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Analysis of Kaposi's sarcoma-associated herpesvirus latent replication using a real-time polymerase chain reaction technique

Authors
Cha, SehoJang, Jun HyeongKim, YejinHwang, Lee RangSeo, Taegun
Issue Date
Nov-2013
Publisher
ELSEVIER SCIENCE BV
Keywords
KSHV; LANA; TR; Latent replication; Real-time PCR
Citation
JOURNAL OF VIROLOGICAL METHODS, v.193, no.2, pp 660 - 666
Pages
7
Indexed
SCI
SCIE
SCOPUS
Journal Title
JOURNAL OF VIROLOGICAL METHODS
Volume
193
Number
2
Start Page
660
End Page
666
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/15335
DOI
10.1016/j.jviromet.2013.07.061
ISSN
0166-0934
1879-0984
Abstract
Kaposi's sarcoma-associated herpesvirus (KSHV) undergoes replication independently via latent and lytic pathways. Latent replication is mediated by latent-associated nuclear antigen (LANA), the sole viral trans element for genome maintenance and replication. According to previous studies, LANA tethers the KSHV genome to the host chromosome during latency and interacts with host factors to ensure proper latent replication. Studies using Southern blot experiments have revealed consistently that vector constructs containing the viral terminal repeat (TR) region as a cis element in latent replication are replicated in the presence of LANA. However, Southern blotting is a time-intensive, complicated technique that requires multiple reagents. In addition, it has a limited ability to detect slight changes in replication efficiency under different conditions owing to its relatively low sensitivity. In the current study, a real-time polymerase chain reaction method was developed for detecting transient KSHV replication and was found to be capable of further identifying several factors that affect latent replication. This technique should provide a useful tool for the detection of KSHV latent replication under various conditions, including overexpression of viral or cellular factors and chemical stimulation. (C) 2013 Elsevier B.V. All rights reserved.
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