Trypanosoma cruzi infectivity assessment in “in vitro” culture systems by automated cell counting
Author
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Liempi Manquel, Ana
Author
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Castillo, Christian
Author
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Cerda Villablanca, Mauricio
Author
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Droguett Ossa, Daniel
Author
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Duaso, Juan
Author
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Barahona, Katherine
Author
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Hernández, Ariane
Author
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Díaz Luján, Cintia
Author
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Fretes, Ricardo
Author
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Härtel, Steffen
Author
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Kemmerling Weis, Ulrike
Admission date
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2015-08-07T13:19:40Z
Available date
dc.date.available
2015-08-07T13:19:40Z
Publication date
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2015
Cita de ítem
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Acta Tropica 143 (2015) 47–50
en_US
Identifier
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0001-706X
Identifier
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DOI: 10.1016/j.actatropica.2014.12.006
Identifier
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https://repositorio.uchile.cl/handle/2250/132474
General note
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Artículo de publicación ISI
en_US
Abstract
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Chagas disease is an endemic, neglected tropical disease in Latin America that is caused by the protozoan
parasite Trypanosoma cruzi. In vitro models constitute the first experimental approach to study the
physiopathology of the disease and to assay potential new trypanocidal agents.
Here, we report and describe clearly the use of commercial software (MATLAB®) to quantify T. cruzi
amastigotes and infected mammalian cells (BeWo) and compared this analysis with the manual one.
There was no statistically significant difference between the manual and the automatic quantification
of the parasite; the two methods showed a correlation analysis r2 value of 0.9159. The most significant
advantage of the automatic quantification was the efficiency of the analysis. The drawback of this automated
cell counting method was that some parasites were assigned to the wrong BeWo cell, however
this data did not exceed 5% when adequate experimental conditions were chosen.
We conclude that this quantification method constitutes an excellent tool for evaluating the parasite
load in cells and therefore constitutes an easy and reliable ways to study parasite infectivity
en_US
Patrocinador
dc.description.sponsorship
1120230 (UK) 1120579 (SH),
and 3140447 (MC) from FONDECYT, FONDEFD0711019 (SH), the
Chilean Millennium Science Initiative (ICM, P09-015-F) (SH/MC),
the Universidad de Chile URedes Project: BioMed-HPC (SH), the
Latin American Cancer Research Network (US-LACRN) (SH/MC),
CONICYT-PBCT Anillo ACT112 and CONICYT/MINCYT 2011-595-
CH/11/08