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Development and evaluation of a 28S rRNA gene-based nested PCR assay for P. falciparum and P. vivax

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dc.contributor.author Garg, Shilpi
dc.contributor.author Saxena, Vishal
dc.contributor.author Das, Ashis
dc.date.accessioned 2021-09-27T16:27:32Z
dc.date.available 2021-09-27T16:27:32Z
dc.date.issued 2013-04-12
dc.identifier.uri https://www.tandfonline.com/doi/full/10.1179/2047773213Y.0000000090
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/xmlui/handle/123456789/2361
dc.description.abstract The 28S rRNA gene was amplified and sequenced from P. falciparum and P. vivax isolates collected from northwest India. Based upon the sequence diversity of the Plasmodium 28SrRNA gene in comparison with its human counterpart, various nested polymerase chain reaction (PCR) primers were designed from the 3R region of the 28SrRNA gene and evaluated on field isolates. This is the first report demonstrating the utility of this gene for species-specific diagnosis of malaria for these two species, prevalent in India. The initial evaluation on 363 clinical isolates indicated that, in comparison with microscopy, which showed sensitivity and specificity of 85·39% and 100% respectively, the sensitivity and specificity of the nested PCR assay was found to be 99·08% and 100% respectively. This assay was also successful in detecting mixed infections that are undetected by microscopy. Our results demonstrate the utility of the 28S rRNA gene as a diagnostic target for the detection of the major plasmodial species infecting humans. en_US
dc.language.iso en en_US
dc.publisher Taylor & Francis en_US
dc.subject Biology en_US
dc.subject 28S rRNA gene en_US
dc.subject Plasmodium detection en_US
dc.subject Malaria diagnosis en_US
dc.subject Surveillance tools en_US
dc.title Development and evaluation of a 28S rRNA gene-based nested PCR assay for P. falciparum and P. vivax en_US
dc.type Article en_US


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