Staphylococcus aureus RNAIII coordinately represses the synthesis of virulence factors and the transcription regulator Rot by an antisense mechanism

被引:351
作者
Boisset, Sandrine
Geissmann, Thomas
Huntzinger, Eric
Fechter, Pierre
Bendridi, Nadia
Possedko, Maria
Chevalier, Clement
Helfer, Anne Catherine
Benito, Yvonne
Jacquier, Alain
Gaspin, Christine
Vandenesch, Francois
Romby, Pascale [1 ]
机构
[1] Univ Strasbourg 1, CNRS, Inst Biol Mol & Cellulaire, Architecture & React lARN, F-67084 Strasbourg, France
[2] Univ Lyon 1, Fac Laennec, Ctr Natl Reference Staphylocoques, INSERM,E0230, F-69008 Lyon, France
[3] Inst Pasteur, CNRS, URA 2171, Unite Genet Interact Macromol, F-75724 Paris, France
[4] INRA, UR875, Unite Biometrie & Intelligence Artificielle, F-31326 Castanet Tolosan, France
关键词
regulatory RNA; translational repression; antisense regulation; RNase III; virulence; Staphylococcus aureus;
D O I
10.1101/gad.423507
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
RNAIII is the intracellular effector of the quorum-sensing system in Staphylococcus aureus. It is one of the largest regulatory RNAs (514 nucleotides long) that are known to control the expression of a large number of virulence genes. Here, we show that the 3' domain of RNAIII coordinately represses at the post- transcriptional level, the expression of mRNAs that encode a class of virulence factors that act early in the infection process. We demonstrate that the 3' domain acts primarily as an antisense RNA and rapidly anneals to these mRNAs, forming long RNA duplexes. The interaction between RNAIII and the mRNAs results in repression of translation initiation and triggers endoribonuclease III hydrolysis. These processes are followed by rapid depletion of the mRNA pool. In addition, we show that RNAIII and its 3' domain mediate translational repression of rot mRNA through a limited number of base pairings involving two loop-loop interactions. Since Rot is a transcriptional regulatory protein, we proposed that RNAIII indirectly acts on many downstream genes, resulting in the activation of the synthesis of several exoproteins. These data emphasize the multitude of regulatory steps affected by RNAIII and its 3' domain in establishing a network of S. aureus virulence factors.
引用
收藏
页码:1353 / 1366
页数:14
相关论文
共 46 条
[1]   fhlA repression by OxyS RNA:: Kissing complex formation at two sites results in a stable antisense-target RNA complex [J].
Argaman, L ;
Altuvia, S .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 300 (05) :1101-1112
[2]   New vector for efficient allelic replacement in naturally nontransformable, low-GC-content, gram-positive bacteria [J].
Arnaud, M ;
Chastanet, A ;
Débarbouillé, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 2004, 70 (11) :6887-6891
[3]  
BALABAN N, 1995, FEMS MICROBIOL LETT, V133, P155, DOI 10.1016/0378-1097(95)00356-A
[4]   trans-Complementation of a Staphylococcus aureus agr mutant by Staphylococcus lugdunensis agr RNAIII [J].
Benito, Y ;
Lina, G ;
Greenland, T ;
Etienne, J ;
Vandenesch, F .
JOURNAL OF BACTERIOLOGY, 1998, 180 (21) :5780-5783
[5]   Probing the structure of RNAIII, the Staphylococcus aureus agr regulatory RNA, and identification of the RNA domain involved in repression of protein A expression [J].
Benito, Y ;
Kolb, FA ;
Romby, P ;
Lina, G ;
Etienne, J ;
Vandenesch, F .
RNA, 2000, 6 (05) :668-679
[6]   No detectable effect of RNA-binding protein Hfq absence in Staphylococcus aureus [J].
Bohn, Chantal ;
Rigoulay, Candice ;
Bouloc, Philippe .
BMC MICROBIOLOGY, 2007, 7
[7]   Analysis of SD sequences in completed microbial genomes: Non-SD-led genes are as common as SD-led genes [J].
Chang, Bill ;
Halgamuge, Saman ;
Tang, Sen-Lin .
GENE, 2006, 373 :90-99
[8]   DIMINISHED VIRULENCE OF A SAR(-)/AGR(-) MUTANT OF STAPHYLOCOCCUS-AUREUS IN THE RABBIT MODEL OF ENDOCARDITIS [J].
CHEUNG, AL ;
EBERHARDT, KJ ;
CHUNG, E ;
YEAMAN, MR ;
SULLAM, PM ;
RAMOS, M ;
BAYER, AS .
JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (05) :1815-1822
[9]   Comparative proteomics of Staphylococcus aureus and the response of methicillin-resistant and methicillin-sensitive strains to Triton X-100 [J].
Cordwell, SJ ;
Larsen, MR ;
Cole, RT ;
Walsh, BJ .
MICROBIOLOGY-SGM, 2002, 148 :2765-2781
[10]   Identification of genes controlled by the essential YycG/YycF two-component system of Staphylococcus aureus [J].
Dubrac, S ;
Msadek, T .
JOURNAL OF BACTERIOLOGY, 2004, 186 (04) :1175-1181