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      Characterization of antennal sensilla, larvae morphology and olfactory genes of Melipona scutellaris stingless bee

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          Abstract

          There is growing evidence in the literature suggesting that caste differentiation in the stingless bee, Melipona scutellaris, and other bees in the genus Melipona, is triggered by environmental signals, particularly a primer pheromone. With the proper amount of food and a chemical stimulus, 25% of females emerge as queens, in agreement with a long-standing “two loci/two alleles model” proposed in the 1950s. We surmised that these larvae must be equipped with an olfactory system for reception of these chemical signals. Here we describe for the first time the diversity of antennal sensilla in adults and the morphology of larvae of M. scutellaris. Having found evidence for putative olfactory sensilla in larvae, we next asked whether olfactory proteins were expressed in larvae. Since the molecular basis of M. scutellaris is still unknown, we cloned olfactory genes encoding chemosensory proteins (CSP) and odorant-binding proteins (OBPs) using M. scutellaris cDNA template and primers designed on the basis CSPs and OBPs previously reported from the European honeybee, Apis mellifera. We cloned two CSP and two OBP genes and then attempted to express the proteins encoded by these genes. With a recombinant OBP, MscuOBP8, and a combinatorial single-chain variable fragment antibody library, we generated anti-MscuOBP8 monoclonal antibody. By immunohistochemistry we demonstrated that the anti-MscuOBP8 binds specifically to the MscuOBP8. Next, we found evidence that MscuOBP8 is expressed in M. scutellaris larvae and it is located in the mandibular region, thus further supporting the hypothesis of olfactory function in immature stages. Lastly, molecular modeling suggests that MscuOBP8 may function as a carrier of primer pheromones or other ligands.

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          Genome-wide analysis of the odorant-binding protein gene family in Drosophila melanogaster.

          Olfaction is of considerable importance to many insects in behaviors critical for survival and reproduction, including location of food sources, selection of mates, recognition of colony con-specifics, and determination of oviposition sites. An ubiquitous, but poorly understood, component of the insect's olfactory system is a group of odorant-binding proteins (OBPs) that are present at high concentrations in the aqueous lymph surrounding the dendrites of olfactory receptor neurons. OBPs are believed to shuttle odorants from the environment to the underlying odorant receptors, for which they could potentially serve as odorant presenters. Here we show that the Drosophila genome carries 51 potential OBP genes, a number comparable to that of its odorant-receptor genes. We find that the majority (73%) of these OBP-like genes occur in clusters of as many as nine genes, in contrast to what has been observed for the Drosophila odorant-receptor genes. Two of the presumptive OBP gene clusters each carries an odorant-receptor gene. We also report an intriguing subfamily of 12 putative OBPs that share a unique C-terminal structure with three conserved cysteines and a conserved proline. Members of this subfamily have not previously been described for any insect. We have performed phylogenetic analyses of the OBP-related proteins in Drosophila as well as other insects, and we discuss the duplication and divergence of the genes for this large family. [The sequence data from this study have been submitted to FlyBase. Annotations for these sequences are available as supplementary material at http://www.genome.org.]
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            Function and evolution of a gene family encoding odorant binding-like proteins in a social insect, the honey bee (Apis mellifera).

            The remarkable olfactory power of insect species is thought to be generated by a combinatorial action of two large protein families, G protein-coupled olfactory receptors (ORs) and odorant binding proteins (OBPs). In olfactory sensilla, OBPs deliver hydrophobic airborne molecules to ORs, but their expression in nonolfactory tissues suggests that they also may function as general carriers in other developmental and physiological processes. Here we used bioinformatic and experimental approaches to characterize the OBP-like gene family in a highly social insect, the Western honey bee. Comparison with other insects shows that the honey bee has the smallest set of these genes, consisting of only 21 OBPs. This number stands in stark contrast to the more than 70 OBPs in Anopheles gambiae and 51 in Drosophila melanogaster. In the honey bee as in the two dipterans, these genes are organized in clusters. We show that the evolution of their structure involved frequent intron losses. We describe a monophyletic subfamily of OBPs where the diversification of some amino acids appears to have been accelerated by positive selection. Expression profiling under a wide range of conditions shows that in the honey bee only nine OBPs are antenna-specific. The remaining genes are expressed either ubiquitously or are tightly regulated in specialized tissues or during development. These findings support the view that OBPs are not restricted to olfaction and are likely to be involved in broader physiological functions.
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              Chemosensory proteins in the honey bee: Insights from the annotated genome, comparative analyses and expressional profiling.

              Small chemosensory proteins (CSPs) belong to a conserved, but poorly understood protein family that has been implicated in transporting chemical stimuli within insect sensilla. However, their expression patterns suggest that these molecules are also critical for other functions including early development. Here we used both bioinformatics and experimental approaches to characterize the CSP gene family in a social insect, the Western honey bee Apis mellifera, and then compared its members to CSPs in other arthropods. The number of CSPs in the honey bee genome (six) is similar to that found in the sequenced dipteran species (four-seven), but is much lower than the number of CSPs in the moth or in the beetle (around 20 each). These differences seem to be the result of lineage specific expansions. Our analysis of CSPs in a number of arthropods reveals a conserved gene family found in both Mandibulates and Chelicerates. Expressional profiling in diverse tissues and throughout development reveals broader than expected patterns of expression with none of the CSPs restricted to the antennae and one found only in the queen ovaries and in embryos. We conclude that CSPs are multifunctional context-dependent proteins involved in diverse cellular processes ranging from embryonic development to chemosensory signal transduction. Some CSPs may function in cuticle synthesis, consistent with their evolutionary origins in the arthropods.
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                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                19 April 2017
                2017
                : 12
                : 4
                : e0174857
                Affiliations
                [1 ]Department of Molecular and Cellular Biology, University of California-Davis, Davis, California, United States of America
                [2 ]Laboratório de Genética, Instituto de Genética e Bioquímica, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brasil
                [3 ]Laboratório de Nanobiotecnologia, Instituto de Genética e Bioquímica, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brasil
                [4 ]Department of Medical Microbiology and Immunology, University of California-Davis, Davis, California, United States of America
                [5 ]Laboratório de Immunopatologia, Instituto de Ciências Biomédicas, Universidade Federal de Uberlândia, Uberlândia, Minas Gerais, Brasil
                USDA Agricultural Research Service, UNITED STATES
                Author notes

                Competing Interests: This work was supported in part by unrestricted gifts from Bedoukian Research, Inc., and Fuji Flavor, Inc., to the University of California-Davis, according to university policy: http://research.ucdavis.edu/industry/partner-with-uc-davis/building-u-icollaborations/ research-transactions/industry-opportunities/gifts-industry/. Support from commercial funder does not alter the authors' adherence to all the PLOS ONE policies on sharing data and materials.

                • Conceptualization: WSL CUV WJC.

                • Funding acquisition: WJC LRG CUV WSL.

                • Investigation: WJC PTF AMB LRG KC NMS ECBA CUV WSL.

                • Supervision: CUV WSL.

                • Writing – original draft: WJC CUV WSL.

                • Writing – review & editing: WSL WJC CUV.

                [¤]

                Current address: Department of Entomology, Pennsylvania State University, University Park, Pennsylvania, United States of America

                Article
                PONE-D-16-46011
                10.1371/journal.pone.0174857
                5396885
                28423045
                3557402d-159b-4909-821a-dc4fb429b155
                © 2017 Carvalho et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 19 November 2016
                : 16 March 2017
                Page count
                Figures: 7, Tables: 2, Pages: 22
                Funding
                Funded by: CAPES
                Award Recipient :
                Funded by: CNPq
                Award Recipient :
                Funded by: FAPEMIG
                Award Recipient :
                Funded by: Bedoukian Research Inc.
                Award Recipient :
                Funded by: Fuji Flavor Co. Ltd.
                Award Recipient :
                Research reported in this publication was supported in part by Brazil’s Coordination for the Improvement of Higher Education Personnel (CAPES) and The Brazilian National Council for Scientific and Technological Development (CNPq) through scholarships under the Brazil’s Science Mobility Program for WJC and CU-V at UC Davis, Bedoukian Research Inc., through a Research Agreement that supported KC at UC Davis, the State Funding Agency of Minas Gerais and gifts from various donors, including Bedoukian Research, Inc., and Fuji Flavor Co., Ltd. (Japan), made to UC Davis to support WSL’s research program. Chimera is developed by the Resource for Biocomputing, Visualization, and Informatics at the University of California, San Francisco, supported by NIGMS P41-GM103311. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
                Categories
                Research Article
                Biology and Life Sciences
                Developmental Biology
                Life Cycles
                Larvae
                Biology and Life Sciences
                Biochemistry
                Proteins
                Odorant Binding Proteins
                Biology and Life Sciences
                Zoology
                Animal Anatomy
                Antennae (Animal Physiology)
                Biology and Life Sciences
                Zoology
                Animal Physiology
                Antennae (Animal Physiology)
                Biology and Life Sciences
                Biochemistry
                Proteins
                Recombinant Proteins
                Research and Analysis Methods
                Immunologic Techniques
                Immunoassays
                Enzyme-Linked Immunoassays
                Biology and Life Sciences
                Organisms
                Animals
                Invertebrates
                Arthropoda
                Insects
                Hymenoptera
                Bees
                Honey Bees
                Biology and Life Sciences
                Organisms
                Animals
                Invertebrates
                Arthropoda
                Insects
                Hymenoptera
                Bees
                Biology and Life Sciences
                Molecular Biology
                Molecular Biology Techniques
                Molecular Biology Assays and Analysis Techniques
                Gene Expression and Vector Techniques
                Protein Expression
                Research and Analysis Methods
                Molecular Biology Techniques
                Molecular Biology Assays and Analysis Techniques
                Gene Expression and Vector Techniques
                Protein Expression
                Custom metadata
                The data underlying the findings in this manuscript were deposited in GenBank under accession numbers: KT965292, KT965293, KT965294, and KT965295 for MscuCSP2, MscuCSP6, MscuOBP4 and MscuOPB8, respectively. All relevant data are within the paper.

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