A real-time PCR diagnostic method for detection of Naegleria fowleri

被引:19
|
作者
Madarova, Lucia [1 ]
Trnkova, Katarina [1 ]
Feikova, Sona [1 ]
Klement, Cyril [1 ]
Obernauerova, Margita [2 ]
机构
[1] Reg Author Publ Hlth Banska Bystr, Dept Mol Biol, Banska Bystrica 97556, Slovakia
[2] Comenius Univ, Fac Nat Sci, Dept Microbiol & Virol, Bratislava, Slovakia
关键词
Naegleria fowleri; Diagnosis; Real-time PCR; Hybridization probes; POLYMERASE-CHAIN-REACTION; LIVING AMEBA NAEGLERIA; MELTING-CURVE ANALYSIS; NESTED PCR; BALAMUTHIA-MANDRILLARIS; QUANTITATIVE DETECTION; ACANTHAMOEBA SPP; DNA; IDENTIFICATION; DIFFERENTIATION;
D O I
10.1016/j.exppara.2009.11.001
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
Naegleria fowleri is a free-living amoeba that can cause primary amoebic meningoencephalitis (PAM). While, traditional methods for diagnosing PAM still rely on culture, more current laboratory diagnoses exist based on conventional PCR methods; however, only a few real-time PCR processes have been described as yet. Here, we describe a real-time PCR-based diagnostic method using hybridization fluorescent labelled probes, with a LightCycler instrument and accompanying software (Roche), targeting the Naegleria fowleri Mp2Cl5 gene sequence. Using this method, no cross reactivity with other tested epidemiologically relevant prokaryotic and eukaryotic organisms was found. The reaction detection limit was 1 copy of the Mp2Cl5 DNA sequence. This assay could become useful in the rapid laboratory diagnostic assessment of the presence or absence of Naegleria fowleri. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:37 / 41
页数:5
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