Literature DB >> 17098918

Antimicrobial-resistant enteric bacteria from dairy cattle.

Ashish A Sawant1, Narasimha V Hegde, Beth A Straley, Sarah C Donaldson, Brenda C Love, Stephen J Knabel, Bhushan M Jayarao.   

Abstract

A study was conducted to understand the descriptive and molecular epidemiology of antimicrobial-resistant gram-negative enteric bacteria in the feces of healthy lactating dairy cattle. Gram-negative enteric bacteria resistant to ampicillin, florfenicol, spectinomycin, and tetracycline were isolated from the feces of 35, 8, 5, and 42% of 213 lactating cattle on 74, 39, 9, 26, and 82% of 23 farms surveyed, respectively. Antimicrobial-resistant gram-negative bacteria accounted for 5 (florfenicol) to 14% (tetracycline) of total gram-negative enteric microflora. Nine bacterial species were isolated, of which Escherichia coli (87%) was the most predominant species. MICs showing reduced susceptibility to ampicillin, ceftiofur, chloramphenicol, florfenicol, spectinomycin, streptomycin, and tetracycline were observed in E. coli isolates. Isolates exhibited resistance to ampicillin (48%), ceftiofur (11%), chloramphenicol (20%), florfenicol (78%), spectinomycin (18%), and tetracycline (93%). Multidrug resistance (> or =3 to 6 antimicrobials) was seen in 40% of E. coli isolates from healthy lactating cattle. Of 113 tetracycline-resistant E. coli isolates, tet(B) was the predominant resistance determinant and was detected in 93% of isolates, while the remaining 7% isolates carried the tet(A) determinant. DNA-DNA hybridization assays revealed that tet determinants were located on the chromosome. Pulsed-field gel electrophoresis revealed that tetracycline-resistant E. coli isolates (n = 99 isolates) belonged to 60 subtypes, which is suggestive of a highly diverse population of tetracycline-resistant organisms. On most occasions, E. coli subtypes, although shared between cows within the herd, were confined mostly to a dairy herd. The findings of this study suggest that commensal enteric E. coli from healthy lactating cattle can be an important reservoir for tetracycline and perhaps other antimicrobial resistance determinants.

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Year:  2006        PMID: 17098918      PMCID: PMC1797124          DOI: 10.1128/AEM.01551-06

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  51 in total

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2.  The multiple nature of the animal protein factor.

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3.  Examination of heat stress and stage of lactation (early versus late) on fecal shedding of E. coli O157:H7 and Salmonella in dairy cattle.

Authors:  T S Edrington; C L Schultz; K J Genovese; T R Callaway; M L Looper; K M Bischoff; J L McReynolds; R C Anderson; D J Nisbet
Journal:  Foodborne Pathog Dis       Date:  2004       Impact factor: 3.171

4.  Clinical efficacy of florfenicol in the treatment of calf respiratory tract infections.

Authors:  V Aslan; M Maden; O Erganis; F M Birdane; M Corlu
Journal:  Vet Q       Date:  2002-02       Impact factor: 3.320

Review 5.  Cephalosporin resistance among animal-associated Enterobacteria: a current perspective.

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8.  A herd level analysis of urinary tract infection in dairy cattle.

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9.  A survey on antibiotic usage in dairy herds in Pennsylvania.

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10.  Trends in antibacterial susceptibility of mastitis pathogens during a seven-year period.

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  52 in total

1.  Antimicrobial resistance in mastitis, respiratory and enteric bacteria isolated from ruminant animals from the Atlantic Provinces of Canada from 1994-2013.

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2.  Prevalence of Antimicrobial Resistance and Transfer of Tetracycline Resistance Genes in Escherichia coli Isolates from Beef Cattle.

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3.  Molecular detection of virulence genes and multi-drug resistance patterns in Escherichia coli (STEC) in clinical bovine mastitis: Alborz province, Iran.

Authors:  M Tavakoli; H Pourtaghi
Journal:  Iran J Vet Res       Date:  2017       Impact factor: 1.376

4.  Selection pressure required for long-term persistence of blaCMY-2-positive IncA/C plasmids.

Authors:  Murugan Subbiah; Eva M Top; Devendra H Shah; Douglas R Call
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5.  Fecal cultivable aerobic microbiota of dairy cows and calves acting as reservoir of clinically relevant antimicrobial resistance genes.

Authors:  João Pedro Rueda Furlan; Lucas David Rodrigues Dos Santos; Micaela Santana Ramos; Inara Fernanda Lage Gallo; Eliana Guedes Stehling
Journal:  Braz J Microbiol       Date:  2020-04-03       Impact factor: 2.476

6.  Relatedness of Escherichia coli strains with different susceptibility phenotypes isolated from swine feces during ampicillin treatment.

Authors:  D Bibbal; V Dupouy; M F Prère; P L Toutain; A Bousquet-Mélou
Journal:  Appl Environ Microbiol       Date:  2009-03-06       Impact factor: 4.792

7.  Influence of therapeutic ceftiofur treatments of feedlot cattle on fecal and hide prevalences of commensal Escherichia coli resistant to expanded-spectrum cephalosporins, and molecular characterization of resistant isolates.

Authors:  John W Schmidt; Dee Griffin; Larry A Kuehn; Dayna M Brichta-Harhay
Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

8.  Role of ceftiofur in selection and dissemination of blaCMY-2-mediated cephalosporin resistance in Salmonella enterica and commensal Escherichia coli isolates from cattle.

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9.  Effect of subtherapeutic administration of antibiotics on the prevalence of antibiotic-resistant Escherichia coli bacteria in feedlot cattle.

Authors:  T W Alexander; L J Yanke; E Topp; M E Olson; R R Read; D W Morck; T A McAllister
Journal:  Appl Environ Microbiol       Date:  2008-05-23       Impact factor: 4.792

10.  Influence of antibiotic selection on genetic composition of Escherichia coli populations from conventional and organic dairy farms.

Authors:  Seth T Walk; Janice M Mladonicky; Jaclyn A Middleton; Anthony J Heidt; Julie R Cunningham; Paul Bartlett; Kenji Sato; Thomas S Whittam
Journal:  Appl Environ Microbiol       Date:  2007-08-17       Impact factor: 4.792

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