Haemolymph Components of Infected & None Infected Lymnaea snails with Xiphidiocercariae
Abstract
Background: In this study the haemolymph components of infected and none infected Lymnaea gedrosiana with xiphidiocercaria larvae was compared.
Methods: Five hundred Fifty Lymnaea snails were collected from Ilam and Mazandaran provinces, Iran, during 2008-2009. The snails were transported to the lab at Tehran University of Medical Sciences and their cercarial sheddings were studied. Haemolmyphs of snails were extracted and cells were counted using haemocytometer and cell-surface carbohydrate were recognized by conjugated lectin (Lentil). Haemolymph protein concentrations were measured by Bradford protein assay method and soluble protein compositions were determined on sodium dodecyl sulphate polyacrilamide gel electrophoresis (SDS-PAGE).
Result: From the 550 examined Lymnaea snails for cercariae, 27 snails were infected with xiphidiocercariae. Mean of haemolymph cells (haemocyte) number were obtained 93480±2.43 (cells/ml) for none infected snails (25 snail) and 124560±2800 (cells/ml) for infected snails (25 snail). Mannose carbohydrate was recognized on haemocyte of none infected and infected snails. Mean of protein concentration of haemolymph plasma was obtained as 1354 ± 160 μg/ml (1.4 mg/ml) for none infected snails (25 snails) and 1802±138 μg/ml (1.8 mg/ml) for infected snail (25 snails). Comparing to none infected snails, the SDS-PAGE results of haemolymph plasma of infected snails, showed an extra protein band (70 kDa). The results showed a significant difference between the amounts and the kinds of proteins in haemolymph of infected and none infected snails.
Conclusion: This information might be useful to understand of parasite detection, adhesion, engulfment and antigen agglutination by snail.
Chingwena G, Mukaratirwa S, Kristensen TK, Chimbari M. Larval trematode infections in freshwater snails from the Highveld and Lowveld areas of Zimbabwe . J Helminthology.2002; 76: 283–293.
Bezerra JCB, Becker W, Zelck UE. A comparative study of the organic acid content of the hemolymph of schistosoma mansoni-resistant and susceptible strains of biomphalaria glabrata. Mem Inst Oswaldo Cruz, Rio de Janeiro. 1997; 92(3): 421-425.
Rupprecht H, Becker W, Schwanbek A. Alterations in hemolymph components in Biomphalaria glabrata during longterm infection with Schistosoma mansoni. Parasitol Res. 1989; 75(3):233-7.
Loker ES. Alterations in Biomphalaria glabrata plasma induced by infection with the digenetic trematode Echinostoma paraensei. J Parasitol. 1987; 73(3):503-13.
Farahnak A, Dabagh N. Adhesion of Cercaria (Larva of Helminth Parasites) to Host by Lectins- carbohydrates bonds as a Model for Evaluation of Schistosoma Entrance Mechanisms in Cercarial Dermatitis. Iranian J Publ Health. 2008; 37(2): 59-63.
Stewart CS. The Trematodes. M.C. Dubuque, Iowa: Brown Company Publisher; 1970.
Malek ETA. Laboratory guide and notes for medical malacology. Minneapolis: Burgess Pub. Co.; 1962.
Caprette DR. Experimental bioscience; Laboratory methods: Using a Counting Chamber [online]; 2007. Available from: http://www.ruf.rice.edu/~bioslabs/meth ods/microscopy/cellcounting.html.
Maizels RM, Blaxter ML, Robertson BD, Selkirk ME. Parasite antigen and parasite genes: A laboratory manual for molecular parasitology.1st ed. Cambridge: Cambridge University Press; 1991,pp 93-94.
Moema EB, King PH, Baker C. Cercariae developing in Lymnaea natalensis Krauss, 1848 collected in the vicinity of Pretoria, Gauteng Province, South Africa. J Vet Res. 2008; 75(3):215-23.
Narayanan R, Venkateswararao P. Effect of xiphidiocercarial infection on oxidation of glycolytic and Krebs cycle intermediates in Lymnaea luteola (Mollusca). J Invertebr Pathol.1980; 36(1): 21-24.
Reddy BR, Rao PV. Effect of xiphidiocercarial infection on the purine nucleotide cycle activity in the freshwater pulmonate snail, Lymnaea luteola. J Invertebr Pathol.1992; 60(2): 117-120.
El-Emam MA, Ebeid FA. Effect of Schistosoma mansoni infection, starvation and molluscicides on acid phosphate, transaminases and total protein in tissues and hemolymph of Biomphalaria alexandrina. J Egypt Soc Parasitol. 1989; 19(1):139-47.
Sminia T, Knaap W. The internal defence system of the freshwater snail. Developmental & Comparative Immunology. 1981; 5, Supplement 1: 87-97.
Mohamed AH. Characterization of surface lectins binding and SDS-PAGE protein patterns of Biomphalaria alexandrina haemocytes infected with Schistosoma mansoni. J Egypt Soc Parasitol. 2005; 35(2):615-30.
Weis WI, Drickamer K. Structural basis of lectin-carbohydrate recognition. Annu Rev Biochem. 1996; 65:441-73.
Amen RI, Tijnagel JM, Knaap WPW, Meuleman EA, Klerk ES, Sminia T. Effects of Trichobilharzia ocellata on hemocytes of Lymnaea stagnalis. Dev Comp Immunol. 1991; 15(3):105-15.
Knaap WPW, Doderer A, Boerrigter- Barendsen H, Sminia T. Some Properties of an Agglutinin in the Haemolymph of the Pond snail Lymnaea stagnalis. Biol bull.1982; 162: 404-412.
Horák P, Knaap WPW. Lectins in snail-trematode immune interactions: a review. FoliaParasitológica.1997; 44:161-172.
Files | ||
Issue | Vol 6 No 1 (2011) | |
Section | Articles | |
Keywords | ||
Cercaria Lymnaea Haemolymph Xiphidiocercariae |
Rights and permissions | |
This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License. |