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Calcium carbonate mineralization is essential for biofilm formation and lung colonization

Biofilms are differentiated microbial communities held together by an extracellular matrix. μCT X-ray revealed structured mineralized areas within biofilms of lung pathogens belonging to two distant phyla – the proteobacteria Pseudomonas aeruginosa and the actinobacteria Mycobacterium abscessus. Fur...

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Autores principales: Cohen-Cymberknoh, Malena, Kolodkin-Gal, Dror, Keren-Paz, Alona, Peretz, Shani, Brumfeld, Vlad, Kapishnikov, Sergey, Suissa, Ronit, Shteinberg, Michal, McLeod, Daniel, Maan, Harsh, Patrauchan, Marianna, Zamir, Gideon, Kerem, Eitan, Kolodkin-Gal, Ilana
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062676/
https://www.ncbi.nlm.nih.gov/pubmed/35521519
http://dx.doi.org/10.1016/j.isci.2022.104234
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author Cohen-Cymberknoh, Malena
Kolodkin-Gal, Dror
Keren-Paz, Alona
Peretz, Shani
Brumfeld, Vlad
Kapishnikov, Sergey
Suissa, Ronit
Shteinberg, Michal
McLeod, Daniel
Maan, Harsh
Patrauchan, Marianna
Zamir, Gideon
Kerem, Eitan
Kolodkin-Gal, Ilana
author_facet Cohen-Cymberknoh, Malena
Kolodkin-Gal, Dror
Keren-Paz, Alona
Peretz, Shani
Brumfeld, Vlad
Kapishnikov, Sergey
Suissa, Ronit
Shteinberg, Michal
McLeod, Daniel
Maan, Harsh
Patrauchan, Marianna
Zamir, Gideon
Kerem, Eitan
Kolodkin-Gal, Ilana
author_sort Cohen-Cymberknoh, Malena
collection PubMed
description Biofilms are differentiated microbial communities held together by an extracellular matrix. μCT X-ray revealed structured mineralized areas within biofilms of lung pathogens belonging to two distant phyla – the proteobacteria Pseudomonas aeruginosa and the actinobacteria Mycobacterium abscessus. Furthermore, calcium chelation inhibited the assembly of complex bacterial structures for both organisms with little to no effect on cell growth. The molecular mechanisms promoting calcite scaffold formation were surprisingly conserved between the two pathogens as biofilm development was similarly impaired by genetic and biochemical inhibition of calcium uptake and carbonate accumulation. Moreover, chemical inhibition and mutations targeting mineralization significantly reduced the attachment of P. aeruginosa to the lung, as well as the subsequent damage inflicted by biofilms to lung tissues, and restored their sensitivity to antibiotics. This work offers underexplored druggable targets for antibiotics to combat otherwise untreatable biofilm infections.
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spelling pubmed-90626762022-05-04 Calcium carbonate mineralization is essential for biofilm formation and lung colonization Cohen-Cymberknoh, Malena Kolodkin-Gal, Dror Keren-Paz, Alona Peretz, Shani Brumfeld, Vlad Kapishnikov, Sergey Suissa, Ronit Shteinberg, Michal McLeod, Daniel Maan, Harsh Patrauchan, Marianna Zamir, Gideon Kerem, Eitan Kolodkin-Gal, Ilana iScience Article Biofilms are differentiated microbial communities held together by an extracellular matrix. μCT X-ray revealed structured mineralized areas within biofilms of lung pathogens belonging to two distant phyla – the proteobacteria Pseudomonas aeruginosa and the actinobacteria Mycobacterium abscessus. Furthermore, calcium chelation inhibited the assembly of complex bacterial structures for both organisms with little to no effect on cell growth. The molecular mechanisms promoting calcite scaffold formation were surprisingly conserved between the two pathogens as biofilm development was similarly impaired by genetic and biochemical inhibition of calcium uptake and carbonate accumulation. Moreover, chemical inhibition and mutations targeting mineralization significantly reduced the attachment of P. aeruginosa to the lung, as well as the subsequent damage inflicted by biofilms to lung tissues, and restored their sensitivity to antibiotics. This work offers underexplored druggable targets for antibiotics to combat otherwise untreatable biofilm infections. Elsevier 2022-04-11 /pmc/articles/PMC9062676/ /pubmed/35521519 http://dx.doi.org/10.1016/j.isci.2022.104234 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Cohen-Cymberknoh, Malena
Kolodkin-Gal, Dror
Keren-Paz, Alona
Peretz, Shani
Brumfeld, Vlad
Kapishnikov, Sergey
Suissa, Ronit
Shteinberg, Michal
McLeod, Daniel
Maan, Harsh
Patrauchan, Marianna
Zamir, Gideon
Kerem, Eitan
Kolodkin-Gal, Ilana
Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title_full Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title_fullStr Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title_full_unstemmed Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title_short Calcium carbonate mineralization is essential for biofilm formation and lung colonization
title_sort calcium carbonate mineralization is essential for biofilm formation and lung colonization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9062676/
https://www.ncbi.nlm.nih.gov/pubmed/35521519
http://dx.doi.org/10.1016/j.isci.2022.104234
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