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首页> 外文期刊>International Journal of Molecular Sciences >Identification of Pathogenicity-Related Genes in Biofilm-Defective Acidovorax citrulli by Transposon Tn5 Mutagenesis
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Identification of Pathogenicity-Related Genes in Biofilm-Defective Acidovorax citrulli by Transposon Tn5 Mutagenesis

机译:转座子Tn5诱变鉴定生物膜缺陷性柠檬酸嗜酸菌的致病性相关基因

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Biofilm formation is important for virulence of a large number of plant pathogenic bacteria. Indeed, some virulence genes have been found to be involved in the formation of biofilm in bacterial fruit blotch pathogen Acidovorax citrulli. However, some virulent strains of A. citrulli were unable to format biofilm, indicating the complexity between biofilm formation and virulence. In this study, virulence-related genes were identified in the biofilm-defective strain A1 of A. citrulli by using Tn5 insertion, pathogenicity test, and high-efficiency thermal asymmetric interlaced PCR (hiTAIL-PCR). Results from this study indicated that 22 out of the obtained 301 mutants significantly decreased the virulence of strain A1 compared to the wild-type. Furthermore, sequence analysis indicated that the obtained 22 mutants were due to the insertion of Tn5 into eight genes, including Aave 4244 (cation diffusion facilitator family transporter), Aave 4286 (hypothetical protein), Aave 4189 (alpha/beta hydrolase fold), Aave 1911 (IMP dehydrogenase/GMP reductase domain), Aave 4383 (bacterial export proteins, family 1), Aave 4256 (Hsp70 protein), Aave 0003 (histidine kinase, DNA gyrase B, and HSP90-like ATPase), and Aave 2428 (pyridoxal-phosphate dependent enzyme). Furthermore, the growth of mutant Aave 2428 was unaffected and even increased by the change in incubation temperature, NaCl concentration and the pH of the LB broth, indicating that this gene may be directly involved in the bacterial virulence. Overall, the determination of the eight pathogenicity-related genes in strain A1 will be helpful to elucidate the pathogenesis of biofilm-defective A. citrulli.
机译:生物膜的形成对于大量植物病原细菌的毒性很重要。确实,已经发现某些毒力基因参与了细菌性水果斑病病原体Acidovorax citrulli中生物膜的形成。但是,一些有毒的柠檬曲霉菌株无法形成生物膜,表明生物膜形成和毒力之间的复杂性。在这项研究中,通过使用Tn5插入,致病性测试和高效热不对称交错PCR(hiTAIL-PCR),在柑桔曲霉的生物膜缺陷菌株A1中鉴定了毒力相关基因。这项研究的结果表明,与野生型相比,获得的301个突变体中有22个显着降低了菌株A1的毒力。此外,序列分析表明,获得的22个突变体是由于将Tn5插入八个基因,包括Aave 4244(阳离子扩散促进子家族转运蛋白),Aave 4286(假设蛋白),Aave 4189(α/β水解酶折叠),Aave 1911(IMP脱氢酶/ GMP还原酶结构域),Aave 4383(细菌输出蛋白,家族1),Aave 4256(Hsp70蛋白),Aave 0003(组氨酸激酶,DNA促旋酶B和HSP90样ATPase)和Aave 2428(吡rid醛) -磷酸盐依赖性酶)。此外,突变体Aave 2428的生长不受孵化温度,NaCl浓度和LB肉汤pH的变化的影响甚至增加,表明该基因可能直接参与细菌的致病性。总体而言,确定菌株A1中的8个致病性相关基因将有助于阐明生物膜缺陷性柑桔曲霉的发病机理。

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