RESEARCH PAPER
Tick distribution along animal tracks: implication for preventative medicine
 
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1
Pavol Jozef Safarik University, Kosice, Slovak Republic
2
Department of Systematic Zoology, Faculty of Biology, Adam Mickiewicz University, Poznań, Poland
3
CREAF, Cerdanyola del Valles, Catalonia, Spain
4
Institute of Zoology, Poznań University of Life Sciences, Poznań, Poland
5
Research & Development Centre, HiProMine S.A., Robakowo, Poland
6
Institute of Parasitology, Slovak Academy of Sciences, Kosice, Slovak Republic
7
Department of preclinical sciences and infectious diseases, Poznań University of Life Sciences, Poznań, Poland
CORRESPONDING AUTHOR
Krzysztof Dudek   

Institute of Zoology, Wojska Polskiego, 60-625 Poznań, Poland
 
Ann Agric Environ Med. 2018;25(2):360–363
KEYWORDS
TOPICS
ABSTRACT
Introduction:
Tick abundance and the prevalence of the pathogens they carry have been increasing worldwide in the last decades, and is projected to increase even further. Despite the fact that problem is global, there still remain many gaps in the diagnosis and treatment of tick-borne diseases. The best protection from tick-borne pathogens, therefore, is prevention and avoidance of bites. Ticks mobility is limited so that their spatial distribution is strongly correlated with the presence of, especially with large mammals. In this study, the hypothesis was tested that tick abundance is higher on animal tracks in the forests than in adjacent habitats. This is an important issue because there are still several human habits and practices that can decrease the zoonoses risk. For example, during recreation in forest, people should always walk on the paths (including narrow animal’s tracks) instead of wading through bushes.

Material and methods:
Flagging of animal trails and near control transects were performed simultaneously. Next, collected ticks were counted, sexed and aged.

Results:
The abundance of ticks was almost 5-fold (Ixodes ricinus) and 3-fold (Dermacentor spp.) higher on animal trails than on adjacent control transects.

Conclusions:
The results obtained support the hypothesis that ticks are more abundant on pathways than in adjacent habitats. Most likely, the pattern emerges because large mammals, like deer, which are the most important ticks hosts, use forest paths to move across the landscape and frequently move along the same routes. This research sends an important public message that these forest trails are hotspots of disease risk and should be avoided.

 
REFERENCES (48)
1.
Jongejan F, Uilenberg G. The global importance of ticks. Parasitol. 2004; 129(S1): S3-S14.
 
2.
Burgdorfer W, Barbour AG, Hayes SF, Benach JL, Grunwaldt E, Davis JP. Lyme disease-a tick-borne spirochetosis? Science 1982; 216(4552): 1317–1319.
 
3.
Víchová B, Horská M, Blaňarová L, Švihran M, Andersson M, Peťko B. First molecular identification of Babesia gibsoni in dogs from Slovakia, central Europe. Ticks and Tick-Borne Dis. 2016; 7(1): 54–59.
 
4.
Lindquist L, Vapalahti O. Tick-borne encephalitis. The Lancet 2008; 371(9627): 1861–1871.
 
5.
Kjemtrup A, Conrad P. Human babesiosis: an emerging tick-borne disease. Int J Parasitol. 2000; 30(12): 1323–1337.
 
6.
Estrada-Peña A, de La Fuente J. Species interactions in occurrence data for a community of tick-transmitted pathogens. Scientific Data 2016; 3: 160056.
 
7.
Víchová B, Majláthová V, Nováková M, Stanko M, Hviščová I, Pangrácová L, Chrudimský T, Čurlík J, Peťko B. Anaplasma infections in ticks and reservoir host from Slovakia. Infect Genet Evol. 2014; 22: 265–272.
 
8.
Dautel H, Dippel C, Oehme R, Hartelt K, Schettler E. Evidence for an increased geographical distribution of Dermacentor reticulatus in Germany and detection of Rickettsia sp. RpA4. Int J Med Microbiol. 2006; 296: 149–156.
 
9.
Gray J, Dautel H, Estrada-Peña A, Kahl O, Lindgren E. Effects of climate change on ticks and tick-borne diseases in Europe. Interdiscip Perspect Infect Dis. 2009; 2009: 593232. doi: 10.1155/2009/593232. Epub 2009 Jan 4.
 
10.
Randolph SE. To what extent has climate change contributed to the recent epidemiology of tick-borne diseases? Vet Parasitol. 2010; 167(2): 92–94.
 
11.
Földvári G, Široký P, Szekeres S, Majoros G, Sprong H. Dermacentor reticulatus: a vector on the rise. Parasit Vectors. 2016; 9(1): 314.
 
12.
Jones CG, Ostfeld RS, Richard MP, Schauber EM, Wolff JO. Chain reactions linking acorns to gypsy moth outbreaks and Lyme disease risk. Science 1998; 279(5353): 1023–1026.
 
13.
Randolph SE. The shifting landscape of tick-borne zoonoses: tick-borne encephalitis and Lyme borreliosis in Europe. Philos Trans R Soc Lond B Biol Sci. 2001; 356(1411): 1045–1056.
 
14.
Estrada Peña A. The relationships between habitat topology, critical scales of connectivity and tick abundance Ixodes ricinus in a heterogeneous landscape in northern Spain. Ecography 2003; 26(5): 661–671.
 
15.
Ostfeld RS, Canham CD, Oggenfuss K, Winchcombe RJ, Keesing F. Climate, deer, rodents, and acorns as determinants of variation in Lyme-disease risk. PLoS Biol. 2006; 4(6):e145.
 
16.
Bogdziewicz M, Szymkowiak J. Oak acorn crop and Google search volume predict Lyme disease risk in temperate Europe. Basic Appl Ecol. 2016; 17(4): 300–307.
 
17.
Ostfeld R. Lyme disease: the ecology of a complex system: OUP USA; 2010.
 
18.
Gray J. A carbon dioxide trap for prolonged sampling of Ixodes ricinus L. populations. Exp Appl Acarol. 1985; 1(1): 35–44.
 
19.
Carroll J, Schmidtmann E. Dispersal of blacklegged tick (Acari: Ixodidae) nymphs and adults at the woods–pasture interface. J Med Entomol. 1996; 33(4): 554–558.
 
20.
Ostfeld RS, Hazler KR, Cepeda OM. Temporal and spatial dynamics of Ixodes scapularis (Acari: Ixodidae) in a rural landscape. J Med Entomol. 1996; 33(1): 90–95.
 
21.
Kugeler K, Jordan R, Schulze T, Griffith K, Mead P. Will Culling White Tailed Deer Prevent Lyme Disease? Zoonoses and Public Health 2015.
 
22.
Pérez de León AA, Teel PD, Li A, Ponnusamy L, Roe RM. Advancing integrated tick management to mitigate burden of tick-borne diseases. Outlooks on Pest Management 2014; 25(6): 382–389.
 
23.
Dantas-Torres F, Chomel BB, Otranto D. Ticks and tick-borne diseases: a One Health perspective. Trends Parasitol. 2012; 28(10): 437–446.
 
24.
Rabinowitz P, Conti L. Links among human health, animal health, and ecosystem health. Ann Rev Public Health 2013; 34: 189–204.
 
25.
Carroll J, Schmidtmann E. Tick sweep: modification of the tick drag-flag method for sampling nymphs of the deer tick (Acari: Ixodidae). J Med Entomol. 1992; 29(2): 352–355.
 
26.
Zeileis A, Kleiber C, Jackman S. Regression models for count data in R. J Stat Softw. 2008; 27(8): 1–25.
 
27.
Jackman S. pscl: Classes and Methods for R Developed in the Political Science. R package version 1.4.9. In.: Stanford, California: Computational Laboratory, Stanford University. Department of Political Science, Stanford University. Available: http://pscl. stanford. ed u. Accessed; 2015.
 
28.
Team RDC: R. A language and environment for statistical computing. Vienna: R Foundation for Statistical Computing;. In.; 2016.
 
29.
Zuur A, Ieno E, Walker N, Saveliev A, Smith G. Mixed Effects Models and Extensions in Ecology with R. Springer Science+. 2009.
 
30.
Burnham KP, Anderson DR. Model selection and multimodel inference: a practical information-theoretic approach: Springer Science & Business Media; 2003.
 
31.
Barton K. Multi-model inference. R package version 1.10. 0. 2014. In.; 2016.
 
32.
Arnold TW: Uninformative parameters and model selection using Akaike’s Information Criterion. J Wildl Manage. 2010; 74(6): 1175–1178.
 
33.
Vor T, Kiffner C, Hagedorn P, Niedrig M, Rühe F. Tick burden on European roe deer (Capreolus capreolus). Exp Appl Acarol. 2010; 51(4): 405–417.
 
34.
Wilson ML, Telford III SR, Piesman J, Spielman A. Reduced abundance of immature Ixodes dammini (Acari: Ixodidae) following elimination of deer. J Med Entomol. 1988; 25(4): 224–228.
 
35.
Medlock J, Shuttleworth H, Copley V, Hansford K, Leach S. Woodland biodiversity management as a tool for reducing human exposure to Ixodes ricinus ticks: A preliminary study in an English woodland. J Vect Ecol. 2012; 37(2): 307–315.
 
36.
Oliver Jr JH. Biology and systematics of ticks (Acari: Ixodida). Annu Rev Ecol Syst. 1989; 20(1): 397–430.
 
37.
Kiewra D, Czulowska A. Evidence for an increased distribution range of Dermacentor reticulatus in south-west Poland. Exp Appl Acarol. 2013; 59(4): 501–506.
 
38.
Vassallo M, Pichon B, Cabaret J, Figureau C, Pérez-Eid C. Methodology for sampling questing nymphs of Ixodes ricinus (Acari: Ixodidae), the principal vector of Lyme disease in Europe. J Med Entomol. 2000; 37(3): 335–339.
 
39.
Rubel F, Brugger K, Pfeffer M, Chitimia-Dobler L, Didyk YM, Leverenz S, Dautel H, Kahl O. Geographical distribution of Dermacentor marginatus and Dermacentor reticulatus in Europe. Ticks Tick Borne Dis. 2016; 7(1): 224–233.
 
40.
Horobik V, Keesing F, Ostfeld RS. Abundance and Borrelia burgdorferi-infection prevalence of nymphal Ixodes scapularis ticks along forest–field edges. EcoHealth 2006; 3(4): 262–268.
 
41.
Mihalca A, Gherman C, Magdaş C, Dumitrache M, Györke A, Sándor A, Domşa C, Oltean M, Mircean V, Mărcuţan D. Ixodes ricinus is the dominant questing tick in forest habitats in Romania: the results from a countrywide dragging campaign. Exp Appl Acarol. 2012; 58(2): 175–182.
 
42.
Due C, Fox W, Medlock JM, Pietzsch M, Logan JG. Tick bite prevention and tick removal. BMJ 2013; 347: f7123.
 
43.
Estrada-Peña An. Forecasting habitat suitability for ticks and prevention of tick-borne diseases. Vet Parasitol. 2001; 98(1): 111–132.
 
44.
Fish D: Environmental risk and prevention of Lyme disease. Am J Med. 1995; 98(4): 2S-9S.
 
45.
Piesman J, Eisen L. Prevention of tick-borne diseases. Annu Rev Entomol. 2008; 53: 323–343.
 
46.
Estrada-Peña A. Distribution, abundance, and habitat preferences of Ixodes ricinus (Acari: Ixodidae) in northern Spain. J Med Entomol. 2001; 38(3): 361–370.
 
47.
Ginsberg HS, Ewing CP. Habitat distribution of Ixodes dammini (Acari: Ixodidae) and Lyme disease spirochetes on Fire island, New York. J Med Entomol. 1989; 26(3): 183–189.
 
48.
Szekeres S, Lügner J, Fingerle V, Margos G, Földvári G. Prevalence of Borrelia miyamotoi and Borrelia burgdorferi sensu lato in questing ticks from a recreational coniferous forest of East Saxony, Germany. Ticks Tick Borne Dis. 2017; 8(6): 922–927.
 
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