<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>230(1)</volume><submitter>Kalizang'oma A</submitter><pubmed_abstract>&lt;h4>Background&lt;/h4>Streptococcus pneumoniae serotype 3 remains a problem globally. Malawi introduced 13-valent pneumococcal conjugate vaccine (PCV13) in 2011, but there has been no direct protection against serotype 3 carriage. We explored whether vaccine escape by serotype 3 is due to clonal expansion of a lineage with a competitive advantage.&lt;h4>Methods&lt;/h4>The distribution of serotype 3 Global Pneumococcal Sequence Clusters (GPSCs) and sequence types (STs) globally was assessed using sequences from the Global Pneumococcal Sequencing Project. Whole-genome sequences of 135 serotype 3 carriage isolates from Blantyre, Malawi (2015-2019) were analyzed. Comparative analysis of the capsule locus, entire genomes, antimicrobial resistance, and phylogenetic reconstructions were undertaken. Opsonophagocytosis was evaluated using serum samples from vaccinated adults and children.&lt;h4>Results&lt;/h4>Serotype 3 GPSC10-ST700 isolates were most prominent in Malawi. Compared with the prototypical serotype 3 capsular polysaccharide locus sequence, 6 genes are absent, with retention of capsule polysaccharide biosynthesis. This lineage is characterized by increased antimicrobial resistance and lower susceptibility to opsonophagocytic killing.&lt;h4>Conclusions&lt;/h4>A serotype 3 variant in Malawi has genotypic and phenotypic characteristics that could enhance vaccine escape and clonal expansion after post-PCV13 introduction. Genomic surveillance among high-burden populations is essential to improve the effectiveness of next-generation pneumococcal vaccines.</pubmed_abstract><journal>The Journal of infectious diseases</journal><pagination>e189-e198</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11272040</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Clonal Expansion of a Streptococcus pneumoniae Serotype 3 Capsule Variant Sequence Type 700 With Enhanced Vaccine Escape Potential After 13-Valent Pneumococcal Conjugate Vaccine Introduction.</pubmed_title><pmcid>PMC11272040</pmcid><pubmed_authors>Lourenco J</pubmed_authors><pubmed_authors>Obolski U</pubmed_authors><pubmed_authors>French N</pubmed_authors><pubmed_authors>Mwalukomo TS</pubmed_authors><pubmed_authors>Roalfe L</pubmed_authors><pubmed_authors>Demetriou H</pubmed_authors><pubmed_authors>Brown C</pubmed_authors><pubmed_authors>Msefula J</pubmed_authors><pubmed_authors>Goldblatt D</pubmed_authors><pubmed_authors>Chan JM</pubmed_authors><pubmed_authors>Heyderman RS</pubmed_authors><pubmed_authors>Chaguza C</pubmed_authors><pubmed_authors>Kalizang'oma A</pubmed_authors><pubmed_authors>Kamng'ona A</pubmed_authors><pubmed_authors>Swarthout TD</pubmed_authors></additional><is_claimable>false</is_claimable><name>Clonal Expansion of a Streptococcus pneumoniae Serotype 3 Capsule Variant Sequence Type 700 With Enhanced Vaccine Escape Potential After 13-Valent Pneumococcal Conjugate Vaccine Introduction.</name><description>&lt;h4>Background&lt;/h4>Streptococcus pneumoniae serotype 3 remains a problem globally. Malawi introduced 13-valent pneumococcal conjugate vaccine (PCV13) in 2011, but there has been no direct protection against serotype 3 carriage. We explored whether vaccine escape by serotype 3 is due to clonal expansion of a lineage with a competitive advantage.&lt;h4>Methods&lt;/h4>The distribution of serotype 3 Global Pneumococcal Sequence Clusters (GPSCs) and sequence types (STs) globally was assessed using sequences from the Global Pneumococcal Sequencing Project. Whole-genome sequences of 135 serotype 3 carriage isolates from Blantyre, Malawi (2015-2019) were analyzed. Comparative analysis of the capsule locus, entire genomes, antimicrobial resistance, and phylogenetic reconstructions were undertaken. Opsonophagocytosis was evaluated using serum samples from vaccinated adults and children.&lt;h4>Results&lt;/h4>Serotype 3 GPSC10-ST700 isolates were most prominent in Malawi. Compared with the prototypical serotype 3 capsular polysaccharide locus sequence, 6 genes are absent, with retention of capsule polysaccharide biosynthesis. This lineage is characterized by increased antimicrobial resistance and lower susceptibility to opsonophagocytic killing.&lt;h4>Conclusions&lt;/h4>A serotype 3 variant in Malawi has genotypic and phenotypic characteristics that could enhance vaccine escape and clonal expansion after post-PCV13 introduction. Genomic surveillance among high-burden populations is essential to improve the effectiveness of next-generation pneumococcal vaccines.</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Jul</publication><modification>2026-04-21T03:25:40.81Z</modification><creation>2025-04-19T14:49:48.516Z</creation></dates><accession>S-EPMC11272040</accession><cross_references><pubmed>39052729</pubmed><doi>10.1093/infdis/jiae040</doi></cross_references></HashMap>