Various microbial taxa couple arsenic transformation to nitrogen and carbon cycling in paddy soils.

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Xin-Di Zhao, Zi-Yu Gao, Jingjing Peng, Konstantinos T Konstantinidis, Si-Yu Zhang
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引用次数: 0

Abstract

Background: Arsenic (As) metabolism pathways and their coupling to nitrogen (N) and carbon (C) cycling contribute to elemental biogeochemical cycling. However, how whole-microbial communities respond to As stress and which taxa are the predominant As-transforming bacteria or archaea in situ remains unclear. Hence, by constructing and applying ROCker profiles to precisely detect and quantify As oxidation (aioA, arxA) and reduction (arrA, arsC1, arsC2) genes in short-read metagenomic and metatranscriptomic datasets, we investigated the dominant microbial communities involved in arsenite (As(III)) oxidation and arsenate (As(V)) reduction and revealed their potential pathways for coupling As with N and C in situ in rice paddies.

Results: Five ROCker models were constructed to quantify the abundance and transcriptional activity of short-read sequences encoding As oxidation (aioA and arxA) and reduction (arrA, arsC1, arsC2) genes in paddy soils. Our results revealed that the sub-communities carrying the aioA and arsC2 genes were predominantly responsible for As(III) oxidation and As(V) reduction, respectively. Moreover, a newly identified As(III) oxidation gene, arxA, was detected in genomes assigned to various phyla and showed significantly increased transcriptional activity with increasing soil pH, indicating its important role in As(III) oxidation in alkaline soils. The significant correlation of the transcriptional activities of aioA with the narG and nirK denitrification genes, of arxA with the napA and nirS denitrification genes and of arrA/arsC2 with the pmoA and mcrA genes implied the coupling of As(III) oxidation with denitrification and As(V) reduction with methane oxidation. Various microbial taxa including Burkholderiales, Desulfatiglandales, and Hyphomicrobiales (formerly Rhizobiales) are involved in the coupling of As with N and C metabolism processes. Moreover, these correlated As and N/C genes often co-occur in the same genome and exhibit greater transcriptional activity in paddy soils with As contamination than in those without contamination.

Conclusions: Our results revealed the comprehensive detection and typing of short-read sequences associated with As oxidation and reduction genes via custom-built ROCker models, and shed light on the various microbial taxa involved in the coupling of As and N and C metabolism in situ in paddy soils. The contribution of the arxA sub-communities to the coupling of As(III) oxidation with nitrate reduction and the arsC sub-communities to the coupling of As(V) reduction with methane oxidation expands our knowledge of the interrelationships among As, N, and C cycling in paddy soils. Video Abstract.

各种微生物类群将砷转化与稻田土壤中的氮和碳循环联系起来。
背景:砷(As)代谢途径及其与氮(N)和碳(C)循环的耦合有助于元素生物地球化学循环。然而,整个微生物群落如何应对砷胁迫以及哪些类群是原位砷转化的主要细菌或古细菌仍不清楚。因此,通过构建和应用 ROCker 图谱来精确检测和量化短读数元基因组和元转录组数据集中的砷氧化(aioA、arxA)和砷还原(arrA、arsC1、arsC2)基因,我们研究了参与亚砷酸盐(As(III))氧化和砷酸盐(As(V))还原的主要微生物群落,并揭示了它们在稻田中将砷与氮和碳原位耦合的潜在途径:结果:我们构建了五个 ROCker 模型,以量化水稻田土壤中编码砷氧化(aioA 和 arxA)和砷还原(arrA、arsC1 和 arsC2)基因的短读序列的丰度和转录活性。我们的研究结果表明,携带 aioA 和 arsC2 基因的亚群落分别主要负责 As(III) 氧化和 As(V) 还原。此外,在不同门类的基因组中发现了一个新鉴定的 As(III)氧化基因 arxA,其转录活性随着土壤 pH 值的增加而显著增加,表明它在碱性土壤中的 As(III)氧化过程中发挥着重要作用。aioA 的转录活性与 narG 和 nirK 反硝化基因、arxA 的转录活性与 napA 和 nirS 反硝化基因、arrA/arsC2 的转录活性与 pmoA 和 mcrA 基因之间存在明显的相关性,这意味着 As(III)氧化与反硝化以及 As(V)还原与甲烷氧化之间存在耦合关系。包括 Burkholderiales、Desulfatiglandales 和 Hyphomicrobiales(前根瘤菌)在内的各种微生物类群都参与了 As 与氮和碳代谢过程的耦合。此外,这些与砷和氮/碳相关的基因往往同时出现在同一基因组中,并且在受砷污染的稻田土壤中比在未受砷污染的土壤中表现出更强的转录活性:我们的研究结果揭示了通过定制的 ROCker 模型对与砷氧化和还原基因相关的短读序列的全面检测和分型,并揭示了参与水稻田土壤中砷与氮和碳原位代谢耦合的各种微生物类群。arxA 亚群落对 As(III) 氧化与硝酸盐还原耦合的贡献以及 arsC 亚群落对 As(V) 还原与甲烷氧化耦合的贡献扩展了我们对水稻田土壤中 As、N 和 C 循环之间相互关系的认识。视频摘要。
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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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