26 research outputs found
Fungal endophytes from arid areas of Andalusia: high potential sources for antifungal and antitumoral agents
Native plant communities from arid areas present distinctive characteristics to survive in extreme
conditions. The large number of poorly studied endemic plants represents a unique potential
source for the discovery of novel fungal symbionts as well as host-specific endophytes not yet
described. The addition of adsorptive polymeric resins in fungal fermentations has been seen to
promote the production of new secondary metabolites and is a tool used consistently to generate
new compounds with potential biological activities. A total of 349 fungal strains isolated from 63
selected plant species from arid ecosystems located in the southeast of the Iberian Peninsula, were
characterized morphologically as well as based on their ITS/28S ribosomal gene sequences. The fungal
community isolated was distributed among 19 orders including Basidiomycetes and Ascomycetes,
being Pleosporales the most abundant order. In total, 107 different genera were identified being
Neocamarosporium the genus most frequently isolated from these plants, followed by Preussia and
Alternaria. Strains were grown in four different media in presence and absence of selected resins to
promote chemical diversity generation of new secondary metabolites. Fermentation extracts were
evaluated, looking for new antifungal activities against plant and human fungal pathogens, as well
as, cytotoxic activities against the human liver cancer cell line HepG2. From the 349 isolates tested,
126 (36%) exhibited significant bioactivities including 58 strains with exclusive antifungal properties
and 33 strains with exclusive activity against the HepG2 hepatocellular carcinoma cell line. After LCMS
analysis, 68 known bioactive secondary metabolites could be identified as produced by 96 strains,
and 12 likely unknown compounds were found in a subset of 14 fungal endophytes. The chemical
profiles of the differential expression of induced activities were compared. As proof of concept, ten
active secondary metabolites only produced in the presence of resins were purified and identified. The
structures of three of these compounds were new and herein are elucidated.This work was supported by Fundación MEDINA and the Andalusian Government grant
RNM-7987 ‘Sustainable use of plants and their fungal parasites from arid regions of Andalucía for new molecules
useful for antifungals and neuroprotectors’
Ευρετικές προσεγγίσεις του μοναδιάστατου προβλήματος πακετοποίησης
Article 59.1, of the International Code of Nomenclature for Algae, Fungi, and Plants (ICN; Melbourne Code), which addresses the nomenclature of pleomorphic fungi, became effective from 30 July 2011. Since that date, each fungal species can have one nomenclaturally correct name in a particular classification. All other previously used names for this species will be considered as synonyms. The older generic epithet takes priority over the younger name. Any widely used younger names proposed for use, must comply with Art. 57.2 and their usage should be approved by the Nomenclature Committee for Fungi (NCF). In this paper, we list all genera currently accepted by us in Dothideomycetes (belonging to 23 orders and 110 families), including pleomorphic and non-pleomorphic genera. In the case of pleomorphic genera, we follow the rulings of the current ICN and propose single generic names for future usage. The taxonomic placements of 1261 genera are listed as an outline. Protected names and suppressed names for 34 pleomorphic genera are listed separately. Notes and justifications are provided for possible proposed names after the list of genera. Notes are also provided on recent advances in our understanding of asexual and sexual morph linkages in Dothideomycetes. A phylogenetic tree based on four gene analyses supported 23 orders and 75 families, while 35 families still lack molecular data
Parastagonosporella fallopiae gen. et sp. nov. (Phaeosphaeriaceae) on Fallopia convolvulus from Iran
Bezerromycetales and Wiesneriomycetales ord. nov. (class Dothideomycetes), with two novel genera to accommodate endophytic fungi from Brazilian cactus
During a survey of endophytic fungi from the cactus Tacinga inamoena in a Brazilian tropical
dry forest (Caatinga) some undescribed ascomycetous fungi were isolated. These fungi are
characterized by superficial and immersed, globose to subglobose, smooth or hairy
ascomata, bitunicate asci, and muriformly septate, ellipsoidal ascospores. Multigene
phylogenetic analyses using sequences from partial ITS, SSU and LSU nrDNA and the
translation elongation factor 1-alpha gene (tef1) demonstrated a monophyletic clade
accommodating these endophytic fungi in the class Dothideomycetes, closely related to the
order Tubeufiales. Based on morphological features and phylogenetic analyses, these fungi
could not be placed in the order Tubeufiales, in the new order Wiesneriomycetales, or any
other known genus in the class Dothideomycetes. Thus, two new genera (Bezerromyces,
with B. brasiliensis and B. pernambucoensis, and Xiliomyces with X. brasiliensis), a new
family (Bezerromycetaceae) and a new order (Bezerromycetales) are introduced to
accommodate these novel taxa. Our phylogenetic analyses also demonstrated that the clade
accommodating Wiesneriomycetaceae represents a new order, here introduced as
Wiesneriomycetales.Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) (Process
203132/2014-9), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)
and Fundação de Amparo à Ciência e Tecnologia de Pernambuco (FACEPE) of Brazil.http://link.springer.com/journal/115572018-04-30hb2017Microbiology and Plant Patholog
Outline of Fungi and fungus-like taxa – 2021
This paper provides an updated classification of the Kingdom Fungi (including fossil fungi) and fungus-like taxa. Five-hundred and twenty-three (535) notes are provided for newly introduced taxa and for changes that have been made since the previous outline. In the discussion, the latest taxonomic changes in Basidiomycota are provided and the classification of Mycosphaerellales are broadly discussed. Genera listed in Mycosphaerellaceae have been confirmed by DNA sequence analyses, while doubtful genera (DNA sequences being unavailable but traditionally accommodated in Mycosphaerellaceae) are listed in the discussion. Problematic genera in Glomeromycota are also discussed based on phylogenetic results