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比较严重婴幼儿龋儿童的唾液和牙本质微生物组与无龋儿童的唾液微生物组。

Comparison of the salivary and dentinal microbiome of children with severe-early childhood caries to the salivary microbiome of caries-free children.

机构信息

School of Microbiology, University College Cork, Room 447 Food Science Building, Cork, Ireland.

Cork University Dental School & Hospital, Cork University Hospital, Wilton, Cork, Ireland.

出版信息

BMC Oral Health. 2019 Jan 14;19(1):13. doi: 10.1186/s12903-018-0693-1.


DOI:10.1186/s12903-018-0693-1
PMID:30642327
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6332856/
Abstract

BACKGROUND: The main objectives of this study were to describe and compare the microbiota of 1) deep dentinal lesions of deciduous teeth of children affected with severe early childhood caries (S-ECC) and 2) the unstimulated saliva of these children and 3) the unstimulated saliva of caries-free children, and to compare microbiota compositional differences and diversity of taxa in these sampled sites. METHODS: Children with S-ECC and without S-ECC were recruited. The saliva of all children with and without S-ECC was sampled along with the deep dentinal microbiota from children affected by S-ECC. The salivary microbiota of children affected by S-ECC (n = 68) was compared to that of caries-free children (n = 70), by Illumina MiSeq sequencing of 16S rRNA amplicons. Finally, the caries microbiota of deep dentinal lesions of those children with S-ECC was investigated. RESULTS: Using two beta diversity metrics (Bray Curtis dissimilarity and UniFrac distance), the caries microbiota was found to be distinct from that of either of the saliva groups (caries-free & caries-active) when bacterial abundance was taken into account. However, when the comparison was made by measuring only presence and absence of bacterial taxa, all three microbiota types separated. While the alpha diversity of the caries microbiota was lowest, the diversity difference between the caries samples and saliva samples was statistically significant (p < 0.001). The major phyla of the caries active dentinal microbiota were Firmicutes (median abundance value 33.5%) and Bacteroidetes (23.2%), with Neisseria (10.3%) being the most abundant genus, followed by Prevotella (10%). The caries-active salivary microbiota was dominated by Proteobacteria (median abundance value 38.2%) and Bacteroidetes (27.8%) with the most abundant genus being Neisseria (16.3%), followed by Porphyromonas (9.5%). Caries microbiota samples were characterized by high relative abundance of Streptococcus mutans, Prevotella spp., Bifidobacterium and Scardovia spp. CONCLUSIONS: Distinct differences between the caries microbiota and saliva microbiota were identified, with separation of both salivary groups (caries-active and caries-free) whereby rare taxa were highlighted. While the caries microbiota was less diverse than the salivary microbiota, the presence of these rare taxa could be the difference between health and disease in these children.

摘要

背景:本研究的主要目的是描述和比较 1)患有严重婴幼儿龋(S-ECC)儿童的深牙本质病变和 2)这些儿童的非刺激性唾液与 3)无龋儿童的非刺激性唾液的微生物群,并比较这些采样部位的微生物群组成差异和分类群多样性。

方法:招募了患有 S-ECC 和不患有 S-ECC 的儿童。从患有 S-ECC 的儿童中采集了所有患有 S-ECC 和不患有 S-ECC 儿童的非刺激性唾液以及深牙本质微生物群。通过 Illumina MiSeq 测序 16S rRNA 扩增子,比较了患有 S-ECC 的儿童(n=68)的唾液微生物群与无龋儿童(n=70)的唾液微生物群。最后,研究了患有 S-ECC 的儿童深牙本质病变中的龋病微生物群。

结果:使用两种 beta 多样性指标(Bray Curtis 不相似性和 UniFrac 距离),当考虑细菌丰度时,发现龋病微生物群与任何一种唾液组(无龋和有龋)都不同。然而,当仅通过测量细菌分类群的存在和不存在来进行比较时,所有三种微生物群类型都分开了。虽然龋病微生物群的 alpha 多样性最低,但龋病样本和唾液样本之间的多样性差异具有统计学意义(p<0.001)。活跃牙本质龋病微生物群的主要门是厚壁菌门(中位数丰度值 33.5%)和拟杆菌门(23.2%),其中奈瑟菌(10.3%)是最丰富的属,其次是普雷沃氏菌(10%)。活跃唾液龋病微生物群主要由变形菌门(中位数丰度值 38.2%)和拟杆菌门(27.8%)组成,最丰富的属是奈瑟菌(16.3%),其次是卟啉单胞菌(9.5%)。龋病微生物群样本的特征是变形链球菌、普雷沃氏菌、双歧杆菌和 Scardovia 属的相对丰度较高。

结论:确定了龋病微生物群和唾液微生物群之间的显著差异,并且分离了两组唾液(有龋和无龋),从而突出了稀有分类群的存在。虽然龋病微生物群的多样性低于唾液微生物群,但这些稀有分类群的存在可能是这些儿童健康和疾病之间的差异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/e77bea049bb8/12903_2018_693_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/a1a65488b64f/12903_2018_693_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/4c6808d5994e/12903_2018_693_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/7ecfb69e6f33/12903_2018_693_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/97d858450eb3/12903_2018_693_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/148a861a0f41/12903_2018_693_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/e77bea049bb8/12903_2018_693_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/a1a65488b64f/12903_2018_693_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/4c6808d5994e/12903_2018_693_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/7ecfb69e6f33/12903_2018_693_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/97d858450eb3/12903_2018_693_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/148a861a0f41/12903_2018_693_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6deb/6332856/e77bea049bb8/12903_2018_693_Fig6_HTML.jpg

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[6]
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