<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Fang Q</submitter><funding>National Natural Science Foundation of China</funding><pagination>e0008022</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9044933</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>7(2)</volume><pubmed_abstract>We isolated and characterized a novel phage from hospital sewage, P13, able to lyse ST11 K47 carbapenem-resistant Klebsiella pneumoniae (CRKP), a major CRKP lineage. P13 formed a large lytic plaque (3.0 to 6.0 mm in diameter) in double-layer LB agar after overnight coculture with its host bacterial strain. A translucent halo formed when the culture was prolonged to 48 h. P13 showed a narrow host range only lysing ST11 K47 CRKP with a burst size of around 167 PFU/cell and exhibited broad pH and thermal stability. Genome sequencing showed that P13 contains no virulence, lysogenic or antimicrobial resistance genes, making this lytic phage a potential agent for phage therapy. Transmission electron microscopy showed that P13 exhibited typical morphology of the family &lt;i>Podoviridae&lt;/i> with an </pubmed_abstract><journal>mSphere</journal><pubmed_title>Lytic Phages against ST11 K47 Carbapenem-Resistant Klebsiella pneumoniae and the Corresponding Phage Resistance Mechanisms.</pubmed_title><pmcid>PMC9044933</pmcid><funding_grant_id>81861138055</funding_grant_id><pubmed_authors>Fang Q</pubmed_authors><pubmed_authors>Zong Z</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lytic Phages against ST11 K47 Carbapenem-Resistant Klebsiella pneumoniae and the Corresponding Phage Resistance Mechanisms.</name><description>We isolated and characterized a novel phage from hospital sewage, P13, able to lyse ST11 K47 carbapenem-resistant Klebsiella pneumoniae (CRKP), a major CRKP lineage. P13 formed a large lytic plaque (3.0 to 6.0 mm in diameter) in double-layer LB agar after overnight coculture with its host bacterial strain. A translucent halo formed when the culture was prolonged to 48 h. P13 showed a narrow host range only lysing ST11 K47 CRKP with a burst size of around 167 PFU/cell and exhibited broad pH and thermal stability. Genome sequencing showed that P13 contains no virulence, lysogenic or antimicrobial resistance genes, making this lytic phage a potential agent for phage therapy. Transmission electron microscopy showed that P13 exhibited typical morphology of the family &lt;i>Podoviridae&lt;/i> with an </description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Apr</publication><modification>2026-06-07T07:32:22.025Z</modification><creation>2025-04-04T21:00:26.074Z</creation></dates><accession>S-EPMC9044933</accession><cross_references><pubmed>35255715</pubmed><doi>10.1128/msphere.00080-22</doi></cross_references></HashMap>