Generation of HIV-1 and Internal Control Transcripts as Standards for an In-House Quantitative Competitive RT-PCR Assay to Determine HIV-1 Viral Load

Human immunodeficiency virus type-1 (HIV-1) viral load is useful for monitoring disease progression in HIV-infected individuals. We generated RNA standards of HIV-1 and internal control (IC) by in vitro transcription and evaluated its performance in a quantitative reverse transcription polymerase chain reaction (qRT-PCR) assay. HIV-1 and IC standards were obtained at high RNA concentrations, without DNA contamination. When these transcripts were included as standards in a qRT-PCR assay, it was obtained a good accuracy (±0.5 log10 unit of the expected results) in the quantification of the HIV-1 RNA international standard and controls. The lower limit detection achieved using these standards was 511.0 IU/mL. A high correlation (r = 0.925) was obtained between the in-house qRT-PCR assay and the NucliSens easyQ HIV-1 test (bioMerieux) for HIV-1 RNA quantitation with clinical samples (N = 14). HIV-1 and IC RNA transcripts, generated in this study, proved to be useful as standards in an in-house qRT-PCR assay for determination of HIV-1 viral load.


Introduction
The quantitation of human immunodeficiency virus type-1 (HIV-1) RNA is a crucial factor to help clinicians decide whether to stop or continue antiretroviral combinations after switching or starting antiretroviral drug therapy [1]. In addition, it is a useful biological marker to study HIV dynamics [2,3], host/virus interaction, HIV evolution, and the progression of the acquired immunodeficiency syndrome (AIDS) [4,5].
There are three major methodologies available for viral load quantitation. The reverse transcriptase-polymerase chain reaction (RT-PCR), the nucleic acid sequence-based amplification (NASBA) and a signal amplification methodology termed branched-chain DNA (bDNA) technique [6]. In the past recent years there have been new reported viral load assays that have incorporated the real-time detection, such as the COBAS TaqMan HIV-1 test from Roche Diagnostics [7], which utilizes real-time PCR technology [8] and the NucliSens EasyQ HIV-1 from bioMerieux, which uses molecular beacon for the real-time detection [9]. In spite of the advantages that offer the use of the real-time PCR, which helps reducing the possibility of contamination, increasing the assay sensitivity, and improving the turnaround time [10], commercially available real-time PCR assays are just as expensive as the more standard nucleic acid viral load tests and also rely on expensive, often dedicated equipment, that can only be used for these assays [10,11]. For this reason, inexpensive and technologically simpler assays are still needed in resource-limited countries, where the new technology and equipments are currently not available.
For the development of an in-house quantitative competitive RT-PCR assay (qRT-PCR) for the estimation of HIV-1 viral load, it is necessary to obtain an HIV-1 RNA external control (calibration curve) and an internal quantitation control (IC), which is added to the specimen at a known concentration before RNA extraction. The IC can be differentiated from the viral target sequences and serves to compensate for variability in RNA extraction and also to indicate substances in serum or plasma that may be inhibitory to PCR amplification [12]. Although chemical synthesis up to a length of about 80 nucleotides is possible, yields decrease rapidly and costs become prohibitive. A good alternative is to produce the RNA by in vitro transcription with T7 RNA polymerase [13]. RNA synthesis by in vitro transcription using phage T7 RNA polymerase allows preparation of milligram quantities of RNA for biochemical, biophysical, and structural investigations [14].
In this study, we generated RNA standards with HIV-1 and internal control sequences, using in vitro transcription method and evaluated its performance in a qRT-PCR for determining HIV-1 viral load.

Materials and Methods
2.1. RNA Isolation. RNA was extracted from 200 µL of human serum or plasma by the guanidinium isothiocyanateacid phenol method [17] with modifications [18]. The RNA pellets were resuspended in 20 µL of diethylpyrocarbonate-(DEPC-) treated water.

Amplification of HIV-1 RNA by RT-PCR.
A fragment of 120 bp located in the 5 LTR region of the HIV-1 genome was amplified from RNA isolated from an HIV-1 subtype-B-infected serum, by RT-PCR. The cDNA synthesis by RT and amplification by PCR were carried out in a single tube in a reaction mixture of 25 µL using 5 µL of the isolated RNA. The reaction contained 25 pmol of each of the primers HIV1-Q3 and HIV1-Biot-Q4 (Table 1) that correspond to the long terminal repeat (LTR) region of the HIV-1 genome, Go Taq buffer, 1.5 mM MgCl 2 , 250 µM of each dNTPs, 3.6 u of AMV-RT, 9 u of RNasin ribonuclease inhibitor, and 1.05 u of Go Taq Flexi DNA polymerase (all from Promega, USA). The reaction was carried out in a thermocycler (Eppendorf, Hamburg, Germany). The amplified product was checked by hybridization using a probe complementary to the amplified HIV-1 fragment (HIV1-S) ( Table 1).

Amplification of the Internal Control (IC) Fragment.
A fragment of 120 bp was amplified by PCR, from a plasmid that contained the sequence of the p-64K protein of Neisseria meningitidis, flanked by the sequences of binding to sense and antisense primers (HIV1-Q3 and HIV1-Biot-Q4, resp.). The PCR reaction was done using the same conditions described above and the primers IC-1 and IC-2 (Table 1).

Cloning of the Amplified HIV-1 and IC Fragments into the pGEM-T Vector.
The amplified HIV-1 and IC fragments were gel-purified using the Wizard SV Gel and PCR Clean-Up System (Promega, USA) and cloned into the pGEM-T vector following the manufacturer's instructions (pGEM-T and pGEM-T Easy Vector Systems, Promega, USA). Escherichia coli XL-1 blue cells were transformed with the products of the ligation reactions and plated on Luria-Bertani-(LB-) ampicillin plate to select the transformed colonies. The plasmid DNA was isolated and purified from the colonies using the Wizard plus SV Minipreps DNA Purification System (Promega, USA), and PCR amplified to check the orientation of the cloned HIV-1 and IC fragments. The PCR reactions were performed using 25 pmol of the T7 Promoter primer from Promega, USA (Table 1) and 25 pmol of HIV1-Biot-Q4 primer. The correct orientation of the HIV-1 and IC fragments into the pGEM-T vector must generate a PCR band of 189 bp.

In Vitro Transcription.
Two batches of the pGEM-HIV1 and pGEM-IC plasmids were linearized with Mlu1 enzyme (Promega, USA). The correspondent HIV-1 and IC RNAs were obtained from 1 µg of pGEM-HIV1 and pGEM-IC plasmids using 50 u of T7 RNA polymerase (Promega, USA) in presence of 0.75 mM of each rNTPs (Promega, USA), transcription buffer (Promega, USA) in a 50 µL reaction, according to the procedure optimized in our laboratory, described in [19]. After transcription, 2 or 4 u of RNase free DNase (Promega, USA) per 1 µg of template DNA, were added for 15 or 30 min at 37 • C to degrade the contaminant DNA. Finally, the HIV-1 and IC transcripts were purified by phenol-chloroform extraction and were precipitated with 2.5 volumes of ethanol 95%. After RNA was washed and dried, it was dissolved in 50 µL of DEPC-treated water.

Determination of RNA Concentration by Optical Density
Measuring. One aliquot of each purified HIV-1 and IC transcripts was diluted 1 : 20 or 1 : 35 with DEPC-treated water and quantitated by measuring the optical density (OD) at 260 nm using the spectrophotometer (GeneQuant II, Pharmacia, USA). The ratio of absorbance at 260 and 280 nm was also obtained for the purified transcripts.
2.6.2. Evaluation of the Quality of the HIV-1 and IC Transcripts by Determining the Presence of RNA and DNA Contamination. The purified HIV-1 and IC transcripts were diluted 1 : 4 in a lysis reagent for preservation at 4 • C [20,21]. For the evaluation of the quality of the HIV-1 and IC transcripts, they were 10-fold serially diluted in lysis reagent from 1 : 4 × 10 3 to 1 : 4 × 10 9 . Isolation of RNA from lysis reagent was performed as described above. In this case, the lysis reagent containing the HIV-1 and IC transcripts was used in a volume of 500 µL per sample.
To simulate the natural sample, in the case of transcripts diluted in lysis reagent, 200 µL of cryosupernatant negative for hepatitis C virus (HCV), human immunodeficiency virus (HIV), and hepatitis B virus (HBV) were added to the mixture. The absence of plasmid template and the presence of RNA in the diluted HIV-1 and IC transcripts were verified through 50 cycles of PCR and RT-PCR, respectively, in mixes of 30 µL, employing HIV1-Q3 and HIV1-Biot-Q4 primers. Several negative and positive RT-PCR and PCR controls were tested. A HIV-, HCV-and HBV-negative cryosupernatant was used as a negative control of each assay. Positive HIV-1 RT-PCR control consisted on a positive HIV-1 plasma sample while the positive HIV-1 and IC PCR controls were the same plasmids used as templates in the in vitro transcription reactions. The amplified products were checked by hybridization using probes complementary to HIV-1 (HIV1-S) and IC (IC-S1) fragments (Table 1).

Determination of the Working Dilution of the IC Transcript in an In-House Quantitative Competitive RT-PCR Assay.
The dilution required for the IC transcript to work optimally as a competitor was determined by titration versus HIV-1positive human plasma calibration curves in a competitive RT-PCR assay described below. The calibration curve was obtained by diluting HIV-1-positive human plasma with high viral load, 10-fold from 10 6 to 10 2 IU/mL. As internal control, we evaluated four dilutions of the IC transcript, using the lysis reagent as diluent (1 : 4 × 10 4 , 1 : 4 × 10 5 , 1 : 4 × 10 6 and 1 : 4 × 10 7 ). Two HIV-1 RNA concentrations of the WHO international standard (IS) 97/656 (NIBSC, South Mimms, Potters Bar, Hertfordshire, UK) 10 3 and 10 4 IU/mL were evaluated in the same experiment. Previously, each vial of the international standard was reconstituted in 1 mL of ultrapure water as instructed by the NIBSC to yield a solution containing 10 5 IU/mL of HIV-1 RNA. The determination coefficient r 2 , the curve slope (b) values, and the accuracy in the quantification of different HIV-1 RNA IS concentrations were taken into account to select the working dilution of the IC transcript.

Determination of the HIV-1 Transcript RNA Concentration.
The RNA concentration of the HIV-1 transcript was determined through the qRT-PCR assay described below using a calibration curve built from the IS 97/650 (NIBSC, South Mimms, Potters Bar, Hertfordshire, UK). Each vial of the international standard was reconstituted in 1 mL of ultrapure water as instructed by the NIBSC to yield a solution containing 363 078.05 IU/mL of HIV-1 RNA. It was diluted 10-fold to obtain the calibration curve (363.08 to 363 078.05 IU/mL). Isolation of RNA from IS or lysis reagent containing the HIV-1 transcript was performed as described above. The lysis reagent containing the IC transcript in its working dilution was used in a volume of 500 µL per sample. The HIV-1 transcript was 10-fold serially diluted from 1 : 4 × 10 7 to 1 : 4 × 10 11 in order to quantify it, and the RNA concentration of the original HIV-1 transcript (IU/mL) was obtained by averaging each value multiplied by the dilution factor. HIV-1 transcript dilutions, where the R value was out of the calibration curve range, were considered non quantifiable.

Evaluation of the HIV-1 and IC Transcripts as Standards in an In-House qRT-PCR Assay for Estimation of HIV-1 Viral Load.
For standardization of the assay, the HIV-1 and IC transcripts were included as standards in an inhouse quantitative competitive RT-PCR assay for estimation of HIV-1 viral load. The IC transcript is a 120-bp RNA fragment, which is similar to the HIV-1 target except for a short and unique internal sequence. This transcript is added to the specimen during sample preparation and is simultaneously amplified by PCR in a competitive reaction. The IC transcript was used into the lysis reagent in its working dilution. In order to build the calibration curve, dilutions of the HIV-1 transcript were made to give 10 3 , 10 4 , 10 5 , 10 6 , and 10 7 IU/mL of HIV-1 RNA. The IS was evaluated pure, 1 : 10, and 1 : 100, and also two samples with very high viral load (HIV1-235 and HIV1-157), previously quantified by the NucliSens EasyQ HIV-1 v1.1 assay (bioMerieux, Boxtel, The Netherlands), were evaluated. Different parameters such as the determination of coefficient r 2 and the accuracy in the quantification of the HIV-1 RNA IS and the two reference samples were measured.

Description of the In-House qRT-PCR Assay.
Following sample preparation and setup of the reaction mixture, reverse transcription and amplification of the target and the internal control were simultaneously performed in the same reaction tube. We added 5 µL of the isolated RNA to 25 µL of an RT-PCR reaction mixture that contained 50 pmol of the HIV1-Q3 and HIV1-Biot-Q4 primers, Go Taq buffer, 1.5 mM MgCl 2 , 250 µM each dNTPs, 3.6 u of AMV-RT, 9 u of RNasin ribonuclease inhibitor, and 1.05 u of Go Taq Flexi DNA polymerase (all from Promega, USA). These reactions were carried out in a thermocycler (Eppendorf AG 22331, Hamburg, Germany) at 45 • C for 30 min followed by 95 • C for 3 min and 50 cycles at 95 • C for 30 s, 58 • C for 30 s, and 72 • C for 30 s. The hybridization and detection of the amplified products were done in the ultramicroenzyme-linked oligosorbent assay (UMELOSA) format [22]. It is a detection system similar to the one used by the Amplicor HIV-1 Monitor Test v1.5, from Roche Diagnostic Systems (Branchburg, NJ, USA) [23], but unlike the colorimetric reaction, we use a fluorescence reading. Following PCR amplification, the HIV-1 and IC amplicons were chemically denatured by the addition of denaturation solution. Aliquots were added, in duplicate, to separate wells of a microwell plate coated with HIV-1-specific (HIV1-S) an IC-specific (IC-S1) probes. HIV-1 and IC amplification products were bound to HIV-1 and IC wells, respectively, by hybridization to the microwell plate-bound probes. Following the hybridization reaction, the microwell plate was washed to remove unbound material and a streptavidinalkaline phosphatase conjugate was added to each well of the plate. The conjugate bound to the biotin-labeled amplicon captured by the plate-bound probes. The plate was washed again to remove unbound conjugate, and a substrate 4-Methylumbelliferyl phosphate (4-MUP) was added to the wells. In the presence of this fluorescent substrate, the bound alkaline phosphatase catalyzes the hydrolysis of 4-MUP to produce a fluorescent signal that is detected by an automated microwell plate reader.
The calibration curve, made from HIV-1 reference sample, HIV-1 IS or HIV-1 transcript, was built by weighted linear regression (WLR) [24] from the common logarithms of theoretical viral loads (log 10 VLt ) and ratios of HIV-1 and IC fluorescence signals (log 10 R). HIV-1 RNA concentrations of transcripts and samples were estimated by interpolating log 10 R in the calibration curve.

Determination of the
In-House qRT-PCR Limit of Detection. The 95% detection limit (LoD) or the sensitivity of the in-house qRT-PCR assay was assessed on dilution series of a WHO IS 97/656 (NIBSC, South Mimms, Potters Bar, Hertfordshire, UK). Each vial of the HIV-1 standard (subtype B) was reconstituted in 1 mL of ultrapure water as instructed by the NIBSC to yield a solution containing 100 000 IU/mL of HIV-1 RNA. It was further diluted in HIV-, HCV-, and HBVnegative plasma, resulting in the following concentrations: 50, 100, 250, 500, 1000, 2500, and 5000 IU/mL. The number of replicas tested varied from 5 to 15, and they were run in different days with different reagent lots and operators. A HIV-, HCV-, and HBV-negative cryosupernatant was included, as a negative control, in each run of the assay. We employed the same transcripts and assay conditions that were used in Section 2.6.5. A positive result was considered when the sample fluorescence value was three-fold the fluorescence value of the negative control. The LoD was estimated by Probit analysis [9,11,25,26], using SPSS version 9.0.

Analysis of the Correlation between the In-House qRT-PCR
and NucliSens EasyQ Assays. We analyzed the correlation between our in-house qRT-PCR assay and the commercial NucliSens EasyQ HIV-1 v1.1 assay (bioMerieux, Boxtel, The Netherlands) using linear regression analysis. The quantified values of 14 clinical plasma samples from antiretroviral drugnaïve and treatment-experienced patients were obtained from the "Pedro Kourí" Tropical Medicine Institute (Havana, Cuba), using the NucliSens EasyQ assay. We employed the same transcripts and assay conditions that were used in Section 2.6.5.

Results and Discussion
Because of HIV-1 variability, we selected and designed primers and probes for the in-house qRT-PCR assay that were based on a highly conserved LTR region of the HIV-1 genome. Instead of the gag gene, the use of the LTR region extends the spectrum of detectable and quantifiable genotypes beyond that of many current assays that are not accurate for testing "exotic" HIV-1 subtypes found mainly in developing countries [11].
To prevent PCR inhibition from interfering with accurate quantification, we designed a competitive internal control that used the same amplification primers as HIV-1 and was detected by a probe of different sequence composition.
We also optimized reaction chemistry to evaluate the RNA standards and to quantify the IS and HIV-1 samples.
The amplified HIV-1 and IC fragments were purified and cloned into the pGEM-T vector. The presence of each band in the T vector was checked by amplification using the HIV1-Q3 and HIV1-Biot-Q4 primers, and the fragment orientation was checked by amplification using the T7 Promoter and HIV1-Biot-Q4 primers. In both cases, we obtained the PCR band at the expected length, indicating the presence and the correct orientation of the HIV-1 and IC fragments into the pGEM-T vector.
The pGEM-HIV1 and pGEM-IC plasmids were in vitro transcribed, and the resultant HIV-1 and IC transcripts (T-HIV1 and T-IC, resp.) were purified. Before being diluted in the lysis reagent, an aliquot of the two batches of each transcript was diluted 1 : 20 or 1 : 35 and quantified by measuring the OD at 260 nm. RNA concentration in µg/mL was obtained ( Table 2).
According to McKenna et al. [14], large-scale in vitro transcription of RNA yields varies with the transcript being produced. Expected yields should fall in the range of 200-1000 µg/mL [14]. In one in vitro reaction, ARN concentration was below the lower limit of the expected range because of some loss of sample occurring during the purification step of the T-IC second transcript. This issue has been described by McKenna et al. during the phenol/chloroform extraction of transcripts although they stated that this step is necessary because far greater loss is incurred if the extraction step is omitted [14]. Sample loss during RNA purification, which rather depends on the technical skills of the analyst, allows us to explain the big yield differences obtained among the same transcript batches. In some cases, we obtained RNA yields over the upper limit of the expected RNA concentration range ( Table 2). The ratio of absorbance at 260 and 280 nm (the A260/280 ratio) is frequently used to assess the purity of RNA and DNA preparations. A low A260/280 ratio indicates contamination by proteins [27]. Data presented in Table 2   107.55 ± 0.36 3.35 ± 0.04 1 : 4 × 10 7 11.87 ± 0.38 3.29 ± 0.01 1 : 4 × 10 8 3.43 ± 0 3 .23 ± 0.11 1 : 4 × 10 9 3.46 ± 0. showed A260/280 ratios from 1.54 to 1.70. Similar results were obtained by Okamoto and Okabe [27] when they used DEPC-treated water to dissolve RNA for performing the spectrophotometric determinations. The authors stated that DEPC-treated water did not affect the absorbance at 260 nm but elevated that at 280 nm [27]. We also evaluated the quality of the HIV-1 and IC transcripts. Transcripts with the highest RNA concentration (T-IC-2 b and T-HIV1-2 b ) were 10-fold serially diluted in lysis reagent from 1 : 4 × 10 3 to 1 : 4 × 10 9 . These dilutions were subjected to RT-PCR to evaluate the presence of specific RNA and also subjected to direct PCR without RT in order to test the DNA contamination. Neither PCR signal was obtained for the IC transcript dilutions tested nor for the highest dilutions of the HIV-1 transcript. Specific RT-PCR signals were obtained for both transcripts ( Table 3).
The use of RNA controls must be absolutely free of plasmid DNA carryover from the in vitro transcription reaction [28]. In this sense, Hazari et al. [28] developed and evaluated a competitive RT-PCR assay for HCV RNA in serum using transcribed thioRNA as internal control. This internal control RNA was tested for DNA contamination, and no signal was obtained using 1 µL of undiluted RNA, containing 10 8 molecules/µL [28]. Westerman et al. [29] developed a quantitative reverse transcription-polymerase chain reaction for measuring a marker for small cell lung carcinoma. A standard curve was constructed from a complementary RNA (cRNA) of the Human achaete-scute homologue 1 (HASH1) protein that was obtained by in vitro transcription. The authors demonstrated that complete removal of contaminating plasmid was essential for accurate quantification, and this was achieved by overnight incubation with RQ1 DNase One during cRNA purification [29].
In order to develop an in-house qRT-PCR assay for HIV-1 RNA and taking into account the very high yields that are obtained in the in vitro transcription reactions [19],   1.29E + 14 1 : 4 × 10 9 1.50E + 14 1 : 4 × 10 10 1.02E + 14 1 : 4 × 10 10 7.05E + 13 1 : 4 × 10 11 2.21E + 14 we used the dilutions of the transcript T-HIV1-2 b in which DNA signal was not obtained. We determined the working dilution of the transcript T-IC-2 b which acts as internal control of an in-house qRT-PCR assay for HIV-1 RNA. Several 10-fold dilutions of positive HIV-1 human plasma were obtained for constructing a calibration curve (10 2 to 10 6 IU/mL), and four dilutions of the transcript T-IC-2 b were evaluated.
As observed in Table 4, the dilution required for the IC transcript to work optimally was 1 : 4 × 10 6 , in which the r 2 and the curve slope reached the maximum value. In the selected IC working dilution, the qRT-PCR assay was able to quantify the two IS concentrations (10 3 and 10 4 IU/mL) accurately, with log 10 differences below ±0.5 log 10 of the expected units (Table 4). As discussed by some authors, a minimally significant change in plasma viremia is considered to be a three-fold or 0.5 log 10 increase or decrease [30][31][32].
HIV-1 transcript was quantified so as to introduce it as standard in the qRT-PCR assay. For this purpose, we used the IS 97/650 to obtain the calibration curve and the transcript T-IC-2 b in its working dilution. Transcript T-HIV1-2 b was 10-fold serially diluted from 1 : 4 × 10 7 to 1 : 4 × 10 11 and quantified using the calibration curve showed in Figure 1.
The RNA concentration estimated for the transcript T-HIV1-2 b was similar to the ones obtained by González et al., in which the log 10 orders of estimated HCV RNA concentrations were higher than 11 for all transcripts they obtained [19]. In our study, we obtained HIV-1 RNA concentrations about 10 14 IU/mL (Table 5), allowing us to use the HIV-1 transcript as standard for quantification purposes in calibration curves that commonly have maximal concentrations with log 10 orders between 5 and 9 [19,29].
HIV-1 and IC transcripts were included as standards in an in-house qRT-PCR assay for estimating the HIV-1 viral load from plasma samples. The calibration curve was built from the HIV-1 transcript (T-HIV1-2 b ), and the transcript (T-IC-2 b ) in its working dilution was used as internal control. Different HIV-1 RNA concentration of the IS and two reference plasma samples with very high viral load were tested to evaluate the accuracy of the assay using these HIV-1 controls. Figure 2 shows the calibration curve obtained with the inclusion of the HIV-1 and IC transcripts as standards. It was obtained a regression line with an r 2 = 0.99. All results were found to be within ±0.5 log 10 unit of the expected  results (Table 6), which is considered not significant for the quantification assay employed [30][31][32]. Similar results were obtained by Muller et al., who evaluated five HIV-1 controls from 10 2 to 5 × 10 4 copies/mL using a quantitative Abbott LCx HIV RNA assay, and all results were found to be within ±0.32 log 10 unit of the expected results [31]. In order to consider if a biological change in the viral load is significant or not, we show here the intra-and inter-assay variability of the assay using three serum samples with different viral load values. These samples were repeated 24 times in this precision study. Precision is defined as the standard deviation of the log-transformed values [9]. In our study, intra-assay precision was 0.  [9]. The percentage of positive results corresponding to each HIV-1 RNA concentration tested by the in-house qRT-PCR assay is shown in Table 7. Using Probit analysis, the concentration of HIV-1 RNA with 95% detection was estimated to be 511.0 IU/mL (95% confidence interval, 433.4-588.6 IU/mL). The LoD for the Amplicor HIV-1 Monitor test v1.5 (Roche Diagnostic Systems, Branchburg, NJ, USA) using the standard specimen preparation procedure was 200 copies/mL [33] or 312.5 IU/mL if we take into account the Roche conversion factor, 0.64 [34]. This Roche test is In-house qRT-PCR assay (log IU/mL) NucliSens EasyQ (log IU/mL) y = 0.937x + 0.142 r 2 = 0.855 r = 0.925 based on a similar assay methodology to that of our in-house qRT-PCR assay.
The sensitivity obtained for our in-house qRT-PCR assay was similar to the one obtained with the NucliSens EasyQ HIV-1 (500.0 IU/mL) using 0.2 mL of input sample volume [10,32].
The analysis of correlation between our in-house qRT-PCR assay and the NucliSens EasyQ HIV-1 test is shown in Figure 3. The correlation between the two assays was high (r = 0.925). A similar correlation coefficient (r = 0.91) was obtained by Choi et al., who compared the NucliSens EasyQ HIV-1 v1.1 (bioMerieux) and RealTime HIV-1 (Abbott) kits [1]. The correlation coefficient of the NucliSens EasyQ HIV-1 kit with the Cobas Amplicor HIV-1 Monitor v1.5 (Roche Diagnostic Systems, Branchburg, NJ, USA) test, which is based on traditional PCR method instead of real-time PCR, was 0.87 [9].
A high correlation between different assays is important because the data on HIV-1 RNA quantitation are collected from various laboratories using different kinds of assay kits nationwide [1]. However, it has been recommended using the same method and also possibly the same laboratory to monitor patients [35].
Human plasma or serum samples can be indistinctly used in our in-house qRT-PCR assay because they were both evaluated, and no significant viral load differences were found between them (data not shown).
It was observed a good linear behavior along the calibration curve built with the transcripts, which reached maximum HIV-1 RNA concentration near 10 7 IU/mL or 7 log 10 ( Figure 2). As discussed by Yao et al., the ability to quantify HIV-1 RNA over a 5 log 10 is important in this kind of assays that are used to evaluate a variety of patient populations with a wide range of viral loads. This is an important asset when a normal clinical laboratory test run includes samples from newly diagnosed untreated patients, who generally have a higher viral load than chronic HIV-1 infected adults. This feature also eliminates the need for reflex repeat testing, improves turnaround time for results, and is associated with significant savings in both technical time and reagent costs [32].
In summary, the HIV-1 and IC transcripts were obtained with the required quality to be used as standards for quantification purposes, considering also the advantage of their long-term stability when stored in the lysis reagent [20,21]. It was obtained a high correlation between our assay and a commercial one. On the other hand, one of the major benefits of our method is cost reduction. Commercially assays are currently offered, even in developing countries, at prices of approximately US $50-$100 per test [10,11]. For our inhouse HIV-1 viral load assay, the net price would be reduced considerably.