Abstract

Following an outbreak of Q fever in a group of students who contracted the infection during a training course on a sheep farm, a detailed investigation of the sheep flock involved was conducted. Of 478 flock animals, 60 Coxiella burnetii ELISA-positive and 60 ELISA-negative ewes were selected for the trial and divided into four groups. A month after the initial ELISA screening, all ewes in the flock (except the control group) were vaccinated. Sequentially collected blood samples were tested with ELISA and PCR; feces, milk, manure, bedding, and soil were tested with PCR. The immune response to the vaccination was 92.7%, while the overall C. burnetii seroprevalence in the flock after the human outbreak was 64.9%. PCR was positive for 0.2% of milk samples and 34.4% of fecal samples of animals from all four trial groups. C. burnetii DNA was not detected in any of the blood samples. Manure was PCR-positive for about 35 months; bedding from the stable was also positive while samples of pasture soil were negative. It appears that extensive cleaning and disinfection combined with vaccination could be regarded as an appropriate approach to control/prevent Q fever in farm settings even in the short term.

Highlights

  • Q fever, a zoonosis caused by Coxiella burnetii, has a worldwide distribution

  • In the group of positive vaccinated ewes, 23.3% of animals became seronegative before vaccination; after vaccination, these animals were found to be seropositive in ELISA 3

  • The aim was to determine the reduction of C. burnetii presence in the environment

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Summary

Introduction

Q fever, a zoonosis caused by Coxiella burnetii, has a worldwide distribution. Even though it is present in a wide range of animal species, including arthropods, it affects mostly ruminants and humans. Acute infections with C. burnetii in humans commonly include a self-limiting febrile episode, pneumonia, or granulomatous hepatitis, while the main clinical manifestation of chronic Q fever is endocarditis [3]. The main route of infection for humans is inhalation of contaminated aerosols or dust containing C. burnetii shed by infected female animals at parturition, when a great number of organisms can be found in fetal fluids and the placenta. After delivery, animals shed C. burnetii via urine, feces, and milk for several months [4,5]. Able to produce highly resistant spore-like forms, C. burnetii can survive in the environment as infectious particles for long periods [6]

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