Anaplasma infections in ticks and reservoir host from Slovakia

•Ticks and animal hosts were screened for the presence of A. phagocytophilum.•Bacterial DNA was confirmed in questing ixodid ticks from all sampling sites.•Tested wild ungulates were infected to a considerable extent.•GroEL isolates from rodents differ from those isolated from wild ungulates.•Europe...

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Veröffentlicht in:Infection, genetics and evolution genetics and evolution, 2014-03, Vol.22, p.265-272
Hauptverfasser: Víchová, Bronislava, Majláthová, Viktória, Nováková, Mária, Stanko, Michal, Hviščová, Ivana, Pangrácová, Lucia, Chrudimský, Tomáš, Čurlík, Ján, Peťko, Branislav
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Sprache:eng
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Zusammenfassung:•Ticks and animal hosts were screened for the presence of A. phagocytophilum.•Bacterial DNA was confirmed in questing ixodid ticks from all sampling sites.•Tested wild ungulates were infected to a considerable extent.•GroEL isolates from rodents differ from those isolated from wild ungulates.•European rodents do not harbour bacterial strains with strong zoonotic potential. Anaplasma phagocytophilum is a worldwide distributed bacterium with a significant medical and veterinary importance. It grows within the phagosome of infected neutrophils and is responsible for human granulocytic anaplasmosis (HGA), tick-borne fever (TBF) of small ruminants and cattle, canine and equine granulocytic anaplasmosis, but infects also a great variety of wildlife species. Wild ungulates and rodents are considered reservoirs of infection in natural foci. The objective of this study was to determine the spectrum of animal species involved in the circulation of A. phagocytophilum in Slovakia and to analyze the variability of obtained nucleotide sequences, in order to determine whether genotypes from Slovakia cluster according to host-species or geographical location. Several animal species and vector ticks were screened for the presence of members of the family Anaplasmataceae using PCR based methods. Additional data on the molecular evidence of Anaplasma ovis and Candidatus Neoehrlichia mikurensis are presented. These pathogens were detected in tested sheep flocks and rodents with the mean infection rates of 8.16% and 10.75%, respectively. A. phagocytophilum was genotyped by 16S rRNA and groEL gene sequencing. Bacterial DNA was confirmed in questing ixodid ticks, in domesticated canine, wild rodents and several species of wild ungulates. In European isolates, 16S rRNA gene does not seem to be an appropriate locus for the analyses of heterogeneity as it is too conservative. Similarly, 16S rRNA isolates from our study did not reveal any polymorphisms. All isolates were identical in overlapped region and showed identity with sequences from ticks, horses or ruminants previously isolated elsewhere in the world. On the other hand, the groESL heat shock operon is widely used for determination of diversity and the analyses have already revealed considerable degree of heterogeneity. Tested ungulates were infected with A. phagocytophilum to a considerable extent. High proportions of red and roe deer tested positive and the rates of infection reached over 60.0%. GroEL sequences from canine
ISSN:1567-1348
1567-7257
DOI:10.1016/j.meegid.2013.06.003