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Anthony P. James

Bio: Anthony P. James is an academic researcher from Queensland University of Technology. The author has contributed to research in topics: Banana streak virus & Colocasia esculenta. The author has an hindex of 9, co-authored 26 publications receiving 604 citations. Previous affiliations of Anthony P. James include Foundation for Research & Technology – Hellas.

Papers
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Journal ArticleDOI
Washington University in St. Louis1, National Institutes of Health2, Georgia State University3, United States Army Medical Research Institute of Infectious Diseases4, Friedrich Loeffler Institute5, Commonwealth Scientific and Industrial Research Organisation6, Columbia University7, University of Texas Medical Branch8, Colorado State University9, Yeshiva University10, University of Queensland11, University of Marburg12, University of Warwick13, Mayo Clinic14, Zhejiang University15, World Health Organization16, Erasmus University Rotterdam17, New York University18, Queensland University of Technology19, Public Health England20, Auckland University of Technology21, Kyoto University22, Huazhong Agricultural University23, Laval University24, Okayama University25, United States Geological Survey26, Northwestern University27, Icahn School of Medicine at Mount Sinai28, Boston University29, Novosibirsk State University30, University of Medicine and Health Sciences31, University of Veterinary Medicine Vienna32, Texas Biomedical Research Institute33, Texas A&M University34, University of Auckland35, University of St Andrews36, University of Melbourne37, Queen's University Belfast38, Centers for Disease Control and Prevention39, University of Freiburg40, Defence Science and Technology Laboratory41, University of Missouri42, Hokkaido University43, Pasteur Institute44, Claude Bernard University Lyon 145, National University of Singapore46, University of Rochester47, Kansas State University48
TL;DR: The updated taxonomy of the order Mononegavirales is presented, with non-Latinized binomial species names replaced all paramyxovirus and pneumovirus species names, thereby accomplishing application of binomial Species names throughout the entire order.
Abstract: In 2017, the order Mononegavirales was expanded by the inclusion of a total of 69 novel species. Five new rhabdovirus genera and one new nyamivirus genus were established to harbor 41 of these species, whereas the remaining new species were assigned to already established genera. Furthermore, non-Latinized binomial species names replaced all paramyxovirus and pneumovirus species names, thereby accomplishing application of binomial species names throughout the entire order. This article presents the updated taxonomy of the order Mononegavirales as now accepted by the International Committee on Taxonomy of Viruses (ICTV).

222 citations

Journal ArticleDOI
TL;DR: In this article, the identification of transgenic Cavendish with resistance to Tropical Race 4 (TR4) was reported, and two lines were transformed with RGA2, a gene isolated from a TR4-resistant diploid banana, and the other with a nematode-derived gene, Ced9.
Abstract: Banana (Musa spp.) is a staple food for more than 400 million people. Over 40% of world production and virtually all the export trade is based on Cavendish banana. However, Cavendish banana is under threat from a virulent fungus, Fusarium oxysporum f. sp. cubense tropical race 4 (TR4) for which no acceptable resistant replacement has been identified. Here we report the identification of transgenic Cavendish with resistance to TR4. In our 3-year field trial, two lines of transgenic Cavendish, one transformed with RGA2, a gene isolated from a TR4-resistant diploid banana, and the other with a nematode-derived gene, Ced9, remain disease free. Transgene expression in the RGA2 lines is strongly correlated with resistance. Endogenous RGA2 homologs are also present in Cavendish but are expressed tenfold lower than that in our most resistant transgenic line. The expression of these homologs can potentially be elevated through gene editing, to provide non-transgenic resistance.

157 citations

Journal ArticleDOI
TL;DR: The results from this study suggest that early activation of the rate‐limiting enzyme in the carotenoid biosynthetic pathway and extended fruit maturation time are essential factors to achieve optimal PVA concentrations in banana fruit.
Abstract: Summary Vitamin A deficiency remains one of the world's major public health problems despite food fortification and supplements strategies. Biofortification of staple crops with enhanced levels of pro-vitamin A (PVA) offers a sustainable alternative strategy to both food fortification and supplementation. As a proof of concept, PVA-biofortified transgenic Cavendish bananas were generated and field trialed in Australia with the aim of achieving a target level of 20 μg/g of dry weight (dw) β-carotene equivalent (β-CE) in the fruit. Expression of a Fe'i banana-derived phytoene synthase 2a (MtPsy2a) gene resulted in the generation of lines with PVA levels exceeding the target level with one line reaching 55 μg/g dw β-CE. Expression of the maize phytoene synthase 1 (ZmPsy1) gene, used to develop “Golden Rice 2”, also resulted in increased fruit PVA levels although many lines displayed undesirable phenotypes. Constitutive expression of either transgene with the maize polyubiquitin promoter increased PVA accumulation from the earliest stage of fruit development. In contrast, PVA accumulation was restricted to the late stages of fruit development when either the banana 1-aminocyclopropane-1-carboxylate oxidase or the expansin 1 promoters were used to drive the same transgenes. Wild-type plants with the longest fruit development time had also the highest fruit PVA concentrations. The results from this study suggest that early activation of the rate-limiting enzyme in the carotenoid biosynthetic pathway, as well as extended fruit maturation time, are essential factors to achieve optimal PVA concentrations in banana fruit.

127 citations

Journal ArticleDOI
TL;DR: This technique was shown to discriminate between integrated and episomal BSV DNA, specifically detecting the latter in several banana cultivars known to contain episomal or integrated sequences of Banana streak Mysore virus, Banana streak OL virus, and Banana streak GF virus.
Abstract: Banana plants are hosts to a large number of Banana streak virus (BSV) species. However, diagnostic methods for BSV are inadequate because of the considerable genetic and serological diversity among BSV isolates and the presence of integrated BSV sequences in some banana cultivars which leads to false positives. In this study, a sequence-nonspecific, rolling-circle amplification (RCA) technique was developed and shown to overcome these limitations for the detection and subsequent characterization of BSV isolates infecting banana. This technique was shown to discriminate between integrated and episomal BSV DNA, specifically detecting the latter in several banana cultivars known to contain episomal or integrated sequences of Banana streak Mysore virus (BSMyV), Banana streak OL virus (BSOLV), and Banana streak GF virus (BSGFV). Using RCA, the presence of BSMyV and BSOLV was confirmed in Australia, while BSOLV, BSGFV, Banana streak Uganda I virus (BSUgIV), Banana streak Uganda L virus (BSUgLV), and Banana streak Uganda M virus (BSUgMV) were detected in Uganda. This is the first confirmed report of episomally-derived BSUglV, BSUgLV, and BSUgMV in Uganda. As well as its ability to detect BSV, RCA was shown to detect two other pararetroviruses, Sugarcane bacilliform virus in sugarcane and Cauliflower mosaic virus in turnip.

78 citations

Journal ArticleDOI
TL;DR: It is demonstrated that sequences with high similarity to BSIMV only were present in several banana cultivars which had tested negative for episomal BSV sequences, and it is proposed that these sequences be recognised as six new species and be designated as Banana streak UA virus, Banana streak UI virus, banana streak UL virus, bananas streak UM virus and Banana streak IM virus.
Abstract: Banana leaf streak disease, caused by several species of Banana streak virus (BSV), is widespread in East Africa. We surveyed for this disease in Uganda and Kenya, and used rolling-circle amplification (RCA) to detect the presence of BSV in banana. Six distinct badnavirus sequences, three from Uganda and three from Kenya, were amplified for which only partial sequences were previously available. The complete genomes were sequenced and characterised. The size and organisation of all six sequences was characteristic of other badnaviruses, including conserved functional domains present in the putative polyprotein encoded by open reading frame (ORF) 3. Based on nucleotide sequence analysis within the reverse transcriptase/ribonuclease H-coding region of open reading frame 3, we propose that these sequences be recognised as six new species and be designated as Banana streak UA virus, Banana streak UI virus, Banana streak UL virus, Banana streak UM virus, Banana streak CA virus and Banana streak IM virus. Using PCR and species-specific primers to test for the presence of integrated sequences, we demonstrated that sequences with high similarity to BSIMV only were present in several banana cultivars which had tested negative for episomal BSV sequences.

43 citations


Cited by
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01 Jun 2012
TL;DR: SPAdes as mentioned in this paper is a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler and on popular assemblers Velvet and SoapDeNovo (for multicell data).
Abstract: The lion's share of bacteria in various environments cannot be cloned in the laboratory and thus cannot be sequenced using existing technologies. A major goal of single-cell genomics is to complement gene-centric metagenomic data with whole-genome assemblies of uncultivated organisms. Assembly of single-cell data is challenging because of highly non-uniform read coverage as well as elevated levels of sequencing errors and chimeric reads. We describe SPAdes, a new assembler for both single-cell and standard (multicell) assembly, and demonstrate that it improves on the recently released E+V-SC assembler (specialized for single-cell data) and on popular assemblers Velvet and SoapDeNovo (for multicell data). SPAdes generates single-cell assemblies, providing information about genomes of uncultivatable bacteria that vastly exceeds what may be obtained via traditional metagenomics studies. SPAdes is available online ( http://bioinf.spbau.ru/spades ). It is distributed as open source software.

10,124 citations

Journal ArticleDOI
07 Nov 2019-Nature
TL;DR: The potential of plant sciences to address post-Green Revolution challenges in agriculture is considered and emerging strategies for enhancing sustainable crop production and resilience in a changing climate are explored.
Abstract: The current trajectory for crop yields is insufficient to nourish the world’s population by 20501. Greater and more consistent crop production must be achieved against a backdrop of climatic stress that limits yields, owing to shifts in pests and pathogens, precipitation, heat-waves and other weather extremes. Here we consider the potential of plant sciences to address post-Green Revolution challenges in agriculture and explore emerging strategies for enhancing sustainable crop production and resilience in a changing climate. Accelerated crop improvement must leverage naturally evolved traits and transformative engineering driven by mechanistic understanding, to yield the resilient production systems that are needed to ensure future harvests. Genetic strategies for improving the yield and sustainability of agricultural crops, and the resilience of crops in the face of biotic and abiotic stresses contingent on projected climate change, are evaluated.

639 citations

Journal ArticleDOI
TL;DR: This review provides a comprehensive overview of the impact of various types of plastids on carotenoid biosynthesis and accumulation, and discusses recent advances in the understanding of the regulatory control ofCarotenogenesis and metabolic engineering ofcarotenoids in light ofplastid types in plants.

388 citations

Journal ArticleDOI
Gaya K. Amarasinghe1, María A. Ayllón2, Yīmíng Bào3, Christopher F. Basler4, Sina Bavari5, Kim R. Blasdell6, Thomas Briese7, Paul Brown, Alexander Bukreyev8, Anne Balkema-Buschmann9, Ursula J. Buchholz10, Camila Chabi-Jesus11, Kartik Chandran12, Chiara Chiapponi, Ian Crozier10, Rik L. de Swart13, Ralf G. Dietzgen14, Olga Dolnik15, Jan Felix Drexler16, Ralf Dürrwald17, William G. Dundon18, W. Paul Duprex19, John M. Dye5, Andrew J. Easton20, Anthony R. Fooks, Pierre Formenty21, Ron A. M. Fouchier13, Juliana Freitas-Astúa22, Anthony Griffiths23, Roger Hewson24, Masayuki Horie25, Timothy H. Hyndman26, Dàohóng Jiāng27, E. W. Kitajima28, Gary P. Kobinger29, Hideki Kondō30, Gael Kurath31, Ivan V. Kuzmin32, Robert A. Lamb33, Antonio Lavazza, Benhur Lee34, Davide Lelli, Eric M. Leroy35, Jiànróng Lǐ36, Piet Maes37, Shin-Yi Lee Marzano38, Ana Moreno, Elke Mühlberger23, Sergey V. Netesov39, Norbert Nowotny40, Norbert Nowotny41, Are Nylund42, Arnfinn Lodden Økland42, Gustavo Palacios5, Bernadett Pályi, Janusz T. Paweska, Susan Payne43, Alice Prosperi, Pedro Luis Ramos-González11, Bertus K. Rima44, Paul A. Rota45, Dennis Rubbenstroth9, Mǎng Shī46, Peter Simmonds47, Sophie J. Smither48, Enrica Sozzi, Kirsten Spann49, Mark D. Stenglein50, David M. Stone, Ayato Takada51, Robert B. Tesh8, Keizō Tomonaga25, Noël Tordo52, Jonathan S. Towner45, Bernadette G. van den Hoogen13, Nikos Vasilakis8, Victoria Wahl, Peter J. Walker14, Lin-Fa Wang53, Anna E. Whitfield54, John V. Williams19, F. Murilo Zerbini55, Tāo Zhāng3, Yong-Zhen Zhang56, Yong-Zhen Zhang57, Jens H. Kuhn10 
Washington University in St. Louis1, Technical University of Madrid2, Beijing Institute of Genomics3, Georgia State University4, United States Army Medical Research Institute of Infectious Diseases5, Commonwealth Scientific and Industrial Research Organisation6, Columbia University7, University of Texas Medical Branch8, Friedrich Loeffler Institute9, National Institutes of Health10, Instituto Biológico11, Albert Einstein College of Medicine12, Erasmus University Rotterdam13, University of Queensland14, University of Marburg15, Humboldt University of Berlin16, Robert Koch Institute17, International Atomic Energy Agency18, University of Pittsburgh19, University of Warwick20, World Health Organization21, Empresa Brasileira de Pesquisa Agropecuária22, Boston University23, Public Health England24, Kyoto University25, Murdoch University26, Huazhong Agricultural University27, University of São Paulo28, Laval University29, Okayama University30, United States Geological Survey31, United States Department of Agriculture32, Northwestern University33, Icahn School of Medicine at Mount Sinai34, Institut de recherche pour le développement35, Ohio State University36, Katholieke Universiteit Leuven37, South Dakota State University38, Novosibirsk State University39, University of Veterinary Medicine Vienna40, University of Medicine and Health Sciences41, University of Bergen42, Texas A&M University43, Queen's University Belfast44, Centers for Disease Control and Prevention45, University of Sydney46, University of Oxford47, Defence Science and Technology Laboratory48, Queensland University of Technology49, Colorado State University50, Hokkaido University51, Pasteur Institute52, National University of Singapore53, North Carolina State University54, Universidade Federal de Viçosa55, Fudan University56, Chinese Center for Disease Control and Prevention57
TL;DR: The updated taxonomy of the order Mononegavirales is presented as now accepted by the International Committee on Taxonomy of Viruses (ICTV).
Abstract: In February 2019, following the annual taxon ratification vote, the order Mononegavirales was amended by the addition of four new subfamilies and 12 new genera and the creation of 28 novel species. This article presents the updated taxonomy of the order Mononegavirales as now accepted by the International Committee on Taxonomy of Viruses (ICTV).

238 citations

Journal ArticleDOI
Washington University in St. Louis1, National Institutes of Health2, Georgia State University3, United States Army Medical Research Institute of Infectious Diseases4, Friedrich Loeffler Institute5, Commonwealth Scientific and Industrial Research Organisation6, Columbia University7, University of Texas Medical Branch8, Colorado State University9, Yeshiva University10, University of Queensland11, University of Marburg12, University of Warwick13, Mayo Clinic14, Zhejiang University15, World Health Organization16, Erasmus University Rotterdam17, New York University18, Queensland University of Technology19, Public Health England20, Auckland University of Technology21, Kyoto University22, Huazhong Agricultural University23, Laval University24, Okayama University25, United States Geological Survey26, Northwestern University27, Icahn School of Medicine at Mount Sinai28, Boston University29, Novosibirsk State University30, University of Medicine and Health Sciences31, University of Veterinary Medicine Vienna32, Texas Biomedical Research Institute33, Texas A&M University34, University of Auckland35, University of St Andrews36, University of Melbourne37, Queen's University Belfast38, Centers for Disease Control and Prevention39, University of Freiburg40, Defence Science and Technology Laboratory41, University of Missouri42, Hokkaido University43, Pasteur Institute44, Claude Bernard University Lyon 145, National University of Singapore46, University of Rochester47, Kansas State University48
TL;DR: The updated taxonomy of the order Mononegavirales is presented, with non-Latinized binomial species names replaced all paramyxovirus and pneumovirus species names, thereby accomplishing application of binomial Species names throughout the entire order.
Abstract: In 2017, the order Mononegavirales was expanded by the inclusion of a total of 69 novel species. Five new rhabdovirus genera and one new nyamivirus genus were established to harbor 41 of these species, whereas the remaining new species were assigned to already established genera. Furthermore, non-Latinized binomial species names replaced all paramyxovirus and pneumovirus species names, thereby accomplishing application of binomial species names throughout the entire order. This article presents the updated taxonomy of the order Mononegavirales as now accepted by the International Committee on Taxonomy of Viruses (ICTV).

222 citations