2020
DOI: 10.1016/j.meegid.2020.104265
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The evolutionary puzzle of Escherichia coli ST131

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Cited by 77 publications
(80 citation statements)
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References 108 publications
(144 reference statements)
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“…The incidence rates and prevalence of ST131 increased over the time period, mostly caused by an influx of subclades C2 with bla CTX-M-15 and C1-M27 with bla CTX-M-27 . Such results reinforce the possible role of CTX-M enzymes in the evolutionary success of ST131 (10). The presence of bla CTX-M-14 among C1-nonM27 isolates did not provide a beneficial advantage to this subclade.…”
Section: Discussionsupporting
confidence: 65%
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“…The incidence rates and prevalence of ST131 increased over the time period, mostly caused by an influx of subclades C2 with bla CTX-M-15 and C1-M27 with bla CTX-M-27 . Such results reinforce the possible role of CTX-M enzymes in the evolutionary success of ST131 (10). The presence of bla CTX-M-14 among C1-nonM27 isolates did not provide a beneficial advantage to this subclade.…”
Section: Discussionsupporting
confidence: 65%
“…The abrupt global expansion of ST131 during the 2000s is unrivaled among human bacteria and is a real-world model for the evolution of antimicrobial-resistant high-risk clones (10). This study describes the clinical features, incidence rates, genomic characteristics, and changes in population structure of ST131 clades causing bloodstream infections in a large centralized region of Canada over an 11-year period (2006-2016).…”
Section: Discussionmentioning
confidence: 99%
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“…Among the five ST131 E. coli isolates, four were genetically close (Figure 1). However, these isolates did not share the same resistome indicating that ST131 is widely distributed independent of the ESBL content as previously observed (Pitout and Finn, 2020). Moreover, the two closest ST131 (S65 and S17-2) possessing the bla CTX−M−27 ESBL gene were recovered one-year apart indicating the persistence or continuing contamination by this clone.…”
Section: Clonal Relationshipmentioning
confidence: 55%
“…The group of aminopenicillins and inhibitor-protected penicillins cannot be used for empirical therapy of UT infections, with the exception of certain cases (for example, the proven gram-positive nature of the disease), due to the high resistance of E. coli throughout the world (on the territory of the Russian Federation it is more than 20%). In addition, the use of these drugs increases the risk of developing microbiological collateral damage (Gupta et al 2011;Grabe et al 2015;Sidorenko et al 2016;Zaycev et al 2019;Bonkat et al 2019;Pitout and Finn 2020).…”
Section: Resultsmentioning
confidence: 99%