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Long-term N fertilization altered C-13-labeled fungal community composition but not diversity in wheat rhizosphere of Chinese black soil

文献类型： 外文期刊

作者： Wang, Qingfeng 1 ; Ma, Mingchao 1 ; Jiang, Xin 1 ; Zhou, Baoku 4 ; Guan, Dawei 1 ; Cao, Fengming 1 ; Chen, Sanfeng 2 ; Li 1 ;

作者机构： 1.Chinese Acad Agr Sci, Inst Agr Resources & Reg Planning, Beijing 100081, Peoples R China

2.China Agr Univ, Coll Biol Sci, Beijing 100094, Peoples R China

3.Minist Agr, Lab Qual & Safety Risk Assessment Microbial Prod, Beijing 100081, Peoples R China

4.Heilongjiang Acad Agr Sci, Inst Soil Fertil & Environm Sources, Harbin 150086, Heilongjiang, Peoples R China

关键词： Rhizosphere fungal composition; Nitrogen fertilization; Stable isotope probing; Root exudates

期刊名称：SOIL BIOLOGY & BIOCHEMISTRY （ 影响因子：7.609； 五年影响因子：8.312 ）

ISSN： 0038-0717

年卷期： 2019 年 135 卷

页码：

收录情况： SCI

摘要： Plant root exudates are considered as critical substrates mediating the interaction between rhizosphere microorganisms and plants. However, little is known about how microbial community response to root exudates under nitrogen (N) fertilization in agroecosystems. Here, we applied stable isotope probing to divide fungi in wheat rhizosphere soil (under 37-year N fertilization regimes) into two biological compartments: C-13-labeled and C-12 labeled fungal communities. High-throughput pyrosequencing was followed to characterize the two biological compartments. Long-term N fertilization changed rhizosphere soil physiochemical properties, and increased the quantity of plant root exudates. C-13-labeled fungi had lower diversity than C-12-labeled fungi. The fungal communities were predominantly composed of Ascomycota and Basidiomycota in both the C-13-labeled and C-12 labeled DNA, and the abundance of those two phyla were higher in C-13-labeled than that in C-12-labeled DNA. The Nonmetric Multidimensional Scaling (NMDS) showed that C-13-labeled and C-12-labeled fungal communities were distinct from each other. Long-term N fertilization altered fungal communities in C-13-labeled DNA, with lower abundance of putative fungal pathogens, and higher abundance of Glomeromycota. Although N fertilization significantly decreased C-12-labeled fungal diversity, no significant differences were detected in C-13-labeled fungal diversity, indicating the microbial species responses to root exudates and fertilization both influenced fungal diversity. In addition, "C-labeled fungal communities were less determined by soil chemical properties than C-12-labeled fungal communities, based on partial Mantel test. Overall, our results revealed that long-term N fertilization, which increased the quantity of plant root exudates, altered "C-labeled fungal community composition, but not changed C-13-labeled fungal diversity in our studied ecosystem.

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