Whole-Genome Sequencing of Klebsiella pneumoniae Isolates to Track Strain Progression in a Single Patient With Recurrent Urinary Tract Infection

被引:9
作者
Wylie, Kristine M. [1 ,2 ]
Wylie, Todd N. [2 ,3 ]
Minx, Patrick J. [2 ]
Rosen, David A. [1 ,4 ]
机构
[1] Washington Univ, Sch Med, Dept Pediat, Div Pediat Infect Dis, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, McDonnell Genome Inst, St Louis, MO USA
[3] Washington Univ, Sch Med, Dept Pediat, Div Gastroenterol Hepatol & Nutr, St Louis, MO 63110 USA
[4] Washington Univ, Sch Med, Dept Mol Microbiol, St Louis, MO 63110 USA
来源
FRONTIERS IN CELLULAR AND INFECTION MICROBIOLOGY | 2019年 / 9卷
基金
美国国家卫生研究院;
关键词
Klebsiella pneumoniae; whole-genome sequencing; single nucleotide variants; urinary tract infection; strain tracking; UROPATHOGENIC ESCHERICHIA-COLI; PERSISTENCE; ASSEMBLIES; MECHANISMS; TABLET;
D O I
10.3389/fcimb.2019.00014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Klebsiella pneumoniae is an important uropathogen that increasingly harbors broad-spectrum antibiotic resistance determinants. Evidence suggests that some same-strain recurrences in women with frequent urinary tract infections (UTIs) may emanate from a persistent intravesicular reservoir. Our objective was to analyze K. pneumoniae isolates collected over weeks from multiple body sites of a single patient with recurrent UTI in order to track ordered strain progression across body sites, as has been employed across patients in outbreak settings. Whole-genome sequencing of 26 K. pneumoniae isolates was performed utilizing the Illumina platform. PacBio sequencing was used to create a refined reference genome of the original urinary isolate (TOP52). Sequence variation was evaluated by comparing the 26 isolate sequences to the reference genome sequence. Whole-genome sequencing of the K. pneumoniae isolates fromsix different body sites of this patient with recurrent UTI demonstrated 100% chromosomal sequence identity of the isolates, with only a small P2 plasmid deletion in a minority of isolates. No single nucleotide variants were detected. The complete absence of single-nucleotide variants from 26 K. pneumoniae isolates from multiple body sites collected over weeks froma patientwith recurrent UTI suggests that, unlike in an outbreak situation with strains collected from numerous patients, other methods are necessary to discern strain progression within a single host over a relatively short time frame.
引用
收藏
页数:5
相关论文
共 31 条
[1]   The Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2018 update [J].
Afgan, Enis ;
Baker, Dannon ;
Batut, Berenice ;
van den Beek, Marius ;
Bouvier, Dave ;
Cech, Martin ;
Chilton, John ;
Clements, Dave ;
Coraor, Nate ;
Gruening, Bjoern A. ;
Guerler, Aysam ;
Hillman-Jackson, Jennifer ;
Hiltemann, Saskia ;
Jalili, Vahid ;
Rasche, Helena ;
Soranzo, Nicola ;
Goecks, Jeremy ;
Taylor, James ;
Nekrutenko, Anton ;
Blankenberg, Daniel .
NUCLEIC ACIDS RESEARCH, 2018, 46 (W1) :W537-W544
[2]   wzi Gene Sequencing, a Rapid Method for Determination of Capsular Type for Klebsiella Strains [J].
Brisse, Sylvain ;
Passet, Virginie ;
Haugaard, Anita Bjork ;
Babosan, Anamaria ;
Kassis-Chikhani, Najiby ;
Struve, Carsten ;
Decre, Dominique .
JOURNAL OF CLINICAL MICROBIOLOGY, 2013, 51 (12) :4073-4078
[3]   Genomic Diversity and Fitness of E. coli Strains Recovered from the Intestinal and Urinary Tracts of Women with Recurrent Urinary Tract Infection [J].
Chen, Swaine L. ;
Wu, Meng ;
Henderson, Jeffrey P. ;
Hooton, Thomas M. ;
Hibbing, Michael E. ;
Hultgren, Scott J. ;
Gordon, Jeffrey I. .
SCIENCE TRANSLATIONAL MEDICINE, 2013, 5 (184)
[4]  
Chin CS, 2016, NAT METHODS, V13, P1050, DOI [10.1038/nmeth.4035, 10.1038/NMETH.4035]
[5]  
Chin CS, 2013, NAT METHODS, V10, P563, DOI [10.1038/nmeth.2474, 10.1038/NMETH.2474]
[6]   Prospective Cohort Study of Microbial and Inflammatory Events Immediately Preceding Escherichia coli Recurrent Urinary Tract Infection in Women [J].
Czaja, C. A. ;
Stamm, W. E. ;
Stapleton, A. E. ;
Roberts, P. L. ;
Hawn, T. R. ;
Scholes, D. ;
Samadpour, M. ;
Hultgren, S. J. ;
Hooton, T. M. .
JOURNAL OF INFECTIOUS DISEASES, 2009, 200 (04) :528-536
[7]   Genome-scale rates of evolutionary change in bacteria [J].
Duchene, Sebastian ;
Holt, Kathryn E. ;
Weill, Francois-Xavier ;
Le Hello, Simon ;
Hawkey, Jane ;
Edwards, David J. ;
Fourment, Mathieu ;
Holmes, Edward C. .
MICROBIAL GENOMICS, 2016, 2 (11) :e000094
[8]   Urinary tract infections: epidemiology, mechanisms of infection and treatment options [J].
Flores-Mireles, Ana L. ;
Walker, Jennifer N. ;
Caparon, Michael ;
Hultgren, Scott J. .
NATURE REVIEWS MICROBIOLOGY, 2015, 13 (05) :269-284
[9]   Consed: a graphical editor for next-generation sequencing [J].
Gordon, David ;
Green, Phil .
BIOINFORMATICS, 2013, 29 (22) :2936-2937
[10]   Gastrointestinal Carriage Is a Major Reservoir of Klebsiella pneumoniae Infection in Intensive Care Patients [J].
Gorrie, Claire L. ;
Mirceta, Mirjana ;
Wick, Ryan R. ;
Edwards, David J. ;
Thomson, Nicholas R. ;
Strugnell, Richard A. ;
Pratt, Nigel F. ;
Garlick, Jill S. ;
Watson, Kerri M. ;
Pilcher, David V. ;
McGloughlin, Steve A. ;
Spelman, Denis W. ;
Jenney, Adam W. J. ;
Holt, Kathryn E. .
CLINICAL INFECTIOUS DISEASES, 2017, 65 (02) :208-215