Evaluation of a norovirus sampling method using sodium dodecyl sulfate/EDTA-pretreated chromatography paper strips

被引:13
作者
Wollants, E
Maes, P
Thoelen, I
Vanneste, F
Rahman, M
Van Ranst, M
机构
[1] Rega Inst, Dept Microbiol & Immunol, Lab Clin & Epidemiol Virol, B-3000 Louvain, Belgium
[2] ICDDR B, Virol Lab, Ctr Hlth & Populat Res, Dhaka, Bangladesh
[3] Univ Leuven, Hosp Gasthuisberg, Dept Lab Med, Diagnost Virol Lab, Louvain, Belgium
关键词
norovirus; calicivirus; chromatography paper strips; RT-PCR;
D O I
10.1016/j.jviromet.2004.08.001
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Noroviruses are the most common cause of nonbacterial gastroenteritis outbreaks. A novel method was tested that utilizes sodium dodecyl sulfate (SDS)/EDTA-pretreated chromatography paper strips to collect and transport norovirus-containing fresh stool samples. As confirmation, the strips were infected with different dilutions of human norovirus-containing faeces and stored at different temperatures (-80, -20, 4 degreesC, room temperature and 37 degreesC). Reverse transcription (RT)-PCR analysis was carried out after storage of the strips for 1, 7, 14, 60, and 120 days. The presence of amplifiable norovirus RNA on the strips was inversely correlated with the duration of storage and the storage temperature. Norovirus RNA remained detectable for a sufficient amount of time at room temperature or even in warmer climatic conditions to allow transportation of the samples from a field site to a reference laboratory using regular postal mail. To prove that viral infectivity was lost upon contact with the SDS/EDTA-treated strips, feline calicivirus F9 (10(7) TCID50/ml) was loaded onto the strips. After elution and dialysis, no cytopatic effect could be observed upon incubation on Crandell-Reese feline kidney cells. The SDS/EDTA-pretreated chromatography filter paper strips are an inexpensive, biosafe and adequate method to collect, transport and store norovirus samples. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 48
页数:4
相关论文
共 16 条
[1]   DETECTION AND DIFFERENTIATION OF ANTIGENICALLY DISTINCT SMALL ROUND-STRUCTURED VIRUSES (NORWALK-LIKE VIRUSES) BY REVERSE TRANSCRIPTION PCR AND SOUTHERN HYBRIDIZATION [J].
ANDO, T ;
MONROE, SS ;
GENTSCH, JR ;
JIN, Q ;
LEWIS, DC ;
GLASS, RI .
JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (01) :64-71
[2]   A feline kidney cell line-based plaque assay for feline calicivirus, a surrogate for Norwalk virus [J].
Bidawid, S ;
Malik, N ;
Adegbunrin, O ;
Sattar, SA ;
Farber, JM .
JOURNAL OF VIROLOGICAL METHODS, 2003, 107 (02) :163-167
[3]   Winter vomiting - Infections due to Norwalk-like viruses are underestimated [J].
Cowden, JM .
BMJ-BRITISH MEDICAL JOURNAL, 2002, 324 (7332) :249-250
[4]   Inactivation of feline calicivirus, a surrogate of norovirus (formerly Norwalk-like viruses), by different types of alcohol in vitro and in vivo [J].
Gehrke, C ;
Steinmann, J ;
Goroncy-Bermes, P .
JOURNAL OF HOSPITAL INFECTION, 2004, 56 (01) :49-55
[5]   Taxonomy of the caliciviruses [J].
Green, KY ;
Ando, T ;
Balayan, MS ;
Berke, T ;
Clarke, IN ;
Estes, MK ;
Matson, DO ;
Nakata, S ;
Neill, JD ;
Studdert, MJ ;
Thiel, HJ .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 :S322-S330
[6]  
Green KY, 1997, ARCH VIROL, P153, DOI 10.1007/BF01243835
[7]  
GREEN KY, 2001, FIELDS VIROLOGY, P847
[8]  
HO MS, 1989, LANCET, V2, P961
[9]   SEQUENCE AND GENOMIC ORGANIZATION OF NORWALK VIRUS [J].
JIANG, X ;
WANG, M ;
WANG, KN ;
ESTES, MK .
VIROLOGY, 1993, 195 (01) :51-61
[10]   The discovery of the 27-nm Norwalk virus: An historic perspective [J].
Kapikian, AZ .
JOURNAL OF INFECTIOUS DISEASES, 2000, 181 :S295-S302