Effects of Dietary Algae Supplementation on Growth, Hepatopancreatic Histopathology, and Disease Resistance in Post-Larval White Shrimp (Litopenaeus vannamei)

Authors

  • Maliwan Kutako Faculty of Marine Technology, Burapha University, Chanthaburi, 22170 Thailand https://orcid.org/0000-0002-3707-6442
  • Sasikarn Prueprak Faculty of Marine Technology, Burapha University, Chanthaburi, 22170 Thailand
  • Piraya Iamsa-ard Faculty of Marine Technology, Burapha University, Chanthaburi, 22170 Thailand
  • Janjarus Watanachote Aquatic Animal Disease Diagnostics and Immunology Research Unit, Burapha University, Chanthaburi, 22170 Thailand
  • Molruedee Sonthi Faculty of Marine Technology, Burapha University, Chanthaburi, 22170 Thailand

Keywords:

Algae, Survivalrate, Histopathology, L. vannamei

Abstract

Algae have been increasingly incorporated into aquaculture feeds as functional additives with dual roles as immunostimulants and growth enhancement. Various species serve as rich reservoirs of essential nutrients and bioactive constituents—such as vitamins, antioxidants, phycocyanin, minerals, amino acids, carotenoids, proteins, and fatty acids—that collectively promote growth and stimulate immunity. A 28-d feeding trial was conducted to assess the impact of different algae-based supplements on growth performance, hepatopancreatic histology, and resistance to Vibrio parahaemolyticus in post-larval Litopenaeus vannamei. Shrimp were divided into 4 groups: control (F0) received the basal diet alone, while treatment groups were fed the basal formulation supplemented with 5 g/kg of dried Ulva sp. (F1), Sargassum sp. (F2), and Spirulina platensis (F3). The results revealed that the F3 group (S. platensis) achieved the greatest improvement in final body weight, weight gain, average daily gain (ADG), and feedconversion ratio (FCR) compared to F0, F1, and F2 (p≤0.05). Following a 168-h V. parahaemolyticus challenge, shrimp in the F3 group exhibited the lowest cumulative mortality rate (6.60 %), significantly lower than that of all other treatments (p≤0.05). Histological examination of the hepatopancreas revealed superior tissueintegrity and a marked reduction in pathogen burden within the F3 group (p≤0.05). In summary, the study highlights the potential of algae as functional additives in shrimp feed demonstrating their capacity to enhance growth performance, induce beneficial histological alterations, and enhance resistance to V. parahaemolyticus. Among the algae tested, S. platensis proved to be the most effective supplement.

References

Abdelkhalek, N.K., Ghazy, E.W., & Abdel-Daim, M.M. (2015). Pharmacodynamic interaction of Spirulina platensis and deltamethrin in freshwater fish Nile tilapia, Oreochromis niloticus: Impact on lipid peroxidation and oxidative stress. Environmental Science and Pollution Research, 22(4), 3023–3031.

Abdel-Razek, N., Khalil, R.H., Afifi, A.A., Alkhuriji, A.F., & Metwally, D.M. (2024). Nutritional innovation using green seaweed (Ulva sp.) and garlic powder extracts for white-leg shrimp (Litopenaeus vannamei) challenged by Vibrio harveyi. Veterinary Medicine and Science, 10(6), e70052.

Ahmed, R.A., Jastaniah, S.D., Alaidaroos, B.A., Shafi, M.E., El-Haroun, E., Abd El-Aziz, Y.M., ... Elfeky, A. (2025). Effects of dietary Spirulina platensis supplementation on growth performance, whole body composition, antioxidant activity, histological alterations, and resistance to Vibrio parahaemolyticus in Pacific white shrimp, Litopenaeus vannamei. Aquaculture Reports, 40, 102606.

Celekli, A., Alslibi, Z.A., & Üseyin Bozkurt, H. (2019). Influence of incorporated Spirulina platensis on the growth of microflora and physiochemical properties of ayran as a functional food. Algal research, 44, 156654.

Cuzon, G.Y., Dos Santos, R. Hew, M., & Poullaouec, G. (2009). Use of Spirulina in shrimp (Penaeus japonicus) diet. Journal of the World Aquaculture Society, 12(2), 292–291.

Dangtip, S., Sirikharin, R., Sanguanrut, P., Thitamadee, S., Sritunyalucksana, K. Taengchaiyaphum, S., Mavichak, R., Proespraiwong, R., & Flegel, T.W. (2015). AP4 method for two-tube nested PCR detection of AHPND isolates of Vibrio parahaemolyticus. Aquaculture Reports, 2, 158–162.

Department of Fisheries. (2024). Fisheries statistics and information, statistics of shrimp culture. Retrieved from https://www4.fisheries.go.th/local/file_document/20250331145630_1_file.pdf

Han, J.E., Tang, K.F., Pantoja, C.R., White, B.L., &. Lightner, D.V. (2015). qPCR assay for detecting and quantifying a virulence plasmid in acute hepatopancreatic necrosis disease (AHPND) due to pathogenic Vibrio parahaemolyticus. Aquaculture, 442, 12–15.

Hejna, M., Dell’Anno, M., Liu, Y., Rossi, L., Aksmann, A., Pogorzelski, G., & Jóźwik, A. (2024). Assessment of the antibacterial and antioxidant activities of algaederived extracts. Scientific Reports, 14(1), 21044.

Immanuel, G., Sivagnanavelmurugan, M., Marudhupandi, T., Radhakrishnan, S., & Palavesam, A. (2012). The effect of fucoidan from brown algae Sargassum wightii on WSSV resistance and immune activity in shrimp Penaeus monodon (Fab). Fish & Shellfish Immunology, 32(4), 551–564.

James, R., Sampath, K., Thangarathinam, R., & Vasudevan, I. (2006). Effects of dietary Spirulina level on growth, fertility, coloration and leucocyte count in red swordtail, Xiphophorus helleri. Israel Journal of Aquaculture, 58(2), 97–104.

Kanjana, K., Radtanatip, T., Asuvapongpatana, S., Withyachumnarnkul, B. & Wongprasert, K. 2011. Solvent extracts of the red algae Gracilaria fishri prevent Vibrio harveyi infections in the black tiger shrimp Penaeus monodon. Fish & Shellfish Immunology, 30(1), 389–396.

Kizhakkekarammal, P.S., Angel, J.R.J., Thirugnanamurthy, S., Suresh, S., Nathamuni, S., Raja, R.A., ... Kondusamy, A. (2022). Effect of dietary C-Phycocyanin on growth, survival, haematology, immune response, gut microbiome and disease resistance of Pacific white shrimp, Penaeus vannamei. Aquaculture Research, 53(17), 6292–6309.

Klongklaew, N., Praiboon, J., Tamtin, M., & Srisapoome, P. (2021). Chemical composition of a hot water crude extract (HWCE) from Ulva Intestinalis and its potential effects on growth performance, immune responses, and resistance to white spot syndrome virus and yellowhead virus in Pacific white shrimp (Litopenaeus vannamei). Fish & Shellfish Immunology, 112, 8–22.

Li, L., Liu, H., & Zhang, P. (2022). Effect of Spirulina meal supplementation on growth performance and feed utilization in fish and shrimp: A meta-analysis. Aquaculture Nutrition, 2022, 8517733.

Li, X., Ringø, E., Hoseinifar, S.H., Lauzon, H.L., Birkbeck, H., & Yang, D., (2019). The adherence and colonization of microorganisms in fish gastrointestinal tract. Reviews in Aquaculture. 11(3), 603–618.

Luiz, G.A., Diniz, F.M., & Pereira, A.M. (2023). Immunostimulants derived from plants and algae to increase resistance of pacific white shrimp (Litopenaeus vannamei) against vibriosis. Studies in Natural Products Chemistry, 77, 297–337.

Ma, K., Bao, Q., Wu, Y., Chen, S., Zhao, S., Wu, H., & Fan J. (2020). Evaluation of microalgae as immunostimulants and recombinant vaccines for diseases prevention and control in aquaculture. Frontiers in Bioengineering and Biotechnology, 8, 590431.

Nolasco-Alzaga, H.R., Monreal-Escalante, E., Gullian-Klanian, M., de Anda-Montañez, J.A., Luna-González, A., Aranceta, F., ... Angulo, C. (2025). Use of immunostimulants in shrimp farming—A bioeconomic perspective. Animals, 15(2), 124.

Patnaik, S., Samocha, T.M., Davis, D.A., Bullis, R.A., & Browdy, C.L. (2006). The use of HUFA-rich algal meals in diets for Litopenaeus vannamei. Aquaculture Nutrition, 12(5), 395–401.

Poolkhet, C., Boonyawiwat, V., Yaemkasem, S., & Kasornchandra, J. (2023). Post-larvae movement network of marine shrimp during the 2013 outbreak of acute hepatopancreatic necrosis disease in Thailand. Preventive Veterinary Medicine, 210, 105796.

Setyawan, A., Hudaidah, S., & Fidyandini, H.P. (2021). Non-specific immune response of Pacific white shrimp Litopenaeus vannamei by supplementation of sodium alginate of Sargassum collected from Lampung Indonesia. In IOP conference series: Earth and Environmental Science (p. 012015). Bristol, UK: IOP Publishing.

Sivakumar, N., Sundararaman, M., Selvakumarand, G.J.I., & Jo, A.R. (2018). Evaluation of growth performance of Penaeus monodon (Fabricius) fed diet with partial replacement of fishmeal by Spirulina platensis (Sp) meal. Indian Journal of Animal Research, 52(12), 1721–1726.

Thanigaivel, S., Chandrasekaran, N., Mukherjee, A., & Thomas, J. (2016). Algae as an alternative therapeutic source for aquatic disease management. Aquaculture, 464, 529–536.

Tran, L., Nunan, L., Redman, R.M., Mohney, L.L., Pantija, C.R., Fitzsimmons, K. & Lightner, D.V. (2013). Determination of the infectious nature of the agent of acute hepatopancreatic necrosis syndrome affecting penaeid shrimp. Diseases of aquatic organisms, 105(1), 45–55.

Watanuki, H., Ota, K., Tassakka, A.C.M.A., Kato, T., & Sakai, M. (2006). Immunostimulant effects of dietary Spirulina platensis on carp, Cyprinus carpio. Aquaculture, 258(1–4), 157–163.

Yudiati, E., Isnansetyo, A., Murwantoko, Ayuningtyas, Triyanto, & Handayani, C.R. (2016). Innate immune-stimulating and immune genes up-regulating activities of three types of alginates from Sargassum siliquosum in Pacific white shrimp, Litopenaeus vannamei. Fish & Shellfish Immunology, 54, 46–53.

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Published

2025-12-22

How to Cite

Kutako, M., Prueprak, S., Iamsa-ard, P., Watanachote, J., & Sonthi, . M. (2025). Effects of Dietary Algae Supplementation on Growth, Hepatopancreatic Histopathology, and Disease Resistance in Post-Larval White Shrimp (Litopenaeus vannamei). Journal of Food Health and Bioenvironmental Science, 18(3), 261–269. retrieved from https://li01.tci-thaijo.org/index.php/sdust/article/view/266872

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