2017
DOI: 10.1038/s41598-017-06143-w
|View full text |Cite
|
Sign up to set email alerts
|

Bivalent DNA vaccine induces significant immune responses against infectious hematopoietic necrosis virus and infectious pancreatic necrosis virus in rainbow trout

Abstract: Infectious hematopoietic necrosis virus (IHNV) and infectious pancreatic necrosis virus (IPNV) are important pathogens of salmon and trout. An active bivalent DNA vaccine was constructed with the glycoprotein gene of Chinese IHNV isolate Sn1203 and VP2–VP3 gene of Chinese IPNV isolate ChRtm213. Rainbow trout (5 g) were vaccinated by intramuscular injection with 1.0 µg of the bivalent DNA vaccine and then challenged with an intraperitoneal injection of IHNV, IPNV, or both, at 30 and 60 days post-vaccination (d.… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

0
16
0

Year Published

2019
2019
2022
2022

Publication Types

Select...
7
2
1

Relationship

0
10

Authors

Journals

citations
Cited by 31 publications
(16 citation statements)
references
References 56 publications
0
16
0
Order By: Relevance
“…The cell line SSP-9 was identified to be useful for developing vaccines against infectious pancreatic necrosis virus (IPNV) and infectious haematopoietic necrosis virus (IHNV) (Saint-Jean et al 2014). EPC cells were used to produce bivalent DNA vaccine p Ch-IHN/IPN against IHNV and IPNV (Xu et al 2017). Cell culture has been very useful in identification and characterization emerging viral infections and understanding host immune responses for easy development of vaccines (Haugland et al 2011).…”
Section: Vaccine Developmentmentioning
confidence: 99%
“…The cell line SSP-9 was identified to be useful for developing vaccines against infectious pancreatic necrosis virus (IPNV) and infectious haematopoietic necrosis virus (IHNV) (Saint-Jean et al 2014). EPC cells were used to produce bivalent DNA vaccine p Ch-IHN/IPN against IHNV and IPNV (Xu et al 2017). Cell culture has been very useful in identification and characterization emerging viral infections and understanding host immune responses for easy development of vaccines (Haugland et al 2011).…”
Section: Vaccine Developmentmentioning
confidence: 99%
“…Remarkably, a recent bivalent DNA vaccine encoding both the G protein of IHNV and VP2–VP3 of IPNV was shown to be highly effective in rainbow trout against individual and simultaneous IHNV and IPNV challenges. In all cases, the RPS was over 90% (Xu et al, 2017b). Multivalent vaccines have an added advantage over multi-DNA vaccination due to lower cost of production, as only one type of plasmid is required to produce multiple immunogenic antigens.…”
Section: Vaccines Against Ihnvmentioning
confidence: 93%
“…Expression of pcIL-34 and pcHrp1 in largemouth bass muscle tissue was confirmed by Western blotting at 21 days p.v. as described previously [48,49]. The muscle tissue of five fish in each experimental group were biopsied at the injection site, homogenized in buffer containing 100 mmol mL −1 Tris-HCl, pH = 6.8; 1.0 mmol mL −1 phenylmethysulfonyl fluoride (PMSF), 6% Sodium dodecyl sulfate (SDS) and 2% β-mercapthoethanol, and then subjected to a 12% SDS-PAGE gel.…”
Section: In Vivo Expression Analysis Of Pcil-34 and Pchrp1 By Westernmentioning
confidence: 99%