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Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa
Although microscopic examination of stool samples remains the reference method for the diagnosis of intestinal protozoal infections, these techniques are time-consuming and require operators who are experienced and well trained. Molecular biology seems to offer performances at least equivalent in te...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
EDP Sciences
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144649/ https://www.ncbi.nlm.nih.gov/pubmed/30230444 http://dx.doi.org/10.1051/parasite/2018049 |
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author | Autier, Brice Belaz, Sorya Razakandrainibe, Romy Gangneux, Jean-Pierre Robert-Gangneux, Florence |
author_facet | Autier, Brice Belaz, Sorya Razakandrainibe, Romy Gangneux, Jean-Pierre Robert-Gangneux, Florence |
author_sort | Autier, Brice |
collection | PubMed |
description | Although microscopic examination of stool samples remains the reference method for the diagnosis of intestinal protozoal infections, these techniques are time-consuming and require operators who are experienced and well trained. Molecular biology seems to offer performances at least equivalent in terms of sensitivity and specificity for certain parasites. This study aimed to compare three multiplex PCR assays on 93 prospectively collected positive stools (prospective cohort) and a panel of 12 more Cryptosporidium-positive samples (Cryptosporidium panel). On the prospective cohort, the sensitivity was 89%, 64% and 41% for Giardia sp. detection for BD Max(TM), G-DiaPara(TM) and RIDA(®)GENE, respectively and 75%, 100% and 100% for C. parvum/hominis detection. The sensitivity of the RIDA(®)GENE assay for all Cryptosporidium species was 100%, and for D. fragilis 71%. All the techniques obtained the same results for E. histolytica detection, with one positive sample. All species in the Cryptosporidium panel were identified by the RIDA(®)GENE PCR. The BD Max(TM) and G-DiaPara(TM) assays detected only C. parvum/hominis with the exception of one positive sample for C. meleagridis. No assay showed satisfactory results for all parasites simultaneously, and the DNA extraction seems to be the critical step. More studies are needed to standardize this procedure. |
format | Online Article Text |
id | pubmed-6144649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | EDP Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-61446492018-09-26 Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa Autier, Brice Belaz, Sorya Razakandrainibe, Romy Gangneux, Jean-Pierre Robert-Gangneux, Florence Parasite Research Article Although microscopic examination of stool samples remains the reference method for the diagnosis of intestinal protozoal infections, these techniques are time-consuming and require operators who are experienced and well trained. Molecular biology seems to offer performances at least equivalent in terms of sensitivity and specificity for certain parasites. This study aimed to compare three multiplex PCR assays on 93 prospectively collected positive stools (prospective cohort) and a panel of 12 more Cryptosporidium-positive samples (Cryptosporidium panel). On the prospective cohort, the sensitivity was 89%, 64% and 41% for Giardia sp. detection for BD Max(TM), G-DiaPara(TM) and RIDA(®)GENE, respectively and 75%, 100% and 100% for C. parvum/hominis detection. The sensitivity of the RIDA(®)GENE assay for all Cryptosporidium species was 100%, and for D. fragilis 71%. All the techniques obtained the same results for E. histolytica detection, with one positive sample. All species in the Cryptosporidium panel were identified by the RIDA(®)GENE PCR. The BD Max(TM) and G-DiaPara(TM) assays detected only C. parvum/hominis with the exception of one positive sample for C. meleagridis. No assay showed satisfactory results for all parasites simultaneously, and the DNA extraction seems to be the critical step. More studies are needed to standardize this procedure. EDP Sciences 2018-09-18 /pmc/articles/PMC6144649/ /pubmed/30230444 http://dx.doi.org/10.1051/parasite/2018049 Text en © B. Autier et al., published by EDP Sciences, 2018 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Autier, Brice Belaz, Sorya Razakandrainibe, Romy Gangneux, Jean-Pierre Robert-Gangneux, Florence Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title | Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title_full | Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title_fullStr | Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title_full_unstemmed | Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title_short | Comparison of three commercial multiplex PCR assays for the diagnosis of intestinal protozoa |
title_sort | comparison of three commercial multiplex pcr assays for the diagnosis of intestinal protozoa |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144649/ https://www.ncbi.nlm.nih.gov/pubmed/30230444 http://dx.doi.org/10.1051/parasite/2018049 |
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