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Small RNA Profiles of Serum Exosomes Derived From Individuals With Latent and Active Tuberculosis.

作者信息

Lyu Lingna, Zhang Xiuli, Li Cuidan, Yang Tingting, Wang Jinghui, Pan Liping, Jia Hongyan, Li Zihui, Sun Qi, Yue Liya, Chen Fei, Zhang Zongde

机构信息

Beijing Key Laboratory for Drug Resistant Tuberculosis Research, Beijing Tuberculosis and Thoracic Tumor Research Institute, Beijing Chest Hospital, Capital Medical University, Beijing, China.

CAS Key Laboratory of Genome Science and Information, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China.

出版信息

Front Microbiol. 2019 May 28;10:1174. doi: 10.3389/fmicb.2019.01174. eCollection 2019.


DOI:10.3389/fmicb.2019.01174
PMID:31191492
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6546874/
Abstract

Tuberculosis (TB) has been the leading lethal infectious disease worldwide since 2014, and about one third of the world's population has a latent TB infection (LTBI). This is largely attributed to the difficulties in diagnosis and treatment of TB and LTBI patients. Exosomes offer a new perspective on investigation of the process of TB infection. In this study, we performed small RNA sequencing to explore small RNA profiles of serum exosomes derived from LTBI and TB patients and healthy controls (HC). Our results revealed distinct miRNA profile of the exosomes in the three groups. We screened 250 differentially expressed miRNAs including 130 specifically expressed miRNAs. Some miRNAs were further validated to be specifically expressed in LTBI (hsa-let-7e-5p, hsa-let-7d-5p, hsa-miR-450a-5p, and hsa-miR-140-5p) and TB samples (hsa-miR-1246, hsa-miR-2110, hsa-miR-370-3P, hsa-miR-28-3p, and hsa-miR-193b-5p). Additionally, we demonstrated four expression panels in LTBI and TB groups, and six expression patterns among the three groups. These specifically expressed miRNAs and differentially expressed miRNAs in different panels and patterns provide potential biomarkers for detection/diagnosis of latent and active TB using exosomal miRNAs. Additionally, we also discovered plenty of small RNAs derived from genomic repetitive sequences, which might play roles in host immune responses along with infection progresses. Overall, our findings provide important reference and an improved understanding about miRNAs and repetitive region-derived small RNAs in exosomes during the infectious process, and facilitate the development of potential molecular targets for detection/diagnosis of latent and active tuberculosis.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/0d67ea145124/fmicb-10-01174-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/2c2be6bd12b8/fmicb-10-01174-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/e79171250c8f/fmicb-10-01174-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/e2f9d7cd5fb2/fmicb-10-01174-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/eac0eb66c1f3/fmicb-10-01174-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/5d20dba7bbec/fmicb-10-01174-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/fe354baf5d9a/fmicb-10-01174-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/0d67ea145124/fmicb-10-01174-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/2c2be6bd12b8/fmicb-10-01174-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/e79171250c8f/fmicb-10-01174-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/e2f9d7cd5fb2/fmicb-10-01174-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/eac0eb66c1f3/fmicb-10-01174-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/5d20dba7bbec/fmicb-10-01174-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/fe354baf5d9a/fmicb-10-01174-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f2f/6546874/0d67ea145124/fmicb-10-01174-g007.jpg

相似文献

[1]
Small RNA Profiles of Serum Exosomes Derived From Individuals With Latent and Active Tuberculosis.

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[2]
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引用本文的文献

[1]
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Microorganisms. 2024-11-23

[2]
Circulating MicroRNAs as Biomarkers for the Early Diagnosis of Lung Cancer and Its Differentiation from Tuberculosis.

Diagnostics (Basel). 2024-11-28

[3]
Integrative analysis of circulating tumor cells (CTCs) and exosomes from small-cell lung cancer (SCLC) patients: a comprehensive approach.

Mol Oncol. 2024-11-22

[4]
Unveiling the promise: Exosomes as game-changers in anti-infective therapy.

Exploration (Beijing). 2024-3-12

[5]
The role of exosomal miRNAs in host pathogen cross-talk as diagnostic and therapeutic biomarkers.

Front Microbiol. 2024-8-8

[6]
Lipopolysaccharide-induced bacterial infection model: microRNA-370-3p participates in the anti-infection response by targeting the macrophage TLR4-NLRP3 caspase-1 cellular pyroptosis pathway.

Int J Immunopathol Pharmacol. 2024

[7]
Exosomal Small RNA Sequencing Profiles in Plasma from Subjects with Latent Infection.

Microorganisms. 2024-7-12

[8]
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J Extracell Biol. 2024-4-12

[9]
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[10]
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本文引用的文献

[1]
Cross-sectional Whole-genome Sequencing and Epidemiological Study of Multidrug-resistant Mycobacterium tuberculosis in China.

Clin Infect Dis. 2019-7-18

[2]
Pan-Genomic Study of Reflecting the Primary/Secondary Genes, Generality/Individuality, and the Interconversion Through Copy Number Variations.

Front Microbiol. 2018-8-17

[3]
A LINE1-Nucleolin Partnership Regulates Early Development and ESC Identity.

Cell. 2018-6-21

[4]
Identification of a plasma microRNA profile in untreated pulmonary tuberculosis patients that is modulated by anti-mycobacterial therapy.

J Infect. 2018-5-7

[5]
Characterization of a novel panel of plasma microRNAs that discriminates between Mycobacterium tuberculosis infection and healthy individuals.

PLoS One. 2017-9-14

[6]
RNA Profiling Analysis of the Serum Exosomes Derived from Patients with Active and Latent Infection.

Front Microbiol. 2017-6-12

[7]
MicroRNA-144-3p inhibits autophagy activation and enhances Bacillus Calmette-Guérin infection by targeting ATG4a in RAW264.7 macrophage cells.

PLoS One. 2017-6-21

[8]
MicroRNA 26a (miR-26a)/KLF4 and CREB-C/EBPβ regulate innate immune signaling, the polarization of macrophages and the trafficking of Mycobacterium tuberculosis to lysosomes during infection.

PLoS Pathog. 2017-5-30

[9]
The Bioinformatics Analysis of Comparative Genomics of Complex (MTBC) Provides Insight into Dissimilarities between Intraspecific Groups Differing in Host Association, Virulence, and Epitope Diversity.

Front Cell Infect Microbiol. 2017-3-21

[10]
Genome-wide mapping of infection-induced SINE RNAs reveals a role in selective mRNA export.

Nucleic Acids Res. 2017-6-2

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