2022
DOI: 10.1016/j.rhisph.2022.100535
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Inoculation with Penicillium citrinum aids ginseng in resisting Fusarium oxysporum by regulating the root and rhizosphere microbial communities

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Cited by 10 publications
(4 citation statements)
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“…The six fungal isolates in our study were identified as F. oxysporum , A. alternata , P. grisea and C. truncatum , species of pathogenic fungi that can infect many different crops (Nguvo & Gao, 2019). F. oxysporum is largely responsible for causing root rot in Sanqi (Fan et al, 2016) as well as in ginseng (Wang, Zhang, Wang, et al, 2022) and soybean (Cruz Jimenez et al, 2018). A. panax has been found to be the main cause of Alternaria leaf spots in ginseng plants (Li et al, 2020).…”
Section: Discussionmentioning
confidence: 99%
“…The six fungal isolates in our study were identified as F. oxysporum , A. alternata , P. grisea and C. truncatum , species of pathogenic fungi that can infect many different crops (Nguvo & Gao, 2019). F. oxysporum is largely responsible for causing root rot in Sanqi (Fan et al, 2016) as well as in ginseng (Wang, Zhang, Wang, et al, 2022) and soybean (Cruz Jimenez et al, 2018). A. panax has been found to be the main cause of Alternaria leaf spots in ginseng plants (Li et al, 2020).…”
Section: Discussionmentioning
confidence: 99%
“…Some Penicillium species are involved in the production of solubilized phosphorus, siderophore, and phytohormones such as indole acetic acid and gibberellic acid, all of which are beneficial to plant health ( Elias et al, 2016 ; Altaf et al, 2018 ). Penicillium species have shown to suppress the root rot disease caused by Fusarium species and promote plant growth ( Wang et al, 2022a ). Fusarium species like F. oxysporum and F. solani are the major cause of tobacco root rot disease ( Yang et al, 2020a ; Gai et al, 2021 ).…”
Section: Discussionmentioning
confidence: 99%
“…Bacterial PCRs were performed in triplicate with 4 µL of 5 × FastPfu Buffer, 2 µL of 2.5 mmol/L dNTPs, 0.8 µL of 5 µmol/L forwards primer, 0.8 µL of 5 µmol/L reverse primer, 0.4 µL of Fastpfu Polymerase, 0.2 µL of bovine serum albumin (BSA), and 10 ng of template DNA in a 20 µL reaction volume. The thermal cycling conditions were described previously (Wang et al 2022a). The PCR products were identified by 2% agarose gel electrophoresis, purified using an AxyPrep DNA gel extraction kit (Axygen, Corning, USA) and quantified using a QuantiFluor ™ -ST Blue Fluorescence Quantification System (Promega, Madison, USA).…”
Section: Methodsmentioning
confidence: 99%