Detection of rotavirus A in sewage samples using multiplex qPCR and an evaluation of the ultracentrifugation and adsorption-elution methods for virus concentration

被引:108
|
作者
Fumian, Tulio M. [1 ]
Leite, Jose Paulo G.
Castello, Alejandro A. [2 ]
Gaggero, Aldo [3 ]
de Caillou, Maria Susana L. [4 ]
Miagostovich, Marize P.
机构
[1] Fiocruz MS, Lab Comparat & Environm Virol, Inst Oswaldo Cruz, BR-21040360 Rio De Janeiro, Brazil
[2] Univ Nacl Quilmes Bernal, Lab Inmunol & Virol, Bernal, Argentina
[3] Univ Chile, Fac Med, ICBM, Programa Virol, Santiago, Chile
[4] Univ Tucuman, Inst Microbiol, San Miguel De Tucuman, Argentina
关键词
Rotavirus A; PP7; Multiplex qPCR; Ultracentrifugation; Adsorption-elution method; HEPATITIS-A-VIRUS; POLYMERASE CHAIN-REACTION; RIO-DE-JANEIRO; REVERSE TRANSCRIPTION-PCR; WASTE-WATER TREATMENT; URBAN SEWAGE; MOLECULAR-DETECTION; TREATMENT-PLANT; RT-PCR; ACUTE GASTROENTERITIS;
D O I
10.1016/j.jviromet.2010.08.017
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Group A rotaviruses (RV-A) are the most common agents of viral gastroenteritis in children worldwide. The goal of this study was to compare two different methods to concentrate RV-A from sewage samples and to improve the detection and quantification of RV-A using a multiplex quantitative PCR assay with an internal control. Both RV-A and the internal control virus, bacteriophage PP7, were seeded into wastewater and then concentrated using either an ultrafiltration-based adsorption-elution protocol or an ultracentrifugation-based protocol. Real time multiplex quantitative PCR was used to quantify the purified RV-A and PP7, and the results of the multiplex assay were compared with the results of the monoplex assays. The ultracentrifugation-based method had a mean recovery rate of 47% (range: 34-60%), while the ultrafiltration-based adsorption-elution method had a mean recovery rate of 3.5% (range: 1.5-5.5%). These results demonstrate that ultracentrifugation is a more appropriate method for recovering RV-A from wastewater. This method together with the multiplex qPCR assay may be suitable for routine laboratory use. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:42 / 46
页数:5
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