Real Time PCR TaqMan assays for detection of polyomaviruses KIV and WUV in clinical samples

被引:22
作者
Bergallo, Massimiliano [1 ]
Terlizzi, Maria Elena [1 ]
Astegiano, Sara [1 ]
Ciotti, Marco [2 ]
Babakir-Mina, Muhammed [2 ]
Perno, Carlo Federico [2 ,3 ]
Cavallo, Rossana [1 ]
Costa, Cristina [1 ]
机构
[1] Univ Turin, Virol Unit, Dept Publ Hlth & Microbiol, I-10126 Turin, Italy
[2] Univ Roma Tor Vergata, Mol Virol Lab, Rome, Italy
[3] Univ Roma Tor Vergata, Dept Expt Med & Biochem Sci, I-00173 Rome, Italy
关键词
Polyomavirus KI; Polyomavirus WU; Real Time polymerase chain reaction; Primer/probe set; IDENTIFICATION; DISEASE; INFECTIONS; VALIDATION; TESTS;
D O I
10.1016/j.jviromet.2009.07.016
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Recently, polyomaviruses KI and WU were identified in the airways of patients with acute respiratory symptoms. The epidemiology and pathogenesis of these two viruses are not fully understood, and the development of molecular assays, such as Real Time PCR, was useful for examining their biology and role in different clinical syndromes. The evaluation of different target regions for the amplification of polyomaviruses KI and WU, comparing published primer/probe sets and sets designed in the laboratory is described and was used for testing 175 clinical specimens (84 stools and 91 tonsils). The results showed that the laboratory designs were more sensitive for the detection of polyomaviruses KI and WU DNA in clinical samples. The choice of the primer/probe set, and primarily of the region for amplification, may be relevant for understanding the pathogenic role of viruses such as polyomaviruses KI and WU. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:69 / 74
页数:6
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