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. 2011;6(10):e26041.
doi: 10.1371/journal.pone.0026041. Epub 2011 Oct 10.

Plasmid metagenome reveals high levels of antibiotic resistance genes and mobile genetic elements in activated sludge

Tong Zhang  1 , Xu-Xiang Zhang, Lin Ye
Affiliations

Plasmid metagenome reveals high levels of antibiotic resistance genes and mobile genetic elements in activated sludge

Tong Zhang et al. PLoS One. 2011.

Abstract

The overuse or misuse of antibiotics has accelerated antibiotic resistance, creating a major challenge for the public health in the world. Sewage treatment plants (STPs) are considered as important reservoirs for antibiotic resistance genes (ARGs) and activated sludge characterized with high microbial density and diversity facilitates ARG horizontal gene transfer (HGT) via mobile genetic elements (MGEs). However, little is known regarding the pool of ARGs and MGEs in sludge microbiome. In this study, the transposon aided capture (TRACA) system was employed to isolate novel plasmids from activated sludge of one STP in Hong Kong, China. We also used Illumina Hiseq 2000 high-throughput sequencing and metagenomics analysis to investigate the plasmid metagenome. Two novel plasmids were acquired from the sludge microbiome by using TRACA system and one novel plasmid was identified through metagenomics analysis. Our results revealed high levels of various ARGs as well as MGEs for HGT, including integrons, transposons and plasmids. The application of the TRACA system to isolate novel plasmids from the environmental metagenome, coupled with subsequent high-throughput sequencing and metagenomic analysis, highlighted the prevalence of ARGs and MGEs in microbial community of STPs.

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Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1
Figure 1. Abundances of bacterial hosts of plasmids in activated sludge of Shatin STP.
Figure 2
Figure 2. Open reading frames (ORFs) on the three plasmids detected in activated sludge of Shatin STP. pST1 structure was identified by assembling the sequencing reads using SOAPdenovo (BGI, Shenzhen, China).
pST2 and pST10 were cloned with culture-independent transposon aided capture system and DNA sequencing were conducted applying the primer walking strategy.
Figure 3
Figure 3. Relative abundances of the three plasmids in activated sludge of Shatin STP.
The relative abundance is given in relation to the total number of sequencing reads and the plasmid coverage was estimated by counting the number of reads aligned at each base.
Figure 4
Figure 4. Relative abundances of various ARGs in activated sludge of Shatin STP.
The relative abundance is given in relation to the total number of ARG-matched reads.
See this image and copyright information in PMC

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