Whole-genome sequencing to control antimicrobial resistance

被引:217
作者
Koeser, Claudio U. [1 ]
Ellington, Matthew J. [2 ]
Peacock, Sharon J. [1 ,2 ,3 ,4 ]
机构
[1] Univ Cambridge, Dept Med, Cambridge CB2 2QQ, England
[2] Publ Hlth England, Clin Microbiol & Publ Hlth Lab, Cambridge, England
[3] Cambridge Univ Hosp Natl Hlth Serv Fdn Trust, Cambridge, England
[4] Wellcome Trust Sanger Inst, Hinxton, England
基金
英国惠康基金;
关键词
whole-genome sequencing; antibiotic resistance; surveillance; diagnostics; MYCOBACTERIUM-TUBERCULOSIS COMPLEX; STAPHYLOCOCCUS-AUREUS; ANTIBIOTIC-RESISTANCE; ISONIAZID RESISTANCE; GENETIC DIVERSITY; MOLECULAR METHODS; ESCHERICHIA-COLI; DRUG-RESISTANCE; SUSCEPTIBILITY; EVOLUTION;
D O I
10.1016/j.tig.2014.07.003
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Following recent improvements in sequencing technologies, whole-genome sequencing (WGS) is positioned to become an essential tool in the control of antibiotic resistance, a major threat in modern healthcare. WGS has already found numerous applications in this area, ranging from the development of novel antibiotics and diagnostic tests through to antibiotic stewardship of currently available drugs via surveillance and the elucidation of the factors that allow the emergence and persistence of resistance. Numerous proof-of-principle studies have also highlighted the value of WGS as a tool for day-to-day infection control and, for some pathogens, as a primary diagnostic tool to detect antibiotic resistance. However, appropriate data analysis platforms will need to be developed before routine WGS can be introduced on a large scale.
引用
收藏
页码:401 / 407
页数:7
相关论文
共 100 条
[31]   Clostridium difficile surveillance: harnessing new technologies to control transmission [J].
Eyre, David W. ;
Walker, A. Sarah .
EXPERT REVIEW OF ANTI-INFECTIVE THERAPY, 2013, 11 (11) :1193-1205
[32]   Diverse Sources of C. difficile Infection Identified on Whole-Genome Sequencing [J].
Eyre, David W. ;
Cule, Madeleine L. ;
Wilson, Daniel J. ;
Griffiths, David ;
Vaughan, Alison ;
O'Connor, Lily ;
Ip, Camilla L. C. ;
Golubchik, Tanya ;
Batty, Elizabeth M. ;
Finney, John M. ;
Wyllie, David H. ;
Didelot, Xavier ;
Piazza, Paolo ;
Bowden, Rory ;
Dingle, Kate E. ;
Harding, Rosalind M. ;
Crook, Derrick W. ;
Wilcox, Mark H. ;
Peto, Tim E. A. ;
Walker, A. Sarah .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 369 (13) :1195-1205
[33]   Detection of Mixed Infection from Bacterial Whole Genome Sequence Data Allows Assessment of Its Role in Clostridium difficile Transmission [J].
Eyre, David W. ;
Cule, Madeleine L. ;
Griffiths, David ;
Crook, Derrick W. ;
Peto, Tim E. A. ;
Walker, A. Sarah ;
Wilson, Daniel J. .
PLOS COMPUTATIONAL BIOLOGY, 2013, 9 (05)
[34]   A pilot study of rapid benchtop sequencing of Staphylococcus aureus and Clostridium difficile for outbreak detection and surveillance [J].
Eyre, David W. ;
Golubchik, Tanya ;
Gordon, N. Claire ;
Bowden, Rory ;
Piazza, Paolo ;
Batty, Elizabeth M. ;
Ip, Camilla L. C. ;
Wilson, Daniel J. ;
Didelot, Xavier ;
O'Connor, Lily ;
Lay, Rochelle ;
Buck, David ;
Kearns, Angela M. ;
Shaw, Angela ;
Paul, John ;
Wilcox, Mark H. ;
Donnelly, Peter J. ;
Peto, Tim E. A. ;
Walker, A. Sarah ;
Crook, Derrick W. .
BMJ OPEN, 2012, 2 (03)
[35]   Phylogenetic polymorphisms in antibiotic resistance genes of the Mycobacterium tuberculosis complex [J].
Feuerriegel, Silke ;
Koeser, Claudio U. ;
Niemann, Stefan .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2014, 69 (05) :1205-1210
[36]   Impact of fgd1 and ddn Diversity in Mycobacterium tuberculosis Complex on In Vitro Susceptibility to PA-824 [J].
Feuerriegel, Silke ;
Koeser, Claudio U. ;
Bau, Davide ;
Ruesch-Gerdes, Sabine ;
Summers, David K. ;
Archer, John A. C. ;
Marti-Renom, Marc A. ;
Niemann, Stefan .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2011, 55 (12) :5718-5722
[37]   Can Molecular Methods Detect 1% Isoniazid Resistance in Mycobacterium tuberculosis? [J].
Folkvardsen, Dorte Bek ;
Svensson, Erik ;
Thomsen, Vibeke O. ;
Rasmussen, Erik Michael ;
Bang, Didi ;
Werngren, Jim ;
Hoffner, Sven ;
Hillemann, Doris ;
Rigouts, Leen .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (05) :1596-1599
[38]   Mycobacterium tuberculosis mutation rate estimates from different lineages predict substantial differences in the emergence of drug-resistant tuberculosis [J].
Ford, Christopher B. ;
Shah, Rupal R. ;
Maeda, Midori Kato ;
Gagneux, Sebastien ;
Murray, Megan B. ;
Cohen, Ted ;
Johnston, James C. ;
Gardy, Jennifer ;
Lipsitch, Marc ;
Fortune, Sarah M. .
NATURE GENETICS, 2013, 45 (07) :784-+
[39]   Bacterial genome sequencing in the clinic: bioinformatic challenges and solutions [J].
Fricke, W. Florian ;
Rasko, David A. .
NATURE REVIEWS GENETICS, 2014, 15 (01) :49-55
[40]   Global phylogeography of Mycobacterium tuberculosis and implications for tuberculosis product development [J].
Gagneux, Sebastien ;
Small, Peter M. .
LANCET INFECTIOUS DISEASES, 2007, 7 (05) :328-337