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Potential interactions between metazoan parasites of the Mayan catfish Ariopsis assimilis and chemical pollution in Chetumal Bay, Mexico

Published online by Cambridge University Press:  12 April 2024

V.M. Vidal-Martínez ,
M.L. Aguirre-Macedo ,
E. Noreña-Barroso ,
G. Gold-Bouchot  and
P.I. Caballero-Pinzón
V.M. Vidal-Martínez*
Affiliation:
Laboratories of Parasitology and Marine Geochemistry, Center for Research and Advanced Studies, National Polytechnic Institute (CINVESTAV-IPN), Carretera Antigua a Progreso Km. 6, C.P. 97310 Mérida, Yucatan, Mexico. Laboratory of Parasitology, Faculty of Natural Sciences, Autonomous University of Queretaro, A.P. 184 Cerro de las Campanas, 76010 Santiago de Querétaro, Querétaro, Mexico.
M.L. Aguirre-Macedo
Affiliation:
Laboratories of Parasitology and Marine Geochemistry, Center for Research and Advanced Studies, National Polytechnic Institute (CINVESTAV-IPN), Carretera Antigua a Progreso Km. 6, C.P. 97310 Mérida, Yucatan, Mexico.
E. Noreña-Barroso
Affiliation:
Laboratories of Parasitology and Marine Geochemistry, Center for Research and Advanced Studies, National Polytechnic Institute (CINVESTAV-IPN), Carretera Antigua a Progreso Km. 6, C.P. 97310 Mérida, Yucatan, Mexico.
G. Gold-Bouchot
Affiliation:
Laboratories of Parasitology and Marine Geochemistry, Center for Research and Advanced Studies, National Polytechnic Institute (CINVESTAV-IPN), Carretera Antigua a Progreso Km. 6, C.P. 97310 Mérida, Yucatan, Mexico.
P.I. Caballero-Pinzón
Affiliation:
Centro de Estudios Tecnológicos del Mar No.10 (CETMAR Chetumal) Boulevard Bahía s/n, 77010 Chetumal, Quintana Roo, Mexico.
*
* Fax: ++52 (999) 9812334 E-mail: [email protected].
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Abstract

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The effect of pollutants on the intensity of infection of metazoan parasites in the Mayan catfish, Ariopsis assimilis was investigated. Data were collected on pollutants and metazoan parasites from 76 catfish from five localities in Chetumal Bay in October, 1996. Nineteen pollutants (pesticides, polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs)) were found in the catfish livers. Heavy metal content was not determined. Nineteen metazoan parasite species were recovered. After controlling for fish length and sampling station, there was a significant negative linear relationship between the intensity of the larval digenean Mesostephanus appendiculatoides and 1,1,1,-trichloro-2,2-bis (4-chlorophenyl) ethane (DDT) concentrations. This negative relationship may be explained either by the effect of the pesticide on the mortality of (i) free-living larval forms, (ii) metacercariae in the fish, (iii) infected fish or (iv) intermediate host snails. There were significant differences between fish parasitized and not parasitized with M. appendiculatoides with respect to their DDT concentrations. There were also significant differences between the variances of the mean Clark's coefficient of condition values between catfish parasitized and not parasitized by M. appendiculatoides, with the variance of non-parasitized catfish being significantly larger. The results provided statistical evidence that DDT has a detrimental effect on M. appendiculatoides infection intensity. Furthermore, the significantly larger variance value of Clark's coefficient for non-parasitized fish suggested that DDT affects both the parasite and general host condition.

Type
Research Article
Information
Journal of Helminthology , Volume 77 , Issue 2 , June 2003 , pp. 173 - 184
Copyright
Copyright © Cambridge University Press 2003

References

Babicek, K. & Danek, J. (1993) Method verification and tests on the efficacy of antihelmintics against immature stages of Fasciola hepatica in laboratory mice. Veterínarni Medícina 36, 51–56.Google Scholar
Bielecki, A. (1985) Influence of phoschlorine, carbadox and copper sulfate on infectivity of Fasciola hepatica larvae. Wiadomości Parazytologiczne 31, 3–25.Google Scholar
Bush, A.O., Lafferty, K.D., Lotz, J.M. & Shostak, A.W. (1997) Parasitology meets ecology on its own terms: Margolis et al. revisited. Journal of Parasitology 83, 575–583.CrossRefGoogle Scholar
D'Amelio, S. & Gerasi, L. (1997) Evaluation of environmental deterioration by analysing fish parasite biodiversity and community structure. Parassitologia 39, 237–242.Google ScholarPubMed
Deustche Gesellschaft für Technische Zusammenarbeit (1995) Catalogue of environmental standards Vol. III. Bundesminister für Wirtschafltiliche Zusammenarbeit und Entwicklung, Eschborn, Germany.Google Scholar
Dušek, L., Gelnar, M. & Šebelová, S. (1998) Biodiversity of parasites in a freshwater environment with respect to pollution: metazoan parasites of chub (Leuciscus cephalus L.) as a model for statistical evaluation. International Journal for Parasitology 28, 1555–1571.CrossRefGoogle Scholar
Gelnar, M., Šebelová, Š., Dušek, L., Koubková, B., Jurajda, P. & Zahrádková, S. (1997) Biodiversity of parasites in freshwater environment in relation to pollution. Parassitologia 39, 189–199.Google ScholarPubMed
Goater, C.P. & Holmes, J.C. (1997) Parasite-mediated natural selection. pp. 9–29 in Clayton, D.H. & Moore, J. (Eds) Host-parasite evolution, general principles and avian models. Oxford, Oxford University Press.CrossRefGoogle Scholar
Gupta, S.C. & Yadav, S.C. (1993) Efficacy of closantel against immature Fasciola gigantica infection in the rabbit. Indian Veterinary Journal 70, 1003–1004.Google Scholar
Holmes, J.C. & Zohar, S. (1990) Pathology and host behaviour. pp. 34–63 in Barnard, C. & Behnke, J.M. (Eds) Parasitism and host behaviour. Oxford, Oxford University Press.Google Scholar
Hudson, P.J. & Dobson, A.P. (1995) Host-parasite processes and demographic consequences. pp. 155–173 in Clayton, D.H. & Moore, J. (Eds) Host-parasite evolution, general principles and avian models. Oxford, Oxford University Press.Google Scholar
INEGI, (1998) Anuario Estadístico del Estado de Quintana Roo. México City, Instituto Nacional de Estadística, Geografía e Informática y Gobierno del Estado de Quintana Roo.Google Scholar
Iwama, G.K. & Greer, G.L. (1980) Effect of a bacterial infection on the toxicity of sodium pentachlorophenate to juvenile coho salmon. Transactions of the American Fisheries Society 109, 290–292.2.0.CO;2>CrossRefGoogle Scholar
Jongman, R.H.G., teer Braak, C.J.F. & van Tongeren, O.F.R. (1995) Data analysis in community and landscape ecology. Cambridge, Cambridge University Press.CrossRefGoogle Scholar
Kennedy, C.R. (1997) Freshwater fish parasites and environmental quality: an overview and caution. Parassitologia 39, 249–254.Google ScholarPubMed
Kumar, A., Deb, A.R., Ansari, M.Z. & Sahai, B.N. (1992) Control of snail vectors of amphistomiasis with various indigenous products. Indian Journal of Animal Sciences 62, 129–131.Google Scholar
Lafferty, K.D. (1997) Environmental parasitology: what can parasites tell us about human impacts on the environment? Parasitology Today 13, 251–255.CrossRefGoogle ScholarPubMed
Lafferty, K.D. & Kuris, A.M. (1999) How environmental stress affects the impacts of parasites. Limnology and Oceanography 44, 925–931.CrossRefGoogle Scholar
Lemly, A.D. & Esch, G.W. (1984) Effects of the trematode Uvulifer ambloplitis on juvenile bluegill sunfish, Lepomis macrochirus: ecological implications. Journal of Parasitology 70, 475–492.CrossRefGoogle Scholar
MAFF/ADAS (1988) A manual of veterinary parasitology. Reference Book 418, Ministry of Agriculture, Fisheries and Food, London, HMSO.Google Scholar
MacKenzie, K., Williams, H.H., Williams, B., McVicar, A.H. & Siddall, R. (1995) Parasites as indicators of water quality and the potential use of helminth transmission in marine pollution studies. Advances in Parasitology 35, 86–144.Google ScholarPubMed
Marcogliese, D.J., Nagler, J.J. & Cyr, D.G. (1998) Effects of exposure to contaminated sediments on the parasite fauna of American plaice (Hipoglossoides platessoides). Bulletin of Environmental Contamination and Toxicology 61, 88–95.CrossRefGoogle Scholar
Moles, A. (1980) Sensitivity of parasitised coho salmon fry to crude oil, toluene, and naphthalene. Transactions of the American Fisheries Society 109, 293–297.2.0.CO;2>CrossRefGoogle Scholar
Morley, N.J., Crane, M. & Lewis, J.W. (2001) Toxicity of cadmium and zinc to Diplostomum spathaceum (Trematoda: Diplostomidae) cercarial survival. International Journal for Parasitology 31, 1211–1217.CrossRefGoogle ScholarPubMed
Mukherjee, R.P. (1973) Toxicity of certain chemicals on the larval stages of some amphistomes of domesticated animals. Indian Veterinary Journal 50, 1076–1082.Google Scholar
Noreña-Barroso, E., Zapata-Pérez, O., Ceja-Moreno, V. & Gold-Bouchot, G. (1998) Hydrocarbon and organochlorine residue concentrations in sediments from Bay of Chetumal, Mexico. Bulletin of Environmental Contamination and Toxicology 61, 80–87.CrossRefGoogle Scholar
Noreña-Barroso, E., Simá-Álvarez, R., Gold-Bouchot, G. & Zapata-Pérez, O. Persistent organic pollutants and histological lesions in Mayan catfish Ariopsis assimilis from the bay of Chetumal, Mexico. Marine Pollution Bulletin (in press).CrossRefGoogle Scholar
Pascoe, D. & Cram, P. (1977) The effect of parasitism on the toxicity of cadmium to the three-spined stickleback, Gasterosteus aculeatus L. Journal of Fish Biology 10, 467–472.CrossRefGoogle Scholar
Qian, G. & Pin, N. (2000) Lead content in the monogenean Ancyrocephalus mogurndae and in different organs of its host, the mandarin fish Siniperca chuasi . China Environmental Science 20, 233–236.Google Scholar
Sagerup, K., Henrikssen, E.O., Skorping, A., Skaare, J.U. & Gabrielsen, G.W. (2000) Intensity of parasitic nematodes increases with organochlorine levels in the glaucous gull. Journal of Applied Ecology 37, 532–539.CrossRefGoogle Scholar
Salgado-Maldonado, G. & Kennedy, C.R. (1997) Richness and similarity of helminth communities in the tropical cichlid fish Cichlasoma urophthalmus from the Yucatan Peninsula, Mexico. Parasitology 114, 581–590.Google Scholar
Salgado-Maldonado, G., Pineda-López, R.F., Vidal-Martínez, V.M. & Kennedy, C.R. (1997) A checklist of the metazoan parasites of cichlid fish from Mexico. Journal of the Helminthological Society of Washington 64, 195–207.Google Scholar
Sarot, D.A. & Perlmutter, A. (1976) The toxicity of zinc to the immune system response of the zebra fish Brachydanio rerio, injected with viral and bacterial antigens. Transactions of the American Fisheries Society 105, 456–459.2.0.CO;2>CrossRefGoogle Scholar
Sericano, J.L., Atlas, E.L., Wade, T.L. & Brooks, J.M. (1990) NOAA's status and trends mussel watch program: chlorinated pesticides and PCBs in oysters (Crassostrea virginica) and sediments from the Gulf of Mexico, 1986–1987. Marine and Environmental Research 29, 161–203.CrossRefGoogle Scholar
Siddall, R. & Des Clers, S. (1995) Effect of sewage sludge on the miracidium and cercaria of Zoogonoides viviparus (Trematoda: Digenea). Helminthologia 31, 143–153.Google Scholar
Sokal, R.R. & Rohlf, F.J. (1981) Biometry. 2nd edn. San Francisco, California, W.H. Freeman and Company.Google Scholar
Soucek, D.J. & Noblet, G.P. (1998) Copper toxicity to the endoparasitic trematode (Posthodiplostomum minimum) relative to physid snail and bluegill sunfish intermediate hosts. Environmental Toxicology and Chemistry 17, 2512–2516.CrossRefGoogle Scholar
Sures, B. & Taraschevski, H. (1995) Cadmium concentrations in two adult acanthocephalans, Pomporhynchus laevis and Acanthocephalus lucii, as compared to their fish hosts and cadmium and lead levels in larvae of A. lucii as compared with their crustacean host. Parasitology Research 81, 494–497.CrossRefGoogle ScholarPubMed
Sures, B., Taraschevski, H. & Rokicki, J. (1997) Lead and cadmium contents of two cestodes, Monobothrium wageneri and Bothriocephalus scorpii, and their fish hosts. Parasitology Research 83, 618–623.CrossRefGoogle ScholarPubMed
Sures, B., Siddall, R. & Taraschevski, H. (1998) Parasites as accumulation indicators of heavy metal pollution. Parasitology Today 15, 16–21.CrossRefGoogle Scholar
ter Braak, C.J.F. & Šmilauer, P. (1998) CANOCO reference manual and user's guide to CANOCO for Windows: software for Canonical Community Ordination (version 4). New York, Microcomputer Power.Google Scholar
Valtonen, E.T., Holmes, J.C. & Koskivaara, M. (1997) Eutrophication, pollution, and fragmentation: effects on parasite communities in roach (Rutilus rutilus) and perch (Perca fluviatilis) in four lakes in central Finland. Canadian Journal of Fisheries and Aquatic Sciences 54, 572–585.CrossRefGoogle Scholar
Varma, T.K., Malviya, H.C., Prasad, A. & Dwidevi, P. (1994) Effect of physicochemical factors upon hatching of different species of paramphistome eggs. Journal of Veterinary Parasitology 8, 31–34.Google Scholar
Vidal-Martínez, V.M., Aguirre-Macedo, M.L. & Kennedy, C.R. (1998) The structuring process of the macroparasite community of an experimental population of Cichlasoma urophthalmus through time. Journal of Helminthology 72, 199–207.CrossRefGoogle ScholarPubMed
Wade, T.L., Brooks, J.L., Kennicutt II, M.C., McDonald, T.J., Sericano, J.L. & Jackson, T.J. (1993) GERG trace organic contaminant analytical techniques. In Sampling and analytical methods of the National Status and Trends Program, National Benthic Surveillance and Mussel Watch projects 1984–1992, Vol. IV. NOAA Technical Memorandum NOS ORCA 71, 121–139.Google Scholar