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Can the use of older-generation beta-lactam antibiotics in livestock production over-select for beta-lactamases of greatest consequence for human medicine? An in vitro experimental model

机译:是否可以在牲畜生产中使用较旧的β-内酰胺抗生素,对人类药物最大后果的β-内酰胺酶进行选择? 体外实验模型

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Though carbapenems are not licensed for use in food animals in the U.S., carbapenem resistance among Enterobacteriaceae has been identified in farm animals and their environments. The objective of our study was to determine the extent to which older-generation β-lactam antibiotics approved for use in food animals in the U.S. might differentially select for resistance to antibiotics of critical importance to human health, such as carbapenems. Escherichia coli (E . coli) strains from humans, food animals, or the environment bearing a single β-lactamase gene (n = 20 each) for bla TEM-1 , bla CMY-2 , and bla CTX-M-* or else bla KPC/IMP/NDM (due to limited availability, often in combination with other bla genes), were identified, along with 20 E . coli strains lacking any known beta-lactamase genes. Baseline estimates of intrinsic bacterial fitness were derived from the population growth curves. Effects of ampicillin (32 μg/mL), ceftriaxone (4 μg/mL) and meropenem (4 μg/mL) on each strain and resistance-group also were assessed. Further, in vitro batch cultures were prepared by mixing equal concentrations of 10 representative E . coli strains (two from each resistance gene group), and each mixture was incubated at 37°C for 24 hours in non-antibiotic cation-adjusted Mueller-Hinton II (CAMH-2) broth, ampicillin + CAMH-2 broth (at 2, 4, 8, 16, and 32 μg/mL) and ceftiofur + CAMH-2 broth (at 0.5, 1, 2, 4, and 8μg/mL). Relative and absolute abundance of resistance-groups were estimated phenotypically. Line plots of the raw data were generated, and non-linear Gompertz models and multilevel mixed-effect linear regression models were fitted to the data. The observed strain growth rate distributions were significantly different across the groups. AmpC strains (i.e., bla CMY-2 ) had distinctly less robust (p 0.05) growth in ceftriaxone (4 μg/mL) compared to extended-spectrum beta-lactamase (ESBL) producers harboring bla CTX-M-* variants. With increasing beta-lactam antibiotic concentrations, relative proportions of ESBLs and CREs were over-represented in the mixed bacterial communities; importantly, this was more pronounced with ceftiofur than with ampicillin. These results indicate that aminopenicillins and extended-spectrum cephalosporins would be expected to propagate carbapenemase-producing Enterobacteriaceae in food animals if and when Enterobacteriaceae from human health care settings enter the food animal environment.
机译:虽然CarbapeNems不被许可用于美国食物动物中的用途,但在农场动物及其环境中鉴定了肠杆菌痤疮之间的Carbapenem抗性。我们研究的目的是确定较旧的β-内酰胺抗生素在美国食物动物中使用的程度可能差异地选择对抗生素的抗生素对人类健康的关键重要性,例如Carbapems。大肠杆菌(例如Coli)来自人,食物动物或轴承的环境的菌株,用于BLA TEM-1,BLA CMY-2和BLA CTX-M- *或其他含有单个β-内酰胺酶基因(n = 20)的环境鉴定BLA KPC / IMP / NDM(由于有限的可用性,通常与其他BLA基因组合),以及20 e。缺乏任何已知的β-内酰胺酶基因的大肠杆菌菌株。内在细菌健身的基线估计来自群体生长曲线。评估了氨苄青霉素(32μg/ ml),头孢哌酮(4μg/ ml)和梅洛宁(4μg/ ml)对每种菌株和抗性组的影响。此外,通过混合等浓度的10个代表性e制备体外批量培养物。大肠杆菌菌株(来自每个抗性基因组的两个),并在37℃下在非抗生素阳离子调节的ueller-hinton II(Camh-2)肉汤中,在37℃下在37℃下温育24小时(Ampicillin + Camh-2肉汤(在2 ,4,8,16和32μg/ ml)和头孢噻呋+ Camh-2肉汤(0.5,1,2,4和8μg/ ml)。相对和绝对丰富的抗性群体估计表型。生成了原始数据的线条图,并将非线性gompertz模型和多级混合效果线性回归模型安装在数据上。观察到的菌株生长速率分布在整个组上有显着差异。与疏忽BLA CTX-M- *变体的扩展β-内酰胺酶(ESBL)生产商相比,AMPC菌株(即BLA CMY-2)具有明显不那么较低的头孢菌(4μg/ mL)的生长(4μg/ mL)。随着β-内酰胺抗生素浓度的增加,ESBLS和CRE的相对比例在混合细菌群落中过于代表;重要的是,这种比氨苄青霉素更明显。这些结果表明,如果来自人类医疗保健环境的肠杆菌薄膜进入食物动物环境,则预期氨基尼霉素和扩展谱头孢菌素将在食物动物中繁殖碳碱酶产生的肠杆菌菌。进入食物动物环境。

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