Literature DB >> 9820838

Improvement of the specificity of enzyme immunoassays for the detection of rotavirus and adenovirus in fecal specimens.

H Rabenau1, B Knoll, R Allwinn, H W Doerr, B Weber.   

Abstract

A variable rate of false-positive results may be observed with commercial enzyme immunoassays (EIAs) for the detection of rotavirus and adenovirus antigen in stool specimens, depending on the quality of the reagents and the presence of potentially interfering substances in stool samples. The present study was performed in an attempt to improve the specificity of current commercial rotavirus and adenovirus EIAs without significant loss of sensitivity by optimizing the cut-off value. A collective of 174 stool samples obtained from children suffering from acute gastroenteritis was tested. Electron microscopy (EM) and PAGE were used as reference methods for rotavirus detection. For the evaluation of the adenovirus kits, virus isolation in cell culture and the polymerase chain reaction served as reference standards. The highest sensitivity for rotavirus and adenovirus detection was achieved by the Ridascreen(R) Rotavirus and Ridascreen Adenovirus. However, the Ridascreen(R) Rotavirus and Ridascreen Adenovirus produced the highest number of false-positive results (n = 9) for each rotavirus and adenovirus detection. Cross-reactivities to coronaviruses and reoviruses were observed with the rotavirus antigen EIAs. For Rotazyme II, Ridascreen Rotavirus and Ridascreen Adenovirus, the specificity could be markedly increased without loss of sensitivity by doubling the cut-off value. For the alternative immunoassays, which were overall more specific, it was not possible to significantly decrease the rate of false-positive results without impairment of sensitivity by raising the cut-off value. In conclusion, at least for some rotavirus and adenovirus antigen EIAs, the cut-off value set by the manufacturer may not permit an optimal differentiation between true-positive and -negative samples. By raising the cut-off value from 50 to 100%, the specificity of two rotavirus antigen and one adenovirus antigen EIA can be improved markedly without significant loss of sensitivity.

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Year:  1998        PMID: 9820838     DOI: 10.1159/000024915

Source DB:  PubMed          Journal:  Intervirology        ISSN: 0300-5526            Impact factor:   1.763


  5 in total

1.  Evaluation of two enzyme immunoassays for detection of human rotaviruses in fecal specimens.

Authors:  B R Eing; G May; H G Baumeister; J E Kühn
Journal:  J Clin Microbiol       Date:  2001-12       Impact factor: 5.948

2.  Sensitive and specific quantitative detection of rotavirus A by one-step real-time reverse transcription-PCR assay without antecedent double-stranded-RNA denaturation.

Authors:  Slavica Mijatovic-Rustempasic; Ka Ian Tam; Tara K Kerin; Jamie M Lewis; Rashi Gautam; Osbourne Quaye; Jon R Gentsch; Michael D Bowen
Journal:  J Clin Microbiol       Date:  2013-07-12       Impact factor: 5.948

3.  Rotavirus infection increases the risk of bacteremia in children with nontyphoid Salmonella gastroenteritis.

Authors:  T-Y Hung; M-C Liu; C-F Hsu; Y-C Lin
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2008-10-24       Impact factor: 3.267

4.  Adenovirus gastroenteritis in Hungary, 2003-2006.

Authors:  K Bányai; P Kisfali; A Bogdán; V Martella; B Melegh; D Erdman; G Szucs
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2009-03-04       Impact factor: 3.267

5.  Discrepancies in viral gastroenteritis diagnosis: an unusual dual reovirus-adenovirus infection case.

Authors:  Miguel O Giordano; Laura C Martinez; Leonardo J Ferreyra; María B Isa; Mirtha Paez Rearte; Jorge V Pavan; Silvia V Nates
Journal:  J Clin Virol       Date:  2005-01       Impact factor: 3.168

  5 in total

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