Contributions of P2-and P22-like prophages to understanding the enormous diversity and abundance of tailed bacteriophages

被引:46
作者
Casjens, Sherwood R. [1 ,2 ]
Grose, Julianne H. [3 ]
机构
[1] Univ Utah, Sch Med, Dept Pathol, Div Microbiol & Immunol, Salt Lake City, UT 84112 USA
[2] Univ Utah, Dept Biol, Salt Lake City, UT 84112 USA
[3] Brigham Young Univ, Dept Mol Biol & Microbiol, Provo, UT 84602 USA
关键词
Bacteriophage; Tailed phage; Prophage; Phage P2; Phage P22; Major capsid protein; Tailspike; Caudovirales; Salmonella; COMPLETE NUCLEOTIDE-SEQUENCE; PHAGE-P22 TAILSPIKE PROTEIN; COMPLETE GENOME SEQUENCE; ENTERICA SEROVAR TYPHIMURIUM; CRYSTAL-STRUCTURE; ESCHERICHIA-COLI; SALMONELLA-TYPHIMURIUM; BURKHOLDERIA-PSEUDOMALLEI; POPULATION-STRUCTURE; BINDING DOMAIN;
D O I
10.1016/j.virol.2016.05.022
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
We identified 9371 tailed phage prophages of 20 known types in reported complete genome sequences of 3298 bacteria in the Salmonella genus. These include 4758 P2 type and 744 P22 type prophages. The latter prophage types were found in the genome sequences of 127 and 24 bacterial host genera, increasing the known host ranges of phages in these groups by 114 and 20 genera, respectively. These prophage nucleotide sequences displayed much more diversity than was previously known from the 48 P2 and 24 P22 type authentic phages whose genomes have been sequenced. More detailed analysis of these prophage sequences indicated that major capsid protein (MCP) gene exchange between tailed phage clusters or types is extremely rare and that P22 prophage-encoded tailspikes correspond perfectly with their hosts' surface polysaccharide structure; thus, MCP and tailspike sequences accurately predict tailed phage type (and thus lifestyle) and host cell surface polysaccharide structure, respectively. (C) 2016 Elsevier Inc. All rights reserved.
引用
收藏
页码:255 / 276
页数:22
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