Responses of rhizosphere and bulk substrate microbiome to wastewater-borne sulfonamides in constructed wetlands with different plant species

根际 微生物群 生物降解 芦苇 人工湿地 生物 湿地 微生物 废水 基质(水族馆) 植物修复 环境化学 基因组 植物 细菌 化学 生态学 环境科学 污染 环境工程 生物化学 生物信息学 遗传学 基因
作者
Ying Man,Jiaxi Wang,N.F.Y. Tam,Xiang Wan,Wenda Huang,Yu Zheng,Jinpeng Tang,Ran Tao,Yang Yang
出处
期刊:Science of The Total Environment [Elsevier BV]
卷期号:706: 135955-135955 被引量:81
标识
DOI:10.1016/j.scitotenv.2019.135955
摘要

Constructed wetlands (CWs) have been used to remove organic pollutants including antibiotics based on the roles of plants and microbial communities, but how rhizosphere and bulk substrate-associated microbiomes respond to antibiotics during biodegradation have seldom been researched. The effects of sulfonamides (SAs) on the microbiome composition in different compartments, namely rhizosphere, near rhizosphere and bulk substrate, in CWs planted with either Cyperus alternifolius, Cyperus papyrus or Juncus effuses were evaluated using specially designed rhizoboxes and 16S rRNA gene high-throughput sequencing. Results revealed that wastewater-borne SAs significantly reduced the microbial biodiversity in CWs, and inhibited the functional bacterial groups related to sulphur and nitrogen cycles. On the contrary, SAs significantly enriched methylotrophs with potential to initially biodegrade SAs, such as Methylosinus, Methylotenera, Methylocaldum and Methylomonas, and such enrichment was more significant in rhizosphere than in bulk substrate. The network analysis indicated that a more complex network in bulk substrate was more fragile to SA stress. The presence of wetland plants significantly influenced the bacterial community structure in CWs, but in the same compartment, the difference among the three plants species was not obvious. Wetland plants ensured the stability of rhizosphere microorganisms and increased their ability to tolerate SA stress. The present study enhances our understanding of the importance of plant-bacteria interactions in CWs and responses of substrate microbiome to antibiotics.
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