Whole-Genome Sequencing Reveals the Contribution of Long-Term Carriers in Staphylococcus aureus Outbreak Investigation

被引:21
作者
Gordon, N. C. [1 ,2 ]
Pichon, B. [3 ]
Golubchik, T. [1 ,2 ]
Wilson, D. J. [1 ,2 ]
Paul, J. [4 ]
Blanc, D. S. [5 ]
Cole, K. [5 ]
Collins, J. [6 ]
Cortes, N. [7 ]
Cubbon, M. [8 ]
Gould, F. K. [6 ]
Jenks, P. J. [9 ]
Llewelyn, M. [8 ,10 ]
Nash, J. Q. [11 ]
Orendi, J. M. [12 ]
Paranthaman, K. [13 ]
Price, J. R. [4 ]
Senn, L. [5 ]
Thomas, H. L. [13 ]
Wyllie, S. [7 ]
Crook, D. W. [1 ,2 ,13 ,14 ]
Peto, T. E. A. [1 ,2 ,14 ]
Walker, A. S. [1 ,2 ,14 ]
Kearns, A. M. [3 ]
机构
[1] John Radcliffe Hosp, Oxford Biomed Res Ctr, Natl Inst Hlth Res, Oxford, England
[2] Univ Oxford, Nuffield Dept Med, Oxford, England
[3] Publ Hlth England, Antimicrobial Resistance & Healthcare Associated, Colindale, England
[4] Royal Sussex Cty Hosp, Publ Hlth England, Brighton, E Sussex, England
[5] Lausanne Univ Hosp, Serv Preventat Med, Lausanne, Switzerland
[6] Newcastle Tyne Hosp NHS Fdn Trust, Newcastle, England
[7] Portsmouth Hosp NHS Trust, Portsmouth, Hants, England
[8] Brighton & Sussex Univ Hosp NHS Trust, Brighton, E Sussex, England
[9] Plymouth Hosp NHS Trust, Plymouth, Devon, England
[10] Brighton & Sussex Med Sch, Falmer, England
[11] East Kent Hosp NHS Fdn Trust, Canterbury, Kent, England
[12] Royal Stoke Univ Hosp, Univ Hosp North Midlands NHS Trust, Stoke On Trent, Staffs, England
[13] Publ Hlth England, London, England
[14] Univ Oxford, Hlth Protect Res Unit Healthcare Associated Infec, Natl Inst Hlth Res, Oxford, England
关键词
MRSA; Staphylococcus aureus; outbreaks; whole-genome sequencing; TRANSMISSION; RESISTANCE; EVOLUTION; CARRIAGE; SPREAD; MRSA; COLONIZATION; DYNAMICS; STRAINS;
D O I
10.1128/JCM.00363-17
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Whole-genome sequencing (WGS) makes it possible to determine the relatedness of bacterial isolates at a high resolution, thereby helping to characterize outbreaks. However, for Staphylococcus aureus, the accumulation of within-host diversity during carriage might limit the interpretation of sequencing data. In this study, we hypothesized the converse, namely, that within-host diversity can in fact be exploited to reveal the involvement of long-term carriers (LTCs) in outbreaks. We analyzed WGS data from 20 historical outbreaks and applied phylogenetic methods to assess genetic relatedness and to estimate the time to most recent common ancestor (TMRCA). The findings were compared with the routine investigation results and epidemiological evidence. Outbreaks with epidemiological evidence for an LTC source had a mean estimated TMRCA (adjusted for outbreak duration) of 243 days (95% highest posterior density interval [HPD], 143 to 343 days) compared with 55 days (95% HPD, 28 to 81 days) for outbreaks lacking epidemiological evidence for an LTC (P < 0.004). A threshold of 156 days predicted LTC involvement with a sensitivity of 0.875 and a specificity of 1. We also found 6/ 20 outbreaks included isolates with differing antimicrobial susceptibility profiles; however, these had only modestly increased pairwise diversity (mean 17.5 single nucleotide variants [SNVs] [95% confidence interval {CI}, 17.3 to 17.8]) compared with isolates with identical antibiograms (12.7 SNVs [95% CI, 12.5 to 12.8]) (P < 0.0001). Additionally, for 2 outbreaks, WGS identified 1 or more isolates that were genetically distinct despite having the outbreak pulsed-field gel electrophoresis (PFGE) pulsotype. The duration-adjusted TMRCA allowed the involvement of LTCs in outbreaks to be identified and could be used to decide whether screening for long-term carriage (e.g., in health care workers) is warranted. Requiring identical antibiograms to trigger investigation could miss important contributors to outbreaks.
引用
收藏
页码:2188 / 2197
页数:10
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