Literature DB >> 6133773

Trypanosoma congolense: susceptibility of cattle to cyclical challenge.

G W Akol, M Murray.   

Abstract

Cattle primed by cyclical infection with Glossina morsitans morsitans infected with cloned derivatives of Trypanosoma congolense and treated with the trypanocidal drug Berenil after 3 or 4 weeks were immune to cyclical challenge with homologous clones 3 to 5 weeks later. In these animals, localized skin reactions (chancres) and parasitemia did not develop. The same results were obtained in cattle given a homologous superinfection without prior treatment. On the other hand, cattle subjected to a cyclical challenge with heterologous clones were completely susceptible as demonstrated by the development of chancres. Immunity to homologous challenge was achieved irrespective of the bloodstream variable antigenic types used to infect the tsetse. It was concluded that for a given serodeme the variable antigen composition of the metacyclic population which develops in the tsetse is constant and characteristic. Immunity to cyclical challenge was also obtained with uncloned stocks, providing the same stock was used for challenge. On the other hand, cattle immune to homologous cyclical challenge with cloned material were not always immune to cyclical challenge with parent stock, indicating that certain stocks consist of more than one serodeme. On the basis of these findings, it may be possible to use the chancre as a marker for serodeme analysis.

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Year:  1983        PMID: 6133773     DOI: 10.1016/0014-4894(83)90036-x

Source DB:  PubMed          Journal:  Exp Parasitol        ISSN: 0014-4894            Impact factor:   2.011


  3 in total

1.  Mechanisms for the elimination of potentially lytic complement-fixing variable surface glycoprotein antibody-complexes in Trypanosoma brucei.

Authors:  D C Russo; D J Williams; D J Grab
Journal:  Parasitol Res       Date:  1994       Impact factor: 2.289

2.  Genetic and expression analysis of cattle identifies candidate genes in pathways responding to Trypanosoma congolense infection.

Authors:  Harry Noyes; Andy Brass; Isaiah Obara; Susan Anderson; Alan L Archibald; Dan G Bradley; Paul Fisher; Abigail Freeman; John Gibson; Michael Gicheru; Laurence Hall; Olivier Hanotte; Helen Hulme; Declan McKeever; Caitriona Murray; Sung Jung Oh; Catriona Tate; Ken Smith; Miika Tapio; John Wambugu; Diana J Williams; Morris Agaba; Stephen J Kemp
Journal:  Proc Natl Acad Sci U S A       Date:  2011-05-18       Impact factor: 11.205

3.  Variant antigen repertoires in Trypanosoma congolense populations and experimental infections can be profiled from deep sequence data using universal protein motifs.

Authors:  Sara Silva Pereira; Aitor Casas-Sánchez; Lee R Haines; Moses Ogugo; Kihara Absolomon; Mandy Sanders; Steve Kemp; Álvaro Acosta-Serrano; Harry Noyes; Matthew Berriman; Andrew P Jackson
Journal:  Genome Res       Date:  2018-07-13       Impact factor: 9.043

  3 in total

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