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Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology

OBJECTIVE: Histopathological studies suggest that parasite load is different between acute and chronic forms of cutaneous leishmaniasis (CL). However, highly sensitive detection methods are still needed to distinguish different forms of leishmaniasis. In the present study, we developed a quantitativ...

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Autores principales: Fekri-SoofiAbadi, Maryam, Fekri, Meisam, moradabadi, Alireza, Vahidi, Reza, Shamsi-Meymandi, Simin, Dabiri, Donya, Dabiri, Shahriar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757515/
https://www.ncbi.nlm.nih.gov/pubmed/31547842
http://dx.doi.org/10.1186/s13104-019-4666-5
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author Fekri-SoofiAbadi, Maryam
Fekri, Meisam
moradabadi, Alireza
Vahidi, Reza
Shamsi-Meymandi, Simin
Dabiri, Donya
Dabiri, Shahriar
author_facet Fekri-SoofiAbadi, Maryam
Fekri, Meisam
moradabadi, Alireza
Vahidi, Reza
Shamsi-Meymandi, Simin
Dabiri, Donya
Dabiri, Shahriar
author_sort Fekri-SoofiAbadi, Maryam
collection PubMed
description OBJECTIVE: Histopathological studies suggest that parasite load is different between acute and chronic forms of cutaneous leishmaniasis (CL). However, highly sensitive detection methods are still needed to distinguish different forms of leishmaniasis. In the present study, we developed a quantitative real-time polymerase chain reaction (PCR) to detect and quantify Leishmania tropica parasites in paraffin-embedded tissue samples. RESULTS: The ability of real-time PCR for leishmania detection was higher than histopathological evaluation. The quantitative real-time PCR (qPCR) quantified parasite loads were highly correlated with microscopic results (r = 0.598; P < 0.001). Among patients, the parasite load was inversely correlated with disease duration (acute CL lesions had very higher parasite load than chronic CL lesions), but there was no difference in the parasite load according to the patients’ age and sex as well as location of the lesions. In contrast to Ridley scoring system (P < 0.001), there were no statistically significant differences in the relative number of parasites among the lupoid and non-lupoid forms of chronic lesions in real-time PCR (P = 0.549), which indicates the superiority of histopathological evaluation for chronic forms differentiation.
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spelling pubmed-67575152019-09-30 Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology Fekri-SoofiAbadi, Maryam Fekri, Meisam moradabadi, Alireza Vahidi, Reza Shamsi-Meymandi, Simin Dabiri, Donya Dabiri, Shahriar BMC Res Notes Research Note OBJECTIVE: Histopathological studies suggest that parasite load is different between acute and chronic forms of cutaneous leishmaniasis (CL). However, highly sensitive detection methods are still needed to distinguish different forms of leishmaniasis. In the present study, we developed a quantitative real-time polymerase chain reaction (PCR) to detect and quantify Leishmania tropica parasites in paraffin-embedded tissue samples. RESULTS: The ability of real-time PCR for leishmania detection was higher than histopathological evaluation. The quantitative real-time PCR (qPCR) quantified parasite loads were highly correlated with microscopic results (r = 0.598; P < 0.001). Among patients, the parasite load was inversely correlated with disease duration (acute CL lesions had very higher parasite load than chronic CL lesions), but there was no difference in the parasite load according to the patients’ age and sex as well as location of the lesions. In contrast to Ridley scoring system (P < 0.001), there were no statistically significant differences in the relative number of parasites among the lupoid and non-lupoid forms of chronic lesions in real-time PCR (P = 0.549), which indicates the superiority of histopathological evaluation for chronic forms differentiation. BioMed Central 2019-09-23 /pmc/articles/PMC6757515/ /pubmed/31547842 http://dx.doi.org/10.1186/s13104-019-4666-5 Text en © The Author(s) 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Note
Fekri-SoofiAbadi, Maryam
Fekri, Meisam
moradabadi, Alireza
Vahidi, Reza
Shamsi-Meymandi, Simin
Dabiri, Donya
Dabiri, Shahriar
Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title_full Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title_fullStr Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title_full_unstemmed Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title_short Ability of real-time PCR for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
title_sort ability of real-time pcr for differential diagnosis of various forms of cutaneous leishmaniasis: a comparative study with histopathology
topic Research Note
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6757515/
https://www.ncbi.nlm.nih.gov/pubmed/31547842
http://dx.doi.org/10.1186/s13104-019-4666-5
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