Leptosphaeria doliolum
Leptosphaeria doliolum (Pers.) Ces. & De Not., Comm. Soc. crittog. Ital. 1(fasc. 4): 234 (1863).
≡ Sphaeria doliolum Pers., Icon. Desc. Fung. Min. Cognit. (Leipzig) 2: 39 (1800).
Index Fungorum number: IF 161618; Facesoffungi number: FoF 00391, Fig. 1
Description: see Ariyawansa et al. (2015).
Material considered: see Ariyawansa et al. (2015).
Fig. 1 Leptosphaeria doliolum (MFLU 14–0565, modified from Fig. 90 in Liu et al. 2015). a, b Appearance of ascomata on host substrate. c Section through ascomata. d Peridium. e, f Asci. g–j Ascospores. Scale bars: a = 200 μm, b, c, e, f = 20 μm, d = 5 μm, g–j = 10 μm.
Importance and distribution
Leptosphaeria is significant for medical and pharmaceutical industry as it produces wide range of secondary compounds (Pedra et al. 2008, 2009).
Quarantine significance
Leptosphaeria is in the list of Quarantine Pests for various countries such as India (Plant Quarantine Regulation of Import into India Order 2003) for protection of Brassica spp. such as broccoli, Brussels sprouts, cabbage, canola, cauliflower, Chinese cabbage, kohlrabi and mustard amongst others. Blackleg caused by L. maculans is a threat to Canada (Canola Council of Canada 2019) and to Sudan (Quarantine Pests decline entry into Sudan 2016).
Biochemical importance of the genus, chemical diversity or applications
Leptosphaeria produces wide range of chemicals such as sirodesmin PL, a non-host selective phytotoxin including deacetylsirodesmin, phomalirazine, sirodesmin H, sirodesmin J, sirodesmin K, Sirodesmin PL, Leptomaculins A, B, C, D, E including 3-oxosilphinene, deacetylleptomaculins C, D, and E, lairdinol A, phomalairdenols A, B, C, D, Phomalairdenones A, B, C, D, selin-11-en-4α−-ol, Sterol metabolites such as 24-methylene dihydrolanosterol, 4,4-dimethyl fecosterol, 4-methyl fecosterol, obtusifoliol, epiergosterol, episterol, ergosta5,7,9(11),22-tetraenol, ergosta-7,22-dienol, Ergosterol, fecosterol Phomapyrone metabolites such as infectopyrone, Phomapyrone A, B, C, D, E, F and G, phomenin B, Phomaligols and other polyketide metabolites phomaligadiones A and B, phomaligin A Phomaligol A, A1 wasabidienones B and E, Polyketide metabolites Hydroxynaphthalene-1-sulfate and bulgarein, 2,4-Dihydroxy-3,6-dimethylbenzaldehyde, 2-[2-(5- Hydroxybenzofuranyl)]-3-(4-hydroxyphenyl)-propanenitrile, 2-hydroxyjuglone, 4-hydroxyscytalone, Flaviolin. Maculansins A and B including brassilexin, cyclobrassinin, Phytoalexins, rutalexin, spirobrassinin. Cerebroside metabolites cerebrosides C and D (Pedra et al. 2008, 2009).
There are 1105 Leptosphaeria epithets in Index Fungorum (2022), but many species have been transferred to other genera such as Amarenomyces, Asterella, Didymolepta, Extrawettsteinina, Kalmusia, Lasiosphaeriopsis, Lautitia, Leptopeltis, Metasphaeria, Mycosphaerella, Nemania, Neocamarosporium, Neomassariosphaeria, Neoventuria, Nodulosphaeria, Ophiobolus, Paraconiothyrium, Paramassariosphaeria, Phaeosphaeria, Phaeospora, Phragmonaevia, Plenodomus, Psammina, Pyrenidium, Setoseptoria, Stagonospora and Stigmatula. Leptosphaeria comprises 605 species known on wide range of hosts such as Achillea millefolium (Asteraceae), Aconitum variegatum (Ranunculaceae), Agrimonia eupatoria (Rosaceae), Ambrosia trifida (Asteraceae), Anaphalis margaritacea (Asteraceae), Angelica sp. (Apiaceae), Aralia racemosa (Araliaceae), Arnica viscosa (Asteraceae), Asclepias incarnata (Apocynaceae) and many more. Leptosphaeria has wide distribution including Asia (Brunei Darussalam, Uzbekistan), Europe (Bulgaria, Denmark, England, Georgia, Germany, Italy, Poland, Romania, Sweden, Ukraine), North America (Canada) and The United States (Alaska, California, Illinois, New York, North Dakota).
References
Ariyawansa HA, Phukhamsakda C, Thambugala KM, Bulgakov TS et al. 2015 – Revision and phylogeny of Leptosphaeriaceae. Fungal Diversity 74, 19–51.
Barr ME. 1987 – New taxa and combinations in the Loculoascomycetes. Mycotaxon 29, 501–505.
Blackleg Strategic Plan in Canada. 2019– https://www.canolacouncil.org/download/215/pages/5227/2019_blackleg_strategic_plan
Dayarathne MC, Phookamsak R, Ariyawansa HA, Jones EBG et al. 2015 – Phylogenetic and morphological appraisal of Leptosphaeria italica sp. nov. (Leptosphaeriaceae, Pleosporales) from Italy. Mycosphere 6, 634–642.
Eriksson OE, Hawksworth DL. 1986 – Outline of the Ascomycetes – 1986. Systema Ascomycetum 5, 185–324.
Eriksson OE, Hawksworth DL.1991– Outline of the Ascomycetes – 1990. Systema Ascomycetum Reprint of Volumes 1–4 (1982–1985) 9, 39–271.
Food and Agriculture Organisation (FAO). 2023 – FAOLEX Database. Plant Quarantine Regulation of Import into India Order 2003.
Höhnel FV. 1909 – Fragmente zur mykologie: VI. Mitteilung (Nr. 182 bis 288). Sber Akademie der Wissenschaften in Wien Mathematisch-Naturwissenschaftliche Classe, Abteilung l 118, 275–452.
Hyde KD, Hongsanan S, Jeewon R, Bhat DJ et al. 2016 – Fungal diversity notes 367–490: taxonomic and phylogenetic contributions to fungal taxa. Fungal Diversity 80, 1–270.
Hyde KD, Jones EBG, Liu JK, Ariyawansa H et al. 2013 – Families of Dothideomycetes. Fungal Diversity 63, 1–313.
Lestari AS, Wanasinghe DN, Gafforov Y, Tennakoon DS et al. 2021–Taxonomy and phylogenetic appraisal of Leptosphaeria chatkalica sp. nov. (Leptosphaeriaceae, Pleosporales) from Uzbekistan. Phytotaxa 520, 155–168. DOI: 10.11646/phytotaxa.520.2.3
Liu JK, Hyde KD, Jones EBG, Ariyawansa HA et al. 2015 – Fungal diversity notes 1–110: taxonomic and phylogenetic contributions to fungal species. Fungal Diversity 72, 1–197.
Müller E. 1950 – Die schweizerischen arten der gattung leptosphaeria und ihrer verwandten. Sydowia 4, 185–319
Pedras MS, Yu Y. 2008 – Stress-driven discovery of metabolites from the phytopathogenic fungus Leptosphaeria maculans: Structure and activity of leptomaculins A–E. Bioorganic & Medicinal Chemistry 16, 8063–8071.
Pedras MS, Yu Y. 2009 – Phytotoxins, Elicitors and Other Secondary Metabolites from Phytopathogenic "Blackleg" Fungi: Structure, Phytotoxicity and Biosynthesis. Natural Product Communications 4, 1291–1304.
Pem D, Jeewon R, Selcuk F, Ulukapi M et al. 2020 – Ribosomal and Protein Gene Phylogeny Reveals Novel Saprobic Fungal Species from Juglans regia and Urtica dioica. Frontiers in Microbiology 11, 1303.
Persoon CH.1800 – Icones et description Fugorum-minus cognitorum 2, 27–67 Lispsiae.
Phookamsak R, Hyde KD, Jeewon R, Bhat DJ et al. 2019 – Fungal diversity notes 929–1035: taxonomic and phylogenetic contributions on genera and species of fungi. Fungal Diversity 95, 1–273.
Quarantine Pests (Fungi) Declined Entry into Sudan = (Zero Tolerance). 2016 – Available at: https://pflanzengesundheit.julius-kuehn.de/dokumente/upload/sd3-2016pest-ware_en.pdf
Schoch CL, Crous PW, Groenewald JZ, Boehm EWA et al. 2009a – A class-wide phylogenetic assessment of Dothideomycetes. Studies in Mycology 64, 1–15.
Shearer CA, Crane JL, Chandra Reddy KR. 1990 – Studies in Leptosphaeria. Lectotypification of Sphaeria Doliolum. Mycologia 82, 496–500.
Zhang Y, Crous PW, Schoch CL, Hyde KD. 2012 – Pleosporales. Fungal Diversity 53, 1–221.
Recent News
Recent paper to be publishedRecent Genus
NothocladosporiumPhillipsiella
Curreya
Recent Species
Nothocladosporium syzygiiPhillipsiella atra
Curreya conorum