Trichoderma Combined with 1-Aminocyclopropane-1-carboxylic acid (ACC) Soil Amendments Modulates the Root Microbiome and Improves Wheat Growth Under Salinity Stress

IF 6.8 Q1 PLANT SCIENCES
Huicheng Zhao , Linqi Zhang , Meiyu Liu , Xinzhen Wang , Abraham Mulu Oljira
{"title":"Trichoderma Combined with 1-Aminocyclopropane-1-carboxylic acid (ACC) Soil Amendments Modulates the Root Microbiome and Improves Wheat Growth Under Salinity Stress","authors":"Huicheng Zhao ,&nbsp;Linqi Zhang ,&nbsp;Meiyu Liu ,&nbsp;Xinzhen Wang ,&nbsp;Abraham Mulu Oljira","doi":"10.1016/j.stress.2025.100785","DOIUrl":null,"url":null,"abstract":"<div><div>Salinity stress in agricultural soils impairs plant defense responses and imposes multiple effects, including ionic imbalance, osmotic and oxidative stress. Consequently, devising and customizing more effective solutions for mitigating salinity stress in crops are vital. The microbial enzyme 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase, which cleaves the ethylene precursor, ACC, is presumed to decrease stress-induced senescence and promote plant growth. In this study, halotolerant <em>Trichoderma viride</em> Th4 was isolated from salt cedar (<em>Tamarix chinensis</em> Lour.) rhizosphere soils and mass-cultured for use as a seed inoculant. ACC soil amendment is thought to promote the proliferation of root-associated microorganisms with ACC deaminase activity. A glasshouse experiment was conducted to determine the effects of <em>T. viride</em> Th4 and ACC, when applied individually or in combination, on the root microbiome communities and physio-biochemical attributes of wheat plants grown in pots containing nonsaline or saline soil. Control (CK) and stress-CK reference pots were also prepared. The highest fungal richness was observed in the roots of plants treated with <em>T. viride</em> Th4, in both nonsaline and saline soils, whereas the highest fungal diversity was observed in the <em>T. viride</em> Th4, ACC, and their coapplication treatments in saline soil. Moreover, ACC soil amendment consistently increased bacterial richness and diversity in the root endosphere, whereas <em>T. viride</em> Th4, ACC, and their coapplication decreased the richness and diversity of the rhizosphere microbiome in saline soil. Individual ACC soil amendment or coapplication with <em>T. viride</em> Th4 increased the abundance of the genus <em>Rhodanobacter</em> and reduced that of the genus <em>Ochrobactrum</em> in the root endosphere of the stressed plants. Saline soil significantly increased sodium (Na<sup>+</sup>) accumulation in wheat roots and shoots. However, <em>T. viride</em> Th4, ACC, and their coapplication reduced the Na<sup>+</sup> content in the roots by 21.5%, 27%, and 9.5%, respectively, and in the shoots by 31.7%, 9.9%, and 23.44%, respectively, compared with the stress CK treatment. Salinity stress also decreased the leaf chlorophyll a content, but <em>T. viride</em> Th4 application or coapplication with ACC increased it by approximately 6.6% and 11.3%, respectively. Furthermore, salinized wheat treated with <em>T. viride</em> Th4 alone or in combination with ACC presented increased activities of superoxide dismutase (SOD; 27.23% and 14.23%, respectively), catalase (CAT; 161.85% and 151.28%, respectively), ascorbate peroxidase (APX; 64.15% and 128.74%, respectively), and guaiacol peroxidase (GPX; 57.61% and 12.38%, respectively) compared with those in the stress CK treatment. Compared with the stress CK treatment, the ACC treatment slightly reduced SOD activity (5.29%) but increased CAT (78.86% and GPX (58.57%) activity. The findings of the present study suggest that <em>T. viride</em> Th4 application alone or in combination with ACC results in increased antioxidant activity and counteracts detrimental effects, thus improving wheat growth. Additionally, our results provide insights into a promising way to leverage plant-beneficial soil microbes to reinforce salinity tolerance in wheat tissues, although the multifaceted synergies between <em>Trichoderma</em> and ACC and their broad-scale applications need to be more fully elucidated.</div></div>","PeriodicalId":34736,"journal":{"name":"Plant Stress","volume":"15 ","pages":"Article 100785"},"PeriodicalIF":6.8000,"publicationDate":"2025-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Plant Stress","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2667064X25000508","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"PLANT SCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Salinity stress in agricultural soils impairs plant defense responses and imposes multiple effects, including ionic imbalance, osmotic and oxidative stress. Consequently, devising and customizing more effective solutions for mitigating salinity stress in crops are vital. The microbial enzyme 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase, which cleaves the ethylene precursor, ACC, is presumed to decrease stress-induced senescence and promote plant growth. In this study, halotolerant Trichoderma viride Th4 was isolated from salt cedar (Tamarix chinensis Lour.) rhizosphere soils and mass-cultured for use as a seed inoculant. ACC soil amendment is thought to promote the proliferation of root-associated microorganisms with ACC deaminase activity. A glasshouse experiment was conducted to determine the effects of T. viride Th4 and ACC, when applied individually or in combination, on the root microbiome communities and physio-biochemical attributes of wheat plants grown in pots containing nonsaline or saline soil. Control (CK) and stress-CK reference pots were also prepared. The highest fungal richness was observed in the roots of plants treated with T. viride Th4, in both nonsaline and saline soils, whereas the highest fungal diversity was observed in the T. viride Th4, ACC, and their coapplication treatments in saline soil. Moreover, ACC soil amendment consistently increased bacterial richness and diversity in the root endosphere, whereas T. viride Th4, ACC, and their coapplication decreased the richness and diversity of the rhizosphere microbiome in saline soil. Individual ACC soil amendment or coapplication with T. viride Th4 increased the abundance of the genus Rhodanobacter and reduced that of the genus Ochrobactrum in the root endosphere of the stressed plants. Saline soil significantly increased sodium (Na+) accumulation in wheat roots and shoots. However, T. viride Th4, ACC, and their coapplication reduced the Na+ content in the roots by 21.5%, 27%, and 9.5%, respectively, and in the shoots by 31.7%, 9.9%, and 23.44%, respectively, compared with the stress CK treatment. Salinity stress also decreased the leaf chlorophyll a content, but T. viride Th4 application or coapplication with ACC increased it by approximately 6.6% and 11.3%, respectively. Furthermore, salinized wheat treated with T. viride Th4 alone or in combination with ACC presented increased activities of superoxide dismutase (SOD; 27.23% and 14.23%, respectively), catalase (CAT; 161.85% and 151.28%, respectively), ascorbate peroxidase (APX; 64.15% and 128.74%, respectively), and guaiacol peroxidase (GPX; 57.61% and 12.38%, respectively) compared with those in the stress CK treatment. Compared with the stress CK treatment, the ACC treatment slightly reduced SOD activity (5.29%) but increased CAT (78.86% and GPX (58.57%) activity. The findings of the present study suggest that T. viride Th4 application alone or in combination with ACC results in increased antioxidant activity and counteracts detrimental effects, thus improving wheat growth. Additionally, our results provide insights into a promising way to leverage plant-beneficial soil microbes to reinforce salinity tolerance in wheat tissues, although the multifaceted synergies between Trichoderma and ACC and their broad-scale applications need to be more fully elucidated.
求助全文
约1分钟内获得全文 求助全文
来源期刊
Plant Stress
Plant Stress PLANT SCIENCES-
CiteScore
5.20
自引率
8.00%
发文量
76
审稿时长
63 days
期刊介绍: The journal Plant Stress deals with plant (or other photoautotrophs, such as algae, cyanobacteria and lichens) responses to abiotic and biotic stress factors that can result in limited growth and productivity. Such responses can be analyzed and described at a physiological, biochemical and molecular level. Experimental approaches/technologies aiming to improve growth and productivity with a potential for downstream validation under stress conditions will also be considered. Both fundamental and applied research manuscripts are welcome, provided that clear mechanistic hypotheses are made and descriptive approaches are avoided. In addition, high-quality review articles will also be considered, provided they follow a critical approach and stimulate thought for future research avenues. Plant Stress welcomes high-quality manuscripts related (but not limited) to interactions between plants and: Lack of water (drought) and excess (flooding), Salinity stress, Elevated temperature and/or low temperature (chilling and freezing), Hypoxia and/or anoxia, Mineral nutrient excess and/or deficiency, Heavy metals and/or metalloids, Plant priming (chemical, biological, physiological, nanomaterial, biostimulant) approaches for improved stress protection, Viral, phytoplasma, bacterial and fungal plant-pathogen interactions. The journal welcomes basic and applied research articles, as well as review articles and short communications. All submitted manuscripts will be subject to a thorough peer-reviewing process.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信