| Literature DB >> 33572469 |
Irene Cano1, John Worswick1, Brian Mulhearn1, David Stone1, Gareth Wood1, Jacqueline Savage1, Richard Paley1.
Abstract
Fluorescence real-time LAMP assays were designed for the orf43 gene of CyHV-3 European genotype and the p4a gene of the CEV genogroup I. A third LAMP assay to detect the ef1a gene of the host common carp was designed as an internal control. The limit of detection was 102 and 103 viral copies under 25 min for CyHV-3 and CEV, respectively. The specificity of the CyHV-3 LAMP assay was 95.6% of 72 fish herpesviruses tested. Sixty-three non-lethal common carp mucus swabs were collected across 16 sites during disease investigations. DNA extractions were performed in under 10 min using the QuickExtract™ digestion buffer. The LAMP amplification of CyHV-3 DNA in mucus swabs from clinical cases was detected from 4 to 13 min in 13 sites, while a co-infection of CyHV-3 and CEV was confirmed by LAMP in a single site. The LAMP results agreed with the results of the reference laboratory. The common carp ef1a was amplified only in 61% of the mucus swabs collected, preventing its use as a robust internal control to distinguish false negatives from invalid tests. After further optimization, these tests could be implemented for border inspection posts surveillance and decentralizing testing during disease outbreaks.Entities:
Keywords: LAMP; carp edema virus; common carp; cyprinid herpesvirus; disease control; fluorescence real-time loop-mediated isothermal amplification; point of care test; skin swab
Year: 2021 PMID: 33572469 PMCID: PMC7916346 DOI: 10.3390/ani11020459
Source DB: PubMed Journal: Animals (Basel) ISSN: 2076-2615 Impact factor: 2.752