Literature DB >> 22429768

Effect of deer density on tick infestation of rodents and the hazard of tick-borne encephalitis. II: population and infection models.

L Bolzoni1, R Rosà, F Cagnacci, A Rizzoli.   

Abstract

Tick-borne encephalitis is an emerging vector-borne zoonotic disease reported in several European and Asiatic countries with complex transmission routes that involve various vertebrate host species other than a tick vector. Understanding and quantifying the contribution of the different hosts involved in the TBE virus cycle is crucial in estimating the threshold conditions for virus emergence and spread. Some hosts, such as rodents, act both as feeding hosts for ticks and reservoirs of the infection. Other species, such as deer, provide important sources of blood for feeding ticks but they do not support TBE virus transmission, acting instead as dead-end (i.e., incompetent) hosts. Here, we introduce an eco-epidemiological model to explore the dynamics of tick populations and TBE virus infection in relation to the density of two key hosts. In particular, our aim is to validate and interpret in a robust theoretical framework the empirical findings regarding the effect of deer density on tick infestation on rodents and thus TBE virus occurrence from selected European foci. Model results show hump-shaped relationships between deer density and both feeding ticks on rodents and the basic reproduction number for TBE virus. This suggests that deer may act as tick amplifiers, but may also divert tick bites from competent hosts, thus diluting pathogen transmission. However, our model shows that the mechanism responsible for the dilution effect is more complex than the simple reduction of tick burden on competent hosts. Indeed, while the number of feeding ticks on rodents may increase with deer density, the proportion of blood meals on competent compared with incompetent hosts may decrease, triggering a decline in infection. As a consequence, using simply the number of ticks per rodent as a predictor of TBE transmission potential could be misleading if competent hosts share habitats with incompetent hosts.
Copyright © 2012 Australian Society for Parasitology Inc. Published by Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22429768     DOI: 10.1016/j.ijpara.2012.02.006

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  27 in total

1.  The role of game (wild boar and roe deer) in the spread of tick-borne encephalitis in the Czech Republic.

Authors:  Bohumir Kriz; Milan Daniel; Cestmir Benes; Marek Maly
Journal:  Vector Borne Zoonotic Dis       Date:  2014-11       Impact factor: 2.133

2.  Molecular detection of apicomplexan protozoa in Hokkaido brown bears (Ursus arctos yesoensis) and Japanese black bears (Ursus thibetanus japonicus).

Authors:  Mohamed Abdallah Mohamed Moustafa; Ayaka Sasaki; Michito Shimozuru; Ryo Nakao; Mariko Sashika; Koji Yamazaki; Shinsuke Koike; Junpei Tanaka; Hiroo Tamatani; Masami Yamanaka; Tsuyoshi Ishinazaka; Toshio Tsubota
Journal:  Parasitol Res       Date:  2020-10-01       Impact factor: 2.289

3.  Candidatus Neoehrlichia mikurensis in rodents in an area with sympatric existence of the hard ticks Ixodes ricinus and Dermacentor reticulatus, Germany.

Authors:  Cornelia Silaghi; Dietlinde Woll; Monia Mahling; Kurt Pfister; Martin Pfeffer
Journal:  Parasit Vectors       Date:  2012-12-07       Impact factor: 3.876

Review 4.  Why is tick-borne encephalitis increasing? A review of the key factors causing the increasing incidence of human TBE in Sweden.

Authors:  Thomas G T Jaenson; Marika Hjertqvist; Tomas Bergström; Ake Lundkvist
Journal:  Parasit Vectors       Date:  2012-08-31       Impact factor: 3.876

5.  Limited Capacity of Deer To Serve as Zooprophylactic Hosts for Borrelia burgdorferi in the Northeastern United States.

Authors:  Heidi K Goethert; Sam R Telford
Journal:  Appl Environ Microbiol       Date:  2022-02-02       Impact factor: 5.005

6.  Climate and environmental change drives Ixodes ricinus geographical expansion at the northern range margin.

Authors:  Solveig Jore; Sophie O Vanwambeke; Hildegunn Viljugrein; Ketil Isaksen; Anja B Kristoffersen; Zerai Woldehiwet; Bernt Johansen; Edgar Brun; Hege Brun-Hansen; Sebastian Westermann; Inger-Lise Larsen; Bjørnar Ytrehus; Merete Hofshagen
Journal:  Parasit Vectors       Date:  2014-01-08       Impact factor: 3.876

Review 7.  Factors affecting the ecology of tick-borne encephalitis in Slovenia.

Authors:  N Knap; T Avšič-Županc
Journal:  Epidemiol Infect       Date:  2015-04-28       Impact factor: 4.434

8.  Making green infrastructure healthier infrastructure.

Authors:  Mare Lõhmus; John Balbus
Journal:  Infect Ecol Epidemiol       Date:  2015-11-27

9.  The three subtypes of tick-borne encephalitis virus induce encephalitis in a natural host, the bank vole (Myodes glareolus).

Authors:  Elina Tonteri; Anja Kipar; Liina Voutilainen; Sirkka Vene; Antti Vaheri; Olli Vapalahti; Åke Lundkvist
Journal:  PLoS One       Date:  2013-12-13       Impact factor: 3.240

10.  History and complexity in tick-host dynamics: discrepancies between 'real' and 'visible' tick populations.

Authors:  Andrew D M Dobson
Journal:  Parasit Vectors       Date:  2014-05-19       Impact factor: 3.876

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