Evaluation of envelope glycoprotein E(rns) of an atypical bovine pestivirus as antigen in a microsphere immunoassay for the detection of antibodies against bovine viral diarrhea virus 1 and atypical bovine pestivirus.

Abstract:

:Atypical bovine pestiviruses are related antigenically and phylogenetically to bovine viral diarrhea viruses (BVDV-1 and BVDV-2), and may cause the same clinical manifestations in animals. Glycoprotein E(rns) of an atypical bovine pestivirus Th/04_KhonKaen was produced in a baculovirus expression system and was purified by affinity chromatography. The recombinant E(rns) protein was used as an antigen in a microsphere immunoassay for the detection of antibodies against BVDV-1 and atypical bovine pestivirus. The diagnostic performance of the new method was evaluated by testing a total of 596 serum samples, and the assay was compared with enzyme-linked immunosorbent assay (ELISA). Based on the negative/positive cut-off median fluorescence intensity (MFI) value of 2800, the microsphere immunoassay had a sensitivity of 100% and specificity of 100% compared to ELISA. The immunoassay was able to detect antibodies against both BVDV-1 and the atypical pestivirus. This novel microsphere immunoassay has the potential to be multiplexed for simultaneous detection of antibodies against different bovine pathogens in a high-throughput and economical way.

journal_name

J Virol Methods

authors

Vijayaraghavan B,Xia H,Harimoorthy R,Liu L,Belák S

doi

10.1016/j.jviromet.2012.06.017

subject

Has Abstract

pub_date

2012-11-01 00:00:00

pages

193-8

issue

2

eissn

0166-0934

issn

1879-0984

pii

S0166-0934(12)00230-3

journal_volume

185

pub_type

杂志文章
  • A modified immunofluorescence test for Epstein-Barr virus-specific IgM antibody.

    abstract::The fluorescent antibody (FA) test for Epstein-Barr virus (EBV)-specific IgM antibody was improved by the use of sodium butyrate to induce a higher level of EBV antigen expression in P3HR-1 slide preparations and by removal of rheumatoid factor (RF) and IgG antibodies from test sera by means of adsorption with suspens...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(85)90004-7

    authors: Harnett GB,Palmer CA,Bucens MR

    更新日期:1985-10-01 00:00:00

  • Characterisation of isolates and strains of citrus tristeza closterovirus using restriction analysis of the coat protein gene amplified by the polymerase chain reaction.

    abstract::Citrus Tristeza Virus (CTV) exists as a large number of distinct strains differing in biological properties and with different distributions in citrus producing countries. Strategies such as eradication or cross protection, aimed at controlling severe variants of the pathogen, require procedures to identify virus stra...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(93)90065-y

    authors: Gillings M,Broadbent P,Indsto J,Lee R

    更新日期:1993-10-01 00:00:00

  • The isolation of the two electrophoretic forms of cowpea mosaic virus using fast protein liquid chromatography.

    abstract::This report describes the first time entire viral capsids have been purified using fast protein liquid chromatography (FPLC) techniques. The FPLC is used here to separate the two electrophoretic forms of cowpea mosaic virus. The capsid forms are shown to be separated by the Mono-Q column without damaging the capsids. ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(87)90011-5

    authors: Smith TJ

    更新日期:1987-07-01 00:00:00

  • Comparison of three different hybridization assays in the quantitative measurement of serum hepatitis B virus DNA.

    abstract::The measurement of hepatitis B virus (HBV) DNA, is important for monitoring and evaluating the efficacy of anti-viral agents in the treatment of patients with chronic hepatitis B. Three different hybridization assays for quantitative measurement of HBV DNA: direct membrane (dot-blot) hybridization, liquid hybridizatio...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(96)02093-9

    authors: Hwang SJ,Lee SD,Lu RH,Chan CY,Lai L,Co RL,Tong MJ

    更新日期:1996-12-01 00:00:00

  • Coupling of foot-and-mouth disease virus to sheep red blood cells using tannic acid for immunological assays.

    abstract::A technique for coupling foot-and-mouth disease virus (FMDV) to tanned sheep red blood cells (SRBC) is reported. Different parameters influencing the procedure were studied. Subtypes C2, C3, O1 and A24 were used as antigens, and guinea pig hyperimmune sera obtained were tested for specific antibody in passive hemagglu...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(88)90131-0

    authors: Pujol CA,Feledi CA,Massouh EJ

    更新日期:1988-08-01 00:00:00

  • Comparison of two hybridization assays for the rapid detection of PCR amplified HSV genome sequences from cerebrospinal fluid.

    abstract::Rapid diagnosis of herpes simplex encephalitis (HSE) can only be achieved by the polymerase chain reaction (PCR). In order to carry out PCR under routine conditions, it is of great importance to establish an easy DNA extraction protocol and especially a rapid and sensitive DNA detection method. In the present study, t...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)90174-0

    authors: Sakrauski A,Weber B,Kessler HH,Pierer K,Doerr HW

    更新日期:1994-12-01 00:00:00

  • A new assay for quantitative detection of hepatitis A virus.

    abstract::Hepatitis A virus (HAV) is mainly transmitted via contaminated food or water or through person-to-person contact. Here, we describe development and evaluation of a reverse transcription droplet digital PCR (RT-ddPCR) and reverse transcription real-time PCR (RT-qPCR) assay for detection of HAV in food and clinical spec...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2020.114010

    authors: Persson S,Alm E,Karlsson M,Enkirch T,Norder H,Eriksson R,Simonsson M,Ellström P

    更新日期:2021-02-01 00:00:00

  • The GPRIME package: computer programs for identifying the best regions of aligned genes to target in nucleic acid hybridisation-based diagnostic tests, and their use with plant viruses.

    abstract::The GPRIME (Group PRIMEr design) programs examine aligned sets of gene sequences to discover homologous regions to be targeted in diagnostic tests. The core program moves a 'window' over the aligned sequences and calculates, at each window position, a 'redundancy value', namely the number of sequences that would repre...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00070-6

    authors: Gibbs A,Armstrong J,Mackenzie AM,Weiller GF

    更新日期:1998-09-01 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

  • Development of loop-mediated isothermal amplification assay for detection of human coronavirus-NL63.

    abstract::Human coronavirus NL63 was identified in 2004 in the Netherlands. Due to the high prevalence and world-wide distribution of this pathogen, it is essential to develop a sensitive and specific detection assay suitable for use in a routine diagnostic laboratory. Techniques based on PCR or real-time PCR are laborious and ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.04.024

    authors: Pyrc K,Milewska A,Potempa J

    更新日期:2011-07-01 00:00:00

  • Analytical evaluation of the microarray-based FluChip-8G Influenza A+B Assay.

    abstract:BACKGROUND:Influenza causes a significant annual disease burden, with characterization of the infecting virus important in clinical and public health settings. Rapid immunoassays are fast but insensitive, whereas real-time RT-PCR is sensitive but susceptible to genetic mutations and often requires multiple serial assay...

    journal_title:Journal of virological methods

    pub_type: 杂志文章,多中心研究

    doi:10.1016/j.jviromet.2019.113686

    authors: Taylor AW,Dawson ED,Blair RH,Johnson JE Jr,Slinskey AH,Smolak AW,Toth E,Liikanen K,Stoughton RS,Smith C,Talbot S,Rowlen KL

    更新日期:2019-11-01 00:00:00

  • Comparative study of peroxidase-labelled IgG and anti-IgG for the detection of measles virus antigens.

    abstract::The immunoperoxidase and immunoblotting techniques were used to detect measles virus antigens in nasopharyngeal samples taken from children visiting the Yaounde Health Centre (Cameroon). In order to make these diagnostic tests simpler, faster and less costly, peroxidase-labelled anti-measles IgG were prepared and comp...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(90)90011-4

    authors: Njayou M,Balla A

    更新日期:1990-07-01 00:00:00

  • Detection and strain differentiation of European bat lyssaviruses using in situ hybridisation.

    abstract::A protocol suitable for the detection of rabies virus and the related European bat lyssaviruses type 1 and 2 is described. In situ hybridisation, employing digoxigenin labelled riboprobes was used for the detection of lyssavirus RNA in mouse-infected brain tissue. The principal advantage of this technique, compared to...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2004.06.020

    authors: Finnegan CJ,Brookes SM,Johnson L,Fooks AR

    更新日期:2004-11-01 00:00:00

  • Presence of enteroviruses in recreational water in Wuhan, China.

    abstract::Contaminated recreational waters pose a public health concern, as the potential for waterborne diseases exists in water contaminated with human fecal waste. Worldwide, bacterial indicators such as Escherichia coli, enterococci, and total and fecal coliform are used as indicators of water quality. However, enteric viru...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.06.028

    authors: Allmann E,Pan L,Li L,Li D,Wang S,Lu Y

    更新日期:2013-11-01 00:00:00

  • Immunostained plaque assay for detection and titration of rabies virus infectivity.

    abstract::The fluorescent antibody test (FAT) is the most commonly used method for detection of the rabies virus (RV). The plaque assay can only be applied to fixed RVs, and cannot be used for street RVs. In this study, plaque formation allowing the determination of both fixed and street RVs was achieved using the immune plaque...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.10.010

    authors: Park JS,Um J,Choi YK,Lee YS,Ju YR,Kim SY

    更新日期:2016-02-01 00:00:00

  • Multiplex real-time PCR for identification of canine parvovirus antigenic types.

    abstract::Canine parvovirus (CPV) is an important disease causing gastroenteritis and/or haemorrhagic gastroenteritis in dogs. There are four antigenic types of CPV reported worldwide viz. CPV 2, CPV 2a, CPV 2b and CPV 2c. The diagnosis of CPV with the identification of the antigen type responsible remains problematic. In the p...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2016.02.013

    authors: Kaur G,Chandra M,Dwivedi PN,Narang D

    更新日期:2016-07-01 00:00:00

  • A novel HIV-1 reporter virus with a membrane-bound Gaussia princeps luciferase.

    abstract::HIV-1 reporter viruses are a critical tool for investigating HIV-1 infection. By having a reporter gene incorporated into the HIV-1 genome, the expressed reporter protein acts as a specific tag, thus enabling specific detection of HIV-1 infected cells. Currently existing HIV-1 reporter viruses utilize reporters for th...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2012.03.028

    authors: Suree N,Koizumi N,Sahakyan A,Shimizu S,An DS

    更新日期:2012-07-01 00:00:00

  • A quantitative assay for measuring human foamy virus using an established indicator cell line.

    abstract::In order to improve the accuracy for detecting human foamy virus (HFV), an indicator cell line was established by co-transfecting baby hamster kidney-21 cells with two plasmids: one containing a G418 antibiotic resistance marker and the other including the luc gene which was placed downstream of the inducible HFV long...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(01)00285-3

    authors: Tai HY,Sun KH,Kung SH,Liu WT

    更新日期:2001-05-01 00:00:00

  • A fast and robust method for full genome sequencing of Porcine Reproductive and Respiratory Syndrome Virus (PRRSV) Type 1 and Type 2.

    abstract::PRRSV is a positive-sense RNA virus with a high degree of genetic variability among isolates. For diagnostic sensitivity and vaccine design it is essential to monitor PRRSV genetic diversity. However, to date only a few full genome sequences of PRRSV isolates have been made publicly available. In the present study, fa...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.07.019

    authors: Kvisgaard LK,Hjulsager CK,Fahnøe U,Breum SØ,Ait-Ali T,Larsen LE

    更新日期:2013-11-01 00:00:00

  • An efficient and rapid influenza gene cloning strategy for reverse genetics system.

    abstract::Influenza reverse genetics plays vital roles in understanding influenza molecular characteristics and vaccine development. However, current influenza reverse genetics heavily depends on restriction enzyme and ligation for gene cloning. The traditional cloning process of influenza eight fragments for virus rescuing gen...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.06.001

    authors: Shao H,Fan Z,Wan Z,Tian X,Chen H,Perez DR,Qin A,Ye J

    更新日期:2015-09-15 00:00:00

  • Multiple primer pairs polymerase chain reaction for the detection of human papillomavirus types.

    abstract::A polymerase chain reaction (PCR) based on the use of multiple primers enabling the simultaneous detection of HPV-6b, -11, -16 and -18 in a single tube reaction was developed and validated on cervico-vaginal specimens, including tissues embedded in paraffin. This PCR setting proved to be specific and sensitive, allowi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(90)90087-v

    authors: Anceschi MM,Falcinelli C,Pieretti M,Cosmi EV

    更新日期:1990-04-01 00:00:00

  • Engineering of the hepatitis C virus helicase for enhanced seroreactivity.

    abstract::Hepatitis C Virus c33, a recombinant protein comprising residues 1192-1457 of NS3 helicase, has been a mainstay of HCV serology for decades. With seven unpaired cysteines, seroreactivity of E. coli expressed c33 is dependant on reductants. While engineering a c33 replacement for new anti-HCV serological tests, we soug...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2018.10.019

    authors: Marohnic CC,Birkenmeyer LG,Bogdan MF,Frias EC,Otis KS,Palafox MAP,McSherry TD,Gregory SD,Zhao C,Gutierrez RA,Prostko JC,Muerhoff AS

    更新日期:2019-02-01 00:00:00

  • Extraction and purification of hepatitis B virus-like M particles from a recombinant Saccharomyces cerevisiae strain using alumina powder.

    abstract::A recombinant hepatitis B surface antigen (HBsAg) has been produced in the yeast Saccharomyces cerevisiae and used as a vaccine against hepatitis B virus (HBV) infection. The present study aimed to optimize the extraction of recombinant virus-like particles (rVLPs) to develop a simple purification procedure based on g...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2012.09.023

    authors: Hadiji-Abbes N,Martin M,Benzina W,Karray-Hakim H,Gergely C,Gargouri A,Mokdad-Gargouri R

    更新日期:2013-01-01 00:00:00

  • Development of universal primers for detection of potato carlaviruses by RT-PCR.

    abstract::To facilitate efficient and accurate detection of potato-infecting carlaviruses, degenerated universal primers were designed based on conserved amino acid and nucleotide sequences. Two sense primers, Car-F1 and Car-F2, were based on the amino acid sequences "SNNMA" and "GLGVPTE", respectively, in the coat protein. The...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.02.004

    authors: Nie X,Bai Y,Molen TA,Desjardins DC

    更新日期:2008-05-01 00:00:00

  • Rapid detection and identification of two lineages of influenza B strains with monoclonal antibodies.

    abstract::Monoclonal antibodies (Mabs) against influenza B virus were obtained by immunizing mice with B/Nagasaki/1/87, one of the strains of the B/Victoria group. Immunoprecipitation analysis revealed that individual Mabs precipitated the nucleoprotein (NP), the matrix protein (M) or the hemagglutinin protein (HA). By using th...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(99)00015-4

    authors: Nakagawa N,Maeda A,Kase T,Kubota R,Okuno Y

    更新日期:1999-04-01 00:00:00

  • Detection of circulating platelet-monocyte complexes in persons infected with human immunodeficiency virus type-1.

    abstract::Activated platelets form transient aggregates with monocytes in circulation and have a half-life of approximately 30-60 min. These complexes are increased in various inflammatory conditions and are an early marker of myocardial infarction. HIV-1 infection is associated with chronic inflammation, and increased CD16⁺ in...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2012.02.005

    authors: Singh MV,Davidson DC,Kiebala M,Maggirwar SB

    更新日期:2012-05-01 00:00:00

  • A small-scale procedure for extracting nucleic acids from woody plants infected with various phytopathogens for PCR assay.

    abstract::The complexity of most nucleic acid extraction procedures limits the number of samples that can be easily processed for analysis by polymerase chain reaction (PCR). A simple, small-scale procedure was developed which can be carried out entirely in 1.5-ml microfuge tubes whereby the container and contents are frozen wi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(97)00190-0

    authors: Zhang YP,Uyemoto JK,Kirkpatrick BC

    更新日期:1998-03-01 00:00:00

  • Serological diagnosis of influenza A and B infections by enzyme immunoassay. Comparison with the complement fixation test.

    abstract::Paired sera from 784 patients with symptoms of acute respiratory disease were examined for antibodies against influenza A, B and parainfluenza (1 and 3) viruses by complement fixation (CF) and enzyme immunoassay (EIA). The internal variation of the EIA test results was low and an increase of 0.250 in absorbance values...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(84)90078-8

    authors: Julkunen I,Kleemola M,Hovi T

    更新日期:1984-08-01 00:00:00

  • A PCR-restriction enzyme technique for determining dengue virus subgroups within serotypes.

    abstract::The polymerase chain reaction (PCR) and restriction enzyme analysis were used to develop a rapid and simple procedure for identifying geographic subgroups of dengue virus within serotypes for epidemiologic investigations. The entire structural protein region of dengue viruses was amplified and the products were digest...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)90122-8

    authors: Vorndam V,Kuno G,Rosado N

    更新日期:1994-07-01 00:00:00

  • Molecular cloning of Indian tomato leaf curl virus genome following a simple method of concentrating the supercoiled replicative form of viral DNA.

    abstract::DNA-A and DNA-B components of the genome of a whitefly transmitted virus causing yellowing and leaf curl in tomato (ITLCV) were cloned following a simple procedure for isolation of the double stranded replicative form of viral DNA from infected tomato plants. The method is based on extraction of total DNA from infecte...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)00122-w

    authors: Srivastava KM,Hallan V,Raizada RK,Chandra G,Singh BP,Sane PV

    更新日期:1995-02-01 00:00:00