Department of Surgery, University of Wisconsin, 1111 Highland Avenue, Madison, 53705 Wisconsin USA.
Microbiome. 2014 Dec 8;2:43. doi: 10.1186/2049-2618-2-43. eCollection 2014.
Benign vocal fold lesions, including cysts, nodules, polyps, and Reinke's edema, are common causes of hoarseness and subsequent voice disorders. Given the prevalence of these lesions, disease etiology and pathophysiology remain unclear and their microbiota has not been studied to date secondary to the paucity of available biopsies for investigation. We sought to characterize and compare the bacterial communities in biopsies of cysts, nodules, polyps, and Reinke's edema collected from patients in Germany and Wisconsin. These samples were then compared to the communities found in healthy saliva and throat samples from the Human Microbiome Project (HMP).
454 pyrosequencing of the V3-V5 regions of the 16S rRNA gene revealed five phyla that explained most of the bacterial diversity, including Firmicutes (73.8%), Proteobacteria (12.7%), Bacteroidetes (9.2%), Actinobacteria (2.1%), and Fusobacteria (1.9%). Every lesion sample, regardless of diagnosis, had operational taxonomic units (OTUs) identified as Streptococcus, with a mean abundance of 68.7%. Most of the lesions, 31 out of 44, were indistinguishable in a principal coordinates analysis (PCoA) due to dominance by OTUs phylogenetically similar to Streptococcus pseudopneumoniae. Thirteen lesions not dominated by S. pseudopneumoniae were more similar to HMP throat and saliva samples, though 12 of them contained Pseudomonas, which was not present in any of the HMP samples. Community structure and abundance could not be correlated with lesion diagnosis or any other documented patient factor, including age, sex, or country of origin.
Dominance by S. pseudopneumoniae could be a factor in disease etiology, as could the presence of Pseudomonas in some samples. Likewise, decreased diversity, as compared to healthy saliva and throat samples, may be associated with disease, similar to disease models in other mucosal sites.
良性声带病变,包括囊肿、结节、息肉和 Reinke 水肿,是导致声音嘶哑和随后的声音障碍的常见原因。鉴于这些病变的普遍性,疾病的病因和病理生理学仍然不清楚,而且迄今为止,由于可供研究的活检标本很少,它们的微生物群尚未得到研究。我们试图描述和比较从德国和威斯康星州患者的囊肿、结节、息肉和 Reinke 水肿活检中采集的细菌群落。然后将这些样本与人类微生物组计划(HMP)中发现的健康唾液和喉咙样本的群落进行比较。
16S rRNA 基因 V3-V5 区的 454 焦磷酸测序显示,五个门解释了大部分细菌多样性,包括厚壁菌门(73.8%)、变形菌门(12.7%)、拟杆菌门(9.2%)、放线菌门(2.1%)和梭杆菌门(1.9%)。每个病变样本,无论诊断如何,都有鉴定为链球菌的操作分类单位(OTU),其丰度平均值为 68.7%。由于与肺炎链球菌亲缘关系相似的 OTU 占主导地位,44 个病变中有 31 个在主坐标分析(PCoA)中无法区分。13 个不受 S. pseudopneumoniae 支配的病变与 HMP 喉咙和唾液样本更为相似,尽管其中 12 个含有不在任何 HMP 样本中存在的铜绿假单胞菌。群落结构和丰度不能与病变诊断或任何其他记录的患者因素相关,包括年龄、性别或原籍国。
肺炎链球菌的主导地位可能是病因的一个因素,某些样本中存在铜绿假单胞菌也是一个因素。同样,与健康唾液和喉咙样本相比,多样性降低可能与疾病相关,类似于其他粘膜部位的疾病模型。