Plant growth-promoting rhizobacterium Bacillus megaterium modulates the expression of antioxidant-related and drought-responsive genes to protect rice (Oryza sativa L.) from drought.

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2024-08-21 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1430546
Sanghun Lee, Jung-Ae Kim, Jeongsup Song, Seonbong Choe, Geupil Jang, Yangseon Kim
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Abstract

Global climate change poses a significant threat to plant growth and crop yield and is exacerbated by environmental factors, such as drought, salinity, greenhouse gasses, and extreme temperatures. Plant growth-promoting rhizobacteria (PGPR) help plants withstand drought. However, the mechanisms underlying PGPR-plant interactions remain unclear. Thus, this study aimed to isolate PGPR, Bacillus megaterium strains CACC109 and CACC119, from a ginseng field and investigate the mechanisms underlying PGPR-stimulated tolerance to drought stress by evaluating their plant growth-promoting activities and effects on rice growth and stress tolerance through in vitro assays, pot experiments, and physiological and molecular analyses. Compared with B. megaterium type strain ATCC14581, CACC109 and CACC119 exhibited higher survival rates under osmotic stress, indicating their potential to enhance drought tolerance. Additionally, CACC109 and CACC119 strains exhibited various plant growth-promoting activities, including phosphate solubilization, nitrogen fixation, indole-3-acetic acid production, siderophore secretion, 1-aminocyclopropane-1-carboxylate deaminase activity, and exopolysaccharide production. After inoculation, CACC109 and CACC119 significantly improved the seed germination of rice (Oryza sativa L.) under osmotic stress and promoted root growth under stressed and non-stressed conditions. They also facilitated plant growth in pot experiments, as evidenced by increased shoot and root lengths, weights, and leaf widths. Furthermore, CACC109 and CACC119 improved plant physiological characteristics, such as chlorophyll levels, and production of osmolytes, such as proline. In particular, CACC109- and CACC119-treated rice plants showed better drought tolerance, as evidenced by their higher survival rates, greater chlorophyll contents, and lower water loss rates, compared with mock-treated rice plants. Application of CACC109 and CACC119 upregulated the expression of antioxidant-related genes (e.g., OsCAT, OsPOD, OsAPX, and OsSOD) and drought-responsive genes (e.g., OsWRKY47, OsZIP23, OsDREB2, OsNAC066, OsAREB1, and OsAREB2). In conclusion, CACC109 and CACC119 are promising biostimulants for enhancing plant growth and conferring resistance to abiotic stresses in crop production. Future studies should conduct field trials to validate these findings under real agricultural conditions, optimize inoculation methods for practical use, and further investigate the biochemical and physiological responses underlying the observed benefits.

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植物生长促进根瘤菌巨型芽孢杆菌调节抗氧化相关基因和干旱响应基因的表达,保护水稻(Oryza sativa L.)免受干旱影响。
全球气候变化对植物生长和作物产量构成重大威胁,而干旱、盐碱化、温室气体和极端温度等环境因素又加剧了这一威胁。植物生长促进根瘤菌(PGPR)有助于植物抵御干旱。然而,PGPR 与植物相互作用的机制仍不清楚。因此,本研究旨在从人参田中分离出 PGPR--巨型芽孢杆菌菌株 CACC109 和 CACC119,并通过体外实验、盆栽实验以及生理和分子分析,评估它们的植物生长促进活性以及对水稻生长和抗逆性的影响,从而研究 PGPR 激发水稻抗旱的机制。与巨杆菌ATCC14581型菌株相比,CACC109和CACC119在渗透胁迫下表现出更高的存活率,表明它们具有增强耐旱性的潜力。此外,CACC109 和 CACC119 菌株还表现出多种植物生长促进活性,包括磷酸盐溶解、固氮、吲哚-3-乙酸生成、苷元分泌、1-氨基环丙烷-1-羧酸脱氨酶活性和外多糖生成。接种后,CACC109 和 CACC119 能显著提高水稻(Oryza sativa L.)在渗透胁迫条件下的种子萌发率,并促进根系在胁迫和非胁迫条件下的生长。在盆栽实验中,它们也促进了植物的生长,表现为嫩枝和根的长度、重量和叶宽都有所增加。此外,CACC109 和 CACC119 还改善了植物的生理特性,如叶绿素水平和渗透溶质(如脯氨酸)的产生。特别是,与模拟处理的水稻植株相比,CACC109 和 CACC119 处理的水稻植株具有更高的存活率、更高的叶绿素含量和更低的失水率,这证明它们具有更好的耐旱性。施用 CACC109 和 CACC119 能上调抗氧化相关基因(如 OsCAT、OsPOD、OsAPX 和 OsSOD)和干旱响应基因(如 OsWRKY47、OsZIP23、OsDREB2、OsNAC066、OsAREB1 和 OsAREB2)的表达。总之,CACC109 和 CACC119 是很有前途的生物刺激剂,可在作物生产中促进植物生长并赋予抗非生物性胁迫的能力。未来的研究应开展田间试验,在实际农业条件下验证这些发现,优化接种方法以利于实际使用,并进一步研究观察到的益处背后的生化和生理反应。
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来源期刊
CiteScore
7.70
自引率
9.60%
发文量
4837
审稿时长
14 weeks
期刊介绍: Frontiers in Microbiology is a leading journal in its field, publishing rigorously peer-reviewed research across the entire spectrum of microbiology. Field Chief Editor Martin G. Klotz at Washington State University is supported by an outstanding Editorial Board of international researchers. This multidisciplinary open-access journal is at the forefront of disseminating and communicating scientific knowledge and impactful discoveries to researchers, academics, clinicians and the public worldwide.
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