ARGs-OAP v2.0 with an expanded SARG database and Hidden Markov Models for enhancement characterization and quantification of antibiotic resistance genes in environmental metagenomes

被引:448
作者
Yin, Xiaole [1 ]
Jiang, Xiao-Tao [1 ]
Chai, Benli [2 ]
Li, Liguan [1 ]
Yang, Ying [3 ]
Cole, James R. [2 ]
Tiedje, James M. [2 ]
Zhang, Tong [1 ]
机构
[1] Univ Hong Kong, Dept Civil Engn, Environm Biotechnol Lab, Hong Kong, Hong Kong, Peoples R China
[2] Michigan State Univ, Dept Plant Soil & Microbial Sci, E Lansing, MI 48824 USA
[3] Sun Yat Sen Univ, Sch Marine Sci, South China Sea Resource Exploitat & Protect Coll, Guangzhou, Guangdong, Peoples R China
关键词
PROTEIN FAMILIES; HUMAN MICROBIOME;
D O I
10.1093/bioinformatics/bty053
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Much global attention has been paid to antibiotic resistance in monitoring its emergence, accumulation and dissemination. For rapid characterization and quantification of antibiotic resistance genes (ARGs) in metagenomic datasets, an online analysis pipeline, ARGs-OAP has been developed consisting of a database termed Structured Antibiotic Resistance Genes (the SARG) with a hierarchical structure (ARGs type-subtype-reference sequence). Results: The new release of the database, termed SARG version 2.0, contains sequences not only from CARD and ARDB databases, but also carefully selected and curated sequences from the latest protein collection of the NCBI-NR database, to keep up to date with the increasing number of ARG deposited sequences. SARG v2.0 has tripled the sequences of the first version and demonstrated improved coverage of ARGs detection in metagenomes from various environmental samples. In addition to annotation of high-throughput raw reads using a similarity search strategy, ARGs-OAP v2.0 now provides model-based identification of assembled sequences using SARGfam, a high-quality profile Hidden Markov Model (HMM), containing profiles of ARG subtypes. Additionally, ARGs-OAP v2.0 improves cell number quantification by using the average coverage of essential single copy marker genes, as an option in addition to the previous method based on the 16S rRNA gene.
引用
收藏
页码:2263 / 2270
页数:8
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