Suppr超能文献

通过培养和直接 qPCR 方法评估奶牛场挤奶机表面细菌细胞密度与抗生素耐药丰度的相关性。

Correlation between Bacterial Cell Density and Abundance of Antibiotic Resistance on Milking Machine Surfaces Assessed by Cultivation and Direct qPCR Methods.

机构信息

Institute of Nutrition and Food Sciences, Department of Food Microbiology and Hygiene, University of Bonn, Friedrich-Hirzebruch-Allee 7, 53115, Bonn, Germany.

Institute for Hygiene and Public Health, University Hospital Bonn, Venusberg-Campus 1, 53127, Bonn, Germany.

出版信息

Microb Ecol. 2023 Oct;86(3):1676-1685. doi: 10.1007/s00248-023-02225-7. Epub 2023 May 11.

Abstract

The relative abundance of antibiotic-resistant bacteria and antibiotic-resistance genes was surveyed for different parts of a milking machine. A cultivation approach based on swab samples showed a highly diverse microbiota, harboring resistances against cloxacillin, ampicillin, penicillin, and tetracycline. This approach demonstrated a substantial cloxacillin resistance of numerous taxa within milking machine microbiota coming along with regular use of cloxacillin for dry-off therapy of dairy cows. For the less abundant tetracycline-resistant bacteria we found a positive correlation between microbial cell density and relative abundance of tetracycline-resistant microorganisms (R = 0.73). This indicated an accelerated dispersion of resistant cells for sampling locations with high cell density. However, the direct quantification of the tetM gene from the swap samples by qPCR showed the reverse relation to bacterial density if normalized against the abundance of 16S rRNA genes (R = 0.88). The abundance of 16S rRNA genes was analyzed by qPCR combined with a propidium monoazide treatment, which eliminates 16S rRNA gene signals in negative controls.

摘要

对挤奶设备的不同部位进行了抗生素耐药菌和抗生素耐药基因的相对丰度调查。基于拭子样本的培养方法显示出高度多样化的微生物群落,对氯唑西林、氨苄西林、青霉素和四环素具有耐药性。该方法表明,由于经常使用氯唑西林对奶牛进行干乳疗法,挤奶设备微生物群落中的许多分类群具有很高的氯唑西林耐药性。对于较少的四环素耐药菌,我们发现微生物细胞密度与四环素耐药微生物的相对丰度之间存在正相关(R=0.73)。这表明在细胞密度高的采样点,耐药细胞的扩散速度加快。然而,如果将 qPCR 从交换样本中直接定量的 tetM 基因与 16S rRNA 基因的丰度进行归一化,则与细菌密度呈反比关系(R=0.88)。16S rRNA 基因的丰度通过 qPCR 与吖啶单脒处理相结合进行分析,该处理消除了阴性对照中的 16S rRNA 基因信号。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61ca/10497690/25459a4371e1/248_2023_2225_Fig1_HTML.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验