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Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors
SIMPLE SUMMARY: In this study, we evaluated the microbiota in resected thymoma samples and identified Sphingomonas and Phenylobacterium as the dominant genera in thymomas. This is the first study that evaluated the microbiota in thymoma and that identified bacterial genera specific to thymoma. Furth...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623653/ https://www.ncbi.nlm.nih.gov/pubmed/34834444 http://dx.doi.org/10.3390/jpm11111092 |
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author | Higuchi, Rumi Goto, Taichiro Hirotsu, Yosuke Otake, Sotaro Oyama, Toshio Amemiya, Kenji Ohyama, Hiroshi Mochizuki, Hitoshi Omata, Masao |
author_facet | Higuchi, Rumi Goto, Taichiro Hirotsu, Yosuke Otake, Sotaro Oyama, Toshio Amemiya, Kenji Ohyama, Hiroshi Mochizuki, Hitoshi Omata, Masao |
author_sort | Higuchi, Rumi |
collection | PubMed |
description | SIMPLE SUMMARY: In this study, we evaluated the microbiota in resected thymoma samples and identified Sphingomonas and Phenylobacterium as the dominant genera in thymomas. This is the first study that evaluated the microbiota in thymoma and that identified bacterial genera specific to thymoma. Furthermore, our study indicates a potential approach for preventing the development of thymoma as a new “precision medicine”. ABSTRACT: The microbiota has been reported to be closely associated with carcinogenesis and cancer progression. However, its involvement in the pathology of thymoma remains unknown. In this study, we aimed to identify thymoma-specific microbiota using resected thymoma samples. Nineteen thymoma tissue samples were analyzed through polymerase chain reaction amplification and 16S rRNA gene sequencing. The subjects were grouped according to histology, driver mutation status in the GTF2I gene, PD-L1 status, and smoking habits. To identify the taxa composition of each sample, the operational taxonomic units (OTUs) were classified on the effective tags with 97% identity. The Shannon Index of the 97% identity OTUs was calculated to evaluate the alpha diversity. The linear discriminant analysis effect size (LEfSe) method was used to compare the relative abundances of all the bacterial taxa. We identified 107 OTUs in the tumor tissues, which were classified into 26 genera. Sphingomonas and Phenylobacterium were identified as abundant genera in almost all the samples. No significant difference was determined in the alpha diversity within these groups; however, type A thymoma tended to exhibit a higher bacterial diversity than type B thymoma. Through the LEfSe analysis, we identified the following differentially abundant taxa: Bacilli, Firmicutes, and Lactobacillales in type A thymoma; Proteobacteria in type B thymoma; Gammaproteobacteria in tumors harboring the GTF2I mutation; and Alphaproteobacteria in tumors without the GTF2I mutation. In conclusion, Sphingomonas and Phenylobacterium were identified as dominant genera in thymic epithelial tumors. These genera appear to comprise the thymoma-specific microbiota. |
format | Online Article Text |
id | pubmed-8623653 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86236532021-11-27 Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors Higuchi, Rumi Goto, Taichiro Hirotsu, Yosuke Otake, Sotaro Oyama, Toshio Amemiya, Kenji Ohyama, Hiroshi Mochizuki, Hitoshi Omata, Masao J Pers Med Article SIMPLE SUMMARY: In this study, we evaluated the microbiota in resected thymoma samples and identified Sphingomonas and Phenylobacterium as the dominant genera in thymomas. This is the first study that evaluated the microbiota in thymoma and that identified bacterial genera specific to thymoma. Furthermore, our study indicates a potential approach for preventing the development of thymoma as a new “precision medicine”. ABSTRACT: The microbiota has been reported to be closely associated with carcinogenesis and cancer progression. However, its involvement in the pathology of thymoma remains unknown. In this study, we aimed to identify thymoma-specific microbiota using resected thymoma samples. Nineteen thymoma tissue samples were analyzed through polymerase chain reaction amplification and 16S rRNA gene sequencing. The subjects were grouped according to histology, driver mutation status in the GTF2I gene, PD-L1 status, and smoking habits. To identify the taxa composition of each sample, the operational taxonomic units (OTUs) were classified on the effective tags with 97% identity. The Shannon Index of the 97% identity OTUs was calculated to evaluate the alpha diversity. The linear discriminant analysis effect size (LEfSe) method was used to compare the relative abundances of all the bacterial taxa. We identified 107 OTUs in the tumor tissues, which were classified into 26 genera. Sphingomonas and Phenylobacterium were identified as abundant genera in almost all the samples. No significant difference was determined in the alpha diversity within these groups; however, type A thymoma tended to exhibit a higher bacterial diversity than type B thymoma. Through the LEfSe analysis, we identified the following differentially abundant taxa: Bacilli, Firmicutes, and Lactobacillales in type A thymoma; Proteobacteria in type B thymoma; Gammaproteobacteria in tumors harboring the GTF2I mutation; and Alphaproteobacteria in tumors without the GTF2I mutation. In conclusion, Sphingomonas and Phenylobacterium were identified as dominant genera in thymic epithelial tumors. These genera appear to comprise the thymoma-specific microbiota. MDPI 2021-10-26 /pmc/articles/PMC8623653/ /pubmed/34834444 http://dx.doi.org/10.3390/jpm11111092 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Higuchi, Rumi Goto, Taichiro Hirotsu, Yosuke Otake, Sotaro Oyama, Toshio Amemiya, Kenji Ohyama, Hiroshi Mochizuki, Hitoshi Omata, Masao Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title | Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title_full | Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title_fullStr | Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title_full_unstemmed | Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title_short | Sphingomonas and Phenylobacterium as Major Microbiota in Thymic Epithelial Tumors |
title_sort | sphingomonas and phenylobacterium as major microbiota in thymic epithelial tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8623653/ https://www.ncbi.nlm.nih.gov/pubmed/34834444 http://dx.doi.org/10.3390/jpm11111092 |
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