Literature DB >> 16820444

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

Jihong Li1, Bruce A McClane.   

Abstract

Clostridium perfringens type A isolates can carry the enterotoxin gene (cpe) on either their chromosome or a plasmid, but food poisoning isolates usually have a chromosomal cpe gene. This linkage between chromosomal cpe isolates and food poisoning has previously been attributed, at least in part, to better high-temperature survival of chromosomal cpe isolates than of plasmid cpe isolates. In the current study we assessed whether vegetative cells and spores of chromosomal cpe isolates also survive better than vegetative cells and spores of plasmid cpe isolates survive when the vegetative cells and spores are subjected to low temperatures. Vegetative cells of chromosomal cpe isolates exhibited about eightfold-higher decimal reduction values (D values) at 4 degrees C and threefold-higher D values at -20 degrees C than vegetative cells of plasmid cpe isolates exhibited. After 6 months of incubation at 4 degrees C and -20 degrees C, the average log reductions in viability for spores of plasmid cpe isolates were about fourfold and about threefold greater, respectively, than the average log reductions in viability for spores from chromosomal cpe isolates. C. perfringens type A isolates carrying a chromosomal cpe gene also grew significantly faster than plasmid cpe isolates grew at 25 degrees C, 37 degrees C, or 43 degrees C. In addition, chromosomal cpe isolates grew at higher maximum and lower minimum temperatures than plasmid cpe isolates grew. Collectively, these results suggest that chromosomal cpe isolates are commonly involved in food poisoning because of their greater resistance to low (as well as high) temperatures for both survival and growth. They also indicate the importance of proper low-temperature storage conditions, as well as heating, for prevention of C. perfringens type A food poisoning.

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Year:  2006        PMID: 16820444      PMCID: PMC1489334          DOI: 10.1128/AEM.00177-06

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


  21 in total

1.  Association of beta2 toxin production with Clostridium perfringens type A human gastrointestinal disease isolates carrying a plasmid enterotoxin gene.

Authors:  Derek J Fisher; Kazuaki Miyamoto; Benjamin Harrison; Shigero Akimoto; Mahfuzur R Sarker; Bruce A McClane
Journal:  Mol Microbiol       Date:  2005-05       Impact factor: 3.501

2.  Phenotypic characterization of enterotoxigenic Clostridium perfringens isolates from non-foodborne human gastrointestinal diseases.

Authors:  R E Collie; J F Kokai-Kun; B A McClane
Journal:  Anaerobe       Date:  1998-04       Impact factor: 3.331

3.  Modeling growth of Clostridium perfringens in pea soup during cooling.

Authors:  Aarieke E I de Jong; Rijkel R Beumer; Marcel H Zwietering
Journal:  Risk Anal       Date:  2005-02       Impact factor: 4.000

4.  Complete sequencing and diversity analysis of the enterotoxin-encoding plasmids in Clostridium perfringens type A non-food-borne human gastrointestinal disease isolates.

Authors:  Kazuaki Miyamoto; Derek J Fisher; Jihong Li; Sameera Sayeed; Shigeru Akimoto; Bruce A McClane
Journal:  J Bacteriol       Date:  2006-02       Impact factor: 3.490

5.  Behavior of Clostridium perfringens at low temperatures.

Authors:  A E I de Jong; F M Rombouts; R R Beumer
Journal:  Int J Food Microbiol       Date:  2004-12-01       Impact factor: 5.277

6.  Comparison of the levels of heat resistance of wild-type, cpe knockout, and cpe plasmid-cured Clostridium perfringens type A strains.

Authors:  Deepa Raju; Mahfuzur R Sarker
Journal:  Appl Environ Microbiol       Date:  2005-11       Impact factor: 4.792

7.  Heat resistance, spore germination, and enterotoxigenicity of Clostridium perfringens.

Authors:  Y Ando; T Tsuzuki; H Sunagawa; S Oka
Journal:  Microbiol Immunol       Date:  1985       Impact factor: 1.955

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

Authors:  J F Kokai-Kun; J G Songer; J R Czeczulin; F Chen; B A McClane
Journal:  J Clin Microbiol       Date:  1994-10       Impact factor: 5.948

9.  "Phoenix phenomenon" in the growth of Clostridium perfringens.

Authors:  S P Shoemaker; M D Pierson
Journal:  Appl Environ Microbiol       Date:  1976-12       Impact factor: 4.792

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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  38 in total

1.  Evaluating the involvement of alternative sigma factors SigF and SigG in Clostridium perfringens sporulation and enterotoxin synthesis.

Authors:  Jihong Li; Bruce A McClane
Journal:  Infect Immun       Date:  2010-07-19       Impact factor: 3.441

2.  Survival of akinetes (resting-state cells of cyanobacteria) in low earth orbit and simulated extraterrestrial conditions.

Authors:  Karen Olsson-Francis; Rosa de la Torre; Martin C Towner; Charles S Cockell
Journal:  Orig Life Evol Biosph       Date:  2009-12       Impact factor: 1.950

3.  The Agr-like quorum-sensing system regulates sporulation and production of enterotoxin and beta2 toxin by Clostridium perfringens type A non-food-borne human gastrointestinal disease strain F5603.

Authors:  Jihong Li; Jianming Chen; Jorge E Vidal; Bruce A McClane
Journal:  Infect Immun       Date:  2011-04-04       Impact factor: 3.441

Review 4.  Sporulation and Germination in Clostridial Pathogens.

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

5.  Comparative effects of osmotic, sodium nitrite-induced, and pH-induced stress on growth and survival of Clostridium perfringens type A isolates carrying chromosomal or plasmid-borne enterotoxin genes.

Authors:  Jihong Li; Bruce A McClane
Journal:  Appl Environ Microbiol       Date:  2006-10-13       Impact factor: 4.792

Review 6.  Inactivation Strategies for Clostridium perfringens Spores and Vegetative Cells.

Authors:  Prabhat K Talukdar; Pathima Udompijitkul; Ashfaque Hossain; Mahfuzur R Sarker
Journal:  Appl Environ Microbiol       Date:  2016-12-15       Impact factor: 4.792

7.  Freshwater suspended sediments and sewage are reservoirs for enterotoxin-positive Clostridium perfringens.

Authors:  Sabrina R Mueller-Spitz; Lisa B Stewart; J Val Klump; Sandra L McLellan
Journal:  Appl Environ Microbiol       Date:  2010-06-25       Impact factor: 4.792

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

Authors:  Daniel Paredes-Sabja; Pathima Udompijitkul; Mahfuzur R Sarker
Journal:  Appl Environ Microbiol       Date:  2009-08-07       Impact factor: 4.792

9.  Clostridium perfringens type A strains carrying a plasmid-borne enterotoxin gene (genotype IS1151-cpe or IS1470-like-cpe) as a common cause of food poisoning.

Authors:  Päivi Lahti; Annamari Heikinheimo; Tuula Johansson; Hannu Korkeala
Journal:  J Clin Microbiol       Date:  2007-11-14       Impact factor: 5.948

10.  Further characterization of Clostridium perfringens small acid soluble protein-4 (Ssp4) properties and expression.

Authors:  Jihong Li; Daniel Paredes-Sabja; Mahfuzur R Sarker; Bruce A McClane
Journal:  PLoS One       Date:  2009-07-17       Impact factor: 3.240

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