<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Hilty M</submitter><funding>Swiss National Science Foundation</funding><funding>NIAID NIH HHS</funding><funding>Wellcome Trust</funding><pagination>3281-94</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC4986459</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(12)</volume><pubmed_abstract>The surrounding capsule of Streptococcus pneumoniae has been identified as a major virulence factor and is targeted by pneumococcal conjugate vaccines (PCV). However, nonencapsulated S. pneumoniae (non-Ec-Sp) have also been isolated globally, mainly in carriage studies. It is unknown if non-Ec-Sp evolve sporadically, if they have high antibiotic nonsusceptiblity rates and a unique, specific gene content. Here, whole-genome sequencing of 131 non-Ec-Sp isolates sourced from 17 different locations around the world was performed. Results revealed a deep-branching classic lineage that is distinct from multiple sporadic lineages. The sporadic lineages clustered with a previously sequenced, global collection of encapsulated S. pneumoniae (Ec-Sp) isolates while the classic lineage is comprised mainly of the frequently identified multilocus sequences types (STs) ST344 (n = 39) and ST448 (n = 40). All ST344 and nine ST448 isolates had high nonsusceptiblity rates to β-lactams and other antimicrobials. Analysis of the accessory genome reveals that the classic non-Ec-Sp contained an increased number of mobile elements, than Ec-Sp and sporadic non-Ec-Sp. Performing adherence assays to human epithelial cells for selected classic and sporadic non-Ec-Sp revealed that the presence of a integrative conjugative element (ICE) results in increased adherence to human epithelial cells (P = 0.005). In contrast, sporadic non-Ec-Sp lacking the ICE had greater growth in vitro possibly resulting in improved fitness. In conclusion, non-Ec-Sp isolates from the classic lineage have evolved separately. They have spread globally, are well adapted to nasopharyngeal carriage and are able to coexist with Ec-Sp. Due to continued use of PCV, non-Ec-Sp may become more prevalent.</pubmed_abstract><journal>Genome biology and evolution</journal><pubmed_title>Global phylogenomic analysis of nonencapsulated Streptococcus pneumoniae reveals a deep-branching classic lineage that is distinct from multiple sporadic lineages.</pubmed_title><pmcid>PMC4986459</pmcid><funding_grant_id>R01 AI106786</funding_grant_id><funding_grant_id>133157</funding_grant_id><funding_grant_id>098051</funding_grant_id><funding_grant_id>083735</funding_grant_id><funding_grant_id>083735/Z/07</funding_grant_id><funding_grant_id>R01 AI106786-01</funding_grant_id><pubmed_authors>Dupasquier M</pubmed_authors><pubmed_authors>de Lencastre H</pubmed_authors><pubmed_authors>Smith-Vaughan H</pubmed_authors><pubmed_authors>Hilty M</pubmed_authors><pubmed_authors>Hanage WP</pubmed_authors><pubmed_authors>Engel H</pubmed_authors><pubmed_authors>Hermans P</pubmed_authors><pubmed_authors>McGee L</pubmed_authors><pubmed_authors>Turner P</pubmed_authors><pubmed_authors>Chewapreecha C</pubmed_authors><pubmed_authors>Endimiani A</pubmed_authors><pubmed_authors>Bruggmann R</pubmed_authors><pubmed_authors>Muhlemann K</pubmed_authors><pubmed_authors>Sa-Leao R</pubmed_authors><pubmed_authors>Parkhill J</pubmed_authors><pubmed_authors>Pluschke G</pubmed_authors><pubmed_authors>Weber J</pubmed_authors><pubmed_authors>Kuffer M</pubmed_authors><pubmed_authors>Campbell S</pubmed_authors><pubmed_authors>Salter SJ</pubmed_authors><pubmed_authors>Low DE</pubmed_authors><pubmed_authors>Eser OK</pubmed_authors><pubmed_authors>Bentley SD</pubmed_authors><pubmed_authors>Diggle M</pubmed_authors><pubmed_authors>Sadowy E</pubmed_authors><pubmed_authors>Wuthrich D</pubmed_authors><pubmed_authors>Hathaway LJ</pubmed_authors><pubmed_authors>Beaudoing E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Global phylogenomic analysis of nonencapsulated Streptococcus pneumoniae reveals a deep-branching classic lineage that is distinct from multiple sporadic lineages.</name><description>The surrounding capsule of Streptococcus pneumoniae has been identified as a major virulence factor and is targeted by pneumococcal conjugate vaccines (PCV). However, nonencapsulated S. pneumoniae (non-Ec-Sp) have also been isolated globally, mainly in carriage studies. It is unknown if non-Ec-Sp evolve sporadically, if they have high antibiotic nonsusceptiblity rates and a unique, specific gene content. Here, whole-genome sequencing of 131 non-Ec-Sp isolates sourced from 17 different locations around the world was performed. Results revealed a deep-branching classic lineage that is distinct from multiple sporadic lineages. The sporadic lineages clustered with a previously sequenced, global collection of encapsulated S. pneumoniae (Ec-Sp) isolates while the classic lineage is comprised mainly of the frequently identified multilocus sequences types (STs) ST344 (n = 39) and ST448 (n = 40). All ST344 and nine ST448 isolates had high nonsusceptiblity rates to β-lactams and other antimicrobials. Analysis of the accessory genome reveals that the classic non-Ec-Sp contained an increased number of mobile elements, than Ec-Sp and sporadic non-Ec-Sp. Performing adherence assays to human epithelial cells for selected classic and sporadic non-Ec-Sp revealed that the presence of a integrative conjugative element (ICE) results in increased adherence to human epithelial cells (P = 0.005). In contrast, sporadic non-Ec-Sp lacking the ICE had greater growth in vitro possibly resulting in improved fitness. In conclusion, non-Ec-Sp isolates from the classic lineage have evolved separately. They have spread globally, are well adapted to nasopharyngeal carriage and are able to coexist with Ec-Sp. Due to continued use of PCV, non-Ec-Sp may become more prevalent.</description><dates><release>2014-01-01T00:00:00Z</release><publication>2014 Dec</publication><modification>2026-05-04T14:50:54.595Z</modification><creation>2019-03-27T02:20:44Z</creation></dates><accession>S-EPMC4986459</accession><cross_references><pubmed>25480686</pubmed><doi>10.1093/gbe/evu263</doi></cross_references></HashMap>