Characterization of a novel T4-type Stenotrophomonas maltophilia virulent phage Smp14

被引:26
作者
Chen, Chiy-Rong
Lin, Ching-Hsuan
Lin, Juey-Wen
Chang, Chi-I
Tseng, Yi-Hsiung [1 ]
Weng, Shu-Fen
机构
[1] Cent Taiwan Univ Sci & Technol, Inst Med Biotechnol, Taichung 406, Taiwan
[2] Natl Chung Hsing Univ, Inst Mol Biol, Taichung 402, Taiwan
[3] Natl Chung Hsing Univ, Inst Biochem, Taichung 402, Taiwan
[4] Natl Pingtung Univ Sci & Technol, Grad Inst Biotechnol, Pingtung 912, Taiwan
关键词
S; maltophilia; virulent phage; T4-type; unknown modified bases; major capsid protein; phylogenetic analysis;
D O I
10.1007/s00203-007-0238-5
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Stenotrophomonas maltophilia (Sm), with most of the isolates being resistant to multidrugs, is an opportunistic bacterium causing nosocomial infections. In this study, a novel virulent Sm phage, Smp14, was characterized. Electron microscopy showed that Smp14 resembled members of Myoviridae and adsorbed to poles of the host cells during infection. It lysed 37 of 87 clinical Sm isolates in spot test, displayed a latent period of ca. 20 min, and had a burst size of ca. 150. Its genome (estimated to be 160 kb by PFGE), containing m4C and two unknown modified bases other than m5C and m6A as identified by HPLC, resisted to digestion with many restriction endonucleases except MseI. These properties indicate that it is a novel Sm phage distinct from the previously reported phiSMA5 which has a genome of 250 kb digestible with various restriction enzymes. Sequencing of a 16 kb region revealed 12 ORFs encoding structural proteins sharing 15-45% identities with the homologues from T4-type phages. SDS-PAGE displayed 20 virion proteins, with the most abundant one being the 39 kDa major capsid protein (gp23), which had the N-terminal 52 amino acids removed. Phylogenetic analysis based on gp23 classified Smp14 into a novel single-membered T4-type subgroup.
引用
收藏
页码:191 / 197
页数:7
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