Evidence map›Paper›PMID 38869727›Full record

ArticleExperimental & applied acarology2024

Bacterial pathogens in Ixodes ricinus collected from lizards Lacerta agilis and Zootoca vivipara in urban areas of Wrocław, SW Poland- preliminary study.

Dagmara Dyczko, Alicja Krysmann, Aleksandra Kolanek, Bartosz Borczyk, Dorota Kiewra

Abstract read
In one paragraph

Article in Experimental & applied acarology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Prevalence ofPathogens (Basel, Switzerland) · 2025
    Article
  4. Animals : an open access journal from MDPI · 2025
    Article
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Dagmara DyczkoDepartment of Microbial Ecology and Acaroentomology, Faculty of Biological Sciences, University of Wrocław, Przybyszewskiego 63/77, Wrocław, 51-148, Poland. dagmara.dyczko@uwr.edu.pl.ORCID http://orcid.org/0000-0003-1601-8726
Alicja KrysmannFaculty of Chemistry, Biotechnology and Food Science, Norwegian University of Life Sciences, NMBU, Ås, Norway.ORCID http://orcid.org/0000-0003-1353-0994
Aleksandra KolanekDepartment of Geoinformatics and Cartography, Institute of Geography and Regional Development, Faculty of Earth Sciences and Environmental Management, University of Wrocław, pl. Uniwersytecki 1, Wrocław, 50-137, Poland.ORCID http://orcid.org/0000-0002-6218-9916
Bartosz BorczykDepartment of Evolutionary Biology and Conservation of Vertebrates, Faculty of Biological Sciences, University of Wrocław, Sienkiewicza 21, Wrocław, 50-335, Poland.ORCID http://orcid.org/0000-0001-9630-1809
Dorota KiewraDepartment of Microbial Ecology and Acaroentomology, Faculty of Biological Sciences, University of Wrocław, Przybyszewskiego 63/77, Wrocław, 51-148, Poland.ORCID http://orcid.org/0000-0002-7208-101X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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 Wrocław (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.

Indexed as

AnaplasmaBorreliaIxodesLizardsRickettsiaAnimalsCitiesFemaleLarvaMaleNymphPolandBacterial pathogensIxodes ricinusLizardsUrban ecologyWrocław

Identifiers

PMID38869727
PMCPMC11269471

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.