Analyze Diet
Vector borne and zoonotic diseases (Larchmont, N.Y.)2015; 15(9); 529-534; doi: 10.1089/vbz.2015.1768

Serologic and Molecular Prevalence of Rickettsia helvetica and Anaplasma phagocytophilum in Wild Cervids and Domestic Mammals in the Central Parts of Sweden.

Abstract: Both Rickettsia helvetica and Anaplasma phagocytophilum are common in Ixodes ricinus ticks in Sweden. Knowledge is limited regarding different animal species' competence to act as reservoirs for these organism. For this reason, blood samples were collected from wild cervids (roe deer, moose) and domestic mammals (horse, cat, dog) in central Sweden, and sera were tested using immunofluorescence assay to detect antibodies against spotted fever rickettsiae using Rickettsia helvetica as antigen. Sera with a titer ≥1:64 were considered as positive, and 23.1% (104/450) of the animals scored positive. The prevalence of seropositivity was 21.5% (23/107) in roe deer, 23.3% (21/90) in moose, 36.5% (23/63) in horses, 22.1% (19/90) in cats, and 17.0% (17/100) in dogs. PCR analysis of 113 spleen samples from moose and sheep from the corresponding areas were all negative for rickettsial DNA. In roe deer, 85% (91/107) also tested seropositive for A. phagocytophilum with a titer cutoff of 1:128. The findings indicate that the surveyed animal species are commonly exposed to rickettsiae and roe deer also to A. phagocytophilum.
Publication Date: 2015-09-18 PubMed ID: 26378972DOI: 10.1089/vbz.2015.1768Google Scholar: Lookup
The Equine Research Bank provides access to a large database of publicly available scientific literature. Inclusion in the Research Bank does not imply endorsement of study methods or findings by Mad Barn.
  • Journal Article
  • Research Support
  • Non-U.S. Gov't

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research discusses the prevalence of two specific organisms, Rickettsia helvetica and Anaplasma phagocytophilum, in both wild (roe deer, moose) and domestic animals (horses, cats, dogs) in central Sweden, shedding light on the potential reservoir competence of these animal species.

Objective

The purpose of this study was to gain more detailed understanding of the reservoir potential of different animal species for Rickettsia helvetica and Anaplasma phagocytophilum, two organisms that are typically found in Ixodes ricinus ticks in Sweden.

Methodology

  • To investigate this, blood samples were collected from various animal species both domestic (such as horses, dogs, and cats) and wild (like roe deer and moose) in the central parts of Sweden.
  • These samples were then tested via an immunofluorescence assay that used Rickettsia helvetica as an antigen in order to detect antibodies against spotted fever rickettsiae.
  • Any samples boasting a titer (a measure indicating the concentration of a substance in a solution) of 1:64 or more were considered positive.
  • A total of 104 out of 450 animals were determined to be positive based on this standard.
  • Moreover, PCR analysis was also carried out on 113 spleen samples from sheep and moose from the same regions, though none of these tested positive for rickettsial DNA.
  • Besides, in roe deer, an additional test was conducted for Anaplasma phagocytophilum, setting the cutoff for a positive result at a titer of 1:128.

Results

  • The instances of seropositivity to Rickettsia helvetica were found to be 21.5% in roe deer, 23.3% in moose, 36.5% in horses, 22.1% in cats, and 17% in dogs.
  • Interestingly, no rickettsial DNA was found in the spleen samples from the moose and sheep.
  • Meanwhile, 85% of the roe deer also tested positive for Anaplasma phagocytophilum, indicating a high level of exposure to this organism in this species.

Conclusion

Based on the results of this study, it can be concluded that the animal species surveyed are commonly exposed to Rickettsia helvetica. Additionally, roe deer were found to be frequently exposed to Anaplasma phagocytophilum as well. This helps broaden our understanding of the prevalence of these organisms in different animal populations, providing valuable insight into potential reservoirs and paths of spread for these pathogens.

Cite This Article

APA
Elfving K, Malmsten J, Dalin AM, Nilsson K. (2015). Serologic and Molecular Prevalence of Rickettsia helvetica and Anaplasma phagocytophilum in Wild Cervids and Domestic Mammals in the Central Parts of Sweden. Vector Borne Zoonotic Dis, 15(9), 529-534. https://doi.org/10.1089/vbz.2015.1768

Publication

ISSN: 1557-7759
NlmUniqueID: 100965525
Country: United States
Language: English
Volume: 15
Issue: 9
Pages: 529-534

Researcher Affiliations

Elfving, Karin
  • 1 Department of Medical Sciences, Unit of Clinical Bacteriology, Uppsala University , Uppsala, Sweden .
  • 5 Center of Clinical Research , Dalarna, Falun, Sweden .
Malmsten, Jonas
  • 3 Department of Clinical Sciences, Division of Reproduction, Swedish University of Agricultural Sciences , Uppsala, Sweden .
  • 4 Department of Pathology and Wildlife Diseases, National Veterinary Institute , Uppsala, Sweden .
Dalin, Anne-Marie
  • 4 Department of Pathology and Wildlife Diseases, National Veterinary Institute , Uppsala, Sweden .
Nilsson, Kenneth
  • 1 Department of Medical Sciences, Unit of Clinical Bacteriology, Uppsala University , Uppsala, Sweden .
  • 2 Department of Medical Sciences, Unit of Infectious Diseases, Uppsala University , Uppsala, Sweden .
  • 5 Center of Clinical Research , Dalarna, Falun, Sweden .

MeSH Terms

  • Anaplasma phagocytophilum / genetics
  • Anaplasma phagocytophilum / immunology
  • Anaplasma phagocytophilum / isolation & purification
  • Animals
  • Animals, Domestic
  • Arachnid Vectors / microbiology
  • Cat Diseases / epidemiology
  • Cats
  • Deer / microbiology
  • Disease Reservoirs / veterinary
  • Dog Diseases / epidemiology
  • Dogs
  • Ehrlichiosis / epidemiology
  • Ehrlichiosis / veterinary
  • Horse Diseases / epidemiology
  • Horses
  • Ixodes / microbiology
  • Rickettsia / genetics
  • Rickettsia / immunology
  • Rickettsia / isolation & purification
  • Rickettsia Infections / epidemiology
  • Rickettsia Infections / veterinary
  • Seroepidemiologic Studies
  • Sheep
  • Sheep Diseases / epidemiology
  • Sweden / epidemiology

Citations

This article has been cited 17 times.
  1. Vauhkonen H, Zakham F, Voutilainen L, Keinänen R, Lind K, Niamsap T, Puonti PT, Castrén RS, Smura T, Joensuu R, Nikkari S, Tonteri E, Vapalahti O, Korhonen EM, Jääskeläinen A, Jääskeläinen AJ, Sironen T, Kinnunen PM. Rickettsia spp. in finnish ixodid ticks. Parasit Vectors 2025 Nov 24;18(1):485.
    doi: 10.1186/s13071-025-07090-6pubmed: 41286942google scholar: lookup
  2. Lesiczka PM, Azagi T, Krawczyk AI, Scott WT Jr, Dirks RP, Simo L, Dobler G, Nijsse B, Schaap PJ, Sprong H, Koehorst JJ. Deep sequencing of 16 Ixodes ricinus ticks unveils insights into their interactions with endosymbionts. mSystems 2025 Jul 22;10(7):e0050725.
    doi: 10.1128/msystems.00507-25pubmed: 40521888google scholar: lookup
  3. Ölmedal G, Toresson L, Nehring M, Hawley J, Vande Woude S, Lappin M. Prevalence of selected infectious agents in Swedish cats with fever and/or anemia compared to cats without fever and/or anemia and to stable/stray cats. Acta Vet Scand 2025 May 9;67(1):23.
    doi: 10.1186/s13028-025-00807-8pubmed: 40341138google scholar: lookup
  4. Geisen V, Pantchev N, Zablotski Y, Kim O, Globokar Vrhovec M, Hartmann K, Bergmann M. Molecular Detection of Anaplasma phagocytophilum in Cats in Europe and Associated Risk Factors. Animals (Basel) 2024 Aug 15;14(16).
    doi: 10.3390/ani14162368pubmed: 39199902google scholar: lookup
  5. Lysholm S, Ådén F, Aspán A, Högberg A, Wensman JJ, Omazic A. Presence of Anaplasma spp. and Their Associated Antibodies in the Swedish Goat Population. Animals (Basel) 2023 Jan 17;13(3).
    doi: 10.3390/ani13030333pubmed: 36766222google scholar: lookup
  6. Wijburg SR, Fonville M, de Bruin A, van Rijn PA, Montizaan MGE, van den Broek J, Sprong H, Rijks JM. Prevalence and predictors of vector-borne pathogens in Dutch roe deer. Parasit Vectors 2022 Mar 5;15(1):76.
    doi: 10.1186/s13071-022-05195-wpubmed: 35248157google scholar: lookup
  7. Atif FA, Mehnaz S, Qamar MF, Roheen T, Sajid MS, Ehtisham-Ul-Haque S, Kashif M, Ben Said M. Epidemiology, Diagnosis, and Control of Canine Infectious Cyclic Thrombocytopenia and Granulocytic Anaplasmosis: Emerging Diseases of Veterinary and Public Health Significance. Vet Sci 2021 Dec 8;8(12).
    doi: 10.3390/vetsci8120312pubmed: 34941839google scholar: lookup
  8. El Hamiani Khatat S, Daminet S, Duchateau L, Elhachimi L, Kachani M, Sahibi H. Epidemiological and Clinicopathological Features of Anaplasma phagocytophilum Infection in Dogs: A Systematic Review. Front Vet Sci 2021;8:686644.
    doi: 10.3389/fvets.2021.686644pubmed: 34250067google scholar: lookup
  9. Gałęcki R, Jaroszewski J, Bakuła T, Galon EM, Xuan X. Molecular Detection of Selected Pathogens with Zoonotic Potential in Deer Keds (Lipoptena fortisetosa). Pathogens 2021 Mar 10;10(3).
    doi: 10.3390/pathogens10030324pubmed: 33801932google scholar: lookup
  10. Springer A, Glass A, Topp AK, Strube C. Zoonotic Tick-Borne Pathogens in Temperate and Cold Regions of Europe-A Review on the Prevalence in Domestic Animals. Front Vet Sci 2020;7:604910.
    doi: 10.3389/fvets.2020.604910pubmed: 33363242google scholar: lookup
  11. Fuehrer HP, Alho AM, Kayikci FN, Shahi Barogh B, Rosa H, Tomás J, Rocha H, Harl J, Madeira de Carvalho L. Survey of Zoonotic and Non-zoonotic Vector-Borne Pathogens in Military Horses in Lisbon, Portugal. Front Vet Sci 2020;7:591943.
    doi: 10.3389/fvets.2020.591943pubmed: 33195629google scholar: lookup
  12. Chisu V, Foxi C, Masu G, D' Amaddio B, Masala G. Detection of potentially pathogenic bacteria from Ixodes ricinus carried by pets in Tuscany, Italy. Vet Rec Open 2020;7(1):e000395.
    doi: 10.1136/vetreco-2020-000395pubmed: 33024565google scholar: lookup
  13. Schäfer I, Kohn B. Anaplasma phagocytophilum infection in cats: A literature review to raise clinical awareness. J Feline Med Surg 2020 May;22(5):428-441.
    doi: 10.1177/1098612X20917600pubmed: 32326861google scholar: lookup
  14. Latrofa MS, Iatta R, Toniolo F, Furlanello T, Ravagnan S, Capelli G, Schunack B, Chomel B, Zatelli A, Mendoza-Roldan J, Dantas-Torres F, Otranto D. A molecular survey of vector-borne pathogens and haemoplasmas in owned cats across Italy. Parasit Vectors 2020 Apr 21;13(1):116.
    doi: 10.1186/s13071-020-3990-xpubmed: 32312323google scholar: lookup
  15. Azagi T, Hoornstra D, Kremer K, Hovius JWR, Sprong H. Evaluation of Disease Causality of Rare Ixodes ricinus-Borne Infections in Europe. Pathogens 2020 Feb 24;9(2).
    doi: 10.3390/pathogens9020150pubmed: 32102367google scholar: lookup
  16. Ebani VV. Serological Evidence of Anaplasma phagocytophilum and Spotted Fever Group Rickettsia spp. Exposure in Horses from Central Italy. Pathogens 2019 Jun 26;8(3).
    doi: 10.3390/pathogens8030088pubmed: 31247976google scholar: lookup
  17. Pennisi MG, Hofmann-Lehmann R, Radford AD, Tasker S, Belák S, Addie DD, Boucraut-Baralon C, Egberink H, Frymus T, Gruffydd-Jones T, Hartmann K, Horzinek MC, Hosie MJ, Lloret A, Lutz H, Marsilio F, Thiry E, Truyen U, Möstl K. Anaplasma, Ehrlichia and Rickettsia species infections in cats: European guidelines from the ABCD on prevention and management. J Feline Med Surg 2017 May;19(5):542-548.
    doi: 10.1177/1098612X17706462pubmed: 28438088google scholar: lookup