Lenka Čechová1, Monika Halánová2, Ingrid Babinská3, Oľga Danišová4, Martin Bartkovský5, Slavomír Marcinčák6, Dana Marcinčáková7, Alexandra Valenčáková8, Lýdia Čisláková9. 1. Department of Epidemiology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia. lenka.cechova@upjs.sk. 2. Department of Epidemiology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia. monika.halanova@upjs.sk. 3. Department of Epidemiology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia. ingrid.babinska@upjs.sk. 4. Department of Biology and Genetics, University of Veterinary Medicine and Pharmacy, Košice, Slovakia. olga.danisova@uvlf.sk. 5. Department of Hygiene and Food Industry Technology, University of Veterinary Medicine and Pharmacy, Košice, Slovakia. martin.bartkovsky@uvlf.sk. 6. Department of Hygiene and Food Industry Technology, University of Veterinary Medicine and Pharmacy, Košice, Slovakia. slavomir.marcincak@uvlf.sk. 7. Department of Pharmacology and Toxicology, University of Veterinary Medicine and Pharmacy, Košice, Slovakia. dana.marcincakova@uvlf.sk. 8. Department of Biology and Genetics, University of Veterinary Medicine and Pharmacy, Košice, Slovakia. alexandra.valencakova@uvlf.sk. 9. Department of Epidemiology, Faculty of Medicine, Pavol Jozef Šafárik University, Košice, Slovakia. lydia.cislakova@upjs.sk.
Abstract
INTRODUCTION: <i>Chlamydia psittaci</i> is an obligate intracellular Gram-negative bacterium causing respiratory disease (chlamydiosis) or asymptomatic carriage in poultry. In humans, it is a zoonotic agent of ornithosis/psittacosis. Due to low awareness of the disease and variable clinical presentation, psittacosis is often remains unrecognised as such by general practitioners. Zoonotic transfer occurs through inhalation of contaminated aerosols, and originates from feathers, faecal material and respiratory tract exudates. OBJECTIVE: The aim of this study was to investigate chickens for the presence of <i>Chlamydia sp</i>. from pharyngeal and cloacal swabs and review the zoonotic risk for humans. MATERIAL AND METHODS: 138 clinically healthy chickens from farms in Slovakia were examined for the presence of <i>Chlamydia sp</i>. The age of the chickens was 6 months. Two different samples were used - pharyngeal swabs and cloacal swabs. Each sample was examined by the molecular PCR method, and in the case of a positive result the identity of the obtained sequences was examined by a BLAST search. RESULTS: Of the total number of 276 examined samples from 138 chickens, 19 (6.9%) showed positivity for <i>C. psittaci</i> infection, 12 (8.7%) which were positive from pharyngeal swabs and 7 (5.1%) from cloacal swabs. None of the chickens were positive in both samples. Phylogenetic examination of the 19 isolates identified in the study, based on the 23S rRNA gene sequence, revealed that the isolates obtained were identical with <i>C. psittaci</i>, and genetically very close to genotypes B and genotype E. CONCLUSIONS: <i>C. psittaci</i> infections are apparently emerging in chickens. Chicken-processing plant employees should be considered a risk group for human psittacosis. There is a need for higher awareness and for efficient risk assessment and management.
INTRODUCTION: <i>Chlamydia psittaci</i> is an obligate intracellular Gram-negative bacterium causing respiratory disease (chlamydiosis) or asymptomatic carriage in poultry. In humans, it is a zoonotic agent of ornithosis/psittacosis. Due to low awareness of the disease and variable clinical presentation, psittacosis is often remains unrecognised as such by general practitioners. Zoonotic transfer occurs through inhalation of contaminated aerosols, and originates from feathers, faecal material and respiratory tract exudates. OBJECTIVE: The aim of this study was to investigate chickens for the presence of <i>Chlamydia sp</i>. from pharyngeal and cloacal swabs and review the zoonotic risk for humans. MATERIAL AND METHODS: 138 clinically healthy chickens from farms in Slovakia were examined for the presence of <i>Chlamydia sp</i>. The age of the chickens was 6 months. Two different samples were used - pharyngeal swabs and cloacal swabs. Each sample was examined by the molecular PCR method, and in the case of a positive result the identity of the obtained sequences was examined by a BLAST search. RESULTS: Of the total number of 276 examined samples from 138 chickens, 19 (6.9%) showed positivity for <i>C. psittaci</i> infection, 12 (8.7%) which were positive from pharyngeal swabs and 7 (5.1%) from cloacal swabs. None of the chickens were positive in both samples. Phylogenetic examination of the 19 isolates identified in the study, based on the 23S rRNA gene sequence, revealed that the isolates obtained were identical with <i>C. psittaci</i>, and genetically very close to genotypes B and genotype E. CONCLUSIONS: <i>C. psittaci</i> infections are apparently emerging in chickens. Chicken-processing plant employees should be considered a risk group for humanpsittacosis. There is a need for higher awareness and for efficient risk assessment and management.