Department of Clinical Laboratory, Shanghai Pulmonary Hospital, School of Medicine, Tongji University, Shanghai, China.
Department of Laboratory Medicine, The First Affiliated Hospital of Wenzhou Medical University, Wenzhou, China.
J Clin Microbiol. 2018 Aug 27;56(9). doi: 10.1128/JCM.00731-18. Print 2018 Sep.
Carbapenem-resistant and hypervirulent strains have emerged recently. These strains are both hypervirulent and multidrug resistant and may also be highly transmissible and able to cause severe infections in both the hospital and the community. Clinical and public health needs require a rapid and comprehensive molecular detection assay to identify and track the spread of these strains and provide timely infection control information. Here, we develop a rapid multiplex PCR assay capable of distinguishing carbapenem-resistant isolates of sequence type 258 (ST258) and ST11, and hypervirulent ST23, ST65/ST375, and ST86 clones, as well as capsular types K1, K2, K locus type 47 (KL47), and KL64, and virulence genes , , , and The assay demonstrated 100% concordance with 118 previously genotyped isolates and revealed different populations of carbapenem-resistant and hypervirulent strains in two collections in China and the United States. The results showed that carbapenem-resistant and hypervirulent strains are still rare in the United States, whereas in China, ∼50% of carbapenem-resistant strains carry and virulence genes, which are largely associated with the epidemic ST11 strains. Similarly, a high prevalence of hypervirulent strains was found in carbapenem-susceptible isolates in two Chinese hospitals, but these primarily belong to ST23, ST65/ST375, and ST86, which are distinct from the carbapenem-resistant strains. Taken together, our results demonstrated that this PCR assay can be a useful tool for molecular surveillance of carbapenem-resistant and hypervirulent strains.
最近出现了耐碳青霉烯和高毒力的菌株。这些菌株不仅具有高毒力和多重耐药性,而且可能具有高度传染性,并能在医院和社区引起严重感染。临床和公共卫生的需要要求快速和全面的分子检测方法来识别和跟踪这些菌株的传播,并提供及时的感染控制信息。在这里,我们开发了一种快速多重 PCR 检测方法,能够区分耐碳青霉烯的 258 型(ST258)和 ST11 型、高毒力的 ST23、ST65/ST375 和 ST86 克隆,以及荚膜类型 K1、K2、K 位型 47(KL47)和 KL64,以及毒力基因 、 、 和 。该检测方法与 118 个先前进行基因分型的分离株具有 100%的一致性,并揭示了来自中国和美国的两个收集物中耐碳青霉烯和高毒力菌株的不同群体。结果表明,耐碳青霉烯和高毒力的 菌株在美国仍然罕见,而在中国,约 50%的耐碳青霉烯菌株携带 和 毒力基因,这些基因主要与流行的 ST11 菌株有关。同样,在中国的两家医院中,在耐碳青霉烯敏感的分离株中也发现了高比例的高毒力菌株,但这些菌株主要属于 ST23、ST65/ST375 和 ST86,与耐碳青霉烯菌株不同。总之,我们的研究结果表明,这种 PCR 检测方法可以作为监测耐碳青霉烯和高毒力 菌株的分子监测的有用工具。