Inhibition of red seabream iridovirus (RSIV) replication by small interfering RNA (siRNA) in a cell culture system
Small interfering RNAs (siRNAs), mediators of a process of sequence-specific gene silencing called RNA interference, have been shown to have activity against a wide range of viruses and are considered to be potential antiviral tools. Here, we describe an antiviral activity of a siRNA that targets th...
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Published in | Antiviral research Vol. 77; no. 2; pp. 142 - 149 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.02.2008
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Abstract | Small interfering RNAs (siRNAs), mediators of a process of sequence-specific gene silencing called RNA interference, have been shown to have activity against a wide range of viruses and are considered to be potential antiviral tools. Here, we describe an antiviral activity of a siRNA that targets the major capsid protein (MCP) gene of red seabream iridovirus (RSIV), a marine fish-pathogenic virus, in a cell culture system. Inhibition of RSIV replication was demonstrated by reduced MCP expression level and reduced RSIV titer. MCP-targeted siRNA (siR-MCP) dose-dependently inhibited the expression of MCP gene in cells that either transiently expressed or stably expressed the MCP gene. At 84 and 96
h after viral infection, siR-MCP reduced the expression of MCP gene by 55.2% and 97.1%, respectively. Transfection with siR-MCP reduced the production of RSIV particles in supernatants of samples infected with RSIV, while the corresponding mismatched siR-MCP (MsiR-MCP) and nsRNA controls did not exhibit this effect. These results show that MCP-targeted siRNA can effectively and specifically inhibit the expression of the target gene and hinder RSIV replication during an
in vitro infection, providing a potential approach for the control of viral diseases in aquaculture. |
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AbstractList | Small interfering RNAs (siRNAs), mediators of a process of sequence-specific gene silencing called RNA interference, have been shown to have activity against a wide range of viruses and are considered to be potential antiviral tools. Here, we describe an antiviral activity of a siRNA that targets the major capsid protein (MCP) gene of red seabream iridovirus (RSIV), a marine fish-pathogenic virus, in a cell culture system. Inhibition of RSIV replication was demonstrated by reduced MCP expression level and reduced RSIV titer. MCP-targeted siRNA (siR-MCP) dose-dependently inhibited the expression of MCP gene in cells that either transiently expressed or stably expressed the MCP gene. At 84 and 96h after viral infection, siR-MCP reduced the expression of MCP gene by 55.2% and 97.1%, respectively. Transfection with siR-MCP reduced the production of RSIV particles in supernatants of samples infected with RSIV, while the corresponding mismatched siR-MCP (MsiR-MCP) and nsRNA controls did not exhibit this effect. These results show that MCP-targeted siRNA can effectively and specifically inhibit the expression of the target gene and hinder RSIV replication during an in vitro infection, providing a potential approach for the control of viral diseases in aquaculture. Small interfering RNAs (siRNAs), mediators of a process of sequence-specific gene silencing called RNA interference, have been shown to have activity against a wide range of viruses and are considered to be potential antiviral tools. Here, we describe an antiviral activity of a siRNA that targets the major capsid protein (MCP) gene of red seabream iridovirus (RSIV), a marine fish-pathogenic virus, in a cell culture system. Inhibition of RSIV replication was demonstrated by reduced MCP expression level and reduced RSIV titer. MCP-targeted siRNA (siR-MCP) dose-dependently inhibited the expression of MCP gene in cells that either transiently expressed or stably expressed the MCP gene. At 84 and 96 h after viral infection, siR-MCP reduced the expression of MCP gene by 55.2% and 97.1%, respectively. Transfection with siR-MCP reduced the production of RSIV particles in supernatants of samples infected with RSIV, while the corresponding mismatched siR-MCP (MsiR-MCP) and nsRNA controls did not exhibit this effect. These results show that MCP-targeted siRNA can effectively and specifically inhibit the expression of the target gene and hinder RSIV replication during an in vitro infection, providing a potential approach for the control of viral diseases in aquaculture. |
Author | Dang, Lua T. Kondo, Hidehiro Hirono, Ikuo Aoki, Takashi |
Author_xml | – sequence: 1 givenname: Lua T. surname: Dang fullname: Dang, Lua T. – sequence: 2 givenname: Hidehiro surname: Kondo fullname: Kondo, Hidehiro – sequence: 3 givenname: Ikuo surname: Hirono fullname: Hirono, Ikuo email: hirono@kaiyodai.ac.jp – sequence: 4 givenname: Takashi surname: Aoki fullname: Aoki, Takashi |
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Keywords | RSIV RNA interference (RNAi) Small interfering RNA (siRNA) MCP Red seabream iridovirus Major capsid protein Cell culture RNA interference Pagrus major siRNA In vitro Protein Virus Gene silencing Vertebrata Iridoviridae Pisces Replication Cell system Capsid Veterinary Iridovirus |
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SubjectTerms | Animals Antibiotics. Antiinfectious agents. Antiparasitic agents Antiviral agents Base Sequence Biological and medical sciences Capsid Proteins - genetics Capsid Proteins - metabolism Cell Line Cells, Cultured Iridovirus Iridovirus - genetics Major capsid protein MCP Medical sciences Pharmacology. Drug treatments Plasmids Red seabream iridovirus Reverse Transcriptase Polymerase Chain Reaction RNA Interference RNA interference (RNAi) RNA, Small Interfering - genetics RSIV Sea Bream - virology Small interfering RNA (siRNA) Transfection Virus Replication - drug effects |
Title | Inhibition of red seabream iridovirus (RSIV) replication by small interfering RNA (siRNA) in a cell culture system |
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