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文蛤外套膜粘液菌群分析及其在弧菌胁迫下的代谢响应研究

王梦甜 付璐璐 姚韩韩 董迎辉

王梦甜,付璐璐,姚韩韩,等. 文蛤外套膜粘液菌群分析及其在弧菌胁迫下的代谢响应研究[J]. 海洋学报,2026,48(x):1–14
引用本文: 王梦甜,付璐璐,姚韩韩,等. 文蛤外套膜粘液菌群分析及其在弧菌胁迫下的代谢响应研究[J]. 海洋学报,2026,48(x):1–14
Wang Mengtian,Fu Lulu,Yao Hanhan, et al. Mantle-Mucus Microbial Communities and Metabolic Responses to Vibrio Stress in the hard clam Meretrix meretrix[J]. Haiyang Xuebao,2026, 48(x):1–14
Citation: Wang Mengtian,Fu Lulu,Yao Hanhan, et al. Mantle-Mucus Microbial Communities and Metabolic Responses to Vibrio Stress in the hard clam Meretrix meretrix[J]. Haiyang Xuebao,2026, 48(x):1–14

文蛤外套膜粘液菌群分析及其在弧菌胁迫下的代谢响应研究

基金项目: 国家科技资源共享服务平台项目课题“国家海洋水产种质资源库-浙江万里学院”;国家现代贝类产业技术体系项目(CARS-49)。
详细信息
    作者简介:

    王梦甜(2001—),女,浙江省金华市人,主要从事贝类分子遗传学研究。E-mail:2664397368@qq.com

    通讯作者:

    姚韩韩(1984—),女,正高级实验师,主要从事贝类分子遗传和繁殖学研究。E-mail:yaohanhan1020@126.com

    董迎辉(1980—),男,教授,主要从事贝类分子育种学研究。E-mail:dongyinghui118@126.com

Mantle-Mucus Microbial Communities and Metabolic Responses to Vibrio Stress in the hard clam Meretrix meretrix

  • 摘要: 文蛤外套膜组织及其粘液在防御病原体中起着重要作用,然而它们自身固有菌群组成和功能与宿主免疫之间的潜在联系尚不清晰。本研究采用16S rRNA基因高通量测序技术,比较分析健康文蛤外套膜组织(M组)与外套膜粘液(N组)的菌群组成及潜在功能,利用非靶向代谢组学(UHPLC-Q-TOF/MS)分析弧菌胁迫下粘液代谢物变化,并通过斯皮尔曼相关性分析联合菌群与代谢物数据,初步探索菌群与宿主免疫的潜在关联。结果显示,外套膜和粘液的菌群存在显著生态位分化:外套膜的菌群丰富度更高,以螺旋体门(Spirochaetota)为绝对优势菌;粘液的菌群均匀度更高,以变形菌门(Proteobacteria)和拟杆菌门(Bacteroidota)为主,并显著富集了弧菌属(Vibrio)、黏着杆菌属(Tenacibaculum)与黄杆菌属(Flavobacterium)等具降解多糖或潜在致病能力的类群。功能预测显示,粘液菌群在半胱氨酸/甲硫氨酸代谢、氧化磷酸化等免疫与能量通路中更为活跃。弧菌胁迫下代谢组结果表明,粘液中存在琥珀酸、丙酸、苯丙氨酸等多种免疫相关代谢物;菌群与代谢物相关性分析揭示了固有微生物与宿主代谢物的紧密联系,如海单胞菌属(Marinomonas)与尿嘧啶强正相关,黄杆菌属与硝酸盐强负相关。综合表明,外套膜-粘液作为一个动态界面微环境,其特定菌群结构可能通过与宿主代谢互作,为机体应对病原体入侵提供了免疫准备。
  • 图  1  文蛤外套膜(M)和粘液(N)菌群的聚类及β多样性分析

    A. 所有样品的稀释曲线;B. 所有样品的Shannon-Wiener曲线;C. 所有样品的等级-丰度曲线;D. 所有样本的物种积累曲线;E. PCoA分析; F. NMDS分析

    Fig.  1  Clustering and β diversity analysis of the mantle (M) and mucus (N) microbiota in M. meretrix

    A. Rarefaction curves of all samples; B. Shannon-Wiener curves of all samples; C. Rank-abundance curves of all samples; D. Species accumulation curves of all samples; E. PCoA analysis; F. NMDS analysis

    图  2  文蛤外套膜(M)和粘液(N)细菌群落的α-多样性指数

    Fig.  2  The α -diversity index of the bacterial communities in the mantle (M) and mucilage (N) in M. meretrix

    图  3  文蛤外套膜(M)和粘液(N)菌群在各分类水平的平均相对丰度分布情况

    A. 门水平上分类组成;B. 科水平上分类组成;C. 属水平上分类组成

    Fig.  3  Average relative abundance distribution of the microbial communities in the mantle(M) and mucus(N) at different taxonomic levels in M. meretrix

    A.Taxonomic composition at the phylum level; B. Taxonomic composition at the family level; C. Taxonomic composition at the genus level

    图  4  文蛤外套膜和粘液菌群在属水平上的组间方差分析柱状图

    “**”表示差异极显著 (P<0.01)

    Fig.  4  Bar chart of intergroup analysis of variance (ANOVA) of the microbiota in the mantle and mucus of M. meretrix at the genus level

    “**” indicates the significant difference in the level of P<0.01

    图  5  文蛤外套膜和粘液菌群LEfSe分析结果

    A.LDA值分布直方图; B. 进化分枝图

    Fig.  5  LEfSe analysis results of the mantle and mucus bacterial communities of M. meretrix

    A. Cladogram; B. Histogram of LDA value distribution.

    图  6  文蛤外套膜和粘液菌群的KEGG代谢途径分析

    A. 二级功能水平;B. 三级功能水平

    Fig.  6  KEGG metabolic pathway analysis of the mantle and mucus microbiota in M. meretrix.

    A. Secondary functional level; B. Tertiary functional level

    图  7  文蛤弧菌胁迫后外套膜组织切片

    A,B. 外套膜区域Masson染色;C,D. 外套膜外褶区域AB-PAS染色。图A、C为对照组,图B、D为副溶血弧菌感染组。CFS:胶原纤维结构,CM:肌纤维和胞质,VS:液态结构,MV:微绒毛,AM:酸性黏液细胞;比例尺为100 μm

    Fig.  7  Histological sections of mantle tissues after Vibrio infection in M. meretrix.

    A, B. Masson's trichrome staining of the mantle region; C, D. Alcian blue-periodic acid-Schiff (AB-PAS) staining of the outer fold region of the mantle. A and C were the control groups, and B and D were the Vibrio infected groups. CFS: collagen fiber structure, CM: cytoplasmic matrix and muscle fibers, VS: liquid (-phase) structure, MV: microvilli, AM: acidic mucus; Scale bar = 100 μm.

    图  8  基于UHPLCQ-TOF/MS的12份粘液样本和3份QC样本分析

    A. 基于正离子模式的主成分分析图;B. 基于正离子模式的样本相关性热图;C. 基于正离子模式的偏最小二乘法判别分析的评分图;D. 基于负离子模式的主成分分析图;E. 基于负离子模式的样本相关性热图;F. 于负离子模式的偏最小二乘法判别分析的评分图

    Fig.  8  12 mucus and 3 quality control (QC) sample analysis based on UHPLC-Q-TOF/MS

    A. Principal component analysis (PCA) score plot in positive ion mode; B. Sample correlation heatmap in positive ion mode; C. Partial least squares-discriminant analysis (PLS-DA) score plot in positive ion mode; D. PCA score plot in negative ion mode; E. Sample correlation heatmap in negative ion mode; F. PLS-DA score plot in negative ion mode

    图  9  基于正、负离子模式Top20代谢物的聚类热图

    C1-C6为对照组;E1-E6为实验组

    Fig.  9  Clustered heatmap of the Top 20 metabolites.

    C1-C6 are the control group;E1-E6 are the experimental group

    图  10  正、负离子模式下差异代谢物的KEGG富集气泡图(A)和MetPA拓扑分析(B)

    Fig.  10  KEGG enrichment bubble chart (A) and MetPA topological analysis (B) of differential metabolites in positive and negative ion modes

    图  11  文蛤外套膜粘液优势菌属与代谢产物的相关性热图

    “*”表示差异显著 (P<0.05),“**”表示差异极显著 (P<0.01),“***”表示差异极显著 (P<0.001)

    Fig.  11  Correlation heatmap between the dominant bacterial genera and metabolites in the mucus of M. meretrix.

    “*” indicates the significant difference in the level of P<0.05, “**” indicates the significant difference in the level of P<0.01, and “***” indicates the significant difference in the level of P<0.001

  • [1] 王如才, 王昭萍, 张建中. 海水贝类养殖学[M]. 青岛: 中国海洋大学出版社, 2008. (查阅网上资料, 未找到对应的标黄作者信息, 请确认)

    Wang Rucai, Wang Zhaoping, Zhang Jianzhong. Aquaculture of Marine Shellfish[M]. Beijing: Ocean University of China Press, 2008. (查阅网上资料, 未找到对应的英文翻译, 请确认)
    [2] Cook D W, Oleary P, Hunsucker J C, et al. Vibrio vulnificus and Vibrio parahaemolyticus in U. S. retail shell oysters: a national survey from June 1998 to July 1999[J]. Journal of Food Protection, 2002, 65(1): 79−87. doi: 10.4315/0362-028X-65.1.79
    [3] Wu C J, Wang Hang, Chan Yilin, et al. Passive immune-protection of small abalone against Vibrio alginolyticus infection by anti-Vibrio IgY-encapsulated feed[J]. Fish & Shellfish Immunology, 2011, 30(4/5): 1042−1048. doi: 10.1016/j.fsi.2011.01.026
    [4] 谢超伊, 宋宏策, 董美云, 等. 长牡蛎外套膜组织着色区和无色区的微生物多样性比较分析[J]. 海洋通报, 2024, 43(2): 188−197.

    Xie Chaoyi, Song Hongce, Dong Meiyun, et al. Comparative analysis of microbial diversity between coloured and colorless areas of Crassostrea gigas mantle[J]. Marine Science Bulletin, 2024, 43(2): 188−197.
    [5] Venier P, Varotto L, Rosani U, et al. Insights into the innate immunity of the Mediterranean mussel Mytilus galloprovincialis[J]. BMC Genomics, 2011, 12(1): 69. doi: 10.1186/1471-2164-12-69
    [6] Beuerlein K, Löhr S, Westermann B, et al. Components of the cellular defense and detoxification system of the common cuttlefish Sepia officinalis (Mollusca, Cephalopoda)[J]. Tissue and Cell, 2002, 34(6): 390−396. doi: 10.1016/S0040816602000708
    [7] 何治江, 贾梦雪, 王锦乙, 等. 厚壳贻贝不同组织中的微生物群落结构[J]. 水产学报, 2022, 46(12): 2421−2431.

    He Zhijiang, Jia Mengxue, Wang Jinyi, et al. Differential distribution of indigenous microbiome in tissues of Mytilus coruscus[J]. Journal of Fisheries of China, 2022, 46(12): 2421−2431.
    [8] Kumar M R, Krishnan K A, Vimexen V. Effect of trace metal contamination in sediments on the bioaccumulation of bivalve Meretrix meretrix[J]. Marine Pollution Bulletin, 2022, 176: 113422. doi: 10.1016/j.marpolbul.2022.113422
    [9] Wang Xiaotian, Zhou Shangjie, Dong Jianhao, et al. The impact of bisphenol A on gill health: a focus on mitochondrial dysfunction induced disorders of energy metabolism and apoptosis in Meretrix petechialis[J]. Aquatic Toxicology, 2025, 279: 107259. doi: 10.1016/j.aquatox.2025.107259
    [10] Zhang Shujing, Jiao Shuang, Liu Dongweu, et al. Characterization of the lipidomic profile of clam Meretrix petechialis in response to Vibrio parahaemolyticus infection[J]. Fish & Shellfish Immunology, 2023, 134: 108602. doi: 10.1016/j.fsi.2023.108602
    [11] Su Rina, Fang Jun, Wang Hongxia, et al. Lipid metabolism changes in clam Meretrix petechialis in response to Vibrio infection and the identification of Vibrio-resistance markers[J]. Aquaculture, 2021, 539: 736611. doi: 10.1016/j.aquaculture.2021.736611
    [12] Dong Li, Wang Hongxia, Bo Haitian, et al. Probiotic potential of gill-symbiotic Endozoicomonas sp. in enhancing vibrio resistance in the clam Meretrix petechialis: a novel approach to sustainable aquaculture[J]. Aquaculture, 2025, 598: 742041. doi: 10.1016/j.aquaculture.2024.742041
    [13] 岳欣. 文蛤弧菌病的病原分析、免疫应答及抗性选育研究[D]. 青岛: 中国科学院研究生院(海洋研究所), 2011.

    Yue Xin. Vibrio disease, anti-vibrio immunity and vibrio-resistance selective breeding of clam Meretrix meretrix[D]. Qingdao: Institute of Oceanology, Chinese Academy of Sciences, 2011.
    [14] Yue Xin, Zhang Shujing, Wang Hongxia, et al. The mud-dwelling clam Meretrix petechialis secretes endogenously synthesized erythromycin[J]. Proceedings of the National Academy of Sciences of the United States of America, 2022, 119(49): e2214150119.
    [15] Lowrey L, Woodhams D C, Tacchi L, et al. Topographical mapping of the rainbow trout (Oncorhynchus mykiss) microbiome reveals a diverse bacterial community with antifungal properties in the skin[J]. Applied and Environmental Microbiology, 2015, 81(19): 6915−6925. doi: 10.1128/AEM.01826-15
    [16] Liu Wenwen, Mo Fengfeng, Jiang Guixian, et al. Stress-induced mucus secretion and its composition by a combination of proteomics and metabolomics of the jellyfish Aurelia coerulea[J]. Marine Drugs, 2018, 16(9): 341. doi: 10.3390/md16090341
    [17] Sinha A K, Laursen M F, Licht T R. Regulation of microbial gene expression: the key to understanding our gut microbiome[J]. Trends in Microbiology, 2025, 33(4): 397−407. doi: 10.1016/j.tim.2024.07.005
    [18] Leng Weijun, Wu Xiaoyun, Shi Tong, et al. Untargeted metabolomics on skin mucus extract of Channa argus against Staphylococcus aureus: antimicrobial activity and mechanism[J]. Foods, 2021, 10(12): 2995. doi: 10.3390/foods10122995
    [19] Ekman D R, Skelton D M, Davis J M, et al. Metabolite profiling of fish skin mucus: a novel approach for minimally-invasive environmental exposure monitoring and surveillance[J]. Environmental Science & Technology, 2015, 49(5): 3091−3100. doi: 10.1021/es505054f
    [20] Ivanova L, Rangel-Huerta O D, Tartor H, et al. Fish skin and gill mucus: a source of metabolites for non-invasive health monitoring and research[J]. Metabolites, 2022, 12(1): 28. doi: 10.3390/metabo12010028
    [21] Edgar R C. UPARSE: highly accurate OTU sequences from microbial amplicon reads[J]. Nature Methods, 2013, 10(10): 996−998. doi: 10.1038/nmeth.2604
    [22] Bokulich N A, Subramanian S, Faith J J, et al. Quality-filtering vastly improves diversity estimates from Illumina amplicon sequencing[J]. Nature Methods, 2013, 10(1): 57−59. doi: 10.1038/nmeth.2276
    [23] Yu H, Rhee M S. Characterization of ready-to-eat fish surface as a potential source of contamination of Vibrio parahaemolyticus biofilms[J]. Food Research International, 2023, 169: 112890. doi: 10.1016/j.foodres.2023.112890
    [24] Subramanian S, MacKinnon S L, Ross N W. A comparative study on innate immune parameters in the epidermal mucus of various fish species[J]. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 2007, 148(3): 256−263. doi: 10.1016/j.cbpb.2007.06.003
    [25] Benhamed S, Guardiola F A, Mars M, et al. Pathogen bacteria adhesion to skin mucus of fishes[J]. Veterinary Microbiology, 2014, 171(1/2): 1−12. doi: 10.1016/j.vetmic.2014.03.008
    [26] Revault J, Desdevises Y, Magnanou É. Link between bacterial communities and contrasted loads in ectoparasitic monogeneans from the external mucus of two wild sparid species (Teleostei)[J]. Animal Microbiome, 2024, 6(1): 42. doi: 10.1186/s42523-024-00329-0
    [27] McKee L S, La Rosa S L, Westereng B, et al. Polysaccharide degradation by the Bacteroidetes: mechanisms and nomenclature[J]. Environmental Microbiology Reports, 2021, 13(5): 559−581. doi: 10.1111/1758-2229.12980
    [28] Ding J Y, Shiu J H, Chen Wenming, et al. Genomic insight into the host-endosymbiont relationship of Endozoicomonas montiporae CL-33T with its coral host[J]. Frontiers in Microbiology, 2016, 7: 251. doi: 10.3389/fmicb.2016.00251
    [29] Meyer J L, Paul V J, Teplitski M. Community shifts in the surface microbiomes of the coral Porites astreoides with unusual lesions[J]. PLoS One, 2014, 9(6): e100316. doi: 10.1371/journal.pone.0100316
    [30] Lucas-Elío P, ElAlami T, Martínez A, et al. Marinomonas mediterranea synthesizes an R-type bacteriocin[J]. Applied And Environmental Microbiology, 2024, 90(1): e01273−23.
    [31] Bertrand C, Martins R, Nunes F, et al. Genomic insights into indole-3-acetic acid catabolism in the marine algae-associated bacterium, Marinomonas sp. NFXS50[J]. Access Microbiology, 2024, 6(9): 000856. v3.
    [32] Kang M, Van Le V, Ko S R, et al. Effect of rainfall in shaping microbial community during Microcystis bloom in Nakdong River, Korea[J]. Science of the Total Environment, 2024, 928: 172482. doi: 10.1016/j.scitotenv.2024.172482
    [33] Wang Hailiang, Sun Bochao, Xie Guosi, et al. Spotlight on a novel bactericidal mechanism and a novel SXT/R391-like integrative and conjugative element, carrying multiple antibiotic resistance genes, in Pseudoalteromonas flavipulchra strain CDM8[J]. Microbiological Research, 2021, 242: 126598. doi: 10.1016/j.micres.2020.126598
    [34] Zhao Na, Deng Qiuxia, Zhu Chunhua, et al. Mucus piRNAs profiles of Vibrio harveyi-infected Cynoglossus semilaevis: a hint for fish disease monitoring[J]. Journal of Fish Diseases, 2022, 45(1): 165−175. doi: 10.1111/jfd.13546
    [35] Conforto E, Vílchez-Gómez L, Parrinello D, et al. Role of mucosal immune response and histopathological study in European eel (Anguilla anguilla L. ) intraperitoneal challenged by Vibrio anguillarum or Tenacibaculum soleae[J]. Fish & Shellfish Immunology, 2021, 114: 330−339. doi: 10.1016/j.fsi.2021.05.011
    [36] Burchard R P, Rittschof D, Bonaventura J. Adhesion and motility of gliding bacteria on substrata with different surface free energies[J]. Applied and Environmental Microbiology, 1990, 56(8): 2529−2534. doi: 10.1128/aem.56.8.2529-2534.1990
    [37] Echeverría-Bugueño M, Avendaño-Herrera R. Tenacibaculum dicentrarchi produce outer membrane vesicles (OMV) that are associated with the cytotoxic effect in rainbow trout head kidney macrophages[J]. Journal of Fish Diseases, 2024, 47(2): e13888. doi: 10.1111/jfd.13888
    [38] Rahman I, Al-Bar A H A, Richard F S, et al. Chemotactic response of Vibrio coralliilyticus to mucus from various coral species[J]. Canadian Journal of Microbiology, 2021, 67(7): 548−552. doi: 10.1139/cjm-2020-0287
    [39] Grognot M, Mittal A, Mah'moud M, et al. Vibrio cholerae motility in aquatic and mucus-mimicking environments[J]. Applied and Environmental Microbiology, 2021, 87(20): e01293−21.
    [40] Wei Yihan, Ma Xi, Zhao Jiangchao, et al. Succinate metabolism and its regulation of host-microbe interactions[J]. Gut Microbes, 2023, 15(1): 2190300. doi: 10.1080/19490976.2023.2190300
    [41] Kuo C H, Ballantyne R, Huang Polin, et al. Sarcodia suae modulates the immunity and disease resistance of white shrimp Litopenaeus vannamei against Vibrio alginolyticus via the purine metabolism and phenylalanine metabolism[J]. Fish & Shellfish Immunology, 2022, 127: 766−777. doi: 10.1016/j.fsi.2022.07.011
    [42] Jiang Ming, Gong Qiyang, Lai Sisi, et al. Phenylalanine enhances innate immune response to clear ceftazidime-resistant Vibrio alginolyticus in Danio rerio[J]. Fish & Shellfish Immunology, 2019, 84: 912−919. doi: 10.1016/j.fsi.2018.10.071
    [43] Zhu Yijun, Dwidar M, Nemet I, et al. Two distinct gut microbial pathways contribute to meta-organismal production of phenylacetylglutamine with links to cardiovascular disease[J]. Cell Host & Microbe, 2023, 31(1): 18−32. e9.
    [44] 尹宏权, 田黎, 付红伟, 等. 海洋细菌Bacillus marinus化学成分分离和结构鉴定[J]. 北京理工大学学报, 2007, 27(5): 460−462.

    Yin Hongquan, Tian Li, Fu Hongwei, et al. Isolation and structure identification of chemical constituents from marine bacteria Bacillus marinus[J]. Transactions of Beijing Institute of Technology, 2007, 27(5): 460−462.
    [45] Gromek S M, Suria A M, Fullmer M S, et al. Leisingera sp. JC1, a bacterial isolate from Hawaiian bobtail squid eggs, produces indigoidine and differentially inhibits vibrios[J]. Frontiers in Microbiology, 2016, 7: 1342. doi: 10.3389/fmicb.2016.01342
    [46] Chen Liping, Xu Haiying, Fu Songzhe, et al. Lishizhenia tianjinensis sp. nov. , isolated from coastal seawater[J]. International Journal of Systematic and Evolutionary Microbiology, 2009, 59(10): 2400−2403.
    [47] Duan Yafei, Wang Yun, Liu Qingsong, et al. Changes in the intestine microbial, digestion and immunity of Litopenaeus vannamei in response to dietary resistant starch[J]. Scientific Reports, 2019, 9(1): 6464. doi: 10.1038/s41598-019-42939-8
    [48] Cadby I T, Faulkner M, Cheneby J, et al. Coordinated response of the Desulfovibrio desulfuricans 27774 transcriptome to nitrate, nitrite and nitric oxide[J]. Scientific Reports, 2017, 7(1): 16228. doi: 10.1038/s41598-017-16403-4
    [49] Bueno E, Sit B, Waldor M K, et al. Anaerobic nitrate reduction divergently governs population expansion of the enteropathogen Vibrio cholerae[J]. Nature Microbiology, 2018, 3(12): 1346−1353. doi: 10.1038/s41564-018-0253-0
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  • 收稿日期:  2026-01-27
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