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中性粒细胞胞外陷阱(NETs)介导的对耐碳青霉烯类超毒力(CR-hvKP)的杀伤作用在糖尿病患者中受损。

Neutrophil extracellular traps (NETs)-mediated killing of carbapenem-resistant hypervirulent (CR-hvKP) are impaired in patients with diabetes mellitus.

机构信息

Department of Clinical Laboratory, Peking University People's Hospital , Beijing, China.

出版信息

Virulence. 2020 Dec;11(1):1122-1130. doi: 10.1080/21505594.2020.1809325.

DOI:10.1080/21505594.2020.1809325
PMID:32865110
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7549946/
Abstract

Carbapenem-resistant hypervirulent (CR-hvKP) have been reported in recent years across Asian countries and pose a serious threat to public health. Neutrophils represent the first line of defense against numerous infectious pathogens, such as CR-hvKP. Neutrophil extracellular traps (NETs) constitute one of the major antimicrobial defense mechanisms in neutrophils against invading pathogens, especially against hvKP. Interestingly, previous studies have demonstrated that patients with type 2 diabetes mellitus (T2D) display elevated levels of NETosis but are vulnerable to infections caused by hvKP. The discrepancy propels us to investigate the role of NETs in hvKP infections in the context of T2D. By utilizing a clinical-derived CR-hvKP strain and a combination of NETs complex detection, phagocytosis testing, NETs killing assay and immunofluorescence, and scanning electron microscope assays, we identified defective NETs-mediated killing of CR-hvKP strain in patients with T2D. Specifically, we show that the impaired NETs-mediated killing in T2D is not due to the decreased NETs formation, as the neutrophils isolated from T2D patients exhibited enhanced NETs formation compared to healthy controls. Further, we demonstrate that the reduced NETs activity does not result from the trapping failure of CR-hvKP, but likely associated with the deficient surface damage conferred by the NETs of T2D patients. Our data provide a novel insight into the defective innate immune response against CR-hvKP in T2D.

摘要

近年来,亚洲国家报告了碳青霉烯类耐药高毒力 (CR-hvKP),这对公共卫生构成了严重威胁。中性粒细胞是抵御多种感染性病原体的第一道防线,如 CR-hvKP。中性粒细胞胞外诱捕网(NETs)是中性粒细胞抵御入侵病原体的主要抗菌防御机制之一,特别是针对 hvKP。有趣的是,先前的研究表明,2 型糖尿病(T2D)患者的 NETosis 水平升高,但易感染 hvKP 引起的感染。这种差异促使我们研究 NETs 在 T2D 背景下对 hvKP 感染的作用。通过利用临床衍生的 CR-hvKP 株和 NETs 复合物检测、吞噬试验、NETs 杀伤试验和免疫荧光、扫描电子显微镜检测相结合,我们确定了 T2D 患者中 CR-hvKP 株的 NETs 介导杀伤作用受损。具体而言,我们表明 T2D 中受损的 NETs 介导杀伤作用不是由于 NETs 形成减少所致,因为与健康对照组相比,T2D 患者的中性粒细胞表现出增强的 NETs 形成。此外,我们证明 NETs 活性的降低不是由于 CR-hvKP 的捕获失败所致,而可能与 T2D 患者的 NETs 赋予的表面损伤不足有关。我们的数据为 T2D 中针对 CR-hvKP 的先天免疫反应受损提供了新的见解。

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