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Data-driven predictions and novel hypotheses about zoonotic tick vectors from the genus Ixodes



With the resurgence of tick-borne diseases such as Lyme disease and the emergence of new tick-borne pathogens such as Powassan virus, understanding what distinguishes vectors from non-vectors, and predicting undiscovered tick vectors is a crucial step towards mitigating disease risk in humans. We aimed to identify intrinsic traits that predict which Ixodes tick species are confirmed or strongly suspected to be vectors of zoonotic pathogens.


We focused on the well-studied tick genus Ixodes from which many species are known to transmit zoonotic diseases to humans. We apply generalized boosted regression to interrogate over 90 features for over 240 species of Ixodes ticks to learn what intrinsic features distinguish zoonotic vectors from non-vector species. In addition to better understanding the biological underpinnings of tick vectorial capacity, the model generates a per species probability of being a zoonotic vector on the basis of intrinsic biological similarity with known Ixodes vector species.


Our model predicted vector status with over 91% accuracy, and identified 14 Ixodes species with high probabilities (80%) of transmitting infections from animal hosts to humans on the basis of their traits. Distinguishing characteristics of zoonotic tick vectors of Ixodes tick species include several anatomical structures that influence host seeking behavior and blood-feeding efficiency from a greater diversity of host species compared to non-vectors.


Overall, these results suggest that zoonotic tick vectors are most likely to be those species where adult females hold a fecundity advantage by producing more eggs per clutch, which develop into larvae that feed on a greater diversity of host species compared to non-vector species. These larvae develop into nymphs whose anatomy are well suited for more efficient and longer feeding times on soft-bodied hosts compared to non-vectors, leading to larger adult females with greater fecundity. In addition to identifying novel, testable hypotheses about intrinsic features driving vectorial capacity across Ixodes tick species, our model identifies particular Ixodes species with the highest probability of carrying zoonotic diseases, offering specific targets for increased zoonotic investigation and surveillance.


Ticks transmit a greater diversity of pathogenic agents than any other arthropod [1] and are responsible for vectoring at least 30 zoonotic infectious diseases worldwide [2]. With global warming, tick-borne diseases are projected to increase even more drastically [3]. Unsurprisingly, a large volume of research is dedicated to understanding tick biology with a bias towards a small fraction of tick species known to vector pathogens from animals to humans (zoonotic vectors). Among the hard-bodied ticks (family Ixodidae), the most species-rich genus, Ixodes, contains 244 species, of which 29 are known zoonotic vectors (Additional file 1: Table S1). Identifying what intrinsic features distinguish effective zoonotic vectors from non-vector species is essential for understanding the biological drivers of vectorial capacity in Ixodes ticks, and for developing preemptive approaches to reducing tick-borne diseases transmitted by Ixodes species in humans.

Our goal was to determine which Ixodes tick species might harbor undiscovered zoonotic pathogens, and to identify intrinsic biological traits of Ixodes ticks that best predict their status as vectors of human zoonotic disease. To achieve this, we applied a machine learning method called generalized boosted regression [4, 5]. This algorithm determines which features are most important for correctly predicting a response variable (here, a binary variable designating whether the Ixodes tick species is a zoonotic vector) by building thousands of linked classification trees that successively improve upon the predictions of the previous tree. An advantage of this approach is that it does not rely on distributional assumptions about the data, and is ideal for high-dimensional ecological data containing hidden, nonlinear interactions, and non-random patterns of missing data [6]. In addition to identifying particular Ixodes tick species as potentially novel (undocumented) vectors of zoonotic diseases, we describe a suite of features suggesting that zoonotic vectors in this group are species whose anatomy and ecology confer a fecundity advantage that results from more efficient feeding of certain life stages from a broad range of host animals.


Data collection

We recorded a binary score for all 244 ticks of the genus Ixodes based on their zoonotic vector status as established by the primary literature and GIDEON database [7], which gives the public health consensus on the status of each Ixodes tick species as vector for one or more zoonotic diseases (Additional file 1: Table S1). We first used a standard reference text [19] to standardize Latin binomials for each Ixodes species, and to collate data on their biomes and host breadth. For remaining anatomical, biological, and additional biogeographical information across three life stages (larvae, nymph, and adult), we searched peer-reviewed primary literature using the Latin binomial of each species (Additional file 1: Table S2). The references reporting all data used in this study can be found in the Citations column of the data file available in the Figshare repository ( The major goal of this work was to identify traits and testable hypotheses about these traits that enable some species to vector zoonotic pathogens compared to others. Thus, data collection was limited to features describing intrinsic biological differences between species (e.g., anatomy, life history metrics, and biomes); less widely available data related to particular drivers of ecological change (e.g., changing patterns of land use, climate) were excluded.


Using similar approaches applied successfully in previous studies [8, 9], we applied generalized boosted regression via the gbm package in R [4, 5, 10]. We built an ensemble of 30,000 trees using tenfold cross-validation (learning rate = 0.00025, interaction depth = 3; all model parameters reported in Additional file 1: Table S3). Boosted regression methods deal robustly with missing data by the method of surrogate splits, which draws from the correlation structure among trait variables for tree building, effectively treating ‘missingness’ as a feature. In addition, we set a minimum threshold of 1% data coverage across tick species as criteria for inclusion in order to remove variables with near-zero coverage, though the difference between using all traits and removing those with less 1% coverage was negligible to model performance. Data were randomly partitioned into training (70%) and test data (30%). Classification accuracy was measured by area under the receiver operator curve (AUC).

Study effort

While many epidemiological metrics (e.g., prevalence of tick-borne disease in humans) are biased by study effort (i.e., the amount of healthcare or research spending per country), data on intrinsic features (e.g., tick body size, egg clutch size) are less subject to such biases. However, if study bias across Ixodes tick species strongly affects data coverage (i.e., biological features are only known for vectors), study bias can influence model results. To diagnose this possibility, we plotted the probability of a Ixodes tick species being a novel vector as a function of citation count, a proxy for study effort (Additional file 2: Figure S1). We also conducted a second boosted regression analysis to determine whether study effort is predictable on the basis of tick species traits (model: citation count ~ intrinsic traits). We found intrinsic traits poorly predicted which Ixodes tick species were highly researched (Additional file 1: Table S3). Although Ixodes tick species that are known vectors for at least one zoonosis have higher citation counts, there are also several Ixodes tick species (vectors and non-vectors) that are reasonably well studied with both low and high probabilities of being zoonotic vectors (Additional file 2: Figure S1). These results confirm that any study bias towards zoonotic vectors does not extend to the tick trait profile reported here, which reflects that of a zoonotic vector rather than that of well studied ticks.


Of 244 Ixodes species, 29 species are currently recognized as vectors of human diseases in the GIDEON database. Our model was able to distinguish vector from non-vector species with over 91% accuracy on withheld test data. The best predictors of zoonotic vector status included host breadth (number of orders and families that a tick species feeds on); tarsus I length of larvae; capitulum lengths of larvae, nymphs, and female adults; scutum length of female adults; egg clutch size; and female body length (Fig. 1, Additional file 1: Table S3).

Fig. 1
figure 1

Partial dependence plots representing the top six most important predictor variables from a generalized boosted regression model predicting tick zoonotic vector status. These partial dependence plots illustrate how ticks that transmit zoonotic diseases have distinctive characteristics from non-vectors. In each plot, the frequency histogram represents the trait values for all tick species (vectors and non-vectors) (left y-axis), and the black line shows the marginal effect of each trait on vector status after accounting for the average effects of all other variables in the model (right y-axis). For example, in panel 1, the majority of Ixodes ticks parasitize hosts from few taxonomic orders (bars), but tick vectors of zoonotic diseases tend to infest hosts from > 4 orders (line)

Compared to non-vectors, Ixodes tick species that vector zoonotic diseases tend to have several distinctive characteristics. First of all, zoonotic vectors have wider host breadth, feeding on host species from five or more families and four or more orders. In addition, the larvae possess shorter tarsus I lengths (the length of the first segment of the first pair of legs; < 0.18 mm), whereas those of non-vectors are generally longer. Larvae and adult female ticks have shorter capitulum lengths than non-vectors, but nymphs exhibit the opposite pattern, with nymphs of zoonotic vector species having longer capitula than non-vectors. Zoonotic vector species were also larger as female adults (scutum length > 1.0 mm, and body length, both while engorged (> 6.0 mm) and unengorged (> 2.5 mm). Adult females of zoonotic vector species also have larger clutches (> 1000 eggs) compared to adult females of non-vector species.

Our model identifies an additional 14 potential Ixodes vector species that share similar trait profiles with the 29 species already recognized as zoonotic vectors. Among these, 10 species are reported in primary literature as possibly parasitizing humans (Table 1). The remaining four species, I. canisuga, I. trichosuri, I. eldaricus, and I. aragaoi, are novel vectors that have not yet been identified as human parasites but reflect > 80% probability of vectoring a zoonotic pathogen.

Table 1 Predicted novel zoonotic Ixodes tick vectors ranked in descending order of probability, and citations of primary literature reporting human infestation by each species


Identifying Ixodes tick species most likely to vector future zoonoses is a critical step toward more effective surveillance and prevention of tickborne disease. Understanding what traits best predict an intrinsic capacity to harbor and transmit zoonotic infections will also facilitate a mechanistic understanding of why some Ixodes tick species are better at acquiring and/or transmitting zoonotic infection compared to other species. Here, we report a profile of tick traits that distinguish zoonotic vectors from non-vectors of Ixodes tick species with > 90% accuracy. On the basis of these traits, our model identifies particular species with high probabilities of vectoring one or more zoonotic diseases as potential targets for increased investigation and surveillance.

The most important predictor of zoonotic vector status in Ixodes ticks was the diversity of vertebrate species parasitized by the tick. This finding is consistent with the general principle that the probability of vectoring a zoonotic disease correlates directly with host range [11, 12]. Several anatomical features were also highly predictive of vector status. Larvae of vector species tend to have shorter tarsus I lengths (length of the first segment of the first pair of legs) compared to non-vectors. The larval stage is important because acquisition of zoonotic pathogens (e.g., Lyme spirochetes) often occurs during the blood meal at this stage [13]. Moreover, if infected at this stage, larvae have two potentially infectious bites through which to transmit pathogens to new hosts, compared to one bite if infected as a nymph. In all three life stages, tarsus I contains many important sensory organs, including Haller’s organ, which promotes habitat-, host-, and mate-seeking behaviors by determining host location, host odors, detecting pheromones, and serving other environmental sensory functions [14]. If the size of Haller’s organ scales allometrically with the length of tarsus I in larvae, tick species with shorter tarsus I lengths than expected for larval body size may indicate a decreased selectivity towards particular host species providing the first blood meal in the tick life cycle. Reduced host selectivity at this stage could lead to more generalized feeding preferences across a wider diversity of host species and environments, increasing the possibility of contact with competent zoonotic hosts that can successfully transmit infection to larval ticks. In a post hoc analysis, we found that ticks with shorter tarsus I lengths at the larval stage indeed fed upon a more diverse host range (infesting hosts from more taxonomic orders) (Additional file 2: Figure S2, p = 0.01, F1,43 = 7.05). This pattern was absent at the other life stages (nymphs: p = 0.96, F1,40 = 0.003; adult females: p = 0.82, F1,79 = 0.05; adult males: p = 0.59, F1,53 = 0.30). In addition to validating comparative patterns across species, future empirical work could explore the relationships between tarsus I and Haller’s organ sizes and their effects on host selectivity in controlled experiments.

Another important trait distinguishing vectors from non-vectors was the capitulum length in larvae, nymphs, and adult females. Capitulum length is determined by hypostome length and salivarium size in ticks. The hypostome is a the ratchet-like anchor within the capitulum that is inserted into the host body [14, 15], and the salivarium is a repository that collects and delivers tick saliva. Tick saliva contains bioactive molecules responsible for facilitating blood meals and can contain zoonotic pathogens such as Borrelia burgdorferi (causative agent of Lyme disease) and Francisella tularensis (causative agent of tularemia), among others [16]. We found that capitulum lengths were shorter in adult female and larval vectors than those of non-vectors, and that capitulum length in nymphal vectors was longer in zoonotic vectors. This pattern is consistent with widely documented patterns of vector competence of Ixodes species that transmit pathogens that cause anaplasmosis, babesiosis, and Lyme disease: of the three developmental stages, the nymphal stage is disproportionately responsible for human transmission [13]. With softer substrates like those encountered in human and other mammal hosts, ticks benefit from a more secure anchor conferred by deeper penetration of mouthparts that comprise the capitulum [15]. Secure attachments lead to increased feeding times, which increase the probability of successful transmission for tick-borne pathogens [15, 16]. Such stage-dependent relationships between capitulum length and feeding behaviors and outcomes (i.e., host breadth, transmission success) present another set of testable hypotheses that, if validated, may suggest that capitulum length at the nymphal stage could be used as an indicator of the vectorial capacity of Ixodes tick species for zoonotic pathogens. In contrast, a shorter capitulum in larval and adult tick vectors may signal more generalized feeding that is less selective for particular host species, with host breadth ranging widely across several taxonomic groups.

Our analysis also suggest that Ixodes tick vectors may have a fecundity advantage over non-vector ticks [17], with larger adult females producing larger clutches. Specifically, body size, scutum length, and clutch size of adult females were all larger for zoonotic vectors compared to non-vectors. Larger body sizes enable the ingestion of larger blood meals from hosts, leading to greater resources available for egg production [18]. Combined, these results suggest that zoonotic Ixodes tick vectors are most likely to be species where adult females produce a larger number of eggs, which develop into larvae that feed on a greater diversity of host species. These larvae may develop into nymphs whose capitula allow for more efficient and longer feeding times on soft-bodied hosts compared to non-vector species, leading to larger adult females with greater fecundity.

Our model identified 14 Ixodes tick species that showed ~ 80% probabilities of being undiscovered vectors of zoonotic disease on the basis of their trait similarity with known Ixodes vector species (Table 1). The majority of these species reside in Nearctic or Palearctic biomes, and all of them are habituated to forest or grassland habitats [19]. Some of the ticks are suspected in the primary literature as being likely disease vectors, but are not currently recognized by the public health community as zoonotic vectors per se. For example, one species, Ixodes acuminatus, is capable of transmitting Borrelia burgdorferi sensu lato, though it is not considered an important vector for human disease in nature, perhaps due to infrequent contact with humans [20]. The saliva of another species, Ixodes rubicundus, causes paralysis in sheep [21], but to our knowledge there is no record of this species transmitting zoonotic infections to humans. Given that many of the 14 predicted Ixodes vectors are understudied and some of them are already suspected to have contact with, and potential health consequences for, humans (Table 1), our study offers new utility for identifying tick species whose intrinsic traits suggest they should be targets for enhanced zoonotic surveillance. In particular, the risk of future tick-borne zoonoses should be monitored in Nearctic and Palearctic regions, which are currently experiencing disproportionately rapid warming [22], and in regions experiencing large-scale ecological changes that are associated with increasing human population densities and declining biodiversity [23, 24]. In addition to informing the biological basis by which some Ixodes ticks vector zoonotic pathogens, our study underscores the crucial importance of basic research on ticks and other arthropod vectors, since understanding the biological underpinnings of transmission will rely fundamentally on understanding intrinsic characteristics distinguishing vector from non-vector species of Ixodes tick species.


This study revealed a number of intrinsic biological traits that are highly predictive of zoonotic vector status in the Ixodes ticks, and suggest hypotheses about anatomical and biological mechanisms underlying vectorial capacity across Ixodes species that now require empirical validation in future work. In general, these distinguishing traits are related to the diversity of hosts species infested by ticks, and suggests that vectorial capacity could be maximized by a suite of features enabling some tick species to feed more efficiently on soft bodied hosts at particular life stages compared to non-vector species. These analyses also reveal several Ixodes species that are currently not recognized as vectors of zoonotic disease, but whose biological profile suggests they should be targets of future surveillance.


  1. Durden LA. Taxonomy, host associations, life cycles and vectorial importance of ticks parasitizing small mammals. In: Morand S, Krasnov BR, Poulin R, editors. Micromammals and macroparasites. Tokyo: Springer; 2006. p. 91–102. Accessed 8 June 2016.

  2. GIDEON. Global infectious diseases and epidemiology online network; 1994. Accessed 10 Feb 2018.

  3. Levi T, Keesing F, Oggenfuss K, Ostfeld RS. Accelerated phenology of blacklegged ticks under climate warming. Phil Trans R Soc B. 2015;370(1665):20130556.

    Article  PubMed  PubMed Central  Google Scholar 

  4. Elith J, Leathwick JR, Hastie T. A working guide to boosted regression trees. J Anim Ecol. 2008;77:802–13.

    Article  CAS  PubMed  Google Scholar 

  5. Ridgeway G. gbm: generalized boosted regression models; 2013. Accessed 15 Aug 2013.

  6. Hastie T, Tibshirani R, Friedman JH. The elements of statistical learning: data mining, inference, and prediction. 2nd ed. New York: Springer; 2009 (Springer Series in Statistics).

    Book  Google Scholar 

  7. Berger SA. GIDEON: a comprehensive Web-based resource for geographic medicine. Int J Health Geogr. 2005;4:10.

    Article  PubMed  PubMed Central  Google Scholar 

  8. Han BA, Schmidt JP, Bowden SE, Drake JM. Rodent reservoirs of future zoonotic diseases. Proc Natl Acad Sci. 2015;112(22):7039–44.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  9. Han BA, Schmidt JP, Alexander LW, Bowden SE, Hayman DTS, Drake JM. Undiscovered bat hosts of filoviruses. PLOS Negl Trop Dis. 2016;10(7):e0004815.

    Article  PubMed  PubMed Central  Google Scholar 

  10. R Core Team. R: a language and environment for statistical computing. Vienna: R Foundation for Statistical Computing; 2014. Accessed 10 Feb 2018.

  11. Davies TJ, Pedersen AB. Phylogeny and geography predict pathogen community similarity in wild primates and humans. Proc R Soc B Biol Sci. 2008;275(1643):1695–701.

    Article  Google Scholar 

  12. Woolhouse MEJ, Gowtage-Sequeria S. Host range and emerging and reemerging pathogens. Emerg Infect Dis. 2005;11(12):1842–7.

    Article  PubMed  PubMed Central  Google Scholar 

  13. Matuschka FR, Fischer P, Heiler M, Blümcke S, Spielman A. Stage-associated risk of transmission of the Lyme disease spirochete by European Ixodes ticks. Parasitol Res. 1992;78(8):695–8.

    Article  CAS  PubMed  Google Scholar 

  14. Sonenshine DE, Roe RM. Biology of Ticks. Vol. 1. OUP USA; 2013. 504 p.

  15. Richter D, Matuschka F-R, Spielman A, Mahadevan L. How ticks get under your skin: insertion mechanics of the feeding apparatus of Ixodes ricinus ticks. Proc R Soc B Biol Sci. 2013;280(1773):20131758.

    Article  Google Scholar 

  16. Reuben Kaufman W. Ticks: physiological aspects with implications for pathogen transmission. Ticks TickBorne Dis. 2010;1(1):11–22.

    Article  Google Scholar 

  17. Shine R. The evolution of large body size in females: a critique of Darwin’s “fecundity advantage” model. Am Nat. 1988;131(1):124–31.

    Article  Google Scholar 

  18. Oliver JH Jr. Biology and systematics of ticks (Acari: Ixodida). Annu Rev Ecol Syst. 1989;20:397–430.

    Article  Google Scholar 

  19. Guglielmone AA, Robbins RG, Apanaskevich DA, Petney TN, Estrada-Peña A, Horak IG. The hard ticks of the world. Dordrecht: Springer; 2014. Accessed 8 June 2016.

  20. Doby JM, Bigaignon G, Launay H, Costil C, Lorvellec O. Presence of Borrelia burgdorferi, agent of tick spirochaetosis, in Ixodes (Exopalpiger) trianguliceps Birula, 1895 and Ixodes (Ixodes) acuminatus Neumann, 1901 (Acari: Ixodidae) and in Ctenophthalmus baeticus arvernus Jordan, 1931 and Megabothris turbidus (Rothschild, 1909) (Insecta: Siphonaptera), ectoparasites of small mammals in forests in western France. Bull Société Fr Parasitol. 1990;8(2):311–22.

    Google Scholar 

  21. Fourie LJ, Petney TN, Horak IG, De Jager C. Seasonal incidence of Karoo paralysis in relation to the infestation density of female Ixodes rubicundus. Vet Parasitol. 1989;33(3–4):319–28.

    Article  CAS  PubMed  Google Scholar 

  22. Sezzere MC, Barry RG. Processes and impacts of arctic amplification: a research synthesis. Global Planet Change. 2011;17:85–96.

    Article  Google Scholar 

  23. Civitello DJ, et al. Biodiversity inhibits parasites: broad evidence for the dilution effect. Proc Natl Acad Sci USA. 2015;112:8667–71.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  24. Keesing F, et al. Impacts of biodiversity on the emergence and transmission of infectious diseases. Nature. 2010;468:647–52.

    Article  CAS  PubMed  Google Scholar 

  25. Horak IG, Fourie LJ, Heyne H, Walker JB, Needham GR. Ixodid ticks feeding on humans in South Africa: with notes on preferred hosts, geographic distribution, seasonal occurrence and transmission of pathogens. Exp Appl Acarol. 2002;27:113–36.

    Article  CAS  PubMed  Google Scholar 

  26. Hillyard P. Ticks of north-west Europe—keys and notes for identification of species. Synopses of the British fauna no. 52. Field Studies Council, Shrewsbury, United Kingdom; 1996.

  27. Piksa K, Nowak-Chmura M, Siuda K. First case of human infestation by the tick Ixodes vespertilionis (Acari: Ixodidae). Int J Acarol. 2013;39:1–2.

    Article  Google Scholar 

  28. Salkeld DJ, Eisen RJ, Antolin MF, Stapp P, Eisen L. Host usage and seasonal activity patterns of Ixodes kingi and I. sculptus (Acari: Ixodidae) nymphs in a Colorado prairie landscape, with a summary of published North American host records for all life stages. J Vector Ecol. 2006;31:168–80.

    Article  PubMed  Google Scholar 

  29. Fedorov VG. Ixodoidea ticks on men in Western Siberia. Med Parazitol. 1968;37:615–6.

    CAS  Google Scholar 

  30. Merten HA, Durden LA. A state-by-state survey of ticks recorded from humans in the United States. J Vector Ecol. 2000;25:102–13.

    CAS  PubMed  Google Scholar 

  31. Filippova NA. Ixodid ticks (Ixodinae). Fauna USSR New Ser. 4 (4). Nauka, Moscow, Leningrad; 1977.

  32. Emchuk EM. Certain biological peculiarities of Ixodes redikorzevi Olen; 1968.

  33. Bursali A, Keskin A, Tekin S. A review of the ticks (Acari: Ixodida) of Turkey: species diversity, hosts and geographical distribution. Exp Appl Acarol. 2012;57:91–104.

    Article  PubMed  Google Scholar 

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Authors’ contributions

LHY and BH conceived the idea, LHY collected and pre-processed data, LHY and BH carried out the analysis, LHY and BH drafted the manuscript. Both authors read and approved the final manuscript.


Authors thank R. Ostfeld and P. Feinberg for comments on earlier versions of this work; A. Schuler, and M. Gillespie for assistance with reference collation and editing; A. Matts, J. Maloney, K. Chen for internship support for LHY at Spackenkill High School.

Competing interests

The authors declare that they have no competing interests.

Availability of data and materials

The data sets supporting the results of this article are available in the Figshare repository: Traits of ticks species from the genus Ixodes (;; Definition of traits of ticks from genus Ixodes (;; Zoonotic vector status of ticks from the genus Ixodes (;

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Correspondence to Barbara A. Han.

Additional files

Additional file 1: Tables S1–S3.

Tables reporting the zoonotic vector status of all 244 Ixodes ticks; A list of all variables include in the boosted regression analysis; and model parameters and performance metrics for boosted regression analyses on vector status and citation count.

Additional file 2: Figures S1, S2.

Figure S1 shows the relationship between citation count and the probability assigned by a boosted regression model of being a zoonotic vector. Figure S2 shows the relationship between diversity of infested hosts and tarsus I length for Ixodes tick species at larval, nymphal, and male and female adult stages.

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Yang, L.H., Han, B.A. Data-driven predictions and novel hypotheses about zoonotic tick vectors from the genus Ixodes. BMC Ecol 18, 7 (2018).

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  • Host range
  • Machine learning
  • Surveillance
  • Transmission
  • Vectorial capacity
  • Hypostome
  • Capitulum
  • Ixodes