Literature DB >> 35347426

The influence of local environmental factors in southwestern Poland on the abundance of Ixodes ricinus and prevalence of infection with Borrelia burgdorferi s.l. and B. miyamotoi.

Dagmara Dyczko1, Dorota Kiewra2, Aleksandra Kolanek3, Paweł Błażej4.   

Abstract

Ticks are important ectoparasites and vectors of pathogens that cause disease in humans and animals. The natural habitat of Ixodes ricinus ticks is forests, which are convenient habitats to search for hosts, including reservoir hosts, and therefore can be an important habitat source of tick-borne pathogens. The aim of the study was to assess the usefulness of detailed forest habitat-type maps to estimate the tick-borne risk at a local scale (Lower Silesia, SW Poland). For the purposes of estimating tick abundance, we used the land cover maps available from the Forest Data Bank. For I. ricinus collection, nine sites located in three forest habitat types were chosen: broadleaf forest, mixed broadleaf and coniferous forest and coniferous forest. Ticks were collected once a month from April to June 2018 and 2019 using the standard flagging method. At each of the nine sites, ticks were collected in four plots, of 100 m2 each. Tick abundance was analysed using general linear mixed models (GLMM). A total of 2196 (10.1/100 m2) ticks were collected, including 2093 Ixodes ricinus (95.3%; 9.6/100 m2), 46 Dermacentor reticulatus (2.1%; 0.2/100 m2) and 57 Haemaphysalis concinna (2.6%; 0.3/100 m2). Among the collected I. ricinus were 589 larvae (28.1%; 2.7/100 m2), 1261 nymphs (60.3%; 5.8/100 m2), 128 females (6.1%; 0.6/100 m2) and 115 males (5.5%; 0.5/100 m2). We found a highly significant effect of forest habitat type on the density of ticks for broadleaf forest (coefficient = 1.87267, p-value = 2.79e - 07). Additionally, a significant influence of air temperature and relative humidity on the abundance of ticks was observed. During spring, the peak activity of I. ricinus was recorded in May and June. For DNA amplification of Borrelia burgdorferi s.l., a nested PCR method was used. Out of 494 I. ricinus, 83 (16.8%) were positive for Borrelia spp. The RFLP method showed the occurrence of five species including four belonging to the B. burgdorferi s.l. complex: B. afzelii (30.1%), B. garinii (38.6%), B. valaisiana (2.4%) and B. lusitaniae (18.1%). Furthermore, B. miyamotoi (9.6%), a species belonging to bacteria that cause relapsing fever as well as co-infection of B. miyamotoi/B.lusitaniae (1.2%) were found. The differences in the infection level of Borrelia spp. between broadleaf forest and mixed broadleaf and coniferous forest were statistically significant.
© 2022. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany, part of Springer Nature.

Entities:  

Keywords:  Borrelia burgdorferi s.l.; Borrelia miyamotoi; Forest habitat types; Ixodes ricinus; Lower Silesia (SW Poland)

Mesh:

Year:  2022        PMID: 35347426     DOI: 10.1007/s00436-022-07493-9

Source DB:  PubMed          Journal:  Parasitol Res        ISSN: 0932-0113            Impact factor:   2.289


  42 in total

1.  Risk factors associated with ixodid tick species distributions in the Basque region in Spain.

Authors:  J F Barandika; E Berriatua; M Barral; R A Juste; P Anda; A L García-Pérez
Journal:  Med Vet Entomol       Date:  2006-06       Impact factor: 2.739

Review 2.  Ticks and tick-borne diseases: a One Health perspective.

Authors:  Filipe Dantas-Torres; Bruno B Chomel; Domenico Otranto
Journal:  Trends Parasitol       Date:  2012-08-17

3.  Distribution, abundance, and habitat preferences of Ixodes ricinus (Acari: Ixodidae) in northern Spain.

Authors:  A Estrada-Peña
Journal:  J Med Entomol       Date:  2001-05       Impact factor: 2.278

4.  Risk of tick-borne bacterial diseases among workers of Roztocze National Park (south-eastern Poland).

Authors:  Ewa Cisak; Jolanta Chmielewska-Badora; Jacek Zwoliński; Angelina Wójcik-Fatla; Jolanta Polak; Jacek Dutkiewicz
Journal:  Ann Agric Environ Med       Date:  2005       Impact factor: 1.447

5.  Tick (Ixodes ricinus) abundance and seasonality at recreational sites in the UK: hazards in relation to fine-scale habitat types revealed by complementary sampling methods.

Authors:  Andrew D M Dobson; Jennifer L Taylor; Sarah E Randolph
Journal:  Ticks Tick Borne Dis       Date:  2011-05-13       Impact factor: 3.744

6.  Modelling and mapping tick dynamics using volunteered observations.

Authors:  Irene Garcia-Martí; Raúl Zurita-Milla; Arnold J H van Vliet; Willem Takken
Journal:  Int J Health Geogr       Date:  2017-11-14       Impact factor: 3.918

7.  Environmental drivers of Ixodes ricinus abundance in forest fragments of rural European landscapes.

Authors:  Steffen Ehrmann; Jaan Liira; Stefanie Gärtner; Karin Hansen; Jörg Brunet; Sara A O Cousins; Marc Deconchat; Guillaume Decocq; Pieter De Frenne; Pallieter De Smedt; Martin Diekmann; Emilie Gallet-Moron; Annette Kolb; Jonathan Lenoir; Jessica Lindgren; Tobias Naaf; Taavi Paal; Alicia Valdés; Kris Verheyen; Monika Wulf; Michael Scherer-Lorenzen
Journal:  BMC Ecol       Date:  2017-09-06       Impact factor: 2.964

8.  Climate of origin affects tick (Ixodes ricinus) host-seeking behavior in response to temperature: implications for resilience to climate change?

Authors:  Lucy Gilbert; Jennifer Aungier; Joseph L Tomkins
Journal:  Ecol Evol       Date:  2014-03-10       Impact factor: 2.912

9.  Using volunteered observations to map human exposure to ticks.

Authors:  Irene Garcia-Marti; Raul Zurita-Milla; Margriet G Harms; Arno Swart
Journal:  Sci Rep       Date:  2018-10-18       Impact factor: 4.379

10.  Research paper on abiotic factors and their influence on Ixodes ricinus activity-observations over a two-year period at several tick collection sites in Germany.

Authors:  Jörn Gethmann; Bernd Hoffmann; Elisa Kasbohm; Jochen Süss; Birgit Habedank; Franz J Conraths; Martin Beer; Christine Klaus
Journal:  Parasitol Res       Date:  2020-03-26       Impact factor: 2.289

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