Optimization of oviposition lure settings to observe populations of Aedes mosquitoes, vectors of arboviruses in La Reunion
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Yang, X., Quam, M. B., Zhang, T. & Sang, S. International burden for dengue and the evolving sample previously 30 years. J. Journey Med. 28, taab146 (2021).
Simmons, C. P., Farrar, J. J., van Vinh Chau, N. & Wills, B. Dengue. N. Engl. J. Med. 366, 1423–1432 (2012).
Brady, O. J. et al. Refining the worldwide spatial limits of dengue virus transmission by evidence-based consensus. PLoS Negl. Trop. Dis. 6, e1760 (2012).
Morin, C. W., Comrie, A. C. & Ernst, Ok. Local weather and dengue transmission: Proof and implications. Environ. Well being Perspect. 121, 1264–1272 (2013).
Brady, O. J. et al. International temperature constraints on Aedes aegypti and Ae. albopictus persistence and competence for dengue virus transmission. Parasites Vectors 7, 338 (2014).
Betanzos-Reyes, Á. F. et al. Affiliation of dengue fever with Aedes spp. abundance and climatological results. Salud Pública de México 60, 12 (2017).
WHO. Dengue and extreme dengue. (2022).
Gubler, D. J. Dengue and dengue hemorrhagic fever. Clin. Microbiol. Rev. 11, 480–496 (1998).
Delatte, H. et al. Aedes albopictus, vecteur des virus du chikungunya et de la dengue à La Réunion : biologie et contrôle. Parasite 15, 3–13 (2008).
Kles, V., Michault, A., Rodhain, F., Mevel, F. & Chastel, C. A serological survey relating to Flaviviridae infections on the island of Reunion (1971–1989). Bull. Soc. Pathol. Exot. 1990(87), 71–76 (1994).
Pierre, V. et al. Epidémie de dengue 1 à la Réunion en 2004. Journal de Veille Sanitaire (2005).
Vincent, M. et al. From the risk to the massive outbreak: dengue on Reunion Island, 2015 to 2018. Eurosurveillance 24, (2019).
Cellule Santé Publique France en Région, ARS. State of affairs de la dengue à La Réunion au 15 décembre 2020. https://www.lareunion.ars.sante.fr/avec-le-retour-de-lete-agissons-des-maintenant-contre-la-dengue (2020).
Agence Régionale de Santé. Communiqué de presse: dengue à La Réunion. State of affairs au 28 juillet 2021. https://www.lareunion.ars.sante.fr/system/recordsdata/2021-07/2021-07-28-Dengue-State of affairs à La Réunion_0.pdf (2021).
Hafsia, S. et al. Overview of dengue outbreaks within the southwestern Indian Ocean and evaluation of things concerned within the shift towards endemicity in Reunion Island: A scientific overview. PLoS Negl. Trop. Dis. 16, e0010547 (2022).
Reiter, P., Fontenille, D. & Paupy, C. Aedes albopictus as an epidemic vector of chikungunya virus: One other rising downside?. Lancet. Infect. Dis 6, 463–464 (2006).
Njenga, M. Ok. et al. Monitoring epidemic Chikungunya virus into the Indian Ocean from East Africa. J. Gen. Virol. 89, 2754–2760 (2008).
Soumahoro, M.-Ok. et al. The Chikungunya epidemic on La Réunion Island in 2005–2006: a cost-of-illness research. PLoS Negl. Trop. Dis. 5, e1197 (2011).
Larrieu, S., Balleydier, E., Renault, P., Baville, M. & Filleul, L. [Epidemiological surveillance du chikungunya on Reunion Island from 2005 to 2011]. Médecine tropicale : Revue du Corps de Santé colonial 72 Spec No, 38–42 (2012).
Soghigian, J. et al. Genetic proof for the origin of Aedes aegypti, the yellow fever mosquito, within the southwestern Indian Ocean. Mol. Ecol. 29, 3593–3606 (2020).
Kotsakiozi, P. et al. Inhabitants construction of a vector of human illnesses: Aedes aegypti in its ancestral vary Africa. Ecol. Evol. 8, 7835–7848 (2018).
MacGregor, M. E. Aedes (Stegomyia) mascarensis, MacGregor: A brand new Mosquito from Mauritius. Bull. Entomol. Res. 14, 409–412 (1924).
Salvan, M. & Mouchet, J. Aedes albopictus et Aedes aegypti à l’Ile de La Réunion. Ann. Soc. Belg. Med. Trop. 74, 323–326 (1994).
Bagny, L., Delatte, H., Quilici, S. & Fontenille, D. Progressive Lower in Aedes aegypti distribution in Reunion Island because the 1900s. J. Med. Entomol. 46, 1541–1545 (2009).
Le Vassal, J. J. paludisme à l’Ile de La Réunion. Per Gli Stud Della Maria 8, 18–27 (1907).
Delatte, H. et al. Geographic distribution and developmental websites of Aedes albopictus (Diptera: Culicidae) throughout a chikungunya epidemic occasion. Vector-Borne Zoon. Dis. 8, 25–34 (2008).
Hamon, J. Etudes biologique et systématique des Culicinae de l’Ile de La Réunion. Mem. Inst. Scient. Madagascar 4, 521–541 (1953).
Bouyer, J. & Lefrançois, T. Boosting the sterile insect method to regulate mosquitoes. Tendencies Parasitol. 30, 271–273 (2014).
Haramboure, M. et al. Modelling the management of Aedes albopictus mosquitoes primarily based on sterile males launch methods in a tropical setting. Ecol. Mannequin. 424, 109002 (2020).
Bouyer, J., Yamada, H., Pereira, R., Bourtzis, Ok. & Vreysen, M. J. B. Phased conditional method for mosquito administration utilizing sterile insect method. Tendencies Parasitol. 36, 325–336 (2020).
Bouyer, J. & Vreysen, M. J. B. Sure, irradiated sterile male mosquitoes will be sexually aggressive!. Tendencies Parasitol. 36, 877–880 (2020).
Group, W. H. Pointers for laboratory and subject testing of mosquito larvicides. WHO/CDS/WHOPES/GCDPP/2005.13 (2005).
World Well being Group and Particular Programme for Analysis and Coaching in Tropical Ailments and World Well being Group. Division of Management of Uncared for Tropical Ailments and World Well being Group. Epidemic and Pandemic Alert. Dengue: Pointers for analysis, therapy, prevention and management. (World Well being Group, 2009).
Yap, H. H. Preliminary report on the colour choice for oviposition by Aedes albopictus (Skuse) within the subject. Southeast Asian J. Trop. Med. Public Well being 6, 1–2 (1975).
Yap, H. H., Lee, C. Y., Chong, N. L., Foo, A. E. S. & Lim, M. P. Oviposition website choice of Aedes albopictus within the laboratory. J. Am. Mosquito Management Assoc. Mosquito Information 11, 128–132 (1995).
Marin, G., Mahiba, B., Arivoli, S. & Tennyson, S. Does color of ovitrap affect the ovipositional choice of Aedes aegypti Linnaeus 1762 (Diptera: Culicidae). Int. J. Mosq. Res 7, 11–15 (2020).
Claudel, I. et al. To bait or to not bait? Optimizing the usage of grownup mosquito traps for monitoring arbovirus vector populations in La Réunion Island. (2022). https://doi.org/10.21203/rs.3.rs-1798972/v1.
Cleveland, W. S. Visualizing information. (Hobart press, 1993).
Lamigueiro, Ó. P. Displaying time collection, spatial, and space-time information with R. (Chapman; Corridor/CRC, 2018).
Yoshioka, M. et al. Weight-reduction plan and density dependent competitors have an effect on larval efficiency and oviposition website choice within the mosquito species Aedes albopictus (Diptera: Culicidae). Parasites Vectors 5, (2012).
Wong, J., Stoddard, S. T., Astete, H., Morrison, A. C. & Scott, T. W. Oviposition website choice by the dengue vector Aedes aegypti and its implications for dengue management. PLoS Negl. Trop. Dis. 5, e1015 (2011).
Hawley, W. A. The biology of aedes albopictus. J. Am. Mosquito Management Assoc. Suppl 1, 1–39 (1988).
Delatte, H., Gimonneau, G., Triboire, A. & Fontenille, D. Affect of temperature on immature improvement, survival, longevity, fecundity, and gonotrophic cycles of Aedes albopictus, vector of Chikungunya and dengue within the Indian Ocean. J. Med. Entomol. 46, 33–41 (2009).
Daugherty, M. P., Alto, B. W. & Juliano, S. A. Invertebrate carcasses as a useful resource for competing Aedes albopictus and Aedes aegypti (Diptera: Culicidae). J. Med. Entomol. 37, 364–372 (2000).
Papaj, D. R. & Rausher, M. D. Particular person variation in host location by phytophagous bugs. Herbivorous Bugs: Host searching for conduct and mechanisms 77–127 (1983).
Valladares, G. & Lawton, J. H. Host-plant choice within the holly leaf-miner: Does mom know finest?. J. Anim. Ecol. 60, 227 (1991).
Ellis, A. M. Incorporating density dependence into the oviposition preference-offspring efficiency speculation. J. Anim. Ecol. 77, 247–256 (2008).
Juliano, S. A., OMeara, G. F., Morrill, J. R. & Cutwa, M. M. Desiccation and thermal tolerance of eggs and the coexistence of competing mosquitoes. Oecologia 130, 458–469 (2002).
Costanzo, Ok. S., Kesavaraju, B. & Juliano, S. A. Situation-specific competion in container mosquitoes: The function of non-competing life-history levels. Ecology 86, 3289–3295 (2005).
Sanchez, M. & Probst, J.-M. Distribution and conservation standing of the Manapany day gecko, Phelsuma inexpectata MERTENS, 1966, an endemic threatened reptile from Réunion Island (Squamata: Gekkonidae). Cahiers scientifiques de l’océan Indien occidental 2, (2011).
Braks, M. A. H., Honório, N. A., Lounibos, L. P., De-Oliveira, R. L. & Juliano, S. A. Interspecific competitors between two invasive species of container mosquitoes, Aedes aegypti and Aedes albopictus (Diptera: Culicidae), in Brazil. Ann. Entomol. Soc. Am. 97, 130–139 (2004).
Moore, C. G. & Fisher, B. R. Competitors in mosquitoes.1 Density and species ratio results on progress, mortality, fecundity, and manufacturing of progress retardant2. Ann. Entomol. Soc. Am. 62, 1325–1331 (1969).
Madeira, N. G., Macharelli, C. A. & Carvalho, L. R. Variation of the Oviposition Preferences of Aedes aegypti in Perform of Substratum and Humidity. Mem. Inst. Oswaldo Cruz 97, 415–420 (2002).
Bellini, R. et al. Use of the sterile insect method towards Aedes albopictus in Italy: first outcomes of a pilot trial. in Space-wide management of insect pests 505–515 (Springer, 2007).
Boussès, P., Dehecq, J. S., Brengues, C. & Fontenille, D. Inventaire actualisé des moustiques (Diptera : Culicidae) de l’île de La Réunion, océan Indien. Bulletin de la Société de pathologie exotique 106, 113–125 (2013).
Zeileis, A., Kleiber, C. & Jackman, S. Regression fashions for rely information in R. J. Stat. Softw. 27, (2008).
Sileshi, G. Deciding on the best statistical mannequin for evaluation of insect rely information through the use of data theoretic measures. Bull. Entomol. Res. 96, 479–488 (2006).
Guthery, F. S., Burnham, Ok. P. & Anderson, D. R. Mannequin choice and multimodel inference: A sensible information-theoretic method. J. Wildl. Manag. 67, 655 (2003).
Hurvich, C. M. & Tsai, C.-L. Mannequin choice for prolonged quasi-likelihood fashions in small samples. Biometrics 51, 1077–1084 (1995).
Burnham, Ok. P. & Anderson, D. R. Mannequin choice and multimodel inference: a sensible information-theoretic method. 496 (Springer-Verlag, 2002).
Manly, B. F. J. Randomization, bootstrap and Monte Carlo strategies in biology. 399 (CRC Press / Chapman & Corridor, 2006). https://doi.org/10.1201/9781315273075.
Holm, S. A easy sequentially rejective a number of take a look at process. Scand. J. Stat. 65–70 (1979).
R Core Crew. R: A Language and Surroundings for Statistical Computing. (R Basis for Statistical Computing, 2022).
Lesnoff, M. & Lancelot, R. aods3: evaluation of overdispersed information utilizing S3 strategies. (2018).
Barton, Ok. MuMIn: Multi-Mannequin Inference. (2022).
Xie, Y., Dervieux, C. & Riederer, E. R Markdown Cookbook. (Chapman; Corridor/CRC, 2020). https://doi.org/10.1201/9781003097471.
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