Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/29535
Title: Altered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosis
Authors: Uludağ Üniversitesi/Tıp Fakültesi/İmmünoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Biyoloji Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Klinik Mikrobiyoloji ve Enfeksiyon Hastalıkları Anabilim Dalı.
Uludağ Üniversitesi/Tıp Fakültesi/Tıbbi Mikrobiyoloji Anabilim Dalı.
0000-0003-0463-6818
0000-0002-5956-8755
Budak, Ferah
Bal, Salih Haldun
Tezcan, Gülçin
Akalın, Halis
Göral, Güher
Oral, Haluk Barbaros
K-7285-2012
AAU-8952-2020
F-4657-2014
F-8554-2017
AAH-3843-2020
6701913697
57191480128
25650627600
57207553671
6603453166
7004498001
Keywords: Immunology
Dendritic cell maturation
B-virus infection
Microrna expression
Gene-expression
Up-regulation
Integrated analysis
Abortus invasion
Down-regulation
Cancer cells
TNF-alpha
Issue Date: 31-Jul-2016
Publisher: Hindawi
Citation: Budak, F. vd. (2016). "Altered expressions of miR-1238-3p, miR-494, miR-6069, and miR-139-3p in the formation of chronic Brucellosis". Journal of Immunology Research, 2016, 1-11.
Abstract: Brucellosis is a zoonotic disease that is still endemic in developing countries. Despite early diagnosis and treatment of patients, chronic infections are seen in 10-30% of patients. In this study, we aimed to investigate the immunological factors that play roles in the transition of brucellosis from acute infection into chronic infection. Here, more than 2000 miRNAs were screened in peripheral blood mononuclear cells (PBMCs) of patients with acute or chronic brucellosis and healthy controls by using miRNA array, and the results of the miRNA array were validated through qRT-PCR. Findings were evaluated using GeneSpring GX (Agilent) 13.0 software and KEGG pathway analysis. Four miRNAs were expressed in the chronic group but were not expressed in acute and control groups. Among these miRNAs, the expression level of miR-1238-3p was increased while miR-494, miR-6069, and miR-1393p were decreased (p< 0.05, fold change > 2). These miRNAs have the potential to be markers for chronic cases. The differentially expressed miRNAs and their predicted target genes involved in endocytosis, regulation of actin cytoskeleton, MAPK signaling pathway, and cytokine-cytokine receptor interaction and its chemokine signaling pathway indicate their potential roles in chronic brucellosis and its progression. It is the first study of miRNA expression analysis of human PBMC to clarify the mechanism of inveteracy in brucellosis.
URI: https://doi.org/10.1155/2016/4591468
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5046029/
http://hdl.handle.net/11452/29535
ISSN: 2314-8861
2314-7156
Appears in Collections:Scopus
Web of Science

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