This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Field, P. R.
Right arrow Articles by Devine, P. L.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Field, P. R.
Right arrow Articles by Devine, P. L.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, April 2000, p. 1645-1647, Vol. 38, No. 4
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Comparison of a Commercial Enzyme-Linked Immunosorbent Assay with Immunofluorescence and Complement Fixation Tests for Detection of Coxiella burnetii (Q Fever) Immunoglobulin M

Peter R. Field,1 Jody L. Mitchell,2 Avelina Santiago,1 David J. Dickeson,1 Sau-Wan Chan,1 David W. T. Ho,1 Alan M. Murphy,3 Andrea J. Cuzzubbo,2 and Peter L. Devine2,*

Centre for Infectious Diseases and Microbiology Laboratory Services, Institute of Clinical Pathology and Medical Research, Westmead,1 PanBio, Brisbane,2 and Viral Diagnostic and Referral Laboratory, North Ryde,3 Australia

Received 6 August 1999/Returned for modification 17 October 1999/Accepted 3 January 2000

A commercially available enzyme-linked immunosorbent assay (ELISA) for the diagnosis of Q fever (PanBio Coxiella burnetii immunoglobulin M [IgM] ELISA, QFM-200) was compared to the indirect fluorescent antibody test (IFAT) for C. burnetii IgM and the complement fixation test (CFT). The ELISA demonstrated 92% agreement with the reference method (IFAT), and gave a sensitivity of 99% (69 of 70 samples) and a specificity of 88% (106 of 121). Specificity can be increased with confirmation by IFAT. CFT was found to have a specificity of 90% (107 of 119), although it was lacking in sensitivity (73%; 51 of 70). No cross-reactivity was observed in the ELISA with serum samples from patients with mycoplasma (n = 6), chlamydia (n = 5), or legionella (n = 4) infections, although 2 of 5 patients with leptospirosis and 1 of 4 samples containing rheumatoid factor (RF) demonstrated positive results in the ELISA. Results indicate that the performance of the PanBio C. burnetii (Q fever) IgM ELISA (F = 187) is superior to that of CFT (F = 163), and consequently the ELISA should be a useful aid in the diagnosis of acute Q fever.


* Corresponding author. Mailing address: PanBio Pty., Ltd., 116 Lutwyche Rd., Windsor 4030, Queensland, Australia. Phone: 61-7-33571177. Fax: 61-7-33571222. E-mail: peter_devine{at}panbio.com.au.


Journal of Clinical Microbiology, April 2000, p. 1645-1647, Vol. 38, No. 4
0095-1137/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Setiyono, A., Ogawa, M., Cai, Y., Shiga, S., Kishimoto, T., Kurane, I. (2005). New Criteria for Immunofluorescence Assay for Q Fever Diagnosis in Japan. J. Clin. Microbiol. 43: 5555-5559 [Abstract] [Full Text]  
  • Thorpe, R., Swanson, S. J (2005). Current Methods for Detecting Antibodies against Erythropoietin and Other Recombinant Proteins. CVI 12: 28-39 [Full Text]  
  • Field, P. R., Santiago, A., Chan, S.-W., Patel, D. B., Dickeson, D., Mitchell, J. L., Devine, P. L., Murphy, A. M. (2002). Evaluation of a Novel Commercial Enzyme-Linked Immunosorbent Assay Detecting Coxiella burnetii-Specific Immunoglobulin G for Q Fever Prevaccination Screening and Diagnosis. J. Clin. Microbiol. 40: 3526-3529 [Abstract] [Full Text]