Abstract
Vector-borne diseases transmitted by mosquitoes and ticks are on the rise. The effective and sustainable control of these arthropod vectors is a puzzling challenge for public health worldwide. In the present review, I attempted to provide a concise and updated overview of the current mosquito and tick research scenario. The wide array of control tools recently developed has been considered, with special reference to those approved by the World Health Organization Vector Control Advisory Group (WHO VCAG), as well as novel ones with an extremely promising potential to be exploited in vector control programs. Concerning mosquitoes, a major focus has been given on genetically modified vectors, eave tubes, attractive toxic sugar baits (ATSB) and biocontrol agents. Regarding ticks, the recent development of highly effective repellents and acaricides (including nanoformulated ones) as well as behavior-based control tools, has been highlighted. In the second part of the review, key research questions about biology and control of mosquitoes and ticks have been critically formulated. A timely research agenda outlining hot issues to be addressed in mosquito and tick research is provided. Overall, it is expected that the present review will contribute to boost research and applications on successful mosquito and tick control strategies, along with an improved knowledge of their biology and ecology.
Keywords: Acaricides, Dengue, Integrated Vector Management, Lyme disease, Malaria, Nanoparticles, Repellents, Zika virus
1. Introduction
The world is now subjected to rapid environmental changes, along with the fast, unintended spread of invasive pests and vectors through commercial and migration routes (Keirans and Durden, 2001, Schaffner et al., 2013, Medlock et al., 2015, Akiner et al., 2016, Kelehear et al., 2017). In this scenario, the effective and sustainable control of arthropod vectors is a puzzling challenge for public health worldwide (Benelli and Duggan, 2018, De Fuentes-Vicente et al., 2018, Fernandes et al., 2018a), with special reference to local communities in developing countries, which experience poor access to adequate diagnostics, prevention and treatment of infectious diseases (Bergquist et al., 2017, Molyneux et al., 2017).
Vector-borne diseases transmitted by mosquitoes and ticks are on the rise (Rosenberg et al., 2018). Despite decades of extensive research efforts, Culicidae still play a crucial role among vectors of medical and veterinary importance (Benelli, 2015, Saifi et al., 2016). The malaria burden is widely recognized for its importance in tropical and subtropical countries. In this context, with about forty Anopheles competent vectors (Fig. 1) (CDC, 2015), it leads to 6.8 million deaths averted globally since 2001, worsened by the fact that the recently released malaria vaccine only showed transient protection (Gosling and von Seidlein, 2016). In addition to this, malaria cases in European countries have been also registered, including fatal ones (Benelli et al., 2018a).
Fig. 1.
Several Anopheles species acting as malaria vectors: (a) Anopheles albimanus, (b) Anopheles arabiensis (c) Anopheles atroparvus, (d) Anopheles farauti, (e) Anopheles funestus, (f) Anopheles gambiae, (g) Anopheles merus, (h) Anopheles minimus, (i) Anopheles plumbeus, (l) Anopheles quadriannulatus, (m) Anopheles sinensis, and (n) Anopheles stephensi (photo credit: A. plumbeus: ECDC; A. stephensi: Dr. W. Collins; others: Dr. J. Gathany, CDC-PHIL).
Furthermore, dengue virus poses at risk 3900 million people in 128 countries (Bhatt et al., 2013, Al-Shami et al., 2014), and lymphatic filariasis is still ranked among the most important neglected tropical diseases (Jambulingam et al., 2016). At the same time – Zika virus outbreaks in the Americas and the Pacific are attracting high public health attention (Petersen et al., 2016, Yakob and Walker, 2016, Benelli and Romano, 2017), due to the arboviral connection with fetal microcephaly and neurological complications, particularly the Guillain–Barré syndrome (Oehler et al., 2014, Benelli and Mehlhorn, 2016). The spread of arboviral diseases is continuous and hard to deal with, as very recently showed by a case of Keystone virus isolated from a Florida teenager with rash and fever (Lednicky et al., 2018).
Ticks are fascinating organisms, which can transmit an extremely high number of infectious agents to humans, livestock, pets, and wildlife (Fig. 2) (Guglielmone et al., 2014, Pantchev et al., 2015, Diuk-Wasser et al., 2016, Banumathi et al., 2017, Boka et al., 2017). Besides the rise in the number of cases of Lyme disease, caused by genospecies of the Borrelia burgdorferi s.l. complex (CDC, 2017), important tick-borne diseases also include anaplasmosis, ehrlichiosis, Rocky Mountain spotted fever, Powassan virus, and babesiosis (Lani et al., 2014, Buckingham, 2015, Ostfeld and Brunner, 2015, Inci et al., 2016, Solano-Gallego et al., 2016, de la Fuente et al., 2017).
Fig. 2.
Ticks act as major vectors of medical and veterinary importance. Among soft ticks, is worthy of mention (a) Ornithodoros hermsi, vectoring a bacterial disease called tick-borne relapsing fever. Hard ticks play a major role as pathogen vectors, including – among others – (b) the Gulf Coast tick, Amblyomma maculatum (female here), (c) the cayenne tick, Amblyomma cajennense (male here), (d) Amblyomma triste (female here), (e) the Rocky Mountain wood tick, Dermacentor andersoni (female here), and (f) the blacklegged deer tick, Ixodes scapularis (engorged female here) (photo credit: courtesy of Dr. J. Gathany, CDC-PHIL, except for I. scapularis, Dr. G. Alpert).
In the present work, I attempted to provide a concise and update overview of the current mosquito and tick research scenario, reinforcing basic opinions of vector experts globally (Fernandes et al., 2018a). The wide array of control tools recently developed has been considered, with special reference to those approved by the WHO Vector Control Advisory Group (WHO VCAG), as well as novel ones with an extremely promising potential to be exploited in Integrated Vector Management (IVM), which suggests making use of the full range of vector control tools available, avoiding “vertical” management structures relying only on one form of vector control (Beier et al., 2008, Benelli and Beier, 2017). In the second part of the article, major research questions about biology and control of mosquitoes and ticks have been critically formulated. Therefore, a research agenda outlining hot issues to be addressed in mosquito and tick research is provided.
2. Control of mosquitoes and ticks – Towards an eco-friendly scenario?
To effectively manage mosquito populations, a rather wide number of control routes have been attempted, including classic applications of chemical pesticides (Strode et al., 2014) as well as microbial ones (e.g., toxins from Bacillus thuringiensis israelensis) (Melo et al., 2016, Alkenani, 2017), wide employ of long-lasting insecticidal nets (LLINs) (Tiono et al., 2015, Hamainza et al., 2016, Tan et al., 2016) and indoor residual spraying (IRS) (West et al., 2014, Paredes-Esquivel et al., 2016), where the latter strongly contributed to malaria decline in sub-Saharan Africa (Benelli and Beier, 2017).
Besides, the development of eco-friendly formulations of novel insecticides (Isman, 2015, Isman, 2017), covering also nanostructured materials (Benelli, 2016a, Benelli, 2016b, Mishra et al., 2018), is rapidly gaining ground, along with the employ of attractive toxic sugar baits (ATSB) (Muller et al., 2010, Beier et al., 2012, Junnila et al., 2015, Qualls et al., 2015, Fiorenzano et al., 2017) and eave tubes (Knols et al., 2016, Sternberg et al., 2016). Travel medicine dedicated a major emphasis to mosquito repellents (Lupi et al., 2013), even this option is of applied significance mostly for tourists visiting regions with endemic vector-borne diseases, but cannot be a long-term solution for local communities living in these regions.
Besides, while biological control agents experienced a slow gradual decline in their applications, linked to the earlier massive detection of non-target effects due to several biocontrol agents (e.g., the mosquitofish, Gambusia affinis Baird and Girard) (Lacey et al., 2015, Benelli et al., 2016a), biotechnological tools are currently considered of high interest. The latter includes genetically modified mosquitoes, Wolbachia-based approaches [successfully used against important Aedes vectors, such as the yellow fever mosquito, Aedes aegypti (L.)], the sterile insect technique (SIT) (Zhang et al., 2015, Bourtzis et al., 2016, Joubert et al., 2016, Wilke et al., 2018).
However, according to the WHO VCAG, there is an urgent need to validate the most promising ones through epidemiological evidences (Wilke et al., 2018). Besides, despite the fast-growing research on the so-called “green” mosquito larvicides (e.g., plant extracts, essential oils, bacterial and fungal metabolites), it is worthy to note that they are not recommended for mosquito control in rural areas (Benelli and Beier, 2017).
A comparable scenario applies well to other important arthropod vectors. The effective and timely management of ticks is crucial to prevent tick-borne diseases (Willadsen, 2006, Drexler et al., 2014, Benelli, 2016c, Dantas-Torres and Otranto, 2016). Decades of intensive research on tick biology and control have strongly contributed to stress the relevance of:
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Timely and reliable molecular identification of tick vectors (Lv et al., 2014a, Lv et al., 2014b, Zhang and Zhang, 2014) and their vertebrate hosts examining tick bloodmeals (Alcaide et al., 2009, Gariepy et al., 2012).
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Vaccine development (de la Fuente et al., 2007, de la Fuente and Contreras, 2015, Lew-Tabor and Valle, 2016).
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Genetic and genomic tools (Mapholi et al., 2014).
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Operations based on the IVM criteria lowering the interactions of ticks with livestock (Ghosh et al., 2006, Ghosh and Nagar, 2014.
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Tick chemoecology manipulation through pheromone-based tools (Sonenshine et al., 2002, Sonenshine, 2006).
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Plant-isolated repellents (Semmler et al., 2011, Benelli et al., 2016b), with a selected number of them now used in commercial formulations.
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Control programs based on the use of biocontrol agents (Samish and Rehacek, 1999, Gindin et al., 2002), including entomopathogenic fungi [e.g., Metarhizium anisopliae (Metchnikoff) Sorokin] (Webster et al., 2015).
However, despite the promising potential of the above-mentioned tools, the majority of tick control operations still rely to the use of synthetic acaricides (Dantas-Torres et al., 2012, Pfister and Armstrong, 2016, Brites-Neto et al., 2017). This leads to severe drawbacks (Estrada-Peña and Salman, 2013), with special reference to fast resistance development in targeted ticks (Abbas et al., 2014, Shyma et al., 2015, Vudriko et al., 2016), hazard risks for mammals (van Wieren et al., 2016), and livestock product contamination by acaricidal residues (Ghosh et al., 2006, Yavuz et al., 2017).
3. Major research questions on mosquitoes
Some of the most relevant research questions about mosquito biology and ecology focused on their impressive ability to adapt to new environments. This is the case, for instance, of the highly invasive species Aedes (Stegomyia) albopictus (Skuse), commonly known as the Asian tiger mosquito. This species has been able to spread and establish in northern Europe (Kraemer et al., 2015), due its huge ecological and physiological plasticity (Bonizzoni et al., 2013). In this framework, researchers can formulate various timely questions, including: which is the updated vectors status of mosquitoes widespread in Europe (Koch et al., 2016)? Besides, the same can apply to other areas worldwide. Also, a relevant research focus has been devoted to which mosquito species are endangering public health in Asian countries subjected to rapid urbanization (Li et al., 2014).
In addition to their well-established role as vectors of highly studied parasites and pathogens, we know relatively little about the potential role of mosquito vectors in spreading other, overlooked, infectious agents. As recently asked by several researchers, along with preliminary research evidences, a timely question is: what we really know about the potential carcinogenic action of some pathogens and parasites vectored by mosquitoes (Lehrer, 2010, Benelli et al., 2016c, Johansson and Ward, 2017, Ward and Benelli, 2017, Ward and Benelli, 2018)?
Some basic facets of mosquito behavioral ecology and biology still needs to be elucidated. For example, it is surprising that – despite our rather wide knowledge on mosquito kairomones – we know little about the volatile compounds mediating swarming and mate recognition (Pitts et al., 2014, Vaníčková et al., 2017).
Furthermore, concerning mosquito control, crucial issues to deal with are: which are the main drawbacks arising from the use of chemical pesticides (Desneux et al., 2007, Chanda et al., 2016, Naqqash et al., 2016, Chang et al., 2017)? How outbreaks of mosquito-borne diseases can be prevented by proper modelling (Cosner et al., 2009, Ajelli, 2017)? Does the latter gives valuable information for vector control operations? Do herbal and microbial products represent a challenging solution to develop novel mosquito repellents and insecticides of commercial interest (Soonwera and Phasomkusolsil, 2015, Pavela and Benelli, 2016a, Pavela and Benelli, 2016b)? Do long-lasting repellent- and insecticide-treated textiles have a promising potential in the fight against mosquitoes and other bloodsucking arthropods (Banks et al., 2014, Abdel-Ghaffar et al., 2015)? Do nanoparticles and nanoformulated pesticides have a real potential in the fight against mosquitoes (Benelli and Lukehart, 2017, Benelli, 2018a)? Which are their modes of action and fate in the aquatic environment (Benelli et al., 2018b,c)? Are they dangerous for human health (Foldbjerg et al., 2015, Benelli et al., 2017a)?
Last, but not least, it has been recently outlined that the management of mosquito vector populations can be achieved also considering the plant species complex characterizing the habitats where mosquitoes live. Indeed, adult mosquitoes can benefit from the large availability of some nectar-rich flowerings, and a significant number of them are invasive species that needs to be managed (Stone et al., 2018).
4. Major research questions on ticks
Notably, a number of research questions outlined for mosquito vectors apply well also on tick research (Fig. 3, Fig. 4). A first good one would be: which is the real vector competence of many overlooked and poorly studied tick species (Estrada-Peña et al., 2017)? This question is of relevance especially in poor and marginalized areas of the world, where people, livestock and pets have limited access to advanced diagnostic tools. This applies both to hard and soft ticks (Manzano-Román et al., 2012).
Fig. 3.
A research agenda for next future mosquito research: key questions to address about mosquito biology and ecology are given in dark grey, while crucial issues about control tool development and validation are given in light grey.
Fig. 4.
A research agenda for next future tick research: key questions to address about tick biology and ecology are given in dark grey, while main issues about control tool development and validation are given in light grey.
Furthermore, despite a wide number of researches available on tick and tick-borne disease ecology (Pfäffle et al., 2013), important facets of their behavior still need to be elucidated. For example, the behavioral asymmetries of ticks during questing and related success, have been investigated only in a species, the castor bean tick, Ixodes ricinus (L.) (Benelli et al., 2018c), where population-level lateralized questing has been detected.
From a control perspective, despite significant efforts to move tick control strategies towards IVM, including the One Health approach (Dantas-Torres et al., 2012, Eisen and Dolan, 2016, Benelli and Duggan, 2018), tick control is still too anchored to the massive use of chemical acaricides. The development of new products with more eco-friendly features [see Ghosh et al., 2015, Benelli et al., 2016b for recent reviews] is lowered by several technical problems, with special reference to the lack of uniform methods to test toxicity on ticks among research groups, as recently pointed out in a systematic review by Benelli and Pavela (2018) as well as by Adenubi et al. (2018). In this framework, can robotics help us to standardize tick testing protocols (Romano et al., 2018)? A preliminary reply has been recently provided by a study developing a mechatronic device that may be used to repeatedly test repellents in association with selected host-borne cues over time (Benelli et al., 2018c).
Concerning biological control tools, it has been stressed the timely importance of basic studies to understand the interactions of entomopathogenic fungi with the components of the livestock skin microenvironment, since this would help to identify suitable fungal strains, and develop improved formulations (Polar et al., 2008).
Above, we referred to herbal preparations that can be used as acaricides and repellents against ticks. Some of these uses have a long ethnobotanical history, with a confirmed efficacy both in medical and veterinary settings (George et al., 2014, Ellse and Wall, 2014, Adenubi et al., 2016, Pavela et al., 2016). However, a long-standing unresolved question in this research field is: do we really need to isolate pure compounds from plants (Tabari et al., 2017)? Or is better and eco-friendlier to avoid further synthesis processes and use the selected whole plant essential oil or extract? In the first case, this allows to skip problems linked with the chemical composition of essential oils and extracts, which is subjected to strong variations according to many biotic and abiotic factors (Heng et al., 2013). However, the first solution is often more expensive and did not permit to exploit the synergistic toxicity effects that occur among the phytochemicals present in complex mixtures (Pavela, 2015a, Pavela, 2015b, Benelli et al., 2017c, Benelli et al., 2017d).
Nanoparticles and close-related nanomaterials have been tested – besides mosquitoes – also against selected tick species, achieving really interesting results (Benelli et al., 2017b). However, also in this case, there are some imperative questions to face. First, do nanoparticles represent a hazardous material for non-target species? Are they suitable to be used to fight ticks infesting livestock and pets? In this framework, which are the possible ecotoxicology implications for large mammals and soil invertebrates? Similar questions are relevant also about the use of photosensitizers as acaricides (Khater et al., 2016).
5. Conclusive remarks and future challenges
Overall, all the questions outlined above urgently need a further replies and research efforts from both public health experts, epidemiologists, parasitologists, biologists, and entomologists, as also recently pointed out by Stone et al. (2018) about research on plant-mosquito interactions, and by Benelli et al., (2018b) concerning the One Health approach in parasitology and ecotoxicology.
As highlighted by Fernandes et al. (2018a), a number of novel tools with a promising potential in arthropod vector control science are being developed. However, more efficient health system infrastructures and entomological capacity are urgently required in endemic countries to ensure an effective management of vector populations.
A research agenda for next future mosquito research is provided in Fig. 3. It summarizes – among the questions raised in the paragraphs above – some crucial ones. Furthermore, research agenda for next future tick research is given in Fig. 4. To my eyes, the future of mosquito and tick research is largely dependent from the close cooperation between various disciplines, since most of the current control tools being developed and later assessed in the field for their real-world efficacy needs a huge mixture of competences and analytical tools from many research fields. This is the case of insecticidal and acaricidal nanomaterials, which requires cooperation from the fields of physics, phytochemistry, as well as vector biology, physiology, behavior and ecology (Benelli, 2018b, Benelli, 2018c). Large networks of scientists with various research expertise, from molecular genetics to population ecology, are also needed for monitoring of invasive species, their DNA barcoding (Zhang and Zhang, 2014, Lv et al., 2014a, Lv et al., 2014b, Murugan et al., 2016, Vadivalagan et al., 2017, Karthika et al., 2018), as well as the reliable evaluation of vector competence potential and molecular patterns of infection in different regions worldwide (Murdock et al., 2014, Vega-Rúa et al., 2014, de la Fuente et al., 2017, Bartholomay and Michel, 2018, Priya et al., 2017). New technology is needed for pathogen detection in bloodsucking arthropods. In this framework, Fernandes et al., (2018b) recently developed a rapid noninvasive detection tool to identify Zika virus in Ae. aegypti mosquitoes, relying to near-infrared spectroscopy.
In conclusion, I am aware that this review cannot fully reflect the high diversity of the ideas and new insights rapidly growing in the field of mosquito and tick research. Furthermore, I hope that it will contribute to boost research and applications on successful mosquito and tick control strategies, along with an improved knowledge about the impact of mosquito and tick biology and ecology, since the latter is limited, but still crucial to ensure proper success of vector control programs in an IVM perspective.
Acknowledgments
Acknowledgements
Four anonymous reviewers kindly improved an earlier version of this Review.
Conflict of interest
The Author declares no competing interests.
Footnotes
Peer review under responsibility of King Saud University.
References
- Abbas R.Z., Zaman M.A., Colwell D.D., Gilleard J., Iqbal Z. Acaricide resistance in cattle ticks and approaches to its management: the state of play. Vet. Parasitol. 2014;203(1):6–20. doi: 10.1016/j.vetpar.2014.03.006. [DOI] [PubMed] [Google Scholar]
- Abdel-Ghaffar F., Al-Quraishy S., Mehlhorn H. Length of tick repellency depends on formulation of the repellent compound (Icaridin = Saltidin®): tests on Ixodes persulcatus and Ixodes ricinus placed on hands and clothes. Parasitol. Res. 2015;114:3041–3045. doi: 10.1007/s00436-015-4506-z. [DOI] [PubMed] [Google Scholar]
- Adenubi O.T., Fasina F.O., McGaw L.J., Eloff J.N., Naidoo V. Plant extracts to control ticks of veterinary and medical importance: A review. S. Afr. J. Bot. 2016;105:178–193. [Google Scholar]
- Adenubi O.T., McGaw L.J., Eloff J.N., Naidoo V. In vitro bioassays used in evaluating plant extracts for tick repellent and acaricidal properties: a critical review. Vet. Parasitol. 2018;254:160–171. doi: 10.1016/j.vetpar.2018.03.008. [DOI] [PubMed] [Google Scholar]
- Ajelli M. Modeling mosquito-borne diseases in complex urban environments. Acta Trop. 2017;176:332–334. doi: 10.1016/j.actatropica.2017.08.026. [DOI] [PubMed] [Google Scholar]
- Akiner M.M., Demirci B., Babuadze G., Robert V., Schaffner F. Spread of the invasive mosquitoes Aedes aegypti and Aedes albopictus in the Black Sea region increases risk of Chikungunya, Dengue, and Zika outbreaks in Europe. PLoS Negl.Trop. Dis. 2016;10(4) doi: 10.1371/journal.pntd.0004664. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Al-Shami S.A., Mahyoub J.A., Hatabbi M., Ahmad A.H., Rawi C.S.M. An update on the incidence of dengue gaining strength in Saudi Arabia and current control approaches for its vector mosquito. Parasites Vectors. 2014;7(1):258. doi: 10.1186/1756-3305-7-258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Alcaide M., Rico C., Ruiz S., Soriguer R., Muñoz J., Figuerola J. Disentangling vector-borne transmission networks: a universal DNA barcoding method to identify vertebrate hosts from arthropod bloodmeals. PLoS One. 2009;4(9) doi: 10.1371/journal.pone.0007092. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Alkenani N.A. Influence of the mixtures composed of slow–release insecticide formulations against Aedes aegypti mosquito larvae reared in pond water. Saudi J. Biol. Sci. 2017;24(6):1181–1185. doi: 10.1016/j.sjbs.2017.02.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Banks S.D., Murray N., Wilder-Smith A., Logan J.G. Insecticide-treated clothes for the control of vector-borne diseases: a review on effectiveness and safety. Med. Vet. Entomol. 2014;28(S1):14–25. doi: 10.1111/mve.12068. [DOI] [PubMed] [Google Scholar]
- Banumathi B., Vaseeharan B., Rajasekar P., Prabhu N.M., Ramasamy P., Murugan K., Canale A., Benelli G. Exploitation of chemical, herbal and nanoformulated acaricides to control the cattle tick, Rhipicephalus (Boophilus) microplus–a review. Vet. Parasitol. 2017;244:102–110. doi: 10.1016/j.vetpar.2017.07.021. [DOI] [PubMed] [Google Scholar]
- Bartholomay L.C., Michel K. Mosquito Immunobiology: The Intersection of Vector Health and Vector Competence. Annu. Rev. Entomol. 2018;63(1):145–167. doi: 10.1146/annurev-ento-010715-023530. [DOI] [PubMed] [Google Scholar]
- Beier J.C., Keating J., Githure J.I., Macdonald M.B., Impoinvil D.E., Novak R.J. Integrated vector management for malaria control. Malar. J. 2008;7:54. doi: 10.1186/1475-2875-7-S1-S4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Beier J.C., Müller G.C., Gu W., Arheart K.L., Schlein Y. Attractive toxic sugar bait (ATSB) methods decimate populations of Anopheles malaria vectors in arid environments regardless of the local availability of favoured sugar-source blossoms. Malar. J. 2012;11:31. doi: 10.1186/1475-2875-11-31. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benelli G. Research in mosquito control: current challenges for a brighter future. Parasitol. Res. 2015;114:2801–2805. doi: 10.1007/s00436-015-4586-9. [DOI] [PubMed] [Google Scholar]
- Benelli G. Plant-mediated biosynthesis of nanoparticles as an emerging tool against mosquitoes of medical and veterinary importance: a review. Parasitol. Res. 2016;115:23–34. doi: 10.1007/s00436-015-4800-9. [DOI] [PubMed] [Google Scholar]
- Benelli G. Green synthesized nanoparticles in the fight against mosquito-borne diseases and cancer—a brief review. Enzyme Microb. Technol. 2016;95:58–68. doi: 10.1016/j.enzmictec.2016.08.022. [DOI] [PubMed] [Google Scholar]
- Benelli G. Tools to fight ticks: A never-ending story? News from the front of green acaricides and photosensitizers. Asian Pacific J. Trop. Dis. 2016;6(8):656–659. [Google Scholar]
- Benelli G. Gold nanoparticles – against parasites and insect vectors. Acta Trop. 2018;178:73–80. doi: 10.1016/j.actatropica.2017.10.021. [DOI] [PubMed] [Google Scholar]
- Benelli G. Mode of action of nanoparticles against insects. Environ. Sci. Pollut. Res. 2018;25:12329–12341. doi: 10.1007/s11356-018-1850-4. [DOI] [PubMed] [Google Scholar]
- Benelli G. Plant-borne compounds and nanoparticles: challenges for medicine, parasitology and entomology. Environ. Sci. Pollut. Res. 2018;25:10149–10150. doi: 10.1007/s11356-017-9960-y. [DOI] [PubMed] [Google Scholar]
- Benelli G., Mehlhorn H. Declining malaria, rising dengue and Zika virus: insights for mosquito vector control. Parasitol. Res. 2016;115:1747–1754. doi: 10.1007/s00436-016-4971-z. [DOI] [PubMed] [Google Scholar]
- Benelli G., Beier J. Current vector control challenges in the fight against malaria. Acta Trop. 2017;174:91–96. doi: 10.1016/j.actatropica.2017.06.028. [DOI] [PubMed] [Google Scholar]
- Benelli G., Romano D. Mosquito vectors of Zika virus. Entomol. Gener. 2017;36:309–318. [Google Scholar]
- Benelli G., Lukehart C.M. Special Issue: Applications of green-synthesized nanoparticles in pharmacology, parasitology and entomology. J. Cluster Sci. 2017;28:1–2. [Google Scholar]
- Benelli G., Pavela R. Repellence of essential oils and selected compounds against ticks – a systematic review. Acta Trop. 2018;179:47–54. doi: 10.1016/j.actatropica.2017.12.025. [DOI] [PubMed] [Google Scholar]
- Benelli G., Duggan M.F. Management of arthropod vector data – Social and ecological dynamics facing the One Health perspective. Acta Trop. 2018;182:80–91. doi: 10.1016/j.actatropica.2018.02.015. [DOI] [PubMed] [Google Scholar]
- Benelli G., Jeffries C.L., Walker T. Biological control of mosquito vectors: past, present and future. Insects. 2016;7:52. doi: 10.3390/insects7040052. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Benelli G., Pavela R., Canale A., Mehlhorn H. Tick repellents and acaricides of botanical origin: a green roadmap to control tick-borne diseases? Parasitol. Res. 2016;115(7):2545–2560. doi: 10.1007/s00436-016-5095-1. [DOI] [PubMed] [Google Scholar]
- Benelli G., Lo Iacono A., Canale A., Mehlhorn H. Mosquito vectors and the spread of cancer: an overlooked connection? Parasitol. Res. 2016;115(6):2131–2137. doi: 10.1007/s00436-016-5037-y. [DOI] [PubMed] [Google Scholar]
- Benelli G., Pavela R., Maggi F., Petrelli R., Nicoletti M. Commentary: making green pesticides greener? The potential of plant products for nanosynthesis and pest control. J. Cluster Sci. 2017;28(1):3–10. [Google Scholar]
- Benelli G., Maggi F., Romano D., Stefanini C., Vaseeharan B., Kumar S. Nanoparticles as effective acaricides against ticks—a review. Ticks Tick-borne Dis. 2017;8(6):821–826. doi: 10.1016/j.ttbdis.2017.08.004. [DOI] [PubMed] [Google Scholar]
- Benelli G., Pavela R., Iannarelli R., Petrelli R., Cappellacci L., Cianfaglione K. Synergized mixtures of Apiaceae essential oils and related plant-borne compounds: larvicidal effectiveness on the filariasis vector Culex quinquefasciatus Say. Ind. Crops Prod. 2017;96:186–195. [Google Scholar]
- Benelli G., Pavela R., Canale A., Cianfaglione K., Ciaschetti G., Conti F. Acute larvicidal toxicity of five essential oils (Pinus nigra, Hyssopus officinalis, Satureja montana, Aloysia citrodora and Pelargonium graveolens) against the filariasis vector Culex quinquefasciatus: synergistic and antagonistic effects. Parasitol. Int. 2017;66(2):166–171. doi: 10.1016/j.parint.2017.01.012. [DOI] [PubMed] [Google Scholar]
- Benelli G., Pombi M., Otranto D. Malaria in Italy – migrants are not the cause. Trends Parasitol. 2018;34:351–354. doi: 10.1016/j.pt.2018.01.002. [DOI] [PubMed] [Google Scholar]
- Benelli G., Maggi F., Pavela R., Murugan K., Govindarajan M., Vaseeharan B. Mosquito control with green nanopesticides: towards the One Health approach? A review of non-target effects. Environ. Sci. Pollut. Res. 2018;25:10184–10206. doi: 10.1007/s11356-017-9752-4. [DOI] [PubMed] [Google Scholar]
- Benelli G., Romano D., Rocchigiani G., Caselli A., Mancianti F., Canale A., Stefanini C. Behavioral asymmetries in ticks – lateralized questing of Ixodes ricinus to a mechatronic apparatus delivering host-borne cues. Acta Trop. 2018;178:176–181. doi: 10.1016/j.actatropica.2017.11.024. [DOI] [PubMed] [Google Scholar]
- Bergquist R., Brattig N.W., Chimbari M.J., Zinsstag J., Utzinger J. Ecohealth research in Africa: Where from—Where to? Acta Trop. 2017;175:1–8. doi: 10.1016/j.actatropica.2017.07.015. [DOI] [PubMed] [Google Scholar]
- Bhatt S., Gething P.W., Brady O.J., Messina J.P., Farlow A.W., Moyes C.L., Myers M.F. The global distribution and burden of dengue. Nature. 2013;496(7446):504. doi: 10.1038/nature12060. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boka O.M., Achi L., Adakal H., Azokou A., Yao P., Yapi Y.G. Review of cattle ticks (Acari, Ixodida) in Ivory Coast and geographic distribution of Rhipicephalus (Boophilus) microplus, an emerging tick in West Africa. Exp. Appl. Acarol. 2017;71(4):355–369. doi: 10.1007/s10493-017-0129-7. [DOI] [PubMed] [Google Scholar]
- Bonizzoni M., Gasperi G., Chen X., James A. The invasive mosquito species Aedes albopictus: current knowledge and future perspectives. Trends Parasitol. 2013;29:460–468. doi: 10.1016/j.pt.2013.07.003. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bourtzis K., Lees R.S., Hendrichs J., Vreysen M.J. More than one rabbit out of the hat: Radiation, transgenic and symbiont-based approaches for sustainable management of mosquito and tsetse fly populations. Acta Trop. 2016;157:115–130. doi: 10.1016/j.actatropica.2016.01.009. [DOI] [PubMed] [Google Scholar]
- Brites-Neto J., Brasil J., de Andrade J., Saqui G.L. Evaluation of an association of alpha-cypermethrin and flufenoxuron for tick control in an area at risk of Brazilian spotted fever. Vet. Parasitol. 2017;238:1–4. doi: 10.1016/j.vetpar.2017.03.002. [DOI] [PubMed] [Google Scholar]
- Buckingham S.C. Tick-borne diseases of the USA: ten things clinicians should know. J. Infect. 2015;71:S88–S96. doi: 10.1016/j.jinf.2015.04.009. [DOI] [PubMed] [Google Scholar]
- CDC, 2015. Anopheles mosquitoes, https://www.cdc.gov/malaria/about/biology/mosquitoes/, Global Health – Division of Parasitic Diseases and Malaria, accessed February 6 2018.
- CDC, 2017. Lyme disease, https://www.cdc.gov/lyme/index.html, Centers for Disease Control and Prevention, National Center for Emerging and Zoonotic Infectious Diseases (NCEZID), Division of Vector-Borne Diseases (DVBD, accessed February 6 2018.
- Chanda E., Thomsen E.K., Musapa M., Kamuliwo M., Brogdon W.G., Norris D.E. An operational framework for insecticide resistance management planning. Emerg. Infect. Dis. 2016;22(5):773. doi: 10.3201/eid2205.150984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chang K.S., Kim H.C., Klein T.A., Ju Y.R. Insecticide resistance and cytochrome-P450 activation in unfed and blood-fed laboratory and field populations of Culex pipiens pallens. J. Pest. Sci. 2017;90(2):759–771. doi: 10.1007/s10340-016-0820-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Cosner C., Beier J.C., Cantrell R.S., Impoinvil D., Kapitanski L., Potts M.D., Troyo A., Ruan S. The effects of human movement on the persistence of vector-borne diseases. J. Theor. Biol. 2009;258:550–560. doi: 10.1016/j.jtbi.2009.02.016. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dantas-Torres F., Otranto D. Best practices for preventing vector-borne diseases in dogs and humans. Trends Parasitol. 2016;32(1):43–55. doi: 10.1016/j.pt.2015.09.004. [DOI] [PubMed] [Google Scholar]
- Dantas-Torres F., Chomel B.B., Otranto D. Ticks and tick-borne diseases: a one health perspective. Trends Parasitol. 2012;28:437–446. doi: 10.1016/j.pt.2012.07.003. [DOI] [PubMed] [Google Scholar]
- De Fuentes-Vicente J.A., Gutiérrez-Cabrera A.E., Flores-Villegas L.A., Lowenberger C., Benelli G., Salazar-Schettino P.M., Córdoba-Aguilar A. What makes an effective Chagas disease vector? Factors underlying Trypanosoma cruzi-triatomine interactions. Acta Trop. 2018;183:23–31. doi: 10.1016/j.actatropica.2018.04.008. [DOI] [PubMed] [Google Scholar]
- de la Fuente J., Contreras M. Tick vaccines: current status and future directions. Expert Rev. Vacc. 2015;14(10):1367–1376. doi: 10.1586/14760584.2015.1076339. [DOI] [PubMed] [Google Scholar]
- de la Fuente J., Almazán C., Canales M., de la Lastra J.M.P., Kocan K.M., Willadsen P. A ten-year review of commercial vaccine performance for control of tick infestations on cattle. Anim. Health Res. Rev. 2007;8(1):23–28. doi: 10.1017/S1466252307001193. [DOI] [PubMed] [Google Scholar]
- de la Fuente J., Antunes S., Bonnet S., Cabezas-Cruz A., Domingos A.G., Estrada-Peña A. Tick-pathogen interactions and vector competence: identification of molecular drivers for tick-borne diseases. Front. Cell. Infect. Microbiol. 2017;7:114. doi: 10.3389/fcimb.2017.00114. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Desneux N., Decourtye A., Delpuech J.M. The sublethal effects of pesticides on beneficial arthropods. Annu. Rev. Entomol. 2007;52:81–106. doi: 10.1146/annurev.ento.52.110405.091440. [DOI] [PubMed] [Google Scholar]
- Diuk-Wasser M.A., Vannier E., Krause P.J. Coinfection by Ixodes tick-borne pathogens: ecological, epidemiological, and clinical consequences. Trends Parasitol. 2016;32(1):30–42. doi: 10.1016/j.pt.2015.09.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Drexler N., Miller M., Gerding J., Todd S., Adams L., Dahlgren F.S. Community-based control of the brown dog tick in a region with high rates of Rocky Mountain spotted fever, 2012–2013. PLoS One. 2014;9(12):e112368. doi: 10.1371/journal.pone.0112368. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Eisen L., Dolan M.C. Evidence for personal protective measures to reduce human contact with blacklegged ticks and for environmentally based control methods to suppress host-seeking blacklegged ticks and reduce infection with Lyme disease spirochetes in tick vectors and rodent reservoirs. J. Med. Entomol. 2016;53(5):1063–1092. doi: 10.1093/jme/tjw103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ellse L., Wall R. The use of essential oils in veterinary ectoparasite control: a review. Med. Vet. Entomol. 2014;28(3):233–243. doi: 10.1111/mve.12033. [DOI] [PubMed] [Google Scholar]
- Estrada-Peña A., Salman M. Current limitations in the control and spread of ticks that affect livestock: a review. Agriculture. 2013;3(2):221–235. [Google Scholar]
- Estrada-Peña, D’Amico A., Palomar G.A.M., Dupraz M., Fonville M., Heylen D. A comparative test of ixodid tick identification by a network of European researchers. Ticks Tick-borne Dis. 2017;8(4):540–546. doi: 10.1016/j.ttbdis.2017.03.001. [DOI] [PubMed] [Google Scholar]
- Fernandes J.N., Moise I.K., Maranto G.L., Beier J.C. Revamping mosquito-borne disease control to tackle future threats. Trends Parasitol. 2018;34(5):359–368. doi: 10.1016/j.pt.2018.01.005. [DOI] [PubMed] [Google Scholar]
- Fernandes J.N., Santos L.M., Chouin-Carneiro T., Pavan M.G., Garcia G.A., David M.R., Beier J.C., Dowell F.E., Marciel-de-Freitas R., Sikulu-Lord M.T. Rapid, noninvasive detection of Zika virus in Aedes aegypti mosquitoes by near-infrared spectroscopy. Sci. Adv. 2018;4(5) doi: 10.1126/sciadv.aat0496. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Fiorenzano J.M., Koehler P.G., Xue R.D. Attractive Toxic Sugar Bait (ATSB) for control of mosquitoes and its impact on non-target organisms: A review. Int. J. Environ. Res. Public Health. 2017;14(4):398. doi: 10.3390/ijerph14040398. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Foldbjerg R., Jiang X., Miclăuş T., Chen C., Autrup H., Beer C. Silver nanoparticles–wolves in sheep's clothing? Toxicol. Res. 2015;4(3):563–575. [Google Scholar]
- Gariepy T.D., Lindsay R., Ogden N., Gregory T.R. Identifying the last supper: utility of the DNA barcode library for bloodmeal identification in ticks. Mol. Ecol. Resour. 2012;12(4):646–652. doi: 10.1111/j.1755-0998.2012.03140.x. [DOI] [PubMed] [Google Scholar]
- George D.R., Finn R.D., Graham K.M., Sparagano O.A. Present and future potential of plant-derived products to control arthropods of veterinary and medical significance. Parasites Vectors. 2014;7(1):28. doi: 10.1186/1756-3305-7-28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ghosh S., Nagar G. Problem of ticks and tick-borne diseases in India with special emphasis on progress in tick control research: a review. J. Vector-borne Dis. 2014;51(4):259. [PubMed] [Google Scholar]
- Ghosh S., Azhahianambi P., de la Fuente J. Control of ticks of ruminants, with special emphasis on livestock farming systems in India: present and future possibilities for integrated control—a review. Exp. Appl. Acarol. 2006;40:49–66. doi: 10.1007/s10493-006-9022-5. [DOI] [PubMed] [Google Scholar]
- Gindin G., Samish M., Zangi G., Mishoutchenko A., Glazer I. The susceptibility of different species and stages of ticks to entomopathogenic fungi. Exp. Appl. Acarol. 2002;28:283–288. doi: 10.1023/a:1025379307255. [DOI] [PubMed] [Google Scholar]
- Ghosh S., Tiwari S.S., Kumar B., Srivastava S., Sharma A.K., Kumar S. Identification of potential plant extracts for anti-tick activity against acaricide resistant cattle ticks, Rhipicephalus (Boophilus) microplus (Acari: Ixodidae) Exp. Appl. Acarol. 2015;66(1):159–171. doi: 10.1007/s10493-015-9890-7. [DOI] [PubMed] [Google Scholar]
- Gosling R., von Seidlein L. The future of the RTS, S/AS01 malaria vaccine: an alternative development plan. PLoS Med. 2016;13(4):e1001994. doi: 10.1371/journal.pmed.1001994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guglielmone A.A., Robbins R.G., Apanaskevich D.A., Petney T.N., Estrada-Peña A., Horak I.G. Springer; Heidelberg: 2014. Hard ticks (Acari: Ixodida: Ixodidae) of the world. [Google Scholar]
- Hamainza B., Sikaala C.H., Moonga H.B., Chanda J., Chinula D., Mwenda M. Incremental impact upon malaria transmission of supplementing pyrethroid-impregnated long-lasting insecticidal nets with indoor residual spraying using pyrethroids or the organophosphate, pirimiphos methyl. Malar. J. 2016;15(1):100. doi: 10.1186/s12936-016-1143-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heng M.Y., Tan S.N., Yong J.W.H., Ong E.S. Emerging green technologies for the chemical standardization of botanicals and herbal preparations. Trends Anal. Chem. 2013;50:1–10. [Google Scholar]
- Isman M.B. A renaissance for botanical insecticides? Pest Manage. Sci. 2015;71(12):1587–1590. doi: 10.1002/ps.4088. [DOI] [PubMed] [Google Scholar]
- Inci A., Yildirim A., Duzlu O., Doganay M., Aksoy S. Tick-borne diseases in Turkey: a review based on one health perspective. PLoS Negl.Trop. Dis. 2016;10(12) doi: 10.1371/journal.pntd.0005021. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Isman M.B. Bridging the gap: Moving botanical insecticides from the laboratory to the farm. –. Ind. Crops Prod. 2017;110:10–14. [Google Scholar]
- Jambulingam P., Subramanian S., de Vlas S.J., Vinubala C., Stolk W.A. Mathematical modelling of lymphatic filariasis elimination programmes in India: required duration of mass drug administration and post-treatment level of infection indicators. Parasites Vectors. 2016;9(1):501. doi: 10.1186/s13071-016-1768-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Johansson O., Ward M. The human immune system’s response to carcinogenic and other infectious agents transmitted by mosquito vectors. Parasitol. Res. 2017;116(1):1–9. doi: 10.1007/s00436-016-5272-2. [DOI] [PubMed] [Google Scholar]
- Joubert D.A., Walker T., Carrington L.B., De Bruyne J.T., Kien D.H.T., Hoang N.L.T. Establishment of a Wolbachia superinfection in Aedes aegypti mosquitoes as a potential approach for future resistance management. PLoS Pathog. 2016;12(2):e1005434. doi: 10.1371/journal.ppat.1005434. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Junnila A., Revay E.E., Müller G.C., Kravchenko V., Qualls W.A., Allen S.A. Efficacy of attractive toxic sugar baits (ATSB) against Aedes albopictus with garlic oil encapsulated in beta-cyclodextrin as the active ingredient. Acta Trop. 2015;152:195–200. doi: 10.1016/j.actatropica.2015.09.006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Karthika P., Vadivalagan C., Thirumurugan D., Kumar R.R., Murugan K., Benelli G. DNA barcoding of five Japanese encephalitis mosquito vectors (Culex fuscocephala, Culex gelidus, Culex tritaeniorhynchus, Culex pseudovishnui and Culex vishnui) Acta Trop. 2018;183:84–91. doi: 10.1016/j.actatropica.2018.04.006. [DOI] [PubMed] [Google Scholar]
- Keirans J.E., Durden L.A. Invasion: exotic ticks (Acari: Argasidae, Ixodidae) imported into the United States. A review and new records. J. Med. Entomol. 2001;38(6):850–861. doi: 10.1603/0022-2585-38.6.850. [DOI] [PubMed] [Google Scholar]
- Kelehear C., Hudson C.M., Mertins J.W., Shine R. First report of exotic ticks (Amblyomma rotundatum) parasitizing invasive cane toads (Rhinella marina) on the Island of Hawai ‘i. Ticks Tick-borne Dis. 2017;8(2):330–333. doi: 10.1016/j.ttbdis.2016.12.010. [DOI] [PubMed] [Google Scholar]
- Khater H., Hendawy N., Govindarajan M., Murugan K., Benelli G. Photosensitizers in the fight against ticks: safranin as a novel photodynamic fluorescent acaricide to control the camel tick Hyalomma dromedarii (Ixodidae) Parasitol. Res. 2016;115:3747–3758. doi: 10.1007/s00436-016-5136-9. [DOI] [PubMed] [Google Scholar]
- Koch L.K., Cunze S., Werblow A., Kochmann J., Dörge D.D., Mehlhorn H., Klimpel S. Modeling the habitat suitability for the arbovirus vector Aedes albopictus (Diptera: Culicidae) in Germany. Parasitol. Res. 2016;115(3):957–964. doi: 10.1007/s00436-015-4822-3. [DOI] [PubMed] [Google Scholar]
- Knols B.G., Farenhorst M., Andriessen R., Snetselaar J., Suer R.A., Osinga A.J. Eave tubes for malaria control in Africa: an introduction. Malar. J. 2016;15(1):404. doi: 10.1186/s12936-016-1452-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kraemer M.U., Sinka M.E., Duda K.A., Mylne A., Shearer F.M., Brady O.J. The global compendium of Aedes aegypti and Ae. albopictus occurrence. Sci. Data. 2015;2 doi: 10.1038/sdata.2015.35. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lacey L.A., Grzywacz D., Shapiro-Ilan D.I., Frutos R., Brownbridge M., Goettel M.S. Insect pathogens as biological control agents: back to the future. J. Invertebr. Pathol. 2015;132:1–41. doi: 10.1016/j.jip.2015.07.009. [DOI] [PubMed] [Google Scholar]
- Lani R., Moghaddam E., Haghani A., Chang L.Y., AbuBakar S., Zandi K. Tick-borne viruses: a review from the perspective of therapeutic approaches. Ticks Tick-borne Dis. 2014;5(5):457–465. doi: 10.1016/j.ttbdis.2014.04.001. [DOI] [PubMed] [Google Scholar]
- Lednicky J.A., White S.K., Stephenson C.J., Cherabuddi K., Loeb J.C., Moussatche N. Keystone virus isolated from a Florida teenager with rash and subjective fever: another endemic arbovirus in the southeastern United States? Clin. Infect. Dis. 2018 doi: 10.1093/cid/ciy485. [DOI] [PubMed] [Google Scholar]
- Lehrer S. Anopheles mosquito transmission of brain tumor. Med. Hypotheses. 2010;74(1):167–168. doi: 10.1016/j.mehy.2009.07.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lew-Tabor A.E., Valle M.R. A review of reverse vaccinology approaches for the development of vaccines against ticks and tick borne diseases. Ticks Tick-borne Dis. 2016;7(4):573–585. doi: 10.1016/j.ttbdis.2015.12.012. [DOI] [PubMed] [Google Scholar]
- Li Y., Kamara F., Zhou G., Puthiyakunnon S., Li C., Liu Y. Urbanization increases Aedes albopictus larval habitats and accelerates mosquito development and survivorship. PLoS Negl.Trop. Dis. 2014;8(11) doi: 10.1371/journal.pntd.0003301. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lupi E., Hatz C., Schlagenhauf P. The efficacy of repellents against Aedes, Anopheles, Culex and Ixodes spp.–A literature review. Travel Med. Infect. Dis. 2013;11(6):374–411. doi: 10.1016/j.tmaid.2013.10.005. [DOI] [PubMed] [Google Scholar]
- Lv J., Wu S., Zhang Y., Chen Y., Feng C., Yuan X. Assessment of four DNA fragments (COI, 16S rDNA, ITS2, 12S rDNA) for species identification of the Ixodida (Acari: Ixodida) Parasites Vectors. 2014;7(1):93. doi: 10.1186/1756-3305-7-93. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lv J., Wu S., Zhang Y., Zhang T., Feng C., Jia G., Lin X. Development of a DNA barcoding system for the Ixodida (Acari: Ixodida) Mitochondrial DNA. 2014;25(2):142–149. doi: 10.3109/19401736.2013.792052. [DOI] [PubMed] [Google Scholar]
- Manzano-Román, R., Díaz-Martín, V., de la Fuente, J., Pérez-Sánchez, R., 2012. Soft ticks as pathogen vectors: distribution, surveillance and control. In: Parasitology. InTech.
- Mapholi N.O., Marufu M.C., Maiwashe A., Banga C.B., Muchenje V., MacNeil M.D. Towards a genomics approach to tick (Acari: Ixodidae) control in cattle: a review. Ticks Tick-borne Dis. 2014;5(5):475–483. doi: 10.1016/j.ttbdis.2014.04.006. [DOI] [PubMed] [Google Scholar]
- Medlock J.M., Hansford K.M., Versteirt V., Cull B., Kampen H., Fontenille D. An entomological review of invasive mosquitoes in Europe. Bull. Entomol. Res. 2015;105(6):637–663. doi: 10.1017/S0007485315000103. [DOI] [PubMed] [Google Scholar]
- Melo A.L.D.A., Soccol V.T., Soccol C.R. Bacillus thuringiensis: mechanism of action, resistance, and new applications: a review. Crit. Rev. Biotechnol. 2016;36(2):317–326. doi: 10.3109/07388551.2014.960793. [DOI] [PubMed] [Google Scholar]
- Mishra P., Tyagi B.K., Chandrasekaran N., Mukherjee A. Biological nanopesticides: a greener approach towards the mosquito vector control. Environ. Sci. Pollut. Res. 2018 doi: 10.1007/s11356-017-9640-y. [DOI] [PubMed] [Google Scholar]
- Molyneux D.H., Savioli L., Engels D. Neglected tropical diseases: progress towards addressing the chronic pandemic. The Lancet. 2017;389(10066):312–325. doi: 10.1016/S0140-6736(16)30171-4. [DOI] [PubMed] [Google Scholar]
- Muller G.C., Beier J.C., Traore S.F., Toure M.B., Traore M.M., Bah S., Doumbia S., Schlein Y. Successful field trial of attractive toxic sugar bait (ATSB) plant-spraying methods against malaria vectors in the Anopheles gambiae complex in Mali West Africa. Malaria J. 2010;9:210. doi: 10.1186/1475-2875-9-210. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murdock C.C., Blanford S., Luckhart S., Thomas M.B. Ambient temperature and dietary supplementation interact to shape mosquito vector competence for malaria. J. Insect Physiol. 2014;67:37–44. doi: 10.1016/j.jinsphys.2014.05.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Murugan K., Vadivalagan C., Karthika P., Panneerselvam C., Paulpandi M., Subramaniam J. DNA barcoding and molecular evolution of mosquito vectors of medical and veterinary importance. Parasitol. Res. 2016;115(1):107–121. doi: 10.1007/s00436-015-4726-2. [DOI] [PubMed] [Google Scholar]
- Naqqash M.N., Gökçe A., Bakhsh A., Salim M. Insecticide resistance and its molecular basis in urban insect pests. Parasitol. Res. 2016;115(4):1363–1373. doi: 10.1007/s00436-015-4898-9. [DOI] [PubMed] [Google Scholar]
- Oehler E., Watrin L., Larre P., Leparc-Goffart I., Lastere S., Valour F. Zika virus infection complicated by Guillain-Barre syndrome–case report, French Polynesia, December 2013. Eurosurveillance. 2014;19(9):20720. doi: 10.2807/1560-7917.es2014.19.9.20720. [DOI] [PubMed] [Google Scholar]
- Ostfeld R.S., Brunner J.L. Climate change and Ixodes tick-borne diseases of humans. Phil. Trans. R. Soc. B. 2015;370(1665):20140051. doi: 10.1098/rstb.2014.0051. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pfäffle M., Littwin N., Muders S.V., Petney T.N. The ecology of tickborne diseases. Int. J. Parasitol. 2013;43:1059–1077. doi: 10.1016/j.ijpara.2013.06.009. [DOI] [PubMed] [Google Scholar]
- Pantchev N., Pluta S., Huisinga E., Nather S., Scheufelen M., Vrhovec M.G. Tick-borne diseases (borreliosis, anaplasmosis, babesiosis) in German and Austrian dogs: Status quo and review of distribution, transmission, clinical findings, diagnostics and prophylaxis. Parasitol. Res. 2015;114(1):19–54. doi: 10.1007/s00436-015-4513-0. [DOI] [PubMed] [Google Scholar]
- Paredes-Esquivel C., Lenhart A., del Río R., Leza M.M., Estrugo M., Chalco E., Miranda M.Á. The impact of indoor residual spraying of deltamethrin on dengue vector populations in the Peruvian Amazon. Acta Trop. 2016;154:139–144. doi: 10.1016/j.actatropica.2015.10.020. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pavela R. Acute toxicity and synergistic and antagonistic effects of the aromatic compounds of some essential oils against Culex quinquefasciatus Say larvae. Parasitol. Res. 2015;114(10):3835–3853. doi: 10.1007/s00436-015-4614-9. [DOI] [PubMed] [Google Scholar]
- Pavela R. Essential oils for the development of eco-friendly mosquito larvicides: a review. Ind. Crops Prod. 2015;76:174–187. [Google Scholar]
- Pavela R., Benelli G. Ethnobotanical knowledge on botanical repellents employed in the African region against mosquito vectors–a review. Exp. Parasitol. 2016;167:103–108. doi: 10.1016/j.exppara.2016.05.010. [DOI] [PubMed] [Google Scholar]
- Pavela R., Benelli G. Essential oils as ecofriendly biopesticides? Challenges and constraints. Trends Plant Sci. 2016;21(12):1000–1007. doi: 10.1016/j.tplants.2016.10.005. [DOI] [PubMed] [Google Scholar]
- Pavela R., Canale A., Mehlhorn H., Benelli G. Application of ethnobotanical repellents and acaricides in prevention, control and management of livestock ticks: a review. Res. Vet. Sci. 2016;109:1–9. doi: 10.1016/j.rvsc.2016.09.001. [DOI] [PubMed] [Google Scholar]
- Petersen E., Wilson M.E., Touch S., McCloskey B., Mwaba P., Bates M. Rapid spread of Zika virus in the Americas-implications for public health preparedness for mass gatherings at the 2016 Brazil Olympic Games. Int. J. Infect. Dis. 2016;44:11–15. doi: 10.1016/j.ijid.2016.02.001. [DOI] [PubMed] [Google Scholar]
- Pfister K., Armstrong R. Systemically and cutaneously distributed ectoparasiticides: a review of the efficacy against ticks and fleas on dogs. Parasites Vectors. 2016;9(1):436. doi: 10.1186/s13071-016-1719-7. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pitts R.J., Mozūraitis R., Gauvin-Bialecki A., Lempérière G. The roles of kairomones, synomones and pheromones in the chemically-mediated behaviour of male mosquitoes. Acta Trop. 2014;132:S26–S34. doi: 10.1016/j.actatropica.2013.09.005. [DOI] [PubMed] [Google Scholar]
- Polar P., Moore D., Kairo M.T., Ramsubhag A. Topically applied myco-acaricides for the control of cattle ticks: overcoming the challenges. Exp. Appl. Acarol. 2008;46:119–148. doi: 10.1007/s10493-008-9170-x. [DOI] [PubMed] [Google Scholar]
- Priya S.P., Sakinah S., Sharmilah K., Hamat R.A., Sekawi Z., Higuchi A., Ling M.P., Nordin S.A., Benelli G., Kumar S.S. Leptospirosis: molecular trial path and immunopathogenesis correlated with malaria and dengue mimetic hemorrhagic infections. Acta Trop. 2017;176:206–223. doi: 10.1016/j.actatropica.2017.08.007. [DOI] [PubMed] [Google Scholar]
- Qualls W.A., Müller G.C., Traore S.F., Traore M.M., Arheart K.L., Doumbia S. Indoor use of attractive toxic sugar bait (ATSB) to effectively control malaria vectors in Mali West Africa. Malaria J. 2015;14(1):301. doi: 10.1186/s12936-015-0819-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Romano D., Stefanini C., Canale A., Benelli G. Artificial blood feeders for mosquito and ticks – where from, where to? Acta Trop. 2018;183:43–56. doi: 10.1016/j.actatropica.2018.04.009. [DOI] [PubMed] [Google Scholar]
- Rosenberg R., Lindsey N.P., Fischer M., Gregory C.J., Hinckley A.F., Mead P.S. Vital signs: trends in reported vectorborne disease cases—United States and territories, 2004–2016. Morb. Mortal. Wkly Rep. 2018;67(17):496. doi: 10.15585/mmwr.mm6717e1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saifi M.A., Alyousif M.S., Amoudi M.A. Anopheline species and their Plasmodium infection status in Aligarh India. Saudi J. Biol. Sci. 2016;23(5):649–653. doi: 10.1016/j.sjbs.2015.01.005. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Samish M., Rehacek J. Pathogens and predators of ticks and their potential in biological control. Annu. Rev. Entomol. 1999;44:159–182. doi: 10.1146/annurev.ento.44.1.159. [DOI] [PubMed] [Google Scholar]
- Schaffner F., Bellini R., Petrić D., Scholte E.J., Zeller H., Rakotoarivony L.M. Development of guidelines for the surveillance of invasive mosquitoes in Europe. Parasites Vectors. 2013;6(1):209. doi: 10.1186/1756-3305-6-209. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Semmler M., Abdel-Ghaffar F., Al-Rasheid K.A., Mehlhorn H. Comparison of the tick repellent efficacy of chemical and biological products originating from Europe and the USA. Parasitol. Res. 2011;108:899–904. doi: 10.1007/s00436-010-2131-4. [DOI] [PubMed] [Google Scholar]
- Shyma K.P., Gupta J.P., Singh V. Breeding strategies for tick resistance in tropical cattle: a sustainable approach for tick control. J. Parasit. Dis. 2015;39(1):1–6. doi: 10.1007/s12639-013-0294-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Soonwera M., Phasomkusolsil S. Efficacy of Thai herbal essential oils as green repellent against mosquito vectors. Acta Trop. 2015;142:127–130. doi: 10.1016/j.actatropica.2014.11.010. [DOI] [PubMed] [Google Scholar]
- Solano-Gallego L., Sainz Á., Roura X., Estrada-Peña A., Miró G. A review of canine babesiosis: the European perspective. Parasit. Vectors. 2016;9(1):336. doi: 10.1186/s13071-016-1596-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sonenshine, D.E., Lane, R.S., Nicholson, W.L., 2002. Ticks (Ixodida). In: Mullen, G., Durden, L. (Eds.), Medical and Veterinary Entomology. Academic San Diego, pp. 517–558.
- Sonenshine D.E. Tick pheromones and their use in tick control. Annu. Rev. Entomol. 2006;51:557–580. doi: 10.1146/annurev.ento.51.110104.151150. [DOI] [PubMed] [Google Scholar]
- Sternberg E.D., Ng’habi K.R., Lyimo I.N., Kessy S.T., Farenhorst M., Thomas M.B. Eave tubes for malaria control in Africa: initial development and semi-field evaluations in Tanzania. Malaria J. 2016;15(1):447. doi: 10.1186/s12936-016-1499-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Stone C.M., Witt A.B., Walsh G.C., Foster W.A., Murphy S.T. Would the control of invasive alien plants reduce malaria transmission? A review. Parasit. Vectors. 2018;11(1):76. doi: 10.1186/s13071-018-2644-8. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Strode C., Donegan S., Garner P., Enayati A.A., Hemingway J. The impact of pyrethroid resistance on the efficacy of insecticide-treated bed nets against African anopheline mosquitoes: systematic review and meta-analysis. PLoS Med. 2014;11(3):e1001619. doi: 10.1371/journal.pmed.1001619. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tabari M.A., Youssefi M.R., Maggi F., Benelli G. Toxic and repellent activity of selected monoterpenoids (thymol, carvacrol and linalool) against the castor bean tick, Ixodes ricinus (Acari: Ixodidae) Vet. Parasitol. 2017;245C:86–91. doi: 10.1016/j.vetpar.2017.08.012. [DOI] [PubMed] [Google Scholar]
- Tan K.R., Coleman J., Smith B., Hamainza B., Katebe-Sakala C., Kean C. A longitudinal study of the durability of long-lasting insecticidal nets in Zambia. Malar. J. 2016;15(1):106. doi: 10.1186/s12936-016-1154-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tiono A.B., Pinder M., N’Fale S., Faragher B., Smith T., Silkey M. The AvecNet Trial to assess whether addition of pyriproxyfen, an insect juvenile hormone mimic, to long-lasting insecticidal mosquito nets provides additional protection against clinical malaria over current best practice in an area with pyrethroid-resistant vectors in rural Burkina Faso: study protocol for a randomised controlled trial. Trials. 2015;16(1):113. doi: 10.1186/s13063-015-0606-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vadivalagan C., Karthika P., Murugan K., Panneerselvam C., Del Serrone P., Benelli G. Exploring genetic variation in haplotypes of the filariasis vector Culex quinquefasciatus (Diptera: Culicidae) through DNA barcoding. Acta Trop. 2017;169:43–50. doi: 10.1016/j.actatropica.2017.01.020. [DOI] [PubMed] [Google Scholar]
- van Wieren, S.E., Braks, M. A., Lahr, J., 2016. Effectiveness and environmental hazards of acaricides applied to large mammals for tick control. In: Ecology and prevention of Lyme borreliosis. Wageningen Academic Publishers, pp. 75–89.
- Vaníčková L., Canale A., Benelli G. Sexual chemoecology of mosquitoes (Diptera, Culicidae): Current knowledge and implications for vector control programs. Parasitol. Int. 2017;66(2):190–195. doi: 10.1016/j.parint.2016.09.010. [DOI] [PubMed] [Google Scholar]
- Vega-Rúa A., Zouache K., Girod R., Failloux A.B., Lourenço-de-Oliveira R. High level of vector competence of Aedes aegypti and Aedes albopictus from ten American countries as a crucial factor in the spread of Chikungunya virus. J. Virol. 2014;88(11):6294–6306. doi: 10.1128/JVI.00370-14. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Vudriko P., Okwee-Acai J., Tayebwa D.S., Byaruhanga J., Kakooza S., Wampande E. Emergence of multi-acaricide resistant Rhipicephalus ticks and its implication on chemical tick control in Uganda. Parasit. Vectors. 2016;9(1):4. doi: 10.1186/s13071-015-1278-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ward M., Benelli G. Avian and simian malaria: do they have a cancer connection? Parasitol. Res. 2017;116(3):839–845. doi: 10.1007/s00436-016-5352-3. [DOI] [PubMed] [Google Scholar]
- Ward M., Benelli G. Culiseta annulata–just a biting nuisance or a deadly foe? Pathogens Glob. Health. 2018;112:96–100. doi: 10.1080/20477724.2017.1397876. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Webster A., Reck J., Santi L., Souza U.A., Dall’Agnol B., Klafke G.M. Integrated control of an acaricide-resistant strain of the cattle tick Rhipicephalus microplus by applying Metarhizium anisopliae associated with cypermethrin and chlorpyriphos under field conditions. Vet. Parasitol. 2015;207(3-4):302–308. doi: 10.1016/j.vetpar.2014.11.021. [DOI] [PubMed] [Google Scholar]
- West P.A., Protopopoff N., Wright A., Kivaju Z., Tigererwa R., Mosha F.W. Indoor residual spraying in combination with insecticide-treated nets compared to insecticide-treated nets alone for protection against malaria: a cluster randomised trial in Tanzania. PLoS Med. 2014;11(4):e1001630. doi: 10.1371/journal.pmed.1001630. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wilke A.B.B., Beier J.C., Benelli G. Transgenic mosquitoes – fact or fiction? Trends Parasitol. 2018;34(6):456–465. doi: 10.1016/j.pt.2018.02.003. [DOI] [PubMed] [Google Scholar]
- Willadsen P. Tick control: thoughts on a research agenda. Vet. Parasitol. 2006;138(1–2):161–168. doi: 10.1016/j.vetpar.2006.01.050. [DOI] [PubMed] [Google Scholar]
- Yakob L., Walker T. Zika virus outbreak in the Americas: the need for novel mosquito control methods. Lancet Glob. Health. 2016;4(3):e148–e149. doi: 10.1016/S2214-109X(16)00048-6. [DOI] [PubMed] [Google Scholar]
- Yavuz O., Aksoy A., Das Y.K., Arslan H.H., Gurler A.T., Yarim G.F. An evaluation of the efficacy, clinical safety, blood levels and milk concentrations of flumethrin and cypermethrin formulations used for tick control in cattle. Large Anim. Rev. 2017;23(3):97–101. [Google Scholar]
- Zhang R.L., Zhang B. Prospects of using DNA barcoding for species identification and evaluation of the accuracy of sequence databases for ticks (Acari: Ixodida) Ticks Tick-borne Dis. 2014;5(3):352–358. doi: 10.1016/j.ttbdis.2014.01.001. [DOI] [PubMed] [Google Scholar]
- Zhang D., Lees R.S., Xi Z., Gilles J.R., Bourtzis K. Combining the sterile insect technique with Wolbachia-based approaches: II-a safer approach to Aedes albopictus population suppression programmes, designed to minimize the consequences of inadvertent female release. PloS One. 2015;10(8):e0135194. doi: 10.1371/journal.pone.0135194. [DOI] [PMC free article] [PubMed] [Google Scholar]




