Anti-inflammatory Activity of Antimicrobial Peptide Papiliocin 3 Derived from the Swallowtail Butterfly, Papilio xuthus

Yong pyo Shin, Joon-Ha Lee, In-woo Kim, M. Seo, Mi-Ae Kim, H. Lee, Minhee Baek, Seong Hyun Kim, Jae‐Sam Hwang
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Abstract

The development of novel peptide antibiotics with potent antimicrobial activity and anti-inflammatory activity is urgently needed. In a previous work, we performed an in-silico analysis of the Papilio xuthus transcriptome to identify putative antimicrobial peptides and identified several candidates. In this study, we investigated the antibacterial and anti-inflammatory activities of papiliocin 3, which was selected bioinformatically based on its physicochemical properties against bacteria and mouse macrophage Raw264.7 cells. Papiliocin 3 showed antibacterial activities against E. coli and S. aureus without inducing hemolysis and decreased the nitric oxide production of the lipopolysaccharide-induced Raw264.7 cells. Moreover, ELISA and Western blot analysis revealed that papiliocin 3 reduced the expression levels of pro-inflammatory enzymes, such as inducible nitric oxide synthase (iNOS), cyclooxygenase-2 (COX-2), and prostaglandin E2 (PGE2). In addition, we examined whether papiliocin 3 could inhibit the expression of pro-inflammatory cytokines (interleukin-6 and interleukin-1β) in LPSinduced Raw264.7 cells. We found that papiliocin 3 markedly reduced the expression level of cytokines through the regulation of mitogen-activated protein kinases (MAPK) and nuclear factor kappa B (NF-κB) signaling. We also confirmed that papiliocin 3 binds to bacterial cell membranes via a specific interaction with lipopolysaccharides. Collectively, these findings suggest that papiliocin 3 could be a promising molecule for development as a novel peptide antibiotic.
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从燕尾蝶中提取的抗菌肽Papiliocin 3的抗炎活性
迫切需要开发具有有效抗菌和抗炎活性的新型多肽抗生素。在之前的工作中,我们对凤蝶(Papilio xuthus)转录组进行了计算机分析,以鉴定推定的抗菌肽,并鉴定了几个候选肽。在本研究中,我们研究了papiliocin 3的抗菌和抗炎活性,根据其对细菌和小鼠巨噬细胞Raw264.7细胞的理化性质,生物信息学上选择了papiliocin 3。Papiliocin 3在不诱导溶血的情况下对大肠杆菌和金黄色葡萄球菌具有抗菌活性,并能降低脂多糖诱导的Raw264.7细胞一氧化氮的产生。此外,ELISA和Western blot分析显示,papiliocin 3降低了促炎酶的表达水平,如诱导型一氧化氮合酶(iNOS)、环氧合酶-2 (COX-2)和前列腺素E2 (PGE2)。此外,我们还检测了papiliocin 3是否能抑制lp诱导的Raw264.7细胞中促炎细胞因子(白细胞介素-6和白细胞介素-1β)的表达。我们发现,papiliocin 3通过调控丝裂原活化蛋白激酶(MAPK)和核因子κB (NF-κB)信号传导,显著降低细胞因子的表达水平。我们还证实,乳突蛋白3通过与脂多糖的特异性相互作用结合到细菌细胞膜上。总的来说,这些发现表明,papiliocin 3可能是一种有前景的新型肽抗生素分子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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