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Bacterial pathogens in Ixodes ricinus collected from lizards Lacerta agilis and Zootoca vivipara in urban areas of Wroclaw, SW Poland- preliminary study.
Dyczko, Dagmara; Krysmann, Alicja; Kolanek, Aleksandra; Borczyk, Bartosz; Kiewra, Dorota.
Afiliação
  • Dyczko D; Department of Microbial Ecology and Acaroentomology, Faculty of Biological Sciences, University of Wroclaw, Przybyszewskiego 63/77, Wroclaw, 51-148, Poland. dagmara.dyczko@uwr.edu.pl.
  • Krysmann A; Faculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, NMBU, Ås, Norway.
  • Kolanek A; Department of Geoinformatics and Cartography, Institute of Geography and Regional Development, Faculty of Earth Sciences and Environmental Management, University of Wroclaw, pl. Uniwersytecki 1, Wroclaw, 50-137, Poland.
  • Borczyk B; Department of Evolutionary Biology and Conservation of Vertebrates, Faculty of Biological Sciences, University of Wroclaw, Sienkiewicza 21, Wroclaw, 50-335, Poland.
  • Kiewra D; Department of Microbial Ecology and Acaroentomology, Faculty of Biological Sciences, University of Wroclaw, Przybyszewskiego 63/77, Wroclaw, 51-148, Poland.
Exp Appl Acarol ; 2024 Jun 13.
Article em En | MEDLINE | ID: mdl-38869727
ABSTRACT
The aim of this study was to determine the level of infection of Ixodes ricinus ticks with pathogens (Borrelia spp., Rickettsia spp., and Anaplasma spp.) collected from Lacerta agilis and Zootoca vivipara lizards in the urban areas of Wroclaw (SW Poland). The study was carried out in July-August 2020. Lizards were caught by a noose attached to a pole or by bare hands, identified by species, and examined for the presence of ticks. Each lizard was then released at the site of capture. Ticks were removed with tweezers, identified by species using keys, and molecular tests were performed for the presence of pathogens. From 28 lizards (17 specimens of Z. vivipara and 11 specimens of L. agilis) a total of 445 ticks, including 321 larvae and 124 nymphs, identified as I. ricinus were collected. A larger number of ticks were obtained from L. agilis compared to Z. vivipara. Molecular tests for the presence of pathogens were performed on 445 specimens of I. ricinus. The nested PCR method for the fla gene allowed the detection of Borrelia spp. in 9.4% of ticks, and it was higher in ticks from L. agilis (12.0%) than from Z. vivipara (1.0%). The RFLP method showed the presence of three species, including two belonging to the B. burgdorferi s.l. complex (B. lusitaniae and B. afzelii), and B. miyamotoi. The overall level of infection of Rickettsia spp. was 19.3%, including 27.2% in ticks collected from Z. vivipara and 17.0% from L. agilis. Sequencing of randomly selected samples confirmed the presence of R. helvetica. DNA of Anaplasma spp. was detected only in one pool of larvae collected from L. agilis, and sample sequencing confirmed the presence of (A) phagocytophilum. The research results indicate the important role of lizards as hosts of ticks and their role in maintaining pathogens in the environment including urban agglomeration as evidenced by the first recorded presence of (B) miyamotoi and (A) phagocytophilum in I. ricinus ticks collected from L. agilis. However, confirmation of the role of sand lizards in maintaining (B) miyamotoi and A. phagocytophilum requires more studies and sampling of lizard tissue.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article