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Integrated biochemical, histological, and transcriptomic analyses reveal dose-dependent effects of sodium alginate on the physiology of Meretrix meretrix
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  • Published: 02 March 2026

Integrated biochemical, histological, and transcriptomic analyses reveal dose-dependent effects of sodium alginate on the physiology of Meretrix meretrix

  • Yuchen Wang1,2 na1,
  • Zhidong Zhang1 na1,
  • Suhua Chen1,
  • Yu Zhang1,
  • Yi Cao1,
  • Yuheng Peng1,2,
  • Jiazhen Zhao1,2,
  • Aihua Chen1 &
  • …
  • Yangping Wu1 

Scientific Reports , Article number:  (2026) Cite this article

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Subjects

  • Biochemistry
  • Cell biology
  • Molecular biology

Abstract

Natural polysaccharides are increasingly explored as functional additives in aquaculture, yet their safe and effective dose windows remain poorly defined in bivalves. Here, we evaluated the dose-dependent effects of sodium alginate ( 0, 10, and 20 mg/L) on the hard clam Meretrix meretrix over a 60-day culture period by integrating growth performance, antioxidant indices, intestinal histology, and hepatopancreas transcriptomics. SA10 consistently produced superior growth, and quadratic regression based on weight gain rate predicted an optimal concentration of 11.14 mg/L. Although SA20 maintained partial growth benefits at later stages, it induced marked intestinal lesions (shortened/disordered villi and impaired goblet cells) and oxidative damage, evidenced by a significant increase in malondialdehyde despite elevated SOD, CAT, and GSH-Px activities. RNA-seq revealed extensive transcriptional remodeling under SA20, identifying 985 DEGs (SA0 vs. SA20) and 728 DEGs (SA10 vs. SA20), with 218 shared core-responsive genes. Enrichment analyses highlighted coordinated regulation of pathways involved in cellular catabolism and redox homeostasis (lysosome, autophagy, phagosome, AMPK signaling, and glutathione metabolism) together with apoptosis-related processes. Notably, apoptosis-associated genes showed an overall suppression pattern (e.g., downregulation of pro-apoptotic caspases) alongside upregulation of inhibitors of apoptosis, suggesting a compensatory survival strategy under high-dose exposure. Collectively, these findings define an effective SA range that supports growth while indicating intestinal and oxidative-stress risks at elevated concentrations, providing a basis for dose optimization in clam aquaculture.

Data availability

The associated BioProject accession number is PRJNA1365470.The project and its metadata are available for review at the following link: https://dataview.ncbi.nlm.nih.gov/object/PRJNA1365470?reviewer=i7j10bqark5h3ckog5hf4vcblm.

References

  1. Wang, Y. et al. Comprehensive assessment of a miRNA-mRNA regulatory network in Meretrix meretrix: Implications for metabolism and autophagy across divergent growth rates. Aquaculture Rep. 40, 102527 (2025).

    Google Scholar 

  2. Khan, M. S. R., Nahar, S., Bhowmik, P., Hasan, M. N. & Rashid, H. O. The survival and growth of adult and juvenile hard clam Meretrix meretrix exposed to variable estuarine salinities in aquarium settings. Res. Agric. Livest. Fisheries. 11 (2), 239–254 (2024).

    Google Scholar 

  3. Zhang, Z. et al. Correlation of morphometric properties to meat yield and fatness index in the red strain of the saltwater hard clam Meretrix meretrix. Plos one, 18(4), e0284730. (2023).

  4. Wen, X. et al. Comparative evaluation of proximate compositions and taste attributes of three Asian hard clams (Meretrix meretrix) with different shell colors. Int. . Food Prop. 23 (1), 400–411 (2020).

    Google Scholar 

  5. Chang, C. C., Huang, . F., Schafferer, C., Lee, . M. & Ho, L. M. Impacts of culture survival rate on culture cost and input factors: Case study of the hard clam (Meretrix meretrix) culture in Yunlin County, Taiwan. . World Aquaculture Soc. 51 (1), 139–158 (2020).

    Google Scholar 

  6. Zhang, Z. et al. Effects of adding EM bacteria and mechanical aeration on water quality, growth and antioxidant status of Meretrix meretrix and Exopalaemon carinicauda farmed in the clam–shrimp polyculture system. Aquac. Res. 53 (5), 1823–1832 (2022).

    Google Scholar 

  7. Wang, Y. et al. Integrated microbiome and metabolome analyses reveal effects of sodium alginate on the growth of Meretrix meretrix. Int. . Biol. Macromol., 145431. (2025).

  8. Shen, Y. et al. Unraveling the web of defense: the crucial role of polysaccharides in immunity. Front. Immunol. 15, 1406213 (2024).

    Google Scholar 

  9. Thuat, N. D. et al. The content, antioxidant activity, and structural characteristics of sodium alginate extracting from Sargassum polycystum grew in Vietnam: Effect of various extraction conditions. . Pharm. Res. Int., 197–206. (2021).

  10. Qin, H. et al. Growth performance, digestive capacity and intestinal health of juvenile spotted seabass (Lateolabrax maculatus) fed dietary laminarin supplement. Front. Mar. Sci. 10, 1242175 (2023).

    Google Scholar 

  11. Abbas, E. M., Al-Souti, A. S., Sharawy, Z. Z., El-Haroun, E. & Ashour, M. Impact of dietary administration of seaweed polysaccharide on growth, microbial abundance, and growth and immune-related genes expression of the pacific whiteleg shrimp (Litopenaeus vannamei). Life 13 (2), 344 (2023).

    Google Scholar 

  12. Zhou, C. et al. Effect of dietary carbohydrate levels on growth performance, body composition, intestinal and hepatic enzyme activities, and growth hormone gene expression of juvenile golden pompano, Trachinotus ovatus. Aquaculture 437, 390–397 (2015).

    Google Scholar 

  13. Wang . et al. Effects of different dietary carbohydrate levels on growth, feed utilization and body composition of juvenile grouper Epinephelus akaara. Aquaculture 459, 143–147 (2016).

  14. Hemre, G. I., Mommsen, T. P. & Krogdahl, Å. Carbohydrates in fish nutrition: effects on growth, glucose metabolism and hepatic enzymes. Aquacult. Nutr. 8 (3), 175–194 (2002).

    Google Scholar 

  15. Hutchins, C. G., Rawles, S. D. & Gatlin Iii, D. M. Effects of dietary carbohydrate kind and level on growth, body composition and glycemic response of juvenile sunshine bass (Morone chrysops× M. saxatilis). Aquaculture 161 (1–4), 187–199 (1998).

    Google Scholar 

  16. Chen, S. et al. fastp: an ultra-fast all-in-one FASTQ preprocessor. Bioinformatics 34 (17), i884–i890 (2018).

    Google Scholar 

  17. Langmead, B. & Salzberg, S. L. Fast gapped-read alignment with Bowtie 2. Nat. Methods. 9 (4), 357–359 (2012).

    Google Scholar 

  18. Kim, D., Langmead, B. & Salzberg, S. L. HISAT: a fast spliced aligner with low memory requirements. Nat. Methods. 12 (4), 357–360 (2015).

    Google Scholar 

  19. Pertea, M. et al. StringTie enables improved reconstruction of a transcriptome from RNA-seq reads. Nat. Biotechnol. 33 (3), 290–295 (2015).

    Google Scholar 

  20. Cui, H. et al. Effects of a highly purified fucoidan from Undaria pinnatifida on growth performance and intestine health status of gibel carp Carassius auratus gibelio. Aquacult. Nutr. 26 (1), 47–59 (2020).

    Google Scholar 

  21. Sotoudeh, E. & Mardani, F. Antioxidant-related parameters, digestive enzyme activity and intestinal morphology in rainbow trout (Oncorhynchus mykiss) fry fed graded levels of red seaweed, Gracilaria pygmaea. Aquacult. Nutr. 24 (2), 777–785 (2018).

    Google Scholar 

  22. Dawood, M. A. O. Nutritional immunity of fish intestines: important insights for sustainable aquaculture. Rev. Aquac. 13, 642–663 (2021).

    Google Scholar 

  23. Islam, S. M., Rohani, M. F. & Shahjahan, M. Probiotic yeast enhances growth performance of Nile tilapia (Oreochromis niloticus) through morphological modifications of intestine. Aquaculture Rep. 21, 100800 (2021).

    Google Scholar 

  24. Gustafsson, . K. & Johansson, M. E. The role of goblet cells and mucus in intestinal homeostasis. Nat. reviews Gastroenterol. Hepatol. 19 (12), 785–803 (2022).

    Google Scholar 

  25. Liu, Y. et al. High dietary non-starch polysaccharides detrimental to nutrient digestibility, digestive enzyme activity, growth performance, and intestinal morphology in largemouth bass, Micropterus salmoides. Front. Nutr. 9, 1015371 (2022).

    Google Scholar 

  26. Wang, T., Xu, R., Qiao, F., Du, Z. Y. & Zhang, M. L. Effects of mannan oligosaccharides (MOS) on glucose and lipid metabolism of largemouth bass (Micropterus salmoides) fed with high carbohydrate diet. Anim. Feed Sci. Technol. 292, 115449 (2022).

    Google Scholar 

  27. Li et al. Effects of arginine supplementation in high-carbohydrate diets on the growth, hematological parameters, and hepatic and skeletal muscle glucose metabolism of juvenile mirror carp (Cyprinus carpio) based on PI3K/Akt signaling pathway. Aquaculture Rep. 39, 102409 (2024).

  28. Sahoo, D. K. et al. Oxidative stress, hormones, and effects of natural antioxidants on intestinal inflammation in inflammatory bowel disease. Front. Endocrinol. 14, 1217165 (2023).

    Google Scholar 

  29. Liu, D. Y., Lou, W. ., Zhang, D. Y. & Sun, S. Y. ROS plays a role in the neonatal rat intestinal barrier damages induced by hyperoxia. BioMed research international, 2020(1), 8819195. (2020).

  30. Wang, B. et al. ROS-induced lipid peroxidation modulates cell death outcome: mechanisms behind apoptosis, autophagy, and ferroptosis. Arch. Toxicol. 97 (6), 1439–1451 (2023).

    Google Scholar 

  31. Guan, G. & Lan, S. Implications of antioxidant systems in inflammatory bowel disease. BioMed research international, 2018(1), 1290179. (2018).

  32. Jiang, W. et al. Effects of different types of non-starch polysaccharides on growth, digestive enzyme activity, intestinal barrier function and antioxidant activity of tilapia (Oreochromis niloticus). Aquaculture Rep. 25, 101198 (2022).

    Google Scholar 

  33. Irato, P. & Santovito, G. Enzymatic and non-enzymatic molecules with antioxidant function. Antioxidants 10 (4), 579 (2021).

    Google Scholar 

  34. Hekmat, A., Saboury, A. A. & Saso, L. Superoxide dismutases inhibitors. In Metalloenzymes (523–531). Academic. (2024).

  35. Gebicka, L. & Krych-Madej, . The role of catalases in the prevention/promotion of oxidative stress. . Inorg. Biochem. 197, 110699 (2019).

  36. Pei, ., Pan, X., Wei, G. & Hua, Y. Research progress of glutathione peroxidase family (GPX) in redoxidation. Front. Pharmacol. 14, 1147414 (2023).

  37. Hu, ., Zhang, . & Wu, S. The growth performance and non-specific immunity of juvenile grass carp (Ctenopharyngodon idella) affected by dietary alginate oligosaccharide. 3 Biotech. 11 (2), 46 (2021).

  38. Xie, . et al. Study on mechanism of synthetic astaxanthin and Haematococcus pluvialis improving the growth performance and antioxidant capacity under acute hypoxia stress of golden pompano (Trachinotus ovatus) and enhancing anti-inflammatory by activating Nrf2-ARE pathway to antagonize the NF-κB pathway. Aquaculture 518, 734657 (2020).

  39. Jianbin, H., Yan, C., Chuanpeng, Z., Xiaolin, H., Zhong, H., Wei, Y., Heizhao, L. Effects of dietary alginate oligosaccharide on growth performance, antioxidative capacity and immune function of juvenile Trachinotus ovatus. South China Fisheries Science, 18(3), 118–128 (2022).

  40. Xie, C. et al. A review on seaweeds and seaweed-derived polysaccharides: Nutrition, chemistry, bioactivities, and applications. Food Reviews Int. 40 (5), 1312–1347 (2024).

    Google Scholar 

  41. Janssens, L. & Stoks, R. Oxidative stress mediates rapid compensatory growth and its costs. Funct. Ecol. 34 (10), 2087–2097 (2020).

    Google Scholar 

  42. Martel, . et al. Hormetic effects of phytochemicals on health and longevity. Trends Endocrinol. Metabolism. 30 (6), 335–346 (2019).

  43. Jingwei, L. et al. Effects of dietary fucoidan on growth performance, digestion, immunity, antioxidant and glucolipid metabolism of juvenile sea cucumber (Apostichopus japonicus) (Journal of fisheries of china, 2025).

  44. Zhou, X. Improving growth, digestion, immunity, and disease resistance of Procrazium clarkii via fucoidan supplementation. (Doctoral dissertation, Yangtze University). https://link.cnki.net/doi/10.26981/d.cnki (2024).

  45. Liu, Y., Huang, H., Fan, ., Zhou, H., Zhang, Y., Cao, Y., Tan, B. Effects of dietary non-starch polysaccharides level on the growth, intestinal flora and intestinal health of juvenile largemouth bass Micropterus salmoides. Aquaculture, 557, 738343 (2022).

  46. Wu, C., Yang, H., Yang, Y., Yuan, Q., Lv, W., Ayana, G. U., Zhang, Q. Dietary Supplementation of Astragalus Polysaccharides Modulates Growth Physiology, Metabolic Homeostasis, and Innate Immune Responses in Rice Field Eels (Monopterus albus). Fishes. 10(5), 213 (2025).

  47. Bakky, M. A. H., Tran, N. T., Zhang, Y. & Li, S. Utilization of marine macroalgae-derived sulphated polysaccharides as dynamic nutraceutical components in the feed of aquatic animals: A review. Aquac. Res. 53 (17), 5787–5808 (2022).

    Google Scholar 

  48. Bhattacharjee, S. & Bhattacharjee, S. ROS and oxidative modification of cellular components. Reactive Oxygen Species Plant. Biology, 81–105. (2019).

  49. Zheng, ., Tan, ., Miao, Y. Y. & Zhang, Q. Extracellular vesicles degradation pathway based autophagy lysosome pathway. Am. . translational Res. 11 (3), 1170 (2019).

  50. Lee, . W., Park, S., Takahashi, Y. & Wang, H. G. The association of AMPK with ULK1 regulates autophagy. PloS one, 5(11), e15394. (2010).

  51. Park, . M., Lee, D. H. & Kim, D. H. Redefining the role of AMPK in autophagy and the energy stress response. Nat. Commun. 14 (1), 2994 (2023).

    Google Scholar 

  52. Shang, L. & Wang, X. AMPK and mTOR coordinate the regulation of Ulk1 and mammalian autophagy initiation. Autophagy 7 (8), 924–926 (2011).

    Google Scholar 

  53. Mahapatra, K. K. et al. The lysosome as an imperative regulator of autophagy and cell death. Cell. Mol. Life Sci., 1–15. (2021).

  54. Settembre, C. & Perera, R. M. Lysosomes as coordinators of cellular catabolism, metabolic signalling and organ physiology. Nat. Rev. Mol. Cell Biol. 25 (3), 223–245 (2024).

    Google Scholar 

  55. Ratto, E. et al. Direct control of lysosomal catabolic activity by mTORC1 through regulation of V-ATPase assembly. Nat. Commun. 13 (1), 4848 (2022).

    Google Scholar 

  56. Tušar, L., Usenik, A., Turk, B. & Turk, D. Mechanisms applied by protein inhibitors to inhibit cysteine proteases. Int. . Mol. Sci. 22 (3), 997 (2021).

    Google Scholar 

  57. Liu, B. et al. Response of microbiota and immune function to different hypotonic stress levels in giant freshwater prawn Macrobrachium rosenbergii post-larvae. Sci. Total Environ. 844, 157258 (2022).

    Google Scholar 

  58. Guo, H. et al. Gene expression of apoptosis-related genes, stress protein and antioxidant enzymes in hemocytes of white shrimp Litopenaeus vannamei under nitrite stress. Comp. Biochem. Physiol. C: Toxicol. Pharmacol. 157 (4), 366–371 (2013).

    Google Scholar 

  59. Tang, D. et al. Toxic effects of metal copper stress on immunity, metabolism and pathologic changes in Chinese mitten crab (Eriocheir japonica sinensis). Ecotoxicology 30, 632–642 (2021).

    Google Scholar 

  60. Lee, H. ., Woo, Y., Hahn, T. W., Jung, Y. M. & Jung, Y. . Formation and maturation of the phagosome: a key mechanism in innate immunity against intracellular bacterial infection. Microorganisms 8 (9), 1298 (2020).

    Google Scholar 

  61. Praefcke, G. . & McMahon, H. T. The dynamin superfamily: universal membrane tubulation and fission molecules? Nat. Rev. Mol. Cell Biol. 5 (2), 133–147 (2004).

    Google Scholar 

  62. Hao, Q. et al. Revelation of benzo (a) pyrene-induced latent toxicity mechanism to intestinal histomorphology and oxidative status for common carp (Cyprinus carpio) through transcriptional and single-cell sequencing. Aquaculture 585, 740712 (2024).

    Google Scholar 

  63. Stockinger, W. & Nohturfft, A. Studying phagocytosis by live-cell scintillation proximity assay. Exocytosis Endocytosis, 147–155. (2008).

  64. Zhang, Y. et al. Insufficient or excessive dietary carbohydrates affect gut health through change in gut microbiota and regulation of gene expression of gut epithelial cells in grass carp (Ctenopharyngodon idella) Vol. 132, 108442 (Fish & Shellfish Immunology, 2023).

  65. Stockinger, W. & Nohturfft, A. Studying phagocytosis by live-cell scintillation proximity assay. Exocytosis Endocytosis, 147–155. (2008).

  66. Wu, G., Lupton, . R., Turner, N. D., Fang, Y. Z. & Yang, S. Glutathione metabolism and its implications for health. . Nutr. 134 (3), 489–492 (2004).

    Google Scholar 

  67. Hayes, . D. & McLellan, L. I. Glutathione and glutathione-dependent enzymes represent a co-ordinately regulated defence against oxidative stress. Free Radic. Res. 31 (4), 273–300 (1999).

    Google Scholar 

  68. Pei, ., Pan, X., Wei, G. & Hua, Y. Research progress of glutathione peroxidase family (GPX) in redoxidation. Front. Pharmacol. 14, 1147414 (2023).

  69. Xiao, W. & Loscalzo, . Metabolic responses to reductive stress. Antioxid. Redox. Signal. 32 (18), 1330–1347 (2020).

  70. Filomeni, G., De Zio, D. & Cecconi, F. Oxidative stress and autophagy: the clash between damage and metabolic needs. Cell. Death Differ. 22 (3), 377–388 (2015).

    Google Scholar 

  71. Ou, X. H. et al. Maternal insulin resistance causes oxidative stress and mitochondrial dysfunction in mouse oocytes. Hum. Reprod. 27 (7), 2130–2145 (2012).

    Google Scholar 

  72. Arandjelovic, S. & Ravichandran, K. S. Phagocytosis of apoptotic cells in homeostasis. Nat. Immunol. 16 (9), 907–917 (2015).

    Google Scholar 

  73. Portt, L., Norman, G., Clapp, C., Greenwood, M. & Greenwood, M. T. Anti-apoptosis and cell survival: a review. Biochim. et Biophys. Acta (BBA)-Molecular Cell. Res. 1813 (1), 238–259 (2011).

    Google Scholar 

  74. Edelblum, K. L., Yan, F., Yamaoka, T. & Polk, B. D. Regulation of apoptosis during homeostasis and disease in the intestinal epithelium. Inflamm. Bowel Dis. 12 (5), 413–424 (2006).

    Google Scholar 

  75. Cohen, G. M. Caspases: the executioners of apoptosis. Biochem. . 326 (1), 1–16 (1997).

    Google Scholar 

  76. Wei, Y., Fan, T. & Yu, M. Inhibitor of apoptosis proteins and apoptosis. Acta Biochim. Biophys. Sin. 40 (4), 278–288 (2008).

    Google Scholar 

  77. Redza-Dutordoir, M. & Averill-Bates, D. A. Activation of apoptosis signalling pathways by reactive oxygen species. Biochim. et Biophys. Acta (BBA)-Molecular Cell. Res. 1863 (12), 2977–2992 (2016).

    Google Scholar 

  78. Kannan, K. & Jain, S. K. Oxidative stress and apoptosis. Pathophysiology 7 (3), 153–163 (2000).

    Google Scholar 

  79. Snezhkina, A. V. et al. ROS generation and antioxidant defense systems in normal and malignant cells. Oxidative Med. Cell. Longev. 2019(1), 6175804 (2019).

    Google Scholar 

  80. Franco, R. & Cidlowski, . A. Apoptosis and glutathione: beyond an antioxidant. Cell. Death Differ. 16 (10), 1303–1314 (2009).

    Google Scholar 

  81. Mukhopadhyay, S., Panda, P. K., Sinha, N., Das, D. N. & Bhutia, S. K. Autophagy and apoptosis: where do they meet? Apoptosis 19, 555–566 (2014).

    Google Scholar 

  82. Napoletano, F., Baron, O., Vandenabeele, P., Mollereau, B. & Fanto, M. Intersections between regulated cell death and autophagy. Trends Cell Biol. 29 (4), 323–338 (2019).

    Google Scholar 

  83. Hunkeler, M., Jin, C. Y. & Fischer, E. S. Structures of BIRC6-client complexes provide a mechanism of SMAC-mediated release of caspases. Science 379 (6637), 1105–1111 (2023).

    Google Scholar 

  84. Dietz, L. et al. Structural basis for SMAC-mediated antagonism of caspase inhibition by the giant ubiquitin ligase BIRC6. Science 379 (6637), 1112–1117 (2023).

    Google Scholar 

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Funding

This work was supported by the “JBGS” Project of Seed Industry Revitalization (Grant No. JBGS [2021] 142); the Key Technology Integration and Extension Program for Modern Agriculture in Jiangsu Province (Grant No. JCTG [2025] 22); the Science and Technology Program for Social and People’s Livelihood in Nantong (Grant No. MSZ2024084); the Agricultural Science and Technology Innovation and Promotion Project in Jiangsu Province (Grant No. 2025-SJCG-005-03).

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  1. Yuchen Wang and Zhidong Zhang contributed equally to this work.

Authors and Affiliations

  1. Marine Economic Shellfish Research and Development Center of Jiangsu Province, Marine Fisheries Research Institute of Jiangsu Province, Nantong, 226007, China

    Yuchen Wang, Zhidong Zhang, Suhua Chen, Yu Zhang, Yi Cao, Yuheng Peng, Jiazhen Zhao, Aihua Chen & Yangping Wu

  2. College of Fisheries and Life Science, Shanghai Ocean University, Shanghai, 201306, China

    Yuchen Wang, Yuheng Peng & Jiazhen Zhao

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  1. Yuchen Wang
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Contributions

YuchenWang: Data curation and writing original draft. Zhidong Zhang: co-first author, Data visualization. Suhua Chen: Enzyme activity detection. Yu Zhang and Yi Cao: Samples preparation. Yujeng Peng:Enzyme activity detection. Jiazhen Zhao: Cultured clams. Aihua Chen: Supervision. Yangping Wu: Conceptualization and funding. We are grateful to Guangzhou Genedenovo Biotechnology Co., Ltd for assisting in sequencing and/or bioinformatics analysis.

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Correspondence to Aihua Chen or Yangping Wu.

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Wang, Y., Zhang, Z., Chen, S. et al. Integrated biochemical, histological, and transcriptomic analyses reveal dose-dependent effects of sodium alginate on the physiology of Meretrix meretrix. Sci Rep (2026). https://doi.org/10.1038/s41598-026-41950-0

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  • Received: 11 November 2025

  • Accepted: 23 February 2026

  • Published: 02 March 2026

  • DOI: https://doi.org/10.1038/s41598-026-41950-0

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Keywords

  • Meretrix meretrix
  • Sodium alginate
  • Dose-dependent effect
  • Transcriptomics
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