Hostname: page-component-8448b6f56d-gtxcr Total loading time: 0 Render date: 2024-04-23T16:35:11.968Z Has data issue: false hasContentIssue false

Faecal egg counts and expulsion dynamics of the whipworm, Trichuris trichiura following self-infection

Published online by Cambridge University Press:  17 March 2015

E.P. Hansen
Affiliation:
Section for Parasitology and Aquatic Diseases, Department of Veterinary Disease Biology, University of Copenhagen, Denmark
A.M. Tejedor
Affiliation:
Section for Parasitology and Aquatic Diseases, Department of Veterinary Disease Biology, University of Copenhagen, Denmark
S.M. Thamsborg
Affiliation:
Section for Parasitology and Aquatic Diseases, Department of Veterinary Disease Biology, University of Copenhagen, Denmark
T.V. Alstrup Hansen
Affiliation:
Section for Parasitology and Aquatic Diseases, Department of Veterinary Disease Biology, University of Copenhagen, Denmark
J.F. Dahlerup
Affiliation:
Department of Hepatology and Gastroenterology, Aarhus University Hospital, 8000Aarhus C, Denmark
P. Nejsum*
Affiliation:
Section for Parasitology and Aquatic Diseases, Department of Veterinary Disease Biology, University of Copenhagen, Denmark
*
*E-mail: pn@sund.ku.dk

Abstract

More than 400 million humans are estimated to be infected with the intestinal helminth parasite, Trichuris trichiura. The infection is chronic in nature and high-intensity infection can lead to colitis, anaemia, Trichuris Dysentery Syndrome and reduced cognitive performance. Single doses of 400 mg albendazole or 500 mg mebendazole (MBZ) are used in mass drug administration programmes, but this has been shown to be insufficient. In this study, worm expulsion dynamics are described after MBZ treatment, given as a multi-dose and single-dose treatment in two separate T. trichiura self-infection studies. Worm expulsion dynamics post-treatment showed a similar pattern regardless of the dose regime, with the first worms observed on day 2 and the last worms expelled on days 9 and 13 post-treatment. Establishment of a chronic infection was observed following the inefficient single-dose treatment. The prepatent period was 13–16 weeks in both studies and worms were found to have a lifespan of at least 1 year and 10 months. These self-infection studies provide key information on the chronicity of T. trichiura infections, expulsion dynamics after anthelmintic treatment and the prepatent period, as well as the fecundity of female worms, which was around 18,000 eggs/female per day.

Type
Research Papers
Copyright
Copyright © Cambridge University Press 2015 

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

Bundy, D.A.P. (1986) Epidemiological aspects of Trichuris and trichuriasis in Caribbean communities. Transactions of the Royal Society of Tropical Medicine and Hygiene 80, 706718.Google Scholar
Bundy, D. & Cooper, E. (1989) Trichuris and trichuriasis in humans. Advances in Parasitology 28, 107173.Google Scholar
Bundy, D.A.P., Thompson, D.E., Cooper, E.S. & Blanchard, J. (1985) Rate of expulsion of Trichuris trichiura with multiple and single dose regimens of albendazole. Transactions of the Royal Society of Tropical Medicine and Hygiene 79, 641644.Google Scholar
Horii, Y. & Usui, M. (1985) Experimental transmission of Trichuris ova from monkeys to man. Transactions of the Royal Society of Tropical Medicine and Hygiene 79, 423.Google Scholar
Keiser, J. & Ützinger, J. (2008) Efficacy of current drugs against soil-transmitted helminth infections. Clinician's Corner 299, 19371948.Google Scholar
Nejsum, P., Roepstorff, A., Jørgensen, C.B., Fredholm, M., Göring, H.H.H., Anderson, T.J.C. & Thamsborg, S.M. (2009) High heritability for Ascaris and Trichuris infection levels in pigs. Heredity 102, 357364.CrossRefGoogle ScholarPubMed
Olsen, A., Namwanje, H., Nejsum, P., Roepstorff, A. & Thamsborg, S.M. (2009) Albendazole and mebendazole have low efficacy against Trichuris trichiura in school-age children in Kabale District, Uganda. Transactions of the Royal Society of Tropical Medicine and Hygiene 103, 443446.CrossRefGoogle ScholarPubMed
Pullan, R.L., Smith, J.L., Jasrasaria, R. & Brooker, S.J. (2014) Global numbers of infection and disease burden of soil transmitted helminth infections in 2010. Parasites & Vectors 7, 37.Google Scholar
Roepstorff, A. & Nansen, P. (1998) Epidemiology, diagnosis and control of helminth parasites of swine. Rome, Food and Agriculture Organization (FAO).Google Scholar
Stear, M.J., Bishop, S.C., Doligalska, M., Duncan, J.L., Holmes, P.H., Irvine, J., McCririe, L., McKellar, Q.A, Sinski, E. & Murray, M. (1995) Regulation of egg production, worm burden, worm length and worm fecundity by host responses in sheep infected with Ostertagia circumcincta . Parasite Immunology 17, 643652.Google Scholar
Stear, M.J., Bairden, K., Duncan, J.L., Holmes, P.H., Park, M., McKellar, Q., Strain, A.S., Murray, M., Bishop, S.C. & Gettinby, G. (1997) How hosts control worms. Nature 389, 2728.Google Scholar
Stephenson, L.S., Holland, C.V. & Cooper, E.S. (2000) The public health significance of Trichuris trichiura . Parasitology 121, S73S95.Google Scholar
WHO (2013) Assessing the efficacy of anthelminthic drugs against schistosomiasis and soil-transmitted helminthiasis. Geneva, World Health Organisation.Google Scholar