| Literature DB >> 27888461 |
Md Bashir Uddin1,2, Byeong-Hoon Lee1, Chamilani Nikapitiya1, Jae-Hoon Kim1, Tae-Hwan Kim1, Hyun-Cheol Lee1, Choul Goo Kim3, Jong-Soo Lee4, Chul-Joong Kim5.
Abstract
Bee venom (BV) from honey bee (Apis Melifera L.) contains at least 18 pharmacologically active components including melittin (MLT), phospholipase A2 (PLA2), and apamin etc. BV is safe for human treatments dose dependently and proven to possess different healing properties including antibacterial and antiparasitidal properties. Nevertheless, antiviral properties of BV have not well investigated. Hence, we identified the potential antiviral properties of BV and its component against a broad panel of viruses. Co-incubation of non-cytotoxic amounts of BV and MLT, the main component of BV, significantly inhibited the replication of enveloped viruses such as Influenza A virus (PR8), Vesicular Stomatitis Virus (VSV), Respiratory Syncytial Virus (RSV), and Herpes Simplex Virus (HSV). Additionally, BV and MLT also inhibited the replication of non-enveloped viruses such as Enterovirus-71 (EV-71) and Coxsackie Virus (H3). Such antiviral properties were mainly explained by virucidal mechanism. Moreover, MLT protected mice which were challenged with lethal doses of pathogenic influenza A H1N1 viruses. Therefore, these results provides the evidence that BV and MLT could be a potential source as a promising antiviral agent, especially to develop as a broad spectrum antiviral agent.Entities:
Keywords: anti-viral activity; bee venom; melittin; virucidal effect
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Year: 2016 PMID: 27888461 PMCID: PMC7091203 DOI: 10.1007/s12275-016-6376-1
Source DB: PubMed Journal: J Microbiol ISSN: 1225-8873 Impact factor: 3.422