Literature DB >> 15566901

Detection of respiratory viruses in nasopharyngeal secretions with immunofluorescence technique for multiplex screening-an evaluation of the Chemicon assay.

K Shen1, G Zhaori, B Zweygberg-Wirgart, M Ying, M Grandien, B Wahren, A Linde.   

Abstract

BACKGROUND: Antigen detection with immunofluorescence is an efficient method for diagnosis of respiratory tract infections, but has previously not allowed for simple screening of many respiratory viruses. Pools of monoclonal antibodies against various respiratory viruses are now available, and are potentially important tools for improvement of antigen detection in nasopharyngeal samples.
OBJECTIVE: To evaluate the commercially available Chemicon immunofluorescence assay (IFA; respiratory viruses panel and identification kit), an indirect IFA containing a pool of monoclonal antibodies for screening for influenza A, B, respiratory syncytial virus (RSV), parainfluenza 1, 2, 3 and adenovirus, and the respective individual antibodies. STUDY
DESIGN: Ninety-six frozen preparations from nasopharyngeal secretions or bronchoalveolar lavages were retrospectively examined with the assay, and the results compared with other IFAs for antigen detection and cell culture isolation obtained in the everyday routine. Nasopharyngeal preparations from 300 children with lower respiratory tract infections at Beijing Children's Hospital during the 1994-1995 winter season were also examined.
RESULTS: The sensitivity of the Chemicon assay compared to the combined results of routine IFA and isolation was 89% and specificity 92%. If five identifications of RSV made with the Chemicon assay alone were regarded to be truly positive, the specificity was 100%. A viral etiology was identified in 105/280 (38%) evaluable samples drawn from the Chinese children (influenza A 20%, RSV 14%, adenovirus 3% and parainfluenza 1, 2 or 3, 7%).
CONCLUSION: One problem with the Chemicon assay was that for around 4-13% of samples there was a non-specific staining in the screening assay, necessitating stainings for verification. Despite this, the assay is an excellent tool for identification of viral respiratory tract infections, giving an increased sensitivity compared to direct immunofluorescence assays.

Entities:  

Year:  1996        PMID: 15566901     DOI: 10.1016/0928-0197(96)00229-2

Source DB:  PubMed          Journal:  Clin Diagn Virol        ISSN: 0928-0197


  4 in total

1.  Simultaneous detection and identification of human parainfluenza viruses 1, 2, and 3 from clinical samples by multiplex PCR.

Authors:  J E Echevarría; D D Erdman; E M Swierkosz; B P Holloway; L J Anderson
Journal:  J Clin Microbiol       Date:  1998-05       Impact factor: 5.948

2.  Simultaneous detection and typing of influenza viruses A and B by a nested reverse transcription-PCR: comparison to virus isolation and antigen detection by immunofluorescence and optical immunoassay (FLU OIA).

Authors:  B Herrmann; C Larsson; B W Zweygberg
Journal:  J Clin Microbiol       Date:  2001-01       Impact factor: 5.948

3.  Isolation & molecular characterization of human parainfluenza virus in Chennai, India.

Authors:  C P Indumathi; P Gunanasekaran; K Kaveri; Kavita Arunagiri; S Mohana; A Khaleefathullah Sheriff; B V SureshBabu; P Padmapriya; R Senthilraja; Gracy Fathima
Journal:  Indian J Med Res       Date:  2015-11       Impact factor: 2.375

4.  Development and evaluation of a real-time nucleic acid sequence based amplification assay for rapid detection of influenza A.

Authors:  Catherine Moore; Sam Hibbitts; Neil Owen; Sally A Corden; Graham Harrison; Julie Fox; Colin Gelder; Diana Westmoreland
Journal:  J Med Virol       Date:  2004-12       Impact factor: 2.327

  4 in total

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