Cargando…
DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR
PCR detection of intestinal protozoa is often restrained by a poor DNA recovery or by inhibitors present in feces. The need for an extraction protocol that can overcome these obstacles is therefore clear. QIAamp® DNA Stool Mini Kit (Qiagen) was evaluated for its ability to recover DNA from oocysts/c...
Autor principal: | |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Korean Society for Parasitology and Tropical Medicine
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096637/ https://www.ncbi.nlm.nih.gov/pubmed/25031466 http://dx.doi.org/10.3347/kjp.2014.52.3.263 |
_version_ | 1782326161916821504 |
---|---|
author | Hawash, Yousry |
author_facet | Hawash, Yousry |
author_sort | Hawash, Yousry |
collection | PubMed |
description | PCR detection of intestinal protozoa is often restrained by a poor DNA recovery or by inhibitors present in feces. The need for an extraction protocol that can overcome these obstacles is therefore clear. QIAamp® DNA Stool Mini Kit (Qiagen) was evaluated for its ability to recover DNA from oocysts/cysts directly from feces. Twenty-five Giardia-positive, 15 Cryptosporidium-positive, 15 Entamoeba histolytica-positive, and 45 protozoa-free samples were processed as control by microscopy and immunoassay tests. DNA extracts were amplified using 3 sets of published primers. Following the manufacturer's protocol, the kit showed sensitivity and specificity of 100% towards Giardia and Entamoeba. However, for Cryptosporidium, the sensitivity and specificity were 60% (9/15) and 100%, respectively. A series of optimization experiments involving various steps of the kit's protocol were conducted using Cryptosporidium-positive samples. The best DNA recoveries were gained by raising the lysis temperature to the boiling point for 10 min and the incubation time of the InhibitEX tablet to 5 min. Also, using a pre-cooled ethanol for nucleic acid precipitation and small elution volume (50-100 µl) were valuable. The sensitivity of the amended protocol to Cryptosporidium was raised to 100%. Cryptosporidium DNA was successfully amplified by either the first or the second primer set. When applied on parasite-free feces spiked with variable oocysts/cysts counts, ≈ 2 oocysts/cysts were theoretically enough for detection by PCR. To conclude, the Qiagen kit with the amended protocol was proved to be suitable for protozoan DNA extraction directly from feces and support PCR diagnosis. |
format | Online Article Text |
id | pubmed-4096637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Korean Society for Parasitology and Tropical Medicine |
record_format | MEDLINE/PubMed |
spelling | pubmed-40966372014-07-16 DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR Hawash, Yousry Korean J Parasitol Original Article PCR detection of intestinal protozoa is often restrained by a poor DNA recovery or by inhibitors present in feces. The need for an extraction protocol that can overcome these obstacles is therefore clear. QIAamp® DNA Stool Mini Kit (Qiagen) was evaluated for its ability to recover DNA from oocysts/cysts directly from feces. Twenty-five Giardia-positive, 15 Cryptosporidium-positive, 15 Entamoeba histolytica-positive, and 45 protozoa-free samples were processed as control by microscopy and immunoassay tests. DNA extracts were amplified using 3 sets of published primers. Following the manufacturer's protocol, the kit showed sensitivity and specificity of 100% towards Giardia and Entamoeba. However, for Cryptosporidium, the sensitivity and specificity were 60% (9/15) and 100%, respectively. A series of optimization experiments involving various steps of the kit's protocol were conducted using Cryptosporidium-positive samples. The best DNA recoveries were gained by raising the lysis temperature to the boiling point for 10 min and the incubation time of the InhibitEX tablet to 5 min. Also, using a pre-cooled ethanol for nucleic acid precipitation and small elution volume (50-100 µl) were valuable. The sensitivity of the amended protocol to Cryptosporidium was raised to 100%. Cryptosporidium DNA was successfully amplified by either the first or the second primer set. When applied on parasite-free feces spiked with variable oocysts/cysts counts, ≈ 2 oocysts/cysts were theoretically enough for detection by PCR. To conclude, the Qiagen kit with the amended protocol was proved to be suitable for protozoan DNA extraction directly from feces and support PCR diagnosis. The Korean Society for Parasitology and Tropical Medicine 2014-06 2014-06-26 /pmc/articles/PMC4096637/ /pubmed/25031466 http://dx.doi.org/10.3347/kjp.2014.52.3.263 Text en © 2014, Korean Society for Parasitology and Tropical Medicine http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Hawash, Yousry DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title | DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title_full | DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title_fullStr | DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title_full_unstemmed | DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title_short | DNA Extraction from Protozoan Oocysts/Cysts in Feces for Diagnostic PCR |
title_sort | dna extraction from protozoan oocysts/cysts in feces for diagnostic pcr |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4096637/ https://www.ncbi.nlm.nih.gov/pubmed/25031466 http://dx.doi.org/10.3347/kjp.2014.52.3.263 |
work_keys_str_mv | AT hawashyousry dnaextractionfromprotozoanoocystscystsinfecesfordiagnosticpcr |