2014
DOI: 10.3354/dao02785
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Detection and application of circular (concatemeric) DNA as an indicator of koi herpesvirus infection

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Cited by 3 publications
(2 citation statements)
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“…The same method of seawater sampling was performed between June 2017 and June 2019 at another bay area (D), where fish surviving RSIVD in 2016 were transferred in April 2017. Heat-inactivated koi herpesvirus (KHV) NRIA0301 isolate ( 57 ) was added to the seawater samples between April 2018 and November 2019 as the external standard virus before the concentration process. Then, the seawater was concentrated using iron flocculation and eDNA was extracted, with minor modifications ( 16 ).…”
Section: Methodsmentioning
confidence: 99%
“…The same method of seawater sampling was performed between June 2017 and June 2019 at another bay area (D), where fish surviving RSIVD in 2016 were transferred in April 2017. Heat-inactivated koi herpesvirus (KHV) NRIA0301 isolate ( 57 ) was added to the seawater samples between April 2018 and November 2019 as the external standard virus before the concentration process. Then, the seawater was concentrated using iron flocculation and eDNA was extracted, with minor modifications ( 16 ).…”
Section: Methodsmentioning
confidence: 99%
“…This process was performed at room temperature between 22°C and 26°C. First, approximately 10 3 copies in 50 µL of heat-inactivated KHV NRIA0301 isolate ( 48 ) were added to the seawater sample as an external standard virus for the internal control of eDNA before the iron flocculation process ( 32 ). The same volume of KHV in a 1.5-mL microtube was placed at room temperature during the iron flocculation process for each sampling batch as a control for copy number reduction during sample treatment.…”
Section: Methodsmentioning
confidence: 99%