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dc.contributor.author
Muñoz Calderon, Arturo Alejandro
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Diaz Bello, Zoraida
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Ramirez, José Luis
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Noya, Oscar
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Alarcón de Noya, Belkisyolé
dc.date.available
2020-07-24T20:43:35Z
dc.date.issued
2019-09
dc.identifier.citation
Muñoz Calderon, Arturo Alejandro; Diaz Bello, Zoraida; Ramirez, José Luis; Noya, Oscar; Alarcón de Noya, Belkisyolé; Nifurtimox response of Trypanosoma cruzi isolates from an outbreak of Chagas disease in Caracas, Venezuela; Malaria Research Centre; Journal Of Vector Borne Diseases; 56; 3; 9-2019; 237-243
dc.identifier.issn
0972-9062
dc.identifier.uri
http://hdl.handle.net/11336/110255
dc.description.abstract
Background & objectives: In Venezuela, Chagas disease (ChD) is considered a serious health problem, with about 6 million people at risk; and acute outbreaks due to oral transmission of Chagas Disease (OChD) are becoming increasingly important. In 2007 there was a major outbreak of OChD and although patients from this episode were treated with nifurtimox (Lampit®—Bayer), about 70% therapeutic failure was registered. These results led us to examine whether parasite’s drug susceptibility was related to this therapeutic failure. Methods: The Trypanosoma cruzi parasites were isolated by haemoculture of the peripheral blood drawn from the pre- and post-nifurtimox treated patients infected in the 2007 OChD outbreak at Caracas, Venezuela. The in vitro assays for drug testing were performed by the MTT methodology followed by calculation of inhibitory concentration-50 (IC50) values. Results: Parasite isolates obtained from the infected patients prior and after nifurtimox treatment when subjected to variable concentrations of the drug showed great heterogeneity in susceptibility with IC50 values ranging from 4.07 ± 1.82 to 94.92 ± 7.24 µM. Interpretation & conclusion: The high heterogeneity in nifurtimox IC50 values in the isolates and clones from the OChD patients, suggests that the therapeutic failure to nifurtimox could be due in part to a phenotypic variability that existed in the wild parasite population at the original source of contamination. Though, further pharmacological studies are needed to confirm the existence of natural nifurtimox resistance in the parasite.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Malaria Research Centre
dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
CHAGAS DISEASE
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ORAL TRANSMISSION
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TRYPANOSOMA CRUZI
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NIFURTIMOX
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Biología Celular, Microbiología
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Ciencias Biológicas
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CIENCIAS NATURALES Y EXACTAS
dc.title
Nifurtimox response of Trypanosoma cruzi isolates from an outbreak of Chagas disease in Caracas, Venezuela
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2020-07-21T21:00:32Z
dc.journal.volume
56
dc.journal.number
3
dc.journal.pagination
237-243
dc.journal.pais
India
dc.description.fil
Fil: Muñoz Calderon, Arturo Alejandro. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina. Universidad Central de Venezuela; Venezuela
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Fil: Diaz Bello, Zoraida. Universidad Central de Venezuela; Venezuela
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Fil: Ramirez, José Luis. Fundacion Instituto de Estudios Avanzados Idea; Venezuela
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Fil: Noya, Oscar. Universidad Central de Venezuela; Venezuela. Ministerio del Poder Popular para la Salud; Venezuela
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Fil: Alarcón de Noya, Belkisyolé. Universidad Central de Venezuela; Venezuela
dc.journal.title
Journal Of Vector Borne Diseases
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.4103/0972-9062.289397
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info:eu-repo/semantics/altIdentifier/url/http://www.jvbd.org/temp/JVectorBorneDis563237-9788681_024308.pdf
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.jvbd.org/downloadpdf.asp?issn=0972-9062;year=2019;volume=56;issue=3;spage=237;epage=243;aulast=Munoz-Calderon;type=2
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