Viral replication is enhanced by an HIV-1 intersubtype recombination-derived Vpu protein

Abstract

Background

Multiple HIV-1 intersubtype recombinants have been identified in human populations. Previous studies from our lab group have shown that the epidemic in Argentina is characterized by the high prevalence of a circulating recombinant form, CRF12_BF, and many related BF recombinant forms. In these genomic structures a recombination breakpoint frequently involved the vpu coding region. Due to the scarce knowledge of Vpu participation in the virion release process and its impact on pathogenesis and of the functional capacities of intersubtype recombinant Vpu proteins, the aim of this work was to perform a comparative analysis on virion release capacity and relative replication capacity among viral variants harboring either a BF recombinant Vpu or a subtype B Vpu.

Results

Our results showed that BF recombinant Vpu was associated to an increased viral particles production when compared to WT B variant in tetherin-expressing cell lines. This observation was tested in the context of a competition assay between the above mentioned variants. The results showed that the replication of the BF Vpu-harboring variant was more efficient in cell cultures than subtype B, reaching a higher frequency in the viral population in a short period of time.

Conclusion

This study showed that as a result of intersubtype recombination, a structurally re-organized HIV-1 Vpu has an improved in vitro capacity of enhancing viral replication, and provides evidence of the changes occurring in this protein function that could play an important role in the successful spread of intersubtype recombinant variants.

Background

Multiple HIV-1 intersubtype recombinants have been identified in human populations. To date, more than 40 circulating recombinant forms (CRFs) have been described (Los Alamos HIV Database). In South American countries such as Argentina and Brazil, the epidemic shows considerable diversity in terms of subtypes and CRFs. Previous studies from our lab group have shown that Argentina is characterized by the co-circulation of intersubtype recombinants, mainly BF [1-7] and subtype B viruses. Nucleotide sequence analyses showed that HIV-1 BF recombinants exhibit diverse mosaic structures and that the prototypic CRF12_BF genome mainly corresponds to subtype F1 with five segments of subtype B distributed all along the genome [1,5,6]. In these genomic structures a recombination breakpoint frequently involved the vpu coding region. The resulting recombinant protein structure exhibits a subtype B membrane-spanning domain and α- helix I, and a subtype F1 α- helix II.

Regarding protein functions, two distinct biological activities have been attributed to Vpu: a) proteasomal degradation of CD4, and b) enhancement of virion release from infected cells. Although the mechanism by which Vpu degrades CD4 is well delineated [8-10], its enhancing effect on virion release is not fully clarified. It was shown that the transmembrane domain of the protein forms cation-selective ion channels in cellular membranes and that this feature might be involved in facilitating virion release [11,12]. Nevertheless, recent studies have shown that Vpu-dependent virion release is related to its capacity to counteract an INFα-inducible host restriction factor known as Bst-2/CD317/tetherin [13-15].

Since data on Vpu participation in the virion release process and its impact on pathogenesis is still incomplete and scarce, and on account of the remarkable protein diversity, and that most studies have been conducted on Vpu protein from subtypes B or C, the present study was aimed at analyzing the virion release capacity of a naturally occurring BF recombinant Vpu, and its comparison with its pure subtype B counterpart. A chimeric variant harboring a naturally occurring BF recombinant vpu coding sequence on a subtype B genetic background (NL4-3) was generated and used for the studies. Our results show that the BF recombinant Vpu is capable of enhancing virion release more efficiently, suggesting an improvement in this function as a consequence of an intersubtype recombination event.

Results

Structural characterization of naturally occurring BF intersubtype recombinant Vpu sequences

A previous study from our lab group found a high percentage of BF recombinant strains (56.9%, n = 283) among drug-naïve newly diagnosed HIV-1 individuals [7]. When re-analyzing this group of samples we found that 109 out of 161 (67.7%) of these recombinant variants exhibited a recombination pattern which involved the vpu coding region. The analysis of these sequences was performed by means of a tool to detect HIV-1 genomic recombinants available online at http://jphmm.gobics.de/, and confirmed by bootscaning analysis (Simplot V3.5.1). Seventy four (68.3%) sequences presented a very similar recombination pattern to that observed in CRF12_BF, where the breakpoint was located between positions 6195 and 6205 of the genomic sequence, according to the HXB2 numbering.

A naturally occurring BF recombinant was selected for the biological analysis. This variant, named CRF12_BF-like, was chosen because it shares a similar recombination pattern to that observed in the prototypic CRF12_BF [1] (Figure 1A) where the membrane-spanning domain and the α-helix I intracytoplasmic domain (positions 1-50), and the α-helix II together with the 10 C-terminal aminoacids (positions 51-81) correspond to subtypes B and F1 respectively. Comparison of its primary amino acid sequences (CRF12_BF vs. CRF12_BF-like) showed that only 9 out of 81 residues (11.1%) differ from each other, i.e. T6I, A22V, S24T, I43L, E58D, F67L, E69D, L72P, and N80I (Figure 1B). An additional analysis performed on 74 recombinant sequences showed that these substitutions did not occur as inherent features of the selected CRF12_BF-like variant. Even more, some of them were highly represented among the naturally occurring recombinants.

Figure 1.

A. Comparison of bootscaning analysis performed on CRF12_BF and CRF12_BF-like showed a similar recombination pattern, with a breakpoint located between α-helix I and II. Reference sequences of subtype B (red), F (black), and A (blue) - out group - were obtained from Los Alamos Database. Plots represent bootstrap values based on 100 re-samplings, supporting branching with reference sequences within a 140 nt window moving in steps of 20 bases.

The structural domains as well as the phosphorylation sites (asterisks) of Vpu are shown in Figure 1B. Underlined residues represent differences between CRF12_BF and CRF-like variant.

C. Diagram depicts the construction step of a chimeric viral genome: vpu coding sequence from a naturally occurring BF intersubtype recombinant variant (named CRF12_BF-like) amplified by PCR from a genomic DNA sample obtained from an infected patient. The use of modified oligonucleotides allowed the introduction of both PacI and Eco47III restriction sites. The purified PCR product was cloned into a commercial vector (pGEM-T) to obtain the pVpuBF plasmid. In parallel, these restriction sites were introduced in pNL4-3 by PCR-based site-directed mutagenesis. After digestion and ligation steps a chimeric variant harboring the Vpu BF sequence into the subtype B genomic background (pNL4-3 VpuBF) was obtained.

A serine residue, either at position 61 or 64 (S61 or S64) has been shown to be involved in the regulation of Vpu degradation process [16]. Neither S61 nor S64 were present in the CRF12_BF-like variant. Additionally, the analysis of B (n = 137), F1 (n = 12) and BF recombinant (n = 120) Vpu sequences (Los Alamos Database) from Argentina, Brazil, and Uruguay showed that S64 was present in 82% and 6.6% of B and BF sequences respectively. This residue was not found among F1 sequences. None of the whole set of sequences harbored the S61 residue.

The comparative analysis of Vpu amino acid sequences performed among the variants used in this work, in terms of protein domains, is shown in Table 1. Most of the differences were found in the α-helix II and C-terminal domains. Of note, net charge of these domains differed among variants. BF has + 4 and - 5 charges in the α-helix I and α-helix II respectively, compared to the + 3 and - 4 charges found in the subtype B variant. The net charge of C-terminal domains remained constant (-1) although amino acid changes were found.

Table 1.

Comparative analysis of amino acid differences between subtype B and CRF12_BF-like variants. Positions are shown according to protein domains.

N-Terminal							Transmembrane					α-Helix I
Positions	3	4	5				7	16	18	24	27	43	46	47
Subtype B	P	-	I				V	I	I	S	I	I	L	I
CRF12_BF-like	S	L	V				L	A	L	T	L	L	I	R
α-Helix II												C-Terminal
Positions	58	60	61	62	63	65	66	67	68	69	70	73	74	75	77	78	81
Subtype B	E	E	V	S	A	V	E	M	G	V	E	H	H	A	W	D	D
CRF12_BF-like	D	D	A	E	E	A	A	-	L	G	G	P	L	I	G	N	I

Functional analysis of BF intersubtype recombinant Vpu

vpu mRNA is correctly synthesized from the BF Vpu harboring-chimeric variant

A chimeric viral genome, named pNL4-3 VpuBF, harboring the CRF12_BF-like Vpu sequence on a pure subtype B (NL4-3) background (Figure 1C), was generated to evaluate the consequences of intersubtype recombination involving the vpu coding region on viral particles release enhancement.

In order to test the vpu mRNA expression, HeLa cell cultures were transfected either with pNL4-3 VpuBF, pNL4-3 VpuB and pNL4-3 ΔVpu plasmids. Forty eight hours post-transfection total mRNA content was obtained from each transfected culture, and vpu mRNA production was evaluated by qualitative RT-PCR. β-actin mRNA was used as control. All transfected cell cultures exhibited comparable expression levels of vpu mRNA (Figure 2).

Figure 2.

Vpu expression was assessed by specific RT-PCR of vpu mRNA after transfection of HeLa cells. Both untransfected (UT) cells and cells transfected with empty vector (NC) were used as control (right panel). Amplification of β-actin mRNA was also evaluated as an internal control (left panel).

BF Vpu correlates with an increased viral release in Vpu-dependent cell line models

This study was aimed at evaluating the impact of BF recombinant Vpu on viral release by transfecting both HeLa and 293T cell lines with pNL4-3 VpuBF, pNL4-3 VpuB and pNL4-3 ΔVpu. As previously described, HIV-1 Vpu is essential for viral replication in certain cell lines (e.g. HeLa) but dispensable in others (e.g. 293T) [13-15,17]. Viral production was monitored by quantifying p24 antigen in cell culture supernatants 24 and 48 h post-transfection.

In HeLa cells, transfection with pNL4-3 VpuBF resulted in a substantially higher p24 antigen concentration in culture supernatant when compared with that of the subtype B counterpart and ΔVpu, at 24 h post-transfection (22.5 pg/ml, 4.9 pg/ml and 0.4 pg/ml respectively). This difference persisted after 48 h post-transfection (114.7 pg/ml vs. 25.6 pg/ml), showing an approximately 4.5-fold increase in p24 production when the intersubtype recombinant protein was present (Figure 3A).

Figure 3.

HeLa (A) and 293T cells (B) were transfected with plasmids pNL4-3 VpuB, pNL4-3 Vpu BF, and pNL4-3 ΔVpu, separately. Viral production was evaluated, using an ELISA assay, by measuring the Gag p24 antigen content in cell culture supernatants 24 and 48 hours post-transfection. Jurkat cells (C) and CEM-GFP (D) were infected with equal MOI of NL4-3 Vpu B, NL4-3 Vpu BF and NL4-3 ΔVpu virus stock, and viral replication was monitored by measuring the virus-associated reverse transcriptase activity in culture supernatants. Error bars indicate standard errors. Results are representative of two independent experiments.

The evaluation of post-transfection viral production in 293T cell cultures with the variants studied showed no significant differences in the p24 content of culture supernatants (Figure 3B), confirming that both pNL4-3 and pNLVpuBF promoted viral release with similar efficiency in this Vpu-independent cell model.

Viral release was also evaluated in Jurkat and CEM-GFP cell lines, both known to constitutively express tetherin [13,18] and representing Vpu-dependent models. As described in the Materials and Methods section, Jurkat and CEM-GFP cell cultures were infected with each viral stock (NL4-3 VpuBF, NL4-3 VpuB, NL4-3 ΔVpu), and viral production kinetics was evaluated by quantitation of virus-associated RT activity in culture supernatants. After 24 h, comparable levels of infection were achieved for each virus in both Jurkat and CEM-GFP cell cultures, evaluated as percentage of p24 (+) or GFP-expressing cells (FACS) respectively (data not shown).

Viral production was significantly higher for the NL4-3 VpuBF in both Jurkat and CEM-GFP cell cultures (1.5-fold and 1.8-fold respectively), when compared to the wild type variant (Figures 3C and 3D).

Relative in vitro replication capacity

The relative replication capacity of WT subtypes B and chimeric BF variants was tested in vitro by performing a competitive dual infection. Both variants were used to infect CEM-GFP cell culture, in duplicate, and maintained up to 21 days post-infection (p.i.). Viral population analysis was performed on days 1, 12 and 21 p.i. by cloning and sequencing the vpu coding region, as described in the Material and Methods section. Of note, subtype B sequences were predominant at the beginning (B/BF ratio: 1.52) but its ratio changed over time; the recombinant variant became more frequent (B/BF ratio: 0.99) at the end of the experiment. B/BF variants ratio at each time point is depicted in Figure 4.

Figure 4.

NL4-3 VpuB and NL4-3 VpuBF viruses were competed against each other by infecting CEM-GFP reporter cells with p24-normalized inocula at 1:1 ratio. Each variant ratio was determined by clonal analysis of viral population present in culture supernatants. Error bars indicate standard errors. Results are representative of two independent experiments.

Discussion

The vpu coding sequence is one of the most variable regions of the HIV-1 genome [19]. It is unknown if this variability and the diversity among different HIV-1 subtypes [20] may have an effect on protein functions, and to what extent this effect may have an impact on HIV-1 transmission and pathogenecity.

A recent report has shown that only HIV-1 strains from the M group express a fully functional Vpu protein and the authors postulate that this may explain the global HIV/AIDS pandemic for the HIV-1 M group [21]. However, most of the structural and functional studies on Vpu have been performed on subtype B proteins. Hence, little is known about the functionality of non-subtype B Vpu, not even about its function as a viral release enhancer. In this work we performed a comparative analysis between subtype B and BF intersubtype recombinant Vpu proteins, focusing on this important function.

The structural analysis carried out on naturally occurring BF recombinant Vpu sequences revealed high conservation of the recombination pattern. This pattern was similar to that observed in the prototypic BF recombinant, CRF12_BF, where the breakpoint is located in the region coding for an amino acid stretch predicted to form a random-coil structure [20]. This region contains two serine residues (S52 and S56), targeted by the casein kinase II, which phosphorylation is an essential step in recruiting the β-TrCP complex and subsequent proteasome-mediated degradation of CD4 [10,22,23]. Recent studies suggest that Vpu may induce internalization and degradation of tetherin by the same pathway [18,24,25].

On the other hand, Vpu degradation is accomplished through a β-TrCP independent mechanism that involves phosphorylation of a serine residue at position 61 or 64. Lack of these residues has been shown to increase the protein stability without affecting the CD4 degradation [16,26]. We have found that S61 was absent in the CRF12_BF and all related BF recombinant Vpu sequences, and that only 6.6% of them presented the S64 residue. Neither CRF12_BF nor the CRF12_BF-like variant harbored S61 or S64, which might suggest that the turnover of the recombinant variants could be different from the pure subtype counterpart, partly explaining at least the higher viral release associated to the former.

It has been shown that an intact transmembrane domain of HIV-1 Vpu is important and sufficient to enhance HIV-1 particle release [12,27]. This domain is a critical determinant of its function since it physically interacts with the BST-2 transmembrane domain leading to its degradation [28,29]. As determined by the comparative analysis of Vpu amino acid sequences performed in this work, 5 amino acid changes were found between the variants studied, and all of the substitutions were conservative, i.e. amino acids belonging to the same chemical group, suggesting a consequent functional conservation of this domain.

Our results showed that BF Vpu increased viral particles production when compared to the WT B variant in tetherin-expressing cell models. As shown in the results obtained from the in vitro competition assay, this difference in viral production might represent an advantage for the virus in terms of replication capacity or fitness.

According to the structural characteristics of the recombinant protein, the interchange of the second half of the Vpu coding sequence, encompassing the α-helix II and the C-terminal segment between subtypes B and F1, may have resulted in an alternative protein form with enhanced regulation capacity of the host cell environment.

Previous molecular studies from our lab group have shown that BF intersubtype recombination frequently affected genomic regions involved in regulating viral gene expression, replication, and interaction with the host immune system [30-35]. Taken together, these results sustain the idea that this phenomenon might have played an important role in the successful spread of the resulting variants, arguing in favor of the intersubtype recombination as a powerful source of variability and adaptation capacity.

As accessory proteins and/or their cellular counterparts are nowadays seen as promising future therapeutic targets [36-39], results presented here contribute to the comprehensive and profound knowledge of protein functions and its variations needed to develop more effective and specific therapeutic agents aimed at blocking viral replication.

Conclusion

As described above, our results show that intersubtype recombination gave rise to a structurally re-organized HIV-1 Vpu variant with an improved capacity of enhancing viral replication, when tested in vitro. Although these results correspond to a single recombinant isolate, it provides evidence on the changes in the protein function that could play a role in the spread of intersubtype recombinant variants, having implications on HIV-1 epidemiology and pathogenesis. These data are also important in the context of future therapeutic approaches.

Methods

Plasmids, cells and viruses

The vpu coding sequence from a naturally occurring BF intersubtype recombinant variant (named CRF12_BF-like) was amplified by PCR from a genomic DNA sample obtained from an infected patient identified in a previous study conducted in Argentina [7]. PCR reaction was carried out by using a high fidelity DNA polymerase (Platinum^® Taq DNA Polymerase High Fidelity, Invitrogen). Oligonucleotides used for the reaction were:

VpuBF/PacI (5'-TTAATTAAGCTTCTCTATCAAAGC-3')

VpuBF/Eco47III (5'-AGCGCTAAAGAAAAATTGTGGGTC-3')

Modifications in the oligonucleotides allowed obtaining a PCR product harboring both PacI and Eco47III restriction sites at the 5' and 3' ends of the vpu coding sequence respectively. The amplicon was subcloned into a commercial vector (pGEM-T^® easy vector, Promega) according to the manufacturer's instructions. The resulting transformants were screened for the insert and the plasmids were sequenced to ensure that BF recombinant vpu sequences and restriction sites were intact. The resulting plasmid was named as pVpuBF.

Insertion of the BF vpu gene into HIV-1 molecular clone pNL4-3 [40] (obtained from Dr Malcolm Martin through the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH) was accomplished in a two-step procedure. The first step involved the introduction of PacI and Eco47III restriction site at the 5' and 3' ends of the pNL4-3 vpu coding sequence respectively, by site-directed mutagenesis. Oligonucleotides used for this step were:

VpuB/PacI (5'-GCTCATCAGAACAGTCAGATTAATTAAGCTTCTCTATCAAAGC-3')

VpuB/Eco47III (5'-GGGATATTGATGATCTGTAGCGCTACAGAAAAATTGTGGGTC-3')

The second step consisted in the replacement of the WT pNL4-3 Vpu coding sequence with the CRF12_BF-like Vpu sequence, followed by reversion of the changes introduced to the original sequence by a new cycle of site-directed mutagenesis. Briefly, both pNL4-3 PacI/Eco47III and pVpuBF were digested with each restriction enzyme. Ligation of the pNL4-3 PacI/Eco47III backbone and the VpuBF PacI/Eco47III insert was performed by T4 ligase (Invitrogen). Oligonucleotides used for the site-directed mutagenesis reaction were:

VpuPacIrevt (5'-GCTCATCAGAACAGTCAGACTCATCAAGCTTCTCTATCAAAGC-3')

VpuEco47IIIrevt (5'-GGGATATTGATGATCTGTAGTGCTACAGAAAAATTGTGGGTC-3')

Again, the resulting transformants were screened for the insert and any possible unwanted changes in the generated plasmid.

Mini and midipreps of selected clones were obtained (QIAgen).

All mutagenesis reactions were performed by using a highly processive DNA polymerase with proofreading 3'-5' exonuclease activity (Platinum^®PfxDNA Polymerase, Invitrogen). Sequencing was performed on an automatic sequencer (Applied Biosystems DNA sequencer 3100) by using the Big Dye Terminator sequencing kit (Amersham, Sweden). Nucleotide sequences were analyzed and manually adjusted using Sequencher 4.0.5 software (Gene Codes Co, USA).

The Vpu-deficient plasmid pNL4-3 ΔVpu[41] (obtained from Dr. Klaus Strebel through the AIDS Research and Reference Reagent Program, Division of AIDS, NIAID, NIH) contains a defective vpu gene, but is otherwise identical to the infectious molecular clone pNL4-3.

HeLa, 293T, MT2, Jurkat T and CEM-GFP cells were used in this study. HeLa and 293T were cultured in DMEM medium (Gibco^®) supplemented with 10% fetal bovine serum (FBS, Gibco^®), 2 mM L-glutamine (Gibco^®), penicillin/streptomycin (100 IU/ml and 100 μg/ml respectively, Gibco^®). MT2 and Jurkat T cells were cultured in RPMI-1640 medium (Gibco^®) supplemented with 10% FBS, 2 mM L-glutamine, 100 U/ml penicillin and 100 μg/ml streptomycin. CEM-GFP cells were cultured in the same medium plus 500 μg/ml G418. Cell lines were obtained through the AIDS Research and Reference Reagent Program.

293T cells transient transfections were carried out using Lipofectamine2000 (Invitrogen) following manufacturer's instructions. For single transfections experiments confluent cells grown in 24-well dish were transfected with 0.8 μg of pNL4-3 Vpu B, pNL4-3 VpuBF and pNL4-3 ΔVpu.

Viral stocks were obtained by infecting MT2 cells. Briefly, 2×10⁶ cells were infected with 1 ml of culture supernatant from 293T cell culture transfections. Afterwards, cells were washed twice with PBS and maintained in culture medium, until CPE was observed. Viral stock titrations (TCID 50/ml values) were performed by using the Reed and Muench method [42].

RT-PCR

HeLa cells transient transfections were carried out using Lipofectamine2000 (Invitrogen) following manufacturer's instructions. For single transfections experiments confluent cells grown in 60 mm Petri dishes were transfected with 8 μg of pNL4-3 Vpu B, pNL4-3 Vpu BF and pNL4-3 ΔVpu. Untransfected cells as well as cells transfected with empty vectors were always used as negative controls.

Total cellular RNA was extracted from 10⁷ cells using Trizol^® reagent (Invitrogen). Three μg of RNA were reverse transcribed using MMLV reverse transcriptase (Invitrogen) and an oligo-dT primer. The mix was supplemented with RNAse inhibitors (Invitrogen) in a final volume of 20 μl. Two μl of cDNA were used for vpu PCR amplification using the following oligonucleotides:

VpuB fw (5'-CCTCTAGATAATGCAACCTATAATAG-3');

VpuB rev (5'-CACGCGTCTACAGATCATCAATATCC-3');

VpuBF fw (5'-CCTCTAGATAATGCAATCTTTAG-3') and

VpuBF rev (5'-CACGCGTCTACAGAATATCAATATTC-3').

PCR amplification of β-actin, used as RNA quality control, was performed by using the following oligonucleotides:

β1 (5'-GGACCTGACTGACTACCTCATGAA-3')

β2 (5'-GATCCACATCTGCTGGAAGGTGG-3').

Vpu recombinant sequences analysis

BF recombinant Vpu sequences were obtained from Los Alamos HIV sequence database. A multiple alignment with reference sequences was performed using Clustal W, and visually corrected with the BioEdit version 5.0.9 program http://www.mbio.ncsu.edu/BioEdit/bioedit.html.

Detection of intersubtype genomic recombination was carried out by a tool available online at http://jphmm.gobics.de. This method uses a probabilistic approach to compare a sequence to a multiple alignment of a sequence family [43]. Recombination analysis was confirmed by bootscanning analysis as implemented in the SimPlot v.3.5.1 program.

HIV-1 production assay: transfections and infections

HeLa and 293T cells were transfected with 0.8 μg of pNL4-3 VpuB, pNL4-3 VpuBF and pNL4-3 ΔVpu together with 0.05 μg of GFP expression vector used as a control for the transfection, using Lipoafectamine2000 (Invitrogen) and following manufacture's instruction. Cell culture supernatants were collected 24 and 48 hours post-transfection. HIV-1 p24 antigen quantitation was performed by means of a commercial ELISA assay (Murex, Abbott).

For viral replication kinetics analysis, 10⁶ logarithmically growing Jurkat or CEM-GFP suspension cells were infected in duplicate with each viral stock (NL4-3 VpuB, NL4-3 VpuBF and NL4-3 ΔVpu) at MOI of 0.01. Afterwards, cells were washed twice with PBS and maintained in culture medium. Cell culture supernatants were harvested at different time points and assayed for RT activity, using the Reverse Transcriptase Colorimetric Assay (Roche) following manufacture's instruction.

Growth competition assay

Competitive growth of NL4-3 Vpu B and NL4-3 Vpu BF viruses was analyzed as recently described [44]. Briefly, 2×10⁶ CEM cells were infected in duplicate with wild-type and the BF chimeric variants at a ratio 1:1. Cells samples were collected at 3 time points (1, 12 and 21 d.p.i.), and genomic DNA was extracted using the QIAamp DNA Mini kit (QIAgen). Vpu coding sequence was PCR amplified from proviral DNA with primers ACC7 (5'-CTATGGCAGGAAGAAGCGGAGA-3') and ZM140E (5'-GGGGTCAACTTTACACATGGCTTT-3'). PCR products were gel-purified (QIAquick gel extraction kit) and cloned into a commercial cloning vector (pGEMT-EASY^®, Promega). Nucleotide sequencing was performed as described above.

Statistical analysis

All data was expressed as mean ± SD unless otherwise stated. Significance (p < 0.05) between means of experiments was evaluated using the Student's t test for independence samples (Primer of Biostatistics version 4.02 software)

Competing interests

The authors declare that they have no competing interests.

Authors' contributions

CDC contributed to the design of the study, to perform the experiments, and to write the manuscript. GD and YG contributed to perform the experiments. CE provided technical support during cloning and sequencing procedures. GT and HS contributed to design the study, data interpretation and discussion. MC contributed to design the study, to supervise experimental design, data interpretation and discussion and to write the manuscript. All authors read and approved the final manuscript.

Acknowledgements

We thank Sergio Mazzini for his excellent work in manuscript editing and language revision, and to Andrea Rubio and Monica Saracco for their technical assistance on automated sequencing and flow cytometry respectively.

CDC, CE, GT, HS and MC were supported by the Argentinean National Research Council (CONICET). This research was partially funded by the Argentinean Agency for the Promotion of Science and Technology (ANPCYT, Grant N° 01276).

YG was supported by a Fogarty International Center/NIH grant through the AIDS International Training and Research Program at Mount Sinai School of Medicine-Argentina Program (Grant # D43TW 001037).