Literature DB >> 26318912

Comparison of the bioMérieux NucliSENS EasyQ HIV-1 v2.0-HIV-1 RNA quantification assay versus Abbott RealTime HIV-1 and Roche Cobas TaqMan HIV-1 v2.0 on current epidemic HIV-1 variants.

Thomas Mourez1, Constance Delaugerre2, Muriel Vray3, Véronique Lemée4, François Simon5, Jean-Christophe Plantier6.   

Abstract

BACKGROUND: An improved version of the bioMérieux NucliSENS(®) EasyQ(®) HIV-1 v2.0 has been introduced to overcome the underquantification observed with previous versions, especially with non-B HIV-1 subtypes.
OBJECTIVES: Comparing bioMérieux NucliSENS(®) EasyQ(®) HIV-1 v2.0 versus Roche Cobas CA/CTM v2.0 and Abbott RealTime HIV-1 assays for HIV-1 group M and non-M (N, O, P) viral load measurement. STUDY
DESIGN: The three assays were tested in parallel on 103HIV-1 group M plasma samples, and on non-group M HIV-1 culture supernatants.
RESULTS: Values obtained for the 103HIV-1 group M plasma samples tested with bioMérieux assay showed good overall correlation compared to the 2 others. The Roche Cobas assay gave higher values than the bioMérieux assay, while Abbott and bioMérieux both displayed similar results. However, analysis showed a wider dispersion in results when comparing the bioMérieux NucliSENS(®) EasyQ(®) HIV-1 v2.0 and the other 2 techniques. All data taken into account, we observed frequent discrepancies in quantification, of the plasma samples and major differences above 1log in 10/72 (13.8%). The quantification of non-M HIV groups in culture supernatant has shown variable results, with better quantification of HIV-O and of HIV-N respectively with the Abbott assay and the bioMérieux assay.
CONCLUSIONS: The bioMérieux NucliSENS(®) EasyQ(®) HIV-1 v2.0 showed improved sensitivity to non-B HIV-M subtypes compared to previous versions. Notwithstanding, we observed frequent discrepancies and a wide dispersion in results when comparing bioMérieux NucliSENS(®) EasyQ(®) HIV-1 v2.0 and the other 2 techniques.
Copyright © 2015 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  Genetic diversity; HIV-1; HIV-O; Quantification; Viral load

Mesh:

Year:  2015        PMID: 26318912     DOI: 10.1016/j.jcv.2015.08.007

Source DB:  PubMed          Journal:  J Clin Virol        ISSN: 1386-6532            Impact factor:   3.168


  5 in total

1.  Field evaluation of an open and polyvalent universal HIV-1/SIVcpz/SIVgor quantitative RT-PCR assay for HIV-1 viral load monitoring in comparison to Abbott RealTime HIV-1 in Cameroon.

Authors:  Emilande Guichet; Avelin Aghokeng; Sabrina Eymard-Duvernay; Nicole Vidal; Ahidjo Ayouba; Eitel Mpoudi Ngole; Eric Delaporte; Laura Ciaffi; Martine Peeters
Journal:  J Virol Methods       Date:  2016-09-05       Impact factor: 2.014

2.  Multiple HIV-1/M + HIV-1/O dual infections and new HIV-1/MO inter-group recombinant forms detected in Cameroon.

Authors:  Fabienne De Oliveira; Thomas Mourez; Aurélia Vessiere; Paul-Alain Ngoupo; Elodie Alessandri-Gradt; François Simon; Dominique Rousset; Jean-Christophe Plantier
Journal:  Retrovirology       Date:  2017-01-13       Impact factor: 4.602

3.  Biomacromolecules as tools and objects in nanometrology-current challenges and perspectives.

Authors:  Payam Hashemi; Luise Luckau; Petra Mischnick; Sarah Schmidt; Rainer Stosch; Bettina Wünsch
Journal:  Anal Bioanal Chem       Date:  2017-08-14       Impact factor: 4.142

4.  ARCHITECT HIV Combo Ag/Ab and RealTime HIV-1 Assays Detect Diverse HIV Strains in Clinical Specimens.

Authors:  Mary A Rodgers; Ana S Vallari; Julie Yamaguchi; Vera Holzmayer; Barbara Harris; Coumba Toure-Kane; Souleymane Mboup; Samar Badreddine; Carole McArthur; Nicaise Ndembi; Dora Mbanya; Lazare Kaptue; Gavin Cloherty
Journal:  AIDS Res Hum Retroviruses       Date:  2018-02-13       Impact factor: 2.205

Review 5.  Current and Future Perspectives on Isothermal Nucleic Acid Amplification Technologies for Diagnosing Infections.

Authors:  Godwin Attah Obande; Kirnpal Kaur Banga Singh
Journal:  Infect Drug Resist       Date:  2020-02-12       Impact factor: 4.003

  5 in total

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