• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

AM16菌株毒力丧失的分子基础。

Molecular basis for loss of virulence in strain AM16.

作者信息

Deng Jiahui, Zhang Ziya, Wang Xingli, Cao Yongni, Huang Huichuan, Wang Mo, Luo Qiong

机构信息

State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan, Yunnan Agricultural University, Kunming, China.

出版信息

Front Plant Sci. 2024 Dec 6;15:1484214. doi: 10.3389/fpls.2024.1484214. eCollection 2024.

DOI:10.3389/fpls.2024.1484214
PMID:39711596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11659016/
Abstract

The rapid virulence variation of () to rice is a big challenge for rice blast control. Even though many studies have been done by scientists all over the world, the mechanism of virulence variation in remains elusive. AM16, an avirulent strain reported in our previous study, provides an excellent entry point to explore the mechanism of virulence variation in . In this study, we found that the and had specific mutations in strain AM16. The AM16 strains overexpressing or (and) allele from strain Guy11 displayed significantly increasing conidiation, functional appressorium formation, and restoring pathogenicity to rice. Moreover, we observed that the strains overexpressing had stronger conidia forming capacity than that of the strains overexpressing , while the appressorium formation rate of strains overexpressing was similar to that of strains overexpressing - , much higher than that of the strains overexpressing . Taken together, our results reveal that the natural mutation of and genes are important, but not the sole cause, for the loss of virulence in strain AM16. The functional difference between Pmk1 and Mac1 in the growth and development of was first discovered, providing new insight into the pathogenic mechanism of .

摘要

()对水稻的毒力快速变异是稻瘟病防治面临的一大挑战。尽管世界各地的科学家已经开展了许多研究,但()毒力变异的机制仍不清楚。AM16是我们之前研究中报道的一种无毒()菌株,为探索()毒力变异机制提供了一个很好的切入点。在本研究中,我们发现AM16菌株中()和()存在特定突变。过表达来自Guy11菌株的()或(和)()等位基因的AM16菌株表现出分生孢子显著增加、功能性附着胞形成以及对水稻致病性的恢复。此外,我们观察到过表达()的菌株比分生孢子形成能力比过表达()的菌株更强,而过表达()的菌株的附着胞形成率与过表达()-()的菌株相似,远高于过表达()的菌株。综上所述,我们的结果表明()和()基因的自然突变是AM16菌株毒力丧失的重要因素,但不是唯一原因。首次发现Pmk1和Mac1在()生长发育中的功能差异,为()致病机制提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/21c9160fd354/fpls-15-1484214-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/f0511b924ffa/fpls-15-1484214-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/345e1af09442/fpls-15-1484214-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/ac5402c1d67b/fpls-15-1484214-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/865f181c8f48/fpls-15-1484214-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/21835988dc5a/fpls-15-1484214-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/21c9160fd354/fpls-15-1484214-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/f0511b924ffa/fpls-15-1484214-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/345e1af09442/fpls-15-1484214-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/ac5402c1d67b/fpls-15-1484214-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/865f181c8f48/fpls-15-1484214-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/21835988dc5a/fpls-15-1484214-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/57c4/11659016/21c9160fd354/fpls-15-1484214-g006.jpg

相似文献

1
Molecular basis for loss of virulence in strain AM16.AM16菌株毒力丧失的分子基础。
Front Plant Sci. 2024 Dec 6;15:1484214. doi: 10.3389/fpls.2024.1484214. eCollection 2024.
2
Anti-Fungal Analysis of DL76 on Conidiation, Appressorium Formation, Growth, Multiple Stress Response, and Pathogenicity in .DL76 对 的产孢、附着胞形成、生长、多重胁迫响应和致病性的抗真菌分析。
Int J Mol Sci. 2022 May 10;23(10):5314. doi: 10.3390/ijms23105314.
3
KLBMPGC81 suppresses appressorium-mediated plant infection by altering the cell wall integrity signaling pathway and multiple cell biological processes in .KLBMPGC81 通过改变细胞壁完整性信号通路和多个细胞生物学过程来抑制 中的附着胞介导的植物感染。
Front Cell Infect Microbiol. 2022 Sep 9;12:983757. doi: 10.3389/fcimb.2022.983757. eCollection 2022.
4
A Pmk1-interacting gene is involved in appressorium differentiation and plant infection in Magnaporthe oryzae.一个与Pmk1相互作用的基因参与稻瘟病菌附着胞的分化和对植物的侵染。
Eukaryot Cell. 2011 Aug;10(8):1062-70. doi: 10.1128/EC.00007-11. Epub 2011 Jun 3.
5
PoRal2 Is Involved in Appressorium Formation and Virulence Pmk1 MAPK Pathways in the Rice Blast Fungus .水稻稻瘟病菌中,Por1参与附着胞形成及毒性Pmk1丝裂原活化蛋白激酶途径。
Front Plant Sci. 2021 Sep 13;12:702368. doi: 10.3389/fpls.2021.702368. eCollection 2021.
6
The Role of Iron Competition in the Antagonistic Action of the Rice Endophyte Streptomyces sporocinereus OsiSh-2 Against the Pathogen Magnaporthe oryzae.铁竞争在水稻内生放线菌 Streptomyces sporocinereus OsiSh-2 拮抗病原菌稻瘟病菌中的作用。
Microb Ecol. 2018 Nov;76(4):1021-1029. doi: 10.1007/s00248-018-1189-x. Epub 2018 Apr 20.
7
A putative PKA phosphorylation site S227 in MoSom1 is essential for infection-related morphogenesis and pathogenicity in Magnaporthe oryzae.假定的 MoSom1 中的 PKA 磷酸化位点 S227 对于稻瘟病菌中的感染相关形态发生和致病性是必需的。
Cell Microbiol. 2021 Oct;23(10):e13370. doi: 10.1111/cmi.13370. Epub 2021 Jul 16.
8
Melanin Promotes Spore Production in the Rice Blast Fungus .黑色素促进稻瘟病菌的孢子产生。
Front Microbiol. 2022 Feb 24;13:843838. doi: 10.3389/fmicb.2022.843838. eCollection 2022.
9
Endocytic protein Pal1 regulates appressorium formation and is required for full virulence of Magnaporthe oryzae.内吞蛋白 Pal1 调控附着胞的形成,是稻瘟病菌完全毒力所必需的。
Mol Plant Pathol. 2022 Jan;23(1):133-147. doi: 10.1111/mpp.13149. Epub 2021 Oct 12.
10
MoSfl1 is important for virulence and heat tolerance in Magnaporthe oryzae.MoSfl1 对稻瘟病菌的毒力和耐热性很重要。
PLoS One. 2011;6(5):e19951. doi: 10.1371/journal.pone.0019951. Epub 2011 May 19.

本文引用的文献

1
The phosphorylation landscape of infection-related development by the rice blast fungus.稻瘟病菌感染相关发育的磷酸化图谱。
Cell. 2024 May 9;187(10):2557-2573.e18. doi: 10.1016/j.cell.2024.04.007.
2
Approaches to Reduce Rice Blast Disease Using Knowledge from Host Resistance and Pathogen Pathogenicity.利用宿主抗性和病原菌致病性知识减少水稻稻瘟病的方法。
Int J Mol Sci. 2023 Mar 5;24(5):4985. doi: 10.3390/ijms24054985.
3
Identification of Elite -Gene Combinations against Blast Disease in Rice Varieties.鉴定水稻品种对稻瘟病的关键基因组合。
Int J Mol Sci. 2023 Feb 16;24(4):3984. doi: 10.3390/ijms24043984.
4
Prospects for rice in 2050.2050 年的水稻前景。
Plant Cell Environ. 2023 Apr;46(4):1037-1045. doi: 10.1111/pce.14565. Epub 2023 Mar 1.
5
Genome Sequence Resource of an Avirulent Field Strain AM16.无毒力田间菌株AM16的基因组序列资源
Plant Dis. 2022 Aug;106(8):2243-2246. doi: 10.1094/PDIS-01-22-0040-A. Epub 2022 Jun 21.
6
Recent Progress in Rice Broad-Spectrum Disease Resistance.水稻广谱抗病性的最新进展。
Int J Mol Sci. 2021 Oct 28;22(21):11658. doi: 10.3390/ijms222111658.
7
Appressorium-mediated plant infection by Magnaporthe oryzae is regulated by a Pmk1-dependent hierarchical transcriptional network.稻瘟病菌附着胞介导的植物侵染受 Pmk1 依赖性层次转录网络调控。
Nat Microbiol. 2021 Nov;6(11):1383-1397. doi: 10.1038/s41564-021-00978-w. Epub 2021 Oct 27.
8
PoRal2 Is Involved in Appressorium Formation and Virulence Pmk1 MAPK Pathways in the Rice Blast Fungus .水稻稻瘟病菌中,Por1参与附着胞形成及毒性Pmk1丝裂原活化蛋白激酶途径。
Front Plant Sci. 2021 Sep 13;12:702368. doi: 10.3389/fpls.2021.702368. eCollection 2021.
9
Molecular virulence determinants of : disease pathogenesis and recent interventions for disease management in rice plant.水稻疾病发病机制的分子毒力决定因素及疾病管理的最新干预措施
Mycology. 2021 Jan 15;12(3):174-187. doi: 10.1080/21501203.2020.1868594. eCollection 2021.
10
Mucin Msb2 cooperates with the transmembrane protein Sho1 in various plant surface signal sensing and pathogenic processes in the poplar anthracnose fungus Colletotrichum gloeosporioides.黏液素 Msb2 与跨膜蛋白 Sho1 在杨树炭疽菌 Colletotrichum gloeosporioides 的各种植物表面信号感应和致病过程中合作。
Mol Plant Pathol. 2021 Dec;22(12):1553-1573. doi: 10.1111/mpp.13126. Epub 2021 Aug 19.