Abstract

Viridans streptococci were obtained from primates (great apes, rhesus monkeys, and ring-tailed lemurs) held in captivity, as well as from free-living animals (chimpanzees and lemurs) for whom contact with humans is highly restricted. Isolates represented a variety of viridans streptococci, including unknown species. Streptococcus oralis was frequently isolated from samples from great apes. Genotypic methods revealed that most of the strains clustered on separate lineages outside the main cluster of human S.oralis strains. This suggests that S.oralis is part of the commensal flora in higher primates and evolved prior to humans. Many genes described as virulence factors in Streptococcuspneumoniae were present also in other viridans streptococcal genomes. Unlike in S.pneumoniae, clustered regularly interspaced short palindromic repeat (CRISPR)-CRISPR-associated protein (Cas) gene clusters were common among viridans streptococci, and many S.oralis strains were type PI-2 (pilus islet 2) variants. S.oralis displayed a remarkable diversity of genes involved in the biosynthesis of peptidoglycan (penicillin-binding proteins and MurMN) and choline-containing teichoic acid. The small noncoding cia-dependent small RNAs (csRNAs) controlled by the response regulator CiaR might contribute to the genomic diversity, since we observed novel genomic islands between duplicated csRNAs, variably present in some isolates. All S.oralis genomes contained a β-N-acetyl-hexosaminidase gene absent in S.pneumoniae, which in contrast frequently harbors the neuraminidases NanB/C, which are absent in S.oralis. The identification of S.oralis-specific genes will help us to understand their adaptation to diverse habitats. IMPORTANCE Streptococcus pneumoniae is a rare example of a human-pathogenic bacterium among viridans streptococci, which consist of commensal symbionts, such as the close relatives Streptococcusmitis and S.oralis. We have shown that S.oralis can frequently be isolated from primates and a variety of other viridans streptococci as well. Genes and genomic islands which are known pneumococcal virulence factors are present in S.oralis and S.mitis, documenting the widespread occurrence of these compounds, which encode surface and secreted proteins. The frequent occurrence of CRISP-Cas gene clusters and a surprising variation of a set of small noncoding RNAs are factors to be considered in future research to further our understanding of mechanisms involved in the genomic diversity driven by horizontal gene transfer among viridans streptococci.

Highlights

  • Viridans streptococci were obtained from primates held in captivity, as well as from free-living animals for whom contact with humans is highly restricted

  • All isolates from primates were initially characterized for their morphologies, antibiotic susceptibilities, 16S rRNAs, and in some cases SDS-PAGE protein patterns of cell lysates and penicillin binding protein (PBP) profiles

  • If a group of isolates obtained from one animal showed properties identical to those listed above, only one isolate was subjected to further analysis by Multilocus sequence typing (MLST)

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Summary

Introduction

Viridans streptococci were obtained from primates (great apes, rhesus monkeys, and ring-tailed lemurs) held in captivity, as well as from free-living animals (chimpanzees and lemurs) for whom contact with humans is highly restricted. Many genes described as virulence factors in Streptococcus pneumoniae were present in other viridans streptococcal genomes. IMPORTANCE Streptococcus pneumoniae is a rare example of a human-pathogenic bacterium among viridans streptococci, which consist of commensal symbionts, such as the close relatives Streptococcus mitis and S. oralis. The frequent occurrence of CRISP-Cas gene clusters and a surprising variation of a set of small noncoding RNAs are factors to be considered in future research to further our understanding of mechanisms involved in the genomic diversity driven by horizontal gene transfer among viridans streptococci. Diversification within the S. pneumoniae lineage has probably occurred during growth of the human population, its primary host [5] This suggests that the diversification of S. mitis and S. oralis took place earlier and that great apes might still harbor S. mitis and S. oralis as part of their commensal flora

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