Literature DB >> 3047352

Growth of pleomorphic Trypanosoma brucei rhodesiense in irradiated inbred mice.

J R Seed1, J Sechelski.   

Abstract

It was shown that irradiation (650 rad) of 7 inbred strains of mice did not block the ability of Trypanosoma brucei rhodesiense to transform from the long slender (LS) to the short stumpy (SS) form or alter the plateau in parasitemia. In addition, it was observed that significant differences in parasitemia levels, in the rate of transformation from the LS to the SS form, as well as in the survival times occurred between the irradiated C3HeB/FeJ and several of the other strains. These differences in the nonspecific ability to control parasitemia appeared to be characteristic for each inbred strain of mice. The resistant strains generally had lower parasitemia than the susceptible strains. However, it was also shown that there is not a one-to-one correlation between the innate ability of a mouse strain to control its initial parasitemia, and the strain's ability to clear the parasitemia or increase its survival time. It was therefore concluded that the hypothesis which states that the ability of an animal to increase nonspecifically the rate of transformation, and therefore to lower the parasitemia, allowing intact animals to respond immunologically and survive longer is either incorrect or incomplete. The results further show that the ability of mice to clear their initial parasitemia by an antibody response is not necessarily correlated with their survival time. Therefore, this study suggests that factors other than an antibody response and the nonspecific control of parasitemia are important in resistance.

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Year:  1988        PMID: 3047352

Source DB:  PubMed          Journal:  J Parasitol        ISSN: 0022-3395            Impact factor:   1.276


  7 in total

1.  Limitation of Trypanosoma brucei parasitaemia results from density-dependent parasite differentiation and parasite killing by the host immune response.

Authors:  K M Tyler; P G Higgs; K R Matthews; K Gull
Journal:  Proc Biol Sci       Date:  2001-11-07       Impact factor: 5.349

Review 2.  New discoveries in the transmission biology of sleeping sickness parasites: applying the basics.

Authors:  Paula MacGregor; Keith R Matthews
Journal:  J Mol Med (Berl)       Date:  2010-06-05       Impact factor: 4.599

3.  Specific uptake of tumor necrosis factor-alpha is involved in growth control of Trypanosoma brucei.

Authors:  S Magez; M Geuskens; A Beschin; H del Favero; H Verschueren; R Lucas; E Pays; P de Baetselier
Journal:  J Cell Biol       Date:  1997-05-05       Impact factor: 10.539

4.  Transcriptomes of newly-isolated Trypanosoma brucei rhodesiense reveal hundreds of mRNAs that are co-regulated with stumpy-form markers.

Authors:  Julius Mulindwa; Clémentine Mercé; Enock Matovu; John Enyaru; Christine Clayton
Journal:  BMC Genomics       Date:  2015-12-29       Impact factor: 3.969

Review 5.  An Overview of Trypanosoma brucei Infections: An Intense Host-Parasite Interaction.

Authors:  Alicia Ponte-Sucre
Journal:  Front Microbiol       Date:  2016-12-26       Impact factor: 5.640

6.  Role of the long slender to short stumpy transition in the life cycle of the african trypanosomes.

Authors:  John Richard Seed; Mary Anne Wenck
Journal:  Kinetoplastid Biol Dis       Date:  2003-06-25

Review 7.  Infections With Extracellular Trypanosomes Require Control by Efficient Innate Immune Mechanisms and Can Result in the Destruction of the Mammalian Humoral Immune System.

Authors:  Stefan Magez; Joar Esteban Pinto Torres; Emmanuel Obishakin; Magdalena Radwanska
Journal:  Front Immunol       Date:  2020-03-11       Impact factor: 7.561

  7 in total

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