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Genetic Evidence for O-Specific Antigen as Receptor of Pseudomonas aeruginosa Phage K8 and Its Genomic Analysis

机译:O特异性抗原作为绿脓杆菌噬菌体K8受体的遗传证据及其基因组分析

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Phage therapy requires the comprehensive understanding of the mechanisms underlying the host-phage interactions. In this work, to identify the genes related to Pseudomonas aeruginosa phage K8 receptor synthesis, 16 phage-resistant mutants were selected from a Tn 5G transposon mutant library of strain PAK. The disrupted genetic loci were identified and they were related to O-specific antigen (OSA) synthesis, including gene wbpR, ssg, wbpV, wbpO , and Y880_RS05480 , which encoded a putative O-antigen polymerase Wzy. The Lipopolysaccharide profile of the Y880_RS05480 mutant was analyzed and shown to lack the O-antigen. Therefore, the data from characterization of Y880_RS05480 by TMHMM and SDS-PAGE silver staining analysis suggest that this locus might encode Wzy. The complete phage K8 genome was characterized as 93879 bp in length and contained identical 1188-bp terminal direct repeats. Comparative genomic analysis showed that phage K8 was highly homologous to members of the genus PaP1-like phages. On the basis of our genetic findings, OSA of P. aeruginosa PAK is proven to be the receptor of phage K8. The highly conserved structural proteins among the genetic closely related phages suggest that they may recognize the same receptor.
机译:噬菌体疗法需要全面理解宿主-噬菌体相互作用的潜在机制。在这项工作中,为了鉴定与铜绿假单胞菌噬菌体K8受体合成有关的基因,从菌株PAK的Tn 5G转座子突变体文库中选择了16个噬菌体抗性突变体。鉴定了破坏的遗传基因座,它们与O特异性抗原(OSA)合成有关,包括基因wbpR,ssg,wbpV,wbpO和Y880_RS05480,它们编码一个假定的O抗原聚合酶Wzy。分析了Y880_RS05480突变体的脂多糖谱,发现缺乏O抗原。因此,通过TMHMM和SDS-PAGE银染分析表征Y880_RS05480的数据表明该基因座可能编码Wzy。完整的噬菌体K8基因组的长度为93879 bp,并包含相同的1188 bp末端直接重复序列。比较基因组分析表明,噬菌体K8与PaP1样噬菌体成员高度同源。根据我们的遗传发现,铜绿假单胞菌PAK的OSA被证明是噬菌体K8的受体。遗传上密切相关的噬菌体中高度保守的结构蛋白表明它们可能识别相同的受体。

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