2021
DOI: 10.1007/s10658-021-02333-5
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Molecular detection of putative pathogens to determine any role in a causal relationship with abnormal vertical growth syndrome of macadamia

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Cited by 4 publications
(2 citation statements)
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“…Prior to the extraction, fungal mycelium was scraped from the PDA plate into a sterile 2 ml microfuge tube and homogenized in a QIAGEN TissueLyser II at a frequency of 30 Hz for 1 min with a sterile 3 mm tungsten carbide bead. To obtain the total fungal community in plant samples, total DNA was extracted from 0.1 g of lyophilized leaf tissue using the CTAB method as described in Zakeel et al (2021a). DNA concentration was measured with a BioDrop spectrophotometer.…”
Section: Methodsmentioning
confidence: 99%
“…Prior to the extraction, fungal mycelium was scraped from the PDA plate into a sterile 2 ml microfuge tube and homogenized in a QIAGEN TissueLyser II at a frequency of 30 Hz for 1 min with a sterile 3 mm tungsten carbide bead. To obtain the total fungal community in plant samples, total DNA was extracted from 0.1 g of lyophilized leaf tissue using the CTAB method as described in Zakeel et al (2021a). DNA concentration was measured with a BioDrop spectrophotometer.…”
Section: Methodsmentioning
confidence: 99%
“…The Australian macadamia industry is threatened by a syndrome known as abnormal vertical growth (AVG), which has an unknown etiology. Recent studies have hypothesized a biotic cause for AVG while dismissing previous hypothesis that AVG is caused by Bacillus megaterium, phytoplasmas or a geminivirus (Zakeel et al, 2020(Zakeel et al, , 2021. AVG is characterized by a vigorous upright growth habit with reduced lateral branching, flower production and nut set (O'Farrell, 2011).…”
Section: Introductionmentioning
confidence: 99%