Literature DB >> 6439844

The IsTaR 1 serodeme of Trypanosoma brucei: development of a new serodeme.

K Stuart, E Gobright, L Jenni, M Milhausen, L Thomashow, N Agabian.   

Abstract

An extensive serodeme of sequentially-isolated antigenic variants of African trypanosomes has been produced from both syringe-passaged and cyclically-transmitted Trypanosoma brucei of the IsTaR 1 clone derived from EATRO 164. The majority of the antigenic variants were isolated from chronically-infected deer mice (Peromyscus leucopus). The pattern of parasitemias during the course of infections initiated with syringe-passaged trypanosomes differed from those initiated with cyclically-transmitted trypanosomes. Trypanosome populations from syringe-passaged (192) and cyclically-transmitted (31) clones were each amplified by growth in lethally-irradiated mice and cryopreserved for retrospective analysis. Five clones derived from a single deer mouse during the first 44 days of infection, and 2 clones derived from an acutely-infected rat were established from these amplified populations. Homogeneous populations were grown in lethally-irradiated rats and mice for antigenic analysis purification of variant-specific glycoprotein. Six of the 7 clones were distinct variants by immunological criteria using antisera derived from whole cells or purified surface glycoproteins. Two clones, one derived from the acutely-infected rat, and the other from the first parasitemia in a chronic infection that was initiated with the former clone, were immunologically identical. Production of these clones established a well-defined serodeme that will allow detailed analysis of antigenic variation.

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Year:  1984        PMID: 6439844

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


  36 in total

1.  Association of two novel proteins, TbMP52 and TbMP48, with the Trypanosoma brucei RNA editing complex.

Authors:  A K Panigrahi; S P Gygi; N L Ernst; R P Igo; S S Palazzo; A Schnaufer; D S Weston; N Carmean; R Salavati; R Aebersold; K D Stuart
Journal:  Mol Cell Biol       Date:  2001-01       Impact factor: 4.272

2.  Kinetoplastid RNA editing does not require the terminal 3' hydroxyl of guide RNA, but modifications to the guide RNA terminus can inhibit in vitro U insertion.

Authors:  M L Burgess; S Heidmann; K Stuart
Journal:  RNA       Date:  1999-07       Impact factor: 4.942

3.  The specificity of nucleotide removal during RNA editing in Trypanosoma brucei.

Authors:  S D Lawson; R P Igo; R Salavati; K D Stuart
Journal:  RNA       Date:  2001-12       Impact factor: 4.942

4.  Four related proteins of the Trypanosoma brucei RNA editing complex.

Authors:  A K Panigrahi; A Schnaufer; N Carmean; R P Igo; S P Gygi; N L Ernst; S S Palazzo; D S Weston; R Aebersold; R Salavati; K D Stuart
Journal:  Mol Cell Biol       Date:  2001-10       Impact factor: 4.272

5.  Maxicircle CR1 transcripts of Trypanosoma brucei are edited and developmentally regulated and encode a putative iron-sulfur protein homologous to an NADH dehydrogenase subunit.

Authors:  A E Souza; P J Myler; K Stuart
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

6.  Guide RNAs for transcripts with developmentally regulated RNA editing are present in both life cycle stages of Trypanosoma brucei.

Authors:  D J Koslowsky; G R Riley; J E Feagin; K Stuart
Journal:  Mol Cell Biol       Date:  1992-05       Impact factor: 4.272

7.  The trypanosome leucine repeat gene in the variant surface glycoprotein expression site encodes a putative metal-binding domain and a region resembling protein-binding domains of yeast, Drosophila, and mammalian proteins.

Authors:  B L Smiley; A W Stadnyk; P J Myler; K Stuart
Journal:  Mol Cell Biol       Date:  1990-12       Impact factor: 4.272

8.  Chimeric and truncated RNAs in Trypanosoma brucei suggest transesterifications at non-consecutive sites during RNA editing.

Authors:  L K Read; R A Corell; K Stuart
Journal:  Nucleic Acids Res       Date:  1992-05-11       Impact factor: 16.971

9.  Quantitation of RNA editing substrates, products and potential intermediates: implications for developmental regulation.

Authors:  G R Riley; P J Myler; K Stuart
Journal:  Nucleic Acids Res       Date:  1995-02-25       Impact factor: 16.971

10.  Editing of Trypanosoma brucei maxicircle CR5 mRNA generates variable carboxy terminal predicted protein sequences.

Authors:  L K Read; K D Wilson; P J Myler; K Stuart
Journal:  Nucleic Acids Res       Date:  1994-04-25       Impact factor: 16.971

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