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Journal of Helminthology Journal of Helminthology

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Monospecific helminth and arthropod infections in an urban population of brown rats from Doha, Qatar

Published online by Cambridge University Press:  22 February 2007

M.A. Abu-Madi ,
J.W. Lewis ,
M. Mikhail ,
M.E. El-Nagger  and
J.M. Behnke
M.A. Abu-Madi*
Affiliation:
Department of Applied Sciences, Faculty of Technology, Qatar University, PO 2713, Doha, Qatar
J.W. Lewis
Affiliation:
School of Biological Sciences, Royal Holloway, University of London, Egham, Surrey, TW20 OEX, UK
M. Mikhail
Affiliation:
Department of Health-Affairs, Ministry of Municipal Affairs and Agriculture, Doha, Qatar: School of Life and Environmental Sciences, University of Nottingham, Nottingham, NG7 2RD, UK
M.E. El-Nagger
Affiliation:
Department of Health-Affairs, Ministry of Municipal Affairs and Agriculture, Doha, Qatar: School of Life and Environmental Sciences, University of Nottingham, Nottingham, NG7 2RD, UK
*
*Fax: 00 974 4655749 E-mail: abumadi:@qu.edu.qa
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Abstract

Parasitic infections were studied for the first time in an urban population of brown rats (Rattus norvegicus) from Doha. Only one species of helminth was found, the cestode Hymenolepis diminuta, and one ectoparasite, the flea Xenopsylla astia, from a sample size of 136 rats (52 males and 84 females). The prevalence of H. diminuta was 17.6%, increasing with host age but not in relation to host sex nor season of capture. Host age was a key factor in influencing abundance of infection, although there was a significant three-way interaction with season and host sex arising through heavy infections in juvenile male rats in the summer. The prevalence of X. astia was 45.6%, although both prevalence and abundance of infestations were season and host age dependent. In the winter prevalence and abundance were similar in both host age and sex groups, but in the summer both parameters of infestation were markedly higher among juveniles compared with adults. We found evidence for some association between these two species: H. diminuta was more prevalent among rats with fleas than among those without, although this association was season-, and independently sex- and age-dependent. There were no quantitative interactions and reasons for this are discussed in relation to the foraging and breeding behaviour of the brown rat in Qatar.

Type
Research Article
Information
Journal of Helminthology , Volume 75 , Issue 4 , December 2001 , pp. 313 - 320
Copyright
Cambridge University Press 2001

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References

Abu-Madi, M.A., Behnke, J.M., Lewis, J.W. & Gilbert, F.S. (1998) Descriptive epidemiology of Heligmosomoides polygyrus in Apodemus sylvaticus from three contrasting habitats in south-east England. Journal of Helminthology 72, 93–100.CrossRefGoogle Scholar
Abu-Madi, M.A., Behnke, J.M., Lewis, J.W. & Gilbert, F.S. (2000) Seasonal and site specific variation in the component community structure of intestinal helminths in Apodemus sylvaticus from three contrasting habitats in south-east England. Journal of Helminthology 74, 7–15.Google ScholarPubMed
Acha, P. & Szyfres, B. (1987) Zoonoses and communicable diseases common to man and animals. 2nd edn. Washington, DC, Pan American Health Organization.Google Scholar
Andreassen, J., Bennet-Jenkin, E.M. & Bryant, C. (1999) Immunology and biochemistry of Hymenolepis diminuta. Advances in Parasitology 42, 223–275.CrossRefGoogle ScholarPubMed
Behnke, J.M., Barnard, C., Hurst, J.L., McGregor, P.K., Gilbert, F. & Lewis, J.W. (1993) The prevalence and intensity of infection with helminth parasites in Mus spretus from the Setubal Peninsula of Portugal. Journal of Helminthology 67, 115–122.CrossRefGoogle ScholarPubMed
Behnke, J.M., Lewis, J.W., Mohd, Zain, S.N. & Gilbert, F.S. (1999) Helminth infections in Apodemus sylvaticus in southern England: interactive effects of host-age, sex and year on prevalence and abundance of infections. Journal of Helminthology 73, 31–44.Google ScholarPubMed
Behnke, J.M., Barnard, C., Mason, N., Harris, P.D., Sherif, N.E., Zalat, S. & Gilbert, F.S. (2000) Intestinal helminths of spiny mice (Acomys cahirinus dimidiatus) from St. Katherine's Protectorate in the Sinai, Egypt. Journal of Helminthology 74, 31–43.Google ScholarPubMed
Brooks, J.E. & Rowe, F.P. (1987) Vector control series: rodents, training and information guide.World Health Organization,Google Scholar
Bundy, D.A.P. (1988) Gender-dependent patterns of infection and disease. Parasitology Today 4, 186–189.CrossRefGoogle Scholar
Chomel, B.B. (1992) Zoonoses of house pets other than dogs, cats and birds. Paediatric Infectious Diseases Journal 11, 479–487.CrossRefGoogle ScholarPubMed
Crawley, M.T. (1993G) GLIM for ecologists. Oxford, Blackwell Scientific Press.Google Scholar
Dash, K.M., Hall, E. & Barger, I.A. (1988) The role of arithmetic and geometric mean worm egg counts in faecal egg count reduction tests and in monitoring strategic drenching programs in sheep. Australian Veterinary Journal 65, 66–68.CrossRefGoogle Scholar
De Clercq, D., Sacko, M., Behnke, J.M., Gilbert, F., Dorny, P. & Vercruysse, J. (1997) Failure of mebendazole in treatment of human hookworm infections in the Southern Region of Mali. American Journal of Tropical Medicine and Hygiene 57, 25–30.CrossRefGoogle ScholarPubMed
Elliott, J.M. (1977) Some methods for the statistical analysis of samples of benthic invertebrates. Cumbria, UK, Freshwater Biological Association.Google Scholar
Erhardova-Kotrla, B. & Daniel, M. (1970) Parasitic worms of small mammals from the region of the mountain regions of the Eastern Hindu Kush. Folia Parasitologica 17, 201–206.Google Scholar
Fahmy, M.A.M., Rifaat, M.A. & Arafa, M.S. (1969) Helminthic infection of the brown rat, Ruttus norvegicus (Berkenhout, 1769) in U.A.R.. Journal of the Egyptian Public Health Association 46, 147–153.Google Scholar
Greenberg, Z. (1969) Helminths of mammals and birds of Israel I. Helminths of Acomys spp. (Rodentia, Murinae). Israel Journal of Zoology 18, 25–38.Google Scholar
Gregory, R.D. (1992) On the interpretation of host-parasite ecology: Heligmosomoides polygyrus (Nematoda) in wild wood mouse (Apodemus sylvaticus) populations. Journal of Zoology 226, 109–121.CrossRefGoogle Scholar
Haukisalmi, V., Henttonen, H. & Tenora, F. (1988) Population dynamics of common are rare helminths in cyclic vole populations. Journal of Animal Ecology 57, 807–825.CrossRefGoogle Scholar
Healing, T.D. & Nowell, F. (1985) Diseases and parasites of woodland rodent populations. Symposia of the Zoological Society of London 55, 193–218.Google Scholar
Kansouh, A.S., El-Zemaity, M.S. & Mikhail, M.W. (1990) Population density of domestic rodents and associates fleas at Dahshour, Giza governorate. Annals of Agricultural Science 35, 543–550.Google Scholar
Kisielewska, K. (1970) Ecological organization of intestinal helminth groupings in Clethrionomys glareolus (Schreb.) (Rodentia). V. Some questions concerning helminth groupings in the host individuals. Acta Parasitologica Polonica 17, 197–208.Google Scholar
Lewis, J.W. (1968) Studies on the helminth parasites of the long-tailed field mouse, Apodemus sylvaticus from Wales. Journal of Zoology 154, 287–312.CrossRefGoogle Scholar
Lewis, J.W. (1987) Helminth parasites of British rodents and insectivores. Mammal Review 17, 81–93.CrossRefGoogle Scholar
Lewis, J.W. & Twigg, G.I. (1972) A study of the internal parasites of small rodents from woodland areas in Surrey. Journal of Zoology 166, 61–77.CrossRefGoogle Scholar
Mafiana, C.F., Osho, M.B., Sam-Wobo, S. (1997) Gastrointestinal helminth parasites of the black rat (Rattus rattus) in Abeokuta, southwest Nigeria. Journal of Helminthology 71, 217–220.CrossRefGoogle ScholarPubMed
Margolis, L., Esch, G.W., Holmes, J.C., Kuris, A.M. & Schad, G.A. (1982) The use of ecological terms in parasitology (report of an ad hoc committee of The American Society of Parasitologists). Journal of Parasitology 68, 131–133.CrossRefGoogle Scholar
Montgomery, S.S.J. & Montgomery, W.I. (1990) Structure, stability and species interactions in helminth communities of wood mice Apodemus sylvaticus. International Journal for Parasitology 20, 225–242.CrossRefGoogle ScholarPubMed
Morris, P. (1972) A review of mammalian age determination methods. Mammal Review 2, 69–104.CrossRefGoogle Scholar
Myers, B.J., Kuntz, R.E. & Wells, W.H. (1962) Helminth parasites of reptiles, birds, and mammals in Egypt VII. Check list of nematodes collected from 1948 to 1955. Canadian Journal of Zoology 40, 531–538.CrossRefGoogle Scholar
Poulin, R. (1993) The disparity between observed and uniform distribution: a new look at parasite aggregation. International Journal for Parasitology 23, 937–944.CrossRefGoogle Scholar
Read, C.P. (1967) Longevity of the tapeworm, Hymenolepis diminuta. Journal of Parasitology 53, 1055–1056.CrossRefGoogle ScholarPubMed
Rifaat, M.A., Mohammed, A.H.H., Mahdi, A.H. & Arafa, M.S. (1969) Some observations on ectoparasites infesting domestic and commensal rodents in U.A.R.. Journal of the Egyptian Public Health Association 44, 97–118.Google ScholarPubMed
Seng, L.T., Liat, L.B., Fong, Y.L. & Krishnasamy, M. (1979) Parasite fauna of the house rat Rattus rattus diardii in Kuala Lumpur and nearby villages. Southeast Asian Journal of Tropical Medicine and Public Health 10, 122–126.Google Scholar
Seong, J.K., Huh, S., Lee, J.S. & Oh, Y.S. (1995) Helminths in Rattus norvegicus in Chunchon, Korea. Korean Journal of Parasitology 33, 235–237.CrossRefGoogle ScholarPubMed
Sinniah, B. (1979) Parasites of some rodents in Malaysia. Southeast Asian Journal of Tropical Medicine and Public Health 10, 115–121.Google ScholarPubMed
Tena, D., Simon, M.P., Gimeno, C., Pomata, M.T.P., Illescas, S., Amondarain, I., Gonzalez, A., Dominguez, J. & Bisquert, J. (1998) Human infection with Hymenolepis diminuta: case report from Spain. Journal of Clinical Microbiology 36, 2375–2376.Google ScholarPubMed
Udonsi, J.K. (1989) Helminth parasites of wild populations of the black rat, Rattus rattus (L.), from urban, rural residential and other ecological areas of Nigeria. Acta Parasitologica Polonica 34, 107–116.Google Scholar
Webster, J.P. & Macdonald, D.W. (1995) Parasites of wild brown rats (Rattus norvegicus) on UK farms. Parasitology 111, 247–255.CrossRefGoogle ScholarPubMed
Welch, J.S. (1972) Parasitology field studies. Twenty Seventh Annual Report for the Queensland Institute of Medical Research, Brisbane (1971) Volume 24.Google Scholar
Werthein, G. & Greenberg, Z. (1970) Notes on helminth parasites of myomorph rodents from Southern Sinai. Journal of Helminthology 44, 243–252.CrossRefGoogle Scholar
Zakaria, M. & Zaghloul, T.M. (1982) Parasitic infection of Rattus norvegicus in Kuwait. Proceedings of the First Symposium on Recent Advances in Rodent Control, Kuwait 136–143.Google Scholar
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