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FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases

BACKGROUND: Influenza, measles, and mumps are common viral infectious diseases in Mongolia. The traditional Mongolian medicine (TMM) classified them as warm disease, and still plays a major role in the diagnoses and treatments. METHODS: To interpret the connotation of the complex theoretical system...

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Autores principales: Li, Li, Wu, Xiaoying, Eerdunchaolu, Qin, Wenyan, Yang, Yuqiu, Wang, Geriletu, He, Huili, Zhang, Husileng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320185/
https://www.ncbi.nlm.nih.gov/pubmed/30572452
http://dx.doi.org/10.1097/MD.0000000000013526
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author Li, Li
Wu, Xiaoying
Eerdunchaolu,
Qin, Wenyan
Yang, Yuqiu
Wang, Geriletu
He, Huili
Zhang, Husileng
author_facet Li, Li
Wu, Xiaoying
Eerdunchaolu,
Qin, Wenyan
Yang, Yuqiu
Wang, Geriletu
He, Huili
Zhang, Husileng
author_sort Li, Li
collection PubMed
description BACKGROUND: Influenza, measles, and mumps are common viral infectious diseases in Mongolia. The traditional Mongolian medicine (TMM) classified them as warm disease, and still plays a major role in the diagnoses and treatments. METHODS: To interpret the connotation of the complex theoretical system in TMM with scientific technique, in this study, a high throughput mass spectrometry was used to identify potential protein markers of TMM symptom types. Fifty venous blood samples were drawn from influenza, measles and mumps patients. Differential proteins between samples of patients diagnosed as immature and mature heat in TMM were detected by mass spectrometry. RESULTS: After proteomics analysis, 1500 proteins and 7619 polypeptides were identified and 1323 in total showed differential expression between those 2 symptom types; then enrichment analysis of the differentially expressed proteins revealed the significant biological functions related to the differentially expressed proteins, including cardiomyopathy, several bacterial and parasitic infections, bacterial invasion of epithelial cells, insulin signaling pathway, and regulation of actin cytoskeleton. The network analysis showed that FBP2 and Talin-1 were critical points and might determine the evolution directions of TMM warm disease symptom. CONCLUSIONS: This study suggests that the identified core differential proteins may be regarded as potential biomarkers, and benefit to evaluate the evolutionary tendency of TMM warm disease symptoms.
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spelling pubmed-63201852019-01-14 FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases Li, Li Wu, Xiaoying Eerdunchaolu, Qin, Wenyan Yang, Yuqiu Wang, Geriletu He, Huili Zhang, Husileng Medicine (Baltimore) Research Article BACKGROUND: Influenza, measles, and mumps are common viral infectious diseases in Mongolia. The traditional Mongolian medicine (TMM) classified them as warm disease, and still plays a major role in the diagnoses and treatments. METHODS: To interpret the connotation of the complex theoretical system in TMM with scientific technique, in this study, a high throughput mass spectrometry was used to identify potential protein markers of TMM symptom types. Fifty venous blood samples were drawn from influenza, measles and mumps patients. Differential proteins between samples of patients diagnosed as immature and mature heat in TMM were detected by mass spectrometry. RESULTS: After proteomics analysis, 1500 proteins and 7619 polypeptides were identified and 1323 in total showed differential expression between those 2 symptom types; then enrichment analysis of the differentially expressed proteins revealed the significant biological functions related to the differentially expressed proteins, including cardiomyopathy, several bacterial and parasitic infections, bacterial invasion of epithelial cells, insulin signaling pathway, and regulation of actin cytoskeleton. The network analysis showed that FBP2 and Talin-1 were critical points and might determine the evolution directions of TMM warm disease symptom. CONCLUSIONS: This study suggests that the identified core differential proteins may be regarded as potential biomarkers, and benefit to evaluate the evolutionary tendency of TMM warm disease symptoms. Wolters Kluwer Health 2018-12-21 /pmc/articles/PMC6320185/ /pubmed/30572452 http://dx.doi.org/10.1097/MD.0000000000013526 Text en Copyright © 2018 the Author(s). Published by Wolters Kluwer Health, Inc. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0
spellingShingle Research Article
Li, Li
Wu, Xiaoying
Eerdunchaolu,
Qin, Wenyan
Yang, Yuqiu
Wang, Geriletu
He, Huili
Zhang, Husileng
FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title_full FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title_fullStr FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title_full_unstemmed FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title_short FBP2 and Talin-1 are potential protein markers for Mongolian medicine symptom evaluation in viral infectious diseases
title_sort fbp2 and talin-1 are potential protein markers for mongolian medicine symptom evaluation in viral infectious diseases
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6320185/
https://www.ncbi.nlm.nih.gov/pubmed/30572452
http://dx.doi.org/10.1097/MD.0000000000013526
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