Plant growth promoting endophytic fungus Aspergillus niger VN2 enhances growth, regulates oxidative stress and protects DNA damage in Vigna radiata under salt stress.

IF 4.2 2区 生物学 Q2 MICROBIOLOGY
Pooja Chauhan, Mandeep Singh, Avinash Sharma, Pooja Chadha, Amarjeet Kaur
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引用次数: 0

Abstract

Background: Plant microbe-interactions contribute in mitigating abiotic environmental stresses in plants. Salinity stress is one of major factor in reducing agricultural productivity. Recently, the use of endophytic fungi has proved as one of the approaches that can help plant growth under salt stress. Therefore, the objective of this study was to isolate halotolerant endophytic fungi and elevate their potential to mitigate salt stress in Vigna radiata.

Methodology: Endophytic fungi were isolated from asymptomatic parts of Vachellia nilotica and screened for plant growth-promoting attributes such as IAA production, phosphate solubilization, siderophore production, and halotolerance. Based on growth-promoting characteristics and halotolerance, Aspergillus niger VN2 was selected and colonized in V. radiata. The colonized plants were exposed to different salt concentrations (150 mM, 200 mM, and 250 mM NaCl) to evaluate the effect of A. niger VN2 in mitigating salt stress. The effects of A. niger VN2 colonization on physiological, biochemical, and molecular parameters were assessed.

Results: In the present study, an endophytic fungus Aspergillus niger VN2 isolated from Vachellia nilotica exhibited good plant growth promotion properties and halotolerance. A. niger VN2 produced IAA (148.32 ± 2.34 µg/ml IAA), solubilized phosphate, and produced hydroxamate type siderophore (72.66% SU). It also exhibited ACC deaminase ability (134.40 ± 5.45µmolα-ketobutyrate/h/mg protein), and could tolerate up to 15% NaCl. Colonization of A. niger VN2 in V. radiata enhanced salt tolerance, and resulted in increased root and shoot length, biomass, leaf number, chlorophyll content, relative water content, and protein content in salt stressed plants. DPPH scavenging and endogenous IAA levels also increased in treated plants. Oxidative stress parameters viz. proline, electrolyte leakage, and malondialdehyde, were found to decrease in VN2 colonized plants. Fluorescent microscopy studies revealed VN2 colonized plants showed increased cell survival and lowered glutathione and hydrogen peroxide under salt stress. Comet assay was used for determining the genoprotective effect of A. niger VN2. Colonization of A. niger VN2 reduced DNA tail length, % tail DNA, tail moment, and olive tail moment in plants exposed to salt stress. The difference in biochemical molecules viz. protein, carbohydrates, lipid, and nucleic acid in colonized and non-colonized plants under salt stress was revealed by FT-IR spectroscopy and validated by PCA, which showed that A. niger VN2 mitigated salt-induced changes, as colonized samples clustered closely under both conditions.

Conclusion: From the current study, it can be concluded that colonization of endophytic fungus A. niger VN2 promotes plant growth and can mitigate salt stress in V. radiata by regulating oxidative stress.

促进植物生长的内生真菌黑曲霉VN2在盐胁迫下促进植物生长、调节氧化应激和保护DNA损伤。
背景:植物微生物相互作用有助于减轻植物的非生物环境胁迫。盐胁迫是降低农业生产力的主要因素之一。近年来,利用内生真菌已被证明是帮助植物在盐胁迫下生长的途径之一。因此,本研究的目的是分离耐盐内生真菌,并提高其缓解盐胁迫的潜力。方法:从无症状部位分离内生真菌,筛选植物生长促进特性,如IAA生产、磷酸盐溶解、铁载体生产和耐盐性。根据黑曲霉的促生特性和耐盐性,选择了黑曲霉VN2,并在辐射弧菌中定殖。采用不同盐浓度(150 mM、200 mM和250 mM NaCl)处理定植植株,评价黑曲霉VN2缓解盐胁迫的效果。评估黑曲霉VN2定殖对小鼠生理、生化和分子参数的影响。结果:从黑曲霉中分离得到的内生真菌黑曲霉VN2具有良好的促植物生长特性和耐盐性。黑曲霉VN2产生IAA(148.32±2.34µg/ml IAA),溶解磷酸盐,产生羟酸型铁载体(72.66% SU)。它还具有ACC脱氨酶能力(134.40±5.45µmolα-酮丁酸酯/h/mg蛋白),并能耐受高达15%的NaCl。黑曲霉VN2侵染辐射紫霉,增强了盐胁迫植物的耐盐性,增加了根冠长、生物量、叶片数、叶绿素含量、相对含水量和蛋白质含量。处理植株的DPPH清除能力和内源IAA水平也有所提高。氧化应激参数脯氨酸、电解质泄漏和丙二醛在VN2定殖植物中降低。荧光显微镜研究显示,VN2定植植物在盐胁迫下细胞存活率增加,谷胱甘肽和过氧化氢含量降低。采用Comet法检测黑曲霉VN2的基因保护作用。黑曲霉VN2定殖降低了盐胁迫下植物的DNA尾长、%尾DNA、尾矩和橄榄尾矩。利用傅里叶变换红外光谱(FT-IR)和主成分分析(PCA)分析了盐胁迫下定植植株和非定植植株在蛋白质、碳水化合物、脂质和核酸等生化分子方面的差异,表明黑曲霉VN2能减轻盐胁迫下定植植株的变化,因为定植样品在两种条件下都紧密聚集。结论:从目前的研究来看,内生真菌黑曲霉VN2的定殖可以促进植物生长,并通过调节氧化应激来缓解辐射曲霉的盐胁迫。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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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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