Bittner Mauricio, Saldı As Soledad, Estévez Claudia, Zaldı Var Mercedes, Marolda Cristina L, Valvano Miguel A, Contreras Inés
Departamento de Bioquı́mica y Biologı́a Molecular, Facultad de Ciencias Quı́micas y Farmacéuticas, Universidad de Chile, PO Box 174, Correo 22, Santiago, Chile1.
Department of Microbiology and Immunology, University of Western Ontario, London, Ontario, Canada N6A 5C12.
Microbiology (Reading). 2002 Dec;148(Pt 12):3789-3799. doi: 10.1099/00221287-148-12-3789.
The authors previously reported increased expression of the Salmonella enterica serovar Typhi (S. typhi) rfaH gene when the bacterial cells reach stationary phase. In this study, using a lacZ fusion to the rfaH promoter region, they demonstrate that growth-dependent regulation of rfaH expression occurs at the level of transcription initiation. It was also observed that production of the lipopolysaccharide (LPS) O-antigen by S. typhi Ty2 correlated with the differential expression of rfaH during bacterial growth. This was probably due to the increased cellular levels of RfaH, since expression of the distal gene in the O-antigen gene cluster of S. typhi Ty2, wbaP, was also increased during stationary growth, as demonstrated by RT-PCR analysis. Examination of the sequences upstream of the rfaH coding region revealed homologies to potential binding sites for the RcsB/RcsA dimer of the RcsC/YopJ/RcsB phosphorelay regulatory system and for the RpoN alternative sigma factor. The expression of the rfaH gene in rpoN and rcsB mutants of S. typhi Ty2 was measured. The results indicate that inactivation of rpoN, but not of rcsB, suppresses the growth-phase-dependent induction of rfaH expression. Furthermore, production of beta-galactosidase mediated by the rfaH-lacZ fusion increased approximately fourfold when bacteria were grown in a nitrogen-limited medium. Nitrogen limitation was also shown to increase the expression of the O-antigen by the wild-type S. typhi Ty2, as demonstrated by a similar electrophoretic profile to that observed during the stationary phase of growth in rich media. It is therefore concluded that the relationship between LPS production and nitrogen limitation parallels the pattern of rfaH regulation under the control of RpoN and is consistent with the idea that RpoN modulates LPS formation via its effect on rfaH gene expression during bacterial growth.
作者之前报道过,当肠炎沙门氏菌伤寒血清型(伤寒杆菌)细胞进入稳定期时,其rfaH基因的表达会增加。在本研究中,通过使用与rfaH启动子区域融合的lacZ,他们证明了rfaH表达的生长依赖性调控发生在转录起始水平。还观察到,伤寒杆菌Ty2产生的脂多糖(LPS)O抗原与细菌生长过程中rfaH的差异表达相关。这可能是由于RfaH的细胞水平增加,因为通过RT-PCR分析表明,伤寒杆菌Ty2的O抗原基因簇中的远端基因wbaP在稳定期生长期间表达也增加。对rfaH编码区上游序列的检查揭示了与RcsC/YopJ/RcsB磷酸化信号转导调节系统的RcsB/RcsA二聚体以及RpoN替代sigma因子的潜在结合位点的同源性。测量了伤寒杆菌Ty2的rpoN和rcsB突变体中rfaH基因的表达。结果表明,rpoN的失活而非rcsB的失活抑制了rfaH表达的生长阶段依赖性诱导。此外,当细菌在氮限制培养基中生长时,由rfaH-lacZ融合介导的β-半乳糖苷酶的产生增加了约四倍。如在丰富培养基中生长的稳定期观察到的类似电泳图谱所示,氮限制也显示会增加野生型伤寒杆菌Ty2的O抗原表达。因此得出结论,LPS产生与氮限制之间的关系与RpoN控制下的rfaH调节模式相似,并且与RpoN在细菌生长过程中通过影响rfaH基因表达来调节LPS形成的观点一致。