Mikkelsen Helga, Ball Geneviève, Giraud Caroline, Filloux Alain
Imperial College London, Division of Cell and Molecular Biology, Centre for Molecular Microbiology and Infection, South Kensington Campus, London, UK.
PLoS One. 2009 Jun 23;4(6):e6018. doi: 10.1371/journal.pone.0006018.
Pseudomonas aeruginosa is a gram-negative pathogenic bacterium with a high adaptive potential that allows proliferation in a broad range of hosts or niches. It is also the causative agent of both acute and chronic biofilm-related infections in humans. Three cup gene clusters (cupA-C), involved in the assembly of cell surface fimbriae, have been shown to be involved in biofilm formation by the P. aeruginosa strains PAO1 or PAK. In PA14 isolates, a fourth cluster, named cupD, was identified within a pathogenicity island, PAPI-I, and may contribute to the higher virulence of this strain. Expression of the cupA genes is controlled by the HNS-like protein MvaT, whereas the cupB and cupC genes are under the control of the RocS1A1R two-component system. In this study, we show that cupD gene expression is positively controlled by the response regulator RcsB. As a consequence, CupD fimbriae are assembled on the cell surface, which results in a number of phenotypes such as a small colony morphotype, increased biofilm formation and decreased motility. These behaviors are compatible with the sessile bacterial lifestyle. The balance between planktonic and sessile lifestyles is known to be linked to the intracellular levels of c-di-GMP with high levels favoring biofilm formation. We showed that the EAL domain-containing PvrR response regulator counteracts the activity of RcsB on cupD gene expression. The action of PvrR is likely to involve c-di-GMP degradation through phosphodiesterase activity, confirming the key role of this second messenger in the balance between bacterial lifestyles. The regulatory network between RcsB and PvrR remains to be elucidated, but it stands as a potential model system to study how the equilibrium between the two lifestyles could be influenced by therapeutic agents that favor the planktonic lifestyle. This would render the pathogen accessible for the immune system or conventional antibiotic treatment.
铜绿假单胞菌是一种革兰氏阴性致病细菌,具有很高的适应潜力,能够在广泛的宿主或生态位中增殖。它也是人类急性和慢性生物膜相关感染的病原体。三个参与细胞表面菌毛组装的cup基因簇(cupA - C)已被证明与铜绿假单胞菌菌株PAO1或PAK的生物膜形成有关。在PA14分离株中,在一个致病岛PAPI - I内鉴定出了第四个基因簇,命名为cupD,它可能导致该菌株具有更高的毒力。cupA基因的表达受HNS样蛋白MvaT控制,而cupB和cupC基因则受RocS1A1R双组分系统的控制。在本研究中,我们表明cupD基因的表达受响应调节因子RcsB的正向调控。因此,CupD菌毛组装在细胞表面,导致多种表型,如小菌落形态、生物膜形成增加和运动性降低。这些行为与固着细菌的生活方式相符。已知浮游生活方式和固着生活方式之间的平衡与细胞内c - 二鸟苷酸水平有关,高水平有利于生物膜形成。我们表明,含EAL结构域的PvrR响应调节因子可抵消RcsB对cupD基因表达的活性。PvrR的作用可能涉及通过磷酸二酯酶活性降解c - 二鸟苷酸,证实了这种第二信使在细菌生活方式平衡中的关键作用。RcsB和PvrR之间的调控网络仍有待阐明,但它是一个潜在的模型系统,可用于研究有利于浮游生活方式的治疗药物如何影响两种生活方式之间的平衡。这将使病原体易于被免疫系统或传统抗生素治疗。