Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro

Herpes simplex virus type 1 (HSV-1) infections are one of the most common diseases in human population. HSV-1 causes subclinical, mild to severe diseases, especially in immunocompromised patients. Acyclovir has been used to reduce manifestations of HSV-1 infections. The extensive use of this drug ha...

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Main Authors: Mehdi Shabani, Bahram Nasr Esfahani, Bahar Sadegh Ehdaei, Sharareh Moghim, Arezoo Mirzaei, Mohammadreza Sharifi, Leili Mouhebat
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2019-01-01
Series:Research in Pharmaceutical Sciences
Subjects:
Online Access:http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2019;volume=14;issue=2;spage=167;epage=174;aulast=Shabani
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author Mehdi Shabani
Bahram Nasr Esfahani
Bahar Sadegh Ehdaei
Sharareh Moghim
Arezoo Mirzaei
Mohammadreza Sharifi
Leili Mouhebat
author_facet Mehdi Shabani
Bahram Nasr Esfahani
Bahar Sadegh Ehdaei
Sharareh Moghim
Arezoo Mirzaei
Mohammadreza Sharifi
Leili Mouhebat
author_sort Mehdi Shabani
collection DOAJ
description Herpes simplex virus type 1 (HSV-1) infections are one of the most common diseases in human population. HSV-1 causes subclinical, mild to severe diseases, especially in immunocompromised patients. Acyclovir has been used to reduce manifestations of HSV-1 infections. The extensive use of this drug has led to the development of resistant strains. Thus, designing a novel anti-herpes drug with different mechanisms of action is urgently needed. Cellular microRNAs (miRNAs) have direct antiviral effects in addition to their regulatory functions. In this study we used a novel miRNA (hsa-miR-7704), expressed in macrophages, to inhibit HSV-1 lytic infection in HeLa cells. Synthesized hsa-miR-7704 mimics were transfected into HSV-1 infected HeLa cell. The inhibitory effects of the miRNA were evaluated by plaque assay, real time polymerase chain reaction and the viral titers were measured by the 50% tissue culture infective dose (TCID50). The viral titer and cell cytopathic effect were dramatically decreased in HeLa cells transfected with hsa-miR-7704 (50 and 100 nM), compared with HSV-1 infected cells alone or transfected with the mock miRNA control. These results suggest that hsa-miR-7704 inhibits HSV-1 replication efficiently in vitro. This may provide an alternative mechanism to prevent HSV-1 infections.
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spelling doaj.art-437296da2b9e48f2be135b17075ae8cb2022-12-21T18:51:33ZengWolters Kluwer Medknow PublicationsResearch in Pharmaceutical Sciences1735-53621735-94142019-01-0114216717410.4103/1735-5362.253364Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitroMehdi ShabaniBahram Nasr EsfahaniBahar Sadegh EhdaeiSharareh MoghimArezoo MirzaeiMohammadreza SharifiLeili MouhebatHerpes simplex virus type 1 (HSV-1) infections are one of the most common diseases in human population. HSV-1 causes subclinical, mild to severe diseases, especially in immunocompromised patients. Acyclovir has been used to reduce manifestations of HSV-1 infections. The extensive use of this drug has led to the development of resistant strains. Thus, designing a novel anti-herpes drug with different mechanisms of action is urgently needed. Cellular microRNAs (miRNAs) have direct antiviral effects in addition to their regulatory functions. In this study we used a novel miRNA (hsa-miR-7704), expressed in macrophages, to inhibit HSV-1 lytic infection in HeLa cells. Synthesized hsa-miR-7704 mimics were transfected into HSV-1 infected HeLa cell. The inhibitory effects of the miRNA were evaluated by plaque assay, real time polymerase chain reaction and the viral titers were measured by the 50% tissue culture infective dose (TCID50). The viral titer and cell cytopathic effect were dramatically decreased in HeLa cells transfected with hsa-miR-7704 (50 and 100 nM), compared with HSV-1 infected cells alone or transfected with the mock miRNA control. These results suggest that hsa-miR-7704 inhibits HSV-1 replication efficiently in vitro. This may provide an alternative mechanism to prevent HSV-1 infections.http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2019;volume=14;issue=2;spage=167;epage=174;aulast=Shabaniantiviral therapy; hsv-1; micro rna; mir-has-7704; mir-sx1.
spellingShingle Mehdi Shabani
Bahram Nasr Esfahani
Bahar Sadegh Ehdaei
Sharareh Moghim
Arezoo Mirzaei
Mohammadreza Sharifi
Leili Mouhebat
Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
Research in Pharmaceutical Sciences
antiviral therapy; hsv-1; micro rna; mir-has-7704; mir-sx1.
title Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
title_full Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
title_fullStr Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
title_full_unstemmed Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
title_short Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
title_sort inhibition of herpes simplex virus type 1 replication by novel hsa mir 7704 in vitro
topic antiviral therapy; hsv-1; micro rna; mir-has-7704; mir-sx1.
url http://www.rpsjournal.net/article.asp?issn=1735-5362;year=2019;volume=14;issue=2;spage=167;epage=174;aulast=Shabani
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