Implementation and evaluation of the Presto combined qualitative real-time assay for Chlamydia trachomatis and Neisseria gonorrhoeae in Rwanda

African Journal of Laboratory Medicine

 
 
Field Value
 
Title Implementation and evaluation of the Presto combined qualitative real-time assay for Chlamydia trachomatis and Neisseria gonorrhoeae in Rwanda
 
Creator Cuylaerts, Vicky De Baetselier, Irith Muvunyi, Claude M. Mwambarange, Lambert Smet, Hilde Rusine, John Musengamana, Viateur van de Wijgert, Janneke Crucitti, Tania
 
Subject Medicine; Clinical Science; Microbiology qPCR; Chlamydia trachomatis; Neisseria gonorrhoeae
Description Background: The Presto combined qualitative real-time assay for Chlamydia trachomatis and Neisseria gonorrhoeae (Presto CT/NG PCR assay) is appealing for developing countries, because it can be used with multiple DNA extraction methods and polymerase chain reaction (PCR) platforms.Objectives: The objective of the study was to implement and evaluate the Presto CT/NG PCR assay at the National Reference Laboratory (NRL) in Kigali, Rwanda, where no real-time PCR assays for the detection of C. trachomatis or N. gonorrhoeae were available.Methods: The Presto CT/NG PCR assay was first evaluated at the Institute of Tropical Medicine (ITM) in Antwerp, Belgium. Next, NRL laboratory technicians were trained to use the assay on their ABI PRISM 7500 real-time PCR instrument and their competencies were assessed prior to trial initiation. During the trial, endocervical swabs were tested at the NRL, with bi-monthly external quality control testing monitored by the ITM. The final NRL results were evaluated against extended gold standard testing at the ITM, consisting of the Abbott m2000 RealTime System with confirmation of positive results by an in-house real-time PCR assay for C. trachomatis or N. gonorrhoeae.Results: Of the 192 samples analysed using the Presto assay at the NRL, 16 samples tested positive for C. trachomatis and 17 tested positive for N. gonorrhoeae; four of these were infected with both. The sensitivity and specificity of the Presto assay were 93.3% (95% confidence interval [CI]: 68.1% – 99.8%) and 99.4% (95% CI: 96.8% – 100%) for C. trachomatis and 100% (95% CI: 76.8% – 100%) and 98.8% (95% CI: 95.8% – 99.9%) for N. gonorrhoeae.Conclusion: C. trachomatis and N. gonorrhoeae testing with the Presto assay was feasible in Kigali, Rwanda, and good performance was achieved.
 
Publisher AOSIS
 
Contributor EDCTP
Date 2019-04-18
 
Type info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion — Head-to-head comparison
Format text/html application/epub+zip application/xml application/pdf
Identifier 10.4102/ajlm.v8i1.739
 
Source African Journal of Laboratory Medicine; Vol 8, No 1 (2019); 6 pages 2225-2010 2225-2002
 
Language eng
 
Relation
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https://ajlmonline.org/index.php/ajlm/article/view/739/1269 https://ajlmonline.org/index.php/ajlm/article/view/739/1268 https://ajlmonline.org/index.php/ajlm/article/view/739/1270 https://ajlmonline.org/index.php/ajlm/article/view/739/1267
 
Coverage Rwanda 2014 Women; reproductive age; African
Rights Copyright (c) 2019 Vicky Cuylaerts, Irith De Baetselier, Claude M. Muvunyi, Lambert Mwambarange, Hilde Smet, John Rusine, Viateur Musengamana, Janneke van de Wijgert, Tania Crucitti https://creativecommons.org/licenses/by/4.0
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