The interaction of nonstructural protein 9 with retinoblastoma protein benefits the replication of genotype 2 porcine reproductive and respiratory syndrome virus in vitro

被引:32
作者
Dong, Jianguo
Zhang, Ning
Ge, Xinna
Zhou, Lei
Guo, Xin
Yang, Hanchun
机构
[1] China Agr Univ, Coll Vet Med, Minist Agr, Key Lab Anim Epidemiol & Zoonosis, Beijing 100193, Peoples R China
[2] China Agr Univ, State Key Lab Agrobiotechnol, Beijing 100193, Peoples R China
基金
中国国家自然科学基金;
关键词
Porcine reproductive and respiratory syndrome virus (PRRSV); Genotype; 2; Nonstructural protein 9 (Nsp9); Retinoblastoma protein (pRb); Interaction; Replication; ADENOVIRUS E1A PROTEINS; TUMOR-SUPPRESSOR; MUTATIONAL ANALYSIS; ECONOMIC-IMPACT; BINDING; RB; DEGRADATION; RNA; COMPLEX; 1-BETA;
D O I
10.1016/j.virol.2014.07.036
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The nonstructural protein 9 (Nsp9) of porcine reproductive and respiratory syndrome virus (PRRSV) is a RNA-dependent RNA polymerase (RdRp) that plays a vital role in viral replication. This study first demonstrated that the Nsp9 of genotype 2 PRRSV interacted with cellular retinoblastoma protein (pRb), and Nsp9 co-localized with pRb in the cytoplasm of PRRSV-infected MARC-145 cells and pulmonary alveolar macrophages (PAMs). Next, the overexpression of truncated pRb was shown to inhibit the PRRSV replication and silencing the pRb gene could facilitate the PRRSV replication in MARC-145 cells. Finally, the pRb level was confirmed to be down-regulated in PRRSV-infected MARC-145 cells, and Nsp9 was shown to promote the pRb degradation by proteasome pathway. These findings indicate that the interaction of Nsp 9 with pRb benefits the replication of genotype 2 PRRSV in vitro, helping to understand the roles of Nsp9 in the replication and pathogenesis of PRRSV. (C) 2014 Elsevier Inc. All rights reserved.
引用
收藏
页码:432 / 440
页数:9
相关论文
共 59 条
[1]   HIV/Simian Immunodeficiency Virus (SIV) Accessory Virulence Factor Vpx Loads the Host Cell Restriction Factor SAMHD1 onto the E3 Ubiquitin Ligase Complex CRL4DCAF1 [J].
Ahn, Jinwoo ;
Hao, Caili ;
Yan, Junpeng ;
Delucia, Maria ;
Mehrens, Jennifer ;
Wang, Chuanping ;
Gronenborn, Angela M. ;
Skowronski, Jacek .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2012, 287 (15) :12550-12558
[2]   Cellular Poly(C) Binding Proteins 1 and 2 Interact with Porcine Reproductive and Respiratory Syndrome Virus Nonstructural Protein 1β and Support Viral Replication [J].
Beura, Lalit K. ;
Dinh, Phat X. ;
Osorio, Fernando A. ;
Pattnaik, Asit K. .
JOURNAL OF VIROLOGY, 2011, 85 (24) :12939-12949
[3]   Porcine Reproductive and Respiratory Syndrome Virus Nonstructural Protein 1β Modulates Host Innate Immune Response by Antagonizing IRF3 Activation [J].
Beura, Lalit K. ;
Sarkar, Saumendra N. ;
Kwon, Byungjoon ;
Subramaniam, Sakthivel ;
Jones, Clinton ;
Pattnaik, Asit K. ;
Osorio, Fernando A. .
JOURNAL OF VIROLOGY, 2010, 84 (03) :1574-1584
[4]   The Coronavirus Endoribonuclease Nsp15 Interacts with Retinoblastoma Tumor Suppressor Protein [J].
Bhardwaj, Kanchan ;
Liu, Pinghua ;
Leibowitz, Julian L. ;
Kao, C. Cheng .
JOURNAL OF VIROLOGY, 2012, 86 (08) :4294-4304
[5]  
Boyer SN, 1996, CANCER RES, V56, P4620
[6]   Retinoblastoma protein directly interacts with and activates the transcription factor NF-IL6 [J].
Chen, PL ;
Riley, DJ ;
ChenKiang, S ;
Lee, WH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :465-469
[7]   THE UBIQUITIN-PROTEASOME PROTEOLYTIC PATHWAY [J].
CIECHANOVER, A .
CELL, 1994, 79 (01) :13-21
[8]   MOLECULAR CHARACTERIZATION OF PORCINE REPRODUCTIVE AND RESPIRATORY SYNDROME VIRUS, A MEMBER OF THE ARTERIVIRUS GROUP [J].
CONZELMANN, KK ;
VISSER, N ;
VANWOENSEL, P ;
THIEL, HJ .
VIROLOGY, 1993, 193 (01) :329-339
[9]   FUNCTIONAL IMPORTANCE OF COMPLEX-FORMATION BETWEEN THE RETINOBLASTOMA TUMOR-SUPPRESSOR FAMILY AND ADENOVIRUS E1A PROTEINS AS DETERMINED BY MUTATIONAL ANALYSIS OF E1A CONSERVED REGION-2 [J].
CORBEIL, HB ;
BRANTON, PE .
JOURNAL OF VIROLOGY, 1994, 68 (10) :6697-6709
[10]   Role of the LXCXE binding site in Rb function [J].
Dahiya, A ;
Gavin, MR ;
Luo, RX ;
Dean, DC .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (18) :6799-6805