Multiplex PCR for specific identification and determination of mating type in Togninia minima (anamorphic Phaeoacremonium aleophilum), a causal agent of esca disease of grapevine

Togninia minima is one of the fungi involved in esca disease of grapevine, worldwide. It has a biallelic heterothallic mating system. A multiplex PCR test was developed that can detect the species as well as the mating type. A T. minima-specific primer set, with expected amplicon size of 500 bp, was designed based on β-tubulin gene sequences. A previously designed degenerate primer set (NcHMG1 and NcHMG2) was successfully used to amplify a fragment of approximately 300 bp from the Mat1-2 gene of T. minima. The obtained sequence showed substantial homology to the Mat1-2 gene sequences of other related ascomycetes. A more specific primer set, with expected amplicon size of 230 bp, was designed based on the same Mat1-2 gene sequence. The specificity of the new primer set was verified on DNA extracted from a set of Phaeoacremonium and other fungal species frequently occurring on grapevine. Both primer sets were combined in a multiplex PCR for the simultaneous identification and determination of mating types of T. minima. A 500 bp amplicon was obtained from all available T. minima isolates and none from the other Phaeoacremonium spp. A 230 bp amplicon confirmed T. minima isolates that have the Mat1-2 allele. The species-specific β-tubulin-based primer set served as an internal control to confirm that the PCR reaction with the mating type primer set had worked properly. The efficacy of the multiplex test was evaluated on 31 isolates of T. minima from different vineyards in the Azarshahr region (East Azerbaijan province, Iran). Isolates of both mating types were found from the sampled areas; however, Mat1-2 isolates were more frequent than Mat1-1 isolates (19:12). This multiplex PCR assay developed can facilitate rapid screening of mating types in populations of T. minima

Macrophomina phaseolina associated with grapevine decline in Iran

Grapevines exhibiting general decline symptoms were observed in July 2012 in Arbatan, a region in Marand county, north-western Iran. Leaf necrosis symptoms were also observed in affected grapevines. Dark brown necrotic lesions and wood discoloration were observed in the vascular tissues of affected cordons. Fungal isolates, all with similar cultural and morphological features, were obtained from symptomatic tissues. Morphological characteristics indicated that the isolates were Macrophomina phaseolina. Sequence analysis of the elongation factor (EF-1α) gene from isolates confirmed this identification, with 100% similarity to the reference M. phaseolina sequences obtained from GenBank. Pathogenicity assays of two M. phaseolina isolates on 2-year-old potted vines (cv. ‘Keshmeshi’) demonstrated that M. phaseolina was pathogenic on grapevine. This study confirmed the association of M. phaseolina with grapevine decline symptoms, and represents the first report of this fungus associated with grapevine trunk diseases in Iran

Multiplex PCR for specific identification and determination of mating type in <em>Togninia minima</em> (anamorphic <em>Phaeoacremonium aleophilum</em>), a causal agent of esca disease of grapevine

<p><em>Togninia minima</em> is one of the fungi involved in esca disease of grapevine, worldwide. It has a biallelic heterothallic mating system. A multiplex PCR test was developed that can detect the species as well as the mating type. A <em>T. minima</em>-specific primer set, with expected amplicon size of 500 bp, was designed based on <em>β-tubulin</em> gene sequences. A previously designed degenerate primer set (NcHMG1 and NcHMG2) was successfully used to amplify a fragment of approximately 300 bp from the <em>Mat1-2</em> gene of <em>T. minima</em>. The obtained sequence showed substantial homology to the <em>Mat1-2</em> gene sequences of other related ascomycetes. A more specific primer set, with expected amplicon size of 230 bp, was designed based on the same <em>Mat1-2</em> gene sequence. The specificity of the new primer set was verified on DNA extracted from a set of <em>Phaeoacremonium</em> and other fungal species frequently occurring on grapevine. Both primer sets were combined in a multiplex PCR for the simultaneous identification and determination of mating types of <em>T. minima</em>. A 500 bp amplicon was obtained from all available <em>T. minima</em> isolates and none from the other <em>Phaeoacremonium</em> spp. A 230 bp amplicon confirmed <em>T. minima</em> isolates that have the <em>Mat1-2</em> allele. The species-specific β-tubulin-based primer set served as an internal control to confirm that the PCR reaction with the mating type primer set had worked properly. The efficacy of the multiplex test was evaluated on 31 isolates of <em>T. minima</em> from different vineyards in the Azarshahr region (East Azerbaijan province, Iran). Isolates of both mating types were found from the sampled areas; however, Mat1-2 isolates were more frequent than Mat1-1 isolates (19:12). This multiplex PCR assay developed can facilitate rapid screening of mating types in populations of <em>T. minima</em>.</p

<em>Macrophomina phaseolina</em> associated with grapevine decline in Iran

Grapevines exhibiting general decline symptoms were observed in July 2012 in Arbatan, a region in Marand county, north-western Iran. Leaf necrosis symptoms were also observed in affected grapevines. Dark brown necrotic lesions and wood discoloration were observed in the vascular tissues of affected cordons. Fungal isolates, all with similar cultural and morphological features, were obtained from symptomatic tissues. Morphological characteristics indicated that the isolates were Macrophomina phaseolina. Sequence analysis of the elongation factor (EF-1α) gene from isolates confirmed this identification, with 100% similarity to the reference M. phaseolina sequences obtained from GenBank. Pathogenicity assays of two M. phaseolina isolates on 2-year-old potted vines (cv. ‘Keshmeshi’) demonstrated that M. phaseolina was pathogenic on grapevine. This study confirmed the association of M. phaseolina with grapevine decline symptoms, and represents the first report of this fungus associated with grapevine trunk diseases in Iran

New secondary metabolites produced by the phytopathogenic fungus Wilsonomyces carpophilus

wo new metabolites possessing the unusual 1-oxa-7-azaspiro[4.4]non-2- ene-4,6-dione core (2, 3) along with the recently described pseurotin A3 (1) were isolated from the pathogenic fungus Wilsonomyces carpophilus(previously named Stigmina carpophila). The producer organism was obtained from Prunus armeniaca collected in Iran and was identified by morphological and molecular phylogenetic methods. The structures of the isolated compounds were elucidated on the basis of extensive NMR spectroscopic analysis, high-resolution mass spectrometry and ECD analysis. The compounds were screened for their antimicrobial, cytotoxic, nematicidal and biofilm inhibition activities but, no significant effect was observed. To the best of our knowledge, this is the first report on the isolation of secondary metabolites produced by W. carpophilus

Cytotoxic, anti-biofilm and antimicrobial polyketides from the plant associated fungus Chaetosphaeronema achilleae.

From extracts of the plant associated fungus Chaetosphaeronema achilleae collected in Iran, a previously unreported isoindolinone named chaetosisoindolinone (1) and a previously undescribed indanone named chaetosindanone (2) were isolated in addition to five known metabolites, 2-(2-acetyl-3,5-dihydroxyphenyl) acetic acid (3), vulculic acid (4), 2-(2-acetyl-3-hydroxy-5-methoxyphenyl)acetic acid (5), curvulin (6), and curvulol (7). Their structures were elucidated on the basis of extensive spectroscopic analysis and high-resolution mass spectrometry. The isolated compounds were tested for their antimicrobial, anti-biofilm, and nematicidal activities. Compound 2 exhibited cytotoxicity against the human breast adenocarcinoma MCF-7 cells with an IC50 value of 1.5 μg/mL. Furthermore, compounds 4 and 7 almost completely inhibited biofilm formation in Staphylococcus aureus at 256 μg/mL. Weak antimicrobial activities were also observed for some of the isolated compounds against Mucor hiemalis, Rhodoturula glutinis, Chromobacterium violaceum, and Staphylococcus aureus

Five Tetramic Acid Derivatives Isolated from the Iranian Fungus Colpoma quercinum CCTU A372

Submerged mycelial cultures of the ascomycete Colpoma&nbsp;quercinum CCTU A372 were found to produce five previously undescribed tetramic acids, for which we propose the trivial names colposetins A–C (1–3) and colpomenoic acids A and B (4 and 5), along with the known compounds penicillide (6) and monodictyphenone (7). The planar structures of 1–5 were determined by high-resolution electrospray ionization mass spectrometry (HR-ESIMS) and extensive 1D and 2D nuclear magnetic resonance (NMR) spectroscopy. Their absolute configurations were determined by the combination of electronic circular dischroism (ECD) analysis, J-based configurational analysis, and a rotating-frame Overhauser effect spectroscopy (ROESY) experiment. Colposetin B displayed weak antimicrobial activity against Bacillus subtilis and Mucor hiemalis (MIC 67 µg/mL)

Simplicilones A and B Isolated from the Endophytic Fungus SPC3.

Two new tetracyclic polyketides with a spirocenter, simplicilones A (1) and B (2) were isolated from the broth-culture of the endophytic fungus Simplicilliumsubtropicum (SPC3) in the course of our screening for new bioactive secondary metabolites. This endophytoic fungus is naturally harboured in the fresh bark of the Cameroonian medicinal plant Duguetia staudtii (Engl. and Diels) Chatrou. The planar structures of the simplicilones were elucidated by MS and 1D as well as 2D NMR spectroscopic techniques. The relative configuration was assigned by NOESY experiments in conjunction with coupling constants; subsequently, the absolute configurations were assigned by the modified Mosher's method. The compounds showed weak cytotoxic effects against the cell line KB3.1 (in vitro cytotoxicity (IC50) = 25 µg/mL for 1, 29 µg/mL for 2), but were inactive against the tested Gram-positive and Gram-negative bacteria as well as fungi

Simplicilones A and B Isolated from the Endophytic Fungus Simplicillium subtropicum SPC3

Two new tetracyclic polyketides with a spirocenter, simplicilones A (1) and B (2) were isolated from the broth-culture of the endophytic fungus Simplicilliumsubtropicum (SPC3) in the course of our screening for new bioactive secondary metabolites. This endophytoic fungus is naturally harboured in the fresh bark of the Cameroonian medicinal plant Duguetia staudtii (Engl. and Diels) Chatrou. The planar structures of the simplicilones were elucidated by MS and 1D as well as 2D NMR spectroscopic techniques. The relative configuration was assigned by NOESY experiments in conjunction with coupling constants; subsequently, the absolute configurations were assigned by the modified Mosher&rsquo;s method. The compounds showed weak cytotoxic effects against the cell line KB3.1 (in vitro cytotoxicity (IC50) = 25 &micro;g/mL for 1, 29 &micro;g/mL for 2), but were inactive against the tested Gram-positive and Gram-negative bacteria as well as fungi

Bioactive Secondary Metabolites from Fungi of the Genus <i>Cytospora</i> Ehrenb. (Ascomycota)

Cytospora is a genus of fungi belonging to the Cytosporaceae family (Sordariomycetes, Ascomycota) considered as a prolific source of specialized metabolites due to their ability to produce diverse secondary metabolites with a broad range of biological activities. Since the first chemical investigation of this genus in the 1980s, further studies have led to the isolation and structural elucidation of several bioactive compounds including cytosporones, nonanolides, macrocyclic dilactones, and terpenoids. This review summarizes, for the first time, the chemical diversity of bioactive secondary metabolites from the genus Cytospora and highlights its potential as an alternative source of secondary metabolites for pharmacological studies. Moreover, this review will serve as a basis for future investigations of compounds of this genus