Literature DB >> 23560425

Increased recognition of non-O157 Shiga toxin-producing Escherichia coli infections in the United States during 2000-2010: epidemiologic features and comparison with E. coli O157 infections.

L Hannah Gould1, Rajal K Mody, Kanyin L Ong, Paula Clogher, Alicia B Cronquist, Katie N Garman, Sarah Lathrop, Carlota Medus, Nancy L Spina, Tameka H Webb, Patricia L White, Katie Wymore, Ruth E Gierke, Barbara E Mahon, Patricia M Griffin.   

Abstract

BACKGROUND: Shiga toxin-producing Escherichia coli (STEC) are an important cause of diarrhea and the major cause of postdiarrheal hemolytic uremic syndrome. Non-O157 STEC infections are being recognized with greater frequency because of changing laboratory practices.
METHODS: Foodborne Diseases Active Surveillance Network (FoodNet) site staff conducted active, population-based surveillance for laboratory-confirmed STEC infections. We assessed frequency and incidence of STEC infections by serogroup and examined and compared demographic factors, clinical characteristics, and frequency of international travel among patients.
RESULTS: During 2000-2010, FoodNet sites reported 2006 cases of non-O157 STEC infection and 5688 cases of O157 STEC infections. The number of reported non-O157 STEC infections increased from an incidence of 0.12 per 100,000 population in 2000 to 0.95 per 100,000 in 2010; while the rate of O157 STEC infections decreased from 2.17 to 0.95 per 100,000. Among non-O157 STEC, six serogroups were most commonly reported: O26 (26%), O103 (22%), O111 (19%), O121 (6%), O45 (5%), and O145 (4%). Non-O157 STEC infections were more common among Hispanics, and infections were less severe than those caused by O157 STEC, but this varied by serogroup. Fewer non-O157 STEC infections were associated with outbreaks (7% versus 20% for O157), while more were associated with international travel (14% versus 3% for O157).
CONCLUSIONS: Improved understanding of the epidemiologic features of non-O157 STEC infections can inform food safety and other prevention efforts. To detect both O157 and non-O157 STEC infections, clinical laboratories should routinely and simultaneously test all stool specimens submitted for diagnosis of acute community-acquired diarrhea for O157 STEC and for Shiga toxin and ensure that isolates are sent to a public health laboratory for serotyping and subtyping.

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Year:  2013        PMID: 23560425     DOI: 10.1089/fpd.2012.1401

Source DB:  PubMed          Journal:  Foodborne Pathog Dis        ISSN: 1535-3141            Impact factor:   3.171


  107 in total

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2.  Identification and characterization of atypical enteropathogenic and Shiga toxin-producing Escherichia coli isolated from ground beef and poultry breast purchased in Botucatu, Brazil.

Authors:  Rodrigo H S Tanabe; Melissa A Vieira; Noelle A B Mariano; Regiane C B Dias; Rafael Ventin da Silva; Caroline M Castro; Luis F Dos Santos; Carlos H Camargo; Ricardo S Yamatogi; Vera L M Rall; Rodrigo T Hernandes
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Review 3.  Laboratory diagnosis of bacterial gastroenteritis.

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Authors:  R P Johnson; B Holtslander; A Mazzocco; S Roche; J L Thomas; F Pollari; K D M Pintar
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Review 5.  Global incidence of human Shiga toxin-producing Escherichia coli infections and deaths: a systematic review and knowledge synthesis.

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6.  Tellurite Resistance in Shiga Toxin-Producing Escherichia coli.

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7.  Pooled Nucleic Acid Amplification Test for Screening of Stool Specimens for Shiga Toxin-Producing Escherichia coli.

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8.  Genetic Relatedness Among Escherichia coli Pathotypes Isolated from Food Products for Human Consumption in Cartagena, Colombia.

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Review 9.  The population genetics of pathogenic Escherichia coli.

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Journal:  Nat Rev Microbiol       Date:  2020-08-21       Impact factor: 60.633

10.  Factors Associated with Shiga Toxin-Producing Escherichia coli Shedding by Dairy and Beef Cattle.

Authors:  Cristina Venegas-Vargas; Scott Henderson; Akanksha Khare; Rebekah E Mosci; Jonathan D Lehnert; Pallavi Singh; Lindsey M Ouellette; Bo Norby; Julie A Funk; Steven Rust; Paul C Bartlett; Daniel Grooms; Shannon D Manning
Journal:  Appl Environ Microbiol       Date:  2016-07-29       Impact factor: 4.792

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