Development of chemiluminescent probe hybridization, RT-PCR and nucleic acid cycle sequencing assays of Sabin type 3 isolates to identify base pair 472 Sabin type 3 mutants associated with vaccine associated paralytic poliomyelitis.

Abstract:

:Sabin type 3 polio vaccine virus is the most common cause of poliovaccine associated paralytic poliomyelitis. Vaccine associated paralytic poliomyelitis cases have been associated with Sabin type 3 revertants containing a single U to C substitution at bp 472 of Sabin type 3. A rapid method of identification of Sabin type 3 bp 472 mutants is described. An enterovirus group-specific probe for use in a chemiluminescent dot blot hybridization assay was developed to identify enterovirus positive viral lysates. A reverse transcription-polymerase chain reaction (RT-PCR) assay producing a 319 bp PCR product containing the Sabin type 3 bp 472 mutation site was then employed to identify Sabin type 3 isolates. Chemiluminescent nucleic acid cycle sequencing of the purified 319 bp PCR product was then employed to identify nucleic acid sequences at bp 472. The enterovirus group probe hybridization procedure and isolation of the Sabin type 3 PCR product were highly sensitive and specific; nucleic acid cycle sequencing corresponded to the known sequence of stock Sabin type 3 isolates. These methods will be used to identify the Sabin type 3 reversion rate from sequential stool samples of infants obtained after the first and second doses of oral poliovirus vaccine.

journal_name

J Virol Methods

authors

Old MO,Logan LH,Maldonado YA

doi

10.1016/s0166-0934(97)00114-6

subject

Has Abstract

pub_date

1997-11-01 00:00:00

pages

109-18

issue

2

eissn

0166-0934

issn

1879-0984

pii

S0166-0934(97)00114-6

journal_volume

68

pub_type

杂志文章
  • A rapid screening assay for detecting individual RNA species in field isolates of rotaviruses.

    abstract::A method is described that allows the rapid screening of field isolates of rotavirus for the detection of specific viral RNA segments. Cloned cDNA copies of viral genomic RNAs are employed for detection in the assay which makes use of the dot-hybridization technique of Thomas (1980). The assay developed was shown to b...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(84)90009-0

    authors: Pedley S,McCrae MA

    更新日期:1984-10-01 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

  • Detection of porcine parvovirus by loop-mediated isothermal amplification.

    abstract::Loop-mediated isothermal amplification is a novel method for rapid amplification of DNA. It has been adopted widely for the detection of virus because of its simplicity, rapidity, and specificity. A loop-mediated isothermal amplification assay was developed for the detection of porcine parvovirus. Four primers specifi...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.10.004

    authors: Chen CM,Cui SJ

    更新日期:2009-02-01 00:00:00

  • Poly A-linked non-isotopic microtiter plate reverse transcriptase assay for sensitive detection of clinical human immunodeficiency virus isolates.

    abstract::A colorimetric reverse transcriptase assay (cRT assay) was developed for quantitative detection of HIV-1. In this format, reverse transcriptase incorporates biotin-labeled dUTP onto oligo-dT primers hybridized to poly A templates. The templates are covalently bound to the surface of microtiter wells. The amount of inc...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(95)00073-5

    authors: Suzuki K,Saito T,Kondo M,Osanai M,Watanabe S,Kano T,Kano K,Imai M

    更新日期:1995-11-01 00:00:00

  • Multiplication of Taura syndrome virus in primary hemocyte culture of shrimp (Penaeus vannamei).

    abstract::The propagation of Taura syndrome virus (TSV) in primary hemocyte culture of Pacific white shrimp (Penaeus vannamei) was investigated. Purified TSV was inoculated into a 24 h old primary hemocyte culture and the development of cytopathic effects was monitored. The cell morphology started changing within 6 h post-inocu...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2010.12.020

    authors: George SK,Kaizer KN,Betz YM,Dhar AK

    更新日期:2011-03-01 00:00:00

  • A facile system for construction of HSV-1 variants: site directed mutation of the UL26 protease gene in HSV-1.

    abstract::A 2-plasmid/4-cosmid-based system of mutagenesis is described for construction of herpes simplex virus type 1 (HSV-1) variants with point mutations in the protease gene. The system was used to reconstruct a mutant virus (V701) with Tyr30 to Phe and Ala48 to Val mutations in HSV-1 protease that exhibits the temperature...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(95)01984-7

    authors: Register RB,Shafer JA

    更新日期:1996-04-05 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

  • Comparative study of the replication of infectious bursal disease virus in DF-1 cell line and chicken embryo fibroblasts evaluated by a new real-time RT-PCR.

    abstract::A real-time RT-PCR method was developed for the detection of infectious bursal disease virus (IBDV). The VP5 gene of IBDV was chosen as the target binding region for a specific TaqMan probe. The results showed that viral genomic copy number could be quantified accurately ranging from 10(8)copies/microL to 10(1)copies/...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.01.001

    authors: Wang Y,Qi X,Gao H,Gao Y,Lin H,Song X,Pei L,Wang X

    更新日期:2009-05-01 00:00:00

  • A rapid assay for Hendra virus IgG antibody detection and its titre estimation using magnetic nanoparticles and phycoerythrin.

    abstract::Detection of Hendra viral IgG antibody in animal sera is useful for surveillance following a virus outbreak. The commonly used enzyme-linked immunosorbent assay and fluorescence-based Luminex assay typically consist of three steps and take at least several hours to complete. We have simplified the procedure to two ste...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2015.05.008

    authors: Gao Y,Pallister J,Lapierre F,Crameri G,Wang LF,Zhu Y

    更新日期:2015-09-15 00:00:00

  • Detection of human virulence signatures in H5N1.

    abstract::A method for detecting the emergence of potential pandemic-causing influenza strains has been developed. The system first uses real-time RT-PCR to detect H5, the highly pathogenic avian influenza subtype most likely to cause a pandemic. Pyrosequencing is then employed to scan for codon changes encoding amino acids kno...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.09.013

    authors: Waybright N,Petrangelo E,Lowary P,Bogan J,Mulholland N

    更新日期:2008-12-01 00:00:00

  • A portable detection assay for Apple stem pitting virus using reverse transcription-recombinase polymerase amplification.

    abstract::A molecular diagnostic assay for the rapid, sensitive and specific detection of Apple stem pitting virus (ASPV) in infected samples, utilizing reverse transcription-recombinase polymerase amplification (RT-RPA) at an isothermal constant temperature of 42 °C and the designed target-specific primers, was developed. The ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2019.113747

    authors: Kim NY,Lee HJ,Jeong RD

    更新日期:2019-12-01 00:00:00

  • Development of a multiplex real-time RT-PCR that allows universal detection of influenza A viruses and simultaneous typing of influenza A/H1N1/2009 virus.

    abstract::On June 11, 2009, the World Health Organization declared that the influenza A/H1N1/2009 virus had become the first influenza pandemic of the 21st century. Rapid detection and differentiation from seasonal and avian influenza would be beneficial for patient management and infection control. It was the aim of this study...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2009.10.006

    authors: Gunson R,Maclean A,Davies E,Bennett S,Miller R,Carman WF

    更新日期:2010-02-01 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

  • Reactivity and amplification efficiency of the NASBA HIV-1 RNA amplification system with regard to different HIV-1 subtypes.

    abstract::In view of the genetic diversity of the human immunodeficiency virus Type 1, we assessed the sensitivity and quantification efficiency of the HIV-1 RNA NASBA amplification system with respect to different HIV-1 subtypes and recombinants. Twenty cell culture supernatants representing 17 HIV-1 group M and 3 group O stra...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(97)00072-4

    authors: Gobbers E,Fransen K,Oosterlaken T,Janssens W,Heyndrickx L,Ivens T,Vereecken K,Schoones R,van de Wiel P,van der Groen G

    更新日期:1997-07-01 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

  • Development and evaluation of a generic tag array to detect and genotype noroviruses in water.

    abstract::Noroviruses are the leading cause of nonbacterial gastroenteritis outbreaks in the United States, some of which are caused by the ingestion of contaminated water. Detection and genotypic characterization of noroviruses is commonly performed by reverse transcription-polymerase chain reaction (RT-PCR) followed by sequen...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.03.010

    authors: Brinkman NE,Fout GS

    更新日期:2009-03-01 00:00:00

  • Detection of foot-and-mouth disease virus RNA in clinical samples and cell culture isolates by amplification of the capsid coding region.

    abstract::Foot-and-mouth disease is one of the most economically important virus diseases of livestock. Two important requirements for the control of this disease are rapid laboratory diagnosis and epidemiological investigation. The use of the polymerase chain reaction method (PCR) to amplify specific nucleic acid regions offer...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/0166-0934(93)90176-r

    authors: Höfner MC,Carpenter WC,Donaldson AI

    更新日期:1993-04-01 00:00:00

  • Quantification of recombinant core-like particles of bluetongue virus using immunosorbent electron microscopy.

    abstract::Immunosorbent electron microscopy was used to quantify recombinant baculovirus-generated bluetongue virus (BTV) core-like particles (CLP) in either purified preparations or lysates of recombinant baculovirus-infected cells. The capture antibody was an anti-BTV VP7 monoclonal antibody. The CLP concentration in purified...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(98)00170-0

    authors: Zheng YZ,Hyatt A,Wang LF,Eaton BT,Greenfield PF,Reid S

    更新日期:1999-06-01 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

  • Comparative detection of rabies RNA by NASBA, real-time PCR and conventional PCR.

    abstract::Five methods for the RNA detection of rabies virus were directly compared in this study. These included conventional nucleic acid sequence-based amplification with electrochemiluminescence (NASBA-ECL) assay, reverse transcription (RT)-heminested (hn) polymerase chain reaction (PCR) and TaqMan real-time RT-PCR using pr...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.05.007

    authors: Wacharapluesadee S,Phumesin P,Supavonwong P,Khawplod P,Intarut N,Hemachudha T

    更新日期:2011-08-01 00:00:00

  • Characterization of a recombinant Newcastle disease virus expressing the green fluorescent protein.

    abstract::A recombinant Newcastle disease virus (NDV) expressing the green fluorescent protein (GFP) was generated by applying reverse genetics techniques. The GFP open reading frame flanked by NDV transcription start and stop sequences was inserted between the fusion (F)- and hemagglutinin-neuraminidase genes in a full-length ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/s0166-0934(02)00247-1

    authors: Engel-Herbert I,Werner O,Teifke JP,Mebatsion T,Mettenleiter TC,Römer-Oberdörfer A

    更新日期:2003-03-01 00:00:00

  • The impact of PCR-generated recombination on diversity estimation of mixed viral populations by deep sequencing.

    abstract::Ultra-deep pyrosequencing (UDPS) of targeted amplicons allows to determine a large number of individual sequence reads from a single PCR product, and this approach is thus extremely valuable for analysis of mixed viral populations. A mixture of genetically distinct DNA templates, however, may lead to the generation of...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2010.07.040

    authors: Görzer I,Guelly C,Trajanoski S,Puchhammer-Stöckl E

    更新日期:2010-10-01 00:00:00

  • Laboratory tests for evaluating the level of attenuation of bluetongue virus.

    abstract::One of the most important steps when preparing a live attenuated vaccine is the assessment of the level of attenuation in target animals. It is costly and time consuming as it requires, on each occasion, a large number of susceptible animals and contained accommodation. This study assessed the consistency of the bovin...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.07.007

    authors: Franchi P,Mercante MT,Ronchi GF,Armillotta G,Ulisse S,Molini U,Di Ventura M,Lelli R,Savini G,Pini A

    更新日期:2008-11-01 00:00:00

  • Construction of replication competent plasmids of hepatitis B virus subgenotypes A1, A2 and D3 with authentic endogenous promoters.

    abstract::Hepatitis B virus (HBV) is hyperendemic to southern Africa, with genotype A of HBV being the predominant genotype, and subgenotype A1 prevailing. Infection with this subgenotype is associated with rapid disease progression, and high frequency of hepatocellular carcinoma development. The objectives of our study was to ...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.03.015

    authors: Bhoola NH,Reumann K,Kew MC,Will H,Kramvis A

    更新日期:2014-07-01 00:00:00

  • Development of SYBR Green based real time PCR assay for detection of monodon baculovirus in Penaeus monodon.

    abstract::Shrimp farming is one of the most important aquaculture activities. Expansion and intensification of shrimp farming has been accompanied with the outbreak of diseases, which threaten the development and sustainability of the industry. Viral diseases are the major challenges faced by shrimp farming industries. The prev...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2014.05.006

    authors: Ramesh Kumar D,Sanjuktha M,Rajan JJ,Ananda Bharathi R,Santiago TC,Alavandi SV,Poornima M

    更新日期:2014-09-01 00:00:00

  • Development of a high-throughput human rhinovirus infectivity cell-based assay for identifying antiviral compounds.

    abstract::Asthma and chronic obstructive pulmonary disease exacerbations are associated with human rhinovirus (HRV) lung infections for which there are no current effective antiviral therapies. To date, HRV infectivity of cells in vitro has been measured by a variety of biochemical and immunological methods. This paper describe...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2011.02.002

    authors: Phillips T,Jenkinson L,McCrae C,Thong B,Unitt J

    更新日期:2011-05-01 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

  • Ovine progressive pneumonia virus capsid is B-cell immunodominant using Western blot analysis: a comparison of sensitivity between Western blot analysis and immunoprecipitation.

    abstract::A Western blot assay was developed and analyzed against the comparable standard, immunoprecipitation of (35)[S]-methionine/cysteine-labeled ovine progressive pneumonia virus (OPPV) proteins, for its ability to detect anti-OPPV antibodies using endpoint titers. Western blot analysis is 12-fold more sensitive in detecti...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2006.06.025

    authors: Myers-Evert DK,Herrmann-Hoesing LM

    更新日期:2006-11-01 00:00:00

  • Real-time RT-PCR (TaqMan) assays for the detection of viruses associated with Rugose wood complex of grapevine.

    abstract::Real-time TaqMan RT-PCR (TaqMan RT-PCR) assays were developed to detect the viruses associated with Rugose wood complex of grapevines. The viruses detected were Rupestris stem pitting-associated virus in the genus Foveavirus, Grapevine virus A, Grapevine virus B and Grapevine virus D in the genus Vitivirus. The coat p...

    journal_title:Journal of virological methods

    pub_type: 杂志文章

    doi:10.1016/j.jviromet.2008.09.005

    authors: Osman F,Rowhani A

    更新日期:2008-12-01 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