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Journal of Clinical Microbiology, April 2000, p. 1645-1647, Vol. 38, No. 4
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.
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
*
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.
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