Cited by 60Vector-borne infectious diseasesBartonella species infections researchViral Infections and Vectors

Detection of selected pathogens in ticks collected from cats and dogs in the Wrocław Agglomeration, South-West Poland

Open access
Król, Nina, Obiegala, Anna, Pfeffer, Martin, Lonc, Elżbieta, Kiewra, Dorota·2016·Parasites & Vectors

Abstract

BACKGROUND: Tick-borne infections are no longer confined to rural areas, they are documented with increasing frequency in urban settlements across the world. They are known to cause diseases in humans as well as in their companion animals. METHODS: During a period of 2 years, from January 2013 until December 2014, ticks were collected from dogs and cats in 18 veterinary clinics in the Wrocław Agglomeration, Poland. In total, 1455 ticks were found on 931 pets: 760 domestic dogs and 171 cats. For molecular examinations 127 I. ricinus ticks (115 females and 12 males) were randomly selected, all collected I. hexagonus (n = 137, 32 females, 98 nymphs, 7 larvae) and all collected D. reticulatus (n = 46, 31 females, 15 males) were taken. Ixodes ricinus and I. hexagonus ticks were tested for Rickettsia spp., Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis and Babesia spp., while D. reticulatus ticks were investigated for Rickettsia spp. and Babesia spp. only. RESULTS: In total, 65.4 % I. ricinus ticks were infected with at least one pathogen. Over 50 % of I. ricinus were positive for Rickettsia spp. (R. helvetica and R. monacensis). The infection level with A. phagocytophilum was 21.3 %. DNA of Cand. N. mikurensis was detected in 8.1 % I. ricinus ticks. Interestingly only female ticks were infected. The prevalence of Babesia spp. was confirmed in 9.0 % of I. ricinus involving the species B. microti and B. venatorum. A total of nineteen double, one triple and two quadruple infections were found in I. ricinus ticks only. Almost 11 % of I. hexagonus ticks were positive for at least one of the tested pathogens. Rickettsia spp. infection was found in 2.2 %, while A. phagocytophilum was detected in 8.1 % of I. hexagonus ticks. Only one nymph was positive for Cand. N. mikurensis and none of I. hexagonus ticks harbored a Babesia spp. Over 60 % of D. reticulatus ticks were positive for rickettsial DNA, exclusively belonging to the species R. raoultii. CONCLUSION: The high tick infestation rates and the prevalence of pathogens found in these ticks demonstrate a serious level of encounter to tick-borne diseases in urban dogs in the Wroclaw area, and provide evidence that dogs and cats themselves may substantially contribute to the circulation of the ticks and pathogens in the urban area.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1186/s13071-016-1632-0

Cites

2 of 2 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • In studies of pet-associated ticks, Rickettsia spp. was detected in 18.4 and 14.1% of Ixodes ticks in Italy and Belgium, respectively, while over 50% of I. ricinus were positive for Rickettsia spp. in Poland and Germany; Dermacentor ticks were pathogen-negative in Belgium, but 39% of D. reticulatus were found to be Rickettsia-positive in the study in Germany.

    “Interestingly, in studies of pet-associated ticks, Rickettsia spp. was detected in 18.4 and 14.1% of Ixodes ticks in Italy and Belgium, respectively, while over 50% of I. ricinus were positive for Rickettsia spp. in Poland and Germany; also, Dermacentor ticks were pathogen-negative in Belgium, but 39% of D. reticulatus were found to be Rickettsia–positive in the study in Germany [20–23].”

    From Tick-borne pathogens in ticks collected from dogs, Latvia, 2011–2016 (2019) · cites this paper as [21]

    Split into 2 atoms — 1 confirmed, 1 partially supported, 0 disputed, 0 misattributed, 0 unverifiable. Expand the claim to see per-atom verdicts.

    Experimental — accuracy not yet measured
  • The spectrum of detected pathogens was compatible to those reported recently in dog-associated ticks collected in Germany, Italy, Belgium and Poland.

    “The spectrum of detected pathogens was compatible to those reported recently in dog-associated ticks collected in Germany, Italy, Belgium and Poland [20–23].”

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 52

  1. [1]Diniz PP Schulz BS Hartmann K Breitschwerdt EB “Candidatus Neoehrlichia mikurensis” infection in a dog from Germany J Clin Microbiol 2011 49 2059 62 10.1128/JCM.02327-10 21367991 PMC3122698 · DOI
  2. [2]Homer MJ Aguilar-Delfin I Telford SR 3rd Krause PJ Persing DH Babesiosis Clin Microbiol Rev 2000 13 3 451 69 10.1128/CMR.13.3.451-469.2000 10885987 PMC88943 · DOI
  3. [3]Li H Jiang JF Liu W Zheng YC Huo QB Tang K Zuo SY Liu K Jiang BG Yang H Cao WC Human infection with Candidatus Neoehrlichia mikurensis China Emerg Infect Dis 2012 18 1636 9 10.3201/eid1810.120594 23017728 PMC3471638 · DOI
  4. [4]Woldehiwet Z The natural history of Anaplasma phagocytophilum Vet Parasitol 2010 167 2-4 108 22 10.1016/j.vetpar.2009.09.013 19811878 · DOI
  5. [5]Oteo JA Portillo A Tick-borne rickettsioses in Europe Ticks Tick Borne Dis 2012 3 271 8 10.1016/j.ttbdis.2012.10.035 23177355 · DOI
  6. [6]Solano-Gallego L Kidd L Trotta M Di Marco M Caldin M Furlanello T Breitschwerdt E Febrile illness associated with Rickettsia conorii infection in dogs from Sicily Emerg Infect Dis 2006 12 1985 8 10.3201/eid1212.060326 17326960 PMC3291343 · DOI
  7. [7]Parola P Paddock CD Socolovschi C Labruna MB Mediannikov O Kernif T Abdad MY Stenos J Bitam I Fournier PE Raoult D Update on tick-borne rickettsioses around the world: a geographic approach Clin Microbiol Rev 2013 26 4 657 702 10.1128/CMR.00032-13 24092850 PMC3811236 · DOI
  8. [8]Ibarra V Oteo JA Portillo A Santibanez S Blanco JR Metola L Rickettsia slovaca infection: DEBONEL/TIBOLA Ann N Y Acad Sci. 2006 1078 206 14 10.1196/annals.1374.040 17114711 · DOI
  9. [9]Podsiadły E Chmielewski T Karbowiak G Kędra E Tylewska-Wierzbanowska S The occurrence of spotted fever rickettsioses and other tick-borne infections in forest workers in Poland Vector Borne Zoonotic Dis 2011 11 985 9 10.1089/vbz.2010.0080 21083370 · DOI
  10. [10]Rymaszewska A Adamska M Molecular evidence of vector-borne pathogens coinfecting dogs from Poland Acta Vet Hung 2011 59 215 23 10.1556/AVet.2011.008 21665575 · DOI
  11. [11]Stańczak J Detection of spotted fever group (SFG) rickettsiae in Dermacentor reticulatus (Acari: Ixodidae) in Poland Int J Med Microbiol 2006 296 Suppl 40 144 8 10.1016/j.ijmm.2006.01.014 16524778 · DOI
  12. [12]Grzeszczuk A Stanczak J Kubica-Biernat B Racewicz M Kruminis-Lozowska W Prokopowicz D Human anaplasmosis in north-eastern Poland: seroprevalence in humans and prevalence in Ixodes ricinus ticks Ann Agric Environ Med 2004 11 99 103 15236505
  13. [13]Welc-Falęciak R Kowalec M Zajkowska J Pancewicz SA Siński E Clinical and molecular features of one case of human infection with Anaplasma phagocytophilum from Podlaskie Province in eastern Poland Ann Agric Environ Med 2015 22 3 414 7 10.5604/12321966.1167704 26403105 · DOI
  14. [14]Skotarczak B Adamska M Supron M Blood DNA analysis for Ehrlichia (Anaplasma) phagocytophila and Babesia spp. in dogs from Northern Poland Acta Vet Brno 2004 73 347 51 10.2754/avb200473030347 · DOI
  15. [16]Welinder-Olsson C Kjellin E Vaht K Jacobsson S Wenneras C First case of human “Candidatus Neoehrlichia mikurensis” infection in a febrile patient with chronic lymphocytic leukemia J Clin Microbiol 2010 48 5 1956 9 10.1128/JCM.02423-09 20220155 PMC2863919 · DOI
  16. [17]Welc-Falęciak R, Siński E, Kowalec M, Zajkowska J, Pancewicz SA. Asymptomatic “Candidatus Neoehrlichia mikurensis” infections in immunocompetent humans. J Clin Microbiol. 2014a;52(8):3072–4. PMC4136151 24899023
  17. [18]Welc-Falęciak R, Kowalec M, Karbowiak G, Bajer A, Behnke JM, Siński E. Rickettsiaceae and Anaplasmataceae infections in Ixodes ricinus ticks from urban and natural forested areas of Poland. Parasit Vectors. 2014b;7:121–10. PMC3994390 24661311
  18. [19]Wójcik-Fatla A Bartosik K Buczek A Dutkiewicz J Babesia microti in adult Dermacentor reticulatus ticks from eastern Poland Vector Borne Zoonotic Dis 2012 12 10 841 3 10.1089/vbz.2011.0904 22651392 · DOI
  19. [20]Kiewra D Stańczak J Richter M Ixodes ricinus ticks (Acari, Ixodidae) as a vector of Borrelia burgdorferi sensu lato and Borrelia miyamotoi in Lower Silesia. Poland--preliminary study Ticks Tick Borne Dis 2014 5 6 892 7 10.1016/j.ttbdis.2014.07.004 25150724 · DOI
  20. [21]Rizzoli A, Silaghi C, Obiegala A, Rudolf I, Hubálek Z, Földvári G, et al. Ixodes ricinus and its transmitted pathogens in urban and peri-urban areas in Europe: New hazards and relevance for public health. Front Public Health. 2014;2:251. PMC4248671 25520947
  21. [22]Hamer SA Tsao JI Walker ED Mansfield LS Foster ES Hickling GJ Use of tick surveys and serosurveys to evaluate pet dogs as a sentinel species for emerging Lyme disease Am J Vet Res 2009 70 1 49 56 10.2460/ajvr.70.1.49 19119948 · DOI
  22. [23]Nowak-Chmura M Siuda K Ticks of Poland review of contemporary issues and latest research Ann Parasitol 2012 58 125 55 23444797
  23. [24]Siuda K, Bliska M, Nowak M. Kleszcze (Acari: Ixodida: Ixodidae) atakujące psy domowe w okolicach Wadowic. Zoonozy: problem nadal aktualny. Conference Materials. Warszawa, 2002; 68. [in Polish].
  24. [25]Zygner W Wedrychowicz H Occurrence of hard ticks in dogs from Warsaw area Ann Agric Environ Med 2006 13 2 355 9 17196014
  25. [27]Martinod S Brossard M Moreau Y Immunity of dogs against Babesia canis, its vector tick Dermacentor reticulatus, and Ixodes ricinus in endemic area J Parasitol 1985 71 3 269 73 10.2307/3282004 4009345 · DOI
  26. [28]Mediannikov O Matsumoto K Samoylenko I Drancourt M Roux V Rydkina E Davoust B Tarasevich I Brouqui P Fournier PE Rickettsia raoultii sp. nov., a spotted fever group rickettsia associated with Dermacentor ticks in Europe and Russia Int J Syst Evol Microbiol 2008 58 1635 9 10.1099/ijs.0.64952-0 18599708 · DOI
  27. [29]Król N Kiewra D Szymanowski M Lonc E The role of domestic dogs and cats in the zoonotic cycles of ticks and pathogens. Preliminary studies in the Wrocław Agglomeration (SW Poland) Vet Parasitol 2015 214 208 12 10.1016/j.vetpar.2015.09.028 26464069 · DOI
  28. [31]Wölfel R Essbauer S Dobler G Diagnostics of tick-borne rickettsioses in Germany: A modern concept for a neglected disease Int J Med Microbiol 2008 298 368 74 10.1016/j.ijmm.2007.11.009 · DOI
  29. [32]Courtney JW Kostelnik LM Zeidner NS Massung RF Multiplex real-time PCR for detection of Anaplasma phagocytophilum and Borrelia burgdorferi J Clin Microbiol 2004 42 3164 8 10.1128/JCM.42.7.3164-3168.2004 15243077 PMC446246 · DOI
  30. [33]Jahfari S Fonville M Hengeveld P Reusken C Scholte EJ Takken W Heyman P Medlock J Heylen D Kleve J Sprong H Prevalence of Neoehrlichia mikurensis in ticks and rodents from north-west Europe Parasit Vectors 2012 5 74 10.1186/1756-3305-5-74 22515314 PMC3395572 · DOI
  31. [34]Silaghi C Woll D Mahling M Pfister K Pfeffer M Candidatus Neoehrlichia mikurensis in rodents in an area with sympatric existence of the hard ticks Ixodes ricinus and Dermacentor reticulatus Parasit Vectors 2012 5 285 10.1186/1756-3305-5-285 23216786 PMC3533915 · DOI
  32. [35]Casati S Sager H Gern L Piffaretti JC Presence of potentially pathogenic Babesia sp. for human in Ixodes ricinus in Switzerland Ann Agric Environ Med 2006 13 65 70 16841874
  33. [36]Roux V Raoult D Phylogenetic analysis of members of the genus Rickettsia using the gene encoding the outer-membrane protein rOmpB (ompB) Int J Syst Evol Microbiol 2000 50 1449 55 10.1099/00207713-50-4-1449 10939649 · DOI
  34. [38]Eichenberger RM Deplazes P Mathis A Ticks on dogs and cats: A pet owner-based survey in a rural town in northeastern Switzerland Ticks Tick-borne Dis 2015 6 267 71 10.1016/j.ttbdis.2015.01.007 25684694 · DOI
  35. [39]Beichel E Petney TN Hassler D Brückner M Maiwald M Tick infestation patterns and prevalence of Borrelia burgdorferi in ticks collected at a veterinary clinic in Germany Vet Parasitol 1996 65 147 55 10.1016/0304-4017(96)00943-0 8916409 · DOI
  36. [40]Smith FD Ballantyne R Morgan ER Wall R Prevalence, distribution and risk associated with tick infestation of dogs in Great Britain Med Vet Entomol 2011 25 377 84 10.1111/j.1365-2915.2011.00954.x 21418263 · DOI
  37. [42]Duh D Slovák M Saksida A Strašek K Petrovec M Avšič-Županc T Molecular detection of Babesia canis in Dermacentor reticulatus ticks collected in Slovakia Biologia 2006 61 2 231 3 10.2478/s11756-006-0035-7 · DOI
  38. [43]Boretti FS Perreten A Meli ML Cattori V Willi B Wengi N Hornok S Honegger H Hegglin D Woelfel R Reusch CE Lutz H Hofmann-Lehmann R Molecular investigations of Rickettsia helvetica infections in dogs, foxes, humans and Ixodes ticks Appl Environ Microbiol 2009 75 3230 7 10.1128/AEM.00220-09 19329665 PMC2681666 · DOI
  39. [44]Nijhof AM Bodaan C Postigo M Nieuwenhuijs H Opsteegh M Franssen L Jebbink F Jongejan F Ticks and associated pathogens collected from domestic animals in The Netherlands Vector Borne Zoonotic Dis 2007 7 1 11 10.1089/vbz.2007.0130 17979540 · DOI
  40. [45]Schreiber C Krücken J Beck S Maaz D Pachnicke S Krieger K Gross M Kohn B von Samson-Himmelstjerna G Pathogens in ticks collected from dogs in Berlin/Brandenburg, Germany Parasit Vectors 2014 7 535 10.1186/s13071-014-0535-1 25441762 PMC4262381 · DOI · Paper page
  41. [46]Stensvold CR Al Marai D O’Brien Andersen L Krogfelt KA Jensen JS Søholt Larsen K Nielsen HV Babesia spp. and other pathogens in ticks recovered from domestic dogs in Denmark Parasit Vectors 2015 8 262 10.1186/s13071-015-0843-0 25951937 PMC4425907 · DOI
  42. [47]Chmielewski T Podsiadly E Karbowiak G Tylewska-Wierzbanowska S Rickettsia spp. in ticks, Poland Emerg Infect Dis 2009 15 3 486 8 10.3201/eid1503.080711 19239772 PMC2681112 · DOI
  43. [48]Stańczak J Racewicz M Michalik J Buczek A Distribution of Rickettsia helvetica in Ixodes ricinus tick populations in Poland Int J Med Microbiol 2008 298 231 4 10.1016/j.ijmm.2007.09.006 · DOI
  44. [49]Mierzejewska E, Welc-Falęciak R, Kowalec M, Alsarraf M, Bajer A. Comparison of prevalence of vector-borne pathogens in Dermacentor reticulatus from eastern and western Poland. The 16th International Symposium ‘Parasitic and Allergic Arthropods – Medical and Sanitarny Significance’. Kazimierz Dolny. 2014:76.
  45. [50]Krücken J Schreiber C Maaz D Kohn M Demeler J Beck S Schein E Olias P Richter D Matuschka FR Pachnicke S Krieger K Kohn B von Samson-Himmelstjerna G A novel high-resolution melt PCR assay discriminates Anaplasma phagocytophilum and “Candidatus Neoehrlichia mikurensis” J Clin Microbiol 2013 51 6 1958 61 10.1128/JCM.00284-13 23576542 PMC3716091 · DOI
  46. [51]Zygner W Jaros S Wędrychowicz H Prevalence of Babesia canis, Borrelia afzelii, and Anaplasma phagocytophilum infection in hard ticks removed from dogs in Warsaw (central Poland) Vet Parasitol 2008 153 139 42 10.1016/j.vetpar.2008.01.036 18328630 · DOI
  47. [52]Sytykiewicz H Karbowiak G Hapunik J Szpechciński A Supergan-Marwicz M Goławska S Sprawka I Czerniewicz P Molecular evidence of Anaplasma phagocytophilum and Babesia microti co-infections in Ixodes ricinus ticks in central-eastern region of Poland Ann Agric Environ Med 2012 19 45 9 22462444
  48. [54]Lempereur L Decat A Caron Y Madder M Claerebout E Saegerman C Losson B First molecular evidence of potentially zoonotic Babesia microti and Babesia sp. EU1 in Ixodes ricinus ticks in Belgium Vector Borne Zoonotic Dis 2011 11 125 30 10.1089/vbz.2009.0189 20575647 · DOI
  49. [55]Cieniuch S Stańczak J Ruczaj A The first detection of Babesia EU1 and Babesia canis canis in Ixodes ricinus ticks (Acari, Ixodidae) collected in urban and rural areas in northern Poland Pol J Microbiol 2009 58 3 231 6 19899616
  50. [56]Leschnik MW Khanakah G Duscher G Wille-Piazzai W Hörweg C Joachim A Stanek G Species, developmental stage and infection with microbial pathogens of engorged ticks removed from dogs and questing ticks Med Vet Entomol 2012 26 4 440 6 10.1111/j.1365-2915.2012.01036.x 22882652 · DOI
  51. [57]Földvári G, Márialigeti M, Solymosi N, Lukács Z, Majoros G, Kósa JP, et al. Hard ticks infesting dogs in Hungary and their infection with Babesia and Borrelia species. Parasitol Res. 2007;101:25–34.
  52. [58]Welc-Falęciak R Rodo A Siński E Bajer A Babesia canis and other tick-borne infections in dogs in Central Poland Vet Parasitol 2009 166 191 8 10.1016/j.vetpar.2009.09.038 19837515 · DOI

Cited by

Sorted by citations

Authors
Król, N., Obiegala, A., Pfeffer, M., Lonc, E., & Kiewra, D.
Affiliations
  • University of Wrocław (PL)
  • Leipzig University (DE)
Corresponding author
Król, Nina
Venue
Parasites & Vectors
Published
2016-06-21
Volume
9
Issue
1
Pages
351-351
ISSN
1756-3305 (ISSN-L)
OpenAlex
W2465310444
Cited by
60
References
2
Citations by year
2026: 2 · 2025: 4 · 2024: 10 · 2023: 8 · 2022: 3 · 2021: 9 · 2020: 7 · 2019: 4 · 2018: 9 · 2017: 4
FWCI
5.84
Type
journal article
Language
en
Open access
Licence
cc-by
Locations
  • Parasites & Vectors (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
Funders
Bayer Animal HealthCare (DE) (TC00685704)
Topics
  • Life Sciences › Immunology and Microbiology › Parasitology › Vector-borne infectious diseases
  • Life Sciences › Immunology and Microbiology › Parasitology › Bartonella species infections research
  • Health Sciences › Medicine › Infectious Diseases › Viral Infections and Vectors
Keywords
tick-borne pathogens, Ixodes ricinus, Ixodes hexagonus, Dermacentor reticulatus, Rickettsia helvetica, Rickettsia monacensis, Anaplasma phagocytophilum, Candidatus Neoehrlichia mikurensis, Babesia microti, Babesia venatorum, co-infection
MeSH terms
Anaplasmataceae, Animals, Arachnid Vectors, Babesia, Cat Diseases, Cats, Dog Diseases, Dogs, Female, Male, Poland, Rickettsia, Tick Infestations, Urban Population, Ixodidae

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review