Construction of an infectious Marek's disease virus bacterial artificial chromosome and characterization of protection induced in chickens.

Abstract:

:Marek's disease virus (MDV) is a highly oncogenic alphaherpesvirus that induces rapid-onset T-cell lymphoma in poultry. The complete genome of the avirulent vaccine strain MDV-814 was cloned as an infectious bacterial artificial chromosome (BAC) using an 8.8-kb fragment containing the self-designed selective marker guanosine phosphoriboxyl transferase. The recombinant virus MDV-814-BAC was generated by co-transfection of a BAC transfer vector and MDV-814 total DNA, and was purified by eight rounds of selective passaging. The infectivity of the BAC DNA clone was validated by MDV reconstitution from chicken embryo fibroblasts transfected with MDV-BAC DNA, which was extracted from electroporated Escherichia coli DH10B cells. In vitro, the BAC-derived virus had similar biological characteristics and growth kinetics as the wild-type parental and recombinant viruses, and chickens immunized with BAC derivatives by various delivery mechanisms acquired protection against virulent MDV challenge. Construction of this MDV-BAC may aid the development of recombinant vaccines-containing multiple antigens.

journal_name

J Virol Methods

authors

Cui HY,Wang YF,Shi XM,An TQ,Tong GZ,Lan DS,He L,Liu CJ,Wang M

doi

10.1016/j.jviromet.2008.10.021

subject

Has Abstract

pub_date

2009-03-01 00:00:00

pages

66-72

issue

1-2

eissn

0166-0934

issn

1879-0984

pii

S0166-0934(08)00382-0

journal_volume

156

pub_type

杂志文章
  • Validation of an r3AB1-FMDV-NSP ELISA to distinguish between cattle infected and vaccinated with foot-and-mouth disease virus.

    abstract::Foot-and-mouth disease (FMD) is a highly contagious disease of cloven-hoofed livestock which has a drastic economic impact for affected countries. Although FMDV is distributed worldwide, many regional programs have been effective eradicating this agent. In Argentina, as in many other regions of South America, the comb...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.09.011

    authors: Jaworski JP,Compaired D,Trotta M,Perez M,Trono K,Fondevila N

    更新日期:2011-12-01 00:00:00

  • Radioimmunoassay of adjuvant-associated porcine parvovirus using a monoclonal antibody in a nitrocellulose membrane system.

    abstract::A quantitative and simple indirect radioimmunoassay (IRIA) was developed for porcine parvovirus (PPV), employing a monoclonal antibody directed against PPV adsorbed to nitrocellulose membrane. The IRIA was equally sensitive to live or inactivated PPV. There was a linear relationship between membrane-bound radioactivit...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(85)90129-6

    authors: Katz JB,van Deusen RA

    更新日期:1985-12-01 00:00:00

  • A refined long RT-PCR technique to amplify complete viral RNA genome sequences from clinical samples: application to a novel hepatitis C virus variant of genotype 6.

    abstract::The goal of this study was to adapt a long RT-PCR technique to amplify large PCR fragments from the genome of hepatitis C virus (HCV) isolates using clinical samples. This was done by using a reverse transcriptase devoid of RNase H activity and a mixture of two antibody-bound thermostable polymerases to combine the hi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2005.01.031

    authors: Lu L,Nakano T,Smallwood GA,Heffron TG,Robertson BH,Hagedorn CH

    更新日期:2005-06-01 00:00:00

  • Development and comparison of strain specific gag and pol real-time PCR assays for the detection of Visna/maedi virus.

    abstract::The aim of this study was the development of gag and pol dual labelled probe real-time PCR and RT PCR assays to quantify the proviral load and the transcripts of the British Visna/maedi virus EV1 strain. Primers and probes were chosen based on the consensus sequences of gag and pol clones representative of EV1 genetic...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2010.01.013

    authors: Carrozza ML,Mazzei M,Bandecchi P,Fraisier C,Pérez M,Suzan-Monti M,de Andrés D,Amorena B,Rosati S,Andrésdottir V,Lujan L,Pepin M,Blacklaws B,Tolari F,Harkiss GD

    更新日期:2010-05-01 00:00:00

  • Expression and purification of bioactive hemagglutinin protein of highly pathogenic avian influenza A (H5N1) in silkworm larvae.

    abstract::The hemagglutinin (HA) of avian influenza viruses plays a very important role in the infection of host cells. In this study, the HA gene of the highly pathogenic avian influenza H5N1 virus was cloned and expressed in silkworm larvae. The expressed recombinant HA (rHA) was purified using fetuin-agarose chromatography a...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.08.040

    authors: Dong J,Harada M,Yoshida S,Kato Y,Murakawa A,Ogata M,Kato T,Usui T,Park EY

    更新日期:2013-12-01 00:00:00

  • Real-time PCR assay to identify variants of Vaccinia virus: implications for the diagnosis of bovine vaccinia in Brazil.

    abstract::Naturally occurring infections of Vaccinia virus (VACV) have been recognized in Brazil during the past 10 years. Human Brazilian Vaccinia virus (BVV) infections typically occur as a zoonosis transferred from affected dairy cows to their handlers. Outbreaks have caused notable economic losses to the rural community in ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.05.028

    authors: de Souza Trindade G,Li Y,Olson VA,Emerson G,Regnery RL,da Fonseca FG,Kroon EG,Damon I

    更新日期:2008-09-01 00:00:00

  • Comparison of four non-radioactive and 35S-based methods for the detection of human papillomavirus DNA by in situ hybridization.

    abstract::Human papillomavirus DNA was detected in 40 condylomatous lesions of various sites (vulva, cervix, larynx, penis and anus) by in situ hybridization using 35S-labelled probes and four non-radioactive probes to compare the various sensitivities of these techniques on the same material (formalin-fixed and paraffin-embedd...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(91)90025-u

    authors: Clavel C,Binninger I,Boutterin MC,Polette M,Birembaut P

    更新日期:1991-08-01 00:00:00

  • Rapid identification of flavivirus using the polymerase chain reaction.

    abstract::A rapid and accurate detection and identification system was developed for flaviviruses that makes use of reverse transcription-polymerase chain reaction (RT-PCR). A primer pair (YF-1 and YF-3), which corresponds to the highly conserved sequence at 3' noncoding region among flaviviruses, was useful for identification ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(93)90020-r

    authors: Tanaka M

    更新日期:1993-03-01 00:00:00

  • Concentration and purification of feline leukaemia virus (FeLV) and its outer envelope protein gp70 by aqueous two-phase systems.

    abstract::The major protective antigens of retroviruses are considered to be their glycosylated envelope proteins. However, the methods commonly employed to enrich and purify virus from culture media such as pelleting and density-gradient centrifugation result in a low recovery of the viral external glycoproteins. This is an ob...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(89)90011-6

    authors: Hammar L,Eriksson S,Malm K,Morein B

    更新日期:1989-04-01 00:00:00

  • A cornucopia of screening and diagnostic techniques for human papillomavirus associated cervical carcinomas.

    abstract::Cervical carcinoma is one of the major consequences of human papillomavirus (HPV) infections. Although HPV infections of cervix do not always progress to cancer, 90% cases of cervical cancer have been found associated with high risk HPV (hrHPV) infection. Usually, HPV infection is asymptomatic; however, this asymptoma...

    journal_title:Journal of virological methods

    pub_type: 杂志文章,评审

    doi:10.1016/j.jviromet.2015.06.015

    authors: Ramzan M,Noor ul Ain,Ilyas S,Umer M,Bano S,Sarwar S,Shahzad N,Shakoori AR

    更新日期:2015-09-15 00:00:00

  • Development of sheep kidney cells with increased resistance to different subgenotypes of BVDV-1 by RNA interference.

    abstract::Bovine viral diarrhea virus (BVDV) should be a ubiquitous viral pathogen to the cattle and sheep industry. This pathogen is responsible for severe economic losses. We previously showed that plasmid-mediated dual short hairpin RNA (shRNA) efficiently inhibit BVDV replication in bovine kidney epithelial (MDBK) cells. In...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.03.014

    authors: Ni W,Qiao J,Ma Q,Wang J,Wang D,Zhao X,Cao Y,Li Q,Hu S,Chen C

    更新日期:2015-06-15 00:00:00

  • Development and application of an indirect ELISA for the detection of antibodies to novel duck reovirus.

    abstract::A novel duck reovirus (N-DRV) disease emerged in China in 2000 and it has become an epidemic genotype. A test for detection of virus-specific antibodies in serum samples would be useful for epidemiological investigations. Currently, Currently, serological assays for N-DRV diagnosis are not available. A test for detect...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.04.012

    authors: Yun T,Chen H,Yu B,Zhang C,Chen L,Ni Z,Hua J,Ye W

    更新日期:2015-08-01 00:00:00

  • Immunogenicity and virulence of attenuated vaccinia virus Tian Tan encoding HIV-1 muti-epitope genes, p24 and cholera toxin B subunit in mice.

    abstract::No effective prophylactic or therapeutic vaccine against HIV-1 in humans is currently available. This study analyzes the immunogenicity and safety of a recombinant attenuated vaccinia virus. A chimeric gene of HIV-1 multi-epitope genes containing CpG ODN and cholera toxin B subunit (CTB) was inserted into Chinese vacc...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.03.007

    authors: Du S,Wang Y,Liu C,Wang M,Zhu Y,Tan P,Ren D,Li X,Tian M,Yin R,Li C,Jin N

    更新日期:2015-07-01 00:00:00

  • Generation of a replication-deficient recombinant human adenovirus type 35 vector using bacteria-mediated homologous recombination.

    abstract::The use of adenovirus type 35 (Ad35) as a vector in vaccine and gene therapy studies is promising due to its broad cell tropism and low seroprevalence in humans. However, to date, a simple and effective system for producing recombinant Ad35 (rAd35) has not been well developed. This report describes a two-plasmid Ad35-...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.06.016

    authors: Wu C,Lei X,Wang J,Hung T

    更新日期:2011-10-01 00:00:00

  • WNV Typer: a server for genotyping of West Nile viruses using an alignment-free method based on a return time distribution.

    abstract::West Nile virus (WNV), genus Flavivirus, family Flaviviridae, is a major cause of viral encephalitis with broad host range and global spread. The virus has undergone a series of evolutionary changes with emergence of various genotypic lineages that are known to differ in type and severity of the diseases caused. Curre...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.12.012

    authors: Kolekar P,Hake N,Kale M,Kulkarni-Kale U

    更新日期:2014-03-01 00:00:00

  • HSV-1 amplicon peptide display vector.

    abstract::There are significant uses for expressing foreign peptide epitopes in viral surface attachment proteins in terms of investigating viral targeting, biology, and immunology. HSV-1 attachment, followed by fusion and entry, is mediated in large part by the binding of viral surface glycoproteins to cell surface receptors, ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(02)00193-3

    authors: Spear MA,Schuback D,Miyata K,Grandi P,Sun F,Yoo L,Nguyen A,Brandt CR,Breakefield XO

    更新日期:2003-01-01 00:00:00

  • Simple and rapid strategy for genetic characterization of influenza B virus reassortants.

    abstract::Genetic reassortment of influenza viruses is widely used for creating viruses with specific phenotypes. Reassortment of two influenza viruses, each with eight RNA segments potentially yields as many as 256 gene segment combinations. Therefore, confirmation that progeny viruses possess genomes corresponding to the spec...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2004.11.024

    authors: Lugovtsev VY,Vodeiko GM,Strupczewski CM,Levandowski RA

    更新日期:2005-03-01 00:00:00

  • Use of non-radioactively labeled DNA probes for the detection of a baculovirus from Penaeus monodon by in situ hybridization on fixed tissue.

    abstract::Clones isolated from a genomic library of the baculovirus PmSNPV (= MBV) were used to prepare DNA probes for detection of PmSNPV in shrimp tissue. Davidson's AFA fixed shrimp tissues were probed using DNA that had been labeled with the hapten, digoxigenin, by an in situ hybridization assay. The DNA probes readily dist...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)90043-4

    authors: Poulos BT,Mari J,Bonami JR,Redman R,Lightner DV

    更新日期:1994-09-01 00:00:00

  • Influenza virus detection with pentabody-activated nanoparticles.

    abstract::A nanoparticle-based immunoassay was developed for the rapid and sensitive detection of avian influenza virus (AIV). In this method, AIV-specific pentabody (pVHH3B) was conjugated to magnetic nanoparticles (MNPs) and used to capture AIV. Gold nanoparticles (GNPs), labelled with the anti-AIV mouse monoclonal antibody 3...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2010.07.024

    authors: Mu B,Huang X,Bu P,Zhuang J,Cheng Z,Feng J,Yang D,Dong C,Zhang J,Yan X

    更新日期:2010-11-01 00:00:00

  • A simple and rapid method for detecting human immunodeficiency virus by PCR.

    abstract::A simple, sensitive and specific method using the polymerase chain reaction (PCR) for amplification of human immunodeficiency virus type 1 (HIV-1) is described. The method involves minimal manipulations. Peripheral blood mononuclear cells (PBMC) were prepared by a rapid Ficoll-Paque gradient method. Lymphocytes were l...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(91)90058-8

    authors: Gibson KM,McLean KA,Clewley JP

    更新日期:1991-05-01 00:00:00

  • Development of a real-time reverse transcription polymerase chain reaction assay for detection of marine caliciviruses (genus Vesivirus).

    abstract::Marine caliciviruses form a distinct lineage within the genus Vesivirus (family Caliciviridae). This group includes vesicular exanthema of swine virus (VESV) and San Miguel sea lion virus (SMSV) and other related viruses which have been proposed to be marine in origin isolated from a variety of terrestrial and marine ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.11.010

    authors: Reid SM,King DP,Shaw AE,Knowles NJ,Hutchings GH,Cooper EJ,Smith AW,Ferris NP

    更新日期:2007-03-01 00:00:00

  • Comparison of hemagglutination inhibition, serum neutralization and ELISA-PVM tests for the detection of antibodies to pneumonia virus of mice in rat sera.

    abstract::Recently, the seroneutralization, hemagglutination inhibition, and the ELISA procedures were used to determine the presence of serum antibody to the pneumonia virus of mice in rat sera. This study was initiated to evaluate the reliability of these procedures to detect specific antibodies in our laboratory animal speci...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(81)90004-5

    authors: Descôteaux JP,Payment P

    更新日期:1981-09-01 00:00:00

  • Development and application of a universal Taqman real-time PCR for quantitation of duck hepatitis B virus DNA.

    abstract::To develop a quantitative assay for universal detection of duck hepatitis B virus (DHBV) DNA, a Taqman real-time fluorescent quantitative polymerase chain reaction (FQ-PCR) assay was developed using primers and probes based on genomic sequences located at nucleotide 241-414 of the DHBV Core region which possesses the ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.03.025

    authors: Wang Y,Li Y,Yang C,Hui L,Han Q,Ma L,Wang Q,Yang G,Liu Z

    更新日期:2013-07-01 00:00:00

  • A clinical virology database for a regional virology service.

    abstract::We describe a laboratory information system employing a virus and chlamydia database developed over seven years which is used by a regional laboratory, performing virus and chlamydia testing. The information system is implemented on a University mainframe computer and accessed by computer terminals in the laboratory. ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(89)90108-0

    authors: Ahmed K,Mahony J,Stiles C,Castriciano S,Chernesky M

    更新日期:1989-12-01 00:00:00

  • Competitive polymerase chain reaction assay for quantitation of HIV-1 DNA and RNA.

    abstract::A quantitative PCR assay for the detection of HIV-1 nucleic acids is described. The assay is based on a competitive internal standard nucleic acid which can be discriminated from target sequences by the presence of a new restriction enzyme site. The method was used to quantitate plasmid molecules containing HIV-1 sequ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(91)90095-h

    authors: Stieger M,Démollière C,Ahlborn-Laake L,Mous J

    更新日期:1991-09-01 00:00:00

  • Rapid diagnosis and quantification of herpes simplex virus with a green fluorescent protein reporter system.

    abstract::A genetically modified cell line (Vero-ICP10-EGFP) was constructed for detection of herpes simplex virus (HSV) by a simple, rapid and direct method. The cell line was developed by stable transfection of Vero cell with a plasmid encoding the green fluorescent protein (GFP) driven by the promoter of the HSV-2 ICP10 gene...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(00)00234-2

    authors: Kung SH,Wang YC,Lin CH,Kuo RL,Liu WT

    更新日期:2000-11-01 00:00:00

  • Detection of wild type and deleted latent membrane protein 1 (LMP1) of Epstein-Barr virus in clinical biopsy material.

    abstract::The latent membrane protein 1 (LMP1) of Epstein-Barr virus (EBV) is one of two postulated viral oncogenic proteins. Sequence variations, and in particular a 30 base pair deletion variant called CAO, may define different disease populations. We developed a panel of rat monoclonal antibodies (MAb) specific for the non-w...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2003.10.015

    authors: Nicholls J,Hahn P,Kremmer E,Fröhlich T,Arnold GJ,Sham J,Kwong D,Grässer FA

    更新日期:2004-03-01 00:00:00

  • Highly sensitive and specific non-radioactive biotinylated probes for dot-blot, Southern and colony hybridizations.

    abstract::We describe a simple method for the incorporation of biotin into nucleic acid probes. This method has been improved and optimized to produce biotinylated DNA probes for the detection of DNA by dot-blot, Southern and colony hybridization techniques. The sensitivity of this method has been particularly improved to allow...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(89)90072-4

    authors: Eweida M,Sit TL,Sira S,AbouHaidar MG

    更新日期:1989-10-01 00:00:00

  • Suitability of autoclaved tap water for preparation of ELISA reagents and washing buffer.

    abstract::The suitability of autoclaved tap water for the preparation of ELISA reagents and washing buffer was compared with that of ultrapure water, in a standard indirect ELISA for the detection of antibodies to pseudorabies virus (PRV). The performance of the assay, using autoclaved tap water (AT-ELISA) compared favourably t...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)90110-4

    authors: Afshar A,Zhao X,Heckert RA,Trotter HC

    更新日期:1994-02-01 00:00:00

  • Detection and quantitation of the new world Squash leaf curl virus by TaqMan real-time PCR.

    abstract::Squash leaf curl diseases are caused by distinct virus species that are separated into two major phylogenetic groups, western and eastern hemisphere groups. The western group includes the new world Squash leaf curl virus (SLCV) which causes major losses to cucurbit production and induces severe stunting and leaf curl ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.04.001

    authors: Abrahamian PE,Abou-Jawdah Y

    更新日期:2013-07-01 00:00:00