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Oviposition signals and their neuroethological correlates in the Culex pipiens complex
Institution:1. Eck Institute for Global Health & Department of Biological Sciences, University of Notre Dame, Notre Dame, IN 46556, USA;2. Center for Research Computing, University of Notre Dame, Notre Dame, IN 46556, USA;1. Institut Pasteur de Tunis, Laboratory of Vector Ecology, 13 Place Pasteur, 1002 Tunis, Tunisia;2. Public Health England, Porton Down, Salisbury, Wiltshire SP4 0JG, UK;3. Department of Public Health Sciences, University of Miami Miller School of Medicine, Miami, FL 33136, USA;1. Faculty of Integrated Human Studies, Kyoto University, Kyoto 606-8501, Japan;2. Medical Mycology Research Center, Chiba University, Chiba, Japan;3. Graduate School of Human and Environmental Studies, Kyoto University, Kyoto, Japan;4. Graduate School of Agriculture, Kyoto University, Kyoto, Japan;1. Laboratory of Chemistry and Physics Multi-scale Approach of Complex Environments, Lorraine University, 1 Bd Arago, 57078 Metz, France;2. Unit Research Animal and Functionality of Animal Products, Lorraine University, 1 Bd Arago, 57078 Metz, France;3. National Institute for Research in Rural Engineering Water and Forestry, BP N10, Ariana 2080, Tunisia;4. Faculty of Sciences of Bizerta, Carthage University, Jarzouna, 7021 Bizerta, Tunisia;1. Department of Vector Biology, Liverpool School of Tropical Medicine, Liverpool L3 5QA, UK;2. Institut Régional de Santé Publique/Université d’Abomey–Calavi, Ouidah, Benin
Abstract:Mosquitoes in the Culex pipiens complex (Diptera: Culicidae), especially Cx. pipiens and Culex quinquefasciatus, have successfully exploited the rapid growth of the human population and globalization to their advantage by successfully utilizing man-made habitats, particularly for oviposition. Culex spp. lay over 100 eggs together in a raft. Each egg in the raft produces an apical droplet containing an oviposition attractant, erythro-6-acetoxy-5-hexadecanolide, commonly referred to as Mosquito Oviposition Pheromone (MOP). Here we present a detailed gas chromatography–mass spectrometry (GC–MS) analysis of the apical droplets from six populations that revealed MOP as the most abundant constituent. Subjecting MOP and the remaining 17 most abundant chemical constituents of the droplets from these populations to a Principal Component Analysis (PCA) resolved the populations into two distinct clusters that contained two populations each of Cx. quinquefasciatus and Culex pipiens molestus. The two Culex pipiens pipiens, however, did not resolve into a single cluster, with the Shasta population sorting closer to Cx. quinquefasciatus. Comparing the PCA scores with the genetic evidence from adult females using available molecular markers that have earlier shown to sort various Culex forms, we found that the molecular data support the PCA clustering pattern. Behavioral investigation of the droplet-induced attraction tested in gravid Cx. quinquefasciatus elicited various degrees of oviposition to the droplets from each population. Overall, droplets from all six populations induced higher attraction compared to controls. A detailed time-course analysis of droplet composition in Cx. quinquefasciatus from 6 to 54 h post egg-laying identified MOP again as the main constituent. Finally, our electrophysiological investigation identified MOP as the only biologically active constituent from of the droplets eliciting responses from female antennae. These studies will aid in global efforts to understand the vector biology and evolution that can be exploited to develop novel vector management strategies.
Keywords:Apical egg droplet chemistry  MOP  GC-EAD  Oviposition behavior  Molecular identification
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