Within-farm dynamics of ESBL/AmpC-producing escherichia coli in veal calves: A longitudinal approach

Journal of Antimicrobial Chemotherapy

Volumn 68, Issue 11, 2013, Pages 2468-2476

  Hordijk, Joost ^a,b   Mevius, Dik J ^a,b   Kant, Arie ^b   Bos, Marian E H ^c   Graveland, Haitske ^c   Bosman, Angela B ^a   Hartskeerl, Cedric M ^a   Heederik, Dick J J ^c   Wagenaar, Jaap A ^a,b  

^a UTRECHT UNIVERSITY   (Netherlands)

^b WAGENINGEN UNIVERSITY   (Netherlands)

^c UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Antimicrobial resistance; Cattle; Faecal carriage

Indexed keywords

AMPICILLIN; BETA LACTAMASE AMPC; CEFOTAXIME; CEFTAZIDIME; CIPROFLOXACIN; COLISTIN; COTRIMOXAZOLE; EXTENDED SPECTRUM BETA LACTAMASE; FLORFENICOL; STREPTOMYCIN; SULFAMETHOXAZOLE;

ANTIBIOTIC RESISTANCE; ANTIBIOTIC SENSITIVITY; ARTICLE; BACTERIUM ISOLATION; CALF (BOVINE); CATTLE; EXTENDED SPECTRUM BETA LACTAMASE PRODUCING ESCHERICHIA COLI; FOOD INTAKE; GENE SEQUENCE; GENOTYPE; METHICILLIN RESISTANT STAPHYLOCOCCUS AUREUS; MINIMUM INHIBITORY CONCENTRATION; MULTIGENE FAMILY; MULTILOCUS SEQUENCE TYPING; NONHUMAN; POLYMERASE CHAIN REACTION; PREVALENCE; PROMOTER REGION; REPLICON; VEAL;

ANTIMICROBIAL RESISTANCE; CATTLE; FAECAL CARRIAGE;

ANIMALS; ANIMALS, DOMESTIC; BETA-LACTAMASES; CATTLE; DNA, BACTERIAL; ESCHERICHIA COLI; ESCHERICHIA COLI INFECTIONS; FECES; GENOTYPE; MOLECULAR EPIDEMIOLOGY; MULTILOCUS SEQUENCE TYPING; PLASMIDS; POLYMERASE CHAIN REACTION; PREVALENCE; TRANSFORMATION, BACTERIAL;

EID: 84886290739     PISSN: 03057453     EISSN: 14602091     Source Type: Journal    
DOI: 10.1093/jac/dkt219     Document Type: Article

References (52)

1. Ewers C, Bethe A, Semmler T et al. Extended-spectrum b-lactamase-producing and AmpC-producing Escherichia coli from livestock and companion animals, and their putative impact on public health: a global perspective Clin Microbiol Infect 2012 18 646-55
2. Paterson DL, Bonomo RA. Extended-spectrum b-lactamases: a clinical update. Clin Microbiol Rev 2005; 18: 657-86.
3. Bush K, Jacoby GA. Updated functional classification of b-lactamases. Antimicrob Agents Chemother 2010; 54: 969-76.
4. Carattoli A. Resistance plasmid families in Enterobacteriaceae. Antimicrob Agents Chemother 2009; 53: 2227-38.
5. Carattoli A. Animal reservoirs for extended spectrum b-lactamase producers. Clin Microbiol Infect 2008; 14 Suppl 1: 117-23.
6. Bortolaia V, Larsen J, Damborg P et al. Potential pathogenicity and host range of extended-spectrum b-lactamase-producing Escherichia coli isolates from healthy poultry. Appl Environ Microbiol 2011; 77: 5830-3.
7. Dierikx C, van Essen-Zandbergen A, Veldman K et al. Increased detection of extended spectrum b-lactamase producing Salmonella enterica and Escherichia coli isolates from poultry. Vet Microbiol 2010; 145: 273-8.
8. Escudero E, Vinue L, Teshager T et al. Resistance mechanisms and farm-level distribution of fecal Escherichia coli isolates resistant to extended-spectrum cephalosporins in pigs in Spain. Res Vet Sci 2010; 88: 83-7.
9. Horton RA, Randall LP, Snary EL et al. Fecal carriage and shedding density of CTX-M extended-spectrum b-lactamase-producing Escherichia coli in cattle, chickens, and pigs: implications for environmental contamination and food production. Appl Environ Microbiol 2011; 77: 3715-9.
10. Zheng H, Zeng Z, Chen S et al. Prevalence and characterisation of CTX-M b-lactamases amongst Escherichia coli isolates from healthy food animals in China. Int J Antimicrob Agents 2012; 39: 305-10.
11. Dierikx C, van der Goot J, Fabri Tet al. Extended-spectrum-b-lactamaseand AmpC-b-lactamase-producing Escherichia coli in Dutch broilers and broiler farmers. J Antimicrob Chemother 2013; 68: 60-7.
12. Leverstein-van Hall MA, Dierikx CM, Cohen Stuart J et al. Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains. Clin Microbiol Infect 2011; 17: 873-80.
13. Geser N, Stephan R, Hachler H. Occurrence and characteristics of extended-spectrum b-lactamase (ESBL) producing Enterobacteriaceae in food producing animals, minced meat and raw milk. BMC Vet Res 2012; 8: 21.
14. Guerra B, Junker E, Schroeter A et al. Phenotypic and genotypic characterization of antimicrobial resistance in German Escherichia coli isolates from cattle, swine and poultry. J Antimicrob Chemother 2003; 52: 489-92.
15. Hiroi M, Yamazaki F, Harada T et al. Prevalence of extended-spectrum b-lactamase-producing Escherichia coli and Klebsiella pneumoniae in food-producing animals. J Vet Med Sci 2012; 74: 189-95.
16. Liebana E, Batchelor M Hopkins KL et al. Longitudinal farm study of extended-spectrum b-lactamase-mediated resistance. J Clin Microbiol 2006; 44: 1630-4.
17. Madec JY, LazizzeraC, Chatre Pet al. Prevalenceof fecal carriage ofacquired expanded-spectrum cephalosporin resistance in Enterobacteriaceae strains fromcattle in France. J ClinMicrobiol 2008; 46: 1566-7.
18. SnowLC,Wearing H, Stephenson B et al. Investigation of the presence of ESBL-producing Escherichia coli in the NorthWalesandWest Midlands areas of the UK in 2007 to 2008 using scanning surveillance. Vet Rec 2011; 169: 656.
19. MARAN 2008. Monitoring of Antimicrobial Resistance and Antibiotic Usage inAnimals in TheNetherlands in (21 March 2013, date last accessed) 2008 http://www.wageningenur.nl/nl/ Expertises-Dienstverlening/Onderzoeksinstituten/central-veterinary-institute/ Publicaties-CVI/MARAN-Rapporten.htm
20. Hoyle DV, Knight HI, Shaw DJ et al. Acquisition and epidemiology of antibiotic-resistant Escherichia coli in a cohort of newborn calves. J Antimicrob Chemother 2004; 53: 867-71.
21. Werckenthin C, Seidl S, Riedl J et al. Escherichia coli isolates from young calves in Bavaria: in vitro susceptibilities to 14 anti-microbial agents. J Vet Med B Infect Dis Vet Public Health 2002; 49: 61-5.
22. Hoyle DV, Shaw DJ, Knight HI et al. Age-related decline in carriage of ampicillin-resistant Escherichia coli in young calves. Appl Environ Microbiol 2004; 70: 6927-30.
23. Hordijk J,Wagenaar J.A., van de G.W.et al. Increasing prevalence and diversity of ESBL/AmpC-type b-lactamase genes in Escherichia coli isolated from veal calves from 1997 to 2010. J Antimicrob Chemother 2013; 68: 1970-3.
24. Dierikx CM, van Duijkeren E, Schoormans A.H.et al. Occurrence and characteristics of extended-spectrum-b-lactamase- and AmpCproducing clinical isolates derived from companion animals and horses. J Antimicrob Chemother 2012; 67: 1368-74.
25. Pé rez-Pé rez FJ, Hanson ND. Detection of plasmid-mediated AmpC b-lactamase genes in clinical isolates by using multiplex PCR. J Clin Microbiol 2002; 40: 2153-62.
26. Voets GM, FluitAC, Scharringa J et al. A set ofmultiplex PCRs for genotypic detection of extended-spectrum b-lactamases, carbapenemases, plasmidmediated AmpC b-lactamases and OXA b-lactamases. Int J Antimicrob Agents 2011; 37: 356-9.
27. Caroff N, Espaze E, Berard I et al. Mutations in the ampC promoter of Escherichia coli isolates resistant to oxyiminocephalosporins without extended spectrum b-lactamase production. FEMS Microbiol Lett 1999; 173: 459-65.28
28. Mulvey MR, Bryce E, Boyd DA et al. Molecular characterization of cefoxitin-resistant Escherichia coli from Canadian hospitals. Antimicrob Agents Chemother 2005; 49: 358-65.
29. Carattoli A, Bertini A, Villa Let al. Identification of plasmids by PCR-based replicon typing. J Microbiol Methods 2005; 63: 219-28.
30. Garcia-Fernandez A, Fortini D, Veldman K et al. Characterization of plasmids harbouring qnrS1, qnrB2 and qnrB19 genes in Salmonella. J Antimicrob Chemother 2009; 63: 274-81.
31. Villa L, Garcia-Fernandez A, Fortini D et al. Replicon sequence typing of IncF plasmids carrying virulence and resistance determinants. J Antimicrob Chemother 2010; 65: 2518-29.
32. Wirth T, Falush D, Lan R et al. Sex and virulence in Escherichia coli: an evolutionary perspective. Mol Microbiol 2006; 60: 1136-51.
33. UCC. Escherichia coli MLST Database (21 March 2013, date last accessed) http://mlst.ucc.ie/mlst/dbs/Ecoli (21 March 2013, date last accessed).
34. EUCAST. http://mic.eucast.org/Eucast2/ (21 March 2013, date last accessed).
35. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing: Twentieth Informational Supplement M100-S20 (Supplemental Table 2A-S1). CLSI,Wayne, PA, USA 2010
36. MARAN Monitoring of Antimicrobial Resistance and Antibiotic Usage in Animals in The Netherlands (21 March 2013, date last accessed) http://www.wageningenur.nl/nl/ Expertises-Dienstverlening/Onderzoeksinstituten/central-veterinary-institute/ Publicaties-CVI/MARAN-Rapporten.htm 2012
37. HoPL, LoWU, YeungMK et al. Dissemination of pHK01-like incompatibility groupIncFIIplasmids encodingCTX-M-14inEscherichiacoli fromhumanand animal sources. Vet Microbiol 2012; 158: 172-9.
38. HoPL, YeungMK, LoWUetal. PredominanceofpHK01-like incompatibility group FII plasmids encoding CTX-M-14 among extended-spectrum b-lactamase-producing Escherichia coli in Hong Kong, 1996-2008. Diagn Microbiol Infect Dis 2012; 73: 182-6.
39. Kim J, Bae IK, Jeong SH et al. Characterization of IncF plasmids carrying the blaCTX-M-14 gene in clinical isolates of Escherichia coli from Korea. J Antimicrob Chemother 2011; 66: 1263-8.
40. Mollenkopf DF, Weeman MF, Daniels JB et al. Variable within- and between-herd diversity of CTX-M cephalosporinase-bearing Escherichia coli isolates from dairy cattle. Appl Environ Microbiol 2012; 78: 4552-60.
41. Stokes MO, Cottell JL, Piddock LJ et al. Detection and characterization of pCT-like plasmid vectors for blaCTX-M-14 in Escherichia coli isolates from humans, turkeys and cattle in England and Wales. J Antimicrob Chemother 2012; 67: 1639-44.42
42. Diestra K, Juan C, Curiao T et al. Characterization of plasmids encoding blaESBL and surrounding genes in Spanish clinical isolates of Escherichia coli and Klebsiella pneumoniae. J Antimicrob Chemother 2009; 63: 60-6.
43. Valverde A, Canton R, Garcillan-Barcia MP et al. Spread of blaCTX-M-14 is driven mainly by IncK plasmids disseminated among Escherichia coli phylogroups A, B1, and D in Spain. Antimicrob Agents Chemother 2009; 53: 5204-12.
44. Oteo J, Diestra K, Juan C et al. Extended-spectrum b-lactamaseproducing Escherichia coli in Spain belong to a large variety of multilocus sequence typing types, including ST10. Int J Antimicrob Agents 2009; 34: 173-6.
45. Khachatryan AR, Hancock DD, Besser TE et al. Role of calf-adapted Escherichia coli in maintenance of antimicrobial drug resistance in dairy calves. Appl Environ Microbiol 2004; 70: 752-7.
46. Brunton LA, Duncan D, Coldham NG et al. A survey of antimicrobial usage on dairy farms and waste milk feeding practices in England and Wales. Vet Rec 2012; 171: 296.
47. Randall RL, Sharma M, Horton R et al. Isolation and characterisation of extended-spectrum b-lactamase CTX-M bacteria fromwaste milk samples from dairy farms in England and Wales in 2011 In: Abstracts of the Twenty-second European Congress of Clinical Microbiology and Infectious Diseases, London, UK 2012 451 Abstract P1641 European Society of Clinical Microbiology and Infectious Diseases, Basel, Switzerland
48. de Jong A, Thomas V, Simjee S et al. Pan-European monitoring of susceptibility to human-use antimicrobial agents in enteric bacteria isolated from healthy food-producing animals. J Antimicrob Chemother 2012; 67: 638-51.
49. Mezghani Maalej S, Rekik Meziou M, Mahjoubi F et al. Epidemiological study of Enterobacteriaceae resistance to colistin in Sfax (Tunisia). Med Mal Infect 2012; 42: 256-63.
50. Morales A.S., Fragoso de A.J., de Moura Gomes VT et al. Colistin resistance in Escherichia coli and Salmonella enterica strains isolated from swine in Brazil. ScientificWorldJournal 2012; 2012: 109795.
51. Wasyl D, Hoszowski A, Zajac M et al. Colistin resistance in Salmonella and Escherichia coli: a statistical approach In: Posters of the Third ASM Conference on Antimicrobial Resistance in Zoonotic Bacteria and Foodborne Pathogens in Animals, Humans and the Environment, Aix-en-Provence, France 2012 Poster 66B. American Society for Microbiology, Washington, DC, USA
52. Graveland H,Wagenaar JA,Verstappen KM.et al. DynamicsofMRSAcarriage in veal calves: a longitudinal field study Prev Vet Med 2012 107 180-6.