21 results on '"Baa-Puyoulet, P"'
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2. Correction to: The genome sequence of the grape phylloxera provides insights into the evolution, adaptation, and invasion routes of an iconic pest
- Author
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Rispe, Claude, Legeai, Fabrice, Nabity, Paul D, Fernández, Rosa, Arora, Arinder K, Baa-Puyoulet, Patrice, Banfill, Celeste R, Bao, Leticia, Barberà, Miquel, Bouallègue, Maryem, Bretaudeau, Anthony, Brisson, Jennifer A, Calevro, Federica, Capy, Pierre, Catrice, Olivier, Chertemps, Thomas, Couture, Carole, Delière, Laurent, Douglas, Angela E, Dufault-Thompson, Keith, Escuer, Paula, Feng, Honglin, Forneck, Astrid, Gabaldón, Toni, Guigó, Roderic, Hilliou, Frédérique, Hinojosa-Alvarez, Silvia, Hsiao, Yi-min, Hudaverdian, Sylvie, Jacquin-Joly, Emmanuelle, James, Edward B, Johnston, Spencer, Joubard, Benjamin, Le Goff, Gaëlle, Le Trionnaire, Gaël, Librado, Pablo, Liu, Shanlin, Lombaert, Eric, Lu, Hsiao-ling, Maïbèche, Martine, Makni, Mohamed, Marcet-Houben, Marina, Martínez-Torres, David, Meslin, Camille, Montagné, Nicolas, Moran, Nancy A, Papura, Daciana, Parisot, Nicolas, Rahbé, Yvan, Lopes, Mélanie Ribeiro, Ripoll-Cladellas, Aida, Robin, Stéphanie, Roques, Céline, Roux, Pascale, Rozas, Julio, Sánchez-Gracia, Alejandro, Sánchez-Herrero, Jose F, Santesmasses, Didac, Scatoni, Iris, Serre, Rémy-Félix, Tang, Ming, Tian, Wenhua, Umina, Paul A, van Munster, Manuella, Vincent-Monégat, Carole, Wemmer, Joshua, Wilson, Alex CC, Zhang, Ying, Zhao, Chaoyang, Zhao, Jing, Zhao, Serena, Zhou, Xin, Delmotte, François, and Tagu, Denis
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Developmental Biology - Abstract
An amendment to this paper has been published and can be accessed via the original article.
- Published
- 2020
3. The genome sequence of the grape phylloxera provides insights into the evolution, adaptation, and invasion routes of an iconic pest
- Author
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Rispe, Claude, Legeai, Fabrice, Nabity, Paul D, Fernández, Rosa, Arora, Arinder K, Baa-Puyoulet, Patrice, Banfill, Celeste R, Bao, Leticia, Barberà, Miquel, Bouallègue, Maryem, Bretaudeau, Anthony, Brisson, Jennifer A, Calevro, Federica, Capy, Pierre, Catrice, Olivier, Chertemps, Thomas, Couture, Carole, Delière, Laurent, Douglas, Angela E, Dufault-Thompson, Keith, Escuer, Paula, Feng, Honglin, Forneck, Astrid, Gabaldón, Toni, Guigó, Roderic, Hilliou, Frédérique, Hinojosa-Alvarez, Silvia, Hsiao, Yi-min, Hudaverdian, Sylvie, Jacquin-Joly, Emmanuelle, James, Edward B, Johnston, Spencer, Joubard, Benjamin, Le Goff, Gaëlle, Le Trionnaire, Gaël, Librado, Pablo, Liu, Shanlin, Lombaert, Eric, Lu, Hsiao-ling, Maïbèche, Martine, Makni, Mohamed, Marcet-Houben, Marina, Martínez-Torres, David, Meslin, Camille, Montagné, Nicolas, Moran, Nancy A, Papura, Daciana, Parisot, Nicolas, Rahbé, Yvan, Lopes, Mélanie Ribeiro, Ripoll-Cladellas, Aida, Robin, Stéphanie, Roques, Céline, Roux, Pascale, Rozas, Julio, Sánchez-Gracia, Alejandro, Sánchez-Herrero, Jose F, Santesmasses, Didac, Scatoni, Iris, Serre, Rémy-Félix, Tang, Ming, Tian, Wenhua, Umina, Paul A, van Munster, Manuella, Vincent-Monégat, Carole, Wemmer, Joshua, Wilson, Alex CC, Zhang, Ying, Zhao, Chaoyang, Zhao, Jing, Zhao, Serena, Zhou, Xin, Delmotte, François, and Tagu, Denis
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Biological Sciences ,Genetics ,Human Genome ,Infection ,Climate Action ,Adaptation ,Biological ,Animal Distribution ,Animals ,Biological Evolution ,Genome ,Insect ,Hemiptera ,Introduced Species ,Vitis ,Arthropod genomes ,Daktulosphaira vitifoliae ,Gene duplications ,Host plant interactions ,Effectors ,Biological invasions ,Developmental Biology ,Biological sciences - Abstract
BackgroundAlthough native to North America, the invasion of the aphid-like grape phylloxera Daktulosphaira vitifoliae across the globe altered the course of grape cultivation. For the past 150 years, viticulture relied on grafting-resistant North American Vitis species as rootstocks, thereby limiting genetic stocks tolerant to other stressors such as pathogens and climate change. Limited understanding of the insect genetics resulted in successive outbreaks across the globe when rootstocks failed. Here we report the 294-Mb genome of D. vitifoliae as a basic tool to understand host plant manipulation, nutritional endosymbiosis, and enhance global viticulture.ResultsUsing a combination of genome, RNA, and population resequencing, we found grape phylloxera showed high duplication rates since its common ancestor with aphids, but similarity in most metabolic genes, despite lacking obligate nutritional symbioses and feeding from parenchyma. Similarly, no enrichment occurred in development genes in relation to viviparity. However, phylloxera evolved > 2700 unique genes that resemble putative effectors and are active during feeding. Population sequencing revealed the global invasion began from the upper Mississippi River in North America, spread to Europe and from there to the rest of the world.ConclusionsThe grape phylloxera genome reveals genetic architecture relative to the evolution of nutritional endosymbiosis, viviparity, and herbivory. The extraordinary expansion in effector genes also suggests novel adaptations to plant feeding and how insects induce complex plant phenotypes, for instance galls. Finally, our understanding of the origin of this invasive species and its genome provide genetics resources to alleviate rootstock bottlenecks restricting the advancement of viticulture.
- Published
- 2020
4. Sawfly genomes reveal evolutionary acquisitions that fostered the mega-radiation of parasitoid and eusocial Hymenoptera
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Oeyen, Jan Philip, Baa-Puyoulet, Patrice, Benoit, Joshua B, Beukeboom, Leo W, Bornberg-Bauer, Erich, Buttstedt, Anja, Calevro, Federica, Cash, Elizabeth I, Chao, Hsu, Charles, Hubert, Chen, Mei-Ju May, Childers, Christopher, Cridge, Andrew G, Dearden, Peter, Dinh, Huyen, Doddapaneni, Harsha Vardhan, Dolan, Amanda, Donath, Alexander, Dowling, Daniel, Dugan, Shannon, Duncan, Elizabeth, Elpidina, Elena N, Friedrich, Markus, Geuverink, Elzemiek, Gibson, Joshua D, Grath, Sonja, Grimmelikhuijzen, Cornelis JP, Große-Wilde, Ewald, Gudobba, Cameron, Han, Yi, Hansson, Bill S, Hauser, Frank, Hughes, Daniel ST, Ioannidis, Panagiotis, Jacquin-Joly, Emmanuelle, Jennings, Emily C, Jones, Jeffery W, Klasberg, Steffen, Lee, Sandra L, Lesný, Peter, Lovegrove, Mackenzie, Martin, Sebastian, Martynov, Alexander G, Mayer, Christoph, Montagné, Nicolas, Moris, Victoria C, Munoz-Torres, Monica, Murali, Shwetha Canchi, Muzny, Donna M, Oppert, Brenda, Parisot, Nicolas, Pauli, Thomas, Peters, Ralph S, Petersen, Malte, Pick, Christian, Persyn, Emma, Podsiadlowski, Lars, Poelchau, Monica F, Provataris, Panagiotis, Qu, Jiaxin, Reijnders, Maarten JMF, von Reumont, Björn Marcus, Rosendale, Andrew J, Simao, Felipe A, Skelly, John, Sotiropoulos, Alexandros G, Stahl, Aaron L, Sumitani, Megumi, Szuter, Elise M, Tidswell, Olivia, Tsitlakidis, Evangelos, Vedder, Lucia, Waterhouse, Robert M, Werren, John H, Wilbrandt, Jeanne, Worley, Kim C, Yamamoto, Daisuke S, van de Zande, Louis, Zdobnov, Evgeny M, Ziesmann, Tanja, Gibbs, Richard A, Richards, Stephen, Hatakeyama, Masatsugu, Misof, Bernhard, and Niehuis, Oliver
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Human Genome ,Genetics ,Life Below Water ,Amino Acid Sequence ,Animals ,Conserved Sequence ,DNA Transposable Elements ,Female ,Gene Dosage ,Genetic Speciation ,Genome ,Insect ,Glycoproteins ,Herbivory ,Host-Parasite Interactions ,Hymenoptera ,Immunity ,Insect Proteins ,Male ,Multigene Family ,Receptors ,Odorant ,Social Behavior ,Vision ,Ocular ,hexamerin ,major royal jelly protein ,microsynteny ,odorant receptor ,opsin ,phytophagy ,Biochemistry and Cell Biology ,Evolutionary Biology ,Developmental Biology - Abstract
The tremendous diversity of Hymenoptera is commonly attributed to the evolution of parasitoidism in the last common ancestor of parasitoid sawflies (Orussidae) and wasp-waisted Hymenoptera (Apocrita). However, Apocrita and Orussidae differ dramatically in their species richness, indicating that the diversification of Apocrita was promoted by additional traits. These traits have remained elusive due to a paucity of sawfly genome sequences, in particular those of parasitoid sawflies. Here, we present comparative analyses of draft genomes of the primarily phytophagous sawfly Athalia rosae and the parasitoid sawfly Orussus abietinus. Our analyses revealed that the ancestral hymenopteran genome exhibited traits that were previously considered unique to eusocial Apocrita (e.g., low transposable element content and activity) and a wider gene repertoire than previously thought (e.g., genes for CO2 detection). Moreover, we discovered that Apocrita evolved a significantly larger array of odorant receptors than sawflies, which could be relevant to the remarkable diversification of Apocrita by enabling efficient detection and reliable identification of hosts.
- Published
- 2020
5. Molecular evolutionary trends and feeding ecology diversification in the Hemiptera, anchored by the milkweed bug genome
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Panfilio, Kristen A, Vargas Jentzsch, Iris M, Benoit, Joshua B, Erezyilmaz, Deniz, Suzuki, Yuichiro, Colella, Stefano, Robertson, Hugh M, Poelchau, Monica F, Waterhouse, Robert M, Ioannidis, Panagiotis, Weirauch, Matthew T, Hughes, Daniel ST, Murali, Shwetha C, Werren, John H, Jacobs, Chris GC, Duncan, Elizabeth J, Armisén, David, Vreede, Barbara MI, Baa-Puyoulet, Patrice, Berger, Chloé S, Chang, Chun-che, Chao, Hsu, Chen, Mei-Ju M, Chen, Yen-Ta, Childers, Christopher P, Chipman, Ariel D, Cridge, Andrew G, Crumière, Antonin JJ, Dearden, Peter K, Didion, Elise M, Dinh, Huyen, Doddapaneni, Harsha Vardhan, Dolan, Amanda, Dugan, Shannon, Extavour, Cassandra G, Febvay, Gérard, Friedrich, Markus, Ginzburg, Neta, Han, Yi, Heger, Peter, Holmes, Christopher J, Horn, Thorsten, Hsiao, Yi-min, Jennings, Emily C, Johnston, J Spencer, Jones, Tamsin E, Jones, Jeffery W, Khila, Abderrahman, Koelzer, Stefan, Kovacova, Viera, Leask, Megan, Lee, Sandra L, Lee, Chien-Yueh, Lovegrove, Mackenzie R, Lu, Hsiao-ling, Lu, Yong, Moore, Patricia J, Munoz-Torres, Monica C, Muzny, Donna M, Palli, Subba R, Parisot, Nicolas, Pick, Leslie, Porter, Megan L, Qu, Jiaxin, Refki, Peter N, Richter, Rose, Rivera-Pomar, Rolando, Rosendale, Andrew J, Roth, Siegfried, Sachs, Lena, Santos, M Emília, Seibert, Jan, Sghaier, Essia, Shukla, Jayendra N, Stancliffe, Richard J, Tidswell, Olivia, Traverso, Lucila, van der Zee, Maurijn, Viala, Séverine, Worley, Kim C, Zdobnov, Evgeny M, Gibbs, Richard A, and Richards, Stephen
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Biological Sciences ,Bioinformatics and Computational Biology ,Genetics ,Human Genome ,Biotechnology ,Amino Acid Sequence ,Animals ,CYS2-HIS2 Zinc Fingers ,Evolution ,Molecular ,Feeding Behavior ,Gene Dosage ,Gene Expression Profiling ,Gene Transfer ,Horizontal ,Genes ,Homeobox ,Genome ,Insect ,Hemiptera ,Pigmentation ,Smell ,Transcription Factors ,Evolution of development ,Gene family evolution ,Gene structure ,Lateral gene transfer ,Phytophagy ,RNAi ,Transcription factors ,Environmental Sciences ,Information and Computing Sciences ,Bioinformatics - Abstract
BackgroundThe Hemiptera (aphids, cicadas, and true bugs) are a key insect order, with high diversity for feeding ecology and excellent experimental tractability for molecular genetics. Building upon recent sequencing of hemipteran pests such as phloem-feeding aphids and blood-feeding bed bugs, we present the genome sequence and comparative analyses centered on the milkweed bug Oncopeltus fasciatus, a seed feeder of the family Lygaeidae.ResultsThe 926-Mb Oncopeltus genome is well represented by the current assembly and official gene set. We use our genomic and RNA-seq data not only to characterize the protein-coding gene repertoire and perform isoform-specific RNAi, but also to elucidate patterns of molecular evolution and physiology. We find ongoing, lineage-specific expansion and diversification of repressive C2H2 zinc finger proteins. The discovery of intron gain and turnover specific to the Hemiptera also prompted the evaluation of lineage and genome size as predictors of gene structure evolution. Furthermore, we identify enzymatic gains and losses that correlate with feeding biology, particularly for reductions associated with derived, fluid nutrition feeding.ConclusionsWith the milkweed bug, we now have a critical mass of sequenced species for a hemimetabolous insect order and close outgroup to the Holometabola, substantially improving the diversity of insect genomics. We thereby define commonalities among the Hemiptera and delve into how hemipteran genomes reflect distinct feeding ecologies. Given Oncopeltus's strength as an experimental model, these new sequence resources bolster the foundation for molecular research and highlight technical considerations for the analysis of medium-sized invertebrate genomes.
- Published
- 2019
6. The transposable element-rich genome of the cereal pest Sitophilus oryzae
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Parisot, Nicolas, Vargas-Chávez, Carlos, Goubert, Clément, Baa-Puyoulet, Patrice, Balmand, Séverine, Beranger, Louis, Blanc, Caroline, Bonnamour, Aymeric, Boulesteix, Matthieu, Burlet, Nelly, Calevro, Federica, Callaerts, Patrick, Chancy, Théo, Charles, Hubert, Colella, Stefano, Da Silva Barbosa, André, Dell’Aglio, Elisa, Di Genova, Alex, Febvay, Gérard, Gabaldón, Toni, Galvão Ferrarini, Mariana, Gerber, Alexandra, Gillet, Benjamin, Hubley, Robert, Hughes, Sandrine, Jacquin-Joly, Emmanuelle, Maire, Justin, Marcet-Houben, Marina, Masson, Florent, Meslin, Camille, Montagné, Nicolas, Moya, Andrés, Ribeiro de Vasconcelos, Ana Tereza, Richard, Gautier, Rosen, Jeb, Sagot, Marie-France, Smit, Arian F. A., Storer, Jessica M., Vincent-Monegat, Carole, Vallier, Agnès, Vigneron, Aurélien, Zaidman-Rémy, Anna, Zamoum, Waël, Vieira, Cristina, Rebollo, Rita, Latorre, Amparo, and Heddi, Abdelaziz
- Published
- 2021
- Full Text
- View/download PDF
7. Proteogenomic reconstruction of organ-specific metabolic networks in an environmental sentinel species, the amphipod Gammarus fossarum.
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Koenig, Natacha, Baa-Puyoulet, Patrice, Lafont, Amélie, Lorenzo-Colina, Isis, Navratil, Vincent, Leprêtre, Maxime, Sugier, Kevin, Delorme, Nicolas, Garnero, Laura, Queau, Hervé, Gaillard, Jean-Charles, Kielbasa, Mélodie, Ayciriex, Sophie, Calevro, Federica, Chaumot, Arnaud, Charles, Hubert, Armengaud, Jean, Geffard, Olivier, and Degli Esposti, Davide
- Abstract
Metabolic pathways are affected by the impacts of environmental contaminants underlying a large variability of toxic effects across different species. However, the systematic reconstruction of metabolic pathways remains limited in environmental sentinel species due to the lack of available genomic data in many taxa of animal diversity. In this study we used a multi-omics approach to reconstruct the most comprehensive map of metabolic pathways for a crustacean model in biomonitoring, the amphipod Gammarus fossarum in order to improve the knowledge of the metabolism of this sentinel species. We revisited the assembly of RNA-seq data by de novo approaches to reduce RNA contaminants and transcript redundancy. We also acquired extensive mass spectrometry shotgun proteomic data on several organs from a reference population of G. fossarum males and females to identify organ-specific metabolic profiles. The G. fossarum metabolic pathway reconstruction (available through the metabolic database GamfoCyc) was performed by adapting the genomic tool CycADS and we identified 377 pathways representing 7630 annotated enzymes, 2610 enzymatic reactions and the expression of 858 enzymes was experimentally validated by proteomics. To our knowledge, our analysis provides for the first time a systematic metabolic pathway reconstruction and the proteome profiles of these pathways at the organ level in this sentinel species. As an example, we show an elevated abundance in enzymes involved in ATP biosynthesis and fatty acid beta-oxidation indicative of the high-energy requirement of the gills, or the key anabolic and detoxification role of the hepatopancreatic caeca, as exemplified by the specific expression of the retinoid biosynthetic pathways and glutathione synthesis. In conclusion, the multi-omics data integration performed in this study provides new resources to investigate metabolic processes in crustacean amphipods and their role in mediating the effects of environmental contaminant exposures in sentinel species. This study provide the first evidence that it is possible to combine multiple omics data to exhaustively describe the metabolic network of a model species in ecotoxicology, Gammarus fossarum , for which a reference genome is not yet available. [Display omitted] • Metabolic pathway systematic reconstruction using transcriptomics of a sentinel freshwater amphipod, Gammarus fossarum. • Creation of an open-access molecular resource for G. fossarum metabolic network at http://arthropodacyc.cycadsys.org • Identification of organ-specific metabolic profiles using high resolution mass spectrometry proteomics [ABSTRACT FROM AUTHOR]
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- 2024
- Full Text
- View/download PDF
8. The transposable element-rich genome of the cereal pest Sitophilus oryzae
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Parisot, N, Vargas-Chavez, C, Goubert, C, Baa-Puyoulet, P, Balmand, S, Beranger, L, Blanc, C, Bonnamour, A, Boulesteix, M, Burlet, N, Calevro, F, Callaerts, P, Chancy, T, Charles, H, Colella, S, Barbosa, ADS, Dell'Aglio, E, Di Genova, A, Febvay, G, Gabaldon, T, Ferrarini, MG, Gerber, A, Gillet, B, Hubley, R, Hughes, S, Jacquin-Joly, E, Maire, J, Marcet-Houben, M, Masson, F, Meslin, C, Montagne, N, Moya, A, Ribeiro de Vasconcelos, AT, Richard, G, Rosen, J, Sagot, M-F, Smit, AFA, Storer, JM, Vincent-Monegat, C, Vallier, A, Vigneron, A, Zaidman-Remy, A, Zamoum, W, Vieira, C, Rebollo, R, Latorre, A, Heddi, A, Parisot, N, Vargas-Chavez, C, Goubert, C, Baa-Puyoulet, P, Balmand, S, Beranger, L, Blanc, C, Bonnamour, A, Boulesteix, M, Burlet, N, Calevro, F, Callaerts, P, Chancy, T, Charles, H, Colella, S, Barbosa, ADS, Dell'Aglio, E, Di Genova, A, Febvay, G, Gabaldon, T, Ferrarini, MG, Gerber, A, Gillet, B, Hubley, R, Hughes, S, Jacquin-Joly, E, Maire, J, Marcet-Houben, M, Masson, F, Meslin, C, Montagne, N, Moya, A, Ribeiro de Vasconcelos, AT, Richard, G, Rosen, J, Sagot, M-F, Smit, AFA, Storer, JM, Vincent-Monegat, C, Vallier, A, Vigneron, A, Zaidman-Remy, A, Zamoum, W, Vieira, C, Rebollo, R, Latorre, A, and Heddi, A
- Abstract
BACKGROUND: The rice weevil Sitophilus oryzae is one of the most important agricultural pests, causing extensive damage to cereal in fields and to stored grains. S. oryzae has an intracellular symbiotic relationship (endosymbiosis) with the Gram-negative bacterium Sodalis pierantonius and is a valuable model to decipher host-symbiont molecular interactions. RESULTS: We sequenced the Sitophilus oryzae genome using a combination of short and long reads to produce the best assembly for a Curculionidae species to date. We show that S. oryzae has undergone successive bursts of transposable element (TE) amplification, representing 72% of the genome. In addition, we show that many TE families are transcriptionally active, and changes in their expression are associated with insect endosymbiotic state. S. oryzae has undergone a high gene expansion rate, when compared to other beetles. Reconstruction of host-symbiont metabolic networks revealed that, despite its recent association with cereal weevils (30 kyear), S. pierantonius relies on the host for several amino acids and nucleotides to survive and to produce vitamins and essential amino acids required for insect development and cuticle biosynthesis. CONCLUSIONS: Here we present the genome of an agricultural pest beetle, which may act as a foundation for pest control. In addition, S. oryzae may be a useful model for endosymbiosis, and studying TE evolution and regulation, along with the impact of TEs on eukaryotic genomes.
- Published
- 2021
9. The genome sequence of the grape phylloxera provides insights into the evolution, adaptation, and invasion routes of an iconic pest
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Rispe, C, Legeai, F, Nabity, PD, Fernandez, R, Arora, AK, Baa-Puyoulet, P, Banfill, CR, Bao, L, Barbera, M, Bouallegue, M, Bretaudeau, A, Brisson, JA, Calevro, F, Capy, P, Catrice, O, Chertemps, T, Couture, C, Deliere, L, Douglas, AE, Dufault-Thompson, K, Escuer, P, Feng, H, Forneck, A, Gabaldon, T, Guigo, R, Hilliou, F, Hinojosa-Alvarez, S, Hsiao, Y-M, Hudaverdian, S, Jacquin-Joly, E, James, EB, Johnston, S, Joubard, B, Le Goff, G, Le Trionnaire, G, Librado, P, Liu, S, Lombaert, E, Lu, H-L, Maibeche, M, Makni, M, Marcet-Houben, M, Martinez-Torres, D, Meslin, C, Montagne, N, Moran, NA, Papura, D, Parisot, N, Rahbe, Y, Lopes, MR, Ripoll-Cladellas, A, Robin, S, Roques, C, Roux, P, Rozas, J, Sanchez-Gracia, A, Sanchez-Herrero, JF, Santesmasses, D, Scatoni, I, Serre, R-F, Tang, M, Tian, W, Umina, PA, van Munster, M, Vincent-Monegat, C, Wemmer, J, Wilson, ACC, Zhang, Y, Zhao, C, Zhao, J, Zhao, S, Zhou, X, Delmotte, F, Tagu, D, Rispe, C, Legeai, F, Nabity, PD, Fernandez, R, Arora, AK, Baa-Puyoulet, P, Banfill, CR, Bao, L, Barbera, M, Bouallegue, M, Bretaudeau, A, Brisson, JA, Calevro, F, Capy, P, Catrice, O, Chertemps, T, Couture, C, Deliere, L, Douglas, AE, Dufault-Thompson, K, Escuer, P, Feng, H, Forneck, A, Gabaldon, T, Guigo, R, Hilliou, F, Hinojosa-Alvarez, S, Hsiao, Y-M, Hudaverdian, S, Jacquin-Joly, E, James, EB, Johnston, S, Joubard, B, Le Goff, G, Le Trionnaire, G, Librado, P, Liu, S, Lombaert, E, Lu, H-L, Maibeche, M, Makni, M, Marcet-Houben, M, Martinez-Torres, D, Meslin, C, Montagne, N, Moran, NA, Papura, D, Parisot, N, Rahbe, Y, Lopes, MR, Ripoll-Cladellas, A, Robin, S, Roques, C, Roux, P, Rozas, J, Sanchez-Gracia, A, Sanchez-Herrero, JF, Santesmasses, D, Scatoni, I, Serre, R-F, Tang, M, Tian, W, Umina, PA, van Munster, M, Vincent-Monegat, C, Wemmer, J, Wilson, ACC, Zhang, Y, Zhao, C, Zhao, J, Zhao, S, Zhou, X, Delmotte, F, and Tagu, D
- Abstract
Background Although native to North America, the invasion of the aphid-like grape phylloxera Daktulosphaira vitifoliae across the globe altered the course of grape cultivation. For the past 150 years, viticulture relied on grafting-resistant North American Vitis species as rootstocks, thereby limiting genetic stocks tolerant to other stressors such as pathogens and climate change. Limited understanding of the insect genetics resulted in successive outbreaks across the globe when rootstocks failed. Here we report the 294-Mb genome of D. vitifoliae as a basic tool to understand host plant manipulation, nutritional endosymbiosis, and enhance global viticulture. Results Using a combination of genome, RNA, and population resequencing, we found grape phylloxera showed high duplication rates since its common ancestor with aphids, but similarity in most metabolic genes, despite lacking obligate nutritional symbioses and feeding from parenchyma. Similarly, no enrichment occurred in development genes in relation to viviparity. However, phylloxera evolved > 2700 unique genes that resemble putative effectors and are active during feeding. Population sequencing revealed the global invasion began from the upper Mississippi River in North America, spread to Europe and from there to the rest of the world. Conclusions The grape phylloxera genome reveals genetic architecture relative to the evolution of nutritional endosymbiosis, viviparity, and herbivory. The extraordinary expansion in effector genes also suggests novel adaptations to plant feeding and how insects induce complex plant phenotypes, for instance galls. Finally, our understanding of the origin of this invasive species and its genome provide genetics resources to alleviate rootstock bottlenecks restricting the advancement of viticulture.
- Published
- 2020
10. The genome sequence of the grape phylloxera provides insights into the evolution, adaptation, and invasion routes of an iconic pest (vol 18, 90, 2020)
- Author
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Rispe, C, Legeai, F, Nabity, PD, Fernandez, R, Arora, AK, Baa-Puyoulet, P, Banfill, CR, Bao, L, Barbera, M, Bouallegue, M, Bretaudeau, A, Brisson, JA, Calevro, F, Capy, P, Catrice, O, Chertemps, T, Couture, C, Deliere, L, Douglas, AE, Dufault-Thompson, K, Escuer, P, Feng, H, Forneck, A, Gabaldon, T, Guigo, R, Hilliou, F, Hinojosa-Alvarez, S, Hsiao, Y-M, Hudaverdian, S, Jacquin-Joly, E, James, EB, Johnston, S, Joubard, B, Le Goff, G, Le Trionnaire, G, Librado, P, Liu, S, Lombaert, E, Lu, H-L, Maibeche, M, Makni, M, Marcet-Houben, M, Martinez-Torres, D, Meslin, C, Montagne, N, Moran, NA, Papura, D, Parisot, N, Rahbe, Y, Lopes, MR, Ripoll-Cladellas, A, Robin, S, Roques, C, Roux, P, Rozas, J, Sanchez-Gracia, A, Sanchez-Herrero, JF, Santesmasses, D, Scatoni, I, Serre, R-F, Tang, M, Tian, W, Umina, PA, van Munster, M, Vincent-Monegat, C, Wemmer, J, Wilson, ACC, Zhang, Y, Zhao, C, Zhao, J, Zhao, S, Zhou, X, Delmotte, F, Tagu, D, Rispe, C, Legeai, F, Nabity, PD, Fernandez, R, Arora, AK, Baa-Puyoulet, P, Banfill, CR, Bao, L, Barbera, M, Bouallegue, M, Bretaudeau, A, Brisson, JA, Calevro, F, Capy, P, Catrice, O, Chertemps, T, Couture, C, Deliere, L, Douglas, AE, Dufault-Thompson, K, Escuer, P, Feng, H, Forneck, A, Gabaldon, T, Guigo, R, Hilliou, F, Hinojosa-Alvarez, S, Hsiao, Y-M, Hudaverdian, S, Jacquin-Joly, E, James, EB, Johnston, S, Joubard, B, Le Goff, G, Le Trionnaire, G, Librado, P, Liu, S, Lombaert, E, Lu, H-L, Maibeche, M, Makni, M, Marcet-Houben, M, Martinez-Torres, D, Meslin, C, Montagne, N, Moran, NA, Papura, D, Parisot, N, Rahbe, Y, Lopes, MR, Ripoll-Cladellas, A, Robin, S, Roques, C, Roux, P, Rozas, J, Sanchez-Gracia, A, Sanchez-Herrero, JF, Santesmasses, D, Scatoni, I, Serre, R-F, Tang, M, Tian, W, Umina, PA, van Munster, M, Vincent-Monegat, C, Wemmer, J, Wilson, ACC, Zhang, Y, Zhao, C, Zhao, J, Zhao, S, Zhou, X, Delmotte, F, and Tagu, D
- Abstract
An amendment to this paper has been published and can be accessed via the original article.
- Published
- 2020
11. Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species
- Author
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Mathers, Thomas, Chen, Yazhou, Kaithakottil, Gemy, Legeai, Fabrice, Mugford, Sam, Baa-Puyoulet, Patrice, Bretaudeau, Anthony, Clavijo, Bernardo, Colella, Stefano, Collin, Olivier, Dalmay, Tamas, Derrien, Thomas, Feng, Honglin, Gabaldón, Toni, Jordan, Anna, Julca, Irene, Kettles, Graeme, Kowitwanich, Krissana, Lavenier, Dominique, Lenzi, Paolo, Lopez-Gomollon, Sara, Loska, Damian, Mapleson, Daniel, Maumus, Florian, Moxon, Simon, Price, Daniel, Sugio, Akiko, van Munster, Manuella, Uzest, Marilyne, Waite, Darren, Jander, Georg, Tagu, Denis, Wilson, Alex, van Oosterhout, Cock, Swarbreck, David, and Hogenhout, Saskia
- Abstract
The prevailing paradigm of host-parasite evolution is that arms races lead to increasing specialisation via genetic adaptation. Insect herbivores are no exception and the majority have evolved to colonise a small number of closely related host species. Remarkably, the green peach aphid, Myzus persicae, colonises plant species across 40 families and single M. persicaeclonal lineages can colonise distantly related plants. This remarkable ability makes M. persicaea highly destructive pest of many important crop species. To investigate the exceptional phenotypic plasticity of M. persicae, we sequenced the M. persicaegenome and assessed how one clonal lineage responds to host plant species of different families. We show that genetically identical individuals are able to colonise distantly related host species through the differential regulation of genes belonging to aphid-expanded gene families. Multigene clusters collectively upregulate in single aphids within two days upon host switch. Furthermore, we demonstrate the functional significance of this rapid transcriptional change using RNA interference (RNAi)-mediated knock-down of genes belonging to the cathepsin B gene family. Knock-down of cathepsin B genes reduced aphid fitness, but only on the host that induced upregulation of these genes. Previous research has focused on the role of genetic adaptation of parasites to their hosts. Here we show that the generalist aphid pest M. persicaeis able to colonise diverse host plant species in the absence of genetic specialisation. This is achieved through rapid transcriptional plasticity of genes that have duplicated during aphid evolution.
- Published
- 2017
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12. CycADS: an annotation database system to ease the development and update of BioCyc databases
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Vellozo, A. F., primary, Veron, A. S., additional, Baa-Puyoulet, P., additional, Huerta-Cepas, J., additional, Cottret, L., additional, Febvay, G., additional, Calevro, F., additional, Rahbe, Y., additional, Douglas, A. E., additional, Gabaldon, T., additional, Sagot, M.-F., additional, Charles, H., additional, and Colella, S., additional
- Published
- 2011
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13. Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species
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Tc, Mathers, Chen Y, Kaithakottil G, Legeai F, Sam Mugford, Baa-Puyoulet P, Bretaudeau A, Clavijo B, Colella S, Collin O, Dalmay T, Derrien T, Feng H, Gabaldón T, Jordan A, Julca I, Gj, Kettles, Kowitwanich K, Lavenier D, and Lenzi P
14. Erratum to: Rapid transcriptional plasticity of duplicated gene clusters enables a clonally reproducing aphid to colonise diverse plant species
- Author
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Mathers, Thomas, Chen, Yazhou, Kaithakottil, Gemy, Legeai, Fabrice, Mugford, Sam, Baa-Puyoulet, Patrice, Bretaudeau, Anthony, Clavijo, Bernardo, Colella, Stefano, Collin, Olivier, Dalmay, Tamas, Derrien, Thomas, Feng, Honglin, Gabaldón, Toni, Jordan, Anna, Julca, Irene, Kettles, Graeme, Kowitwanich, Krissana, Lavenier, Dominique, Lenzi, Paolo, Lopez-Gomollon, Sara, Loska, Damian, Mapleson, Daniel, Maumus, Florian, Moxon, Simon, Price, Daniel, Sugio, Akiko, van Munster, Manuella, Uzest, Marilyne, Waite, Darren, Jander, Georg, Tagu, Denis, Wilson, Alex, van Oosterhout, Cock, Swarbreck, David, and Hogenhout, Saskia
- Published
- 2017
- Full Text
- View/download PDF
15. Annotation of transcription factors, chromatin-associated factors, and basal transcription machinery in the pea aphid, Acyrthosiphon pisum, and development of the ATFdb database, a resource for studies of transcriptional regulation.
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Parisot N, Ribeiro Lopes M, Peignier S, Baa-Puyoulet P, Charles H, Calevro F, and Callaerts P
- Subjects
- Animals, Chromatin metabolism, Chromatin genetics, Genome, Insect, Databases, Genetic, Molecular Sequence Annotation, Insect Proteins genetics, Insect Proteins metabolism, Gene Expression Regulation, Aphids genetics, Aphids metabolism, Transcription Factors metabolism, Transcription Factors genetics
- Abstract
The pea aphid, Acyrthosiphon pisum, is an emerging model system in functional and comparative genomics, in part due to the availability of new genomic approaches and the different sequencing and annotation efforts that the community has dedicated to this important crop pest insect. The pea aphid is also used as a model to study fascinating biological traits of aphids, such as their extensive polyphenisms, their bacteriocyte-confined nutritional symbiosis, or their adaptation to the highly unbalanced diet represented by phloem sap. To get insights into the molecular basis of all these processes, it is important to have an appropriate annotation of transcription factors (TFs), which would enable the reconstruction/inference of gene regulatory networks in aphids. Using the latest version of the A. pisum genome assembly and annotation, which represents the first chromosome-level pea aphid genome, we annotated the complete repertoire of A. pisum TFs and complemented this information by annotating genes encoding chromatin-associated and basal transcription machinery proteins. These annotations were done combining information from the model Drosophila melanogaster, for which we also provide a revisited list of these proteins, and de novo prediction. The comparison between the two model systems allowed the identification of major losses or expansions in each genome, while a deeper analysis was made of ZNF TFs (with certain families expanded in the pea aphid), and the Hox gene cluster (showing reorganization in gene position in the pea aphid compared to D. melanogaster). All annotations are available to the community through the Aphid Transcription Factors database (ATFdb), consolidating the various annotations we generated. ATFdb serves as a valuable resource for gene regulation studies in aphids., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)
- Published
- 2025
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16. At the Gate of Mutualism: Identification of Genomic Traits Predisposing to Insect-Bacterial Symbiosis in Pathogenic Strains of the Aphid Symbiont Serratia symbiotica .
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Renoz F, Foray V, Ambroise J, Baa-Puyoulet P, Bearzatto B, Mendez GL, Grigorescu AS, Mahillon J, Mardulyn P, Gala JL, Calevro F, and Hance T
- Subjects
- Animals, Genome, Bacterial, Genomics, Phylogeny, Serratia, Aphids genetics, Symbiosis
- Abstract
Mutualistic associations between insects and heritable bacterial symbionts are ubiquitous in nature. The aphid symbiont Serratia symbiotica is a valuable candidate for studying the evolution of bacterial symbiosis in insects because it includes a wide diversity of strains that reflect the diverse relationships in which bacteria can be engaged with insects, from pathogenic interactions to obligate intracellular mutualism. The recent discovery of culturable strains, which are hypothesized to resemble the ancestors of intracellular strains, provide an opportunity to study the mechanisms underlying bacterial symbiosis in its early stages. In this study, we analyzed the genomes of three of these culturable strains that are pathogenic to aphid hosts, and performed comparative genomic analyses including mutualistic host-dependent strains. All three genomes are larger than those of the host-restricted S. symbiotica strains described so far, and show significant enrichment in pseudogenes and mobile elements, suggesting that these three pathogenic strains are in the early stages of the adaptation to their host. Compared to their intracellular mutualistic relatives, the three strains harbor a greater diversity of genes coding for virulence factors and metabolic pathways, suggesting that they are likely adapted to infect new hosts and are a potential source of metabolic innovation for insects. The presence in their genomes of secondary metabolism gene clusters associated with the production of antimicrobial compounds and phytotoxins supports the hypothesis that S. symbiotia symbionts evolved from plant-associated strains and that plants may serve as intermediate hosts. Mutualistic associations between insects and bacteria are the result of independent transitions to endosymbiosis initiated by the acquisition of environmental progenitors. In this context, the genomes of free-living S. symbiotica strains provide a rare opportunity to study the inventory of genes held by bacterial associates of insects that are at the gateway to a host-dependent lifestyle., Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest., (Copyright © 2021 Renoz, Foray, Ambroise, Baa-Puyoulet, Bearzatto, Mendez, Grigorescu, Mahillon, Mardulyn, Gala, Calevro and Hance.)
- Published
- 2021
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17. Drosophila-associated bacteria differentially shape the nutritional requirements of their host during juvenile growth.
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Consuegra J, Grenier T, Baa-Puyoulet P, Rahioui I, Akherraz H, Gervais H, Parisot N, da Silva P, Charles H, Calevro F, and Leulier F
- Subjects
- Acetobacter genetics, Acetobacter metabolism, Amino Acids metabolism, Animal Nutritional Physiological Phenomena, Animals, Drosophila melanogaster growth & development, Drosophila melanogaster metabolism, Gastrointestinal Microbiome, Host Microbial Interactions, Lactobacillus genetics, Lactobacillus metabolism, Larva growth & development, Larva metabolism, Larva microbiology, Larva physiology, Metabolic Networks and Pathways, Micronutrients metabolism, Species Specificity, Acetobacter physiology, Drosophila melanogaster microbiology, Drosophila melanogaster physiology, Lactobacillus physiology, Nutritional Requirements physiology
- Abstract
The interplay between nutrition and the microbial communities colonizing the gastrointestinal tract (i.e., gut microbiota) determines juvenile growth trajectory. Nutritional deficiencies trigger developmental delays, and an immature gut microbiota is a hallmark of pathologies related to childhood undernutrition. However, how host-associated bacteria modulate the impact of nutrition on juvenile growth remains elusive. Here, using gnotobiotic Drosophila melanogaster larvae independently associated with Acetobacter pomorumWJL (ApWJL) and Lactobacillus plantarumNC8 (LpNC8), 2 model Drosophila-associated bacteria, we performed a large-scale, systematic nutritional screen based on larval growth in 40 different and precisely controlled nutritional environments. We combined these results with genome-based metabolic network reconstruction to define the biosynthetic capacities of Drosophila germ-free (GF) larvae and its 2 bacterial partners. We first established that ApWJL and LpNC8 differentially fulfill the nutritional requirements of the ex-GF larvae and parsed such difference down to individual amino acids, vitamins, other micronutrients, and trace metals. We found that Drosophila-associated bacteria not only fortify the host's diet with essential nutrients but, in specific instances, functionally compensate for host auxotrophies by either providing a metabolic intermediate or nutrient derivative to the host or by uptaking, concentrating, and delivering contaminant traces of micronutrients. Our systematic work reveals that beyond the molecular dialogue engaged between the host and its bacterial partners, Drosophila and its associated bacteria establish an integrated nutritional network relying on nutrient provision and utilization., Competing Interests: The authors have declared that no competing interests exist.
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- 2020
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18. Draft Genome Sequences of Two Cultivable Strains of the Bacterial Symbiont Serratia symbiotica.
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Renoz F, Ambroise J, Bearzatto B, Baa-Puyoulet P, Calevro F, Gala JL, and Hance T
- Abstract
Serratia symbiotica , one of the most frequent symbiont species in aphids, includes strains that exhibit various lifestyles ranging from free-living to obligate intracellular mutualism. Here, we report the draft genome sequences of two strains, namely, 24.1 and Apa8A1, isolated from aphids of the genus Aphis , consisting of genome sizes of 3,089,091 bp and 3,232,107 bp, respectively. These genome sequences may provide new insights into how mutualistic interactions between bacteria and insects evolve and are shaped., (Copyright © 2020 Renoz et al.)
- Published
- 2020
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19. Bacteriocyte Reprogramming to Cope With Nutritional Stress in a Phloem Sap Feeding Hemipteran, the Pea Aphid Acyrthosiphon pisum .
- Author
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Colella S, Parisot N, Simonet P, Gaget K, Duport G, Baa-Puyoulet P, Rahbé Y, Charles H, Febvay G, Callaerts P, and Calevro F
- Abstract
Nutritional symbioses play a central role in the ability of insects to thrive on unbalanced diets and in ensuring their evolutionary success. A genomic model for nutritional symbiosis comprises the hemipteran Acyrthosiphon pisum , and the gamma-3-proteobacterium, Buchnera aphidicola , with genomes encoding highly integrated metabolic pathways. A. pisum feeds exclusively on plant phloem sap, a nutritionally unbalanced diet highly variable in composition, thus raising the question of how this symbiotic system responds to nutritional stress. We addressed this by combining transcriptomic, phenotypic and life history trait analyses to determine the organismal impact of deprivation of tyrosine and phenylalanine. These two aromatic amino acids are essential for aphid development, are synthesized in a metabolic pathway for which the aphid host and the endosymbiont are interdependent, and their concentration can be highly variable in plant phloem sap. We found that this nutritional challenge does not have major phenotypic effects on the pea aphid, except for a limited weight reduction and a 2-day delay in onset of nymph laying. Transcriptomic analyses through aphid development showed a prominent response in bacteriocytes (the core symbiotic tissue which houses the symbionts), but not in gut, thus highlighting the role of bacteriocytes as major modulators of this homeostasis. This response does not involve a direct regulation of tyrosine and phenylalanine biosynthetic pathway and transporter genes. Instead, we observed an extensive transcriptional reprogramming of the bacteriocyte with a rapid down-regulation of genes encoding sugar transporters and genes required for sugar metabolism. Consistently, we observed continued overexpression of the A. pisum homolog of RRAD, a small GTPase implicated in repressing aerobic glycolysis. In addition, we found increased transcription of genes involved in proliferation, cell size control and signaling. We experimentally confirmed the significance of these gene expression changes detecting an increase in bacteriocyte number and cell size in vivo under tyrosine and phenylalanine depletion. Our results support a central role of bacteriocytes in the aphid response to amino acid deprivation: their transcriptional and cellular responses fine-tune host physiology providing the host insect with an effective way to cope with the challenges posed by the variability in composition of phloem sap.
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- 2018
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20. ArthropodaCyc: a CycADS powered collection of BioCyc databases to analyse and compare metabolism of arthropods.
- Author
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Baa-Puyoulet P, Parisot N, Febvay G, Huerta-Cepas J, Vellozo AF, Gabaldón T, Calevro F, Charles H, and Colella S
- Subjects
- Animals, Molecular Sequence Annotation, Arthropods genetics, Database Management Systems, Databases, Genetic, Internet, Software
- Abstract
Arthropods interact with humans at different levels with highly beneficial roles (e.g. as pollinators), as well as with a negative impact for example as vectors of human or animal diseases, or as agricultural pests. Several arthropod genomes are available at present and many others will be sequenced in the near future in the context of the i5K initiative, offering opportunities for reconstructing, modelling and comparing their metabolic networks. In-depth analysis of these genomic data through metabolism reconstruction is expected to contribute to a better understanding of the biology of arthropods, thereby allowing the development of new strategies to control harmful species. In this context, we present here ArthropodaCyc, a dedicated BioCyc collection of databases using the Cyc annotation database system (CycADS), allowing researchers to perform reliable metabolism comparisons of fully sequenced arthropods genomes. Since the annotation quality is a key factor when performing such global genome comparisons, all proteins from the genomes included in the ArthropodaCyc database were re-annotated using several annotation tools and orthology information. All functional/domain annotation results and their sources were integrated in the databases for user access. Currently, ArthropodaCyc offers a centralized repository of metabolic pathways, protein sequence domains, Gene Ontology annotations as well as evolutionary information for 28 arthropod species. Such database collection allows metabolism analysis both with integrated tools and through extraction of data in formats suitable for systems biology studies.Database URL: http://arthropodacyc.cycadsys.org/., (© The Author(s) 2016. Published by Oxford University Press.)
- Published
- 2016
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21. Tyrosine pathway regulation is host-mediated in the pea aphid symbiosis during late embryonic and early larval development.
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Rabatel A, Febvay G, Gaget K, Duport G, Baa-Puyoulet P, Sapountzis P, Bendridi N, Rey M, Rahbé Y, Charles H, Calevro F, and Colella S
- Subjects
- Animals, Aphids metabolism, Aphids physiology, Aspartate Aminotransferases genetics, Aspartate Aminotransferases metabolism, Biological Transport, Gene Expression Regulation, Developmental, Larva genetics, Larva growth & development, Oligonucleotide Array Sequence Analysis, Aphids embryology, Aphids genetics, Embryonic Development genetics, Gene Expression Profiling, Pisum sativum, Symbiosis, Tyrosine metabolism
- Abstract
Background: Nutritional symbioses play a central role in insects' adaptation to specialized diets and in their evolutionary success. The obligatory symbiosis between the pea aphid, Acyrthosiphon pisum, and the bacterium, Buchnera aphidicola, is no exception as it enables this important agricultural pest insect to develop on a diet exclusively based on plant phloem sap. The symbiotic bacteria provide the host with essential amino acids lacking in its diet but necessary for the rapid embryonic growth seen in the parthenogenetic viviparous reproduction of aphids. The aphid furnishes, in exchange, non-essential amino acids and other important metabolites. Understanding the regulations acting on this integrated metabolic system during the development of this insect is essential in elucidating aphid biology., Results: We used a microarray-based approach to analyse gene expression in the late embryonic and the early larval stages of the pea aphid, characterizing, for the first time, the transcriptional profiles in these developmental phases. Our analyses allowed us to identify key genes in the phenylalanine, tyrosine and dopamine pathways and we identified ACYPI004243, one of the four genes encoding for the aspartate transaminase (E.C. 2.6.1.1), as specifically regulated during development. Indeed, the tyrosine biosynthetic pathway is crucial for the symbiotic metabolism as it is shared between the two partners, all the precursors being produced by B. aphidicola. Our microarray data are supported by HPLC amino acid analyses demonstrating an accumulation of tyrosine at the same developmental stages, with an up-regulation of the tyrosine biosynthetic genes. Tyrosine is also essential for the synthesis of cuticular proteins and it is an important precursor for cuticle maturation: together with the up-regulation of tyrosine biosynthesis, we observed an up-regulation of cuticular genes expression. We were also able to identify some amino acid transporter genes which are essential for the switch over to the late embryonic stages in pea aphid development., Conclusions: Our data show that, in the development of A. pisum, a specific host gene set regulates the biosynthetic pathways of amino acids, demonstrating how the regulation of gene expression enables an insect to control the production of metabolites crucial for its own development and symbiotic metabolism.
- Published
- 2013
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