期刊
APPLIED AND ENVIRONMENTAL MICROBIOLOGY
卷 87, 期 5, 页码 -出版社
AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.02171-20
关键词
biofilm; Pseudomonas aeruginosa; RetS; type III secretion system; YbeY; sRNA
资金
- National Key Research and Development Project of China [2017YFE0125600]
- National Science Foundation of China [31670130, 31970680, 31870130]
- Tianjin Municipal Science and Technology Commission [19JCYBJC24700]
- program of China Scholarships Council [201906200035]
YbeY is a highly conserved RNase in bacteria that plays essential roles in rRNA processing, small RNA regulation, and bacterial responses to environmental stresses. Mutation of the ybeY gene in Pseudomonas aeruginosa leads to dysregulation of secretion system gene expression and biofilm formation, indicating the pleiotropic functions of YbeY in bacterial regulation.
YbeY is a highly conserved RNase in bacteria and plays essential roles in the maturation of 16S rRNA, regulation of small RNAs (sRNAs), and bacterial responses to environmental stresses. Previously, we verified the role of YbeY in rRNA processing and ribosome maturation in Pseudomonas aeruginosa and demonstrated YbeY-mediated regulation of rpoS through an sRNA, ReaL. In this study, we demonstrate that mutation of the ybeY gene results in upregulation of the type Ill secretion system (T3SS) genes as well as downregulation of the type VI secretion system (T6SS) genes and reduction of biofilm formation. By examining the expression of the known sRNAs in P. aeruginosa, we found that mutation of the ybeY gene leads to downregulation of the small RNAs RsmY/Z, which control the T3SS, T6SS, and biofilm formation. Further studies revealed that the reduced levels of RsmY/Z are due to upregulation of retS. Taken together, our results reveal the pleiotropic functions of YbeY and provide detailed mechanisms of YbeY-mediated regulation in P. aeruginosa. IMPORTANCE Pseudomonas aeruginosa causes a variety of acute and chronic infections in humans. The type III secretion system (T3SS) plays an important role in acute infection, and the type VI secretion system (T6SS) and biofilm formation are associated with chronic infections. Understanding of the mechanisms that control the virulence determinants involved in acute and chronic infections will provide clues for the development of effective treatment strategies. Our results reveal a novel RNase-mediated regulation of T3SS, T6SS, and biofilm formation in P. aeruginosa.
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