Characterization and functional prediction of the dental plaque microbiome in patients with alveolar clefts

Front Cell Infect Microbiol. 2024 May 10:14:1361206. doi: 10.3389/fcimb.2024.1361206. eCollection 2024.

Abstract

Introduction: Alveolar cleft (AC) is a common congenital defect in people with cleft lip and palate (CLP). Alveolar bone grafting (ABG) is typically performed during adolescence, resulting in the fissure remaining in the mouth for a longer length of time. Patients with AC have a greater rate of oral diseases such as dental caries than the normal population, and the precise characteristics of the bacterial alterations caused by AC are unknown.

Methods: We recruited a total of 87 subjects and collected dental plaque samples from AC adolescents (AAP), post-operative ABG adolescents (PAP), healthy control adolescents (CAP), AC young adults (AYP), post-operative ABG young adults (PYP), and healthy control young adults (CYP). The sequencing of 16S rRNA genes was performed.

Results: The microbial composition of plaque from alveolar cleft patients differed significantly from age-matched healthy controls. Linear discriminant analysis effect size (LEfSe) analysis revealed that AAP was enriched for Neisseria, Haemophilus, Fusobacterium, Rhodococcus, Aggregatibacter, Gemella, and Porphyromonas, whereas AYP was enriched for Capnocytophaga, Rhodococcus, and Actinomyces-f0332. There were phenotypic differences in facultatively anaerobic, Gram-negative, Gram-positive, and oxidative stress tolerance between the AYP group with longer alveolar cleft and the healthy control group according to Bugbase phenotypic predictions. Alveolar bone grafting did not alter the functional phenotype of alveolar cleft patients but reduced the number of differential genera between alveolar cleft patients and healthy controls at both ages.

Conclusions: Our study systematically characterized the supragingival plaque microbiota of alveolar cleft patients, post-alveolar bone grafting patients, and matched healthy controls in two ages to gain a better understanding of plaque ecology and microbiology associated with alveolar clefts.

Keywords: 16S rRNA sequencing; alveolar bone grafting; alveolar cleft; microbial diversity; supragingival plaque microorganisms.

MeSH terms

  • Adolescent
  • Adult
  • Alveolar Bone Grafting
  • Bacteria* / classification
  • Bacteria* / genetics
  • Bacteria* / isolation & purification
  • Cleft Lip* / microbiology
  • Cleft Palate* / microbiology
  • Dental Plaque* / microbiology
  • Female
  • Humans
  • Male
  • Microbiota* / genetics
  • RNA, Ribosomal, 16S* / genetics
  • Young Adult

Substances

  • RNA, Ribosomal, 16S

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This research was funded by Clinical Research Program of Ninth People’s Hospital, Shanghai Jiao Tong University School of Medicine, grant number No. JYLJ202004.