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Improved multiplex PCR method for the detection of diverse Megalocytivirus in the Korea
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Megalocytivirus is a genus of piscine viruses that belongs to the
Iridoviridae family, and this family comprises red seabream iridovirus
(RSIV), turbot reddish body iridovirus (TRBIV), and infectious spleen
and kidney necrosis virus. RSIV causes high mortality and economic
losses in the rock bream (Oplegnathus fasciatus) Korean aquaculture
industry. The World Organization for Animal Health’s Office
International des Epizooties has provided a manual for RSIV detection.
However, detection against TRBIV has not been confirmed. In this study,
a multiplex PCR method was established to detect two genotypes of
Megalocytivirus, RSIV and TRBIV. New primer pairs were optimized for the
PCR reaction. A mixture of one universal and two specific primer pairs
could amplify three distinct products targeting three different genes.
The sensitivity of the primer pairs was evaluated and results showed a
detection limit of 2.0 105 copies for each target gene. Moreover, the
primer pairs did not amplify any other viruses. The evaluation of
multiplex PCR using 21 RSIV Korean isolates has shown that it can
distinguish two genotypes of Megalocytivirus from 21 RSIV Korean
isolates. Finally, we describe a new multiplex PCR method to detect
different genotypes of Megalocytivirus simultaneously, which makes the
diagnosis of viral diseases occurring in the Korean aquaculture industry
more convenient.
Title: Improved multiplex PCR method for the detection of diverse Megalocytivirus in the Korea
Description:
Megalocytivirus is a genus of piscine viruses that belongs to the
Iridoviridae family, and this family comprises red seabream iridovirus
(RSIV), turbot reddish body iridovirus (TRBIV), and infectious spleen
and kidney necrosis virus.
RSIV causes high mortality and economic
losses in the rock bream (Oplegnathus fasciatus) Korean aquaculture
industry.
The World Organization for Animal Health’s Office
International des Epizooties has provided a manual for RSIV detection.
However, detection against TRBIV has not been confirmed.
In this study,
a multiplex PCR method was established to detect two genotypes of
Megalocytivirus, RSIV and TRBIV.
New primer pairs were optimized for the
PCR reaction.
A mixture of one universal and two specific primer pairs
could amplify three distinct products targeting three different genes.
The sensitivity of the primer pairs was evaluated and results showed a
detection limit of 2.
0 105 copies for each target gene.
Moreover, the
primer pairs did not amplify any other viruses.
The evaluation of
multiplex PCR using 21 RSIV Korean isolates has shown that it can
distinguish two genotypes of Megalocytivirus from 21 RSIV Korean
isolates.
Finally, we describe a new multiplex PCR method to detect
different genotypes of Megalocytivirus simultaneously, which makes the
diagnosis of viral diseases occurring in the Korean aquaculture industry
more convenient.
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