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Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica

BACKGROUND: To compare three molecular methods, PCR-RFLP for internal transcribed spacer, PCR sequencing and high resolution melting analysis shown reliable sensitivity and specificity for detecting Leishmania tropica as a model for cutaneous leishmaniasis (CL) as the perspective overview for scient...

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Autores principales: MOHAMMADI, Mohammad Ali, BAMOROVAT, Mehdi, FASIHI HARANDI, Majid, KARIMI, Tayyebeh, SHARIFI, Iraj, AFLATOONIAN, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527031/
https://www.ncbi.nlm.nih.gov/pubmed/28761481
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author MOHAMMADI, Mohammad Ali
BAMOROVAT, Mehdi
FASIHI HARANDI, Majid
KARIMI, Tayyebeh
SHARIFI, Iraj
AFLATOONIAN, Mohammad Reza
author_facet MOHAMMADI, Mohammad Ali
BAMOROVAT, Mehdi
FASIHI HARANDI, Majid
KARIMI, Tayyebeh
SHARIFI, Iraj
AFLATOONIAN, Mohammad Reza
author_sort MOHAMMADI, Mohammad Ali
collection PubMed
description BACKGROUND: To compare three molecular methods, PCR-RFLP for internal transcribed spacer, PCR sequencing and high resolution melting analysis shown reliable sensitivity and specificity for detecting Leishmania tropica as a model for cutaneous leishmaniasis (CL) as the perspective overview for scientific and economic approaches. METHODS: This study was carried out between 2015 and 2016 in Leishmaniasis Research Center in Kerman University of Medical Sciences, Kerman, Iran. The positives smears (n=50) were obtained from patients referred from the health clinics in a major anthroponotic CL (ACL) focus, southeastern Iran. Only smear preparations with the same grade were selected according to the method described by the WHO for future PCR assays. RESULTS: All three molecular methods had capability to identify positive samples at species level with the same specificity and sensitivity. However, these techniques were different in simplicity, consuming time, and cost effectiveness. Although additional enzymatic process in PCR-RFLP provided good resolution to find Leishmania species but this would cause time and cost increases. CONCLUSION: HRM (high resolution melting) is a relatively new technique that allows direct characterization of PCR amplicons in a closed system with more simplicity, cost effectiveness and time-consuming compared with other PCR-based assays for epidemiological or clinical identification purposes.
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spelling pubmed-55270312017-07-31 Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica MOHAMMADI, Mohammad Ali BAMOROVAT, Mehdi FASIHI HARANDI, Majid KARIMI, Tayyebeh SHARIFI, Iraj AFLATOONIAN, Mohammad Reza Iran J Parasitol Original Article BACKGROUND: To compare three molecular methods, PCR-RFLP for internal transcribed spacer, PCR sequencing and high resolution melting analysis shown reliable sensitivity and specificity for detecting Leishmania tropica as a model for cutaneous leishmaniasis (CL) as the perspective overview for scientific and economic approaches. METHODS: This study was carried out between 2015 and 2016 in Leishmaniasis Research Center in Kerman University of Medical Sciences, Kerman, Iran. The positives smears (n=50) were obtained from patients referred from the health clinics in a major anthroponotic CL (ACL) focus, southeastern Iran. Only smear preparations with the same grade were selected according to the method described by the WHO for future PCR assays. RESULTS: All three molecular methods had capability to identify positive samples at species level with the same specificity and sensitivity. However, these techniques were different in simplicity, consuming time, and cost effectiveness. Although additional enzymatic process in PCR-RFLP provided good resolution to find Leishmania species but this would cause time and cost increases. CONCLUSION: HRM (high resolution melting) is a relatively new technique that allows direct characterization of PCR amplicons in a closed system with more simplicity, cost effectiveness and time-consuming compared with other PCR-based assays for epidemiological or clinical identification purposes. Tehran University of Medical Sciences 2017 /pmc/articles/PMC5527031/ /pubmed/28761481 Text en Copyright© Iranian Society of Parasitology & Tehran University of Medical Sciences http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
MOHAMMADI, Mohammad Ali
BAMOROVAT, Mehdi
FASIHI HARANDI, Majid
KARIMI, Tayyebeh
SHARIFI, Iraj
AFLATOONIAN, Mohammad Reza
Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title_full Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title_fullStr Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title_full_unstemmed Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title_short Comparison of Three PCR-based Methods for Simplicity and Cost Effectiveness Identification of Cutaneous Leishmaniasis Due to Leishmania tropica
title_sort comparison of three pcr-based methods for simplicity and cost effectiveness identification of cutaneous leishmaniasis due to leishmania tropica
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5527031/
https://www.ncbi.nlm.nih.gov/pubmed/28761481
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