PMID- 37275897 OWN - NLM STAT- MEDLINE DCOM- 20230607 LR - 20230607 IS - 1664-3224 (Electronic) IS - 1664-3224 (Linking) VI - 14 DP - 2023 TI - A novel antimicrobial peptide screened by a Bacillus subtilis expression system, derived from Larimichthys crocea Ferritin H, exerting bactericidal and parasiticidal activities. PG - 1168517 LID - 10.3389/fimmu.2023.1168517 [doi] LID - 1168517 AB - Antimicrobial peptides (AMPs) may be the most promising substitute for antibiotics due to their effective antimicrobial activities and multiple function mechanisms against pathogenic microorganisms. In this study, a novel AMP containing 51 amino acids, named Lc1687, was screened from the large yellow croaker (Larimichthys crocea) via a B. subtilis system. Bioinformatics and circular dichroism (CD) analyses showed that Lc1687 is a novel anionic amphiphilic alpha-helical peptide, which was derived from the C-terminal of a Ferritin heavy subunit. The recombinant Lc1687 (named rLc1687) purified from Escherichia coli exhibited strong activities against Gram-positive (Gram+) bacterium Staphylococcus aureus, Gram-negative (Gram-) bacteria Vibrio vulnificus, V. parahaemolyticus, and Scuticociliatida. Scanning electron microscope (SEM) and transmission electron microscopy (TEM) revealed the possible function mechanisms of this peptide, which is to target and disrupt the bacterial cell membranes, including pore-forming, loss of fimbriae, and cytoplasm overflow, whereas gel retardation assay revealed that peptide Lc1687 cannot bind bacterial DNA. The peptide stability analysis showed that rLc1687 acts as a stable antimicrobial agent against Gram+ and Gram- bacteria at temperatures ranging from 25 to 100 degrees C, pH 3-12, and UV radiation time ranging from 15 to 60 min. A hemolytic activity assay confirmed that this peptide may serve as a potential source for clinical medicine development. Taken together, Lc1687 is a novel AMP as it is a firstly confirmed Ferritin fragment with antimicrobial activity. It is also a promising agent for the development of peptide-based antibacterial and anti-parasitic therapy. CI - Copyright (c) 2023 Chen, Lin, Liu, Tang, Wang and Zhang. FAU - Chen, Meiling AU - Chen M AD - Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. FAU - Lin, Nengfeng AU - Lin N AD - Institute of Biotechnology, Fujian Academy of Agricultural Sciences, Fuzhou, China. FAU - Liu, Xiande AU - Liu X AD - Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. FAU - Tang, Xin AU - Tang X AD - Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. FAU - Wang, Zhiyong AU - Wang Z AD - Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. FAU - Zhang, Dongling AU - Zhang D AD - Key Laboratory of Healthy Mariculture for the East China Sea, Ministry of Agriculture and Rural Affairs, Jimei University, Xiamen, China. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20230518 PL - Switzerland TA - Front Immunol JT - Frontiers in immunology JID - 101560960 RN - 0 (Antimicrobial Peptides) RN - 0 (Anti-Bacterial Agents) RN - 0 (Anti-Infective Agents) RN - 0 (Peptides) SB - IM MH - Animals MH - Bacillus subtilis MH - Antimicrobial Peptides MH - Anti-Bacterial Agents/chemistry MH - *Anti-Infective Agents/pharmacology/metabolism MH - Peptides/metabolism MH - *Perciformes/genetics PMC - PMC10232870 OTO - NOTNLM OT - Bacillus subtilis OT - Ferritin heavy subunit OT - Larimichthys crocea. OT - antibacterial OT - antimicrobial peptide OT - antiparasite COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2023/06/05 19:10 MHDA- 2023/06/07 06:42 PMCR- 2023/01/01 CRDT- 2023/06/05 12:23 PHST- 2023/02/17 00:00 [received] PHST- 2023/05/04 00:00 [accepted] PHST- 2023/06/07 06:42 [medline] PHST- 2023/06/05 19:10 [pubmed] PHST- 2023/06/05 12:23 [entrez] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fimmu.2023.1168517 [doi] PST - epublish SO - Front Immunol. 2023 May 18;14:1168517. doi: 10.3389/fimmu.2023.1168517. eCollection 2023.