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棘状链球菌毒力在粘菌变形虫和家蚕模型中的研究。

Studies of Streptococcus anginosus Virulence in Dictyostelium discoideum and Galleria mellonella Models.

机构信息

Department of Microbiology, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Krakow, Poland.

Department of Drug Biotechnology and Bioinformatics, National Medicines Institute, Warsaw, Poland.

出版信息

Infect Immun. 2023 May 16;91(5):e0001623. doi: 10.1128/iai.00016-23. Epub 2023 Apr 25.

Abstract

For many years, Streptococcus anginosus has been considered a commensal colonizing the oral cavity, as well as the gastrointestinal and genitourinary tracts. However, recent epidemiological and clinical data designate this bacterium as an emerging opportunistic pathogen. Despite the reported pathogenicity of S. anginosus, the molecular mechanism underpinning its virulence is poorly described. Therefore, our goal was to develop and optimize efficient and simple infection models that can be applied to examine the virulence of S. anginosus and to study host-pathogen interactions. Using 23 S. anginosus isolates collected from different infections, including severe and superficial infections, as well as an attenuated strain devoid of CppA, we demonstrate for the first time that Dictyostelium discoideum is a suitable model for initial, fast, and large-scale screening of virulence. Furthermore, we found that another nonvertebrate animal model, Galleria mellonella, can be used to study the pathogenesis of S. anginosus infection, with an emphasis on the interactions between the pathogen and host innate immunity. Examining the profile of immune defense genes, including antimicrobial peptides, opsonins, regulators of nodulation, and inhibitors of proteases, by quantitative PCR (qPCR) we identified different immune response profiles depending on the S. anginosus strain. Using these models, we show that S. anginosus is resistant to the bactericidal activity of phagocytes, a phenomenon confirmed using human neutrophils. Notably, since we found that the data from these models corresponded to the clinical severity of infection, we propose their further application to studies of the virulence of S. anginosus.

摘要

多年来,咽峡炎链球菌一直被认为是一种定居于口腔、胃肠道和泌尿生殖道的共生菌。然而,最近的流行病学和临床数据将该细菌指定为一种新兴的机会性病原体。尽管已经报道了咽峡炎链球菌的致病性,但支持其毒力的分子机制仍描述不足。因此,我们的目标是开发和优化高效、简单的感染模型,这些模型可用于研究咽峡炎链球菌的毒力以及宿主-病原体相互作用。

我们使用从不同感染中收集的 23 株咽峡炎链球菌,包括严重和浅表感染,以及缺乏 CppA 的减毒菌株,首次证明了粘菌(Dictyostelium discoideum)是用于快速、大规模筛选毒力的初始模型。此外,我们发现另一种无脊椎动物模型(家蚕)可用于研究咽峡炎链球菌感染的发病机制,重点研究病原体与宿主固有免疫之间的相互作用。通过定量 PCR(qPCR) 研究免疫防御基因(包括抗菌肽、调理素、结节调节因子和蛋白酶抑制剂)的表达谱,我们根据咽峡炎链球菌菌株的不同确定了不同的免疫反应谱。

使用这些模型,我们表明咽峡炎链球菌对吞噬细胞的杀菌活性具有抗性,这一现象通过人类中性粒细胞得到了证实。值得注意的是,由于我们发现这些模型的数据与感染的临床严重程度相对应,因此我们建议进一步将其应用于研究咽峡炎链球菌的毒力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8a0c/10187118/f51460b35826/iai.00016-23-f001.jpg

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