Stable multi-infection of splenocytes during SIV infection - the basis for continuous recombination
© Schultz et al; licensee BioMed Central Ltd. 2012
Received: 13 January 2012
Accepted: 23 April 2012
Published: 23 April 2012
Recombination is an important mechanism in the generation of genetic diversity of the human (HIV) and simian (SIV) immunodeficiency viruses. It requires the co-packaging of divergent RNA genomes into the same retroviral capsid and subsequent template switching during the reverse transcription reaction. By HIV-specific fluorescence in situ hybridization (FISH), we have previously shown that the splenocytes from 2 chronically infected patients with Castelman's disease were multi-infected and thus fulfill the in vivo requirements to generate genetic diversity by recombination. In order to analyze when multi-infection first occurs during a lentivirus infection and how the distribution of multi-infection evolves during the disease course, we now determined the SIV copy numbers from splenocytes of 11 SIVmac251-infected rhesus macaques cross-sectionally covering the time span of primary infection throughout to end-stage immunodeficiency.
SIV multi-infection of single splenocytes was readily detected in all monkeys and all stages of the infection. Single-infected cells were more frequent than double- or triple- infected cells. There was no strong trend linking the copy number distribution to plasma viral load, disease stage, or CD4 cell counts.
SIV multi-infection of single cells is already established during the primary infection phase thus enabling recombination to affect viral evolution in vivo throughout the disease course.
KeywordsSIV FISH Recombination Provirus copy number
The human (HIV) and simian (SIV) immunodeficiency viruses exhibit phenomenal genetic diversity. This diversity is generated by 3 different mechanisms, (i) error-prone replication by the reverse transcriptase that occurs without proofreading , (ii) hypermutation by host mutators of the family of cytidine deaminases [2–6] and (iii) recombination between the viral RNA genomes by template switching . As a result of these processes, a population of virus variants or quasispecies is established within an infected host that is subsequently shaped by processes like fitness competition between variants, immune-mediated activation of infected cells and bottlenecking [8–11].
Due to the structure of the retrovirus particle and the low processivity of the reverse transcriptase, recombination is extraordinary frequent in HIV and SIV . In fact, the number of crossovers during reverse transcription between the two RNA templates that are packaged within one HIV virion has been estimated to be around three or higher per genome [13–16]. Thus any generated single provirus can be expected to have a mosaic structure derived from its two parental viral RNA strands. In comparison, the point mutation rate with approximately 0.25 mutations per genome and replication  is at least a factor of 10 lower.
To have an impact on virus evolution, recombination needs to proceed between non-identical RNA strands. The requirements and biological steps for the generation of such virus particles with non-identical genomes have been described. First, multi-infection of single cells occurs via direct and via cell-mediated entry pathways . Second, the existence of multi-infected cells has been directly shown by HIV-specific fluorescence in situ hybridization (FISH) on splenocytes of infected patients . Third, transcribed HIV RNA genomes are co-packaged into virions at ratios expected from a random distribution . However, the extent of sequence similarity, especially of the dimerization initiation site, influences co-packaging efficiency and consequently the frequency of observable recombinants [21–23].
While features of the basic steps in the generation of HIV/SIV recombinants have been described in various experimental conditions, it is still unknown when multi-infected single cells first appear in vivo during a lentivirus infection and how the distribution of multi-infection evolves during the disease course. To answer these questions, we determined the SIV copy number in splenocytes from SIVmac251-infected rhesus macaques (Macaca mulatta) by specific fluorescence in situ hybridization.
Results and discussion
Multi-infection of single splenocytes of SIV-infected rhesus macaques in all stages of infection
To determine the SIV copy number of splenocytes from SIVmac251-infected animals by FISH, DNA from SIVmac239 was used as a probe. This was possible due to the high sequence homology between SIVmac239 and SIVmac251 . In vitro SIVmac239-infected CEMx174 cells served as positive control to test the sensitivity of the biotin-labelled SIV DNA-probe while un-infected CEMx174 cells as well as spleen cells from an un-infected rhesus macaque were used as negative controls. Only after detecting bright signals in the interphase nuclei of the infected CEMx174 cells with no nonspecific background in the negative samples, the splenocytes of the infected animals were analyzed under the same conditions.
Characteristics of SIVmac251-infected rhesus macaques
Duration of infection (weeks)
Absolute CD4+ T cells (cell/μl)
Plasma viral load (SIV-RNA/ml)
Number of infected cells counted
Relative SIV copy number distribution
7.7 × 103
1740 (I, A)
2.3 × 108
1778 (I, A)
3, 1 × 106
1718, (I, A)
2.6 × 105
To evaluate the efficiency of the FISH assay and the error in our provirus copy number estimates, the technique has to be tested on cells with a defined copy number. For this we used U1 cells that carry 2 HIV provirus copies per genome and performed the assay under identical conditions only using HIV DNA as a probe. This is a valid approach as the base composition and thus the hybridization properties for HIV-1 and SIV are basically identical (HIV-1: A-35,3%, T-22,1%, G-24,4%, C-18,2% and SIV239: A-33,6%, T-22,7%, G-24,7%, C-18,8%). Approximately 10% of U1 cells showed only one copy. Thus it would appear that we underestimated the real values by ~10%. Within the same experiments, we very rarely detected 3 proviruses (< 0.5% of cells). Likewise, using either HIV DNA or SIV DNA as probes, non-infected monkey splenocytes rarely gave a positive signal (< 0.5%) suggesting that the number of false positive events is very small. Extrapolating these findings to the SIV FISH experiments with splenocytes from infected monkeys, the real SIV proviral copy number may be around 10% higher than indicated.
While the sample size of this present study is low and thus has limited statistical power, there was no strong trend between the SIV plasma viral load, the stage of SIV infection, or the CD4 cell count and the relative copy number distribution. For example, monkeys 8179 and 1740 differed more than 104-fold in plasma virus titres but showed a similar provirus distribution in their splenocytes (Table 1). A similar observation was made previously when studying the HIV copy number distributions in splenocytes of 2 seropositive patients with Castleman disease . Notably, in this latter study, the copy number distribution was higher with the majority of cells harbouring 3 to 4 proviruses. While the reason for this difference is unknown, it may well be related to the lymphoproliferative nature of the disease . Nonetheless, with respect to recombination, any cell with a provirus copy number above 1 is able to generate virions with mixed RNA genomes that in the subsequent infection round will result in recombinant progeny.
How are infected splenocytes with multiple proviruses generated? The lack of a clear trend between the plasma viral load and the copy number distribution of this study and that of Jung et al.  suggest that cell-cell transmission events rather than circulating virus itself are the likely viral source. Indeed, infections by viruses deposited on Follicular Dendritic cells  or transferred from Dendritic cells to T cells in the process of antigen-specific stimulation  are highly efficient and may result in the transmission of multiple virions as demonstrated by more recent ex vivo studies [28, 29].
The early onset of SIV multi-infection provides the fundamental mechanistic requirements for recombination to occur already at primary viremia. Indeed, when macaques were inoculated simultaneously with SIVmac239Δvpx or Δvpr and SIVmac239Δnef, the emergence of wild-type virus was detected in blood in as little as 2 weeks post-inoculation [30, 31]. This was due to the large fitness advantage of the recombined wild-type over both deletion mutants. In naturally occurring HIV infections however, only one or very few virus variants are transmitted resulting in a rather homogenous virus population at primary viremia [32, 33]. Consequently, any generated recombinant will remain unnoticed unless a fair degree of sequence diversity is generated over time by error prone replication rounds. This scenario is well documented and shows up in the time-structured sequence networks from HIV patients as well as clonal SIV infections of macaques [34–37].
In summary, SIV multi-infection of single cells within a lymphoid tissue is established during the primary infection phase and observed throughout the entire disease course. As a consequence, recombination events will inevitably occur and contribute to virus evolution.
Splenocytes were analyzed from 11 SIVmac251-infected monkeys that had been used in previously published infection studies . Animals were housed at the German Primate Center under standard conditions and experiments were performed according to the German animal protection law which complies with the European Union guidelines on the use of non-human primates for biomedical research (approval 604.42502/08-02.95, Bezirksregierung Braunschweig). The animals had been infected intravenously with 100 MID50 (monkey infectious dose infecting 50% of recipients) of a SIVmac251-derived virus stock prepared in rhesus monkey peripheral blood mononuclear cells . They were sacrificed at predetermined time points in the acute, post-acute, and early asymptomatic phase without clinical symptoms of immunodeficiency or euthanized due to early signs of AIDS. The eleven animals cover a time range from 2 weeks to 51 weeks post primary infection and a wide range of peripheral CD4 T cell counts (Table 1). The spleens were removed from anesthetized animals, cut into slices, and put into ice-cold Hank's balanced salt solution containing 3% FCS. Spleen tissue was then forced through a 100 μm-mesh metal sieve with forceps. The dissociated material was left to settle for five minutes, and the single cell suspension in the supernatant was collected by centrifugation at 170 g for 10 minutes at 4°C and washed twice. Cells were counted in a Neubauer chamber and stored in liquid nitrogen. For the SIV-specific FISH, the thawed cells were stimulated for 2 days in the presence of 10 μM AZT. The fixed cell nuclei were then hydridized with a biotin-labelled SIVmac239-specific DNA probe that was subsequently detected with a tyramide signal amplification (TSA) system. The fluorescence signals were analysed with an Olympus AX 70 epifluorescence microscope (Olympus Optical, Hamburg Germany). Pictures were documented with a digital camera Hamamatsu DC C4742-95 (Hamamatsu Photonics Deutschland GmbH, Herrsching am Ammersee, Germany) and an ISIS digital imaging analysis system (Metasystems GmbH, Altlussheim Germany). A detailed description of the experimental procedures is given in the Additional file 1 and Additional file 2.
RS was supported by an EMBO Long Term Fellowship. AM was supported by grants from the Deutsche Forschungsgemeinschaft and the Spanish Ministry of Science and Innovation (SAF2010-21336).
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