Author/Authors :
Saber Amoli, Saghar Department of Microbiology - School of Medicine- Babol University of Medical Sciences, Babol, , Zebardast, Arghavan Department of Virology - School of Public Health - Tehran University of Medical Sciences, Tehran , Keyvani, Hossein Department of Virology- School of Medicine - Iran University of Medical Sciences, Tehran , Yahyapour, Yousef Infectious Diseases & Tropical Medicine Research Center- Health Research Institute- Babol University of Medical Sciences, Babol , Ghodsi, Mohammad Department of Neurosurgery - Shariati Hospital - Tehran University of Medical Sciences, Tehran , Maniati, Mahmood School of Medicine - Ahvaz Jundishapur University of Medical Sciences, Ahvaz , Sadeghi, Farzin Cellular & Molecular Biology Research Center - Health Research Institute - Babol University of Medical Sciences, Babol
Abstract :
Background: Due to persistent infections of human central nervous system (CNS),
polyomaviruses have been identified as one of the risk factors for brain tumor development.
Human BK virus is of significant interest due to its experimental neuro-oncogenic potential
and the possible association with CNS neoplasms. However, the results of different studies
are discrepant. In the present study, we aimed to investigate the prevalence of BK virus
genome and quantify BK viral load in Iranian patients with primary and metastatic brain
malignancies.
Methods: To assess the prevalence of BK virus sequences, a total of 58 fresh brain tumors
were examined by quantitative real-time PCR. The BK viral load was determined as viral
copy number per cell.
Results: Of the 58 brain tumor samples BK tumor antigen (TAg) sequences were detected
in 26 (44.8%) of cases. In primary brain tumors, BK virus sequences were recognized more
frequently in schwannomas (15.5%) and meningiomas (12.1%). The mean BK virus TAg
copy number in positive cases was 0.20×10-3±0.27×10-3 (range 0.01×10-3- 0.8×10-3) copies
per cell.
Conclusion: Taken together, in the present study low copy numbers of BK virus TAg gene
was detected in brain tumor cells, which can indicate that BK virus may contribute to tumor
induction by indirect mechanisms or neuro-persistence of this virus without any pathological
consequences