key: cord-0689282-ikomc19t
authors: van Doremalen, Neeltje; Lambe, Teresa; Sebastian, Sarah; Bushmaker, Trenton; Fischer, Robert; Feldmann, Friederike; Haddock, Elaine; Letko, Michael; Avanzato, Victoria A.; Rissanen, Ilona; LaCasse, Rachel; Scott, Dana; Bowden, Thomas A.; Gilbert, Sarah; Munster, Vincent
title: A single-dose ChAdOx1-vectored vaccine provides complete protection against Nipah Bangladesh and Malaysia in Syrian golden hamsters
date: 2019-06-06
journal: PLoS Negl Trop Dis
DOI: 10.1371/journal.pntd.0007462
sha: 6276adaeca8fcd42c9565718ac6bbdc4f97aa10f
doc_id: 689282
cord_uid: ikomc19t

Nipah virus (NiV) is a highly pathogenic re-emerging virus that causes outbreaks in South East Asia. Currently, no approved and licensed vaccine or antivirals exist. Here, we investigated the efficacy of ChAdOx1 NiV(B), a simian adenovirus-based vaccine encoding NiV glycoprotein (G) Bangladesh, in Syrian hamsters. Prime-only as well as prime-boost vaccination resulted in uniform protection against a lethal challenge with NiV Bangladesh: all animals survived challenge and we were unable to find infectious virus either in oral swabs, lung or brain tissue. Furthermore, no pathological lung damage was observed. A single-dose of ChAdOx1 NiV(B) also prevented disease and lethality from heterologous challenge with NiV Malaysia. While we were unable to detect infectious virus in swabs or tissue of animals challenged with the heterologous strain, a very limited amount of viral RNA could be found in lung tissue by in situ hybridization. A single dose of ChAdOx1 NiV(B) also provided partial protection against Hendra virus and passive transfer of antibodies elicited by ChAdOx1 NiV(B) vaccination partially protected Syrian hamsters against NiV Bangladesh. From these data, we conclude that ChAdOx1 NiV(B) is a suitable candidate for further NiV vaccine pre-clinical development.

Introduction ChAdOx1-vectored vaccines fulfil all these requirements, making this a promising platform. The ChAdOx1 vector is a replication-deficient simian adenovirus vector which has been used to produce several vaccines which are now in clinical development. A common feature of these vaccines is their low reactogenicity, strong immunogenicity, and the absence of vector replication after immunization, an important safety feature. In pre-clinical studies a single dose of ChAdOx1 vectored vaccines has been shown to be protective against infection with Rift Valley Fever Virus, Middle East respiratory syndrome coronavirus, Mycobacterium tuberculosis and Zika virus [18] [19] [20] [21] . Large scale manufacturing has been performed for replicationdeficient adenoviral vectored vaccines for Ebola, with one vaccine now licensed and another in advanced clinical development [22, 23] . Further, a simple thermostabilization process allows for vaccine storage at ambient temperatures [24] , removing the need for a cold chain for storage and shipping. We now report on pre-clinical immunogenicity and efficacy testing of ChAd-Ox1 NiV B .

Animal experiment approval was received from the Institutional Animal Care and Use Committee (IACUC) at Rocky Mountain Laboratories. Experiments were performed in an Association for Assessment and Accreditation of Laboratory Animal Care-approved facility by certified staff, following the guidelines and basic principles in the NIH Guide for the Care and Use of Laboratory Animals, the Animal Welfare Act, United States Department of Agriculture and the United States Public Health Service Policy on Humane Care and Use of Laboratory Animals (Protocol # 2017-033E and 2018-035E). The Institutional Biosafety Committee (IBC) approved work with infectious NiV and Hendra virus (HeV) strains under BSL4 conditions and sample inactivation was performed according to IBC-approved standard operating procedures for removal of specimens from high containment.

Henipavirus isolates were obtained from the Special Pathogens Branch of the Centers for Disease Control and Prevention, Atlanta, GA or Public Health Agency, Winnipeg, Canada. NiV Bangladesh (GenBank no. AY988601), NiV Malaysia (GenBank no. AF212302), and HeV (GenBank no. AF017149) have been passaged three, four, and three times in VeroE6 cells respectively. All virus propagation in this manuscript was performed in VeroE6 cells in Dulbecco's modified Eagle's medium (DMEM, Sigma) supplemented with 2% fetal bovine serum (Gibco), 1 mM L-glutamine (Gibco), 50 U/ml penicillin (Gibco), and 50 μg/ml streptomycin (Gibco) (2% DMEM). VeroE6 cells were maintained in DMEM supplemented with 10% fetal bovine serum, 1 mM L glutamine, 50 U/ml penicillin and 50 μg/ml streptomycin.

The glycoprotein (G) gene from Nipah virus (Bangladesh outbreak 2008-2010, Genbank accession number: JN808864.1) was codon optimized for humans and synthesized by GeneArt (Thermo Fisher Scientific). The synthesized G gene was cloned into a transgene expression plasmid comprising a modified human cytomegalovirus immediate early promoter (CMV promoter) with tetracycline operator (TetO) sites and the polyadenylation signal from bovine growth hormone (BGH). The resulting expression cassette was inserted into the E1 locus of a genomic clone of ChAdOx1 using site-specific recombination [25] . The virus was rescued and propagated in T-REx-293 cells (Invitrogen). Purification was by CsCl gradient ultracentrifugation, and the virus was titered as previously described [26] . Doses for vaccination were based on infectious units (IU).

Female Golden Syrian hamsters (4-6 weeks old) were purchased from Envigo. Animals were vaccinated I.M. with 50 μl of 10 8 IU of vaccine or injected I.M. with 50 μl of saline, in each thigh (100 μl total volume). For the homologous challenge vaccine experiment, animals were vaccinated at D-70 and/or D-42. For the heterologous challenge experiment, animals were vaccinated at D-28. Three days prior to vaccination and virus challenge animals were bled via orbital sinus puncture. All animals were challenged with 1000LD 50 of virus in 500 μl DMEM via I.P. inoculation: NiV Bangladesh = 5.3 x 10 5 TCID 50 ; NiV Malaysia = 6.8 x 10 4 TCID 50 ; HeV = 6.0 x 10 3 TCID 50 . We chose the I.P. route as a uniformly lethal challenge route and to be able to compare with previously conducted vaccine experiments [27] . For each study group, 10 hamsters were utilized. Of these, four animals were euthanized 4 (HeV) or 5 (NiV) days post inoculation and the remaining six animals were followed for 28 days post challenge. Weight was recorded daily up to 10 days post infection, and oropharyngeal swabs were taken daily up to 7 days post inoculation in 1 mL of DMEM. Animals were euthanized when >20% of weight loss was recorded, or severe disease signs (e.g. difficulty breathing or paralysis) were observed. Upon euthanasia, blood and tissues were collected and subsequently analyzed for virology and histology as approved by IACUC.

Female Golden Syrian hamsters (4-6 weeks old) were purchased from Envigo. Fifteen animals were vaccinated with either ChAdOx1 NiV B or ChAdOx1 GFP as described above at 56 and 28 days before serum collection. Serum was collected via cardiac puncture, pooled per vaccine group and IgGs were purified using the MAbtrap kit (Sigma) according to manufacturer's instructions from 10 mL of serum. Purified IgGs were filtered through an 0.45μm filter and diluted to 4.5 mL in sterile PBS. Ten hamsters were immunized via I.P. injection using 400 μl per hamster. All animals were challenged as described above one day post treatment. For each study group, 10 hamsters were utilized. Of these, four animals were euthanized 5 days post challenge and the remaining six animals were followed for 56 days post challenge. Weight was recorded daily up to 10 days post challenge, and oropharyngeal swabs were taken daily up to 7 days post inoculation in 1 mL of DMEM. Animals were euthanized when >20% of weight loss was recorded, or severe disease signs (e.g. difficulty breathing or paralysis) were observed. Upon euthanasia, blood and tissues were collected and subsequently analyzed for virology and histology as approved by IACUC.

Virus titrations were performed by end-point titration in VeroE6 cells, which were inoculated with tenfold serial dilutions of virus swab media or tissue homogenates. After 1hr incubation at 37˚C and 5% CO 2 , tissue homogenate dilutions were removed, washed twice with PBS and replaced with 100 μl 2% DMEM. Cytopathic effect was scored at 5 dpi and the TCID 50 was calculated from 4 replicates by the Spearman-Karber method [28] . added to VeroE6 cells and incubated at 37˚C and 5% CO 2 . At 5 dpi, cytopathic effect was scored. The virus neutralization titer was expressed as the reciprocal value of the highest dilution of the serum which still inhibited virus replication.

NiV-G Malaysia (residues E144-T602, gene accession number NC_002728) was cloned into the pHLSEC mammalian expression vector [29] and NiV-F Malaysia (residues G26-D482, gene accession number AY816748.1) was cloned into the pHLSEC vector containing a C-terminal GCNt trimerization motif [30] . The constructs were transiently expressed in human embryonic kidney (HEK) 293T cells in roller bottles, as described previously [29] . Supernatant was harvested 96 hours after transfection and diafiltrated using the AKTA FLUX system (GE Healthcare) against either PBS, pH 7.4 (NiV-G) or buffer containing 10 mM Tris and 150 mM NaCl, pH 8.0 (NiV-F). The proteins were further purified by Ni-NTA immobilized metal-affinity chromatography using His-Trap HP columns (GE Healthcare) followed by size exclusion chromatography. NiV-G was purified using a Superdex 200 10/300 Increase GL column (GE healthcare) equilibrated in PBS pH 7.4 and NiV-F was purified using a Superose 6 Increase 10/ 300 GL column (GE healthcare) equilibrated in 10 mM Tris and 150 mM NaCl pH 8.0.

Maxisorp plates (Nunc) were coated overnight at 4˚C with 5 μg of G or F protein per plate in Carb/Bicarb binding buffer (4.41 g KHCO 3 and 0.75 g Na 2 CO 3 in 1 L distilled water). After blocking with 5% milk in PBS with 0.01% tween (PBST), serum (2x serial diluted starting at 100x dilution) in 5% milk in PBST was incubated at RT for 1 hr. Antibodies were detected using affinity-purified antibody peroxidase-labeled goat-anti-hamster IgG (Fisher, 14-22-06) in 5% milk in PBST and TMB 2-component peroxidase substrate (Seracare) and read at 450 nm. All wells were washed 3x with PBST in between steps. Prior to using F and G proteins based on NiV Malaysia, we established that cross-reactivity with NiV Bangladesh antibodies was sufficient for usage in ELISA by testing sera known to be positive for NiV Bangladesh antibodies.

Necropsies and tissue sampling were performed according to IBC-approved protocols. Harvested tissues were fixed for a minimum of 7 days in 10% neutral-buffered formalin and subsequently embedded in paraffin. Hematoxylin and eosin (H&E) staining and in situ hybridization (ISH) were performed on tissue sections and cell blocks. Detection of NiV and HeV viral RNA was performed using the RNAscope FFPE assay (Advanced Cell Diagnostics Inc., Newark, USA) as previously described [31] and in accordance with the manufacturer's instructions. Briefly, tissue sections were deparaffinized and pretreated with heat and protease before hybridization with target-specific probes for NiV or HeV. Ubiquitin C and the bacterial gene, dapB, were used as positive and negative controls, respectively. Whole-tissue sections for selected cases were stained for NiV and HeV viral RNA, UBC and dapB by the RNAscope VS FFPE assay (RNAscopeVS, Newark, USA) using the Ventana Discovery XT slide autostaining system (Ventana Medical Systems Inc., Tucson, USA). A board-certified veterinary anatomic pathologist evaluated all tissue slides.

Statistical analysis was performed by the Log-rank (Mantel-Cox) test to compare survival curves, and by Welch-corrected one-tailed unpaired student's t-test to compare infectious virus titers in tissue. SEM was calculated for all samples. P-values < 0.05 were significant.

To determine efficacy of the ChAdOx1 NiV B vaccine, we vaccinated groups of 10 hamsters with either a single dose at D-42 or a prime-boost regime at D-70 and D-42. As control groups, we either injected hamsters with ChAdOx1 GFP at D-70 and D-42 or saline at D-42 ( Fig 1A) . Virus neutralizing antibodies could be detected after a single dose of ChAdOx1 NiV B and increased upon a secondary dose (average VN titer ± SEM = 30.5 ± 5.7 after single dose, 91 ± 21 after boost). In contrast, no neutralizing antibodies could be detected in serum obtained from the control groups ( Fig 1B) . All hamsters were challenged with a lethal dose of NiV Bangladesh (1000 LD 50 ) via intraperitoneal inoculation on D0 ( Fig 1A) . All vaccinated animals survived challenge and did not show signs of disease, such as weight loss, at any stage throughout the experiment. This was in contrast to the control groups in which all animals succumbed to disease between D6 and D10 and exhibited weight loss (Fig 1C and 1D) , as well as respiratory and/or neurological signs, including labored breathing and paralyzed hind legs. Statistical analysis demonstrated that survival in the vaccinated groups was significant compared to both control groups (P < 0.0001).

Oropharyngeal swabs were taken daily and assessed for infectious virus by limiting dilution titrations. None of the vaccinated animals shed virus at any timepoint. In contrast, control animals from both groups were found to shed virus at D5 and D6 (Fig 1E) .

Four animals of each group were euthanized at D5 and lung and brain tissue were harvested. Infectious virus could only be detected in lung tissue of animals from both control groups (average titer ± SEM = 3.3 x 10 4 ± 2.5 x 10 4 TCID 50 /g of tissue) and was not detected in any tissue of the vaccinated animals ( Fig 1F) . We did not observe any differences between the two control groups.

Lung and brain tissue harvested at D5 were then evaluated for pathological changes. None of the vaccinated animals displayed pulmonary pathology and no viral RNA was detected in lung tissue by ISH. Control animals developed pulmonary lesions that were indistinguishable between the two groups. These hamsters developed bronchointerstitial pneumonia that was characterized by multifocal inflammatory nodules that were centered on terminal bronchioles and extend into adjacent alveoli. The nodules were composed of large numbers of foamy macrophages and fewer neutrophils and lymphocytes admixed with small amounts of necrotic debris. In most cases hemorrhage, fibrin and edema admixed with inflammatory cells was observed. Edema and fibrin often were extended into surrounding alveoli. Alveoli that were adjacent to areas of inflammation were thickened by fibrin, edema and small numbers of macrophages and neutrophils as previously observed in NiV infected hamsters [32] . There was abundant viral RNA demonstrated by ISH in areas of inflammation (brown staining). The viral RNA was predominantly found in type I pneumocytes but was also multifocally present in vascular and bronchiolar smooth muscle and endothelial cells (Fig 2) .

To determine efficacy of ChAdOx1 NiV B against NiV Malaysia and HeV, groups of 10 hamsters were vaccinated with a single dose of ChAdOx1 NiV B or a single dose of ChAdOx1 GFP at D-28 ( Fig 3A) . As before, virus neutralizing antibodies could be detected after vaccination with ChAdOx1 NiV B but not upon injection with ChAdOx1 GFP (Average VN titer ± SEM = 68.6 ± 13.6) ( Fig 3B) . Subsequently, hamsters were challenged with either NiV Malaysia or HeV (1000 LD 50 ) via intraperitoneal inoculation on D0 (Fig 3A) . All vaccinated animals challenged with NiV Malaysia survived with no signs of disease such as weight loss at any stage throughout the experiment. In contrast, animals challenged with NiV Malaysia that received ChAdOx1 FGP all succumbed to infection between D5 and D6. These animals experienced weight loss and respiratory and neurological signs (Fig 3C and 3D) . Statistical analysis demonstrated that survival in the vaccinated group was significantly different from the control group (P = 0.0012). Oropharyngeal swabs were taken daily and assessed for infectious virus. None of the vaccinated animals challenged with NiV Malaysia shed virus at any timepoint. In contrast, control animals challenged with NiV Malaysia were found to shed virus at D5 and D6 (Fig 3E) .

Four animals from both groups were euthanized at D5 and lung and brain tissue were harvested. Infectious virus could only be detected in lung and brain tissue of animals from the control group (average virus titer lung ± SEM = 1.5 x 10 5 ± 5.2 x 10 4 TCID 50 /g, brain ± SEM = 6.8 x 10 1 ± 4.4 x 10 1 TCID 50 /g) and was not detected in any tissue of the vaccinated animals ( Fig 3F) .

Four out of six vaccinated animals challenged with HeV succumbed to disease between D5 and D7. The two survivors showed minimal weight loss (<2%) and no signs of disease. Animals that received ChAdOx1 FGP all succumbed to HeV infection between D4 and D6. These animals showed weight loss as well as respiratory and neurological signs (Fig 3C and 3D) . Logrank (Mantel-Cox) test demonstrated that survival in the vaccinated group was significant (P = 0.0476) compared to the control group.

Oropharyngeal swabs were taken daily and assessed for infectious virus. None of the vaccinated animals challenged with HeV shed virus at any timepoint. In contrast, control animals challenged with HeV were found to shed virus at D4, D5 and D6 (Fig 3E) .

Four animals from both groups were euthanized at D4 and lung and brain tissue were harvested. Infectious virus was detected in three out of four lungs of the vaccinated animals and all lungs of the control animals (average virus titer ± SEM = 5.2 x 10 5 ± 3.6 x 10 5 and 4.4 x 10 6 ± 2.2 x 10 6 TCID 50 /g tissue for vaccinated and control animals, respectively). No statistical difference in infectious virus titer was found between the two groups using an unpaired onetailed Student's t-test (P = 0.0674). Infectious virus was only detected in brain tissue of animals from the control group (average titer ± SEM = 4.6 x 10 2 ± 2.0 x 10 2 TCID 50 /g) and not in vaccinated animals (Fig 3F) .

Harvested lung tissue was then evaluated for pathological changes. All four groups of hamsters developed pulmonary lesions. All animals challenged with HeV and control animals challenged with NiV Malaysia developed bronchointerstitial pneumonia which was indistinguishable from the lesions described for the control animals in the homologous challenge study. Vaccinated hamsters challenged with NiV Malaysia developed mild to moderate bronchointerstitial pneumonia and did not display any evidence of pulmonary edema, fibrin or hemorrhage. ISH demonstrated viral RNA predominantly in type I pneumocytes and rarely in vascular and bronchiolar smooth muscle and endothelial cells in animals challenged with HeV and control animals challenged with NiV Malaysia. In vaccinated animals challenged with NiV Malaysia, however; there was very little RNA present and only in type I pneumocytes in areas of inflammation (Fig 4) .

Finally, we wanted to assess the protective effect of antibodies elicited after ChAdOx1 NiV B vaccination. Two groups of 15 hamsters were either vaccinated with ChAdOx1 NiV B or injected with ChAdOx1 FGP at D-56 and D-28. All animals were bled at D0 and we collected 13 and 15 mL respectively. IgG was purified from 10 mL pooled serum. Ten animals per group were then injected peritoneally with purified IgG. Animals were challenged with a lethal dose of NiV Bangladesh (1000 LD 50 ) one day post passive transfer ( Fig 5A) . We were unable to detect neutralizing antibodies in serum obtained at D5 from four hamsters from each group. However, serum from animals treated with NiV antibodies was positive by ELISA against NiV G protein, albeit with a lower reciprocal titer than antibodies in serum obtained from single-dose vaccinated animals (Fig 5B) . One out of six animals treated with NiV antibodies succumbed to disease on D11. No weight loss was observed, however the animal showed severe neurological signs. None of the other NiV antibody-treated animals experienced weight loss or signs of disease. Four out of six animals treated with GFP antibodies succumbed to disease between D6 and D8. These animals showed weight loss and respiratory or neurological signs. The two surviving animals did not show any signs of disease throughout the experiment. One of these animals did not seroconvert as measured by ELISA against NiV F and G protein, and it was suspected this animal was not infected. Therefore, this animal was excluded from the survival curve. The log-rank (Mantel-Cox) test demonstrated that survival in the treated group was significant (P = 0.0168) compared to the control group (Fig 5C and 5D) .

Oropharyngeal swabs were taken daily and assessed for infectious virus. Shedding was minimal and found in one animal treated with NiV antibodies on D5, and five animals treated with GFP antibodies between D4 and D6 (Fig 5E) .

Four animals from both groups were euthanized at D5 and lung and brain tissue were harvested. Infectious virus could only be detected in lung tissue of animals treated with GFP antibodies and was not detected in any tissue of the animals treated with NiV antibodies (Fig 5F) .

Lung tissue harvested at D5 was then evaluated for pathological changes. Both groups of hamsters developed pulmonary lesions similar to those described in the homologous challenge study, however; the NiV antibody-treated hamsters developed mild to moderate pulmonary lesions whereas the control animals developed severe lesions. Additionally, none of the NiV antibody-treated hamsters displayed any pulmonary fibrin, edema or hemorrhage. ISH demonstrated viral RNA in type I pneumocytes in areas of inflammation. Abundance of viral RNA was notably less in animals treated with NiV antibodies (Fig 6) .

NiV is a re-emerging infectious disease which causes outbreaks with a high case-fatality rate.

No licensed vaccine against NiV currently exists, and it is therefore key that a safe and effective vaccine be developed. Several vaccine candidates have been explored in different animal models. These can be categorized as subunit vaccines or live-vectored vaccines that target the NiV outer membrane proteins G and/or F. Protection against disease and lethality has been shown in hamsters [27, 33] , pigs [34, 35] , African green monkeys [36] [37] [38] , cats [39] , and ferrets [40, 41] . Efficacy is thought to be mediated by neutralizing antibodies, as passive transfer of ChAdOx1 NiVB efficacy in the Syrian Golden hamster antibodies in naive animals also results in protection against disease [27, 42] . These approaches are promising, but no vaccine candidates have so far been moved into clinical trials.

In the studies presented here, we tested the efficacy of a vaccine based on NiV Bangladesh G protein in a replication-deficient simian adenovirus vector in Syrian hamsters. A primeonly as well as a prime-boost regime protected Syrian hamsters against challenge with a lethal dose of NiV Bangladesh and NiV Malaysia, and partially protected against HeV challenge. Furthermore, antibodies elicited by vaccination alone provided partial protection against a NiV Bangladesh challenge.

Two genetic lineages of NiV have been described; NiV Malaysia and NiV Bangladesh [10] [11] [12] . Although NiV Malaysia has not caused an outbreak in humans since 1999, the virus was isolated from Pteropus vampyrus, Pteropus hypomelanus and Pteropus lylei in Malaysia and Cambodia [43] [44] [45] and another spillover event could occur. Having one vaccine that protects against both lineages of NiV virus would be the easiest and cheapest countermeasure. A singledose vaccination with ChAdOx1 NiV B , which is based on NiV Bangladesh, fully protected Syrian hamsters against lethal disease caused by NiV Malaysia. The G proteins of the NiV strains used in this study are 95.5% pairwise identical on the amino acid level, with 27 amino acid differences scattered throughout the protein. Although we did not see sterile protection against NiV Malaysia, none of the vaccinated animals showed signs of disease and all were protected against lethal disease. These results suggest that ChAdOx1 NiV B could protect against both lineages of NiV.

Like NiV, HeV is a species in the Henipavirus genus and thus we investigated cross-protection of ChAdOx1 NiV B against a lethal challenge with HeV in Syrian hamsters. The G protein of the HeV strain used in this study was 78.2% identical to the ChAdOx1 NiV B G protein; 133 amino acids differ between the two proteins. ChAdOx1 NiV B only protected partially against HeV challenge; four out of six animals did not survive challenge. We observed a non-significant decrease in infectious HeV titer in lung and brain tissue of vaccinated animals compared to control animals. It is possible that disease progression in vaccinated animals is delayed compared to control animals. This is supported by the delay in time to death; whereas the average time to death is 5 days in control animals, it is 6 days in vaccinated animals.

Cross-protection of NiV or HeV vaccines has been studied by other groups as well. An adeno-associated virus vaccine expressing NiV G protein offered 50% protection against a lethal challenge with HeV in hamsters [46] . In contrast, vaccines based on HeV provide full protection against NiV in the ferret and NHP model [36, 41, 47] . Likewise, high levels of crossprotective antibodies were found in sera from HeV-infected individuals, whereas cross-protective antibodies were limited in NiV-infected individuals [48] . This might be caused by induction of a more robust and cross-reactive immune response by native HeV protein compared to NiV protein, as suggested by Bossart et al. [48] .

Human cases of HeV are associated with direct contact with infected horses, the intermediate animal host of HeV, and direct contact with bats or their products has not yet been associated with HeV infection in humans [49] . It is therefore likely that prevention of HeV in horses will completely prevent human cases. Currently, a HeV vaccine (Equivac) is available for horses and fully protects against HeV [50] . Furthermore, the total number of human cases that contracted HeV is relatively low at 7 [13] . Thus, the requirement of a human vaccine for HeV is therefore less urgent than that of a NiV vaccine.

Previous work has shown that the humoral immune response to NiV vaccination is sufficient to protect Syrian hamsters against a lethal challenge with NiV [27, 42] . Likewise, administration of a human neutralizing monoclonal antibody (m102.4) provided full protection against both HeV and NiV in multiple animal models [51, 52] . Administration of purified IgG obtained from ChAdOx1 NiV B vaccinated hamsters provided partial protection against NiV challenge. Furthermore, infectious virus could only be detected in the lungs of control animals and not in the lungs of vaccinated animals, and thus as in previous studies, ChAdOx1 NiV Belicited antibodies are able to provide protection against a lethal challenge with NiV. Although we were able to detect NiV G protein-specific antibodies in serum obtained from NiV antibody-treated animals, the reciprocal titer was much lower than that detected in serum from Syrian hamsters after a single dose of ChAdOx1 NiV B . It is possible that administering a higher dose of IgG would have led to uniform protection.

Two animals treated with IgG purified from animals which received injections with ChAd-Ox1 FGP survived a lethal challenge with NiV Bangladesh. Occasional survival has been observed in the Syrian hamster model [33] . The increased survival rate might however also reflect a non-specific effect of treatment with IgG, which has been reported previously [53] . As the survival rate was significantly different between the NiV IgG-treated group and the control IgG-treated group, the passive transfer experiment shows that antibodies elicited by ChAd-Ox1-NiV B are sufficient for protection against a lethal challenge with NiV.

Animals in the passive transfer experiment were observed for 56 days, to ensure that the two animals that survived would not succumb to disease after 28 days.

The Syrian hamster is a suitable initial small animal model to investigate the efficacy of NiV vaccines, followed by the African green monkey [54] . The immune system of African green monkeys is more like humans than that of hamsters and is therefore seen as a more relevant animal model to test NiV vaccines. Based on the results presented in the current manuscript, future studies are planned to test ChAdOx1 NiV B in African green monkeys, supported by the Coalition for Epidemic Preparedness Innovations (CEPI).

We show that ChAdOx1 NiV B provides complete protection against lethal disease in Syrian hamsters challenged with NiV Bangladesh. Furthermore, ChAdOx1 NiV B vaccination results in complete survival but with limited evidence of viral replication after NiV Malaysia challenge, and partial protection against HeV. Passive transfer of antibodies elicited by ChAdOx1 NiV B vaccination provide partial protection against lethal challenge with NiV Bangladesh.

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We would like to thank the animal care takers for their excellent care of the animals, and Anita Mora for assistance with figures. Benjamin Carrasco provided outstanding assistance with the preparation for animal experiments. Greg Saturday, Kimberly Meade-White and Kathleen Cordova were instrumental in assistance during the animal studies. We thank Benhur Lee for kindly providing the c-DNA for NiV-F.