An Outbreak of Gastroenteritis in Japan due to Escherichia coli O166.
In an outbreak of gastroenteritis on July 23, 1996, in Osaka, Japan, 54 of 91 persons attending a meeting held in an office building on July 22, 1996, became ill. The patients did not eat any common foods except the lunch served at the office. Symptoms were diarrhea in 52 (96%); abdominal pain in 32 (59%); nausea in 8 (15%); fever in 8 (15%); and vomiting in 5 (10%). The mean incubation period was 17 hours.
Stool specimens of 33 patients were examined, and E. coli O166 with an unidentifiable H antigen were isolated from 29 specimens. Laboratory tests for other bacterial pathogens and viruses were negative. The isolates showed the same DNA banding pattern in pulsed-field gel electrophoresis after treatment with the restriction enzymes Xba I or Not I.
The E. coli O166 organisms did not adhere to HEp-2 cells in a localized, diffuse, or enteroaggregative manner and did not give mannose-resistant hemagglutination of human or bovine red blood cells. Although the organisms were further analyzed for expression of known ETEC colonization factors by a dot-blot assay using specific monoclonal antibodies, they did not express CFA/I, CS1, CS2, CS3, CS4, CS5, CS6, CS7, CS17, PCFO159, PCFO166, or CFA/III. In polymerase chain reaction (PCR) tests, the bacteria did not have coding genes for verocytotoxin of enterohemorrhagic E. coli, heat-labile, or heat-stable enterotoxin of ETEC, attachment and effacement (eaeA) of EPEC, or invasion (invE) of enteroinvasive E. coli. Consequently, they are not assigned to any of the recognized diarrheagenic groups of E. coli: EPEC, ETEC, enterohemorrhagic E. coli, emeroinvasive E. coli, EAggEC, and diffusely adhering E. coli. According to the PCR method of Yamamoto et al. (2), however, the organisms possessed the EAST1 gene.
To our knowledge, this is the first report of an outbreak caused by EAST 1-producing E. coli that did not have other well-characterized virulence genes. We believe that these strains should be assigned to a new subgroup of ETEC. Such strains would not be detected in most current surveys for diarrheagenic E. coli, as tests for EAST1 are rarely included. The role of EAST1 in pathogenicity has been controversial. We propose that diarrheal specimens be examined for EASTl-producing E. coli so that the distribution of these organisms worldwide can be determined.
We thank Sylvia M. Scotland, who retired from the Laboratory of Enteric Pathogens, Central Public Health Laboratory, London, for her critical review of the manuscript.
(1.) Savarino SJ, Fasano A, Robertson DC, Levine MM. Enteroaggregative Escherichia coli elaborate a heat-stable enterotoxin demonstrable in an in vitro rabbit intestinal model. J Clin Invest 1991 ;87:1450-5.
(2.) Yamamoto T, Wakisaka N, Sato F, Kato A. Comparison of the nucleotide sequence of enteroaggregative Escherichia coli heat-stable enterotoxin I genes among diarrhea-associated Escherichia coli. FEMS Microbiol Lett 1997;147:89-95.
(3.) Hedberg CW, Savarino SJ, Besser JM, Paulus CJ, Thelen VM, Myers LJ, et al. An outbreak of foodborne illness caused by Escherichia coli O39:NM, an agent not fitting into the existing scheme for classifying diarrheagenic E. coli. J Infect Dis 1997;176:1625-8.
Yoshikazu Nishikawa,(*) Jun Ogasawara,(*) Anna Helander, ([dagger]) and Kosuke Haruki(*)
(*)Osaka City Institute of Public Health and Environmental Sciences, Osaka, Japan; ([dagger])Goteborg University, Sweden
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|Publication:||Emerging Infectious Diseases|
|Article Type:||Brief Article|
|Date:||Mar 1, 1999|
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