The infection of potatoes byPhytophthora infestans during simulated washing and its control using a hot water treatment

Summary A single blighted tuber released on average 1.39 mg ofP. infestans mycelia and sporangia during simulated washing. In subsequent experiments up to 100% of tubers were infected when healthy tubers were washed in a suspension ofP. infestans equivalent to a concentration of 1.65 μg ml⁻¹, i.e. that calculated to be in a commercial washing plant after washing a potato stock with approximately 1% of tubers infected with blight for 4 hours. Immature tubers were more prone to infection during washing than mature tubers. Damaging tubers, irrespective of their maturity, increased the incidence of tuber infection. The viability ofP. infestans isolates was significantly reduced byin vitro immersion in water at 44°C for 5 minutes. The infection of daughter tubers dipped in a suspension ofP. infestans for 3 minutes was prevented when the suspension temperature was 44°C. There was no indication of tuber damage at this temperature.     

Infectious pancreatic necrosis virus in Atlantic salmon, Salmo salar L., post-smolts in the Shetland Isles, Scotland: virus identification, histopathology, immunohistochemistry and genetic comparison with Scottish mainland isolates

During mid-June 1999 peak mortalities of 11% of the total stock per week were seen at a sea cage site of Atlantic salmon, Salmo salar L., post-smolts in the Shetland Isles, Scotland. Virus was isolated on chinook salmon embryo (CHSE) cells in a standard diagnostic test and infectious pancreatic necrosis virus (IPNV) identified by enzyme-linked immunosorbent assay. IPNV was confirmed as serogroup A by a cell immunofluorescent antibody test using the cross-reactive monoclonal antibody AS-1. Four weeks after the main outbreak, virus titres in surviving moribund fish were assayed at >10(10) TCID50 g(-1) kidney. Histopathology of moribund fish was characterized by pancreatic acinar cell necrosis and a marked catarrhal enteritis of the intestinal mucosa. In the liver, necrosis, leucocytic infiltration and a generalized cell vacuolation were noted. IPNV-specific immunostaining was demonstrated in pancreas, liver, heart, gill and kidney tissue. The nucleotide sequence of the coding region of segment A was determined from the Shetland isolate. A 1180 bp fragment of the VP2 gene of this isolate was compared with a 1979 reference isolate from mainland Scottish Atlantic salmon, La/79 and another more recent mainland isolate, 432/00. Both A2 isolates were derived from carrier fish without signs of IPN and serotyped by a plaque neutralization test. The Shetland isolate shows a different nucleotide and amino acid sequence compared with the two isolates from carrier fish. These latter isolates showed identical amino acid sequences in the fragment examined, despite the 21 years separating the isolations. Sequence comparisons with other A2 (Sp) isolates on the database confirm all three Scottish isolates are A2 (Sp).