Protection conferred by a recombinant Marek’s disease virus that expresses the spike protein from infectious bronchitis virus in specific pathogen-free chicken
© Zhang et al.; licensee BioMed Central Ltd. 2012
Received: 9 October 2011
Accepted: 4 May 2012
Published: 4 May 2012
In many countries, the predominant field isolates of infectious bronchitis virus (IBV) have been classified as QX-like strains since 1996. However, no commercial vaccines that are specific for this type of IBV are currently available. Therefore, there is an urgent need to develop novel vaccines that prevent QX-like IBV infection.
A recombinant Marek’s disease virus (MDV), rMDV-S1, that expresses the S1 subunit of the spike (S) protein from the QX-like infectious bronchitis virus (IBV) was constructed by inserting the IBV S1 gene into the genome of the CVI988/Rispens strain of MDV. Specific pathogen-free (SPF) chickens that were vaccinated with rMDV-S1 were protected when challenged with the QX-like IBV. They were observed to have mild clinical signs of disease, a short virus-shedding period and low mortality. Additionally, the rMDV-S1 conferred full protection to chickens against virulent MDV, as did the CVI988/Rispens strain.
Our results demonstrate that rMDV-S1 is an effective and promising recombinant vaccine for the prevention of QX-like IBV infection.
KeywordsInfectious bronchitis virus Spike protein Marek’s disease virus
Infectious bronchitis (IB) is an acute, contagious disease of both layer and broiler chickens. This disease is caused by infectious bronchitis virus (IBV) and has respiratory signs. In hens infected with IBV, decreased egg production and quality are often observed. Some IBV strains are nephropathogenic, and infection with these strains can result in interstitial nephritis and mortality . IBV encodes four major structural proteins: the spike (S) protein, the nucleocapsid (N) protein, the membrane (M) protein, and the envelope (E) protein. The S protein of IBV is initially translated into a precursor glycoprotein that is cleaved post-translationally to form two subunits, S1 and S2 . Most of the virus-neutralizing antibodies target the S1 protein . Currently, both modified live and inactivated vaccines are commercially available . Despite the intensive vaccination efforts, outbreaks of IBV frequently occur due to the persistence of different IBV serotypes. These serotypes arise from point mutations, insertions, deletions, and RNA recombination . Multiple distinct genetic groups of IBV have been reported, but since 1996, the predominant field isolates in China have been classified as QX-like (LX4-type) [4–8]. QX-like IBVs are circulating in almost all of the countries in Europe, and these variants are frequently associated with cases of nephritis and false layer syndrome in chickens [9–14]. Clearly, QX-like IBVs are a serious threat to the poultry industry. However, no vaccines against QX-like IBVs are commercially available. Therefore, there is an urgent need to develop vaccines that can prevent QX-like IBV infection.
Marek’s disease (MD) is a transmissible, malignant T-cell lymphoma in chickens caused by Marek’s disease virus (MDV) . MDV strains are classified into the following three serotypes: Gallid herpesvirus 2 (MDV serotype 1), Gallid herpesvirus 3 (MDV serotype 2), and Meleagrid herpesvirus 1 (MDV serotype 3/herpesvirus of turkeys) . All of the pathogenic strains of the virus are included in serotype 1, and they range from highly virulent to weakly virulent strains. These strains, such as CVI988/Rispens, may be attenuated by extensive serial passage in tissue culture, with loss of pathogenic properties but retention of immunogenicity. The CVI988/Rispens strain provides good protection against challenge even with the newly discovered highly virulent pathotype of MDV .
MDV has several ideal characteristics that make it useful as a vector for recombinant vaccine. MDV infection results in a persistent infection, and because it is transmitted cell to cell, the virus is not susceptible to maternal antibodies. Furthermore, the virus has a large genome with several regions that are not essential for viral replication, which are suitable for the insertion of foreign genes . In the present study, a recombinant MDV (rMDV) expressing the S1 protein from QX-like IBV (rMDV-S1) was constructed, and the protective efficacy of the virus as a vaccine against both IBV and MDV in SPF chickens was investigated.
Construction of the transfer vector
Construction and characterization of the recombinant viruses
The rMDV-S1 virus was genetically stable after 30 sequential passages in CEFs.
Induction of the IBV antibody response
Protection against IBV challenge
Morbidity and mortality of vaccinated chickens after challenge with the IBV CK/CH/JS/06II strain
Virus isolation from tracheal swabs or from the kidneys of vaccinated chickens after challenge with the IBV CK/CH/JS/06II strain
Isolation of virus★
Days post-virus challenge
Bodyweight changes of vaccinated chickens after challenge with the IBV CK/CH/JS/06II strain
49.5 ± 0.8 a (n = 20)
259.6 ± 10.9 a (n = 20)
433.0 ± 29.8 a (n = 19)
49.4 ± 0.7 a (n = 20)
256.6 ± 11.4 a (n = 20)
395.7 ± 48.7 b (n = 14)
49.5 ± 1.1 a (n = 20)
258.8 ± 10.9 a (n = 20)
391.6 ± 50.9 b (n = 14)
Protection against MDV challenge
Protective efficacy of the rMDV-S1 virus against MDV RB1B challenge
Antigenic variation among IBV strains is common [3, 18–28]. Due to the regular emergence of antigenic variants, the occurrence of disease and the use of vaccines will vary by geographical region. According to phylogenetic analysis by Han et al., most of the recently described IBV isolates were from 9 distinct genetic groups, and the predominant group was the QX-like strain [6, 29]. In China, the commonly used IBV vaccine strains, such as H120, H52 and M41, are all Mass-type vaccines, and the S1 gene sequence similarity is low compared with the currently circulating IBV strains . This result could explain why the increasing number of vaccination failures. Thus, developing novel vaccines against QX-like IBVs is necessary [5, 19, 23].
The construction of a recombinant virus vector-based vaccine is a good option to develop IBV vaccines that are specific to new IBV serotypes. Fowlpox viruses that express the IBV S1 gene have been reported previously [30–32], and all of these vaccines have been described to confer protection against viral challenge with homotypic IBV strains and some heterotypic IBV strains in SPF chickens. However, the protective efficacy that is conferred by recombinant fowlpox viruses could be diminished in commercial chickens due to the presence of maternal antibodies against fowlpox virus [33, 34]. In fact, fowlpox vaccines are widely used in commercial chickens, which hinder the application of recombinant vaccines that are based on fowlpox virus vectors. Compared with other viral vectors, the CVI988/Rispens has several unique advantages. The CVI988/Rispens is the most effective MD vaccine obtained thus far . Additionally, the CVI988/Rispens can persistently infect chickens, which results in the continuous expression of inserted, heterologous antigens . Finally, the CVI988/Rispens can be used to inoculate one-day-old chickens to establish an early immunity.
Although the rMDV-S1 vaccinated group induced a low level antibody response until 4 weeks post-vaccination, but the level of antibody increased more rapidly compared to the control groups following IBV challenge. Additionally, chickens vaccinated with rMDV-S1 were observed to have a shorter virus-shedding period and a greater increase in bodyweight. These results suggested that rMDV-S1 immunization could induce an efficient primary immune response that was specific to the expressed S1 protein. When the chickens were challenged with IBV, the primed B cells could rapidly differentiate into plasma cells, thus permitting the production of higher titers of IBV-specific circulating antibody within a shorter period of time. This finding is important for the establishment of an early-stage active immune response against IBV infection.
We constructed a recombinant MDV, called rMDV-S1, that expressed the S1 protein of a QX-like IBV. Vaccination with rMDV-S1 conferred good protection in SPF chickens against both IBV and MDV challenge. Taken together, rMDV-S1 is a promising vaccine candidate for the control of infection by QX-like IBVs: the major IBV genotype currently circulating in many countries.
Materials and Methods
Viruses, SPF chicken embryos and chickens
The CVI988/Rispens strain of MDV was used as the vector for the construction of the recombinant virus, and the virulent RB1B strain of MDV was used as the challenge virus. MDVs were propagated in secondary CEFs in Medium 199 supplemented with 3% newborn calf serum (Thermo Fisher Scientific).
The QX-like IBV strain CK/CH/JS/06II was used for S1 gene [GenBank: EU031526] amplification and as the challenge virus. The challenge dose was determined in a previous experiment in SPF chickens. This dose (2 × 103.5 EID50 per chicken) could induce clinical signs, including death, beginning on day 2 post-challenge.
SPF chicken embryos were purchased from Merial-Vital Laboratory Animal Technology Co., Ltd. (Beijing, China). SPF chickens were hatched from SPF embryos and reared in negative-pressure isolators. Feed and water were available ad libitum. This study was conducted in strict accordance with the recommendations given in the Guide for the Care and Use of Laboratory Animals of the National Research Council. The animal care and use committee of Yangzhou University approved all experiments and procedures conducted on the animals (approval ID: SYXK (Su) 2007-0005).
Construction of the transfer vector
Construction of rMDV
The recombinant virus was produced by calcium phosphate-mediated transfection of secondary CEFs that were cultured in a 60-mm dish with 100 ng of the pUP-LTR-EGFP-S1-DOWN transfer vector and 10 μg of CVI988/Rispens genomic DNA . The transfected CEFs were cultured at 37°C in 5% CO2 for 5–7 days until viral plaques were visible. Viral plaques that expressed EGFP were identified by fluorescence microscopy (Leica DM RIB). These plaques were subsequently scraped from the monolayer using a micropipette containing a small amount of 0.25% trypsin. The cells were then aspirated, trypsinized into a single cell suspension, and passaged repeatedly. This process was repeated until all of the visible plaques were fluorescent. The resulting intermediate recombinant virus rMDV-EGFP-S1 was then amplified in CEFs.
Genomic DNA from the rMDV-EGFP-S1 virus was prepared as described above, and the EGFP gene between the two loxP sites was excised with Cre recombinase (New England BioLabs), which ensured that the S1 gene was placed immediately downstream of the LTR promoter. The genomic DNA from rMDV-EGFP-S1, in which the EGFP gene had been excised, was used for subsequent transfection experiments to generate new recombinant viruses that contained no reporter gene. The resulting non-fluorescent rMDV, called rMDV-S1, was screened and purified as described above. The complete process is illustrated in Figure 7c.
PCR Identification of rMDV-S1
Primers S1-F and S1-R were used to amplify the inserted S1 gene from rMDV-S1. To further verify the correct orientation of the S1 gene, the primer PLTR-F (5′-ATCGGCATCAAGAGCAGG-3′) was designed according the sequence of the LTR promoter in combination with the primer S1-R that would amplify a 2.0-kb DNA fragment that comprised part of the LTR promoter sequence and the entire S1 gene sequence if the recombinant virus was engineered correctly. To verify whether the recombination event occurred at the expected location in the genome of the CVI988/Rispens vector, four other primers, designated Geno-F (5′-GCGTAGCCAGACCGCACCA-3′), Geno-R (5′-GCCTGAATAAAGACCGACA-3′), PLTR-R (5′-ATTGGCTCAGTATGATAGTTC-3′) and S1-F2 (5′-TTGCCACGTCAAGGAAGC-3′), were designed. The binding site for Geno-F was located upstream of the left homologous arm (153275–153293 nt in the CVI988/Rispens genome), and Geno-R was located downstream of the right homologous arm (154958–154976 nt in the CVI988/Rispens genome). PLTR-R and S1-F2 were located in the LTR promoter and the S1 gene, respectively. A detailed PCR scheme is illustrated in Figure 7d.
CEFs were harvested, and the total cellular RNA was prepared using TRIzol reagent (Invitrogen) after 48 hours of infection with either the rMDV-S1 or CVI988/Rispens. Total RNA was treated with DNase I (New England BioLabs) to eliminate any genomic DNA contamination and was then reverse-transcribed using oligo (dT)15 primers (Takara, Dalian, China). Subsequently, the S1 gene was amplified with primers S1-F and S1-R as described above. A positive control reaction using the transfer vector pUP-LTR-EGFP-S1-DOWN as the amplification template was performed. Additionally, a reaction with DNase I-treated total RNA as the amplification template was included in the RT-PCR analysis to check for DNA contamination.
Indirect immunofluorescence assay (IFA)
CEFs were grown in a 24-well tissue culture plate and infected with rMDV-S1 or the CVI988/Rispens (100 PFU/well) vector. After incubation for 48 h at 37°C, these cells were fixed for 15 min with methanol-acetone (1:1) and incubated for 30 min in the presence of a 5 μg/ml dilution of a chicken anti-IBV polyclonal antibody that was prepared via multiple immunizations of SPF chickens with the Mass-type IBV antigen (China Institute of Veterinary Drug Control, Beijing, China) and a 7.5 μg/ml dilution of fluorescein-conjugated rabbit anti-chicken IgY (H+L) (Thermo Fisher Scientific) at 37°C. After each step, the cells were washed three times for 5 min with PBS. The cells were overlaid with 90% glycerol containing 25 mg/ml 1,4 diazabicyclo[2.2.2]octane (Sigma-Aldrich). The binding of the fluorescein-conjugated, secondary antibodies was analyzed by fluorescent microscopy (Leica DM RIB).
Genetic stability of rMDV
The rMDV-S1 was sequentially passaged in CEFs to determine the genetic stability of the virus. As described above, the genomic DNA from passages 5, 10, 15, 20, 25 and 30 were extracted and used as a template for amplification of the S1 gene. IFAs were also applied to confirm the expression of the S1 gene in each passage.
Protective efficacy of rMDV vaccination against IBV
Sixty, one-day-old SPF white Leghorn chickens were divided into 3 groups with 20 chickens in each group. The chickens were raised in individual isolators under negative pressure. Two groups were inoculated subcutaneously on the back of the neck with 5 × 103 PFU of rMDV-S1 or CVI988/Rispens. The third group was mock-injected with PBS. An additional 10 chickens were raised separately to serve as the healthy controls.
Serum was collected weekly after vaccination until the chickens were challenged. Pre-vaccination serum was also collected. Serum samples were assayed in single dilutions (1:500) using an Infectious Bronchitis Virus Antibody Test Kit (IDEXX, ME, USA) according to the manufacturer’s instructions. S/P ratios that were greater than 0.2 were considered positive.
Four weeks after immunization, chickens from each group were challenged by the ocular-nasal administration of 2 × 103.5 EID50 of the IBV CK/CH/JS/06II strain in 200 μl PBS per chicken. Any clinical disease symptoms, including death, beginning on day 2 post-challenge were recorded. On days 2, 4, 6, 8, 10, and 12 post-challenge, tracheal swabs were collected and used for virus isolation from 10 randomly selected chickens from each group. Dead chickens were necropsied immediately, and the live chickens from each group were euthanized 14 days post-challenge. The kidney tissues from all chickens were collected for virus isolation and pathological examination. Each chicken was weighed at 1-day-old, pre-challenge and at two weeks post-challenge.
The tracheal swabs and 20% tissue suspensions were freeze-thawed three times and centrifuged at 1000 × g. After centrifugation, the resulting supernatant was used to inoculate the allantoic cavity of 10-day-old SPF chicken embryos. After 96 hours, the allantoic fluid was collected, and any pathological changes in the embryos were recorded. The samples were considered positive for IBV isolation if the embryos appeared to be congestive, dropsical or hemorrhagic or if they developed urate deposition . Otherwise, the embryos were inoculated for three blind passages. Allantoic fluid from the chicken embryos was collected and analyzed using RT-PCR as described above.
The collected kidney tissues were fixed in 10% neutral buffered formalin. The tissues were processed by standard histological procedures, embedded in paraffin, and cut into 5-mm sections. All of the sections were stained with hematoxylin and eosin (H&E).
Protective efficacy of rMDV vaccination against MDV
The differences in morbidity, mortality and virus-shedding period from the tracheal swaps and kidneys between each group were compared using the χ 2 test. The difference in the increase in body weight (means ± SE) between each group was analyzed by Student’s t tests. The increase in bodyweight was analyzed by ANOVA. All statistical analyses were performed using the SPSS software (version 17.0. SPSS Inc., IL, USA).
Marek’s disease virus
Infectious bronchitis virus
Chick embryo fibroblasts
Indirect immunofluorescence assay
Phosphate buffered saline..
We are grateful to Dr. Songshu Meng and Dr. Daxin Peng for helpful discussion. We also thank Dr. Xiaobo Wang for the necropsy and analysis of tissue samples. This work was supported by the earmarked fund for Modern Agro-industry Technology Research System (CARS-41-K08), project 31101815 supported by National Natural Science Foundation of China, grants from Yangzhou University (2009CXJ036 and 2010CXJ058), the Program for Changjiang Scholars and Innovative Research Team in University (IRT0978), and a project funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions.
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