The polyphagous shot hole borer (PSHB), an ambrosia beetle (Coleoptera: Curculeonidae: Scolytinae) native to Asia, together with its fungal symbiont Fusarium euwallaceae, has emerged as an important invasive pest killing avocado and other trees in Israel and the United States. The PSHB is one of three cryptic species in the Euwallacea fornicatus species complex, the taxonomy of which remains to be resolved. The surge in the global spread of invasive forest pests such as the PSHB has led to the development of programmes utilising sentinel tree plantings to record new host-pest interactions. During routine surveys of tree health in botanical gardens of South Africa undertaken as part of a sentinel project, an ambrosia beetle/fungal associate was detected damaging Platanus x acerifolia (London Plane) in the KwaZulu-Natal National Botanical Gardens, Pietermaritzburg. Identification of the beetle by sequencing part of the mitochondrial cytochrome oxidase c subunit 1 (COI) gene confirmed its identity as PSHB, and specifically one of the invasive haplotypes of the beetle. The associated fungus F. euwallaceae was identified based on phylogenetic analysis of elongation factor (EF 1α) sequences. Koch's postulates have confirmed the pathogenicity of fungal isolates to P. x acerifolia. This is the first report of PSHB and its fungal symbiont causing Fusarium dieback in South Africa. This report also represents the first verified case of a damaging invasive forest pest detected in a sentinel planting project, highlighting the importance of such studies. Given the potential impact these species present to urban trees, native biodiversity and agriculture, both the PSHB and its fungal symbiont should be included in invasive species regulations in South Africa.
The plant pathogenic asexual fungus Thielaviopsis basicola (Ascomycota) causes black root rot on many important agricultural and ornamental plant species. Since its first description in 1850, this species has had a tumultuous taxonomic history, being classified in many different genera. Thus far, DNA‐based techniques have not played a significant role in identification of T. basicola and have been used only to confirm its placement in the Microascales. This investigation reconsidered the phylogenetic placement of T. basicola, using DNA sequence data for six different gene regions. It included 41 isolates identified as T. basicola from 13 geographical locations worldwide. Phylogenetic analyses showed that these isolates grouped in a well‐supported lineage distinct from other genera in the Ceratocystidaceae, here described as Berkeleyomyces gen. nov. The data also provided robust evidence that isolates of T. basicola include a cryptic sister species. As a result, this report provides a new combination as B. basicola comb. nov. and introduces a new species as B. rouxiae sp. nov.
Draft genomes of the species Annulohypoxylon stygium, Aspergillus mulundensis, Berkeleyomyces basicola (syn. Thielaviopsis basicola), Ceratocystis smalleyi, two Cercospora beticola strains, Coleophoma cylindrospora, Fusarium fracticaudum, Phialophora cf. hyalina and Morchella septimelata are presented. Both mating types (MAT1-1 and MAT1-2) of Cercospora beticola are included. Two strains of Coleophoma cylindrospora that produce sulfated homotyrosine echinocandin variants, FR209602, FR220897 and FR220899 are presented. The sequencing of Aspergillus mulundensis, Coleophoma cylindrospora and Phialophora cf. hyalina has enabled mapping of the gene clusters encoding the chemical diversity from the echinocandin pathways, providing data that reveals the complexity of secondary metabolism in these different species. Overall these genomes provide a valuable resource for understanding the molecular processes underlying pathogenicity (in some cases), biology and toxin production of these economically important fungi.
An order, family and genus are validated, seven new genera, 35 new species, two new combinations, two epitypes, two lectotypes, and 17 interesting new host and / or geographical records are introduced in this study. Validated order, family and genus: Superstratomycetales and Superstratomycetaceae (based on Superstratomyces). New genera: Haudseptoria (based on Haudseptoria typhae); Hogelandia (based on Hogelandia lambearum); Neoscirrhia (based on Neoscirrhia osmundae); Nothoanungitopsis (based on Nothoanungitopsis urophyllae); Nothomicrosphaeropsis (based on Nothomicrosphaeropsis welwitschiae); Populomyces (based on Populomyces zwinianus); Pseudoacrospermum (based on Pseudoacrospermum goniomae). New species: Apiospora sasae on dead culms of Sasa veitchii (Netherlands); Apiospora stipae on dead culms of Stipa gigantea (Spain); Bagadiella eucalyptorum on leaves of Eucalyptus sp. (Australia); Calonectria singaporensis from submerged leaf litter (Singapore); Castanediella neomalaysiana on leaves of Eucalyptus sp. (Malaysia); Colletotrichum pleopeltidis on leaves of Pleopeltis sp. (South Africa); Coniochaeta deborreae from soil (Netherlands); Diaporthe durionigena on branches of Durio zibethinus (Vietnam); Floricola juncicola on dead culm of Juncus sp. (France); Haudseptoria typhae on leaf sheath of Typha sp. (Germany); Hogelandia lambearum from soil (Netherlands); Lomentospora valparaisensis from soil (Chile); Neofusicoccum mystacidii on dead stems of Mystacidium capense (South Africa); Neomycosphaerella guibourtiae on leaves of Guibourtia sp. (Angola); Niesslia neoexosporioides on dead leaves of Carex paniculata (Germany); Nothoanungitopsis urophyllae on seed capsules of Eucalyptus urophylla (South Africa); Nothomicrosphaeropsis welwitschiae on dead leaves of Welwitschia mirabilis (Namibia); Paracremonium bendijkiorum from soil (Netherlands); Paraphoma ledniceana on dead wood of Buxus sempervirens (Czech Republic); Paraphoma salicis on leaves of Salix cf. alba (Ukraine); Parasarocladium wereldwijsianum from soil (Netherlands); Peziza ligni on masonry and plastering (France); Phyllosticta phoenicis on leaves of Phoenix reclinata (South Africa); Plectosphaerella slobbergiarum from soil (Netherlands); Populomyces zwinianus from soil (Netherlands); Pseudoacrospermum goniomae on leaves of Gonioma kamassi (South Africa); Pseudopyricularia festucae on leaves of Festuca californica (USA); Sarocladium sasijaorum from soil (Netherlands); Sporothrix hypoxyli in sporocarp of Hypoxylon petriniae on Fraxinus wood (Netherlands); Superstratomyces albomucosus on Pycnanthus angolensis (Netherlands); Superstratomyces atroviridis on Pinus sylvestris (Netherlands); Superstratomyces flavomucosus on leaf of Hakea multilinearis (Australia); Superstratomyces tardicrescens from human eye specimen (USA); Taeniolella platani on twig of Platanus hispanica (Germany), and Tympanis pini on twigs of Pinus sylvestris (Spain).
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