Real-time RT-PCR differentiation and quantitation of infectious bursal disease virus strains using dual-labeled fluorescent probes.

Abstract:

:A real-time RT-PCR assay was developed utilizing dual-labeled fluorescent probes binding to VP4 sequence that are specific to the classical (Cl), variant (V) and very virulent (vv) strains of infectious bursal disease virus (IBDV). The assay was highly sensitive and could detect as little as 3 x 10(2) to 3 x 10(3) copies of viral template. Viral genomic copy number could be accurately assayed over a broad range of 7-8 logs of viral genome. The variant sequence-specific probe was found to be highly specific in detecting isolates classified as variant A, D, E, G and GLS-5, and did not react with classical strains. A total of 130 field and experimental variant strain isolates were tested using this assay. The classical sequence-specific probe also demonstrated high sensitivity and specificity, and positively detected a total of 87 STC isolates, both field and experimental isolates, while differentiating between isolates that were variant and classical strains. The very virulent sequence-specific probe detected positively the Holland vvIBDV isolate and did not react with classical or variant strains. Rapid identification of viral strain is a primary concern to poultry flock health programs to ensure administered vaccines will protect against current strains of virus circulating in the flock. The ability to quantify virus concurrently is also of assistance in identifying the progression of disease outbreaks within the flock.

journal_name

J Virol Methods

authors

Peters MA,Lin TL,Wu CC

doi

10.1016/j.jviromet.2005.03.009

subject

Has Abstract

pub_date

2005-07-01 00:00:00

pages

87-95

issue

1

eissn

0166-0934

issn

1879-0984

pii

S0166-0934(05)00090-X

journal_volume

127

pub_type

杂志文章
  • Novel post-translational modifications of the hemagglutinin and neuraminidase proteins of avian influenza virus expressed by Kluyveromyces lactis.

    abstract::Avian influenza virus (AIV) is an enveloped virus with segmented RNA that belongs to the Orthomyxoviridae. Recently, avian influenza virus isolates have not only posed a significant threat to the poultry industry but also serious public health concerns. The full-length viral hemagglutinin (HA), neuraminidase (NA) or b...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.05.006

    authors: Tsai SM,Chiang YC,Chin LT,Liu HJ,Wang CY

    更新日期:2011-08-01 00:00:00

  • Relationship between plant virus concentration and infectivity: a 'growth curve' model.

    abstract::A logistic ('growth curve') model is formulated and applied to the relationship between numbers of infections (local lesions) produced by a virus on inoculated plants and the concentration of the virus in the inoculum. This model has the advantages of being simple, data-based and therefore not founded on limiting post...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(87)90084-x

    authors: Gokhale DV,Bald JG

    更新日期:1987-12-01 00:00:00

  • Optimization of an in situ hybridization technique for the detection of foot-and-mouth disease virus in bovine tissues using the digoxigenin system.

    abstract::An in situ hybridization technique has been optimised for use on paraffin-embedded sections of tissues collected from cattle infected experimentally with foot-and-mouth disease virus type O1BFS. Tissue was collected 5 days after infection by direct contact. In situ hybridization was carried out using an RNA probe corr...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(94)00153-8

    authors: Woodbury EL,Ilott MC,Brown CC,Salt JS

    更新日期:1995-01-01 00:00:00

  • Rapid subtyping of H9N2 influenza virus by a triple reverse transcription polymerase chain reaction.

    abstract::The aim of this study was to develop a rapid, cost-saving triple reverse transcription polymerase chain reaction (triple RT-PCR) for subtyping H9N2 avian influenza viruses (AIVs). The three primer pairs for amplification of target sequences of nucleoprotein (NP), hemagglutinin (HA) and neuraminidase (NA) genes, respec...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.01.026

    authors: Chen HT,Zhang J,Ma LN,Ma YP,Ding YZ,Wang M,Liu XT,Zhang YG,Liu YS

    更新日期:2009-06-01 00:00:00

  • Cytomegalovirus quantification in plasma with Abbott RealTime CMV and Roche Cobas Amplicor CMV assays.

    abstract::We assessed the performance of Abbott RealTime CMV assay (ARC) compared to Roche Cobas Amplicor CMV Monitor Test (RCM) for quantification of CMV in plasma of transplant patients. Commercial panels were used to test linearity, precision and interference and 83 clinical samples were used for the accuracy and precision a...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.08.010

    authors: Tremblay MA,Rodrigue MA,Deschênes L,Boivin G,Longtin J

    更新日期:2015-12-01 00:00:00

  • Immunodiagnosis of Prune dwarf virus using antiserum produced to its recombinant coat protein.

    abstract::Certification represents the first line of defense against fruit tree viruses. For certification or surveys dealing with large number of samples, ELISA is still considered the technique of choice and requires a continuous supply of good quality antibodies. Prune dwarf virus (PDV) is among the major viruses affecting s...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2004.05.013

    authors: Abou-Jawdah Y,Sobh H,Cordahi N,Kawtharani H,Nemer G,Maxwell DP,Nakhla MK

    更新日期:2004-10-01 00:00:00

  • Development of a novel protocol for generating flavivirus reporter particles.

    abstract::Infection with West Nile virus (WNV), a mosquito-borne flavivirus, is a growing public and animal health concern worldwide. Prevention, diagnosis and treatment strategies for the infection are urgently required. Recently, viral reverse genetic systems have been developed and applied to clinical WNV virology. We develo...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.08.002

    authors: Fernández IV,Okamoto N,Ito A,Fukuda M,Someya A,Nishino Y,Sasaki N,Maeda A

    更新日期:2014-11-01 00:00:00

  • Simultaneous detection of five different DNA targets by real-time Taqman PCR using the Roche LightCycler480: Application in viral molecular diagnostics.

    abstract::One of the most interesting aspects of real-time PCR based on the detection of fluorophoric labeled oligonucleotides is the possibility of being able to detect conveniently multiple targets in the same PCR reaction. Recently, Roche Diagnostics launched a real-time PCR platform, the LightCycler480 (LC480), which should...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.12.007

    authors: Molenkamp R,van der Ham A,Schinkel J,Beld M

    更新日期:2007-05-01 00:00:00

  • Characterization of isolates of Citrus tristeza virus by sequential analyses of enzyme immunoassays and capillary electrophoresis-single-strand conformation polymorphisms.

    abstract::Citrus tristeza virus (CTV) is the causal agent of tristeza disease, which is one of the most devastating diseases of citrus crops worldwide. This paper describes a method for the rapid detection and genotyping of naturally spreading CTV isolates. This method uses ELISA or dot-blot immunological tests to detect trees ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2012.01.015

    authors: Licciardello G,Raspagliesi D,Bar-Joseph M,Catara A

    更新日期:2012-05-01 00:00:00

  • Efficient transfer of HTLV-1 tax gene in various primary and immortalized cells using a flap lentiviral vector.

    abstract::Human T cell leukemia virus type 1 (HTLV-1) causes two major diseases: adult T-cell leukemia-lymphoma and tropical spastic paraparesis/HTLV-1 associated myelopathy (TSP/HAM). In order to understand the involvement of Tax protein in HTLV-1 pathogenesis, we constructed a HIV-1 based lentiviral vector containing the cent...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(02)00097-6

    authors: Royer-Leveau C,Mordelet E,Delebecque F,Gessain A,Charneau P,Ozden S

    更新日期:2002-08-01 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

  • Preservation of RNA and destruction of infectivity in microdissected brain tissues of Lewis rats infected with the Borna disease virus.

    abstract::Laser microdissection combined with real-time RT-PCR presents an advanced tool to quantify particular RNA species in defined tissue areas. Dealing with infectious tissue samples increases the need to overcome the risk of infectivity and contamination during laser microdissection. Here, an useful method to control infe...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.03.024

    authors: Porombka D,Herzog S,Baumgärtner W,Herden C

    更新日期:2006-08-01 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

  • Disparate detection outcomes for anti-HCV IgG and HCV RNA in dried blood spots.

    abstract::Dried blood spots (DBS) expedite the collection, storage and shipping of blood samples, thereby facilitating large-scale serologic studies. We evaluated the sensitivity of anti-HCV IgG testing and HCV-RNA quantitation using freshly prepared and stored DBS derived from HCV-infected patients. Protocols for elution were ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.10.018

    authors: Tejada-Strop A,Drobeniuc J,Mixson-Hayden T,Forbi JC,Le NT,Li L,Mei J,Terrault N,Kamili S

    更新日期:2015-02-01 00:00:00

  • A comparison of reverse transcriptase and antigen capture assays for the detection of HIV.

    abstract::HIV antigen capture assay (ELISA) and reverse transcriptase assay were compared for the detection of HIV. Purified virus and the supernatant of infected cells were used for this study. Antigen capture assay was found to be at least one hundred times more sensitive than the RT assay, and for a large number of samples e...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(88)90044-4

    authors: Lee YS

    更新日期:1988-05-01 00:00:00

  • Indirect measurement of Epstein-Barr virus neutralising antibodies by ELISA.

    abstract::A rapid and effective ELISA for measuring Epstein-Barr virus (EBV)-neutralizing antibodies in human sera was devised to replace the existing cumbersome method involving the inhibition of fetal cord blood B-cell transformation by the virus. The new method will be invaluable for assessing antibody responses in human sub...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00054-8

    authors: Wilson AD,Morgan AJ

    更新日期:1998-07-01 00:00:00

  • Highly sensitive immunoassays for detection of barley stripe mosaic virus and beet necrotic yellow vein virus.

    abstract::Enzyme immunoassays based on the use of monoclonal antibodies (MAbs) were developed for the detection of the barley stripe mosaic virus (BSMV) and the beet necrotic yellow vein virus (BNYVV). Assays employing conjugates of MAbs to horseradish peroxidase (HRP) were compared to systems with biotinylated MAbs and strepta...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(95)01962-6

    authors: Sukhacheva E,Novikov V,Plaksin D,Pavlova I,Ambrosova S

    更新日期:1996-02-01 00:00:00

  • Specificity of two HIV screening tests detecting simultaneously HIV-1 p24 antigen and antibodies to HIV-1 and -2.

    abstract::This study aimed at assessing the specificity of the Elecsys® HIV combi PT in comparison to the ARCHITECT® HIV Ag/Ab Combo. With both of these assays, 3997 unselected sera from patients of a tertiary health care centre in Basel, Switzerland, were screened for HIV. Reactive sera were reanalysed on the VIDAS® HIV Duo Ul...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2017.09.005

    authors: Blaich A,Buser A,Stöckle M,Gehringer C,Hirsch HH,Battegay M,Klimkait T,Frei R

    更新日期:2017-11-01 00:00:00

  • A vaccinia-virus-free reverse genetics system for infectious hematopoietic necrosis virus.

    abstract::Reverse genetics system is a powerful tool to study the function of a particular gene. The currently available reverse genetics system for Novirhabdovirus is based on vaccinia-driven T7 RNA polymerase expression. An improved system for the recovery of infectious hematopoietic necrosis virus (IHNV) was developed which ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2010.03.023

    authors: Ammayappan A,Lapatra SE,Vakharia VN

    更新日期:2010-08-01 00:00:00

  • Microarray-based assay for the detection of genetic variations of structural genes of West Nile virus.

    abstract::Adaptation through fixation of spontaneous mutations in the viral genome is considered to be one of the important factors that enable recurrent West Nile virus (WNV) outbreaks in the U.S. Genetic variations can alter viral phenotype and virulence, and degrade the performance of diagnostic and screening assays, vaccine...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.09.015

    authors: Grinev A,Daniel S,Laassri M,Chumakov K,Chizhikov V,Rios M

    更新日期:2008-12-01 00:00:00

  • Development and validation of a novel SYBR Green real-time RT-PCR assay for the detection of classical swine fever virus evaluated on different real-time PCR platforms.

    abstract::Classical swine fever is a highly contagious viral disease that causes significant economic losses in pig production on a global scale. The rapid dissemination of the virus and the variability of the clinical signs merit the development of swift and accurate classical swine fever virus (CSFV) detection methods, which ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.03.022

    authors: Pérez LJ,Díaz de Arce H,Tarradas J,Rosell R,Perera CL,Muñoz M,Frías MT,Nuñez JI,Ganges L

    更新日期:2011-06-01 00:00:00

  • Filter in situ hybridisation: an evaluation of the FISH technique for HPV detection in cervical swabs.

    abstract::The filter in situ hybridisation (FISH) method for detection of HPV in cervical swabs was evaluated against the Southern blot technique on concomitant cervical biopsies. Of 73 biopsies, HPV 16 DNA sequences were found in 26 biopsies and HPV 18 sequences in 2 biopsies. Analysis by FISH of the corresponding smears detec...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(89)90014-1

    authors: Hørding U,Sebbelov A,Daugaard S,Bock JE,Norrild B

    更新日期:1989-04-01 00:00:00

  • Diagnosis of measles by fluorescent antibody and culture of nasopharyngeal secretions.

    abstract::An indirect fluorescent antibody test (IFA) was evaluated using commercial mouse anti-measles monoclonal antibody and FITC-labeled goat anti-mouse immunoglobulin. For measles isolation, specimens were inoculated into Rhesus monkey kidney (RMK) cells and, when available, CV-1 cells. 381 specimens were tested by IFA and...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(91)90022-r

    authors: Smaron MF,Saxon E,Wood L,McCarthy C,Morello JA

    更新日期:1991-06-01 00:00:00

  • Detection of novel swine origin influenza A virus (H1N1) by real-time nucleic acid sequence-based amplification.

    abstract::Rapid detection of novel swine origin influenza A virus (S-OIV) (H1N1) is crucial for timely implementation of infection control measures. In this study, a haemagglutinin (HA) gene-based real-time nucleic acid sequence-based amplification (NASBA) assay was developed for the specific detection of S-OIV (H1N1). The assa...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.10.025

    authors: Ge Y,Cui L,Qi X,Shan J,Shan Y,Qi Y,Wu B,Wang H,Shi Z

    更新日期:2010-02-01 00:00:00

  • Inferring viral population structures using heteroduplex mobility and DNA sequence analyses.

    abstract::Heteroduplex mobility (HMA) and tracking assays (HTA) are used to assess genetic relationships between DNA molecules. While distinguishing relationships between clonal or nearly clonal molecules is relatively straightforward, inferring population structures is more complex. To address this issue, HIV-1 quasispecies wi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.08.012

    authors: Shankarappa R,Mullins JI

    更新日期:2013-12-01 00:00:00

  • A new system to measure and compare hepatitis C virus replication capacity using full-length, replication competent viruses.

    abstract::Measuring the in vitro replication capacity of viruses is an important tool for assessing the effects of selective pressure of immune responses and drug therapy. Measuring hepatitis C virus (HCV) replication capacity utilizing primarily sub-genomic reporter constructs is limited. To overcome some of these limitations ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.08.009

    authors: Lassmann B,Arumugaswami V,Chew KW,Lewis MJ

    更新日期:2013-12-01 00:00:00

  • Analysis of the expression profiles of Marek's disease virus-encoded microRNAs by real-time quantitative PCR.

    abstract::MicroRNAs (miRNAs) are a large class of endogenous approximately 22-nucleotide long non-coding RNAs involved in post-transcriptional silencing of gene expression by translational repression or direct cleavage of the target mRNAs. Several hundreds of miRNAs have now been identified in a wide range of organisms includin...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.02.005

    authors: Xu H,Yao Y,Zhao Y,Smith LP,Baigent SJ,Nair V

    更新日期:2008-05-01 00:00:00

  • Sensitive and accurate quantitation of hepatitis B virus DNA using a kinetic fluorescence detection system (TaqMan PCR).

    abstract::The laboratory diagnosis of hepatitis B virus (HBV) infection is based mainly on serological assays. Yet the detection and quantitation of viral DNA is necessary when addressing directly the question of infectivity or when monitoring the viral load during therapy. Standard hybridization assays allow for exact quantita...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(99)00154-8

    authors: Weinberger KM,Wiedenmann E,Böhm S,Jilg W

    更新日期:2000-03-01 00:00:00

  • Enzyme-linked fluorescence immunoassays using beta-galactosidase and antibodies covalently bound to polystyrene plates.

    abstract::A solid-phase enzyme-linked immunoassay using a fluorogenic substrate (4-methylumbelliferyl-beta-D-galactopyranoside) was developed. Antibodies were covalently linked to glutaraldehyde-activated 96-well aminopolystyrene plates. Antigens from test samples were adsorbed to the solid phase and detected using antibodies c...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(81)90050-1

    authors: Neurath AR,Strick N

    更新日期:1981-10-01 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