Doan Thuy, Akileswaran Lakshmi, Andersen Dallin, Johnson Benjamin, Ko Narae, Shrestha Angira, Shestopalov Valery, Lee Cecilia S, Lee Aaron Y, Van Gelder Russell N
Department of Ophthalmology, University of Washington, Seattle, Washington, United States.
Evelyn F. and William L. McKnight Vision Research Center, Bascom Palmer Eye Institute, Department of Ophthalmology, University of Miami, Miami, Florida, United States.
Invest Ophthalmol Vis Sci. 2016 Oct 1;57(13):5116-5126. doi: 10.1167/iovs.16-19803.
To characterize the ocular surface microbiome of healthy volunteers using a combination of microbial culture and high-throughput DNA sequencing techniques.
Conjunctival swab samples from 107 healthy volunteers were analyzed by bacterial culture, 16S rDNA gene deep sequencing (n = 89), and biome representational in silico karyotyping (BRiSK; n = 80). Swab samples of the facial skin (n = 42), buccal mucosa (n = 50), and environmental controls (n = 27) were processed in parallel. 16S rDNA gene quantitative PCR was used to calculate the bacterial load in each site. Bacteria were characterized by site using principal coordinate analysis of metagenomics data. BRiSK data were analyzed for presence of fungi and viruses.
Corynebacteria, Propionibacteria, and coagulase-negative Staphylococci were the predominant organisms identified by all three techniques. Quantitative 16S PCR demonstrated approximately 0.1 bacterial 16S rDNA/human actin copy on the ocular surface compared with greater than 10 16S rDNA/human actin copy for facial skin or the buccal mucosa. The conjunctival bacterial community structure is distinct compared with the facial skin (R = 0.474, analysis of similarities P = 0.0001), the buccal mucosa (R = 0.893, P = 0.0001), and environmental control samples (R = 0.536, P = 0.0001). 16S metagenomics revealed substantially more bacterial diversity on the ocular surface than other techniques, which appears to be artifactual. BRiSK revealed presence of torque teno virus (TTV) on the healthy ocular surface, which was confirmed by direct PCR to be present in 65% of all conjunctiva samples tested.
Relative to adjacent skin or other mucosa, healthy ocular surface microbiome is paucibacterial. Its flora are distinct from adjacent skin. Torque teno virus is a frequent constituent of the ocular surface microbiome. (ClinicalTrials.gov number, NCT02298881.).
运用微生物培养和高通量DNA测序技术相结合的方法,对健康志愿者的眼表微生物群进行特征分析。
对107名健康志愿者的结膜拭子样本进行细菌培养、16S rDNA基因深度测序(n = 89)和生物群落代表性虚拟核型分析(BRiSK;n = 80)。同时对面部皮肤(n = 42)、颊黏膜(n = 50)和环境对照样本(n = 27)的拭子样本进行平行处理。采用16S rDNA基因定量PCR计算每个部位的细菌载量。利用宏基因组学数据的主坐标分析按部位对细菌进行特征分析。对BRiSK数据进行真菌和病毒存在情况分析。
棒状杆菌属、丙酸杆菌属和凝固酶阴性葡萄球菌是所有三种技术鉴定出的主要微生物。定量16S PCR显示,眼表每人类肌动蛋白拷贝约有0.1个细菌16S rDNA,而面部皮肤或颊黏膜每人类肌动蛋白拷贝大于10个16S rDNA。结膜细菌群落结构与面部皮肤(R = 0.474,相似性分析P = 0.0001)、颊黏膜(R = 0.893,P = 0.0001)和环境对照样本(R = 0.536,P = 0.0001)相比有明显差异。16S宏基因组学显示眼表细菌多样性比其他技术检测到的要多得多,这似乎是人为造成的。BRiSK显示健康眼表存在细小病毒B19,直接PCR证实所有检测的结膜样本中有65%存在该病毒。
相对于相邻皮肤或其他黏膜而言,健康眼表微生物群细菌数量较少。其菌群与相邻皮肤不同。细小病毒B19是眼表微生物群的常见组成部分。(临床试验注册号,NCT02298881。)