2016
DOI: 10.1016/j.aquaculture.2015.08.025
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Stability of Ostreid herpesvirus-1 (OsHV-1) and assessment of disinfection of seawater and oyster tissues using a bioassay

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Cited by 34 publications
(23 citation statements)
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“…Other studies showed that an OsVH-1 infected tissue preparation remained infectious for 54 h at 16°C compared to 33 h at 25°C (Martenot et al 2015) and that OsHV-1 in seawater re tained infectivity for 2 d at 20°C (Hick et al 2016). Previously infected oysters showed high survival, and low quantities of OsHV-1 µVar DNA were detected when held at <14°C, but high mortality and in creased quantity of OsHV-1 µVar DNA occurred when these oysters were subsequently exposed to 21°C .…”
Section: Introductionmentioning
confidence: 99%
“…Other studies showed that an OsVH-1 infected tissue preparation remained infectious for 54 h at 16°C compared to 33 h at 25°C (Martenot et al 2015) and that OsHV-1 in seawater re tained infectivity for 2 d at 20°C (Hick et al 2016). Previously infected oysters showed high survival, and low quantities of OsHV-1 µVar DNA were detected when held at <14°C, but high mortality and in creased quantity of OsHV-1 µVar DNA occurred when these oysters were subsequently exposed to 21°C .…”
Section: Introductionmentioning
confidence: 99%
“…Observations on the stability of OsHV‐1 μVar in laboratory conditions demonstrate that the virus is unlikely to survive more than two days at 20°C in the seawater (Hick et al . ). The dispersal distance of this virus in seawater has been shown to be limited by viral shedding and decay rates, which are influenced by environmental parameters, such as temperature and ultraviolet radiation (Wommack & Colwell ; Mojica & Brussaard ).…”
Section: Oshv‐1 Virus and Its Variants Associated With Oyster Mortalimentioning
confidence: 97%
“…Experimental infection of C. gigas D-larvae with OsHV-1 was conducted according to the protocol outlined in Burge and Friedman (2012). Experiments involving OsHV-1 were conducted in a physical containment level 2 (PC2) facility at the Sydney Institute of Marine and all waste arising from experiments was decontaminated by heat sterilization (autoclaved at 121 o C for 15 min (Hick et al, 2016). Briefly, gill and mantle tissue from OsHV-1 infected and non-infected adult C. gigas was homogenized in 10-volumes of sterile seawater containing 1000 units.ml -1 of penicillin and 1 mg.ml -1 of streptomycin, clarified by centrifugation and 0.2 µm filtered to prepare OsHV-1 and control homogenates, respectively (Burge and Friedman, 2012;Renault et al, 2011).…”
Section: Oysters Immune Challenge and Mating Trialsmentioning
confidence: 99%