Literature DB >> 9774607

Enhancement of the AMPLICOR enterovirus PCR test with a coprecipitant.

E W Taggart1, C L Byington, D R Hillyard, J E Robison, K C Carroll.   

Abstract

The incorporation of a commercially available coprecipitant into the AMPLICOR enterovirus PCR test specimen preparation enhanced the sensitivity and reproducibility of this assay. Fifty-five previously tested archived cerebrospinal fluids (CSF) specimens were tested in a blind study in duplicate with and without Pellet Paint coprecipitant (Novagen, Inc., Madison, Wis.). Of these specimens, 26 had previously been determined to be positive and 29 had previously been determined to be negative. All previously positive CSF specimens were positive when Pellet Paint was used and only 18 were positive without Pellet Paint. No previously negative specimens were positive on repeat testing with or without Pellet Paint. The background signal was not affected by the addition of Pellet Paint. These data support the utility of a coprecipitant in minimizing false-negative results.

Mesh:

Year:  1998        PMID: 9774607      PMCID: PMC105343     

Source DB:  PubMed          Journal:  J Clin Microbiol        ISSN: 0095-1137            Impact factor:   5.948


  10 in total

1.  Reverse transcription and DNA amplification by a Thermus thermophilus DNA polymerase.

Authors:  T W Myers; D H Gelfand
Journal:  Biochemistry       Date:  1991-08-06       Impact factor: 3.162

2.  Reproducibility of AMPLICOR enterovirus PCR test results.

Authors:  H A Rotbart
Journal:  J Clin Microbiol       Date:  1997-12       Impact factor: 5.948

3.  The complete nucleotide sequence of coxsackievirus B4 and its comparison to other members of the Picornaviridae.

Authors:  O Jenkins; J D Booth; P D Minor; J W Almond
Journal:  J Gen Virol       Date:  1987-07       Impact factor: 3.891

4.  Enzymatic amplification of beta-globin genomic sequences and restriction site analysis for diagnosis of sickle cell anemia.

Authors:  R K Saiki; S Scharf; F Faloona; K B Mullis; G T Horn; H A Erlich; N Arnheim
Journal:  Science       Date:  1985-12-20       Impact factor: 47.728

5.  Specific synthesis of DNA in vitro via a polymerase-catalyzed chain reaction.

Authors:  K B Mullis; F A Faloona
Journal:  Methods Enzymol       Date:  1987       Impact factor: 1.600

6.  Nonisotopic oligomeric probes for the human enteroviruses.

Authors:  H A Rotbart; P S Eastman; J L Ruth; K K Hirata; M J Levin
Journal:  J Clin Microbiol       Date:  1988-12       Impact factor: 5.948

7.  Diagnosis of enteroviral meningitis by using PCR with a colorimetric microwell detection assay.

Authors:  H A Rotbart; M H Sawyer; S Fast; C Lewinski; N Murphy; E F Keyser; J Spadoro; S Y Kao; M Loeffelholz
Journal:  J Clin Microbiol       Date:  1994-10       Impact factor: 5.948

8.  Comparison of cell culture with an immunoperoxidase kit for rapid diagnosis of herpes simplex virus infections.

Authors:  V C Salmon; B K Michaels; R B Turner
Journal:  Diagn Microbiol Infect Dis       Date:  1984-09       Impact factor: 2.803

9.  Complete nucleotide sequences of all three poliovirus serotype genomes. Implication for genetic relationship, gene function and antigenic determinants.

Authors:  H Toyoda; M Kohara; Y Kataoka; T Suganuma; T Omata; N Imura; A Nomoto
Journal:  J Mol Biol       Date:  1984-04-25       Impact factor: 5.469

Review 10.  Enteroviral infections of the central nervous system.

Authors:  H A Rotbart
Journal:  Clin Infect Dis       Date:  1995-04       Impact factor: 9.079

  10 in total
  2 in total

1.  Quantitative PCR method for diagnosis of citrus bacterial canker.

Authors:  J Cubero; J H Graham; T R Gottwald
Journal:  Appl Environ Microbiol       Date:  2001-06       Impact factor: 4.792

2.  Improvement of AMPLICOR human immunodeficiency virus type 1 viral load test (version 1.5) by addition of a coprecipitant during the RNA isolation step.

Authors:  Min Xu; Yung Chan; Steven H Fischer; Alan T Remaley
Journal:  J Clin Microbiol       Date:  2002-07       Impact factor: 5.948

  2 in total

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