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[M. Immunology-29]



             A Novel Peptide from Spider Venom, Lycotoxin-Pa4a, Exhibits


                          Antibacterial and Anti-inflammatory Activity




                 Min Kyoung Shin¹, In-Wook Hwang¹, Yunkyung Kim¹, Seung-Tae Kim², Jung-Suk Sung¹˙*

         ¹Department of Life Science, Dongguk University-Seoul, Goyang 10326, Republic of Korea, ²Life and Environment

                             Research Institute, Konkuk University, Seoul 05029, Republic of Korea




        Since the threat of the drug-resistant bacteria is increasing, antimicrobial peptides (AMPs) are drawing attention as
        a new source of antibiotics. Animal venom comprises diverse components with bioactivity, including antibacterial

        and  neuromodulatory  effects.  In  search  of  the  novel  peptide  with  functionality,  the  transcriptome  library  was

        constructed through RNA sequencing of the venom gland of the spider Pardosa astrigera. A sequence that showed
        homology with known-peptides derived from spiders was selected via in silico analysis, and renamed as Lycotoxin-
        Pa4a. The peptide inhibited both gram-positive and gram-negative bacteria by disrupting the outer and cytoplasmic

        membrane of the bacteria. Also, Lycotoxin-Pa4a exhibited anti-inflammatory activity via modulating the expression
        of inflammatory mediators through the inactivation of mitogen-activated protein kinase signaling. In this study, a

        novel peptide Lycotixin-Pa4a was identified as AMP with anti-inflammatory activity and suggested the potential
        development  of  new  antibiotics  and  understanding  of  utilizing  venomous  biological  resources.  [This  work  was

        supported  by  a  grant  from  the  National  Institute  of  Biological  Resources  (NIBR),  funded  by  the  Ministry  of
        Environment (MOE) of the Republic of Korea (NIBR202009201)]
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