- Research article
- Open Access
A dengue receptor as possible genetic marker of vector competence in Aedes aegypti
© Mercado-Curiel et al; licensee BioMed Central Ltd. 2008
Received: 11 January 2008
Accepted: 15 July 2008
Published: 15 July 2008
Vector competence refers to the intrinsic permissiveness of an arthropod vector for infection, replication and transmission of a virus. Notwithstanding studies of Quantitative Trait Loci (QTL) that influence the ability of Aedes aegypti midgut (MG) to become infected with dengue virus (DENV), no study to date has been undertaken to identify genetic markers of vector competence. Furthermore, it is known that mosquito populations differ greatly in their susceptibility to flaviviruses. Differences in vector competence may, at least in part, be due to the presence of specific midgut epithelial receptors and their identification would be a significant step forward in understanding the interaction of the virus with the mosquito. The first interaction of DENV with the insect is through proteins in the apical membrane of the midgut epithelium resulting in binding and receptor-mediated endocytosis of the virus, and this determines cell permissiveness to infection. The susceptibility of mosquitoes to infection may therefore depend on their specific virus receptors. To study this interaction in Ae. aegypti strains that differ in their vector competence for DENV, we investigated the DS3 strain (susceptible to DENV), the IBO-11 strain (refractory to infection) and the membrane escape barrier strain, DMEB, which is infected exclusively in the midgut epithelial cells.
(1) We determined the MG proteins that bind DENV by an overlay protein binding assay (VOPBA) in Ae. aegypti mosquitoes of the DS3, DMEB and IBO-11 strains. The main protein identified had an apparent molecular weight of 67 kDa, although the protein identified in the IBO-11 strain showed a lower mass (64 kDa). (2) The midgut proteins recognized by DENV were also determined by VOPBA after two-dimensional gel electrophoresis. (3) To determine whether the same proteins were identified in all three strains, we obtained polyclonal antibodies against R67 and R64 and tested them against the three strains by immunoblotting; both antibodies recognized the 67 and 64 kDa proteins, corroborating the VOPBA results. (4) Specific antibodies against both proteins were used for immunofluorescent location by confocal microscopy; the antibodies recognized the basal lamina all along the MG, and cell membranes and intercellular spaces from the middle to the end of the posterior midgut (pPMG) in the neighborhood of the hindgut. (5) Quantitative analysis showed more intense fluorescence in DS3 and DMEB than in IBO-11. (6) The viral envelope antigen was not homogeneously distributed during MG infection but correlated with MG density and the distribution of R67/R64.
In this paper we provide evidence that the 67 kDa protein (R67/R64), described previously as a DENV receptor, is related to vector competence in Ae. aegypti. Consequently, our results strongly suggest that this protein may be a marker of vector competence for DENV in Ae. aegypti mosquitoes.
DENV is a Flavivirus within the Arboviruses class, more than 500 of which have so far been identified. DENV is distributed worldwide in tropical and subtropical countries in association with its mosquito vector Ae. aegypti. Dengue infection ranges from self-limited asymptomatic or mild illness (dengue fever, DF) to a severe hemorrhagic disease (dengue hemorrhagic fever, DHF) that can progress to dengue shock syndrome (DSS) characterized by circulatory failure .
More than fifty million dengue infection cases occur every year , resulting in approximately 24,000 deaths due to DSS. In Mexico , 45,748 cases of DF and 10,501 of DHF were reported from 2004 to 2006. Although DEN is the most common vector-borne viral disease, few studies have investigated the complex relationship between DENV and Ae. aegypti through their genetic characteristics.
Transmission of infection depends on DENV virulence, host immunity and the susceptibility of the mosquito to infection. Susceptibility will depend on the interaction between the mosquito and DENV: the interaction between midgut (MG) cell membrane receptors and the virus envelope glycoprotein is the initial step  in receptor-mediated endocytosis [5, 6]. This essential step determines cell permissiveness to infection. Furthermore, it is known that populations of Ae. aegypti differ greatly in their susceptibility to DENV [7–10] and this variability is determined by the effects of several genes [11, 12]. It has also been proposed  that the infection barriers in the mosquitoes are the MG infection barrier (MIB), which prevents DENV infection of MG epithelial cells, and the MG escape barrier (MEB), which prevents DENV from leaving the MG and infecting peripheral tissues, limiting the infection to MG cells. Three Ae. aegypti strains differing in DENV vector competence were selected: the susceptible DS3 strain lacks MIB and MEB, so 95–100% of these mosquitoes have disseminated infection ; the DMEB strain has MEB, and although 85% of them are infected in the MG epithelial cells, 27% develop a disseminated infection ; and the refractory strain, IBO-11, has MIB . Differences in vector competence may, at least in part, be due to the presence of specific MG epithelial receptors and their identification would be a significant step forward in understanding the interaction of the virus with the mosquito vector with possible implications for vector surveillance and control of virus transmission.
Fc gamma receptor-mediated entry of infectious DENV immune complexes into human monocytes/macrophages is hypothesized to be a key event in the pathogenesis of DHF [15–18]. However, this mechanism does not explain virus entry in primary infections or in cells with non-Fc receptors such as those of mosquitoes [19, 20].
Putative non-Fc gamma receptors differ in chemical structure ; proteins [22–34] or glycoproteins ; heparan sulfates  and LPS/CD14-associated binding proteins  have been proposed as cellular receptors for DENV. We have previously shown that the four serotypes of DENV mainly recognize two proteins with apparent molecular weights of 80 and 67 kDa [24, 29] from Ae. albopictus C6/36 cells and Ae. aegypti MG. Although a variety of receptors have been described in many studies, the mechanism by which the virus enters the cell is unknown.
A study of receptors in the DS3, DMEB and IBO-11 strains will allow us to determine whether they are related to the susceptibility of Ae. aegypti to DENV infection and transmission, and consequently whether they may serve as genetic markers of vector competence. To date, none have been described. Knowledge of one or more genes responsible for susceptibility will help in designing new control strategies that may prevent DENV infection and dissemination in the mosquito vector .
Therefore, the objective of this work was to determine whether DENV receptors from Ae. aegypti MG are related to vector competence. The aim was to identify the proteins recognized by DENV in three Ae. aegypti strains that differ in their susceptibility to infection.
Identification of DENV binding proteins in MG from DS3, DMEB and IBO-11by VOPBA
Identification of R67 and R64 in DS3, DMEB and IBO-11by immunoblotting
Thus, we found that the differences observed by VOPBA (Figure 1A) were not due to differences in the affinity of R67 and R64 for DENV, but may have been due to differences in the amounts of R67 and R64 in MG from each strain. Each specific band in the membranes was analyzed by densitometry and normalized to actin as control of the quantity of protein loaded on to each lane.
Distribution of R67/R64 in Aedes aegyptimidgut
Time-course of DENV infection in Aedes aegyptimidgut
We analyzed the time-course of infection all along the MG in order to determine the density and distribution of DENV and its binding proteins at the outset of the infective process.
DENV reached the epithelial cells in all strains 5 h after infection, before the peritrophic matrix (PM) was formed. The distribution of DENV in the IBO-11 strain was similar to the other strains until 5 h, but virus density decreased with incubation time; the fluorescence had very low intensity at 13 h after infection; and at 26 h and 14 days after infection it had completely disappeared in 80% of the analyzed MGs.
In the DS3 and DMEB strains the fluorescence was very similar in each region analyzed at all times after infection; the infection increased with time and viral envelope antigen was apparent in the BL from 5 h until 14 days after infection irrespective of the distribution in epithelial cells (evident in panel 5J).
Importantly, the highest fluorescence intensity observed in the MG at the beginning of infection (26 h after infection) was very similar to that observed by immunofluorescence assays using anti-R67/R64 antibody. All infected or non-infected MGs stained with pre-immune serum showed no-fluorescence (results not-shown).
The relationships between DENV and its arthropod vector Ae. aegypti are crucial, and analysis of host cell responses to flavivirus infection of mosquito vectors is particularly important for understanding the maintenance and transmission of the disease. Mosquito populations differ in their susceptibility to flavivirus development, termed "vector competence", reflecting the different barriers encountered by the virus from its entry into the mosquito to its release in the saliva. Factors such as specific mosquito receptors on the epithelial cells as well as differential viral replication in the mosquito are critical for vector competence in addition to other genes as has been exhibited by the QTL studies . In the laboratory we have three mosquito strains with different susceptibilities to DENV infection (DS3, DMEB and IBO-11) and these have allowed us to determine whether MG cell receptors for DENV may be markers of vector competence.
A possible explanation for the wide spectrum of DENV receptors in host cells may be that different cell types have been used; alternatively, the reported proteins may not all be cell membrane components. Increasing evidence [33, 40] suggests that DENV interacts differently with mammalian and mosquito cells; accordingly, we have studied the molecules that serve as true DENV receptors in the MG of Ae. aegypti. We previously showed by VOPBA  that the four serotypes of DENV mainly recognized two membrane proteins with apparent molecular weights of 80 (R80) and 67 (R67) kDa in Ae. albopictus C6/36 cells and Ae. aegypti MG.
Both of these receptors were detected in the MG of strains DS3, DMEB and IBO-11 in this study, although IBO-11 displayed a protein with a slightly lower apparent molecular weight (64 kDa) in addition to the 67 kDa protein, and the quantity of R67 was much lower than in the other two strains. R67 and R64 seem to be the same protein, because both are recognized by polyclonal anti-R67 and anti-R64 antibodies from the DS3 and IBO-11 strains. The size difference was also detected by two dimensional gels (Figure 2). Munoz et al.  and Mercado-Curiel et al.  showed that anti-R67 antibody inhibited DENV infection more strongly than anti-R80 in C6/36 cells. This is in agreement with the present results, since R80 was recognized in all three strains with no apparent change, suggesting that although this protein participates in DENV binding; its role may be different. It will be necessary future studies to determine R80 function during mosquito virus infection. Difference between R67 and R64 will be the objective of future studies, since they may be attributable to many facts such as post-translational modifications, different splicing or a deletion in the coding region.
Studies of the vector competence of Ae. aegypti for DENV are typically qualitative, involving the detection of viral antigens in the MG and the head. This is the first study to scan DENV infection and R67 protein distribution thoroughly along the entire MG, taking into account that MG contains morphologically different epithelial cells  with different biochemical characteristics [42, 43]. Previous studies have not determined DENV distribution in detail; most of them have concerned virus titer (presence or absence) in the whole mosquito MG [44–49].
R67/R64 were not homogeneously distributed over the epithelial cells along the MG in the three strains; they were mainly present in the cell membrane and behind the intercellular spaces in the region named pPMG, which extends from middle to the end of the posterior MG in the neighborhood of the hindgut. The quantity of R67/R64 in the pPMG region was noticeably higher in DS3 and DMEB than in the IBO-11 strain (Figure 4). The receptor distribution was similar to the distribution of infection at the outset. Moreover, we observed a correlation among receptor abundance, presence of DENV and mosquito strain susceptibility (Figures 4 and 8).
Analysis of the time course of DENV infection from the beginning to 14 days gave insight into the earliest events in DENV infection of the MG in the three strains. MG infection diminished by 14 days post-infection, as described previously . We also observed that MGs from the different strains showed a difference in the degree of infection, depending on the susceptibility of the strain. For example, the IBO-11 strain showed almost no fluorescence after 26 days.
Interestingly, DMEB strain showed increase in infection up to the 26 h in all the three MG regions infection, having the maximal virus accumulation in the pPMG and then diminished by 336 h post-infection compare to the susceptible strain DS3 that have the maximal virus accumulation in aPMG at 14 days post-infection. These results also display a statistically significative MG infection increase from the first 5 h post-infection to 26 h in DS3 and DMEB strains (**p < 0.05). Moreover, IBO-11 strain exhibited a significative decrease (**p < 0.05) of MG infection from 5 to 336 h post-infection. Furthermore, virus infection of IBO-11 strain was almost completely abolish (*p < 0.05, Figure 8) compared to DS3 and DMEB strains from 13 to 336 h post-infection.
Recently, the Ae. aegypti genome has been sequenced . This will facilitate the identification of genes encoding the R67/R64 DENV receptors, which could be important for influencing the MG infection barrier (MIB). This is in agreement with Miller and Mitchell , who showed that susceptibility, depends on multiple genes. They selected refractory or highly susceptible strains and obtained progeny with intermediate susceptibility, which suggests that alleles at vector competence loci act additively. Bosio et al.  proposed a significant additive genetic effect in MIB and demonstrated that the DENV titer in the MG and head did not correlate with the rate of infection. They also showed that the heritability for virus titer in tissues (MG or head) were almost identical in different strains of Ae. aegypti formosus; and showed that the amount of virus in the MG did not determine if virus was disseminated, which hypothetical may be due to the presence or absence of DENV receptors. In the present study we also observed similar maximum levels of DENV in the DS3 and DMEB strains, suggesting that genes that influence the virus titer have minimal impact on overall vector competence.
Further studies are needed to explain the fact that the DMEB strain, which has MEB, showed the presence of DENV in the BL all along the MG throughout the time course examined. The lack of infection in peripheral tissues may have been mainly due to the lack of cell receptors, or to additional factors specific to the kind of cell that allows DENV to infect those organs.
Ae. aegypti seems to be the most vulnerable link in the transmission chain; at present there is no genetic marker of vector competence for DENV. Such a marker would be very important in the design of new mosquito control strategies, such as campaigns focused on natural populations that could be easily identified by their high DENV susceptibility, in order to prevent dengue epidemics.
Our results may suggest that R67/R64 from the Ae. aegypti MG could be used as a vector competence marker, since those proteins are the main ones involved in the recognition of DENV by MG cells. The amount of these proteins in the MG varied proportionally to mosquito vector competence and their distribution along the MG correlated with the distribution of DENV infection.
DEN-2 Jamaica strain was expanded in Vero cells, purified from the culture supernatants as previously described [52, 53] and kept frozen at -70°C pending for use. Briefly, Vero cells were cultured at 37°C, 2% CO2 in Dulbecco's Modified Eagle's Medium (DMEM; HyClone, Logan, Utah, USA) supplemented with 5% heat-inactivated fetal bovine serum (FBS; Gibco BRL, Gaithersburg, MD, USA), 100 units/ml of penicillin and 100 μg/ml of streptomycin. Vero cells were infected with 0.2 ml of DEN-2 inoculum with an input MOI of 600 PFU/plate and incubated for 10 days; DEN-2 was purified from the clarified supernatants by a 30/60% sucrose step gradient. Titers of virus stocks made in LLC-MK2 cells  were 8 × 108 PFU/ml.
Mosquitoes (DS3, DMEB and IBO-11 strains) were laboratory-reared and maintained at 28°C and 80% RH with a 12 h photoperiod using standard mosquito-rearing procedures . They were fed with blood meals to maintain the strains and the eggs were collected in water cups containing paper filters.
Mosquito infection and midgut dissection
Mosquitoes (DS3, DMEB and IBO-11 strains) were infected via an artificial membrane feeder . Briefly, the blood meal consisted of equal parts of virus suspension, washed sheep erythrocytes and FBS in 10% sucrose. It was incubated at 38°C for 15 min, then placed in membrane feeders covered with hog gut and maintained at a constant temperature of 37°C. Mosquitoes (250, 3–4 days old) were starved of sucrose and deprived of water for 30 hours prior to blood feeding. They were allowed to feed for 45–60 minutes. Fully engorged females were selected and held in the insectary.
The entire MG was dissected from 25 mosquitoes at 5, 13, 26 h and 14 days after feeding. The procedure was carried out in 10 μl phosphate buffered saline (PBS). The MG was rinsed twice and resuspended in 10 μl of PBS. MGs were immunolabeled with a specific antibody against DEN-2 envelope protein E (anti-DEN-2 protein E).
All experiments included control mosquitoes fed with a blood meal without virus. MGs from non-infected mosquitoes were also used to obtain protein extracts and were examined by immunofluorescence with anti-R67.
DEN-2 affinity chromatography
Purified DEN-2 was bound covalently to 1 g CNBr-activated Sepharose™ 4B (Amersham Pharmacia Biotech) as described previously . The DEN-2-Sepharose™ 4B column was either used immediately or stored in 0.002% sodium azide at 4°C pending for use.
Protein extracts were obtained by homogenizing MGs (300/ml from the DS3 and IBO-11 strains) in buffer E (50 mM Tris-HCl, pH 7.2, 1 mM EDTA, 0.05% v/v Triton X-100) containing a protease inhibitor cocktail (Sigma-Aldrich P8340). To obtain the soluble proteins, the homogenate was centrifuged for 10 min at 10,000 rpm at 4°C.
Each MG protein extract (1 mg) was applied to the DEN-2-Sepharose™ 4B column (1 ml) equilibrated in buffer E and washed with the same buffer. The DEN-2 binding proteins were eluted with buffer E containing 0.5 M NaCl. Fractions of 0.5 ml were collected and the protein content was monitored by the Bradford method . The retained and eluted proteins were precipitated with acetone, resuspended in a 10 μl buffer E/protease inhibitor cocktail (Sigma-Aldrich P8340) and analyzed by 10% sodium dodecylate sulfate polyacrylamide gel electrophoresis (SDS-PAGE) .
Preparation of specific polyclonal antibodies against DEN-2 protein E, R67 and R64
To obtain specific anti-DEN-2 protein E, 10% SDS-PAGE was performed with purified DEN-2 and the corresponding 52 kDa band from the silver-stained gel was excised and used to immunize BALB/c mice as described below.
Proteins retained and eluted from the DEN-2-Sepharose™ 4B column were separated by 10% SDS-PAGE. After silver staining, the 64 or 67 kDa band was excised, cut into small pieces, suspended in PBS and mixed with an equal volume of Titer-Max adjuvant (CytRx Vaxcel Inc., Norcross, GA) to immunize two groups of BALB/c mice and obtain specific antibodies against R67 or R64 from DS3 or IBO-11 strain Ae. aegypti MGs.
Pre-immune sera were obtained before immunization. The mice received a booster fifteen days after the first immunization. They were bled after thirty days and the sera were stored at -70°C until use. Negative controls using pre-immune sera were included in all assays. All immunofluorescence and immunoblotting results were reproducible using either anti-R67 or R64 from either DS3 or IBO-11.
Immunofluorescence with anti-DEN-2 protein E and anti-R67
After the MGs were dissected from the different strains and different infection times, including non-infected mosquitoes as negative control; they were fixed for 2 h in 4% p-formaldehyde (Sigma-Aldrich Corporation), washed with PBS, 0.2% PBT (5% BSA, 0.2% Triton X-100 in PBS), incubated overnight at 4°C with anti-DEN-2 protein E diluted 1:75 or anti-R67 diluted 1:40, washed with 0.1% PBT (0.1% Triton X-100), incubated for 2 h with 1:500 FITC goat anti/mouse (Zymed Laboratories Inc. S. San Francisco, CA USA), stained with 1 μg/ml propidium iodide (Sigma-Aldrich Corporation), and then washed with 0.1% PBT. Finally, each MG was placed individually on a glass slide with a Vecta Shield (Vector Laboratories). All preparations were examined by confocal microscopy (TCS SP5 Leica Microsystems).
Confocal microscopy analysis
Confocal Image was captured using a Leica confocal microscope scanning system. The confocal microscope was set up for all the experiments as follow: speed 400 Hz, PMT1-746, PMT2-933, potency 1/3 and laser 26%. Fluorescence evaluation was made using a 64× (NA 0.3) objective. The lens is raised to its maximum specified height. The detector is secured on the stage and centered grossly using either laser fluorescent or light. The detector position is then adjusted more accurately to achieve maximum signal intensity by using the microscope's x/y joystick. The CLSM zoom factor is set from 8 to 32 to reduce the beam scan and to focus it into the "sweet spot" of the detector.
A series of 30 successive sections were recorded along the optical axis of the microscope over a range of the specimen planes with a depth separation of 1 μm for each one of the three different MG regions (Cardia/AMG, aPMG, pPMG) and mosquito strains, comprising a total of 3 series of 30 slices. Then each confocal fluorescence images was divided in areas of 1000 μm2. This was done for every time and each mosquito strain.
The Leica software (1997–2002, Leica Microsystems Heidelberg GmbH) was used to evaluate all images. ANOVA statistic analysis was conducted for all the data.
Results represent the analysis of at least 20 MGs for each infection time and for each mosquito strain in four independent experiments.
The means and standard errors of means (S.E.M.) were calculated for all groups. The data was subjected to a two-way analysis of variance (ANOVA) by General Linear Model followed by All Pairwise Multiple Comparison Procedures (Student-Newman-Keuls Method) to determine whether means were significantly different among them. All P values less than 0.05 were considered to indicate statistical significance. All the statistics were carried out in SigmaStat 2.03 software and data plotted in SigmaPlot 2001.
2D gel electrophoresis
Midguts (300) from each strain were solubilized in 125 μl of IPG strip rehydration buffer (8 M urea, 2% CHAPS, 10 mM DTT, 0.2% Bio-Lyte) at room temperature and centrifuged at 10,000 rpm for 10 min. The resulting supernatants, containing approximately 936 μg protein for DS3, 1080 μg for DMEB and 1143 μg for IBO-11, were used to rehydrate each ReadyStrip IPG, pH range 3–10, 7 cm (BioRad Laboratories, Hercules, CA, USA) under passive conditions overnight at 4°C in the focusing tray (Mini-PROTEAN 3 cell). Subsequently, IEF was carried out as recommended by the manufacturer (2 h at 4000 V with a gradient until a total of 10000 volt-hour was reached).
The strips were removed from the focusing tray and incubated for 15 min in 1 ml equilibration buffer I (50 mM Tris-HCl, pH 8.8, 6 M urea, 2% SDS, 30% glycerol, 1% DTT) and 15 min in equilibration buffer II (6 M urea, 0.375 M Tris-HCl, pH 8.8, 2% SDS, 20% glycerol, 2.5% w/v iodoacetamide). They were washed with distilled water and placed on the top of the second dimension gel (10% SDS-PAGE). Molecular weight markers were applied to small pieces of chromatography paper and inserted next to each strip on the top of the gel, then the strips and markers were sealed with ReadyPrep Overlay Agarose (0.5% low melting point agarose in 1X Tris/Glycine/SDS and 0.003% Bromophenol Blue). The second dimension was developed at a constant 150 V (Mini Protean 3, BioRad Laboratories, Hercules, CA, USA). The gels were silver stained or used for 2D VOPBA as described below.
1D and 2D virus overlay protein binding assay (VOPBA)
MG protein extracts (35 μg) from each strain, or 72 μg for DS3, 59 μg for DMEB and 155 μg for IBO-11, were obtained as mentioned above by DEN-2 affinity chromatography and separated by 10% SDS-PAGE. Two dimensional gels were developed with approximately 1000 μg protein from MGs of each strain. All the gels were blotted on to polyvinylidine difluoride (PVDF) membranes using the WetBlot technique (BioRad Laboratories, Hercules, CA, USA) in transfer buffer (15.6 mM Tris-HCl, 120 mM glycine, 20% methanol). After transfer was complete, VOPBA was performed as previously described . Briefly, the membrane was blocked for 1 h at room temperature with 5% skim milk in TBS (100 mM Tris-HCl, 0.15% NaCl), incubated overnight with purified DEN-2, washed with TTBS (100 mM Tris-HCl, 0.15% NaCl, 0.2% Tween 20) and incubated overnight with 1:200 anti-DEN-2 protein E at 4°C. Mouse anti-rat brain actin Mab (generously provided by Dr. Manuel Hernandez-Hernandez from the department of Cell Biology, Centro de Investigación y de Estudios Avanzados del IPN, Mexico) diluted 1:50 was also included in the VOPBA from 1D gels. The epitope recognized by this MAb is conserved among all actins. After washing with TTBS, the membrane was incubated for 2 h at room temperature with 1:1000 alkaline phosphatase (AP) labeled goat anti-mouse (Zymed Laboratories Inc. S. San Francisco, CA USA) and the reactive proteins were visualized by color development with the chromogenic substrate BCIP/NBT.
Immunoblotting with anti-R67 and anti-R64
MG protein extracts from the DS3, DMEB and IBO-11 strains were separated by 10% SDS-PAGE, transferred to PVDF membranes (BioRad Laboratories, Hercules, CA, USA) and incubated with anti-R67 or anti-R64 diluted 1:75 in TBS (100 mM Tris-HCl, 0.15% NaCl). In addition, anti-actin antibodies diluted 1:50 in TBS were used. The membranes were incubated for 2 h at room temperature with the secondary antibody, AP goat anti-mouse (Zymed Laboratories Inc., San Francisco, CA, USA) diluted 1:1000, and color was developed as recommended by the manufacturer and described above.
We acknowledge the M. Sc. Maria Leticia Avila Ramirez for statistical analysis. Doctor Alvaro Diaz-Badillo is gratefully acknowledged for their help during the development of this research. This research was supported by the United States Public Health Service Grant AI 45430 sub grant G-46321.
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