Acidianus Tailed Spindle Virus: a New Archaeal Large Tailed Spindle Virus Discovered by Culture-Independent Methods

被引:28
作者
Hochstein, Rebecca A. [1 ,3 ]
Amenabar, Maximiliano J. [1 ,3 ]
Munson-McGee, Jacob H. [1 ,3 ]
Boyd, Eric S. [1 ,3 ,4 ]
Young, Mark J. [2 ,3 ]
机构
[1] Montana State Univ, Dept Microbiol & Immunol, Bozeman, MT 59717 USA
[2] Montana State Univ, Dept Plant Sci & Plant Pathol, Bozeman, MT 59717 USA
[3] Montana State Univ, Thermal Biol Inst, Bozeman, MT 59717 USA
[4] Montana State Univ, NASA Astrobiol Inst, Bozeman, MT 59717 USA
基金
美国国家航空航天局; 美国国家科学基金会;
关键词
LEUCINE-RICH REPEAT; HOST INTERACTIONS; ECOLOGICAL DRIVERS; SINGLE-CELL; IDENTIFICATION; EVOLUTIONARY; DIVERSITY; SOFTWARE; GENOME; METAGENOMICS;
D O I
10.1128/JVI.03098-15
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The field of viral metagenomics has expanded our understanding of viral diversity from all three domains of life (Archaea, Bacteria, and Eukarya). Traditionally, viral metagenomic studies provide information about viral gene content but rarely provide knowledge about virion morphology and/or cellular host identity. Here we describe a new virus, Acidianus tailed spindle virus (ATSV), initially identified by bioinformatic analysis of viral metagenomic data sets from a high-temperature (80 degrees C) acidic (pH 2) hot spring located in Yellowstone National Park, followed by more detailed characterization using only environmental samples without dependency on culturing. Characterization included the identification of the large tailed spindle virion morphology, determination of the complete 70.8-kb circular double-stranded DNA (dsDNA) viral genome content, and identification of its cellular host. Annotation of the ATSV genome revealed a potential three-domain gene product containing an N-terminal leucine-rich repeat domain, followed by a likely posttranslation regulatory region consisting of high serine and threonine content, and a C-terminal ESCRT-III domain, suggesting interplay with the host ESCRT system. The host of ATSV, which is most closely related to Acidianus hospitalis, was determined by a combination of analysis of cellular clustered regularly interspaced short palindromic repeat (CRISPR)/Cas loci and dual viral and cellular fluorescence in situ hybridization (viral FISH) analysis of environmental samples and confirmed by culture-based infection studies. This work provides an expanded pathway for the discovery, isolation, and characterization of new viruses using culture-independent approaches and provides a platform for predicting and confirming virus hosts.
引用
收藏
页码:3458 / 3468
页数:11
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