THE VECTOR – TICK

TBEV isolates from Slovenia belong to the European subtype (TBEV-Eu) and the virus is transmitted by I. ricinus ticks [Reference Avsic-Zupanc15–Reference Kmet and Likar17]. I. ricinus can be throughout Europe, from Ireland to the Ural Mountains and from Scandinavia to northern Africa, although the spread of the virus is limited to endemic areas in central and eastern Europe, part of Scandinavia and the Balkan region [Reference Estrada-Pena18, Reference Suss19]. Over such an extensive area of distribution I. ricinus encounters a variety of environmental conditions, which challenge its endurance and adaptability. The life cycle of the tick ranges from 2 to 6 years, depending on the climate; the cold climates of the north provide a longer life cycle than the warm climates of the south, since the duration of favorable conditions in the latter is significantly shorter [Reference Gray20]. The three active stages each require a single host, from which they feed on blood for several days [Reference Gray20, Reference Randolph21]. After completing a bloodmeal, the tick then detaches, hides in the undergrowth and the larvae and nymphs moult, while the female adults produce eggs [Reference Randolph21, Reference Gray22]. Development from one stage to the next takes about a year but can be longer or shorter depending on environmental conditions. There have been changes in the distribution of the tick in Europe in past decades and there appear to be many driving factors for changes in the altitudinal and latitudinal spread of I. ricinus [Reference Medlock23]. One of these is climate change, where increased temperatures and rainfall influence both the developmental period and winter survival of ticks, as well as causing changes in the forest and wildlife management and structure [Reference Danielova24, Reference Rizzoli25] .

Even though Slovenia is a relatively small country in terms of its geographical area, there is considerable diversity of both climate and habitat types. The conditions influencing tick dynamics are consequently also very variable and are the cause of different patterns of seasonal activity [Reference Knap26]. Ticks were sampled monthly by flagging the vegetation at eight locations in Slovenia from April 2005 to September 2008 [Reference Knap26, Reference Durmisi27]. The most common tick found throughout the country was I. ricinus. In only one location were two other species confirmed, Dermacentor reticulatus and Haemaphysalis concinna. The majority of the country has bimodal seasonal activity of I. ricinus, with the first peak occurring in the spring months (April, May, June) and the second peak occurring in the autumn months (September or October) (Fig. 1). Only the coastal region offers a climate that enables unimodal seasonal activity, with one peak extending from autumn, through winter, to the early spring months. Only occasionally can larvae be found during the early summer months in this region. I. ricinus ticks find their hosts by climbing vegetation and waiting for the host to walk by. In such a position, ticks are exposed to multiple environmental factors and are especially sensitive to desiccation when the relative humidity drops below 80% [Reference Randolph and Storey28]. Saturation deficit was calculated since it gives an integrated measure of the drying power of the atmosphere [Reference Knap26, Reference Perret29, Reference Thornthwaite30] and its changes compared with the rate of change of nymph density during the period of decline. It was confirmed that warmer drier weather was associated with a very rapid decline in nymph density [Reference Knap26], confirming the direct influence of weather on tick dynamics. The analysis was performed only for nymphs, since sampling by flagging is most efficient for this tick stage. Larvae quest closer to the ground, since their limited fat supply makes water stress a greater problem and they are consequently harder to reach by flagging [Reference Mejlon and Jaenson31]. Adult ticks are least sensitive to water stress. They are thus able to quest higher and can therefore be picked up quickly but also loosened from the flag faster. However, even when taking the sampling bias into account, we found that, during the 4-year sampling period, while all other sampling sites provided larvae and nymphs simultaneously (during the spring months), we never encountered large numbers of larvae and nymphs at the same time at the sub-Mediterranean, coastal location. The seasonal synchrony of immature stages has been established as the condition for tick co-feeding and therefore a potentially high virus transmission rate [Reference Randolph32]. Our sampling data suggest that co-feeding of ticks on rodents is very likely to occur in most of Slovenia, while it is unlikely to occur at the coastal location. The virus transmission rate between tick stages is therefore significantly impaired at the coastal location (Fig. 1).

Fig. 1.

Seasonal variation in the number of larvae (- - -), nymph (–––) and adult () I. ricinus/100 m² on two selected sampling sites in Slovenia. Črni Kal, a sub-Mediterranean coastal sampling site; Mozirje, continental Slovenia.

The sampled ticks collected during the 4-year period at eight different locations in Slovenia were screened for the presence of TBEV RNA by real-time RT–PCR [Reference Schwaiger and Cassinotti33]. Sampling sites were selected on the basis of the previously recognized incidence of TBE [Reference Durmisi27]. Studies performed in Europe have established that 0–5% of I. ricinus ticks are infected with TBEV, depending on the sampling area, screened tick stage and TBEV detection method [Reference Carpi34–Reference Suss36]. Our study established that 0·3% of ticks were infected with TBEV (Table 1), although the infection rate varied from 2% in areas with a high incidence of the disease, to 0% where cases are never or only rarely confirmed [Reference Durmisi27]. Moreover, inter-annual variation was evident in all of the sampling sites at which TBEV was detected in ticks (Table 1).

Table 1.

Rate of infection in I. ricinus ticks, number of positive and tested pools and tested individuals at eight sampling sites in Slovenia collected from 2005 to 2008

Adult ticks (0·75%) had a higher infection rate than nymphs (0·18%; χ ², P = 8·4 × 10⁻⁵) and slightly more males (0·81%) harboured the virus than females (0·68%; χ ², P > 0·05). Since the analysed ticks were questing ticks, the rate of infection is connected to the probability of acquiring the virus during feeding in previous stages, which explains why the rate of infection is higher in adult ticks, which have fed twice before [Reference Randolph21].

Ticks in which TBEV infection was confirmed were found only at locations at which analysis of seasonal dynamics showed that co-feeding of nymphs and larvae was possible due to seasonal synchrony of immature tick stages (Fig. 1). Co-feeding, in addition to direct TBEV transmission from a viraemic animal to the tick and transtadial and transovarial transmission, is recognized as one of the most important paths of TBEV transmission between ticks, and a high rate of infected ticks consequently causes higher TBE incidence [Reference Labuda10, Reference Lindquist and Vapalahti37]. I. ricinus ticks are widely and densely distributed in most of Slovenia and exhibit a dynamic that makes co-feeding possible (Fig. 1). In areas in which the seasonal synchrony of nymphs and larvae does not occur, there were no or very few TBE cases (Črni Kal, Murska Šuma, Table 1) [Reference Durmisi27].

Additionally to I. ricinus ticks, D. reticulatus and H. concinna ticks were collected in one location in Slovenia. Although the virus has been demonstrated in D. reticulatus ticks in other countries and laboratory experiments have confirmed the ability of both types of ticks to transmit the virus [Reference Kozuch38, Reference Randolph39], TBEV was not detected in these two species in Slovenia. In contrast to the I. ricinus ticks, only adult D. reticulatus quest for hosts by climbing vegetation. Nymphs and larvae are thus rarely found by flagging vegetation. Even the life cycle of this species is significantly different. Since the development from egg to adult animal only takes 1 year, there is less overlap between the ticks active stages during their life cycle, so co-feeding is unlikely to occur [Reference Randolph39, Reference Gray40]. H. concinna also has a specific scheme of seasonal dynamics, which does not support co-feeding transmission [Reference Kozuch38, Reference Szell41]. The importance of these two species of ticks for transmission of TBEV in the foci is probably therefore minimal.

THE TICK HOSTS

Each of the three active stages of the I. ricinus tick requires a vertebrate host to provide a bloodmeal, which is necessary for further development. The selection of tick host may be determined by the tick's questing height [Reference Randolph21]. Larvae quest close to the ground and feed mostly on small mammals, which are also good hosts for the nymphs. All three tick stages can be found on larger hosts, such as wild cervids, cattle and other animals [Reference Jaenson42]. Furthermore, these large hosts are the most important host for adult reproductive ticks [Reference Jaenson42]. Host density directly influences the density of ticks, whereby the density of adult female tick hosts in particular (e.g. deer) can be a limiting factor or can influence the expansion and abundance of the I. ricinus population [Reference Gray20, Reference Jaenson42].

Small mammals are important hosts in the tick life cycle and also play an important role in facilitating TBEV transmission between ticks. They enable non-viraemic transmission by co-feeding infected nymphs and uninfected larvae [Reference Labuda10] and also develop sufficient viraemia to support direct transmission of the virus to feeding ticks [Reference Achazi43–Reference Kozuch45]. By contrast, deer are not competent hosts for TBEV transmission, since they do not develop sufficient viraemia for transmission, although they are an important factor in the TBEV enzootic cycle since they support tick populations [Reference Labuda13, Reference Rizzoli25, Reference Knap and Avsic-Zupanc46]. Theoretical and empirical studies have demonstrated that TBEV amplification can occur when a certain host threshold density is achieved [Reference Cagnacci47, Reference Bolzoni48]. Transmission of TBEV by co-feeding has been suggested, due to a large number of ticks feeding on a single deer in very close proximity, but no experimental or direct evidence exists to support such a hypothesis [Reference Jaenson49, Reference Vor50].

Previous studies on wildlife and the abundance of ticks have produced inconclusive results concerning a connection between TBE incidence and deer density [Reference Rizzoli25, Reference Vor50, Reference Ostfeld51]. A study performed in Slovenia demonstrated a link between the abundance of deer and the number of TBE patients [Reference Knap and Avsic-Zupanc46]. Roe deer and red deer numbers have been increasing in past decades, as well as the incidence of TBE. A temporal connection was significant in cases of both host groups. Since such connections may be a result of coincidental factors, an additional spatial analysis was performed. The analysis established that roe deer density is not associated with the incidence of TBE but that the red deer density is significantly connected to TBE incidence in Slovenia. The study confirmed that fewer people contract TBE in areas with a lower red deer density. The density of roe deer in Slovenia is very high compared to neighbouring countries, such as Italy, where a connection between roe deer and TBE incidence has been established [Reference Rizzoli25, Reference Knap and Avsic-Zupanc46]. In Slovenia, the average density of roe deer is 8·79 head/km², which might exceed the threshold beyond which host density has a measurable effect on the incidence of TBE [Reference Knap and Avsic-Zupanc46, Reference Erhatič52]. Nevertheless, roe deer should not be neglected in further research, since evidence from studies in other countries supports their important role in the circulation of the virus in nature [Reference Rizzoli25, Reference Jaenson42, Reference Knap and Avsic-Zupanc46]. However, it is important to note that the density of red deer has been increasing since the 1970s, both in Slovenia and in other European countries [Reference Knap and Avsic-Zupanc46]. Red deer, too, which almost became extinct in the 19th century, are currently increasing in abundance due to shooting restrictions and artificial restocking [Reference Knap and Avsic-Zupanc46]. Why the connection between TBEV and red deer is more pronounced than the connection with other deer species remains unknown but further studies elucidating the red deer–tick host characteristics and analysing the preferred red deer habitat and behavioural features are needed to explain the connection.

Rodents are the most studied vertebrate host group in connection with the TBEV enzootic cycle, especially the yellow-necked mouse (Apodemus flavicollis) and the bank vole (Myodes glareolus). These species are most abundant in areas in which TBE incidence is high and both are excellent hosts for the nymphal and larval tick stages. They are often considered bridge hosts for TBEV between the two subadult tick stages due to co-feeding transmission [Reference Labuda10, Reference Randolph, Gern and Nuttall11, Reference Labuda53].

A study was performed in Slovenia analysing TBEV infection patterns in naturally infected wild rodents [Reference Knap44]. Rodents were trapped from 1990 to 2009 throughout Slovenia. Live traps were used and animals were euthanized and the internal organs and blood harvested, and stored at -70 °C. Rodent sera were screened for the presence of TBEV antibodies as described previously and samples from almost 700 rodents were screened for the presence of TBEV RNA [Reference Knap44]. TBEV-specific antibodies were detected in 5·53% of investigated rodent sera but the prevalence differed significantly according to the rodent species (Table 2) and the investigated region (Fig. 2).

Fig. 2.

Map of Slovenia indicating the incidence of tick-borne encephalitis (TBE) in Slovenian municipalities and the sampling sites of rodents, where specific antibodies against TBEV were detected (•) or not detected (▴) in rodent sera.

Table 2.

Prevalence of infection of rodent species captured in Slovenia from 1990 to 2009

The prevalence of infection was highest in bank voles (12·54%); a lower prevalence was detected in Apodemus sp. rodents (4·04%). Several of the animals in which TBEV antibodies were present were still in the viraemic phase or had detectable viral RNA in their organs [Reference Knap44]. Although previous studies indicated that the viraemic phase only lasts a couple of days, more recent studies have shown that viraemia can be detected for weeks or month after the initial infection. Recent studies have shown that some vole species (M. glareolus and Microtus arvalis) can develop persistent TBE infection, without apparent clinical symptoms in the majority of infected animals [Reference Achazi43, Reference Tonteri54]. Especially prolonged continuation of TBEV in the brain tissue of infected animals (both naturally and experimentally) [Reference Achazi43, Reference Knap44, Reference Tonteri54] might indicate a more crucial role of certain rodent species in the enzootic cycle of TBEV, a role that extends beyond the important tick host function.

HUMANS AND THE ENVIRONMENT

Two sets of factors influence TBE endemicity. One set influences the increased ability of the virus to be transmitted between different hosts while the other set increases the relative risk, namely the risk of humans coming into contact with the infected tick [Reference Sumilo55]. Both sets of factors are influenced by human interventions and activity in nature.

Direct interventions, which include modifications of the forest area, and an increase or abandonment of agricultural areas, can influence both tick and tick hosts [Reference Šumilo56]. Abandoned agricultural fields are good habitats for rodents and increased A. flavicollis and M. glareolus populations are an important step in the TBEV enzootic cycle. Additionally, more forests again provide more suitable habitats for the TBEV vector, the tick, I. ricinus, as well as its hosts, i.e. deer, rodents and other vertebrate animals [Reference Šumilo56]. More than 60% of Slovenia is covered by forests. Analysis of statistical data in past decades has shown that the forest area has been increasing and agricultural land has been slightly decreasing. We were able to confirm a correlation between forest area and TBE incidence (Pearson's correlation coefficient: r = 0·640, P < 0·0001), but were unable to confirm a connection between agricultural land and TBE (Pearson's correlation coefficient: r = −0·201, P = 0·204) (Fig. 3). Although a negative correlation between decreasing agricultural areas and the incidence of TBE is indicated, no straightforward correlation could be confirmed. The influence of deer abundance control was described in the previous section but there are other influences of human interventions on host populations that need to be investigated. One example is changes in rodent populations due to forest and agricultural land management. Changes in farmed crops could influence small mammal populations. On the other hand, pesticide use could influence tick populations directly. Many of these factors have already been researched and their influence established [Reference Randolph57]. It is therefore important to recognize these factors, which synergistically act to increase the zoonotic risk of infection as well as influencing the exposure of humans to risk.

Fig. 3.

Correlation between tick-borne encephalitis (TBE) incidence and (a) forest areas (m²) and (b) agricultural land areas (m²).

Human behaviuor influences TBE incidence, since it can trigger actions that increase the contact of people with infected ticks. One example is good weather, which increases the time spent outdoors, therefore the chance of an encounter between ticks and humans is significantly increased [Reference Randolph58]. This happened in 2006, when a long warm autumn provided favourable weather for outdoor recreational activities and a spike in TBE incidence can be observed during that period [Reference Randolph58]. Additionally, it has been indicated that background socioeconomic conditions also impact on TBE incidence [Reference Godfrey and Randolph59]. For example, both unemployment and an increase in household expenditure on food can generate an increase in the number of TBE cases [Reference Godfrey and Randolph59]. A study performed in Slovenia on vaccination against TBE indicated that being in middle- or high-income groups increases the chances of people being vaccinated [Reference Grgic-Vitek and Klavs3]. People also tend to be more aware of the risk of TBE and, consequently, increasingly cautious when coming from a higher-income population. High-risk behaviour in Slovenia has been shown to include leisure-time activities, mushroom and berry picking, and farming [Reference Blasko-Markic and Socan60].

The genetic variability of TBEV was studied in Slovenian patients, as well as in rodents and tick populations. TBEV E and NS5 protein gene sequences were obtained and the correlation between phylogenetic and geographical clustering was investigated and confirmed [Reference Fajs16]. At the same time, it was established in this study that the majority of patients become infected in relative proximity to their homes [Reference Fajs16, Reference Zeman and Benes61]. Therefore, human behaviour should not be neglected in studies of TBE, since it can significantly alter the incidence. The ecological factors that influence such changes should also be identified as far as possible.