<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Minhas V</submitter><funding>Swiss National Science Foundation</funding><funding>European Research Council</funding><funding>Deutsche Forschungsgemeinschaft</funding><funding>Helmut Horten Stiftung</funding><pagination>e3001990</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9910801</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>21(1)</volume><pubmed_abstract>Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called "fratricins" such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a choline-binding protein (CBP) that binds to phosphorylcholine residues found on wall and lipoteichoic acids (WTA and LTA) that together with PGN are major constituents of the pneumococcal cell wall. Competent pneumococci are protected against fratricide by producing the immunity protein ComM. How competence and fratricide contribute to virulence is unknown. Here, using a genome-wide CRISPRi-seq screen, we show that genes involved in teichoic acid (TA) biosynthesis are essential during competence</pubmed_abstract><journal>PLoS biology</journal><pubmed_title>Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence.</pubmed_title><pmcid>PMC9910801</pmcid><funding_grant_id>771534-PneumoCaTChER</funding_grant_id><funding_grant_id>HA 3125/5-2</funding_grant_id><funding_grant_id>198903</funding_grant_id><funding_grant_id>GI 979/1-2</funding_grant_id><funding_grant_id>771534</funding_grant_id><funding_grant_id>310030_200792,310030_192517, 40AR40_185533, 51NF40_180541</funding_grant_id><funding_grant_id>PP00P3_198903</funding_grant_id><pubmed_authors>Costa C</pubmed_authors><pubmed_authors>Havarstein LS</pubmed_authors><pubmed_authors>Synefiaridou D</pubmed_authors><pubmed_authors>Baldry M</pubmed_authors><pubmed_authors>Straume D</pubmed_authors><pubmed_authors>Sirard JC</pubmed_authors><pubmed_authors>Gisch N</pubmed_authors><pubmed_authors>Liu X</pubmed_authors><pubmed_authors>Domenech A</pubmed_authors><pubmed_authors>Perez C</pubmed_authors><pubmed_authors>Cebrero G</pubmed_authors><pubmed_authors>Veening JW</pubmed_authors><pubmed_authors>Brendel M</pubmed_authors><pubmed_authors>Minhas V</pubmed_authors><pubmed_authors>Hammerschmidt S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Competence remodels the pneumococcal cell wall exposing key surface virulence factors that mediate increased host adherence.</name><description>Competence development in the human pathogen Streptococcus pneumoniae controls several features such as genetic transformation, biofilm formation, and virulence. Competent bacteria produce so-called "fratricins" such as CbpD that kill noncompetent siblings by cleaving peptidoglycan (PGN). CbpD is a choline-binding protein (CBP) that binds to phosphorylcholine residues found on wall and lipoteichoic acids (WTA and LTA) that together with PGN are major constituents of the pneumococcal cell wall. Competent pneumococci are protected against fratricide by producing the immunity protein ComM. How competence and fratricide contribute to virulence is unknown. Here, using a genome-wide CRISPRi-seq screen, we show that genes involved in teichoic acid (TA) biosynthesis are essential during competence</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Jan</publication><modification>2025-05-18T11:38:49.588Z</modification><creation>2025-04-06T18:40:29.183Z</creation></dates><accession>S-EPMC9910801</accession><cross_references><pubmed>36716340</pubmed><doi>10.1371/journal.pbio.3001990</doi></cross_references></HashMap>