Exploring Post-Treatment Reversion of Antimicrobial Resistance in Enteric Bacteria of Food Animals as a Resistance Mitigation Strategy

被引:7
作者
Volkova, Victoriya V. [1 ]
KuKanich, Butch [2 ]
Riviere, Jim E. [2 ]
机构
[1] Kansas State Univ, Coll Vet Med, Inst Computat Comparat Med, Dept Diagnost Med Pathobiol, Manhattan, KS 66506 USA
[2] Kansas State Univ, Coll Vet Med, Inst Computat Comparat Med, Dept Anat & Physiol, Manhattan, KS 66506 USA
关键词
pre-harvest food safety; antimicrobial use in livestock; antimicrobial resistance in bacteria of animal origin; antimicrobial resistance ecology; population pharmacokinetics; BETA-LACTAMASE INDUCTION; FECAL ESCHERICHIA-COLI; GROWTH PROMOTER; BEEF-CATTLE; IN-VITRO; ANTIBIOTIC-RESISTANCE; WITHDRAWAL TIMES; DAIRY-CATTLE; PHARMACOKINETICS; CEFTIOFUR;
D O I
10.1089/fpd.2016.2152
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Antimicrobial drug use in food animals is associated with an elevation in relative abundance of bacteria resistant to the drug among the animal enteric bacteria. Some of these bacteria are potential foodborne pathogens. Evidence suggests that at least in the enteric nontype-specific Escherichia coli, after treatment the resistance abundance reverts to the background pre-treatment levels, without further interventions. We hypothesize that it is possible to define the distribution of the time period after treatment within which resistance to the administered drug, and possibly other drugs in case of coselection, in fecal bacteria of the treated animals returns to the background pre-treatment levels. Furthermore, it is possible that a novel resistance mitigation strategy for microbiological food safety could be developed based on this resistance reversion phenomenon. The strategy would be conceptually similar to existing antimicrobial drug withdrawal periods, which is a well-established and accepted mitigation strategy for avoiding violative drug residues in the edible products from the treated animals. For developing resistance-relevant withdrawals, a mathematical framework can be used to join the necessary pharmacological, microbiological, and animal production components to project the distributions of the post-treatment resistance reversion periods in the production animal populations for major antimicrobial drug classes in use. The framework can also help guide design of empirical studies into the resistance-relevant withdrawal periods and development of mitigation approaches to reduce the treatment-associated elevation of resistance in animal enteric bacteria. We outline this framework, schematically and through exemplar equations, and how its components could be formulated.
引用
收藏
页码:610 / 617
页数:8
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