Literature DB >> 30971463

Evaluation of the ELITe InGenius PCR Platform for Detection of Mycoplasma pneumoniae.

Arthur H Totten1, Sixto M Leal2, Amy E Ratliff2, Li Xiao3, Donna M Crabb2, Ken B Waites4.   

Abstract

Mycoplasma pneumoniae is the leading cause of bacterial community-acquired pneumonia in persons of all ages. Due to the fastidious nature of this bacterium and the necessary specialized growth media, nucleic acid amplification testing is currently the most reliable means for patient diagnostics. Analytical sensitivity, specificity, reproducibility, and clinical performance of the ELITe InGenius automated PCR platform with its MGB Alert M. pneumoniae real-time PCR research use only reagents (ELITechGroup, Inc., Bothell, WA) were compared with those of a laboratory-developed real-time PCR assay targeting repMp1 for detection of M. pneumoniae The ELITe InGenius PCR assay successfully detected 31 distinct M. pneumoniae clinical isolates and reference strains, and there was no cross-reactivity with other mollicutes, Gram-positive bacteria, or Gram-negative bacteria. In testing 223 clinical samples, the ELITe InGenius PCR showed 95.79% and 99.22% positive and negative agreement with the repMp1 assay, respectively. Additionally, the ELITech platform showed 98.91% positive and 96.95% negative predictive values, and there was no significant difference detected between the two assays (McNemar's test, P = 0.375). The ELITe InGenius PCR assay limit of detection was 0.16 CFU/PCR test or 4.16 genome copies (GCs)/test. Accuracy, instrument ease-of-use, and decreased hands-on time make the ELITe InGenius platform suitable for detection of M. pneumoniae directly from clinical specimens.
Copyright © 2019 American Society for Microbiology.

Entities:  

Keywords:  ELITe InGenius; Mycoplasma pneumoniaezzm321990; PCR; molecular detection; respiratory

Mesh:

Year:  2019        PMID: 30971463      PMCID: PMC6535612          DOI: 10.1128/JCM.00287-19

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


  14 in total

1.  Analysis of three different repeated DNA elements present in the P1 operon of Mycoplasma pneumoniae: size, number and distribution on the genome.

Authors:  K Ruland; R Wenzel; R Herrmann
Journal:  Nucleic Acids Res       Date:  1990-11-11       Impact factor: 16.971

2.  Sensitive detection of Mycoplasma pneumoniae in human respiratory tract samples by optimized real-time PCR approach.

Authors:  Roger Dumke; Nicol Schurwanz; Matthias Lenz; Markus Schuppler; Christian Lück; Enno Jacobs
Journal:  J Clin Microbiol       Date:  2007-05-30       Impact factor: 5.948

3.  Sequence variations in RepMP2/3 and RepMP4 elements reveal intragenomic homologous DNA recombination events in Mycoplasma pneumoniae.

Authors:  Emiel B M Spuesens; Minoushka Oduber; Theo Hoogenboezem; Marcel Sluijter; Nico G Hartwig; Annemarie M C van Rossum; Cornelis Vink
Journal:  Microbiology       Date:  2009-04-23       Impact factor: 2.777

4.  Evaluation of five commercial real-time PCR assays for detection of Mycoplasma pneumoniae in respiratory tract specimens.

Authors:  A Touati; A Benard; A Ben Hassen; C M Bébéar; S Pereyre
Journal:  J Clin Microbiol       Date:  2009-04-29       Impact factor: 5.948

Review 5.  Mycoplasma pneumoniae from the Respiratory Tract and Beyond.

Authors:  Ken B Waites; Li Xiao; Yang Liu; Mitchell F Balish; T Prescott Atkinson
Journal:  Clin Microbiol Rev       Date:  2017-07       Impact factor: 26.132

Review 6.  Molecular methods for the detection of Mycoplasma and ureaplasma infections in humans: a paper from the 2011 William Beaumont Hospital Symposium on molecular pathology.

Authors:  Ken B Waites; Li Xiao; Vanya Paralanov; Rose M Viscardi; John I Glass
Journal:  J Mol Diagn       Date:  2012-07-20       Impact factor: 5.568

7.  Evaluation of five real-time PCR assays for detection of Mycoplasma pneumoniae.

Authors:  Roger Dumke; Enno Jacobs
Journal:  J Clin Microbiol       Date:  2014-09-10       Impact factor: 5.948

8.  Evaluation of Toxoplasma ELITe MGB Real-Time PCR Assay for Diagnosis of Toxoplasmosis.

Authors:  Florence Robert-Gangneux; Marie-Pierre Brenier-Pinchart; Hélène Yera; Sorya Belaz; Emmanuelle Varlet-Marie; Patrick Bastien
Journal:  J Clin Microbiol       Date:  2017-02-15       Impact factor: 5.948

9.  Comparison of the illumigene Mycoplasma DNA amplification assay and culture for detection of Mycoplasma pneumoniae.

Authors:  Amy E Ratliff; Lynn B Duffy; Ken B Waites
Journal:  J Clin Microbiol       Date:  2014-01-15       Impact factor: 5.948

10.  Comparative evaluation of six commercialized multiplex PCR kits for the diagnosis of respiratory infections.

Authors:  Sylvie Pillet; Marina Lardeux; Julia Dina; Florence Grattard; Paul Verhoeven; Jérôme Le Goff; Astrid Vabret; Bruno Pozzetto
Journal:  PLoS One       Date:  2013-08-23       Impact factor: 3.240

View more
  3 in total

1.  Evaluation of Commercial Molecular Diagnostic Methods for Detection and Determination of Macrolide Resistance in Mycoplasma pneumoniae.

Authors:  Sixto M Leal; Arthur H Totten; Li Xiao; Donna M Crabb; Amy Ratliff; Lynn B Duffy; Karen B Fowler; Emily Mixon; Jonas M Winchell; Maureen H Diaz; Alvaro J Benitez; Bernard J Wolff; Xuan Qin; Y-W Tang; Mark Gonzalez; Raj Selvarangan; Tao Hong; Edward Brooks; Steve Dallas; T Prescott Atkinson; Xiaotian Zheng; Jennifer Dien Bard; Ken B Waites
Journal:  J Clin Microbiol       Date:  2020-05-26       Impact factor: 5.948

2.  Mycoplasma pneumoniae infection mimicking tuberculous pleurisy in a young woman: a case report and literature review.

Authors:  Peng Wen; Min Wei; Xue Guo; Yu-Rong Xu
Journal:  J Int Med Res       Date:  2020-04       Impact factor: 1.671

3.  Metabolomic analysis reveals potential biomarkers and the underlying pathogenesis involved in Mycoplasma pneumoniae pneumonia.

Authors:  Jieqiong Li; Laurence Don Wai Luu; Xiaoxia Wang; XiaoDai Cui; Xiaolan Huang; Jin Fu; Xiong Zhu; Zhenjun Li; Yi Wang; Jun Tai
Journal:  Emerg Microbes Infect       Date:  2022-12       Impact factor: 7.163

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.