In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication

Feline Infectious Peritonitis (FIP) is a severe fatal immune-augmented disease in cat population. It is caused by FIP virus (FIPV), a virulent mutant strain of Feline Enteric Coronavirus (FECV). Current treatments and prophylactics are not effective. The in vitro antiviral properties of five circula...

Full description

Saved in:
Bibliographic Details
Main Authors: Choong, Oi Kuan, Mehrbod, Parvaneh, Tejo, Bimo Ario, Omar, Abdul Rahman
Format: Article
Language:English
Published: Hindawi Publishing Corporation 2014
Online Access:http://psasir.upm.edu.my/id/eprint/38005/1/38005.pdf
http://psasir.upm.edu.my/id/eprint/38005/
http://www.hindawi.com/journals/bmri/2014/654712/abs/
Tags: Add Tag
No Tags, Be the first to tag this record!
Institution: Universiti Putra Malaysia
Language: English
id my.upm.eprints.38005
record_format eprints
spelling my.upm.eprints.380052015-12-18T07:51:13Z http://psasir.upm.edu.my/id/eprint/38005/ In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication Choong, Oi Kuan Mehrbod, Parvaneh Tejo, Bimo Ario Omar, Abdul Rahman Feline Infectious Peritonitis (FIP) is a severe fatal immune-augmented disease in cat population. It is caused by FIP virus (FIPV), a virulent mutant strain of Feline Enteric Coronavirus (FECV). Current treatments and prophylactics are not effective. The in vitro antiviral properties of five circular Triple-Helix Forming Oligonucleotide (TFO) RNAs (TFO1 to TFO5), which target the different regions of virulent feline coronavirus (FCoV) strain FIPV WSU 79-1146 genome, were tested in FIPV-infected Crandell-Rees Feline Kidney (CRFK) cells. RT-qPCR results showed that the circular TFO RNAs, except TFO2, inhibit FIPV replication, where the viral genome copy numbers decreased significantly by 5-fold log10 from 1014 in the virus-inoculated cells to 109 in the circular TFO RNAs-transfected cells. Furthermore, the binding of the circular TFO RNA with the targeted viral genome segment was also confirmed using electrophoretic mobility shift assay. The strength of binding kinetics between the TFO RNAs and their target regions was demonstrated by NanoITC assay. In conclusion, the circular TFOs have the potential to be further developed as antiviral agents against FIPV infection. Hindawi Publishing Corporation 2014 Article PeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/38005/1/38005.pdf Choong, Oi Kuan and Mehrbod, Parvaneh and Tejo, Bimo Ario and Omar, Abdul Rahman (2014) In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication. BioMed Research International, 2014. art. no. 654712. pp. 1-8. ISSN 2314-6133; ESSN: 2314-6141 http://www.hindawi.com/journals/bmri/2014/654712/abs/ 10.1155/2014/654712
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
description Feline Infectious Peritonitis (FIP) is a severe fatal immune-augmented disease in cat population. It is caused by FIP virus (FIPV), a virulent mutant strain of Feline Enteric Coronavirus (FECV). Current treatments and prophylactics are not effective. The in vitro antiviral properties of five circular Triple-Helix Forming Oligonucleotide (TFO) RNAs (TFO1 to TFO5), which target the different regions of virulent feline coronavirus (FCoV) strain FIPV WSU 79-1146 genome, were tested in FIPV-infected Crandell-Rees Feline Kidney (CRFK) cells. RT-qPCR results showed that the circular TFO RNAs, except TFO2, inhibit FIPV replication, where the viral genome copy numbers decreased significantly by 5-fold log10 from 1014 in the virus-inoculated cells to 109 in the circular TFO RNAs-transfected cells. Furthermore, the binding of the circular TFO RNA with the targeted viral genome segment was also confirmed using electrophoretic mobility shift assay. The strength of binding kinetics between the TFO RNAs and their target regions was demonstrated by NanoITC assay. In conclusion, the circular TFOs have the potential to be further developed as antiviral agents against FIPV infection.
format Article
author Choong, Oi Kuan
Mehrbod, Parvaneh
Tejo, Bimo Ario
Omar, Abdul Rahman
spellingShingle Choong, Oi Kuan
Mehrbod, Parvaneh
Tejo, Bimo Ario
Omar, Abdul Rahman
In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
author_facet Choong, Oi Kuan
Mehrbod, Parvaneh
Tejo, Bimo Ario
Omar, Abdul Rahman
author_sort Choong, Oi Kuan
title In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
title_short In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
title_full In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
title_fullStr In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
title_full_unstemmed In vitro antiviral activity of circular triple helix forming oligonucleotide RNA towards feline infectious peritonitis virus replication
title_sort in vitro antiviral activity of circular triple helix forming oligonucleotide rna towards feline infectious peritonitis virus replication
publisher Hindawi Publishing Corporation
publishDate 2014
url http://psasir.upm.edu.my/id/eprint/38005/1/38005.pdf
http://psasir.upm.edu.my/id/eprint/38005/
http://www.hindawi.com/journals/bmri/2014/654712/abs/
_version_ 1643832122591412224