European multicenter evaluation of commercial enzyme immunoassays for detecting norovirus antigen in fecal samples

被引:65
作者
Gray, Jim J.
Kohli, Evelyne
Ruggeri, Franco M.
Vennema, Harry
Sanchez-Fauquier, Alicia
Schreier, Eckart
Gallimore, Chris I.
Iturriza-Gomara, Miren
Giraudon, Helene
Pothier, Pierre
Di Bartolo, Ilaria
Inglese, Nadia
de Bruin, Erwin
van der Veer, Bas
Moreno, Silvia
Montero, Vanessa
de Llano, Mari C.
Hoehne, Marina
Diedrich, Sabine M.
机构
[1] Hlth Protect Agcy, Ctr Infect, Virus Reference Dept, Enter Virus Unit, London NW9 5HT, England
[2] CHU Brocage, Virol Lab, F-21034 Dijon, France
[3] Ist Super Sanita, Dipartimento Sanita Alimentare & Anim, I-00161 Rome, Italy
[4] Natl Inst Publ Hlth & Environm, Diagnost Lab Infect Dis & Perinatal Screening, NL-3720 BA Bilthoven, Netherlands
[5] Inst Salud Carlos III, Ctr Nacl Microbiol, Madrid, Spain
[6] Robert Koch Inst, Dept Mol Epidemiol Viral Pathogens, D-1000 Berlin, Germany
关键词
D O I
10.1128/CVI.00214-07
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
A total of 2,254 fecal samples were tested in a European multicenter evaluation of commercially available norovirus antigen detection assays. Two commercial enzyme immunoassays, IDEIA Norovirus (Oxoid; Thermo Fisher Scientific, Ely, United Kingdom) and RIDASCREEN Norovirus (R-Biopharm, Darmstadt, Germany), were included in the evaluation, and their performance was compared with the results of reverse transcription-PCR (RT-PCR). Included in the evaluation were samples collected in sporadic cases of gastroenteritis, samples from outbreaks in which two or more samples were collected, well-characterized samples representing genotypes currently cocirculating within Europe, and samples collected from patients with gastroenteritis caused by a pathogen other than norovirus. The sensitivities and specificities of the IDEIA Norovirus and RIDASCREEN Norovirus assays were 58.93 and 43.81% and 93.91 and 96.37%, respectively, compared with RT-PCR. The sensitivities of both assays for outbreak investigations improved when six or more samples from an outbreak were examined. The IDEIA Norovirus assay exhibited reactivity to a broader range of norovirus genotypes than the RIDASCREEN Norovirus assay, which showed genotype-dependent sensitivities. The results indicate that, if used, these assays should serve as screening assays and the results should be confirmed by RT-PCR.
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页码:1349 / 1355
页数:7
相关论文
共 25 条
[1]   Detection of Norwalk virus and other genogroup 1 human caliciviruses by a monoclonal antibody, recombinant-antigen-based immunoglobulin M capture enzyme immunoassay [J].
Brinker, JP ;
Blacklow, NR ;
Estes, MK ;
Moe, CL ;
Schwab, KJ ;
Herrmann, JE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1998, 36 (04) :1064-1069
[2]   Evaluation and comparison of two commercial enzyme-linked immunosorbent assay kits for detection of antigenically diverse human noroviruses in stool samples [J].
Burton-MacLeod, JA ;
Kane, EM ;
Beard, RS ;
Hadley, LA ;
Glass, RI ;
Ando, T .
JOURNAL OF CLINICAL MICROBIOLOGY, 2004, 42 (06) :2587-2595
[3]   Diagnosis of Norovirus outbreaks by commercial ELISA or RT-PCR [J].
de Bruin, Erwin ;
Duizer, Erwin ;
Vennema, Harry ;
Koopmans, Marion P. G. .
JOURNAL OF VIROLOGICAL METHODS, 2006, 137 (02) :259-264
[4]   Evaluation of the Dako IDEIA norovirus EIA assay for detection of norovirus using faecal specimens from Australian gastroenteritis outbreaks [J].
Dimitriadis, A ;
Bruggink, LD ;
Marshall, JA .
PATHOLOGY, 2006, 38 (02) :157-165
[5]   Evaluation of a commercial enzyme immunoassay for detection of norovirus in outbreak specimens [J].
Dimitriadis, A ;
Marshall, JA .
EUROPEAN JOURNAL OF CLINICAL MICROBIOLOGY & INFECTIOUS DISEASES, 2005, 24 (09) :615-618
[6]   The role of environmental contamination with small round structured viruses in a hospital outbreak investigated by reverse-transcriptase polymerase chain reaction assay [J].
Green, J ;
Wright, PA ;
Gallimore, CI ;
Mitchell, O ;
Morgan-Capner, P ;
Brown, DWG .
JOURNAL OF HOSPITAL INFECTION, 1998, 39 (01) :39-45
[7]   BROADLY REACTIVE REVERSE-TRANSCRIPTASE POLYMERASE CHAIN-REACTION FOR THE DIAGNOSIS OF SRSV-ASSOCIATED GASTROENTERITIS [J].
GREEN, J ;
GALLIMORE, CI ;
NORCOTT, JP ;
LEWIS, D ;
BROWN, DWG .
JOURNAL OF MEDICAL VIROLOGY, 1995, 47 (04) :392-398
[8]   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
[9]   A predominant role for Norwalk-like viruses as agents of epidemic gastroenteritis in Maryland nursing homes for the elderly [J].
Green, KY ;
Belliot, G ;
Taylor, JL ;
Valdesuso, J ;
Lew, JF ;
Kapikian, AZ ;
Lin, FYC .
JOURNAL OF INFECTIOUS DISEASES, 2002, 185 (02) :133-146
[10]   POLYMERASE CHAIN-REACTION DETECTION OF SMALL ROUND-STRUCTURED VIRUSES FROM 2 RELATED HOSPITAL OUTBREAKS OF GASTROENTERITIS USING INOSINE-CONTAINING PRIMERS [J].
GREEN, SM ;
LAMBDEN, PR ;
DENG, Y ;
LOWES, JA ;
LINEHAM, S ;
BUSHELL, J ;
ROGERS, J ;
CAUL, EO ;
ASHLEY, CR ;
CLARKE, IN .
JOURNAL OF MEDICAL VIROLOGY, 1995, 45 (02) :197-202