<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(5)</volume><submitter>Dogan O</submitter><pubmed_abstract>We proposed the hypothesis that high-risk clones of colistin-resistant K. pneumoniae (ColR-Kp) possesses a high number of virulence factors and has enhanced survival capacity against the neutrophil activity. We studied virulence genes of ColR-Kp isolates and neutrophil response in 142 patients with invasive ColR-Kp infections. The ST101 and ST395 ColR-Kp infections had higher 30-day mortality (58%, p = 0.005 and 75%, p = 0.003). The presence of yersiniabactin biosynthesis gene (ybtS) and ferric uptake operon associated gene (kfu) were significantly higher in ST101 (99%, p ≤ 0.001) and ST395 (94%, p &lt; 0.012). Being in ICU (OR: 7.9; CI: 1.43-55.98; p = 0.024), kfu (OR:27.0; CI: 5.67-179.65; p &lt; 0.001) and ST101 (OR: 17.2; CI: 2.45-350.40; p = 0.01) were found to be predictors of 30-day morta</pubmed_abstract><journal>Biology</journal><pagination>436</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8155863</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Virulence Determinants of Colistin-Resistant K. pneumoniae High-Risk Clones.</pubmed_title><pmcid>PMC8155863</pmcid><pubmed_authors>Dogan O</pubmed_authors><pubmed_authors>Demiray A</pubmed_authors><pubmed_authors>Sahin OE</pubmed_authors><pubmed_authors>Ergonul O</pubmed_authors><pubmed_authors>Atac N</pubmed_authors><pubmed_authors>Kilicoglu BK</pubmed_authors><pubmed_authors>Can F</pubmed_authors><pubmed_authors>Karahuseyinoglu S</pubmed_authors><pubmed_authors>Gonen M</pubmed_authors><pubmed_authors>Vatansever C</pubmed_authors><pubmed_authors>Albayrak O</pubmed_authors></additional><is_claimable>false</is_claimable><name>Virulence Determinants of Colistin-Resistant K. pneumoniae High-Risk Clones.</name><description>We proposed the hypothesis that high-risk clones of colistin-resistant K. pneumoniae (ColR-Kp) possesses a high number of virulence factors and has enhanced survival capacity against the neutrophil activity. We studied virulence genes of ColR-Kp isolates and neutrophil response in 142 patients with invasive ColR-Kp infections. The ST101 and ST395 ColR-Kp infections had higher 30-day mortality (58%, p = 0.005 and 75%, p = 0.003). The presence of yersiniabactin biosynthesis gene (ybtS) and ferric uptake operon associated gene (kfu) were significantly higher in ST101 (99%, p ≤ 0.001) and ST395 (94%, p &lt; 0.012). Being in ICU (OR: 7.9; CI: 1.43-55.98; p = 0.024), kfu (OR:27.0; CI: 5.67-179.65; p &lt; 0.001) and ST101 (OR: 17.2; CI: 2.45-350.40; p = 0.01) were found to be predictors of 30-day morta</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 May</publication><modification>2025-04-18T16:06:33.584Z</modification><creation>2022-02-10T14:47:38.337Z</creation></dates><accession>S-EPMC8155863</accession><cross_references><pubmed>34068937</pubmed><doi>10.3390/biology10050436</doi></cross_references></HashMap>