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      Identifying genomic changes associated with insecticide resistance in the dengue mosquito Aedes aegypti by deep targeted sequencing

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          Abstract

          The capacity of mosquitoes to resist insecticides threatens the control of diseases such as dengue and malaria. Until alternative control tools are implemented, characterizing resistance mechanisms is crucial for managing resistance in natural populations. Insecticide biodegradation by detoxification enzymes is a common resistance mechanism; however, the genomic changes underlying this mechanism have rarely been identified, precluding individual resistance genotyping. In particular, the role of copy number variations (CNVs) and polymorphisms of detoxification enzymes have never been investigated at the genome level, although they can represent robust markers of metabolic resistance. In this context, we combined target enrichment with high-throughput sequencing for conducting the first comprehensive screening of gene amplifications and polymorphisms associated with insecticide resistance in mosquitoes. More than 760 candidate genes were captured and deep sequenced in several populations of the dengue mosquito Ae. aegypti displaying distinct genetic backgrounds and contrasted resistance levels to the insecticide deltamethrin. CNV analysis identified 41 gene amplifications associated with resistance, most affecting cytochrome P450s overtranscribed in resistant populations. Polymorphism analysis detected more than 30,000 variants and strong selection footprints in specific genomic regions. Combining Bayesian and allele frequency filtering approaches identified 55 nonsynonymous variants strongly associated with resistance. Both CNVs and polymorphisms were conserved within regions but differed across continents, confirming that genomic changes underlying metabolic resistance to insecticides are not universal. By identifying novel DNA markers of insecticide resistance, this study opens the way for tracking down metabolic changes developed by mosquitoes to resist insecticides within and among populations.

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          Most cited references81

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          Trimmomatic: a flexible trimmer for Illumina sequence data

          Motivation: Although many next-generation sequencing (NGS) read preprocessing tools already existed, we could not find any tool or combination of tools that met our requirements in terms of flexibility, correct handling of paired-end data and high performance. We have developed Trimmomatic as a more flexible and efficient preprocessing tool, which could correctly handle paired-end data. Results: The value of NGS read preprocessing is demonstrated for both reference-based and reference-free tasks. Trimmomatic is shown to produce output that is at least competitive with, and in many cases superior to, that produced by other tools, in all scenarios tested. Availability and implementation: Trimmomatic is licensed under GPL V3. It is cross-platform (Java 1.5+ required) and available at http://www.usadellab.org/cms/index.php?page=trimmomatic Contact: usadel@bio1.rwth-aachen.de Supplementary information: Supplementary data are available at Bioinformatics online.
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            Fast and accurate short read alignment with Burrows–Wheeler transform

            Motivation: The enormous amount of short reads generated by the new DNA sequencing technologies call for the development of fast and accurate read alignment programs. A first generation of hash table-based methods has been developed, including MAQ, which is accurate, feature rich and fast enough to align short reads from a single individual. However, MAQ does not support gapped alignment for single-end reads, which makes it unsuitable for alignment of longer reads where indels may occur frequently. The speed of MAQ is also a concern when the alignment is scaled up to the resequencing of hundreds of individuals. Results: We implemented Burrows-Wheeler Alignment tool (BWA), a new read alignment package that is based on backward search with Burrows–Wheeler Transform (BWT), to efficiently align short sequencing reads against a large reference sequence such as the human genome, allowing mismatches and gaps. BWA supports both base space reads, e.g. from Illumina sequencing machines, and color space reads from AB SOLiD machines. Evaluations on both simulated and real data suggest that BWA is ∼10–20× faster than MAQ, while achieving similar accuracy. In addition, BWA outputs alignment in the new standard SAM (Sequence Alignment/Map) format. Variant calling and other downstream analyses after the alignment can be achieved with the open source SAMtools software package. Availability: http://maq.sourceforge.net Contact: rd@sanger.ac.uk
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              A new mathematical model for relative quantification in real-time RT-PCR.

              M. Pfaffl (2001)
              Use of the real-time polymerase chain reaction (PCR) to amplify cDNA products reverse transcribed from mRNA is on the way to becoming a routine tool in molecular biology to study low abundance gene expression. Real-time PCR is easy to perform, provides the necessary accuracy and produces reliable as well as rapid quantification results. But accurate quantification of nucleic acids requires a reproducible methodology and an adequate mathematical model for data analysis. This study enters into the particular topics of the relative quantification in real-time RT-PCR of a target gene transcript in comparison to a reference gene transcript. Therefore, a new mathematical model is presented. The relative expression ratio is calculated only from the real-time PCR efficiencies and the crossing point deviation of an unknown sample versus a control. This model needs no calibration curve. Control levels were included in the model to standardise each reaction run with respect to RNA integrity, sample loading and inter-PCR variations. High accuracy and reproducibility (<2.5% variation) were reached in LightCycler PCR using the established mathematical model.
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                Author and article information

                Journal
                Genome Res
                Genome Res
                genome
                genome
                GENOME
                Genome Research
                Cold Spring Harbor Laboratory Press
                1088-9051
                1549-5469
                September 2015
                September 2015
                : 25
                : 9
                : 1347-1359
                Affiliations
                [1 ]Laboratoire d'Ecologie Alpine (LECA), CNRS, UMR 5553, 38041 Grenoble Cedex 9, France;
                [2 ]Université Grenoble–Alpes, 38041 Grenoble Cedex 9, France;
                [3 ]Environmental and Systems Biology (BEeSy), Université Grenoble–Alpes, 38041 Grenoble Cedex 9, France;
                [4 ]Unité d'Entomologie Médicale, Institut Pasteur de la Guyane, 97306 Cayenne Cedex, France;
                [5 ]Pôle Rhône Alpes de Bioinformatique, Université Lyon 1, 69100 Villeurbanne, France;
                [6 ]Institut de Recherche pour le Développement (IRD), Maladies Infectieuses et Vecteurs, Ecologie, Génétique, Evolution et Contrôle (IRD 224-CNRS 5290 UM1-UM2), 34394 Montpellier Cedex 5, France;
                [7 ]Department of Entomology, Faculty of Agriculture, Kasetsart University, Lat Yao Chatuchak Bangkok 10900, Thailand;
                [8 ]Center for Advanced Studies for Agriculture and Food, Kasetsart University Institute for Advanced Studies, Kasetsart University, Bangkok 10900, Thailand (CASAF, NRU-KU, Thailand);
                [9 ]Bureau of Vector Borne Diseases, Department of Disease Control, Ministry of Public Health, Mueang, Nonthaburi 11000, Thailand;
                [10 ]Vector Biology Group, Liverpool School of Tropical Medicine, L35QA Liverpool, United Kingdom
                Author notes
                Article
                9509184
                10.1101/gr.189225.115
                4561493
                26206155
                6f8ee8f1-c16c-49a0-a590-b9bb69639bea
                © 2015 Faucon et al.; Published by Cold Spring Harbor Laboratory Press

                This article, published in Genome Research, is available under a Creative Commons License (Attribution-NonCommercial 4.0 International), as described at http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 5 January 2015
                : 30 June 2015
                Page count
                Pages: 13
                Funding
                Funded by: Centre National de la Recherche Scientifique (CNRS) http://dx.doi.org/10.13039/501100004794
                Award ID: APEGE 2013
                Funded by: French Institut de Microbiologie et Maladies Infectieuses
                Award ID: IMMI 109764
                Funded by: Grenoble-Alpes University
                Funded by: Center for Advanced Studies for Agriculture and Food, Institute for Advanced Studies, Kasetsart University
                Funded by: Thailand Research Fund http://dx.doi.org/10.13039/501100004396
                Award ID: 5558002
                Award ID: 5380102
                Funded by: Kasetsart University Research and Development Institute (KURDI) http://dx.doi.org/10.13039/501100005621
                Categories
                Research

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