Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period
Mannheimia haemolytica isolated from feedlot cattle were tested for tulathromycin resistance. Cattle were sampled over a three-year period, starting 12 months after approval of tulathromycin for prevention and treatment of bovine respiratory disease. Nasopharyngeal samples from approximately 5,814...
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Frontiers Media S.A.
2013-10-01
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Online Access: | http://journal.frontiersin.org/Journal/10.3389/fmicb.2013.00297/full |
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author | Trevor W. Alexander Shaun R. Cook Cassidy L. Klima Ed eTopp Tim A. McAllister |
author_facet | Trevor W. Alexander Shaun R. Cook Cassidy L. Klima Ed eTopp Tim A. McAllister |
author_sort | Trevor W. Alexander |
collection | DOAJ |
description | Mannheimia haemolytica isolated from feedlot cattle were tested for tulathromycin resistance. Cattle were sampled over a three-year period, starting 12 months after approval of tulathromycin for prevention and treatment of bovine respiratory disease. Nasopharyngeal samples from approximately 5,814 cattle were collected when cattle entered feedlots (N = 4) and again from the same cattle after ≥ 60 d on feed. The antimicrobial use history for each animal was recorded. Mannheimia haemolytica was isolated from 796 (13.7%) entry samples and 1,038 (20.6%) ≥ 60 d samples. Of the cattle positive for M. haemolytica, 18.5%, 2.9%, and 2.4% were administered therapeutic concentrations of tulathromycin, tilmicosin, or tylosin tartrate, respectively. In addition, 13.2% were administered subtherapeutic concentrations of tylosin phosphate in feed. In years one and two, no tulathromycin-resistant M. haemolytica were detected, whereas 5 isolates (0.4%) were resistant in year three. These resistant isolates were collected from three cattle originating from a single pen, were all serotype 1, and were genetically related (≥ 89% similarity) according to pulsed-field gel electrophoreses patterns. The five tulathromycin-resistant isolates were multi-drug resistant also exhibiting resistance to oxytetracycline, tilmicosin, ampicillin, or penicillin. The macrolide resistance genes erm(42), erm(A), erm(B), erm(F), erm(X) and msr(E)-mph(E), were not detected in the tulathromycin-resistant M. haemolytica. This study showed that tulathromycin resistance in M. haemolytica from a general population of feedlot cattle in western Canada was low and did not change over a three-year period after tulathromycin was approved for use in cattle. |
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spelling | doaj.art-b82d61c69ab041a4a831b1ccd7c1f4592022-12-22T03:37:12ZengFrontiers Media S.A.Frontiers in Microbiology1664-302X2013-10-01410.3389/fmicb.2013.0029765709Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year periodTrevor W. Alexander0Shaun R. Cook1Cassidy L. Klima2Ed eTopp3Tim A. McAllister4Agriculture and Agri-Food CanadaAgriculture and Agri-Food CanadaAgriculture and Agri-Food CanadaAgriculture and Agri-Food CanadaAgriculture and Agri-Food CanadaMannheimia haemolytica isolated from feedlot cattle were tested for tulathromycin resistance. Cattle were sampled over a three-year period, starting 12 months after approval of tulathromycin for prevention and treatment of bovine respiratory disease. Nasopharyngeal samples from approximately 5,814 cattle were collected when cattle entered feedlots (N = 4) and again from the same cattle after ≥ 60 d on feed. The antimicrobial use history for each animal was recorded. Mannheimia haemolytica was isolated from 796 (13.7%) entry samples and 1,038 (20.6%) ≥ 60 d samples. Of the cattle positive for M. haemolytica, 18.5%, 2.9%, and 2.4% were administered therapeutic concentrations of tulathromycin, tilmicosin, or tylosin tartrate, respectively. In addition, 13.2% were administered subtherapeutic concentrations of tylosin phosphate in feed. In years one and two, no tulathromycin-resistant M. haemolytica were detected, whereas 5 isolates (0.4%) were resistant in year three. These resistant isolates were collected from three cattle originating from a single pen, were all serotype 1, and were genetically related (≥ 89% similarity) according to pulsed-field gel electrophoreses patterns. The five tulathromycin-resistant isolates were multi-drug resistant also exhibiting resistance to oxytetracycline, tilmicosin, ampicillin, or penicillin. The macrolide resistance genes erm(42), erm(A), erm(B), erm(F), erm(X) and msr(E)-mph(E), were not detected in the tulathromycin-resistant M. haemolytica. This study showed that tulathromycin resistance in M. haemolytica from a general population of feedlot cattle in western Canada was low and did not change over a three-year period after tulathromycin was approved for use in cattle.http://journal.frontiersin.org/Journal/10.3389/fmicb.2013.00297/fullCattleMannheimia haemolyticaantimicrobial resistancetulathromycinfeedlot |
spellingShingle | Trevor W. Alexander Shaun R. Cook Cassidy L. Klima Ed eTopp Tim A. McAllister Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period Frontiers in Microbiology Cattle Mannheimia haemolytica antimicrobial resistance tulathromycin feedlot |
title | Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period |
title_full | Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period |
title_fullStr | Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period |
title_full_unstemmed | Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period |
title_short | Susceptibility to tulathromycin in Mannheimia haemolytica isolated from feedlot cattle over a three-year period |
title_sort | susceptibility to tulathromycin in mannheimia haemolytica isolated from feedlot cattle over a three year period |
topic | Cattle Mannheimia haemolytica antimicrobial resistance tulathromycin feedlot |
url | http://journal.frontiersin.org/Journal/10.3389/fmicb.2013.00297/full |
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