Volume 10, Number 10—October 2004
Escherichia coli O157 Cluster Evaluation
Highlight and copy the desired format.
|EID||Gupta A, Hunter SB, Bidol SA, Dietrich S, Kincaid J, Salehi E, et al. Escherichia coli O157 Cluster Evaluation. Emerg Infect Dis. 2004;10(10):1856-1858. https://dx.doi.org/10.3201/eid1010.040374|
|AMA||Gupta A, Hunter SB, Bidol SA, et al. Escherichia coli O157 Cluster Evaluation. Emerging Infectious Diseases. 2004;10(10):1856-1858. doi:10.3201/eid1010.040374.|
|APA||Gupta, A., Hunter, S. B., Bidol, S. A., Dietrich, S., Kincaid, J., Salehi, E....Brooks, J. T. (2004). Escherichia coli O157 Cluster Evaluation. Emerging Infectious Diseases, 10(10), 1856-1858. https://dx.doi.org/10.3201/eid1010.040374.|
We investigated a multistate cluster of Escherichia coli O157:H7 isolates; pulsed-field gel electrophoresis subtyping, using a single enzyme, suggested an epidemiologic association. An investigation and additional subtyping, however, did not support the association. Confirmation E. coli O157 clusters with two or more restriction endonucleases is necessary before public health resources are allocated to follow-up investigations.
Escherichia coli O157:H7 is an important cause of foodborne infections estimated to cause 73,000 illnesses and 60 deaths annually in the United States (1). Implementation of pulsed-field gel electrophoresis (PFGE) molecular subtyping has greatly improved E. coli O157:H7 surveillance and detection of outbreaks (2). PFGE subtyping was initially used to identify related isolates and support epidemiologic associations during outbreak investigations. Public health laboratories in the United States now routinely subtype all E. coli O157:H7 isolates by PFGE as part of a national molecular subtyping network (PulseNet) (2) after this practice proved instrumental in identifying outbreaks not detected by traditional epidemiologic methods (3). PulseNet laboratories initially digest isolates with a single enzyme and compare the resulting PFGE patterns by using commercial software (BioNumerics, St. Martens-Latem, Belgium) to determine whether patterns are shared by multiple isolates. These patterns are then communicated electronically to the Centers for Disease Control and Prevention (CDC) (Atlanta, GA), where PFGE patterns of isolates from different states are definitively compared. PulseNet policy states that isolates with potential epidemiologic significance that have indistinguishable patterns with a primary enzyme, should be digested with a secondary enzyme before extensive epidemiologic investigations are undertaken. Indistinguishable patterns should also be confirmed by submission to a central database (2). However, time constraints and the availability of sufficient resources prevent some laboratories from adhering to this policy.
On July 5, 2000, the Michigan Department of Community Health’s laboratory notified CDC of a cluster of five E. coli O157:H7 isolates, collected from May 25 to June 21, 2000, which shared an indistinguishable XbaI PFGE pattern. PulseNet staff confirmed that these isolates’ patterns were indistinguishable and designated the pattern as PulseNet pattern EXHX01.0047. In 2000, this PFGE pattern represented approximately 2% of the E. coli O157 patterns in the PulseNet database. These Michigan isolates possessed genes only for Shiga toxin 2 (stx2) but not Shiga toxin 1 (stx1); approximately 30% of E. coli O157 isolates sent to CDC since 1983 expressed only stx2. From July through September 2000, six states (California, Michigan, New Jersey, New York, Ohio, and Texas) reported a total of 64 E. coli O157 isolates with PulseNet pattern EXHX01.0047, a value that exceeding expectation for this time of year and that prompted an epidemiologic investigation. Not all of these patterns were submitted to CDC’s central database for confirmation. Fifty-one of these isolates were probed for Shiga toxin genes, and all possessed only stx2. Illness onsets ranged from April 1 through August 21, 2000, with a notable increase after late May 2000. The median age of case-patients was 13 years (range 1–91), and 38 (60%) were female; 36 (57%) of 64 were hospitalized, and hemolytic uremic syndrome developed in 9 (14%).
To determine the source of these E. coli O157:H7 infections, six state health departments (California, Michigan, New Jersey, New York, Ohio, and Texas) and CDC initiated an epidemiologic investigation. Informed consent was obtained from all patients or their parents or guardians and human experimentation guidelines of the U.S. Department of Health and Human Services were followed. These data were collected as part of an outbreak investigation and therefore were exempt from formal institutional review board aprovals.
Through hypothesis-generating interviews with 19 infected persons, 11 food exposures were reported by >50% of interviewees or were reported in substantial excess relative to that food’s frequency of consumption in the general population (4). In a case-control study that used a survey instrument that focused on these 11 food exposures, controls were matched to case-patients by sex and age group, and were asked about exposures during the same 5-day period before the matching case-patient’s illness onset. Controls were contacted and identified by using sequential-digit dialing beginning with the matching patient’s telephone number.
Twenty-eight case-patients and 69 matched controls were enrolled (2.46 controls per patient). The median age was 13.5 years and 50% were female; case-patients did not differ significantly from controls in terms of sex or age. In matched univariate analysis by using logistic regression with stratification (LogXact version 2.1.1, Cytel Software Corporation, Cambridge, MA), only broccoli was significantly associated with illness (matched odds ratio [mOR] 3.65, p = 0.04); 14 (58%) of 24 case-patients, and 19 (31%) of 62 controls reported eating broccoli. Although none of the three foods that contained ground beef were individually associated with illness, consumption of “any hamburger” (a composite variable) was significant (mOR 7.30, p = 0.01), reported by 20 (87%) of 23 patients and 28 (55%) of 51 controls. In multivariate analysis, only eating “any hamburger” remained significantly associated with illness (OR = 6.13, p = 0.02).
Ground beef eaten by case-patients was recovered from three households; samples from two households (in New Jersey and California) yielded E. coli O157:H7 isolates that were indistinguishable from PulseNet pattern EXHX01.0047. One of these isolates was tested for Shiga toxin and produced only stx2. Using information from these two cases and additional information regarding likely ground beef sources for the original Michigan cases, the U.S. Department of Agriculture performed a traceback; however, an extensive investigation did not identify any common supplier for the two samples of ground beef.
We performed a retrospective review of available isolate patterns received by the PulseNet national database after the case-control study and traceback had been completed. Four additional states (Florida, Indiana, Massachusetts, and Washington) had reported E. coli O157 isolates with XbaI patterns that were indistinguishable from PulseNet pattern EXHX01.0047. Among the 46 submitted XbaI patterns from states reporting a possible match to PulseNet pattern EXHX01.0047, analysis at CDC indicated that 38 were indistinguishable and that 6 differed by one band from the PulseNet pattern EXHX01.0047 (Figure 1). Furthermore, among the 38 isolates confirmed as PulseNet pattern EXHX01.0047, digestion of 13 isolates with the restriction enzyme BlnI produced PFGE patterns that sorted into multiple distinct clusters (Figure 2).
Identifying outbreaks of E. coli O157:H7 infections by routinely subtyping isolates using PFGE is a relatively new phenomenon (2,3). Traditionally, PFGE has been used to support or refute the likelihood of epidemiologic relatedness among case-patients and suspect food vehicles in epidemiologic investigations. In this instance, the converse occurred; the results of routine PFGE subtyping (XbaI) of E. coli O157:H7 isolates prompted a large, multistate epidemiologic investigation. Isolates were potentially related because 1) the PFGE patterns obtained with one restriction enzyme (XbaI) were reported to be indistinguishable and a relatively uncommon pattern, and 2) the isolates shared a Shiga toxin profile that was relatively uncommon among E. coli O157 (stx2 only). A rigorous case-control study implicated a widely consumed food vehicle responsible for multiple past outbreaks of E. coli O157 infections: ground beef (5). This study and the isolation of two E. coli O157 with matching PFGE patterns from ground beef consumed by case-patients prompted two extensive traceback investigations. However, no common source could be identified. Subsequent digestion of patient isolates with a second enzyme showed that they were actually part of multiple, small clusters and that the illnesses were thus unlikely to be related to a common source.
Investigation of suspected multistate outbreaks requires substantial public health resources (6). This investigation involved more than 50 federal, state, and local staff. E. coli O157:H7 infections can cause serious and potentially life-threatening illness that may also engender legal action. Public health authorities must ensure that linkage of illnesses to an outbreak be as complete and accurate as possible. Rapid identification of the infections’ source can avert many potential illnesses. Earlier studies demonstrated the value of subtyping E. coli O157:H7 isolates with two or more restriction endonuclease digestions or using other subtyping methods, such as phage typing, to determine whether such isolates are truly related, even if these isolates have produced matching patterns using a single enzyme digestion (7–9). More recently, in the absence of epidemiologic data, single enzyme PFGE has been found to be a poor measure of genetic relatedness (10). Since 1998, the PulseNet Task Force has recommended the use of at least two enzyme digestions for optimal subtyping of E. coli O157 isolates. However, because of resource limitations, many state and local public health laboratories initially subtype E. coli O157 isolates with XbaI enzyme and perform subtyping with a second enzyme only if clusters are identified and personnel and resources are in place to do so. This investigation lends further support to the conclusion that when clusters of E. coli O157 are detected on the basis of subtyping data only (i.e., in the absence of any epidemiologic data), digestion with two or more endonucleases is warranted, even if the isolates appear to share a primary enzyme pattern or possess other microbiologic evidence of clonality (e.g., Shiga toxin profile). Furthermore, these findings underscore the importance of having a centralized database team that can rapidly verify reports of clusters from participating PulseNet laboratories and assist in determining whether isolates are likely to be part of an outbreak and whether a rapid, large-scale epidemiologic investigation and traceback would be warranted.
Dr. Gupta is currently at Johns Hopkins University, Division of Infectious Diseases. Her research interests include enteric diseases and HIV clinical care and treatment research in India
We acknowledge the many people at CDC, USDA, and state and local health departments who contributed their time and efforts to this investigation. A special thanks to Keith Pilot, Sylvia Matiuk, Maria Lidicker, Dianna J. Schoonmaker-Bopp, Deborah Shea, Jeffrey Higa, and Sharon Abbott.
Funding or support was provided by CDC’s Emerging Infections Programs and Food Safety Office.
- Mead PS, Slutsker L, Dietz V, McCaig LF, Bresee JS, Shapiro C, Food-related illness and death in the United States. Emerg Infect Dis. 1999;5:607–25.
- Swaminathan B, Barrett TJ, Hunter SB, Tauxe RV. PulseNet: the molecular subtyping network for foodborne bacterial disease surveillance, United States. Emerg Infect Dis. 2001;7:382–9.
- Bender JB, Hedberg CW, Besser JM, Boxrud DJ, MacDonald KL, Osterholm MT. Surveillance by molecular subtype for Escherichia coli O157:H7 infections in Minnesota by molecular subtyping. N Engl J Med. 1997;337:388–94.
- Centers for Disease Control and Prevention. Foodborne Diseases Active Surveillance Network (FoodNet): population survey atlas of exposures: 1998–2000. Atlanta: The Centers; 2000.
- Slutsker L, Ries AA, Greene KD, Wells JG, Hutwagner L, Griffin PM. Escherichia coli O157: H7 diarrhea in the United States: clinical and epidemiologic features. Ann Intern Med. 1997;126:505–13.
- Elbasha EH, Fitzsimmons TD, Meltzer MI. Costs and benefits of a subtype-specific surveillance system for identifying Escherichia coli O157:H7 outbreaks. Emerg Infect Dis. 2000;6:293–7.
- Barrett TJ, Lior H, Green JH, Khakhria R, Wells JG, Bell BP, Laboratory investigation of a multistate food-borne outbreak of Escherichia coli O157:H7 by using pulsed-field gel electrophoresis and phage typing. J Clin Microbiol. 1994;32:3013–7.
- Proctor ME, Kurzynski T, Koschmann C, Archer JR, Davis JP. Four strains of Escherichia coli O157:H7 isolated from patients during an outbreak of disease associated with ground beef: importance of evaluating multiple colonies from an outbreak-associated product. J Clin Microbiol. 2002;40:1530–3.
- Preston MA, Johnson W, Khakhria R, Borczyk A. Epidemiologic subtyping of Escherichia coli serogroup O157 strains isolated in Ontario by phage typing and pulsed-field gel electrophoresis. J Clin Microbiol. 2000;38:2366–8.
- Davis MA, Hancock DD, Besser TE, Call DR. Evaluation of pulsed-field gel electrophoresis as a tool for determining the degree of genetic relatedness between strains of Escherichia coli O157:H7. J Clin Microbiol. 2003;41:1843–9.
- Figure 1. XbaI-generated pulsed-field gel electrophoresis patterns for Escherihia coli O157 isolates reported as indistinguishable from PulseNet pattern EXHX01.0047.
- Figure 2. BlnI-generated pulsed-field gel electrophoresis patterns for Esscherichia coli O157 isolates that generated patterns indistinguishable from PulseNet pattern EXHX01.0047 by using XbaI.
Please use the form below to submit correspondence to the authors or contact them at the following address:
Amita Gupta: Johns Hopkins University, Division of Infectious Diseases, 1830 East Monument Street, Room 450E, Baltimore, MD 21287, USA; fax 410-614-8488
Comment submitted successfully, thank you for your feedback.
The conclusions, findings, and opinions expressed by authors contributing to this journal do not necessarily reflect the official position of the U.S. Department of Health and Human Services, the Public Health Service, the Centers for Disease Control and Prevention, or the authors' affiliated institutions. Use of trade names is for identification only and does not imply endorsement by any of the groups named above.
- Page created: April 11, 2011
- Page last updated: April 11, 2011
- Page last reviewed: April 11, 2011
- Centers for Disease Control and Prevention,
National Center for Emerging and Zoonotic Infectious Diseases (NCEZID)
Office of the Director (OD)