Flue-cured tobacco intercropping with insectary floral plants improves rhizosphere soil microbial communities and chemical properties of flue-cured tobacco.

IF 4 2区 生物学 Q2 MICROBIOLOGY
Jin Zhong, Wenze Pan, Shenglan Jiang, Yanxia Hu, Guangyuan Yang, Ke Zhang, Zhenyuan Xia, Bin Chen
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引用次数: 0

Abstract

Background: Continuous cropping of the same crop leads to land degradation. This is also called the continuous-cropping obstacle. Currently, intercropping tobacco with other crops can serve as an effective strategy to alleviate continuous cropping obstacles.

Results: In this study, tobacco K326 and insectary floral plants were used as materials, and seven treatments of tobacco monoculture (CK), tobacco intercropped with Tagetes erecta, Vicia villosa, Fagopyrum esculentum, Lobularia maritima, Trifolium repens, and Argyranthemum frutescens respectively, were set up to study their effects on rhizosphere soil chemical properties and composition and structure of rhizosphere soil microbial community of tobacco. The 16 S rRNA gene and ITS amplicons were sequenced using Illumina high-throughput sequencing. tobacco/insectary floral plants intercropping can influence rhizosphere soil chemical properties, which also change rhizosphere microbial communities. The CK and treatment groups tobacco rhizosphere soil microorganisms had significantly different genera, such as tobacco intercropping with T. repens and A. frutescens significantly increased the number of Fusarium and intercropping T. erecta, V. villosa, L. maritima, T. repens, and A. frutescens significantly increased the number of Sphingomonas and unknown Gemmatimonadaceae. Additionally, intercropping T. erecta, V. villosa and L. maritima changed the rhizosphere fungal and bacteria community and composition of tobacco and the positive correlation between tobacco rhizosphere the genera of fungi and bacterial were greater than CK. The pathway of the carbohydrate metabolism, amino acid metabolism, and energy metabolism in rhizosphere bacteria were significantly decreased after continuous cropping. Fungal symbiotic trophic and saprophytic trophic were significantly increased after intercropping V. villosa, L. maritima and plant pathogen and animal pathogen were increased after intercropping T. repens and A. frutescens. Additionally, bacterial and fungal communities significantly correlated with soil chemical properties, respectively.

Conclusion: This study reveals that intercropping tobacco with insectary floral plants, particularly T. erecta, V. villosa, L. maritima and A. frutescens significantly affects soil chemical properties and alters rhizosphere microbial communities, increasing the abundance of certain microbial genera. Additionally, intercropping enhances pathways related to carbohydrate, amino acid, and energy metabolism in rhizosphere bacteria. These findings suggest that intercropping could provide a promising strategy to overcome challenges associated with continuous tobacco cropping by regulating the rhizosphere environment.

烟草与昆虫花卉植物间作可改善根瘤土壤微生物群落和烟草的化学特性。
背景:连续种植同一种作物会导致土地退化。这也被称为连作障碍。目前,烟草与其他作物间作可以作为缓解连作障碍的有效策略:本研究以烟草 K326 和昆虫花卉植物为材料,分别设置了烟草单作(CK)、烟草与直立万寿菊(Tagetes erecta)、野漆(Vicia villosa)、Fagopyrum esculentum、Lobularia maritima、Trifolium repens 和 Argyranthemum frutescens 七种处理,研究它们对烟草根圈土壤化学性质和根圈土壤微生物群落组成与结构的影响。利用 Illumina 高通量测序技术对 16 S rRNA 基因和 ITS 扩增子进行了测序。烟草/虫媒花植物间作会影响根圈土壤的化学性质,也会改变根圈微生物群落。CK 组和处理组烟草根圈土壤微生物具有显著的不同属,如烟草间作 T. repens 和 A. frutescens 显著增加了镰刀菌的数量,而间作 T. erecta、V. villosa、L. maritima、T. repens 和 A. frutescens 显著增加了 Sphingomonas 和未知 Gemmatimonadaceae 的数量。此外,间作 T. erecta、V. villosa 和 L. maritima 改变了烟草根圈真菌和细菌群落和组成,烟草根圈真菌和细菌属之间的正相关性大于 CK。连作后,根圈细菌的碳水化合物代谢、氨基酸代谢和能量代谢途径明显减少。间作 V. villosa 和 L. maritima 后,真菌共生营养体和吸食营养体明显增加,间作 T. repens 和 A. frutescens 后,植物病原体和动物病原体增加。此外,细菌和真菌群落分别与土壤化学性质显著相关:本研究揭示了烟草与昆虫花卉植物间作,特别是直立鸢尾、V. villosa、L. maritima 和 A. frutescens 会显著影响土壤化学性质并改变根瘤菌群落,增加某些微生物属的丰度。此外,间作还能增强根瘤菌中与碳水化合物、氨基酸和能量代谢有关的途径。这些研究结果表明,通过调节根圈环境,间作套种可以为克服烟草连作带来的挑战提供一种有前途的策略。
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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