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Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology
In Algeria, Leishmania infantum, Leishmania major, and Leishmania killicki (Leishmania tropica) are responsible for cutaneous leishmaniosis. We established a murine model of L. killicki infection to investigate its infective capacity, some immunophysiopathological aspects, and its suitability for ph...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754473/ https://www.ncbi.nlm.nih.gov/pubmed/26949705 http://dx.doi.org/10.1155/2016/7985104 |
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author | Eddaikra, Naouel Kherachi Djenad, Ihcene Benbetka, Sihem Benikhlef, Razika Aït-Oudhia, Khatima Moulti-Mati, Farida Oury, Bruno Sereno, Denis Harrat, Zoubir |
author_facet | Eddaikra, Naouel Kherachi Djenad, Ihcene Benbetka, Sihem Benikhlef, Razika Aït-Oudhia, Khatima Moulti-Mati, Farida Oury, Bruno Sereno, Denis Harrat, Zoubir |
author_sort | Eddaikra, Naouel |
collection | PubMed |
description | In Algeria, Leishmania infantum, Leishmania major, and Leishmania killicki (Leishmania tropica) are responsible for cutaneous leishmaniosis. We established a murine model of L. killicki infection to investigate its infective capacity, some immunophysiopathological aspects, and its suitability for pharmacological purposes. Following the injection of L. major or L. killicki metacyclic promastigotes in the ear dermis of BALB/c mice, the course of infection was followed. The infection with L. killicki caused slower lesion formation than with L. major. The presence of L. killicki or L. major DNA and parasites was detected in the ear dermis and in lymph nodes, spleen, and liver. Lesions induced by L. killicki were nonulcerative in their aspect, whereas those caused by L. major were highly ulcerative and necrotic, which matches well with the lesion phenotype reported in humans for L. killicki and L. major, respectively. The treatment of L. killicki lesions by injection of Glucantime® significantly reduced the lesion thickness and parasite burden. Ear dermal injection of BALB/c mice constitutes a model to study lesions physiopathology caused by L. killicki and presents interest for in vivo screening of new compounds against this pathogen, emerging in Algeria. |
format | Online Article Text |
id | pubmed-4754473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-47544732016-03-06 Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology Eddaikra, Naouel Kherachi Djenad, Ihcene Benbetka, Sihem Benikhlef, Razika Aït-Oudhia, Khatima Moulti-Mati, Farida Oury, Bruno Sereno, Denis Harrat, Zoubir Biomed Res Int Research Article In Algeria, Leishmania infantum, Leishmania major, and Leishmania killicki (Leishmania tropica) are responsible for cutaneous leishmaniosis. We established a murine model of L. killicki infection to investigate its infective capacity, some immunophysiopathological aspects, and its suitability for pharmacological purposes. Following the injection of L. major or L. killicki metacyclic promastigotes in the ear dermis of BALB/c mice, the course of infection was followed. The infection with L. killicki caused slower lesion formation than with L. major. The presence of L. killicki or L. major DNA and parasites was detected in the ear dermis and in lymph nodes, spleen, and liver. Lesions induced by L. killicki were nonulcerative in their aspect, whereas those caused by L. major were highly ulcerative and necrotic, which matches well with the lesion phenotype reported in humans for L. killicki and L. major, respectively. The treatment of L. killicki lesions by injection of Glucantime® significantly reduced the lesion thickness and parasite burden. Ear dermal injection of BALB/c mice constitutes a model to study lesions physiopathology caused by L. killicki and presents interest for in vivo screening of new compounds against this pathogen, emerging in Algeria. Hindawi Publishing Corporation 2016 2016-02-02 /pmc/articles/PMC4754473/ /pubmed/26949705 http://dx.doi.org/10.1155/2016/7985104 Text en Copyright © 2016 Naouel Eddaikra et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Eddaikra, Naouel Kherachi Djenad, Ihcene Benbetka, Sihem Benikhlef, Razika Aït-Oudhia, Khatima Moulti-Mati, Farida Oury, Bruno Sereno, Denis Harrat, Zoubir Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title | Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title_full | Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title_fullStr | Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title_full_unstemmed | Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title_short | Development of a Murine Infection Model with Leishmania killicki, Responsible for Cutaneous Leishmaniosis in Algeria: Application in Pharmacology |
title_sort | development of a murine infection model with leishmania killicki, responsible for cutaneous leishmaniosis in algeria: application in pharmacology |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4754473/ https://www.ncbi.nlm.nih.gov/pubmed/26949705 http://dx.doi.org/10.1155/2016/7985104 |
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