Literature DB >> 3601446

Potential value of localized skin reactions (chancres) induced by Trypanosoma congolense transmitted by Glossina morsitans centralis for the analysis of metacyclic trypanosome populations.

R H Dwinger, M Murray, S K Moloo.   

Abstract

Goats infected with Trypanosoma congolense transmitted by Glossina morsitans centralis and then treated with the trypanocidal drug diminazene aceturate are immune to tsetse-transmitted infection with a homologous, but not heterologous trypanosome clone. Immune animals fail to develop localized skin reactions (chancres) and do not become infected, whereas on heterologous challenge chancres appear followed by parasitaemia. In this study, the feasibility of using chancre reactions to characterize several different metacyclic populations of T. congolense was evaluated. Provided goats were immunized, it was found that the chancre reaction could be used to distinguish different populations of T. congolense. However, problems were encountered when attempts were made to induce immunity against more than one trypanosome population. When goats were infected by tsetse flies with four antigenically unrelated metacyclic populations of T. congolense, either simultaneously or at 4 day intervals, adequate immunological priming was not always achieved. In fact, goats exposed to superinfection 8 to 12 days after a primary infection did not develop chancres or an immune response to the second infection (although they were immune to the organism used for primary infection). Following trypanocidal treatment these animals were subsequently completely susceptible to homologous infection with the metacyclic population used for superinfection, indicating that some form of interference phenomenon effective at the level of the skin appears to prevent or delay the development of the second trypanosome population following superinfection of infected animals.

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Year:  1987        PMID: 3601446     DOI: 10.1111/j.1365-3024.1987.tb00513.x

Source DB:  PubMed          Journal:  Parasite Immunol        ISSN: 0141-9838            Impact factor:   2.280


  8 in total

1.  Parasite-specific T-cell responses of trypanotolerant and trypanosusceptible cattle during infection with Trypanosoma congolense.

Authors:  J N Flynn; M Sileghem; D J Williams
Journal:  Immunology       Date:  1992-04       Impact factor: 7.397

2.  The role of the macrophage in induction of immunosuppression in Trypanosoma congolense-infected cattle.

Authors:  J N Flynn; M Sileghem
Journal:  Immunology       Date:  1991-10       Impact factor: 7.397

3.  Nitric oxide synthesis is depressed in Bos indicus cattle infected with Trypanosoma congolense and Trypanosoma vivax and does not mediate T-cell suppression.

Authors:  K Taylor; V Lutje; B Mertens
Journal:  Infect Immun       Date:  1996-10       Impact factor: 3.441

4.  CD5+ B lymphocytes are the main source of antibodies reactive with non-parasite antigens in Trypanosoma congolense-infected cattle.

Authors:  J Buza; M Sileghem; P Gwakisa; J Naessens
Journal:  Immunology       Date:  1997-10       Impact factor: 7.397

5.  Involvement of gamma delta T cells in immunity to trypanosomiasis.

Authors:  J N Flynn; M Sileghem
Journal:  Immunology       Date:  1994-09       Impact factor: 7.397

6.  Mapping of quantitative trait loci controlling trypanotolerance in a cross of tolerant West African N'Dama and susceptible East African Boran cattle.

Authors:  O Hanotte; Y Ronin; M Agaba; P Nilsson; A Gelhaus; R Horstmann; Y Sugimoto; S Kemp; J Gibson; A Korol; M Soller; A Teale
Journal:  Proc Natl Acad Sci U S A       Date:  2003-06-12       Impact factor: 11.205

7.  Non-invasive in vivo study of the Trypanosoma vivax infectious process consolidates the brain commitment in late infections.

Authors:  Simon D'Archivio; Alain Cosson; Mathieu Medina; Thierry Lang; Paola Minoprio; Sophie Goyard
Journal:  PLoS Negl Trop Dis       Date:  2013-01-03

8.  Transcriptional profiling of cattle infected with Trypanosoma congolense highlights gene expression signatures underlying trypanotolerance and trypanosusceptibility.

Authors:  Grace M O'Gorman; Stephen D E Park; Emmeline W Hill; Kieran G Meade; Paul M Coussens; Morris Agaba; Jan Naessens; Stephen J Kemp; David E MacHugh
Journal:  BMC Genomics       Date:  2009-05-01       Impact factor: 3.969

  8 in total

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