da Costa Rosa Thamirys, de Almeida Neves Aline, Azcarate-Peril M Andrea, Divaris Kimon, Wu Di, Cho Hunyong, Moss Kevin, Paster Bruce J, Chen Tsute, B Freitas-Fernandes Liana, Fidalgo Tatiana K S, Tadeu Lopes Ricardo, Valente Ana Paula, R Arnold Roland, de Aguiar Ribeiro Apoena
Department of Pediatric Dentistry, Fluminense Federal University, Nova Friburgo, Brazil.
Department of Pediatric Dentistry, Rio de Janeiro Federal University, Brazil.
J Oral Microbiol. 2021 Jun 16;13(1):1886748. doi: 10.1080/20002297.2021.1886748.
: This experimental study investigated bacterial microbiome and metabolome longitudinal changes associated with enamel caries lesion progression and arrest. : We induced natural caries activity in three caries-free volunteers prior to four premolar extractions for orthodontic reasons. The experimental model included placement of a modified orthodontic band on smooth surfaces and a mesh on occlusal surfaces. We applied the caries-inducing protocol for 4- and 6-weeks, and subsequently promoted caries lesion arrest via a 2-week toothbrushing period. Lesions were verified clinically and quantitated via micro-CT enamel density measurements. The biofilm microbial composition was determined via 16S rRNA gene Illumina sequencing and NMR spectrometry was used for metabolomics. : Biofilm maturation and caries lesion progression were characterized by an increase in Gram-negative anaerobes, including and was associated caries lesion progression, while a more equal distribution of characterized arrest. Lactate, acetate, pyruvate, alanine, valine, and sugars were more abundant in mature biofilms compared to newly formed biofilms. : These longitudinal bacterial microbiome and metabolome results provide novel mechanistic insights into the role of the biofilm in caries progression and arrest and offer promising candidate biomarkers for validation in future studies.
本实验研究调查了与釉质龋损进展和静止相关的细菌微生物组和代谢组的纵向变化。我们在三名无龋志愿者身上诱导自然龋活性,之后出于正畸原因拔除四颗前磨牙。实验模型包括在光滑表面放置改良正畸带,在咬合面放置网。我们应用致龋方案4周和6周,随后通过为期2周的刷牙期促进龋损静止。通过临床检查验证病变,并通过显微CT釉质密度测量进行定量。通过16S rRNA基因Illumina测序确定生物膜微生物组成,并使用核磁共振光谱法进行代谢组学分析。生物膜成熟和龋损进展的特征是革兰氏阴性厌氧菌增加,包括[具体菌名缺失],且与龋损进展相关,而[具体菌名缺失]分布更均匀则表征龋损静止。与新形成的生物膜相比,成熟生物膜中的乳酸、乙酸、丙酮酸、丙氨酸、缬氨酸和糖类更为丰富。这些纵向细菌微生物组和代谢组结果为生物膜在龋病进展和静止中的作用提供了新的机制见解,并为未来研究中的验证提供了有前景的候选生物标志物。