Leishmania AFLP: Paving the way towards improved molecular assays and markers of diversity

被引:20
|
作者
Odiwuor, Samwel [1 ,2 ,3 ]
Vuylsteke, Marnik [4 ,5 ]
De Doncker, Simonne [1 ]
Maes, Ilse [1 ]
Mbuchi, Margaret [2 ]
Dujardin, Jean-Claude [1 ,3 ]
Van der Auwera, Gert [1 ]
机构
[1] Inst Trop Med, Dept Parasitol, B-2000 Antwerp, Belgium
[2] Kenya Govt Med Res Ctr, Clin Res Ctr, Nairobi, Kenya
[3] Univ Antwerp, Dept Biomed Sci, B-2020 Antwerp, Belgium
[4] VIB, Dept Plant Syst Biol, Ghent, Belgium
[5] Univ Ghent, Dept Plant Biotechnol & Genet, B-9000 Ghent, Belgium
关键词
Leishmania donovani; Leishmania infantum; Diversity; Phylogeny; AFLP; Fingerprint; LENGTH POLYMORPHISM AFLP; DONOVANI COMPLEX; VISCERAL LEISHMANIASIS; PHYLOGENETIC NETWORKS; INFANTUM; CLASSIFICATION; EVOLUTION; HOMOPLASY; GENOTYPES; TAXONOMY;
D O I
10.1016/j.meegid.2011.03.008
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Diversity, phylogenetic, and population genetic studies of the genus Leishmania, causative agent of leishmaniasis, nowadays generally involve multilocus microsatellite and multilocus sequence typing. Even though these are well established and useful applications, amplified fragment length polymorphisms (AFLP) can provide complementary information. In addition, as the technique essentially probes the entire genome at random, without prior sequence knowledge, it is ideally suited as a screening tool for molecular markers linked with biological and clinical traits. We developed an AFLP protocol adapted to the Leishmania genome, tested its repeatability, and validated it on a panel of samples from the Leishmania donovani complex previously analyzed by multiple molecular tests. The technique proved highly reproducible, and showed that genetic relationships between L. donovani strains generally reflect geographic distance. Four main groups were identified: Leishmania infantum, African L. donovani, Indian L. donovani, and a mixed group consisting of L. donovani from India and Africa. Results were highly congruent with previous analyses on essentially the same sample set, indicating that the developed assay produces trustworthy data. This opens possibilities for application in studies of speciation and population dynamics. Moreover, it allows random screening of the entire Leishmania genome for linkage with biological and clinical parasite properties, such as fitness, drug resistance, and disease profile. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:960 / 967
页数:8
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