da Silva Neto José F, Koide Tie, Abe Cecília M, Gomes Suely L, Marques Marilis V
Departamento de Microbiologia, Instituto de Ciências Biomédicas, Universidade de São Paulo, Av. Prof. Lineu Prestes 1374, 05508-000 São Paulo, SP, Brazil.
Arch Microbiol. 2008 Mar;189(3):249-61. doi: 10.1007/s00203-007-0314-x. Epub 2007 Nov 6.
The phytopathogen Xylella fastidiosa produces long type IV pili and short type I pili involved in motility and adhesion. In this work, we have investigated the role of sigma factor sigma(54) (RpoN) in the regulation of fimbrial biogenesis in X. fastidiosa. An rpoN null mutant was constructed from the non-pathogenic citrus strain J1a12, and microarray analyses of global gene expression comparing the wild type and rpoN mutant strains showed few genes exhibiting differential expression. In particular, gene pilA1 (XF2542), which encodes the structural pilin protein of type IV pili, showed decreased expression in the rpoN mutant, whereas two-fold higher expression of an operon encoding proteins of type I pili was detected, as confirmed by quantitative RT-PCR (qRT-PCR) analysis. The transcriptional start site of pilA1 was determined by primer extension, downstream of a sigma(54)-dependent promoter. Microarray and qRT-PCR data demonstrated that expression of only one of the five pilA paralogues, pilA1, was significantly reduced in the rpoN mutant. The rpoN mutant made more biofilm than the wild type strain and presented a cell-cell aggregative phenotype. These results indicate that sigma(54) differentially regulates genes involved in type IV and type I fimbrial biogenesis, and is involved in biofilm formation in X. fastidiosa.
植物病原体木质部难养菌(Xylella fastidiosa)产生参与运动性和黏附作用的长型IV菌毛和短型I菌毛。在本研究中,我们调查了σ因子σ⁵⁴(RpoN)在木质部难养菌菌毛生物合成调控中的作用。从非致病性柑橘菌株J1a12构建了rpoN缺失突变体,通过对野生型和rpoN突变体菌株进行全基因组基因表达的微阵列分析,发现很少有基因表现出差异表达。特别是,编码IV型菌毛结构菌毛蛋白的pilA1基因(XF2542)在rpoN突变体中表达降低,而定量逆转录聚合酶链反应(qRT-PCR)分析证实,编码I型菌毛蛋白的一个操纵子的表达则检测到高出两倍。通过引物延伸确定了pilA1的转录起始位点,位于一个依赖于σ⁵⁴的启动子下游。微阵列和qRT-PCR数据表明,在rpoN突变体中,五个pilA旁系同源基因中只有一个pilA1的表达显著降低。rpoN突变体比野生型菌株形成更多生物膜,并呈现细胞间聚集表型。这些结果表明,σ⁵⁴差异调节参与IV型和I型菌毛生物合成的基因,并参与木质部难养菌的生物膜形成。