Literature DB >> 11283067

Evaluation of the NucliSens Basic Kit for detection of Chlamydia trachomatis and Neisseria gonorrhoeae in genital tract specimens using nucleic acid sequence-based amplification of 16S rRNA.

J B Mahony1, X Song, S Chong, M Faught, T Salonga, J Kapala.   

Abstract

We evaluated a new RNA amplification and detection kit, the NucliSens Basic Kit (Organon Teknika), for the detection of Chlamydia trachomatis and Neisseria gonorrhoeae in genitourinary specimens. The Basic Kit provides an open platform for RNA amplification and detection and contains isolation reagents for nucleic acid extraction, nucleic acid sequence-based amplification (NASBA) reagents (enzymes and buffers), and a generic ruthenium-labeled probe for electrochemiluminescent (ECL) detection of amplified product. Using freshly purified and titrated stocks of C. trachomatis and N. gonorrhoeae and in vitro-generated RNA transcripts for sensitivity determinations, the Basic Kit detected 1 inclusion-forming unit of C. trachomatis, 1 CFU of N. gonorrhoeae, and 100 RNA molecules of 16S rRNA for both bacteria. The clinical performance of the Basic Kit was evaluated by testing a total of 250 specimens for N. gonorrhoeae by culture and NASBA and a total of 96 specimens for C. trachomatis by PCR and NASBA. The Basic Kit detected 139 of 142 N. gonorrhoeae culture-positive specimens and gave a negative result for 73 of 74 culture-negative specimens, for a sensitivity and specificity of 97.9 and 98.7%, respectively. For C. trachomatis, the Basic Kit detected 24 of 24 PCR-positive specimens and gave a negative result for 71 of 72 PCR-negative specimens, for a sensitivity and specificity of 100 and 98.6%, respectively. The Basic Kit also detected specimens containing both N. gonorrhoeae and C. trachomatis, using a multiplex NASBA assay using primers for both bacteria. The NucliSens Basic Kit offers a versatile platform for the development of sensitive RNA detection assays for sexually transmitted diseases.

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Year:  2001        PMID: 11283067      PMCID: PMC87950          DOI: 10.1128/JCM.39.4.1429-1435.2001

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


  29 in total

1.  Rapid and simple method for purification of nucleic acids.

Authors:  R Boom; C J Sol; M M Salimans; C L Jansen; P M Wertheim-van Dillen; J van der Noordaa
Journal:  J Clin Microbiol       Date:  1990-03       Impact factor: 5.948

2.  Ability of commercial ligase chain reaction and PCR assays to diagnose Chlamydia trachomatis infections in men by testing first-void urine.

Authors:  M A Chernesky; S Chong; D Jang; K Luinstra; J Sellors; J B Mahony
Journal:  J Clin Microbiol       Date:  1997-04       Impact factor: 5.948

3.  Nucleotide sequence of a 16S ribosomal RNA gene from Neisseria gonorrhoeae.

Authors:  R Rossau; L Heyndrickx; H Van Heuverswyn
Journal:  Nucleic Acids Res       Date:  1988-07-11       Impact factor: 16.971

4.  Detection of Neisseria gonorrhoeae and Chlamydia trachomatis in genitourinary specimens from men and women by a coamplification PCR assay.

Authors:  K A Crotchfelt; L E Welsh; D DeBonville; M Rosenstraus; T C Quinn
Journal:  J Clin Microbiol       Date:  1997-06       Impact factor: 5.948

5.  Urinary inhibitors of polymerase chain reaction and ligase chain reaction and testing of multiple specimens may contribute to lower assay sensitivities for diagnosing Chlamydia trachomatis infected women.

Authors:  M A Chernesky; D Jang; J Sellors; K Luinstra; S Chong; S Castriciano; J B Mahony
Journal:  Mol Cell Probes       Date:  1997-08       Impact factor: 2.365

6.  Comparison of manual Amplicor PCR, Cobas Amplicor PCR, and LCx assays for detection of Chlamydia trachomatis infection in women by using urine specimens.

Authors:  R Pasternack; P Vuorinen; T Pitkäjärvi; M Koskela; A Miettinen
Journal:  J Clin Microbiol       Date:  1997-02       Impact factor: 5.948

7.  Detection of Chlamydia trachomatis, Neisseria gonorrhoeae, Ureaplasma urealyticum, and Mycoplasma genitalium in First-void Urine Specimens by Multiplex Polymerase Chain Reaction.

Authors: 
Journal:  Mol Diagn       Date:  1997-09

8.  Performance of transcription-mediated amplification and ligase chain reaction assays for detection of chlamydial infection in urogenital samples obtained by invasive and noninvasive methods.

Authors:  A Stary; E Schuh; M Kerschbaumer; B Götz; H Lee
Journal:  J Clin Microbiol       Date:  1998-09       Impact factor: 5.948

9.  Evaluation of ligase chain reaction for use with urine for identification of Neisseria gonorrhoeae in females attending a sexually transmitted disease clinic.

Authors:  K R Smith; S Ching; H Lee; Y Ohhashi; H Y Hu; H C Fisher; E W Hook
Journal:  J Clin Microbiol       Date:  1995-02       Impact factor: 5.948

10.  Monitoring of Chlamydia trachomatis infections after antibiotic treatment using RNA detection by nucleic acid sequence based amplification.

Authors:  S A Morré; P T Sillekens; M V Jacobs; S de Blok; J M Ossewaarde; P van Aarle; B van Gemen; J M Walboomers; C J Meijer; A J van den Brule
Journal:  Mol Pathol       Date:  1998-06
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  16 in total

Review 1.  Characteristics and applications of nucleic acid sequence-based amplification (NASBA).

Authors:  Birgit Deiman; Pierre van Aarle; Peter Sillekens
Journal:  Mol Biotechnol       Date:  2002-02       Impact factor: 2.695

2.  Prospective study of use of PCR amplification and sequencing of 16S ribosomal DNA from cerebrospinal fluid for diagnosis of bacterial meningitis in a clinical setting.

Authors:  Tim Schuurman; Richard F de Boer; Anna M D Kooistra-Smid; Anton A van Zwet
Journal:  J Clin Microbiol       Date:  2004-02       Impact factor: 5.948

3.  Nucleotide sequence-based multitarget identification.

Authors:  T Vinayagamoorthy; Kirk Mulatz; Roger Hodkinson
Journal:  J Clin Microbiol       Date:  2003-07       Impact factor: 5.948

4.  A novel sequence-specific RNA quantification method using nicking endonuclease, dual-labeled fluorescent DNA probe, and conformation-interchangeable oligo-DNA.

Authors:  Kazufumi Hosoda; Tomoaki Matsuura; Hiroshi Kita; Norikazu Ichihashi; Koji Tsukada; Itaru Urabe; Tetsuya Yomo
Journal:  RNA       Date:  2008-01-29       Impact factor: 4.942

5.  The laboratory diagnosis of Neisseria gonorrhoeae.

Authors:  Lai-King Ng; Irene E Martin
Journal:  Can J Infect Dis Med Microbiol       Date:  2005-01       Impact factor: 2.471

6.  Label-Free Pathogen Detection by a Deoxyribozyme Cascade with Visual Signal Readout.

Authors:  Adam J Reed; Ryan P Connelly; Allison Williams; Maithi Tran; Byoung-Shik Shim; Hyeryun Choe; Yulia V Gerasimova
Journal:  Sens Actuators B Chem       Date:  2018-11-29       Impact factor: 7.460

7.  Specific and sensitive detection of Neisseria gonorrhoeae in clinical specimens by real-time PCR.

Authors:  C W M Geraats-Peters; M Brouwers; P M Schneeberger; A G M van der Zanden; S M Bruisten; G Weers-Pothoff; C H E Boel; A J C van den Brule; H G Harmsen; M H A Hermans
Journal:  J Clin Microbiol       Date:  2005-11       Impact factor: 5.948

8.  Use of PCR and reverse line blot hybridization assay for rapid simultaneous detection and serovar identification of Chlamydia trachomatis.

Authors:  Likuan Xiong; Fanrong Kong; Hua Zhou; Gwendolyn L Gilbert
Journal:  J Clin Microbiol       Date:  2006-04       Impact factor: 5.948

9.  Detection of Chlamydia trachomatis by isothermal ramification amplification method: a feasibility study.

Authors:  Wandi Zhang; Menashi Cohenford; Brian Lentrichia; Henry D Isenberg; Elkin Simson; Hengjin Li; Jizu Yi; David Y Zhang
Journal:  J Clin Microbiol       Date:  2002-01       Impact factor: 5.948

10.  Prevalence of Chlamydia infection among women visiting a gynaecology outpatient department: evaluation of an in-house PCR assay for detection of Chlamydia trachomatis.

Authors:  Achchhe L Patel; Divya Sachdev; Poonam Nagpal; Uma Chaudhry; Subash C Sonkar; Suman L Mendiratta; Daman Saluja
Journal:  Ann Clin Microbiol Antimicrob       Date:  2010-09-08       Impact factor: 3.944

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