The relation of NCCR variations and host transcription factors gene regulation in BK polyomavirus infected kidney transplant patients

被引:3
|
作者
Sahragard, Ilnaz [1 ]
Mohammadi, Ali [1 ]
Yaghobi, Ramin [2 ,5 ]
Pakfetrat, Maryam [3 ]
Afshari, Afsoon [3 ]
Sharifi, Hassan [4 ]
Ghaemi, Mehran [1 ]
机构
[1] Shiraz Univ, Sch Vet Med, Dept Pathobiol, Shiraz, Iran
[2] Shiraz Univ Med Sci, Shiraz Transplant Res Ctr, Shiraz, Iran
[3] Shiraz Univ Med Sci, Shiraz Nephrourol Res Ctr, Shiraz, Iran
[4] Shiraz Univ, Sch Vet Med, Dept Clin Sci, Shiraz, Iran
[5] Shiraz Univ Med Sci, Shiraz Transplant Res Ctr, Res Tower,Khalili St, Shiraz, Iran
关键词
BKPyV; NCCR; TCR; Kidney transplantation; Nephropathy; NONCODING CONTROL REGION; SEQUENCE VARIATIONS; NUCLEAR FACTOR; VIRUS; REPLICATION; PROTEINS; PROMOTER; SP1;
D O I
10.1016/j.gene.2023.147567
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: BK polyomavirus (BKPyV) infection in immunocompromised patients can led to polyomavirusassociated 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 inactive 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, NF & kappa;B, 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.
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页数:10
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