Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment

Background. Microbes have been shown to contribute to gastric cancer (GC), gastric bacteria and viruses are associated with gastric carcinogenesis. However, the relationship between gastric fungi and GC is still unclear. Our aim was to evaluate the gastric fungal microbiota in the GC microenvironmen...

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Main Authors: Zhenzhan Zhang, Hao Feng, Yaopeng Qiu, Zhou Xu, Qingfeng Xie, Wenfu Ding, Hao Liu, Guoxin Li
Format: Article
Language:English
Published: Wiley 2022-01-01
Series:Journal of Immunology Research
Online Access:http://dx.doi.org/10.1155/2022/6011632
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author Zhenzhan Zhang
Hao Feng
Yaopeng Qiu
Zhou Xu
Qingfeng Xie
Wenfu Ding
Hao Liu
Guoxin Li
author_facet Zhenzhan Zhang
Hao Feng
Yaopeng Qiu
Zhou Xu
Qingfeng Xie
Wenfu Ding
Hao Liu
Guoxin Li
author_sort Zhenzhan Zhang
collection DOAJ
description Background. Microbes have been shown to contribute to gastric cancer (GC), gastric bacteria and viruses are associated with gastric carcinogenesis. However, the relationship between gastric fungi and GC is still unclear. Our aim was to evaluate the gastric fungal microbiota in the GC microenvironment. Methods. Gastric fungal microbiome profiling was performed with internal transcribed spacer (ITS) rDNA sequencing in primary tumor and corresponding paired normal mucosal tissues from 61 GC patients. Differences in microbial composition, taxa diversity, and predicted function were further analyzed. Results. Dysbiosis of gastric mucosal fungal microbiome was observed between the tumor and normal groups in GC. The tumor group had a higher abundance of certain taxa than the normal group. In the taxa classification, the abundances of Pezizomycetes, Sordariales, Chaetomiaceae, and Rozellomycota were lower in the tumor group than in the normal group. At the genus level, Solicoccozyma (P=0.033) was found in higher abundance and was differentially enriched in the tumor group with Lefse analysis. Additionally, Solicoccozyma accounted for 0.3% of gastric fungi in the GC microenvironment. Twenty-seven of the 61 GC patients showed positive Solicoccozyma expression in tumors. Solicoccozyma-positive expression in tumors was associated with the Bormann classification and nerve invasion. Solicoccozyma was considered a gastric fungal marker to classify stage I and stage II-IV GC patients with an area under the receiver-operating curve (AUC) of 0.7061, as well as to classify the nerve invasive and nonnerve invasive tumors from GC patients with an AUC of 0.6978. Functional prediction indicated that the positive expression of Solicoccozyma in tumors was associated with the amino acid- and carbohydrate-related metabolic pathways in GC. Conclusions. This study revealed a novel perspective on the role of Solicoccozyma in tumors and a theoretical basis for therapeutic targets against GC.
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spelling doaj-art-45174597d42f48c6a0bda2ecc2001c2a2025-02-03T06:01:51ZengWileyJournal of Immunology Research2314-71562022-01-01202210.1155/2022/6011632Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer MicroenvironmentZhenzhan Zhang0Hao Feng1Yaopeng Qiu2Zhou Xu3Qingfeng Xie4Wenfu Ding5Hao Liu6Guoxin Li7Department of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorDepartment of General Surgery & Guangdong Provincial Key Laboratory of Precision Medicine for Gastrointestinal TumorBackground. Microbes have been shown to contribute to gastric cancer (GC), gastric bacteria and viruses are associated with gastric carcinogenesis. However, the relationship between gastric fungi and GC is still unclear. Our aim was to evaluate the gastric fungal microbiota in the GC microenvironment. Methods. Gastric fungal microbiome profiling was performed with internal transcribed spacer (ITS) rDNA sequencing in primary tumor and corresponding paired normal mucosal tissues from 61 GC patients. Differences in microbial composition, taxa diversity, and predicted function were further analyzed. Results. Dysbiosis of gastric mucosal fungal microbiome was observed between the tumor and normal groups in GC. The tumor group had a higher abundance of certain taxa than the normal group. In the taxa classification, the abundances of Pezizomycetes, Sordariales, Chaetomiaceae, and Rozellomycota were lower in the tumor group than in the normal group. At the genus level, Solicoccozyma (P=0.033) was found in higher abundance and was differentially enriched in the tumor group with Lefse analysis. Additionally, Solicoccozyma accounted for 0.3% of gastric fungi in the GC microenvironment. Twenty-seven of the 61 GC patients showed positive Solicoccozyma expression in tumors. Solicoccozyma-positive expression in tumors was associated with the Bormann classification and nerve invasion. Solicoccozyma was considered a gastric fungal marker to classify stage I and stage II-IV GC patients with an area under the receiver-operating curve (AUC) of 0.7061, as well as to classify the nerve invasive and nonnerve invasive tumors from GC patients with an AUC of 0.6978. Functional prediction indicated that the positive expression of Solicoccozyma in tumors was associated with the amino acid- and carbohydrate-related metabolic pathways in GC. Conclusions. This study revealed a novel perspective on the role of Solicoccozyma in tumors and a theoretical basis for therapeutic targets against GC.http://dx.doi.org/10.1155/2022/6011632
spellingShingle Zhenzhan Zhang
Hao Feng
Yaopeng Qiu
Zhou Xu
Qingfeng Xie
Wenfu Ding
Hao Liu
Guoxin Li
Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
Journal of Immunology Research
title Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
title_full Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
title_fullStr Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
title_full_unstemmed Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
title_short Dysbiosis of Gastric Mucosal Fungal Microbiota in the Gastric Cancer Microenvironment
title_sort dysbiosis of gastric mucosal fungal microbiota in the gastric cancer microenvironment
url http://dx.doi.org/10.1155/2022/6011632
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