Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis

Abstract Background This study aimed to investigate the differences in the microbiota composition of serum exosomes from patients with acute and chronic cholecystitis. Method Exosomes were isolated from the serum of cholecystitis patients through centrifugation and identified and characterized using...

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Main Authors: Qing Zhu, Min-Xian Li, Ming-Chin Yu, Qi-Wen Ma, Ming-Jie Huang, Chun-Wei Lu, Chun-Bing Chen, Wen-Hung Chung, Chih-Jung Chang
Format: Article
Language:English
Published: BMC 2024-04-01
Series:BMC Microbiology
Subjects:
Online Access:https://doi.org/10.1186/s12866-024-03269-6
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author Qing Zhu
Min-Xian Li
Ming-Chin Yu
Qi-Wen Ma
Ming-Jie Huang
Chun-Wei Lu
Chun-Bing Chen
Wen-Hung Chung
Chih-Jung Chang
author_facet Qing Zhu
Min-Xian Li
Ming-Chin Yu
Qi-Wen Ma
Ming-Jie Huang
Chun-Wei Lu
Chun-Bing Chen
Wen-Hung Chung
Chih-Jung Chang
author_sort Qing Zhu
collection DOAJ
description Abstract Background This study aimed to investigate the differences in the microbiota composition of serum exosomes from patients with acute and chronic cholecystitis. Method Exosomes were isolated from the serum of cholecystitis patients through centrifugation and identified and characterized using transmission electron microscopy and nano-flow cytometry. Microbiota analysis was performed using 16S rRNA sequencing. Results Compared to patients with chronic cholecystitis, those with acute cholecystitis exhibited lower richness and diversity. Beta diversity analysis revealed significant differences in the microbiota composition between patients with acute and chronic cholecystitis. The relative abundance of Proteobacteria was significantly higher in exosomes from patients with acute cholecystitis, whereas Actinobacteria, Bacteroidetes, and Firmicutes were significantly more abundant in exosomes from patients with chronic cholecystitis. Furthermore, functional predictions of microbial communities using Tax4Fun analysis revealed significant differences in metabolic pathways such as amino acid metabolism, carbohydrate metabolism, and membrane transport between the two patient groups. Conclusions This study confirmed the differences in the microbiota composition within serum exosomes of patients with acute and chronic cholecystitis. Serum exosomes could serve as diagnostic indicators for distinguishing acute and chronic cholecystitis.
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spelling doaj.art-d8d47e4ce40040b08022f21d3d0b91fe2024-04-21T11:10:42ZengBMCBMC Microbiology1471-21802024-04-0124111210.1186/s12866-024-03269-6Altered microbiome of serum exosomes in patients with acute and chronic cholecystitisQing Zhu0Min-Xian Li1Ming-Chin Yu2Qi-Wen Ma3Ming-Jie Huang4Chun-Wei Lu5Chun-Bing Chen6Wen-Hung Chung7Chih-Jung Chang8Department of Surgery, Xiamen Chang Gung Hospital Hua Qiao UniversityDepartment of Surgery, Xiamen Chang Gung Hospital Hua Qiao UniversityDepartment of Surgery, Xiamen Chang Gung Hospital Hua Qiao UniversitySchool of Medicine and Medical Research Center, Xiamen Chang Gung Hospital Hua Qiao UniversitySchool of Medicine and Medical Research Center, Xiamen Chang Gung Hospital Hua Qiao UniversityDrug Hypersensitivity Clinical and Research Center, Department of Dermatology, Chang Gung Memorial HospitalDrug Hypersensitivity Clinical and Research Center, Department of Dermatology, Chang Gung Memorial HospitalSchool of Medicine and Medical Research Center, Xiamen Chang Gung Hospital Hua Qiao UniversitySchool of Medicine and Medical Research Center, Xiamen Chang Gung Hospital Hua Qiao UniversityAbstract Background This study aimed to investigate the differences in the microbiota composition of serum exosomes from patients with acute and chronic cholecystitis. Method Exosomes were isolated from the serum of cholecystitis patients through centrifugation and identified and characterized using transmission electron microscopy and nano-flow cytometry. Microbiota analysis was performed using 16S rRNA sequencing. Results Compared to patients with chronic cholecystitis, those with acute cholecystitis exhibited lower richness and diversity. Beta diversity analysis revealed significant differences in the microbiota composition between patients with acute and chronic cholecystitis. The relative abundance of Proteobacteria was significantly higher in exosomes from patients with acute cholecystitis, whereas Actinobacteria, Bacteroidetes, and Firmicutes were significantly more abundant in exosomes from patients with chronic cholecystitis. Furthermore, functional predictions of microbial communities using Tax4Fun analysis revealed significant differences in metabolic pathways such as amino acid metabolism, carbohydrate metabolism, and membrane transport between the two patient groups. Conclusions This study confirmed the differences in the microbiota composition within serum exosomes of patients with acute and chronic cholecystitis. Serum exosomes could serve as diagnostic indicators for distinguishing acute and chronic cholecystitis.https://doi.org/10.1186/s12866-024-03269-6CholecystitisExosomesMicrobiota composition16S rRNA sequencing
spellingShingle Qing Zhu
Min-Xian Li
Ming-Chin Yu
Qi-Wen Ma
Ming-Jie Huang
Chun-Wei Lu
Chun-Bing Chen
Wen-Hung Chung
Chih-Jung Chang
Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
BMC Microbiology
Cholecystitis
Exosomes
Microbiota composition
16S rRNA sequencing
title Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
title_full Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
title_fullStr Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
title_full_unstemmed Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
title_short Altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
title_sort altered microbiome of serum exosomes in patients with acute and chronic cholecystitis
topic Cholecystitis
Exosomes
Microbiota composition
16S rRNA sequencing
url https://doi.org/10.1186/s12866-024-03269-6
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