Multi-center evaluation of one commercial and 12 in-house real-time PCR assays for detection of Mycoplasma pneumoniae

Detection of Mycoplasma pneumoniae by real-time PCR is not yet standardized across laboratories. We have implemented a standardization protocol to compare the performance of thirteen commercial and in-house approaches. Despite differences on threshold values of samples, all assays were able to detec...

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Veröffentlicht in:Diagnostic microbiology and infectious disease 2017-06, Vol.88 (2), p.111-114
Hauptverfasser: Dumke, Roger, Benitez, Alvaro J., Chalker, Victoria, Gullsby, Karolina, Henrich, Birgit, Hidalgo-Grass, Carlos, Hoogenboezem, Theo, Kese, Darja, Loens, Katherine, Maaskant, Jolanda, Michael-Gayego, Ayelet, Moses, Allon E., Nir-Paz, Ran, Pas, Suzan D., Pereyre, Sabine, Petersen, Randi F., Rosenblatt, Meike, van Rossum, Annemarie M.C., Uldum, Søren A., Unger, Wendy W.J., Ursi, Dominique, Winchell, Jonas M., Bebear, Cecile
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Sprache:eng
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Zusammenfassung:Detection of Mycoplasma pneumoniae by real-time PCR is not yet standardized across laboratories. We have implemented a standardization protocol to compare the performance of thirteen commercial and in-house approaches. Despite differences on threshold values of samples, all assays were able to detect at least 20M. pneumoniae genomes per reaction. •We compared 13 real-time PCR assays to detect M. pneumoniae.•Participating laboratories used identical DNA samples and a standardized protocol.•All assays were able to detect at least 20 genomes per reaction.
ISSN:0732-8893
1879-0070
1879-0070
DOI:10.1016/j.diagmicrobio.2017.03.004