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第一代头孢菌素治疗金黄色葡萄球菌引起的小鼠乳腺炎的乳腺内疗效。

The intramammary efficacy of first generation cephalosporins against Staphylococcus aureus mastitis in mice.

机构信息

Laboratory of Biochemistry, Ghent University, Salisburylaan 133, 9820 Merelbeke, Belgium.

出版信息

Vet Microbiol. 2012 Nov 9;160(1-2):141-50. doi: 10.1016/j.vetmic.2012.05.017. Epub 2012 May 22.

Abstract

Staphylococcus aureus-induced mastitis in cattle causes important financial losses in the dairy industry due to lower yield and bad milk quality. Although S. aureus is susceptible to many antimicrobials in vitro, treatment often fails to cure the infected udder. Hence, comprehensive evaluation of antimicrobials against S. aureus mastitis is desirable to direct treatment strategies. The mouse mastitis model is an elegant tool to evaluate antimicrobials in vivo while circumventing the high costs associated with bovine experiments. An evaluation of the antimicrobial efficacy of the intramammary (imam) applied first generation cephalosporins cefalexin, cefalonium, cefapirin and cefazolin, was performed using the S. aureus mouse mastitis model. In vivo determination of the effective dose 2log(10) (ED(2log10)), ED(4log10), protective dose 50 (PD(50)) and PD(100) in mouse mastitis studies, support that in vitro MIC data of the cephalosporins did not fully concur with the in vivo clinical outcome. Cefazolin was shown to be the most efficacious first generation cephalosporin to treat S. aureus mastitis whereas the MIC data indicate that cefalonium and cefapirin were more active in vitro. Changing the excipient for imam application from mineral oil to miglyol 812 further improved the antimicrobial efficacy of cefazolin, confirming that the excipient can influence the in vivo efficacy. Additionally, statistical analysis of the variation of S. aureus-infected, excipient-treated mice from fourteen studies emphasizes the strength of the mouse mastitis model as a fast, cost-effective and highly reproducible screening tool to assess the efficacy of antimicrobial compounds against intramammary S. aureus infection.

摘要

金黄色葡萄球菌引起的奶牛乳腺炎会给奶业造成重大经济损失,因为这会降低产量和牛奶质量。尽管金黄色葡萄球菌在体外对许多抗生素敏感,但治疗往往无法治愈感染的乳房。因此,需要对治疗金黄色葡萄球菌乳腺炎的抗生素进行综合评估,以指导治疗策略。小鼠乳腺炎模型是一种在体内评估抗生素的良好工具,同时避免了与牛实验相关的高成本。使用金黄色葡萄球菌小鼠乳腺炎模型评估了第一代头孢菌素头孢氨苄、头孢洛宁、头孢匹林和头孢唑林的经乳腺(imam)应用的抗菌功效。在小鼠乳腺炎研究中,体内测定有效剂量 2log(10)(ED(2log10))、ED(4log10)、保护剂量 50(PD(50))和 PD(100),支持头孢菌素的体外 MIC 数据与体内临床结果不完全一致。头孢唑林是治疗金黄色葡萄球菌乳腺炎最有效的第一代头孢菌素,而 MIC 数据表明头孢洛宁和头孢匹林在体外更活跃。将 imam 应用的赋形剂从矿物油改为 Miglyol 812 进一步提高了头孢唑林的抗菌功效,证实赋形剂会影响体内功效。此外,对 14 项研究中感染金黄色葡萄球菌、赋形剂处理的小鼠的变异进行的统计分析强调了小鼠乳腺炎模型作为一种快速、具有成本效益和高度可重复的筛选工具的优势,可用于评估抗 intramammary S. aureus 感染的抗菌化合物的功效。

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