A Regulatory sRNA rli41 is Implicated in Cell Adhesion, Invasion and Pathogenicity in Listeria monocytogenes
文献类型： 外文期刊
作者： Wang, L. X. 1 ; Ji, C. H. 1 ; Ning, C. C. 1 ; Liu, Y. C. 2 ; Li, Z. Y. 1 ; Sun, Y. Q. 1 ; Xia, X. Z. 1 ; Cai, X. P. 3 ; Meng, Q. L. 1 ; Qiao, J. 1 ;
作者机构： 1.Shihezi Univ, Coll Anim Sci & Technol, Shihezi 832003, Xinjiang, Peoples R China
2.Xinjiang Acad Agr & Reclamat Sci, State Key Lab Sheep Genet Improvement & Hlth Prod, Shihezi 832000, 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; sRNA rli41; peptidoglycan-binding protein; virulence
期刊名称：APPLIED BIOCHEMISTRY AND MICROBIOLOGY （ 影响因子：0.8； 五年影响因子：1.1 ）
ISSN： 0003-6838
年卷期： 2022 年 58 卷 SUPPL 1 期
页码：
收录情况： SCI
摘要： Small regulatory RNAs (sRNAs) play important roles as post-transcriptional regulators throughout the life activities of bacteria. To explore the roles of the regulatory sRNA rli41 identified in Listeria monocytogenes (LM), we analyzed the molecular characteristics and expression profiles of sRNA rli41 during cell infection. Then the deletion strain LM-Delta rli41 and complementation strain LM-Delta rli41-rli41 were constructed and used to investigate the effects of deficiency of rli41 gene on the adhesion, invasion and pathogenicity of LM. Furthermore, sRNA rli41-regulated potential target genes were predicted in silico, followed by the verification of sRNA-mRNA interaction using a dual plasmid reporter system. The results revealed that sRNA rli41 was highly conserved in LM and its expression level was 15.78-fold up-regulated during cell infection as compared to extracellular environment. Compared with the parental strain and complementation strain, cell adhesion and invasion of the deletion strain were significantly reduced. Moreover, LD50 of LM increased and the pathogenicity weakened significantly due to the deficiency of rli41 genes. Additionally, sRNA rli41 could complementarily base pairing with lmo2178 mRNA 5'-UTR, which could facilitate the expression of peptidoglycan-binding protein Lmo2178, which in turn promotes the cell adhesion, invasion and pathogenicity of LM. Taken together, these findings demonstrated for the first time that the regulatory sRNA rli41 is implicated in cell adhesion, invasion and pathogenicity by modulating the expression of virulence factor Lmo2178 in LM.
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