4.6 Article

Transcriptomic Responses to Coaggregation between Streptococcus gordonii and Streptococcus oralis

期刊

出版社

AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.01558-21

关键词

bioinformatics; coaggregation; oral streptococci; Streptococcus gordonii; Streptococcus oralis; transcriptome; biofilms

资金

  1. Ministry of Higher Education and Scientific Research (Iraq)
  2. EPSRC [EP/J004111/2, EP/N031962/1]
  3. NSFC International Young Scientists Fund [31750110452]
  4. WenzhouKean University [5000105]
  5. EPSRC [EP/N031962/1, EP/J004111/2] Funding Source: UKRI

向作者/读者索取更多资源

Cell-cell adhesion among oral bacteria, particularly Streptococcus gordonii and Streptococcus oralis, plays a crucial role in the development of polymicrobial communities like dental plaque. Gene regulation in response to coaggregation differs between S. gordonii and S. oralis, with specific genes involved in amino acid biosynthesis and transporters being upregulated. These distinct responses to coaggregation highlight the importance of understanding interspecies interactions in biofilm development and dental health maintenance.
Cell-cell adhesion between oral bacteria plays a key role in the development of polymicrobial communities such as dental plaque. Oral streptococci such as Streptococcus gordonii and Streptococcus oralis are important early colonizers of dental plaque and bind to a wide range of different oral microorganisms, forming multi-species clumps or coaggregates. S. gordonii actively responds to coaggregation by regulating gene expression. To further understand these responses, we assessed gene regulation in S. gordonii and S. oralis following coaggregation in 25% human saliva. Coaggregates were formed by mixing, and after 30 min, RNA was extracted for dual transcriptome sequencing (RNA-Seq) analysis. In S. oralis, 18 genes (6 upregulated and 12 downregulated) were regulated by coaggregation. Significantly downregulated genes encoded functions such as amino acid and antibiotic biosynthesis, ribosome, and central carbon metabolism. In total, 28 genes were differentially regulated in Streptococcus gordonii (25 upregulated and 3 downregulated). Many genes associated with transporters and a two-component (NisK/SpaK) regulatory system were upregulated following coaggregation. Our comparative analyses of S. gordonii-S. oralis with different previously published S. gordonii pairings (S. gordonii-Fusobacterium nucleatum and S. gordonii-Veillonella parvula) suggest that the gene regulation is specific to each pairing, and responses do not appear to be conserved. This ability to distinguish between neighboring bacteria may be important for S. gordonii to adapt appropriately during the development of complex biofilms such as dental plaque. IMPORTANCE Dental plaque is responsible for two of the most prevalent diseases in humans, dental caries and periodontitis. Controlling the formation of dental plaque and preventing the transition from oral health to disease requires a detailed understanding of microbial colonization and biofilm development. Streptococci are among the most common colonizers of dental plaque. This study identifies key genes that are regulated when oral streptococci bind to one another, as they do in the early stages of dental plaque formation. We show that specific genes are regulated in two different oral streptococci following the formation of mixed-species aggregates. The specific responses of S. gordonii to coaggregation with S. oralis are different from those to coaggregation with other oral bacteria. Targeting the key genes that are upregulated during interspecies interactions may be a powerful approach to control the development of biofilm and maintain oral health.

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