IRTA, Centro de San Carlos de la Rápita, San Carlos de la Rápita, 43540 Tarragona, Spain.
Scottish Fish Immunology Research Centre, University of Aberdeen, Zoology Building, Tillydrone Avenue, Aberdeen AB24 2TZ, Scotland, UK.
Fish Shellfish Immunol. 2017 Oct;69:200-210. doi: 10.1016/j.fsi.2017.08.026. Epub 2017 Aug 24.
Antimicrobial peptides (AMPs), components of innate immunity, play an important role in protecting fish. In this study we report the molecular cloning of full open reading frames and characterization of expression of three AMP genes (β-defensin (defb), hepcidin (hep2), piscidin (pisc) in meagre (Argyrosomus regius). A phylogenetic analysis of the expressed sequences obtained shows the defensin isoform forms a clade with the other members of the beta class of this family, hepcidin corresponds to hepcidin 2, and piscidin corresponds to class I of its respective family. Gene expression profiles of AMPs was investigated, by means of quantification of mRNA in nine development stages, from 8 days post-hatching (dph) to accomplishment of juvenile form (120 dph). During development it was demonstrated defb, hep2, pisc were expressed in all stages of larval development and in juvenile tissues (kidney, spleen gut and gill). Moreover, expression patterns suggest the expression levels of theses AMPs are influenced by live prey (rotifer, Artemia) and first intake of commercial diet. Induction experiments in vivo (24 h) and in vitro (4, 12, 24 h) with PAMPs (LPS, poly (I:C), β-glucan) revealed significant changes in gene expression of the three AMP genes, in kidney, spleen, gut and gill. However, expression profiles differed in magnitude and time course response. defb expression shows a similar trend in vivo and in vitro in kidney at 24 h after LPS and β-glucan stimulation. The hep2 expression levels were up-regulated upon β-glucan challenge in vivo, more in gut and gills than kidney, while in vitro hep2 expression was up-regulated in kidney cells by LPS, poly (I:C), β-glucan (4 h). pisc expression was up-regulated in kidney cells, splenocytes by β-glucan, but in gill cells by poly (I:C) and β-glucan in vivo. However, pisc expression was upregulated in kidney cells by β-glucan and gill cells by LPS at 4 post-stimulation in vitro. These data suggest that AMPs play an important role in defense against pathogens, with each AMP having differing efficacies against specific types of microorganisms, although follow-up studies focusing on the biological activities in fish are needed.
抗菌肽 (AMPs) 作为先天免疫的组成部分,在保护鱼类方面发挥着重要作用。在本研究中,我们报告了三个 AMP 基因(β-防御素 (defb)、hepcidin (hep2)、piscidin (pisc))的全长开放阅读框的分子克隆和表达特征,在牙鲆(Argyrosomus regius)中。获得的表达序列的系统发育分析表明,防御素同工型与该家族β类的其他成员形成一个分支,hepcidin 对应于 hepcidin 2,piscidin 对应于其各自家族的 I 类。通过在 8 天孵化后(dph)至完成幼体形式(120 dph)的 9 个发育阶段的 mRNA 定量,研究了 AMPs 的基因表达谱。在幼虫发育的所有阶段和幼体组织(肾脏、脾脏、肠道和鳃)中均检测到 defb、hep2、pisc 的表达。此外,表达模式表明这些 AMPs 的表达水平受活饵料(轮虫、卤虫)和首次摄入商业饲料的影响。体内(24 小时)和体外(4、12、24 小时)用 PAMP(LPS、聚(I:C)、β-葡聚糖)进行的诱导实验表明,三种 AMP 基因在肾脏、脾脏、肠道和鳃中的基因表达发生了显著变化。然而,表达谱在幅度和时间过程反应上存在差异。在 LPS 和 β-葡聚糖刺激后 24 小时,defb 在体内和体外的肾脏中的表达趋势相似。在体内,β-葡聚糖刺激后,hep2 的表达水平上调,在肠道和鳃中比肾脏中更为明显,而在体外,LPS、聚(I:C)和β-葡聚糖在肾脏细胞中上调 hep2 表达(4 小时)。pisc 在 β-葡聚糖的刺激下,在肾脏细胞和脾细胞中表达上调,但在体内的鳃细胞中则由聚(I:C)和β-葡聚糖上调。然而,在体外,β-葡聚糖刺激后 4 小时,pisc 在肾脏细胞和鳃细胞中上调。这些数据表明,AMP 在抵御病原体方面发挥着重要作用,每种 AMP 对特定类型的微生物都有不同的功效,尽管需要进一步研究聚焦于鱼类的生物学活性。