Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector

Many Newcastle disease virus (NDV) strains have been developed as vectors to express a foreign gene (FG) for vaccine and gene therapy purposes. A majority of these NDV vectors express only a single FG or two FGs from suboptimal insertion sites in the NDV genome, obtaining various levels of FG expres...

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Main Authors: Lei He, Zhenyu Zhang, Qingzhong Yu
Format: Article
Language:English
Published: MDPI AG 2020-06-01
Series:Proceedings
Subjects:
NDV
Online Access:https://www.mdpi.com/2504-3900/50/1/9
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spelling doaj-3582ff3e801d4d2db09e22ca72abf7f52020-11-25T03:10:35ZengMDPI AGProceedings2504-39002020-06-01509910.3390/proceedings2020050009Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy VectorLei He0Zhenyu Zhang1Qingzhong Yu2College of Animal Science and Technology, Henan University of Science and Technology, LuoYang 471003, ChinaUSDA-ARS, US National Poultry Research Center, Athens, GA 30605, USAUSDA-ARS, US National Poultry Research Center, Athens, GA 30605, USAMany Newcastle disease virus (NDV) strains have been developed as vectors to express a foreign gene (FG) for vaccine and gene therapy purposes. A majority of these NDV vectors express only a single FG or two FGs from suboptimal insertion sites in the NDV genome, obtaining various levels of FG expression. To improve the FG expression, we generated NDV LaSota vaccine strain-based recombinant viruses to express two FGs, green fluorescent protein (GFP) and red fluorescent protein (RFP) genes, from the identified optimal insertion sites, through a combination of the independent transcription unit (ITU) and the internal ribosomal entry site (IRES) dependent expression approaches. Biological assessments showed that these recombinants expressing two FGs were slightly attenuated with approximately one order of magnitude lower in virus titers than those containing a single FG. The FG expression efficiencies from two-FG viruses were also lower than those from the single-FG viruses. However, the expression of two FGs from the optimal insertion sites was significantly (<i>p</i><i> </i>< 0.05) higher than those from the suboptimal insertion sites. The expression of FGs through the ITU approach was approximately 4-fold more efficient than that through the IRES-dependent approach. These results suggest that the NDV LaSota vector could efficiently express two FGs from the identified optimal insertions sites. The ITU strategy could be used for the expression of a higher amount of FG products, whereas the IRES tactic might be useful when a lower amount of FG products are needed.https://www.mdpi.com/2504-3900/50/1/9NDVforeign genesGFP and RFPoptimal insertion sitesco-expressionmultivalent vector
collection DOAJ
language English
format Article
sources DOAJ
author Lei He
Zhenyu Zhang
Qingzhong Yu
spellingShingle Lei He
Zhenyu Zhang
Qingzhong Yu
Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
Proceedings
NDV
foreign genes
GFP and RFP
optimal insertion sites
co-expression
multivalent vector
author_facet Lei He
Zhenyu Zhang
Qingzhong Yu
author_sort Lei He
title Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
title_short Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
title_full Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
title_fullStr Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
title_full_unstemmed Expression of Two Foreign Genes from the Optimal Insertion Sites of Newcastle Disease Virus Vector for Use as a Multivalent Vaccine and Gene Therapy Vector
title_sort expression of two foreign genes from the optimal insertion sites of newcastle disease virus vector for use as a multivalent vaccine and gene therapy vector
publisher MDPI AG
series Proceedings
issn 2504-3900
publishDate 2020-06-01
description Many Newcastle disease virus (NDV) strains have been developed as vectors to express a foreign gene (FG) for vaccine and gene therapy purposes. A majority of these NDV vectors express only a single FG or two FGs from suboptimal insertion sites in the NDV genome, obtaining various levels of FG expression. To improve the FG expression, we generated NDV LaSota vaccine strain-based recombinant viruses to express two FGs, green fluorescent protein (GFP) and red fluorescent protein (RFP) genes, from the identified optimal insertion sites, through a combination of the independent transcription unit (ITU) and the internal ribosomal entry site (IRES) dependent expression approaches. Biological assessments showed that these recombinants expressing two FGs were slightly attenuated with approximately one order of magnitude lower in virus titers than those containing a single FG. The FG expression efficiencies from two-FG viruses were also lower than those from the single-FG viruses. However, the expression of two FGs from the optimal insertion sites was significantly (<i>p</i><i> </i>< 0.05) higher than those from the suboptimal insertion sites. The expression of FGs through the ITU approach was approximately 4-fold more efficient than that through the IRES-dependent approach. These results suggest that the NDV LaSota vector could efficiently express two FGs from the identified optimal insertions sites. The ITU strategy could be used for the expression of a higher amount of FG products, whereas the IRES tactic might be useful when a lower amount of FG products are needed.
topic NDV
foreign genes
GFP and RFP
optimal insertion sites
co-expression
multivalent vector
url https://www.mdpi.com/2504-3900/50/1/9
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