Cazer Casey L, Ducrot Lucas, Volkova Victoriya V, Gröhn Yrjö T
Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Cornell UniversityIthaca, NY, United States.
Department of Diagnostic Medicine/Pathobiology, Institute of Computational Comparative Medicine, College of Veterinary Medicine, Kansas State UniversityManhattan, KS, United States.
Front Microbiol. 2017 Sep 20;8:1753. doi: 10.3389/fmicb.2017.01753. eCollection 2017.
Antimicrobial use in beef cattle can increase antimicrobial resistance prevalence in their enteric bacteria, including potential pathogens such as . These bacteria can contaminate animal products at slaughterhouses and cause food-borne illness, which can be difficult to treat if it is due to antimicrobial resistant bacteria. One potential intervention to reduce the dissemination of resistant bacteria from feedlot to consumer is to impose a withdrawal period after antimicrobial use, similar to the current withdrawal period designed to prevent drug residues in edible animal meat. We investigated tetracycline resistance in generic in the bovine large intestine during and after antimicrobial treatment by building a mathematical model of oral chlortetracycline pharmacokinetics-pharmacodynamics and population dynamics. We tracked three subpopulations (susceptible, intermediate, and resistant) during and after treatment with each of three United States chlortetracycline indications (liver abscess reduction, disease control, disease treatment). We compared the proportion of resistant before antimicrobial use to that at several time points after treatment and found a greater proportion of resistant enteric after the current withdrawal periods than prior to treatment. In order for the proportion of resistant in the median beef steer to return to the pre-treatment level, withdrawal periods of 15 days after liver abscess reduction dosing (70 mg daily), 31 days after disease control dosing (350 mg daily), and 36 days after disease treatment dosing (22 mg/kg bodyweight for 5 days) are required in this model. These antimicrobial resistance withdrawal periods would be substantially longer than the current U.S. withdrawals of 0-2 days or Canadian withdrawals of 5-10 days. One published field study found similar time periods necessary to reduce the proportion of resistant following chlortetracycline disease treatment to those suggested by this model, but additional carefully designed field studies are necessary to confirm the model results. This model is limited to biological processes within the cattle and does not include resistance selection in the feedlot environment or co-selection of chlortetracycline resistance following other antimicrobial use.
肉牛使用抗菌药物会增加其肠道细菌中的抗菌药物耐药性流行率,包括诸如……等潜在病原体。这些细菌会在屠宰场污染动物产品,并导致食源性疾病,如果是由抗菌药物耐药菌引起的,这种疾病可能难以治疗。一种减少耐药菌从饲养场传播到消费者的潜在干预措施是在使用抗菌药物后设定停药期,类似于目前为防止食用动物肉中出现药物残留而设计的停药期。我们通过建立口服金霉素药代动力学 - 药效学和大肠杆菌种群动态的数学模型,研究了抗菌治疗期间及之后牛大肠中普通大肠杆菌的四环素耐药性。我们在美国三种金霉素适应症(减少肝脓肿、疾病控制、疾病治疗)治疗期间及之后跟踪了三个大肠杆菌亚群(敏感、中等耐药和耐药)。我们比较了使用抗菌药物前耐药大肠杆菌的比例与治疗后几个时间点的比例,发现当前停药期后耐药肠道大肠杆菌的比例高于治疗前。为了使中等体重肉牛体内耐药大肠杆菌的比例恢复到治疗前水平,在该模型中,减少肝脓肿给药(每日70毫克)后需要15天的停药期,疾病控制给药(每日350毫克)后需要31天,疾病治疗给药(5天内每日22毫克/千克体重)后需要36天。这些抗菌药物耐药性停药期将大大长于美国目前的0 - 2天停药期或加拿大的5 - 10天停药期。一项已发表的实地研究发现,金霉素疾病治疗后降低耐药大肠杆菌比例所需的时间与该模型建议的时间相似,但需要更多精心设计的实地研究来证实模型结果。该模型仅限于牛体内的生物学过程,不包括饲养场环境中的耐药性选择或其他抗菌药物使用后金霉素耐药性的共选择。