Affiliation:
1. Department of Molecular Genetics and Biochemistry, University of Pittsburgh School of Medicine, Pittsburgh, Pennsylvania 15261,1 and
2. TechLab, Inc., Corporate Research Center, Blacksburg, Virginia 240602
Abstract
ABSTRACT
Clostridium perfringens
type A isolates producing enterotoxin (CPE) are an important cause of food poisoning and non-food-borne human gastrointestinal (GI) diseases, including antibiotic-associated diarrhea (AAD). Recent studies suggest that
C. perfringens
type A food poisoning is caused by
C. perfringens
isolates carrying a chromosomal
cpe
gene, while CPE-associated non-food-borne GI diseases, such as AAD, are caused by plasmid
cpe
isolates. Those putative relationships, obtained predominantly with European isolates, were tested in the current study by examining 34
cpe
-positive,
C. perfringens
fecal isolates from North American cases of food poisoning or AAD. These North American disease isolates were all classified as type A using a multiplex PCR assay. Furthermore, restriction fragment length polymorphism and pulsed-field gel electrophoresis genotyping analyses showed the North American AAD isolates included in this collection all have a plasmid
cpe
gene, but the North American food poisoning isolates all carry a chromosomal
cpe
gene. Western blotting demonstrated CPE expression by nearly all of these disease isolates, confirming their virulence potential. These findings with North American isolates provide important new evidence that, regardless of geographic origin or date of isolation, plasmid
cpe
isolates cause most CPE-associated AAD cases and chromosomal
cpe
isolates cause most
C. perfringens
type A food poisoning cases. These findings hold importance for the development of assays for distinguishing cases of CPE-associated food-borne and non-food-borne human GI illnesses and also identify potential epidemiologic tools for determining the reservoirs for these illnesses.
Publisher
American Society for Microbiology
Cited by
118 articles.
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