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新鲜和冷冻猪盲肠样本中多粘菌素耐药性筛选的选择性培养与定量聚合酶链反应的互补性

Complementarity of Selective Culture and qPCR for Colistin Resistance Screening in Fresh and Frozen Pig Cecum Samples.

作者信息

Miguela-Villoldo Pedro, Moreno Miguel A, Hernández Marta, Rodríguez-Lázaro David, Gallardo Alejandro, Borge Carmen, Quesada Alberto, Domínguez Lucas, Ugarte-Ruiz María

机构信息

VISAVET Health Surveillance Centre, Universidad Complutense, Madrid, Spain.

Departamento de Sanidad Animal, Facultad de Veterinaria, Universidad Complutense, Madrid, Spain.

出版信息

Front Microbiol. 2020 Nov 9;11:572712. doi: 10.3389/fmicb.2020.572712. eCollection 2020.

Abstract

Retrospective studies involving the screening of frozen stored collections of samples are commonplace when a new threat emerges, but it has been demonstrated that the freeze-thaw process can affect bacterial viability. The study of colistin-resistant bacteria in human and animal samples is an example of this issue. In this study, we compared culture-based and PCR-based methods for analyzing relative occurrence and diversity of colistin-resistant bacteria in caecal samples to determine the most appropriate method for frozen samples. Thus, 272 samples from the caecal contents of healthy pigs were tested before and after a 6-month freezing period. A selective medium was used when traditional isolation of colistin-resistant bacteria was tested, while a real-time SYBR Green I PCR assay was applied for quantification. The number of samples with colistin-resistant isolates was higher in fresh samples (247/272) than in frozen ones (67/272) and showed a higher diversity of colistin-resistant genera. PCR identification of colistin resistance genes evidenced that was the most prevalent gene and was detected for the first time in pigs from Spanish animal production. The number of samples with -carrying bacteria after a freezing period decreased, while real-time quantitation of the gene showed similar values in frozen and fresh samples. Therefore, when frozen cecal samples need to be analyzed, molecular detection of DNA could be the best option to provide a highly representative frame of the initial population present in the sample, and culture-based methods might be a useful complement to study colistin resistance levels.

摘要

当出现新的威胁时,涉及筛查冷冻保存样本集的回顾性研究很常见,但已证明冻融过程会影响细菌活力。对人类和动物样本中耐黏菌素细菌的研究就是这个问题的一个例子。在本研究中,我们比较了基于培养和基于PCR的方法,以分析盲肠样本中耐黏菌素细菌的相对发生率和多样性,从而确定适用于冷冻样本的最佳方法。因此,对来自健康猪盲肠内容物的272个样本在冷冻6个月前后进行了检测。在测试传统分离耐黏菌素细菌时使用了选择性培养基,同时应用实时SYBR Green I PCR测定法进行定量。耐黏菌素分离株样本的数量在新鲜样本(247/272)中高于冷冻样本(67/272),并且显示出耐黏菌素属的更高多样性。对耐黏菌素抗性基因的PCR鉴定证明, 是最普遍的基因,并且在西班牙动物生产的猪中首次检测到 。冷冻期后携带 细菌的样本数量减少,而 基因的实时定量在冷冻和新鲜样本中显示出相似的值。因此,当需要分析冷冻盲肠样本时,DNA的分子检测可能是提供样本中初始菌群高度代表性框架的最佳选择,而基于培养的方法可能是研究耐黏菌素抗性水平的有用补充。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0324/7680854/160d13619ad1/fmicb-11-572712-g001.jpg

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