描述与严重儿童早期龋齿有关的乳酸杆菌的多样性:研究方案。

Yihong Li, Silvia Argimón, Catherine N Schön, Prakaimuk Saraithong, Page W Caufield
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引用次数: 0

摘要

几十年来,乳酸杆菌一直与龋齿有关;然而,人们对这一细菌群在龋齿病因学方面的了解仅限于定量阐释。如今,尽管口腔乳酸杆菌的分类很复杂,但明确鉴定口腔乳酸杆菌的种类已经成为可能。在此,我们介绍一种结合了培养和基因方法的方法,以确定和描述严重儿童早期龋齿(S-ECC)患儿口腔中乳酸杆菌群的多样性和丰度。这项研究邀请了在纽约市贝尔维尤医院儿科牙科诊所寻求牙科治疗的 80 名 3 至 6 岁儿童(40 名 S-ECC 儿童和 40 名无龋儿童)参加。研究人员从主要照顾者那里获得了有关社会人口信息和口腔健康行为的临床数据。这些数据包括详细的牙科检查、儿童病史和问卷调查。从每个儿童口中采集非刺激性唾液和龈上牙菌斑样本,并在选择性培养基上进行培养,以定量检测乳酸杆菌的含量。乳酸杆菌菌种筛选程序包括在每个平板上随机选择 50 个菌落,从每个菌落中提取 DNA,并通过任意引物聚合酶链反应(AP-PCR)进行基因分型。每个独特的乳酸杆菌 AP-PCR 基因型都将通过 16S rRNA 基因测序分析进行分类评估。通过将 16S rRNA 序列与核糖体数据库和人类口腔微生物组数据库进行比较,确定乳酸杆菌的种类。同时,同一组临床样本将分别进行基因组 DNA 分离、乳酸杆菌属特异性引物的 16S rRNA 扩增、测序以及分类鉴定,并采用定制的流水线进行属和种的鉴定。这些乳酸杆菌的分布和系统发育差异将在患有或未患有 S-ECC 的儿童之间进行比较。本研究的主要目标之一是制定口腔中乳酸杆菌的鉴定和特征描述研究方案。未来的龋病风险评估可包括与 S-ECC 相关的乳酸杆菌计数(定量)和乳酸杆菌物种的特定致龋基因特征的存在/不存在(定性)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Characterizing Diversity of Lactobacilli Associated with Severe Early Childhood Caries: A Study Protocol.

Characterizing Diversity of Lactobacilli Associated with Severe Early Childhood Caries: A Study Protocol.

Characterizing Diversity of Lactobacilli Associated with Severe Early Childhood Caries: A Study Protocol.

Lactobacilli have been consistently associated with dental caries for decades; however, knowledge of this group of bacteria in the etiology of the disease is limited to quantitative elucidation. Nowadays, explicit identification of oral Lactobacillus species is possible, despite their taxonomic complexity. Here we describe a combined approach involving both cultivation and genetic methods to ascertain and characterize the diversity and abundance of the Lactobacillus population in the oral cavities of children with severe early childhood caries (S-ECC). Eighty 3- to 6-year-old children (40 S-ECC and 40 caries free) who were seeking dental care at the Pediatric Dental Clinic of Bellevue Hospital in New York City were invited to participate in this study. Clinical data on socio-demographic information and oral health behavior were obtained from the primary caregiver. The data included a detailed dental examination, children's medical history, and a questionnaire survey. Combined non-stimulated saliva and supra-gingival plaque samples were collected from each child and cultivated on selective media for quantitative measures of lactobacilli levels. The procedure for Lactobacillus species screening will include the random selection of 50 colonies per plate, extraction of DNA from each colony, and genotyping by arbitrarily primed polymerase chain reaction (AP-PCR). Each unique Lactobacillus AP-PCR genotype will be selected for taxonomic assessment by 16S rRNA gene sequencing analysis. Lactobacillus species will be identified by comparing the 16S rRNA sequences with the Ribosomal Database and the Human Oral Microbiome Database. Meanwhile, the same set of clinical samples will be independently subjected to genomic DNA isolation, 16S rRNA amplification with Lactobacillus genus-specific primers, sequencing, and taxonomic identification, both at genus and species levels with a customized pipeline. The distribution and phylogenetic differences of these Lactobacillus species will be compared between children with or without S-ECC. One of the main objectives of this study is to establish a study protocol for the identification and characterization of lactobacilli in the oral cavity. Future caries risk assessments can include lactobacilli counts (quantitative) and the presence/absence of specific cariogenic genetic signatures of a Lactobacillus species (qualitative) associated with S-ECC.

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