Slaughterhouse effluent discharges into rivers not responsible for environmental occurrence of enteroaggregative escherichia coli

Veterinary Microbiology

Volumn 168, Issue 2-4, 2014, Pages 451-454

  Bibbal, Delphine ^a   Kérourédan, Monique ^a   Loukiadis, Estelle ^b   Scheutz, Flemming ^c   Oswald, Eric ^d   Brugère, Hubert ^a  

^a University of Toulouse III   (France)

^b UNIVERSITÉ DE LYON   (France)

^c STATENS SERUM INSTITUT   (Denmark)

^d TOULOUSE UNIVERSITY HOSPITAL   (France)

Author keywords

Cattle; E. coli; EAEC; Effluent; Slaughterhouse; STEC

Indexed keywords

RIVER WATER;

AGRICULTURAL SLURRY; AGRICULTURAL WASTE; ARTICLE; BACTERIAL GENE; BACTERIAL STRAIN; BACTERIUM CONTAMINATION; BACTERIUM DETECTION; BACTERIUM ISOLATE; CATTLE; EFFLUENT; ENTEROAGGREGATIVE ESCHERICHIA COLI; FRANCE; GENETIC MARKER; NONHUMAN; POLYMERASE CHAIN REACTION SYSTEM; RIVER; SLAUGHTERHOUSE; SLUDGE; WASTE WATER;

ANIMALIA; BOS; ESCHERICHIA COLI;

CATTLE; E. COLI; EAEC; EFFLUENT; SLAUGHTERHOUSE; STEC;

ABATTOIRS; ANIMALS; DISEASE OUTBREAKS; ENVIRONMENTAL EXPOSURE; ESCHERICHIA COLI; ESCHERICHIA COLI INFECTIONS; ESCHERICHIA COLI PROTEINS; EUROPE; POLYMERASE CHAIN REACTION; RIVERS; SHIGA-TOXIGENIC ESCHERICHIA COLI; WASTE WATER;

EID: 84892537317     PISSN: 03781135     EISSN: 18732542     Source Type: Journal    
DOI: 10.1016/j.vetmic.2013.11.042     Document Type: Article

References (26)

1. Aurass P., Prager R., Flieger A. EHEC/EAEC O104:H4 strain linked with the 2011 German outbreak of haemolytic uremic syndrome enters into the viable but non-culturable state in response to various stresses and resuscitates upon stress relief. Environ. Microbiol. 2011, 13:3139-3148.
2. Auvray F., Dilasser F., Bibbal D., Kerouredan M., Oswald E., Brugere H. French cattle is not a reservoir of the highly virulent enteroaggregative Shiga toxin-producing Escherichia coli of serotype O104:H4. Vet. Microbiol. 2012, 158:443-445.
3. Bernier C., Gounon P., Le Bouguenec C. Identification of an aggregative adhesion fimbria (AAF) type III-encoding operon in enteroaggregative Escherichia coli as a sensitive probe for detecting the AAF-encoding operon family. Infect. Immun. 2002, 70:4302-4311.
4. Boisen N., Scheutz F., Rasko D.A., Redman J.C., Persson S., Simon J., Kotloff K.L., Levine M.M., Sow S., Tamboura B., Toure A., Malle D., Panchalingam S., Krogfelt K.A., Nataro J.P. Genomic characterization of enteroaggregative Escherichia coli from children in Mali. J. Infect. Dis. 2012, 205:431-444.
5. Cassar C.A., Ottaway M., Paiba G.A., Futter R., Newbould S., Woodward M.J. Absence of enteroaggregative Escherichia coli in farmed animals in Great Britain. Vet. Rec. 2004, 154:237-239.
6. Cerna J.F., Nataro J.P., Estrada-Garcia T. Multiplex PCR for detection of three plasmid-borne genes of enteroaggregative Escherichia coli strains. J. Clin. Microbiol. 2003, 41:2138-2140.
7. China B., Pirson V., Mainil J.G. Typing of bovine attaching and effacing Escherichia coli by multiplex in vitro amplification of virulence-associated genes. Appl. Environ. Microbiol. 1996, 62:3462-3465.
8. Clermont O., Bonacorsi S., Bingen E. Rapid and simple determination of the Escherichia coli phylogenetic group. Appl. Environ. Microbiol. 2000, 66:4555-4558.
9. CLSI Performance standards for antimicrobial susceptibility testing, 17th informational supplement. Document M100-S17 2007, Clinical and Laboratory Standards Institute, Wayne, PA.
10. Cortes C., De la Fuente R., Blanco J., Blanco M., Blanco J.E., Dhabi G., Mora A., Justel P., Contreras A., Sanchez A., Corrales J.C., Orden J.A. Serotypes, virulence genes and intimin types of verotoxin-producing Escherichia coli and enteropathogenic E. coli isolated from healthy dairy goats in Spain. Vet. Microbiol. 2005, 110:67-76.
11. Hamelin K., Bruant G., El-Shaarawi A., Hill S., Edge T.a., Bekal S., Fairbrother J.M., Harel J., Maynard C., Masson L., Brousseau R. A virulence and antimicrobial resistance DNA microarray detects a high frequency of virulence genes in Escherichia coli isolates from Great Lakes recreational waters. Appl. Environ. Microbiol. 2006, 72:4200-4206.
12. Hamelin K., Bruant G., El-Shaarawi A., Hill S., Edge T.a., Fairbrother J., Harel J., Maynard C., Masson L., Brousseau R. Occurrence of virulence and antimicrobial resistance genes in Escherichia coli isolates from different aquatic ecosystems within the St. Clair River and Detroit River areas. Appl. Environ. Microbiol. 2007, 73:477-484.
13. Harrington S.M., Dudley E.G., Nataro J.P. Pathogenesis of enteroaggregative Escherichia coli infection. FEMS Microbiol. Lett. 2006, 254:12-18.
14. Karch H., Denamur E., Dobrindt U., Finlay B.B., Hengge R., Johannes L., Ron E.Z., Tonjum T., Sansonetti P.J., Vicente M. The enemy within us: lessons from the 2011 European Escherichia coli O104:H4 outbreak. EMBO Mol. Med. 2012, 4:841-848.
15. Loukiadis E., Kerouredan M., Beutin L., Oswald E., Brugere H. Characterization of Shiga toxin gene (stx)-positive and intimin gene (eae)-positive Escherichia coli isolates from wastewater of slaughterhouses in France. Appl. Environ. Microbiol. 2006, 72:3245-3251.
16. Monecke S., Mariani-Kurkdjian P., Bingen E., Weill F.X., Baliere C., Slickers P., Ehricht R. Presence of enterohemorrhagic Escherichia coli ST678/O104:H4 in France prior to 2011. Appl. Environ. Microbiol. 2011, 77:8784-8786.
17. Morabito S., Karch H., Mariani-Kurkdjian P., Schmidt H., Minelli F., Bingen E., Caprioli A. Enteroaggregative, Shiga toxin-producing Escherichia coli O111:H2 associated with an outbreak of hemolytic-uremic syndrome. J. Clin. Microbiol. 1998, 36:840-842.
18. Nataro J.P., Kaper J.B., Robins-Browne R., Prado V., Vial P., Levine M.M. Patterns of adherence of diarrheagenic Escherichia coli to HEp-2 cells. Pediatr. Infect. Dis. J. 1987, 6:829-831.
19. Orskov F., Orskov I. Escherichia coli serotyping and disease in man and animals. Can. J. Microbiol. 1992, 38:699-704.
20. Paddock Z.D., Bai J., Shi X., Renter D.G., Nagaraja T.G. Detection of Escherichia coli O104 in the feces of feedlot cattle by a multiplex PCR assay designed to target major genetic traits of the virulent hybrid strain responsible for the 2011 German outbreak. Appl. Environ. Microbiol. 2013, 79:3522-3525.
21. Rasko D.A., Webster D.R., Sahl J.W., Bashir A., Boisen N., Scheutz F., Paxinos E.E., Sebra R., Chin C.S., Iliopoulos D., Klammer A., Peluso P., Lee L., Kislyuk A.O., Bullard J., Kasarskis A., Wang S., Eid J., Rank D., Redman J.C., Steyert S.R., Frimodt-Moller J., Struve C., Petersen A.M., Krogfelt K.A., Nataro J.P., Schadt E.E., Waldor M.K. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N. Engl. J. Med. 2011, 365:709-717.
22. Savarino S.J., McVeigh A., Watson J., Cravioto A., Molina J., Echeverria P., Bhan M.K., Levine M.M., Fasano A. Enteroaggregative Escherichia coli heat-stable enterotoxin is not restricted to enteroaggregative E. coli. J. Infect. Dis. 1996, 173:1019-1022.
23. Seto K., Taguchi M., Kobayashi K., Kozaki S. Biochemical and molecular characterization of minor serogroups of Shiga toxin-producing Escherichia coli isolated from humans in Osaka prefecture. J. Vet. Med. Sci. 2007, 69:1215-1222.
24. Uber A.P., Trabulsi L.R., Irino K., Beutin L., Ghilardi A.C., Gomes T.A., Liberatore A.M., de Castro A.F., Elias W.P. Enteroaggregative Escherichia coli from humans and animals differ in major phenotypical traits and virulence genes. FEMS Microbiol. Lett. 2006, 256:251-257.
25. Wieler L.H., Semmler T., Eichhorn I., Antao E.M., Kinnemann B., Geue L., Karch H., Guenther S., Bethe A. No evidence of the Shiga toxin-producing E. coli O104:H4 outbreak strain or enteroaggregative E. coli (EAEC) found in cattle faeces in northern Germany, the hotspot of the 2011 HUS outbreak area. Gut Pathog. 2011, 3:17.
26. Zhao S., White D.G., Ge B., Ayers S., Friedman S., English L., Wagner D., Gaines S., Meng J. Identification and characterization of integron-mediated antibiotic resistance among Shiga toxin-producing Escherichia coli isolates. Appl. Environ. Microbiol. 2001, 67:1558-1564.