Phagocytic response and phenoloxidase activity of the hemocytes of Bellamya bengalensis exposed to synthetic fenvalerate

Автор: Mukherjee S., Mandal Ch.

Журнал: Журнал стресс-физиологии и биохимии @jspb

Статья в выпуске: 3 т.19, 2023 года.

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Background: Bellamya bengalensis is an important bioresource of the freshwater ecosystem of India. This edible mollusc is filter feeder, indigenous diet of human, poultry and fishery. Natural habitat of this freshwater gastropod mollusc bears the risk of contamination by agricultural pesticide fenvalerate, a synthetic type II pyrethroid. Hemocytes are the immuno effector cells of molluscs which are affected by environmental toxins or pathogenic microorganisms. Hemocytes perform various types of immunological functions such as phagocytosis, cytotoxic response etc. Results: Experimental exposure of fenvalerate resulted in impairment of phagocytic efficacy and alteration in the generation of phenoloxidase in B. bengalensis. Conclusion: The alteration of phagocytic response and generation of phenoloxidase of hemocytes, exposed to experimental concentrations of fenvalerate under static laboratory condition have been determined to establish as biomarker of aquatic toxicity in toxin contaminated natural habitat.

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Fenvalerate, mollusc, phagocytosis, phenoloxidase

Короткий адрес: https://sciup.org/143180561

IDR: 143180561

Список литературы Phagocytic response and phenoloxidase activity of the hemocytes of Bellamya bengalensis exposed to synthetic fenvalerate

  • Adema C.M., Vander Knaap W.P.W. and Sminia, T. (1991) Molluscan hemocytes mediated cytotoxicity: role of reacting oxygen intermediates. Crit. Rev. Aquat.Sci, 4, 201- 223.
  • Anderson R. S. (1993) Modulation of nonspecific immunity by environmental stressors. In: Advances in Fisheries Science J. A. Couch and J. W. Fournie (ed.), Pathobiology of Marine and Estuarine Organisms London: CRC Press, pp. 483-510.
  • Auffret M., Mujdzic, N., Corporeau C. and Moraga D. (2002) Xenobiotic induced immunomodulation in the European flat oyster, Ostrea edulis. Mar. Environ. Res., 54, 585-589.
  • Baby R.L., Hasan I., Kabir K.A. and Naser, M.N. (2010) Nutrient analysis of some commercially important molluscs of Bangladesh. J. Sci. Res., 2(2), 390396.
  • Carballal M. J., Lopez C., Azevedo C. and Villalba A. (1997) In vitro study of phagocytic ability of Mytilus galloprovincialis Lmk. hemocytes. Fish Shellfish Immunol., 7, 403-416.
  • Cerenius L. and Soderhall K. (2004) The prophenoloxidase activating system in invertebrates. Immunol. Rev., 198, 116-126.
  • Chakraborty S., Ray M. and Ray, S. (2009) Evaluation of phagocytic activity and nitric oxide generation by molluscan hemocytes as biomarkers of inorganic arsenic exposure. Biomarkers., 14(8), 539-546.
  • Cima, F., Matozzo, V., Marin, M. G. and Ballarin, L. (2000) Hemocytes of the clam Tapes philippinarum (Adams and Reeve, 1850): morphofunctional characterization. Fish Shellfish Immunol., 10, 677693.
  • Elssner A., Carter J.E., Yunger T.M. and Wewers, M.D. (2004) HIV-1 infection does not impair human alveolar macrophage phagocytic function unless combined with cigarette smoking. Chest., 125, 1071-1076.
  • Gielens C. (2006) Location of intrinsic and inducible phenoloxidase activity in molluscan hemocyanin. Biochem. Biophy. Res. Com., 348, 1138-1144.
  • Gonzalez A.L., Martinez M.A.N., Albores F.V., Valle F.A., and Mungaray M.R. (2003) Phenoloxidase activity in larval and juvenile homogenates and adult plasma and hemocytes of bivalve molluscs. Fish Shellfish Immunol., 15, 275-282.
  • Lacoste A., Malham S.K., Cueff A., Jalabert F., Gelebart F. and Poulet S.A. (2001) Evidence for a form of adrenergic response to stress in the mollusc Crassostrea gigas. J. Exp. Biol., 204, 1247-1255.
  • Muñoz P., Meseguer J. and Ángeles Esteban M. (2006) Phenoloxidase activity in three commercial bivalve species. changes due to natural infestation with Perkinsus atlanticus. Fish Shellfish Immunol., 20, 12-19.
  • Nappi A. J. and Christensen B. M. (2005) Melanogenesis and associated cytotoxic reactions: applications to insect innate immunity. Insect Biochem. Mol. Biol., 35, 443 - 459.
  • Oliver L.M. and Fisher W.S. (1999) Appraisal of prospective bivalve immunomarkers. Biomarker., 4, 510-530.
  • Prabhakar A.K. and Roy, S.P (2009) Ethnomedicinal uses of some shellfishes by people of Kosi river basin in North Bihar, India. Ethno. Med., 3(1), 1-4.
  • Rao N.V.S. and Dey A. (1989) Freshwater molluscs in aquaculture. In: Director (ed.), Handbook: Freshwater molluscs of India. Zool. Surv. India., pp, 225-82.
  • Raut S.K. (1991) Laboratory rearing of medically and economically important molluscs. In M. S. Jalpaiguri (ed.), Snails, flukes and man.. Z. S. I. Pub, pp.79-83.
  • Ray D.E. and Forshaw P.J. (2000) Pyrethroid insecticides: poisoning syndromes, synergies, and therapy. Clin. Toxicol., 38 (2), 95-101.
  • Ray M., Bhunia A.S., Bhunia N.S. and Ray, S. (2013) Density shift, morphological damage, lysosomal fragility and apoptosis of hemocytes of Indian molluscs exposed to pyrethroid pesticides. Fish Shellfish Immunol., 35, 499-512.
  • Sinderman C.J. (1984) Fish and environmental impacts. Arch. Fisch Wiss. Berlin., 35, 125-160.
  • Singh M. and Narkhede S.D. (2012) Role of fenvalerate on growth and yield of cotton (Gossypium hirsutum L.). Sc. Res. Re., 2(3), 281-285.
  • Sminia T. (1972) Structure and function of blood and connective tissue cells of the freshwater pulmonate Lymnaea stagnalis studies by electron microscopy and enzyme histochemistry. Z. Zellforsch. Mikrosk. Anat., 130, 497-526.
  • Sung H.H., Chang H.J., Her C.H., Chang, J.C. and Song, Y.L. (1998) Phenoloxidase activity of hemocytes derived from Penaeus monodon and Macrobrachium rosenbergii. J.Invertebr.Pathol.,7, 26-33.
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