4.1 Article

Virulence of Lactobacillus spp. misidentified as Enterococcus faecalis from children's carious dentine

Journal

ACTA ODONTOLOGICA SCANDINAVICA
Volume 80, Issue 1, Pages 21-28

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/00016357.2021.1934534

Keywords

Lactobacillus; dental caries; Enterococcus faecalis; virulence; misidentification

Funding

  1. Fundacao Carlos Chagas Filho de Amparoa Pesquisa do Estado do Rio de Janeiro (FAPERJ)
  2. ProReitoria de Pesquisa, Pos-Graduacao e Inovacao/Plano de Desenvolvimento Institucional/Universidade Federal Fluminense (PROPPI/PDI/UFF)
  3. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq)

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No Enterococcus faecalis were found in children's carious lesions, but all Lactobacillus misidentified as Enterococcus (LME) isolates showed important virulence traits such as biofilm formation and high acidogenicity.
Objective: This study aimed to search for Enterococcus faecalis in children's deep carious dentine and characterize their virulence traits. Material and Methods: Eight isolates from 15 carious molars identified by 16S rDNA species-specific PCR as E. faecalis were included. These eight isolates were subject to identification by MALDI-TOF and characterized regarding: (i) bacterial aggregation and biofilm formation on polystyrene and glass, with/without saliva, as single or dual-species (associated to Streptococcus mutans); (ii) environmental pH measurement before and after 24 h incubation; (iii) acidogenicity; (iv) gelatinase production; (v) macrophage adherence; and (vi) toxicity towards Caenorhabditis elegans. Statistical analyses were performed using two-way ANOVA/Tukey or Fisher's exact tests. Results: All isolates initially identified as E. faecalis by PCR were correctly identified as Lactobacillus by MALDI-TOF, being designated as Lactobacillus misidentified as Enterococcus (LME). These isolates produced biofilm in the presence of saliva and in the dual-species assays. Bacterial aggregation was only observed in the dual-species model. After 24 h, environmental pH dropped from 7.5 to 4.5 for seven of eight isolates, and to 4.0 in all dual-species models. LME isolates were acidogenic, none of them produced gelatinase or adhered to macrophages, but all presented toxicity towards C. elegans. Conclusions: No E. faecalis were identified in the children's caries lesions. All LME isolates presented important virulence traits, including biofilm formation and high acidogenicity, which cause enamel demineralization, that might increase the risk of dental caries in children carrying LME. Thus, the correct identification and in-depth virulence characterization of microorganisms isolated from dental caries are important to understand the dynamics of this disease.

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