Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico

Introduction: Entamoeba histolytica, E. dispar, and E. moshkovskii are morphologically identical, but intestinal amebiasis is caused only by E. histolytica. Mexico is among the countries with high amebae infection rates, although the contribution of pathogenic amoeba to the total detected cases rem...

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Main Authors: Sandra Aguayo-Patrón, Reyna Castillo-Fimbres, Luis Quihui-Cota, Ana María Calderón de la Barca
Format: Article
Language:English
Published: The Journal of Infection in Developing Countries 2017-10-01
Series:Journal of Infection in Developing Countries
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Online Access:https://jidc.org/index.php/journal/article/view/9350
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author Sandra Aguayo-Patrón
Reyna Castillo-Fimbres
Luis Quihui-Cota
Ana María Calderón de la Barca
author_facet Sandra Aguayo-Patrón
Reyna Castillo-Fimbres
Luis Quihui-Cota
Ana María Calderón de la Barca
author_sort Sandra Aguayo-Patrón
collection DOAJ
description Introduction: Entamoeba histolytica, E. dispar, and E. moshkovskii are morphologically identical, but intestinal amebiasis is caused only by E. histolytica. Mexico is among the countries with high amebae infection rates, although the contribution of pathogenic amoeba to the total detected cases remains unknown, especially in the northwestern dry region. Therefore, the aim of this study was to identify the actual prevalence of E. histolytica using real-time polymerase chain reaction (PCR) in schoolchildren of  northwestern Mexico. Methodology: Participants were children from five public elementary schools in the low-socioeconomic-level suburban areas of Hermosillo, Sonora, Mexico. One stool sample was collected from each child and analyzed by the Faust technique for Entamoeba spp. and by real-time PCR for E. histolytica. Results: Analysis of stool  samples from 273 children (9.0 ± 1.5 years of age) resulted in 25 (9.2%) positive for E. histolytica/E. dispar/E. moshkovskii by the Faust technique; of these, 3 were positive for E. histolytica by real-time PCR. In addition, 2 samples that were negative for E. histolytica/E. dispar/E. moshkovskii by the Faust technique were positive by real-time PCR. Conclusions: The actual prevalence of E. histolytica in our study population was 1.8%, which is lower than those reported in previous studies in other Mexican regions.
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spelling doaj-art-b73a63648a974fec9d53d561fddbfa982025-08-20T03:52:43ZengThe Journal of Infection in Developing CountriesJournal of Infection in Developing Countries1972-26802017-10-01111010.3855/jidc.9350Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest MexicoSandra Aguayo-Patrón0Reyna Castillo-Fimbres1Luis Quihui-Cota2Ana María Calderón de la Barca3Centro de Investigación en Alimentación y Desarrollo A. C., Hermosillo, Sonora, MéxicoCentro de Investigación en Alimentación y Desarrollo A. C., Hermosillo, Sonora, MéxicoCentro de Investigación en Alimentación y Desarrollo A. C., Hermosillo, Sonora, MéxicoCentro de Investigación en Alimentación y Desarrollo A. C., Hermosillo, Sonora, México Introduction: Entamoeba histolytica, E. dispar, and E. moshkovskii are morphologically identical, but intestinal amebiasis is caused only by E. histolytica. Mexico is among the countries with high amebae infection rates, although the contribution of pathogenic amoeba to the total detected cases remains unknown, especially in the northwestern dry region. Therefore, the aim of this study was to identify the actual prevalence of E. histolytica using real-time polymerase chain reaction (PCR) in schoolchildren of  northwestern Mexico. Methodology: Participants were children from five public elementary schools in the low-socioeconomic-level suburban areas of Hermosillo, Sonora, Mexico. One stool sample was collected from each child and analyzed by the Faust technique for Entamoeba spp. and by real-time PCR for E. histolytica. Results: Analysis of stool  samples from 273 children (9.0 ± 1.5 years of age) resulted in 25 (9.2%) positive for E. histolytica/E. dispar/E. moshkovskii by the Faust technique; of these, 3 were positive for E. histolytica by real-time PCR. In addition, 2 samples that were negative for E. histolytica/E. dispar/E. moshkovskii by the Faust technique were positive by real-time PCR. Conclusions: The actual prevalence of E. histolytica in our study population was 1.8%, which is lower than those reported in previous studies in other Mexican regions. https://jidc.org/index.php/journal/article/view/9350Entamoeba histolyticareal-time PCRreal time PCRschool childrenschoolchildrenidentification
spellingShingle Sandra Aguayo-Patrón
Reyna Castillo-Fimbres
Luis Quihui-Cota
Ana María Calderón de la Barca
Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
Journal of Infection in Developing Countries
Entamoeba histolytica
real-time PCR
real time PCR
school children
schoolchildren
identification
title Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
title_full Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
title_fullStr Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
title_full_unstemmed Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
title_short Use of real-time polymerase chain reaction to identify Entamoeba histolytica in schoolchildren from northwest Mexico
title_sort use of real time polymerase chain reaction to identify entamoeba histolytica in schoolchildren from northwest mexico
topic Entamoeba histolytica
real-time PCR
real time PCR
school children
schoolchildren
identification
url https://jidc.org/index.php/journal/article/view/9350
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