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2020 | 30 | 2 | 150-168
Article title

Immune response of shrimp Peneaus monodon against Vibrio parahaemolyticus

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Abstracts
EN
The study was carried out on impact of vibriosis by using Vibrio parahaemolyticus in Peneaus monodon Fabricius, 1798, collected from Nagapattinam. The impact was studied on heamatological and biochemical parameters. Feeds were prepared by coating probiotic strains of B. firmus and B. coagulans. Laboratory investigations were carried out concerning impact of pathogenic Vibrio parahaemolyticus of total count, differential count, Nitroblue tetrazolium activity, Prophenoloxidase activity and bacterial clearance in P. monodon. Total heamocyte was enumerated in vibriosis by induced shrimps, all results showing an increase in total haemocyte count after the time of infection. After feeding, the total heamocyte count was 1442 cells/cu·mm in control animals, in B. coagulans supplemented animals 2757 cells/cu.mm and in B. firmus was 2448 cell/cu·mm. After feed supplementation the shrimps were infected with V. parahaemolyticus and their impact on total haemocyte count was assessed in all three groups. In control, the total haemocyte count was increased with 2560 cells/cu·mm, whereas in B. coagulansis 5126 cells/cu·mm, and in B. firmusis 4697cells/cu·mm. Two-way Analysis of Variance for total haemocyte count in normal and infected haemolymph showed a significant variation. The control samples recorded the lowest, and after infection B. coagulans supplemented animals recorded maximum counts among three groups. Differential count was evaluated by studying the three types of cells. There was not much variation in the percentage of cells, but a slight decrease was observed in the hyaline cells after 24 hours of infection. The NBT activity was 1.4 (NBT activity) in control animals, 2.7 in B. coagulans and 2.4 in B. firmus supplemented animals. Maximum reduction was observed in control animals with 0.92, 1.7 in B. coagulans and 1.4 in B. firmus supplemented animals. There was an initial spurt of vibrios when cultured in selective medium TCBS in all three treatments and gradual decrease in the vibrios count during 24 hours observation.
Discipline
Year
Volume
30
Issue
2
Pages
150-168
Physical description
Contributors
  • Department of Zoology, Periyar E.V.R College, Tiruchirappalli – 620 023, Tamil Nadu, India
author
  • Department of Zoology, Periyar E.V.R College, Tiruchirappalli – 620 023, Tamil Nadu, India
  • Center of Advanced Study in Marine Biology, Faculty of Marine Sciences, Annamalai University, Parangipettai - 608 502, Tamil Nadu, India
  • Department of Zoology, St. Joseph University, Virgin Town, Ikishe, Model Village, Dimapur – 797 115 Nagaland, India
author
  • Department of Zoology, St. Joseph University, Virgin Town, Ikishe, Model Village, Dimapur – 797 115 Nagaland, India
References
  • [1] Johansson MW and K Soderhall (1989) Cellular immunity in crustacean and the proPo system. Parasitology Today 5: 171-176
  • [2] Bachere E, Mialhe E and Rodrigvez J (1995) Identification of defense effectors in the hemolymph of crustaceans with particular reference to the shrimp Penaeus japonicus (Bate): prospects and application. Fish Shellfish Immunol 5: 597-612
  • [3] Smith JV and K Soderhall (1983) Inductionofdeganulation and lysis of haemocytes in the fresh water crayfish, Astacusastacus by components of the prophenoloxidase activating system in vitro. Cell and Tissue Research 233: 295-303
  • [4] Bell KL and Smith VJ (1993) Invitro superoxide production by hyaline cells of the shore crab Carcinusmaenas (L.). Dev Comp Immunol 17: 211-219
  • [5] Arakawa T (1995) Superoxide generative reaction in insect haemolymphandits mimic model system with surfactants in vitro. Insect Biochem Molec Biol 25: 247-253
  • [6] Nappi AJ, E Vass, F Frey and Y Carton (1995) Superoxide generation in Drosophila during melanotic encapsulation of parasites. Eur J Cell Biol 68: 450-456
  • [7] Soderhall K and Cerenius L (1998) Role of the prophenolooxidase-activating system in invertebrate immunity. Curr Opin Immunol 10: 23-28
  • [8] Dikkeboom R, van der Knaap WPW and Meuleman EA (1987) Hemocytes of the pond snail Lymnaeas tagnalis generate reactive forms of oxygen. J Inverteber Pathol 49: 321-331
  • [9] Adema C, Van der Knaap, Sminia WPW (1991) Molluscan haemocyte medicated cytotoxicity the role of reactive oxygen intermediates. Rev Aquat Sci 4: 204-223
  • [10] Larson KG, Roberson BS and Hetrick FM (1989) Effect of environmental pollutants on the chemiluminescence of hemocytes from the American oyster Crassostreavirginica. Dis Aquat Org 6: 131-136
  • [11] Bachere E, Noel T and Mialhe E (1991) Effects of environmental pollutants and chemotherapeutic agents on the chemiluminescence of the hemocytes from the oyster Crassosfreagiges. Eur Aquacult Soc Spec. Publ Dublin 14-15
  • [12] Hervio D, Bachere E, Mialhe E and Grizel H (1989) Chemiluminescent responses of ostrea edulis and Creassastreagigashemocytes to Bonamiaostrea (Aseetospora). Dev Comp Immunol 13 (4): 449
  • [13] Smith VJ and NA Rateliffe (1980) Cellular defence reaction of the shore crab, Carcinusmaenas (L): in vive hemocytic and histopathological responses to injected bacteria. Journal of Invertebrate Pathology 35: 65-74
  • [14] Song YL and Heich YT (1994) Immunostimulation of tiger Shrimp (Penaeus monodon) hemocytes for generation of microbicidal substances: analysis of reactive oxygen species. Dev Comp Immunol 18(3): 201-209
  • [15] Song YL, Cheng W and CH Wang (1993) Isolation and characterization of Vibrio damsela infections for cultured shrimp in Taiwan. Journal of Invertebrate Pathology 61: 24-31
  • [16] Kreger AS (1984) Cytolytic activity and virulence of Vibrio damsela. Infection and Immunity 44: 326-331
  • [17] Tsing A, Arcier JM and M Brehelin (1989) Haemocytes of penaeids and palaemonidshrimps: morphology, cytochemistry and hemograms. Journal of Invertebrate Pathology 53: 64-77
  • [18] Martin GG, Hose JE, Omori S, Chong C, Hoodbho T and N Mckrell (1991) Localization and roles of coagulation and transglutaminase in hemolymph coagulation in decapod crustanceans. Comparative Bio chemistry, and Physiology 100: 517-522
  • [19] Anderson IG, Shamsudin MN, Shariff M and Nash G (1988) Bacterial septicemia in juvenile tiger shrimp, Peneaus monodonculture in Malaysian brackish water ponds. Asian Fisheries science 2(1): 93-108
  • [20] Persson M, Cerenices L and K Soderhall (1987) The influence of haemocyte number on the disease resistance of the resh water crayfish Pacifastaacusleniusculus Dana, to the parasitic fungus Aphanomycesastaci. Journal of fish Diseases 10: 471-477
  • [21] Smith VJ and Johnston PA (1992) Differential haemotoxic effect of PCB congeners in the common shrimp. Crangon crangon. Comp Biochem Physiol 101: 641-649
  • [22] Le Moullac G and Haffner P (2000) Environmental factors affecting immune responses in Crustacea. Aquaculture 191: 121-131
  • [23] Cheng W and Chen JC (2001) Effects of intrinsic and extrinsic factors on the haemocyte profile of the prawn, Macrobrachium rosenbergii. Fish Shellfish Immunol 11: 53-63
  • [24] Cheng TC (1988) In vivo effects of heavy metals on cellular defence mechanisms of Crassostreavirginica: Total and differential cell counts. J Invertebr Pathol 51: 215-220
  • [25] Suresh K and A Mohandass (1990) Effect of sublethal concentrations of copper on haemocyte number in bivalves. J Inverteber Pathol 55: 325-331
  • [26] Martin GG, Hose JE, Minka G and S Rosen berg (1996) Clearance of bacteria injected in to the hemolymph of the ridgeback prawn, Sicyoniaingentis (Crustacea: Decapoda): role of the hematopoietic tissue. Journal of Morphology 227: 227-233
  • [27] Anggraeni MS and Owens L (2000) The haemocytic of lymphoid organ spheroid cells in the penacid prawn Penaeus monodon. Diseases of Aquatic organisms 40: 85-92
  • [28] Alday-Sanz V, Roque A and Turn bull JF (2002) Clearance mechanisms of vireo vulnificus biotype in the black tiger shrimp, Penaeus monodon. Diseases of Aquatic Organisms, 11; 48(2): 91-9
  • [29] Factor JR and M Naar (1990) The digestive system of the lobster, Homarusamaricanus: II: Terminal hepatic arterioles of the disgestive gland. Journal of Morphology 206: 283-291
  • [30] Johnson PT (1987) A review of fixed phayocytic and pinocytotic cell of decapod crustaceans, with remarks on hemocytes. Developmental and Comparative Immunology 11: 679-704.
  • [31] Johnson PT (1980) Histology of the blue crab Callinectessapidus.A model for the Decapoda. New York: Praeger 440.
  • [32] Oka M (1969) Studies on Penaeus Orientolis Kishinouye-VIII. Structure of the newly found lymphoid organ. Bulletin of the Japanese Society of Scientific Fisheries 35: 245-250
  • [33] Martin GG, Hose JE and JJ Kim (1987) Structure of hematopoietic nodules in the ridgback prawn, Sicyoniaingentis: light and electron microscopic observation. Journal of Morphology 192: 193-204
  • [34] Hose JE, Martin GG, Tiu S and N Mekrell (1992) pattern of hemocyte production and release throughout the molt cycle in the penaeid shrimp Sicyoniaingentis. Biological Bulletin 183: 185-199
  • [35] Ven de Braak CBT, Botterblom MHA, Taverne N, Van der knaap WPW and JHWM Robout (2002) The role of the haematopoietic tissue in haemocyte production and maturation in the black tiger shrimp (Penaeus monodon). Fish & Shell fish immunology, 12: 253-272
  • [36] Johnson PT (1976) Bacterial infection in the blue crab, Callinectessapiduscarse of infection and histopathology. Journal of invertebrate pathology 28: 25-36
  • [37] Fontaine CT and DV Lightner (1974) Observations on the phagocytosis and climination o fcarmine particles in to the abdominal musculature of the white shrimp, Penaeus setiferus. Journal of Invertebrate Pathology 24: 141-148
  • [38] Cornick JW and JE Stewart (1968) Interaction of the pathogen Gaffkyahomari with natural agglutinin. Journal of the Fisheries Research Board of Canada 25: 695-709.
  • [39] Factor JR and J Beckman (1990) The digestive system of the lobster, Homarusamaricanus: III. Removal of foreign particles from the blood by fixed phayocytes of the digestive gland. Journal of morphology 206: 293-302.
  • [40] Rahmayani, Herman Hamdani, Junianto, A. Mahdiana Izza, Difference Effect of Mouth Width Size and Operating Depth of Sodo (Push net) on the Catch of Rebon Shrimp (Acetes indicus H. Milne Edwards, 1830) in Tanah Kuning Waters, North Kalimantan, Indonesia. World Scientific News 133 (2019) 121-131
  • [41] Karunasagar I, Otta SK and Karunasagar (1996) Application of Vibrio vaccine in shrimp culture. Fish chimes 16: 49-50.
  • [42] Song YL and Sung HH (1990) Enhancement of growth in tiger shrimp (Penaeus monodon) by bacteria prepared from Vibrio vulnificus. Bull Eur Assoc pathol 10: 98-99.
  • [43] Holmblad T and Soderhall K (1999) Cell adhesion molecules and antioxidative enzymes in a crustacean, possible role in immunity. Aquaculture 172: 117-123
  • [44] Le Moullac G, Soyez C, Saulnier D, Ansquer D, Avarre JC and Levy P (1998) Effect of hypoxia stress on the immune responseand the resistance to vibriosis of the shrimp Penaeus stylirostris. Fish Shellfish Immunol 8: 621-629
  • [45] Cheng W, Liu CH, Hsu JP and Chen JC (2002) Effect of hypoxia on the immune response of giant freshwater prawn Macrobrachium rosenbergiiand its susceptibility to pathogen Enterococcus. Fish Shellfish Immunol 13: 351-365
  • [46] Cheng W and Chen JC (2002) The virulence of Enterococcus to freshwater prawn Macrobrachium rosenbergiiand its immuneresistance under ammonia stress. Fish Shellfish Immunol 12: 97-109.
  • [47] Seralathan Janani, Abdul Salam Asaraf Ali, Selva Mohan Harshini, Balaraman Deivasigamani, Pitchai Sampathkumar, Sadasivam Senthil Kumar (2017) Evaluation of toxicity reduction in textile effluent by different treatment protocols involving marine diatom Odontella aurita on freshwater fish Labeo rohita. Journal of Water Process Engineering, 20: 232-242
  • [48] Marcelo Munoz, Ricardo Cedeno, Jenny Rodríguez, Wil P.W van der Knaap, Eric Mialhe and Evelyne Bachere (2000) Measurement of reactive oxygen intermediate production in Haemocytes of the Penaeid shrimp. Penaeus Vannamei, 193 (1-3): 87-107
Document Type
article
Publication order reference
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YADDA identifier
bwmeta1.element.psjd-65528233-f3fc-4546-822f-0816b6962694
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