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Analytical and clinical performance of a Chikungunya qRT-PCR for Central and South America.


ABSTRACT: Chikungunya was introduced into the Americas in 2015 causing a pandemic across the continent. Testing during the acute phase of infection relies on qRT-PCR, but available assays have a number of limitations. A qRT-PCR assay specific to the chikungunya E1 gene was designed using sequence data from contemporary strains. A probit analysis established the 95% limit of detection as 19.6 copies per reaction. We compared the assay with a US Centers for Disease Control (CDC) chikungunya qRT-PCR as the reference standard. The assay had a sensitivity and specificity of 98.4% and 100% in 90 samples retrospectively collected in Guatemala. In a further 74 febrile samples prospectively collected in Ecuador and Guatemala the test had a sensitivity and specificity of 100% and 98.4%, respectively. Sequencing the nsp4 gene of the discordant positive sample indicated the presence of chikungunya RNA, and mismatches to the primer binding sites of the CDC assay.

SUBMITTER: Edwards T 

PROVIDER: S-EPMC5560405 | biostudies-literature | 2017 Sep

REPOSITORIES: biostudies-literature

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Analytical and clinical performance of a Chikungunya qRT-PCR for Central and South America.

Edwards Thomas T   Del Carmen Castillo Signor Leticia L   Williams Christopher C   Larcher Clément C   Espinel Mauricio M   Theaker Jane J   Donis Evelin E   Cuevas Luis E LE   Adams Emily R ER  

Diagnostic microbiology and infectious disease 20170608 1


Chikungunya was introduced into the Americas in 2015 causing a pandemic across the continent. Testing during the acute phase of infection relies on qRT-PCR, but available assays have a number of limitations. A qRT-PCR assay specific to the chikungunya E1 gene was designed using sequence data from contemporary strains. A probit analysis established the 95% limit of detection as 19.6 copies per reaction. We compared the assay with a US Centers for Disease Control (CDC) chikungunya qRT-PCR as the r  ...[more]

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