Hostname: page-component-76fb5796d-45l2p Total loading time: 0 Render date: 2024-04-27T03:25:37.157Z Has data issue: false hasContentIssue false

Heavy metal concentrations in the freshwater snail Biomphalaria alexandrina uninfected or infected with cercariae of Schistosoma mansoni and/or Echinostoma liei in Egypt: the potential use of this snail as a bioindicator of pollution

Published online by Cambridge University Press:  28 May 2013

O.M.S. Mostafa
Affiliation:
Biology Department, Faculty of Science, King Khaled University, PO Box 9004, Abha, Saudi Arabia Zoology Department, Faculty of Science, Ain Shams University, Abbassia 11566, Cairo, Egypt
A.-T.H. Mossa*
Affiliation:
Environmental Toxicology Research Unit (ETRU), Pesticide Chemistry Department, National Research Centre, Tahrir Street, PO Box 12311, Dokki, Cairo, Egypt
H.M.A. El Einin
Affiliation:
Medical Malacology Department, Theodor Bilharz Research Institute, PO Box 30, Imbaba, Giza, Egypt
*
*Fax: (202)-33370931 E-mail: abdeltawab.mossa@yahoo.com

Abstract

In spite of using aquatic snails as bioindicators for water pollution, little attention has been paid to the effect of parasitism upon the concentration of heavy metals (Al, Cd, Cu, Fe, Mn, Pb and Zn) in these organisms. The present study therefore aimed to compare the concentrations of heavy metals in trematode-infected Biomphalaria alexandrina collected from Kafer Alsheikh and Menofia provinces, Egypt, with uninfected snails from the same sites, in order to assess the effect of parasitism on the use of these snails as bioindicators. The concentrations of heavy metals in the soft parts and shells of snails were measured by flame atomic absorption spectrometry. The results showed that the heavy metal profile in snails infected with Echinostoma liei was very different from that in snails infected with Schistosoma mansoni. The total concentration of heavy metals in E. liei-infected snails collected from Kafer Alsheikh or Menofia province was greater than in uninfected snails. In contrast, the total concentration of heavy metals in S. mansoni-infected snails was reduced compared with uninfected snails. In conclusion, the status of snails with respect to parasitic infection must be taken into consideration when these snails are used as bioindicators.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2013 

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Abd Allah, A.T., Wanas, M.Q.S. & Thompson, S.N. (1997) Effects of heavy metals on survival and growth of Biomphalaria glabrata Say (Gastropoda: Pulmonata) and interaction with schistosome infection. Journal of Molluscan Studies 63, 7986.Google Scholar
Abdel-Shafy, H.I., Abo-El-Wafa, O. & Azzam, A.M. (1987) Role of fertilizer wastewater on the contamination of Ismailia Canal by heavy metals. International Conference on Heavy Metals in the Environment, New Orleans, pp. 454456.Google Scholar
Aisemberg, J., Nahabedian, D.E., Wider, E.A. & Guerrero, N.R.V. (2005) Comparative study on two freshwater invertebrates for monitoring environmental lead exposure. Toxicology 210, 4553.Google Scholar
Ansaldo, M., Nahabedian, D.E., Di Fonzo, C. & Wider, E.A. (2009) Effect of cadmium, lead and arsenic on the oviposition, hatching and embryonic survival of Biomphalaria glabrata. Science of the Total Environment 407, 19231928.CrossRefGoogle ScholarPubMed
Elder, J.F. & Collins, J.J. (1991) Freshwater molluscs as indicators of bioavailability and toxicity of metals in surface-water systems. Reviews of Environmental Contamination and Toxicology 22, 3779.Google Scholar
Evans, D.W., Irwin, S.W.B. & Fitzpatrick, S. (2001) The effect of digenean (Platyhelminthes) infections on heavy metal concentration in Littorina littorea. Journal of the Marine Biological Association of the United Kingdom 81, 349350.Google Scholar
Gabrashanska, M., Damyanova, A. & Kanev, I. (1991) Mineral compostion of Echinostoma revolutum (Froelich, 1802) and its host Lymnaea stagnalis (L.). Khelminthologia 31, 37(in Bulgarian with English summary).Google Scholar
Hassan, A.H. (2008) Effects of digenean larval infection on metallic ions of the shells and soft parts of their intermediate host snail Lanistes carinatus. Journal of the Egyptian Society of Parasitology 38, 805812.Google Scholar
Hoang, T.C. & Rand, G.M. (2009) Exposure routes of copper: short term effects on survival, weight, and uptake in Florida apple snails (Pomacea paludosa). Chemosphere 76, 407414.Google Scholar
Kaufer, S.W., Chejlava, M., Fried, B. & Sherma, J. (2002) Effects of Euhaplorchis californiensis (Trematoda) infection on metallic ions in the host snail Cerithidea californica (Gastropoda). Parasitology Research 88, 10801082.Google Scholar
Layman, L.R., Dory, A.C., Koehnlein, K.M., Fried, B. & Sherma, J. (1996) Effects of Echinostoma trivolvis (Trematoda) infection on metallic ions in the host snail Helisoma trivolvis (Gastropoda). Parasitology Research 82, 1921.CrossRefGoogle ScholarPubMed
Ma, T.W., Zhu, C., Wang, G.Y., Zhou, K., Peng, J.Y. & Liu, J. (2010) Bioaccumulation of sediment heavy metals in Bellamya aeruginosa and its relations with the metals geochemical fractions. Ying Yong Sheng Tai Xue Bao 21, 734742.Google Scholar
Marcogliese, D.J. & Pietrock, M. (2011) Combined effects of parasites and contaminants on animal health: parasites do matter. Trends in Parasitology 27, 123130.Google Scholar
Morley, N.J., Crane, M. & Lewis, J.W. (2002) Toxic effects of cadmium and zinc on the transmission of Echinoparyphium recurvatum cercariae. Journal of Helminthology 76, 157163.Google Scholar
Morley, N.J., Crane, M. & Lewis, J.W. (2004) Influence of cadmium exposure on the incidence of first intermediate host encystment by Echinoparyphium recurvatum cercariae in Lymnaea peregra. Journal of Helminthology 78, 329332.CrossRefGoogle ScholarPubMed
Mostafa, O.M.S. (2008) Effects of Fasciola gigantica experimental infection on some inorganic elements in the snail host Lymnaea natalensis. Experimental Parasitology 118, 468471.Google Scholar
Mostafa, O.M.S. & Dajem, S.M. (2010) Effects of Schistosoma mansoni experimental infection on some inorganic elements in the snail host Biomphalaria alexandrina. Journal of the Egyptian Society of Parasitology 40, 197204.Google ScholarPubMed
Mostafa, O.M.S., Bakry, F.A., Sleem, S.H. & El-Dafrawy, S.M. (2001) The influence of Schistosoma mansoni and/or Echinostoma liei infection on the tissue soluble proteins of Biomphalaria alexandrina. Egyptian Journal of Zoology 37, 3343.Google Scholar
Ong, J.H.L., Chejlava, M., Fried, B., Koehnlein, K.M., Bosavage, G.L. & Sherma, J. (2004) Effects of Schistosoma mansoni infection on inorganic elements in the snail Biomphalaria glabrata. Journal of Helminthology 78, 343346.Google Scholar
Pokora, Z., Szilman, P. & Pokora, I. (1993) Histochemical estimation of zinc accumulation in hepato-pancreatic gland cells of the snail Lymnaea stagnalis (L.) after subacute poisoning with zinc acetate considering infection with Digenea larvae. Wiadomości Parazytologiczne 39, 225232.Google Scholar
Salice, C.J. & Roesijadi, G. (2002) Resistance to cadmium and parasite infection are inversely related in two strains of a freshwater gastropod. Environmental Toxicology and Chemistry 21, 13981403.Google Scholar
Siwela, A.H., Nyathi, C.B. & Naik, Y.S. (2010) A comparison of metal levels and antioxidant enzymes in freshwater snails, Lymnaea natalensis, exposed to sediment and water collected from Wright Dam and Lower Mguza Dam, Bulawayo, Zimbabwe. Ecotoxicology and Environmental Safety 73, 17281732.Google Scholar
Soliman, M.F.M. (2009) Fasciola gigantica: cercarial shedding pattern from Lymnaea natalensis after long-term exposure to cadmium at different temperatures. Experimental Parasitology 121, 307311.CrossRefGoogle ScholarPubMed
Spatz, L., Vidigal, T.H.D.A., Silva, M.C.A., Cappa, S.M.G. & Carvalho, O.S. (2000) Characterization of Biomphalaria orbignyi, B. peregrina and B. oligoza by polymerase chain reaction and restriction enzyme digestion of the internal transcribed spacer region of the RNA ribosomal gene. Memórias do Instituto Oswaldo Cruz 95, 807814.Google Scholar
Sullivan, J.T. & Palmieri, J.R. (1979) Effect of duration and intensity of infection with Echinostoma audyi on survival of Lymnaea rubiginosa exposed to copper sulfate. Journal of Parasitology 65, 5054.Google Scholar
Sures, B. (2006) How parasitism and pollution affect the physiological homeostasis of aquatic hosts. Journal of Helminthology 80, 151157.Google Scholar
Vidigal, T.H., Spatz, L., Nunes, D.N., Simpson, A.J.G., Carvalho, O.S. & Neto, E.D. (1998) Biomphalaria sp. Identification of the intermediate snail hosts of Schistosoma mansoni by polymerase chain reaction amplification and restriction enzyme digestion of the ribosomal RNA gene intergenic spacer. Experimental Parasitology 89, 180187.Google Scholar
Vidigal, T.H., Caldeira, R.L., Simpson, A.J.G. & Carvalho, O.S. (2000) Further studies on the molecular systematics of Biomphalaria snails from Brazil. Memórias do Instituto Oswaldo Cruz 95, 5766.Google Scholar