Comprehensive microbiome analysis of tonsillar crypts in IgA nephropathy

• Published in: Nephrology, dialysis, transplantation Vol. 32; no. 12; pp. 2072 - 2079
• Main Authors: Watanabe, Hirofumi, Goto, Shin, Mori, Hiroshi, Higashi, Koichi, Hosomichi, Kazuyoshi, Aizawa, Naotaka, Takahashi, Nao, Tsuchida, Masafumi, Suzuki, Yusuke, Yamada, Takuji, Horii, Arata, Inoue, Ituro, Kurokawa, Ken, Narita, Ichiei
• Format: Journal Article
• Language: English
• Published: England 01.12.2017
• Subjects: Adult; Child; Female; Glomerulonephritis, IGA - genetics; Glomerulonephritis, IGA - microbiology; Glomerulonephritis, IGA - pathology; Glomerulonephritis, IGA - surgery; Humans; Hyperplasia - genetics; Hyperplasia - microbiology; Hyperplasia - pathology; Hyperplasia - surgery; Male; Microbiota - genetics; Palatine Tonsil - metabolism; Palatine Tonsil - microbiology; RNA, Bacterial - genetics; RNA, Ribosomal, 16S - genetics; Tonsillectomy; Tonsillitis - genetics; Tonsillitis - microbiology; Tonsillitis - pathology; Tonsillitis - surgery; tonsil; recurrent tonsillitis; IgA nephropathy; 16S ribosomal RNA; microbiome
• DOI: 10.1093/ndt/gfw343
• ISSN: 0931-0509

Immunoglobulin A nephropathy (IgAN) is the most prevalent primary chronic glomerular disease, in which the mucosal immune response elicited particularly in the tonsils or intestine has been estimated to be involved in the development of the disease. To explore the relationship between IgAN and bacterial flora in the tonsils, we conducted a comprehensive microbiome analysis. We enrolled 48 IgAN patients, 21 recurrent tonsillitis (RT) patients without urine abnormalities and 30 children with tonsillar hyperplasia (TH) who had undergone tonsillectomy previously. Genomic DNA from tonsillar crypts of each patient was extracted, and V4 regions of the 16S ribosomal RNA gene were amplified and analysed using a high-throughput multiplexed sequencing approach. Differences in genus composition among the three study groups were statistically analysed by permutational multivariate analysis of variance and visualized by principal component analysis (PCA). Substantial diversity in bacterial composition was detected in each sample. Prevotella spp., Fusobacterium spp., Sphingomonas spp. and Treponema spp. were predominant in IgAN patients. The percentage of abundance of Prevotella spp., Haemophilus spp., Porphyromonas spp. and Treponema spp. in IgAN patients was significantly different from that in TH patients. However, there was no significant difference in the percentage of abundance of any bacterial genus between IgAN and RT patients. PCA did not distinguish IgAN from RT, although it discriminated TH. No significant differences in microbiome composition among the groups of IgAN patients according to clinicopathological parameters were observed. Similar patterns of bacteria are present in tonsillar crypts of both IgAN and RT patients, suggesting that the host response to these bacteria might be important in the development of IgAN.