Comparative study of endophytic bacterial strains from non-host crops for enhancing plant growth and managing early blight in tomato.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Frontiers in Microbiology Pub Date : 2024-11-06 eCollection Date: 2024-01-01 DOI:10.3389/fmicb.2024.1487653
Aditya Kukreti, Chethana Bangi Siddabasappa, Prasannakumar Muthakapalli Krishnareddy, Pramesh Devanna, Yashavanth Basavapatna Subbanna, Manjunatha Channappa, Namburi Karunakar Reddy, Abeer Hashem, Mashail Fahad Alsayed, Elsayed Fathi Abd Allah
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引用次数: 0

Abstract

Bacillus pseudomycoides, Paenibacillus polymyxa, and B. velezensis are potent bacterial endophytes, which typically exhibit host-specific interactions. However, comparative studies of these endophytes in vitro and in planta in non-host crops are lacking. Therefore, in this study, we evaluated the potential of endophytes B. pseudomycoides strain HP3d, P. polymyxa strain PGSS1, B. velezensis strain A6, and P42, isolated from various crop ecosystems in promoting plant growth and inducing systemic resistance against early blight disease in tomato. In vitro, endophytes exhibited 44.44-55.56% and 37.50-87.50% inhibition of Alternaria solani in dual culture and volatilome bioassay, respectively. In the glasshouse, individual and combined applications via seed treatment (ST), seedling dip (SD), and foliar spray (FS) significantly enhanced shoot growth (23.63-57.61%), root growth (43.27-118.23%), number of leaves (77.52-93.58%), number of shoots (33.42-45.28%) and root dry matter (42.17-43.86%), reducing early blight (PDI) by 70.95-76.12% compared to uninoculated control. Enzymatic activities, including such as polyphenol oxidase (30-40 fold), peroxidase (65.00-75.00 fold), superoxide dismutase (34.20-37.20 fold) and phenylalanine ammonia-lyase (44.44-45.56 fold) were elevated post-inoculation in endophytes treated tomato plants challenged with A. solani compared to control treated only with A. solani and declined after the fifth day. The total chlorophyll content declined from the 0th to the 10th day, but endophyte treated plants exhibited lesser reductions (2.03-2.09) than uninoculated control. Field trials confirmed the glasshouse findings, showing reduced early blight and improved growth parameters in tomato where the ST + SD + FS combination emerged as the most effective treatment for all endophytes showing 1.06-1.88 fold increase in fruit yield per plant and 28.92-32.52% decrease in PDI compared to untreated control. Thus, the study highlights the broad-spectrum potential of these strains in promoting plant growth and controlling early blight in tomato, demonstrating non-host specificity. These endophytes offer eco-friendly alternatives to chemical pesticides, supporting sustainable agriculture. Their success in field trials suggests the potential for commercialization and large-scale use across diverse crops and pave the way for further interdisciplinary research to optimize their application in integrated pest management strategies.

非寄主作物内生细菌菌株在促进植物生长和控制番茄早疫病方面的比较研究。
假丝酵母菌、多粘芽孢杆菌和维氏芽孢杆菌都是强效的细菌内生体,通常会与寄主发生特异性相互作用。然而,目前还缺乏对这些内生菌在体外和植物体内与非寄主作物的比较研究。因此,在本研究中,我们评估了从各种作物生态系统中分离出来的内生菌 B. pseudomycoides 菌株 HP3d、P. polymyxa 菌株 PGSS1、B. velezensis 菌株 A6 和 P42 在促进植物生长和诱导对番茄早疫病的系统抗性方面的潜力。在体外,内生菌在双重培养和挥发性生物测定中对Alternaria solani的抑制率分别为44.44%-55.56%和37.50%-87.50%。在玻璃温室中,通过种子处理(ST)、浸种(SD)和叶面喷洒(FS)单独或联合施用,与未接种对照相比,能显著提高嫩枝生长(23.63-57.61%)、根系生长(43.27-118.23%)、叶片数(77.52-93.58%)、嫩枝数(33.42-45.28%)和根系干物质(42.17-43.86%),降低早疫病(PDI)70.95-76.12%。经内生菌处理的番茄植株在接种后的酶活性,包括多酚氧化酶(30-40 倍)、过氧化物酶(65.00-75.00 倍)、超氧化物歧化酶(34.20-37.20 倍)和苯丙氨酸氨化酶(44.44-45.56 倍),与只用茄黄萎病菌处理的对照组相比均有所提高,并在第五天后下降。总叶绿素含量从第 0 天到第 10 天一直在下降,但内生菌处理过的植株比未接种的对照植株叶绿素含量的下降幅度要小(2.03-2.09)。田间试验证实了玻璃温室的研究结果,番茄早疫病减少,生长参数改善,ST + SD + FS 组合成为所有内生菌最有效的处理方法,与未处理的对照相比,每株果实产量增加 1.06-1.88 倍,PDI 下降 28.92-32.52%。因此,这项研究强调了这些菌株在促进植物生长和控制番茄早疫病方面的广谱潜力,证明了它们的非寄主特异性。这些内生菌提供了化学农药的生态友好型替代品,支持可持续农业。它们在田间试验中取得的成功表明,它们具有商业化和大规模应用于多种作物的潜力,并为进一步开展跨学科研究,优化它们在病虫害综合防治战略中的应用铺平了道路。
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
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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