Hemingway, J. & Ranson, H. Insecticide resistance in insect vectors of human disease. Annu. Rev. Entomol. 45, 371–391 (2000).
Google Scholar
Liu, N. Insecticide resistance in mosquitoes: impact, mechanisms, and research directions. Annu. Rev. Entomol. 60, 537–559 (2015).
Google Scholar
Roush, R. T. Occurrence, genetics and management of insecticide resistance. Parasitol. Today 9, 174–179 (1993).
Google Scholar
Sternberg, E. D. & Thomas, M. B. Insights from agriculture for the management of insecticide resistance in disease vectors. Evol. Appl. 11, 404–414 (2018).
Google Scholar
Raymond, M., Berticat, C., Weill, M., Pasteur, N. & Chevillon, C. Insecticide resistance in the mosquito Culex pipiens: what have we learned about adaptation? in Microevolution Rate, Pattern, Process 287–296 (Springer, 2001).
Parker-Crockett, C., Connelly, C. R., Siegfried, B. & Alto, B. W. Influence of pyrethroid resistance on vector competency for Zika virus by Aedes aegypti (Diptera: Culicidae). J. Med. Entomol. 2, 19 (2021).
Muturi, E. J., Kim, C., Alto, B. W., Berenbaum, M. R. & Schuler, M. A. Larval environmental stress alters Aedes aegypti competence for Sindbis virus. Trop. Med. Int. Heal. 16, 955–964 (2011).
Google Scholar
James, R. R. & Xu, J. Mechanisms by which pesticides affect insect immunity. J. Invertebr. Pathol. 109, 175–182 (2012).
Google Scholar
Hauser, G., Thiévent, K. & Koella, J. C. Consequences of larval competition and exposure to permethrin for the development of the rodent malaria Plasmodium berghei in the mosquito Anopheles gambiae. Parasit. Vectors 13, 1–11 (2020).
Google Scholar
Hauser, G. & Koella, J. C. Larval exposure to a pyrethroid insecticide and competition for food modulate the melanisation and antibacterial responses of adult Anopheles gambiae. Sci. Rep. 10, 1–8 (2020).
Google Scholar
Devillers, J. Fate and ecotoxicological effects of pyriproxyfen in aquatic ecosystems. Environ. Sci. Pollut. Res. 27, 16052–16068 (2020).
Google Scholar
Nijhout, H. F. & Williams, C. M. Control of moulting and metamorphosis in the tobacco hornworm, Manduca sexta (L.): growth of the last-instar larva and the decision to pupate. J. Exp. Biol. 61, 481–491 (1974).
Google Scholar
Nijhout, H. F. & Wheeler, D. E. Juvenile hormone and the physiological basis of insect polymorphisms. Q. Rev. Biol. 57, 109–133 (1982).
Google Scholar
Ishaaya, I. & Horowitz, A. R. Novel phenoxy juvenile hormone analog (pyriproxyfen) suppresses embryogenesis and adult emergence of sweetpotato whitefly (Homoptera: Aleyrodidae). J. Econ. Entomol. 85, 2113–2117 (1992).
Google Scholar
Ali, A., Nayar, J. K. & Xue, R.-D. Comparative toxicity of selected larvicides and insect growth regulators to a Florida laboratory population of Aedes albopictus. J. Am. Mosq. Control Assoc. 11, 72–76 (1995).
Google Scholar
Maoz, D. et al. Community effectiveness of pyriproxyfen as a dengue vector control method: a systematic review. PLoS Negl. Trop. Dis. 11, e0005651 (2017).
Google Scholar
Hustedt, J. C., Boyce, R., Bradley, J., Hii, J. & Alexander, N. Use of pyriproxyfen in control of Aedes mosquitoes: a systematic review. PLoS Negl. Trop. Dis. 14, e0008205 (2020).
Google Scholar
Alomar, A. A., Eastmond, B. H. & Alto, B. W. The effects of exposure to pyriproxyfen and predation on Zika virus infection and transmission in Aedes aegypti. PLoS Negl. Trop. Dis. 14, e0008846 (2020).
Google Scholar
Alomar, A. A. & Alto, B. W. Mosquito responses to lethal and nonlethal effects of predation and an insect growth regulator. Ecosphere 12, e03452 (2021).
Google Scholar
Devine, G. J. et al. Using adult mosquitoes to transfer insecticides to Aedes aegypti larval habitats. Proc. Natl. Acad. Sci. 106, 11530–11534 (2009).
Google Scholar
Mains, J. W., Brelsfoard, C. L. & Dobson, S. L. Male mosquitoes as vehicles for insecticide. PLoS Negl. Trop. Dis. 9, e0003406 (2015).
Google Scholar
Buckner, E. A., Williams, K. F., Marsicano, A. L., Latham, M. D. & Lesser, C. R. Evaluating the vector control potential of the In2Care® mosquito trap against Aedes aegypti and Aedes albopictus under semifield conditions in Manatee County, Florida. J. Am. Mosq. Control Assoc. 33, 193–199 (2017).
Google Scholar
Fiaz, M. et al. Pyriproxyfen, a juvenile hormone analog, damages midgut cells and interferes with behaviors of Aedes aegypti larvae. Peer J. 7, e7489 (2019).
Google Scholar
Kamal, H. A. & Khater, E. I. M. The biological effects of the insect growth regulators; pyriproxyfen and diflubenzuron on the mosquito Aedes aegypti. J. Egypt Soc. Parasitol. 40, 565–574 (2010).
Google Scholar
Yadav, K., Dhiman, S., Acharya, B. N., Ghorpade, R. R. & Sukumaran, D. Pyriproxyfen treated surface exposure exhibits reproductive disruption in dengue vector Aedes aegypti. PLoS Negl. Trop. Dis. 13, e0007842 (2019).
Google Scholar
Moltini-Conclois, I., Stalinski, R., Tetreau, G., Després, L. & Lambrechts, L. Larval exposure to the bacterial insecticide Bti enhances dengue virus susceptibility of adult Aedes aegypti mosquitoes. Insects 9, 193 (2018).
Google Scholar
Mordecai, E. A. et al. Thermal biology of mosquito-borne disease. Ecol. Lett. 22, 1690–1708 (2019).
Google Scholar
Heugens, E. H. W., Hendriks, A. J., Dekker, T., van Straalen, N. M. & Admiraal, W. A review of the effects of multiple stressors on aquatic organisms and analysis of uncertainty factors for use in risk assessment. Crit. Rev. Toxicol. 31, 247–284 (2001).
Google Scholar
Zhu, J. & Noriega, F. G. The role of juvenile hormone in mosquito development and reproduction. Adv. In Insect Phys. 51, 93–113 (2016).
Google Scholar
El-Shazly, M. M. & Refaie, B. M. Larvicidal effect of the juvenile hormone mimic pyriproxyfen on Culex pipiens. J. Am. Mosq. Control Assoc. News 18, 321–328 (2002).
Google Scholar
Moura, L., de Nadai, B. L. & Corbi, J. J. What does not kill it does not always make it stronger: High temperatures in pyriproxyfen treatments produce Aedes aegypti adults with reduced longevity and smaller females. J. Asia. Pac. Entomol. 23, 529–535 (2020).
Google Scholar
Powell, J. R. & Tabachnick, W. J. History of domestication and spread of Aedes aegypti-a review. Mem. Inst. Oswaldo Cruz 108, 11–17 (2013).
Google Scholar
Baud, D., Gubler, D. J., Schaub, B., Lanteri, M. C. & Musso, D. An update on Zika virus infection. Lancet 390, 2099–2109 (2017).
Google Scholar
He, D., Gao, D., Lou, Y., Zhao, S. & Ruan, S. A comparison study of Zika virus outbreaks in French Polynesia, Colombia and the State of Bahia in Brazil. Sci. Rep. 7, 1–6 (2017).
Google Scholar
Winokur, O. C., Main, B. J., Nicholson, J. & Barker, C. M. Impact of temperature on the extrinsic incubation period of Zika virus in Aedes aegypti. PLoS Negl. Trop. Dis. 14, 150 (2020).
Google Scholar
Glushakova, L. G. et al. Optimization of cationic (Q)-paper for detection of arboviruses in infected mosquitoes. J. Virol. Methods 261, 71–79 (2018).
Google Scholar
Burkett-Cadena, N. D. et al. Evaluation of the honey-card technique for detection of transmission of arboviruses in Florida and comparison with sentinel chicken seroconversion. J. Med. Entomol. 53, 1449–1457 (2016).
Google Scholar
Alto, B. W. et al. Transmission risk of two chikungunya lineages by invasive mosquito vectors from Florida and the Dominican Republic. PLoS Negl. Trop. Dis. 11, e0005724 (2017).
Google Scholar
Bustin, S. A. Absolute quantification of mRNA using real-time reverse transcription polymerase chain reaction assays. J. Mol. Endocrinol. 25, 169–193 (2000).
Google Scholar
Nasci, R. S. The size of emerging and host-seeking Aedes aegypti and the relation of size to blood-feeding success in the field. J. Am. Mosq. Control Assoc. 2, 61–62 (1986).
Google Scholar
Van Handel, E. & Day, J. F. Correlation between wing length and protein content of mosquitoes. J. Am. Mosq. Control Assoc. 5, 180–182 (1989).
Google Scholar
Grill, C. P. & Juliano, S. A. Predicting species interactions based on behaviour: predation and competition in container-dwelling mosquitoes. J. Anim. Ecol. 6, 63–76 (1996).
Google Scholar
Chandrasegaran, K. & Juliano, S. A. How do trait-mediated non-lethal effects of predation affect population-level performance of mosquitoes?. Front. Ecol. Evol. 7, 25 (2019).
Google Scholar
Knecht, H., Richards, S. L., Balanay, J. A. G. & White, A. V. Impact of mosquito age and insecticide exposure on susceptibility of Aedes albopictus (Diptera: Culicidae) to Infection with Zika Virus. Pathogens 7, 67 (2018).
Google Scholar
Öhlund, P., Lundén, H. & Blomström, A. L. Insect-specific virus evolution and potential effects on vector competence. Virus Genes 55, 127–137 (2019).
Google Scholar
Antonio, G. E., Sanchez, D., Williams, T. & Marina, C. F. Paradoxical effects of sublethal exposure to the naturally derived insecticide spinosad in the dengue vector mosquito, Aedes aegypti. Pest Manag. Sci. Former. Pestic. Sci. 65, 323–326 (2009).
Google Scholar
Muturi, E. J. & Alto, B. W. Larval environmental temperature and insecticide exposure alter Aedes aegypti competence for arboviruses. Vector-Borne Zoonotic Dis. 11, 1157–1163 (2011).
Google Scholar
Alto, B. W. & Lord, C. C. Transstadial effects of Bti on traits of Aedes aegypti and infection with dengue virus. PLoS Negl. Trop. Dis. 10, e0004370 (2016).
Google Scholar
Jirakanjanakit, N. et al. Influence of larval density or food variation on the geometry of the wing of Aedes (Stegomyia) aegypti. Trop. Med. Int. Heal. 12, 1354–1360 (2007).
Google Scholar
Polson, K. A., Brogdon, W. G., Rawlins, S. C. & Chadee, D. D. Impact of environmental temperatures on resistance to organophosphate insecticides in Aedes aegypti from Trinidad. Rev. Panam. Salud Pública 32, 1–8 (2012).
Google Scholar
Glunt, K. D., Oliver, S. V., Hunt, R. H. & Paaijmans, K. P. The impact of temperature on insecticide toxicity against the malaria vectors Anopheles arabiensis and Anopheles funestus. Malar. J. 17, 1–8 (2018).
Google Scholar
Benelli, G., Wilke, A. B. B., Bloomquist, J. R., Desneux, N. & Beier, J. C. Overexposing mosquitoes to insecticides under global warming: a public health concern?. Sci. Total Environ. 762, 143069 (2021).
Google Scholar
Alto, B. W. & Bettinardi, D. Temperature and dengue virus infection in mosquitoes: independent effects on the immature and adult stages. Am. J. Trop. Med. Hyg. 88, 497–505 (2013).
Google Scholar
Mourya, D. T., Yadav, P. & Mishra, A. C. Effect of temperature stress on immature stages and susceptibility of Aedes aegypti mosquitoes to chikungunya virus. Am. J. Trop. Med. Hyg. 70, 346–350 (2004).
Google Scholar
Adelman, Z. N. et al. Cooler temperatures destabilize RNA interference and increase susceptibility of disease vector mosquitoes to viral infection. PLoS Negl Trop Dis 7, e2239 (2013).
Google Scholar
Hardy, J. L., Meyer, R. P., Presser, S. B. & Milby, M. M. Temporal variations in the susceptibility of a semi-isolated population of Culex tarsalis to peroral infection with western equine encephalomyelitis and St. Louis encephalitis viruses. Am. J. Trop. Med. Hyg. 42, 500–511 (1990).
Google Scholar
Kay, B. H., Fanning, I. A. N. D. & Mottram, P. Rearing temperature influences flavivirus vector competence of mosquitoes. Med. Vet. Entomol. 3, 415–422 (1989).
Google Scholar
Westbrook, C. J., Reiskind, M. H., Pesko, K. N., Greene, K. E. & Lounibos, L. P. Larval environmental temperature and the susceptibility of Aedes albopictus Skuse (Diptera: Culicidae) to chikungunya virus. Vector-Borne Zoonotic Dis. 10, 241–247 (2010).
Google Scholar
Gotelli, N. J. A Primer of Ecology (Sinauer Associate. Inc., 2001).
Source: Ecology - nature.com
