Trypanosoma vivax:: Characterization of the spliced-leader gene of a Brazilian stock and species-specific detection by PCR amplification of an intergenic spacer sequence

被引:56
作者
Ventura, RM
Paiva, F
Silva, RAMS
Takeda, GR
Buck, GA
Teixeira, MMG [1 ]
机构
[1] Univ Sao Paulo, Inst Ciencias Biomed, Dept Parasitol, BR-05508900 Sao Paulo, Brazil
[2] Univ Fed Mato Grosso do Sul, Ctr Ciencias Biol & Saude, Dept Patol, Campo Grande, MS USA
[3] Virginia Commonwealth Univ, Dept Microbiol & Immunol, Richmond, VA 23298 USA
基金
巴西圣保罗研究基金会;
关键词
Trypanosoma vivax; South American trypanosomes; Salivaria; mini-exon gene; diagnosis; genetic relatedness; cattle trypanosomes;
D O I
10.1006/expr.2001.4641
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 sequence of the spliced-leader gene repeat of a Brazilian Trypanosoma vivax stock from cattle showed high similarity to sequences of West African T. vivax in both intron and intergenic sequences. This is the first evidence based on DNA sequences of close-relatedness between Brazilian and West African T. vivax stocks. A T. vivax-specific diagnostic PCR assay based on spliced-leader gene intergenic sequences was able to amplify DNA from T. vivax stocks from South America (Brazil, Bolivia, and Colombia) and West Africa. Species-specificity of this method was confirmed by results obtained by testing 15 other trypanosomes, including other species and subspecies that can also infect cattle. The PCR assay developed presented high sensitivity, detecting the DNA content of only one parasite and also revealing T. vivax infection in asymptomatic animals without detectable parasitemia by microhematocrit or in Giemsa-stained blood smears. Use of crude preparations from field-blood samples collected on both filter paper and glass slides as DNA template suggested that this method could be useful for the diagnosis of T. vivax in large epidemiological studies. (C) 2001 Academic Press.
引用
收藏
页码:37 / 48
页数:12
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