{"id":1074705,"date":"2022-05-25T04:56:11","date_gmt":"2022-05-25T08:56:11","guid":{"rendered":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/uncategorized\/insecticide-resistant-anopheles-gambiae-have-enhanced-longevity-but-reduced-reproductive-fitness-and-a-longer-first-gonotrophic-cycle-scientific\/"},"modified":"2022-05-25T04:56:11","modified_gmt":"2022-05-25T08:56:11","slug":"insecticide-resistant-anopheles-gambiae-have-enhanced-longevity-but-reduced-reproductive-fitness-and-a-longer-first-gonotrophic-cycle-scientific","status":"publish","type":"post","link":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-longevity\/insecticide-resistant-anopheles-gambiae-have-enhanced-longevity-but-reduced-reproductive-fitness-and-a-longer-first-gonotrophic-cycle-scientific\/","title":{"rendered":"Insecticide resistant Anopheles gambiae have enhanced longevity but reduced reproductive fitness and a longer first gonotrophic cycle | Scientific&#8230;"},"content":{"rendered":"<p><p>WHO. World malaria report 2020: 20 years of global progress and challenges. (2020).<\/p>\n<p>Ranson, H. et al. Pyrethroid resistance in African anopheline mosquitoes: What are the implications for malaria control? Trends Parasitol 27. <a href=\"https:\/\/doi.org\/10.1016\/j.pt.2010.08.004\" rel=\"nofollow\">https:\/\/doi.org\/10.1016\/j.pt.2010.08.004<\/a> (2011).<\/p>\n<p>Hemingway, J. & Ranson, H. Insecticide resistance in insect vectors of human disease. Annu. Rev. Entomol. 45, 371391 (2000).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Alout, H., Roche, B., Dabir, R. K. & Cohuet, A. Consequences of insecticide resistance on malaria transmission. PLoS Pathog. 13, e1006499 (2017).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Afrane, Y. A., Zhou, G., Lawson, B. W., Githeko, A. K. & Yan, G. Effects of microclimatic changes due to deforestation on the survivorship and reproductive fitness of anopheles gambiae in Western Kenya Highlands. . Am. J. Trop. Med. Hyg. 74, 772778 (2006).<\/p>\n<p>Lardeux, F. J., Tejerina, R. H., Quispe, V. & Chavez, T. K. A physiological time analysis of the duration of the gonotrophic cycle of Anopheles pseudopunctipennis and its implications for malaria transmission in Bolivia. Malar. J. 7, 117 (2008).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Afrane, Y. A., Little, T. J., Lawson, B. W., Githeko, A. K. & Yan, G. Deforestation increases the vectorial capacity of anopheles gambiae giles to transmit Malaria in the Western Kenya Highlands. Emerg. Infect. Dis. 10, 15331538 (2008).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Alout, H., Roche, B., Dabir, R. K. & Cohuet, A. J. P. p. Consequences of insecticide resistance on malaria transmission. 13, e1006499 (2017).<\/p>\n<p>Vzilier, J., Nicot, A., Gandon, S. & Rivero, A. J. P. o. t. R. S. B. B. S. Plasmodium infection decreases fecundity and increases survival of mosquitoes. 279, 40334041 (2012).<\/p>\n<p>McCarroll, L., Hemingway, J. J. I. b. & biology, m. Can insecticide resistance status affect parasite transmission in mosquitoes? 32, 1345 (2002).<\/p>\n<p>Platt, N. et al. Target-site resistance mutations (kdr and RDL), but not metabolic resistance, negatively impact male mating competiveness in the malaria vector Anopheles gambiae. 115, 243252 (2015).<\/p>\n<p>Nouage, L. et al. Influence of GST-and P450-based metabolic resistance to pyrethroids on blood feeding in the major African malaria vector Anopheles funestus. (2020).<\/p>\n<p>Rigby, L. M. et al. Identifying the fitness costs of a pyrethroid-resistant genotype in the major arboviral vector Aedes aegypti. 13, 112 (2020).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Tchouakui, M. et al. Fitness costs of the glutathione S-transferase epsilon 2 (L119F-GSTe2) mediated metabolic resistance to insecticides in the major African malaria vector Anopheles funestus. 9, 645 (2018).<\/p>\n<p>Kumar, S. et al. Diminished reproductive fitness associated with the deltamethrin resistance in an Indian strain of dengue vector mosquito. Aedes aegypti L. 26, 5564 (2009).<\/p>\n<p>                    Google Scholar                <\/p>\n<p>Nkahe, D. L. et al. Fitness cost of insecticide resistance on the life-traits of a Anopheles coluzzii population from the city of Yaound. Cameroon. 5, 171. <a href=\"https:\/\/doi.org\/10.12688\/wellcomeopenres.16039.2\" rel=\"nofollow\">https:\/\/doi.org\/10.12688\/wellcomeopenres.16039.2<\/a> (2020).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Machani, M. G. et al. Phenotypic, genotypic and biochemical changes during pyrethroid resistance selection in Anopheles gambiae mosquitoes. Sci. Rep. 10, 19063. <a href=\"https:\/\/doi.org\/10.1038\/s41598-020-75865-1\" rel=\"nofollow\">https:\/\/doi.org\/10.1038\/s41598-020-75865-1<\/a> (2020).<\/p>\n<p>CAS    Article    PubMed    PubMed Central                        Google Scholar                <\/p>\n<p>WHO. World Malaria Report 2016. Geneva: World Health Organization (2016).<\/p>\n<p>Shute, G. T. A method of maintaining colonies of east african strains of anopheles gambiae. Ann. Trop. Med. Parasitol. 50, 9294. <a href=\"https:\/\/doi.org\/10.1080\/00034983.1956.11685743\" rel=\"nofollow\">https:\/\/doi.org\/10.1080\/00034983.1956.11685743<\/a> (1956).<\/p>\n<p>CAS    Article    PubMed                        Google Scholar                <\/p>\n<p>Knols, B. G. et al. MalariaSphere: A greenhouse-enclosed simulation of a natural Anopheles gambiae (Diptera: Culicidae) ecosystem in western Kenya. Malar. J. 1, 19 (2002).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Afrane, Y. A., Zhou, G., Lawson, B. W., Githeko, A. K. & Yan, G. Life-table analysis of Anopheles arabiensis in western Kenya highlands: Effects of land covers on larval and adult survivorship. Am. J. Trop. Med. Hyg. 77, 660666 (2007).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Ranson, H. & Lissenden, N. Insecticide resistance in African Anopheles mosquitoes: A worsening situation that needs urgent action to mantain malaria control. Parasites Vectors 32, 187196 (2016).<\/p>\n<p>CAS                        Google Scholar                <\/p>\n<p>Klowden, M. J. & Briegel, H. Mosquito gonotrophic cycle and multiple feeding potential: Contrasts between Anopheles and Aedes (Diptera: Culicidae). J. Med. Entomol. 31, 618622 (1994).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Mebrahtu, Y. B., Norem, J. & Taylor, M. Inheritance of larval resistance to permethrin in Aedes aegypti and association with sex ratio distortion and life history variation. Am. J. Trop. Med. Hyg. 56, 456465 (1997).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Ma, Z., Gulia-Nuss, M., Zhang, X. & Brown, M. R. Effects of the botanical insecticide, Toosendanin, on blood digestion and egg production by female Aedes aegypti (Diptera: Culicidae): topical application and ingestion. J. Med. Entomol. 50, 112121 (2013).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Gulia-Nuss, M., Robertson, A. E., Brown, M. R. & Strand, M. R. Insulin-like peptides and the target of rapamycin pathway coordinately regulate blood digestion and egg maturation in the mosquito Aedes aegypti. PLoS ONE 6, e20401 (2011).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Martins, A. J., Bellinato, D. F., Peixoto, A. A., Valle, D. & Lima, J. B. P. Effect of insecticide resistance on development, longevity and reproduction of field or laboratory selected Aedes aegypti populations. PLoS ONE 7, e31889 (2012).<\/p>\n<p>CAS    Article                        Google Scholar                <\/p>\n<p>Sy, F. A., Faye, O., Diallo, M. & Dia, I. Effects of insecticide resistance on the reproductive potential of two sub-strains of the malaria vector Anopheles coluzzii. J. Vector Borne Dis. 56, 207211. <a href=\"https:\/\/doi.org\/10.4103\/0972-9062.289401\" rel=\"nofollow\">https:\/\/doi.org\/10.4103\/0972-9062.289401<\/a> (2019).<\/p>\n<p>CAS    Article    PubMed                        Google Scholar                <\/p>\n<p>de Oliveira, C. D., Tadei, W. P., Abdalla, F. C., Paolucci Pimenta, P. F. & Marinotti, O. Multiple blood meals in Anopheles darlingi (Diptera: Culicidae). J. Vector Ecol. 37, 351358 (2012).<\/p>\n<p>Norris, L. C., Fornadel, C. M., Hung, W.-C., Pineda, F. J. & Norris, D. E. Frequency of multiple blood meals taken in a single gonotrophic cycle by Anopheles arabiensis mosquitoes in Macha, Zambia. Am. J. Trop. Med. Hyg. 83, 33 (2010).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Oliver, S. V. & Brooke, B. D. The effect of multiple blood-feeding on the longevity and insecticide resistant phenotype in the major malaria vector Anopheles arabiensis (Diptera: Culicidae). Parasit. Vectors 7, 112 (2014).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Lardeux, F., Loayza, P., Bouchit, B. & Chavez, T. Host choice and human blood index of Anopheles pseudopunctipennis in a village of the Andean valleys of Bolivia. Malar. J. 6, 114 (2007).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Farjana, T. & Tuno, N. Multiple blood feeding and host-seeking behavior in Aedes aegypti and Aedes albopictus (Diptera: Culicidae). J. Med. Entomol. 50, 838846 (2013).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Osoro, J. K. et al. Insecticide resistance exerts significant fitness costs in immature stages of Anopheles gambiae in western Kenya. Malar. J. 20, 17 (2021).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Telang, A., Frame, L. & Brown, M. R. Larval feeding duration affects ecdysteroid levels and nutritional reserves regulating pupal commitment in the yellow fever mosquito Aedes aegypti (Diptera: Culicidae). J. Exp. Biol. 210, 854864. <a href=\"https:\/\/doi.org\/10.1242\/jeb.02715\" rel=\"nofollow\">https:\/\/doi.org\/10.1242\/jeb.02715<\/a> (2007).<\/p>\n<p>Article    PubMed                        Google Scholar                <\/p>\n<p>Belinato, T. A., Martins, A. J. & Valle, D. Fitness evaluation of two Brazilian Aedes aegypti field populations with distinct levels of resistance to the organophosphate temephos. Mem. Inst. Oswaldo Cruz 107, 916922 (2012).<\/p>\n<p>Article                        Google Scholar                <\/p>\n<p>Brito, L. P. et al. Assessing the effects of Aedes aegypti kdr mutations on pyrethroid resistance and its fitness cost. PLoS ONE 8, e60878 (2013).<\/p>\n<p>MathSciNet    CAS    Article                        Google Scholar                <\/p>\n<p><!-- Auto Generated --><\/p>\n<p>Continue reading here:<br \/>\n<a target=\"_blank\" href=\"https:\/\/www.nature.com\/articles\/s41598-022-12753-w\" title=\"Insecticide resistant Anopheles gambiae have enhanced longevity but reduced reproductive fitness and a longer first gonotrophic cycle | Scientific...\" rel=\"noopener\">Insecticide resistant Anopheles gambiae have enhanced longevity but reduced reproductive fitness and a longer first gonotrophic cycle | Scientific...<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"<p> WHO. World malaria report 2020: 20 years of global progress and challenges <a href=\"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/transhuman-news-blog\/human-longevity\/insecticide-resistant-anopheles-gambiae-have-enhanced-longevity-but-reduced-reproductive-fitness-and-a-longer-first-gonotrophic-cycle-scientific\/\">Continue reading <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":9,"featured_media":0,"comment_status":"closed","ping_status":"closed","sticky":false,"template":"","format":"standard","meta":{"footnotes":""},"categories":[24],"tags":[],"class_list":["post-1074705","post","type-post","status-publish","format-standard","hentry","category-human-longevity"],"_links":{"self":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1074705"}],"collection":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts"}],"about":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/types\/post"}],"author":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/users\/9"}],"replies":[{"embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/comments?post=1074705"}],"version-history":[{"count":0,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/posts\/1074705\/revisions"}],"wp:attachment":[{"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/media?parent=1074705"}],"wp:term":[{"taxonomy":"category","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/categories?post=1074705"},{"taxonomy":"post_tag","embeddable":true,"href":"https:\/\/www.euvolution.com\/prometheism-transhumanism-posthumanism\/wp-json\/wp\/v2\/tags?post=1074705"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}