Cargando…
A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas
The aim of this study was to characterize the mycobiome associated with oral squamous-cell carcinoma (OSCC). DNA was extracted from 52 tissue biopsies (cases: 25 OSCC; controls: 27 intra-oral fibro-epithelial polyps [FEP]) and sequenced for the fungal internal transcribed spacer 2 region using Illum...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678454/ https://www.ncbi.nlm.nih.gov/pubmed/29152157 http://dx.doi.org/10.1080/20002297.2017.1385369 |
_version_ | 1783277437533028352 |
---|---|
author | Perera, Manosha Al-hebshi, Nezar Noor Perera, Irosha Ipe, Deepak Ulett, Glen C. Speicher, David J. Chen, Tsute Johnson, Newell W. |
author_facet | Perera, Manosha Al-hebshi, Nezar Noor Perera, Irosha Ipe, Deepak Ulett, Glen C. Speicher, David J. Chen, Tsute Johnson, Newell W. |
author_sort | Perera, Manosha |
collection | PubMed |
description | The aim of this study was to characterize the mycobiome associated with oral squamous-cell carcinoma (OSCC). DNA was extracted from 52 tissue biopsies (cases: 25 OSCC; controls: 27 intra-oral fibro-epithelial polyps [FEP]) and sequenced for the fungal internal transcribed spacer 2 region using Illumina™ 2 x300bp chemistry. Merged reads were classified to species level using a BLASTN-algorithm with UNITE’s named species sequences as reference. Downstream analyses were performed using QIIME™ and linear discriminant analysis effect size. A total of 364 species representing 160 genera and two phyla (Ascomycota and Basidiomycota) were identified, with Candida and Malassezia making up 48% and 11% of the average mycobiome, respectively. However, only five species and four genera were detected in ≥50% of the samples. The species richness and diversity were significantly lower in OSCC. Genera Candida, Hannaella, and Gibberella were overrepresented in OSCC; Alternaria and Trametes were more abundant in FEP. Species-wise, Candida albicans, Candida etchellsii, and a Hannaella luteola–like species were enriched in OSCC, while a Hanseniaspora uvarum–like species, Malassezia restricta, and Aspergillus tamarii were the most significantly abundant in FEP. In conclusion, a dysbiotic mycobiome dominated by C. albicans was found in association with OSCC, a finding worth further investigation. |
format | Online Article Text |
id | pubmed-5678454 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-56784542017-11-17 A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas Perera, Manosha Al-hebshi, Nezar Noor Perera, Irosha Ipe, Deepak Ulett, Glen C. Speicher, David J. Chen, Tsute Johnson, Newell W. J Oral Microbiol Original Article The aim of this study was to characterize the mycobiome associated with oral squamous-cell carcinoma (OSCC). DNA was extracted from 52 tissue biopsies (cases: 25 OSCC; controls: 27 intra-oral fibro-epithelial polyps [FEP]) and sequenced for the fungal internal transcribed spacer 2 region using Illumina™ 2 x300bp chemistry. Merged reads were classified to species level using a BLASTN-algorithm with UNITE’s named species sequences as reference. Downstream analyses were performed using QIIME™ and linear discriminant analysis effect size. A total of 364 species representing 160 genera and two phyla (Ascomycota and Basidiomycota) were identified, with Candida and Malassezia making up 48% and 11% of the average mycobiome, respectively. However, only five species and four genera were detected in ≥50% of the samples. The species richness and diversity were significantly lower in OSCC. Genera Candida, Hannaella, and Gibberella were overrepresented in OSCC; Alternaria and Trametes were more abundant in FEP. Species-wise, Candida albicans, Candida etchellsii, and a Hannaella luteola–like species were enriched in OSCC, while a Hanseniaspora uvarum–like species, Malassezia restricta, and Aspergillus tamarii were the most significantly abundant in FEP. In conclusion, a dysbiotic mycobiome dominated by C. albicans was found in association with OSCC, a finding worth further investigation. Taylor & Francis 2017-10-27 /pmc/articles/PMC5678454/ /pubmed/29152157 http://dx.doi.org/10.1080/20002297.2017.1385369 Text en © 2017 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Perera, Manosha Al-hebshi, Nezar Noor Perera, Irosha Ipe, Deepak Ulett, Glen C. Speicher, David J. Chen, Tsute Johnson, Newell W. A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title | A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title_full | A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title_fullStr | A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title_full_unstemmed | A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title_short | A dysbiotic mycobiome dominated by Candida albicans is identified within oral squamous-cell carcinomas |
title_sort | dysbiotic mycobiome dominated by candida albicans is identified within oral squamous-cell carcinomas |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5678454/ https://www.ncbi.nlm.nih.gov/pubmed/29152157 http://dx.doi.org/10.1080/20002297.2017.1385369 |
work_keys_str_mv | AT pereramanosha adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT alhebshinezarnoor adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT pererairosha adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT ipedeepak adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT ulettglenc adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT speicherdavidj adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT chentsute adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT johnsonnewellw adysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT pereramanosha dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT alhebshinezarnoor dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT pererairosha dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT ipedeepak dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT ulettglenc dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT speicherdavidj dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT chentsute dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas AT johnsonnewellw dysbioticmycobiomedominatedbycandidaalbicansisidentifiedwithinoralsquamouscellcarcinomas |