Scarpari Leandra M, Lambais Marcio R, Silva Denise S, Carraro Dirce M, Carrer Helaine
Departamento de Solos e Nutrição de Plantas, ESALQ, Universidade de São Paulo, Caixa Postal 9, 13418-900, Piracicaba, SP, Brazil.
FEMS Microbiol Lett. 2003 May 16;222(1):83-92. doi: 10.1016/S0378-1097(03)00251-9.
Xylella fastidiosa is the causal agent of economically important plant diseases, including citrus variegated chlorosis and Pierce's disease. Hitherto, there has been no information on the molecular mechanisms controlling X. fastidiosa-plant interactions. To determine whether predicted open reading frames (ORFs) encoding putative pathogenicity-related factors were expressed by X. fastidiosa 9a5c cells grown at low (LCD) and high cell density (HCD) conditions in liquid modified PW medium, reverse Northern blot hybridization and reverse transcription-polymerase chain reaction (RT-PCR) experiments were performed. Our results indicated that ORFs XF2344, XF2369, XF1851 and XF0125, encoding putative Fur, GumC, a serine-protease and RsmA, respectively, were significantly suppressed at HCD conditions. In contrast, ORF XF1115, encoding putative RpfF, was significantly induced at HCD conditions. Expressions of ORFs XF2367, XF2362 and XF0290, encoding putative GumD, GumJ and RpfA, respectively, were detected only at HCD conditions, whereas expression of ORF XF0287, encoding putative RpfB was detected only at LCD conditions. Bioassays with an Agrobacterium traG::lacZ reporter system indicated that X. fastidiosa does not synthesize N-acyl-homoserine lactones, whereas bioassays with a diffusible signal factor (DSF)-responsive Xanthomonas campestris pv. campestris mutant indicate that X. fastidiosa synthesizes a molecule similar to DSF in modified PW medium. Our data also suggest that the synthesis of the DSF-like molecule and fastidian gum by X. fastidiosa is affected by cell density in vitro.
木质部难养菌是包括柑橘杂色黄化病和皮尔斯病在内的具有重要经济影响的植物病害的病原体。迄今为止,尚无关于控制木质部难养菌与植物相互作用分子机制的信息。为了确定编码假定致病相关因子的预测开放阅读框(ORF)是否在液体改良PW培养基中低细胞密度(LCD)和高细胞密度(HCD)条件下生长的木质部难养菌9a5c细胞中表达,进行了反向Northern印迹杂交和逆转录聚合酶链反应(RT-PCR)实验。我们的结果表明,分别编码假定的Fur、GumC、一种丝氨酸蛋白酶和RsmA的ORF XF2344、XF2369、XF1851和XF0125在HCD条件下被显著抑制。相反,编码假定的RpfF的ORF XF1115在HCD条件下被显著诱导。分别编码假定的GumD、GumJ和RpfA的ORF XF2367、XF2362和XF0290的表达仅在HCD条件下被检测到,而编码假定的RpfB的ORF XF0287的表达仅在LCD条件下被检测到。用根癌农杆菌traG::lacZ报告系统进行的生物测定表明,木质部难养菌不合成N-酰基高丝氨酸内酯,而用可扩散信号因子(DSF)响应的野油菜黄单胞菌野油菜致病变种突变体进行的生物测定表明,木质部难养菌在改良PW培养基中合成一种类似于DSF的分子。我们的数据还表明木质部难养菌合成DSF样分子和苛求菌胶受体外细胞密度的影响。