Jingyu Li

Prof. Jingyu Li


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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29 January 2024 in Frontiers in Microbiology
Verified
Journal Article
Open access
XDXiaomin Duan
Xiaomin Duan
JLJiajia Li
Jiajia Li
WHWangping He
Wangping He
JHJingjing Huang
Jingjing Huang
WXWanxiang Xiong
Wanxiang Xiong
JLJingyu Li
Jingyu Li
Introduction: Mossy biocrust represents a stable stage in the succession of biological soil crust in arid and semi-arid areas, providing a microhabitat that maintains microbial diversity. However, the impact of mossy biocrust rhizoid soil and different particle sizes within the mossy biocrust layer and sublayer on microbial diversity and soil enzyme activities remains unclear.Methods: This study utilized Illumina MiSeq sequencing and high-throughput fluorometric technique to assess the differences in microbial diversity and soil extracellular enzymes between mossy biocrust rhizoid soil and different particle sizes within the mossy biocrust sifting and sublayer soil.Results: The results revealed that the total organic carbon (TOC), total nitrogen (TN), ammonium (NH4+) and nitrate (NO3−) in mossy biocrust rhizoid soil were the highest, with significantly higher TOC, TN, and total phosphorus (TP) in mossy biocrust sifting soil than those in mossy biocrust sublayer soil. Extracellular enzyme activities (EAAs) exhibited different responses to various soil particle sizes in mossy biocrust. Biocrust rhizoid soil (BRS) showed higher C-degrading enzyme activity and lower P-degrading enzyme activity, leading to a significant increase in enzyme C: P and N: P ratios. Mossy biocrust soils were all limited by microbial relative nitrogen while pronounced relative nitrogen limitation and microbial maximum relative carbon limitation in BRS. The diversity and richness of the bacterial community in the 0.2 mm mossy biocrust soil (BSS0.2) were notably lower than those in mossy biocrust sublayer, whereas the diversity and richness of the fungal community in the rhizoid soil were significantly higher than those in mossy biocrust sublayer. The predominant bacterial phyla in mossy biocrust were Actinobacteriota, Protebacteria, Chloroflexi, and Acidobacteriota, whereas in BSS0.2, the predominant bacterial phyla were Actinobacteriota, Protebacteria, and Cyanobacteria. Ascomycota and Basidiomycota were dominant phyla in mossy biocrust. The bacterial and fungal community species composition exhibited significant differences. The mean proportions of Actinobacteriota, Protebacteria, Chloroflexi, Acidobacteriota, Acidobacteria, Cyanobacteria, and Bacteroidota varied significantly between mossy biocrust rhizoid and different particle sizes of mossy biocrust sifting and sublayer soil (p < 0.05). Similarly, significant differences (p < 0.05) were observed in the mean proportions of Ascomycota, Basidiomycota, and Glomeromycota between mossy biocrust rhizoid and different particle sizes within the mossy biocrust sifting and sublayer soil. The complexity and connectivity of bacterial and fungal networks were higher in mossy biocrust rhizoid soil compared with different particle sizes within the mossy biocrust sifting and sublayer soil.Discussion: These results offer valuable insights to enhance our understanding of the involvement of mossy biocrust in the biogeochemical cycle of desert ecosystems.

26 May 2017 in Annals of Microbiology
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Journal Article
Closed access
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JLJingyu Li
Jingyu Li
YZYi-Fei Zhang
Yi-Fei Zhang
ZYZhou Yang
Zhou Yang
MWMeng Wang
Meng Wang

1 January 2018 in Biodiversity Science
Verified
Journal Article
Open access
JLJingyu Li
Jingyu Li
JLJianli Liu
Jianli Liu
XZXiu Zhang
Xiu Zhang
MWMeng Wang
Meng Wang
ZYZhou Yang
Zhou Yang
YZYifei Zhang
Yifei Zhang

1 January 2020 in Biodiversity Science
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Journal Article
Closed access
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XJXinying Jin
Xinying Jin
XZXiaochong Zhang
Xiaochong Zhang
DJDuo Jin
Duo Jin
YCYun Chen
Yun Chen
JLJingyu Li
Jingyu Li

1 June 2024 in Plant Disease
Verified
Journal Article
Closed access
JWJiawei Wang
Jiawei Wang
RYRui Yang
Rui Yang
JLJianli Liu
Jianli Liu
JLJingyu Li
Jingyu Li
SCShui hong Chen
Shui hong Chen
Ammopiptanthus mongolicus is the only evergreen broad-leaved shrub in the desert region of Northwest China, which is one of the dominant species in the desert vegetation of the region, playing an important role in maintaining the stability of the local desert ecosystem. A. mongolicus is also very hardy and drought resistant and can survive extreme temperatures (Liu et al. 2013; Yang et al. 2022). The large-scale death of A. mongolicus could cause desertification in the region. Two months after the discovery of Fusarium verticillioides causing blight on A. mongolicus in Etuoke county, Inner Mongolia Autonomous Region in September 2023 (Yang et al. 2024), a large number of A. mongolicus plants with symptoms of blights were found in Lingwu city, Ningxia Hui Autonomous Region, China (106.442368°E, 37.734026°N) in November 2023. The incidence of diseased plants in this field was about 30%. The field symptoms in Lingwu city were similar to those observed in Etuoke county. The diseased leaves initially turned yellow, then wilted and dehisced, eventually resulting in plant death (Figure 1). The roots of the diseased plants were cut diagonally and the central cylinder showed a brown color (Figure 2). In order to investigate whether the death of A. mongolicus was caused by the same pathogen as those identified previously, 30 roots were collected from 10 diseased plants. After rinsing and surface sterilization (70% ethanol for 3 min and 2.5% NaClO for 5 min, rinsed 3 times with sterile distilled water), diseased tissues (10×10 mm) were placed on potato dextrose agar (PDA) (3 pieces per plate) and incubated from 3 to 5 days at 25°C. The strain AmP5 was isolated and used for further study. After 3 days on PDA medium, fungal colonies were white to milky, the undersides of the cultures were yellowish to orange-brown (Figure 3). After 7 days on synthetic nutrient-poor agar (SNA), microconidia were ovoidal or with a rounded apex and truncate base, 10.5 ± 1.5 μm × 1.6 ± 0.2 μm (×400). The macroconidia were slightly curved or arcuate, 40.5 ± 3.5 μm × 5 ± 0.5 μm (×400) (Figure 4) (Šišić et al. 2018). The pathogen was confirmed to be Neocosmospora pisi by multigene phylogenetic analysis of TEF, RPB1 and RPB2 genes using primers EF1/EF2, F5/G2R and 5F2/11AR, respectively (O'Donnell et al. 2022). The sequences of PCR products were deposited in GenBank with accession numbers OR944631 (RPB1), OR988086 (TEF) and OR988087 (RPB2), respectively. The results of pairwise alignment in Fusarioid-ID database (Crous et al. 2021) showed 99.84% similarity and 83.96% overlap of the EF1-α sequence to the corresponding sequence LR583636 of ex-epitype CBS 123669 of Neocosmospora pisi (syn. Fusarium solani f. sp. pisi), 99.72% similarity and 85.66% overlap of the RPB1 sequence to the corresponding sequence MW834242 of ex-epitype CBS 123669 of N. pisi, and 99.47% similarity and 78.26% overlap of RPB2 sequence to the corresponding sequence LR583862 of ex-epitype CBS 123669 of N. pisi. Moreover, the result of polyphasic identification in the Fusarioid-ID database also showed EF1-a, RPB1, and RPB2 sequences had 99.15% similarity to the corresponding sequences of CBS 1233669. The pathogenicity of AmP5 was tested on potted 64 days old seedlings A. mongolicus plants. The roots of 3 seedlings were inoculated with conidial suspension (1×106 /ml), and another 3 used as controls were inoculated with sterile water, by gently peeling off the soil around the roots during inoculation, and pouring the conidial suspension around the roots (10 ml/seedling). All plants were placed in a growth chamber at 18-25℃ (10 h light; 14 h dark). After incubation for 3-5 days, the symptoms similar to those observed in the field (Figure 5), including brown rot of steles (Figure 6), developed on plants inoculated with conidial suspension, whereas no symptoms were observed on the control plants. The same pathogen was reisolated from inoculated roots and confirmed as N. pisi based on morphological and molecular analyses (TEF, RPB1 and RPB2). To our knowledge, this is the first report of blight on A. mongolicus caused by N. pisi in China. This study also indicates that blight on A. mongolicus can be caused by different fungal pathogens. Blight caused by different pathogens may have different in terms of control measures and pathogenic mechanisms, so the study of blight caused by different pathogens is of profound value.

27 January 2025 in Agronomy
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Journal Article
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HZHong Zhang
Hong Zhang
MBMingsheng Bai
Mingsheng Bai
YGYufei Gou
Yufei Gou
TCTianyu Chang
Tianyu Chang
JWJiayuan Wei
Jiayuan Wei
JLJianli Liu
Jianli Liu
In the transitional region between agriculture and livestock rearing in northern China, planting forage crops in rows among fruit trees as feed in orchards represents an effective strategy for enhancing the ecological environment while addressing the increasing demand for livestock feed. Nonetheless, the impact of short-term mowing of cover forage crops for livestock feed on the quality of soil remains unclear. A two-year field experiment was conducted in Ziziphus jujuba cv. “Lingwuchangzao” orchards located in Lingwu County, Ningxia Hui Autonomous Region, in arid and semi-arid Northwest China. The experiment consisted of four treatments: (A) clean tillage (CK), (B) plantation with Lolium perenne (LP), (C) plantation with Trifolium repens (TR), and (D) plantation with Vicia villosa (VV).The results showed that short-term intercropping of forage crops may lead to a reduction in most soil nutrients in Z. jujuba cv. “Lingwuchangzao” orchards, particularly in the 0–20 cm soil layer. However, intercropping with TR can mitigate this declining trend and may even enhance nutrient levels within the 0–40 cm depth. Furthermore, intercropping of forage crops had a more pronounced effect on the α-diversity of fungal communities than on bacterial communities. This practice also altered the relative abundance of bacterial genera such as Sphingomonas, Bacillus, and Flavobacterium in the 20–40 cm depth and dominant fungal genera Fusarium and Mortierella in the 0–20 cm soil layer. The effects of soil physicochemical properties on bacterial communities were more significant than those on fungal communities.These results indicate that the short-term intercropping of forage crops in Z. jujuba cv. “Lingwuchangzao” orchards in arid and semi-arid Northwest China have varying impacts depending on the type of forage crop used.