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Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae

Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems. Biofilms attach to the surfaces of either living or nonliving objects and protect bacteria against antibiotics and a host’s immune system....

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Autores principales: Liu, Yan, Pan, Chao, Ye, Lijun, Si, Yue, Bi, Changhao, Hua, Xiaoting, Yu, Yunsong, Zhu, Li, Wang, Hengliang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Microbiology 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289706/
https://www.ncbi.nlm.nih.gov/pubmed/32522779
http://dx.doi.org/10.1128/mSphere.00336-20
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author Liu, Yan
Pan, Chao
Ye, Lijun
Si, Yue
Bi, Changhao
Hua, Xiaoting
Yu, Yunsong
Zhu, Li
Wang, Hengliang
author_facet Liu, Yan
Pan, Chao
Ye, Lijun
Si, Yue
Bi, Changhao
Hua, Xiaoting
Yu, Yunsong
Zhu, Li
Wang, Hengliang
author_sort Liu, Yan
collection PubMed
description Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems. Biofilms attach to the surfaces of either living or nonliving objects and protect bacteria against antibiotics and a host’s immune system. Here, a novel type of biofilm (the “R-biofilm”) is reported. These biofilms were formed by clinically isolated Klebsiella pneumoniae strains following double-stranded-DNA breaks (DSBs), while undamaged bacteria did not form classic biofilms even in the later stages of growth. R-biofilms had a fixed ring-like or discoid shape with good ductility and could protect many living bacterial cells within. We show that extracellular proteins and DNAs released, probably by dead bacteria, were the core structural materials of R-biofilms. We anticipate that novel signaling pathways besides the bacterial SOS response are involved in R-biofilm formation. The observations in this study suggest a limitation to the use of the currently popular Cas9-mediated bactericidal tools to eliminate certain bacteria because the resulting DSBs may lead to the formation of these protective R-biofilms. IMPORTANCE Many pathogenic bacteria can form biofilm matrices that consist of complex molecules such as polysaccharides, proteins, and DNA. These biofilms help the bacteria to infect and colonize a host. Such biofilms may attach and develop on the surfaces of indwelling medical devices or other supportive environments. This study found that following double-strand breaks in their DNA, Klebsiella pneumoniae cells can form a novel type of biofilm with ring-like or discoid morphology. This biofilm structure, named the “R-biofilm,” helps protect the bacteria against adverse conditions such as exposure to ethanol, hydrogen peroxide, and UV radiation.
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spelling pubmed-72897062020-06-25 Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae Liu, Yan Pan, Chao Ye, Lijun Si, Yue Bi, Changhao Hua, Xiaoting Yu, Yunsong Zhu, Li Wang, Hengliang mSphere Observation Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems. Biofilms attach to the surfaces of either living or nonliving objects and protect bacteria against antibiotics and a host’s immune system. Here, a novel type of biofilm (the “R-biofilm”) is reported. These biofilms were formed by clinically isolated Klebsiella pneumoniae strains following double-stranded-DNA breaks (DSBs), while undamaged bacteria did not form classic biofilms even in the later stages of growth. R-biofilms had a fixed ring-like or discoid shape with good ductility and could protect many living bacterial cells within. We show that extracellular proteins and DNAs released, probably by dead bacteria, were the core structural materials of R-biofilms. We anticipate that novel signaling pathways besides the bacterial SOS response are involved in R-biofilm formation. The observations in this study suggest a limitation to the use of the currently popular Cas9-mediated bactericidal tools to eliminate certain bacteria because the resulting DSBs may lead to the formation of these protective R-biofilms. IMPORTANCE Many pathogenic bacteria can form biofilm matrices that consist of complex molecules such as polysaccharides, proteins, and DNA. These biofilms help the bacteria to infect and colonize a host. Such biofilms may attach and develop on the surfaces of indwelling medical devices or other supportive environments. This study found that following double-strand breaks in their DNA, Klebsiella pneumoniae cells can form a novel type of biofilm with ring-like or discoid morphology. This biofilm structure, named the “R-biofilm,” helps protect the bacteria against adverse conditions such as exposure to ethanol, hydrogen peroxide, and UV radiation. American Society for Microbiology 2020-06-10 /pmc/articles/PMC7289706/ /pubmed/32522779 http://dx.doi.org/10.1128/mSphere.00336-20 Text en Copyright © 2020 Liu 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 Observation
Liu, Yan
Pan, Chao
Ye, Lijun
Si, Yue
Bi, Changhao
Hua, Xiaoting
Yu, Yunsong
Zhu, Li
Wang, Hengliang
Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title_full Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title_fullStr Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title_full_unstemmed Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title_short Nonclassical Biofilms Induced by DNA Breaks in Klebsiella pneumoniae
title_sort nonclassical biofilms induced by dna breaks in klebsiella pneumoniae
topic Observation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7289706/
https://www.ncbi.nlm.nih.gov/pubmed/32522779
http://dx.doi.org/10.1128/mSphere.00336-20
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