Observations on polymerase chain reaction amplification of infectious bursal disease virus dsRNA.

Abstract:

:Two methods for denaturing double stranded (ds)RNA of infectious bursal disease virus for the purpose of reverse transcribing it were compared: Heat denaturation at 65 degrees C in the presence of DMSO and in the absence of DMSO. As part of the analysis, the nature of cDNA in the two preparations was examined by polymerase chain reaction (PCR) amplification, firstly by varying the number of cycles of PCR, and secondly by re-amplification of serial dilutions of the reaction products. The results show that denaturation of dsRNA in the presence of DMSO (method 1) is superior to denaturation without DMSO (method 2) judging by the yield of a specific PCR fragment after 30 cycles, and that the products of method 2 can be re-amplified, albeit poorly, with the generation of heterologous products.

journal_name

J Virol Methods

authors

Qian B,Kibenge FS

doi

10.1016/0166-0934(94)90081-7

subject

Has Abstract

pub_date

1994-04-01 00:00:00

pages

237-42

issue

1-2

eissn

0166-0934

issn

1879-0984

pii

0166-0934(94)90081-7

journal_volume

47

pub_type

杂志文章
  • Chemical inactivation of hepatitis B virus: the effect of disinfectants on virus-associated DNA polymerase activity, morphology and infectivity.

    abstract::The inactivation of hepatitis B virus (HBV) using two commercially available disinfectants was analysed. Indirect evidence of virus inactivation was obtained by examining the decrease in HBV-associated DNA polymerase and HBcAg activities after treatment with increasing concentrations of disinfectant. Inactivation was ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(83)90003-4

    authors: Howard CR,Dixon J,Young P,van Eerd P,Schellekens H

    更新日期:1983-09-01 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

  • Consensus oligonucleotide primers for the detection of GB virus C in human cryptogenic hepatitis.

    abstract::Recently, sequences from a putative member of the Flaviviridae, GB virus C (GBV-C), were isolated from the serum of patients with cryptogenic hepatitis. These sequences were 83-99% identical at the nucleotide level. Because of the divergence between these GBV-C isolates, it is likely that the PCR-based detection assay...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(95)01956-1

    authors: Leary TP,Muerhoff AS,Simons JN,Pilot-Matias TJ,Erker JC,Chalmers ML,Schlauder GG,Dawson GJ,Desai SM,Mushahwar IK

    更新日期:1996-01-01 00:00:00

  • Validation of a modified commercial assay for the detection of rubella-specific IgG in oral fluid for use in population studies.

    abstract::Matching serum and oral fluid (saliva) samples were collected from 369 subjects in Tunisia in 2002, from a city in the north and a rural district in the south. Rubella-specific IgG was detected in sera by commercial ELISA (Dade Behring) and in matching oral fluids by two methods, a previously described IgG-capture ELI...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2003.09.008

    authors: Ben Salah A,Zaâtour A,Pomery L,Cohen BJ,Brown DW,Andrews N

    更新日期:2003-12-01 00:00:00

  • Classification of hepatitis B virus genotypes by the PCR-Invader method with genotype-specific probes.

    abstract::Hepatitis B virus is a worldwide public health problem. A simple and effective test to identify viral genotypes would greatly aid efforts to understand and control the spread of this disease. A serial invasive signal amplification reaction assay (PCR-Invader assay) was developed for distinguishing the known eight geno...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.07.014

    authors: Tadokoro K,Kobayashi M,Yamaguchi T,Suzuki F,Miyauchi S,Egashira T,Kumada H

    更新日期:2006-12-01 00:00:00

  • Development and evaluation of a line probe assay for rapid typing of influenza viruses and detection of the H274Y mutation.

    abstract::Adequate treatment of influenza requires identification of viral type as well as detection of mutation(s) conferring drug resistance. Reverse hybridization-based line probe assays (LiPA) can be performed using several probes immobilized on nitrocellulose, strips enabling LiPA to determine simultaneously viral subtypes...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2012.06.018

    authors: Miyoshi-Akiyama T,Akasaka Y,Oogane T,Kondo Y,Matsushita T,Funatogawa K,Kirikae T

    更新日期:2012-11-01 00:00:00

  • Infectivity enhancement of different HIV-1-based lentiviral pseudotypes in presence of the cationic amphipathic peptide LAH4-L1.

    abstract::Lentiviral vectors (LVs) are promising delivery systems for gene therapy. To enhance the efficiency of target cell transduction by LVs, protocols often include the addition of culture additives. In this study, the cationic amphipathic peptide LAH4-L1 (KKALLAHALHLLALLALHLAHALKKA), a DNA transfection agent, was evaluate...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.02.005

    authors: Fenard D,Genries S,Scherman D,Galy A,Martin S,Kichler A

    更新日期:2013-05-01 00:00:00

  • Expression and spectroscopic analysis of a mutant hepatitis B virus onco-protein HBx without cysteine residues.

    abstract::Chronic infection of the hepatitis B virus (HBV) is one of the causes leading to liver cancer. The 3.2kb genome of HBV encodes four proteins: core antigen, surface antigen, a DNA polymerase and the X protein (HBx). The biological functions of HBx are not fully understood. It has been shown that HBx is a potent trans-a...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2005.01.022

    authors: Rui E,Moura PR,Gonçalves Kde A,Kobarg J

    更新日期:2005-06-01 00:00:00

  • Evaluation of the efficacy of disinfectants against Puumala hantavirus by real-time RT-PCR.

    abstract::Puumala virus, a hantavirus belonging to the Bunyaviridae family, causes a human disease known as nephropathia epidemica, a mild form of hemorrhagic fever with renal syndrome. The implementation of effective decontamination procedures is critical in hantavirus research to minimize the risk of personnel exposure. This ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.11.037

    authors: Maes P,Li S,Verbeeck J,Keyaerts E,Clement J,Van Ranst M

    更新日期:2007-04-01 00:00:00

  • Accurate virus quantitation using a Scanning Transmission Electron Microscopy (STEM) detector in a scanning electron microscope.

    abstract::A method for accurate quantitation of virus particles has long been sought, but a perfect method still eludes the scientific community. Electron Microscopy (EM) quantitation is a valuable technique because it provides direct morphology information and counts of all viral particles, whether or not they are infectious. ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2017.06.014

    authors: Blancett CD,Fetterer DP,Koistinen KA,Morazzani EM,Monninger MK,Piper AE,Kuehl KA,Kearney BJ,Norris SL,Rossi CA,Glass PJ,Sun MG

    更新日期:2017-10-01 00:00:00

  • Novel and highly sensitive SYBR® Green real-time pcr for poxvirus detection in odontocete cetaceans.

    abstract::Poxviruses are emerging pathogens in cetaceans, temporarily named 'Cetaceanpoxvirus' (CePV, family Poxviridae), classified into two main lineages: CePV-1 in odontocetes and CePV-2 in mysticetes. Only a few studies performed the molecular detection of CePVs, based on DNA-polymerase gene and/or DNA-topoisomerase I gene ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2018.06.002

    authors: Sacristán C,Catão-Dias JL,Ewbank AC,Ferreira-Machado E,Neves E,Santos-Neto EB,Azevedo A,Laison-Brito J Jr,De Castilho PV,Daura-Jorge FG,Simões-Lopes PC,Carballo M,García-Párraga D,Sánchez-Vizcaíno JM,Esperón F

    更新日期:2018-09-01 00:00:00

  • Simple serological diagnosis of arboviruses: a simplified diluent system for Japanese encephalitis virus hemagglutination-inhibition tests using formalinized chick erythrocytes.

    abstract::Formalinized chick erythrocytes agglutinated with Japanese encephalitis virus antigens over a wider range of pH (6.0-7.2) than fresh erythrocytes (pH 6.4-6.8). The virus antigens were unstable below pH 7.0 and therefore the use of the formalinized erythrocytes made it possible for a one-diluent system of the hemagglut...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(80)90026-9

    authors: Ito H,Iwasa S

    更新日期:1980-01-01 00:00:00

  • Detection of viruses in environmental samples: suitability of commercial rotavirus and adenovirus test kits.

    abstract::Commercially marketed kits are now available for rapid viral assay of clinical specimens. This study was conducted to determine the suitability of these kits for use in environmental testing. Eight rotavirus kits and one enteric adenovirus kit were screened for sensitivity using simian rotavirus SA11, human rotavirus ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(93)90098-c

    authors: Dahling DR,Wright BA,Williams FP Jr

    更新日期:1993-12-15 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

  • Determination of hepatitis C virus genotype by Pyrosequencing.

    abstract::A simple sequencing-based assay is described for genotyping of hepatitis C virus (HCV). RT-PCR was employed to amplify a 237-nucleotide-long fragment from the 5' untranslated region (UTR) of the genome using one biotinylated and one normal primer. Subsequent to capture of the PCR products on streptavidin-coated beads,...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(03)00068-5

    authors: Elahi E,Pourmand N,Chaung R,Rofoogaran A,Boisver J,Samimi-Rad K,Davis RW,Ronaghi M

    更新日期:2003-05-01 00:00:00

  • Development of a fluorogenic RT-PCR system for quantitative identification of dengue virus serotypes 1-4 using conserved and serotype-specific 3' noncoding sequences.

    abstract::A fluorogenic reverse transcriptase-polymerase chain reaction (RT-PCR) system was developed for use as a rapid diagnostic test for determining dengue viremia. The dengue virus 3'-noncoding sequence was utilized to formulate serotype-specific RT-PCR assays for quantitative identification of the four different dengue vi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(01)00280-4

    authors: Houng HS,Chung-Ming Chen R,Vaughn DW,Kanesa-thasan N

    更新日期:2001-06-01 00:00:00

  • Comparison of a conventional HIV 1/2 line immunoassay with a rapid confirmatory HIV 1/2 assay.

    abstract::The performance of the rapid confirmatory HIV 1/2 assay Geenius was compared with the conventional HIV 1/2 line immunoblot (INNO-LIA HIV I/II Score). One hundred HIV 1/2 confirmed positive samples from donors and patients and 136 negative screening samples from blood donors were evaluated with both assays. A 20 member...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.05.010

    authors: Tinguely C,Schild-Spycher T,Bahador Z,Gowland P,Stolz M,Niederhauser C

    更新日期:2014-09-01 00:00:00

  • Detection and quantitation of HTLV-1 and HTLV-2 mRNA species by real-time RT-PCR.

    abstract::HTLV-1 and HTLV-2 are highly related delta-retroviruses that infect and transform T-lymphocytes, but have distinct pathogenic properties. HTLV replication and survival requires the expression of multiple gene products from an unspliced and a series of highly related alternatively spliced mRNA species. To date, the com...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2007.01.023

    authors: Li M,Green PL

    更新日期:2007-06-01 00:00:00

  • An enzymatic virus-like particle assay for sensitive detection of virus entry.

    abstract::A viral entry assay where a beta-lactamase reporter protein fused to the influenza matrix protein-1 (BlaM1) is packaged as a structural component into influenza virus-like particles (VLPs) is described. The Bla reporter is released upon fusion with target cells and can be detected in live cells by flow cytometry, micr...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.10.020

    authors: Tscherne DM,Manicassamy B,García-Sastre A

    更新日期:2010-02-01 00:00:00

  • Comparison between serum and saliva for the detection of hepatitis A virus RNA.

    abstract::Due to the ease of collection, oral fluid is being investigated as an alternative to serum for diagnostic and epidemiological purposes. However, for prospective studies involving hepatitis A virus (HAV) RNA detection, a standard methodology must be developed. In the present study, nested RT-PCR and real-time PCR were ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2007.10.020

    authors: Amado LA,Villar LM,de Paula VS,Gaspar AM

    更新日期:2008-03-01 00:00:00

  • A new generic real-time reverse transcription polymerase chain reaction assay for vesiviruses; vesiviruses were not detected in human samples.

    abstract::Different viruses belonging to the genus Vesivirus infect a broad range of animals, and cause gastroenteritis, vesicular skin lesions, hemorrhagic disease, respiratory diseases and other conditions. A recent report on Vesivirus viremia, as detected by PCR, in samples from patients with hepatitis of unknown etiology in...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.12.008

    authors: Svraka S,Duizer E,Egberink H,Dekkers J,Vennema H,Koopmans M

    更新日期:2009-04-01 00:00:00

  • Green fluorescent protein as a probe of rotational mobility within bacteriophage T4.

    abstract::Green fluorescent protein (GFP) was targeted into bacteriophage T4 heads and proheads as a probe of the internal environment. Targeting was accomplished with internal protein III (IPIII) fusion proteins or capsid targeting sequence (CTS)-tagged proteins, where CTS is the 10-amino acid residue CTS of IPIII. Recombinant...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(00)00166-x

    authors: Mullaney JM,Thompson RB,Gryczynski Z,Black LW

    更新日期:2000-07-01 00:00:00

  • Chicken single-chain variable fragments against the SARS-CoV spike protein.

    abstract::The major concern for severe acute respiratory syndrome (SARS), caused by the SARS-associated coronavirus (SARS-CoV), is the lack of diagnostic and therapeutic agents. Using a phage display technology in a chicken system, high-affinity monoclonal antibody fragments against the SARS-CoV spike protein were characterized...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2007.06.010

    authors: Lee YC,Leu SJ,Hu CJ,Shih NY,Huang IJ,Wu HH,Hsieh WS,Chiang BL,Chiu WT,Yang YY

    更新日期:2007-12-01 00:00:00

  • Characterization of the mixture of genotypes of a Citrus tristeza virus isolate by reverse transcription-quantitative real-time PCR.

    abstract::A multiplex real-time PCR assay was developed to detect and quantify the Citrus tristeza virus (CTV) genotypic mixture present in infected plants. CTV isolate FS627, a complex Florida isolate containing T36, T30 and VT genotypes and its aphid transmitted subisolates was used. The relative quantitative assay was carrie...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.12.001

    authors: Ananthakrishnan G,Venkataprasanna T,Roy A,Brlansky RH

    更新日期:2010-03-01 00:00:00

  • Detection of dengue virus RNA using nucleic acid hybridization.

    abstract::Conditions for using slot-blot nucleic acid hybridization to quantitatively detect dengue-2 virus using a radiolabelled cDNA probe, pVV17, were determined. As little as 11 plaque-forming units of virus were detected using a hybridization mixture without formamide and performing the test at 70 degrees C. While predomin...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(87)90097-8

    authors: Henchal EA,Narupiti S,Feighny R,Padmanabhan R,Vakharia V

    更新日期:1987-02-01 00:00:00

  • Development of a genome copy specific RT-qPCR assay for divergent strains of type 2 porcine reproductive and respiratory syndrome virus.

    abstract::Porcine reproductive and respiratory syndrome virus (PRRSV) became a significant pathogen of swine upon its emergence in the late 1980s and since then has exemplified a rapidly evolving, constantly re-emerging pathogen. In addition to the challenges faced in development of vaccines and diagnostics, research on the bas...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.02.007

    authors: Spear A,Faaberg KS

    更新日期:2015-06-15 00:00:00

  • A flow-through cell counting assay for point-of-care enumeration of CD4 T-cells.

    abstract::CD4 T-cell count is a priority for staging HIV disease and guiding clinical management as part of HIV care. Conventional CD4 T-cell enumeration methods based on flow cytometry are expensive, require well-trained personnel, and are challenging to use in rural, resource-scarce areas. A simple CD4 T-cell count test that ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2019.05.012

    authors: Bystryak S,Bandwar RP,Santockyte R

    更新日期:2019-09-01 00:00:00

  • Fluorescent poliovirus for flow cytometric cell surface binding studies.

    abstract::Specific cell-surface binding is the essential first step for cellular invasion by viruses. To understand this process, various methods to evaluate binding properties of viruses to cells have been developed. However, many rely on radioactive labeling or indirect immunofluorescence. The development of a novel fluoresce...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2005.08.011

    authors: Freistadt MS,Eberle KE

    更新日期:2006-06-01 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 one-step centrifugal ultrafiltration method to concentrate enteric viruses from wastewater.

    abstract::A one-step centrifugal ultrafiltration method was developed to enhance rapid detection of human enteric viruses and co-occurring viruses in wastewater. Samples were collected pre- and post-UV treatment at two full-scale tertiary municipal wastewater treatment plants in Calgary, Canada. Viruses were concentrated from 1...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2016.09.010

    authors: Qiu Y,Lee BE,Ruecker NJ,Neumann N,Ashbolt N,Pang X

    更新日期:2016-11-01 00:00:00