Comparison of molecular diagnostic approaches for the detection and differentiation of the intestinal protist Blastocystis sp. in humans
Identifikátory výsledku
Kód výsledku v IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F22%3A00569079" target="_blank" >RIV/60077344:_____/22:00569079 - isvavai.cz</a>
Nalezeny alternativní kódy
RIV/68081766:_____/22:00558113 RIV/60076658:12310/22:43905006 RIV/00064203:_____/22:10444203 RIV/00216208:11130/22:10444203
Výsledek na webu
<a href="https://www.parasite-journal.org/articles/parasite/full_html/2022/01/parasite220019/parasite220019.html" target="_blank" >https://www.parasite-journal.org/articles/parasite/full_html/2022/01/parasite220019/parasite220019.html</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1051/parasite/2022029" target="_blank" >10.1051/parasite/2022029</a>
Alternativní jazyky
Jazyk výsledku
angličtina
Název v původním jazyce
Comparison of molecular diagnostic approaches for the detection and differentiation of the intestinal protist Blastocystis sp. in humans
Popis výsledku v původním jazyce
Blastocystis is the most commonly found intestinal protist in the world. Accurate detection and differentiation of Blastocystis including its subtypes (arguably species) are essential to understand its epidemiology and role in human health. We compared (i) the sensitivity of conventional PCR (cPCR) and qPCR in a set of 288 DNA samples obtained from stool samples of gut-healthy individuals, and (ii) subtype diversity as detected by next-generation sequencing (NGS) versus Sanger sequencing. Real-time PCR resulted in more positive samples than cPCR, revealing high fecal load of Blastocystis based on the quantification curve in most samples. In subtype detection, NGS was largely in agreement with Sanger sequencing but showed higher sensitivity for mixed subtype colonization within one host. This fact together with use of the combination of qPCR and NGS and obtaining information on the fecal protist load will be beneficial for epidemiological and surveillance studies.
Název v anglickém jazyce
Comparison of molecular diagnostic approaches for the detection and differentiation of the intestinal protist Blastocystis sp. in humans
Popis výsledku anglicky
Blastocystis is the most commonly found intestinal protist in the world. Accurate detection and differentiation of Blastocystis including its subtypes (arguably species) are essential to understand its epidemiology and role in human health. We compared (i) the sensitivity of conventional PCR (cPCR) and qPCR in a set of 288 DNA samples obtained from stool samples of gut-healthy individuals, and (ii) subtype diversity as detected by next-generation sequencing (NGS) versus Sanger sequencing. Real-time PCR resulted in more positive samples than cPCR, revealing high fecal load of Blastocystis based on the quantification curve in most samples. In subtype detection, NGS was largely in agreement with Sanger sequencing but showed higher sensitivity for mixed subtype colonization within one host. This fact together with use of the combination of qPCR and NGS and obtaining information on the fecal protist load will be beneficial for epidemiological and surveillance studies.
Klasifikace
Druh
J<sub>imp</sub> - Článek v periodiku v databázi Web of Science
CEP obor
—
OECD FORD obor
30310 - Parasitology
Návaznosti výsledku
Projekt
<a href="/cs/project/GA22-04837S" target="_blank" >GA22-04837S: Vztahy mezi prvoky a bakteriomem ve střevním ekosystému domácích psů a jejich majitelů při přechodu na moderní životní styl</a><br>
Návaznosti
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Ostatní
Rok uplatnění
2022
Kód důvěrnosti údajů
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Údaje specifické pro druh výsledku
Název periodika
Parasite
ISSN
1252-607X
e-ISSN
1776-1042
Svazek periodika
29
Číslo periodika v rámci svazku
MAY
Stát vydavatele periodika
FR - Francouzská republika
Počet stran výsledku
7
Strana od-do
30
Kód UT WoS článku
000803306000001
EID výsledku v databázi Scopus
2-s2.0-85131203128