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建立一种四重 qRT-PCR 检测方法,用于同时鉴定高毒力和耐碳青霉烯的.

Development of a quadruple qRT-PCR assay for simultaneous identification of hypervirulent and carbapenem-resistant .

机构信息

Savid Medical School, University of Chinese Academy of Sciences , Beijing, China.

Shenzhen Key Laboratory of Pathogen and Immunity, Shenzhen Clinical Research Center for infectious disease, Shenzhen Third People's Hospital, Second Hospital Affiliated to Southern University of Science and Technology , Shenzhen, Guangdong, China.

出版信息

Microbiol Spectr. 2024 Jan 11;12(1):e0071923. doi: 10.1128/spectrum.00719-23. Epub 2023 Dec 7.

Abstract

Globally, the increasing number of hypervirulent (hvKp) and carbapenem-resistant Kp (CR-Kp) infections poses a huge public health challenge with high morbidity and mortality. Worrisomely, due to the mobility of elements carrying virulence and drug-resistance genes, the increasing prevalence of CR-hvKp has also been found with an overwhelming mortality rate in recent years. However, the current detection methods for hvKp and CR-Kp have many disadvantages, such as long turnaround time, complex operation, low sensitivity, and specificity. Herein, a more sensitive, rapid, single-reaction, and multiplex quantitative real-time PCR was developed and validated to differentiate the circulating lineages of Kp with excellent performance in sensitivity and specificity, providing a useful tool for the differential diagnosis and the surveillance of the circulating Kp.

摘要

全球范围内,高毒力 (hvKp) 和耐碳青霉烯类肠杆菌科 (CR-Kp) 感染的数量不断增加,给公共卫生带来了巨大挑战,导致高发病率和高死亡率。令人担忧的是,由于携带毒力和耐药基因的元素的可移动性,近年来 CR-hvKp 的流行率也在不断增加,死亡率令人震惊。然而,目前 hvKp 和 CR-Kp 的检测方法存在许多缺点,例如检测时间长、操作复杂、灵敏度和特异性低。在此,开发并验证了一种更敏感、快速、单反应和多重实时定量 PCR 方法,用于区分肠杆菌科的流行株,该方法在灵敏度和特异性方面具有优异的性能,为鉴别诊断和监测流行的肠杆菌科提供了一种有用的工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0065/10783029/abc5bc21227c/spectrum.00719-23.f001.jpg

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