2022
DOI: 10.1128/spectrum.00570-22
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Aminotransferase SsAro8 Regulates Tryptophan Metabolism Essential for Filamentous Growth of Sugarcane Smut Fungus Sporisorium scitamineum

Abstract: Sugarcane smut caused by the basidiomycete fungus S. scitamineum leads to massive economic losses in sugarcane plantation globally. Dikaryotic hyphae formation (filamentous growth) and biofilm formation are two important aspects in S. scitamineum pathogenesis, yet the molecular regulation of these two processes was not as extensively investigated as that in the model pathogenic fungi, e.g., Candida albicans , Ustilago maydis … Show more

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Cited by 8 publications
(8 citation statements)
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“…Double‐joint PCR was performed to construct the fragment for the replacement of the target gene by the hygromycin ( HPT ) or zeocin ( ZEO , Invitrogen) resistance gene following a previously described strategy (Yu et al, 2004 ). Polyethylene glycol (PEG)‐mediated protoplast transformation was used to delete and complement target genes following established protocols (Chang et al, 2019 ; Cui et al, 2022 ). For the generation of deletion mutants, the flanking DNA (1 kb 5′ and 3′) of the resident target gene was amplified by PCR using genomic DNA of S. scitamineum strain MAT‐1 as the template and the HPT gene was amplified using plasmid pEX2 (Wang et al, 2019 ) as the template.…”
Section: Methodsmentioning
confidence: 99%
See 1 more Smart Citation
“…Double‐joint PCR was performed to construct the fragment for the replacement of the target gene by the hygromycin ( HPT ) or zeocin ( ZEO , Invitrogen) resistance gene following a previously described strategy (Yu et al, 2004 ). Polyethylene glycol (PEG)‐mediated protoplast transformation was used to delete and complement target genes following established protocols (Chang et al, 2019 ; Cui et al, 2022 ). For the generation of deletion mutants, the flanking DNA (1 kb 5′ and 3′) of the resident target gene was amplified by PCR using genomic DNA of S. scitamineum strain MAT‐1 as the template and the HPT gene was amplified using plasmid pEX2 (Wang et al, 2019 ) as the template.…”
Section: Methodsmentioning
confidence: 99%
“…Double-joint PCR was performed to construct the fragment for the replacement of the target gene by the hygromycin (HPT) or zeocin (ZEO, Invitrogen) resistance gene following a previously described strategy (Yu et al, 2004). Polyethylene glycol (PEG)-mediated protoplast transformation was used to delete and complement target genes following established protocols (Chang et al, 2019;Cui et al, 2022).…”
Section: Plasmid Construction and Fungal Transformationmentioning
confidence: 99%
“…The lack of efficient and simple virulence detection method is one of the main reasons for the lag in the S. scitamineum research. Traditionally, the pathogenicity assay of S. scitamineum involves soaking sugarcane buds with fungal teliospores or injection of teliospores or mixed sporidia of both mating types into meristematic tissue of sugarcane sprouts derived from stalk cuttings or tissue cultures ( Sun et al, 2019 ; Zhu et al, 2019 ; Cui et al, 2022 ). These methods have been used to characterize the virulence and physiological race differentiation of S. scitamineum ( Deng et al, 2018 ) and to determine the pathogenicity of S. scitamineum mutant strains ( Wang et al, 2019 ; Cai et al, 2021 , 2022 ; Shen et al, 2022 ).…”
Section: Introductionmentioning
confidence: 99%
“…Expression of host miRNAs in B. bassiana has been shown to significantly enhance fungal virulence against insecticide-resistant mosquitoes. Engineered fungal entomopathogen B. bassiana, that produces host immunosuppressive miRNAs, can effectively suppress the host Toll immune response and facilitate fungal infection [107]. This pathogenmediated RNAi (pmRNAi)-based approach provides an innovative strategy not only to enhance the efficacy of fungal insecticides but also to minimize the possibility of resistance development.…”
Section: Introducing Insecticidal Molecules Into Mosquitomentioning
confidence: 99%