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The relation of NCCR variations and host transcription factors gene regulation in BK polyomavirus infected kidney transplant patients.
Sahragard, Ilnaz; Mohammadi, Ali; Yaghobi, Ramin; Pakfetrat, Maryam; Afshari, Afsoon; Sharifi, Hassan; Ghaemi, Mehran.
Affiliation
  • Sahragard I; Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
  • Mohammadi A; Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
  • Yaghobi R; Shiraz Transplant Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. Electronic address: yaghoobir@sums.ac.ir.
  • Pakfetrat M; Shiraz Nephro-Urology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Afshari A; Shiraz Nephro-Urology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • Sharifi H; Department of Clinical Sciences, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
  • Ghaemi M; Department of Pathobiology, School of Veterinary Medicine, Shiraz University, Shiraz, Iran.
Gene ; 878: 147567, 2023 Aug 20.
Article in En | MEDLINE | ID: mdl-37330024
ABSTRACT

BACKGROUND:

BK polyomavirus (BKPyV) infection in immunocompromised patients can led to polyomavirus-associated nephropathy (BKPyVAN) especially after kidney transplantation. The polyomavirus genome contains enhancer elements that are important transcription activators. In this study, the association between viral and host gene expression and NCCR variations was evaluated in kidney transplant recipients (KTRs) with BKPyV active, and BKPyV in-active infection. METHODS AND

RESULTS:

Blood samples were collected from selected KTRs who divided to patients with active and in-active BKPyV infection. Transcriptional control region (TCR) anatomy was compared to the genomic sequence of archetype BKPyV strain WW using nested PCR method and sequencing. The expression level of some transcription factor genes was evaluated using in-house Real-time PCR (SYBR Green) technique. Most changes were observed after TCR anatomy detection in the Q and P blocks. The expression level of VP1 and LT-Ag viral genes were significantly higher in patients with active infection compared with non-infected ones. Transcription factor genes SP1, NF1, SMAD, NFκB, P53, PEA3, ETS1, AP2, NFAT and AP1 were significantly higher in BKPyV active group in comparison in-active and control groups. The analyses revealed that viral load level and mutations frequency has significant correlation.

CONCLUSIONS:

Based on the results, increasing of NCCR variations were associated with higher viral load of BKPyV especially in Q block. Host transcriptional factors and viral genes all had higher express level in active BKPyV patients versus no in-active ones. Detection of the relation between NCCR variation and BKPyV severity in KTRs need to be confirmed in further complicated studies.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Transplantation / BK Virus / Polyomavirus Infections Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Gene Year: 2023 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Kidney Transplantation / BK Virus / Polyomavirus Infections Type of study: Diagnostic_studies Limits: Humans Language: En Journal: Gene Year: 2023 Document type: Article Affiliation country: