Patent Application
20230147673
This patent application claims the benefit and priority of Chinese Patent Application No. 202111318523.7, entitled “Recombinant Herpesvirus of Turkeys (HVT) and Preparation Method and Use Thereof” filed on Nov. 9, 2021, the disclosure of which is incorporated by reference herein in its entirety as part of the present application.
The present disclosure belongs to the technical field of genetic engineering vaccines, in particular to a construction method of a recombinant herpesvirus of turkeys (HVT) strain using CRISPR-Cas9 technology. The recombinant virus strain may provide desirable protection as a vaccine.
As a recently emerging gene editing technology, the CRISPR-Cas9 system has achieved great success in efficient generation of genetically engineered cells and animal models. The CRISPR-Cas9 system is also used to edit genomes of various large DNA viruses, including herpes simplex virus, adenovirus, pseudorabies virus, poxvirus, guinea pig cytomegalovirus, and duck enteritis virus.
Herpesvirus of turkeys (HVT) has been widely used as a vaccine vector to express heterologous antigens of various avian diseases. These vaccines provide desirable and long-lasting immunity against the Marek's disease virus (MDV), and gene-dependent viruses inserted into vectors. However, these recombinant HVT vaccines are mainly produced by conventional homologous recombination in virus-infected cells, or by recombination in bacterial artificial chromosomes (BACs) from which a full-length genome is cloned. These methods are inefficient for producing recombinant viruses, resulting in time-consuming production of the recombinant vaccines. It is of broad technical prospects in efficiently editing genomes of avian herpesviruses using the CRISPR-Cas9 system to quickly generate recombinant viruses.
The insertion sites of HVT for exogenous genes that have been reported include US2, US10, UL45/46, HVT065/066, and TK. The multiple defenses with one vaccine can be achieved by discovering novel sites for HVT to express the exogenous genes, and constructing HVT-based live vector vaccines inserting various exogenous genes based on the existing insertion sites. This method has broad market prospects.
An objective of the present disclosure is to provide a site HVT005/HVT006 where an exogenous gene is inserted into a HVT.
An aspect of the present disclosure provides a recombinant HVT, in which an exogenous gene is inserted in a spacer region between an HVT005 region and an HVT006 region of an HVT genome; and the exogenous gene is selected from a gene derived from the group consisting of a Newcastle disease virus (NDV), an avian influenza virus (AIV), and an infectious bursal disease virus (IBDV);
in some embodiments, the AIV is selected from an H9N2 subtype AIV, an H5N1 subtype AIV, an H7N7 subtype AIV, an H5N2 subtype AIV, an H7N2 subtype AIV, and an H9N1 subtype AIV; and the NDV is selected from a VII type NDV, a II type NDV, and a III type NDV; and
in some embodiments, the exogenous gene is selected from an NDV F gene, an AIV HA gene, and an IBDV VP2 gene.
In some embodiments, the spacer region between an HVT005 region and an HVT006 region of an HVT genome is located between 8,867 nt and 9,319 nt of the HVT, and has a nucleotide sequence preferably set forth in SEQ ID NO: 1.
In some embodiments, the NDV F gene is a complete open reading frame (ORF) of a VII type NDV F gene, and has a cleavage site replaced with a cleavage site of a live vaccine (La Sota strain) of Newcastle disease in chicken.
In some embodiments, the nucleotide sequence of the NDV F gene has a nucleotide sequence set forth in SEQ ID NO: 2.
In some embodiments, an expression cassette of the NDV F gene is ligated successively by an mCMV promoter, the NDV F gene and an SV40 poly A.
In some embodiments, the AIV HA gene is a complete ORF of an H9N2 subtype AIV HA gene.
In some embodiments, the nucleotide sequence of the H9N2 subtype AIV HA gene is set forth in SEQ ID NO: 3.
In some embodiments, an expression cassette of the H9N2 subtype AIV HA gene is ligated successively by an mCMV promoter, the exogenous gene and an SV40 poly A.
The present disclosure further provides a method for preparing the recombinant HVT, including the following steps:
S1) Construction of a CRISPR-Cas9 plasmid:
S1-1) designing an sgRNA sequence for the spacer region between an HVT005 region and an HVT006 region, in which the sgRNA sequence is set forth in SEQ ID NO: 7, TCATATACTGAATCGTAGGG (SEQ ID NO: 7); and
S1-2) synthesizing a plus-strand HVT005/006-sgRNA-F and a minus-strand HVT005/006-sgRNA-R according to the designed sgRNA sequence, and conducting annealing to form a dsDNA, and inserting the dsDNA into a vector to obtain the CRISPR-Cas9 plasmid; in which
sequences of the plus-strand HVT005/006-sgRNA-F and the minus-strand HVT005/006-sgRNA-R are set forth in SEQ ID NO: 8 and SEQ ID NO: 9, respectively:
S2) constructing a donor vector plasmid including an expression cassette of the exogenous gene;
S3) construction and purification of a recombinant HVT: co-transfecting a pX459-sgA plasmid, the CRISPR-Cas9 plasmid and the donor vector plasmid into primary chicken embryo fibroblasts (CEFs), inoculating with an HVT, followed by culturing until the primary CEFs are cytopathic; and conducting purification to obtain a primary recombinant HVT; and
S4) removing a green fluorescent protein (GFP) in the primary recombinant HVT obtained in step S3) to obtain the recombinant HVT.
In some embodiments, step S2) includes specifically the following steps:
S2-1) inserting the exogenous gene into a pcDNA3.1-SfiI vector to obtain a pcDNA3.1-SfiI-exogenous gene vector; and
S2-2) ligating an expression cassette of the exogenous gene in the pcDNA3.1-SfiI-exogenous gene vector into a pT-sgA-GFP vector through an SfiI restriction site to obtain a pT-sgA-GFP-exogenous gene vector.
In some embodiments, step S4) includes specifically the following steps: transfecting a pcDNA3.1-Cre plasmid in the primary CEFs, inoculating with the primary recombinant HVT obtained in step S3) and conducting culture until the primary CEFs are cytopathic, followed by purification through virus spotting to obtain a recombinant virus rHVT-exogenous gene.
The present disclosure further provides use of the recombinant HVT in preparation of a vaccine for preventing avian influenza and/or Newcastle disease and/or infectious bursal disease.
The present disclosure further provides a vaccine for preventing avian influenza and/or Newcastle disease and/or infectious bursal disease, including the recombinant HVT.
The present disclosure further provides a method for inserting an exogenous gene in an HVT, including inserting the exogenous gene into an HVT genome using a CRISPR-Cas9 technology; in which
the exogenous gene is inserted into a spacer region between an HVT005 region and an HVT006 region of the HVT genome;
In some embodiments, an insertion site is located between 8,867 nt and 9,319 nt in the spacer region between an HVT005 region and an HVT006 region of the HVT genome, and the nucleotide sequence of the insertion is set forth in SEQ ID NO: 1; and
In some embodiments, the CRISPR-Cas9 technology is achieved by construction of a CRISPR-Cas9 plasmid, including:
S1-1) designing an sgRNA sequence for the spacer region between an HVT005 region and an HVT006 region, in which the sgRNA sequence is set forth in SEQ ID NO: 7, TCATATACTGAATCGTAGGG SEQ ID NO: 7; and
S1-2) synthesizing a plus-strand HVT005/006-sgRNA-F and a minus-strand HVT005/006-sgRNA-R according to the designed sgRNA sequence, and conducting annealing to form a dsDNA, and inserting the dsDNA into a vector to obtain the CRISPR-Cas9 plasmid; where
sequences of the plus-strand HVT005/006-sgRNA-F and the minus-strand HVT005/006-sgRNA-R are set forth in SEQ ID NO: 8 and SEQ ID NO: 9, respectively:
The present disclosure provides a site for inserting an exogenous gene into an HVT genome, that is, the exogenous gene is inserted into a spacer region between an HVT005 region and an HVT006 region of the HVT genome. More specifically, the insertion site is located between 8,867 nt and 9,319 nt in the spacer region between an HVT005 region and an HVT006 region of the HVT genome, and has a nucleotide sequence set forth in SEQ ID NO: 1.
The present disclosure provides a CRISPR/Cas9-based sgRNA guide sequence HVT005/006-sgRNA targeting a HVT005-HVT006 spacer region.
In the present disclosure, the NDV F gene is a complete ORF of a VII type NDV F gene, and has a cleavage site replaced with a cleavage site of a live vaccine (La Sota strain) of Newcastle disease in chicken. The nucleotide sequence of the NDV F gene is set forth in SEQ ID NO: 2. An expression cassette of the NDV F gene is ligated successively by an mCMV promoter, the exogenous gene and an SV40 poly A.
In the present disclosure, the AIV HA gene is a complete ORF of an H9N2 subtype AIV HA gene, having a nucleotide sequence set forth in SEQ ID NO: 3. In some embodiments, an expression cassette the H9N2 subtype AIV HA gene is ligated successively by an mCMV promoter, the exogenous gene and an SV40 poly A.
The mCMV promoter is a mouse-derived mCMV promoter, with a nucleotide sequence set forth in SEQ ID NO: 4. The nucleotide sequence of the SV40 poly A is set forth in SEQ ID NO: 5.
A construction method of a recombinant HVT expressing an NDV F protein, including the following steps: inserting an exogenous gene into an HVT genome using CRISPR-Cas9 technology, and conducting screening and purification to obtain a recombinant virus, namely the recombinant HVT expressing an NDV F protein.
The construction method of the recombinant HVT expressing an NDV F protein includes specifically the following steps:
(1) construction of a CRISPR-Cas9 plasmid, pX330-HVT05/06-sgRNA:
1) designing and synthesizing an sgRNA sequence for an HVT005/006 target site; in which a specific sequence is HVT005/006-sgRNA: TCATATACTGAATCGTAGGG (SEQ ID NO: 7);
2) annealing synthesized HVT005/006-sgRNA-F and HVT005/006-sgRNA-R sequences to form a dsDNA, and inserting the dsDNA into a pX330 vector (purchased from YouBio) to construct the pX330-HVT05/06-sgRNA;
(2) construction of a donor vector pT-sgA-GFP-F:
1) inserting an F gene fragment into a pcDNA3.1-SfiI vector (referring to 2.2.2.1 of Example) to obtain a pcDNA3.1-SfiI-F vector; and
2) ligating an expression cassette of the F gene in the pcDNA3.1-SfiI-F vector into a pT-sgA-GFP vector through an SfiI restriction site (referring to 2.2.3 of Example) to obtain the pT-sgA-GFP-F vector; and
(3) construction and purification of a recombinant HVT, rHVT-F:
1) co-transfecting a pX459-sgA plasmid (referring to 1.1 of Example), a pT-sgA-GFP-F plasmid (referring to 2.2 of Example) and a pX330-HVT005/006-sgRNA plasmid (referring to 2.1 of Example) into primary chickens embryo fibroblasts (CEFs), inoculating with an HVT FC126 strain, conducting culture at 37° C. until the primary CEFs are cytopathic, followed by purification through virus spotting to obtain a recombinant virus rHVT-GFP-F; and
2) transfecting a plasmid pcDNA3.1-Cre (purchased from YouBio) into the primary CEFs, inoculating with the recombinant virus rHVT-GFP-F, conducting culture at 37° C. until the primary CEFs are cytopathic, followed by conducting purification through virus spotting to obtain the recombinant virus rHVT-F, namely the recombinant HVT expressing an NDV F protein.
A construction method of a recombinant HVT expressing an AIV HA protein is the same as the construction method of a recombinant HVT expressing an NDV F protein but the F gene is replaced by the HA gene. Other pathogen-related protective antigen genes can also be constructed according to the same method.
1. In the present disclosure, it is found for the first time that the spacer region between the HVT005 region and the HVT006 region can be used as an insertion site for the exogenous gene of the HVT. The NDV F gene and the AIV HA gene are inserted into the spacer region between the HVT005 region and the HVT006 region of the HVT genome using CRISPR/Cas9 technology, and a vaccine candidate is obtained for prevention of Newcastle disease and avian influenza in chicken.
2. Compared with common homologous recombination, BAC homologous recombination and other technical means, the CRISPR/Cas9 gene knock-in technology is more effective and rapid, which is helpful for rapid construction of an MDV-based recombinant vaccine.
3. The CRISPR/Cas9 is a simple knock-in method, and the designed sgRNA sequence along with the donor plasmid may efficiently insert the target sites.
The present disclosure will be described in detail below by taking construction of rHVT-F and rHVT-HA as an example.
1. Materials
1.1. Strains, Plasmids and Antibodies
An HVT FC-126 vaccine strain, an NDV genotype VII JS strain and an AIV H9N2 (2019) strain were identified and preserved by the Key Laboratory of Avian Preventive Medicine, Ministry of Education, Yangzhou University. All the strains were purchased therefrom.
Plasmids: pX330, pX459, pcDNA3.1 and pcDNA3.1-Cre plasmids were purchased from a website of Hunan Keai Medical Equipment Co., Ltd. (YouBio). The pGEM®-T Easy Vector Systems were purchased from Promega. A plasmid pCMV-N-GFP was purchased from Beyotime Biotechnology. A plasmid pX459-sgA was constructed and preserved by the Key Laboratory of Avian Preventive Medicine, Ministry of Education, Yangzhou University; the plasmid pX459-sgA was obtained by ligating an sgA sequence into the pX459 plasmid through a BbsI restriction site (referring to Knock-in of large reporter genes in human cells via CRISPR/Cas9-induced homology-dependent and independent DNA repair, https://doi.org/10.1093/nar/gkw064).
Antibodies: anti-HA (H9) monoclonal antibody 2G4 (referring to “Identification and Analysis of Critical Amino Acids Mutations in Epitopes in Hemagglutinin and Neuraminidase of H9N2 Influenza Virus in the Pressure of Antibody”, Zhimin Wan) and anti-F (NDV) monoclonal antibody 1D10 (referring to “Characteristics and Preliminary Application of Anti-Newcastle Disease Virus Fusion Protein Monoclonal Antibody”, Qiangian Wang) were prepared and preserved by the Key Laboratory of Avian Preventive Medicine, Ministry of Education, Yangzhou University.
2. Methods
2.1. Target Site Design and sgRNA Sequence Synthesis
An exogenous gene was inserted into an HVT005-HVT006 spacer region within the HVT; referring to an HVT005-HVT006 spacer region sequence of a full gene sequence of an HVT FC126 strain (accession number: AF291866) registered in the GenBank, a target-site-based sgRNA was designed using a sgRNA design website (http://crispr.mit.edu/) to obtain a sgRNA sequence.
A base CACC was added at 5′-end of the sgRNA guide sequence, and a first base T was replaced with G to form a plus-strand sgRNA sequence; the designed sgRNA sequence was reverse-complemented, and a base AAAC was added to the 5′-end to form a minus-strand sgRNA sequence.
2.2. Construction of a Targeting Vector:
(1) synthesized HVT005/006-sgRNA-F and HVT005/006-sgRNA-R sequences were annealed to form a dsDNA, in which a reaction system was as follows:
The above system was shaken, centrifuged and placed in a PCR instrument. The PCR protocol consisted of 30 min at 37° C., 5 min at 95° C., gradient cooling at 5° C./min, and then 10 min at 4° C.
(2) The pX330 vector was digested with a BbsI enzyme for linearization, in which a reaction system was as follows:
After incubation at 37° C. for 2 h, a linearized vector pX330 was excised and recovered.
(3) An annealed dsDNA was ligated with the linearized vector pX330, in which a reaction system was as follows:
The above system was shaken, centrifuged, and ligated at 16° C. overnight to obtain a ligated product.
(4) 50 μL of DH5α competent cells (purchased from Nanjing Vazyme Biotech Co., Ltd.) were mixed well with 10 μL of the ligated product, followed by conducting incubation on ice for 30 min. The above mixture was treated in a water bath at 42° C. for 90 sec, and a tube was quickly inserted into ice and allowed to stand for 3 min. 800 μL of an anti-LB-free medium was added to the tube, followed by incubation on a shaker (37° C./150 rpm) for 1 h; 200 μL of a bacterial solution was pipetted and spread evenly on a solid medium containing ampicillin (50 μg/mL) prepared in advance, followed by inverted incubation at 37° C., and transformed clones were formed at 14 h to 16 h.
(5) A plasmid was extracted, and primers were designed according to the vector pX330 and the sgRNA sequence for PCR identification.
PCR System
The reaction program was as follows: 95° C. for 5 min; 35 cycles of 95° C. for 30 sec, 60° C. for 30 sec, and then 72° C. for 30 sec; and 72° C. for 10 min.
After the reaction, electrophoresis was conducted with 1% agarose gel (
2.2. Construction of a Donor Vector pT-sgA-GFP-F
2.2.1. Amplification of NDV F Gene
Overlap PCR primers were designed for an F gene sequence of an NDV genotype VII and an F gene cleavage site sequence of an NDV La Sota strain. Primer sequences were as follows:
PCR amplification was conducted on a left fragment of the F gene and a right fragment of the F gene taking a reverse-transcribed cDNA of the NDV genotype VII as a template, and using F(overlap)left-F and F(overlap)left-R, F(overlap)right-F and F(overlap)right-R as primers, respectively; and overlap PCR amplification was conducted on an F gene fragment after replacement of the cleavage site using the left fragment of the F gene and the right fragment of the F gene as templates, and using F(overlap)left-F and F(overlap)right-R were used as primers. The F gene fragment after replacement of the cleavage site had a nucleotide sequence set forth in SEQ ID NO: 2.
Primers were designed with Primer Premier 5.0 software, and an NotI restriction sites were introduced upstream and downstream. Primer sequences were as follows:
The PCR amplification was conducted on the F gene using the F gene fragment after replacement of the cleavage site as a template, and using NotI-F-F and NotI-F-R as primers; electrophoresis was conducted with 1% agarose gel after the reaction, and a target band was recovered for later use.
2.2.2. Construction of an Eukaryotic Expression Vector pcDNA3.1-SfiI-F
2.2.2.1. Construction of a Plasmid pcDNA3.1-SfiI
An mCMV+polyA element for gene sequence synthesis (NheI+SfiI+mCMV+NotI+SV40ployA+SfiI+PmeI) was synthesized, in which an mCMV sequence referred to a mouse cytomegalovirus genome (Murid herpesvirus 1 strain Smith, complete genome, GenBank: GU305914.1, 184,336 nt to 182,946 nt), and the entire element had a nucleotide sequence set forth in SEQ ID NO: 6.
The sequence fragment of mCMV+polyA for gene synthesis was double-digested with NheI and PmeI, and ligated into a pcDNA3.1 plasmid through NheI and PmeI restriction sites to obtain a plasmid pcDNA3.1-SfiI.
2.2.2.2. Construction of a Plasmid pcDNA3.1-SfiI-F
PCR gel recovery products of the F gene in 2.2.1 and the plasmid pcDNA3.1-SfiI were digested with the NotI; after conducting 1% gel electrophoresis, the gel was cut to recover a linearized pcDNA3.1-SfiI-NotI vector and an NotI-F gene fragment. The recovered pcDNA3.1-SfiI-NotI fragment and the NotI-F gene fragment were ligated to construct the plasmid pcDNA3.1-SfiI-F.
2.2.3. Construction of a Donor Vector pT-sgA-GFP-F
2.2.3.1. Construction of a Plasmid pT-sgA
A gene sequence (sgA+loxP+PacI+LoxP+SfiI+spacer+SfiI+sgA) was synthesized, in which primers were as follows; sgA-SfiI-F and sgA-SfiI-R were annealed to form dsDNA fragments, and the fragments were ligated into a pGEM-T-easy vector to obtain a pT-sgA vector.
2.2.3.2. Construction of a Plasmid pT-sgA-GFP
The following primers were designed for a GFP expression cassette:
The GFP expression cassette (PacI+CMV promoter+GFP+SV40PolyA+PacI) was amplified using a pCMV-N-GFP plasmid as a template, and using PacI-GFP-F and PacI-GFP-R as primers, and then ligated through a PacI restriction site into a pT-sgA plasmid to obtain the pT-sgA-GFP plasmid.
2.2.3.3. Construction of a Plasmid pT-sgA-GFP-F
The plasmids pcDNA3.1-SfiI-F and pT-sgA-GFP were digested with the SfiI, followed by conducting 1% gel electrophoresis, and an SfiI-F fragment in the pcDNA3.1-SfiI-F vector and a linearized pT-sgA-GFP vector were recovered by gel cutting. The recovered SfiI-F fragment and the pT-sgA-GFP-SfiI fragment were ligated to construct the plasmid pT-sgA-GFP-F.
2.3. Construction of a Donor Vector pT-sgA-GFP-HA
2.3.1. Amplification of AIV HA Gene
Primers were designed with Primer Premier 5.0 software, and an NotI restriction sites were introduced upstream and downstream. Primer sequences were as follows:
The PCR amplification was conducted on the HA gene using an AIV H9N2 (2019) strain cDNA as a template, and using NotI-HA-F and NotI-HA-R as primers; 1% agarose gel electrophoresis was conducted after the reaction, and a target band was recovered for later use.
The HA gene had a nucleotide sequence set forth in SEQ ID NO: 3.
2.3.2. Construction of an Eukaryotic Expression Vector pcDNA3.1-SfiI-HA
PCR gel recovery products of the HA gene in 2.3.1 and the plasmid pcDNA3.1-SfiI (referring to 2.2.2.1 in Example) were digested with the NotI; after conducting 1% gel electrophoresis, the gel was cut to recover a linearized pcDNA3.1-SfiI vector and an NotI-HA gene fragment. The recovered pcDNA3.1-SfiI-NotI fragment and the NotI-HA fragment were ligated to construct the plasmid pcDNA3.1-SfiI-HA.
2.3.3. Construction of a Donor Vector pT-sgA-GFP-HA
The plasmids pcDNA3.1-SfiI-HA and pT-sgA-GFP (referring to 2.2.3.2 in Example) were digested with the SfiI, followed by conducting 1% gel electrophoresis, and an SfiI-HA fragment in the pcDNA3.1-SfiI-HA vector and a linearized pT-sgA-GFP vector were recovered by gel cutting. The recovered SfiI-HA fragment and the pT-sgA-GFP-SfiI fragment were ligated to construct the plasmid pT-sgA-GFP-HA.
2.4. Construction of a Recombinant HVT for Expressing GFP and F Proteins, rHVT-GFP-F
2.4.1. Cell Transfection
Before transfection, primary CEF cells were prepared, in which the cells were grown in a 24-well cell culture plate with an M199 medium containing 5% fetal bovine serum; when the cells grew to 80% of a monolayer, they were transfected with TransIT-X2 according to instructions of the TransIT-X2 transfection reagent (Mirusbio), in which a transfection system of each well included 0.25 μg of plasmid pX459-sgA, 0.25 μg of plasmid pT-sgA-GFP-F and 0.25 μg of plasmid pX330-HVT005/006-sgRNA.
2.4.2. Virus Infection
8 h to 12 h after the transfection, the cells were infected with the HVT, in which the virus in each well had an amount of 5,000 PFU. After incubation for 2 d to 3 d at 37° C. and 5% CO2, cells in 1 well were digested with trypsin and inoculated on 2 new CEF 6-well cell culture plates. After incubation for 3 d to 4 d at 37° C. and 5% CO2, the cells were observed under a fluorescence microscope, and viral plaques were selected with green fluorescence.
2.4.3. Purification of a Recombinant Virus rHVT-GFP-F
The cells were observed under the fluorescence microscope, the viral plaques with green fluorescence were marked using a marker, and labeled green fluorescence-containing cells were selected by trypsin digestion, and inoculated on a secondary CEF monolayer cells, followed by incubation at 37° C. and 5% CO2 for 3 d to 4 d; the above steps were repeated until all plaques showed fluorescence, and a completely-purified recombinant virus was named rHVT-GFP-F (shown in
2.5. Construction of a Recombinant HVT for Expressing GFP and HA Proteins, rHVT-GFP-HA
2.5.1. Cell Transfection
Before transfection, primary CEF cells were prepared, in which the cells were grown in a 24-well cell culture plate with an M199 medium containing 5% fetal bovine serum; when the cells grew to 80% of a monolayer, they were transfected with TransIT-X2 according to instructions of the TransIT-X2 transfection reagent (Mirusbio), in which a transfection system of each well included 0.25 μg of plasmid pX459-sgA, 0.25 μg of plasmid pT-sgA-GFP-HA and 0.25 μg of plasmid pX330-HVT005/006-sgRNA.
2.5.2. Virus Infection
8 h to 12 h after the transfection, the cells were infected with the HVT, in which the virus in each well had an amount of 5,000 PFU. After incubation for 2 d to 3 d at 37° C. and 5% CO2, cells in 1 well were digested with trypsin and inoculated on 2 new CEF 6-well cell culture plates. After incubation for 3 d to 4 d at 37° C. and 5% CO2, the cells were observed under a fluorescence microscope, and viral plaques were selected with green fluorescence.
2.5.3. Purification of a Recombinant Virus rHVT-GFP-HA
The cells were observed under the fluorescence microscope, the viral plaques with green fluorescence were marked using a marker, and labeled green fluorescence-containing cells were selected by trypsin digestion, and inoculated on a secondary CEF monolayer cells, followed by incubation at 37° C. and 5% CO2 for 3 d to 4 d; the above steps were repeated until all plaques showed fluorescence, and a completely-purified recombinant virus was named rHVT-GFP-HA (shown in
2.6. Construction of a Recombinant HVT for Expressing an F Protein, rHVT-F
2.6.1. Cell Transfection
Before transfection, primary CEF cells were prepared, where the cells were grown in a 24-well cell culture plate with an M199 medium containing 5% fetal bovine serum; when the cells grew to 80% of a monolayer, they were transfected with TransIT-X2 according to instructions of the TransIT-X2 transfection reagent (Mirusbio), in which a transfection system of each well included 0.5 μg of plasmid pcDNA3.1-Cre.
2.6.2. Virus Infection
8 h to 12 h after the transfection, the cells were infected with the rHVT-GFP-F, in which the virus in each well had an amount of 5,000 PFU. After incubation for 2 d to 3 d at 37° C. and 5% CO2, cells in 1 well were digested with trypsin and inoculated on 2 new CEF 6-well cell culture plates. After incubation for 3 d to 4 d at 37° C. and 5% CO2, the cells were observed under a fluorescence microscope, and viral plaques were selected without green fluorescence.
2.6.3. Purification of a Recombinant Virus rHVT-F
The cells were observed under the fluorescence microscope, the viral plaques without green fluorescence were marked using a marker, and labeled pathological cells were selected by trypsin digestion, and inoculated on a secondary CEF monolayer cells, followed by incubation at 37° C. and 5% CO2 for 3 d to 4 d; the above steps were repeated until all plaques showed no fluorescence, and a completely-purified recombinant virus was named rHVT-F.
2.7. Construction of a Recombinant HVT for Expressing an HA Protein, rHVT-HA
2.7.1. Cell Transfection
Before transfection, primary CEF cells were prepared, in which the cells were grown in a 24-well cell culture plate with an M199 medium containing 5% fetal bovine serum; when the cells grew to 80% of a monolayer, they were transfected with TransIT-X2 according to instructions of the TransIT-X2 transfection reagent (Mirusbio), in which a transfection system of each well included 0.5 μg of plasmid pcDNA3.1-Cre.
2.7.2. Virus Infection
8 h to 12 h after the transfection, the cells were infected with the rHVT-GFP-HA, in which the virus in each well had an amount of 5,000 PFU. After incubation for 2 d to 3 d at 37° C. and 5% CO2, cells in 1 well were digested with trypsini and inoculated on 2 new CEF 6-well cell culture plates. After incubation for 3 d to 4 d at 37° C. and 5% CO2, the cells were observed under a fluorescence microscope, and viral plaques were selected without green fluorescence.
2.7.3. Purification of a Recombinant Virus rHVT-HA
The cells were observed under the fluorescence microscope, the viral plaques without green fluorescence were marked using a marker, and labeled pathological cells were selected by trypsin digestion, and inoculated on a secondary CEF monolayer cells, followed by incubation at 37° C. and 5% CO2 for 3 d to 4 d; the above steps were repeated until all plaques showed no fluorescence, and a completely-purified recombinant virus was named rHVT-HA.
2.8. Identification of the Recombinant Virus and Detection of Passage Stability
2.8.1. Indirect Immunofluorescence Assay (IFA)
The recombinant virus rHVT-F strain, the recombinant virus rHVT-HA strain and an HVT parental virus were inoculated into a 24-well cell culture plate covered with monolayer CEF, followed by incubation at 37° C. and 5% CO2; after the cells had typical plaques, the medium was discarded, and the cells were fixated with a cold fixative solution of acetone:ethanol (3:2) for 10 min, and washed twice with a PBS; 500 μL (1:200 dilution) of a 1D10 monoclonal antibody was added to the wells inoculated with the rHVT-F strain, 500 μL (1:200 dilution) of a 2G4 monoclonal antibody was added to the wells inoculated with the rHVT-HA strain, 500 μL (1:200 dilution) of the 1D10 monoclonal antibody was added to one well inoculated with the HVT strain, and 500 μL (1:200 dilution) of the 2G4 monoclonal antibody was added to the other well inoculated with the HVT strain. The cells were incubated for 1 h in a constant-temperature incubator at 37° C., and washed three times with the PBS; 500 μL (1:800 dilution) of an Alexa Fluor® 594 goat anti-mouse IgG antibody was added to each well, followed by incubation in a 37° C. incubator for 1 h, and then washing three times with the PBS; the cells were observed under a fluorescence microscope. It was showed that specific red fluorescence appeared in the wells infected with the rHVT-F and rHVT-HA strains (shown in
2.8.2. PCR Detection of the Passage Stability
The rHVT-F strain and the rHVT-HA strain were continuously passed on CEF for 15 generations, and the genome of the recombinant virus was extracted every 5 generations; PCR was conducted using the extracted genome as a template and HVT-005/006-F and HVT-005/006-R as primers, and target bands of about 3,500 bp were amplified, respectively (shown in
3. The rHVT-F Strain as a Vaccine
3.1. Amplification of the rHVT-F Strain
CEFs were inoculated into several T75 cell flasks, and inoculated with rHVT-F after 1 d of incubation, and each flask was inoculated with 50,000 PFU of the virus. After inoculation, the virus growth was observed every day; generally, 48 h to 72 h after inoculation, when more than 70% of the monolayer cells had typical cytopathic effects, the cell medium was discarded, and after washing with PBS once, the cells were digested with an appropriate amount of trypsin; when the monolayer cells shrank and were about to separate from the bottle wall, the trypsin was discarded, and the digestion was terminated using an equal amount of a cell medium containing 5% bovine serum. The cells were pipetted with a pipette to make the cells all detached from the bottle wall; after being collected by centrifugation, the cells were resuspended with a cryoprotectant (a cell medium containing 15% bovine serum and 10% DMSO), divided into cryovials at −70° C., and transferred to liquid nitrogen for storage on a second day.
3.2. Immunization of the rHVT-F Strain
18 1-day-old SPF chickens were randomly divided into two groups, namely an rHVT-F group and a challenge control group; in which the rHVT-F group was inoculated with 2,000 PFU/chicken of an rHVT-F recombinant vaccine by intraperitoneal injection at 1 day old, while the challenge control group was inoculated with a vaccine dilution. The two groups of chickens were challenged with a virulent NDV F48E8 strain by intramuscular injection at 28-day-old, with a challenge dosage of 105 ELD50/chicken. After the challenge, the incidence and mortality of the chickens in each group were observed and counted every day for two weeks.
3.3. Challenge Protection Effects of rHVT-F Strain-Immunized Chickens
The incidence and mortality of the chickens in each group are shown in the table below. It could be seen that the chickens in the rHVT-F group had a challenge protection rate reaching 100%, while the challenge control group had a challenge protection rate of 0%.
The results of immune protection evaluation showed that the chickens had a desirable immune protection effect against the virulent NDV strain after immunization with the recombinant HVT, rHVT-F strain.
| Number | Date | Country | Kind |
|---|---|---|---|
| 202111318523.7 | Nov 2021 | CN | national |
