揭示中国各地土壤巨型病毒的生境偏好、生态驱动因素、潜在宿主和辅助代谢作用

IF 13.8 1区 生物学 Q1 MICROBIOLOGY Microbiome Pub Date : 2024-07-22 DOI:10.1186/s40168-024-01851-8
Jie-Liang Liang, Shi-wei Feng, Pu Jia, Jing-li Lu, Xinzhu Yi, Shao-ming Gao, Zhuo-hui Wu, Bin Liao, Wen-sheng Shu, Jin-tian Li
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引用次数: 0

摘要

人们越来越相信,土壤巨型病毒通过感染各种真核生物对生态功能产生深远影响。然而,人们对它们的生物地理学和生态学仍然知之甚少。本研究分析了来自中国5种生境类型(农田、森林、草地、戈壁沙漠和矿山荒地)的333个土壤元基因组,发现了隶属于9个科的533个不同的巨病毒系统型,从而大大扩展了土壤巨病毒的多样性。在这九个科中,以胸腺病毒科的种类最多。大多数系统型在不同生境类型中呈现异质性分布,其中矿山荒地中独特系统型的比例非常高。系统型的丰度与其环境范围呈负相关。在已发表的全球表土元基因组数据集中,共检测到本研究中发现的 76 个系统型。在气候、地理、土壤和生物特征中,土壤真核生物被认为是不同生境类型巨型病毒群落β多样性的最重要驱动因素。此外,共现网络分析揭示了巨型病毒系统型与真核生物(原生动物、真菌和藻类)之间的一些配对关系。对从我们的元基因组中回收的 44 个中高质量巨型病毒基因组的分析不仅发现了它们高度共享的功能,还发现了它们与碳、硫和磷循环相关的新型辅助代谢基因。这些发现扩展了我们对土壤巨型病毒的多样性、栖息地偏好、生态驱动力、潜在宿主和辅助代谢的了解。
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Unraveling the habitat preferences, ecological drivers, potential hosts, and auxiliary metabolism of soil giant viruses across China
Soil giant viruses are increasingly believed to have profound effects on ecological functioning by infecting diverse eukaryotes. However, their biogeography and ecology remain poorly understood. In this study, we analyzed 333 soil metagenomes from 5 habitat types (farmland, forest, grassland, Gobi desert, and mine wasteland) across China and identified 533 distinct giant virus phylotypes affiliated with nine families, thereby greatly expanding the diversity of soil giant viruses. Among the nine families, Pithoviridae were the most diverse. The majority of phylotypes exhibited a heterogeneous distribution among habitat types, with a remarkably high proportion of unique phylotypes in mine wasteland. The abundances of phylotypes were negatively correlated with their environmental ranges. A total of 76 phylotypes recovered in this study were detectable in a published global topsoil metagenome dataset. Among climatic, geographical, edaphic, and biotic characteristics, soil eukaryotes were identified as the most important driver of beta-diversity of giant viral communities across habitat types. Moreover, co-occurrence network analysis revealed some pairings between giant viral phylotypes and eukaryotes (protozoa, fungi, and algae). Analysis of 44 medium- to high-quality giant virus genomes recovered from our metagenomes uncovered not only their highly shared functions but also their novel auxiliary metabolic genes related to carbon, sulfur, and phosphorus cycling. These findings extend our knowledge of diversity, habitat preferences, ecological drivers, potential hosts, and auxiliary metabolism of soil giant viruses.
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来源期刊
Microbiome
Microbiome MICROBIOLOGY-
CiteScore
21.90
自引率
2.60%
发文量
198
审稿时长
4 weeks
期刊介绍: Microbiome is a journal that focuses on studies of microbiomes in humans, animals, plants, and the environment. It covers both natural and manipulated microbiomes, such as those in agriculture. The journal is interested in research that uses meta-omics approaches or novel bioinformatics tools and emphasizes the community/host interaction and structure-function relationship within the microbiome. Studies that go beyond descriptive omics surveys and include experimental or theoretical approaches will be considered for publication. The journal also encourages research that establishes cause and effect relationships and supports proposed microbiome functions. However, studies of individual microbial isolates/species without exploring their impact on the host or the complex microbiome structures and functions will not be considered for publication. Microbiome is indexed in BIOSIS, Current Contents, DOAJ, Embase, MEDLINE, PubMed, PubMed Central, and Science Citations Index Expanded.
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