Transcriptome analysis of Listeria monocytogenes identifies three groups of genes differently regulated by PrfA

被引:269
作者
Milohanic, E
Glaser, P
Coppée, JY
Frangeul, L
Vega, Y
Vázquez-Boland, JA
Kunst, F
Cossart, P
Buchrieser, C
机构
[1] Inst Pasteur, Lab Genom Microorganismes Pathogenes, F-75724 Paris 15, France
[2] Inst Pasteur, Unite Interact Bacteries Cellules, F-75724 Paris 15, France
[3] Inst Pasteur, Plateau Tech Puces ADN, F-75724 Paris 15, France
[4] Univ Leon, Grp Patogenesis Mol & Genom Bacteriana, Fac Vet, E-24071 Leon, Spain
关键词
D O I
10.1046/j.1365-2958.2003.03413.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
PrfA is the major regulator of Listeria virulence gene expression. This protein is a member of the Crp/Fnr family of transcription regulators. To gain a deeper understanding of the PrfA regulon, we constructed a whole-genome array based on the complete genome sequence of Listeria monocytogenes strain EGDe and evaluated the expression profiles of the wild-type EGDe and a prfA -deleted mutant (EGDe DeltaprfA). Both strains were grown at 37degreesC in brain-heart infusion broth (BHI) and BHI supplemented with either activated charcoal, a compound known to enhance virulence gene expression, or cellobiose, a sugar reported to downregulate virulence gene expression in spite of full expression of PrfA. We identified three groups of genes that are regulated differently. Group I comprises, in addition to the 10 already known genes, two new genes, lmo2219 and lmo0788, both positively regulated and preceded by a putative PrfA box. Group II comprises eight negatively regulated genes: lmo0278 is preceded by a putative PrfA box, and the remaining seven genes (lmo0178-lmo0184 ) are organized in an operon. Group III comprises 53 genes, of which only two (lmo0596 and lmo2067) are preceded by a putative PrfA box. Charcoal addition induced upregulation of group I genes but abolished regulation by PrfA of most group III genes. In the presence of cellobiose, all the group I genes were downregulated, whereas group III genes remained fully activated. Group II genes were repressed in all conditions tested. A comparison of the expression profiles between a second L. monocytogenes strain (P14), its spontaneous mutant expressing a constitutively active PrfA variant (P14prfA*) and its corresponding prfA-deleted mutant (P14DeltaprfA ) and the EGDe strain revealed interesting strain-specific differences. Sequences strongly similar to a sigma B-dependent promoter were identified upstream of 22 group III genes. These results suggest that PrfA positively regulates a core set of 12 genes preceded by a PrfA box and probably expressed from a sigma A-dependent promoter. In contrast, a second set of PrfA-regulated genes lack a PrfA box and are expressed from a sigma B-dependent promoter. This study reveals that PrfA can act as an activator or a repressor and suggests that PrfA may directly or indirectly activate different sets of genes in association with different sigma factors.
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页码:1613 / 1625
页数:13
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