Antibacterial and Anti-Inflammatory Effects of Novel Peptide Toxin from the Spider Pardosa astrigeraopen access
- Authors
- Shin, Min Kyoung; Hwang, In-Wook; Kim, Yunkyung; Kim, Seung Tae; Jang, Wonhee; Lee, Seungki; Bang, Woo Young; Bae, Chang-Hwan; Sung, Jung-Suk
- Issue Date
- Jul-2020
- Publisher
- MDPI
- Keywords
- Pardosa astrigera; spider venom gland; transcriptome; in silico analysis; antibacterial peptide; anti-inflammation
- Citation
- Antibiotics, v.9, no.7, pp 1 - 13
- Pages
- 13
- Indexed
- SCIE
SCOPUS
- Journal Title
- Antibiotics
- Volume
- 9
- Number
- 7
- Start Page
- 1
- End Page
- 13
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/57837
- DOI
- 10.3390/antibiotics9070422
- ISSN
- 2079-6382
2079-6382
- Abstract
- The prevalence of antibiotic-resistant bacteria has become an immediate threat to public health. Antimicrobial peptides are attracting attention as a new source of antibiotics due to their ability to prevent drug-resistances with fewer side effects. Spider venom is composed of various bioactive substances with multiple functionalities such as antimicrobial and anti-inflammatory effects. Here, RNA sequencing was conducted on the venom gland of the spiderPardosa astrigera,and a potential toxin peptide with antibacterial properties was selected via homology and in silico analysis. A novel toxin, Lycotoxin-Pa4a, inhibited both gram-negative and gram-positive bacteria by disrupting the outer and bacterial cytoplasmic membrane. Moreover, the peptide downregulated the expression of pro-inflammatory mediators while upregulating the level of anti-inflammatory cytokine by inactivating mitogen-activated protein kinase signaling in a lipopolysaccharide-stimulated murine macrophage cell line. In this research, we identified a novel peptide toxin, Lycotoxin-pa4a, with antibacterial and anti-inflammatory properties, suggesting its potential for the development of a new antibiotics, as well as offering insights into the utilization of biological resources.
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Collections - College of Life Science and Biotechnology > Department of Life Science > 1. Journal Articles

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