Particle Assembly and Ultrastructural Features Associated with Replication of the Lytic Archaeal Virus Sulfolobus Turreted Icosahedral Virus

被引:82
作者
Brumfield, Susan K. [1 ,2 ,3 ]
Ortmann, Alice C. [7 ,8 ]
Ruigrok, Vincent [1 ,2 ,3 ]
Suci, Peter [1 ,4 ,5 ,6 ]
Douglas, Trevor [2 ,3 ,6 ]
Young, Mark J. [1 ,2 ,3 ,6 ]
机构
[1] Montana State Univ, Dept Plant Sci & Plant Pathol, Bozeman, MT 59717 USA
[2] Montana State Univ, Thermal Biol Inst, Bozeman, MT 59717 USA
[3] Montana State Univ, Ctr Bioinspired Nanomat, Bozeman, MT 59717 USA
[4] Montana State Univ, Ctr Biofilm Engn, Bozeman, MT 59717 USA
[5] Montana State Univ, Dept Biochem & Chem, Bozeman, MT 59717 USA
[6] Montana State Univ, Dept Microbiol, Bozeman, MT 59717 USA
[7] Univ S Alabama, Mobile, AL 36688 USA
[8] Dauphin Isl Sea Lab, Dauphin Isl, AL USA
基金
美国国家科学基金会;
关键词
DOUBLE-STRANDED DNA; HALOARCULA-HISPANICA; CRENARCHAEAL VIRUSES; ELECTRON MICROSCOPY; BACTERIOPHAGE PRD1; HALOPHILIC ARCHAEA; INTERNAL-MEMBRANE; BACTERIAL-VIRUSES; HYPERSALINE LAKE; PROTEIN;
D O I
10.1128/JVI.02668-08
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Little is known about the replication cycle of archaeal viruses. We have investigated the ultrastructural changes of Sulfolobus solfataricus P2 associated with infection by Sulfolobus turreted icosahedral virus (STIV). A time course of a near synchronous STIV infection was analyzed using both scanning and transmission electron microscopy. Assembly of STIV particles, including particles lacking DNA, was observed within cells, and fully assembled STIV particles were visible by 30 h postinfection (hpi). STIV was determined to be a lytic virus, causing cell disruption beginning at 30 hpi. Prior to cell lysis, virus infection resulted in the formation of pyramid-like projections from the cell surface. These projections, which have not been documented in any other host-virus system, appeared to be caused by the protrusion of the cell membrane beyond the bordering S-layer. These structures are thought to be sites at which progeny virus particles are released from infected cells. Based on these observations of lysis, a plaque assay was developed for STIV. From these studies we propose an overall assembly model for STIV.
引用
收藏
页码:5964 / 5970
页数:7
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