2007
DOI: 10.1093/jac/dkm402
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Changes in antimicrobial susceptibility in a population of Salmonella enterica serovar Dublin isolated from cattle in Japan from 1976 to 2005

Abstract: These data suggest that the introduction of nalidixic acid in veterinary medicine seemed to affect the susceptibilities of Salmonella Dublin among the cattle population in Japan, whereas the introduction of enrofloxacin has not caused any additional effect. The prudent use of antimicrobials in the veterinary field should be continuously stressed.

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Cited by 13 publications
(8 citation statements)
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“…The ArcAB-TolC efflux pumps are important for triclosan resistance [ 11 ] and these pumps have also been shown to directly contribute to flouroquinolone (e.g. ENR) resistance in Salmonella [ 40 , 41 ]. The efflux systems EmrAB and ArcEF have been shown to be important for both triclosan resistance [ 10 ] and trimethoprim resistance [ 42 ].…”
Section: Discussionmentioning
confidence: 99%
“…The ArcAB-TolC efflux pumps are important for triclosan resistance [ 11 ] and these pumps have also been shown to directly contribute to flouroquinolone (e.g. ENR) resistance in Salmonella [ 40 , 41 ]. The efflux systems EmrAB and ArcEF have been shown to be important for both triclosan resistance [ 10 ] and trimethoprim resistance [ 42 ].…”
Section: Discussionmentioning
confidence: 99%
“…Construction of gene replacement vectors and generation of deletion mutants. To generate deletion mutants of SGI3, the pco gene cluster, and the cus gene cluster, gene replacement was performed as described previously (52) with slight modifications. Detailed methods for the construction of gene replacement vectors can be found in the supplemental material.…”
Section: Methodsmentioning
confidence: 99%
“…To generate deletion mutants of SGI3, pco gene cluster, and cus gene cluster, gene replacement was performed as described previously (40) with slight modifications. For SGI3, upstream and downstream regions of SGI3 were amplified and connected by three continuous PCRs for the insert fragment as described below to construct a gene replacement vector.…”
Section: Methodsmentioning
confidence: 99%