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一种新型小 RNA 有助于抑制猪链球菌 2 的细胞链长和抗吞噬能力。

A novel small RNA contributes to restrain cellular chain length and anti-phagocytic ability in Streptococcus suis 2.

机构信息

School of Life Science and Technology, China Pharmaceutical University, Nanjing, China; Research Institute for Medicine of Nanjing Command, Nanjing, China.

Research Institute for Medicine of Nanjing Command, Nanjing, China.

出版信息

Microb Pathog. 2019 Dec;137:103730. doi: 10.1016/j.micpath.2019.103730. Epub 2019 Sep 6.

Abstract

Streptococcus suis serotype 2 (SS2) is an important porcine and human pathogen. Regulatory small non-coding RNAs (sRNAs) play an essential role in diverse physiological processes, although they remain poorly understood in SS2. In this study, we identified eight novel sRNAs through a combination of computational strategies and experimental identification. To explore roles of these novel sRNAs, sRNA34 was preferentially selected to assess phenotypes of the deletion strain in vitro and in vivo. The inactivation of sRNA34 significantly elongated the cellular chain, remarkably increased sensitivity to phagocytosis by RAW264.7, and attenuated virulence in a mouse infection model. Transcriptomic analysis revealed that inactivation of sRNA34 altered expression of multiple genes contributing to cellular chain formation and elongation, indicating a potential mechanism of sRNA34 in maintaining proper bacterial chain length to resist phagocytosis by the host cell. In summary, sRNA34 is a novel sRNA that contributes to cellular chain regulation and the anti-phagocytosis ability of SS2.

摘要

猪链球菌 2 型(SS2)是一种重要的猪和人类病原体。调控性小非编码 RNA(sRNA)在各种生理过程中发挥着重要作用,但它们在 SS2 中的作用仍知之甚少。在这项研究中,我们通过计算策略和实验鉴定相结合,鉴定了 8 个新的 sRNA。为了探索这些新的 sRNA 的作用,我们优先选择 sRNA34 来评估缺失菌株在体外和体内的表型。sRNA34 的失活显著延长了细胞链,显著增加了 RAW264.7 吞噬的敏感性,并在小鼠感染模型中减弱了毒力。转录组分析表明,sRNA34 的失活改变了多个与细胞链形成和伸长有关的基因的表达,表明 sRNA34 可能通过维持适当的细菌链长来抵抗宿主细胞的吞噬作用。总之,sRNA34 是一种新的 sRNA,它有助于 SS2 的细胞链调控和抗吞噬作用。

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