Weber Nicolai Rosager1, Nielsen Jens Peter2, Jorsal Sven Erik Lind3, Haugegaard Svend4, Denwood Matthew5, Pedersen Ken Steen6. 1. University of Copenhagen, Faculty of Health and Medical Sciences, Department of Large Animal Sciences, Grønnegårdsvej 2, 1870, Frederiksberg C, Denmark. Electronic address: weber@sund.ku.dk. 2. University of Copenhagen, Faculty of Health and Medical Sciences, Department of Large Animal Sciences, Grønnegårdsvej 2, 1870, Frederiksberg C, Denmark. Electronic address: jpni@sund.ku.dk. 3. National Veterinary Institute, Technical University of Denmark, Bülowsvej 27, 1870, Frederiksberg C, Denmark. Electronic address: selj@vet.dtu.dk. 4. Laboratory for Pig Diseases, Danish Pig Research Centre, Vinkelvej 13, 8620, Kjellerup, Denmark. Electronic address: svh@seges.dk. 5. University of Copenhagen, Faculty of Health and Medical Sciences, Department of Large Animal Sciences, Grønnegårdsvej 2, 1870, Frederiksberg C, Denmark. Electronic address: md@sund.ku.dk. 6. University of Copenhagen, Faculty of Health and Medical Sciences, Department of Large Animal Sciences, Grønnegårdsvej 2, 1870, Frederiksberg C, Denmark; Øvet A/S, Køberupvej 33, 4700, Næstved, Denmark. Electronic address: ken@oevet.dk.
Abstract
INTRODUCTION: The prudent use of antibiotics in veterinary medicine necessitates the selection of antibiotic compounds with narrow-spectrums targeted against the specific pathogens involved. The same pathotype of enterotoxigenic E. coli (ETEC) was recently found both in diarrhoeic pigs and in samples from the pen floor where the pigs were housed. The first objective of this study was to compare resistance profiles from ETEC isolates and Non-ETEC isolates. The second objective was to evaluate the agreement between resistance profiles of ETEC isolated from pen floor samples and from individual rectal samples from pigs. Across three Danish pig herds, faecal samples were collected from the floors of 31 pens that had a within-pen diarrhoea prevalence of >25%, and from rectal samples of 93 diarrhoeic nursery pigs from the same pens. A total of 380 E. coli isolates were analysed by PCR and classified as ETEC when genes for adhesin factors and enterotoxins were detected. Minimum inhibitory concentrations of 13 antimicrobial agents were determined by the broth micro dilution method. Isolates were classified as resistant based on clinical breakpoints. RESULTS: Based on logistic regression models, the odds of Non-ETEC isolates (n=291) being pan-susceptible were significantly higher compared to ETEC isolates (n=89), (P<0.001, OR=20.22, CI95%=6.35-64.35). The odds of ETEC isolates having multidrug resistance were significantly higher compared to Non-ETEC isolates (p<0.001, OR: 7.21, CI95%: 2.87-18.10). The odds of an isolate being resistant were significantly higher in ETEC isolates compared to Non-ETEC isolates for ampicillin (p<0.001), apramycin (p=0.003), sulphamethoxazole (p<0.001) and trimethoprim (p<0.001). No overlap of resistance patterns between the three study herds was observed in the sampled ETEC isolates. In addition, there was generally good or excellent agreement when comparing resistance profiles from isolates from the same pen (pen floor and pig samples), and perfect agreement (Kappa=1.000, SE=0.316) was observed for ampicillin, apramycin, gentamycin, sulphamethoxazole, tetracycline and trimethoprim. CONCLUSIONS: We found that ETEC isolates were more resistant than Non-ETEC isolates. Furthermore, this study indicates that resistance testing of ETEC isolates from pen floor samples can be used as a convenient sampling method for resistance testing and in the selection of clinically relevant antimicrobial agents in the treatment of diarrhoeic pigs. The herd-level variation of resistance in ETEC isolates emphasises the importance of performing antimicrobial susceptibility testing at farm level when selecting antimicrobial agents for the treatment of E. coli-related diarrhoea.
INTRODUCTION: The prudent use of antibiotics in veterinary medicine necessitates the selection of antibiotic compounds with narrow-spectrums targeted against the specific pathogens involved. The same pathotype of enterotoxigenic E. coli (ETEC) was recently found both in diarrhoeic pigs and in samples from the pen floor where the pigs were housed. The first objective of this study was to compare resistance profiles from ETEC isolates and Non-ETEC isolates. The second objective was to evaluate the agreement between resistance profiles of ETEC isolated from pen floor samples and from individual rectal samples from pigs. Across three Danish pig herds, faecal samples were collected from the floors of 31 pens that had a within-pen diarrhoea prevalence of >25%, and from rectal samples of 93 diarrhoeic nursery pigs from the same pens. A total of 380 E. coli isolates were analysed by PCR and classified as ETEC when genes for adhesin factors and enterotoxins were detected. Minimum inhibitory concentrations of 13 antimicrobial agents were determined by the broth micro dilution method. Isolates were classified as resistant based on clinical breakpoints. RESULTS: Based on logistic regression models, the odds of Non-ETEC isolates (n=291) being pan-susceptible were significantly higher compared to ETEC isolates (n=89), (P<0.001, OR=20.22, CI95%=6.35-64.35). The odds of ETEC isolates having multidrug resistance were significantly higher compared to Non-ETEC isolates (p<0.001, OR: 7.21, CI95%: 2.87-18.10). The odds of an isolate being resistant were significantly higher in ETEC isolates compared to Non-ETEC isolates for ampicillin (p<0.001), apramycin (p=0.003), sulphamethoxazole (p<0.001) and trimethoprim (p<0.001). No overlap of resistance patterns between the three study herds was observed in the sampled ETEC isolates. In addition, there was generally good or excellent agreement when comparing resistance profiles from isolates from the same pen (pen floor and pig samples), and perfect agreement (Kappa=1.000, SE=0.316) was observed for ampicillin, apramycin, gentamycin, sulphamethoxazole, tetracycline and trimethoprim. CONCLUSIONS: We found that ETEC isolates were more resistant than Non-ETEC isolates. Furthermore, this study indicates that resistance testing of ETEC isolates from pen floor samples can be used as a convenient sampling method for resistance testing and in the selection of clinically relevant antimicrobial agents in the treatment of diarrhoeic pigs. The herd-level variation of resistance in ETEC isolates emphasises the importance of performing antimicrobial susceptibility testing at farm level when selecting antimicrobial agents for the treatment of E. coli-related diarrhoea.
Authors: Patrick Kindle; Katrin Zurfluh; Magdalena Nüesch-Inderbinen; Sereina von Ah; Xaver Sidler; Roger Stephan; Dolf Kümmerlen Journal: Porcine Health Manag Date: 2019-02-28
Authors: I Holmer; C M Salomonsen; S E Jorsal; L B Astrup; V F Jensen; B Borck Høg; K Pedersen Journal: BMC Vet Res Date: 2019-12-11 Impact factor: 2.741