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New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction

BACKGROUND: Leishmania is the parasitic protozoan responsible for leishmaniases, a disease that can cause a range of cutaneous, mucosal, and visceral infections. Two subgenera L. Viannia and L. Leishmania are known to infect humans in the tropics and subtropics of the Americas. The aim of the presen...

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Autores principales: Calvopiña, Manuel, Fonseca-Carrera, David, Villacrés-Granda, Irina, Toapanta, Alberto, Chiluisa-Guacho, Carlos, Bastidas-Caldes, Carlos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Tehran University of Medical Sciences 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597875/
https://www.ncbi.nlm.nih.gov/pubmed/37886249
http://dx.doi.org/10.18502/ijpa.v18i3.13758
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author Calvopiña, Manuel
Fonseca-Carrera, David
Villacrés-Granda, Irina
Toapanta, Alberto
Chiluisa-Guacho, Carlos
Bastidas-Caldes, Carlos
author_facet Calvopiña, Manuel
Fonseca-Carrera, David
Villacrés-Granda, Irina
Toapanta, Alberto
Chiluisa-Guacho, Carlos
Bastidas-Caldes, Carlos
author_sort Calvopiña, Manuel
collection PubMed
description BACKGROUND: Leishmania is the parasitic protozoan responsible for leishmaniases, a disease that can cause a range of cutaneous, mucosal, and visceral infections. Two subgenera L. Viannia and L. Leishmania are known to infect humans in the tropics and subtropics of the Americas. The aim of the present study was to develop a new pair of primers for the two subgenera and test in clinical samples. METHODS: We designed two new pairs of primers for a PCR method from two conserved genes, cysteine proteinase B (cpb) and N-acetylglucosamine-6-phosfate deacetylase-like protein (nagA), as specific markers for those two respective subgenera. Primers were tested with 16 microscopical positive clinical samples from the Amazon region of Ecuador obtained in 2010–2020 period. RESULTS: The cpb presented a band of 172 bp and the nagA a band of 300 bp, thus clearly differentiating L. viannia from L. leishmania. Additionally, primers identified and differentiated the clinical samples in the two subgenera. CONCLUSION: The new primers targeting different two genes and standardized in a PCR assay could identified and differentiated Leishmania parasites at subgenus level. This protocol could be used for Leishmania genus identification and diagnosis at the subgenus level and for determining the parasite’s geographical distribution where different Leishmania subgenera are found in the same area.
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spelling pubmed-105978752023-10-26 New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction Calvopiña, Manuel Fonseca-Carrera, David Villacrés-Granda, Irina Toapanta, Alberto Chiluisa-Guacho, Carlos Bastidas-Caldes, Carlos Iran J Parasitol Original Article BACKGROUND: Leishmania is the parasitic protozoan responsible for leishmaniases, a disease that can cause a range of cutaneous, mucosal, and visceral infections. Two subgenera L. Viannia and L. Leishmania are known to infect humans in the tropics and subtropics of the Americas. The aim of the present study was to develop a new pair of primers for the two subgenera and test in clinical samples. METHODS: We designed two new pairs of primers for a PCR method from two conserved genes, cysteine proteinase B (cpb) and N-acetylglucosamine-6-phosfate deacetylase-like protein (nagA), as specific markers for those two respective subgenera. Primers were tested with 16 microscopical positive clinical samples from the Amazon region of Ecuador obtained in 2010–2020 period. RESULTS: The cpb presented a band of 172 bp and the nagA a band of 300 bp, thus clearly differentiating L. viannia from L. leishmania. Additionally, primers identified and differentiated the clinical samples in the two subgenera. CONCLUSION: The new primers targeting different two genes and standardized in a PCR assay could identified and differentiated Leishmania parasites at subgenus level. This protocol could be used for Leishmania genus identification and diagnosis at the subgenus level and for determining the parasite’s geographical distribution where different Leishmania subgenera are found in the same area. Tehran University of Medical Sciences 2023 /pmc/articles/PMC10597875/ /pubmed/37886249 http://dx.doi.org/10.18502/ijpa.v18i3.13758 Text en © 2023 Calvopiña et al. Published by Tehran University of Medical Sciences. https://creativecommons.org/licenses/by-nc/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International license (https://creativecommons.org/licenses/by-nc/4.0/). Non-commercial uses of the work are permitted, provided the original work is properly cited.
spellingShingle Original Article
Calvopiña, Manuel
Fonseca-Carrera, David
Villacrés-Granda, Irina
Toapanta, Alberto
Chiluisa-Guacho, Carlos
Bastidas-Caldes, Carlos
New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title_full New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title_fullStr New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title_full_unstemmed New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title_short New Primers for Detection and Differentiation between Leishmania viannia and L. leishmania Subgenera by Polymerase Chain Reaction
title_sort new primers for detection and differentiation between leishmania viannia and l. leishmania subgenera by polymerase chain reaction
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10597875/
https://www.ncbi.nlm.nih.gov/pubmed/37886249
http://dx.doi.org/10.18502/ijpa.v18i3.13758
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