Comparative analysis of Chlamydia bacteriophages reveals variation localized to a putative receptor binding domain.

T. Read, C. Fraser, R. Hsia, P. Bavoil
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引用次数: 33

Abstract

Three recently discovered ssDNA Chlamydia-infecting microviruses, phiCPG1, phiAR39, and Chp2, were compared with the previously characterized phage from avian C. psittaci, Chp1. Although the four bacteriophages share an identical arrangement of their five main genes, Chpl has diverged significantly in its nucleotide and protein sequences from the other three, which form a closely related group. The VP1 major viral capsid proteins of phiCPG1 and phiAR39 (from guinea pig-infecting C. psittaci and C. pneumoniae, respectively) are almost identical. However, VP1 of ovine C. psittaci phage Chp2 shows a high rate of nucleotide sequence change localized to a region encoding the "IN5" loop of the protein, thought to be a potential receptor-binding site. Phylogenetic analysis suggests that the ORF4 replication initiation protein is evolving faster than the other phage proteins. phiCPG1, phiAR39, and Chp2 are closely related to an ORF4 homolog inserted in the C. pneumoniae chromosome. This sequence analysis opens the way toward understanding the host-range and evolutionary history of these phages.
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衣原体噬菌体的比较分析显示变异定位于一个假定的受体结合域。
我们将最近发现的三种ssDNA衣原体感染微病毒phiCPG1、phiAR39和Chp2与先前鉴定的禽鹦鹉热螺旋体Chp1噬菌体进行了比较。虽然这四种噬菌体的五个主要基因排列相同,但Chpl在核苷酸和蛋白质序列上与其他三种噬菌体有明显的差异,这三种噬菌体形成了一个密切相关的群体。phiCPG1和phicar39的VP1主要病毒衣壳蛋白(分别来自豚鼠感染的鹦鹉螺c和肺炎c)几乎相同。然而,羊鹦鹉螺噬菌体Chp2的VP1显示出高速率的核苷酸序列变化,该区域编码该蛋白的“IN5”环,被认为是潜在的受体结合位点。系统发育分析表明,ORF4复制起始蛋白比其他噬菌体蛋白进化得更快。phiCPG1、phiAR39和Chp2与插入到肺炎球菌染色体上的ORF4同源物密切相关。这种序列分析为了解这些噬菌体的宿主范围和进化历史开辟了道路。
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