Cellular adaptation of Clostridioides difficile to high salinity encompasses a compatible solute‐responsive change in cell morphology. (17th February 2022)
- Record Type:
- Journal Article
- Title:
- Cellular adaptation of Clostridioides difficile to high salinity encompasses a compatible solute‐responsive change in cell morphology. (17th February 2022)
- Main Title:
- Cellular adaptation of Clostridioides difficile to high salinity encompasses a compatible solute‐responsive change in cell morphology
- Authors:
- Michel, Annika‐Marisa
Borrero‐de Acuña, José Manuel
Molinari, Gabriella
Ünal, Can Murat
Will, Sabine
Derksen, Elisabeth
Barthels, Stefan
Bartram, Wiebke
Schrader, Michel
Rohde, Manfred
Zhang, Hao
Hoffmann, Tamara
Neumann‐Schaal, Meina
Bremer, Erhard
Jahn, Dieter - Abstract:
- Summary: Infections by the pathogenic gut bacterium Clostridioides difficile cause severe diarrhoeas up to a toxic megacolon and are currently among the major causes of lethal bacterial infections. Successful bacterial propagation in the gut is strongly associated with the adaptation to changing nutrition‐caused environmental conditions; e.g. environmental salt stresses. Concentrations of 350 mM NaCl, the prevailing salinity in the colon, led to significantly reduced growth of C . difficile . Metabolomics of salt‐stressed bacteria revealed a major reduction of the central energy generation pathways, including the Stickland‐fermentation reactions. No obvious synthesis of compatible solutes was observed up to 24 h of growth. The ensuing limited tolerance to high salinity and absence of compatible solute synthesis might result from an evolutionary adaptation to the exclusive life of C . difficile in the mammalian gut. Addition of the compatible solutes carnitine, glycine‐betaine, γ‐butyrobetaine, crotonobetaine, homobetaine, proline‐betaine and dimethylsulfoniopropionate restored growth (choline and proline failed) under conditions of high salinity. A bioinformatically identified OpuF‐type ABC‐transporter imported most of the used compatible solutes. A long‐term adaptation after 48 h included a shift of the Stickland fermentation‐based energy metabolism from the utilization to the accumulation of l ‐proline and resulted in restored growth. Surprisingly, salt stress resulted inSummary: Infections by the pathogenic gut bacterium Clostridioides difficile cause severe diarrhoeas up to a toxic megacolon and are currently among the major causes of lethal bacterial infections. Successful bacterial propagation in the gut is strongly associated with the adaptation to changing nutrition‐caused environmental conditions; e.g. environmental salt stresses. Concentrations of 350 mM NaCl, the prevailing salinity in the colon, led to significantly reduced growth of C . difficile . Metabolomics of salt‐stressed bacteria revealed a major reduction of the central energy generation pathways, including the Stickland‐fermentation reactions. No obvious synthesis of compatible solutes was observed up to 24 h of growth. The ensuing limited tolerance to high salinity and absence of compatible solute synthesis might result from an evolutionary adaptation to the exclusive life of C . difficile in the mammalian gut. Addition of the compatible solutes carnitine, glycine‐betaine, γ‐butyrobetaine, crotonobetaine, homobetaine, proline‐betaine and dimethylsulfoniopropionate restored growth (choline and proline failed) under conditions of high salinity. A bioinformatically identified OpuF‐type ABC‐transporter imported most of the used compatible solutes. A long‐term adaptation after 48 h included a shift of the Stickland fermentation‐based energy metabolism from the utilization to the accumulation of l ‐proline and resulted in restored growth. Surprisingly, salt stress resulted in the formation of coccoid C . difficile cells instead of the typical rod‐shaped cells, a process reverted by the addition of several compatible solutes. Hence, compatible solute import via OpuF is the major immediate adaptation strategy of C . difficile to high salinity‐incurred cellular stress. … (more)
- Is Part Of:
- Environmental microbiology. Volume 24:Number 3(2022)
- Journal:
- Environmental microbiology
- Issue:
- Volume 24:Number 3(2022)
- Issue Display:
- Volume 24, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 24
- Issue:
- 3
- Issue Sort Value:
- 2022-0024-0003-0000
- Page Start:
- 1499
- Page End:
- 1517
- Publication Date:
- 2022-02-17
- Subjects:
- Microbial ecology -- Periodicals
Environmental Microbiology -- Periodicals
579.17 - Journal URLs:
- http://firstsearch.oclc.org ↗
http://firstsearch.oclc.org/journal=1462-2912;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1462-2920/issues ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=emi ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/1462-2920.15925 ↗
- Languages:
- English
- ISSNs:
- 1462-2912
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3791.522600
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 21323.xml