Prevalence of Coxiella burnetii in environmental samples collected from cattle farms in Eastern and Central Poland (2011–2012)

• Published in: Veterinary microbiology 2014-12, Vol.174 (3-4), p.600-606
• Main Authors: Bielawska-Drózd, Agata, Cieślik, Piotr, Mirski, Tomasz, Gaweł, Jerzy, Michalski, Aleksander, Niemcewicz, Marcin, Bartoszcze, Michał, Żakowska, Dorota, Lasocki, Krzysztof, Knap, Józef, Kocik, Janusz
• Format: Article
• Language: English
• Subjects: Animals; Base Sequence; Cattle; Cattle Diseases - epidemiology; Cattle Diseases - microbiology; Cell Line; Coxiella burnetii; Coxiella burnetii - genetics; Coxiella burnetii - immunology; Coxiella burnetii - isolation & purification; Environment; Environmental samples; Enzyme-Linked Immunosorbent Assay - veterinary; Female; Genotype; IS1111; Multi spacer typing; Multilocus Sequence Typing - veterinary; Phylogeny; Poland - epidemiology; Prevalence; Q Fever - epidemiology; Q Fever - microbiology; Q Fever - veterinary; Real-time PCR; Sequence Analysis, DNA - veterinary; Zoonosis
• ISSN: 0378-1135; 1873-2542
• DOI: 10.1016/j.vetmic.2014.09.034

•Coxiella burnetii as a highly dangerous pathogen for animals and humans.•Adaptation of real time PCR method for monitoring of livestock farms.•ELISA and CFT for serological screening.•MST method as a convenient tool for genotyping of C. burnetii. Coxiella burnetii is the etiologic agent of Q fever. It may occur as two different morphological forms, a large cell variant (LCV) and a small cell variant (SCV). The SCV is characterized by unique resistance to physical and chemical factors and may survive in the environment for many months. The objective of this study was to examine environmental samples for the presence of C. burnetii using real-time PCR in areas where Q fever was previously reported and in randomly selected animal farms where Q fever was not reported. The samples were collected in the following provinces in Poland: Lublin, Subcarpathian and Masovian. Monitoring was performed with real-time PCR and serological methods. Of the 727 environmental samples, 33 (4.54%) contained the multi-copy insertion sequence IS1111, which is specific for C. burnetii. Subsequently, the presence of C. burnetii antibodies was determined using serological tests in selected herds in which positive genetic results were obtained. Serological analyses of 169 serum samples using CFT and ELISA were performed on Polish black-and-white Holstein-Friesian cows and one cow imported from Denmark. Using the CFT method, 11 samples were positive for phase I antibodies and six were positive for phase II antibodies. Moreover, in two cases, the presence of antibodies specific for both phase I and phase II antigens of C. burnetii was detected. However, of the 169 examined serum samples, 20 were positive by ELISA test, of which six were also positive by CFT. Additionally, multi spacer typing (MST) of isolated C. burnetii strains was performed. The MST results identified two new genotypes in Poland, ST3 and ST6. The results indicate that continued research regarding spread of this pathogen within a country is necessary.