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A Small Regulatory RNA, Rli82, Is Involved in the Motility and Pathogenicity of Listeria monocytogenes

文献类型： 外文期刊

作者： Ji, Chunhui 1 ; Li, Nengxiu 1 ; Jiao, Jian 1 ; Sun, Yaoqiang 1 ; Zuo, Yufei 1 ; Huang, Xin 2 ; Huang, Xiaoxing 1 ; Li, Zhiyuan 1 ; Li, Yaling 1 ; Leng, Qingwen 1 ; Cai, Xuepeng 3 ; Meng, Qingling 1 ; Qiao, Jun 1 ;

作者机构： 1.Shihezi Univ, Coll Anim Sci & Technol, Shihezi, Xinjiang, Peoples R China

2.Xinjiang Acad Agr & Reclamat Sci, Inst Anim Sci & Vet Res, Shihezi, Xinjiang, Peoples R China

3.Chinese Acad Agr Sci, Lanzhou Vet Res Inst, State Key Lab Vet Etiol Biol, Lanzhou 730046, Gansu, Peoples R China

关键词： Listeria monocytogenes; Regulatory sRNA; Rli82; Motility; Pathogenicity

期刊名称：JUNDISHAPUR JOURNAL OF MICROBIOLOGY （ 影响因子：0.6； 五年影响因子：0.7 ）

ISSN： 2008-3645

年卷期： 2023 年 16 卷 9 期

页码：

收录情况： SCI

摘要： Background: Listeria monocytogenes (LM) is a facultative intracellular pathogen that causes food-borne infections in humans and animals. To invade and multiply within host cells, LM utilizes various strategies to precisely modulate its gene expression and to adapt to the in vivo environment.Objectives: To investigate the regulatory roles of Rli82 sRNA in the motility and pathogenicity of LM EGD-e.Methods: The Rli82 gene knock-out mutant strain, LM-ARli82, and the complementation strain, LM-ARli82/Rli82, were constructed using homologous recombination technology, and their motility and virulence, respectively, were determined. Moreover, the potential target mRNA regulated by Rli82 was predicted using TargetRNA2 software, and then the interaction between the target mRNA and Rli82 was verified by the two-plasmid reporter system.Results: The results showed that the motility of LM-ARli82 was significantly increased at 25 degrees C, facilitated by the production of more flagella than LM EGD-e and LM-ARli82/Rli82. Furthermore, LD50 in LM-ARli82-infected mice was significantly increased as compared to LM EGD-e and LM-ARli82/Rli82, suggesting that the virulence of LM was weakened when the Rli82 gene was deleted. In addition, the mRNA level of flaA was not significantly elevated, but flaA protein was significantly higher in LM-ARli82 than in LM EGD-e and LM-ARli82/Rli82, suggesting that Rli82 might modulate the translation of flaA mRNA at the post-transcriptional level.Conclusions: Taken together, our findings for the first time revealed that Rli82 sRNA might be involved in the modulation of the expression of flaA protein, thereby influencing the mobility and pathogenicity of LM.

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