Next Article in Journal
Genotypic Characterization of Carbapenem-Resistant Klebsiella pneumoniae Isolated from an Egyptian University Hospital
Previous Article in Journal
In Vivo Role of Two-Component Regulatory Systems in Models of Urinary Tract Infections
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Editorial

Tick and Tick-Borne Diseases: New Problems Providing New Possible Solutions

by
Olivier Andre Sparagano
Department of Infectious Diseases and Public Health, Jockey Club College of Veterinary Medicine and Life Sciences, City University of Hong Kong, Hong Kong SAR, China
Pathogens 2023, 12(1), 120; https://doi.org/10.3390/pathogens12010120
Submission received: 4 January 2023 / Accepted: 9 January 2023 / Published: 11 January 2023
Ticks and tick-borne diseases are responsible for enormous losses in animal and human life, which do not seem to become better as new data show surprising connections. For instance, tick bites (from Ixodes ricinus) were linked to new red meat allergies in patients ([1] such patients with IgE against galactose-α-1,3-galactose (known as α-Gal) showed severe allergic reactions after consumption of red meat).
It is also not completely clear how pathogens from different infection sources work together but a recent paper on patients with high hospitalization rates showed that such patients also had a high prevalence of antibodies against Borrelia, a possible coincidence of disabling or confusing the patient’s immune system to allow other pathogens to proliferate more easily [2], or unclear synergies between infectious agents? This could be a similar scenario between some HIV patients showing the highest prevalence of tick-borne pathogens [3]. These multiple, unrelated and complex infections are putting pressure on medical practitioners and veterinarians to successfully treat them, while co-infections between tick-borne pathogens, possibly transmitted by the same tick species, are creating a public-health problem to tackle [4,5,6].
Furthermore, ticks on their own are developing resistance, making it more difficult to prevent their proliferation or treat their infestations. Tick resistance to traditional treatments is not uncommon [7,8], creating a conundrum for practitioners but also opening new opportunities using plant-derived products [9].
Tick-borne pathogens are found in many different host species, from wildlife animals [10] to animals in zoos [11], some carrying zoonotic pathogens, putting at risk the workers looking after such animals.
It is important to identify the key risk factors and practices that can prevent or influence tick development. First, we need to find a consensus on taxonomy keys, where there has not always been full agreement between national taxonomic books [12]. Second, understanding the risk factors and practices (Knowledge, Attitude and Practice) from animal owners would ensure clarity in risk factors to be dealt with as a priority [13,14,15].
With such a development and ticks colonizing new areas, it is clear than new tick-surveillance systems are needed to raise the alarm as soon as they colonize a new bio-ecosystem. Surveillance of ticks and tick-borne diseases has been well documented [16,17] and modelling can help in such an empiric approach [18].
Climate change, a buzzword used perhaps too often and not appropriately all the time, seems to impact tick adaptation [19,20,21].
Not all is lost, as further genome sequencing allows us to better understand how to develop new drugs or new tick vaccines, including a lot of research now on the tick gut microbiome to also evaluate the potential of indirectly knocking down ticks through their own microbiome.
The tick vaccine did not start well but a lot was learnt from the first Boophilus-microplus (now known as Rhipicephalus (Boophilus) microplus)-related vaccines and new possibilities are emerging, meaning a tick vaccine could be available in the next few years [22,23] and an understanding of the tick immune system and tick immunobiology [24] is allowing us to prepare counter attacks.
The host–pathogen relationship could also provide new treatments if we also add the tick saliva microbiome [25] and tick gut microbiome to the equation [26,27].
A One-Health approach has to be kept in mind to avoid developing new treatment, which could work against ticks but be detrimental to animals, humans and their environment [28,29], while other parameters, such as biotic factors, should also be considered in the complex fight against ticks and the pathogens they can carry and transmit [30,31,32].
In conclusion, and hopefully as a way forward, we need to develop consensus diagnostics and methodologies [33], sharing data, not only molecular diagnostics, standardization [34], informative reviews [35] and international collaborations [36].
More challenges and successes are on the way, which we, as a united scientific community, must be ready for.

Conflicts of Interest

The author declares no conflict of interest.

References

  1. Hamsten, C.; Starkhammar, M.; Tran, T.A.T.; Johansson, M.; Bengtsson, U.; Ahlén, G.; Sällberg, M.; Gronlund, H.; van Hage, M. Identification of galactose-a-1,3-galactose in the gastrointestinal tract of the tick Ixodes ricinus; possible relationship with red meat allergy. Allergy 2013, 68, 549–552. [Google Scholar] [CrossRef]
  2. Szewczyk-Dąbrowska, A.; Budziar, W.; Harhala, M.; Baniecki, K.; Pikies, A.; Jędruchniewicz, N.; Kaźmierczak, Z.; Gembara, K.; Klimek, T.; Witkiewicz, W.; et al. Correlation between COVID-19 severity and previous exposure of patients to Borrelia spp. Sci. Rep. 2022, 12, 15944. [Google Scholar] [CrossRef] [PubMed]
  3. Šimeková, K.; Soják, Ľ.; Víchová, B.; Balogová, L.; Jarošová, J.; Antolová, D. Parasitic and Vector-Borne Infections in HIV-Positive Patients in Slovakia—Evidence of an Unexpectedly High Occurrence of Anaplasma phagocytophilum. Pathogens 2021, 10, 1557. [Google Scholar] [CrossRef] [PubMed]
  4. Carvalho Mattos Ferreira, G.; Andrighetto Canozzi, M.E.; Peripolli, V.; de Paula Moura, G.; Sánchez, J.; Nogueira Martins, C.E. Prevalence of bovine Babesia spp., Anaplasma marginale, and their co-infections in Latin America: Systematic review-meta-analysis. Ticks Tick-Borne Dis. 2022, 12, 101967. [Google Scholar] [CrossRef] [PubMed]
  5. Silaghi, C.; Fröhlich, J.; Reindl, H.; Hamel, D.; Rehbein, S. Anaplasma phagocytophilum and Babesia Species of Sympatric Roe Deer (Capreolus capreolus), Fallow Deer (Dama dama), Sika Deer (Cervus nippon) and Red Deer (Cervus elaphus) in Germany. Pathogens 2020, 9, 968. [Google Scholar] [CrossRef]
  6. Kuibagarov, M.; Makhamed, R.; Zhylkibayev, A.; Erdikulov, M.; Abdrakhmanov, S.; Kozhabayev, M.; Akhmetollayev, I.; Mukanov, K.; Ryskeldina, A.; Ramankulov, Y.; et al. Theileria and Babesia infection in cattle—First molecular survey in Kazakhstan. Ticks Tick-Borne Dis. 2023, 14, 102078. [Google Scholar] [CrossRef]
  7. Gupta, S.; Kumar, S. Detection of Deltamethrin Resistance in Cattle Tick, Rhipicephalus microplus Collected in Western Haryana State of India. J. Arthropod. Borne Dis. 2022, 15, 389–396. [Google Scholar] [CrossRef]
  8. Mkize, N.; Maiwashe, A.; Dzama, K.; Dube, B.; Mapholi, N. Suitability of GWAS as a Tool to Discover SNPs Associated with Tick Resistance in Cattle: A Review. Pathogens 2021, 10, 1604. [Google Scholar] [CrossRef]
  9. Torrents, J.; Morel, N.; Rossner, M.V.; Martínez, N.C.; Nava, S. A comparison of two in vitro bioassays to detect resistance of the cattle tick Rhipicephalus microplus to fipronil. Vet. Parasitol. 2023, 37, 100816. [Google Scholar] [CrossRef]
  10. Chao, L.-L.; Chen, T.-H.; Shih, C.-M. First zootiological survey of Amblyomma geoemydae ticks in northern Taiwan. Exp. Appl. Acarol. 2022, 88, 349. [Google Scholar] [CrossRef]
  11. Pittermannová, P.; Žákovská, A.; Váňa, P.; Marková, J.; Treml, F.; Černíková, L.; Budíková, M.; Bártová, E. Wild Small Mammals and Ticks in Zoos—Reservoir of Agents with Zoonotic Potential? Pathogens 2021, 10, 777. [Google Scholar] [CrossRef] [PubMed]
  12. Sparagano, O.A.E.; Carelli, G.; Ceci, L.; Shkap, V.; Molad, T.; Vitale, F.; Loria, G.R.; Reale, S.; Caracappa, S.; Bouattour, A.; et al. Pan Mediterranean Comparison for the molecular detection of Theileria annulata. Ann. N. Y. Acad. Sci. 2002, 969, 73–77. [Google Scholar] [CrossRef] [PubMed]
  13. Asif, M.; Ben Said, M.; Vinueza, R.L.; Leon, R.; Ahmad, N.; Parveen, A.; Khan, A.; Ejaz, A.; Ali, M.; Khan, A.U.; et al. Seasonal Investigation of Anaplasma marginale Infection in Pakistani Cattle Reveals Hematological and Biochemical Changes, Multiple Associated Risk Factors and msp5 Gene Conservation. Pathogens 2022, 11, 1261. [Google Scholar] [CrossRef]
  14. Hussain, S.; Hussain, A.; Ho, J.; Li, J.; George, D.; Rehman, A.; Zeb, J.; Sparagano, O. An Epidemiological survey regarding ticks and tick-borne diseases among livestock owners in Punjab, Pakistan: A One Health Context. Pathogens 2021, 10, 361. [Google Scholar] [CrossRef] [PubMed]
  15. Ribeiro, R.; Eze, J.I.; Gilbert, L.; Macrae, A.; Duncan, A.; Baughan, J.; Gunn, G.; Auty, H. Linking human tick bite risk with tick abundance in the environment: A novel approach to quantify tick bite risk using orienteers in Scotland. Ticks Tick-Borne Dis. 2023, 14, 102109. [Google Scholar] [CrossRef]
  16. Guillot, C.; Bouchard, C.; Buhler, K.; Dumas, A.; Milord, F.; Ripoche, M.; Pelletier, R.; Leighton, P.A. Sentinel Surveillance Contributes to Tracking Lyme Disease Spatiotemporal Risk Trends in Southern Quebec, Canada. Pathogens 2022, 11, 531. [Google Scholar] [CrossRef]
  17. Pasternak, A.R.; Palli, S.R. County-level surveillance for the lone star tick, Amblyomma americanum, and its associated pathogen, Ehrlichia chaffeensis, in Kentucky. Ticks Tick-Borne Dis. 2023, 14, 102072. [Google Scholar] [CrossRef]
  18. Zannou, O.M.; Ouedraogo, A.S.; Biguezoton, A.S.; Abatih, E.; Coral-Almeida, M.; Farougou, S.; Yao, K.P.; Lempereur, L.; Saegerman, C. Models for Studying the Distribution of Ticks and Tick-Borne Diseases in Animals: A Systematic Review and a Meta-Analysis with a Focus on Africa. Pathogens 2021, 10, 893. [Google Scholar] [CrossRef]
  19. Chávez-Larrea, M.A.; Cholota-Iza, C.; Medina-Naranjo, V.; Yugcha-Díaz, M.; Ron-Román, J.; Martin-Solano, S.; Gómez-Mendoza, G.; Saegerman, C.; Reyna-Bello, A. Detection of Babesia spp. in High Altitude Cattle in Ecuador, Possible Evidence of the Adaptation of Vectors and Diseases to New Climatic Conditions. Pathogens 2021, 10, 1593. [Google Scholar] [CrossRef]
  20. Fernández-Ruiz, N.; Estrada-Peña, A. Towards New Horizons: Climate Trends in Europe Increase the Environmental Suitability for Permanent Populations of Hyalomma marginatum (Ixodidae). Pathogens 2021, 10, 95. [Google Scholar] [CrossRef]
  21. Gray, J.S.; Ogden, N.H. Ticks, Human Babesiosis and Climate Change. Pathogens 2021, 10, 1430. [Google Scholar] [CrossRef] [PubMed]
  22. Arocho Rosario, C.M.; Miller, R.J.; Klafke, G.M.; Coates, C.; Grant, W.E.; Samenuk, G.; Yeater, K.; Tidwell, J.; Bach, S.; Pérez de León, A.A.; et al. Interaction between anti-tick vaccine and a macrocyclic lactone improves acaricidal efficacy against Rhipicephalus (Boophilus) microplus (Canestrini) (Acari: Ixodidae) in experimentally infested cattle. Vaccine 2022, 40, 6795–6801. [Google Scholar] [CrossRef] [PubMed]
  23. Harrington, D.; Canales, M.; de la Fuente, J.; Robinson, K.; Guy, J.; Sparagano, O. Immunisation with recombinant proteins subolesin and Bm86 for the control of Dermanyssus gallinae in poultry. Vaccine 2009, 27, 4056–4063. [Google Scholar] [CrossRef] [PubMed]
  24. Aguilar-Díaz, H.; Quiroz-Castañeda, R.E.; Salazar-Morales, K.; Cossío-Bayúgar, R.; Miranda-Miranda, E. Tick Immunobiology and Extracellular Traps: An Integrative Vision to Control of Vectors. Pathogens 2021, 10, 1511. [Google Scholar] [CrossRef]
  25. Jacobs, M.B.; Grasperge, B.J.; Doyle-Meyers, L.A.; Embers, M.E. Borrelia burgdorferi Migration Assays for Evaluation of Chemoattractants in Tick Saliva. Pathogens 2022, 11, 530. [Google Scholar] [CrossRef] [PubMed]
  26. Hussain, S.; Perveen, N.; Hussain, A.; Song, B.; Aziz, M.U.; Zeb, J.; Li, J.; George, D.; Cabezas-Cruz, A.; Sparagano, O.A. The symbiotic continuum within ticks: Opportunities for disease control? Front. Microbiol. 2022, 13, 854803. [Google Scholar] [CrossRef] [PubMed]
  27. Benelli, G. Pathogens Manipulating Tick Behavior—Through a Glass, Darkly. Pathogens 2020, 9, 664. [Google Scholar] [CrossRef]
  28. Dantas-Torres, F.; Chomel, B.B.; Otranto, D. Ticks and tick-borne diseases: A One Health perspective. Trends Parasitol. 2012, 28, 437–446. [Google Scholar] [CrossRef]
  29. Charles, R.A.; Bermúdez, S.; Banović, P.; Alvarez, D.O.; Díaz-Sánchez, A.A.; Corona-González, B.; Etter, E.M.C.; Rodríguez González, I.; Ghafar, A.; Jabbar, A.; et al. Ticks and Tick-Borne Diseases in Central America and the Caribbean: A One Health Perspective. Pathogens 2021, 10, 1273. [Google Scholar] [CrossRef]
  30. Chandra, S.; Šlapeta, J. Biotic Factors Influence Microbiota of Nymph Ticks from Vegetation in Sydney, Australia. Pathogens 2020, 9, 566. [Google Scholar] [CrossRef]
  31. Gillingham, E.L.; Medlock, J.M.; Macintyre, H.; Phalkey, R. Modelling the current and future temperature suitability of the UK for the vector Hyalomma marginatum (Acari: Ixodidae). Ticks Tick-Borne Dis. 2022, 14, 102112. [Google Scholar] [CrossRef]
  32. Estrada-Peña, A.; Cabezas-Cruz, A.; Obregón, D. Resistance of Tick Gut Microbiome to Anti-Tick Vaccines, Pathogen Infection and Antimicrobial Peptides. Pathogens 2020, 9, 309. [Google Scholar] [CrossRef] [PubMed]
  33. Estrada-Peña, A.; Cevidanes, A.; Sprong, H.; Millán, J. Pitfalls in Tick and Tick-Borne Pathogens Research, Some Recommendations and a Call for Data Sharing. Pathogens 2021, 10, 712. [Google Scholar] [CrossRef] [PubMed]
  34. Sparagano, O.; Foldvari, G.; Derdakova, M.; Kazimirova, M. New challenges posed by ticks and tick-borne diseases. Biologia 2022, 77, 1497–1501. [Google Scholar] [CrossRef]
  35. Ghafar, A.; Abbas, T.; Rehman, A.; Sandhu, Z.-U.-D.; Cabezas-Cruz, A.; Jabbar, A. Systematic Review of Ticks and Tick-Borne Pathogens of Small Ruminants in Pakistan. Pathogens 2020, 9, 937. [Google Scholar] [CrossRef]
  36. Esteve-Gasent, M.D.; Rodríguez-Vivas, R.I.; Medina, R.F.; Ellis, D.; Schwartz, A.; Cortés Garcia, B.; Hunt, C.; Tietjen, M.; Bonilla, D.; Thomas, D.; et al. Research on Integrated Management for Cattle Fever Ticks and Bovine Babesiosis in the United States and Mexico: Current Status and Opportunities for Binational Coordination. Pathogens 2020, 9, 871. [Google Scholar] [CrossRef]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Sparagano, O.A. Tick and Tick-Borne Diseases: New Problems Providing New Possible Solutions. Pathogens 2023, 12, 120. https://doi.org/10.3390/pathogens12010120

AMA Style

Sparagano OA. Tick and Tick-Borne Diseases: New Problems Providing New Possible Solutions. Pathogens. 2023; 12(1):120. https://doi.org/10.3390/pathogens12010120

Chicago/Turabian Style

Sparagano, Olivier Andre. 2023. "Tick and Tick-Borne Diseases: New Problems Providing New Possible Solutions" Pathogens 12, no. 1: 120. https://doi.org/10.3390/pathogens12010120

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop