Comparative performance evaluation of four commercial multiplex real-time PCR assays for the detection of the diarrhoea-causing protozoa Cryptosporidium hominis/parvum, Giardia duodenalis and Entamoeba histolytica

dc.contributor.authorPaulos Viñas, Silvia
dc.contributor.authorSaugar, José M.
dc.contributor.authorLucio, Aída de
dc.contributor.authorFuentes, Isabel
dc.contributor.authorMateo Barrientos, María
dc.contributor.authorCarmena, David
dc.date.accessioned2019-07-08T06:59:40Z
dc.date.available2019-07-08T06:59:40Z
dc.date.issued2019
dc.description.abstractBackground Multiplex molecular panels are relentlessly replacing conventional methods for the detection of enteric pathogens from stool samples in clinical and research laboratories. Here we evaluated four commercial multiplex real-time PCR assays for the detection of Cryptosporidium hominis/parvum, Giardia duodenalis and Entamoeba histolytica. Methods The diagnostic performance of the Gastroenteritis/Parasite Panel I (Diagenode), the RIDAGENE Parasitic Stool Panel (R-Biopharm), the Allplex Gastrointestinal Parasite Panel 4 (Seegene) and the FTD Stool Parasites (Fast Track) real-time PCR methods was assessed against a reference panel of 126 well-characterized DNA samples including Cryptosporidium hominis (n = 29), Cryptosporidium parvum (n = 3), Giardia duodenalis (n = 47), Entamoeba histolytica (n = 3), other parasite species (n = 20), and apparently healthy subjects (n = 24). Principal findings Obtained diagnostic sensitivities ranged from 53–88% for Cryptosporidium hominis/parvum, and from 68–100% for G. duodenalis. The R-Biopharm method achieved the best performance for the detection of Cryptosporidium hominis/parvum both in terms of diagnostic sensitivity (87.5%) and detection limit (a 100-fold increase compared to other tests). The Fast Track method was particularly suited for the detection of G. duodenalis, achieving a 100% sensitivity and a detection limit at least 10-fold superior. Detection of E. histolytica was similarly achieved by all compared methods except Diagenode. Conclusions Diagnostic performance varied largely depending on the method used and the targeted pathogen species. Factors including test sensitivity/specificity, cost, patient population surveyed, laboratory workflow, and diagnostic algorithm should be carefully considered when choosing the most appropriate multiplex PCR platform.spa
dc.description.filiationUEMspa
dc.description.impact2.740 JCR (2019) Q2, 27/71 Multidisciplinary Sciencesspa
dc.description.impact1.023 SJR (2019) Q1, 10/145 Multidisciplinaryspa
dc.description.impactNo data IDR 2019spa
dc.description.sponsorshipSin financiaciónspa
dc.identifier.citationPaulos, S., Saugar, J. M., Lucio, A., Fuentes, I., Mateo, M., & Carmena, D. (2019). Comparative performance evaluation of four commercial multiplex real-time PCR assays for the detection of the diarrhoea-causing protozoa Cryptosporidium hominis/parvum, Giardia duodenalis and Entamoeba histolytica. PloS One, 14(4), 1-11. https://doi.org/10.1371/journal.pone.0215068spa
dc.identifier.doi10.1371/journal.pone.0215068
dc.identifier.issn1932-6203
dc.identifier.urihttp://hdl.handle.net/11268/8087
dc.language.isoengspa
dc.peerreviewedSispa
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional*
dc.rights.accessRightsopen accessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subject.uemEtiología médicaspa
dc.subject.uemHecesspa
dc.subject.uemAnálisis clínicosspa
dc.subject.unescoPatologíaspa
dc.subject.unescoAnálisis bioquímicospa
dc.titleComparative performance evaluation of four commercial multiplex real-time PCR assays for the detection of the diarrhoea-causing protozoa Cryptosporidium hominis/parvum, Giardia duodenalis and Entamoeba histolyticaspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublication8dc32f1e-dba8-4b55-8c78-fdbc2dfb627d
relation.isAuthorOfPublication.latestForDiscovery8dc32f1e-dba8-4b55-8c78-fdbc2dfb627d

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