联系我们 加入收藏
 
年期检索 高级检索
33
2025年8月14日 星期四
农业生物技术学报  2025, Vol. 33 Issue (5): 1090-1105    DOI: 10.3969/j.issn.1674-7968.2025.05.013
  研究论文与报告 本期目录 | 过刊浏览 | 高级检索 |
绿鳍马面鲀肝表达抗菌肽-2基因的鉴定、表达及抗菌机制初探
扈艺凡, 魏博崛, 张艺榕, 李长红*, 陈炯
宁波大学 海洋学院 生物化学与分子生物学实验室,宁波 315832
Identification, Expression and Preliminary Antimicrobial Mechanism of Liver-expressed Antimicrobial Peptide 2 Gene in Black Scraper (Thamnaconus modestus)
HU Yi-Fan, WEI Bo-Jue, ZHANG Yi-Rong, LI Chang-Hong*, CHEN Jiong
Laboratory of Biochemistry and Molecular Biology, School of Marine Sciences, Ningbo University, Ningbo 315832, China
全文: PDF (14040 KB)   HTML (1 KB) 
输出: BibTeX | EndNote (RIS)      
摘要 肝表达抗菌肽2 (liver-expressed antimicrobial peptide 2, LEAP-2)是一种阳离子抗菌肽,是动物先天免疫的重要组分。本研究通过转录组测序获得绿鳍马面鲀(Thamnaconus modestus) TmLEAP-2ATmLEAP-2C的cDNA序列,序列分析显示,二者分别编码103和79个氨基酸,分子量分别为11.18和9.14 kD;TmLEAP-2ATmLEAP-2C分别与大黄鱼(Larimichthys crocea)的LEAP-2ALEAP-2C同源性最高,分别为72.8%和62.5%。系统进化树分析表明,TmLEAP-2ATmLEAP-2C分别与大黄鱼LEAP-2ALEAP-2C进化相关性最高。qPCR分析表明,TmLEAP-2ATmLEAP-2C mRNA都主要在肝中表达,并且溶藻弧菌(Vibrio alginolyticus)感染诱导了二者在肝中的表达。TmLEAP-2A成熟肽(TmLEAP-2AP46)仅对创伤弧菌(V. vulnificus)有抑制活性,TmLEAP-2C成熟肽(TmLEAP-2CP39)对溶藻弧菌和创伤弧菌均有抑制活性。进一步研究发现,TmLEAP-2CP39对溶藻弧菌的基因组DNA有水解作用,并且溶藻弧菌与TmLEAP-2CP39孵育后,对碘化吡啶的摄取增强,活细胞比例大幅下降。扫描电镜(scanning electron microscopy, SEM)观察结果显示,TmLEAP-2CP39孵育后溶藻弧菌形态不完整,细胞膜表面出现皱缩,大部分菌体表面甚至有凹陷或孔洞形成;透射电镜(transmission electron microscopy, TEM)观察结果显示,TmLEAP-2CP39孵育后溶藻弧菌细胞膜不仅明显皱缩,而且大部分菌体膜质发生分离,细胞膜破裂,内容物外泄。以上结果说明,TmLEAP-2A和TmLEAP-2C与溶藻弧菌感染密切相关,但仅TmLEAP-2C在体外对溶藻弧菌有抑菌活性,且可通过破坏溶藻弧菌细胞膜的完整性和水解基因组DNA (genomic DNA, gDNA),来发挥直接的抗菌作用。研究结果不仅丰富了鱼类抗菌肽知识,也为鱼类抗菌肽类药物的研发提供了理论基础。
服务
把本文推荐给朋友
加入我的书架
加入引用管理器
E-mail Alert
RSS
作者相关文章
扈艺凡
魏博崛
张艺榕
李长红
陈炯
关键词 肝表达抗菌肽-2 (LEAP-2)绿鳍马面鲀溶藻弧菌基因表达抗菌活性    
Abstract:Liver-expressed antimicrobial peptide 2 (LEAP-2) is a cationic antimicrobial peptide that plays a crucial role in the innate immunity of animals. The cDNA sequences of TmLEAP-2A and TmLEAP-2C were identified through transcriptome sequencing in black scraper (Thamnaconus modestus) in this study. Sequence analysis indicated that TmLEAP-2A and TmLEAP-2C encoded 103 and 79 amino acids, respectively, with molecular weights of 11.18 and 9.14 kD. TmLEAP-2A and TmLEAP-2C exhibited the highest amino acid homology with LEAP-2A and LEAP-2C from the large yellow croaker (Larimichthys crocea), at 72.8% and 62.5% respectively. Phylogenetic tree analysis showed that TmLEAP-2A and TmLEAP-2C had the closest evolutionary correlation with LEAP-2A and LEAP-2C in large yellow croaker respectively. qPCR analysis showed that both TmLEAP-2A and TmLEAP-2C were predominately expressed in the liver. Further, their expression levels were significantly induced by infection with Vibrio alginolyticus in liver of black scraper. TmLEAP-2A mature peptide (TmLEAP-2AP46) only exhibited inhibitory activity against V. vulnificus, while TmLEAP-2C mature peptide (TmLEAP-2CP39) exhibited inhibitory activity against both V. alginolyticus and V. vulnificus. Further research demonstrated that TmLEAP-2CP39 exhibited a hydrolytic effect on the genome of V. alginolyticus. Following incubation with TmLEAP-2CP39, V. alginolyticus showed increased uptake of propidium iodide, indicating a significant reduction in the proportion of viable cells. Scanning electron microscopy (SEM) observations revealed that treatment with TmLEAP-2CP39 resulted in altered morphology of V. alginolyticus, characterized by surface wrinkles and the presence of depressions or holes on most bacterial cells. Additionally, transmission electron microscopy (TEM) analysis revealed that, after treatment with TmLEAP-2CP39, the cell membrane of V. alginolyticus exhibited pronounced wrinkling, significant separation from the cytoplasm, rupturing of the membrane, and notable leakage of cellular contents. Overall, TmLEAP-2A and TmLEAP-2C were found to be closely associated with V. alginolyticus infection; however, only TmLEAP-2C demonstrated antibacterial activity against V. alginolyticus in vitro. TmLEAP-2C exerted direct antibacterial effects by disrupting the integrity of the bacterial cell membrane and hydrolyzing genomic DNA (gDNA) within V. alginolyticus cells. These findings not only enhance the understanding of fish antimicrobial peptides but also provide a theoretical foundation for the research and development of fish-derived antimicrobial peptide drugs.
Key wordsLiver-expressed antimicrobial peptide 2 (LEAP-2)    Thamnaconus modestus    Vibrio alginolyticus    Gene expression    Antimicrobial activity
收稿日期: 2024-10-11     
中图分类号: S917.4
基金资助:国家自然科学基金(32173004); 浙江省自然科学基金(LY21C190003); 宁波市自然科学基金(2023J110)
通讯作者: *lichanghong0716@163.com   
引用本文:   
扈艺凡, 魏博崛, 张艺榕, 李长红, 陈炯. 绿鳍马面鲀肝表达抗菌肽-2基因的鉴定、表达及抗菌机制初探[J]. 农业生物技术学报, 2025, 33(5): 1090-1105.
HU Yi-Fan, WEI Bo-Jue, ZHANG Yi-Rong, LI Chang-Hong, CHEN Jiong. Identification, Expression and Preliminary Antimicrobial Mechanism of Liver-expressed Antimicrobial Peptide 2 Gene in Black Scraper (Thamnaconus modestus). 农业生物技术学报, 2025, 33(5): 1090-1105.
链接本文:  
https://journal05.magtech.org.cn/Jwk_ny/CN/10.3969/j.issn.1674-7968.2025.05.013     或     https://journal05.magtech.org.cn/Jwk_ny/CN/Y2025/V33/I5/1090
 
版权所有 © 2014 《农业生物技术学报》编辑部   京ICP备11035905号-3
地址:北京市海淀区圆明园西路2号中国农业大学生命科学楼1053室 邮编:100193
电话:010-62733684 传真:010-62731615 E-mail: nsjxb@cau.edu.cn