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Fatty acid composition and lipid profiles as chemotaxonomic markers of phytopathogenic fungi Puccinia malvacearum and P. glechomatis
Institution:1. Department of Botany, Mycology and Ecology, Institute of Biological Sciences, Faculty of Biology and Biotechnology, Maria Curie-Sk?odowska University, Akademicka 19, 20-033, Lublin, Poland;2. Retired, James Hutton Institute, Invergowrie, Dundee DD2 5DA, Scotland, UK;3. Core Facility Metabolomics, Leibniz-Institute for Farm Animal Biology (FBN), Wilhelm-Stahl-Allee 2, 18196, Dummerstorf, Germany;4. Department of Genetics and Microbiology, Institute of Biological Science, Faculty of Biology and Biotechnology, Maria Curie-Sk?odowska University, Akademicka 19 St, 20-033, Lublin, Poland;1. Laboratory of Emerging Fungal Pathogens, Department of Microbiology, Immunology, and Parasitology, Discipline of Cellular Biology, Federal University of São Paulo (UNIFESP), São Paulo, 04023062, Brazil;2. Department of Medicine, Discipline of Infectious Diseases, Federal University of São Paulo (UNIFESP), São Paulo, 04023062, Brazil;3. Department of Medical Mycology, Westerdijk Fungal Biodiversity Institute, Uppsalalaan 8, 3584CT, Utrecht, the Netherlands;4. Department of Medical Microbiology, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, the Netherlands;5. Laboratory of Medical Mycology, Jining No. 1 People''s Hospital, Jining, Shandong, People''s Republic of China;6. Infectious Diseases Postgraduate Program, Center for Research in Medical Mycology, Federal University of Espírito Santo (UFES), Espírito Santo, Brazil;7. Mycology Unit of the Infectious Diseases Hospital F.J. Muñiz, Reference Center of Mycology of Buenos Aires City, Buenos Aires, Argentina;8. Department of Veterinary Dermatology, Nihon University College of Bioresource Sciences, Fujisawa, Kanagawa, Japan;9. Dermatology Service, Mycology Department, Hospital General de México, “Dr. Eduardo Liceaga”, Mexico City, Mexico;1. Dipartimento di Scienze, Università ‘Roma Tre’, Viale G. Marconi 446 – 00146, Rome, Italy;2. Dipartimento di Scienze Ecologiche e Biologiche (DEB), Università degli Studi della Tuscia, Largo dell’Università Snc – 01100, Viterbo, Italy;1. School of Life Science, Chongqing University, Chongqing, 400030, People’s Republic of China;2. Instituty of Tobacco Scientific and Technology of Chongqing, Chongqing, 400030, People’s Republic of China;1. Division of Fruit Tree Production Reseach, Institute of Fruit Tree and Tea Science, NARO, 92-24 Shimokuriyagawa, Morioka, Iwate, 020-0123, Japan;2. School of Pharmacy, Nihon University, 7-7-1 Narashinodai, Funabashi, Chiba, 274-8555, Japan;1. School of Biological Science and Technology, University of Jinan, Jinan, China;2. State Key Laboratory of Biobased Material and Green Papermaking, Qilu University of Technology, Shandong Academy of Sciences, Jinan, China;3. Maize Research Institute, Shandong Academy of Agricultural Sciences, Jinan, China
Abstract:The analysis of the overall fatty acid pattern as well as their distribution in various lipid classes of phytopathogenic fungi Puccinia malvacearum and P. glechomatis are considered as chemotaxonomic biomarkers. Puccinia malvacearum on Alcea rosea and P. glechomatis on Glechoma hederacea collected from plants grown in various localities were analysed to determine their fatty acid composition. Both species synthesised significant amounts of saturated palmitic and stearic acids as well as 9,10-epoxy-octadecanoic acid, which rarely occurs in the nature. Both species synthesised hydroxy FAs including 9,10-dihydroxy octadecanoic acid and long-chain 2-hydroxy fatty acids.2-hydroxy 18:0 and 3-hydroxy 20:0 fatty acids were present only in P. malvacearum spores, and these may be the chemotaxonomic markers of the species. Ultra-high performance liquid chromatography mass spectrometry was performed for a comparative lipidomic analysis of P. malvacearum and P. glechomatis. The results revealed the complexity of molecular lipid species of these fungi. P. malvacearum and P. glechomatis lipids were characterised by the presence of a high number of triglyceride (TG) species. 9,10-epoxy octadecanoic fatty acid was found in TGs. Among the many types of oxidised TGs identified in P. glechomatis lipids, the most abundant species corresponds to TG(22:5+6O_17:0_18:2). P. malvacearum and P. glechomatis produced various ceramide species with different FAs from 14 to 24 chain-length. Unusual lipids like (O-acyl)-ω-hydroxy FA 18:0/18:0 in P. glechomatis and (O-acyl)-ω-hydroxy FA 18:0/20:0 and 18:0/22:0 in P. malvacearum were detected. The analysis of the polar lipid composition showed the presence of phosphatidylcholine and phosphatidylethanolamine as the main phospholipid classes of Puccinia spp. with the highest diversity of molecular species. Other phospholipids phosphatidic acid, phosphatidylglycerol phosphatidylserine and phosphatidylinositol were present in smaller amounts.The diversity of the neutral and polar lipid composition and fatty acid profile of P. malvacearum and P. glechomatis can be used in chemotaxonomic studies.
Keywords:Epoxy-octadecanoic fatty acid  Lipidomic analysis  Rust fungi
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