Literature DB >> 21595949

Multi-source analysis reveals latitudinal and altitudinal shifts in range of Ixodes ricinus at its northern distribution limit.

Solveig Jore1, Hildegunn Viljugrein, Merete Hofshagen, Hege Brun-Hansen, Anja B Kristoffersen, Karin Nygård, Edgar Brun, Preben Ottesen, Bente K Sævik, Bjørnar Ytrehus.   

Abstract

BACKGROUND: There is increasing evidence for a latitudinal and altitudinal shift in the distribution range of Ixodes ricinus. The reported incidence of tick-borne disease in humans is on the rise in many European countries and has raised political concern and attracted media attention. It is disputed which factors are responsible for these trends, though many ascribe shifts in distribution range to climate changes. Any possible climate effect would be most easily noticeable close to the tick's geographical distribution limits. In Norway- being the northern limit of this species in Europe- no documentation of changes in range has been published. The objectives of this study were to describe the distribution of I. ricinus in Norway and to evaluate if any range shifts have occurred relative to historical descriptions.
METHODS: Multiple data sources - such as tick-sighting reports from veterinarians, hunters, and the general public - and surveillance of human and animal tick-borne diseases were compared to describe the present distribution of I. ricinus in Norway. Correlation between data sources and visual comparison of maps revealed spatial consistency. In order to identify the main spatial pattern of tick abundance, a principal component analysis (PCA) was used to obtain a weighted mean of four data sources. The weighted mean explained 67% of the variation of the data sources covering Norway's 430 municipalities and was used to depict the present distribution of I. ricinus. To evaluate if any geographical range shift has occurred in recent decades, the present distribution was compared to historical data from 1943 and 1983.
RESULTS: Tick-borne disease and/or observations of I. ricinus was reported in municipalities up to an altitude of 583 metres above sea level (MASL) and is now present in coastal municipalities north to approximately 69°N.
CONCLUSION: I. ricinus is currently found further north and at higher altitudes than described in historical records. The approach used in this study, a multi-source analysis, proved useful to assess alterations in tick distribution.

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Year:  2011        PMID: 21595949      PMCID: PMC3123645          DOI: 10.1186/1756-3305-4-84

Source DB:  PubMed          Journal:  Parasit Vectors        ISSN: 1756-3305            Impact factor:   3.876


  28 in total

1.  Incidence from coincidence: patterns of tick infestations on rodents facilitate transmission of tick-borne encephalitis virus.

Authors:  S E Randolph; D Miklisová; J Lysy; D J Rogers; M Labuda
Journal:  Parasitology       Date:  1999-02       Impact factor: 3.234

2.  Occurrence of ticks infected by tickborne encephalitis virus and Borrelia genospecies in mountains of the Czech Republic.

Authors:  M Daniel; B Kriz; V Danielova; J Materna; N Rudenko; J Holubova; L Schwarzova; M Golovchenko
Journal:  Euro Surveill       Date:  2005-03-31

Review 3.  Fundamental processes in the evolutionary ecology of Lyme borreliosis.

Authors:  Klaus Kurtenbach; Klára Hanincová; Jean I Tsao; Gabriele Margos; Durland Fish; Nicholas H Ogden
Journal:  Nat Rev Microbiol       Date:  2006-08-07       Impact factor: 60.633

4.  Tick-borne encephalitis in Sweden and climate change.

Authors:  E Lindgren; R Gustafson
Journal:  Lancet       Date:  2001-07-07       Impact factor: 79.321

5.  Tick surveillance in Great Britain.

Authors:  Lisa J Jameson; Jolyon M Medlock
Journal:  Vector Borne Zoonotic Dis       Date:  2010-09-17       Impact factor: 2.133

6.  The range of Ixodes ricinus and the risk of contracting Lyme borreliosis will increase northwards when the vegetation period becomes longer.

Authors:  Thomas G T Jaenson; Elisabet Lindgren
Journal:  Ticks Tick Borne Dis       Date:  2010-12-13       Impact factor: 3.744

7.  Geographical distribution, host associations, and vector roles of ticks (Acari: Ixodidae, Argasidae) in Sweden.

Authors:  T G Jaenson; L Tälleklint; L Lundqvist; B Olsen; J Chirico; H Mejlon
Journal:  J Med Entomol       Date:  1994-03       Impact factor: 2.278

Review 8.  Evidence that climate change has caused 'emergence' of tick-borne diseases in Europe?

Authors:  Sarah E Randolph
Journal:  Int J Med Microbiol       Date:  2004-04       Impact factor: 3.473

9.  Altitudinal patterns of tick and host abundance: a potential role for climate change in regulating tick-borne diseases?

Authors:  Lucy Gilbert
Journal:  Oecologia       Date:  2009-08-15       Impact factor: 3.225

Review 10.  Tick-borne encephalitis incidence in Central and Eastern Europe: consequences of political transition.

Authors:  Sarah E Randolph
Journal:  Microbes Infect       Date:  2007-12-23       Impact factor: 2.700

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  67 in total

1.  Forest classes and tree cover gradient: tick habitat in encroached areas of southern Norway.

Authors:  S O Vanwambeke; J Van Doninck; J Artois; R K Davidson; P Meyfroidt; S Jore
Journal:  Exp Appl Acarol       Date:  2015-12-21       Impact factor: 2.132

2.  Lyme neuroborreliosis and bird populations in northern Europe.

Authors:  Atle Mysterud; Dieter J A Heylen; Erik Matthysen; Aïda Lopez Garcia; Solveig Jore; Hildegunn Viljugrein
Journal:  Proc Biol Sci       Date:  2019-05-29       Impact factor: 5.349

Review 3.  Changing distributions of ticks: causes and consequences.

Authors:  Elsa Léger; Gwenaël Vourc'h; Laurence Vial; Christine Chevillon; Karen D McCoy
Journal:  Exp Appl Acarol       Date:  2012-09-27       Impact factor: 2.132

4.  Relative density of host-seeking ticks in different habitat types of south-western Slovakia.

Authors:  Mária Kazimírová; Zuzana Hamšíková; Elena Kocianová; Giovanni Marini; Michala Mojšová; Lenka Mahríková; Lenka Berthová; Mirko Slovák; Roberto Rosá
Journal:  Exp Appl Acarol       Date:  2016-02-29       Impact factor: 2.132

5.  Assessment of using recombinant Ixodes ricinus AV422 saliva protein for confirmation of tick bites in hunting dogs as naturally infested hosts.

Authors:  Darko Mihaljica; Dragana Marković; Željko Radulović; Albert Mulenga; Sanja Ćakić; Ratko Sukara; Zorana Milanović; Snežana Tomanović
Journal:  Exp Appl Acarol       Date:  2017-08-24       Impact factor: 2.132

6.  The Density of the Lyme Disease Vector, Ixodes scapularis (Blacklegged Tick), Differs Between the Champlain Valley and Green Mountains, Vermont.

Authors:  David Allen; Benjamin Borgmann-Winter; Laura Bashor; Jeremy Ward
Journal:  Northeast Nat (Steuben)       Date:  2019-07-24       Impact factor: 0.583

7.  Presence of host-seeking Ixodes ricinus and their infection with Borrelia burgdorferi sensu lato in the Northern Apennines, Italy.

Authors:  Charlotte Ragagli; Alessandro Mannelli; Cecilia Ambrogi; Donal Bisanzio; Leonardo A Ceballos; Elena Grego; Elisa Martello; Marco Selmi; Laura Tomassone
Journal:  Exp Appl Acarol       Date:  2016-03-10       Impact factor: 2.132

8.  How general are generalist parasites? The small mammal part of the Lyme disease transmission cycle in two ecosystems in northern Europe.

Authors:  Atle Mysterud; Vetle Malmer Stigum; Harald Linløkken; Anders Herland; Hildegunn Viljugrein
Journal:  Oecologia       Date:  2019-05-06       Impact factor: 3.225

9.  First evidence of Ixodiphagus hookeri (Hymenoptera: Encyrtidae) parasitization in Finnish castor bean ticks (Ixodes ricinus).

Authors:  Jani Jukka Sormunen; Ella Sippola; Kari Mikael Kaunisto; Eero Juhani Vesterinen; Ilari Eerikki Sääksjärvi
Journal:  Exp Appl Acarol       Date:  2019-11-19       Impact factor: 2.132

10.  Parasite load and seasonal migration in red deer.

Authors:  Atle Mysterud; Lars Qviller; Erling L Meisingset; Hildegunn Viljugrein
Journal:  Oecologia       Date:  2015-10-08       Impact factor: 3.225

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