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. 2025 Mar 26;14(4):342.
doi: 10.3390/biology14040342.

The Presence of Bacterial and Protozoan Pathogens in Wild Fallow Deer (Dama dama) from a Protected Area in Central Italy

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The Presence of Bacterial and Protozoan Pathogens in Wild Fallow Deer (Dama dama) from a Protected Area in Central Italy

Valentina Virginia Ebani et al. Biology (Basel). .

Abstract

Wild ruminants often harbor pathogens transmissible to other animals and humans, but their epidemiological role is not always defined for all microorganisms. In this survey, spleens, kidneys, and hearts sampled from 162 fallow deer (Dama dama) were subjected to molecular analyses to detect bacterial (Anaplasma phagocytophilum, Borrelia burgdorferi s.l., Brucella spp., Chlamydia abortus, Coxiella burnetii, Francisella tularensis, Leptospira spp.) and protozoan (piroplasms, Neospora caninum, Toxoplasma gondii) pathogens. Five (3.08%) spleens were positive for A. phagocytophilum, and twelve (7.40%) spleens were positive for Theileria cervi. The remaining pathogens investigated were not detected, and no coinfections were found. The analyzed animals do not seem to have a relevant role in the spreading of these pathogens; however, monitoring is pivotal to understand the epidemiological scenarios and take appropriate preventive measures in areas frequently visited by people.

Keywords: Anaplasma phagocytophilum; Theileria cervi; fallow deer; pathogens.

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Conflict of interest statement

The authors declare no conflicts of interest.

Figures

Figure 1
Figure 1
Map of the study area. Light green line represents a border of the study area, while star represents the leaning tower.

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References

    1. Silaghi C., Fröhlich J., Reindl H., Hamel D., Rehbein S. Anaplasma phagocytophilum and Babesia Species of Sympatric Roe Deer (Capreolus capreolus), Fallow Deer (Dama dama), Sika Deer (Cervus nippon) and Red Deer (Cervus elaphus) in Germany. Pathogens. 2020;9:968. doi: 10.3390/pathogens9110968. - DOI - PMC - PubMed
    1. Wijburg S.R., Fonville M., de Bruin A., van Rijn P.A., Montizaan M.G.E., van den Broek J., Sprong H., Rijks J.M. Prevalence and predictors of vector-borne pathogens in Dutch roe deer. Parasites Vectors. 2022;15:76. doi: 10.1186/s13071-022-05195-w. - DOI - PMC - PubMed
    1. Middlebrook E.A., Romero A.T., Bett B., Nthiwa D., Oyola S.O., Fair J.M., Bartlow A.W. Identification and distribution of pathogens coinfecting with Brucella spp., Coxiella burnetii and Rift Valley fever virus in humans, livestock and wildlife. Zoonoses Public Health. 2022;69:175–194. doi: 10.1111/zph.12905. - DOI - PMC - PubMed
    1. Dashti A., Köster P.C., Bailo B., de Las Matas A.S., Habela M.Á., Rivero-Juarez A., Vicente J., Serrano E., Arnal M.C., de Luco D.F., et al. Occurrence and limited zoonotic potential of Cryptosporidium spp., Giardia duodenalis, and Balantioides coli infections in free-ranging and farmed wild ungulates in Spain. Res. Vet. Sci. 2023;159:189–197. doi: 10.1016/j.rvsc.2023.04.020. - DOI - PubMed
    1. Ciuti S., Apollonio M. Ecological sexual segregation in fallow deer (Dama dama): A multisptial and multiptemporal approach. Behav. Ecol. Sociobiol. 2008;62:1747–1759.

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