2016
DOI: 10.1016/j.plaphy.2015.11.003
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Identification and utilization of a new Erysiphe necator isolate NAFU1 to quickly evaluate powdery mildew resistance in wild Chinese grapevine species using detached leaves

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Cited by 34 publications
(31 citation statements)
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“…It is worth noticing that Erysisphe declined sharply in B, from 93% (Y11) in July to 1% (Y13) in October. This finding was consistent with an earlier report, which indicated that grapevine powdery mildew is one of the most damaging fungal diseases and it often occurs during July [ 42 ], suggesting that grapevine powdery mildew in B is quite serious and needs proper preventive measures [ 43 44 ]. Meanwhile, Erysisphe was found in Z. Interestingly, the Penicillium increased from 2% (Y11) to 44% (Y13), had become a dominant genus in B of Y samples in October.…”
Section: Resultssupporting
confidence: 93%
“…It is worth noticing that Erysisphe declined sharply in B, from 93% (Y11) in July to 1% (Y13) in October. This finding was consistent with an earlier report, which indicated that grapevine powdery mildew is one of the most damaging fungal diseases and it often occurs during July [ 42 ], suggesting that grapevine powdery mildew in B is quite serious and needs proper preventive measures [ 43 44 ]. Meanwhile, Erysisphe was found in Z. Interestingly, the Penicillium increased from 2% (Y11) to 44% (Y13), had become a dominant genus in B of Y samples in October.…”
Section: Resultssupporting
confidence: 93%
“…5b), and detached leaves of these plants were inoculated with the powdery mildew isolate En. NAFU1 33 15 days after transplantation. Leaves inoculated with En.…”
Section: Powdery Mildew-triggered Mesophyll Cell Death Cell Wall Appmentioning
confidence: 99%
“…Four MLO-edited lines, CM3G1-51 and -91 and CM3G2-30 and -40, were assessed for resistance to powdery mildew. The transgenic mutant and nontransgenic control lines were inoculated with the powdery mildew isolate En NAFU1 as described previously 33 . For detached leaf inoculation, CM3G2-30, CM3G1-51, and wild-type (WT) plants were used at 15 days after transplantation from the subculture medium.…”
Section: Pathogen Inoculation and Evaluation Of Resistance To Powderymentioning
confidence: 99%
“…Light microscopy can distinguish hyphae, appressoria, conidia and conidiophores, while haustoria cannot be monitored (Cadle-Davidson et al, 2010). Also confocal scanning electron microscopy (SEM) and low-temperature scanning electron microscopy (LTSEM) have been used to study E. necator (Carver et al, 1994; Cadle-Davidson et al, 2010; Gadoury et al, 2012; Ramming et al, 2012; Gao et al, 2016). Stainings successfully employed are: i) Coomassie blue, to monitor conidium germination and infiltration into host cells (Ramming et al, 2011; Ramming et al, 2012), ii) Trypan blue, to label the plant dead cells, following conidium germination, hyphae growth, and conidiophore emergence (Gao et al, 2016); iii) Aniline blue, to follow the infection using bright microscopy (Fekete et al, 2009; Gao et al, 2012a) as well as to localise the spores using fluorescence (Vanacker et al, 2000; Pessina et al, 2016).…”
Section: Disease Descriptionmentioning
confidence: 99%