Development of Polycistronic Baculovirus Surface Display Vectors to Simultaneously Express Viral Proteins of Porcine Reproductive and Respiratory Syndrome and Analysis of Their Immunogenicity in Swine

Author:

Hsu Chao-Yu12,Jang Yun3,Huang Wei-Ru34,Wang Chi-Young5ORCID,Wen Hsiao-Wei6ORCID,Tsai Pei-Chien7,Yang Cheng-Yao8ORCID,Munir Muhammad9ORCID,Liu Hung-Jen234710ORCID

Affiliation:

1. Department of Medical Research, Tungs’ Taichung Metroharbor Hospital, Taichung 435, Taiwan

2. Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung 402, Taiwan

3. Institute of Molecular Biology, National Chung Hsing University, Taichung 402, Taiwan

4. The iEGG and Animal Biotechnology Center, National Chung Hsing University, Taichung 402, Taiwan

5. Department of Veterinary Medicine, National Chung Hsing University, Taichung 402, Taiwan

6. Department of Food Science and Biotechnology, National Chung Hsing University, Taichung 402, Taiwan

7. Department of Life Sciences, National Chung Hsing University, Taichung 402, Taiwan

8. Graduate Institute of Veterinary Pathobiology, National Chung Hsing University, Taichung 402, Taiwan

9. Division of Biomedical and Life Sciences, Faculty of Health and Medicine, Lancaster University, Lancaster LA1 4YW, UK

10. Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung 402, Taiwan

Abstract

To simultaneously express and improve expression levels of multiple viral proteins of a porcine reproductive and respiratory syndrome virus (PRRSV), polycistronic baculovirus surface display vectors were constructed and characterized. We engineered polycistronic baculovirus surface display vectors, namely, pBacDual Display EGFP(BacDD)-2GP2-2GP4 and pBacDD-4GP5N34A/N51A (mtGP5), which simultaneously express and display the ectodomain of His-tagged GP2-gp64TM-CTD, His-tagged GP4-gp64TM-CTD, and His-tagged mtGP5-gp64TM-CTD fusion proteins of PRRSV on cell membrane of Sf-9 cells. Specific pathogen-free (SPF) pigs were administered intramuscularly in 2 doses at 21 and 35 days of age with genetic recombinant baculoviruses-infected cells. Our results revealed a high level of ELISA-specific antibodies, neutralizing antibodies, IL-4, and IFN-γ in SPF pigs immunized with the developed PRRSV subunit vaccine. To further assess the co-expression efficiency of different gene combinations, pBacDD-GP2-GP3-2GP4 and pBacDD-2mtGP5-2M constructs were designed for the co-expression of the ectodomain of His-tagged GP2-gp64TM-CTD, His-tagged GP3-gp64TM-CTD, and His-tagged GP4-gp64TM-CTD proteins as well as the ectodomain of His-tagged mtGP5-gp64TM-CTD and His-tagged M-gp64TM-CTD fusion proteins of PRRSV. To develop an ELISA assay for detecting antibodies against PRRSV proteins, the sequences encoding the ectodomain of the GP2, GP3, GP4, mtGP5, and M of PRRSV were amplified and subcloned into the pET32a vector and expressed in E. coli. In this work, the optimum conditions for expressing PRRSV proteins were evaluated, and the results suggested that 4 × 105 of Sf-9 cells supplemented with 7% fetal bovine serum and infected with the recombinant baculoviruses at an MOI of 20 for three days showed a higher expression levels of the protein. Taken together, the polycistronic baculovirus surface display system is a useful tool to increase expression levels of viral proteins and to simultaneously express multiple viral proteins of PRRSV for the preparation of subunit vaccines.

Funder

Ministry of Science and Technology of Taiwan

The iEGG and Animal Biotechnology Center from The Feature Areas Research Center Program within the framework of the Higher Education Sprout Project by the Ministry of Education (MOE) in Taiwan

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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