Foot-and-mouth disease virus utilizes an autophagic pathway during viral replication

被引:93
作者
O'Donnell, Vivian [1 ,2 ]
Pacheco, Juan M. [1 ]
LaRocco, Michael [1 ]
Burrage, Tom [1 ,3 ]
Jackson, William [4 ]
Rodriguez, Luis L. [1 ]
Borca, Manuel V. [1 ]
Baxt, Barry [1 ]
机构
[1] ARS, Foreign Anim Dis Res Unit, USDA, Plum Isl Anim Dis Ctr, Greenport, NY 11944 USA
[2] Univ Connecticut, Dept Pathobiol & Vet Sci, Storrs, CT 06269 USA
[3] USDA ARS, Plum Isl Anim Dis Ctr, Dept Homeland Secur, Greenport, NY 11944 USA
[4] Med Coll Wisconsin, Dept Microbiol & Mol Genet, Milwaukee, WI 53226 USA
关键词
FMDV; Picornavirus; Virus-cell interaction; Autophagy; LC3; ENDOPLASMIC-RETICULUM; CELLULAR AUTOPHAGY; PROTEINS; CELLS; PERSISTENCE; SUBVERSION; ULTRASTRUCTURE; LOCALIZATION; ENTEROVIRUS; EXPRESSION;
D O I
10.1016/j.virol.2010.10.042
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Foot-and-mouth disease virus (FMDV) is the type species of the Aphthovirus genus within the Picornaviridae family. Infection of cells with positive-strand RNA viruses results in a rearrangement of intracellular membranes into viral replication complexes. The origin of these membranes remains unknown; however induction of the cellular process of autophagy is beneficial for the replication of poliovirus, suggesting that it might be advantageous for other picornaviruses. By using confocal microscopy we showed in FMDV-infected cells co-localization of non-structural viral proteins 2B, 2C and 3A with LC3 (an autophagosome marker) and viral structural protein VP1 with Atg5 (autophagy-related protein), and LC3 with LAMP-1. Importantly, treatment of FMDV-infected cell with autophagy inducer rapamycin, increased viral yield, and inhibition of autophagosomal pathway by 3-methyladenine or small-interfering RNAs, decreased viral replication. Altogether, these studies strongly suggest that autophagy may play an important role during the replication of FMDV. Published by Elsevier Inc.
引用
收藏
页码:142 / 150
页数:9
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