2012
DOI: 10.3791/3895-v
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Sexual Development and Ascospore Discharge in <em>Fusarium graminearum</em>

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Cited by 7 publications
(7 citation statements)
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“…In outcrosses, we fertilized female strains grown on carrot agar plates with 1 ml of conidial suspension (1 × 10 6 conidia/ml) derived from male strains. We assayed ascospore discharge as described in ( 69 ). We measured conidiation in 5-day-old liquid carboxymethylcellulose cultures and assayed spore germination and germ tube growth in liquid YEPD (1% yeast extract, 2% peptone, 2% dextrose) medium for 12 hours using freshly harvested conidia or ascospores.…”
Section: Methodsmentioning
confidence: 99%
“…In outcrosses, we fertilized female strains grown on carrot agar plates with 1 ml of conidial suspension (1 × 10 6 conidia/ml) derived from male strains. We assayed ascospore discharge as described in ( 69 ). We measured conidiation in 5-day-old liquid carboxymethylcellulose cultures and assayed spore germination and germ tube growth in liquid YEPD (1% yeast extract, 2% peptone, 2% dextrose) medium for 12 hours using freshly harvested conidia or ascospores.…”
Section: Methodsmentioning
confidence: 99%
“…meridionale are both homothallic; thus, individual strains can produce fertile perithecia without requiring a compatible mate. Sexual fertility was assessed based on the ability of each isolate to produce perithecia and ascospores on carrot agar following a standard protocol with some modifications (Cavinder et al, 2012). Carrot agar plates (6 cm in diameter) were inoculated by placing a 5‐μL drop of a spore suspension (10 4 macroconidia/mL) of each isolate in the centre.…”
Section: Methodsmentioning
confidence: 99%
“…Conidia produced by each strain were filtrated through four layers of lens tissue and their concentration was measured using a haemocytometer. For sexual reproduction assays, mycelial plugs (5‐mm diameter) of each strain/mutant were placed on the centre of CA plates (6‐cm in diameter) and incubated at 25°C in the dark for 7 days; subsequently, the aerial hyphae were removed with sterile toothpicks, and the resulting plates were covered with 1 mL 2.5% Tween 20 and incubated under bright fluorescent lights at 22–25°C for 2 weeks (Cavinder et al, 2012). Perithecia were observed by a stereofluorescence microscope (SMZ25; Nikon).…”
Section: Methodsmentioning
confidence: 99%