http://orcid.org/0000-0003-1765-0002
Figures
Abstract
Background
The liver fluke Opisthorchis viverrini infects several million people in Southeast Asia. Adult flukes live in the bile ducts of humans, where they cause hepatobiliary pathology, including cholangiocarcinoma. Here, we investigated the potential of extracellular vesicles (EVs) secreted by the fluke and defined recombinant proteins derived from EVs to generate protective immunity in a hamster vaccination-challenge model.
Methodology/Principal findings
EVs isolated from the excretory-secretory products of O. viverrini and two recombinant EV surface proteins encoding the large extracellular loops (LEL) of Ov-TSP-2 (rOv-TSP-2) and Ov-TSP-3 (rOv-TSP-3) were adjuvanted and used to vaccinate hamsters intraperitoneally followed by challenge infection with O. viverrini metacercariae. The number of adult flukes recovered from hamsters immunized with EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 were significantly reduced compared to control animals vaccinated with adjuvant alone. The number of eggs per gram feces was also significantly reduced in hamsters vaccinated with rOv-TSP-2 compared to controls, but no significant differences were found in the other groups. The average length of worms recovered from hamsters vaccinated with EVs, rOv-TSP-2 and rOv-TSP-3 was significantly shorter than that of worms recovered from the control group. Anti-EV IgG levels in serum and bile were significantly higher in hamsters vaccinated with EVs compared to control hamsters both pre- and post-challenge. In addition, levels of anti-rOv-TSP antibodies in the serum and bile were significantly higher than control hamsters both pre- and post-challenge. Finally, antibodies against rOv-TSP-2 and rOv-TSP-3 blocked uptake of EVs by human primary cholangiocyte in vitro, providing a plausible mechanism by which these vaccines exert partial efficacy and reduce the intensity of O. viverrini infection.
Author summary
Cholangiocarcinoma (CCA) is a significant public health problem in countries throughout Southeast Asia. In these areas CCA has a strong association with chronic infection with the food-borne liver fluke Opisthorchis viverrini. Current control of the infection relies on chemotherapy and health education, however these approaches are not sustainable in isolation. Hence, there is an urgent need for a vaccine against this neglected tropical disease. A vaccine against O. viverrini would confer anti-cancer protection in similar fashion to the acclaimed vaccine for human papillomavirus and cervical cancer. Toward this goal, secreted extracellular vesicles (EVs) of O. viverrini and recombinant proteins from the surface of EVs were generated and tested as vaccines in a hamster challenge model. Vaccination of hamsters with EVs and recombinant proteins induced production of antibodies in serum and bile, and those antibodies blocked uptake of EVs by primary bile duct cells in vitro. Challenge of vaccinated hamsters with infective stage flukes markedly reduced adult fluke recovery compared to the adjuvant control group. This is the first report of successful vaccination of hamsters with O. viverrini EVs and recombinant vesicle surface proteins, and provides proof-of-concept for development of subunit vaccines for this carcinogenic infection.
Citation: Chaiyadet S, Sotillo J, Krueajampa W, Thongsen S, Brindley PJ, Sripa B, et al. (2019) Vaccination of hamsters with Opisthorchis viverrini extracellular vesicles and vesicle-derived recombinant tetraspanins induces antibodies that block vesicle uptake by cholangiocytes and reduce parasite burden after challenge infection. PLoS Negl Trop Dis 13(5): e0007450. https://doi.org/10.1371/journal.pntd.0007450
Editor: Mar Siles-Lucas, IRNASA, CSIC, SPAIN
Received: January 4, 2019; Accepted: May 9, 2019; Published: May 28, 2019
Copyright: © 2019 Chaiyadet et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This research was financially supported by a project grant from the National Health and Medical Research Council of Australia (NHMRC), grant identification number APP1085309, and the National Cancer Institute, National Institute of Health, grant number 5R01CA164719-03 and 2R01CA164719-06A1. AL acknowledges support from a NHMRC senior principal research fellowship (1117504). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
The human liver fluke Opisthorchis viverrini is endemic in different countries of Southeast Asia including Thailand, Lao PDR, Cambodia, southern part of Vietnam and Myanmar [1, 2]. Furthermore, liver fluke infection is associated with a high incidence of liver pathology including cholangiocarcinoma (CCA) [3, 4]. Current control efforts rely on drug treatment and health education; however, they are not sustainable [5, 6]. Hence, it is essential to develop new interventions for long-term protection against O. viverrini infection, and a vaccine approach is an attractive strategy to reduce parasite burden and achieve ultimate eradication of the parasite.
O. viverrini-induced hepatobiliary damage is multi-factorial, and includes several factors such as mechanical damage of the epithelium by the suckers of the worm, secreted parasite metabolites [7, 8] and different immunopathological processes [9]. The metabolic products of O. viverrini are highly immunogenic and stimulate immunopathology [8], and include tegumental and secreted proteins comprising more than 300 proteins [10]. In addition to secretion of soluble protein, we have previously reported that O. viverrini secretes exosome-like extracellular vesicles (Ov-EVs) [11]. EVs are 40–100 nm in size and of endocytic origin; they are enriched in various lipids, nucleic acids and proteins including tetraspanins, heat shock protein and actin [12]. O. viverrini tetraspanins (Ov-TSPs), belonging to both the CD9 and CD63 families, were found to be enriched in Ov-EVs and abundantly expressed on the outermost tegument of adult worms [13, 14]. Ov-TSPs play an important role in dynamic host-parasite interactions, particularly maintenance of tegument membrane integrity, and their suppression using RNA interference results in a vacuolated tegument in vitro [13, 14]. EVs have been used as protective vaccines in mouse models of intestinal helminths, including the nematodes, Trichuris muris [15] and Heligmosomoides polygyrus [16] and the trematode, Echinostoma caproni [17]. Given the abundance of tetraspanins on the surface of fluke EVs [18, 19] and the ability of antibodies against Ov-TSP-1 to block uptake of EVs by host cells [13], we propose that fluke TSPs could be used as vaccines to interrupt host-parasite communication [20]. Moreover, TSPs from the surface of schistosomes have proven to be efficacious vaccines in animal models of blood fluke infection [21].
In the present study we assessed the vaccine potential of O. viverrini EVs and recombinant Ov-TSPs derived from the EVs surface and the ability of antibodies from vaccinated animals to block EVs uptake by host cells.
Materials and methods
Preparation of O. viverrini metacercariae
O. viverrini metacercariae were prepared as previously described [22]. Briefly, cyprinid fishes from natural sources were homogenized with a blender and the homogenized fish was added to pepsin solution (0.25% pepsin powder, 15% HCl in normal saline solution—NSS) at a ratio of 1:3, followed by incubation at 37°C for 1 hour to enable digestion. The digested solution was filtered through 1,000, 300, and 106 μm meshes. The debris obtained by filtering with the 106 μm mesh was washed and repeatedly sedimented with NSS until clear. Sediments were examined for metacercariae under a dissecting microscope. O. viverrini metacercariae were collected and stored in sterile NSS at 4°C until used.
Production of recombinant Ov-TSP-2 and -3 and rabbit antisera
The large extracellular loop (LEL) from Ov-TSP-2 and Ov-TSP-3 were recombinantly produced as fusions with thioredoxin (TRX) using the plasmid pET32a+ (Novagen, USA) in Escherichia coli and purified as previously described [19]. New Zealand rabbits were immunized with rOv-TSP-2 or -3 and antisera was collected as previously described [19].
Isolation of O. viverrini extracellular vesicles (Ov-EVs)
EVs were isolated from the excretory/secretory (ES) products released by adult O. viverrini (OvES) as described previously with modifications [11, 23, 24]. Briefly, O. viverrini adult worms were cultured in RPMI-1640 containing 1% glucose, antibiotics (Penicillin-Streptomycin 100 μg, Invitrogen, USA) and the 1 μM protease inhibitor E64 (Thermo Scientific, USA). Worms were maintained in vitro at 37°C and supernatants containing the OvES were collected twice each day for up to 7 days and centrifuged at 2,090 g for 10 min to remove the eggs. OvES was concentrated and buffer exchanged to 1x PBS using a 10 kDa cut-off purification column (Amicon, Merk Millipore, USA). One (1) ml of concentrated OvES was centrifuged at 500 g, 2,000 g, 4,000 g and 12,000 g for 30 min each to remove cell debris. The supernatant was filtered using a 0.22 μm filter (Sartorius, Germany), and subsequently pelleted by ultracentrifugation at 110,000 g for 3 hours. The OptiPrep density gradient ultracentrifugation (ODG) was prepared by diluting a 60% Iodixanol solution (Sigma Aldrich, USA) with 0.25 M sucrose in 10 mM Tris-HCl, pH 7.2 to make 40%, 20%, 10% and 5% iodixanol solutions and then 1.0 ml of these solutions was layered in decreasing density in an ultracentrifuge tube. Pelleted O. viverrini EVs (Ov-EVs) were layered on top of the gradient and further centrifuged at 110,000 g for 18 h at 4°C. The fractions with a density of 1.12–1.24 g/mL were pooled and buffer exchanged to PBS using 100 kDa cut-off purification columns (Amicon, Merk Millipore, USA) and resuspended in 200 μl of PBS.
Vaccination and challenge of hamsters
Male Syrian golden hamsters 6–8 weeks-old were used for vaccination studies. Sample size was calculated using two sample inference for comparing two means (https://www.stat.ubc.ca/~rollin/stats/ssize/n2.html) [25]. A sample size of n = 9 was selected on the assumption of a vaccine trial resulting in a mean of 40 worms per hamster for μ1 (adjuvant control) and 25 worms per hamster for μ2 (test group), σ = 11, two-sided test, with α = 0.05 and power of 0.80. A total of 45 hamsters were divided into 5 groups (9 hamsters/group) including 1) vaccinated with 10 μg of Ov-EVs, 2) vaccinated with 50 μg of rOv-LEL-TSP-2, 3) vaccinated with 50 μg of rOv-LEL-TSP-3, 4) vaccinated with 50 μg of rOv-LEL-TSP-2 plus 50 μg of rOv-LEL-TSP-3. Both EVs and recombinant proteins were formulated with an equal volume of a colloidal suspension of aluminium hydroxide gel (alum) (Invivogen, USA) and CpG ODN 1826 (10 μg) (Invivogen, USA). A fifth group of hamsters were injected with 10 μg of alum/CpG only (adjuvant control group) as a control group. Vaccines were injected intraperitoneally on days 0, 14 and 28; and hamsters were challenged with 50 metacercariae via the oral route on day 42 (2 weeks after last vaccination). Hamsters were finally sacrificed at 8 weeks post-challenge. Blood was collected for serum by heart puncture after euthanasia and bile was collected from the gall bladder. Whole livers were collected to investigate the number of flukes.
Faecal egg counts and worm recovery
Faeces from individual hamsters from each group were collected 6 weeks after challenge, and eggs per gram feces (EPG) were counted and calculated using a modified formalin-ether acetate technique [26]. Briefly, 2 grams of hamster feces were fixed in 10 ml of 10% formalin solution, filtered through two layers of gauze, the filtered solution centrifuged at 500 g for 2 minutes, and the supernatant discarded. The pellet was re-suspended with 7 ml of 10% formalin, vigorously mixed with 3 ml ethyl acetate and then centrifuged at 500 g for 5 minutes. The pellet was dissolved in 1 ml of 10% formalin solution and examined in duplicate under light microscopy at 400x magnification. EPG was calculated as follows: (average of number eggs x total drops of fecal solution)/ g of feces. Whole livers from the hamsters were dissected in NSS and adult worms were collected and counted. The percent reduction of worm recovery was calculated as previously described [27]: % Worm reduction = ((Wc–We) / Wc) x 100 (Wc = worm burden in control group, We = worm burden in experiment group). To measure worm length, 21.4–42.2% of the total worms recovered from each group were randomly selected. Worms were washed three times with NSS and fixed in pre-warmed 10% formalin. Worms were photographed under microscopy and worm length was measured using NIS-Element software (Nikon, Japan).
Indirect ELISA for specific IgG
Specific IgG against rOv-TSP-2, rOv-TSP-3, OvES, or Ov-EVs was measured in the serum and bile by indirect ELISA. Hamster serum and bile were collected as described above. Polystyrene flat bottom96-well ELISA plates (NUNC-F96, Fisher Scientific, USA) were coated with 100 μl of rOv-TSP-2 or rOv-TSP-3 or OvES (1 μg/ml) or Ov-EVs (2 μg/ml) overnight at 4°C in coating buffer (0.05 M Na2CO3/NaHCO3, pH 9.6). Plates were washed with PBS 0.05% Tween-20 (PBST) and, then, blocked with 200 μl 5% skim milk in PBST for 2 hours at 37°C. One hundred (100) μl of sera (1:2,000 in PBST/2% skim milk) or bile (1:200 in PBST/2% skim milk) were added and incubated for 2 hours at 37°C. The plates were washed with PBST and probed with 100 μl of anti-hamster IgG conjugate HRP (BioRad, USA) (1:2000 in PBST for serum and 1:1,000 for bile). After washing with PBST, the plates were developed by adding 50 μl TMB (Thermo Fisher Scientific, USA) for 20 minutes, and reaction was stopped by adding 50 μl of 2N H2SO4. The colorimetric reaction was read at a wavelength of 450 nm on a Spectra Max microplate reader (Molecular Devices, USA).
Western blot
Five (5) μg of OvES, OvEVs, OvES depleted of OvEVs, rOv-TSP-2 and rOv-TSP3 were loaded and electrophoresed in a 15% SDS-PAGE gel and proteins were transferred to a nitrocellulose membrane (Mini Trans-Blot Cell, Bio-Rad, USA). Membranes were probed with vaccinated hamster serum (1:200) by incubation at 4°C overnight followed by incubation with anti-hamster IgG-HRP (1:1,000) at 25°C for 2 h. The reaction color was developed by adding Luminata Forte Western HRP Substrate (Millipore, USA).
Blocking of O. viverrini EVs internalization by host cells
Five (5) μg of Ov-EVs were labeled with PKH67 (Sigma-aldrich, USA) following the manufacturer’s instructions and incubated with anti-Ov-TSP-2 or -TSP-3 rabbit sera [19], with vaccinated hamster sera (Ov-TSP-2, Ov-TSP-3, Ov-TSP-2 plus -3 and Ov-EVs) or with control sera (adjuvant alone) at a 1:2.5 dilution for 1 hour at room temperature. Ov-EVs-antibody complexes were washed by 1x PBS using 100 kDa cut-off purification columns (Amicon, Merk Millipore, USA) and cultured with H69 cells for 2 hours. Nuclei were stained with 2 μg/ml of Hoechst (Invitrogen, USA) for 15 minutes. The image was taken using a Carl Zeiss confocal microscope (LSM800, USA) at 200x of the original magnification. Thirty cells from 2 biological replicates were analyzed for fluorescence intensity using imageJ version 1.50i.
Statistical analysis
All data are represented as mean ± SD of three independent experiments using Graphpad Prism Software Version 6.03 (www.graphpad.com). Data from worm burden, EPG, worm length, ELISA experiments and fluorescence intensity were evaluated by Student’s t-test.
Ethics statement
Male Syrian (golden) hamsters (Mesocricetus auratas) were reared at the animal facilities of the Faculty of Medicine, Khon Kaen University. Experimentation protocols were approved by the Animal Ethics Committee of Khon Kaen University according to the Ethics of Animal Experimentation of the National Research Council of Thailand, with the approval number ACUC KKU 10/2559.
Results
O. viverrini tetraspanin antibodies inhibit internalization of Ov-EVs by human cholangiocytes
H69 human cholangiocytes actively internalize Ov-EVs [11]. Co-culture of fluorescently labeled Ov-EVs with antisera from rabbits vaccinated with rOv-TSP-2 and rOv-TSP-3 resulted in 91% (****P<0.0001) and 77% (****P<0.0001) reductions respectively in uptake of EVs by cells compared to control cells that were cultured with pre-immunization rabbit serum (Fig 1).
PKH67-labeled Ov-EVs were incubated with rabbit antisera to rOv-TSP-2 or rOv-TSP-3 or pre-immunization serum prior to co-culture with H69 cholangiocytes. Panel A = rabbit pre-immunization serum, panel B = rabbit antiserum to rOv-TSP-2 1:2.5, panel C = rabbit antiserum to rOv-TSP-3 1:2.5. Panel D shows fluorescence intensity at 490 nm (green channel). The nuclei were stained by Hoechst (blue color) (**** P<0.0001).
IgG levels in the serum and bile of hamsters vaccinated with Ov-EVs and rOv-TSPs
Hamsters vaccinated with Ov-EVs showed a significant increase in serum IgG against OvES (Fig 2A) and Ov-EVs (Fig 2B) when compared with pre-immunization sera and sera from the adjuvant control group (P<0.0001). On the other hand, the IgG levels against OvES post-vaccination but pre-challenge in hamsters vaccinated with rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 were not statistically significant compared to the adjuvant control group (S1 Fig).
Serum IgG was measured from hamsters immunized with Ov-EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 at pre-immunization, pre-challenge and post-challenge. The IgG levels were measured against OvES (A), Ov-EVs (B), rOv-TSP-2 (C) and rOv-TSP-3 (D). Results represent the mean absorbance measured at 450 nm for each group. Significant differences are denoted by an asterisk over the bar (**** P<0.0001).
The total serum IgG against rOv-TSP-2 in hamsters immunized with rOv-TSP-2 and rOv-TSP-2+rOv-TSP-3 was significantly higher at pre-challenge and post-challenge compared to pre-immunization and adjuvant control sera (P<0.0001) (Fig 2C).
Likewise, the serum IgG against rOv-TSP-3 levels in hamsters immunized with Ov-EVs, rOv-TSP-3 or rOv-TSP-2+rOv-TSP-3 were significantly higher pre- and post-challenge than pre-immunization and adjuvant control sera (P<0.0001) (Fig 2D).
Total bile IgG against OvES was significantly higher post-vaccination but pre-challenge in hamsters vaccinated with Ov-EVs (P< 0.05), rOv-TSP-2 (P<0.01) and rOv-TSP-2+rOv-TSP-3 (P<0.01) when compared with adjuvant control bile, while IgG levels in post-challenge samples were significantly higher in rOv-TSP-2 (P<0.001) and rOv-TSP-2+rOv-TSP-3 (P<0.0001) vaccinated groups than in the adjuvant group (Fig 3A).
Bile IgG was measured by ELISA at pre-challenge and post-challenge against OvES (A), rOv-TSP-2 (B) and rOv-TSP-3 (C). Results represent the mean absorbance measured at 450 nm for each group. Significant differences are denoted by an asterisk over the bar (**** P<0.0001, *** P<0.001, ** P<0.01, * P<0.05).
IgG levels against rOv-TSP-2 in the bile of hamsters immunized with rOv-TSP-2 and rOv-TSP-2+rOv-TSP-3 were significantly higher than bile IgG from the adjuvant control group (Fig 3B). Furthermore, the IgG levels in the bile of rOv-TSP-2+rOv-TSP-3 vaccinated animals were significantly (P<0.05) higher at pre-challenge and post-challenge compared to the same samples from the adjuvant group. In the Ov-EVs vaccinated group, bile IgG levels against rOv-TSP-2 post-challenge were higher than those obtained pre-challenge (P<0.05) and in the adjuvant control groups, but these differences did not reach significance (Fig 3B).
IgG antibody levels in bile against rOv-TSP-3 were not statistically different in the pre-challenge or post-challenge samples in any group when compared to the adjuvant group (Fig 3C).
Vaccination with Ov-EVs and Ov-TSPs decreased worm burden in hamsters challenged with O. viverrini
Hamsters immunized with Ov-EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 had significantly lower worm burdens than the control group post-challenge (P<0.05) (Fig 4A). The number of worms was reduced by 27% (P<0.05), 34% (P<0.01), 30% (P<0.001) and 21% (P<0.001) respectively when compared with the adjuvant control group (Fig 4A). Furthermore, mean EPG in hamsters vaccinated with Ov-EVs and rOv-TSP-2 were reduced by 32% (P<0.01) and 41% (P<0.001) respectively compared to the adjuvant control group (Fig 4B). Vaccination with rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 had no effect on EPG when compared with the control group (Fig 4B).
Panel A, Worm burden from each hamster and worm reduction rate in hamsters vaccinated with O. viverrini EVs (Ov-EVs), rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 and control alum/CpG (adjuvant). ** P<0.01, *** P<0.001, **** P<0.0001. Panel B = Number of eggs per gram of feces (EPG) from each vaccinated hamster with mean and SD bar shown (** P<0.01, *** P<0.001).
Growth retardation of worms recovered from hamsters vaccinated with Ov-EVs and rOv-TSPs
The body length of recovered worms from hamsters vaccinated with Ov-EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 was significantly (P<0.001) shorter than worms recovered from the control adjuvant group (Fig 5A). The average length of examined worms from hamsters vaccinated with Ov-EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3 was 2.92±0.55, 2.93±0.50, 3.01±0.61, 2.82 ±0.51 mm, respectively while the average length of worms from control adjuvant group was 33.89±0.77 mm. A representation of the morphology of the worms from each group is shown in Fig 5B.
The body length of 21.4–42.2% of randomly selected worms recovered from each experimental group of vaccinated hamsters was measured using the NIS-element program (A). Flukes from vaccinated animals were significantly shorter than those from hamsters that received adjuvant alone (B).
Sera from vaccinated hamsters recognize O. viverrini proteins
OvES, OvES depleted of EVs (dEVs), rOv-TSP-2 and rOv-TSP-3 were probed with a pooled serum from each group of vaccinated hamsters by western blot. OvES was only detected by pre-challenge serum from the Ov-EVs vaccinated group. The rOv-TSP-2 protein was detected by pooled sera from pre-challenge hamsters vaccinated with rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3, while the rOv-TSP-3 protein was recognized by pooled sera from hamsters vaccinated with Ov-EVs, rOv-TSP-2, rOv-TSP-3 and rOv-TSP-2+rOv-TSP-3. As expected, none of the samples were detected by pooled serum from hamsters vaccinated with adjuvant alone (S2A Fig). Post-challenge sera from all vaccinated groups reacted against all samples (OvES, rOv-TSP-2, rOv-TSP-3, dEVs and Ov-EVs), indicating that the native extracts (OvES and EVs) as well as recombinant TSP-2 and TSP-3 are immunogenic in the course of a natural infection (S2B Fig).
Antibodies of vaccinated hamsters block uptake of Ov-EVs by host cells
PKH67-labelled Ov-EVs were incubated with pooled sera of hamsters vaccinated with rOv-TSP-2, rOv-TSP-3, rOv-TSP-2+rOv-TSP-3, Ov-EVs and from the control groups at a dilution of 1:2.5 before being cultured with H69 cholangiocytes. Ov-EVs uptake was significantly reduced more than 77% and 72% after incubation with rOv-TSP-2 and rOv-TSP -3 vaccinated hamster serum, respectively (Fig 6C, 6D and 6G) when compared with pre-immunization serum and serum from the adjuvant group (Fig 6A). Likewise, antisera to rOv-TSP-2+rOv-TSP-3 and antisera to Ov-EVs blocked Ov-EVs internalization by cholangicytes by more than 80% (Fig 6E, 6F and 6G).
PKH67 labeled Ov-EVs was incubated with hamster antisera to rOv-TSP-2 or rOv-TSP-3 or rOv-TSP-2+rOv-TSP-3 or adjuvant or pre-immunization prior to co-culture with H69 cholangiocytes. Panel A = hamster pre-immunized serum, panel B = Adjuvant hamster serum, panel C = hamster antiserum to rOv-TSP-2, panel D = hamster antiserum to rOv-TSP-3, panel E = hamster antiserum to rOv-TSP-2 plus -3 and panel F = hamster antiserum to Ov-EVs. Panel G shows fluorescence intensity of internalization at 490 nm (green channel). The nuclei were stained by Hoechst (blue color) (**** P<0.0001).
Discussion
The presence of EVs in OvES products precipitated the hypothesis that these vesicles are important in host-parasite communication and immunopathogenesis [11]. EVs have also been characterized in others trematodes such as Echinostoma caproni [28], Fasciola hepatica [29] and Schistosoma spp. [18, 30, 31]. Moreover, other helminths such as the gastrointestinal nematodes H. polygyrus [16, 32] and N. brasiliensis [33] also secrete EVs enriched in specific proteins and miRNAs and can suppress the immunological response in vivo.
In the present study we have shown that immunization of hamsters with Ov-EVs reduced both worms burden and egg production, and that IgG antibody levels specific to Ov-EVs were significantly raised in serum and in bile of vaccinated hamsters. The development of the adult parasites was significantly hampered in hamsters vaccinated with Ov-EVs, as demonstrated by stunted parasite growth in vaccinated hamsters. Other groups have also studied the ability of EVs to control trematode and other helminth infections. For instance, purified EVs from Echinostoma caproni used to vaccinate mice prior to parasite challenge resulted in elevated antibody (IgG) responses but vaccination did not reduce the number of adult worms in the gut after challenge infection [17]. Vaccination of mice with EVs from the nematode H. polygyrus resulted in worm reduction of 82% [16].
The use of native helminth EVs as vaccines is not feasible due to the difficulty in culturing sufficient numbers of worms to collect the required amount of EVs material, however the utility of sera from EVs-vaccinated animals as a discovery tool is evident. With that in mind, we reasoned that proteins that are abundant on the surface of Ov-EVs might impart protective immunity by blocking fluke EVs-host cell interactions. To our knowledge, this is the first report of vaccination with recombinant proteins specifically aimed at inducing antibodies against EVs surface proteins and subsequent blocking of EVs uptake by host cells.
Ov-TSP-2 and Ov-TSP-3 are members of the CD63 family of tetraspanins and have been shown to be abundantly expressed in the O. viverrini tegument as well as enriched in Ov-EVs [11]. Vaccination of hamsters with rOv-TSP-2 and rOv-TSP-3 strong IgG responses that were readily detectable in both sera and bile–the fluid surrounding adult flukes in the biliary tract. The presence of specific IgG in the bile might be a result of diffusion from the blood vessels into the gall bladder where they impact on resident flukes. Previous vaccine studies have used crude O. viverrini antigens to immunize hamsters prior to challenge with metacercariae [6], but to our knowledge this is the first report of successful vaccination of hamsters with O. viverrini recombinant antigens. The utility of tetraspanins as helminth vaccines is evident in schistosomiasis where Sm-TSP-2 is one of the leading vaccine candidates for a human schistosomiasis vaccine [21] and has recently completed phase 1 clinical trials [34].
Antibodies against proteins specific to the Ov-EVs membrane such as the TSPs from sera from vaccinated animals (pre-challenge) significantly blocked EVs internalization by cholangiocytes. These antibodies might block the ability of the parasite to communicate with its host, thereby impairing the establishment and growth of the parasite by interrupting its ability to suppress inflammation. Worms recovered from vaccinated animals were stunted, supporting this hypothesis. It has been previously shown that blocking Ov-EVs internalization decreases the levels of IL-6 (a cytokine heavily implicated in the development of fibrosis) and cell proliferation [11]. We suggest that antibodies specific to the Ov-EVs surface may be performing neutralizing roles by blocking the ability of fluke EVs to hijack host cholangiocytes and interfere with induction of wound healing processes that repair damaged biliary tissue [35, 36] and promote long-term survival of the flukes. Clearly, other molecular mechanisms that are independent of EVs are utilized by liver flukes to communicate with their hosts, including proteins, peptides, glycans and lipids that direct interact with host cells [37].
In contrast to our findings reported herein where antibodies to EV surface TSPs block uptake of vesicles by cholangiocytes, a recent report described enhanced uptake by macrophages of F. hepatica EVs in the presence of antibodies against a CD63-like TSP on the vesicle surface [38]. This is likely due to opsonisation of EVs and FcR-mediated uptake by antigen presenting cells [16, 38] as opposed to distinct EV uptake by non-phagocytic target cells such as cholangiocytes that we describe herein.
In summary, immunization with rOv-TSP-2 and Ov-EVs elicit robust antibody responses which is key for protection against fluke infection, resulting in reduction of worms and egg burden. Moreover, antibodies produced against rOv-TSP-2 significantly blocked internalization of Ov-EVs by cholangiocytes. The tetraspanin proteins present in the membrane of EVs are key in cell contact and uptake [39], and impairing this interaction could be blocking important host-parasite interactions affecting the survival of the parasite. This is the first study to determine the vaccine efficacy of Ov-EVs or the recombinant tetraspanins rOv-TSP-2 and rOv-TSP-3 against a challenge infection with metacercariae of O. viverrini in hamsters, and it supports the notion that targeting interactions between fluke EVs and their mammalian host cells holds promise for the discovery of novel vaccine candidates.
Supporting information
S1 Fig. Serum IgG against Ov-ES of vaccinated hamsters.
ELISA showing IgG levels against Ov-ES of pre-immunized, pre-challenge or post-challenge hamster sera from each vaccinated group.
https://doi.org/10.1371/journal.pntd.0007450.s001
(TIF)
S2 Fig. Western blot analysis of the recognition of O. viverrini proteins by sera from vaccinated hamsters.
OvES, rOv-TSP-2, rOv-TSP-3, Ov-ES-depleted EVs (dEVs) and Ov-EVs were probed with pre-challenge hamster sera (A) or post-challenge hamster sera from each vaccination group (B).
https://doi.org/10.1371/journal.pntd.0007450.s002
(TIF)
Acknowledgments
We thank laboratory staffs of the Department of Parasitology and Tropical Disease Research Laboratory, Department of Pathology, Faculty of Medicine, Khon Kaen University for technical supports.
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