Cargando…

Evaluation of microscopy and PCR for detection of Dientamoeba fragilis

INTRODUCTION: Dientamoeba fragilis (D. fragilis) diagnosis is an intestinal protozoan parasite globally found in rural and urban areas and is attracting a growing interest. Its prevalence in stool varies from 0.2% to more than 19% depending upon the population studied. MATERIALS AND METHODS: This st...

Descripción completa

Detalles Bibliográficos
Autores principales: Tolba, Mona Mohamed, Allam, Amal Farahat, Khalil, Safia Saleh, Elshouki, Wagdy Makram, Shehab, Amel Youssef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832490/
https://www.ncbi.nlm.nih.gov/pubmed/36643979
http://dx.doi.org/10.4103/tp.tp_93_21
_version_ 1784868067442950144
author Tolba, Mona Mohamed
Allam, Amal Farahat
Khalil, Safia Saleh
Elshouki, Wagdy Makram
Shehab, Amel Youssef
author_facet Tolba, Mona Mohamed
Allam, Amal Farahat
Khalil, Safia Saleh
Elshouki, Wagdy Makram
Shehab, Amel Youssef
author_sort Tolba, Mona Mohamed
collection PubMed
description INTRODUCTION: Dientamoeba fragilis (D. fragilis) diagnosis is an intestinal protozoan parasite globally found in rural and urban areas and is attracting a growing interest. Its prevalence in stool varies from 0.2% to more than 19% depending upon the population studied. MATERIALS AND METHODS: This study was based on the examination of 100 stool samples of randomly referred cases in a rural area in Motobus district, Kafr El-Sheikh governorate, Egypt. Our aim was to investigate the presence of D. fragilis in stool of the examined individuals using conventional polymerase chain reaction (PCR) compared to wet mount and trichrome stain with confirmation of infection by transmission electron microscopy. RESULTS: D. fragilis was detected in 13/100 of the stool samples examined using wet mount smears, while trichrome stain detected 17/100. Conventional PCR diagnosed 41 cases of D. fragilis in the studied group. A very good agreement was found between wet mount and trichrome stain for diagnosing D. fragilis, while there was fair agreement between conventional PCR and both microscopy methods. Transmission electron microscope was performed on pooled positive samples that revealed the internal structures of D. fragilis trophozoite with its characteristic nucleus. CONCLUSIONS: PCR technique was superior to microscopy for the detection of D. fragilis. Trichrome stain remains vital for microscopic diagnosis.
format Online
Article
Text
id pubmed-9832490
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Wolters Kluwer - Medknow
record_format MEDLINE/PubMed
spelling pubmed-98324902023-01-12 Evaluation of microscopy and PCR for detection of Dientamoeba fragilis Tolba, Mona Mohamed Allam, Amal Farahat Khalil, Safia Saleh Elshouki, Wagdy Makram Shehab, Amel Youssef Trop Parasitol Original Article INTRODUCTION: Dientamoeba fragilis (D. fragilis) diagnosis is an intestinal protozoan parasite globally found in rural and urban areas and is attracting a growing interest. Its prevalence in stool varies from 0.2% to more than 19% depending upon the population studied. MATERIALS AND METHODS: This study was based on the examination of 100 stool samples of randomly referred cases in a rural area in Motobus district, Kafr El-Sheikh governorate, Egypt. Our aim was to investigate the presence of D. fragilis in stool of the examined individuals using conventional polymerase chain reaction (PCR) compared to wet mount and trichrome stain with confirmation of infection by transmission electron microscopy. RESULTS: D. fragilis was detected in 13/100 of the stool samples examined using wet mount smears, while trichrome stain detected 17/100. Conventional PCR diagnosed 41 cases of D. fragilis in the studied group. A very good agreement was found between wet mount and trichrome stain for diagnosing D. fragilis, while there was fair agreement between conventional PCR and both microscopy methods. Transmission electron microscope was performed on pooled positive samples that revealed the internal structures of D. fragilis trophozoite with its characteristic nucleus. CONCLUSIONS: PCR technique was superior to microscopy for the detection of D. fragilis. Trichrome stain remains vital for microscopic diagnosis. Wolters Kluwer - Medknow 2022 2022-11-24 /pmc/articles/PMC9832490/ /pubmed/36643979 http://dx.doi.org/10.4103/tp.tp_93_21 Text en Copyright: © 2022 Tropical Parasitology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Original Article
Tolba, Mona Mohamed
Allam, Amal Farahat
Khalil, Safia Saleh
Elshouki, Wagdy Makram
Shehab, Amel Youssef
Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title_full Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title_fullStr Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title_full_unstemmed Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title_short Evaluation of microscopy and PCR for detection of Dientamoeba fragilis
title_sort evaluation of microscopy and pcr for detection of dientamoeba fragilis
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832490/
https://www.ncbi.nlm.nih.gov/pubmed/36643979
http://dx.doi.org/10.4103/tp.tp_93_21
work_keys_str_mv AT tolbamonamohamed evaluationofmicroscopyandpcrfordetectionofdientamoebafragilis
AT allamamalfarahat evaluationofmicroscopyandpcrfordetectionofdientamoebafragilis
AT khalilsafiasaleh evaluationofmicroscopyandpcrfordetectionofdientamoebafragilis
AT elshoukiwagdymakram evaluationofmicroscopyandpcrfordetectionofdientamoebafragilis
AT shehabamelyoussef evaluationofmicroscopyandpcrfordetectionofdientamoebafragilis