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Clinical evaluation of a low cost, in-house developed real-time RT-PCR human immunodeficiency virus type 1 (HIV-1) quantitation assay for HIV-1 infected patients.


ABSTRACT:

Objectives

HIV-1 viral quantitation is essential for treatment monitoring. An in-house assay would decrease financial barriers to access.

Materials and methods

A real-time competitive RT-PCR in house assay (Sing-IH) was developed in Singapore. Using HXB2 as reference, the assay's primers and probes were designed to generate a 183-bp product that overlaps a portion of the LTR region and gag region. A competitive internal control (IC) was included in each assay to monitor false negative results due to inhibition or human error. Clinical evaluation was performed on 249 HIV-1 positive patient samples in comparison with the commercially available Generic HIV Viral Load assay. Correlation and agreement of results were assessed for plasma HIV-1 quantification with both assays.

Results

The assay has a lower limit of detection equivalent to 126 copies/mL of HIV-1 RNA and a linear range of detection from 100-1000000 copies/mL. Comparative analysis with reference to the Generic assay demonstrated good agreement between both assays with a mean difference of 0.22 log10 copies/mL and 98.8% of values within 1 log10 copies/mL range. Furthermore, the Sing-IH assay can quantify HIV-1 group M subtypes A-H and group N isolates adequately, making it highly suitable for our region, where subtype B and CRF01_AE predominate.

Conclusions

With a significantly lower running cost compared to commercially available assays, the broadly sensitive Sing-IH assay could help to overcome the cost barriers and serve as a useful addition to the currently limited HIV viral load assay options for resource-limited settings.

SUBMITTER: Kaur P 

PROVIDER: S-EPMC3945479 | biostudies-literature | 2014

REPOSITORIES: biostudies-literature

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Publications

Clinical evaluation of a low cost, in-house developed real-time RT-PCR human immunodeficiency virus type 1 (HIV-1) quantitation assay for HIV-1 infected patients.

Kaur Palvinder P   Khong Wei Xin WX   Wee Sue Yuen SY   Tan Eng Lee EL   Pipper Juergen J   Koay Evelyn E   Ng Kah Ying KY   Yap Joe Kwan JK   Chew Kuan Kiat KK   Tan Mei Ting MT   Leo Yee Sin YS   Inoue Masafumi M   Ng Oon Tek OT  

PloS one 20140306 3


<h4>Objectives</h4>HIV-1 viral quantitation is essential for treatment monitoring. An in-house assay would decrease financial barriers to access.<h4>Materials and methods</h4>A real-time competitive RT-PCR in house assay (Sing-IH) was developed in Singapore. Using HXB2 as reference, the assay's primers and probes were designed to generate a 183-bp product that overlaps a portion of the LTR region and gag region. A competitive internal control (IC) was included in each assay to monitor false nega  ...[more]

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