Highly Variable Streptococcus oralis Strains Are Common among Viridans Streptococci Isolated from Primates

  • Denapaite D
  • Rieger M
  • Köndgen S
  • et al.
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Abstract

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 . 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. 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 Streptococcus pneumoniae 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 Streptococcus mitis 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.

Figures

  • FIG 1 MLSA trees of strains from this study and reference strains. (A) A neighbor-joining tree was constructed using the concatenated sequences of the MLSA loci from 44 strains of this study combined with sequences of 427 strains from the study of Bishop et al. (8). In addition, MLSA genes were extracted from the genomes of S. tigurinus AZ_3a (GCF_000344275.1), S. dentisani 7747 (GCF_000382805.1), S. sinensis HKU4 (GCF_000767835.1), S. oligofermentans AS1.3089 (CP004409.1), and S. downei F0415 (GCA_000180055.1) (strains included in addition to those from the study by Bishop et al. [8] are shaded gray). Viridans group reference and type strains are framed. The Anginosus group of viridans streptococci is shaded gray and the Salivarius group orange. The color key for reference strains and isolates from primates is indicated on the right. Mdg, Madagascar. (B) Neighbor-joining tree of the Streptococcus sp. cluster of strains from Madagascar lemurs (blue circles in the square in panel A) magnified to show more clearly the clustering of the strains. Bootstrap values (percentages) are based on 1,000 replications. The bar refers to genetic divergence as calculated by the MEGA software.
  • FIG 2 Phylogenetic trees of S. oralis and S. mitis strains. (A) Tree generated by MLSA loci of S. oralis from this study and sequences of S. oralis strains, S. tigurinus AZ_3a, and S. dentisani 7747 from the MLSA tree shown in Fig. 1. Gray shading, cluster of isolates from rhesus monkeys; pink shading, lineages consisting of primate isolates only. One S. mitis strain from the study of Bishop et al. (8), VS58, was included for comparison. Red letters indicate the subgroup of IgA protease-negative S. oralis isolates specified in reference 8. Bootstrap values (percentages) are based on 1,000 replications. (B) Phylogenetic relationship of primate isolates, including 38 isolates from zoo animals determined by MLST (7) but excluding ddl, combined with sequences of 119 human isolates (S. oralis, S. mitis, and S. pneumoniae) from different geographic locations (10) (isolate numbers are preceded by Hu for Hungary, RSA for South Africa, S for Spain, HK for Hong Kong, and B for Germany). Lineages within the S. oralis cluster containing only isolates from primates are shaded in dark blue. Bootstrap values (percentages) are based on 500 replications. The bar refers to genetic divergence as calculated by the MEGA software.
  • FIG 3 Comparison of TetM-containing genetic elements in two genomes from rhesus monkeys with those of S. pneumoniae Spain 23F-1 (Sp 23F) and S. oralis Uo5 (So Uo5). Red, tetM; green, ermB; blue, homology to Enterococcus faecium plasmid pM7M2 genes. xis is the excisionase gene (black); the integrase is a pseudogene in S. pneumoniae (dashed arrow). Gray areas indicate BLASTn matches between sequences.
  • FIG 4 CRISPR-Cas gene clusters in streptococcal genomes. The five classes (designated 1 to 5) of CRISPR-Cas gene clusters identified in the genomes of this study are shown; representative genomes containing these clusters are indicated on the left. The annotation given by the RAST server (http://rast.nmpdr.org/) was used. Red, Cas1 genes; blue, Cas2 genes; S. sp, Streptococcus sp.
  • FIG 5 Comparison of PitB genes deduced from pilus clusters in streptococcal genomes. The phylogenetic tree was generated with MEGA6 using the Clustal alignment. PitB of S. pneumoniae SpTCH8431/19A and S. oralis ATCC 10557 represent the closest tBLASTn matches to PitB from S. oralis Uo5. The pilus cluster of S. oralis Uo5 is shown below. Red, pitB. The bar indicates changes per nucleotide position. pitA and pitB, pilus proteins; sipA, essential for pilin biosynthesis; srtG1 and srtG2, sortases. White genes mark conserved flanking genes outside the pilus cluster.
  • FIG 6 Distribution of PBP3 homologs in streptococcal genomes. A phylogenetic tree was constructed from deduced protein sequences from PBP3 D,D-carboxypeptidases using the MEGA6 software and muscle alignment. Proteins with at least one unusual active-site motif, indicating a nonfunctional PBP, are marked by asterisks, and partial sequences indicated by P bootstrap values (percentages) are based on 1,000 replications. The bar refers to genetic divergence as calculated by the MEGA software.
  • FIG 7 Mosaic PBPs in S. mitis and S. oralis. Mosaic gene structures were deduced by comparison to S. oralis ATCC 35037 PBP genes. Sequences that are highly similar to each other (<5% difference) are shown in the same color; sequences of different colors diverge from each other by at least 15%. Light gray, divergence from S. oralis ATCC 35037 of approximately 5%; dark gray, divergence by >15%; arrowheads, mutations within or close to active-site motifs which are shown on top; solid-line box, PBPs from free-living chimpanzees; dashed box, PBPs from human isolates with high-level penicillin resistance. The amino acid numbers are those of PBPs from sensitive S. pneumoniae strains.
  • FIG 8 Neuraminidases and a conserved -N-acetyl-hexosaminidase in S. pneumoniae, S. mitis, and S. oralis. The phylogenetic tree was generated with MEGA6 using the muscle alignment from the genomes used in this study and selected S. pneumoniae genomes. NanA, NanB, and NanC are indicated. p, partial sequences; BAH, putative -N-acetyl-hexosaminidase. Bootstrap values (percentages) are based on 1,000 replications. The bar refers to genetic divergence as calculated by the MEGA software.

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Denapaite, D., Rieger, M., Köndgen, S., Brückner, R., Ochigava, I., Kappeler, P., … Hakenbeck, R. (2016). Highly Variable Streptococcus oralis Strains Are Common among Viridans Streptococci Isolated from Primates. MSphere, 1(2). https://doi.org/10.1128/msphere.00041-15

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