Effect of Chestnut Wood Polyphenols on Growth, Survival, and Disease Resistance in Pacific White Shrimp (Litopenaeus vannamei Boone, 1931)

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Natnicha Chongprachavat
Arunothai Keetanon
Pakawat Poldetch
Tirawat Rairat
Lalitphan Kitsanayanyong
Phongchate Pichitkul
Niti Chuchird

Abstract

Chestnut wood polyphenols (CWP) represent a natural feed additive with potential antibacterial and immunostimulant properties. This study evaluated the in vitro antibacterial activity of CWP against Photobacterium damselae subsp. damselae (PDD) and its effects on the growth performance, immune responses, and disease resistance of Pacific white shrimp (Litopenaeus vannamei Boone, 1931). The minimum inhibitory concentration and minimum bactericidal concentration of CWP against PDD were 10 µg·mL⁻¹ and 20 µg·mL⁻¹, respectively. In the feeding trial, shrimp (initial weight, 5.58±0.19 g) were given diets supplemented with CWP at 0 (control), 1, 3, or 5 g·kg feed⁻¹ for 30 days. The results indicate that dietary CWP significantly improved survival rates and feed conversion ratios in a dose-dependent manner, with the highest survival (92.00±4.00%) and lowest FCR (0.99±0.04) observed in the 5 g·kg feed⁻¹ group. In addition, CWP supplementation notably reduced intestinal Vibrio spp. counts and enhanced superoxide dismutase activity, while the immune parameters, including total hemocyte count, phagocytic activity, and phenoloxidase activity, remained unaffected. Following experimental challenge with PDD, shrimp fed 5 g·kg feed⁻¹ CWP exhibited higher survival (70.00%) compared to the control group (43.33%). On day 7 post-challenge, attenuation of PDD-associated lesions in the hepatopancreas and muscle by dietary CWP was revealed by histopathological examination. These findings thus demonstrate that dietary supplementation with CWP, particularly at 5 g·kg feed⁻¹, enhances growth performance and immune responses, while reducing pathogenic bacterial loads and improving disease resistance in Pacific white shrimp.

Article Details

How to Cite
Chongprachavat, N., Keetanon, A., Poldetch, P., Rairat, T., Kitsanayanyong, L., Pichitkul, P., & Chuchird, N. (2026). Effect of Chestnut Wood Polyphenols on Growth, Survival, and Disease Resistance in Pacific White Shrimp (Litopenaeus vannamei Boone, 1931). Journal of Fisheries and Environment, 50(2), 28–41. retrieved from https://li01.tci-thaijo.org/index.php/JFE/article/view/270980
Section
Research Article

References

American Public Health Association (APHA). 2017. Standard Methods for the Examination of Water and Wastewater, 23rd ed. American Public Health Association, American Water Works Association and Water Environment Federation, Washington, D.C., USA. 1545 pp.

Ashour, M.L., A. Al-Souti, M.M. Mabrouk, M.A.E. Naiel and E.M. Younis. 2024. A commercial seaweed extract increases growth performance, immune responses, and related gene expressions in whiteleg shrimp (Litopenaeus vannamei). Aquaculture Reports 35: 102154. DOI: 10.1016/j.aqrep.2024.102154.

Bell, T.A. and D.V. Lightner. 1988. A Handbook of Normal Penaeid Shrimp Histology. World Aquaculture Society, Baton Rouge, Los Angeles, USA. 114 pp.

Bolívar-Ramírez, N.C., A.S. Mallmann, D.D. Schleder, C. Machado and W.Q. Seiffert. 2022. Tannins as a food additive in Pacific white shrimp diet. Aquaculture 556: 738232. DOI: 10.1016/j.aquaculture.2022.738232.

Borges, A., C. Ferreira, M.J. Saavedra and M. Simões. 2013. Antibacterial activity and mode of action of ferulic and gallic acids against pathogenic bacteria. Microbial Drug Resistance 19(4): 256–265. DOI: 10.1089/mdr.2012.0244.

Cabello, F.C., H.P. Godfrey, A. Tomova, L. Ivanova, H. Dölz, A. Millanao and A.H. Buschmann. 2013. Antimicrobial use in aquaculture re-examined: its relevance to antimicrobial resistance and to animal and human health. Environmental Microbiology 15(7): 1917–1942. DOI: 10.1111/1462-2920.12134.

Chaweepack, T., S. Chaweepack, B. Muenthaisong, L. Ruangpan and K. Nagata. 2015. Effect of galangal (Alpinia galanga Linn.) extract on the expression of immune-related genes and Vibrio harveyi resistance in Pacific white shrimp (Litopenaeus vannamei). Aquaculture International 23(3): 705–719. DOI: 10.1007/s10499-014-9822-2.

Chen, Y.T., C.L. Kuo, C.C. Wu, C.H. Liu and S. Hsieh. 2023. Effects of Panax notoginseng water extract on immune responses and digestive enzymes in white shrimp Litopenaeus vannamei. Animals 13(7): 1131. DOI: 10.3390/ani13071131.

Chuchird, N., N. Chongprachavat, W. Suanploy, L. Kitsanayanyong, P. Phansawat, A. Keetanon, P. Wimanhaemin and T. Rairat. 2024. Investigation of pale shrimp disease in Pacific white shrimp (Litopenaeus vannamei) caused by Photobacterium damselae subsp. damselae in low salinity culture conditions. Aquaculture Reports 39: 102416. DOI: 10.1016/j.aqrep.2024.102416.

Chuchird, N., J. Hantrathin, P. Pichitkul, C. C. Chou and T. Rairat. 2026. Effect of different top-coating materials on minimizing drug leaching from medicated feed in shrimp aquaculture. Journal of Veterinary Pharmacology and Therapeutics 49 (3): 317–323. DOI: 10.1111/jvp.70043.

Clinical and Laboratory Standards Institute (CLSI). 2020. Methods for Antimicrobial Broth Dilution and Disk Diffusion Susceptibility Testing of Bacteria Isolated from Aquatic Animals, 2nd ed. CLSI guideline VET03. Clinical and Laboratory Standards Institute, Pennsylvania, USA. 100 pp.

Daglia, M. 2012. Polyphenols as antimicrobial agents. Current Opinion in Biotechnology 23(2): 174–181. DOI: 10.1016/j.copbio.2011.08.007.

Food and Agriculture Organization of the United Nations (FAO). 2024. The State of World Fisheries and Aquaculture 2024 – Blue Transformation in Action. Food and Agriculture Organization of the United Nations, Rome, Italy. 232 pp.

Farha, A.K., Q.Q. Yang, G. Kim, H.B. Li, F. Zhu, H.Y. Liu, R.Y. Gan and H. Corke. 2020. Tannins as an alternative to antibiotics. Food Bioscience 38: 100751. DOI: 10.1016/j.fbio.2020.100751.

Gong, H., Z. Qin, Z. Chen, J. Li and Z. Chang. 2022. Effects of dietary tannic acid on growth, digestion, immunity and resistance to ammonia stress, and intestinal microbial community in Pacific white shrimp (Litopenaeus vannamei). Fishes 7(6): 327. DOI: 10.3390/fishes7060327.

Hasanthi, M., S. Jo, H. Kim, G.S. Yun and Y. Lee. 2024. Dietary supplementation of micelle silymarin enhances the antioxidant status, innate immunity, growth performance, resistance against Vibrio parahaemolyticus infection, and gut morphology in Pacific white shrimp (Litopenaeus vannamei). Animal Feed Science and Technology 311: 115953. DOI: 10.1016/j.anifeedsci.2024.115953.

Holmblad, T. and K. Söderhäll. 1999. Cell adhesion molecules and antioxidative enzymes in a crustacean, possible role in immunity. Aquaculture 172(1–2): 111–123. DOI: 10.1016/S0044-8486(98)00446-3.

Huang, H.T., Y.F. Hu, Z.H. Liao, Y.R. Lin and Y.Y. Chen. 2024. Dietary supplementation with hydrolyzable tannin improves nonspecific immune responses, intestinal morphology, and disease resistance against Vibrio alginolyticus in whiteleg shrimp. Aquaculture Research 2024: 3486022. DOI: 10.1155/2024/3486022.

Itami, T., Y. Takahashi, E. Tsuchihira, H. Igusa and M. Kondo. 1994. Enhancement of disease resistance of kuruma prawn Penaeus japonicus and increase in phagocytic activity of prawn hemocytes after oral administration of β-1,3-glucan (Schizophyllan). In: The Third Asian Fisheries Forum (eds. L.M. Chou, A.D. Munro, J.J. Lam, et al.), pp. 375–378. Asian Fisheries Society, Manila, Philippines.

Jiravanichpaisal, P., B.L. Lee and K. Söderhäll. 2006. Cell-mediated immunity in arthropods: hematopoiesis, coagulation, melanization and opsonization. Immunobiology 211(4): 213–236. DOI: 10.1016/j.imbio.2005.10.015.

Jory, D. 2019. Shrimps. In: Aquaculture: Farming Aquatic Animals and Plants, 3rd ed. (eds. J.S. Lucas, P.C. Southgate and C.S. Tucker), pp. 499–525. John Wiley and Sons Ltd, Chichester, West Sussex, UK.

Lowry, O.H., N.J. Rosebrough, A.L. Farr and R.J. Randall. 1951. Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry 193(1): 265–275. DOI: 10.1016/S0021-9258(19)52451-6.

Mantaring, S.D.A., J.R.K. Delos Santos, R. Estrella, J.P.G. Jose, I.J.L. Castro, U.G. Bigol and J.P.M.D. Guzman. 2024. Terminalia catappa L. leaf extract interferes with biofilm formation of Vibrio parahaemolyticus and enhances immune response of Penaeus vannamei against acute hepatopancreatic necrosis disease (AHPND). Aquaculture 579: 740266. DOI: 10.1016/j.aquaculture.2023.740266.

Megat Rusydi, M.R. and A. Azrina. 2012. Effect of germination on total phenolic, tannin and phytic acid contents in soy bean and peanut. International Food Research Journal 19(2): 673–677.

Niyamosatha, H., N. Chuchird and T. Rairat. 2015. Effect of dietary polyphenol-rich feed additive from grape pomace on growth, survival and tolerance to Vibrio infection in Pacific white shrimp (Litopenaeus vannamei). Journal of Fisheries and Environment 39(2): 1–9.

Novriadi, R., O.D.S. Hasan, K. Nguyen, S.J. Davies and Z.G. Panjaitan. 2023. Functional effects of hydrolyzable tannins on the growth, health status, and hepatopancreas histology of Pacific white shrimp Penaeus vannamei reared under commercial pond conditions. Aquaculture Research 2023: 6644113. DOI: 10.1155/2023/6644113.

Prapaiwong, T., W. Srakaew, C. Wachirapakorn and C. Jarassaeng. 2021. Effects of hydrolyzable tannin extract obtained from sweet chestnut wood (Castanea sativa Mill.) against bacteria causing subclinical mastitis in Thai Friesian dairy cows. Veterinary World 14(9): 2427–2433. DOI: 10.14202/vetworld.2021.2427-2433.

Reverter, M., N. Bontemps, D. Lecchini, B. Banaigs and P. Sasal. 2014. Use of plant extracts in fish aquaculture as an alternative to chemotherapy: current status and future perspectives. Aquaculture 433: 50–61. DOI: 10.1016/j.aquaculture.2014.05.048.

Smeriglio, A., D. Barreca, E. Bellocco and D. Trombetta. 2016. Proanthocyanidins and hydrolysable tannins: occurrence, dietary intake and pharmacological effects. British Journal of Pharmacology 174(11): 1244–1262. DOI: 10.1111/bph.13630.

Song, Y.L. and Y.T. Hsieh. 1994. Immunostimulation of tiger shrimp (Penaeus monodon) hemocytes for generation of microbicidal substances: analysis of reactive oxygen species. Developmental and Comparative Immunology 18(3): 201–209. DOI: 10.1016/0145-305X(94)90012-4.

Songsangjinda, P. 2019. Handbook on Intensive Farming of Pacific White Shrimp (Litopenaeus vannamei). Department of Fisheries, Minister of Agriculture and Cooperatives, Bangkok, Thailand. 49 pp. (in Thai)

Söderhäll, K. and L. Häll. 1984. Lipopolysaccharide-induced activation of prophenoloxidase activating system in crayfish haemocyte lysate. Biochimica et Biophysica Acta - General Subjects 797(1): 99–104. DOI: 10.1016/0304-4165(84)90387-8.

Vanichkul, K., N. Areechon, N. Kongkathip, P. Srisapoome and N. Chuchird. 2010. Immunological and bactericidal effects of turmeric (Curcuma longa Linn.) extract in Pacific white shrimps (Litopenaeus vannamei Boone). Agriculture and Natural Resources 44(5): 850–858.

Wimanhaemin, P., N. Chuchird, T. Rairat, A. Keetanon and P. Phansawat. 2025. Effects of polyphenol-rich sugarcane extract on growth performance, survival, immune responses, and resistance to Vibrio parahaemolyticus and white spot syndrome virus infections of Pacific white shrimp (Litopenaeus vannamei). Journal of the World Aquaculture Society 56(1): e13110. DOI: 10.1111/jwas.13110.

Wolfe, K., X. Wu and R.H. Liu. 2003. Antioxidant activity of apple peels. Journal of Agricultural and Food Chemistry 51(3): 609–614. DOI: 10.1021/jf020782a.

Yu, Z., G. Liu, S.L. Li, Y. Hong and S. Zhao. 2024. Effects of fermented pomegranate peel polyphenols on the growth performance, immune response, hepatopancreatic health, and disease resistance in white shrimp (Litopenaeus vannamei). Aquaculture Nutrition 2024(1): 9966772. DOI: 10.1155/anu/9966772.