Membrane association of a nonconserved viral protein confers virus ability to extend its host range

被引:21
作者
Kang, Sung-Hwan [1 ]
Bak, Aurelie [1 ]
Kim, Ok-Kyung [1 ]
Folimonova, Svetlana Y. [1 ]
机构
[1] Univ Florida, Dept Plant Pathol, Gainesville, FL 32611 USA
基金
美国国家科学基金会;
关键词
Citrus tristeza virus; Virus movement; Plant virus; CITRUS-TRISTEZA-VIRUS; ENDOPLASMIC-RETICULUM; MOSAIC-VIRUS; MOVEMENT PROTEIN; RNA; CLOSTEROVIRUS; INFECTION; LOCALIZATION; EVOLUTION; SEQUENCE;
D O I
10.1016/j.virol.2015.03.047
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Citrus tristeza virus (CTV), the largest and most complex member of the family Closteroviridae, encodes a unique protein, p33, which shows no homology with other known proteins, however, plays an important role in virus pathogenesis. In this study, we examined some of the characteristics of p33. We show that p33 is a membrane-associated protein that is inserted into the membrane via a transmembrane helix formed by hydrophobic amino acid residues at the C-terminal end of the protein. Removal of this transmembrane domain (TMD) dramatically altered the intracellular localization of p33. Moreover, the TMD alone was sufficient to confer membrane localization of an unrelated protein. Finally, a CTV variant that produced a truncated p33 lacking the TMD was unable to infect sour orange, one of the selected virus hosts, which infection requires p33, suggesting that membrane association of p33 is important for the ability of CTV to extend its host range. (C) 2015 Elsevier Inc. All rights reserved.
引用
收藏
页码:208 / 217
页数:10
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