<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Leitner DR</submitter><funding>NIAID NIH HHS</funding><funding>Life Sciences Research Foundation (LSRF)</funding><funding>Howard Hughes Medical Institute (HHMI)</funding><funding>HHS | NIH | National Institute of Allergy and Infectious Diseases (NIAID)</funding><pagination>e0343324</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11796348</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>Bacteria have evolved diverse strategies to ensure survival under nutrient-limited conditions, where rapid energy generation is not achievable. Here, we performed a transposon insertion site sequencing loss-of-function screen to identify &lt;i>Vibrio cholerae&lt;/i> genes that promote pathogen fitness in stationary phase. We discovered that the &lt;u>m&lt;/u>aintenance of &lt;u>l&lt;/u>ipid &lt;u>a&lt;/u>symmetry (Mla) pathway, which is crucial for transferring phospholipids from the outer to the inner membrane, is critical for stationary phase fitness. Competition experiments with barcoded and fluorophore labeled wild-type (WT) and &lt;i>mlaE&lt;/i> mutant &lt;i>V. cholerae&lt;/i> revealed that the Mla pathway promotes re-expansion from 48 h stationary phase cultures. The mutant defect in transitioning out of stationary pha</pubmed_abstract><journal>mBio</journal><pubmed_title>The Mla pathway promotes &amp;lt;i&amp;gt;Vibrio cholerae&amp;lt;/i&amp;gt; re-expansion from stationary phase.</pubmed_title><pmcid>PMC11796348</pmcid><funding_grant_id>R37 AI042347</funding_grant_id><funding_grant_id>AI-042347</funding_grant_id><funding_grant_id>R01 AI042347</funding_grant_id><funding_grant_id>Zingl-2024HHMI</funding_grant_id><pubmed_authors>Waldor MK</pubmed_authors><pubmed_authors>Leitner DR</pubmed_authors><pubmed_authors>Zingl FG</pubmed_authors><pubmed_authors>Zhang H</pubmed_authors><pubmed_authors>Morano AA</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Mla pathway promotes &amp;lt;i&amp;gt;Vibrio cholerae&amp;lt;/i&amp;gt; re-expansion from stationary phase.</name><description>Bacteria have evolved diverse strategies to ensure survival under nutrient-limited conditions, where rapid energy generation is not achievable. Here, we performed a transposon insertion site sequencing loss-of-function screen to identify &lt;i>Vibrio cholerae&lt;/i> genes that promote pathogen fitness in stationary phase. We discovered that the &lt;u>m&lt;/u>aintenance of &lt;u>l&lt;/u>ipid &lt;u>a&lt;/u>symmetry (Mla) pathway, which is crucial for transferring phospholipids from the outer to the inner membrane, is critical for stationary phase fitness. Competition experiments with barcoded and fluorophore labeled wild-type (WT) and &lt;i>mlaE&lt;/i> mutant &lt;i>V. cholerae&lt;/i> revealed that the Mla pathway promotes re-expansion from 48 h stationary phase cultures. The mutant defect in transitioning out of stationary pha</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-04T02:10:04.072Z</modification><creation>2025-04-04T02:10:04.072Z</creation></dates><accession>S-EPMC11796348</accession><cross_references><pubmed>39714184</pubmed><doi>10.1128/mbio.03433-24</doi></cross_references></HashMap>