Long-term shedding and clonal turnover of enterohemorrhagic Escherichia coli O157 in diarrheal diseases

To investigate the length of time that Shiga-like toxin-producing Escherichia coli O157 is excreted after the onset of diarrhea, 456 serial stool specimens were obtained from 53 children. E. coli O157 cells were identified by the use of DNA probes followed by agglutination with a specific antiserum. Specimens were collected until three consecutive stool samples (collected within 9 days) were negative for E. coli O157. The median durations of shedding were 13 days (range, 2 to 62 days) in patients with diarrhea or hemorrhagic colitis and 21 days (range, 5 to 124 days) in patients that developed hemolytic uremic syndrome. In 36 (68%) of the patients, only the first culture was O157 positive, and the three cultures that followed were negative. In 7 (13%) of the patients, E. coli O157 cells were shed for more than 32 days after the onset of diarrhea; these long-term shedders were clinically asymptomatic by the end of this period. In 12 patients, one or two serial O157-negative cultures, obtained up to 8 days after a positive culture, were followed by another positive culture. Comparison of the first and last E. coli O157 isolates by pulsed-field gel electrophoresis revealed that in three of the seven long-term shedders, pulsed-field gel electrophoresis types varied. In two cases, a Shiga-like toxin gene was apparently lost during infection. The observation of long-term shedding accompanied by genotypic turnover has epidemiological and diagnostic implications.

[1]  J. H. Green,et al.  Laboratory investigation of a multistate food-borne outbreak of Escherichia coli O157:H7 by using pulsed-field gel electrophoresis and phage typing , 1994, Journal of clinical microbiology.

[2]  H. Karch,et al.  An outbreak due to enterohaemorrhagic Escherichia coli O157:H7 in a children day care centre characterized by person-to-person transmission and environmental contamination. , 1994, Zentralblatt fur Bakteriologie : international journal of medical microbiology.

[3]  C. Siddons,et al.  A comparison of immunomagnetic separation and direct culture for the isolation of verocytotoxin-producing Escherichia coli O157 from bovine faeces. , 1994, Journal of medical microbiology.

[4]  J. Heesemann,et al.  Variants of Shiga-like toxin II constitute a major toxin component in Escherichia coli O157 strains from patients with haemolytic uraemic syndrome. , 1994, Journal of medical microbiology.

[5]  H. König,et al.  The role of Escherichia coli O 157 infections in the classical (enteropathic) haemolytic uraemic syndrome: Results of a Central European, multicentre study , 1993, Epidemiology and Infection.

[6]  M. Osterholm,et al.  Transmission of Escherichia coli O157:H7 infection in Minnesota child day-care facilities. , 1993, JAMA.

[7]  Update: multistate outbreak of Escherichia coli O157:H7 infections from hamburgers--western United States, 1992-1993. , 1993, MMWR. Morbidity and mortality weekly report.

[8]  J. Wells,et al.  A Waterborne Outbreak in Missouri of Escherichia coli O157:H7 Associated with Bloody Diarrhea and Death , 1992, Annals of Internal Medicine.

[9]  J. Heesemann,et al.  Frequent loss of Shiga-like toxin genes in clinical isolates of Escherichia coli upon subcultivation , 1992, Infection and immunity.

[10]  H. Karch,et al.  DNA fingerprinting of Escherichia coli O157:H7 strains by pulsed-field gel electrophoresis , 1992, Journal of clinical microbiology.

[11]  F. Gunzer,et al.  Molecular detection of sorbitol-fermenting Escherichia coli O157 in patients with hemolytic-uremic syndrome , 1992, Journal of clinical microbiology.

[12]  H. Karch,et al.  A biotyping scheme for Shiga-like (Vero) toxin-producing Escherichia coli O157 and a list of serological cross-reactions between O157 and other gram-negative bacteria. , 1992, Zentralblatt fur Bakteriologie : international journal of medical microbiology.

[13]  C. Siddons,et al.  An improved selective medium for the isolation of Escherichia coli O157. , 1991, Journal of medical microbiology.

[14]  R. Tauxe,et al.  The epidemiology of infections caused by Escherichia coli O157:H7, other enterohemorrhagic E. coli, and the associated hemolytic uremic syndrome. , 1991, Epidemiologic reviews.

[15]  P. Tarr,et al.  Escherichia coli 0157:H7 and the Hemolytic Uremic Syndrome: Importance of Early Cultures in Establishing the Etiology , 1990 .

[16]  H. Karch,et al.  Evaluation of oligonucleotide probes for identification of shiga-like-toxin-producing Escherichia coli , 1989, Journal of clinical microbiology.

[17]  H. Lior,et al.  HOSPITAL-ACQUIRED ESCHERICHIA COLI 0157:H7 ASSOCIATED HAEMOLYTIC URAEMIC SYNDROME IN A NURSE , 1988, The Lancet.

[18]  B. Rowe,et al.  HAEMORRHAGIC COLITIS AND VERO-CYTOTOXIN-PRODUCING ESCHERICHIA COLI IN ENGLAND AND WALES , 1987, The Lancet.

[19]  Philip Smith,et al.  Escherichia coli O157:H7 diarrhea in a nursing home: clinical, epidemiological, and pathological findings. , 1986, The Journal of infectious diseases.

[20]  J. Wells,et al.  Hemolytic uremic syndrome and diarrhea associated with Escherichia coli 0157:H7 in a day care center , 1986 .

[21]  S. Ratnam,et al.  Sorbitol-MacConkey medium for detection of Escherichia coli O157:H7 associated with hemorrhagic colitis , 1986, Journal of clinical microbiology.

[22]  J. Wells,et al.  Hemolytic uremic syndrome and diarrhea associated with Escherichia coli O157:H7 in a day care center. , 1986, The Journal of pediatrics.

[23]  J. Wells,et al.  Hemorrhagic colitis associated with a rare Escherichia coli serotype. , 1983, The New England journal of medicine.

[24]  H. Lior,et al.  CYTOTOXIC ESCHERICHIA COLI 0157:H7 ASSOCIATED WITH HAEMORRHAGIC COLITIS IN CANADA , 1983, The Lancet.