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      Meta-Analysis of Aedes aegypti Expression Datasets: Comparing Virus Infection and Blood-Fed Transcriptomes to Identify Markers of Virus Presence

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          Abstract

          The mosquito Aedes aegypti (L.) is vector of several arboviruses including dengue, yellow fever, chikungunya, and more recently zika. Previous transcriptomic studies have been performed to elucidate altered pathways in response to viral infection. However, the intrinsic coupling between alimentation and infection were unappreciated in these studies. Feeding is required for the initial mosquito contact with the virus and these events are highly dependent. Addressing this relationship, we reinterrogated datasets of virus-infected mosquitoes with two different diet schemes (fed and unfed mosquitoes), evaluating the metabolic cross-talk during both processes. We constructed coexpression networks with the differentially expressed genes of these comparison: virus-infected versus blood-fed mosquitoes and virus-infected versus unfed mosquitoes. Our analysis identified one module with 110 genes that correlated with infection status (representing ~0.7% of the A. aegypti genome). Furthermore, we performed a machine-learning approach and summarized the infection status using only four genes (AAEL012128, AAEL014210, AAEL002477, and AAEL005350). While three of the four genes were annotated as hypothetical proteins, AAEL012128 gene is a membrane amino acid transporter correlated with viral envelope binding. This gene alone is able to discriminate all infected samples and thus should have a key role to discriminate viral infection in the A. aegypti mosquito. Moreover, validation using external datasets found this gene as differentially expressed in four transcriptomic experiments. Therefore, these genes may serve as a proxy of viral infection in the mosquito and the others 106 identified genes provides a framework to future studies.

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          Most cited references40

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          First report of autochthonous transmission of Zika virus in Brazil

          In the early 2015, several cases of patients presenting symptoms of mild fever, rash, conjunctivitis and arthralgia were reported in the northeastern Brazil. Although all patients lived in a dengue endemic area, molecular and serological diagnosis for dengue resulted negative. Chikungunya virus infection was also discarded. Subsequently, Zika virus (ZIKV) was detected by reverse transcription-polymerase chain reaction from the sera of eight patients and the result was confirmed by DNA sequencing. Phylogenetic analysis suggests that the ZIKV identified belongs to the Asian clade. This is the first report of ZIKV infection in Brazil.
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            Fast R Functions for Robust Correlations and Hierarchical Clustering.

            Many high-throughput biological data analyses require the calculation of large correlation matrices and/or clustering of a large number of objects. The standard R function for calculating Pearson correlation can handle calculations without missing values efficiently, but is inefficient when applied to data sets with a relatively small number of missing data. We present an implementation of Pearson correlation calculation that can lead to substantial speedup on data with relatively small number of missing entries. Further, we parallelize all calculations and thus achieve further speedup on systems where parallel processing is available. A robust correlation measure, the biweight midcorrelation, is implemented in a similar manner and provides comparable speed. The functions cor and bicor for fast Pearson and biweight midcorrelation, respectively, are part of the updated, freely available R package WGCNA.The hierarchical clustering algorithm implemented in R function hclust is an order n(3) (n is the number of clustered objects) version of a publicly available clustering algorithm (Murtagh 2012). We present the package flashClust that implements the original algorithm which in practice achieves order approximately n(2), leading to substantial time savings when clustering large data sets.
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              An evolutionary conserved function of the JAK-STAT pathway in anti-dengue defense.

              Here, we show that the major mosquito vector for dengue virus uses the JAK-STAT pathway to control virus infection. Dengue virus infection in Aedes aegypti mosquitoes activates the JAK-STAT immune signaling pathway. The mosquito's susceptibility to dengue virus infection increases when the JAK-STAT pathway is suppressed through RNAi depletion of its receptor Domeless (Dome) and the Janus kinase (Hop), whereas mosquitoes become more resistant to the virus when the negative regulator of the JAK-STAT pathway, PIAS, is silenced. The JAK-STAT pathway exerts its anti-dengue activity presumably through one or several STAT-regulated effectors. We have identified, and partially characterized, two JAK-STAT pathway-regulated and infection-responsive dengue virus restriction factors (DVRFs) that contain putative STAT-binding sites in their promoter regions. Our data suggest that the JAK-STAT pathway is part of the A. aegypti mosquito's anti-dengue defense and may act independently of the Toll pathway and the RNAi-mediated antiviral defenses.
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                Author and article information

                Contributors
                URI : http://frontiersin.org/people/u/462651
                URI : http://frontiersin.org/people/u/495451
                URI : http://frontiersin.org/people/u/488980
                URI : http://frontiersin.org/people/u/137460
                URI : http://frontiersin.org/people/u/44277
                URI : http://frontiersin.org/people/u/484625
                URI : http://frontiersin.org/people/u/486089
                Journal
                Front Bioeng Biotechnol
                Front Bioeng Biotechnol
                Front. Bioeng. Biotechnol.
                Frontiers in Bioengineering and Biotechnology
                Frontiers Media S.A.
                2296-4185
                11 January 2018
                2017
                : 5
                : 84
                Affiliations
                [1] 1Instituto Gonçalo Moniz, Fundação Oswaldo Cruz (FIOCRUZ) , Salvador, Brazil
                [2] 2Post-Graduation Program in Biotechnology in Health and Investigative Medicine, Fundação Oswaldo Cruz (FIOCRUZ) , Salvador, Brazil
                [3] 3Federal University of Technology—Paraná, UTFPR, Campus Cornélio Procópio , Cornélio Procópio, Brazil
                [4] 4Federal University of Uberlândia , Patos de Minas, Brazil
                [5] 5Post-Graduation Program in Health Sciences, School of Medicine, Federal University of Bahia , Salvador, Brazil
                [6] 6Post-Graduation Program in Applied Computation, Universida de Estadual de Feira de Santana , Feira de Santana, Brazil
                Author notes

                Edited by: Diana Elizabeth Marco, National Scientific Council (CONICET), Argentina

                Reviewed by: Xianwen Ren, Peking University, China; Anna Honko, Data Sciences International, United States

                *Correspondence: Kiyoshi Ferreira Fukutani, ferreirafk@ 123456gmail.com ; Artur Trancoso Lopo de Queiroz, artur.queiroz@ 123456bahia.fiocruz.br

                Present address: Kiyoshi Ferreira Fukutani, Department of Biochemistry and Immunology, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, São Paulo, Brazil

                These authors have contributed equally to the work.

                §These authors are co-first author’s.

                Specialty section: This article was submitted to Bioinformatics and Computational Biology, a section of the journal Frontiers in Bioengineering and Biotechnology

                Article
                10.3389/fbioe.2017.00084
                5768613
                29376049
                bc89dc28-6830-4535-affd-a2f64bb4c5e5
                Copyright © 2018 Fukutani, Kasprzykowski, Paschoal, Gomes, Barral, de Oliveira, Ramos and Queiroz.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 23 October 2017
                : 15 December 2017
                Page count
                Figures: 7, Tables: 1, Equations: 0, References: 57, Pages: 13, Words: 8466
                Funding
                Funded by: Fundação de Amparo à Pesquisa do Estado da Bahia 10.13039/501100006181
                Award ID: JCB0004/2013
                Funded by: Fundação de Amparo à Pesquisa do Estado de São Paulo 10.13039/501100001807
                Award ID: 2017/03491-6
                Funded by: Conselho Nacional de Desenvolvimento Científico e Tecnológico 10.13039/501100003593
                Award ID: 454505/2014-0
                Categories
                Bioengineering and Biotechnology
                Original Research

                aedes aegypti,alimentation,blood-feeding,meta-analysis,transcriptomics,vector-borne diseases,virus infection

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