IHPE, University Montpellier, CNRS, Ifremer, University Perpignan Via Domitia, 34090 Montpellier, France.
Centre de Biophysique Moléculaire UPR4301 CNRS, 45071 Orléans, France.
Mar Drugs. 2022 Nov 26;20(12):745. doi: 10.3390/md20120745.
Big defensins are two-domain antimicrobial peptides (AMPs) that have highly diversified in mollusks. -BigDefs are expressed by immune cells in the oyster , and their expression is dampened during the Pacific Oyster Mortality Syndrome (POMS), which evolves toward fatal bacteremia. We evaluated whether -BigDefs contribute to the control of oyster-associated microbial communities. Two -BigDefs that are representative of molecular diversity within the peptide family, namely -BigDef1 and -BigDef5, were characterized by gene cloning and synthesized by solid-phase peptide synthesis and native chemical ligation. Synthetic peptides were tested for antibacterial activity against a collection of culturable bacteria belonging to the oyster microbiota, characterized by 16S sequencing and MALDI Biotyping. We first tested the potential of -BigDefs to control the oyster microbiota by injecting synthetic -BigDef1 into oyster tissues and analyzing microbiota dynamics over 24 h by 16S metabarcoding. -BigDef1 induced a significant shift in oyster microbiota β-diversity after 6 h and 24 h, prompting us to investigate antimicrobial activities in vitro against members of the oyster microbiota. Both -BigDef1 and -BigDef5 were active at a high salt concentration (400 mM NaCl) and showed broad spectra of activity against bacteria associated with pathologies. Antimicrobial specificity was observed for both molecules at an intra- and inter-genera level. Remarkably, antimicrobial spectra of -BigDef1 and -BigDef5 were complementary, and peptides acted synergistically. Overall, we found that primary sequence diversification of -BigDefs has generated specificity and synergy and extended the spectrum of activity of this peptide family.
大防御素是一类具有两亲性结构的抗菌肽(AMPs),在软体动物中高度多样化。大防御素由牡蛎中的免疫细胞表达,在太平洋牡蛎死亡综合征(POMS)期间其表达受到抑制,POMS 会发展为致命性菌血症。我们评估了大防御素是否有助于控制牡蛎相关微生物群落。我们通过基因克隆对两种具有代表性的大防御素家族分子多样性的大防御素(-BigDef1 和 -BigDef5)进行了特征描述,分别通过固相肽合成和天然化学连接合成。通过 16S 测序和 MALDI Biotyping 对属于牡蛎微生物群的可培养细菌进行了抗菌活性测试。我们首先通过向牡蛎组织中注射合成的 -BigDef1 来测试大防御素控制牡蛎微生物群的潜力,并通过 16S 代谢组学分析 24 小时内微生物组动态。-BigDef1 在 6 小时和 24 小时后引起牡蛎微生物组β多样性的显著变化,促使我们研究体外对牡蛎微生物群成员的抗菌活性。-BigDef1 和 -BigDef5 在高盐浓度(400 mM NaCl)下均具有活性,并表现出对与疾病相关的细菌的广谱活性。在属内和属间水平都观察到两种分子的抗菌特异性。值得注意的是,-BigDef1 和 -BigDef5 的抗菌谱具有互补性,并且肽类具有协同作用。总体而言,我们发现大防御素的一级序列多样化产生了特异性和协同性,并扩展了该肽家族的活性谱。