Inhibition of herpes simplex virus type 1 replication by novel hsa-miR-7704 in vitro
Autor: | Mehdi Shabani, Bahram Nasr Esfahani, Bahar Sadegh Ehdaei, Sharareh Moghim, Arezoo Mirzaei, Mohammadreza Sharifi, Leili Mouhebat |
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Jazyk: | angličtina |
Rok vydání: | 2019 |
Předmět: | |
Zdroj: | Research in Pharmaceutical Sciences, Vol 14, Iss 2, Pp 167-174 (2019) |
Druh dokumentu: | article |
ISSN: | 1735-5362 1735-9414 |
DOI: | 10.4103/1735-5362.253364 |
Popis: | 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. |
Databáze: | Directory of Open Access Journals |
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