Differential oral microbiome in nonhuman primates from periodontitis-susceptible and periodontitis-resistant matrilines.

IF 2.8 3区 医学 Q1 DENTISTRY, ORAL SURGERY & MEDICINE Molecular Oral Microbiology Pub Date : 2023-04-01 DOI:10.1111/omi.12377
Jeffrey L Ebersole, Sreenatha Kirakodu, Octovio Gonzalez
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引用次数: 2

Abstract

Rhesus monkeys (n = 36) exhibiting a healthy periodontium at baseline were used to induce progressing periodontitis through ligature placement around premolar/molar teeth. Bacterial samples were collected at baseline, 0.5, 1, and 3 months of disease and at 5 months for disease resolution. The animals were distributed into two groups (18/group): 3-7 years (young) and 12-23 years (adult) and stratified based upon matriline susceptibility to periodontitis (PDS, susceptible; PDR, resistant). A total of 444 operational taxonomic units (OTUs) with 100 microbes representing a core microbiome present in ≥75% of the samples were identified. Only 48% of the major phylotypes overlapped in the PDS and PDR samples. Different OTU abundance patterns were seen in young animals from the PDS and PDR matrilines, with qualitative similarities during disease and the relative abundance of phylotypes becoming less diverse. In adults, 23 OTUs were increased during disease in PDS samples and 24 in PDR samples; however, only five were common between these groups. Greater diversity of OTU relative abundance at baseline was observed with adult compared to young oral samples from both the PDS and PDR groups. With disease initiation (2 weeks), less diversity of relative abundance and some distinctive increases in specific OTUs were noted. By 1 month, there was considerable qualitative homogeneity in the major OTUs in both groups; however, by 3 months, there was an exacerbation of both qualitative and quantitative differences in the dominant OTUs between the PDS and PDR samples. These results support that some differences in disease expression related to matriline (familial) periodontitis risk may be explained by microbiome features.

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牙周炎易感和抗牙周炎母系非人灵长类动物口腔微生物组的差异。
36只牙周组织健康的恒河猴通过在前磨牙/磨牙周围结扎来诱导进展性牙周炎。在基线、0.5个月、1个月和3个月以及疾病消退5个月时收集细菌样本。实验动物被分为两组(18只/组):3-7岁(幼龄)和12-23岁(成年),并根据母系对牙周炎的易感性(PDS,易感;PDR、耐药)。总共鉴定出444个操作分类单位(otu),其中100个微生物代表核心微生物组,存在于≥75%的样品中。在PDS和PDR样本中,只有48%的主要种型重叠。在来自PDS和PDR母系的幼畜中发现了不同的OTU丰度模式,在疾病期间具有定性相似性,并且种型的相对丰度变得不那么多样化。在成人中,PDS样本中有23个OTUs在疾病期间增加,PDR样本中有24个OTUs在疾病期间增加;然而,这两组人中只有五种是共同的。与来自PDS和PDR组的年轻口腔样本相比,在基线时观察到成人的OTU相对丰度更大的多样性。随着疾病开始(2周),发现相对丰度的多样性减少,特异性otu明显增加。到1个月时,两组的主要otu在质量上有相当大的同质性;然而,到3个月时,PDS和PDR样本间优势otu的定性和定量差异加剧。这些结果支持一些与母系(家族)牙周炎风险相关的疾病表达差异可以用微生物组特征来解释。
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来源期刊
Molecular Oral Microbiology
Molecular Oral Microbiology DENTISTRY, ORAL SURGERY & MEDICINE-MICROBIOLOGY
CiteScore
6.50
自引率
5.40%
发文量
46
审稿时长
>12 weeks
期刊介绍: Molecular Oral Microbiology publishes high quality research papers and reviews on fundamental or applied molecular studies of microorganisms of the oral cavity and respiratory tract, host-microbe interactions, cellular microbiology, molecular ecology, and immunological studies of oral and respiratory tract infections. Papers describing work in virology, or in immunology unrelated to microbial colonization or infection, will not be acceptable. Studies of the prevalence of organisms or of antimicrobials agents also are not within the scope of the journal. The journal does not publish Short Communications or Letters to the Editor. Molecular Oral Microbiology is published bimonthly.
期刊最新文献
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