Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/594
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dc.contributor.authorVaidya, Tushar-
dc.date.accessioned2015-06-16T07:11:15Z-
dc.date.available2015-06-16T07:11:15Z-
dc.date.issued2008-05-
dc.identifier.urihttp://hdl.handle.net/123456789/594-
dc.description.abstractWe have developed a highly accurate and sensitive real-time polymerase chain reaction (PCR) assay to detect and quantify Leishmania parasites. The assay targets GP63, a highly conserved gene in Leishmania. We demonstrate that, with a single assay, we are able to detect and quantify several species of Leishmania. Our assay system detects Leishmania donovani and Leishmania major down to 0.1 parasite. The dynamic range of the assay extends over 6 log cycles of target, with an average correlation coefficient >0.988. In addition, we utilize a simple approach to distinguish between Leishmania species causing diverse spectra of disease. We have also used this assay to follow the course of cutaneous disease in CBA/CaJ mice, known to be resistant to L. major. The assay is sensitive enough to quantify parasite load in the absence of overt lesions and reveals a systemic distribution of Leishmania, which has implications for our understanding of the diseaseen_US
dc.publisherElsevieren_US
dc.titleDevelopment of a real-time polymerase chain reaction assay for the quantification of Leishmania species and the monitoring of systemic distribution of the pathogenen_US
dc.contributor.coauthorVaranasi, Vineeth-
dc.contributor.coauthorRath, Satyajit-
dc.contributor.coauthorTupperwar, Nitin-
dc.keywordReal-time PCR; Leishmaniasis; Quantitation; Systemic infection; Tissue distributionen_US
dc.journalDiagnostic Microbiology and Infectious Diseaseen_US
dc.volumeno61en_US
dc.issueno1en_US
dc.pages23-30en_US
Appears in Collections:Immuno Biology-II, Publications

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