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Yersiniabactin, Colibactin and Wider Resistome Contribute to Enhanced Virulence and Persistence of KPC-2-Producing Klebsiella pneumoniae CG258 in South America

https://doi.org/10.1101/435750
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Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/nmi2.40openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.diagmicrobio.2012.04.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.diagmicrobio.2015.03.012openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.gene.2004.05.008openalex-snapshot
Sequencing and analysis of the large virulence plasmid pLVPK of Klebsiella pneumoniae CG43
inferredcites →https://doi.org/10.1016/j.jgar.2013.06.001openalex-snapshot
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Characterisation of the first KPC-2-producing Klebsiella pneumoniae ST340 from Peru
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inferredcites →https://doi.org/10.1098/rstb.2014.0083openalex-snapshot
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inferredcites →https://doi.org/10.1099/jmm.0.000711openalex-snapshot
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Phenotypic and genotypic ınvestigation of virulence factors in Klebsiella pneumoniae strains ısolated from ventilator-associated pneumonia (VAP) cases
inferred← citeshttps://doi.org/10.1101/2019.12.20.884395openalex-snapshot
Applying Nanopore sequencing to a One-Health scenario for colistin resistance transmission among pigs, cows and the farmer
inferred← citeshttps://doi.org/10.11606/t.9.2019.tde-26082019-103040openalex-snapshot
Comparative analysis of >i /i< belonging to the endemic high-risk clonal group CG258
inferred← citeshttps://doi.org/10.17605/osf.io/2f8w7openalex-snapshot
Preprint - Applying Nanopore sequencing to a One-Health scenario for colistin resistance transmission among pigs, cows and the farmer
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