Literature DB >> 10425151

Plasmodium falciparum: population genetic analysis by multilocus enzyme electrophoresis and other molecular markers.

S B Abderrazak1, B Oury, A A Lal, M F Bosseno, P Force-Barge, J P Dujardin, T Fandeur, J F Molez, F Kjellberg, F J Ayala, M Tibayrenc.   

Abstract

Abderrazak, S. B., Oury, B, Lal, A. A., Bosseno, M.-F., Force-Barge, P., Dujardin, J.-P., Fandeur, T., Molez, J.-F., Kjellberg, F., Ayala, F. J., and Tibayrenc, M. 1999. Plasmodium falciparum: Population genetic analysis by multilocus enzyme electrophoresis and other molecular markers. Experimental Parasitology 92, 232-238. The population structure of Plasmodium falciparum, the agent of malignant malaria, is uncertain. We have analyzed multilocus enzyme electrophoresis (MLEE) polymorphisms at 7-12 gene loci in each of four populations (two populations in Burkina Faso, one in Sudan, one in Congo), plus one "cosmopolitan" sample consisting of parasite cultures from 15 distant localities in four different continents. We have also performed random amplified polymorphic DNA analysis (RAPD) and restriction fragment length polymorphism (RFLP) and characterized gene varia tion at four antigen genes in the Congo population. All genetic assays show abundant genetic variability in all populations analyzed. With the isoenzyme assays, strong linkage disequilibrium is apparent in at least two local populations, the Congo population and one population from Burkina Faso, as well as in the cosmopolitan sample, and less definitely in the other Burkina Faso population. However, no linkage disequilibrium is detected in the Congo population with the molecular assays. We failed to detect any nonrandom association between the different kinds of genetic markers; that is, MLEE with RAPD or RFLP, RAPD with RFLP, and so on. Although isoenzyme data show statistical departures from panmictic expectations, these results suggest that in the areas under survey, P. falciparum populations do not undergo predominant clonal evolution and show no clear-cut subdivisions, un like Trypanosoma cruzi, Leishmania sp., and other major parasitic species. We discuss the epidemiological and taxonomical significance of these results. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10425151     DOI: 10.1006/expr.1999.4424

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


  4 in total

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Journal:  Proc Natl Acad Sci U S A       Date:  2005-11-21       Impact factor: 11.205

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Authors:  L Urdaneta; A Lal; C Barnabe; B Oury; I Goldman; F J Ayala; M Tibayrenc
Journal:  Proc Natl Acad Sci U S A       Date:  2001-05-22       Impact factor: 11.205

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Authors:  Zeinab Annan; Patrick Durand; Francisco J Ayala; Céline Arnathau; Parfait Awono-Ambene; Frédéric Simard; Fabien G Razakandrainibe; Jacob C Koella; Didier Fontenille; François Renaud
Journal:  Proc Natl Acad Sci U S A       Date:  2007-04-30       Impact factor: 11.205

4.  High genetic complexity but low relatedness in Plasmodium falciparum infections from Western Savannah Highlands and coastal equatorial Lowlands of Cameroon.

Authors:  Ngoh Ines Atuh; Damian Nota Anong; Fru-Cho Jerome; Eniyou Oriero; Nuredin Ibrahim Mohammed; Umberto D'Alessandro; Alfred Amambua-Ngwa
Journal:  Pathog Glob Health       Date:  2021-07-26       Impact factor: 3.735

  4 in total

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