Zhang Qing, Yang Jida, Fu Chengxiu, Yang Yanli, Liu Xia, Deng Sihe
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The results showed that R. solanacearum infection led to significant changes in the composition and functions of bacterial and fungal communities in the potato rhizosphere, with various microbial properties (including α,β-diversity, species composition, and community ecological functions) all being driven by R. solanacearum infection. The relative abundance of some beneficial microorganisms in the potato rhizosphere, including Firmicutes, Bacillus, Pseudomonas, and Mortierella, decreased as the duration of infection increased. Moreover, the related microbial communities played a significant role in basic metabolism and signal transduction; however, the functions involved in soil C, N, and P transformation weakened. This study provides new insights into the dynamic changes in the composition and functions of potato rhizosphere microbial communities at different stages of R. solanacearum infection to adapt to the growth promotion or disease suppression strategies of host plants, which may provide guidance for formulating future strategies to regulate microbial communities for the integrated control of soil-borne plant diseases.</p>","PeriodicalId":20173,"journal":{"name":"Plant Pathology Journal","volume":"40 5","pages":"498-511"},"PeriodicalIF":1.8000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11471926/pdf/","citationCount":"0","resultStr":"{\"title\":\"Ralstonia solanacearum Infection Drives the Assembly and Functional Adaptation of Potato Rhizosphere Microbial Communities.\",\"authors\":\"Zhang Qing, Yang Jida, Fu Chengxiu, Yang Yanli, Liu Xia, Deng Sihe\",\"doi\":\"10.5423/PPJ.OA.06.2024.0086\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Bacterial wilt caused by Ralstonia solanacearum is a destructive disease that affects potato production, leading to severe yield losses. 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引用次数: 0
摘要
由 Ralstonia solanacearum 引起的细菌枯萎病是影响马铃薯生产的一种毁灭性病害,会导致严重的产量损失。目前,人们对 R. solanacearum 感染不同阶段马铃薯根瘤微生物群落的组成和功能适应性的变化知之甚少。在本研究中,我们利用扩增子和元基因组测序方法,分析了马铃薯根瘤菌感染四个阶段中细菌和真菌群落组成和功能的变化。结果表明,R. solanacearum 感染导致马铃薯根瘤菌群中细菌和真菌群落的组成和功能发生了显著变化,各种微生物特性(包括α、β-多样性、物种组成和群落生态功能)均受 R. solanacearum 感染的影响。随着感染持续时间的延长,马铃薯根瘤菌圈中一些有益微生物的相对丰度降低,其中包括真菌、芽孢杆菌、假单胞菌和莫蒂尔菌。此外,相关微生物群落在基础代谢和信号转导中发挥了重要作用,但参与土壤碳、氮、磷转化的功能却减弱了。本研究为了解马铃薯根瘤菌感染不同阶段根瘤微生物群落组成和功能的动态变化,以适应寄主植物的生长促进或病害抑制策略提供了新的见解,可为今后制定微生物群落调控策略,综合防治土传植物病害提供指导。
Ralstonia solanacearum Infection Drives the Assembly and Functional Adaptation of Potato Rhizosphere Microbial Communities.
Bacterial wilt caused by Ralstonia solanacearum is a destructive disease that affects potato production, leading to severe yield losses. Currently, little is known about the changes in the assembly and functional adaptation of potato rhizosphere microbial communities during different stages of R. solanacearum infection. In this study, using amplicon and metagenomic sequencing approaches, we analyzed the changes in the composition and functions of bacterial and fungal communities in the potato rhizosphere across four stages of R. solanacearum infection. The results showed that R. solanacearum infection led to significant changes in the composition and functions of bacterial and fungal communities in the potato rhizosphere, with various microbial properties (including α,β-diversity, species composition, and community ecological functions) all being driven by R. solanacearum infection. The relative abundance of some beneficial microorganisms in the potato rhizosphere, including Firmicutes, Bacillus, Pseudomonas, and Mortierella, decreased as the duration of infection increased. Moreover, the related microbial communities played a significant role in basic metabolism and signal transduction; however, the functions involved in soil C, N, and P transformation weakened. This study provides new insights into the dynamic changes in the composition and functions of potato rhizosphere microbial communities at different stages of R. solanacearum infection to adapt to the growth promotion or disease suppression strategies of host plants, which may provide guidance for formulating future strategies to regulate microbial communities for the integrated control of soil-borne plant diseases.