BacWGSTdb, a database for genotyping and source tracking bacterial pathogens

被引:161
作者
Ruan, Zhi [1 ]
Feng, Ye [1 ,2 ]
机构
[1] Zhejiang Univ, Sch Med, Sir Run Run Shaw Hosp, Hangzhou 310016, Zhejiang, Peoples R China
[2] Zhejiang Univ, Sch Med, Inst Translat Med, Hangzhou 310029, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
BY-GENE APPROACH; ACINETOBACTER-BAUMANNII; CLINICAL MICROBIOLOGY; MLST; PROSPECTS; COMPLEX;
D O I
10.1093/nar/gkv1004
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Whole genome sequencing has become one of the routine methods in molecular epidemiological practice. In this study, we present BacWGSTdb (http://bacdb.org/BacWGSTdb), a bacterial whole genome sequence typing database which is designed for clinicians, clinical microbiologists and hospital epidemiologists. This database borrows the population structure from the current multi-locus sequence typing (MLST) scheme and adopts a hierarchical data structure: species, clonal complex and isolates. When users upload the pre-assembled genome sequences to BacWGSTdb, it offers the functionality of bacterial genotyping at both traditional MLST and whole-genome levels. More importantly, users are told which isolates in the public database are phylogenetically close to the query isolate, along with their clinical information such as host, isolation source, disease, collection time and geographical location. In this way, BacWGSTdb offers a rapid and convenient platform for worldwide users to address a variety of clinical microbiological issues such as source tracking bacterial pathogens.
引用
收藏
页码:D682 / D687
页数:6
相关论文
共 30 条
[1]   The multilocus sequence typing network: mlst.net [J].
Aanensen, DM ;
Spratt, BG .
NUCLEIC ACIDS RESEARCH, 2005, 33 :W728-W733
[2]   Molecular Epidemiology of Carbapenem-Nonsusceptible Acinetobacter baumannii in the United States [J].
Adams-Haduch, Jennifer M. ;
Onuoha, Ezenwa O. ;
Bogdanovich, Tatiana ;
Tian, Guo-Bao ;
Marschall, Jonas ;
Urban, Carl M. ;
Spellberg, Brad J. ;
Rhee, Diane ;
Halstead, Diane C. ;
Pasculle, Anthony W. ;
Doi, Yohei .
JOURNAL OF CLINICAL MICROBIOLOGY, 2011, 49 (11) :3849-3854
[3]   GenBank [J].
Benson, Dennis A. ;
Clark, Karen ;
Karsch-Mizrachi, Ilene ;
Lipman, David J. ;
Ostell, James ;
Sayers, Eric W. .
NUCLEIC ACIDS RESEARCH, 2015, 43 (D1) :D30-D35
[4]   Rapid bacterial genome sequencing: methods and applications in clinical microbiology [J].
Bertelli, C. ;
Greub, G. .
CLINICAL MICROBIOLOGY AND INFECTION, 2013, 19 (09) :803-813
[5]   Transforming clinical microbiology with bacterial genome sequencing [J].
Didelot, Xavier ;
Bowden, Rory ;
Wilson, Daniel J. ;
Peto, Tim E. A. ;
Crook, Derrick W. .
NATURE REVIEWS GENETICS, 2012, 13 (09) :601-612
[6]   Next-generation sequencing technologies and their impact on microbial genomics [J].
Forde, Brian M. ;
O'Toole, Paul W. .
BRIEFINGS IN FUNCTIONAL GENOMICS, 2013, 12 (05) :440-453
[7]   NCBIBLAST: a better web interface [J].
Johnson, Mark ;
Zaretskaya, Irena ;
Raytselis, Yan ;
Merezhuk, Yuri ;
McGinnis, Scott ;
Madden, Thomas L. .
NUCLEIC ACIDS RESEARCH, 2008, 36 :W5-W9
[8]  
Jolley KA, 2013, EUROSURVEILLANCE, V18, P41
[9]   Using multilocus sequence typing to study bacterial variation: prospects in the genomic era [J].
Jolley, Keith A. ;
Maiden, Martin C. J. .
FUTURE MICROBIOLOGY, 2014, 9 (05) :623-630
[10]   BIGSdb: Scalable analysis of bacterial genome variation at the population level [J].
Jolley, Keith A. ;
Maiden, Martin C. J. .
BMC BIOINFORMATICS, 2010, 11