Solid phase reverse passive hemadsorption test for hepatitis B surface antigen.

Abstract:

:A solid phase reverse passive hemadsorption test (SP-RPHAd) for hepatitis B surface antigen detection is described. It was compared with a commercial reverse passive hemagglutination assay (Hepatest, Wellcome, U.K.). SP-RPHAd is four-fold less expensive than Hepatest and undiluted sera can be used instead of eight-fold diluted sera without risk of non-specific hemagglutination. Thus, the threshold of detection is lowered to about 5 ng/ml by SP-RPHAd.

journal_name

J Virol Methods

authors

Duverlie G,Driencourt M,Roussel C,Daniel P

doi

10.1016/0166-0934(87)90115-7

subject

Has Abstract

pub_date

1987-11-01 00:00:00

pages

107-12

issue

2-3

eissn

0166-0934

issn

1879-0984

pii

0166-0934(87)90115-7

journal_volume

18

pub_type

杂志文章
  • Differential expression of two isolates of beak and feather disease virus capsid protein in Escherichia coli.

    abstract::Expression of recombinant beak and feather disease virus (BFDV) capsid-associated protein (Cap) has relied on inefficient techniques that typically produce low yields or use specialized expression systems, which greatly increase the cost and expertise required for mass production. An Escherichia coli system was used t...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.01.020

    authors: Patterson EI,Swarbrick CM,Roman N,Forwood JK,Raidal SR

    更新日期:2013-04-01 00:00:00

  • The use of biotin-conjugated antisera in immunoassays for plant viruses.

    abstract::Biotin-conjugated antisera to two strains of sugarcane mosaic virus and erysimum latent virus were used to detect the viruses in extracts of infected plants. Two methods, enzyme-linked immunosorbent assays and electroblot immunoassays, were used. The antisera were found to be sufficiently sensitive for detection of th...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(86)90075-3

    authors: Hewish DR,Shukla DD,Gough KH

    更新日期:1986-04-01 00:00:00

  • Removal of lactate dehydrogenase-elevating virus from human-in-mouse breast tumor xenografts by cell-sorting.

    abstract::Lactate dehydrogenase-elevating virus (LDV) can infect transplantable mouse tumors or xenograft tumors in mice through LDV-contaminated mouse biological materials, such as Matrigel, or through mice infected with LDV. LDV infects specifically mouse macrophages and alters immune system and tumor phenotype. The tradition...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.02.015

    authors: Liu H,Bockhorn J,Dalton R,Chang YF,Qian D,Zitzow LA,Clarke MF,Greene GL

    更新日期:2011-05-01 00:00:00

  • A rapid assay for evaluation of antiviral activity against coxsackie virus B3, influenza virus A, and herpes simplex virus type 1.

    abstract::In order to identify new potential antiviral drugs, small amounts of extracts or compounds have to be examined for cytotoxicity and antiviral activity in primary screening using a rapid, easy, inexpensive, and highly standardised test system. In this study, high-throughput cytopathic effect (CPE) inhibitory assays wer...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(01)00305-6

    authors: Schmidtke M,Schnittler U,Jahn B,Dahse H,Stelzner A

    更新日期:2001-06-01 00:00:00

  • Susceptibility of bovine mesenchymal stem cells to bovine herpesvirus 4.

    abstract::Bovine herpesvirus 4 (BoHV-4) is a gamma herpesvirus with no clear disease association. Previous studies have demonstrated that macrophages can harbour persistent BoHV-4. Since mesenchymal stem cells in bone marrow regulate the differentiation and proliferation of adjacent haematopoietic precursors, such as macrophage...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2005.02.019

    authors: Donofrio G,Colleoni S,Galli C,Lazzari G,Cavirani S,Flammini CF

    更新日期:2005-08-01 00:00:00

  • Sensitive analytic ELISAs for subclass herpes virus IgG.

    abstract::The subclass distribution of antiviral antibodies to three herpes viruses was studied in a population of healthy blood donors. Subclassification by monoclonal antibodies led to the identification of certain viral IgG patterns. IgG1 appeared to be formed in response to almost all CMV, HSV-1 and VZV infections. A higher...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(85)90061-8

    authors: Gilljam G,Sundqvist VA,Linde A,Pihlstedt P,Eklund AE,Wahren B

    更新日期:1985-03-01 00:00:00

  • A method for coupling cytomegalovirus antigens to aldehyde-fixed erythrocytes for use in passive hemagglutination.

    abstract::A method for coupling cytomegalovirus (CMV) antigens to aldehyde-fixed erythrocytes for use in a passive hemagglutination assay for antibody to CMV is described. This method uses acid buffer instead of tannic acid for coupling CMV-complement fixation (CF) antigen to the stabilized cells. The coated cells are stable fo...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(83)90002-2

    authors: Ikram H,Prince AM

    更新日期:1983-09-01 00:00:00

  • A RT-PCR assay for the differential diagnosis of vesicular viral diseases of swine.

    abstract::A RT-PCR assay based on specific amplification of RNA sequences from each of the etiological agents of three important vesicular diseases that affect swine, foot-and-mouth disease virus (FMDV), swine vesicular disease virus (SVDV), and vesicular stomatitis virus (VSV), was developed. Genotype-specific primers that amp...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00032-9

    authors: Núñez JI,Blanco E,Hernández T,Gómez-Tejedor C,Martín MJ,Dopazo J,Sobrino F

    更新日期:1998-06-01 00:00:00

  • Development of a TaqMan-based real-time RT-PCR assay for the detection of SADS-CoV associated with severe diarrhea disease in pigs.

    abstract::Swine acute diarrhea syndrome coronavirus (SADS-CoV) is a novel coronavirus which was first reported in southern China in 2017. It can cause severe diarrhea disease in pigs. In order to detect this new emerging virus rapidly and reliably, a TaqMan-based real-time RT-PCR assay was established in this study. Specific pr...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2018.02.002

    authors: Zhou L,Sun Y,Wu JL,Mai KJ,Chen GH,Wu ZX,Bai Y,Li D,Zhou ZH,Cheng J,Wu RT,Zhang XB,Ma JY

    更新日期:2018-05-01 00:00:00

  • Easy-to-use rapid gene amplification method for direct detection of RNA and DNA viruses in sera and feces from various animals.

    abstract::The development of rapid and simple gene amplification tests is required for detection of pathogens to prevent transmission of infectious diseases between animals or from animals to humans. An easy-to-use rapid gene amplification method that can directly detect RNA and DNA viruses in clinical samples was developed. Th...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.01.019

    authors: Segawa T,Kobayashi Y,Sase Y,Itou T,Suzuki M,Endoh T,Nakanishi T,Sakai T

    更新日期:2014-06-01 00:00:00

  • A plasmid-based reverse genetics system for mammalian orthoreoviruses driven by a plasmid-encoded T7 RNA polymerase.

    abstract::Mammalian orthoreoviruses (reoviruses) have served as highly useful models for studies of virus replication and pathogenesis. The development of a plasmid-based reverse genetics system represented a major breakthrough in reovirus research. The current reverse genetics systems for reoviruses rely on the expression of T...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2013.10.023

    authors: Komoto S,Kawagishi T,Kobayashi T,Ikizler M,Iskarpatyoti J,Dermody TS,Taniguchi K

    更新日期:2014-02-01 00:00:00

  • Formation of subviral particles of the capsid protein VP2 of infectious bursal disease virus and its application in serological diagnosis.

    abstract::Infectious bursal disease virus (IBDV) is an immunosuppressive disease of young chicken characterized by severe depletion of B-lymphocytes in the bursa of Fabricius. To provide antigen for diagnostic tests, its major structural protein VP2 was expressed in the yeast Saccharomyces cerevisiae. Electron microscopy of pur...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.11.020

    authors: Dey S,Upadhyay C,Madhan Mohan C,Kataria JM,Vakharia VN

    更新日期:2009-04-01 00:00:00

  • The influence of incubation time on adenovirus quantitation in A549 cells by most probable number.

    abstract::Cell culture based assays used to detect waterborne viruses typically call for incubating the sample for at least two weeks in order to ensure that all the culturable virus present is detected. Historically, this estimate was based, at least in part, on the length of time used for detecting poliovirus. In this study, ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2016.09.002

    authors: Cashdollar JL,Huff E,Ryu H,Grimm AC

    更新日期:2016-11-01 00:00:00

  • Detection of dengue viral RNA by microplate hybridization.

    abstract::Dengue virus infection is a major public health problem throughout tropical countries. In endemic areas, dengue hemorrhagic fever (DHF) or dengue shock syndrome (DSS) are common complications resulting in death. However, serological confirmation of dengue-related illness is often complicated and time-consuming. Detect...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(95)00026-q

    authors: Ruiz BH,Zamora MP,Liu S

    更新日期:1995-08-01 00:00:00

  • Rapid typing of influenza viruses using super high-speed quantitative real-time PCR.

    abstract::The development of a rapid and sensitive system for detecting influenza viruses is a high priority for controlling future epidemics and pandemics. Quantitative real-time PCR is often used for detecting various kinds of viruses; however, it requires more than 2h per run. Detection assays were performed with super high-...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.08.015

    authors: Sakurai A,Nomura N,Nanba R,Sinkai T,Iwaki T,Obayashi T,Hashimoto K,Hasegawa M,Sakoda Y,Naito A,Morizane Y,Hosaka M,Tsuboi K,Kida H,Kai A,Shibasaki F

    更新日期:2011-12-01 00:00:00

  • Simultaneous detection of two independent antigens by double staining with two mouse monoclonal antibodies.

    abstract::Simultaneous detection of two antigens by immunostaining usually requires primary antibodies from two different species or a hapten modification of one of the antibodies if they are from the same species. A novel double staining method is described for immunodetection of two independent antigens using two mouse monocl...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00048-2

    authors: Teramoto N,Szekely L,Pokrovskaja K,Hu LF,Yoshino T,Akagi T,Klein G

    更新日期:1998-07-01 00:00:00

  • Demonstration of calicivirus in human faeces by immunosorbent and immunogold-labelling electron microscopy methods.

    abstract::Immunosorbent electron microscopy (ISEM) and immuno-gold staining (IGS) electron microscopy methods have been applied to human faeces, shown by direct electron microscopy (EM) to contain calicivirus. Caliciviruses were successfully trapped on grids coated with positive rabbit or human antisera against calicivirus, but...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(86)90034-0

    authors: Kjeldsberg E

    更新日期:1986-11-01 00:00:00

  • Development of a non-radioactive gene probe by PCR for detection of white spot syndrome virus (WSSV).

    abstract::Combining primers created from the sequence information of two baculo-like viruses of penaeid shrimp, Baculovirus penaei (BP) and Monodon baculovirus (MBV), produced a 750 bp band on a 0.8% agarose gel using White Spot Syndrome Virus (WSSV), from Penaeus monodon, as the DNA template. The PCR fragment was ligated to a ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(96)02128-3

    authors: Nunan LM,Lightner DV

    更新日期:1997-01-01 00:00:00

  • Real-time PCR assay for specific detection of cowpox virus.

    abstract::The species cowpox virus (CPXV), genus Orthopoxvirus (OPV), consists of isolates highly variable in their biological properties and their genotypes. A TaqMan PCR assay for the specific detection of CPXV DNA based on sequences of the ORF D11L has been developed recently. (Gavrilova et al., 2010; Shchelkunov et al., 201...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.10.004

    authors: Maksyutov RA,Gavrilova EV,Meyer H,Shchelkunov SN

    更新日期:2015-01-01 00:00:00

  • An assay for quantifying infectious HIV particles.

    abstract::A method for assessing the number of infectious particles in preparations of HIV has been developed. Virus was mixed with cells to allow binding of virus. The cells were then cast in an agar gel to block any further transfer of virus between the cells. After 4 days of incubation the cells initially infected with HIV e...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(90)90133-z

    authors: Tjøtta E,Hungnes O,Grinde B

    更新日期:1990-02-01 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

  • Universal diagnostic RT-PCR protocol for arboviruses.

    abstract::A selected number of PCR protocols were evaluated to determine if they could serve as a universal protocol for detecting and identifying all arboviruses. In this study, four parameters that affect the efficacy of RT-PCR (RNA extraction method, choice of reverse transcriptase, choice of DNA polymerase and thermocycling...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00003-2

    authors: Kuno G

    更新日期:1998-05-01 00:00:00

  • Competitive polymerase chain reaction using an internal standard: application to the quantitation of viral DNA.

    abstract::A general strategy for the construction of an internal standard for the polymerase chain reaction (PCR) is described together with its application in the evaluation of clinical samples. This internal standard is a plasmid containing a modified target sequence that is co-amplified with the native target using the same ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(92)90099-y

    authors: Telenti A,Imboden P,Germann D

    更新日期:1992-09-01 00:00:00

  • Expression of Coxsackievirus B4 proteins VP0 and 2C in Escherichia coli and generation of virus protein recognizing antisera.

    abstract::Coxsackievirus B4 (CBV-4) capsid protein VP0 and non-structural 2C protein were expressed and purified using a glutathione-S-transferase (GST) fusion protein expression system. We used a full-size CBV-4 cDNA as a template to amplify the genes by polymerase chain reaction (PCR). The genes were cloned into expression ve...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(97)00150-x

    authors: Härkönen T,Hovi T,Roivainen M

    更新日期:1997-12-01 00:00:00

  • A solvent-free, rapid and simple virus RNA-release method for potato leafroll virus detection in aphids and plants by reverse transcription polymerase chain reaction.

    abstract::A one-step, rapid and economical method for potato leafroll virus (PLRV) RNA release that is applicable to the use on a microcentrifuge scale is described. Discs (3-6 mm diameter) from leaves, petioles, stems, and tubers of potato plants were incubated in microcentrifuge tubes with detergent solution. The supernatants...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(99)00102-0

    authors: Singh RP

    更新日期:1999-12-01 00:00:00

  • Development of a real-time RT-PCR assay for a novel influenza A (H1N1) virus.

    abstract::A pandemic caused by a novel influenza A virus (H1N1) poses a serious public health threat. In this study, a real-time reverse transcriptase PCR (RT-PCR) assay based on the hemagglutinin gene was developed that discriminates the novel H1N1 from swine influenza virus, seasonal H1N1/H3N2 virus and the highly pathogenic ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.09.021

    authors: Jiang T,Kang X,Deng Y,Zhao H,Li X,Yu X,Yu M,Qin E,Zhu Q,Yang Y,Qin C

    更新日期:2010-02-01 00:00:00

  • PG-4 cell plaque assay for xenotropic murine leukemia virus.

    abstract::Xenotropic murine leukemia virus (X-MuLV) is often used in retrovirus elimination studies involving rodent cells. Currently, X-MuLV is measured using a focus-forming assay on mink (MiCl1 S+L-) or cat (PG-4 S+L-) cell lines. An easier and quicker PG-4 cell plaque assay, which retains the statistical reproducibility of ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(99)00064-6

    authors: Li Z,Blair M,Thorner L

    更新日期:1999-08-01 00:00:00

  • FMDV replicons encoding green fluorescent protein are replication competent.

    abstract::The study of replication of viruses that require high bio-secure facilities can be accomplished with less stringent containment using non-infectious 'replicon' systems. The FMDV replicon system (pT7rep) reported by Mclnerney et al. (2000) was modified by the replacement of sequences encoding chloramphenicol acetyl-tra...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.08.020

    authors: Tulloch F,Pathania U,Luke GA,Nicholson J,Stonehouse NJ,Rowlands DJ,Jackson T,Tuthill T,Haas J,Lamond AI,Ryan MD

    更新日期:2014-12-01 00:00:00

  • Chemiluminescent microtiter method for detecting PCR amplified HIV-1 DNA.

    abstract::A rapid and sensitive method for detecting HIV-1 DNA sequences amplified by polymerase chain reaction (PCR) is described. The method uses solution phase hybridization for rapid and efficient annealing between digoxigenin-labeled targets and biotinylated capture probes. Hybrids containing biotin are captured onto strep...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(92)90174-c

    authors: Suzuki K,Okamoto N,Watanabe S,Kano T

    更新日期:1992-07-01 00:00:00

  • Evaluation of cell viability dyes in antiviral assays with RNA viruses that exhibit different cytopathogenic properties.

    abstract::Studies were conducted to determine the performance of four dyes in assessing antiviral activities of compounds against three RNA viruses with differing cytopathogenic properties. Dyes included alamarBlue® measured by absorbance (ALB-A) and fluorescence (ALB-F), neutral red (NR), Viral ToxGlo™ (VTG), and WST-1. Viruse...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2017.03.012

    authors: Smee DF,Hurst BL,Evans WJ,Clyde N,Wright S,Peterson C,Jung KH,Day CW

    更新日期:2017-08-01 00:00:00