Periodontal Pathogens' strategies disarm neutrophils to promote dysregulated inflammation

Mol Oral Microbiol. 2021 Apr;36(2):103-120. doi: 10.1111/omi.12321. Epub 2020 Dec 31.

Abstract

Periodontitis is an irreversible, chronic inflammatory disease where inflammophilic pathogenic microbial communities accumulate in the gingival crevice. Neutrophils are a major component of the innate host response against bacterial challenge, and under homeostatic conditions, their microbicidal functions typically protect the host against periodontitis. However, a number of periodontal pathogens developed survival strategies to evade neutrophil microbicidal functions while promoting inflammation, which provides a source of nutrients for bacterial growth. Research on periodontal pathogens has largely focused on a few established species: Tannerella forsythia, Treponema denticola, Fusobacterium nucleatum, Aggregatibacter actinomycetemcomitans, and Porphyromonas gingivalis. However, advances in culture-independent techniques have facilitated the identification of new bacterial species in periodontal lesions, such as the two Gram-positive anaerobes, Filifactor alocis and Peptoanaerobacter stomatis, whose characterization of pathogenic potential has not been fully described. Additionally, there is not a full understanding of the pathogenic mechanisms used against neutrophils by organisms that are abundant in periodontal lesions. This presents a substantial barrier to the development of new approaches to prevent or ameliorate the disease. In this review, we first summarize the neutrophil functions affected by the established periodontal pathogens listed above, denoting unknown areas that still merit a closer look. Then, we review the literature on neutrophil functions and the emerging periodontal pathogens, F. alocis and P. stomatis, comparing the effects of the emerging microbes to that of established pathogens, and speculate on the contribution of these putative pathogens to the progression of periodontal disease.

Keywords: Filifactor alocis; emerging oral pathogen; human neutrophils; periodontitis.

Publication types

  • Research Support, N.I.H., Extramural
  • Review

MeSH terms

  • Aggregatibacter actinomycetemcomitans
  • Clostridiales*
  • Humans
  • Inflammation
  • Neutrophils*
  • Porphyromonas gingivalis
  • Treponema denticola

Supplementary concepts

  • Filifactor alocis
  • Peptoanaerobacter stomatis