芽孢杆菌在叶根层的应用通过改变叶片内生菌群落和植物生理,介导低温胁迫下茶树的恢复。

IF 4 2区 生物学 Q2 MICROBIOLOGY
Xiao Han, Yaozong Shen, Litao Sun, Jiazhi Shen, Yilin Mao, Kai Fan, Shuangshuang Wang, Zhaotang Ding, Yu Wang
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引用次数: 0

摘要

背景:在冬季,茶树极易受到低温冻害。春季茶树活力的迅速恢复对茶叶的产量和品质至关重要。一些研究报道,粘液芽孢杆菌可以提高植物的抗逆性。然而,低温胁迫对茶树活力恢复的影响尚未见报道。本研究首先采用不同浓度的粘液芽孢杆菌对茶叶进行喷雾处理,利用16S rRNA高通量测序技术研究了不同处理对茶叶内生菌种群的影响。同时,对不同处理茶树叶片的土壤和植物分析仪发育值(SPAD)、PS II最大光化学量子产率(Fv/Fm)、超氧化物歧化酶(SOD)等生理指标进行了测定和分析,并研究了它们与细菌群落的相关性。结果:微生物学结果显示,不同浓度黏液芽孢杆菌(T1、T2、T3)处理的叶片内生菌种群多样性均高于对照组(CK),其中T2处理的多样性最高。所有样品的优势菌门为变形菌门、放线菌门、厚壁菌门和拟杆菌门。在门水平上,乳杆菌处理后叶片放线菌门、厚壁菌门和拟杆菌门的相对丰度显著高于对照。在属水平上,粘螺旋藻处理叶片中Paenibacillus、Nocardioides和Marmoricola的相对丰度显著高于对照。不同浓度的黏液双歧杆菌对叶片内生菌种群的分布有影响。在细菌功能水平上,观察到丰富的代谢功能特征,包括氨基酸的运输和代谢,以及能量的产生和转化,表明茶树叶片样品中的细菌代谢趋于旺盛。黏液双歧杆菌处理显著提高了茶树抗氧化酶活性和渗透物含量,促进了低温胁迫后茶树Fv/Fm的恢复,提高了茶叶对低温胁迫的抗性,从而促进了茶树的恢复。结论:本研究表明,在低温胁迫下,粘螺旋藻能显著改变茶树叶片内生菌群体的群落结构,提高茶树叶片抗氧化酶活性和渗透物含量,促进叶片光合作用的快速恢复,从而有利于茶树叶片的恢复。本研究为茶树在实际生产中的应用提供了理论依据,也为低温胁迫下茶树的恢复提供了新的思路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phyllospheric application of Bacillus mucilaginosus mediates the recovery of tea plants exposed to low-temperature stress by alteration of leaf endophytic community and plant physiology.

Background: In winter, tea plants are highly susceptible to low-temperature freezing damage. The rapid recovery of tea plant vigor in spring is crucial for tea yield and quality. Some studies have reported that Bacillus mucilaginosus could improve the stress resistance of plants. However, there were no reports on the effect of B. mucilaginosus on the recovery of tea plant vigor after low-temperature stress. This study firstly used different concentrations of B. mucilaginosus to spray tea leaves and used 16S rRNA high-throughput sequencing technology to study the impact of different treatments on tea leaf endophytic populations. Meanwhile, physiological indexes such as Soil and plant analyzer development values (SPAD), maximum photochemical quantum yield of PS II (Fv/Fm), and superoxide dismutase (SOD) were measured and analyzed in tea plant leaves of different treatments, and the correlation between them and the bacterial community was studied.

Results: Microbial results showed that the diversity of leaf endophytic populations treated with different concentrations of Bacillus mucilaginosus (T1, T2, T3) was higher than that in control group (CK) leaves, and T2 treatment had the highest diversity. The dominant bacterial phyla of all samples were Proteobacteria, Actinobacteriota, Firmicutes, and Bacteroidota. At the phylum level, the relative abundance of Actinobacteriota, Firmicutes, and Bacteroidota in leaves treated with B. mucilaginosus was significantly higher than that in the control. At the genus level, the relative abundance of Paenibacillus, Nocardioides, and Marmoricola in leaves treated with B. mucilaginosus was significantly higher than that in the control. Different concentrations of B. mucilaginosus affected the distribution of leaf endophytic populations. At the level of bacterial function, abundant metabolic functional features were observed, including amino acid transport and metabolism, as well as energy production and conversion, indicating that bacterial metabolism in tea plant leaf samples tends to be vigorous. The treatment with B. mucilaginosus significantly increased the activity of antioxidant enzymes and osmolyte content, promoted the recovery of Fv/Fm in tea plants after low-temperature stress, and improved the resistance of tea leaves to low-temperature stress, thereby promoting recovery.

Conclusions: This study showed that B. mucilaginosus could significantly change the community structure of leaf endophytic populations, and increase antioxidant enzyme activity and osmolyte content in tea plants after low-temperature stress, promoting the rapid recovery of photosynthesis, and thereby benefiting the recovery of tea plant leaves. This study provided a theoretical basis for the application of B. mucilaginosus in practical production and also provided new ideas for the recovery of tea plants exposed to low-temperature stress.

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来源期刊
BMC Microbiology
BMC Microbiology 生物-微生物学
CiteScore
7.20
自引率
0.00%
发文量
280
审稿时长
3 months
期刊介绍: BMC Microbiology is an open access, peer-reviewed journal that considers articles on analytical and functional studies of prokaryotic and eukaryotic microorganisms, viruses and small parasites, as well as host and therapeutic responses to them and their interaction with the environment.
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