Siegal Nora, Gutowski Michal, Akileswaran Lakshmi, Beauchamp Norman J, Ding Lien-Chieh, Chambers Christopher B, Van Gelder Russell N
Department of Ophthalmology, University of Washington School of Medicine, Campus Box 359608, 325 9th Avenue, Seattle, WA, 98104, USA.
Department of Ophthalmology, Oregon Health Sciences University, Portland, OR, USA.
Sci Rep. 2021 Jul 28;11(1):15366. doi: 10.1038/s41598-021-92642-w.
The human ocular surface hosts a paucibacterial resident microbiome and virome. The factors contributing to homeostasis of this mucosal community are presently unknown. To determine the impact of ocular enucleation and prosthesis placement on the ocular surface microbiome, we sampled conjunctival swabs from 20 anophthalmic and 20 fellow-eye intact conjunctiva. DNA was extracted and subjected to quantitative 16S rDNA PCR, biome representational karyotyping (BRiSK), and quantitative PCR (qPCR) confirmation of specific organisms. 16S ribosomal qPCR revealed equivalent bacterial loads between conditions. Biome representational in silico karyotyping (BRiSK) demonstrated comparable bacterial fauna between anophthalmic and intact conjunctiva. Both torque teno virus and Merkel cell polyoma virus (MCPyV) were detected frequently in healthy and anophthalmic conjunctiva. By qPCR, MCPyV was detected in 19/20 anophthalmic samples compared with 5/20 fellow eyes. MCPyV copy number averaged 891 copies/ng in anophthalmic conjunctiva compared with 193 copies/ng in fellow eyes (p < 0.001). These results suggest that enucleation and prosthesis placement affect the ocular surface flora, particularly for the resident virome. As MCPyV has been shown to be the etiologic cause of Merkel cell carcinoma, understanding the mechanisms by which the ocular surface regulates this virus may have clinical importance.
人类眼表存在少量常驻微生物群和病毒组。目前尚不清楚促成这个黏膜群落稳态的因素。为了确定眼球摘除术和义眼植入对眼表微生物群的影响,我们从20名无眼球患者和20名健侧眼结膜采集了结膜拭子样本。提取DNA并进行16S rDNA定量PCR、生物群落代表性核型分析(BRiSK)以及特定微生物的定量PCR(qPCR)确认。16S核糖体qPCR显示不同条件下细菌载量相当。生物群落代表性计算机模拟核型分析(BRiSK)表明无眼球结膜和完整结膜的细菌种类相当。在健康结膜和无眼球结膜中均频繁检测到细小病毒B19和默克尔细胞多瘤病毒(MCPyV)。通过qPCR检测,在20份无眼球样本中有19份检测到MCPyV,而健侧眼中只有5份检测到。无眼球结膜中MCPyV拷贝数平均为891拷贝/纳克,健侧眼中为193拷贝/纳克(p < 0.001)。这些结果表明眼球摘除术和义眼植入会影响眼表菌群,尤其是常驻病毒组。由于MCPyV已被证明是默克尔细胞癌的病因,了解眼表调节这种病毒的机制可能具有临床意义。