2018
DOI: 10.1016/j.aquaculture.2017.12.001
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The first instance of HPR-deleted ISAV detection in eviscerated, fresh salmon at a Chinese entry-exit port

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Cited by 5 publications
(3 citation statements)
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“…The mortality incident was reported to be caused by sea lice treatment. No suspicion of ISA was reported; however, ISAV was detected in exported salmon fillets, originating from this farm, at entry inspection to China (Xiao et al, 2018). This finding was later confirmed by RT-qPCR testing of stored frozen filets by the Norwegian Veterinary Institute.…”
mentioning
confidence: 67%
“…The mortality incident was reported to be caused by sea lice treatment. No suspicion of ISA was reported; however, ISAV was detected in exported salmon fillets, originating from this farm, at entry inspection to China (Xiao et al, 2018). This finding was later confirmed by RT-qPCR testing of stored frozen filets by the Norwegian Veterinary Institute.…”
mentioning
confidence: 67%
“…The focus is on information (geographical occurrence, variants, transmission and reservoirs) that can be obtained from phylogenetic analysis of segment six from high (HPRΔ) and low (HPR0) virulent ISA viruses from fresh and sea water in Norway, Scotland, Faeroe Islands and Chile. This segment has been used in several earlier studies of the relationship between existing ISA viruses and for inferring short and long distance transmission [33, 34, 37, 41, 43, 46, 48, 49, 51, 52, 53, 55, 58, 70, 71, 72]. Admittedly, the change from low to high virulent variants of ISA viruses is, based on existing knowledge, dependent on mutational changes in both segment five (fusion protein, F, gene) and segment six (hemagglutinin-esterase, HE, gene) [49, 50, 53, 56, 57, 58], but all HPRΔ variants have so far been of higher virulence than HPR0 variants.…”
Section: Discussionmentioning
confidence: 99%
“…® Total RNA Kit (Omega Bio‐tek) according to the manufacturer's instructions. First‐strand cDNA from the HPR and segment 5 putative cleavage site regions was synthesized using Moloney murine leukaemia virus reverse transcriptase (Promega) with the specific primers S5_Fw (TACAACGGAAAGGATTAAGACTG), S5_Rv (TCTCCCTCTAGCAGCAGGTTC), HPR_3_Fw (5’‐GCCCAGACATTGACTGGAGATG‐3’) and 18_HPR_Rv (5’‐GATGGTGGAATTCTACCTCTAGACTTGTA‐3’) (Xiao et al., 2018). Subsequently, the transcribed cDNA was used as a template in PCR using GoTaq® Green Master Mix (Promega) with the same primers used in cDNA synthesis for either segment 5 or 6.…”
Section: Methodsmentioning
confidence: 99%