Many factors are involved in determining the latitudinal and altitudinal spread of the important tick vector Ixodes ricinus (Acari: Ixodidae) in Europe, as well as in changes in the distribution within its prior endemic zones. This paper builds on published literature and unpublished expert opinion from the VBORNET network with the aim of reviewing the evidence for these changes in Europe and discusses the many climatic, ecological, landscape and anthropogenic drivers. These can be divided into those directly related to climatic change, contributing to an expansion in the tick’s geographic range at extremes of altitude in central Europe, and at extremes of latitude in Scandinavia; those related to changes in the distribution of tick hosts, particularly roe deer and other cervids; other ecological changes such as habitat connectivity and changes in land management; and finally, anthropogenically induced changes. These factors are strongly interlinked and often not well quantified. Although a change in climate plays an important role in certain geographic regions, for much of Europe it is non-climatic factors that are becoming increasingly important. How we manage habitats on a landscape scale, and the changes in the distribution and abundance of tick hosts are important considerations during our assessment and management of the public health risks associated with ticks and tick-borne disease issues in 21st century Europe. Better understanding and mapping of the spread of I. ricinus (and changes in its abundance) is, however, essential to assess the risk of the spread of infections transmitted by this vector species. Enhanced tick surveillance with harmonized approaches for comparison of data enabling the follow-up of trends at EU level will improve the messages on risk related to tick-borne diseases to policy makers, other stake holders and to the general public.

Ticks (Acari: Ixodidae) transmit a wide variety of pathogens to vertebrates including viruses, bacteria, protozoa and helminthes. Tick-borne pathogens are believed to be responsible for more than 100,000 cases of illness in humans throughout the world. Ticks are considered to be second worldwide to mosquitoes as vectors of human diseases, but they are the most important vectors of disease-causing pathogens in domestic and wild animals. Infection and development of pathogens in both tick and vertebrate hosts are mediated by molecular mechanisms at the tick-pathogen interface. These mechanisms, involving traits of both ticks and pathogens, include the evolution of common and species-specific characteristics. The molecular characterization of the tick-pathogen interface is rapidly advancing and providing new avenues for the development of novel control strategies for both tick infestations and their associated pathogens.

Zoonotic tick-borne diseases are an increasing health burden in Europe and there is speculation that this is partly due to climate change affecting vector biology and disease transmission. Data on the vector tickIxodes ricinussuggest that an extension of its northern and altitude range has been accompanied by an increased prevalence of tick-borne encephalitis. Climate change may also be partly responsible for the change in distribution ofDermacentor reticulatus. Increased winter activity of I. ricinusis probably due to warmer winters and a retrospective study suggests that hotter summers will change the dynamics and pattern of seasonal activity, resulting in the bulk of the tick population becoming active in the latter part of the year. Climate suitability models predict that eight important tick species are likely to establish more northern permanent populations in a climate-warming scenario. However, the complex ecology and epidemiology of such tick-borne diseases as Lyme borreliosis and tick-borne encephalitis make it difficult to implicate climate change as the main cause of their increasing prevalence. Climate change models are required that take account of the dynamic biological processes involved in vector abundance and pathogen transmission in order to predict future tick-borne disease scenarios.

This work is intended as a consensus list of valid tick names, following recent revisionary studies, wherein we recognize 896 species of ticks in 3 families. The Nuttalliellidae is monotypic, containing the single entity Nuttalliella namaqua. The Argasidae consists of 193 species, but there is widespread disagreement concerning the genera in this family, and fully 133 argasids will have to be further studied before any consensus can be reached on the issue of genus-level classification. The Ixodidae comprises 702 species in 14 genera: Amblyomma (130 species, of which 17 were formerly included in Aponomma, a genus that is still considered valid by some authors), Anomalohimalaya (3), Bothriocroton (7, all previously included in Aponomma), Cosmiomma (1), Cornupalpatum (1), Compluriscutula (1), Dermacentor (34, including the single member of the former genus Anocentor, which is still considered valid by some authors), Haemaphysalis (166), Hyalomma (27), Ixodes (243), Margaropus (3), Nosomma (2), Rhipicentor (2) and Rhipicephalus (82, including 5 species from the former genus Boophilus, which is still considered valid by some authors). We regard six names as invalid: Amblyomma laticaudae Warburton, 1933 is a synonym of Amblyomma nitidum Hirst & Hirst, 1910; Bothriocroton decorosum (Koch, 1867) is a synonym of B. undatum (Fabricius, 1775); Haemaphysalis vietnamensis Hoogstraal & Wilson, 1966 is a synonym of H. colasbelcouri (Santos Dias, 1958); Haemaphysalis xinjiangensis Teng, 1980 is a synonym of H. danieli Č erný & Hoogstraal, 1977; Hyalomma erythraeum Tonelli-Rondelli, 1932 is a synonym of H. impeltatum Schulze and Schlottke, 1930 and Rhipicephalus hoogstraali Kolonin, 2009 was not described according to the rules of the International Code of Zoological Nomenclature.

Ticks and the pathogens they transmit constitute a growing burden for human and animal health worldwide. Vector competence is a component of vectorial capacity and depends on genetic determinants affecting the ability of a vector to transmit a pathogen. These determinants affect traits such as tick-host-pathogen and susceptibility to pathogen infection. Therefore, the elucidation of the mechanisms involved in tick-pathogen interactions that affect vector competence is essential for the identification of molecular drivers for tick-borne diseases. In this review, we provide a comprehensive overview of tick-pathogen molecular interactions for bacteria, viruses and protozoa affecting human and animal health. Additionally, the impact of tick microbiome on these interactions was considered. Results show that different pathogens evolved similar strategies such as manipulation of the immune response to infect vectors and facilitate multiplication and transmission. Furthermore, some of these strategies may be used by pathogens to infect both tick and mammalian host. Identification of interactions that promote tick survival, spread and pathogen transmission provides the opportunity to disrupt these interactions and lead to a reduction in tick burden and the prevalence of tick-borne diseases. Targeting some of the similar mechanisms used by the pathogens for infection and transmission by ticks may assist in development of preventative strategies against multiple tick-borne diseases.