Rapid identification of Leishmania complexes by a real-time PCR assay

被引:66
|
作者
Wortmann, G
Hochberg, L
Houng, HH
Sweeney, C
Zapor, M
Aronson, N
Weina, P
Ockenhouse, CF
机构
[1] Walter Reed Army Med Ctr, Infect Dis Serv, Washington, DC 20307 USA
[2] Walter Reed Army Inst Res, Dept Entomol, Silver Spring, MD USA
[3] Walter Reed Army Inst Res, Dept Viral Dis, Silver Spring, MD USA
[4] Uniformed Serv Univ Hlth Sci, Div Infect Dis, Bethesda, MD 20814 USA
[5] Walter Reed Army Inst Res, Dept Expt Therapeut, Silver Spring, MD USA
[6] Walter Reed Army Inst Res, Dept Immunol, Silver Spring, MD USA
来源
关键词
D O I
10.4269/ajtmh.2005.73.999
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
A real-time PCR assay for the detection of four Leishmania complexes (L. Viannia, L. mexicana, L. donovani/infantum, and L. major) was developed and evaluated. The assay was developed to detect the glucosephosphate isomerase gene and capitalizes on DNA sequence variability within that gene for Leishmania complex identification. Primer/probe sets were created and tested against a panel of 21 known negative controls and on DNA extracted from cultured promastigotes or from tissue biopsies from patients with cutaneous leishmaniasis. The assay was highly specific, as no amplification products were detected in the negative control samples while simultaneously retaining a high degree of complex-specific diagnostic accuracy for cultured organisms and patient clinical samples. Real-time PCR offers rapid (within hours) identification of Leishmania to the complex level and provides a useful molecular tool to assist both epidemiologists and clinicians.
引用
收藏
页码:999 / 1004
页数:6
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