Intraperitoneal injection of virulent infectious pancreatic necrosis virus (IPNV) into yearling brook trout Salvelinus fontinalis induced an asynlptomatic, chronic w u s infection that persisted for at least 76 wk post-lnlection (wpl) in spite of the production of a strong humoral immune response. At 8 wpi, 100 % of the fish in one of the injected groups were IPNV camers, as determined by organ and feces samphng. At 76 wpi. 95 % of the fish remained IPNV carriers. Vertical transmission of IPNV to progeny occurred, but the fry mortality rate, the prevalence of IPNV-infechon, and mean IPNV titres were low. Hence, vertical transm~ssion 1s not recommended a s a criterion for evaluating the efficacy of broodstock immunization. The IPNV carner state in yearlings that had survived a &rect mmersion in IPNV as fry was equivalent to that induced in yearlings by injection, in terms of the number of IPNV-infected organs per fish and the prevalence and titre of IPNV in the visceral organs when fish were sampled at 73 and 76 wpi, respectively. However, the Injected yearlings mounted a stronger humoral immune response to IPNV that the fish surviving the direct unmersion. Smce the IPNV camer state induced by injechon was nearly indistinguishable from the natural IPNV carner state, intraperitoneal injechon can be used as a challenge protocol for broodstock immunization tnals.
A staphylococcal coagglutination test was developed for the rapid detection of infectious hematopoietic necrosis virus (IHNV) in cell cultures and infected fish. The test could be completed in 15 min but required a minimum IHNV titer of 106 PFU/ml to obtain a positive reaction. All IHNV isolates, representing the five electropherotypes taken from a wide variety of species and different geographic ranges, caused coagglutination of Staphylococcus aureus cells sensitized with rabbit polyclonal serum against the Round Butte IHNV isolate. The coagglutination reaction was blocked by preincubation of IHNV with homologous antiserum, and IHNV did not cause coagglutination of S. aureus cells sensitized with normal rabbit serum. In specificity tests, cells sensitized with rabbit anti-IHNV serum or normal serum did not coagglutinate in the presence of infectious pancreatic necrosis virus, viral hemorrhagic septicemia virus, cell culture medium components, or media from cultures of cell lines of salmonid and nonsalmonid origin. Most importantly, the coagglutination test was able to detect and identify IHNV directly from experimentally infected rainbow trout fry, the organs of naturally infected adult kokanee salmon and winter steelhead trout, and ovarian fluids of the winter steelhead trout. The coagglutination test is very suitable for field use, since it is inexpensive, simple to interpret, sensitive, and rapid and requires no specialized equipment.
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