2020
DOI: 10.1016/j.ijantimicag.2020.105931
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Investigation of possible clonal transmission of carbapenemase-producing Klebsiella pneumoniae complex member isolates in Denmark using core genome MLST and National Patient Registry Data

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Cited by 8 publications
(3 citation statements)
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“…Overall, 35 studies (83.3%) restricted attempts to identify transmission routes to the same hospital unit during a defined period. 9,[11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][29][30][31][32][33][34][35][36][37][38][40][41][42][44][45][46][47] Only 7 studies (16.7%) examined other possible routes such as medical procedures or healthcare workers. [3][4][5]10,28,39,43 Several studies were notable for uncovering otherwise unidentified transmissions, which is the main goal of WGS surveillance.…”
Section: Resultsmentioning
confidence: 99%
“…Overall, 35 studies (83.3%) restricted attempts to identify transmission routes to the same hospital unit during a defined period. 9,[11][12][13][14][15][16][17][18][19][20][21][22][23][24][25][26][27][29][30][31][32][33][34][35][36][37][38][40][41][42][44][45][46][47] Only 7 studies (16.7%) examined other possible routes such as medical procedures or healthcare workers. [3][4][5]10,28,39,43 Several studies were notable for uncovering otherwise unidentified transmissions, which is the main goal of WGS surveillance.…”
Section: Resultsmentioning
confidence: 99%
“…Here, we aim to study the epidemiology and genomic characteristics of CRKP in Henan by making use of whole-genome sequencing (WGS), multilocus sequence typing (MLST), and core genome multilocus sequence typing (cgMLST) ( 10 , 11 ). With cgMLST, heterogeneous isolates of the same sequence type (ST) can be further classified, and linkage in clonal transmission can be inferred, as demonstrated previously ( 12 ). With whole-genome sequence data, it is also possible to identify and type outer membrane polysaccharide capsule antigen (K) and lipopolysaccharide (LPS; O) loci and thus predict clinically relevant antigen types ( 13 ).…”
Section: Introductionmentioning
confidence: 93%
“…In determining possible commonalities, patients may be assumed to have short duration (<90 days) of transmissibility with bacterial pathogens after the initial clinical infection. [1][2][3] However, some studies suggest that this assumption may not always hold true, potentially leading to the exclusion of patients as sources of transmission during outbreak investigations. [4][5][6][7] To accurately determine the length of infectiousness and transmission for bacterial pathogens, an ideal study would use serial whole genome sequencing (WGS) to identify genetically related isolates over a prospective period from individual patients.…”
Section: Introductionmentioning
confidence: 99%