2021
DOI: 10.1016/j.fgb.2021.103612
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Regulation of conidiation, polarity growth, and pathogenicity by MrSte12 transcription factor in entomopathogenic fungus, Metarhizium rileyi

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Cited by 9 publications
(10 citation statements)
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“…Penetration of the host cuticle is essential for filamentous fungal pathogens to successfully infect the host. Fus3/Kss1 MAPK cascade and its downstream TF Ste12‐like are required for appressorium formation/function, penetration of host cuticle/pathogenicity in some fungal pathogens 10,11,14,20,21,26,27,53 . In this study, we provided the direct evidence in vivo that Fus3/Kss1 MAPK (Bbmpk1) interacted with Ste12‐like (BbSte12) in the nucleus in the insect fungal pathogen, B. bassiana .…”
Section: Discussionmentioning
confidence: 85%
See 1 more Smart Citation
“…Penetration of the host cuticle is essential for filamentous fungal pathogens to successfully infect the host. Fus3/Kss1 MAPK cascade and its downstream TF Ste12‐like are required for appressorium formation/function, penetration of host cuticle/pathogenicity in some fungal pathogens 10,11,14,20,21,26,27,53 . In this study, we provided the direct evidence in vivo that Fus3/Kss1 MAPK (Bbmpk1) interacted with Ste12‐like (BbSte12) in the nucleus in the insect fungal pathogen, B. bassiana .…”
Section: Discussionmentioning
confidence: 85%
“…In yeast, transcription factor (TF) Ste12 acts as a target of both of Fus3 and Kss1 MAPK cascades, which coordinates with Far1, Dig1 and Dig2, and Tec1 for regulation of mating and invasive/pseudohyphal growth, respectively 17,18 . Ste12‐like has been also identified in filamentous fungi, which regulates appressorium formation, cell wall penetration and pathogenicity, as well as fungal development and differentation 17,19,20 . Fus3/Kss1‐MAPK has also been shown to interact with Ste12‐like with in vitro tests from the fungal pathogens Fusarium graminearum and Metarhizium robertsii 21,22 .…”
Section: Introductionmentioning
confidence: 99%
“…In D. dactyloides , the Δ Ddste12 mutant had defects for conidiation, and the number of conidia decreased by only 19.7% compared to the WT strains ( 34 ). The absence of Ste12 caused conidia to be produced only under the condition of 0.4 M KCl in the growth medium, in Metarhizium rileyi ( 40 ). Similarly, conidia yield was decreased in the Δ ste12 mutant of S. turcica ( 35 ), and A. oryzae ( 25 ).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, Ste12 is involved in virulence and is necessary for Candida glabrata to produce pseudomycelia in nitrogen-deficient cultures ( 44 ). Similarly, Ste12 is essential for pathogenicity in several pathogenic fungi, such as F. graminearum ( 36 ), F. oxysporum ( 26 ), M. grisea ( 30 ), M. rileyi ( 40 ), and S. turcica ( 35 ). Recently, orthologous Ste12 was identified in the two NT fungi D. dactyloides and A. oligospora (strain TWF154); disruption of the Ddaste12 gene in D. dactyloides disabled the cell inflation of constricting rings and led to an inability to capture nematodes ( 34 ).…”
Section: Discussionmentioning
confidence: 99%
“…The deficiency of MrSte50 and MrOpy2 strains do not produce appressoria [ 42 ]. Furthermore, the complete or nearly complete loss ability of differentiation to appressoria is caused by the deletion of the transcription factor Ste12 in M. acridum , M. rileyi , and M. robertsii [ 43 , 44 , 45 ]. MrSte12 positively regulates the expression of the transcription factor MrAFTF1 through MrFus3 [ 45 ].…”
Section: The Early Phase Interactionmentioning
confidence: 99%