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Microbiomes of the normal middle ear and ears with chronic otitis media

中耳 中耳炎 微生物群 医学 厚壁菌 听力学 生物 外科 生物信息学 16S核糖体RNA 遗传学 基因
作者
Shujiro Minami,Hideki Mutai,Tomoko Suzuki,Arata Horii,Naoki Oishi,Koichiro Wasano,Motoyasu Katsura,Fujinobu Tanaka,Tetsuya Takiguchi,Masato Fujisawa,Kimitaka Kaga
出处
期刊:Laryngoscope [Wiley]
卷期号:127 (10) 被引量:57
标识
DOI:10.1002/lary.26579
摘要

Objective The aim of this study was to profile and compare the middle ear microbiomes of human subjects with and without chronic otitis media. Study Design Prospective multicenter cohort study. Methods All consecutive patients undergoing tympanoplasty surgery for chronic otitis media or ear surgery for conditions other than otitis media were recruited. Sterile swab samples were collected from the middle ear mucosa during surgery. The variable region 4 of the 16S rRNA gene in each sample were amplified using region‐specific primers adapted for the Illumina MiSeq sequencer (Illumina, CA, USA)). The sequences were subjected to local blast and classified using Metagenome@KIN (World Fusion, Tokyo, Japan). Results In total, 155 participants were recruited from seven medical centers. Of these, 88 and 67 had chronic otitis media and normal middle ears, respectively. The most abundant bacterial phyla on the mucosal surfaces of the normal middle ears were Proteobacteria, followed by Actinobacteria, Firmicutes, and Bacteroidetes. The children and adults with normal middle ears differed significantly in terms of middle ear microbiomes. Subjects with chronic otitis media without active inflammation (dry ear) had similar middle ear microbiomes as the normal middle ears group. Subjects with chronic otitis media with active inflammation (wet ear) had a lower prevalence of Proteobacteria and a higher prevalence of Firmicutes than the normal middle ears. Conclusion The human middle ear is inhabited by more diverse microbial communities than was previously thought. Alteration of the middle ear microbiome may contribute to the pathogenesis of chronic otitis media with active inflammation. Level of Evidence 2b. Laryngoscope , 127:E371–E377, 2017
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