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Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries

BACKGROUND: Prompt laboratory diagnosis and initiation of treatment are effective components of leishmaniasis control. Detection of Leishmania parasites by ex-vivo culture of lesion scrapings is considered a definitive diagnostic method preceding initiation of treatment. OBJECTIVE: A pilot study to...

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Autores principales: Tasew, Geremew, Kebede, Amha, Wolday, Dawit, Gadisa, Endalamaw, Britton, Sven, Eidsmo, Liv, Akuffo, Hannah
Formato: Texto
Lenguaje:English
Publicado: CoAction Publishing 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792165/
https://www.ncbi.nlm.nih.gov/pubmed/20027250
http://dx.doi.org/10.3402/gha.v2i0.2046
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author Tasew, Geremew
Kebede, Amha
Wolday, Dawit
Gadisa, Endalamaw
Britton, Sven
Eidsmo, Liv
Akuffo, Hannah
author_facet Tasew, Geremew
Kebede, Amha
Wolday, Dawit
Gadisa, Endalamaw
Britton, Sven
Eidsmo, Liv
Akuffo, Hannah
author_sort Tasew, Geremew
collection PubMed
description BACKGROUND: Prompt laboratory diagnosis and initiation of treatment are effective components of leishmaniasis control. Detection of Leishmania parasites by ex-vivo culture of lesion scrapings is considered a definitive diagnostic method preceding initiation of treatment. OBJECTIVE: A pilot study to find alternative medium that could reduce the cost of culturing from patient lesions for diagnosing leishmaniasis. METHOD: GALF-1 medium was formulated in our lab from locally available inexpensive solutions and powders in the presence of urine from healthy individuals. Amastigote to promastigote transformation, recovery of parasites after cryopreservation, cost and mass cultivation was compared using the following media: GALF-1, RPMI 1640, and conventional Locke's semi-solid medium (LSSM), a modifications of Novy–MacNeal–Nicolle culture media, which uses Locke's solution as an overlay RESULTS: GALF-1 preparation was cheap and the components available in low-income countries such as Ethiopia. Preparation was simple, not requiring autoclaving and extra distilled water. GALF-1 was able to transform amastigotes from Ethiopian patients’ samples and could be used to cultivate promastigotes in large quantities. GALF-1 decreased Leishmania culture costs by ∼80–95% compared to LSSM and RPMI 1640, respectively. Promastigotes cultured with GALF-1 could be cryopreserved in liquid nitrogen with comparable re-culture potential. CONCLUSION: Affordability of diagnostic assays is a key issue for endemic resource-poor countries and the possibility to cut the cost of the efficient culture method for diagnosis through the use of inexpensive, locally formulated reagents could improve the diagnosis of leishmaniasis in Ethiopia and in other low-income countries.
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spelling pubmed-27921652009-12-21 Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries Tasew, Geremew Kebede, Amha Wolday, Dawit Gadisa, Endalamaw Britton, Sven Eidsmo, Liv Akuffo, Hannah Glob Health Action Short Communication BACKGROUND: Prompt laboratory diagnosis and initiation of treatment are effective components of leishmaniasis control. Detection of Leishmania parasites by ex-vivo culture of lesion scrapings is considered a definitive diagnostic method preceding initiation of treatment. OBJECTIVE: A pilot study to find alternative medium that could reduce the cost of culturing from patient lesions for diagnosing leishmaniasis. METHOD: GALF-1 medium was formulated in our lab from locally available inexpensive solutions and powders in the presence of urine from healthy individuals. Amastigote to promastigote transformation, recovery of parasites after cryopreservation, cost and mass cultivation was compared using the following media: GALF-1, RPMI 1640, and conventional Locke's semi-solid medium (LSSM), a modifications of Novy–MacNeal–Nicolle culture media, which uses Locke's solution as an overlay RESULTS: GALF-1 preparation was cheap and the components available in low-income countries such as Ethiopia. Preparation was simple, not requiring autoclaving and extra distilled water. GALF-1 was able to transform amastigotes from Ethiopian patients’ samples and could be used to cultivate promastigotes in large quantities. GALF-1 decreased Leishmania culture costs by ∼80–95% compared to LSSM and RPMI 1640, respectively. Promastigotes cultured with GALF-1 could be cryopreserved in liquid nitrogen with comparable re-culture potential. CONCLUSION: Affordability of diagnostic assays is a key issue for endemic resource-poor countries and the possibility to cut the cost of the efficient culture method for diagnosis through the use of inexpensive, locally formulated reagents could improve the diagnosis of leishmaniasis in Ethiopia and in other low-income countries. CoAction Publishing 2009-10-22 /pmc/articles/PMC2792165/ /pubmed/20027250 http://dx.doi.org/10.3402/gha.v2i0.2046 Text en © 2009 Geremew Tasew et al. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Tasew, Geremew
Kebede, Amha
Wolday, Dawit
Gadisa, Endalamaw
Britton, Sven
Eidsmo, Liv
Akuffo, Hannah
Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title_full Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title_fullStr Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title_full_unstemmed Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title_short Low-cost liquid medium for in vitro cultivation of Leishmania parasites in low-income countries
title_sort low-cost liquid medium for in vitro cultivation of leishmania parasites in low-income countries
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2792165/
https://www.ncbi.nlm.nih.gov/pubmed/20027250
http://dx.doi.org/10.3402/gha.v2i0.2046
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