Different molecular responses of Mytilus mantle to lipopolysaccharide and peptidoglycan challenges

IF 3.9 2区 农林科学 Q1 FISHERIES Fish & shellfish immunology Pub Date : 2025-03-02 DOI:10.1016/j.fsi.2025.110246
Zilin Yang , Pingling Cao , Wenhui Xiao , Fang Song , Xiaoshan Wu , Xiaolin Zhang , Jianyu He , Isabella Buttino , Xiaojun Yan , Zhi Liao
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Abstract

Mytilus live in water as sessile filter feeders, and the mantle tissue plays an important role in their immune defense. However, the overall knowledge of the immunity of this tissue remains limited. Peptidoglycan (PGN) and lipopolysaccharide (LPS) are the most representative microbe-associated molecular patterns (MAMPs) that play roles in the immune stimulation of host cells. In the present study, ultra-performance liquid chromatography tandem mass spectrometry (UPLC-MS/MS)-based metabolomic analysis was performed to understand the precise regulatory mechanism at the molecular level in the Mytilus mantle in response to PGN and LPS stress. Moreover, the antioxidant ability and free amino acid composition of the mantle, and the antimicrobial activities of mantle mucus were evaluated. Our results revealed that LPS and PGN stresses had different effects on the mantle's free amino acid composition and antioxidant ability, and the mantle mucus' antimicrobial activity. Both PGN and LPS stress-induced alterations in amino acids, phospholipids, fatty acids, nucleotides, and their derivatives in the mantle. PGN injection activated the amino acid-related metabolism, and inhibited the lipid-related metabolisms in the mantle, while LPS injection activated the amino acid-related metabolisms and inhibited the arachidonic acid metabolism in the mantle compared to that in the control group. In addition, activation of the mTOR and FoxO signaling pathways and inhibition of lipid-related metabolism were observed in PGN vs. LPS. In addition, PGN injection induced the upregulation of fosfomycin and deoxynojirimycin in the mantle compared to LPS injection. Our study highlights the different responses at the metabolomic level of the mussel mantle to different MAMPs and the potential application of metabolites that specifically respond to PGN and LPS challenges in mussels as biomarkers.
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贻贝壳对脂多糖和肽聚糖的不同分子反应
贻贝是生活在水中的滤食性动物,其被膜组织在其免疫防御中起着重要的作用。然而,对这种组织的免疫的总体认识仍然有限。肽聚糖(PGN)和脂多糖(LPS)是在宿主细胞免疫刺激中发挥作用的最具代表性的微生物相关分子模式(MAMPs)。本研究通过超高效液相色谱串联质谱(UPLC-MS/MS)代谢组学分析,了解Mytilus mantle在分子水平上对PGN和LPS胁迫的精确调控机制。此外,还对其抗氧化能力、游离氨基酸组成以及黏液的抗菌活性进行了评价。结果表明,LPS和PGN胁迫对地幔游离氨基酸组成和抗氧化能力以及地幔黏液的抗菌活性有不同的影响。PGN和LPS胁迫诱导了地幔中氨基酸、磷脂、脂肪酸、核苷酸及其衍生物的改变。与对照组相比,注射PGN激活了氨基酸相关代谢,抑制了膜内脂质相关代谢;注射LPS激活了氨基酸相关代谢,抑制了膜内花生四烯酸代谢。此外,在PGN与LPS的对比中,观察到mTOR和FoxO信号通路的激活和脂质相关代谢的抑制。此外,与LPS注射相比,PGN注射诱导地幔中磷霉素和脱氧诺吉里霉素的表达上调。我们的研究强调了贻贝在代谢组学水平上对不同MAMPs的不同反应,以及在贻贝中作为生物标志物特异性响应PGN和LPS挑战的代谢物的潜在应用。
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来源期刊
Fish & shellfish immunology
Fish & shellfish immunology 农林科学-海洋与淡水生物学
CiteScore
7.50
自引率
19.10%
发文量
750
审稿时长
68 days
期刊介绍: Fish and Shellfish Immunology rapidly publishes high-quality, peer-refereed contributions in the expanding fields of fish and shellfish immunology. It presents studies on the basic mechanisms of both the specific and non-specific defense systems, the cells, tissues, and humoral factors involved, their dependence on environmental and intrinsic factors, response to pathogens, response to vaccination, and applied studies on the development of specific vaccines for use in the aquaculture industry.
期刊最新文献
Editorial introduction: Advancing immunological insights for sustainable mediterranean aquaculture. Corrigendum to "Bacillus coagulans controls grass carp overwintering syndrome through the intestinal microbiota-metabolite-immunity network" [Fish Shellfish Immunol. 169 (2026) 111084]. Exploring the pathogenesis of Anophryoides haemophila infection: impacts on immune responses in American lobster (Homarus americanus). The Class B Scavenger Receptor 2 Act as a Proviral Factor in Largemouth Bass Ranavirus infection. Grass carp pyruvate kinase PKM acts as a key viral helper by orchestrating NS80-mediated VIB formation and multifaceted inhibition of the RLR-IFN-STAT1 antiviral cascade.
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