<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Khan UB</submitter><funding>Rosetrees</funding><funding>Wellcome Trust</funding><pagination>544</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10044541</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(3)</volume><pubmed_abstract>&lt;i>Streptococcus agalactiae&lt;/i> or group B streptococcus (GBS) is a leading cause of neonatal sepsis and increasingly found as an invasive pathogen in older patient populations. Beta-lactam antibiotics remain the most effective therapeutic with resistance rarely reported, while the majority of GBS isolates carry the tetracycline resistance gene &lt;i>tet(M)&lt;/i> in fixed genomic positions amongst five predominant clonal clades. In the UK, GBS resistance to clindamycin and erythromycin has increased from 3% in 1991 to 11.9% (clindamycin) and 20.2% (erythromycin), as reported in this study. Here, a systematic investigation of antimicrobial resistance genomic content sought to fully characterise the associated mobile genetic elements within phenotypically resistant GBS isolates from 193 invasive </pubmed_abstract><journal>Antibiotics (Basel, Switzerland)</journal><pubmed_title>Genomic Analysis Reveals New Integrative Conjugal Elements and Transposons in GBS Conferring Antimicrobial Resistance.</pubmed_title><pmcid>PMC10044541</pmcid><funding_grant_id>M683</funding_grant_id><pubmed_authors>Spiller OB</pubmed_authors><pubmed_authors>Sands K</pubmed_authors><pubmed_authors>Lo S</pubmed_authors><pubmed_authors>Khan UB</pubmed_authors><pubmed_authors>Jauneikaite E</pubmed_authors><pubmed_authors>Portal EAR</pubmed_authors><pubmed_authors>Chalker VJ</pubmed_authors></additional><is_claimable>false</is_claimable><name>Genomic Analysis Reveals New Integrative Conjugal Elements and Transposons in GBS Conferring Antimicrobial Resistance.</name><description>&lt;i>Streptococcus agalactiae&lt;/i> or group B streptococcus (GBS) is a leading cause of neonatal sepsis and increasingly found as an invasive pathogen in older patient populations. Beta-lactam antibiotics remain the most effective therapeutic with resistance rarely reported, while the majority of GBS isolates carry the tetracycline resistance gene &lt;i>tet(M)&lt;/i> in fixed genomic positions amongst five predominant clonal clades. In the UK, GBS resistance to clindamycin and erythromycin has increased from 3% in 1991 to 11.9% (clindamycin) and 20.2% (erythromycin), as reported in this study. Here, a systematic investigation of antimicrobial resistance genomic content sought to fully characterise the associated mobile genetic elements within phenotypically resistant GBS isolates from 193 invasive </description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Mar</publication><modification>2026-04-08T14:17:27.706Z</modification><creation>2025-02-19T02:38:23.495Z</creation></dates><accession>S-EPMC10044541</accession><cross_references><pubmed>36978411</pubmed><doi>10.3390/antibiotics12030544</doi></cross_references></HashMap>