Molecular characterization of field isolates of human pathogenic trypanosomes

被引:14
作者
Gibson, W [1 ]
机构
[1] Univ Bristol, Sch Biol Sci, Bristol BS8 1UG, Avon, England
关键词
Trypanosoma brucei rhodesiense; Trypanosoma brucei gambiense; epidemiology; drug resistance; genetic markers;
D O I
10.1046/j.1365-3156.2001.00711.x
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The accurate identification of each of the three subspecies of Trypanosoma brucei remains a challenging problem in the epidemiology of sleeping sickness. Advances in molecular characterization have revealed a much greater degree of heterogeneity within the species than previously supposed. Only group 1 T. b. gambiense stands out as a separate entity, defined by several molecular markers. T. b. rhodesiense is generally too similar to sympatric T. b. brucei strains to be distinguished from them by any particular molecular markers. Nevertheless, characterization of trypanosome isolates from humans and other animals has allowed the identification of potential reservoir hosts of T. b. rhodesiense. The recent discovery of a gene for human serum resistance may provide a useful marker for T. b. rhodesiense in the future. There have been few attempts to find associations between genetic markers and other biological characters, except human infectivity. However, virulence or fly transmissibility have been correlated with molecular markers in some instances.
引用
收藏
页码:401 / 406
页数:6
相关论文
共 68 条
[31]   HYBRID FORMATION BETWEEN AFRICAN TRYPANOSOMES DURING CYCLICAL TRANSMISSION [J].
JENNI, L ;
MARTI, S ;
SCHWEIZER, J ;
BETSCHART, B ;
LEPAGE, RWF ;
WELLS, JM ;
TAIT, A ;
PAINDAVOINE, P ;
PAYS, E ;
STEINERT, M .
NATURE, 1986, 322 (6075) :173-175
[32]   Characterization of Trypanosoma brucei gambiense isolates using restriction fragment length polymorphisms in 5 variant surface glycoprotein genes [J].
Kanmogne, GD ;
Stevens, JR ;
Asonganyi, T ;
Gibson, WC .
ACTA TROPICA, 1996, 61 (03) :239-254
[33]   Genetic heterogeneity in the Trypanosoma brucei gambiense genome analysed by random amplification of polymorphic DNA [J].
Kanmogne, GD ;
Stevens, JR ;
Asonganyi, T ;
Gibson, WC .
PARASITOLOGY RESEARCH, 1996, 82 (06) :535-541
[34]   Genetic diversity among Trypanosoma brucei rhodesiense isolates from Tanzania [J].
Komba, EK ;
Kibona, SN ;
Ambwene, AK ;
Stevens, JR ;
Gibson, WC .
PARASITOLOGY, 1997, 115 :571-579
[35]   PEDIGREES OF EDINBURGH TRYPANOSOMA (TRYPANOZOON) ANTIGENIC TYPES-(ETAT) [J].
LUMSDEN, WHR ;
HERBERT, WJ .
TRANSACTIONS OF THE ROYAL SOCIETY OF TROPICAL MEDICINE AND HYGIENE, 1975, 69 (02) :205-208
[36]   SENSITIVE DETECTION OF TRYPANOSOMES IN TSETSE-FLIES BY DNA AMPLIFICATION [J].
MASIGA, DK ;
SMYTH, AJ ;
HAYES, P ;
BROMIDGE, TJ ;
GIBSON, WC .
INTERNATIONAL JOURNAL FOR PARASITOLOGY, 1992, 22 (07) :909-918
[37]   ISOZYME VARIABILITY OF TRYPANOSOMA-BRUCEI S-L - GENETIC, TAXONOMIC, AND EPIDEMIOLOGIC SIGNIFICANCE [J].
MATHIEUDAUDE, F ;
TIBAYRENC, M .
EXPERIMENTAL PARASITOLOGY, 1994, 78 (01) :1-19
[38]   IDENTIFICATION OF TRYPANOSOMA-BRUCEI-GAMBIENSE GROUP-I BY A SPECIFIC KINETOPLAST DNA-PROBE [J].
MATHIEUDAUDE, F ;
BICARTSEE, A ;
BOSSENO, MF ;
BRENIERE, SF ;
TIBAYRENC, M .
AMERICAN JOURNAL OF TROPICAL MEDICINE AND HYGIENE, 1994, 50 (01) :13-19
[39]   Susceptibility of Ugandan Trypanosoma brucei rhodesiense isolated from man and animal reservoirs to diminazene, isometamidium and melarsoprol [J].
Matovu, E ;
Iten, M ;
Enyaru, JCK ;
Schmid, C ;
Lubega, GW ;
Brun, R ;
Kaminsky, R .
TROPICAL MEDICINE & INTERNATIONAL HEALTH, 1997, 2 (01) :13-18
[40]  
MEHLITZ D, 1982, TROPENMED PARASITOL, V33, P113