The role of the humoral immune response in the molecular evolution of the envelope C2, V3 and C3 regions in chronically HIV-2 infected patients
© Borrego et al; licensee BioMed Central Ltd. 2008
Received: 29 May 2008
Accepted: 08 September 2008
Published: 08 September 2008
This study was designed to investigate, for the first time, the short-term molecular evolution of the HIV-2 C2, V3 and C3 envelope regions and its association with the immune response. Clonal sequences of the env C2V3C3 region were obtained from a cohort of eighteen HIV-2 chronically infected patients followed prospectively during 2–4 years. Genetic diversity, divergence, positive selection and glycosylation in the C2V3C3 region were analysed as a function of the number of CD4+ T cells and the anti-C2V3C3 IgG and IgA antibody reactivity
The mean intra-host nucleotide diversity was 2.1% (SD, 1.1%), increasing along the course of infection in most patients. Diversity at the amino acid level was significantly lower for the V3 region and higher for the C2 region. The average divergence rate was 0.014 substitutions/site/year, which is similar to that reported in chronic HIV-1 infection. The number and position of positively selected sites was highly variable, except for codons 267 and 270 in C2 that were under strong and persistent positive selection in most patients. N-glycosylation sites located in C2 and V3 were conserved in all patients along the course of infection. Intra-host variation of C2V3C3-specific IgG response over time was inversely associated with the variation in nucleotide and amino acid diversity of the C2V3C3 region. Variation of the C2V3C3-specific IgA response was inversely associated with variation in the number of N-glycosylation sites.
The evolutionary dynamics of HIV-2 envelope during chronic aviremic infection is similar to HIV-1 implying that the virus should be actively replicating in cellular compartments. Convergent evolution of N-glycosylation in C2 and V3, and the limited diversification of V3, indicates that there are important functional constraints to the potential diversity of the HIV-2 envelope. C2V3C3-specific IgG antibodies are effective at reducing viral population size limiting the number of virus escape mutants. The C3 region seems to be a target for IgA antibodies and increasing N-linked glycosylation may prevent HIV-2 envelope recognition by these antibodies. Our results provide new insights into the biology of HIV-2 and its relation with the human host and may have important implications for vaccine design.
The etiologic agents of AIDS, HIV-1 and HIV-2, are two distinct human lentiviruses with similar structural and genomic organization but sharing only 50% of genetic similarity . Compared to HIV-1, the infection by HIV-2 is associated with better prognosis, slower disease progression and transmission, longer latency period and reduced mortality rate [2–6]. Moreover, most HIV-2 patients have normal CD4+ T cell counts and low or undetectable plasmatic viral levels [7, 8]. Two possible explanations for these differences may be the slower replication capacity of HIV-2 and a more efficient immune control of HIV-2 [9–13].
The env gene codes for the viral envelope glycoproteins, which are responsible for HIV entry into cells . Rapid evolutionary changes and high genetic variability are two major characteristics of the HIV env gene . In HIV-1 infection, conflicting associations have been reported between disease status and within-patient env gene evolution. Hence, some studies have shown that genetic diversity and divergence from the infecting strain increase during HIV-1 infection but become stable or even decrease in the advanced stage of disease, with the lower CD4+ T cell counts and progression to AIDS [16–18]. Other authors have shown that higher genetic diversity and divergence are found in patients with rapid progression to disease than in slow- or non-progressors [19, 20]. There is also a positive correlation between viral replication and intrahost HIV-1 evolution in elite controllers and long-term nonprogressors .
The number of studies investigating within-patient HIV-2 molecular evolution and their association with clinical and immunological evolution is limited. In one transversal study, we have shown that the genetic diversity of the HIV-2 env may be directly related to the period of infection . Longitudinal studies performed in Senegal have shown that higher variability in the env V3 region is generally found in patients with faster disease progression to AIDS  and that in elite controllers (patients infected for ≈ 10 years with normal CD4+ T cell counts without antiretroviral therapy and with low or undetectable viral load) the rate of env gene diversification may be positively associated with the rate of CD4+ T cell number decrease .
Higher rate of molecular evolution, with predominance of nonsynonymous amino acid substitutions, tends to occur in regions of the HIV-1 env gene submitted to strong selective pressure from the immune system [15, 25–28]. A structure of particular importance in this process is the V3 loop of the surface glycoprotein which is essential for HIV coreceptor usage [29–32] and for inducing the production of neutralizing and nonneutralizing antibodies in HIV infected individuals . Neutralizing antibody responses, both autologous [34–36] and heterologous [36, 37] may be more common in HIV-2 than in HIV-1 infection. Still, little is known about the role of humoral immunity in the evolution of the HIV-2 env gene. In the present study we analyze, for the first time, the molecular evolution of the env C2V3C3 regions in chronically HIV-2 infected patients over a two to four year period in the context of their antibody response (IgG and IgA) against the same envelope region.
Virological and immunological characterization of the patients
Year of diagnosis
CD4+ T cells/μl
Antibody reactivity against C2V3C3 (OD/cut-off)
Quantification of HIV-2 plasma viremia
HIV-2 viremia in the plasma was quantified with a quantitative-competitive RT-PCR assay as described elsewhere .
DNA extraction, PCR amplification, cloning and sequencing
PBMCs from all patients were co-cultivated with normal PBMCs to try to isolate virus . At the end of the culture period, which is when the culture was positive (mean, 15 days), cells were harvested and DNA was extracted with the Wizard® Genomic DNA Purification kit (Promega) for subsequent analysis. A fragment of the C2V3C3 region (378 bp) of the HIV-2 env gene was amplified in a nested Polymerase Chain Reaction (PCR) as described previously . PCR fragments were cloned into pCR®4-TOPO® vector (Invitrogen) and transformed into One Shot® Match1™-T1R competent cells (Invitrogen). Cloned plasmids were extracted , purified and sequenced using BigDye Terminator Cycle sequencing kit (Applied Biosystems), with M13 Forward and Reverse primers, and an automated sequencer (ABI Prism 3100, Applied Biosystems). For each patient an average of 13 clones (range 7–21) was sequenced per sampling year.
Sequence analysis and phylogenetic studies
The nucleotide sequences were aligned using Clustal X  and manual adjustments were made using Genedoc . Genetic distances between sequences were calculated using the maximum composite likelihood method implemented in the MEGA version 4 . Inter- and intra-sample synonymous (dS) and nonsynonymous (dN) distances were estimated using the modified Nei-Gojobory method with the Jukes-Cantor correction, also implemented in the MEGA software package.
Maximum likelihood analyses  were performed using the best-fit model of molecular evolution estimated by Modeltest under the Akaike information criterion . The chosen model was TVM+G+I. Tree searches were conducted in PAUP version 4.0 using the nearest-neighbor interchange (NNI) and tree bisection and reconnection (TBR) heuristic search strategies , and bootstrap resampling . The nucleotide divergence rate was estimated using an adaptation of the methodology previously described by Salazar-Gonzalez et al. . Firstly, maximum likelihood trees were constructed for each patient using all clonal sequences from each time point and rooted with the consensus sequences from other patients. Then, assuming a molecular clock, the branch lengths between the leafs and the root of the tree were calculated by using Branchlength Calculator  and plotted against time in years.
Natural selection of specific amino acids was examined using Codeml, models M0 and M3, with the HYPHY package . Potential N-glycosylation sites were identified using N-Glycosite . The entropy at each position in protein alignment was measured with Shannon Entropy .
Humoral antibody response against the env C2V3C3 regions
IgG and IgA antibody response against the env C2V3C3 region was quantified with the ELISA-HIV2 test developed in our laboratory, as described elsewhere with some modifications . Briefly, microtiter plates (96-well) were coated with rgp36 and rpC2-C3 by overnight incubation at 4°C and blocked with 1% gelatine in Tris-buffered saline (TBS). HIV-2-positive plasma samples were added to the antigen coated wells at a 1:100 dilution. Bound antibodies were detected by using alkaline phosphatase (AP)-conjugated goat anti-human IgG (diluted 1:2000 in TBS) or horseradish peroxidase (HPR)-conjugated rabbit anti-human IgA (diluted 1:2000 in phosphate-buffer saline) (Sigma-Aldrich). The colour was developed using p-nitrophenilphosphate (p-NPP Tablets, Sigma-Aldrich) as chromogenic substrate to AP and o-phenylenediamine dihydrochloride (OPD) to HPR. Optical density (OD) was measured with an automated microplate reader LP 400 (Bio-Rad) at 405 and 492 nm against a reference wavelength of 620 nm. The clinical cut-off value of the assay, calculated as the mean OD value of HIV-seronegative samples plus three times the standard deviation [SD], was determined using samples from healthy HIV-seronegative subjects. The results of the assay are expressed quantitatively as ODclinical sample(S)/ODcut-off(CO) ratios. For ratio values >1 the sample is considered as seroreactive.
Statistical analysis was performed in GraphPad Prism version 4.00 for Windows (GraphPad Software), with a level of significance of 5%. For the inter-patient statistical analysis across time, only information obtained from one time point (one sample) per patient was considered in order to guarantee the independence of the data analyzed. Thus, to maximize the number of observations in the analysis, we chose the first sample (first time point) available for each patient. Nonparametric tests were used to compare means and medians between variables: paired data was analyzed with Wilcoxon-matched pairs test and Friedman test; unpaired variables were tested with Mann Whitney U test and Kruskal-Wallis test. To study how two variables varied together linear regression was performed and Spearman correlation coefficients were computed. Finally, Deming linear regression was used to study the overall variation (slopes) of intra-patient data with time (longitudinal analysis).
GenBank accession numbers
Sequences have been assigned the following GenBank accession numbers: EU358115–EU358499, EU358501, EU358504, EU358507, EU358509, EU358513, EU358517, EU358519–EU358521, EU358524, EU358525, EU358527–EU358531, EU358533, EU358536–EU358538, EU358541, EU358543, EU358546–EU358549, EU358551–EU358567, EU360797–EU360799.
Phylogenetic relationships, genetic diversity and divergence
The mean evolutionary distance between different nucleotide sequences from each sample/year (nucleotide diversity) was 2.1% (standard deviation = 1.1) (additional file 1). Nucleotide diversity was neither associated with clinical status (2.1% mean median genetic distance in AIDS patients vs 1.4% in the other patients; p = 0.203) nor with plasma viremia (2.3% in viremic patients vs 1.8% in aviremic patients; p = 0.386) (n = 18).
Considering the first and the last samples of each patient, nucleotide diversity increased along the course of infection in all patients, except for patient PTHCC5 (additional file 1). Shannon's entropy was used to measure the relative amino acid variability in our set of sequences . The sum of entropy values of the amino acid alignments varied between regions (p < 0.001), being significantly lower for the V3 region (p < 0.001) and higher for the C2 region (p < 0.005) (additional file 1).
Within-patient nucleotide divergence rate was on average 0.014 substitutions per site per year for the C2V3C3 region, but it varied widely between patients (SD = 0.011). There was no association between the divergence rate and the variation in the number of CD4+ T cells over time (Deming regression analysis, F = 0.058, p = 0.816). Likewise, the divergence rate of the C2V3C3 regions was not related with the level of IgG antibodies produced against the homologous peptide over time (F = 0.192, p = 0.675).
Selection analysis and adaptation rate of the C2, V3, and C3 regions
Glycosylation of the HIV-2 env C2-C3 region
Molecular evolution of the C2, V3 and C3 regions as a function of the antibody response
In this study we have examined, for the first time, the molecular evolution of the envelope C2, V3 and C3 regions during chronic HIV-2 infection and its correlation with the antibody response against the same regions. Our cohort was constituted by long-term infected patients showing, in general, low CD4+ T cell counts and undetectable plasma viremia.
Nucleotide diversity increased with time in all but one patient with values similar to those obtained in an earlier study performed with HIV-2 elite controllers (2.1%, this study, vs 1.7%; p = 0.3440) . This value is also similar to the 2.5% median diversity reported for chronically HIV-1 infected patients  and to the 3.0% mean diversity reported for some long-term nonprogressors with low viral load .
In phylogenetic analysis we found low quasispecies complexity in most patients, i.e. virus populations from most patients were mostly homogeneous during the follow up period. This was expected since HIV-2 is generally seen as a slowly evolving virus and over a short period of time one would expect to observe few evolutionary changes [22, 24, 59]. However, in three patients there was evidence for segregation of virus quasispecies according to the year of infection, which implies high rate of evolutionary change and immune selection in these patients [15, 60]. Consistent with this, we found that the nucleotide divergence rate varied widely between patients. Moreover, the average nucleotide divergence rate (0.014 substitutions per site per year) was very high when compared to that reported for HIV-2 elite controllers (mean, 0.23%)  and for HIV-1 long-term non progressors with low plasma viral load (mean, 0.27%) . Even though we could not detect any association between nucleotide divergence and the number of CD4+ T cells, the higher net divergence observed in our patients might be related to their high immune deterioration, as higher genetic divergence is generally found in HIV-1 rapid progressors compared to slow- or non-progressors [19, 20]. In fact, the 0.014 annual divergence rate found in our patients is similar to that found in chronically HIV-1 infected patients (between 1.0% and 1.5% per year) [17, 58]. In conclusion, the sampling schedule used in our study, and possibly the fact that we have analyzed the virus present inside the cells and not in the plasma, has enabled us to demonstrate that the evolutionary dynamics of HIV-2 during chronic infection is surprisingly similar to HIV-1. This implies that HIV-2 is actively replicating during chronic infection, possibly in the lymphoid tissue, as in HIV-2 patients the mononuclear cells in the lymph nodes are heavily infected, even more than the mononuclear cells in the peripheral blood [61, 62]. Future studies of HIV-2 nucleotide divergence should include also the virus populations present in the lymphoid tissue and other cellular compartments (e.g. GI tract).
Despite the high nucleotide divergence rate, most of the substitutions were of a synonymous nature such that the dN/dS ratio of the C2V3C3 region was always below one and, most importantly, it decreased over time in most patients. These results are in agreement with previous reports that have examined the C2V3C3 region [22, 24] and with the observation that, globally, the HIV-2 env gene is under purifying selection . Consistent with previous studies of a cross-sectional nature, we found that C2 and C3, but not V3, were the fastest evolving regions at the nucleotide and amino acid level contributing significantly to the high within-patient nucleotide divergence rate [22, 63]. The conservation of the V3 region in vivo implies that in HIV-2, as in HIV-1, this region is submitted to strong structural and conformational constraints which are probably related to its crucial functional roles at the level of coreceptor binding and cell entry [29–32].
It is probable that adaptation to immune pressure is the main driver of the rapid intra-host evolution of the C2 and C3 regions in HIV-2 [15, 25, 58, 60, 64–66]. Indeed, we found that most of the amino acids under selection are located in C2, including the two amino acids that are under strongest positive selection in all patients (positions 267 and 270). Moreover, selection at these two sites persisted for at least two years in the majority of the patients which is a clear indication that they are under continued immune pressure in vivo [60, 67]. The equivalent amino acids in HIV-1 are not under positive selection , are located in the hidden surface of envelope glycoprotein complex  and define a cytotoxic T cell epitope . Thus, our results also suggest that the antigenic presentation of the C2, and perhaps the C3 region (see below), in the envelope complex of HIV-2 differs substantially from that of HIV-1.
Glycans on HIV-1 envelope protein play an important role in the folding of the glycoproteins, in infection and in evasion from the host immune response (reviewed in ). We found that, as for HIV-1 [51, 58], the majority of potential N-glycosylation sites were concentrated in the C2 region. The four N-glycosylation sites in C2 and the site in the beginning of V3 were highly conserved in all patients throughout infection which is strongly indicative of convergent evolution at these glycosylation hotspots and suggests an unexpected constraint on the potential diversity of the HIV-2 envelope [70, 71]. The convergent evolution of glycosylation sites may have important implications for both vaccine design and antiviral therapeutic .
To try to identify the immune correlates of the molecular evolution of HIV-2 C2, V3 and C3 regions we have looked into all possible associations between the number of CD4+ T cells or the IgA and IgG antibody levels and different parameters that reflect viral molecular evolution. In longitudinal analysis there was no significant association between the number of CD4+ T cells and nucleotide diversity, amino acid entropy, nucleotide divergence, dN/dS ratio and number of positively selected sites. These results are in partial contrast to those of MacNeil et al. , who found a direct association between the rates of HIV-2 diversification and rates of CD4+ T cell decline in long-term non progressors followed for a decade in Senegal. The short term follow-up and the associated modest variation in the number of CD4 + T cells might have prevented the detection of this type of association in our patients.
Strikingly, however, there was a close relationship between virus diversification and evolution and C2V3C3-specific antibody response over time. In fact, higher IgG response was significantly associated with lower viral variability at the nucleotide and amino acid levels as well as with lower frequency of nonsynonymous substitutions. These results imply that the anti-C2V3C3 IgG antibodies are effective at reducing viral population size limiting the number of virus escape mutants . This is in striking contrast to the majority of acute and chronic HIV-1 infections where the virus quickly escapes from anti-V3 and anti-C3 autologous neutralizing antibodies [33, 73–76]. Consistent with the lower capacity of HIV-2 to escape from C2V3C3- neutralizing antibodies when compared to HIV-1, we found that on average HIV-2 has a five-fold lower adaptation rate in vivo than HIV-1 (1 positively selected site per year vs 5 sites per year) [60, 77]. The HIV-2 low adaptation rate may be related to its low replicative capacity and low plasma viral load [12, 13, 78]. Overall, these results provide support for a crucial role of neutralizing antibody response in the effective containment of viral replication in HIV-2 infection in vivo .
Surprisingly, in some patients addition of glycans to the C3 region was associated with a reduction in the IgA immunogenicity of the C2V3C3 region. Envelope-specific plasma IgA antibodies, mostly binding to the gp36 transmembrane glycoprotein, have been found to neutralize HIV-2 . Increasing the number of N-glycans in the envelope gp120 surface glycoprotein, or varying the position of glycosylation sites, has been associated with escape from IgG neutralizing antibody response in simian immunodeficiency virus (SIV) and HIV-1 infection [57, 80–82]. Hence, one plausible explanation for the inverse association between IgA response and N-glycosylation is that the C3 envelope region induces IgA neutralizing antibodies to which HIV-2 escapes through the occlusion of the C3 region with N-linked glycans. This may have important implications for vaccine design. Ongoing studies will determine whether C2V3C3- specific IgA antibodies present in these patients effectively neutralize their autologous virus.
The evolutionary dynamics of HIV-2 envelope during chronic and highly suppressed infection is surprisingly similar to HIV-1 implying that the virus is actively replicating in cellular compartments. Convergent evolution of N-glycosylation in C2 and V3, as well as the limited diversification of V3, indicates however that there are important functional constraints to the potential diversity of the HIV-2 envelope. HIV-2 envelope diversification is inversely related to the C2V3C3-specific IgG antibody response over time implying that these antibodies are effective at reducing viral population size, limiting the number of virus escape mutants. The C3 region seems to be a target for IgA antibodies and increasing N-linked glycosylation may prevent HIV-2 envelope recognition by these antibodies. Our results provide new insights into the biology of HIV-2 and its relation with the human host and may have important implications for vaccine design.
This work was supported by Fundação para a Ciência e Tecnologia (project POCTI/ESP/48045). Pedro Borrego is supported by a PhD grant from Fundação para a Ciência e Tecnologia.
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