Cited by 17Oral microbiology and periodontitis researchNeutrophil, Myeloperoxidase and Oxidative MechanismsBacterial biofilms and quorum sensing

Effect of salivary agglutination on oral streptococcal clearance by human polymorphonuclear neutrophil granulocytes

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Itzek, A., Chen, Z., Merritt, J., Kreth, J.·2017·Molecular Oral Microbiology

Abstract

Summary: Salivary agglutination is an important host defense mechanism to aggregate oral commensal bacteria as well as invading pathogens. Saliva flow and subsequent swallowing more easily clear aggregated bacteria compared with single cells. Phagocytic clearance of bacteria through polymorphonuclear neutrophil granulocytes also seems to increase to a certain extent with the size of bacterial aggregates. To determine a connection between salivary agglutination and the host innate immune response by phagocytosis, an in vitro agglutination assay was developed reproducing the average size of salivary bacterial aggregates. Using the oral commensal Streptococcus gordonii as a model organism, the effect of salivary agglutination on phagocytic clearance through polymorphonuclear neutrophil granulocytes was investigated. Here we describe how salivary aggregates of S. gordonii are readily cleared through phagocytosis, whereas single bacterial cells showed a significant delay in being phagocytosed and killed. Furthermore, before phagocytosis the polymorphonuclear neutrophil granulocytes were able to induce a specific de‐aggregation, which was dependent on serine protease activity. The data presented suggest that salivary agglutination of bacterial cells leads to an ideal size for recognition by polymorphonuclear neutrophil granulocytes. As a first line of defense, these phagocytic cells are able to recognize the aggregates and de‐aggregate them via serine proteases to a more manageable size for efficient phagocytosis and subsequent killing in the phagolysosome. This observed mechanism not only prevents the rapid spreading of oral bacterial cells while entering the bloodstream but would also avoid degranulation of involved polymorphonuclear neutrophil granulocytes, so preventing collateral damage to nearby tissue.

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  • Coaggregation of oral pathogens by postbiotic lactobacilli

    Golletz, P., Jensen, S. D., Collignon, M., Hall, C., Khamas, A. B., Møllebjerg, A., Schlafer, S., Meyer, R. L., & Tykwinska, K. (2025) · Journal of oral microbiology · doi:10.1080/20002297.2025.2508483 · Cited by 10 · see citing works

    “For example, studies in the oral cavity have shown that large coaggregates are removed more easily than smaller aggregates or planktonic cells [7], and saliva components can cause aggregation in the form of saliva-mediated agglutination [6].”

Authors
Itzek, A., Chen, Z., Merritt, J., & Kreth, J.
Affiliations
  • University of Oklahoma Health Sciences Center (US)
  • Oregon Health & Science University (US)
Corresponding author
Kreth, J.
Venue
Molecular Oral Microbiology
Publisher
Wiley
Published
2016-07-10
Volume
32
Issue
3
Pages
197-210
ISSN
  • 2041-1006 (ISSN-L)
  • 2041-1014
OpenAlex
W2403271685
Cited by
17
References
55
Citations by year
2026: 1 · 2025: 2 · 2024: 2 · 2023: 5 · 2022: 2 · 2020: 3 · 2019: 1 · 2018: 1
FWCI
0.99
Type
journal article
Language
en
Open access
Locations
  • Molecular Oral Microbiology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
Funders
National Institutes of Health (DE021726, DE018893, DE022083)
Topics
  • Health Sciences › Dentistry › Periodontics › Oral microbiology and periodontitis research
  • Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Bacterial biofilms and quorum sensing
Keywords
Streptococcus gordonii, phagocytosis, bacterial aggregates, serine protease, innate immune defense, oral commensal bacteria, neutrophil degranulation
MeSH terms
Agglutination, Humans, Immunity, Innate, Mouth, Neutrophils, Phagocytosis, Saliva, Streptococcus gordonii, Serine Proteases

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