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Authordc.contributor.authorLiempi Manquel, Ana 
Authordc.contributor.authorCastillo, Christian 
Authordc.contributor.authorCerda Villablanca, Mauricio 
Authordc.contributor.authorDroguett Ossa, Daniel 
Authordc.contributor.authorDuaso, Juan 
Authordc.contributor.authorBarahona, Katherine 
Authordc.contributor.authorHernández, Ariane 
Authordc.contributor.authorDíaz Luján, Cintia 
Authordc.contributor.authorFretes, Ricardo 
Authordc.contributor.authorHärtel, Steffen 
Authordc.contributor.authorKemmerling Weis, Ulrike 
Admission datedc.date.accessioned2015-08-07T13:19:40Z
Available datedc.date.available2015-08-07T13:19:40Z
Publication datedc.date.issued2015
Cita de ítemdc.identifier.citationActa Tropica 143 (2015) 47–50en_US
Identifierdc.identifier.issn0001-706X
Identifierdc.identifier.otherDOI: 10.1016/j.actatropica.2014.12.006
Identifierdc.identifier.urihttps://repositorio.uchile.cl/handle/2250/132474
General notedc.descriptionArtículo de publicación ISIen_US
Abstractdc.description.abstractChagas 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 infectivityen_US
Patrocinadordc.description.sponsorship1120230 (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/11/08en_US
Lenguagedc.language.isoenen_US
Publisherdc.publisherElsevieren_US
Type of licensedc.rightsAtribución-NoComercial-SinDerivadas 3.0 Chile*
Link to Licensedc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/cl/*
Keywordsdc.subjectTrypanosoma cruzien_US
Keywordsdc.subjectInfectivityen_US
Keywordsdc.subjectQuantificationen_US
Títulodc.titleTrypanosoma cruzi infectivity assessment in “in vitro” culture systems by automated cell countingen_US
Document typedc.typeArtículo de revista


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Atribución-NoComercial-SinDerivadas 3.0 Chile
Except where otherwise noted, this item's license is described as Atribución-NoComercial-SinDerivadas 3.0 Chile