Noguera-Julian Marc, Guillén Yolanda, Peterson Jessica, Reznik David, Harris Erica V, Joseph Sandeep J, Rivera Javier, Kannanganat Sunil, Amara Rama, Nguyen Minh Ly, Mutembo Simon, Paredes Roger, Read Timothy D, Marconi Vincent C
IrsiCaixa AIDS Research Institute, Badalona University Autònoma de Barcelona, Bellaterra University de Vic-University Central de Catalunya, Vic, Catalonia, Spain Division of Infectious Diseases, Emory University School of Medicine Infectious Diseases Program, Grady Health System Department of Biology, Emory University, O. Wayne Rollins Research Center Department of Global Health, Emory University Rollins School of Public Health, Atlanta, GA Ministry of Health, Zambia Unitat VIH, Hosp. University Germans Trias i Pujol, Badalona, Catalonia, Spain.
Medicine (Baltimore). 2017 Mar;96(12):e5821. doi: 10.1097/MD.0000000000005821.
HIV-associated periodontal diseases (PD) could serve as a source of chronic inflammation. Here, we sought to characterize the oral microbial signatures of HIV+ and HIV- individuals at different levels of PD severity.This cross-sectional study included both HIV+ and HIV- patients with varying degrees of PD. Two tooth, 2 cheek, and 1 saliva samples were obtained for microbiome analysis. Mothur/SILVADB were used to classify sequences. R/Bioconductor (Vegan, PhyloSeq, and DESeq2) was employed to assess overall microbiome structure differences and differential abundance of bacterial genera between groups. Polychromatic flow cytometry was used to assess immune activation in CD4 and CD8 cell populations.Around 250 cheek, tooth, and saliva samples from 50 participants (40 HIV+ and 10 HIV-) were included. Severity of PD was classified clinically as None/Mild (N), Moderate (M), and Severe (S) with 18 (36%), 16 (32%), and 16 (32%) participants in each category, respectively. Globally, ordination analysis demonstrated clustering by anatomic site (R2 = 0.25, P < 0.001). HIV status and PD severity showed a statistically significant impact on microbiome composition but only accounted for a combined 2% of variation. HIV+ samples were enriched in genera Abiotrophia, Neisseria, Kingella, and unclassified Neisseriaceae and depleted in Leptotrichia and Selenomonas. The Neisseria genus was consistently enriched in HIV+ participants regardless of sampling site and PD level. Immune markers were altered in HIV+ participants but did not show association with the oral microbiome.HIV-associated changes in oral microbiome result in subtle microbial signatures along different stages of PD that are common in independent oral anatomic sites.
与人类免疫缺陷病毒(HIV)相关的牙周疾病(PD)可能是慢性炎症的一个来源。在此,我们试图在不同PD严重程度水平上,对HIV阳性和HIV阴性个体的口腔微生物特征进行表征。这项横断面研究纳入了不同程度PD的HIV阳性和HIV阴性患者。采集了两颗牙齿、两处颊部和一份唾液样本用于微生物组分析。使用Mothur/SILVADB对序列进行分类。运用R/Bioconductor(Vegan、PhyloSeq和DESeq2)来评估总体微生物组结构差异以及组间细菌属的差异丰度。采用多色流式细胞术评估CD4和CD8细胞群体中的免疫激活情况。
纳入了来自50名参与者(40名HIV阳性和10名HIV阴性)的约250份颊部、牙齿和唾液样本。PD的严重程度在临床上分为无/轻度(N)、中度(M)和重度(S),每类分别有18名(36%)、16名(32%)和16名(32%)参与者。总体而言,排序分析显示按解剖部位聚类(R2 = 0.25,P < 0.001)。HIV状态和PD严重程度对微生物组组成有统计学上的显著影响,但仅占变异的2%。HIV阳性样本中嗜养菌属、奈瑟菌属、金氏菌属和未分类的奈瑟菌科富集,而纤毛菌属和月形单胞菌属减少。无论采样部位和PD水平如何,HIV阳性参与者中奈瑟菌属始终富集。HIV阳性参与者的免疫标志物发生了改变,但未显示与口腔微生物组相关。
HIV相关的口腔微生物组变化导致了在PD不同阶段常见的、独立口腔解剖部位中微妙的微生物特征。