Phosphate amendment drives bloom of RNA viruses after soil wet-up

IF 10.3 1区 农林科学 Q1 SOIL SCIENCE Soil Biology & Biochemistry Pub Date : 2025-06-01 Epub Date: 2025-03-18 DOI:10.1016/j.soilbio.2025.109791
Ella T. Sieradzki , G. Michael Allen , Jeffrey A. Kimbrel , Graeme W. Nicol , Christina Hazard , Erin Nuccio , Steven J. Blazewicz , Jennifer Pett-Ridge , Gareth Trubl
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Abstract

Soil rewetting after a dry period results in a surge of activity and succession in both microbial and DNA virus communities. Less is known about the response of RNA viruses to soil rewetting—while they are highly diverse and widely distributed in soil, they remain understudied. We hypothesized that RNA viruses would show temporal succession following rewetting and that phosphate amendment would influence their trajectory, as viral proliferation may cause phosphorus limitation. Using 39 time-resolved metatranscriptomes and amplicon data, 2190 RNA viral populations were identified across five phyla, with 26 % of these predicted to infect bacteria, and 11 % fungi. Only 1.2 % of viral populations had annotated capsid genes, suggesting most persist via intracellular replication without a free virion phase. Phosphate amendment altered RNA viral community composition within the first week and amended vs. unamended communities remained distinguishable for up to three weeks. While the overall host community remained stable, certain bacterial populations showed reduced abundance in phosphate-amended soils, likely due to increased viral lysis, as RNA bacteriophages proliferated significantly. Notably, 60 % of the viruses with increased abundance under phosphate amendment belonged to basal Lenarviricota clades rather than well-known groups like Leviviricetes. We estimate RNA bacteriophage infections may affect 107–109 bacteria per gram of soil, aligning with the total bacterial population (107–1010 g−1 soil), suggesting that RNA phages significantly influence bacterial communities post-wet-up, with phosphorus availability modulating this effect.
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土壤湿化后,磷酸盐的修正促使RNA病毒大量繁殖
干旱期后土壤再湿润导致微生物和DNA病毒群落的活动和演替激增。我们对RNA病毒对土壤再湿润的反应知之甚少——尽管它们在土壤中高度多样化且分布广泛,但它们仍未得到充分研究。我们假设RNA病毒在重新润湿后会表现出时间演替,并且磷酸盐的修正会影响它们的轨迹,因为病毒增殖可能导致磷限制。利用39个时间分辨的亚转录组和扩增子数据,在5个门中鉴定出2190个RNA病毒群体,其中26%预计感染细菌,11%感染真菌。只有1.2%的病毒种群具有带注释的衣壳基因,这表明大多数病毒在没有游离病毒粒子期的情况下通过细胞内复制持续存在。磷酸盐修饰在第一周内改变了RNA病毒群落组成,并且修饰与未修饰的群落在长达三周的时间内仍然可以区分。虽然总体宿主群落保持稳定,但某些细菌种群在磷酸盐修正土壤中的丰度下降,可能是由于RNA噬菌体显著增殖,病毒裂解增加。值得注意的是,在磷酸盐修饰下丰度增加的病毒中,有60%属于基础的Lenarviricota分支,而不是像Leviviricetes这样众所周知的群体。我们估计每克土壤中RNA噬菌体感染可能影响107-109个细菌,这与细菌总数(107-1010 g−1土壤)一致,表明RNA噬菌体在湿润后显著影响细菌群落,磷的有效性调节了这种影响。
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来源期刊
Soil Biology & Biochemistry
Soil Biology & Biochemistry 农林科学-土壤科学
CiteScore
16.90
自引率
9.30%
发文量
312
审稿时长
49 days
期刊介绍: Soil Biology & Biochemistry publishes original research articles of international significance focusing on biological processes in soil and their applications to soil and environmental quality. Major topics include the ecology and biochemical processes of soil organisms, their effects on the environment, and interactions with plants. The journal also welcomes state-of-the-art reviews and discussions on contemporary research in soil biology and biochemistry.
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