- Open Access
HIV-1 subtype C transmitted founders modulate dendritic cell inflammatory responses
Retrovirology volume 17, Article number: 17 (2020)
Heterosexual transmission remains the main route of HIV-1 transmission and female genital tract (FGT) inflammation increases the risk of infection. However, the mechanism(s) by which inflammation facilitates infection is not fully understood. In rhesus macaques challenged with simian immunodeficiency virus, dendritic cell (DC) mediated recruitment of CD4+ T cells to the FGT was critical for infection. The aim of this study was to delineate the mechanisms underlying DC-mediated HIV infection by comparing chemokine and pro-inflammatory cytokine production in response to transmitted founder (TF) and chronic infection (CI) Envelope (Env) pseudotyped viruses (PSV).
Monocyte-derived DCs (MDDCs) were stimulated with PSV and recombinant gp140 representing matched TF and CI pairs of four individuals and cytokine secretion measured by multiplex immuno-assay. We found that 4/9 Env induced robust MDDC inflammatory responses and of those, three were cloned from TFs. Overall, TF Env induced MDDCs from healthy donors to secrete higher concentrations of inflammatory cytokines and chemokines than those from CI, suggesting TF Env were better inducers of inflammation. Assessing the signalling pathway associated with inflammatory cytokines, we found that PSV of matched TF and CI variants and a gp140 clone activated ERK and JNK to similar levels. Recombinant soluble DC-SIGN inhibited cytokine release and activation of ERK by PSV, suggesting that Env-DC-SIGN binding was partly involved in MDDC stimulation. Therefore, Env clones might differentially stimulate MDDC immune responses via alternative, yet unidentified signalling pathways.
Overall, this could suggest that the genetics of the virus itself influences inflammatory responses during HIV infection. In the absence of pre-existing infections, induction of greater inflammatory response by TFs might favour virus survival within the healthy FGT by driving an influx of target cells to sites of infection while suppressing immune responses via IL-10.
Inflammation of the female genital tract (FGT) facilitates HIV-1 transmission [1,2,3]. This could be because of mechanical damage to the protective mucosal barrier or the influx of T cells, macrophages and dendritic cells (DCs) to the FGT mucosa [2, 4]. Recruitment of HIV-permissive cells to the FGT might allow for rapid infection, transport to lymph nodes and unchecked viral replication. Haaland et al.  found that infection by multiple variants was associated with FGT inflammation. However, in the vast majority of cases, productive clinical infection is due to a single variant, the transmitted founder (TF) despite the presence of multiple variants in the donor [5, 6]. These findings suggest that not all variants are able to overcome an intact mucosal barrier and it has long been hypothesised that TF Envelope (Env) might provide a selective advantage during transmission. A number of studies [7, 8] to identify the elusive transmission motif have thus far suggested that only R5 tropism and potentially some Env N-glycosylation might consistently be associated with TFs [9,10,11,12]. The link between FGT inflammation, infection by TFs in the presence of an intact mucosal barrier and Env structure and function has yet to be elucidated.
In a previous study, when rhesus macaques were inoculated with simian immunodeficiency virus (SIV), DCs secreted inflammatory cytokines and chemokines (IFN-γ MIP-1α, MIP-1β, and MIP-3 α,) that recruited CCR5+ target cells to the local mucosa leading to enhanced infection . Moreover, when DC inflammatory immune responses (IR) were inhibited using anti-inflammatory glycerol monolaurate, animals were protected against SIV infection . This suggested that similar to other pathogens, HIV-1 deregulation of DC cytokine secretion might play an important role in transmission [14, 15].
It was also found that when HIV-1 Env binds to DC-SIGN it triggers trans-infection of CD4+ T cells, deregulation of DC function, prevention of DC maturation and inhibition of IL-12 expression [16,17,18]. In addition, when monocyte derived DCs (MDDCs) were exposed to HIV-1, IL-10 secretion [19, 20] was enhanced while the release of IL-12 and its capacity to stimulate T cell proliferation was inhibited . Cohort studies showed that concentrations of pro-inflammatory cytokines, IL-8, IL-1 and TNF-α, and pleiotropic cytokines such as IL-10 and IL-6 were found to be abnormally high in plasma of HIV infected patients with a concomitant decrease in IL-2, IL-12 and IFN-γ levels [22,23,24,25,26,27,28,29,30,31,32]. Moreover, cervico-vaginal lavages (CVL) of HIV infected women sampled within weeks of infection had significantly elevated levels of IL-6, IL-10, and IL-12, compared to HIV negative women whereas, IL-1α, IL-1β, IL-8, IL-6, IP10 and IL-10 were increased in plasma of the same patients [22, 33]. We had previously shown that MDDCs exposed to Env of TFs secreted higher levels of IL-10 than those stimulated with Env isolated from variants during chronic stages of infection (CI) . To understand the role of HIV-1 subtype C Env in local inflammatory responses that might lead to new HIV infections, we investigated whether HIV subtype C Env isolated during acute infection (AI) and CI induce distinctive inflammatory responses in healthy MDDCs.
Previous findings suggested that binding of Env to DC-SIGN triggered different signalling pathways which culminated in alternative outcomes. For instance, HIV Env binding to MDDCs via DC-SIGN led to increased Rho-GTPase activity required for the formation of virological synapses  whereas the expression of full-length HIV transcripts required Toll-like receptor-8 (TLR-8) . Binding of gp120 to DC-SIGN led to IL-10 secretion via the activation and phosphorylation of ERK  and DC-SIGN-mediated modulation of TLR-dependent activation of NF-kB . Shan et al.  suggested that virus genetics influenced whether MDDCs secreted IL-10 after exposure to gp120. Furthermore, Wilflingseder et al.  suggested that HIV-1 gp120 differentially activated ERK1/2 and p38 MAPK which lead to alternative DC phenotypes. Together, these findings suggested that different Env clones might differentially activate MAPKs, leading to alternative DC IR that either favour virus clearance or HIV-1 transmission. Therefore, this study hypothesised that in the absence of a pre-existing FGT inflammatory response TF Env modulates DC IR that initiate the recruitment of HIV-permissive cells, leading to productive clinical HIV infection.
MDDC secretion of inflammatory cytokines and chemokines in response to HIV-1
During an antigenic challenge, DCs secrete a combination of soluble mediators which together with co-stimulatory molecules may influence the strength and breadth of the IR [40, 41]. Therefore, in addition to the anti-inflammatory cytokine IL-10 (Fig. 1a) , we also determined the effect of PSV on MDDC secretion of pro-inflammatory cytokines (TNF-α, IL-6, IL-1β, IL-12p40) (Fig. 1b–e) and chemokines (MIP-1α, MIP-1β, IL-8) (Fig. 1f–h). MDDCs from healthy donors were stimulated with PSV of four TF (C1, C7, C12 and C15) and matched CI Env (C2, C8, C13, C14 and C16) and cytokines were measured by Luminex. Stimulation of IL-8 release was highly variable between donors in response to the different clones and all PSV clones seemed to be poor inducers of IL-12p40 relative to the background control. On the other hand, C7, C12, C14 and C15 were better stimulators of TNF-α, IL-6, MIP-1α, MIP-1β and IL-8 secretion than the negative control with the respective cytokine and chemokine concentrations ranging from 26–200, 55–955; 845–1446; 80–361 and 7285–287,334 pg/mL. C7 and C12 induced the secretion of significantly higher concentrations of TNF-α (p = 0.0086, p = 0.0043) IL-6 (p = 0.031, p = 0.031), MIP-1α (p = 0.055, p = 0.016) and IL-8 (p = 0.055, p = 0.031) (Fig. 1).
To determine overall inflammatory response patterns, hierarchical clustering and exploratory factor analysis were performed of all the cytokines and chemokines induced by all PSV Env tested. Most of the cytokines clustered together in Factor 1, with pro-inflammatory cytokines (IL-6 and TNF-α), chemokines (MIP-1α and MIP-1β) and anti-inflammatory IL-10 grouping together (Fig. 2a and Table 1). IL-8 and IL-1β were closely related and grouped together in Factor 2 (Table 1). Although IL-12p40 clustered more closely with Factor 1 than Factor 2, this cytokine had the greatest degree of uniqueness (Table 1) and clustered separately in the unsupervised hierarchical exploratory analysis (Fig. 2a). Therefore, the release of IL-6, TNF-α, MIP-1α, MIP-1β and IL-10 by MDDCs in response to PSV seemed to be linked.
PSV clustered into two groups: those that tended to induce high levels of cytokines (upper three rows) and those that were weak stimulators of MDDC cytokine release (lower six rows) (Fig. 2a). PCA was used to generate principal component scores for each PSV, representing overall pro-inflammatory cytokine responses (TNF-α, IL-6, IL-1β) (Fig. 2b) and overall chemokine responses (MIP-1α, IL-8 and MIP-1β) (Fig. 2c). C1, C7, C12, C13, C14, and C15 had significantly higher pro-inflammatory component scores compared to the control (Fig. 2b I). Of these six clones, four represented TF variants whereas two were CI Env from the same participant. For the chemokine component scores, only C7 and C12, both TF, had significantly higher scores than controls after adjusting for multiple comparisons (Fig. 2c I).
Transmitted founder Envelopes preferentially induced MDDC secretion of inflammatory cytokines and chemokines
Cytokine induction seemed to be associated with time post-infection as C7, C12 and to a lesser extent, C15, three of the four best inducers of cytokine release were cloned from TF variants (Fig. 1). For example, CAP206C7 and CAP210C12, induced the secretion of more TNF-α (p = 0.013) and IL-6 (p = 0.06) than their matched CI clones, CAP206C8, CAP210C13 and CAP210C14 (Fig. 1b, c). Furthermore, TF Env seemed to be better inducers of inflammation as all TF clones, C1, C7, C12, and C15 had higher pro-inflammatory component scores than the control (Fig. 2b) and TFs C7 and C12 proinflammatory scores were significantly greater than their corresponding CI (p = 0.0152 and 0.0043 respectively). Only C12 had a significantly higher chemokine score (p = 0.028) than its matched CI counterpart (Fig. 2a). In addition, only TF PSV had a tendency to induce IL-1β although this did not reach significance. When clones were grouped according to time of sampling, both the pro-inflammatory (Fig. 2b II) and chemokine (Fig. 2c II) component scores of TF and CI clones were significantly higher than the controls and TF values were greater than that of the CI clones, although the difference did not reach significance.
To circumvent experimental and donor variation between biological repeats, PSV were grouped into TF and CI variants and the concentration of each cytokine was expressed relative to the background of each biological repeat before comparing the median values. Overall, TF PSV were better at inducing each cytokine than their matched CI clone. MDDCs stimulated with TF Env tended to release two–eightfold higher concentrations of all cytokines, compared to levels induced by CI PSV that increased by only two–fourfold above background (Fig. 3).
The role of DC-SIGN in MDDC secretion of inflammatory cytokines and chemokines
In a previous study we stimulated MDDCs with PSV in the presence of recombinant DC-SIGN to determine whether IL-10 release was due to Env-DC-SIGN binding. DC-SIGN inhibition was shown to lower the secretion of IL-10 by MDDCs . As pro-inflammatory cytokines and some chemokines grouped together with IL-10 in the hierarchical clustering, we determined whether recombinant DC-SIGN would also inhibit the release of the other inflammation modulators. Two matched clones (C12 and C13) were selected that represented the best and weakest inducers of proinflammatory cytokines and chemokines. Inhibition of C12 PSV DC-SIGN interaction with recombinant DC-SIGN significantly reduced MDDC secretion of IL-6 and TNF-α levels while inhibition of chemokine secretion did not reach statistical significance (Fig. 4). On the contrary, inhibition of MDDC cytokine and chemokine secretion in response to C13, the matched CI clone of C12, was not observed. This is likely due to C13 being a very poor inducer of all cytokines and chemokines, limiting the detection of changes in cytokine and chemokine concentrations in the presence of recombinant DC-SIGN. However, we cannot exclude that preparation of recombinant protein did not co-purify contaminants or alter the structure of soluble DC-SIGN which might have influenced its binding to Env. Despite these limitations, apparent inhibition of cytokine release in the presence of recombinant DC-SIGN suggests that DC-SIGN-Env interactions are important.
Envelope activation of MAPK kinase signalling
As TF and CI PSV seemed to differ in their ability to induce MDDC secretion of cytokines and chemokines, we hypothesized that differences in Env structure might activate either alternative signaling pathways or elicit a more robust response due to higher affinity binding with cell-surface receptors. Previous studies showed that gp120 protein stimulated MDDC ERK phosphorylation, impaired maturation of DCs and induced inflammation . To investigate if PSV Env differentially activated MAPK signaling pathways, pERK levels were detected by WB after stimulation of MDDCs with C12, C13, C14, C15 and C16 PSVs. These clones were selected because they stimulated MDDCs to secrete different levels of cytokines and chemokines which might be reflected in changes in pERK levels. LPS was included as a positive control in this experiment because it has been shown to stimulate ERK phosphorylation . PSV clones stimulated an increase in pERK levels relative to the control, although only LPS induced pERK to statistically significant levels (Fig. 5a). When we also employed flow cytometry based analysis to follow Env-mediated increased protein phosphorylation in MDDCs, LPS, C12 and C13 induced a twofold increase in phosphorylation of ERK and JNK over the control (data not shown). Therefore, although C13 PSV is a poor inducer of cytokine and chemokine secretion, it is able to stimulate both ERK and JNK phosphorylation. To confirm that Env was essential for the activation of ERK and JNK, purified gp140 was used to stimulate MDDCs. C12 gp140 stimulated MDDCs to phosphorylate ERK and JNK similar to C12 PSV although only LPS induced MDDCs to generate significantly higher levels of pERK and pJNK compared to background (Fig. 5b, c). When C12 PSV DC-SIGN interaction was inhibited by recombinant DC-SIGN, MDDC pERK levels decreased significantly (Fig. 5d), suggesting that DC-SIGN interactions in part were contributing to ERK activation, in line with our findings regarding IL-10  and inflammatory cytokine secretion (Fig. 4). Therefore, the ability of C12 PSV and gp140 to induce MDDC activation of ERK and JNK may in part involve interactions between DC-SIGN and Env although we cannot rule out the influence of other DC receptors.
Therefore, Env and DC-SIGN interactions are potentially involved in both the activation of ERK and the stimulation of MDDCs to release cytokines. However, a statistically significant correlation between the activation of MAPK signaling pathways and the extent to which clones induced the secretion of cytokines and chemokines was not observed. For example, C12 and C13 PSV both induced the phosphorylation of ERK and JNK but only C12 induced significant increases in secretion of cytokine and chemokines by MDDC. It is thus possible that Env binding to DC-SIGN activates not only MAPKs but also an unidentified signaling pathway(s) linked to cytokine secretion.
Inflammation in the FGT is associated with increased risk of HIV infection,  multiple variant transmission,  and infection by less infectious virus . However, the underlying mechanisms and causes of inflammation in a healthy genital mucosa are not fully understood. HIV may directly induce inflammatory responses needed to facilitate the establishment of infection  or inflammation may be pre-existing, caused by factors such as sexually transmitted infections (STIs) [2, 46] and dysbiosis . In rhesus macaques, it has been shown that DCs play a critical role in the early stages of SIV infection by producing chemotactic cytokines that recruit CD4+ T cell targets for SIV infection . It is thus possible that DCs play a similar role during the early stages of HIV infection. To investigate this, we compared inflammatory cytokine and chemokine production by MDDCs in response to pseudotyped Env cloned longitudinally from women infected with a single HIV variant.
IL-10, MIP-1α, MIP 1β, IL-6, and IL-8 grouped together when exploratory factor analysis was used to classify the cytokines, suggesting their functions influenced one another. It is tempting to consider that the observed DC IR might provide an advantage during transmission as three of the four clones that induced the release of high levels of cytokine were AI clones. Li et al.  found that a few days following macaque inoculation, pDCs just beneath the endocervix expressed high levels of MIP-1α, MIP-1β, MIP-3a, IFN-α and IFN-β and the chemokine levels were associated with enhanced SIV infection (13). Given their chemoattractant function it is possible that increased chemokine secretion helped to recruit CCR5 expressing cells to areas of infection, thereby facilitating viral replication. This was in fact seen with the influx of CD4+ cells to local infectious foci as early as 1–3 days post viral inoculation. Moreover, inhibition of inflammation by application of glycerol monolaurate significantly reduced target cells and inflammatory cytokines in the genital areas .
When matched pairs of Env were compared, the mean proinflammatory and chemokine scores for TFs were higher than those of CI clones. HIV-1 subtype C TF Env might have the advantage of skewing DC inflammatory responses in their favour to facilitate transmission. The in vivo “cytokine storm” associated with acute HIV-1 infection supports the suggestion that increased inflammatory responses favour viral replication most likely through the recruitment of HIV permissive cells [22, 47]. However, this might not be true for all TFs, and the absence of this advantage might have consequences later during infection. Of note, the TF of the fourth matched pair, that did not induce an inflammatory cytokine profile, was cloned from a slow progressor . However, although it is tempting to speculate that TF variants have a selective advantage of inducing inflammatory responses in the FGT, our sample size is too small to reach definite conclusions.
The pathogenic products of Mycobacterium tuberculosis and HIV-1 (ManLAM and gp120 mannose residues, respectively) induced Raf-1 phosphorylation and activated Raf-1 promoted HIV-1 gene expression in DCs . Gringhuis et al. [38, 49] found that binding of ManLAM to DC-SIGN activated Raf-1 of the Ras-Raf-MEK-MAPK pathway which resulted in NF-kB-stimulated expression of cytokine genes, including IL-10. Furthermore, Env mediated activation of ERK1/2 and p38 MAPK differed between Env clones  suggesting that MAPK signalling via Raf-1 might be differentially activated by HIV-1 variants. To determine whether some Env were better able to activate MAPK, with concomitant aberrant cytokine profiles, we determined whether the Env clones were able to stimulate the phosphorylation of MDDC ERK and JNK.
Following PSV and gp140 stimulation of MDDCs, we detected varied phosphorylation of the MAPKs across the clones. There was no overall significant correlation between MDDC cytokine secretion and ERK activation possibly due to the small sample size in conjunction with the high variation between MDDC donor responses. C13 consistently failed to induce MDDCs to secrete cytokines above that of background and yet this clone was able to stimulate ERK phosphorylation. Similarly, C16 PSV was also unable to stimulate MDDC inflammatory response but did increase pERK levels. This suggests that cytokine secretion in response to HIV is modulated by more than one MDDC signalling mechanism. Blocking Env-DC-SIGN interaction inhibited cytokine release and ERK phosphorylation, demonstrating that DC-SIGN is involved in triggering the inflammatory response. We cannot exclude the possibility that recombinant soluble DC-SIGN and anti-DC-SIGN antibodies non-specifically inhibited MDDC signalling pathways independent of DC-SIGN and/or that Env binds to alternative receptors. However, we have reported that PSV bound Raji cells via DC-SIGN and MDDC-associated virus trans-infected TZM-bl cells, confirming Env and DC-SIGN interactions . Furthermore, we showed that PSV binding to Raji-DC-SIGN cells varied between clones, suggesting that differences in Env structure might influence the interaction with DC-SIGN which could activate alternative signalling molecules. Variation in Env N-glycan structures do alter binding affinity to DC-SIGN which changes its ability to interact with more than one signalling molecule . However, the mechanism of how this occurs remains unknown .
Although inflammation within the FGT is linked to HIV-1 infection [3, 52], the factors initiating the “cytokine storm” are unknown and may depend on several factors. Here we show that in the absence of pre-existing inflammation, the virus itself could modulate MDDC inflammatory responses via its Env glycoprotein interaction with DC-SIGN. Furthermore, although based on a small sample size, single variant TF PSV tended to stimulate higher levels of inflammatory cytokines and chemokines compared to CI PSVs, suggesting that DC IR could play a role in HIV transmission.
Materials and methods
Full-length envelope (env) from four HIV positive women (CAP45, CAP206, CAP210 and CAP239) sampled 2–5 weeks post-infection (wpi) (AI) with follow up longitudinal samples collected 2–3 years post infection (ypi) (CI) were used for this study (Table 1) (Accession numbers: JX976722.1, KC863497.1, FJ443390.1, 47:KC833437.1, KJ700457.1, DQ435683.1, KC863280.1, KC863276.1, FJ443142.1, HQ625601, HQ625600.1, FJ443357.1, HQ625599.1, KC863388.1, HQ625599.1 (www.ncbi.nlm.nih.gov). Single genome amplification (SGA) and sequencing indicated that all participants were infected with a single variant at transmission . Nine functional Env clones (numbered C1, C2, C7, C8, and C12-C16), a subset of 36 generated from SGA—derived PCR products, were cloned into pcDNA/his-topo (Invitrogen) or pTarget (Promega) mammalian expression vectors according to manufacturer’s instructions. The functional clones selected in this study were sampled from four participants infected with a single variant at 2–5 wpi with follow-up 2–3 years later . The CI clones (C2, C8, C13 and C14) were selected because they had N-glycosylation profiles identical to the consensus sequence of circulating variants at CI. Potential N-glycosylation (PNG) frequency analysis was carried out on 36 matched Env consensus sequences from AI and CI (accession numbers: (JX976651.1, FJ443216.1, FJ443182.1, FJ443984.1, KC894137.1, KC863412.1, JN681229.1, KC863558.1, KC863493.1, KC863519.1, KC863542.1, KC833437.1, HQ625599.1, KC863410.1, JX976681.1, HQ625602.1, KC863457.1, HQ625605.1, FJ443279.1, FJ443963.1, KF996701.1) and random subtype C sequences (www.ncbi.nlm.nih.gov).
Human embryonic kidney (HEK) 293T and TZM-bl cells were maintained in Dulbecco modified Eagle high glucose medium (DMEM) (Lonza, Whitehead Scientific). TZM-bl cells were obtained through the NIH AIDS Reagent Program (ARP), Division of AIDS, NIAID from Dr. John C. Kappes, Dr. Xiaoyun Wu and Tranzyme Inc . All cells were grown in a humidified incubator at 37 °C with 5% CO2 and growth media were supplemented with 10% fetal bovine serum (FBS) (PAA, Biocom Biotech), 1 U/mL penicillin and 1 µg/mL streptomycin (P/S) (Lonza, Whitehead Scientific).
Pseudovirus (PSV) was prepared by co-transfection of HEK 293T cells with 2.5 µg of env and 5 µg of pSG3ΔEnv plasmids with PEI transfection reagent at a 1:3 DNA: PEI ratio. Culture medium was harvested 48 h later, filtered through a 0.22 µm pore sized filter and FBS was adjusted to 20% and stored at − 70 °C. The concentration of PSV was determined by a chemiluminescent ELISA (Aalto Bio-reagents) and TROPIX® detection system (CDP-Star®, Applied Biosystems). PSV titre was determined by infecting TZM-bl cells for 48 h with known p24 concentration and relative luminescence units (RLU) were compared between Env pseudotyped virus and pSG3ΔEnv PSV infected cells (background) and a titre resulting in 50 X RLU above background was used for MDDC stimulation.
Gp140 production from CHO cells
Full-length env was truncated before the transmembrane domain and gp140 was produced as described in Lumngwena et al. . Briefly, Env was expressed in non-adherent CHO cells to maximise expression while preserving N- glycosylation patterns introduced by HEK 293 cells . Culture medium was harvested 72 h post-transfection and gp140 purified by affinity chromatography using Galanthus nivalis lectin Sepharose (Vector Labs, Burlingame, CA) diluted fivefold with unliganded Sepharose 4B (GE Healthcare) before dialysis with HEPES, pH 7.4, 150 mM NaCl.
Generation of MDDC
Peripheral blood mononuclear cells (PBMC) were isolated from buffy coats of healthy blood donors using Ficoll-Hypaque (Sigma-Aldrich). Monocytes isolated from PBMCs by positive selection using CD14+ coated beads (130-050-201 Miltenyi, USA or Biochom Biotech, S.A) were seeded in serum-free medium and allowed to adhere to tissue culture dishes for 2 h at 37 °C, 5% CO2. Non-adherent cells were removed and differentiation medium, supplemented with 1000 U/ml GM-CSF (PHC2013, Biosource), and 500 U/ml recombinant human IL-4 (PHC0045, Biosource) was added to the cells and every other day for 6 days.
Monocyte derived dendritic cell stimulation
Either PSV (50X) or purified gp140 (2 µg/ml) was used to stimulate 2 × 106 cells/mL monocyte derived dendritic cells (MDDC) in 200 µl final volume of culture medium containing 2% AB human serum (H1513, Sigma), 1% P/S (Sigma Aldrich), 1% non-essential amino acids (Gibco-Life technologies, USA), 1% sodium pyruvate (Gibco, USA) and 1% l-glutamine (Sigma Aldrich) in RPMI for 24 h. Following stimulation, the plates were centrifuged at 2000 rpm for 10 min and the culture supernatants collected and stored at − 80℃. Prior to stimulation of MDDCs with PSV, MDDCs were pre-incubated with recombinant DC-SIGN (Donation from Dr Arthos) for 1 h at ambient temperature in the presence of 2 mM Ca2+, and then at 37 °C for an additional hour.
Purification of soluble DC-SIGN
DC-SIGN was cloned into pET22b and expressed in E coli as inclusion bodies . Recombinant DC-SIGN was refolded by rapid dilution in renaturation buffer (0.5 M Arginine, 5 mM Cysteamine, 1 mM Cystamine, 0.1 M Tris–HCl, pH 8.0) and purified by ion-exchange (15Q) and Superdex 200 HR size exclusion chromatography .
Luminex multiplex assay for cytokine quantification
The level of cytokines released by MDDCs into the culture supernatants was quantified using Luminex suspension array technology with cytokine-specific antibody-immobilized magnetic beads (Millipore, USA). Biotinylated secondary antibodies and streptavidin–phycoerythrin conjugates were used to determine Mean Fluorescence Intensity (MFI) using a Luminex platform (Bio-rad, USA).
Phosphorylation of MAP Kinase
MDDCs were rested for 2 h, stimulated with pre-titred PSV or gp140 for 15 min, fixed with 2% paraformaldehyde in PBS, permeabilized and stained with fluorescently conjugated antibodies to ERK and JNK and phosphorylation was detected by flow cytometry. Alternatively, phosphorylation of MAPKs was detected by Western blotting (WB). MDDCs were washed with pre-warmed PBS and lysed (RIPA buffer containing protease and phosphatase inhibitors) after stimulation and 30 μg cell lysate was loaded per well for WB. DC-SIGN binding was inhibited by pre-incubation of MDDCs with anti-DC-SIGN Mab for 2 h at 37 °C (Clone DCN46, ARP 7682).
Cytokine measurements (pg/ml) of at least 3 biological repeats were compared by Mann–Whitney test for non-paired events and Wilcoxon matched test for pairwise comparison of paired events (GraphPad Prism 5.0). A P value < 0.05 was considered as statistically significant. P values were adjusted for multiple comparisons by the false discovery rate (FDR) step down procedure. Flow cytometry raw data was analysed by Flowjo 9.6, while the intensity of WB bands was compared by densitometry analysis using the Image lab™ software on a Chemi DocTm (Bio-rad) imaging system. Principal component analysis (PCA; in STATA™) was used to reduce the complexity of the dataset and to examine the relationship between PSV and different cytokine functions (chemokine and pro-inflammatory cytokines). Exploratory factor analysis and unsupervised hierarchical clustering (in R) were used to determine the relatedness and uniqueness of the cytokines secreted. The cytokines secreted by MDDCs in response to PSV stimulation were scored in R using factor loading and the degree of variance between cytokines was determined by the eigenvalues. The principal factor method was used and the number of retained factors was determined using the Kaiser’s criterion.
Availability of data and materials
The datasets generated during and/or analysed during the current study are available in the ZivaHub repository, https://zivahub.uct.ac.za/account/home#/data.
Female genital tract
Phosphate buffered saline
Mitogen activated protein kinases
Extracellular regulated kinase
Janus N Kinase
Monocyte derived dendritic cells
Potential N-glycosylation Site
Peripheral blood mononuclear cells
DC specific intracellular adhesion molecule (ICAM) 3 grabbing non-integrin
Single genome amplification
Fetal bovine serum
human embryonic kidney cells
Simian immunodeficiency virus
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ZW was funded by a TTK20100723000013129 Grant from the National Research Foundation and a 13/25 Grant from the Poliomyelitis Research Foundation. EN was funded by a Carnegie Corporation ‘Developing the Next Generation of Academics’ Scholarship/Fellowship, HIV Research Trust Scholarship, Company of Biologists Travelling Fellowship, National Research Foundation and Poliomyelitis Research Foundation bursaries. CC and JA are supported by the intramural Research Program of the National Institutes of Allergy and Infectious Diseases, NIH. For all funded individuals the funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Ethics approval and consent to participate
Buffy coats were obtained from the Western Province blood bank and as all donors were anonymous, there was no need to obtain informed consent. The protocol was approved by the University of Cape Town Ethics in Research Committee of the Faculty of Science, SFREC 003_2012 and University of Cape Town Human Research Ethics Committee of the Faculty of Health Sciences, HREC554/2017.
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Lumngwena, E.N., Metenou, S., Masson, L. et al. HIV-1 subtype C transmitted founders modulate dendritic cell inflammatory responses. Retrovirology 17, 17 (2020). https://doi.org/10.1186/s12977-020-00526-0
- HIV-subtype C Env
- Transmitter/Founder Envelopes
- Inflammatory responses
- Virus survival