Literature DB >> 1730264

Plasmodium berghei: in vivo generation and selection of karyotype mutants and non-gametocyte producer mutants.

C J Janse1, J Ramesar, F M van den Berg, B Mons.   

Abstract

We previously reported that karyotype and gametocyte-producer mutants spontaneously arose during in vivo asexual multiplication of Plasmodium berghei. Here we studied the rate of selection of these mutants in vivo. Gametocyte production and karyotype pattern were established at regular intervals during prolonged periods of asexual multiplication of clone 8417 of P. berghei. We found that karyotype mutants and mutants which do not produce gametocytes can replace the original high-producer parasites of clone 8417 within several weeks. The time at which mutants became predominant in the population in different experiments, however, differed greatly. Mutants with intermediate or low gametocyte production were not found. In experimentally mixed infections, containing parasites from two clones from different strains (clone 8417 of the ANKA strain; clone 1 of the K173 strain), high-producer parasites of clone 8417 were overgrown by parasites of the nonproducer clone. Nonproducer mutants from the originally high-producer clone 8417, however, were able to coexist with parasites of the nonproducer clone. These results demonstrate that in our experiments nonproducer parasites had a strong selective advantage during asexual multiplication compared to high producers. All karyotype mutants which became predominant in our experiments were nonproducers. In two experiments a change in karyotype coincided with the loss of gametocyte production which may suggest a causal relationship between these events.

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Year:  1992        PMID: 1730264     DOI: 10.1016/0014-4894(92)90133-u

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


  15 in total

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2.  Targeted terminal deletions as a tool for functional genomics studies in Plasmodium.

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Review 3.  Genome plasticity in Plasmodium.

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4.  Infection with Plasmodium berghei boosts antibody responses primed by a DNA vaccine encoding gametocyte antigen Pbs48/45.

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Journal:  Infect Immun       Date:  2006-04       Impact factor: 3.441

5.  Optimized protocols for improving the likelihood of cloning recombinant progeny from Plasmodium yoelii genetic crosses.

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Review 6.  Human red blood cell-adapted Plasmodium knowlesi parasites: a new model system for malaria research.

Authors:  Christof Grüring; Robert W Moon; Caeul Lim; Anthony A Holder; Michael J Blackman; Manoj T Duraisingh
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8.  Proteomic and genetic analyses demonstrate that Plasmodium berghei blood stages export a large and diverse repertoire of proteins.

Authors:  Erica M Pasini; Joanna A Braks; Jannik Fonager; Onny Klop; Elena Aime; Roberta Spaccapelo; Thomas D Otto; Matt Berriman; Jan A Hiss; Alan W Thomas; Matthias Mann; Chris J Janse; Clemens H M Kocken; Blandine Franke-Fayard
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9.  The ETRAMP family member SEP2 is expressed throughout Plasmodium berghei life cycle and is released during sporozoite gliding motility.

Authors:  Chiara Currà; Marco Di Luca; Leonardo Picci; Carina de Sousa Silva Gomes dos Santos; Inga Siden-Kiamos; Tomasino Pace; Marta Ponzi
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10.  A developmental defect in Plasmodium falciparum male gametogenesis.

Authors:  F Guinet; J A Dvorak; H Fujioka; D B Keister; O Muratova; D C Kaslow; M Aikawa; A B Vaidya; T E Wellems
Journal:  J Cell Biol       Date:  1996-10       Impact factor: 10.539

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