镇痛解热对乙酰氨基酚微生物降解过程中对氨基酚的普遍积累:一个新的宏基因组视角。

IF 13.8 1区 生物学 Q1 MICROBIOLOGY
Chao-Fan Yin, Piaopiao Pan, Tao Li, Xin Song, Ying Xu, Ning-Yi Zhou
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引用次数: 0

摘要

背景:对乙酰氨基酚是一种广泛使用的镇痛和解热药物,由于其在全球范围内的广泛生产和消费增加,特别是在COVID-19大流行期间,已成为一种重要的水生微污染物。其高水溶性导致其普遍存在于污水处理厂(WWTPs)中,对环境和人类健康构成重大风险。生物处理是去除这类污染物的一种很有前途的方法。尽管之前的研究已经分离出了降解对乙酰氨基酚的纯培养物并提出了分解代谢途径,但微生物与对乙酰氨基酚之间的相互作用、对乙酰氨基酚降解基因的分布特征以及对乙酰氨基酚在现实环境中的基因驱动命运在很大程度上仍未被探索。结果:在全国20个污水处理厂的水样中,19个水样中检出对乙酰氨基酚,浓度范围为0.06 ~ 29.20 nM。然而,对氨基酚是一种毒性更强的代谢物,在所有样品中检测到的浓度都明显更高(23.93至108.68 nM),这表明WWTPs中存在分解代谢瓶颈。对上述20个样本和全球数据集的宏基因组分析显示,与下游酶相比,初始对乙酰氨基酚酰胺酶的丰度始终较高,这可能解释了瓶颈的原因。同时,基于基因组的分类揭示了初始酰胺酶与放线菌群的密切相关性,表明其降解模式依赖于物种。此外,新分离的Rhodococcus sp. NyZ502(放线菌)鉴定出一种独特的酰胺酶ApaA,它代表了WWTPs中主要的酰胺酶类别。在推测的酰胺酶中观察到显著的系统发育和结构多样性,表明在WWTPs中有多种对乙酰氨基酚水解潜力。结论:本研究增强了我们对扑热息痛的环境命运的认识,并突出了全球污水处理厂对乙酰氨基酚降解过程中可能发生的基因失衡驱动的生态风险。视频摘要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The universal accumulation of p-aminophenol during the microbial degradation of analgesic and antipyretic acetaminophen in WWTPs: a novel metagenomic perspective.

Background: Acetaminophen, a widely used analgesic and antipyretic drug, has become a significant aquatic micro-pollutant due to its extensive global production and increased consumption, particularly during the COVID-19 pandemic. Its high-water solubility leads to its pervasive presence in wastewater treatment plants (WWTPs), posing substantial risks to the environment and human health. Biological treatment is one of the promising approaches to remove such pollutants. Although previous studies have isolated acetaminophen-degrading pure cultures and proposed catabolic pathways, the interactions between microbiotas and acetaminophen, the distribution feature of acetaminophen degradation genes, and the gene-driven fate of acetaminophen in the real-world environment remain largely unexplored.

Results: Among the water samples from 20 WWTPs across China, acetaminophen was detected from 19 samples at concentrations ranging from 0.06 to 29.20 nM. However, p-aminophenol, a more toxic metabolite, was detected in all samples at significantly higher concentrations (23.93 to 108.68 nM), indicating the presence of a catabolic bottleneck in WWTPs. Metagenomic analysis from both the above 20 samples and global datasets revealed a consistently higher abundance of initial acetaminophen amidases compared to downstream enzymes, potentially having explained the reason for the bottleneck. Meanwhile, a close correlation between initial amidases and Actinomycetota revealed by genome-based taxonomy suggests a species-dependent degradation pattern. Additionally, a distinct amidase ApaA was characterized by newly isolated Rhodococcus sp. NyZ502 (Actinomycetota), represents a predominant category of amidase in WWTPs. Significant phylogenetic and structural diversity observed among putative amidases suggest versatile acetaminophen hydrolysis potential in WWTPs.

Conclusions: This study enhances our understanding of acetaminophen's environmental fate and highlights the possible occurrence of ecological risks driven by imbalanced genes in the process of acetaminophen degradation in global WWTPs. Video Abstract.

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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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