Literature DB >> 19666724

Inorganic phosphate and sodium ions are cogerminants for spores of Clostridium perfringens type A food poisoning-related isolates.

Daniel Paredes-Sabja1, Pathima Udompijitkul, Mahfuzur R Sarker.   

Abstract

Clostridium perfringens type A isolates carrying a chromosomal copy of the enterotoxin (cpe) gene are involved in the majority of food poisoning (FP) outbreaks, while type A isolates carrying a plasmid-borne cpe gene are involved in C. perfringens-associated non-food-borne (NFB) gastrointestinal diseases. To cause diseases, C. perfringens spores must germinate and return to active growth. Previously, we showed that only spores of FP isolates were able to germinate with K(+) ions. We now found that the spores of the majority of FP isolates, but none of the NFB isolates, germinated with the cogerminants Na(+) and inorganic phosphate (NaP(i)) at a pH of approximately 6.0. Spores of gerKA-KC and gerAA mutants germinated to a lesser extent and released less dipicolinic acid (DPA) than did wild-type spores with NaP(i). Although gerKB spores germinated to a similar extent as wild-type spores with NaP(i), their rate of germination was lower. Similarly, gerO and gerO gerQ mutant spores germinated slower and released less DPA than did wild-type spores with NaP(i). In contrast, gerQ spores germinated to a slightly lesser extent than wild-type spores but released all of their DPA during NaP(i) germination. In sum, this study identified NaP(i) as a novel nutrient germinant for spores of most FP isolates and provided evidence that proteins encoded by the gerKA-KC operon, gerAA, and gerO are required for NaP(i)-induced spore germination.

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Year:  2009        PMID: 19666724      PMCID: PMC2753063          DOI: 10.1128/AEM.00822-09

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  28 in total

1.  Ionic germination of spores of Bacillus megaterium QM B 1551.

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Journal:  Arch Mikrobiol       Date:  1962

2.  Further comparison of temperature effects on growth and survival of Clostridium perfringens type A isolates carrying a chromosomal or plasmid-borne enterotoxin gene.

Authors:  Jihong Li; Bruce A McClane
Journal:  Appl Environ Microbiol       Date:  2006-07       Impact factor: 4.792

3.  Molecular characterization of Clostridium perfringens isolates from humans with sporadic diarrhea: evidence for transcriptional regulation of the beta2-toxin-encoding gene.

Authors:  Ben Harrison; Deepa Raju; Helen S Garmory; Moira M Brett; Richard W Titball; Mahfuzur R Sarker
Journal:  Appl Environ Microbiol       Date:  2005-12       Impact factor: 4.792

4.  Evidence that the enterotoxin gene can be episomal in Clostridium perfringens isolates associated with non-food-borne human gastrointestinal diseases.

Authors:  R E Collie; B A McClane
Journal:  J Clin Microbiol       Date:  1998-01       Impact factor: 5.948

5.  Identification and characterization of sporulation-dependent promoters upstream of the enterotoxin gene (cpe) of Clostridium perfringens.

Authors:  Y Zhao; S B Melville
Journal:  J Bacteriol       Date:  1998-01       Impact factor: 3.490

6.  Analysis of core housekeeping and virulence genes reveals cryptic lineages of Clostridium perfringens that are associated with distinct disease presentations.

Authors:  Alejandro P Rooney; James L Swezey; Robert Friedman; David W Hecht; Carol W Maddox
Journal:  Genetics       Date:  2006-02-19       Impact factor: 4.562

7.  Comparison of Western immunoblots and gene detection assays for identification of potentially enterotoxigenic isolates of Clostridium perfringens.

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Journal:  J Clin Microbiol       Date:  1994-10       Impact factor: 5.948

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Authors:  C L Duncan; D H Strong
Journal:  Appl Microbiol       Date:  1968-01

9.  Sporulation and enterotoxin production by mutants of Clostridium perfringens.

Authors:  C L Duncan; D H Strong; M Sebald
Journal:  J Bacteriol       Date:  1972-04       Impact factor: 3.490

10.  The enterotoxin gene (cpe) of Clostridium perfringens can be chromosomal or plasmid-borne.

Authors:  E Cornillot; B Saint-Joanis; G Daube; S Katayama; P E Granum; B Canard; S T Cole
Journal:  Mol Microbiol       Date:  1995-02       Impact factor: 3.501

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  11 in total

Review 1.  Sporulation and Germination in Clostridial Pathogens.

Authors:  Aimee Shen; Adrianne N Edwards; Mahfuzur R Sarker; Daniel Paredes-Sabja
Journal:  Microbiol Spectr       Date:  2019-11

2.  The Clostridium perfringens germinant receptor protein GerKC is located in the spore inner membrane and is crucial for spore germination.

Authors:  Saeed Banawas; Daniel Paredes-Sabja; George Korza; Yunfeng Li; Bing Hao; Peter Setlow; Mahfuzur R Sarker
Journal:  J Bacteriol       Date:  2013-09-06       Impact factor: 3.490

Review 3.  Germinants and Their Receptors in Clostridia.

Authors:  Disha Bhattacharjee; Kathleen N McAllister; Joseph A Sorg
Journal:  J Bacteriol       Date:  2016-09-22       Impact factor: 3.490

4.  Spore Cortex Hydrolysis Precedes Dipicolinic Acid Release during Clostridium difficile Spore Germination.

Authors:  Michael B Francis; Charlotte A Allen; Joseph A Sorg
Journal:  J Bacteriol       Date:  2015-04-27       Impact factor: 3.490

Review 5.  Clostridium perfringens Sporulation and Sporulation-Associated Toxin Production.

Authors:  Jihong Li; Daniel Paredes-Sabja; Mahfuzur R Sarker; Bruce A McClane
Journal:  Microbiol Spectr       Date:  2016-06

6.  Clostridioides difficile SpoVAD and SpoVAE Interact and Are Required for Dipicolinic Acid Uptake into Spores.

Authors:  Marko Baloh; Joseph A Sorg
Journal:  J Bacteriol       Date:  2021-08-23       Impact factor: 3.490

7.  Dipicolinic Acid Release by Germinating Clostridium difficile Spores Occurs through a Mechanosensing Mechanism.

Authors:  Michael B Francis; Joseph A Sorg
Journal:  mSphere       Date:  2016-12-14       Impact factor: 4.389

8.  Analysis of the Spore Membrane Proteome in Clostridium perfringens Implicates Cyanophycin in Spore Assembly.

Authors:  Hualan Liu; W Keith Ray; Richard F Helm; David L Popham; Stephen B Melville
Journal:  J Bacteriol       Date:  2016-05-27       Impact factor: 3.490

9.  Transcriptional analysis of temporal gene expression in germinating Clostridium difficile 630 endospores.

Authors:  Marcin Dembek; Richard A Stabler; Adam A Witney; Brendan W Wren; Neil F Fairweather
Journal:  PLoS One       Date:  2013-05-15       Impact factor: 3.240

10.  Bile acid recognition by the Clostridium difficile germinant receptor, CspC, is important for establishing infection.

Authors:  Michael B Francis; Charlotte A Allen; Ritu Shrestha; Joseph A Sorg
Journal:  PLoS Pathog       Date:  2013-05-09       Impact factor: 6.823

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