Cargando…

Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study

PURPOSE: Syphilis is a sexually transmitted bacterial infection caused by Treponema pallidum (T. pallidum), which can lead to chronic morbidity and adverse complications. In clinical practice, serofast status (SF) patients present with clinical symptoms that are very similar to those of healthy indi...

Descripción completa

Detalles Bibliográficos
Autores principales: Liu, Jinquan, Zhang, Ruihua, Lian, Tingting, Chen, Zuoxi, Zhang, Rui-Li, Wang, Qianqiu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124566/
https://www.ncbi.nlm.nih.gov/pubmed/37101664
http://dx.doi.org/10.2147/IJGM.S404545
_version_ 1785029863313244160
author Liu, Jinquan
Zhang, Ruihua
Lian, Tingting
Chen, Zuoxi
Zhang, Rui-Li
Wang, Qianqiu
author_facet Liu, Jinquan
Zhang, Ruihua
Lian, Tingting
Chen, Zuoxi
Zhang, Rui-Li
Wang, Qianqiu
author_sort Liu, Jinquan
collection PubMed
description PURPOSE: Syphilis is a sexually transmitted bacterial infection caused by Treponema pallidum (T. pallidum), which can lead to chronic morbidity and adverse complications. In clinical practice, serofast status (SF) patients present with clinical symptoms that are very similar to those of healthy individuals or syphilis-cured patients, and often require prolonged follow-up for diagnosis. Currently, there is increasing interest in the potential of plasma exosome-derived miRNA as a biomarker for the detection of infectious diseases. In this study, we aimed to explore the diagnostic potential of miRNA in SF and its possible biological implications. PATIENTS AND METHODS: Exosome-derived miRNAs were isolated from peripheral plasma samples obtained from 20 patients with secondary syphilis (SS), SF, serologically cured syphilis (SC), and healthy controls (HC), and differentially expressed miRNAs (DEmiRNAs) were identified by microarray analysis. Prediction of potential target genes, functional annotation, gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were then performed. The expression of selected miRNAs was confirmed in 37 patients by quantitative reverse transcription polymerase chain reaction (RT-qPCR). A receiver operating characteristic (ROC) analysis was performed to evaluate the diagnostic performance of these miRNAs in differentiating syphilis from HC or SC. RESULTS: The expression profile of plasma exosome-derived miRNA was discovered in individuals with SF through microarray analysis. The targeted genes of DEmiRNAs were found to be involved in diverse biological processes according to GO and KEGG analysis, such as regulation of transcription, mitochondria, Golgi, immune system, apoptosis, Ras signaling pathway, etc. Using RT-qPCR validation, miR-1273g-3p, miR-4485-5p, miR-197-3p, and miR-1908-3p showed significant upregulation in patients with SF. These miRNAs exhibited a superior diagnostic ability, either individually or combined, to distinguish SF from SC or HC. CONCLUSION: The DEmiRNAs in plasma exosomes may play a role in the pathogenesis of SF and have the potential to become a noble and effective diagnostic method.
format Online
Article
Text
id pubmed-10124566
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-101245662023-04-25 Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study Liu, Jinquan Zhang, Ruihua Lian, Tingting Chen, Zuoxi Zhang, Rui-Li Wang, Qianqiu Int J Gen Med Original Research PURPOSE: Syphilis is a sexually transmitted bacterial infection caused by Treponema pallidum (T. pallidum), which can lead to chronic morbidity and adverse complications. In clinical practice, serofast status (SF) patients present with clinical symptoms that are very similar to those of healthy individuals or syphilis-cured patients, and often require prolonged follow-up for diagnosis. Currently, there is increasing interest in the potential of plasma exosome-derived miRNA as a biomarker for the detection of infectious diseases. In this study, we aimed to explore the diagnostic potential of miRNA in SF and its possible biological implications. PATIENTS AND METHODS: Exosome-derived miRNAs were isolated from peripheral plasma samples obtained from 20 patients with secondary syphilis (SS), SF, serologically cured syphilis (SC), and healthy controls (HC), and differentially expressed miRNAs (DEmiRNAs) were identified by microarray analysis. Prediction of potential target genes, functional annotation, gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were then performed. The expression of selected miRNAs was confirmed in 37 patients by quantitative reverse transcription polymerase chain reaction (RT-qPCR). A receiver operating characteristic (ROC) analysis was performed to evaluate the diagnostic performance of these miRNAs in differentiating syphilis from HC or SC. RESULTS: The expression profile of plasma exosome-derived miRNA was discovered in individuals with SF through microarray analysis. The targeted genes of DEmiRNAs were found to be involved in diverse biological processes according to GO and KEGG analysis, such as regulation of transcription, mitochondria, Golgi, immune system, apoptosis, Ras signaling pathway, etc. Using RT-qPCR validation, miR-1273g-3p, miR-4485-5p, miR-197-3p, and miR-1908-3p showed significant upregulation in patients with SF. These miRNAs exhibited a superior diagnostic ability, either individually or combined, to distinguish SF from SC or HC. CONCLUSION: The DEmiRNAs in plasma exosomes may play a role in the pathogenesis of SF and have the potential to become a noble and effective diagnostic method. Dove 2023-04-20 /pmc/articles/PMC10124566/ /pubmed/37101664 http://dx.doi.org/10.2147/IJGM.S404545 Text en © 2023 Liu et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Liu, Jinquan
Zhang, Ruihua
Lian, Tingting
Chen, Zuoxi
Zhang, Rui-Li
Wang, Qianqiu
Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title_full Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title_fullStr Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title_full_unstemmed Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title_short Plasma Exosome-Derived microRNAs Profiles in Patients with Serofast Status: A Cross-Sectional Study
title_sort plasma exosome-derived micrornas profiles in patients with serofast status: a cross-sectional study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10124566/
https://www.ncbi.nlm.nih.gov/pubmed/37101664
http://dx.doi.org/10.2147/IJGM.S404545
work_keys_str_mv AT liujinquan plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy
AT zhangruihua plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy
AT liantingting plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy
AT chenzuoxi plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy
AT zhangruili plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy
AT wangqianqiu plasmaexosomederivedmicrornasprofilesinpatientswithserofaststatusacrosssectionalstudy