Polymerase chain reaction assay based on a highly repeated sequence of Schistosoma haematobium:: A potential tool for monitoring schistosome-infested water

被引:91
作者
Hamburger, J
He-Na
Abbasi, I
Ramzy, RM
Jourdane, J
Ruppel, A
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Sch, Kuvin Ctr Study Infect & Trop Dis, IL-91120 Jerusalem, Israel
[2] Shanghai Med Univ, Shanghai 200032, Peoples R China
[3] Ain Shams Univ, Cairo, Egypt
[4] Univ Perpignan, F-66025 Perpignan, France
[5] Univ Heidelberg, D-6900 Heidelberg, Germany
关键词
D O I
10.4269/ajtmh.2001.65.907
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
We have cloned from Schistosoma haematobium genome a repeated sequence, the DraI repeated sequence, which consists of tandemly arranged 121-bp-long units and which is highly abundant (similar to15% of the S. haematobium genome). By these features, the DraI repeat is similar to the Sm1-7 sequence of Schistosoma mansoni previously described by us. However, their nucleotide sequences are profoundly different. Polymerase chain reaction (PCR) primers were designed on the basis of the DraI sequence information and were used in a PCR assay by which as little as 10 fg of schistosomal DNA as well as individual cercariae were detected. The DraI repeat cross-hybridized with DNA from Schistosoma bovis, Schistosoma magrebowiei, Schistosoma mattheei, Schistosoma curassoni, and Schistosoma intercalation, but not with DNA from S. mansoni nor from Trichobilharzia ocellata and Echinostoma sp. A potential value of this PCR assay is suggested for monitoring free-living cercariae and infected snails only in bodies free of cross-hybridizing species.
引用
收藏
页码:907 / 911
页数:5
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