Potential for mercury methylation by Asgard archaea in mangrove sediments

生物 古细菌 变形菌纲 甲基汞 基因组 微生物 Mercury(编程语言) 浮霉菌门 基因 厚壁菌 生态学 细菌 16S核糖体RNA 遗传学 γ蛋白杆菌 生物累积 程序设计语言 计算机科学
作者
Cui‐Jing Zhang,Yu‐Rong Liu,Guihong Cha,Yang Liu,Xinquan Zhou,Zhongyi Lu,Jie Pan,Mingwei Cai,Meng Li
出处
期刊:The ISME Journal [Springer Nature]
卷期号:17 (3): 478-485 被引量:11
标识
DOI:10.1038/s41396-023-01360-w
摘要

Methylmercury (MeHg) is a potent neurotoxin that bioaccumulates along food chains. The conversion of MeHg from mercury (Hg) is mediated by a variety of anaerobic microorganisms carrying hgcAB genes. Mangrove sediments are potential hotspots of microbial Hg methylation; however, the microorganisms responsible for Hg methylation are poorly understood. Here, we conducted metagenomic and metatranscriptomic analyses to investigate the diversity and distribution of putative microbial Hg-methylators in mangrove ecosystems. The highest hgcA abundance and expression occurred in surface sediments in Shenzhen, where the highest MeHg concentration was also observed. We reconstructed 157 metagenome-assembled genomes (MAGs) carrying hgcA and identified several putative novel Hg-methylators, including one Asgard archaea (Lokiarchaeota). Further analysis of MAGs revealed that Deltaproteobacteria, Euryarchaeota, Bacteroidetes, Chloroflexi, and Lokiarchaeota were the most abundant and active Hg-methylating groups, implying their crucial role in MeHg production. By screening publicly available MAGs, 104 additional Asgard MAGs carrying hgcA genes were identified from a wide range of coast, marine, permafrost, and lake sediments. Protein homology modelling predicts that Lokiarchaeota HgcAB proteins contained the highly conserved amino acid sequences and folding structures required for Hg methylation. Phylogenetic tree revealed that hgcA genes from Asgard clustered with fused hgcAB genes, indicating a transitional stage of Asgard hgcA genes. Our findings thus suggest that Asgard archaea are potential novel Hg-methylating microorganisms and play an important role in hgcA evolution.

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