- Letter to the Editor
- Open Access
A large-scale screening for the taiga tick, Ixodes persulcatus, and the meadow tick, Dermacentor reticulatus, in southern Scandinavia, 2016
- Lene Jung Kjær1Email authorView ORCID ID profile,
- Arnulf Soleng2,
- Kristin Skarsfjord Edgar2,
- Heidi Elisabeth H. Lindstedt2,
- Katrine Mørk Paulsen3, 4,
- Åshild Kristine Andreassen3,
- Lars Korslund5,
- Vivian Kjelland5, 6,
- Audun Slettan5,
- Snorre Stuen7,
- Petter Kjellander8,
- Madeleine Christensson8,
- Malin Teräväinen8,
- Andreas Baum9,
- Anastasia Isbrand10,
- Laura Mark Jensen1,
- Kirstine Klitgaard10 and
- René Bødker1
© The Author(s) 2019
- Received: 13 May 2019
- Accepted: 3 July 2019
- Published: 9 July 2019
The taiga tick, Ixodes persulcatus, has previously been limited to eastern Europe and northern Asia, but recently its range has expanded to Finland and northern Sweden. The species is of medical importance, as it, along with a string of other pathogens, may carry the Siberian and Far Eastern subtypes of tick-borne encephalitis virus. These subtypes appear to cause more severe disease, with higher fatality rates than the central European subtype. Until recently, the meadow tick, Dermacentor reticulatus, has been absent from Scandinavia, but has now been detected in Denmark, Norway and Sweden. Dermacentor reticulatus carries, along with other pathogens, Babesia canis and Rickettsia raoultii. Babesia canis causes severe and often fatal canine babesiosis, and R. raoultii may cause disease in humans. We collected 600 tick nymphs from each of 50 randomly selected sites in Denmark, southern Norway and south-eastern Sweden in August–September 2016. We tested pools of 10 nymphs in a Fluidigm real time PCR chip to screen for I. persulcatus and D. reticulatus, as well as tick-borne pathogens. Of all the 30,000 nymphs tested, none were I. persulcatus or D. reticulatus. Our results suggest that I. persulcatus is still limited to the northern parts of Sweden, and have not expanded into southern parts of Scandinavia. According to literature reports and supported by our screening results, D. reticulatus may yet only be an occasional guest in Scandinavia without established populations.
- Taiga tick
- Ixodes persulcatus
- Siberian and Far Eastern tick-borne encephalitis
- meadow tick
- Dermacentor reticulatus
- southern Scandinavia
- range expansion
Letter to the Editor
Tick-borne diseases pose a risk to both humans and animals [1–3], and there is a concern that the increase in incidence and geographical range reported over the last decades [4–8] may be an effect of climate change impacting vectors and their associated pathogens [9, 10]. In Europe, and especially Scandinavia, the main vector of disease-causing pathogens in humans, pets and other large mammals is the castor bean tick Ixodes ricinus [6, 7]. The closely related taiga tick, Ixodes persulcatus, has previously been limited to eastern Europe and northern Asia , but within the last 15 years, the species has expanded its range, both in eastern Europe [12, 13] but also towards western Europe [11, 12, 14]. Ixodes persulcatus was recorded in the western parts of Finland in 2004  and 2008 , and in northern Sweden in 2015 . Ixodes persulcatus may carry the Siberian and Far Eastern subtypes of the tick-borne encephalitis virus (TBEV) along with a range of other pathogens [11, 16, 17]. The Siberian and Far Eastern subtypes of TBEV have been reported to cause more severe symptoms than the European sub-type [17–19], although there is speculation that this may be due to other factors such as clinical alert and reporting [17, 19].
The meadow tick, Dermacentor reticulatus, is endemic to Europe , and is currently spreading to new geographical areas [20–22]. Dermacentor reticulatus was previously absent from Scandinavia , but has been found on migrating birds in Norway as early as 2003–2005 , and potentially in 2009, as Babesia canis was detected in a dog from the Oslo area that had not travelled abroad, indicating that D. reticulatus was present in the area . In Sweden, single D. reticulatus has been identified in 2010 in the region of Skåne, in 2012 on a dog that had been abroad and then again two more times in the region of Skåne in 2017 . In Denmark, D. reticulatus was found on a migrating golden jackal (Canis aureus) in 2017 , and again in 2018 on a dog that was returning from a trip to Slovakia with its owner . Dermacentor reticulatus carries several pathogens presently absent in Scandinavia, but the most concerning involve B. canis and Rickettsia raoultii. Babesia canis causes canine babesiosis in dogs with a high risk of death . Rickettsia raoultii poses a zoonotic health concern as it may cause disease in humans .
We morphologically examined the 30,000 ticks to ensure that they were all nymphs. We aggregated 30,000 collected nymphs into 60 pools of 10 for each site and used the BioMark real-time PCR system (Fluidigm, San Francisco, California, USA) for high-throughput microfluidic RT-PCR. The method is thoroughly described in Klitgaard et al.  and Michelet et al. . Along with 18 different pathogens, we simultaneously screened each pool for presence of D. reticulatus, I. persulcatus and I. ricinus, as described and validated by Michelet et al. . The Fluidigm chip has been used for surveillance of tick-borne pathogens and exotic tick species on both flagged ticks and on ticks removed from imported animals in Denmark since 2014. The chip has previously detected D. reticulatus on a migrating golden jackal .
With this equation, we assume that if I. persulcatus/D. reticulatus constitute a proportion higher or equal to prev in all nymphs collected and the PCR is 100% sensitive in pool sizes of 10, we can then be 95% certain that we would detect at least one positive pool. With 600 ticks per site and all pools negative, we are therefore 95% certain that the proportion of I. persulcatus/D. reticulatus at each given site was lower than 0.5%, given the reasonable assumption that the 600 nymphs represent a random sample drawn from a much larger population at the site. Likewise, if the 30.000 nymphs collected in total were a random sample from the entire area, we would be 95% certain that the proportion of I. persulcatus/D. reticulatus would be lower than 0.01%. Therefore, if the two species are individually introduced by e.g. migrating birds to the region, they constitute less than one out of 10,000 flagged nymphs. However, if the two species are not just randomly introduced individuals but instead have become established breeding populations then they are likely to have a spatially clustered distribution in the area. With small clusters the probability of detecting a cluster by screening 50 sites is just 5.8% at a 95% certainty level, assuming the proportion of the species in a cluster is high enough to be detected with a sensitivity of 100% when 600 nymphs are tested per site. Thus, the existence of spatially limited clusters of locally breeding I. persulcatus or D. reticulatus in the area cannot be excluded with reasonable certainty, despite the large number of nymphs analysed.
Although there is no evidence for an increased northward distribution of permanent viable populations of I. ricinus in Norway , studies from Sweden have found I. ricinus to have expanded northwards compared to historical data , possibly due to climate change [9, 10]. Thus, a potential spread of I. persulcatus further south in Scandinavia and establishment of D. reticulatus within the Scandinavian region could also be expected. Further tick surveillance studies in Scandinavia should acknowledge the possibility of I. persulcatus/D. reticulatus becoming established further in this region, and thus the possibility of infections with the Siberian and Far Eastern subtypes of TBEV, B. canis, R. raoultii and other pathogens related to these two tick species. It may be advisable to carry out targeted surveillance by flagging at sites with reported cases of B. canis in dogs and Siberian and Far Eastern subtypes of TBE in humans without recent travel histories. Alternatively, it may be recommendable to initiate citizen science projects  as local breeding populations of I. persulcatus and D. reticulatus will be difficult to detect by random surveillance. Our results suggest that I. persulcatus and D. reticulatus may not be established in southern Scandinavia.
We thank Simon Friis-Wandall, Mette Frimodt Hansen, Caroline Greisen, Ana Carolina Cuellar, Najmul Haider, Leif Kristian Sortedal, Philip Thomassen Neset, Preben Ottesen, Alaka Lamsal, Ruchika Shakya, Martin Strnad, Hanne Quarsten, Sølvi Noraas, Åslaug Rudjord Lorentzen, Chiara Bertacco, Kevin Hohwald, Catharina Schmidt, Coco de Koning, and Wenche Okstad for assistance in the field. We would also like to thank the Danish Ministry of the Environment, The Forest and Nature Agency as well as many private landowners for allowing us access to their properties to conduct our sampling.
This study was funded by the Interreg V Program (the ScandTick Innovation project, Grant number 20200422), and the Danish Veterinary and Food Administration.
LJK planned and managed the fieldwork set-up, performed fieldwork in Denmark and contributed to field work in Sweden, analysed the data and drafted the manuscript. RB planned the original study, contributed to analysis and drafting the manuscript. AS, KSE, HEHL, KMP, AKA, LK, VK, AS and SS organised and conducted fieldwork in Norway and contributed to drafting the manuscript. PK, MC and MT organised and conducted to fieldwork in Sweden and contributed to drafting the manuscript. AB contributed to analysis and drafting the manuscript. AI and KK performed DNA preparation and the PCR assays and contributed to drafting the manuscript. LMJ contributed to fieldwork, DNA preparation, PCR assays and drafting the manuscript. All authors read and approved the final manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
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