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A potential marker in brucellosis, long non coding RNA IFNG-AS1.
Gheitasi, Reza; Jourghasemi, Sanaz; Pakzad, Iraj; Hosseinpour Sarmadi, Vahid; Samieipour, Yazdan; Sekawi, Zamberi; Azizi Jalilian, Farid.
Afiliación
  • Gheitasi R; Department of Immunology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
  • Jourghasemi S; Department of Immunology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.
  • Pakzad I; Department Microbiology, Faculty of Medicine and Clinical Microbiology Research Center, Ilam University of Medical Sciences, Ilam, Iran.
  • Hosseinpour Sarmadi V; Department of Immunology, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran.
  • Samieipour Y; Institute of Virology, Technical University of Munich, Munich, Germany.
  • Sekawi Z; Department of Medical Microbiology and Parasitology, Faculty of Medicine and Health Sciences, University Putra Malaysia, 43400, Serdang, Selangor, Malaysia.
  • Azizi Jalilian F; Department of Medical Virology, Faculty of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran. azizifarid@gmail.com.
Mol Biol Rep ; 46(6): 6495-6500, 2019 Dec.
Article en En | MEDLINE | ID: mdl-31595441
ABSTRACT
Brucellosis is the most common bacterial zoonotic infection. This pathogen may survive and sustain in host. The aim of this study is to define relationship between long noncoding (lnc) RNA-IFNG-AS1 and interferon gamma (IFN-γ) in different groups of patients with brucellosis compared to control group. In this study, associations of lncRNA IFNG-AS1 expression with secretion of IFN-γ level in Sixty patients with brucellosis, which were divided into 3 groups (acute, chronic and relapse groups), as a case group were compared with 20 subjects with negative serological tests and brucellosis clinical manifestation as a control group. In this regard, RNA were extracted from isolated peripheral blood mononuclear cells (PBMCs). LncRNA IFNG-AS1, T-box transcription factor (T-bet) and IFN-γ expressions were detected using quantitative polymerase chain reaction (qPCR). Serum level IFN-γ was assessed using enzyme linked immunosorbent assay (ELISA). The results showed that expression level of LncRNA IFNG-AS1, T-bet and IFN-γ increased significantly in all patient groups in compared to healthy subjects (P < 0.0001, P < 0.01, P < 0.001). However, there was no significant difference in T-bet expression between chronic and healthy groups (P = 0.98). Additionally, further analysis revealed that the serum level of IFN-γ in acute and relapsed groups were higher than control group (P < 0.0001, P < 0.001). The effective role of IFNG-AS1 in many protective actions, including enhancing the expression of INF-γ in the immune response of brucellosis patients, revealed new potential marker, LncRNA IFNG-AS1 in screening, diagnosis or treatment of brucellosis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Brucelosis / Marcadores Genéticos / Regulación hacia Arriba / ARN Largo no Codificante Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Biol Rep Año: 2019 Tipo del documento: Article País de afiliación: Irán

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Brucelosis / Marcadores Genéticos / Regulación hacia Arriba / ARN Largo no Codificante Tipo de estudio: Observational_studies / Risk_factors_studies Límite: Adolescent / Adult / Aged / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Mol Biol Rep Año: 2019 Tipo del documento: Article País de afiliación: Irán