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Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains
Capsular polysaccharide (CPS) genes and pilus islands encode important virulence factors for group B Streptococcus (GBS) genomes. This study aims to detect phylogenetic inconsistency in CPS genes and pilus islands in GBSs and to explore its relationship with invasiveness. A total of 1016 GBS genomes...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567417/ https://www.ncbi.nlm.nih.gov/pubmed/33067737 http://dx.doi.org/10.1007/s10096-020-04067-4 |
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author | Lin, Enze Zou, Shengmei Wang, Yue Lee, Chien-Chung Chiu, Cheng-Hsun Feng, Ye |
author_facet | Lin, Enze Zou, Shengmei Wang, Yue Lee, Chien-Chung Chiu, Cheng-Hsun Feng, Ye |
author_sort | Lin, Enze |
collection | PubMed |
description | Capsular polysaccharide (CPS) genes and pilus islands encode important virulence factors for group B Streptococcus (GBS) genomes. This study aims to detect phylogenetic inconsistency in CPS genes and pilus islands in GBSs and to explore its relationship with invasiveness. A total of 1016 GBS genomes were downloaded from the NCBI public database. The multi-locus sequence typing (MLST) and Bayesian analysis of Population Structure (BAPS) analyses were both conducted for phylogeny construction. Serotyping and pilus typing were determined in silico using the genomic sequences. The CPS and pilus typing results were generally consistent with MLST and BAPS clustering. GBS isolates of serotype II and of the PI-1 + PI-2b and PI-2a types were more prone to phylogenetic inconsistency than the others. Isolates of serotype Ib and of PI-1 + PI-2a were more likely to appear as colonizing strains, whereas PI-2b was more likely to appear in invasive strains. For serotype V, phylogenetic inconsistency occurred more commonly in colonizing isolates, while for serotype III, the opposite occurred. The present study profiles for the first time the phylogenetic inconsistency of CPS genes and pilus islands in global GBS isolates, which is helpful for infection control and the development of new vaccines for the prevention of GBS occurrence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-020-04067-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-7567417 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-75674172020-10-19 Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains Lin, Enze Zou, Shengmei Wang, Yue Lee, Chien-Chung Chiu, Cheng-Hsun Feng, Ye Eur J Clin Microbiol Infect Dis Original Article Capsular polysaccharide (CPS) genes and pilus islands encode important virulence factors for group B Streptococcus (GBS) genomes. This study aims to detect phylogenetic inconsistency in CPS genes and pilus islands in GBSs and to explore its relationship with invasiveness. A total of 1016 GBS genomes were downloaded from the NCBI public database. The multi-locus sequence typing (MLST) and Bayesian analysis of Population Structure (BAPS) analyses were both conducted for phylogeny construction. Serotyping and pilus typing were determined in silico using the genomic sequences. The CPS and pilus typing results were generally consistent with MLST and BAPS clustering. GBS isolates of serotype II and of the PI-1 + PI-2b and PI-2a types were more prone to phylogenetic inconsistency than the others. Isolates of serotype Ib and of PI-1 + PI-2a were more likely to appear as colonizing strains, whereas PI-2b was more likely to appear in invasive strains. For serotype V, phylogenetic inconsistency occurred more commonly in colonizing isolates, while for serotype III, the opposite occurred. The present study profiles for the first time the phylogenetic inconsistency of CPS genes and pilus islands in global GBS isolates, which is helpful for infection control and the development of new vaccines for the prevention of GBS occurrence. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10096-020-04067-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2020-10-16 2021 /pmc/articles/PMC7567417/ /pubmed/33067737 http://dx.doi.org/10.1007/s10096-020-04067-4 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Lin, Enze Zou, Shengmei Wang, Yue Lee, Chien-Chung Chiu, Cheng-Hsun Feng, Ye Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title | Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title_full | Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title_fullStr | Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title_full_unstemmed | Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title_short | Phylogeny, recombination, and invasiveness of group B Streptococcus revealed by genomic comparisons of its global strains |
title_sort | phylogeny, recombination, and invasiveness of group b streptococcus revealed by genomic comparisons of its global strains |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7567417/ https://www.ncbi.nlm.nih.gov/pubmed/33067737 http://dx.doi.org/10.1007/s10096-020-04067-4 |
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