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首页> 外文期刊>Journal of general plant pathology >Identification of potential virulence genes in Erwinia chrysanthemi 3937: transposon insertion into plant-upregulated genes
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Identification of potential virulence genes in Erwinia chrysanthemi 3937: transposon insertion into plant-upregulated genes

机译:菊花欧文氏菌3937中潜在毒力基因的鉴定:转座子插入植物上调基因

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Erwinia chrysanthemi 3937 is a soft-rotting plant pathogen in Enterobacteriaceae. It attacks a wide range of plant host species. Previously, we identified dozens of E. chrysanthemi 3937 genes induced during plant infection by microarray differential display. Here, we have mutated plant-upregulated and putatively plant-upregulated genes in E. chrysanthemi 3937 using a transposon insertion method. Of 57 mutants produced, 8 were significantly reduced in maceration in African violet leaves. These 8 E. chrysanthemi genes are similar to Escherichia coli purU (formyltetrahydrofolate deformylase; ASAP20623) and wcaJ (undecaprenylphosphate glucosephosphotransferase; ASAP18556), Bacillus subtilis dltA (o-alanine-D-alanyl carrier protein ligase; ASAP19406), Pseudomonas syringae PSPTO2912 (ABC transporter, periplasmic glutamine-binding protein; ASAP15639), Pseudomonas aeruginosa pheC (cyclohexadienyl dehydratase; ASAP19773), P. syringae syrE (peptide synthase; AS API 9989), Vibrio vulnificus VV12303 (unknown protein; ASAP18555), and Yersinia pestis speD (5-adenosylmethionine decarboxylase; ASAP20536). In some of the genes, possible roles in virulence could be postulated based on the functions of their homologues. This work demonstrated that a low proportion of pathogenicity-related genes were among the plant-upregulated genes of E. chrysanthemi 3937. This study and further dissection of these putative virulence genesshould lead to new insights into infection mechanisms in pathogens.
机译:菊花欧文氏菌3937是肠杆菌科的一种软腐病植物病原体。它攻击多种植物宿主物种。以前,我们通过微阵列差异显示技术鉴定了数十种植物感染过程中诱导的大肠杆菌E. chrysanthemi 3937基因。在这里,我们已经使用转座子插入方法突变了菊花E. chrysanthemi 3937中植物上调的基因和推定的植物上调的基因。在产生的57个突变体中,有8个突变体在非洲紫罗兰叶中的浸渍显着减少。这8个菊花大肠杆菌基因与大肠杆菌purU(甲酰基四氢叶酸甲酰基化酶; ASAP20623)和wcaJ(十一烯磷酸葡萄糖葡萄糖磷酸转移酶; ASAP18556),枯草芽孢杆菌dltA(邻丙氨酸-D-丙氨酸基载体蛋白连接酶;转运蛋白,周质谷氨酰胺结合蛋白; ASAP15639),铜绿假单胞菌pheC(环己二烯基脱水酶; ASAP19773),丁香假单胞菌syrE(肽合酶; AS API 9989),创伤弧菌VV12303(未知蛋白; ASAP18555D病原体(5)和Y -腺苷甲硫氨酸脱羧酶; ASAP20536)。在某些基因中,可以根据其同源物的功能推测其在毒力中的可能作用。这项工作表明,致病性相关基因的比例很低,在大肠杆菌E. chrysanthemi 3937的基因中。这项研究以及对这些推定的致病力基因的进一步剖析,应该对病原体的感染机制产生新的认识。

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