Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts

Clostridium difficile spores play a pivotal role in the transmission of infectious diarrhoea, but in order to cause disease spores must complete germination and return to vegetative cell growth. While the mechanisms of spore germination are well understood in Bacillus, knowledge of C. difficile germ...

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Main Authors: Heeg, Daniela, Burns, David A., Cartman, Stephen T., Minton, Nigel P.
Format: Article
Published: Public Library of Science 2012
Online Access:https://eprints.nottingham.ac.uk/2538/
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author Heeg, Daniela
Burns, David A.
Cartman, Stephen T.
Minton, Nigel P.
author_facet Heeg, Daniela
Burns, David A.
Cartman, Stephen T.
Minton, Nigel P.
author_sort Heeg, Daniela
building Nottingham Research Data Repository
collection Online Access
description Clostridium difficile spores play a pivotal role in the transmission of infectious diarrhoea, but in order to cause disease spores must complete germination and return to vegetative cell growth. While the mechanisms of spore germination are well understood in Bacillus, knowledge of C. difficile germination remains limited. Previous studies have shown that bile salts and amino acids play an important role in regulating the germination response of C. difficile spores. Taurocholate, in combination with glycine, can stimulate germination, whereas chenodeoxycholate has been shown to inhibit spore germination in a C. difficile clinical isolate. Our recent studies of C. difficile sporulation characteristics have since pointed to substantial diversity among different clinical isolates. Consequently, in this study we investigated how the germination characteristics of different C. difficile isolates vary in response to bile salts. By analysing 29 isolates, including 16 belonging to the BI/NAP1/027 type, we show that considerable diversity exists in both the rate and extent of C. difficile germination in response to rich medium containing both taurocholate and glycine. Strikingly, we also show that although a potent inhibitor of germination for some isolates, chenodeoxycholate does not inhibit the germination, or outgrowth, of all C. difficile strains. Finally, we provide evidence that components of rich media may induce the germination of C. difficile spores, even in the absence of taurocholate. Taken together, these data suggest that the mechanisms of C. difficile spore germination in response to bile salts are complex and require further study. Furthermore, we stress the importance of studying multiple isolates in the future when analysing the nutrients or chemicals that either stimulate or inhibit C. difficile spore germination.
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spelling nottingham-25382020-05-04T16:32:25Z https://eprints.nottingham.ac.uk/2538/ Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts Heeg, Daniela Burns, David A. Cartman, Stephen T. Minton, Nigel P. Clostridium difficile spores play a pivotal role in the transmission of infectious diarrhoea, but in order to cause disease spores must complete germination and return to vegetative cell growth. While the mechanisms of spore germination are well understood in Bacillus, knowledge of C. difficile germination remains limited. Previous studies have shown that bile salts and amino acids play an important role in regulating the germination response of C. difficile spores. Taurocholate, in combination with glycine, can stimulate germination, whereas chenodeoxycholate has been shown to inhibit spore germination in a C. difficile clinical isolate. Our recent studies of C. difficile sporulation characteristics have since pointed to substantial diversity among different clinical isolates. Consequently, in this study we investigated how the germination characteristics of different C. difficile isolates vary in response to bile salts. By analysing 29 isolates, including 16 belonging to the BI/NAP1/027 type, we show that considerable diversity exists in both the rate and extent of C. difficile germination in response to rich medium containing both taurocholate and glycine. Strikingly, we also show that although a potent inhibitor of germination for some isolates, chenodeoxycholate does not inhibit the germination, or outgrowth, of all C. difficile strains. Finally, we provide evidence that components of rich media may induce the germination of C. difficile spores, even in the absence of taurocholate. Taken together, these data suggest that the mechanisms of C. difficile spore germination in response to bile salts are complex and require further study. Furthermore, we stress the importance of studying multiple isolates in the future when analysing the nutrients or chemicals that either stimulate or inhibit C. difficile spore germination. Public Library of Science 2012-02-22 Article PeerReviewed Heeg, Daniela, Burns, David A., Cartman, Stephen T. and Minton, Nigel P. (2012) Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts. PLoS ONE, 7 (2). e32381/1-e32381/9. ISSN 1932-6203 http://www.plosone.org/article/info%3Adoi%2F10.1371%2Fjournal.pone.0032381 doi:10.1371/journal.pone.0032381 doi:10.1371/journal.pone.0032381
spellingShingle Heeg, Daniela
Burns, David A.
Cartman, Stephen T.
Minton, Nigel P.
Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title_full Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title_fullStr Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title_full_unstemmed Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title_short Spores of Clostridium difficile clinical isolates display a diverse germination response to bile salts
title_sort spores of clostridium difficile clinical isolates display a diverse germination response to bile salts
url https://eprints.nottingham.ac.uk/2538/
https://eprints.nottingham.ac.uk/2538/
https://eprints.nottingham.ac.uk/2538/