<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Zhang Y</submitter><funding>Shanghai Municipal health commission</funding><funding>China Key Scientific Grant Program</funding><pagination>2994</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9106066</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>27(9)</volume><pubmed_abstract>The antibiotic resistance rates of &lt;i>Klebsiella pneumoniae&lt;/i> have been steadily increasing in recent years. Nevertheless, the metabolic features of the drug-resistant &lt;i>Klebsiella pneumoniae&lt;/i> and its associated benefits for bacterial pathogenicity are far from expounded. This study aims to unravel the unique physiological and metabolic properties specific to drug-resistant &lt;i>K. pneumoniae&lt;/i>. Using scanning electron microscopy (SEM), we observed a thicker extracellular mucus layer around a drug-resistant &lt;i>K. pneumonia&lt;/i> strain (Kp-R) than a drug-sensitive &lt;i>K. pneumonia&lt;/i> strain (Kp-S). Kp-R also produced more capsular polysaccharide (CPS) and biofilm, and appeared to have a significant competitive advantage when co-cultured with Kp-S. Moreover, Kp-R was easier to adhere to</pubmed_abstract><journal>Molecules (Basel, Switzerland)</journal><pubmed_title>Inosine and D-Mannose Secreted by Drug-Resistant &lt;i>Klebsiella pneumoniae&lt;/i> Affect Viability of Lung Epithelial Cells.</pubmed_title><pmcid>PMC9106066</pmcid><funding_grant_id>GWV-10.1-XK01, 201940300</funding_grant_id><funding_grant_id>No.2021YFC0122500</funding_grant_id><pubmed_authors>Shen J</pubmed_authors><pubmed_authors>Gu S</pubmed_authors><pubmed_authors>Guan W</pubmed_authors><pubmed_authors>Shu F</pubmed_authors><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhang Y</pubmed_authors><pubmed_authors>Xiao W</pubmed_authors><pubmed_authors>Xie L</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Wang J</pubmed_authors><pubmed_authors>Tang Y</pubmed_authors><pubmed_authors>Zhou Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Inosine and D-Mannose Secreted by Drug-Resistant &lt;i>Klebsiella pneumoniae&lt;/i> Affect Viability of Lung Epithelial Cells.</name><description>The antibiotic resistance rates of &lt;i>Klebsiella pneumoniae&lt;/i> have been steadily increasing in recent years. Nevertheless, the metabolic features of the drug-resistant &lt;i>Klebsiella pneumoniae&lt;/i> and its associated benefits for bacterial pathogenicity are far from expounded. This study aims to unravel the unique physiological and metabolic properties specific to drug-resistant &lt;i>K. pneumoniae&lt;/i>. Using scanning electron microscopy (SEM), we observed a thicker extracellular mucus layer around a drug-resistant &lt;i>K. pneumonia&lt;/i> strain (Kp-R) than a drug-sensitive &lt;i>K. pneumonia&lt;/i> strain (Kp-S). Kp-R also produced more capsular polysaccharide (CPS) and biofilm, and appeared to have a significant competitive advantage when co-cultured with Kp-S. Moreover, Kp-R was easier to adhere to</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 May</publication><modification>2025-04-22T11:53:36.319Z</modification><creation>2024-10-15T17:48:34.471Z</creation></dates><accession>S-EPMC9106066</accession><cross_references><pubmed>35566345</pubmed><doi>10.3390/molecules27092994</doi></cross_references></HashMap>