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一种水解探针PCR检测法的介绍,用于对耐甲氧西林金黄色葡萄球菌进行高通量筛查,并具备包含或排除检测银色葡萄球菌的能力。

Introduction of a hydrolysis probe PCR assay for high-throughput screening of methicillin-resistant Staphylococcus aureus with the ability to include or exclude detection of Staphylococcus argenteus.

作者信息

Bogestam Katja, Vondracek Martin, Karlsson Mattias, Fang Hong, Giske Christian G

机构信息

Department of clinical microbiology, Karolinska University Hospital, Stockholm, Sweden.

Division of microbiology, Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden.

出版信息

PLoS One. 2018 Feb 9;13(2):e0192782. doi: 10.1371/journal.pone.0192782. eCollection 2018.

Abstract

Many countries using sensitive screening methods for detection of carriage of methicillin-resistant Staphylococcus aureus (MRSA) have a sustained low incidence of MRSA infections. For diagnostic laboratories with high sample volumes, MRSA screening requires stability, low maintenance and high performance at a low cost. Herein we designed oligonucleotides for a new nuc targeted hydrolysis probe PCR to replace the standard in-house nuc SybrGreen PCR assay. This new, more time-efficient, PCR assay resulted in a 40% increase in daily sample capacity, with maintained high specificity and sensitivity. The assay was also able to detect Staphylococcus aureus clonal cluster 75 (CC75) lineage strains, recently re-classified as Staphylococcus argenteus, with a sensitivity considerably increased compared to our previous assay. While awaiting consensus if the CC75 lineage of S. aureus should be considered as S. argenteus, and whether methicillin-resistant S. argenteus should be included in the MRSA definition, many diagnostic laboratories need to update their MRSA assay sensitivity/specificity towards this lineage/species. The MRSA screening assay presented in this manuscript is comprised of nuc oligonucleotides separately targeting S. aureus and CC75 lineage strains/S. argenteus, thus providing high user flexibility for the detection of CC75 lineage strains/S. argenteus.

摘要

许多采用灵敏筛选方法检测耐甲氧西林金黄色葡萄球菌(MRSA)携带情况的国家,MRSA感染发病率持续处于较低水平。对于样本量较大的诊断实验室而言,MRSA筛查需要具备稳定性、低维护成本且高性能的低成本检测方法。在此,我们设计了用于新型nuc靶向水解探针PCR的寡核苷酸,以取代标准的内部nuc SybrGreen PCR检测方法。这种新型的、更高效省时的PCR检测方法使每日样本处理量提高了40%,同时保持了高特异性和高灵敏度。该检测方法还能够检测金黄色葡萄球菌克隆复合体75(CC75)谱系菌株,该菌株最近被重新分类为银色葡萄球菌,与我们之前的检测方法相比,其灵敏度有了显著提高。在等待关于金黄色葡萄球菌CC75谱系是否应被视为银色葡萄球菌,以及耐甲氧西林银色葡萄球菌是否应纳入MRSA定义的共识期间,许多诊断实验室需要更新其针对该谱系/物种的MRSA检测方法的灵敏度/特异性。本论文中介绍的MRSA筛查检测方法由分别靶向金黄色葡萄球菌和CC75谱系菌株/银色葡萄球菌的nuc寡核苷酸组成,从而为检测CC75谱系菌株/银色葡萄球菌提供了高度的用户灵活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7fd8/5806904/7f062a80b1ca/pone.0192782.g001.jpg

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