Gp63 gene polymorphism and population structure of Leishmania donovani complex:: influence of the host selection pressure?

被引:39
作者
Guerbouj, S
Victoir, K
Guizani, I
Seridi, N
Nuwayri-Salti, N
Belkaid, M
Ben Ismail, R
Le Ray, D
Dujardin, JC
机构
[1] Prins Leopold Inst Trop Geneeskunde, Protozool Unit, B-2000 Antwerp, Belgium
[2] Inst Pasteur, Lab Epidemiol & Ecol Parasitaire, Tunis 1002, Tunisia
[3] Inst Pasteur Algerie, Algiers, Algeria
[4] Amer Univ Beirut, Beirut, Lebanon
关键词
immunogen; polymorphism; selection; diagnosis;
D O I
10.1017/S0031182000007125
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
The gp63 encoding genes were characterized bq PCR-RFLP in 35 isolates representative of the Leishmania donovani complex (L. infantum, L. donovani, L. archibaldi and L. chagnsi), with special attention to Mediterranean L, infantum from different geographical origins, and in separate groups from Old World Leishmania (L.,major, L. tropica and L. aethiopica). The aim was to evaluate how the possible selective pressure by the host on these important surface proteins would influence structuring of our sample. Comparison was carried out with the structure obtained (i) from reported isoenzyme data, characters supposed to vary neutrally, and (ii) from PCR-RFLP analysis of gp63 inter-genic regions, containing non-translated spacers and regulatory genes. Polymorphism within the gp63-encoding region, was much higher than in gp63 inter-genic regions. In the gp63 intra-genic dendrogram, the 4 species of L. donovani complex were discriminated and quite distinct from outgroups. Within L. infantum, geographical structuring was observed and did not overlap with the structure built-up from isoenzymes and inter-genic data. These results support the idea of a strong host-selection on gp63, at vector level but most of all at vertebrate (human or dog) immunological level. Furthermore. they illustrate how the nature of genetic characters may influence the perception of population structuring.
引用
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页码:25 / 35
页数:11
相关论文
共 34 条
[1]  
ARNEDO PA, 1994, REV SANIDAD HIGIENE, V68, P481
[2]   EVOLUTION OF THE GENUS LEISHMANIA AS REVEALED BY COMPARISONS OF NUCLEAR-DNA RESTRICTION FRAGMENT PATTERNS [J].
BEVERLEY, SM ;
ISMACH, RB ;
PRATT, DM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (02) :484-488
[3]   GENES ENCODING THE MAJOR SURFACE GLYCOPROTEIN IN LEISHMANIA ARE TANDEMLY LINKED AT A SINGLE CHROMOSOMAL LOCUS AND ARE CONSTITUTIVELY TRANSCRIBED [J].
BUTTON, LL ;
RUSSELL, DG ;
KLEIN, HL ;
MEDINAACOSTA, E ;
KARESS, RE ;
MCMASTER, WR .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1989, 32 (2-3) :271-283
[4]   POCKET BLOTTING - A METHOD FOR TRANSFERRING NUCLEIC-ACIDS ONTO NYLON MEMBRANES [J].
CUNY, G ;
VEAS, F ;
ROIZES, G .
ANALYTICAL BIOCHEMISTRY, 1991, 193 (01) :45-48
[5]   INTERGENIC REGION TYPING (IRT) - A RAPID MOLECULAR APPROACH TO THE CHARACTERIZATION AND EVOLUTION OF LEISHMANIA [J].
CUPOLILLO, E ;
GRIMALDI, G ;
MOMEN, H ;
BEVERLEY, SM .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1995, 73 (1-2) :145-155
[6]   DIAGNOSIS OF NEW-WORLD LEISHMANIASIS - SPECIFIC DETECTION OF SPECIES OF THE LEISHMANIA-BRAZILIENSIS COMPLEX BY AMPLIFICATION OF KINETOPLAST DNA [J].
DEBRUIJN, MHL ;
BARKER, DC .
ACTA TROPICA, 1992, 52 (01) :45-58
[7]  
FELSENSTEIN J, 1984, EVOLUTION, V38, P16, DOI 10.1111/j.1558-5646.1984.tb00255.x
[8]  
FERNANDEZ F, 1994, VIS TECNOL, V2, P66
[9]   Cloning of the gp63 surface protease of Leishmania infantum - Differential post-translational modifications correlated with different infective forms [J].
GonzalezAseguinolaza, G ;
Almazan, F ;
Rodriguez, JF ;
Marquet, A ;
Larraga, V .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 1997, 1361 (01) :92-102
[10]   Population structure of pathogens: The role of immune selection [J].
Gupta, S ;
Anderson, RM .
PARASITOLOGY TODAY, 1999, 15 (12) :497-501