DNA vaccines encoding viral glycoproteins induce nonspecific immunity and mr protein synthesis in fish

被引:140
作者
Kim, CH [1 ]
Johnson, MC [1 ]
Drennan, JD [1 ]
Simon, BE [1 ]
Thomann, E [1 ]
Leong, JAC [1 ]
机构
[1] Oregon State Univ, Dept Microbiol, Ctr Salmon Dis Res, Corvallis, OR 97331 USA
关键词
D O I
10.1128/JVI.74.15.7048-7054.2000
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Protective immunity by vaccination with plasmid DNA encoding a viral glycoprotein (G) has long been assumed to result from the induction of a specific immune response. We report here that the initial protection may be due to the induction of alpha/beta interferon, with long-term protection due to a specific response to the encoded viral G, DNA vaccines encoding the Gs of three serologically unrelated fish rhabdoviruses were used to vaccinate rainbow trout against a lethal challenge with infectious hematopoietic necrosis virus (IHNV). All three vaccines, each encoding the G gene of either IHNV (IHNV-G), snakehead rhabdovirus (SHRV) (SHRV-G), or spring viremia of carp virus (SVCV) (SVCV-G), elicited protective immunity against IHNV, Vaccinated fish were challenged at 30 or 70 days postvaccination with lethal doses of IHNV. At 30 days postvaccination, only 5% of fish that had received any of the G vaccines died, whereas more than 50% of the control fish succumbed to virus challenge. When fish were vaccinated and challenged at 70 days postvaccination, only 12% of the IHNV-G-vaccinated fish died compared to 68% for the SHRV-G- and 76% for the SVCV-G-vaccinated fish, Assays for trout Mr protein, an indicator of alpha/beta interferon induction, shelved that only fish vaccinated with a G containing plasmid produced high levels of Mx protein in the kidneys and liver. Interestingly, at day 7 after virus challenge, all of the fish vaccinated with the IHNV-G plasmid were negative for Mr, but the SHRV-G- and SVCV-G-vaccinated fish still shelved detectable levels of Mx. These results suggest that DNA vaccines in fish induce an early, nonspecific antiviral protection mediated by an alpha/beta interferon and, later, a specific immune response.
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收藏
页码:7048 / 7054
页数:7
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