Cultivating crayfish (Procambarus clarkii) significantly enhances the quantity and diversity of soil microorganisms: evidence from the comparison of rice-wheat and rice-crayfish rotation models.

IF 4 2区 生物学 Q2 MICROBIOLOGY Frontiers in Microbiology Pub Date : 2025-02-03 eCollection Date: 2025-01-01 DOI:10.3389/fmicb.2025.1528883
Hui Xu, Dan Wang, Xuguang Li, Jiajia Li, Yu Xu, Zhiqiang Xu
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Abstract

Integrated farming of rice (IFA), as a time-honored agricultural model, can effectively increase agricultural productivity and provide ecological benefits. Rice-wheat rotation and rice-crayfish (Procambarus clarkii) rotation are two most widely applied IFA patterns in China. In this study, we compared the differences in soil microbial communities and predicted their functions in these two IFA models by sequencing the 16s rRNA and analyzing the bioinformation. The results showed that crayfish farming effectively increased the abundance and diversity of soil microorganisms. The main differentially abundant phyla between the two groups were Actinobacteriota, Bacteroidota, and Desulfobacterota, while the main differentially abundant genera were Bacteroidetes_vadinHA17, Sphingomonas, and Thiobacillus. The Similarity Percentages (SIMPER) analysis indicated that these species also had the highest contribution to the differences in microbial composition between the two groups. Random forest prediction analysis was employed to identify potential biomarkers to distinguish the two microbial communities. Actinobacteriota, Desulfobacterota, and Spirochaetota were identified as potential biomarker phyla. Streptomyces, Kribbella, and Paludibacter could serve as potential biomarker genera. Functional Annotation of Prokaryotic Taxa (FAPROTAX) analysis revealed that the dominant bacterial functions in the rice-wheat rotation model were aerobic chemoheterotrophy and chemoheterotrophy. In contrast, the bacterial functions in the rice-crayfish rotation model were more diverse, primarily including methylotrophy, human pathogens all and methanotrophy. The results of co-occurrence network analysis showed that crayfish farming enhanced the modularity of the soil microbial community, and revealed that the microbial network in rice-wheat soil had fewer nodes and more edges, which implying more internal connections. In conclusion, the wheat planting and crayfish farming drove significant differences in the soil microbial communities of paddy fields, with Actinobacteriota and Desulfobacterota identified as potential biomarkers. Compared to wheat cultivation, the rotation system incorporating crayfish farming enhanced the richness and diversity of soil microbial species and functions, increased the modularity of the microbial community, and promoted the presence of keystone species with connecting roles. Our study would not only clarify the effects of different IFA models on soil microbial communities, and should also provide valuable insights for future adjusting cropping patterns and controlling current soil microbial ecological problems.

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克拉氏原螯虾(Procambarus clarkii)的养殖显著提高了土壤微生物的数量和多样性:来自水稻-小麦和水稻-小龙虾轮作模式比较的证据。
水稻综合耕作作为一种历史悠久的农业模式,能够有效提高农业生产力,提供生态效益。水稻-小麦轮作和水稻-小龙虾(克氏原螯虾)轮作是中国应用最广泛的两种IFA模式。本研究通过16s rRNA测序和生物信息分析,比较了两种IFA模型中土壤微生物群落的差异,并对其功能进行了预测。结果表明,养殖小龙虾有效地增加了土壤微生物的丰度和多样性。两组间主要差异菌门为放线菌门(Actinobacteriota)、拟杆菌门(Bacteroidota)和脱硫菌门(Desulfobacterota),主要差异菌属为Bacteroidetes_vadinHA17、鞘氨单胞菌门(Sphingomonas)和硫杆菌门(Thiobacillus)。相似性百分比(SIMPER)分析表明,这些物种对两组微生物组成差异的贡献最大。采用随机森林预测分析鉴定潜在的生物标志物,以区分两种微生物群落。放线菌门、脱硫菌门和螺旋藻门被确定为潜在的生物标志物门。链霉菌、Kribbella和Paludibacter可以作为潜在的生物标记属。原核分类群功能注释(FAPROTAX)分析显示,在水稻-小麦轮作模式中,细菌的优势功能是有氧化养和化养异养。相比之下,在水稻-小龙虾轮换模式中,细菌的功能更为多样化,主要包括甲基化、人类病原体和甲烷化。共现网络分析结果表明,小龙虾养殖增强了土壤微生物群落的模块化,水稻-小麦土壤微生物网络节点较少,边缘较多,内部联系较多。综上所述,种植小麦和养殖小龙虾导致稻田土壤微生物群落存在显著差异,放线菌群和脱硫菌群被确定为潜在的生物标志物。与小麦轮作相比,小龙虾轮作提高了土壤微生物种类和功能的丰富度和多样性,增加了微生物群落的模块化,促进了具有连接作用的关键物种的存在。本研究不仅阐明了不同IFA模型对土壤微生物群落的影响,而且为未来调整种植方式和控制当前土壤微生物生态问题提供了有价值的见解。
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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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