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Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant

Pseudomonas aeruginosa biofilms represent a major threat to health care. Rugose small colony variants (RSCV) of P. aeruginosa, isolated from chronic infections, display hyperbiofilm phenotype. RSCV biofilms are highly resistant to antibiotics and host defenses. This work shows that RSCV biofilm aggr...

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Autores principales: Deng, Binbin, Ghatak, Subhadip, Sarkar, Subendu, Singh, Kanhaiya, Das Ghatak, Piya, Mathew-Steiner, Shomita S., Roy, Sashwati, Khanna, Savita, Wozniak, Daniel J., McComb, David W., Sen, Chandan K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997594/
https://www.ncbi.nlm.nih.gov/pubmed/32058950
http://dx.doi.org/10.1016/j.isci.2020.100827
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author Deng, Binbin
Ghatak, Subhadip
Sarkar, Subendu
Singh, Kanhaiya
Das Ghatak, Piya
Mathew-Steiner, Shomita S.
Roy, Sashwati
Khanna, Savita
Wozniak, Daniel J.
McComb, David W.
Sen, Chandan K.
author_facet Deng, Binbin
Ghatak, Subhadip
Sarkar, Subendu
Singh, Kanhaiya
Das Ghatak, Piya
Mathew-Steiner, Shomita S.
Roy, Sashwati
Khanna, Savita
Wozniak, Daniel J.
McComb, David W.
Sen, Chandan K.
author_sort Deng, Binbin
collection PubMed
description Pseudomonas aeruginosa biofilms represent a major threat to health care. Rugose small colony variants (RSCV) of P. aeruginosa, isolated from chronic infections, display hyperbiofilm phenotype. RSCV biofilms are highly resistant to antibiotics and host defenses. This work shows that RSCV biofilm aggregates consist of two distinct bacterial subpopulations that are uniquely organized displaying contrasting physiological characteristics. Compared with that of PAO1, the extracellular polymeric substance of RSCV PAO1ΔwspF biofilms presented unique ultrastructural characteristics. Unlike PAO1, PAO1ΔwspF released fragmented extracellular DNA (eDNA) from live cells. Fragmented eDNA, thus released, was responsible for resistance of PAO1ΔwspF biofilm to disruption by DNaseI. When added to PAO1, such fragmented eDNA enhanced biofilm formation. Disruption of PAO1ΔwspF biofilm was achieved by aurine tricarboxylic acid, an inhibitor of DNA-protein interaction. This work provides critical novel insights into the contrasting structural and functional characteristics of a hyperbiofilm-forming clinical bacterial variant relative to its own wild-type strain.
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spelling pubmed-69975942020-02-05 Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant Deng, Binbin Ghatak, Subhadip Sarkar, Subendu Singh, Kanhaiya Das Ghatak, Piya Mathew-Steiner, Shomita S. Roy, Sashwati Khanna, Savita Wozniak, Daniel J. McComb, David W. Sen, Chandan K. iScience Article Pseudomonas aeruginosa biofilms represent a major threat to health care. Rugose small colony variants (RSCV) of P. aeruginosa, isolated from chronic infections, display hyperbiofilm phenotype. RSCV biofilms are highly resistant to antibiotics and host defenses. This work shows that RSCV biofilm aggregates consist of two distinct bacterial subpopulations that are uniquely organized displaying contrasting physiological characteristics. Compared with that of PAO1, the extracellular polymeric substance of RSCV PAO1ΔwspF biofilms presented unique ultrastructural characteristics. Unlike PAO1, PAO1ΔwspF released fragmented extracellular DNA (eDNA) from live cells. Fragmented eDNA, thus released, was responsible for resistance of PAO1ΔwspF biofilm to disruption by DNaseI. When added to PAO1, such fragmented eDNA enhanced biofilm formation. Disruption of PAO1ΔwspF biofilm was achieved by aurine tricarboxylic acid, an inhibitor of DNA-protein interaction. This work provides critical novel insights into the contrasting structural and functional characteristics of a hyperbiofilm-forming clinical bacterial variant relative to its own wild-type strain. Elsevier 2020-01-09 /pmc/articles/PMC6997594/ /pubmed/32058950 http://dx.doi.org/10.1016/j.isci.2020.100827 Text en © 2020 The Authors http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Deng, Binbin
Ghatak, Subhadip
Sarkar, Subendu
Singh, Kanhaiya
Das Ghatak, Piya
Mathew-Steiner, Shomita S.
Roy, Sashwati
Khanna, Savita
Wozniak, Daniel J.
McComb, David W.
Sen, Chandan K.
Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title_full Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title_fullStr Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title_full_unstemmed Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title_short Novel Bacterial Diversity and Fragmented eDNA Identified in Hyperbiofilm-Forming Pseudomonas aeruginosa Rugose Small Colony Variant
title_sort novel bacterial diversity and fragmented edna identified in hyperbiofilm-forming pseudomonas aeruginosa rugose small colony variant
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6997594/
https://www.ncbi.nlm.nih.gov/pubmed/32058950
http://dx.doi.org/10.1016/j.isci.2020.100827
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