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BpsR Modulates Bordetella Biofilm Formation by Negatively Regulating the Expression of the Bps Polysaccharide

机译:BpsR通过负调节Bps多糖的表达来调节Bordetella生物膜的形成。

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摘要

Bordetella bacteria are Gram-negative respiratory pathogens of animals, birds, and humans. A hallmark feature of some Bordetella species is their ability to efficiently survive in the respiratory tract even after vaccination. Bordetella bronchiseptica and Bordetella pertussis form biofilms on abiotic surfaces and in the mouse respiratory tract. The Bps exopolysaccharide is one of the critical determinants for biofilm formation and the survival of Bordetella in the murine respiratory tract. In order to gain a better understanding of regulation of biofilm formation, we sought to study the mechanism by which Bps expression is controlled in Bordetella. Expression of bpsABCD (bpsA-D) is elevated in biofilms compared with levels in planktonically grown cells. We found that bpsA-D is expressed independently of BvgAS. Subsequently, we identified an open reading frame (ORF), BB1771 (designated here bpsR), that is located upstream of and in the opposite orientation to the bpsA-D locus. BpsR is homologous to the MarR family of transcriptional regulators. Measurement of bpsA and bpsD transcripts and the Bps polysaccharide levels from the wild-type and the ΔbpsR strains suggested that BpsR functions as a repressor. Consistent with enhanced production of Bps, the bpsR mutant displayed considerably more structured biofilms. We mapped the bpsA-D promoter region and showed that purified BpsR protein specifically bound to the bpsA-D promoter. Our results provide mechanistic insights into the regulatory strategy employed by Bordetella for control of the production of the Bps polysaccharide and biofilm formation.
机译:博德特氏菌是动物,鸟类和人类的革兰氏阴性呼吸道病原体。一些博德特氏菌物种的标志性特征是即使在接种疫苗后它们也能在呼吸道中有效存活。支气管博德氏杆菌和百日咳博德氏杆菌在非生物表面和小鼠呼吸道中形成生物膜。 Bps胞外多糖是决定生物膜形成和博德特氏菌在鼠呼吸道中存活的关键因素之一。为了更好地理解生物膜形成的调控,我们试图研究在博德特氏菌中控制Bps表达的机制。与浮游生长细胞中的水平相比,生物膜中bpsABCD(bpsA-D)的表达升高。我们发现bpsA-D的表达独立于BvgAS。随后,我们确定了一个开放阅读框(ORF),即BB1771(在此指定为bpsR),其位于bpsA-D基因座的上游并与之相反。 BpsR与转录调节子MarR家族同源。对野生型和ΔbpsR菌株的bpsA和bpsD转录本以及Bps多糖水平的测量表明,BpsR充当阻遏物。与提高Bps的产量一致,bpsR突变体显示出更多的结构化生物膜。我们绘制了bpsA-D启动子区域,并显示纯化的BpsR蛋白与 bpsA-D 启动子特异性结合。我们的研究结果为 Bordetella 为控制Bps多糖的产生和生物膜形成所采用的调节策略提供了机械方面的见识。

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