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Dive into the research topics where Daniel S.T. Hughes is active.

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Featured researches published by Daniel S.T. Hughes.


Nature | 2012

Butterfly genome reveals promiscuous exchange of mimicry adaptations among species

Kanchon K. Dasmahapatra; James R. Walters; Adriana D. Briscoe; John W. Davey; Annabel Whibley; Nicola J. Nadeau; Aleksey V. Zimin; Daniel S.T. Hughes; Laura Ferguson; Simon H. Martin; Camilo Salazar; James J. Lewis; Sebastian Adler; Seung-Joon Ahn; Dean A. Baker; Simon W. Baxter; Nicola Chamberlain; Ritika Chauhan; Brian A. Counterman; Tamas Dalmay; Lawrence E. Gilbert; Karl H.J. Gordon; David G. Heckel; Heather M. Hines; Katharina Hoff; Peter W. H. Holland; Emmanuelle Jacquin-Joly; Francis M. Jiggins; Robert T. Jones; Durrell D. Kapan

The evolutionary importance of hybridization and introgression has long been debated. Hybrids are usually rare and unfit, but even infrequent hybridization can aid adaptation by transferring beneficial traits between species. Here we use genomic tools to investigate introgression in Heliconius, a rapidly radiating genus of neotropical butterflies widely used in studies of ecology, behaviour, mimicry and speciation. We sequenced the genome of Heliconius melpomene and compared it with other taxa to investigate chromosomal evolution in Lepidoptera and gene flow among multiple Heliconius species and races. Among 12,669 predicted genes, biologically important expansions of families of chemosensory and Hox genes are particularly noteworthy. Chromosomal organization has remained broadly conserved since the Cretaceous period, when butterflies split from the Bombyx (silkmoth) lineage. Using genomic resequencing, we show hybrid exchange of genes between three co-mimics, Heliconius melpomene, Heliconius timareta and Heliconius elevatus, especially at two genomic regions that control mimicry pattern. We infer that closely related Heliconius species exchange protective colour-pattern genes promiscuously, implying that hybridization has an important role in adaptive radiation.


Nucleic Acids Research | 2012

VectorBase: improvements to a bioinformatics resource for invertebrate vector genomics

Karine Megy; Scott J. Emrich; Daniel Lawson; David E. Campbell; Emmanuel Dialynas; Daniel S.T. Hughes; Gautier Koscielny; Christos Louis; Robert M. MacCallum; Seth Redmond; Andrew Sheehan; Pantelis Topalis; Derek Wilson

VectorBase (http://www.vectorbase.org) is a NIAID-supported bioinformatics resource for invertebrate vectors of human pathogens. It hosts data for nine genomes: mosquitoes (three Anopheles gambiae genomes, Aedes aegypti and Culex quinquefasciatus), tick (Ixodes scapularis), body louse (Pediculus humanus), kissing bug (Rhodnius prolixus) and tsetse fly (Glossina morsitans). Hosted data range from genomic features and expression data to population genetics and ontologies. We describe improvements and integration of new data that expand our taxonomic coverage. Releases are bi-monthly and include the delivery of preliminary data for emerging genomes. Frequent updates of the genome browser provide VectorBase users with increasing options for visualizing their own high-throughput data. One major development is a new population biology resource for storing genomic variations, insecticide resistance data and their associated metadata. It takes advantage of improved ontologies and controlled vocabularies. Combined, these new features ensure timely release of multiple types of data in the public domain while helping overcome the bottlenecks of bioinformatics and annotation by engaging with our user community.


Nature Communications | 2016

Unique features of a global human ectoparasite identified through sequencing of the bed bug genome

Joshua B. Benoit; Zach N. Adelman; Klaus Reinhardt; Amanda Dolan; Monica Poelchau; Emily C. Jennings; Elise M. Szuter; Richard W. Hagan; Hemant Gujar; Jayendra Nath Shukla; Fang Zhu; M. Mohan; David R. Nelson; Andrew J. Rosendale; Christian Derst; Valentina Resnik; Sebastian Wernig; Pamela Menegazzi; Christian Wegener; Nicolai Peschel; Jacob M. Hendershot; Wolfgang Blenau; Reinhard Predel; Paul R. Johnston; Panagiotis Ioannidis; Robert M. Waterhouse; Ralf Nauen; Corinna Schorn; Mark Christoph Ott; Frank Maiwald

The bed bug, Cimex lectularius, has re-established itself as a ubiquitous human ectoparasite throughout much of the world during the past two decades. This global resurgence is likely linked to increased international travel and commerce in addition to widespread insecticide resistance. Analyses of the C. lectularius sequenced genome (650 Mb) and 14,220 predicted protein-coding genes provide a comprehensive representation of genes that are linked to traumatic insemination, a reduced chemosensory repertoire of genes related to obligate hematophagy, host–symbiont interactions, and several mechanisms of insecticide resistance. In addition, we document the presence of multiple putative lateral gene transfer events. Genome sequencing and annotation establish a solid foundation for future research on mechanisms of insecticide resistance, human–bed bug and symbiont–bed bug associations, and unique features of bed bug biology that contribute to the unprecedented success of C. lectularius as a human ectoparasite.


Genome Biology | 2016

Genome of the Asian longhorned beetle (Anoplophora glabripennis), a globally significant invasive species, reveals key functional and evolutionary innovations at the beetle-plant interface

Duane D. McKenna; Erin D. Scully; Yannick Pauchet; Kelli Hoover; Roy Kirsch; Scott M. Geib; Robert F. Mitchell; Robert M. Waterhouse; Seung Joon Ahn; Deanna Arsala; Joshua B. Benoit; Heath Blackmon; Tiffany Bledsoe; Julia H. Bowsher; André Busch; Bernarda Calla; Hsu Chao; Anna K. Childers; Christopher Childers; Dave J. Clarke; Lorna Cohen; Jeffery P. Demuth; Huyen Dinh; HarshaVardhan Doddapaneni; Amanda Dolan; Jian J. Duan; Shannon Dugan; Markus Friedrich; Karl M. Glastad; Michael A. D. Goodisman

BackgroundRelatively little is known about the genomic basis and evolution of wood-feeding in beetles. We undertook genome sequencing and annotation, gene expression assays, studies of plant cell wall degrading enzymes, and other functional and comparative studies of the Asian longhorned beetle, Anoplophora glabripennis, a globally significant invasive species capable of inflicting severe feeding damage on many important tree species. Complementary studies of genes encoding enzymes involved in digestion of woody plant tissues or detoxification of plant allelochemicals were undertaken with the genomes of 14 additional insects, including the newly sequenced emerald ash borer and bull-headed dung beetle.ResultsThe Asian longhorned beetle genome encodes a uniquely diverse arsenal of enzymes that can degrade the main polysaccharide networks in plant cell walls, detoxify plant allelochemicals, and otherwise facilitate feeding on woody plants. It has the metabolic plasticity needed to feed on diverse plant species, contributing to its highly invasive nature. Large expansions of chemosensory genes involved in the reception of pheromones and plant kairomones are consistent with the complexity of chemical cues it uses to find host plants and mates.ConclusionsAmplification and functional divergence of genes associated with specialized feeding on plants, including genes originally obtained via horizontal gene transfer from fungi and bacteria, contributed to the addition, expansion, and enhancement of the metabolic repertoire of the Asian longhorned beetle, certain other phytophagous beetles, and to a lesser degree, other phytophagous insects. Our results thus begin to establish a genomic basis for the evolutionary success of beetles on plants.


BMC Biology | 2017

The house spider genome reveals an ancient whole-genome duplication during arachnid evolution.

Evelyn E. Schwager; Prashant P. Sharma; Thomas H. Clarke; Daniel J. Leite; Torsten Wierschin; Matthias Pechmann; Yasuko Akiyama-Oda; Lauren Esposito; Jesper Bechsgaard; Trine Bilde; Alexandra D. Buffry; Hsu Chao; Huyen Dinh; HarshaVardhan Doddapaneni; Shannon Dugan; Cornelius Eibner; Cassandra G. Extavour; Peter Funch; Jessica E. Garb; Luis B. Gonzalez; Vanessa L. González; Sam Griffiths-Jones; Yi Han; Cheryl Y. Hayashi; Maarten Hilbrant; Daniel S.T. Hughes; Ralf Janssen; Sandra L. Lee; Ignacio Maeso; Shwetha C. Murali

BackgroundThe duplication of genes can occur through various mechanisms and is thought to make a major contribution to the evolutionary diversification of organisms. There is increasing evidence for a large-scale duplication of genes in some chelicerate lineages including two rounds of whole genome duplication (WGD) in horseshoe crabs. To investigate this further, we sequenced and analyzed the genome of the common house spider Parasteatoda tepidariorum.ResultsWe found pervasive duplication of both coding and non-coding genes in this spider, including two clusters of Hox genes. Analysis of synteny conservation across the P. tepidariorum genome suggests that there has been an ancient WGD in spiders. Comparison with the genomes of other chelicerates, including that of the newly sequenced bark scorpion Centruroides sculpturatus, suggests that this event occurred in the common ancestor of spiders and scorpions, and is probably independent of the WGDs in horseshoe crabs. Furthermore, characterization of the sequence and expression of the Hox paralogs in P. tepidariorum suggests that many have been subject to neo-functionalization and/or sub-functionalization since their duplication.ConclusionsOur results reveal that spiders and scorpions are likely the descendants of a polyploid ancestor that lived more than 450 MYA. Given the extensive morphological diversity and ecological adaptations found among these animals, rivaling those of vertebrates, our study of the ancient WGD event in Arachnopulmonata provides a new comparative platform to explore common and divergent evolutionary outcomes of polyploidization events across eukaryotes.


Genome Biology | 2016

The whole genome sequence of the Mediterranean fruit fly, Ceratitis capitata (Wiedemann), reveals insights into the biology and adaptive evolution of a highly invasive pest species

Alexie Papanicolaou; Marc F. Schetelig; Peter Arensburger; Peter W. Atkinson; Joshua B. Benoit; Kostas Bourtzis; Pedro Castañera; John P. Cavanaugh; Hsu Chao; Christopher Childers; Ingrid Curril; Huyen Dinh; HarshaVardhan Doddapaneni; Amanda Dolan; Shannon Dugan; Markus Friedrich; Giuliano Gasperi; Scott M. Geib; Georgios Georgakilas; Richard A. Gibbs; Sarah D. Giers; Ludvik M. Gomulski; Miguel González-Guzmán; Ana Guillem-Amat; Yi Han; Artemis G. Hatzigeorgiou; Pedro Hernández-Crespo; Daniel S.T. Hughes; Jeffery W. Jones; Dimitra Karagkouni

The Mediterranean fruit fly (medfly), Ceratitis capitata, is a major destructive insect pest due to its broad host range, which includes hundreds of fruits and vegetables. It exhibits a unique ability to invade and adapt to ecological niches throughout tropical and subtropical regions of the world, though medfly infestations have been prevented and controlled by the sterile insect technique (SIT) as part of integrated pest management programs (IPMs). The genetic analysis and manipulation of medfly has been subject to intensive study in an effort to improve SIT efficacy and other aspects of IPM control. The 479 Mb medfly genome is sequenced from adult flies from lines inbred for 20 generations. A high-quality assembly is achieved having a contig N50 of 45.7 kb and scaffold N50 of 4.06 Mb. In-depth curation of more than 1800 messenger RNAs shows specific gene expansions that can be related to invasiveness and host adaptation, including gene families for chemoreception, toxin and insecticide metabolism, cuticle proteins, opsins, and aquaporins. We identify genes relevant to IPM control, including those required to improve SIT. The medfly genome sequence provides critical insights into the biology of one of the most serious and widespread agricultural pests. This knowledge should significantly advance the means of controlling the size and invasive potential of medfly populations. Its close relationship to Drosophila, and other insect species important to agriculture and human health, will further comparative functional and structural studies of insect genomes that should broaden our understanding of gene family evolution.


Nature Communications | 2015

Lucilia cuprina genome unlocks parasitic fly biology to underpin future interventions

Clare A. Anstead; Pasi K. Korhonen; Neil D. Young; Ross S. Hall; Aaron R. Jex; Shwetha C. Murali; Daniel S.T. Hughes; Siu F. Lee; Trent Perry; Andreas J. Stroehlein; Brendan R. E. Ansell; Bert Breugelmans; Andreas Hofmann; Jiaxin Qu; Shannon Dugan; Sandra L. Lee; Hsu Chao; Huyen Dinh; Yi Han; Harsha Doddapaneni; Kim C. Worley; Donna M. Muzny; Panagiotis Ioannidis; Robert M. Waterhouse; Evgeny M. Zdobnov; P. J. James; Neil H. Bagnall; Andrew C. Kotze; Richard A. Gibbs; Stephen Richards

Lucilia cuprina is a parasitic fly of major economic importance worldwide. Larvae of this fly invade their animal host, feed on tissues and excretions and progressively cause severe skin disease (myiasis). Here we report the sequence and annotation of the 458-megabase draft genome of Lucilia cuprina. Analyses of this genome and the 14,544 predicted protein-encoding genes provide unique insights into the flys molecular biology, interactions with the host animal and insecticide resistance. These insights have broad implications for designing new methods for the prevention and control of myiasis.


Molecular Biology and Evolution | 2017

Evolutionary History of Chemosensory-Related Gene Families across the Arthropoda

Seong-il Eyun; Ho Young Soh; Marijan Posavi; James B. Munro; Daniel S.T. Hughes; Shwetha C. Murali; Jiaxin Qu; Shannon Dugan; Sandra L. Lee; Hsu Chao; Huyen Dinh; Yi Han; HarshaVardhan Doddapaneni; Kim C. Worley; Donna M. Muzny; Eun-Ok Park; Joana C. Silva; Richard A. Gibbs; Stephen Richards; Carol Eunmi Lee

Abstract Chemosensory-related gene (CRG) families have been studied extensively in insects, but their evolutionary history across the Arthropoda had remained relatively unexplored. Here, we address current hypotheses and prior conclusions on CRG family evolution using a more comprehensive data set. In particular, odorant receptors were hypothesized to have proliferated during terrestrial colonization by insects (hexapods), but their association with other pancrustacean clades and with independent terrestrial colonizations in other arthropod subphyla have been unclear. We also examine hypotheses on which arthropod CRG family is most ancient. Thus, we reconstructed phylogenies of CRGs, including those from new arthropod genomes and transcriptomes, and mapped CRG gains and losses across arthropod lineages. Our analysis was strengthened by including crustaceans, especially copepods, which reside outside the hexapod/branchiopod clade within the subphylum Pancrustacea. We generated the first high-resolution genome sequence of the copepod Eurytemora affinis and annotated its CRGs. We found odorant receptors and odorant binding proteins present only in hexapods (insects) and absent from all other arthropod lineages, indicating that they are not universal adaptations to land. Gustatory receptors likely represent the oldest chemosensory receptors among CRGs, dating back to the Placozoa. We also clarified and confirmed the evolutionary history of antennal ionotropic receptors across the Arthropoda. All antennal ionotropic receptors in E. affinis were expressed more highly in males than in females, suggestive of an association with male mate-recognition behavior. This study is the most comprehensive comparative analysis to date of CRG family evolution across the largest and most speciose metazoan phylum Arthropoda.


BMC Biology | 2017

Genomic innovations, transcriptional plasticity and gene loss underlying the evolution and divergence of two highly polyphagous and invasive Helicoverpa pest species

Stephen L. Pearce; David F. Clarke; Peter D. East; Samia Elfekih; Karl H.J. Gordon; Lars S. Jermiin; Angela McGaughran; John G. Oakeshott; Alexie Papanikolaou; Omaththage P. Perera; Rahul V. Rane; Stephen Richards; Weetek Tay; Tom Walsh; Alisha Anderson; Craig Anderson; Sassan Asgari; Philip G. Board; Anne Bretschneider; Peter M. Campbell; Thomas Chertemps; John T. Christeller; Chris Coppin; Sharon Downes; G Duan; Claire Farnsworth; Robert T. Good; Libin Han; Y. C Han; Klas Hatje

BackgroundHelicoverpa armigera and Helicoverpa zea are major caterpillar pests of Old and New World agriculture, respectively. Both, particularly H. armigera, are extremely polyphagous, and H. armigera has developed resistance to many insecticides. Here we use comparative genomics, transcriptomics and resequencing to elucidate the genetic basis for their properties as pests.ResultsWe find that, prior to their divergence about 1.5 Mya, the H. armigera/H. zea lineage had accumulated up to more than 100 more members of specific detoxification and digestion gene families and more than 100 extra gustatory receptor genes, compared to other lepidopterans with narrower host ranges. The two genomes remain very similar in gene content and order, but H. armigera is more polymorphic overall, and H. zea has lost several detoxification genes, as well as about 50 gustatory receptor genes. It also lacks certain genes and alleles conferring insecticide resistance found in H. armigera. Non-synonymous sites in the expanded gene families above are rapidly diverging, both between paralogues and between orthologues in the two species. Whole genome transcriptomic analyses of H. armigera larvae show widely divergent responses to different host plants, including responses among many of the duplicated detoxification and digestion genes.ConclusionsThe extreme polyphagy of the two heliothines is associated with extensive amplification and neofunctionalisation of genes involved in host finding and use, coupled with versatile transcriptional responses on different hosts. H. armigera’s invasion of the Americas in recent years means that hybridisation could generate populations that are both locally adapted and insecticide resistant.


Nature Ecology and Evolution | 2018

Hemimetabolous genomes reveal molecular basis of termite eusociality

Mark C. Harrison; Evelien Jongepier; Hugh M. Robertson; Nicolas Arning; Tristan Bitard-Feildel; Hsu Chao; Christopher P. Childers; Huyen Dinh; HarshaVardhan Doddapaneni; Shannon Dugan; Johannes Gowin; Carolin Greiner; Yi Han; Haofu Hu; Daniel S.T. Hughes; Ann Kathrin Huylmans; Carsten Kemena; Lukas P.M. Kremer; Sandra L. Lee; Alberto Lopez-Ezquerra; Ludovic Mallet; Jose M. Monroy-Kuhn; Annabell Moser; Shwetha C. Murali; Donna M. Muzny; Saria Otani; Maria Dolors Piulachs; Monica Poelchau; Jiaxin Qu; Florentine Schaub

Around 150 million years ago, eusocial termites evolved from within the cockroaches, 50 million years before eusocial Hymenoptera, such as bees and ants, appeared. Here, we report the 2-Gb genome of the German cockroach, Blattella germanica, and the 1.3-Gb genome of the drywood termite Cryptotermes secundus. We show evolutionary signatures of termite eusociality by comparing the genomes and transcriptomes of three termites and the cockroach against the background of 16 other eusocial and non-eusocial insects. Dramatic adaptive changes in genes underlying the production and perception of pheromones confirm the importance of chemical communication in the termites. These are accompanied by major changes in gene regulation and the molecular evolution of caste determination. Many of these results parallel molecular mechanisms of eusocial evolution in Hymenoptera. However, the specific solutions are remarkably different, thus revealing a striking case of convergence in one of the major evolutionary transitions in biological complexity.Eusociality evolved independently in Hymenoptera and in termites. Here, the authors sequence genomes of the German cockroach and a drywood termite and provide insights into the evolutionary signatures of termite eusociality.

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Hsu Chao

Baylor College of Medicine

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Huyen Dinh

Baylor College of Medicine

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Shannon Dugan

Baylor College of Medicine

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Shwetha C. Murali

Baylor College of Medicine

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Yi Han

Baylor College of Medicine

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Richard A. Gibbs

Baylor College of Medicine

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Christopher Childers

United States Department of Agriculture

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Jiaxin Qu

Baylor College of Medicine

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