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10 results for “Phyllosticta”
Phyllosticta citricarpa ̶ Pest Report and Datasheet to support ranking of EU candidate priority pests
<p>These two files are part of the outputs produced under the mandate <a href="http://registerofquestions.efsa.europa.eu/roqFrontend/wicket/page?1-1.ILinkListener-contentPane-listContainer-pageable-21-mandateNumberLnk">M-2017-0056</a> of the European Commission requesting EFSA for technical assistance in the field of quarantine pests qualifying as priority pests as by Article 6(2) of the Regulation (EU) 2016/2031 <em>on protective measures against pests of plants</em>.</p> <p>Under the mandate EFSA produced: i) 1 methodology report (DOI available at the field "Related/alternate identifiers"), ii) 28 datasheets, one for each of the 28 candidate pests, and iii) 28 pest reports supporting the information provided in the datasheets.</p> <p>EFSA wishes to acknowledge the contribution of Trond Rafoss, Christian Vernière, Antonio Vicent to the EKE and the review conducted by Jaime Cubero.</p>
FIGURE 3 in Morphological and multi-gene phylogenetic analyses of two new species of Phyllosticta (Phyllostictaceae, Botryosphaeriales) from Southwestern China
FIGURE 3. Phyllosticta ovalina (IFRD 9478, holotype). a. Microfungi on leaf litter. b–c. Ascomata on leaf surface. d–e. Vertical section of ascomata. f–i. Asci. j–n. Ascospores (i in cotton blue). Scale bars: b = 500 μm, c = 100 μm, d = 50 μm, f–i = 20 μm, j–n = 10 μm.
FIGURE 1 in Morphological and multi-gene phylogenetic analyses of two new species of Phyllosticta (Phyllostictaceae, Botryosphaeriales) from Southwestern China
FIGURE 1. Phylogram of Phyllosticta resulting from a maximum likelihood analysis based on a combined matrix of ITS, LSU and TEF1 loci. The tree is artificially rooted to B. obtusa (CMW 8232). ML bootstrap values (left, ML-BS ≥ 50%) and Bayesian posterior probabilities (right, BYPP ≥ 0.9) are given at the nodes. New species of this study are indicated using red font and their associated support is bolded.
FIGURE 2 in Morphological and multi-gene phylogenetic analyses of two new species of Phyllosticta (Phyllostictaceae, Botryosphaeriales) from Southwestern China
FIGURE 2. Phyllosticta savannaensis (IFRD 9476, holotype). a. Microfungi on leaf litter. b–c. Ascomata on leaf surface. d–e. Vertical section of ascomata. f–i. Asci (i in cotton blue). j–n. Ascospores (m, n in cotton blue). Scale bars: b = 1000 μm, c= 500 μm, d = 100 μm, e, g–i = 30 μm, f = 50 μm, j–n = 10 μm.
FIGURE 2 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China
FIGURE 2. The first of 2496 equally most parsimonious trees obtained from a heuristic search with 1000 random taxon additions of the ITS, ACT, TEF-1 and GPDH sequences using PAUP v. 4.0b10. The scale bar shows 20 changes. Bootstrap support values for maximum parsimony (MPBS) and maximum likelihood (MLBS)(equal to or above 50 %)were shown. Thickened branches represent significant Bayesian posterior probability (≥90%). A hyphen (–) indicates the value lower than 50%. The tree is rooted Botryosphaeria dothidea.An asterisk (*) indicates the ex-type strains. Novel sequences are printed in bold.
FIGURE 1. The most parsimonious trees obtained from a heuristic search with 1000 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China
FIGURE 1. The most parsimonious trees obtained from a heuristic search with 1000 random taxon additions of the LSU sequences using PAUP v. 4.0b10. The scale bar shows 5 changes. Bootstrap support values for maximum parsimony (MP) and Bayesian posterior probabilities above 0.90are shown. A hyphens (–) indicates the value lower than 50% (BS) or 0.90 (PP). The tree is rooted to Botryosphaeria dothidea. Ex-type/ex-epitype isolates are marked by an asterisk *. Novel sequences are in boldface.
FIGURE 3 in Phyllosticta species from banana (Musa sp.) in Chongqing and Guizhou Provinces, China
FIGURE 3.Phyllosticta musaechinensis (CQ12097, holotype).a. Symptom of disease. b. Pycnidia on infected leaf of Musa sp. c, d. Ostiole of pycnidium. e. Pycnidium and conidiogenous cell. f–h. Conidia. i. Conidia on colony. j. Conidiogenous cell in culture. k. Conidia from culture. l–n. Culture on PDA. Scale bars: e = 50µm, f–h, j, k = 20 µm, n = 5 mm.
Mating-type locus rearrangements and shifts in thallism states in Citrus-associated Phyllosticta species
<p>Files related to the manuscript published in to Fungal Genetics and Biology (<a href="https://doi.org/10.1016/j.fgb.2020.103444">https://doi.org/10.1016/j.fgb.2020.103444</a>), with preprint available in bioRxiv (https://doi.org/10.1101/2020.04.14.040725).</p> <p>Contains:</p> <p>- 03 genome assemblies: Phyllosticta capitalensis LGMF01, Phyllosticta citribraziliensis LGMF08 and Phyllosticta citricarpa LGMF06;</p> <p>- 14 protein-coding gene annotation based in 14 Phyllosticta genomes;</p> <p>- Mating-type locus annotation from the 14 Phyllosticta strains in GBK format, and related FASTA sequences;</p>
Supplementary material 1 from: Zhang Z, Liu X, Zhang X, Meng Z (2022) Morphological and phylogenetic analyses reveal two new species and a new record of Phyllosticta (Botryosphaeriales, Phyllostictaceae) from Hainan, China. MycoKeys 91: 1-23. https://doi.org/10.3897/mycokeys.91.84803
The combined ITS, LSU, tef1, ACT and GAPDH sequences
Downregulated d-limonene transgenic orange trees with increased linalool content showed resistance to Phyllosticta citricarpa
GEO Series GSE99295. Citrus; Citrus sinensis. 18 samples. Type: Expression profiling by array.
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