Matson Eric G, Thompson M Greg, Humphrey Samuel B, Zuerner Richard L, Stanton Thad B
Enteric Diseases and Food Safety Research Unit, National Animal Disease Center, Agricultural Research Service, United States Department of Agriculture, 2300 Dayton Road, Ames, IA 50010, USA.
J Bacteriol. 2005 Sep;187(17):5885-92. doi: 10.1128/JB.187.17.5885-5892.2005.
VSH-1 is a mitomycin C-inducible prophage of the anaerobic spirochete Brachyspira hyodysenteriae. Purified VSH-1 virions are noninfectious, contain random 7.5-kb fragments of the bacterial genome, and mediate generalized transduction of B. hyodysenteriae cells. In order to identify and sequence genes of this novel gene transfer agent (GTA), proteins associated either with VSH-1 capsids or with tails were purified by sodium dodecyl sulfate-polyacrylamide gel electrophoresis. The N-terminal amino acid sequences of 11 proteins were determined. Degenerate PCR primers were designed from the amino acid sequences and used to amplify several VSH-1 genes from B. hyodysenteriae strain B204 DNA. A lambda clone library of B. hyodysenteriae B204 DNA was subsequently screened by Southern hybridization methods and used to identify and sequence overlapping DNA inserts containing additional VSH-1 genes. VSH-1 genes spanned 16.3 kb of the B. hyodysenteriae chromosome and were flanked by bacterial genes. VSH-1 identified genes and unidentified, intervening open reading frames were consecutively organized in head (seven genes), tail (seven genes), and lysis (four genes) clusters in the same transcriptional direction. Putative lysis genes encoding endolysin (Lys) and holin proteins were identified from sequence and structural similarities of their translated protein products with GenBank bacteriophage proteins. Recombinant Lys protein hydrolyzed peptidoglycan purified from B. hyodysenteriae cells. The identified VSH-1 genes exceed the DNA capacity of VSH-1 virions and do not encode traditional bacteriophage early functions involved in DNA replication. These genome properties explain the noninfectious nature of VSH-1 virions and further confirm its resemblance to known prophage-like, GTAs of other bacterial species, such as the GTA from Rhodobacter capsulatus. The identification of VSH-1 genes will enable analysis of the regulation of this GTA and should facilitate investigations of VSH-1-like prophages from other Brachyspira species.
VSH-1是猪痢疾短螺旋体这种厌氧螺旋体的一种丝裂霉素C诱导型原噬菌体。纯化后的VSH-1病毒粒子没有感染性,包含细菌基因组随机的7.5 kb片段,并介导猪痢疾短螺旋体细胞的普遍性转导。为了鉴定和测序这种新型基因转移因子(GTA)的基因,通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳纯化了与VSH-1衣壳或尾部相关的蛋白质。测定了11种蛋白质的N端氨基酸序列。根据氨基酸序列设计了简并PCR引物,并用于从猪痢疾短螺旋体B204菌株DNA中扩增几个VSH-1基因。随后通过Southern杂交方法筛选了猪痢疾短螺旋体B204 DNA的λ克隆文库,并用于鉴定和测序包含其他VSH-1基因的重叠DNA插入片段。VSH-基因跨越猪痢疾短螺旋体染色体的16.3 kb,两侧是细菌基因。VSH-1鉴定出的基因以及未鉴定出的、居间的开放阅读框在头部(7个基因)、尾部(7个基因)和裂解(4个基因)簇中以相同的转录方向连续排列。从其翻译后的蛋白质产物与GenBank噬菌体蛋白质的序列和结构相似性中鉴定出了编码内溶素(Lys)和孔蛋白的推定裂解基因。重组Lys蛋白水解了从猪痢疾短螺旋体细胞中纯化的肽聚糖。鉴定出的VSH-1基因超过了VSH-1病毒粒子的DNA容量,并且不编码参与DNA复制的传统噬菌体早期功能。这些基因组特性解释了VSH-1病毒粒子的非感染性本质,并进一步证实了它与其他细菌物种中已知的类原噬菌体GTA(如来自荚膜红细菌的GTA)的相似性。VSH-1基因的鉴定将有助于分析这种GTA的调控,并应促进对来自其他短螺旋体物种的VSH-1样原噬菌体的研究。