Cargando…

Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival

The viable but non culturable (VBNC) state is a condition in which bacterial cells are viable and metabolically active, but resistant to cultivation using a routine growth medium. We investigated the ability of V. parahaemolyticus to form VBNC cells, and to subsequently become resuscitated. The abil...

Descripción completa

Detalles Bibliográficos
Autores principales: Wagley, Sariqa, Morcrette, Helen, Kovacs-Simon, Andrea, Yang, Zheng R., Power, Ann, Tennant, Richard K., Love, John, Murray, Neil, Titball, Richard W., Butler, Clive S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837498/
https://www.ncbi.nlm.nih.gov/pubmed/33439894
http://dx.doi.org/10.1371/journal.ppat.1009194
_version_ 1783642967968317440
author Wagley, Sariqa
Morcrette, Helen
Kovacs-Simon, Andrea
Yang, Zheng R.
Power, Ann
Tennant, Richard K.
Love, John
Murray, Neil
Titball, Richard W.
Butler, Clive S.
author_facet Wagley, Sariqa
Morcrette, Helen
Kovacs-Simon, Andrea
Yang, Zheng R.
Power, Ann
Tennant, Richard K.
Love, John
Murray, Neil
Titball, Richard W.
Butler, Clive S.
author_sort Wagley, Sariqa
collection PubMed
description The viable but non culturable (VBNC) state is a condition in which bacterial cells are viable and metabolically active, but resistant to cultivation using a routine growth medium. We investigated the ability of V. parahaemolyticus to form VBNC cells, and to subsequently become resuscitated. The ability to control VBNC cell formation in the laboratory allowed us to selectively isolate VBNC cells using fluorescence activated cell sorting, and to differentiate subpopulations based on their metabolic activity, cell shape and the ability to cause disease in Galleria mellonella. Our results showed that two subpopulations (P1 and P2) of V. parahaemolyticus VBNC cells exist and can remain dormant in the VBNC state for long periods. VBNC subpopulation P2, had a better fitness for survival under stressful conditions and showed 100% revival under favourable conditions. Proteomic analysis of these subpopulations (at two different time points: 12 days (T12) and 50 days (T50) post VBNC) revealed that the proteome of P2 was more similar to that of the starting microcosm culture (T0) than the proteome of P1. Proteins that were significantly up or down-regulated between the different VBNC populations were identified and differentially regulated proteins were assigned into 23 functional groups, the majority being assigned to metabolism functional categories. A lactate dehydrogenase (lldD) protein, responsible for converting lactate to pyruvate, was significantly upregulated in all subpopulations of VBNC cells. Deletion of the lactate dehydrogenase (RIMD2210633:ΔlldD) gene caused cells to enter the VBNC state significantly more quickly compared to the wild-type, and adding lactate to VBNC cells aided their resuscitation and extended the resuscitation window. Addition of pyruvate to the RIMD2210633:ΔlldD strain restored the wild-type VBNC formation profile. This study suggests that lactate dehydrogenase may play a role in regulating the VBNC state.
format Online
Article
Text
id pubmed-7837498
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-78374982021-02-02 Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival Wagley, Sariqa Morcrette, Helen Kovacs-Simon, Andrea Yang, Zheng R. Power, Ann Tennant, Richard K. Love, John Murray, Neil Titball, Richard W. Butler, Clive S. PLoS Pathog Research Article The viable but non culturable (VBNC) state is a condition in which bacterial cells are viable and metabolically active, but resistant to cultivation using a routine growth medium. We investigated the ability of V. parahaemolyticus to form VBNC cells, and to subsequently become resuscitated. The ability to control VBNC cell formation in the laboratory allowed us to selectively isolate VBNC cells using fluorescence activated cell sorting, and to differentiate subpopulations based on their metabolic activity, cell shape and the ability to cause disease in Galleria mellonella. Our results showed that two subpopulations (P1 and P2) of V. parahaemolyticus VBNC cells exist and can remain dormant in the VBNC state for long periods. VBNC subpopulation P2, had a better fitness for survival under stressful conditions and showed 100% revival under favourable conditions. Proteomic analysis of these subpopulations (at two different time points: 12 days (T12) and 50 days (T50) post VBNC) revealed that the proteome of P2 was more similar to that of the starting microcosm culture (T0) than the proteome of P1. Proteins that were significantly up or down-regulated between the different VBNC populations were identified and differentially regulated proteins were assigned into 23 functional groups, the majority being assigned to metabolism functional categories. A lactate dehydrogenase (lldD) protein, responsible for converting lactate to pyruvate, was significantly upregulated in all subpopulations of VBNC cells. Deletion of the lactate dehydrogenase (RIMD2210633:ΔlldD) gene caused cells to enter the VBNC state significantly more quickly compared to the wild-type, and adding lactate to VBNC cells aided their resuscitation and extended the resuscitation window. Addition of pyruvate to the RIMD2210633:ΔlldD strain restored the wild-type VBNC formation profile. This study suggests that lactate dehydrogenase may play a role in regulating the VBNC state. Public Library of Science 2021-01-13 /pmc/articles/PMC7837498/ /pubmed/33439894 http://dx.doi.org/10.1371/journal.ppat.1009194 Text en © 2021 Wagley et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wagley, Sariqa
Morcrette, Helen
Kovacs-Simon, Andrea
Yang, Zheng R.
Power, Ann
Tennant, Richard K.
Love, John
Murray, Neil
Titball, Richard W.
Butler, Clive S.
Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title_full Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title_fullStr Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title_full_unstemmed Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title_short Bacterial dormancy: A subpopulation of viable but non-culturable cells demonstrates better fitness for revival
title_sort bacterial dormancy: a subpopulation of viable but non-culturable cells demonstrates better fitness for revival
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7837498/
https://www.ncbi.nlm.nih.gov/pubmed/33439894
http://dx.doi.org/10.1371/journal.ppat.1009194
work_keys_str_mv AT wagleysariqa bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT morcrettehelen bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT kovacssimonandrea bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT yangzhengr bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT powerann bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT tennantrichardk bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT lovejohn bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT murrayneil bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT titballrichardw bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival
AT butlerclives bacterialdormancyasubpopulationofviablebutnonculturablecellsdemonstratesbetterfitnessforrevival