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Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria
Leishmaniasis is a protozoal vector-borne disease that affects both humans and animals. In the Mediterranean Basin, the primary reservoir hosts of Leishmania spp. are mainly rodents and canids. Lipidomic approaches have allowed scientists to establish Leishmania spp. lipid profiles for the identific...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781279/ https://www.ncbi.nlm.nih.gov/pubmed/35056040 http://dx.doi.org/10.3390/pathogens11010092 |
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author | Bouabid, Cyrine Yamaryo-Botté, Yoshiki Rabhi, Sameh Bichiou, Haifa Hkimi, Chaima Bouglita, Wafa Chaouach, Melek Eddaikra, Naouel Ghedira, Kais Guizani-Tabbane, Lamia Botté, Cyrille Y. Rabhi, Imen |
author_facet | Bouabid, Cyrine Yamaryo-Botté, Yoshiki Rabhi, Sameh Bichiou, Haifa Hkimi, Chaima Bouglita, Wafa Chaouach, Melek Eddaikra, Naouel Ghedira, Kais Guizani-Tabbane, Lamia Botté, Cyrille Y. Rabhi, Imen |
author_sort | Bouabid, Cyrine |
collection | PubMed |
description | Leishmaniasis is a protozoal vector-borne disease that affects both humans and animals. In the Mediterranean Basin, the primary reservoir hosts of Leishmania spp. are mainly rodents and canids. Lipidomic approaches have allowed scientists to establish Leishmania spp. lipid profiles for the identification of cell stage specific biomarkers, drug mechanisms of action, and host immune response. Using an in silico approach of global network interaction between genes involved in fatty acid (FA) synthesis followed by the GC-MS approach, we were able to characterize the fatty acid profiles of L. major derived from human and rodent hosts. Our results revealed that the lipid profile of L. major showed similarities and differences with those already reported for other Leishmania species. Phospholipids are the predominant lipid class. FA composition of rodent parasites was characterized by a lower abundance of the precursor C18:2(n-6). One of the rodent clones, which also expressed the lowest lipid abundance in PL and TAG, was the least sensitive clone to the miltefosine drug and has the lowest infection efficiency. Our findings suggest that the lipid composition variation may explain the response of the parasite toward treatment and their ability to infect their host. |
format | Online Article Text |
id | pubmed-8781279 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-87812792022-01-22 Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria Bouabid, Cyrine Yamaryo-Botté, Yoshiki Rabhi, Sameh Bichiou, Haifa Hkimi, Chaima Bouglita, Wafa Chaouach, Melek Eddaikra, Naouel Ghedira, Kais Guizani-Tabbane, Lamia Botté, Cyrille Y. Rabhi, Imen Pathogens Article Leishmaniasis is a protozoal vector-borne disease that affects both humans and animals. In the Mediterranean Basin, the primary reservoir hosts of Leishmania spp. are mainly rodents and canids. Lipidomic approaches have allowed scientists to establish Leishmania spp. lipid profiles for the identification of cell stage specific biomarkers, drug mechanisms of action, and host immune response. Using an in silico approach of global network interaction between genes involved in fatty acid (FA) synthesis followed by the GC-MS approach, we were able to characterize the fatty acid profiles of L. major derived from human and rodent hosts. Our results revealed that the lipid profile of L. major showed similarities and differences with those already reported for other Leishmania species. Phospholipids are the predominant lipid class. FA composition of rodent parasites was characterized by a lower abundance of the precursor C18:2(n-6). One of the rodent clones, which also expressed the lowest lipid abundance in PL and TAG, was the least sensitive clone to the miltefosine drug and has the lowest infection efficiency. Our findings suggest that the lipid composition variation may explain the response of the parasite toward treatment and their ability to infect their host. MDPI 2022-01-14 /pmc/articles/PMC8781279/ /pubmed/35056040 http://dx.doi.org/10.3390/pathogens11010092 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Bouabid, Cyrine Yamaryo-Botté, Yoshiki Rabhi, Sameh Bichiou, Haifa Hkimi, Chaima Bouglita, Wafa Chaouach, Melek Eddaikra, Naouel Ghedira, Kais Guizani-Tabbane, Lamia Botté, Cyrille Y. Rabhi, Imen Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title | Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title_full | Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title_fullStr | Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title_full_unstemmed | Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title_short | Fatty Acid Profiles of Leishmania major Derived from Human and Rodent Hosts in Endemic Cutaneous Leishmaniasis Areas of Tunisia and Algeria |
title_sort | fatty acid profiles of leishmania major derived from human and rodent hosts in endemic cutaneous leishmaniasis areas of tunisia and algeria |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8781279/ https://www.ncbi.nlm.nih.gov/pubmed/35056040 http://dx.doi.org/10.3390/pathogens11010092 |
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