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      Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Inhibits RNA-Mediated Gene Silencing by Targeting Ago-2

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          Abstract

          Porcine reproductive and respiratory syndrome virus (PRRSV) infection strongly modulates the host’s immune response. The RNA silencing pathway is an intracellular innate response to viral infections. However, it is unknown whether PRRSV interacts with cellular RNA silencing to facilitate the viral infection. Here, we report for the first time the interaction between PRRSV and RNA silencing in both the porcine macrophages and African green monkey kidney cell line (MARC-145) cell line, which were derived from African green monkey kidney cells and highly permissive for PRRSV infection. Our data demonstrated that PRRSV suppressed RNA silencing induced by short-hairpin (sh) RNA, double-strand (ds) RNA and microRNA (miRNA) and downregulated the expression of argonaute protein-2 (Ago-2), which is a key protein of the RNA silencing pathway in animal cells. Further, exogenous introduction of siRNA and shRNA downregulated Dicer or Ago-2 proteins of the cellular RNA silencing apparatus in MARC-145 cells and porcine macrophages, which, in turn, increased the viral replication and titers. The viral non-structure protein 1α (nsp-1α) and nsp11 of PRRSV were identified as the suppressors for cellular RNA silencing (RSSs) to downregulate the Ago-2 protein. Our results identify that PRRSV, through its nsp proteins, suppresses the cellular RNA silencing apparatus in favor of viral infection and supports a co-evolutionary process of the virus and the cellular RNA silencing process.

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          Most cited references30

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          Mechanisms of gene silencing by double-stranded RNA.

          Double-stranded RNA (dsRNA) is an important regulator of gene expression in many eukaryotes. It triggers different types of gene silencing that are collectively referred to as RNA silencing or RNA interference. A key step in known silencing pathways is the processing of dsRNAs into short RNA duplexes of characteristic size and structure. These short dsRNAs guide RNA silencing by specific and distinct mechanisms. Many components of the RNA silencing machinery still need to be identified and characterized, but a more complete understanding of the process is imminent.
            • Record: found
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            Human Argonaute2 mediates RNA cleavage targeted by miRNAs and siRNAs.

            Argonaute proteins associate with small RNAs that guide mRNA degradation, translational repression, or a combination of both. The human Argonaute family has eight members, four of which (Ago1 through Ago4) are closely related and coexpressed in many cell types. To understand the biological function of the different Ago proteins, we set out to determine if Ago1 through Ago4 are associated with miRNAs as well as RISC activity in human cell lines. Our results suggest that miRNAs are incorporated indiscriminately of their sequence into Ago1 through Ago4 containing microRNPs (miRNPs). Purification of the FLAG/HA-epitope-tagged Ago containing complexes from different human cell lines revealed that endonuclease activity is exclusively associated with Ago2. Exogenously introduced siRNAs also associate with Ago2 for guiding target RNA cleavage. The specific role of Ago2 in guiding target RNA cleavage was confirmed independently by siRNA-based depletion of individual Ago members in combination with a sensitive positive-readout reporter assay.
              • Record: found
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              Nidovirales: a new order comprising Coronaviridae and Arteriviridae.

              D Cavanagh (1997)

                Author and article information

                Contributors
                Role: Academic Editor
                Journal
                Viruses
                Viruses
                viruses
                Viruses
                MDPI
                1999-4915
                23 October 2015
                October 2015
                : 7
                : 10
                : 5539-5552
                Affiliations
                [1 ]College of Animal Science and Veterinary Medicine, Jilin University, Changchun 130062, China; chenjing519@ 123456126.com
                [2 ]Henan Provincial Key Laboratory of Animal Immunology, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China; shixibao@ 123456aliyun.com (X.S.); nongkewangli@ 123456163.com (L.W.); luojun593@ 123456aliyun.com (J.L.); rgd999@ 123456163.com (R.D.)
                [3 ]College of Life Sciences, Henan Normal University, Xinxiang 453007, China; zhangxiaozhuan0103@ 123456126.com (X.Z.); yanghong@ 123456htu.cn (H.Y.); Ljt66882004@ 123456126.com (J.L.)
                [4 ]Department of Bioengineering, Zhengzhou University, Zhengzhou 450000, China; pingaw@ 123456126.com
                [5 ]College of Veterinary Medicine and Animal Science, Henan Agricultural University, Zhengzhou 450002, China
                Author notes
                [†]

                These authors contributed equally to this work.

                [* ]Correspondence: zhanggaiping2003@ 123456163.com (G.Z.); xingguangxu@ 123456163.com (G.X.); Tel.: +86-371-6355-0369 (G.Z.); +86-371-6575-6056 (G.X.); Fax: +86-371-6355-8998 (G.Z.)
                Article
                viruses-07-02893
                10.3390/v7102893
                4632401
                26512690
                a5cbef22-54e9-41f8-abba-44df2c14bbf9
                © 2015 by the authors; licensee MDPI, Basel, Switzerland.

                This article is an open access article distributed under the terms and conditions of the Creative Commons by Attribution (CC-BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 03 August 2015
                : 08 October 2015
                Categories
                Article

                Microbiology & Virology
                porcine reproductive and respiratory syndrome virus (prrsv),rna silencing,non-structure protein 1α (nsp1α),nsp11,ago-2,j0101

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