Distribution of Antibodies to Coxiella burnetii in Patients with Unknown Fever and Atypical Pneumonia.
- Author:
Man Suck PARK
1
;
Mi Yeoun PARK
;
Yung Oh SHIN
Author Information
1. Laboratory of Rickettsial and Zoonotic Diseases, Department of Bacteriology, National Institute of Health, 5 Nokbeon-dong, Eunpyeong-gu, Seoul, Korea. pmansuk@nih.go.kr
- Publication Type:Original Article
- Keywords:
Q fever;
Coxiella burnetii;
Laboratory diagnosis;
Anti-phase II antigen;
PCR
- MeSH:
Abattoirs;
Animals;
Antibodies*;
Clinical Laboratory Techniques;
Coxiella burnetii*;
Coxiella*;
Diagnosis;
Fever*;
Fluorescent Antibody Technique, Indirect;
Humans;
Immunoglobulin A;
Immunoglobulin G;
Immunoglobulin M;
Korea;
Plasmids;
Pneumonia*;
Polymerase Chain Reaction;
Q Fever;
Sensitivity and Specificity
- From:Journal of Bacteriology and Virology
2003;33(4):307-315
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
Coxiella burnetii is the causative agent of Q fever worldwide in human and animals. While several clinical cases of Q fever were reported in Korea till the middle of 1990s, nobody has reported a case thereafter. However possibilities for an outbreak have still been raised. In this study, antibody titers to C. burnetii in patients with unknown fever and atypical pneumonia were tested by an indirect immunofluorescence method using the phase II antigen. In addition, the validity of a PCR method in indentifying C. burnetii directly from human sera was tested. Among the 560 specimens from atypical pneumonia patients, 23 sera (4.29%) reacted positively to the phase II antigen of C. burnetii. IgG antiphase II antigen titers were 1:16 in 16, 1:32 in 2, 1:64 in 2, 1:128 in 2, and > or =1:256 in one serum. IgM and IgA antibodies anti-phase II antigen were detected in 6 and 3 sera at 1:16, respectively. And each two sera had IgM antibodies at 1:32 and 1:64. Anti-phase II antigen IgG antibody titers in the patients with unknown fever were 1:16 in 5, 1:32 in 2, 1:128 in 1, and 1:256 in 3 sera. However, IgM antibody wasn't detected in this group. Of the 202 sera from abattoir workers, 5 (2.47%) reacted with phase II antigen. Among 448 sera of healthy controls, anti-phase II antigen IgG titer of 1:16 was found in 7 and 1:32 in 1 and 1:64 in 3 sera. In the case of IgM titer, two sera were reactive at 1:16 and 1:32, each. Significant differences among the test groups were not noted in the present study. The PCR assay to detect C. burnetii com-1 and plasmid genes did not show reliable specificity and sensitivity for the diagnosis of Q fever. So, the usefulness of the PCR for laboratory diagnosis of Q fever still remains controversial.
