Literature DB >> 15109427

Enterotoxin-producing Escherichia coli O169:H41, United States.

Mark E Beatty1, Cheryl A Bopp, Joy G Wells, Kathy D Greene, Nancy D Puhr, Eric D Mintz.   

Abstract

From 1996 to 2003, 16 outbreaks of enterotoxigenic Escherichia coli (ETEC) infections in the United States and on cruise ships were confirmed. E. coli serotype O169:H41 was identified in 10 outbreaks and was the only serotype in 6. This serotype was identified in 1 of 21 confirmed ETEC outbreaks before 1996.

Entities:  

Mesh:

Year:  2004        PMID: 15109427      PMCID: PMC3322800          DOI: 10.3201/eid1003.030268

Source DB:  PubMed          Journal:  Emerg Infect Dis        ISSN: 1080-6040            Impact factor:   6.883


Enterotoxigenic Escherichia coli (ETEC) is an important cause of diarrhea in the developing world and among travelers and is increasingly recognized as a cause of outbreaks in the United States (). Dalton et al. reviewed confirmed ETEC outbreaks that occurred both in the United States and among passengers on cruise ships that docked in U.S. ports from 1975 through 1995 (). Twenty-one such outbreaks caused by 17 different ETEC serotypes occurred during this period; 7 (33%) occurred among cruise ship passengers (). Because laboratory tests for the identification of ETEC are not widely available, outbreaks caused by ETEC may escape recognition, and healthcare workers may miss opportunities for treatment and prevention. To improve recognition of ETEC outbreaks, Dalton proposed that specimens from outbreaks of gastroenteritis that meet certain criteria be referred for ETEC testing at a public health reference laboratory. These outbreaks include those for which routine stool cultures have not yielded an etiologic agent and those which are characterized by an incubation period of 24 to 48 hours, a duration of illness >60 hours, and a diarrhea-to-vomiting prevalence ratio of >2.5 ().

The Study

For the 8-year period 1996 through 2003, we reviewed all suspected ETEC outbreaks solely or jointly investigated by the Foodborne and Diarrheal Diseases Branch at the Centers for Disease Control and Prevention (CDC). In accordance with Dalton et al., we defined a confirmed ETEC outbreak as one in which ETEC isolates of the same serotype were isolated from >3 ill persons and no other viral or bacterial pathogens were identified, or one in which ETEC isolates of the same serotype were isolated from >10 ill persons and no more than one other bacterial or viral pathogen was identified in a single stool specimen. Stool specimens collected during these investigations were routinely cultured for Salmonella, Shigella, Campylobacter, E. coli O157:H7, Yersinia, and Vibrio spp. In many instances, these specimens were also tested for Noroviruses. To identify ETEC, patient specimens were plated to MacConkey agar, and individual colonies or sweeps of confluent growth were tested by polymerase chain reaction (PCR) for heat-labile (LT) and heat-stable (ST) enterotoxin genes (). Using standard methods, we serotyped LT- or ST-positive isolates for O and H antigens. ETEC isolates were tested by the disk-diffusion method for susceptibility to ampicillin, amoxicillin/clavulanic acid, ceftriaxone, chloramphenicol, ciprofloxacin, gentamicin, kanamycin, nalidixic acid, streptomycin, sulfisoxazole, tetracycline, and trimethoprim-sulfamethoxazole (). A PCR–restriction fragment length polymorphism test was used to identify the H41 gene in selected nonmotile E. coli O169 isolates ().

Conclusions

During the 8-year study period, CDC received isolates from 59 outbreaks for ETEC testing. Sixteen met the criteria for our definition of a confirmed ETEC outbreak; three occurred on international cruise ships that docked in U.S. ports and 12 occurred in the United States (Table). We identified ETEC in specimens from six other outbreaks that did not meet these criteria, either because ETEC isolates of the same serotype were isolated from only two persons (n = 2) or because we isolated additional bacterial pathogens from the specimens (n = 4).
Table

Characteristics of enterotoxigenic Escherichia coli (ETEC) outbreaks,a United States, 1996–2003

No.Mo/yLocationSetting
(reference)Presumed sourceNo ill% Diarrhea (bloody)% VomitingMedian incubation, h (range)Median illness duration, days (range)No isolatesSerotype/toxin typebAntimicrobial resistancec
1
3/96
Caribbean
Cruise ship
Drinking water
652
98 (9)
19


6
O169:H41/ST
Tc
1
O6:H16/ LT,ST
Sensitive
1
O27:H7/ST
St, Su, Tc
1
O34:H10/ST
Tc
2
4/97
Caribbean
Cruise ship (5)
Drinking water, ice
429
100 (6)
14

>3
8
O169:H41/ST
Tc
3
O148:H28/ LT,ST
Tc
1
O78:H12/ST
Ch, St, Su, Tc, TmS
1
O27:H7/ST
St, Su, Tc
3
4/97
California
Restaurant
Beans, enchilada, tacos, rice, tortilla chips
41
95
17
24 (5–85)
2 (0.3–4)
11
O27:H7/ST
Sensitive
4
6/97
Massachusetts
Boxed lunch
Tomato, mozzarella salad
33
97
33
48 (24–96)
3.7 (1-7)
5
O25:NM/ST
Sensitive
5
7/97
Minnesota
Catered party
Fresh vegetables
15
100
13
37 (8-158)
3.2 (0.4–6)
4
O169:H41/ST
Tc
6
4/98
Mexico-Hawaii
Cruise ship

397
96
33


3
O6:H16/ LT,ST
Sensitive
1
O6:H16/ LT,ST
St, Tc
2
O169:H41/ST
Tc
1
O148:H28/ LT,ST
St, Su, Tc
1
O148:H28/ LT,ST
Tc
1
O27:H7/ST
St, Su, Tc
7
6/98
Illinois
Catered parties
Potato, macaroni, egg salads
916
100
8
50 (40–76)
5 (2–9)
11
O6:H16/ LT,ST
Sensitive
8
8/98
Minnesota
Restaurant (6)
Parsley
66
100 (0)
6
25
8
7
O6:H16/ LT,ST
Ap, St, Su, Tc
1
O159:H4/LT
Ap, St, Su, Tc, TmS
1
O27:H7/ST
St, Su, Tc
9
9/98
Minnesota
Restaurant

5
100 (0)
0
48
6
3
O169:H41/ST
St, Su, Tc
10
5/00
Washington
Cruise ship
Basil
100
100
5
40 (27–67)
10 (0.5–21)
3
O169:H41/ST
Tc
11
6/00
New York
Banquet

40
97 (0)
3
48 (24–96)
3 (1–8)
5
O169:H41/ST
Tc
12
7/00
Utah
Wedding rehearsal

45
100
29
33 (18–59)
2.3 (1–3)
5
O27:H7/ST
St, Su, Tc
13
7/01
Wisconsin
Catered party
Quesadillas, fajitas, nacho chips, beans
21
100

38 (9–70)
6 (1–8)
3
O169:H41/ST
Tc
14
8/01
Illinois
Catered party

24
100
0


3
O169:H41/ST
Ap, Tc
1
O169:H41/ST
Tc
2
O6:H16/LT,ST
Sensitive
1
O25:NM/ST
Ap
15
10/02
Oregon
Catered party
Garlic chicken lasagna
40
98 (13)
15
72 (24–144)
5
3
O27:H7/ST
St, Su,Tc
168/03TennesseeCatered partyCatfish, coleslaw4181 (0)522.5120169:H49Tc

aAn outbreak is defined as ≥3 ill persons infected with the same ETEC serotype and no other viral or bacterial pathogens, or >10 ill persons with the same serotype and no more than one other bacterial or viral pathogen identified.
bNM, nonmotile; LT, heat-labile toxin; ST, heat-stable toxin.
cAp, ampicillin; Amc, amoxicillin/clavulanic acid; Ch, chloramphenicol; St, streptomycin; Su, sulfisoxazole; Tc, tetracycline; TmS, trimethoprim-sulfamethoxazole.

aAn outbreak is defined as ≥3 ill persons infected with the same ETEC serotype and no other viral or bacterial pathogens, or >10 ill persons with the same serotype and no more than one other bacterial or viral pathogen identified.
bNM, nonmotile; LT, heat-labile toxin; ST, heat-stable toxin.
cAp, ampicillin; Amc, amoxicillin/clavulanic acid; Ch, chloramphenicol; St, streptomycin; Su, sulfisoxazole; Tc, tetracycline; TmS, trimethoprim-sulfamethoxazole. The 16 ETEC outbreaks had a median of 41 ill persons per outbreak (range 5−916), for a total of 2,865 patients. From 81% to 100% of ill persons in each outbreak reported diarrhea; less frequently reported symptoms included abdominal cramps (66%–90%), fever (0%–73%), nausea (44%–70%), and vomiting (0%–33%). In the 15 outbreaks in which diarrhea and vomiting were reported, the median “diarrhea-to-vomiting prevalence ratio” (the percentage of patients who reported diarrhea divided by the percentage of patients who reported vomiting) was 7.7 (range 2.9–undefined: The upper limit of the range is undefined because in two outbreaks all ill persons interviewed denied vomiting). In nine outbreaks with sufficient data, incubation periods among individual patients were 5–158 hours. The median incubation period was 24–48 hours for 10 of the 12 outbreaks for which it could be calculated. The duration of illness, reported in 11 outbreaks, was 0.3–21 days. The median duration of illness was >60 hours in 11 of the 13 outbreaks for which it could be calculated. A vehicle was implicated in 11 (69%) outbreaks. Unbottled ship’s water or beverages containing ice prepared on board the ship were implicated in the two outbreaks on cruise ships that had docked in foreign ports. Although no problems with chlorination of bunkered water were documented in these two outbreaks, this problem has been seen in previous waterborne ETEC outbreaks aboard cruise ships (). Basil served on board ship was implicated as the source of ETEC in the remaining cruise ship outbreak (on a ship that docked only in U.S. ports). One other outbreak was attributed to a fresh herb (parsley) served raw (). Salads made with raw vegetables were implicated in four other domestic outbreaks. If we define a strain as each ETEC serotype identified during an outbreak that has a unique antimicrobial resistance pattern, we identified a total of 30 strains representing eight different serotypes in specimens from the 16 outbreaks (Table). In five outbreaks, we isolated more than one ETEC serotype. Heat-stable toxin (ST)-producing E. coli O169:H41 was the most commonly identified serotype. This serotype was identified as the only pathogen in specimens from six outbreaks in the United States and was identified along with other ETEC serotypes in four additional outbreaks. Three of these four outbreaks occurred on cruise ships. In 21 previously reported ETEC outbreaks, E. coli O169:H41 had been isolated only once, from an outbreak that occurred among international cruise ship passengers in 1995, in which another ETEC serotype predominated (). By all of the basic epidemiologic and clinical characteristics that we analyzed, outbreaks in which E. coli O169:H41 was identified alone, or in combination with other serotypes, did not appear to differ from outbreaks in which this emerging strain was not identified. Resistance to antimicrobial agents remained common among ETEC isolates (Table). Twenty-four (80%) of the 30 strains were resistant to tetracycline, 11 (38%) were resistant to sulfisoxazole, 4 (13%) were resistant to ampicillin, and 2 (7%) were resistant to trimethoprim-sulfamethoxazole. All strains of O169:H41 were resistant to tetracycline, and two were also resistant to at least one additional antimicrobial drug. Only two outbreaks were caused exclusively by pan-sensitive ETEC strains (7%). A comparison of ETEC outbreaks reported to CDC from 1996 through 2003 with those from previous years shows that outbreaks on cruise ships and in the United States continue to occur and that antimicrobial resistance among ETEC isolates remains common. Raw vegetables and herbs have been increasingly implicated as the vehicles for ETEC outbreaks in recent years. This finding is in keeping with an increase in produce-associated outbreaks among other foodborne bacterial pathogens (). Finally, a new ETEC serotype, ST-producing O169:H41, has become predominant. The first report of O169:H41 was in association with a foodborne outbreak in 1991 in Japan, where this serotype continues to be isolated (–). Hamada reported four outbreaks that occurred from June 1997 to August 1998; the largest of these outbreaks had a 57% attack rate and resulted in approximately 2,800 cases. All four outbreaks occurred at either restaurants or catered events (). Contaminated wakame seaweed was implicated in one of the outbreaks and considered the likely cause in another (). Nishakawa et al. report that O169:H41 has become the most prevalent ETEC serotype in Japan (). In 1995, CDC detected this serotype for the first time during an outbreak on a Caribbean cruise ship. It was identified during two additional Caribbean cruise ship outbreaks before causing a domestic outbreak in Minnesota in 1997. In addition to being identified in 10 of the 16 ETEC outbreaks that met our criteria, O169:H41 was also a predominant serotype in 4 of the 6 ETEC outbreaks that did not meet our criteria for a confirmed outbreak, either because the serotype was isolated from two persons only or because an additional pathogen was also isolated in the outbreak. The emergence and eventual predominance of O169:H41 in the United States and Japan may have important implications for ETEC vaccine producers. Nishikawa et al. characterized strains of O169:H41 from Japan and reported that they are not clonal and that they possess a novel colony-forming factor (). From 1996 through 1999, laboratory-confirmed ETEC outbreaks represented 0.2% of all foodborne outbreaks reported to CDC (). This number is likely to be an underestimate because special diagnostic tests are required to confirm ETEC. Seventy-one percent of outbreaks of foodborne illness reported to CDC during this period were of unknown cause. In a previous study, Hall et al. demonstrated that the epidemiologic and clinical syndrome in 1.1% of outbreaks of unknown cause reported to CDC from 1982 through 1989 was compatible with infections caused by ETEC or STEC (). ETEC is also responsible for some episodes of sporadic diarrheal disease. When researchers systematically looked for it, they isolated ETEC from 1.4% of stool samples from patients visiting urban and rural health maintenance organization clinics in Minnesota for diarrhea (). Our data suggest that the clinical criteria proposed by Dalton et al. for suspecting ETEC as a cause of an outbreak of unknown cause (median incubation 24–48 hours, mean or median duration >60 hours, and diarrhea-to-vomiting prevalence ratio >2.5) remain valid. The epidemiology of ETEC outbreaks in the United States is changing, but the incidence of these outbreaks does not appear to be decreasing. Researchers cannot use routine stool cultures to detect ETEC, and delays in stool sample collection for >7 days greatly reduces yield (,). For outbreaks that meet the clinical profile and for which routine stool diagnostic tests have not yielded an enteric pathogen, physicians and public health authorities should send E. coli isolates to reference laboratories, such as CDC, for ETEC testing.
  11 in total

1.  Outbreaks of heat stable enterotoxin-producing Escherichia coli O169 in the Kinki district in Japan: epidemiological analysis by pulsed-field gel electrophoresis.

Authors:  K Hamada; H Tsuji; K Shimada
Journal:  Jpn J Infect Dis       Date:  1999-08       Impact factor: 1.362

2.  Travelers' diarrhea and toxigenic Escherichia coli.

Authors:  S L Gorbach; B H Kean; D G Evans; D J Evans; D Bessudo
Journal:  N Engl J Med       Date:  1975-05-01       Impact factor: 91.245

3.  Epidemiologic profiling: evaluating foodborne outbreaks for which no pathogen was isolated by routine laboratory testing: United States, 1982-9.

Authors:  J A Hall; J S Goulding; N H Bean; R V Tauxe; C W Hedberg
Journal:  Epidemiol Infect       Date:  2001-12       Impact factor: 2.451

4.  Enterotoxigenic Escherichia coli and Reovirus-like agent in rural Bangladesh.

Authors:  R W Ryder; D A Sack; A Z Kapikian; J C McLaughlin; J Chakraborty; A S Mizanur Rahman; M H Merson; J G Wells
Journal:  Lancet       Date:  1976-03-27       Impact factor: 79.321

5.  Outbreaks of enterotoxigenic Escherichia coli infection in American adults: a clinical and epidemiologic profile.

Authors:  C B Dalton; E D Mintz; J G Wells; C A Bopp; R V Tauxe
Journal:  Epidemiol Infect       Date:  1999-08       Impact factor: 2.451

6.  Traveler's diarrhea at sea: three outbreaks of waterborne enterotoxigenic Escherichia coli on cruise ships.

Authors:  N A Daniels; J Neimann; A Karpati; U D Parashar; K D Greene; J G Wells; A Srivastava; R V Tauxe; E D Mintz; R Quick
Journal:  J Infect Dis       Date:  2000-04-13       Impact factor: 5.226

7.  Molecular characterization of the gene encoding H antigen in Escherichia coli and development of a PCR-restriction fragment length polymorphism test for identification of E. coli O157:H7 and O157:NM.

Authors:  P I Fields; K Blom; H J Hughes; L O Helsel; P Feng; B Swaminathan
Journal:  J Clin Microbiol       Date:  1997-05       Impact factor: 5.948

8.  Heat-stable enterotoxin-producing Escherichia coli O169:H41 in Japan.

Authors:  Y Nishikawa; M Hanaoka; J Ogasawara; N P Moyer; T Kimura
Journal:  Emerg Infect Dis       Date:  1995 Apr-Jun       Impact factor: 6.883

9.  Concurrent outbreaks of Shigella sonnei and enterotoxigenic Escherichia coli infections associated with parsley: implications for surveillance and control of foodborne illness.

Authors:  Timothy S Naimi; Julie H Wicklund; Sonja J Olsen; Gerard Krause; Joy G Wells; Joanne M Bartkus; David J Boxrud; Maureen Sullivan; Heidi Kassenborg; John M Besser; Eric D Mintz; Michael T Osterholm; Craig W Hedberg
Journal:  J Food Prot       Date:  2003-04       Impact factor: 2.077

10.  Epidemiology and properties of heat-stable enterotoxin-producing Escherichia coli serotype O169:H41.

Authors:  Y Nishikawa; A Helander; J Ogasawara; N P Moyer; M Hanaoka; A Hase; A Yasukawa
Journal:  Epidemiol Infect       Date:  1998-08       Impact factor: 2.451

View more
  20 in total

1.  The use of clinical profiles in the investigation of foodborne outbreaks in restaurants: United States, 1982-1997.

Authors:  C W Hedberg; K L Palazzi-Churas; V J Radke; C A Selman; R V Tauxe
Journal:  Epidemiol Infect       Date:  2007-03-05       Impact factor: 2.451

2.  Bacteriological and epidemiological characteristics of enterotoxigenic Escherichia coli isolated in Tokyo, Japan, between 1966 and 2009.

Authors:  Noriko Konishi; Hiromi Obata; Chie Monma; Akiko Nakama; Akemi Kai; Takao Tsuji
Journal:  J Clin Microbiol       Date:  2011-07-13       Impact factor: 5.948

3.  EtpB is a pore-forming outer membrane protein showing TpsB protein features involved in the two-partner secretion system.

Authors:  Albano C Meli; Maria Kondratova; Virginie Molle; Laurent Coquet; Andrey V Kajava; Nathalie Saint
Journal:  J Membr Biol       Date:  2009-08-27       Impact factor: 1.843

Review 4.  Enterotoxigenic Escherichia coli Infections.

Authors:  James M Fleckenstein; F Matthew Kuhlmann
Journal:  Curr Infect Dis Rep       Date:  2019-03-04       Impact factor: 3.725

5.  Molecular Determinants of Enterotoxigenic Escherichia coli Heat-Stable Toxin Secretion and Delivery.

Authors:  Yuehui Zhu; Qingwei Luo; Sierra M Davis; Chase Westra; Tim J Vickers; James M Fleckenstein
Journal:  Infect Immun       Date:  2018-10-25       Impact factor: 3.441

Review 6.  Recent advances in understanding enteric pathogenic Escherichia coli.

Authors:  Matthew A Croxen; Robyn J Law; Roland Scholz; Kristie M Keeney; Marta Wlodarska; B Brett Finlay
Journal:  Clin Microbiol Rev       Date:  2013-10       Impact factor: 26.132

7.  Characterization of unstable pEntYN10 from enterotoxigenic Escherichia coli (ETEC) O169:H41.

Authors:  Erika Ban; Yuka Yoshida; Mitsuko Wakushima; Takeaki Wajima; Takashi Hamabata; Naoki Ichikawa; Hiroyuki Abe; Yasuhiko Horiguchi; Yukiko Hara-Kudo; Eriko Kage-Nakadai; Taro Yamamoto; Takayuki Wada; Yoshikazu Nishikawa
Journal:  Virulence       Date:  2015       Impact factor: 5.882

8.  Identification of a two-partner secretion locus of enterotoxigenic Escherichia coli.

Authors:  James M Fleckenstein; Koushik Roy; Julia F Fischer; Michael Burkitt
Journal:  Infect Immun       Date:  2006-04       Impact factor: 3.441

9.  Importance of heat-labile enterotoxin in colonization of the adult mouse small intestine by human enterotoxigenic Escherichia coli strains.

Authors:  Kenneth P Allen; Mildred M Randolph; James M Fleckenstein
Journal:  Infect Immun       Date:  2006-02       Impact factor: 3.441

10.  Genotypic and phenotypic profiles of enterotoxigenic Escherichia coli associated with acute diarrhea in Tunis, Tunisia.

Authors:  Nazek Al-Gallas; Saleh Med Abbassi; Assia Ben Hassan; Ridha Ben Aissa
Journal:  Curr Microbiol       Date:  2007-06-06       Impact factor: 2.188

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.