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dc.contributor.authorChohan, Bhavna H
dc.contributor.authorEmery, Sandra
dc.contributor.authorWamalwa, Dalton
dc.contributor.authorJohn-Stewart, Grace
dc.contributor.authorMajiwa, Maxwel
dc.contributor.authorNg'ayo, Musa
dc.contributor.authorFroggett, Steve
dc.contributor.authorOverbaugh, Julie
dc.date.accessioned2013-04-10T05:54:55Z
dc.date.available2013-04-10T05:54:55Z
dc.date.issued2011
dc.identifier.citationBMC Pediatr. 2011; 11: 18.en
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050718/
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/15564
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/21332984
dc.descriptionFull texten
dc.description.abstractBackground The aim of this study was to develop an economical 'in-house' single round polymerase chain reaction (PCR) assay using filter paper-dried blood spots (FP-DBS) for early infant HIV-1 diagnosis and to evaluate its performance in an African setting. Methods An 'in-house' single round PCR assay that targets conserved regions in the HIV-1 polymerase (pol) gene was validated for use with FP-DBS; first we validated this assay using FP-DBS spiked with cell standards of known HIV-1 copy numbers. Next, we validated the assay by testing the archived FP-DBS (N = 115) from infants of known HIV-1 infection status. Subsequently this 'in-house' HIV-1 pol PCR FP-DBS assay was then established in Nairobi, Kenya for further evaluation on freshly collected FP-DBS (N = 186) from infants, and compared with findings from a reference laboratory using the Roche Amplicor® HIV-1 DNA Test, version 1.5 assay. Results The HIV-1 pol PCR FP-DBS assay could detect one HIV-1 proviral copy in 38.7% of tests, 2 copies in 46.9% of tests, 5 copies in 72.5% of tests and 10 copies in 98.1% of tests performed with spiked samples. Using the archived FP-DBS samples from infants of known infection status, this assay was 92.8% sensitive and 98.3% specific for HIV-1 infant diagnosis. Using 186 FP-DBS collected from infants recently defined as HIV-1 positive using the commercially available Roche Amplicor v1.5 assay, 178 FP-DBS tested positive by this 'in-house' single-round HIV-1 pol PCR FP-DBS PCR assay. Upon subsequent retesting, the 8 infant FP-DBS samples that were discordant were confirmed as HIV-1 negative by both assays using a second blood sample. Conclusions HIV-1 was detected with high sensitivity and specificity using both archived and more recently collected samples. This suggests that this 'in-house' HIV-1 pol FP-DBS PCR assay can provide an alternative cost-effective, reliable and rapid method for early detection of HIV-1 infection in infants.en
dc.language.isoenen
dc.subjectHIV-1en
dc.subjectInfantsen
dc.subjectPolymerase chain reactionen
dc.titleEvaluation of a single round polymerase chain reaction assay using dried blood spots for diagnosis of HIV-1 infection in infants in an African settingen
dc.typeArticleen
local.publisherDepartment of Medical Microbiologyen
local.publisherDepartment of Paediatricsen


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