Bungowannah Pestivirus Chimeras as Novel Double Marker Vaccine Strategy against Bovine Viral Diarrhea Virus

被引:4
作者
Koethe, Susanne [1 ]
Koenig, Patricia [1 ]
Wernike, Kerstin [1 ]
Schulz, Jana [2 ]
Reimann, Ilona [1 ]
Beer, Martin [1 ]
机构
[1] Friedrich Loeffler Inst, Inst Diagnost Virol, Fed Res Inst Anim Hlth, D-17493 Greifswald Insel Riems, Germany
[2] Friedrich Loeffler Inst, Inst Epidemiol, Fed Res Inst Anim Hlth, D-17493 Greifswald Insel Riems, Germany
关键词
BVDV; pestivirus; DIVA vaccine; BuPV; chimera; N-pro; E-rns; modified live vaccine; inactivated vaccine; SWINE-FEVER VIRUS; GLYCOPROTEIN E-RNS; N-PRO; CELL TROPISM; PIGS; ERADICATION; ENVELOPE; CATTLE; RNASE; IDENTIFICATION;
D O I
10.3390/vaccines10010088
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Marker or DIVA (differentiation of infected from vaccinated animals) vaccines are beneficial tools for the eradication of animal diseases in regions with a high prevalence of the designated disease. Bovine viral diarrhea virus (BVDV)-1 (syn. Pestivirus A) is a flavivirus that infects predominantly cattle resulting in major economic losses. An increasing number of countries have implemented BVDV eradication programs that focus on the detection and removal of persistently infected cattle. No efficient marker or DIVA vaccine is yet commercially available to drive the eradication success, to prevent fetal infection and to allow serological monitoring of the BVDV status in vaccinated farms. Bungowannah virus (BuPV, species Pestivirus F), a related member of the genus Pestivirus with a restricted prevalence to a single pig farm complex in Australia, was chosen as the genetic backbone for a marker vaccine candidate. The glycoproteins E1 and E2 of BuPV were substituted by the heterologous E1 and E2, which are major immunogens, of the BVDV-1 strain CP7. In addition, the candidate vaccine was further attenuated by the introduction of a deletion within the N-pro protein coding sequence, a major type I interferon inhibitor. Immunization of cattle with the chimeric vaccine virus BuPV_Delta N-pro_E1E2 CP7 (modified live or inactivated) followed by a subsequent experimental challenge infection confirmed the safety of the prototype strain and provided a high level of clinical protection against BVDV-1. The serological discrimination of vaccinated cattle could be enabled by the combined detection of BVDV-1 E2- in the absence of both BVDV NS3- and BVDV E-rns-specific antibodies. The study demonstrates for the first time the generation and application of an efficient BVDV-1 modified double marker vaccine candidate that is based on the genetic background of BuPV accompanied by commercially available serological marker ELISA systems.
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页数:16
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