Acknowledgement
This study was carried out with support of Research on technology to discriminated damage from natural disasters of aquaculture organisms (R2023041) of National Institute of Fisheries Science (NIFS).
References
- Alexander CG, Hindley JPR. The mechanism of food ingestion by the banana prawn, Penaeus merguiensis. Mar Behav Physiol. 1985;12:33-46. https://doi.org/10.1080/10236248509378631
- Bae SH, Kim BR, Kang BJ, Tsutsui N, Okutsu T, Shinji J, et al. Molecular cloning of prophenoloxidase and the effects of dietary β-glucan and rutin on immune response in hemocytes of the fleshy shrimp, Fenneropenaeus chinensis. Fish Shellfish Immunol. 2012;33:597-604. https://doi.org/10.1016/j.fsi.2012.06.034
- Brune DE, Schwartz G, Eversole AG, Collier JA, Schwedler TE. Intensification of pond aquaculture and high rate photosynthetic systems. Aquac Eng. 2003;28:65-86. https://doi.org/10.1016/S0144-8609(03)00025-6
- Chen JC, Ting YY, Lin JN, Lin MN. Lethal effects of ammonia and nitrite on Penaeus chinensis juveniles. Mar Biol. 1990;107:427-31. https://doi.org/10.1007/BF01313424
- Cox SL, Jeffs AG, Davis M. Developmental changes in the mouthparts of juvenile Caribbean spiny lobster, Panulirus argus: implications for aquaculture. Aquaculture. 2008;283:168-74. https://doi.org/10.1016/j.aquaculture.2008.07.019
- Cox SL, Johnston DJ. Developmental changes in foregut functioning of packhorse lobster, Jasus (Sagmariasus) verreauxi (Decapoda : Palinuridae), phyllosoma larvae. Mar Freshw Res. 2004;55:145-53. https://doi.org/10.1071/MF03175
- Crab R, Chielens B, Wille M, Bossier P, Verstraete W. The effect of different carbon sources on the nutritional value of bioflocs, a feed for Macrobrachium rosenbergii postlarvae. Aquac Res. 2010;41:559-67. https://doi.org/10.1111/j.1365-2109.2009.02353.x
- Crab R, Defoirdt T, Bossier P, Verstraete W. Biofloc technology in aquaculture: beneficial effects and future challenges. Aquaculture. 2012;356-357:351-6. https://doi.org/10.1016/j.aquaculture.2012.04.046
- Crain JA. Functional morphology of prey ingestion by Placetron wosnessenskii Schalfeew zoeae (Crustacea: Anomura: Lithodidae). Biol Bull. 1999;197:207-18. https://doi.org/10.2307/1542616
- Ekasari J, Azhar MH, Surawidjaja EH, Nuryati S, De Schryver P, Bossier P. Immune response and disease resistance of shrimp fed biofloc grown on different carbon sources. Fish Shellfish Immunol. 2014;41:332-9. https://doi.org/10.1016/j.fsi.2014.09.004
- Factor JR. Morphology of the mouthparts of larval lobsters, Homarus americanus (Decapoda: Nephropidae), with special emphasis on their setae. Biol Bull. 1978;154:383-408. https://doi.org/10.2307/1541067
- Farmer AS. The functional morphology of the mouthparts and pereiopods of Nephrops norvegicus (L.) (Decapoda: Nephropidae). J Nat Hist. 1974;8:121-42. https://doi.org/10.1080/00222937400770091
- Garm A. Mechanical functions of setae from the mouth apparatus of seven species of decapod crustaceans. J Morphol. 2004a;260:85-100. https://doi.org/10.1002/jmor.10213
- Garm A. Revising the definition of the crustacean seta and setal classification systems based on examinations of the mouthpart setae of seven species of decapods. Zool J Linn Soc. 2004b;142:233-52. https://doi.org/10.1111/j.1096-3642.2004.00132.x
- Gorman MJ, Paskewitz SM. Serine proteases as mediators of mosquito immune responses. Insect Biochem Mol Biol. 2001;31:257-62. https://doi.org/10.1016/S0965-1748(00)00145-4
- Hargreaves JA. Photosynthetic suspended-growth systems in aquaculture. Aquac Eng. 2006;34:344-63. https://doi.org/10.1016/j.aquaeng.2005.08.009
- Hobbie JE, Daley RJ, Jasper S. Use of nucleopore filters for counting bacteria by fluorescence microscopy. Appl Environ Microbiol. 1977;33:1225-8. https://doi.org/10.1128/aem.33.5.1225-1228.1977
- Hu Q, Lu J. Preliminary analysis of the relation of growth of Penaeus orientalis Kishinouye with environmental factors. Donghai Mar Sci. 1990;8:58-62.
- Huang TS, Wang H, Lee SY, Johansson MW, Soderhall K, Cerenius L. A cell adhesion protein from the crayfish Pacifastacus leniusculus, a serine proteinase homologue similar to Drosophila masquerade. J Biol Chem. 2000;275:9996-10001. https://doi.org/10.1074/jbc.275.14.9996
- Huang X, Zhou H, Zhang H. The effect of Sargassum fusiforme polysaccharide extracts on vibriosis resistance and immune activity of the shrimp, Fenneropenaeus chinensis. Fish Shell-fish Immunol. 2006;20:750-7. https://doi.org/10.1016/j.fsi.2005.09.008
- Janeway CA Jr, Medzhitov R. Innate immune recognition. Annu Rev Immunol. 2002;20:197-216. https://doi.org/10.1146/annurev.immunol.20.083001.084359
- Jang IK, Jun JC, Jo GJ, Cho YR, Seo HC, Kim BL, et al. Polyculture of fleshy shrimp Fenneropenaeus chinensis and white shrimp Litopenaeus vannamei with river puffer Takifugu obscurus in shrimp ponds. J Aquac. 2007;20:278-88.
- Jang IK, Meng XH, Seo HC, Cho YR, Kim BR, Ayyaru G, et al. A TaqMan real-time PCR assay for quantifying white spot syndrome virus (WSSV) infections in wild broodstock and hatchery-reared postlarvae of fleshy shrimp, Fenneropenaeus chinensis. Aquaculture. 2009;287:40-5. https://doi.org/10.1016/j.aquaculture.2008.10.038
- Jang IK, Pang Z, Yu J, Kim SK, Seo HC, Cho YR. Selectively enhanced expression of prophenoloxidase activating enzyme 1 (PPAE1) at a bacteria clearance site in the white shrimp, Litopenaeus vannamei. BMC Immunol. 2011b;12:70.
- Jang IK, Suriakala K, Kim JS, Meng XH, Choi TJ. A TaqMan real-time PCR assay for quantifying type III hepatopancreatic parvovirus infections in wild broodstocks and hatchery-reared postlarvae of Fenneropenaeus chinensis in Korea. J Microbiol Biotechnol. 2011a;21:1109-15. https://doi.org/10.4014/jmb.1107.07009
- Jiang H, Wang Y, Yu XQ, Zhu Y, Kanost M. Prophenoloxidase-activating proteinase-3 (PAP-3) from Manduca sexta hemolymph: a clip-domain serine proteinase regulated by serpin-1J and serine proteinase homologs. Insect Biochem Mol Biol. 2003;33:1049-60. https://doi.org/10.1016/S0965-1748(03)00123-1
- Jimenez-Vega F, Vargas-Albores F, Soderhall K. Characterisation of a serine proteinase from Penaeus vannamei haemocytes. Fish Shellfish Immunol. 2005;18:101-8. https://doi.org/10.1016/j.fsi.2004.02.001
- Johnston DJ, Alexander CG. Functional morphology of the mouthparts and alimentary tract of the slipper lobster Thenus orientalis (Decapoda: Scyllaridae). Mar Freshw Res. 1999;50:213-23. https://doi.org/10.1071/MF98089
- Kent M, Browdy CL, Leffler JW. Consumption and digestion of suspended microbes by juvenile Pacific white shrimp Litopenaeus vannamei. Aquaculture. 2011;319:363-8. https://doi.org/10.1016/j.aquaculture.2011.06.048
- Kim SK, Guo Q, Jang IK. Effect of biofloc on the survival and growth of the postlarvae of three penaeids (Litopenaeus vannamei, Fenneropenaeus chinensis, and Marsupenaeus japonicus) and their biofloc feeding efficiencies, as related to the morphological structure of the third maxilliped. J Crustacean Biol. 2015;35:41-50. https://doi.org/10.1163/1937240X-00002304
- Kim SK, Jang IK, Kim SR, Jeon JC, Kim SK. Effects of artificial substrates on the growth and immunology of postlarvae of Marsupenaeus japonicus (Spence Bate, 1888) (Decapoda: Dendrobranchiata: Penaeidae) reared in biofloc. J Crustacean Biol. 2021;41:ruab044.
- Kim SK, Pang Z, Seo HC, Cho YR, Samocha T, Jang IK. Effect of bioflocs on growth and immune activity of Pacific white shrimp, Litopenaeus vannamei postlarvae. Aquac Res. 2014;45:362-71. https://doi.org/10.1111/are.12319
- Kirchman D, Sigda J, Kapuscinski R, Mitchell R. Statistical analysis of the direct count method for enumerating bacteria. Appl Environ Microbiol. 1982;44:376-82. https://doi.org/10.1128/aem.44.2.376-382.1982
- Kunze J, Anderson DT. Functional morphology of the mouthparts and gastric mill in the hermit crabs Clibanarius taeniatus (Milne Edwards), Clibanarius virescens (Krauss), Paguristes squamosus McCulloch and Dardanus setifer (Milne-Edwards) (Anomura: Paguridae). Mar Freshw Res. 1979;30:683-722. https://doi.org/10.1071/MF9790683
- Lee SY, Lee BL, Soderhall K. Processing of crayfish hemocyanin subunits into phenoloxidase. Biochem Biophys Res Commun. 2004;322:490-6. https://doi.org/10.1016/j.bbrc.2004.07.145
- Lee SY, Soderhall K. Characterization of a pattern recognition protein, a masquerade-like protein, in the freshwater crayfish Pacifastacus leniusculus. J Immunol. 2001;166:7319-26. https://doi.org/10.4049/jimmunol.166.12.7319
- Liltved H, Cripps SJ. Removal of particle-associated bacteria by prefiltration and ultraviolet irradiation. Aquac Res. 1999;30:445-50. https://doi.org/10.1046/j.1365-2109.1999.00349.x
- Livak KJ, Schmittgen TD. Analysis of relative gene expression data using real-time quantitative PCR and the 2-ΔΔCT method. Methods. 2001;25:402-8. https://doi.org/10.1006/meth.2001.1262
- Loker ES, Adema CM, Zhang SM, Kepler TB. Invertebrate immune systems: not homogeneous, not simple, not well understood. Immunol Rev. 2004;198:10-24. https://doi.org/10.1111/j.0105-2896.2004.0117.x
- McConaugha J. Alternative feeding mechanisms in megalopae of the blue crab Callinectes sapidus. Mar Biol. 2002;140:1227-33. https://doi.org/10.1007/s00227-002-0781-1
- Medzhitov R, Janeway C Jr. Innate immune recognition: mechanisms and pathways. Immunol Rev. 2000;173:89-97. https://doi.org/10.1034/j.1600-065X.2000.917309.x
- Meng XH, Jang IK, Seo HC, Cho YR. A TaqMan real-time PCR assay for survey of white spot syndrome virus (WSSV) infections in Litopenaeus vannamei postlarvae and shrimp of farms in different grow-out seasons. Aquaculture. 2010;310:32-37. https://doi.org/10.1016/j.aquaculture.2010.10.010
- Nishida S, Quigley BD, Booth JD, Nemoto T, Kittaka J. Comparative morphology of the mouthparts and foregut of the final-stage phyllosoma, puerulus, and postpuerulus of the rock lobster Jasus edwardsii (Decapoda: Palinuridae). J Crustacean Biol. 1990;10:293-305. https://doi.org/10.2307/1548488
- Rawlings ND, Barrett AJ. Families of cysteine peptidases. Methods Enzymol. 1994;244:461-86. https://doi.org/10.1016/0076-6879(94)44034-4
- Ray AJ, Lewis BL, Browdy CL, Leffler JW. Suspended solids removal to improve shrimp (Litopenaeus vannamei) production and an evaluation of a plant-based feed in minimal-exchange, super intensive culture systems. Aquaculture. 2010;299:89-98. https://doi.org/10.1016/j.aquaculture.2009.11.021
- Samocha TM, Patnaik S, Speed M, Ali AM, Burger JM, Almeida RV, et al. Use of molasses as carbon source in limited discharge nursery and grow-out systems for Litopenaeus vannamei. Aquac Eng. 2007;36:184-91. https://doi.org/10.1016/j.aquaeng.2006.10.004
- Shi XZ, Zhao XF, Wang JX. Molecular cloning and expression analysis of chymotrypsin-like serine protease from the Chinese shrimp, Fenneropenaeus chinensis. Fish Shellfish Immunol. 2008;25:589-97. https://doi.org/10.1016/j.fsi.2008.07.011
- Sriphaijit T, Flegel TW, Senapin S. Characterization of a shrimp serine protease homolog, a binding protein of yellow head virus. Dev Comp Immunol. 2007;31:1145-58. https://doi.org/10.1016/j.dci.2007.03.005
- Suthers IM. Functional morphology of the mouthparts and gastric mill in Penaeus plebejus Hess (Decapoda : Penaeidea). Aust J Mar Freshw Res. 1984;35:785-92. https://doi.org/10.1071/MF9840785
- Tyler ER, Adams S, Mallon EB. An immune response in the bumblebee, Bombus terrestris leads to increased food consumption. BMC Physiol. 2006;6:6.
- Zhang MM, Xu Y, Kim S, Wu Q, Qi Z, Pang Z, et al. Molecular characterization, structure and expression analysis of a Ras-related nuclear (Ran) gene in white shrimp, Litopenaeus vannamei. Int J Agric Biol. 2019;21:11-8