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

Bibliographic Data

ID19529486
AuthorsGeremew Tasew (0000-0002-2797-824X, Karolinska Institutet), Amha Kebede (0000-0001-5536-9671, Ethiopian Public Health Institute), Dawit Wolday (0000-0002-1181-1461, Ethiopian Public Health Institute), Endalamaw Gadisa (0000-0002-5179-6278, Armauer Hansen Research Institute), Sven Britton (Karolinska University Hospital), Liv Eidsmo (0000-0001-9237-8374, Karolinska University Hospital), Hannah Akuffo (0000-0003-1854-3591, Karolinska Institutet, corresponding author)
Year2009
Volume2
Issue1
Pages2046
Publication date2009-11-11
Peer ReviewedYes
Open AccessYes
TypeARTICLE
VenueGlobal Health Action (JOURNAL)
Journal identifiersISSN: 1654-9716 • E-ISSN: 1654-9880
PublisherInforma UK Limited (PUBLISHER • GB)
DOI10.3402/gha.v2i0.2046
PMID20027250
PMCIDPMC2792165
OpenAlexW2142464362
LanguageEN
References cited17

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 approximately 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

Amastigote · Biology · Cryopreservation · Leishmania · Leishmania major · Leishmaniasis · Liquid culture · Parasite hosting · Computer Science · Medicine · Parasites and Host Interactions · Research on Leishmaniasis Studies · Trypanosoma species research and implications · Immunology

Citation velocityhistorical
Highly citedNo
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