzed the adaptation of two pairs of P. aeruginosa strains with the same MLST type isolated from two critical COVID-19 patients by combining sequencing analysis and phenotypic assays. Both P. aeruginosa strains were found to turn on alginate biosynthesis and attenuate type VI secretion system (T6SS) during short-term colonization in the COVID-19 patients, which results in excessive biofilm formation and virulence reduction-two distinct markers for chronic infections. The macrophage cytotoxicity test and intracellular reactive oxygen species measurement confirmed that the adapted P. aeruginosa strains reduced their virulence towards host cells and are better to escape from host immune clearance than their ancestors. CONCLUSION: Our study suggests that SARS-CoV-2 infection can create a lung environment that allow rapid adaptive evolution of bacterial pathogens with genetic traits suitable for chronic infections. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13578-022-00748-z. BioMed Central 2022-02-09 /pmc/articles/PMC8827185/ /pubmed/35139898 http://dx.doi.org/10.1186/s13578-022-00748-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Qu, Jiuxin
Cai, Zhao
Duan, Xiangke
Zhang, Han
Cheng, Hang
Han, Shuhong
Yu, Kaiwei
Jiang, Zhaofang
Zhang, Yingdan
Liu, Yang
Bai, Fang
Liu, Yingxia
Liu, Lei
Yang, Liang
Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title_full Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title_fullStr Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title_full_unstemmed Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title_short Pseudomonas aeruginosa modulates alginate biosynthesis and type VI secretion system in two critically ill COVID-19 patients
title_sort pseudomonas aeruginosa modulates alginate biosynthesis and type vi secretion system in two critically ill covid-19 patients
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8827185/
https://www.ncbi.nlm.nih.gov/pubmed/35139898
http://dx.doi.org/10.1186/s13578-022-00748-z
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