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Genomic analysis reveals the molecular basis for capsule loss in the group B Streptococcus population.

TitleGenomic analysis reveals the molecular basis for capsule loss in the group B Streptococcus population.
Publication TypeJournal Article
Year of Publication2015
AuthorsRosini, R, Campisi, E, De Chiara, M, Tettelin, H, Rinaudo, D, Toniolo, C, Metruccio, M, Guidotti, S, Sørensen, UBSkov, Kilian, M, Ramirez, M, Janulczyk, R, Donati, C, Grandi, G, Margarit, I
Corporate AuthorsDEVANI Consortium
JournalPLoS One
Volume10
Issue5
Paginatione0125985
Date Published2015
ISSN1932-6203
KeywordsAnimals, Bacterial Capsules, Bacterial Proteins, Base Sequence, Cattle, DNA, Bacterial, Female, Humans, Mastitis, Bovine, Multilocus Sequence Typing, Polymorphism, Single Nucleotide, Sequence Alignment, Sequence Analysis, DNA, Streptococcal Infections, Streptococcus agalactiae
Abstract

The human and bovine bacterial pathogen Streptococcus agalactiae (Group B Streptococcus, GBS) expresses a thick polysaccharide capsule that constitutes a major virulence factor and vaccine target. GBS can be classified into ten distinct serotypes differing in the chemical composition of their capsular polysaccharide. However, non-typeable strains that do not react with anti-capsular sera are frequently isolated from colonized and infected humans and cattle. To gain a comprehensive insight into the molecular basis for the loss of capsule expression in GBS, a collection of well-characterized non-typeable strains was investigated by genome sequencing. Genome based phylogenetic analysis extended to a wide population of sequenced strains confirmed the recently observed high clonality among GBS lineages mainly containing human strains, and revealed a much higher degree of diversity in the bovine population. Remarkably, non-typeable strains were equally distributed in all lineages. A number of distinct mutations in the cps operon were identified that were apparently responsible for inactivation of capsule synthesis. The most frequent genetic alterations were point mutations leading to stop codons in the cps genes, and the main target was found to be cpsE encoding the portal glycosyl transferase of capsule biosynthesis. Complementation of strains carrying missense mutations in cpsE with a wild-type gene restored capsule expression allowing the identification of amino acid residues essential for enzyme activity.

DOI10.1371/journal.pone.0125985
Alternate JournalPLoS One
PubMed ID25946017
PubMed Central IDPMC4422693