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Fungal Diversity in Europe, 3rd Edition

A special issue of Journal of Fungi (ISSN 2309-608X). This special issue belongs to the section "Fungal Evolution, Biodiversity and Systematics".

Deadline for manuscript submissions: 31 March 2025 | Viewed by 1003

Special Issue Editor

Special Issue Information

Dear Colleagues, 

Since the Convention on Biological Diversity (CBD) in Rio de Janeiro (1992), fungi have become increasingly important in our daily lives. Although 30 years have passed since the first national and regional checklists and redlists were published, knowledge about fungi is still fragmented. In addition, there is a clear knowledge gap between Northern European and Mediterranean countries as well as North African countries bordering the Mediterranean Sea. This Special Issue aims to produce data on the distribution and ecology of fungi and on conservation strategies in order to provide an up-to-date picture not only to researchers but also to ordinary citizens who are increasingly involved in safeguarding ecosystems and biodiversity.

Prof. Giuseppe Venturella
Guest Editor

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Keywords

  • fungi checklists
  • Europe
  • diversity
  • ecology
  • conservation

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Published Papers (1 paper)

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Research

13 pages, 1931 KiB  
Article
Molecular Biodiversity in Fusarium subglutinans and F. temperatum: A Valuable Tool to Distinguish the Two Sister Species and Determine the Beauvericin Chemotype
by Antonia Susca, Alessandra Villani, Miriam Haidukowski, Filomena Epifani, Antonio F. Logrieco and Antonio Moretti
J. Fungi 2024, 10(11), 785; https://doi.org/10.3390/jof10110785 - 13 Nov 2024
Viewed by 719
Abstract
Fusarium subglutinans and F. temperatum are widely distributed maize pathogens recognized as distinct species with a species-specific chemotype based on patterns of mycotoxins. Recent comparative genomic analysis revealed that genomes of both species carry a complete beauvericin (Bea) biosynthetic genes cluster, [...] Read more.
Fusarium subglutinans and F. temperatum are widely distributed maize pathogens recognized as distinct species with a species-specific chemotype based on patterns of mycotoxins. Recent comparative genomic analysis revealed that genomes of both species carry a complete beauvericin (Bea) biosynthetic genes cluster, but the key gene Bea1 in F. subglutinans is not functional likely due to a large insertion (NRPS22ins) and multiple mutations (SNP298 and SNP528). We used the recently published genome sequences for these species to develop PCR markers for investigating the distribution of three main mutations in the Bea1 gene in a large collection of strains of both species from around the world. We also designed a PCR assay for a rapid and reliable discrimination of both species in the evaluation of crop exposure to mycotoxins. Overall, our results showed that SNP528 was the most common mutation, followed by NRPS22ins and SNP298. Moreover, phylogenetic analyses suggest that non-synonymous SNPs have occurred first, and that the resulting inactivation of BEA production has caused the accumulation of other polymorphisms, including the NRPS22ins, in the entire gene-coding region. The screening for genetic differences between these species could guide future crop management strategies. Full article
(This article belongs to the Special Issue Fungal Diversity in Europe, 3rd Edition)
Show Figures

Figure 1

Figure 1
<p>Species tree inferred by ML analysis of <span class="html-italic">Tef1</span> gene. Values on branches indicate bootstrap values based on 1000 replicates. Reference isolates are indicated by R. The tree is rooted with <span class="html-italic">F. proliferatum</span> (NRRL 62905) according to Fumero et al.’s (2020) study [<a href="#B13-jof-10-00785" class="html-bibr">13</a>].</p>
Full article ">Figure 2
<p>PCR amplifications with species-specific primer pairs targeting (<b>a</b>) <span class="html-italic">F. subglutinans</span> (subF/subR) and (<b>b</b>) <span class="html-italic">F. temperatum</span> (tempF/tempR). * GeneRuler 1 kb DNA Ladder.</p>
Full article ">Figure 3
<p>Microevolution in the beauvericin gene cluster of <span class="html-italic">F. subglutinans</span> and <span class="html-italic">F. temperatum</span>. White numbers in the circles indicate the number of strains. The black letters with colors alone indicate the geographical origin: A: Argentina, As: Australia, Au: Austria, G: Germany, I: Italy, N: Netherland, P: Poland, Se: Serbia, Sl: Slovakia, Sw: Switzerland, T: Turkey, U: USA.</p>
Full article ">Figure 4
<p>Phylogenetic tree based on the combined sequences (1022 bp) of SNP298 and SNP528 regions. Data were obtained from 93 strains. Sequences were aligned using MUSCLE as implemented in MEGAX. The evolutionary history was inferred using the maximum likelihood method as implemented in IQ-Tree, with the substitution model K2P + R2. Numbers on branches indicates bootstrap values based on 1000 pseudoreplicates. The tree is rooted with <span class="html-italic">F. proliferatum</span> (NRRL62905) according to Fumero et al.’s (2020) study [<a href="#B13-jof-10-00785" class="html-bibr">13</a>]. *: strains with SNP298; °: strains with SNP528.</p>
Full article ">Figure 5
<p>Phylogenetic tree based on the combined sequences (1671 bp) of SNP298, SNP528, and NRPS22ins. Data were obtained from a subset of 39 strains. Sequences were aligned using MUSCLE as implemented in MEGAX. The evolutionary history was inferred using the maximum likelihood method as implemented in IQ-Tree, with substitution model K2P + G4. Numbers on branches indicate bootstrap values based on 1000 pseudoreplicates. The tree is rooted with <span class="html-italic">F. proliferatum</span> (NRRL62905) according to Fumero et al.’s (2020) study [<a href="#B13-jof-10-00785" class="html-bibr">13</a>]. <sup>a</sup> strains with SNP528; * strains with SNP298; Bold: strains with 184 bp insertion.</p>
Full article ">
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