Abstract

Coxiella burnetii is the causative agent of acute and chronic Q fever in humans. Although the isolates studied so far showed a difference in virulence potential between those causing the two forms of the disease, implying a difference in their proteomic profile, the methods used so far to diagnose the two forms of the disease do not provide sufficient discriminatory capability, and human infections may be often misdiagnosed. The aim of the current study was to identify the outer membrane Com1 (CBU_1910) as a candidate protein for serodiagnostics of Q fever. The protein was cloned, expressed, purified, and used as an antigen in ELISA. The protein was then used for the screening of sera from patients suffering from chronic Q fever endocarditis, patients whose samples were negative for phase I immunoglobulin G (IgG), patients for whom at least one sample was positive for phase I IgG, and patients suffering from any kind of rheumatoid disease. Blood donors were used as the control group. Following statistical analysis, 92.4% (122/132) of the samples tested agreed with the negative clinical diagnosis, and 72.2% (26/36) agreed with the positive clinical diagnosis. Moreover, a significant correlation to the presence of the disease (p = 0.00) was calculated. The results support the idea that a Com1 antigen-based serodiagnostic test may be useful for differential diagnosis of chronic Q fever. Further studies are required to compare more immunogenic proteins of the bacterium against samples originating from patients suffering from different forms of the disease.

Highlights

  • Q fever is a zoonosis caused by the, until recently obligatory, intracellular bacterium Coxiella burnetii [1]

  • We identified and determined antigenic proteins which could be used for the development of a chronic Q fever-specific ELISA and evolve into a fast immunochromatographic kit

  • The interest of this study lies in the search for a reliable serological diagnostic tool for the differential diagnosis of Q fever

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Summary

Introduction

Q fever is a zoonosis caused by the, until recently obligatory, intracellular bacterium Coxiella burnetii [1]. The fact that the pathogen is primarily spread by contaminated aerosols and can travel via wind to large distances due to its small size, as well as its remarkable viability against environmental conditions and its extremely low infection dose, the originally strong belief that Q fever is a strictly occupational disease is starting to decline. As proof of this statement comes the Netherlands Q fever outbreak in 2009 during which more than 4000 Q fever cases were reported [2].

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