罗伯特绿僵菌mrr -lac3和mrr -lcc2调控条件和成熟,增强对非生物胁迫的耐受性和致病性。

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Qiaoyun Wu, Yingying Ye, Yiran Liu, Yufan He, Xing Li, Siqi Yang, Tongtong Xu, Xiufang Hu, Guohong Zeng
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引用次数: 0

摘要

漆酶作为多铜氧化酶的一种,在昆虫病原真菌中发挥着多种生物学作用,增强了昆虫病原真菌的生存、发育和致病性。然而,漆酶在这些真菌中起作用的机制仍未得到充分研究。在这项研究中,我们从罗伯特绿僵菌中鉴定了两个漆酶编码基因Mr-lac3和Mr-lcc2,这两个基因在萌发过程中都是高表达的。敲除Mr-lac3和Mr-lcc2后,robertsii的分生孢子产量显著增加。此外,与野生型菌株相比,ΔMr-lac3和ΔMr-lcc2中与分生途径相关的上游调控因子的相对表达量在分生过程中显著上调,表明Mr-lac3和Mr-lcc2负向调控分生孢子的形成。qRT-PCR分析发现,Mr-lac3和Mr-lcc2受Mr-Pks1、Mr-EthD、Mlac1等色素合成基因簇调控,并提供反馈调控,共同控制色素合成。此外,ΔMr-lac3和ΔMr-lcc2显著降低了分生孢子中海藻糖的含量,增加了对细胞壁扰动剂(如刚果红和愈创木酚)的敏感性,从而导致对非生物胁迫的耐受性显著降低。综上所述,漆酶Mr-lac3和Mr-lcc2负调控分生孢子形成,正调控分生孢子成熟,从而增强对非生物胁迫的耐受性和致病性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mr-lac3 and Mr-lcc2 in Metarhizium robertsii Regulate Conidiation and Maturation, Enhancing Tolerance to Abiotic Stresses and Pathogenicity.

As a type of multicopper oxidase, laccases play multiple biological roles in entomopathogenic fungi, enhancing their survival, development, and pathogenicity. However, the mechanisms by which laccases operate in these fungi remain under-researched. In this study, we identified two laccase-encoding genes, Mr-lac3 and Mr-lcc2, from Metarhizium robertsii, both of which are highly expressed during conidiation. Knocking out Mr-lac3 and Mr-lcc2 resulted in a significant increase in the conidial yields of M. robertsii. Furthermore, the relative expression levels of upstream regulators associated with the conidiation pathway were markedly up-regulated in ΔMr-lac3 and ΔMr-lcc2 compared to the wild-type strain during conidiation, indicating that Mr-lac3 and Mr-lcc2 negatively regulate conidia formation. qRT-PCR analyses revealed that Mr-lac3 and Mr-lcc2 are regulated by the pigment synthesis gene cluster, including Mr-Pks1, Mr-EthD, and Mlac1, and they also provide feedback regulation to jointly control pigment synthesis. Additionally, ΔMr-lac3 and ΔMr-lcc2 significantly reduced the trehalose content in conidia and increased the sensitivity to cell wall-perturbing agents, such as Congo red and guaiacol, which led to a marked decrease in tolerance to abiotic stresses. In conclusion, the laccases Mr-lac3 and Mr-lcc2 negatively regulate conidia formation while positively regulating conidial maturation, thereby enhancing tolerance to abiotic stresses and pathogenicity.

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来源期刊
Journal of Fungi
Journal of Fungi Medicine-Microbiology (medical)
CiteScore
6.70
自引率
14.90%
发文量
1151
审稿时长
11 weeks
期刊介绍: Journal of Fungi (ISSN 2309-608X) is an international, peer-reviewed scientific open access journal that provides an advanced forum for studies related to pathogenic fungi, fungal biology, and all other aspects of fungal research. The journal publishes reviews, regular research papers, and communications in quarterly issues. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. Therefore, there is no restriction on paper length. Full experimental details must be provided so that the results can be reproduced.
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