Literature DB >> 8757868

Regulated expression of Clostridium perfringens enterotoxin in naturally cpe-negative type A, B, and C isolates of C. perfringens.

J R Czeczulin1, R E Collie, B A McClane.   

Abstract

Clostridium perfringens enterotoxin (CPE), the virulence factor responsible for symptoms associated with C. perfringens type A food poisoning, is produced by enterotoxigenic C. perfringens type A isolates when these bacteria sporulate in the gastrointestinal tract. Less than 5% of the global C. perfringens population apparently carries the cpe gene. To assess the distribution of cpe-regulatory factors, we investigated whether the cpe gene of a C. perfringens food poisoning isolate can be expressed and properly regulated (i.e., expressed in a sporulation-associated manner) when transformed into naturally cpe-negative C. perfringens isolates. Sporulation-associated CPE expression was observed when low-copy-number plasmids carrying either a 5.7-kb DNA insert, containing the cpe open reading frame plus >1 kb each of upstream and downstream flanking sequences from C. perfringens food poisoning isolate NCTC 8239, or a 1.6-kb insert, containing only the cpe open reading frame of NCTC 8239, were electroporated into cpe-negative C. perfringens type A, B, and C isolates. Northern (RNA) blot analysis demonstrated that the sizes of the cpe message in the transformants and the naturally enterotoxigenic C. perfringens NCTC 8239 were similar and that this message was detectable only in sporulating cultures of the transformants or NCTC 8239. These studies strongly suggest that many, if not all, cpe-negative C. perfringens isolates (including type B isolates, which are not known to naturally express CPE) produce a factor(s) involved in normal (i.e., sporulation-associated) transcriptional regulation of CPE expression by C. perfringens food poisoning isolates. These findings are consistent with this CPE-regulatory factor(s) also regulating the expression of other genes in C. perfringens.

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Year:  1996        PMID: 8757868      PMCID: PMC174222          DOI: 10.1128/iai.64.8.3301-3309.1996

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  23 in total

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Authors:  U Finckh; P A Lingenfelter; D Myerson
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2.  Factors involved in the electroporation-induced transformation of Clostridium perfringens.

Authors:  S P Allen; H P Blaschek
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Review 3.  Transition-state regulators: sentinels of Bacillus subtilis post-exponential gene expression.

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4.  Genomic diversity and organization of virulence genes in the pathogenic anaerobe Clostridium perfringens.

Authors:  B Canard; B Saint-Joanis; S T Cole
Journal:  Mol Microbiol       Date:  1992-06       Impact factor: 3.501

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Authors:  B A McClane
Journal:  Toxicology       Date:  1994-02-28       Impact factor: 4.221

6.  A complex array of Hpr consensus DNA recognition sequences proximal to the enterotoxin gene in Clostridium perfringens type A.

Authors:  S Brynestad; L A Iwanejko; G S Stewart; P E Granum
Journal:  Microbiology       Date:  1994-01       Impact factor: 2.777

7.  Cloning, nucleotide sequencing, and expression of the Clostridium perfringens enterotoxin gene in Escherichia coli.

Authors:  J R Czeczulin; P C Hanna; B A McClane
Journal:  Infect Immun       Date:  1993-08       Impact factor: 3.441

8.  Evidence that an approximately 50-kDa mammalian plasma membrane protein with receptor-like properties mediates the amphiphilicity of specifically bound Clostridium perfringens enterotoxin.

Authors:  E U Wieckowski; A P Wnek; B A McClane
Journal:  J Biol Chem       Date:  1994-04-08       Impact factor: 5.157

Review 9.  Molecular genetics and pathogenesis of Clostridium perfringens.

Authors:  J I Rood; S T Cole
Journal:  Microbiol Rev       Date:  1991-12

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Authors:  J Sloan; T A Warner; P T Scott; T L Bannam; D I Berryman; J I Rood
Journal:  Plasmid       Date:  1992-05       Impact factor: 3.466

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  32 in total

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Authors:  J F Kokai-Kun; B A McClane
Journal:  Infect Immun       Date:  1997-03       Impact factor: 3.441

Review 3.  Sporulation and Germination in Clostridial Pathogens.

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4.  Genotyping of enterotoxigenic Clostridium perfringens fecal isolates associated with antibiotic-associated diarrhea and food poisoning in North America.

Authors:  S G Sparks; R J Carman; M R Sarker; B A McClane
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5.  The Clostridium perfringens germinant receptor protein GerKC is located in the spore inner membrane and is crucial for spore germination.

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6.  Clostridium perfringens type E animal enteritis isolates with highly conserved, silent enterotoxin gene sequences.

Authors:  S J Billington; E U Wieckowski; M R Sarker; D Bueschel; J G Songer; B A McClane
Journal:  Infect Immun       Date:  1998-09       Impact factor: 3.441

7.  Two novel membrane proteins, TcpD and TcpE, are essential for conjugative transfer of pCW3 in Clostridium perfringens.

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8.  Carbon catabolite repression of type IV pilus-dependent gliding motility in the anaerobic pathogen Clostridium perfringens.

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9.  Multiplex PCR genotyping assay that distinguishes between isolates of Clostridium perfringens type A carrying a chromosomal enterotoxin gene (cpe) locus, a plasmid cpe locus with an IS1470-like sequence, or a plasmid cpe locus with an IS1151 sequence.

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10.  SleC is essential for cortex peptidoglycan hydrolysis during germination of spores of the pathogenic bacterium Clostridium perfringens.

Authors:  Daniel Paredes-Sabja; Peter Setlow; Mahfuzur R Sarker
Journal:  J Bacteriol       Date:  2009-02-13       Impact factor: 3.490

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