Aedes aegypti saliva impairs M1-associated proinflammatory phenotype without promoting or affecting M2 polarization of murine macrophages
During the feeding process, the mouthparts of hematophagous mosquitoes break the skin barrier and probe the host tissue to find the blood. The saliva inoculated in this microenvironment modulates host hemostasis, inflammation and adaptive immune responses. However, the mechanisms involved in these biological activities remain poorly understood and few studies explored the potential roles of mosquito saliva on the individual cellular components of the immune system. Here, we report the immunomodulatory activities of Aedes aegypti salivary cocktail on murine peritoneal macrophages.
The salivary gland extract (SGE) of Ae. aegypti inhibited the production of nitric oxide and inflammatory cytokines such as interleukin-6 (IL-6) and IL-12, as well as the expression of inducible nitric oxide synthase and NF-κB by murine macrophages stimulated by lipopolysaccharide (LPS) plus interferon-γ (IFN-γ). The spare respiratory capacity, the phagocytic and microbicidal activities of these macrophages were also reduced by Ae. aegypti SGE. These phenotypic changes are consistent with SGE suppressing the proinflammatory program of M1 macrophages. On the other hand, Ae. aegypti SGE did not influence M2-associated markers (urea production, arginase-1 and mannose receptor-1 expression), either in macrophages alternatively activated by IL-4 or in those classically activated by LPS plus IFN-γ. In addition, Ae. aegypti SGE did not display any cytokine-binding activity, nor did it affect macrophage viability, thus excluding supposed experimental artifacts.
Given the importance of macrophages in a number of biological processes, our findings help to enlighten how vector saliva modulates vertebrate host immunity.
KeywordsAedes aegypti Saliva Macrophages Inflammation M1/M2 polarization microbicidal activity
analysis of variance
cluster of differentiation
- Con A
enzyme-linked immunosorbent assay
fetal bovine serum
nitric oxide synthase
mitogen-activated protein kinases
Roswell Park Memorial Institute Medium
standard error of the mean
salivary gland extract
Tris-buffered saline with Tween
tumor necrosis factor-α
When attempting to feed on a vertebrate host, the mouthparts of females Aedes aegypti (Linnaeus, 1762) are inserted into the skin, the primary interface between the body and the environment, and “probe” the tissue to find a suitable vessel or a hemorrhagic pool . During the process, mosquito saliva is inoculated in this microenvironment, assisting in the location of blood vessels and counteracting molecules and resident cells responsible for the host’s hemostasis, inflammatory and adaptive immune responses [2, 3]. While the anticoagulant, antiplatelet and vasodilatory activities of Ae. aegypti saliva are addressed in much of the scientific literature [4, 5, 6, 7, 8, 9], the role of the species’ salivary components on immune cells remains largely unknown.
In addition to its role as a physical barrier, the skin is now recognized as an immunological organ according to the concept introduced by Dr J. W. Streilein  and further developed by himself and many others [11, 12, 13, 14, 15]. Among the resident immune response-associated cells in the skin are keratinocytes, mast cells, T lymphocytes (α/β and γ/δ T cells), innate lymphoid cells, dendritic cells, and macrophages. Given the limitation to isolate these cells directly from the skin or study them in situ under real life situations, in vitro models represent valuable tools and have been extensively employed to evaluate the effects of Ae. aegypti salivary components on the phenotype and functions of these cells. Thus, the production of cytokines by keratinocytes , dendritic cells  and mast cells  in response to inflammatory or infectious stimuli was impaired in the presence of Ae. aegypti salivary gland extract (SGE). Likewise, some reports showed a decrease in the polyclonal and antigen-specific proliferation of T cells in the presence of the mosquito’s SGE [19, 20, 21, 22] and this effect was due to the induction of caspase-3 and caspase-8-dependent cell death .
Macrophages play an important role in the onset, maintenance and resolution of inflammatory responses. As one of the major resident cell type in skin [11, 12, 13, 14, 15, 23], macrophages also participate in the arthropod vector-vertebrate host interactions, being probably among the first cells exposed to the saliva released during the blood-feeding. Given the restricted information on the role of mosquito salivary components directly on these cells, a more detailed study focused in the activity of Ae. aegypti SGE on several parameters of macrophage function is strongly needed. To date, only two studies explored the activity of Ae. aegypti salivary components on these cells, both in murine peritoneal macrophages [17, 24]. Macrophages from C3H/HeJ mice infected with West Nile virus or Sindbis virus expressed decreased levels of mRNA to interferon-β (IFN-β) and inducible nitric oxide synthase (iNOS) in the presence of Ae. aegypti SGE. In the absence of infection, Ae. aegypti SGE reduced the basal levels of interleukin (IL)-12 and increased IL-10 mRNA expression in these cells . Macrophages from C57BL/6 mice, incubated with synthetic cecropins identified in the Ae. aegypti genome, decreased the production of nitric oxide (NO) and inflammatory cytokines, and inhibited the expression of iNOS, mitogen-activated protein kinases (MAPKs) and nuclear factor-κB (NF-κB) in lipopolysaccharide (LPS) stimulated macrophages . However, data on the effect of Ae. aegypti salivary components in other aspects of macrophage biology are still lacking. Here, we addressed some of these missing aspects by evaluating the role of Ae. aegypti SGE on parameters associated with macrophage polarization to the M1 and M2 profiles.
Female C57BL/6 mice, 6–10-week-old, were bred and maintained at the Isogenic Breeding Unit of the Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, Brazil. During all manipulation procedures, animals were maintained under specific pathogen-free conditions and kept under controlled temperature and luminosity, with food and water ad libitum.
Preparation of Ae. aegypti SGE
Aedes aegypti mosquitoes (male and female) were reared in an insectary at the Department of Parasitology, Institute of Biomedical Sciences, University of Sao Paulo, Brazil where they were fed and mated as previously described . Five- to eight-day-old female adult mosquitoes were used as a source of salivary glands to prepare the SGE as described .
Macrophage isolation and M1/M2 polarization
Mice were intraperitoneally injected with 1 ml of 4% sterile thioglycolate medium (Becton, Dickinson and Company, Sparks, MD, USA). After 4 days, the animals were euthanized and the peritoneal cavity lavage was collected with 3 ml of cold sterile phosphate-buffered saline (PBS). After centrifugation (300×g for 5 min at 4 °C), the cell-free supernatant was discarded, the cell pellet was suspended in RPMI 1640 medium (Gibco Invitrogen, Grand Island, NY, USA), diluted in Turk’s solution (4 mg/l gentian violet in 3% acetic acid), and the number of cells was determined by optical microscopy in a Neubauer’s chamber. A suspension containing 1.5 × 106 cells/ml was prepared in RPMI 1640 medium, distributed into sterile 96-well plates in aliquots of 100 μl/well and incubated for 2 h at 37 °C and 5% CO2 for macrophage adhesion. Cell monolayers were carefully washed 3 times with warm PBS (at 30 °C) to remove nonadherent cells, and the adherent cells were incubated once more with complete medium [RPMI 1640 supplemented with 10% heat-inactivated fetal bovine serum (FBS), 2 mM l-glutamine, 100 units/ml penicillin, 100 µg/ml streptomycin, 25 mM HEPES and 2.5 × 105 M 2-mercaptoethanol] and cultured overnight at 37 °C and 5% CO2. In the next day, the wells were subjected to a new washing step with warm PBS and the adherent cells (macrophages) were stimulated as it follows.
Macrophages prepared as described above were maintained in complete medium (control group) or preincubated with Ae. aegypti SGE (concentrations indicated in each figure) for 1 h. Then, macrophages were polarized either to a M1 profile by activation with 10 ng/ml of ultrapure LPS (InvivoGen, San Diego, CA, USA) plus 10 ng/ml of murine IFN-γ (Sigma-Aldrich, St. Louis, MO, USA) or to a M2 profile by incubation with 20 ng/ml of murine IL-4 (Sigma-Aldrich). As suggested by the “Macrophage Activation and Polarization: Nomenclature and Experimental Guidelines”, these cells will be often referred as M(LPS+IFN-γ) or M(IL-4) for M1 and M2, respectively .
Following euthanasia, spleens from naive mice were aseptically removed and transferred into individual tubes containing 5 ml of RPMI 1640 medium. The organ was macerated by pressing the spleens through a 40-μm pore-size cell strainer (BD Falcon, Franklin Lakes, NJ, USA) with the aid of a sterile syringe plunger. Cells were centrifuged at 300×g for 5 min at 4 °C, the supernatant was discarded and the red blood cells were lysed by ACK Lysing Buffer (Gibco Invitrogen). After further washings, the cells were resuspended in complete medium, diluted in Turk’s solution, counted in a Neubauer’s chamber and used as described below.
Nitric oxide (NO) and cytokine determination
Macrophage cultures were prepared and polarized to M1 or M2 profile as described above. Cell-free supernatant was collected after 48 h and nitrite (NO2−), a stable and product of NO oxidation, was evaluated in the culture supernatant by Griess reaction as previously described [27, 28]. Briefly, equal volumes of the supernatants and the Griess reagent (1% sulfanilamide in 5% phosphoric acid and 0.1% N-(1-Naphthyl) ethylenediamine dihydrochloride, v/v) were mixed and incubated for 10 min at room temperature. The optical density of each well was evaluated at 554 nm in a spectrophotometer (SpectraMax M3, Molecular Devices, San Jose, CA, USA) and NO2− concentrations were deduced from a standard curve prepared with sodium nitrite (NaNO2) concentrations dissolved in complete medium.
Macrophage cultures were prepared and polarized to a M1 profile as described above. Cell-free supernatant was collected either after 6 h [for quantification of tumor necrosis factor-α (TNF-α)] or after 48 h (for quantification of IL-6, IL-10 and IL-12). The levels of the cytokines IL-10, IL-12 (p70) and TNF-α in the culture supernatants were assayed by BD OptEIA™ ELISA sets (BD Biosciences, San Diego, CA, USA) and the levels of IL-6 were evaluated by DuoSet ELISA (R&D Systems, Minneapolis, MN, USA), according to the manufacturers’ recommendations. Values were expressed as pg/ml deduced from standard curves of recombinant cytokines ran in parallel. The detection limit for each cytokine analyzed was: 15.6 pg/ml (IL-6 and TNF-α); 31.3 pg/ml (IL-10); and 62.5 pg/ml (IL-12).
Assessment of cell viability
Peritoneal macrophages and total spleen cells were prepared as described above and maintained in complete medium (control group) or preincubated with different concentrations of Ae. aegypti SGE (final concentration: 1 to 40 μg/ml) for 1 h. Macrophages were stimulated with LPS plus IFN-γ (final concentration: 10 ng/ml each) and lymphocytes (used as a control) were stimulated with 0.5 μg/ml concanavalin A (Con A, Sigma-Aldrich). Concomitantly, 25 µl of 0.01% resazurin (prepared in complete medium) were added to all wells. Cell viability was evaluated after 48 h of culture by reading the culture absorbance at 570 and 600 nm in a plate reader and the results are expressed as the difference between those readings as described [20, 29, 30].
Peritoneal macrophages and total spleen cells were prepared as described above and maintained in complete medium (control group) or incubated with different concentrations of Ae. aegypti SGE for 4 h. Then, cells were transferred to polypropylene tubes (12 × 75 mm) and centrifuged at 300×g for 5 min at 4 °C. After discarding the supernatant, macrophage samples were stained with fluorescence-conjugated anti-F4/80 (BioLegend, San Diego, CA, USA) and anti-CD11b (BD Biosciences) and lymphocyte samples were stained with fluorescence-conjugated anti-CD3 (BioLegend) and anti-CD19 (BD Biosciences) diluted in flow cytometry buffer (PBS containing 1% FBS) for 30 min at 4 °C in the dark. Cells were then washed twice with annexin buffer (10 mM HEPES, 140 mM NaCl, 0.25 mM CaCl) and centrifuged 300×g for 5 min at 4 °C. The cell pellet was resuspended in 100 μl of annexin buffer and 5 μl of annexin V-FITC (BioLegend) were added to each sample, which was then incubated in the dark for 10 min at room temperature. Cells were immediately acquired by a FACSCanto II flow cytometer (BD Biosciences) to evaluate the percentage of annexin V+ cells in each population. Data was analyzed using the FlowJo software, version 10.0.5 (Tree Star Inc., Ashland, OR, USA).
Real-time cell metabolism assay
In another set of experiments, the real-time analysis of mitochondrial oxygen consumption rate (OCR) was evaluated by a Seahorse XFe24 Extracellular Flux Analyzer (Agilent, Santa Clara, CA, USA). Peritoneal macrophages were prepared as described and seeded in sterile 24-well Seahorse culture plates at a density of 1.5 × 105 cells/well. Nonadherent cells were removed by two cycles of washing (after 2 and 24 h) as described before and adherent cells were maintained in complete medium (control group) or preincubated with Ae. aegypti SGE (40 μg/ml) for 16 h. Cells were then washed 3 times, equilibrated in assay medium and placed in the equipment following the manufacturer’s instructions. Basal OCR as well as the response to the sequential addition of oligomycin [1 μg/ml – for ATP synthase (complex V) inhibition], carbonyl cyanide m-chlorophenyl hydrazone (CCCP; 4.5 μM – for maximal respiratory capacity) and rotenone/ antimycin A [1 μM each – for mitochondrial (complex I and III, respectively) inhibition] was recorded.
M1 and M2 macrophages were polarized as described above. After 48 h, cells were collected, washed three times with cold PBS and the cell pellet was resuspended in RIPA lysis buffer (150 mM NaCl, 1% NP40, 0.1% SDS, 50 mM Tris; pH 8.0) and subjected to three freeze-thaw cycles at −20 °C and 37 °C, respectively. Then, the samples were centrifuged at 14,000×g for 5 min at 4 °C and the supernatant was transferred to a new tube. Arginase activity was evaluated in cell lysates as previously described . Urea production by arginase was determined spectrophotometrically at 550 nm and calculated using a standard curve generated with urea. Aliquots of the cell lysate were used for protein quantification using BCA Protein Assay Kit (Thermo Fisher Scientific, Rockford, IL, USA), according to the manufacturer’s recommendations. A standard curve with known concentrations of urea was prepared and the rate of urea production divided by the protein concentration of each sample was used as an index for arginase activity.
Western blot assays
M1 and M2 macrophages were polarized as described above. After 24 h, cells were then washed three times with cold PBS and lysed with RIPA buffer supplemented with 1% phosphatase inhibitors (100 mM sodium fluoride and 100 mM sodium orthovanadate) and with 1% protease inhibitor (Sigma-Aldrich). The lysate supernatant was collected after 10 min of incubation on ice, centrifuged at 14,000×g for 10 min at 4 °C and the protein concentration was determined using the BCA Protein Assay Kit (Thermo Fisher Scientific) according to the manufacturer’s instructions.
The entire electrophoresis and transfer processes were performed with reagents and equipment from Invitrogen (Carlsbad, CA, USA). Electrophoresis was performed in a Bolt™ system, according to the manufacturer’s instructions. The equivalent of 15 μg proteins from each sample were diluted in Bolt™ Sample Reducing Agent and Bolt™ LDS Sample Buffer, heated to 70 °C for 10 min and separated by electrophoresis in a Bolt™ Bis-Tris Plus 4–12% gel under a constant current of 200 V for 35 min. The separated proteins were transferred to a nitrocellulose membrane using the iBlot® Dry Blotting System and then was blocked with TBS-T buffer (Tris-buffered saline, 0.1% Tween-20) containing 10% FBS for 2 h. Membranes were washed three times with TBS-T (5 min per wash) and incubated overnight at 4 °C with the following rabbit monoclonal antibodies: anti-iNOS (Cell Signaling Technology, Danvers, MA, USA; 1:10,000), anti-phospho-NF-κB p65 (Cell Signaling Technology; 1:1,000), anti-arginase-1 (Cell Signaling Technology; 1:1,000) and anti-mannose receptor-1 (Proteintech, Chicago, IL, USA; 1:1,000). After further washing, the membranes were incubated for 2 h at room temperature with anti-rabbit secondary antibodies (1:3,000) conjugated with horseradish peroxidase (Cell Signaling Technology). Immunoreactive bands were stained using the chemiluminescent ECL Detection Kit (Thermo Fisher Scientific) and visualized in a photodocumentation system (G:BOX, Syngene, Cambridge, UK). Lastly, the membranes were then washed and incubated for 30 min with anti-β-actin conjugated with horseradish peroxidase (1:10,000) (Sigma-Aldrich) and visualized using ECL Detection Kit as described above. The density of the bands was analyzed with DigiDoc1000 software (Alpha Innotech Corporation, San Leandro, CA, USA). The values were normalized by the total of β-actin present in each sample and expressed as arbitrary units.
Cytokine-binding activity of SGE
High-binding flat bottom 96-well plates (Costar, Cambridge, MA, USA) were coated with anti-mouse IL-6 or anti-IL-12 antibody diluted in carbonate buffer (0.1 M, pH 9.6) overnight at 4 °C. Then, the wells were washed, incubated with blocking buffer (10% FBS in PBS) for 1 h at room temperature and washed again. Serial dilutions of IL-6 and IL-12 (3.9–500 pg/ml), previously incubated for 2 h at 37 °C with blocking buffer only or with different concentrations of SGE (1, 5 and 10 µg/ml), were added to the wells and incubated at room temperature for 2 h. After new washing, the bound IL-6 or IL-12 was detected using a solution containing biotinylated anti-mouse IL-6 or IL-12 antibody plus streptavidin-peroxidase for 1 h. Finally, wells were washed again, the chromogenic substrate (TMB Substrate Reagent Set, BD Biosciences) was added and the plate was incubated at room temperature for 30 min in a dark place for developing color. Reaction was stopped by addition of 1M H3PO4. The optical density of the wells was read at 450 nm in a spectrophotometer (Molecular Devices).
Direct binding assay
High-binding flat bottom 96-well plates (Costar, Cambridge, MA, USA) were coated with SGE (10 µg/ml), anti-mouse IL-6 or anti-IL-12 antibody diluted in carbonate buffer (0.1 M, pH 9.6) overnight at 4 °C. After the washing and blocking steps performed as described above, serial dilutions of IL-6 and IL-12 (3.9–500 pg/ml) were added to the wells and incubated at room temperature for 2 h. After new washing, the bound IL-6 or IL-12 was detected as described above. Reaction was stopped by addition of 1M H3PO4. The optical density of the wells was read at 450 nm in a spectrophotometer (Molecular Devices).
Escherichia coli phagocytosis and killing
Macrophage cultures were prepared as described above and maintained in complete medium without antibiotics (control group) or in the presence of Ae. aegypti SGE (final concentration: 40 μg/ml) for 1 h. In one set of experiments, the cells were stimulated with E. coli strain ATCC 25992 at a multiplicity of infection (MOI) of 10 at 37 °C and 5% CO2 for 5 h to evaluate bacterial killing. The medium was collected at the end of the experiment, serially diluted, and then plated on McConkey agar. After 24 h of incubation at 37 °C, plates that displayed isolated colonies were subjected to counting for determination of colony-forming units. In another set of experiments, the cells were incubated with green fluorescent E. coli from EZCell™ Phagocytosis Assay Kit (BioVision, San Francisco, CA, USA) for 1 h. At the end of the assay, macrophages were recovered from the plate using cold PBS, stained with fluorescence-conjugated anti-F4/80, and acquired on FACSCanto II flow cytometer (BD Biosciences). E. coli uptake rate and the median fluorescence intensity (MFI) of macrophages from both groups were analyzed by the FlowJo software (Tree Star Inc.).
Statistical analysis of differences between means of experimental groups was performed using Student’s t-test (for comparison of two groups) or analysis of variance (ANOVA) followed by Tukey’s post-test (for three or more groups). A value of P < 0.05 was considered statistically significant. Data are expressed as the mean ± standard error of the mean (SEM).
Aedes aegypti SGE inhibits NO production and iNOS expression in classically activated macrophages
Aedes aegypti SGE induces viability changes in murine lymphocytes, but not in macrophages
To confirm the refractoriness of macrophages to SGE-induced cell death, we performed a viability assay largely used for cells and microorganisms [36, 37, 38, 39]. The presence of SGE on spleen cell cultures (largely comprised of lymphocytes) significantly reduced the cell viability in a concentration–dependent manner, starting at SGE concentrations as low as 1 μg/ml (data not shown) and maximal at 40 μg/ml (F(2,15) = 1793, P < 0.0001; Fig. 2d). On the other hand, when M(LPS+IFN-γ) were incubated under the same conditions, no changes in their viability was observed at any of the SGE concentrations tested (F(2,15) = 3.148, P = 0.0722; Fig. 2e).
Aedes aegypti SGE decreases spare respiratory capacity in macrophages
Cytokine production by classically activated macrophages (M1) is selectively modulated by Ae. aegypti SGE
We next evaluated the expression of phosphorylated NF-κB in these cells to better characterize the mechanisms leading to this modulatory response. Western blot analysis revealed a constitutive expression of this transcriptional factor in macrophages maintained in medium only or in SGE-containing medium. For M(LPS+IFN-γ) samples, augmented expression of phosphorylated NF-κB was observed, while the presence of SGE in the culture reduced its expression to control levels (Fig. 4d). Densitometry analysis of Western blot data showed that this inhibition was statistically significant (F(3,4) = 9.776, P = 0.0259; Fig. 4e).
Aedes aegypti salivary components do not bind IL-6 or IL-12
M1, but not to M2 polarization, is impaired by Ae. aegypti SGE
Aedes aegypti SGE suppresses bacterial internalization and microbicidal activity by macrophages
Since the demonstration that macrophages could be “alternatively” activated in the presence of IL-4 , several works expanded this universe and different nomenclatures were proposed to reflect the multitude of macrophage phenotypes and functions shaped by environmental cues associated to health and disease states [47, 48, 49, 50, 51, 52]. The term “macrophage polarization” is currently used to express the net result of these conditions, although most researchers in the field agree that given the heterogeneity and plasticity of macrophages, efforts are required to standardize the polarization terminology so that immunologists can speak a common language . Aligned with this viewpoint, in the present work, macrophages activated by LPS plus IFN-γ were interchangeably referred as M1 or M(LPS+IFN-γ) while macrophages activated by IL-4 were referred as M2 or M(IL-4).
Our results revealed that the presence of Ae. aegypti SGE in the culture reduced iNOS expression and NO production by M(LPS+IFN-γ). In addition, the presence of Ae. aegypti SGE in M(LPS+IFN-γ) cultures also decreased IL-6 and IL-12 production while increasing IL-10 production by these cells, and these changes were associated to diminished expression of phosphorylated NF-κB. Similar inhibition of proinflammatory phenotype was observed in murine macrophages infected with West Nile virus or Sindbis virus in the presence of Ae. aegypti SGE  and in murine macrophages stimulated by LPS in the presence of Ae. aegypti salivary cecropins . Interestingly, the downmodulation of iNOS/NO axis in macrophages is also reported for saliva from ticks [53, 54, 55, 56], triatomines , sandflies [58, 59, 60, 61, 62], horseflies  and other mosquito species , suggesting that the activation of this antimicrobial pathway is a common target for saliva of hematophagous arthropods. Similarly, inflammatory cytokine production and NF-κB signaling were impaired in bone marrow-derived murine macrophages infected by Zika virus in the presence of LTRIN, an Ae. aegypti salivary molecule recently identified and characterized . Likewise, this anti-inflammatory phenotype was also found in the presence of salivary components of many blood-feeding arthropods [53, 56, 66, 67, 68, 69]. Despite the characterization of cytokine/chemokine binding proteins in tick saliva [40, 41, 42, 43], Ae. aegypti salivary molecules seem to directly modulate macrophage biology since no binding of SGE to IL-6 or IL-12 was detected, thus discarding experimental artifacts in our assays.
Salivary preparations from some blood-feeding arthropods were shown to induce death of different cell types. For example, Lutzomyia longipalpis SGE induces neutrophil apoptosis , while Armigeres subalbatus SGE does the same to macrophages . Our group has shown that Ae. aegypti SGE induces selective death of naive T cells, but not memory T cells, by a caspase-3- and caspase-8-dependent mechanism . Contrary to that observed for T and B cells, the absence of changes in the annexin V binding or in the viability of macrophages incubated in the presence of SGE suggests that cell death is not the mechanism by which the Ae. aegypti saliva modulates the M1 phenotype. The reason for this selectivity is not known, but it might represent differences between lymphocyte and macrophage proliferative rates and susceptibility to cell death. Although some studies revealed that macrophage proliferation has an impact on the homeostatic maintenance  and in inflammatory conditions [72, 73], these cells are generally depicted as terminally differentiated and usually dye at the end of their life span. On the contrary, lymphocytes undergo extensive proliferation and death during development of immature stages as well as following activation of mature cells. Thus, cell death events are part of lymphocyte life-cycle in order to eliminate cells that display high affinity antigen receptors for self-antigens or cannot respond to antigens, and also during the contraction phase of immune responses . In this way, a recent comprehensive review highlighted the control of apoptosis by the BCL-2 family of proteins and their differential role on promoting or inhibiting apoptosis depending on the stimuli, the tissue/cell type and the proliferative rate of the cells . The contribution of members of the BCL-2 family on SGE-induced lymphocyte death is a topic of interest for future studies.
The fact that Ae. aegypti SGE does not affect the viability of macrophages suggests that changes in the NO and proinflammatory cytokine production, as well as the expression of intracellular proteins associated to these mediators, could be due to a modulatory effect on cell metabolism. Thus, the dynamics of mitochondrial OCR in macrophages maintained in medium or incubated with SGE was evaluated and revealed a profile that was similar to that described by other studies [76, 77, 78]. No changes were observed in the basal OCR or ATP-independent OCR of macrophages incubated with SGE. However, the maximal OCR and, consequently, the spare respiratory capacity, were both decreased in macrophages incubated with SGE. These divergent metabolic responses suggest that mitochondrial respiration of macrophages in the presence of Ae. aegypti salivary molecules may be associated to the inhibition of M1 inflammatory mediators.
Considering the markers involved in either M1 or M2 polarization, we evaluated whether the presence of SGE in the culture could interfere in the polarization to each phenotype. M1 macrophages metabolize l-arginine to NO through the iNOS while M2 macrophages upregulate arginase-1 levels that shift the l-arginine metabolism to l-ornithine, having urea as the final product, in addition to upregulating mannose receptor. Indeed, we confirmed the NO production by M(LPS+IFN-γ) but not M(IL-4) or resting macrophages, as well as the increased urea production and arginase-1 expression by M(IL-4), when compared to resting macrophages or M(LPS+IFN-γ). Interestingly, the presence of Ae. aegypti SGE in the cultures decreased NO production by M(LPS+IFN-γ) but did not alter urea production or arginase-1 and mannose receptor-1 expression by these cells. However, we still cannot rule out an indirect effect of Ae. aegypti salivary components on M2 polarization in vivo. It is known that Ae. aegypti bites induce IL-4 expression at the skin site and the mosquito saliva has a molecule called SAAG-4, capable of programming CD4+ T cells to express IL-4 . Our group also demonstrated that the exposure of Ae. aegypti bites followed by intranasal challenge with SGE was able to induce the production of IL-4, IL-5 and IL-13 in the lung environment associated to high IgE levels, eosinophil migration and mucus production, evidencing the development of a local Th2 response . Taken together, our data suggests that Ae. aegypti SGE interferes in the polarization of M1 macrophages, without affecting the polarization to M2 phenotype in vitro, but other parameters need to be further investigated to confirm these results in vivo.
In addition to their role in the inflammatory process, an effective M1 response is known to possess cytostatic and/or cytotoxic effects against a number of pathogens. Here, we confirmed that E. coli uptake and killing by M(LPS+IFN-γ) were both impaired in the presence of Ae. aegypti SGE. Among the effector mediators produced by macrophages, NO is the deepest understood, providing protection against viruses, bacteria, fungi, protozoa and helminths . Macrophages are also among the main targets for the arboviruses transmitted by Ae. aegypti; thus, it is plausible to hypothesize that the enhancement of viral transmission by salivary components is associated to their ability to divert the development of a full M1 response. In fact, NO presents antiviral activities in vivo and in vitro by direct and indirect mechanisms in different disease models [82, 83, 84]. However, for Ae. aegypti-borne arboviruses, the role of NO in limiting viral replication was shown only for dengue virus to date [85, 86, 87], but none of these studies employed murine macrophages. Indeed, our attempts to observe a productive infection of peritoneal murine macrophages with dengue virus have failed so far (data not shown). On the other hand, mosquito studies showed that the presence of a NO donor totally blocked the replication of dengue virus in the hemolymph of a susceptible Ae. aegypti strain, while an iNOS inhibitor turned a resistant Anopheles albimanus strain permissive to the virus replication .
Finally, two previous studies presented elegant insights that are crucial to understand the potential biological relevance of our findings on the Ae. aegypti-vertebrate host interactions in vivo. Marinotti et al.  demonstrated that a successful blood meal depletes ~50% of the total protein from the salivary glands of Ae. aegypti. In our hands, one salivary gland pair (SGP) from a five- to eight-day-old Ae. aegypti adult female corresponds to 2–4 μg total protein (A. Sá-Nunes, personal communication). Considering that the feeding lesion would have an effective volume of 10 μl , the local concentration of saliva inoculated might reach 100–200 μg/ml of protein, about 2.5- to 5-fold the highest concentration used in our assays. Likewise, Wasserman et al.  presented a theoretical calculation by which the saliva inoculated by one mosquito was assumed to diffuse through a 1-mm spherical radius, affecting a 4.2 μl volume in the skin. Considering the amount of saliva injected and reingested by the mosquito during the blood meal, the authors calculate that one bite would leave 0.3–0.4 salivary gland pair (SGP) equivalent in the skin, resulting in an effective concentration of saliva as high as 30–70 SGP equivalent/ml at the bite site. Thus, the 40 μg/ml concentration used in our experimental conditions would correspond to 10–20 SGP equivalent/ml and therefore, it is also in the physiological range to modulate the macrophages in the microenvironment of the bite site. Whether this immunomodulatory zone created by the inoculated saliva is able to facilitate arbovirus infection in vivo nearby the bite site, it remains to be elucidated.
The present study reinforces the immunomodulatory role of Ae. aegypti salivary components on the vertebrate immune cells. Particularly, we report here changes in the pattern of cytokine production, in the expression of effector molecules involved with the activation of these cells, in parameters of cell metabolism and in the microbial uptake/killing by M1-polarized macrophages, with no effects on M2 polarization in vitro. These findings open avenues for studies aimed at determining whether macrophage polarization plays any role in the transmission of arbovirus by Ae. aegypti.
The authors would like to thank Sandra Alexandre (Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, Brazil) for her technical assistance with salivary gland collection and SGE preparation, Dr. Eliane Esteves (Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, Brazil) for her essential help with the manuscript formatting, Camille Cristine Caldeira da Silva (Institute of Chemistry, University of Sao Paulo, Sao Paulo, SP, Brazil) for her technical assistance with the Seahorse XFe24 Extracellular Flux Analyzer, Dr Sonia Jancar (Department of Immunology, Institute of Biomedical Sciences, University of Sao Paulo, Sao Paulo, SP, Brazil) for discussion and support and Dr. Carlo José Freire de Oliveira (Department of Microbiology, Immunology and Parasitology, Institute of Natural and Biological Sciences, Federal University of Triângulo Mineiro, Uberaba, MG, Brazil) for the critical reading of the manuscript.
MSB and ASN conceived the study. MSB, MTF, EHM, AAS and ASN designed the experiments. MSB, PGL, MTF, EHM, LRF, MLC and ASN generated biological samples. MSB, PGL, MTF, EHM and ASN performed the experiments. MSB, PGL, MTF, EHM, LRF, JOM, MLC, AAS and ASN analyzed data. MSB, MTF and ASN performed statistic data analysis. JOM, MJC, AAS and ASN contributed with reagents/materials/analysis tools. MSB and ASN wrote the paper. All authors read and approved the final manuscript.
This study was financed in part by Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP; Grant # 2015/22934-0, 2016/04921-1 and 2017/11540-7), Instituto Nacional de Ciência e Tecnologia em Entomologia Molecular, Conselho Nacional de Desenvolvimento Científico e Tecnológico (INCT-EM/CNPq; Grant # 465678/2014-9) and the Núcleo de Pesquisa em Moléculas Bioativas de Artrópodes Vetores, University of Sao Paulo (NAP–MOBIARVE/USP, Grant # 12.1.17661.1.7). MSB received a PhD fellowship from FAPESP (Grant # 2013/12467-0). MTF and EHM received postdoctoral fellowships from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) - Finance Code 001.
Ethics approval and consent to participate
All the experiments were carried out in accordance with internationally recognized guidelines and in agreement with the Brazilian Federal Law 11,794 (Arouca Law), Decree 6,899 and on the Normative Resolutions published by the National Council for the Control of Animal Experimentation (CONCEA), approved by the Institutional Animal Care and Use Committee (IACUC) under the protocol numbers 140/2011 and 148/2011.
Consent for publication
The authors declare that they have no competing interests.
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