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  1. Article ; Online: Rational attenuation of canine distemper virus (CDV) to develop a morbillivirus animal model that mimics measles in humans.

    Schmitz, Katharina S / Rennick, Linda J / Tilston-Lunel, Natasha L / Comvalius, Anouskha D / Laksono, Brigitta M / Geers, Daryl / van Run, Peter / de Vries, Rory D / de Swart, Rik L / Duprex, W Paul

    Journal of virology

    2024  Volume 98, Issue 3, Page(s) e0185023

    Abstract: Morbilliviruses are members of the family Paramyxoviridae and are known for their ability to cause systemic disease in a variety of mammalian hosts. The prototypic morbillivirus, measles virus (MeV), infects humans and still causes morbidity and ... ...

    Abstract Morbilliviruses are members of the family Paramyxoviridae and are known for their ability to cause systemic disease in a variety of mammalian hosts. The prototypic morbillivirus, measles virus (MeV), infects humans and still causes morbidity and mortality in unvaccinated children and young adults. Experimental infection studies in non-human primates have contributed to the understanding of measles pathogenesis. However, ethical restrictions call for the development of new animal models. Canine distemper virus (CDV) infects a wide range of animals, including ferrets, and its pathogenesis shares many features with measles. However, wild-type CDV infection is almost always lethal, while MeV infection is usually self-limiting. Here, we made five recombinant CDVs, predicted to be attenuated, and compared their pathogenesis to the non-attenuated recombinant CDV in a ferret model. Three viruses were insufficiently attenuated based on clinical signs, fatality, and systemic infection, while one virus was too attenuated. The last candidate virus caused a self-limiting infection associated with transient viremia and viral dissemination to all lymphoid tissues, was shed transiently from the upper respiratory tract, and did not result in acute neurological signs. Additionally, an in-depth phenotyping of the infected white blood cells showed lower infection percentages in all lymphocyte subsets when compared to the non-attenuated CDV. In conclusion, infection models using this candidate virus mimic measles and can be used to study pathogenesis-related questions and to test interventions for morbilliviruses in a natural host species.IMPORTANCEMorbilliviruses are transmitted via the respiratory route but cause systemic disease. The viruses use two cellular receptors to infect myeloid, lymphoid, and epithelial cells. Measles virus (MeV) remains an important cause of morbidity and mortality in humans, requiring animal models to study pathogenesis or intervention strategies. Experimental MeV infections in non-human primates are restricted by ethical and practical constraints, and animal morbillivirus infections in natural host species have been considered as alternatives. Inoculation of ferrets with wild-type canine distemper virus (CDV) has been used for this purpose, but in most cases, the virus overwhelms the immune system and causes highly lethal disease. Introduction of an additional transcription unit and an additional attenuating point mutation in the polymerase yielded a candidate virus that caused self-limiting disease with transient viremia and virus shedding. This rationally attenuated CDV strain can be used for experimental morbillivirus infections in ferrets that reflect measles in humans.
    MeSH term(s) Animals ; Dogs ; Humans ; Disease Models, Animal ; Distemper/virology ; Distemper Virus, Canine/genetics ; Ferrets ; Measles/pathology ; Measles virus/genetics ; Morbillivirus/genetics ; Morbillivirus Infections/pathology ; Primates ; Viremia
    Language English
    Publishing date 2024-02-28
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/jvi.01850-23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: FeMV is a cathepsin-dependent unique morbillivirus infecting the kidneys of domestic cats.

    Nambulli, Sham / Rennick, Linda J / Acciardo, Andrew S / Tilston-Lunel, Natasha L / Ho, Gregory / Crossland, Nicholas A / Hardcastle, Kathy / Nieto, Betsy / Bainbridge, Graeme / Williams, Tracey / Sharp, Claire R / Duprex, W Paul

    Proceedings of the National Academy of Sciences of the United States of America

    2022  Volume 119, Issue 43, Page(s) e2209405119

    Abstract: Feline morbillivirus (FeMV) is a recently discovered pathogen of domestic cats and has been classified as a morbillivirus in ... ...

    Abstract Feline morbillivirus (FeMV) is a recently discovered pathogen of domestic cats and has been classified as a morbillivirus in the
    MeSH term(s) Amino Acids ; Animals ; Cathepsins/genetics ; Cats ; Furin ; Hemagglutinins ; Humans ; Kidney ; Morbillivirus/genetics ; Morbillivirus Infections/veterinary
    Chemical Substances Amino Acids ; Hemagglutinins ; Cathepsins (EC 3.4.-) ; Furin (EC 3.4.21.75)
    Language English
    Publishing date 2022-10-17
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't ; Research Support, N.I.H., Extramural
    ZDB-ID 209104-5
    ISSN 1091-6490 ; 0027-8424
    ISSN (online) 1091-6490
    ISSN 0027-8424
    DOI 10.1073/pnas.2209405119
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article ; Online: A measles-vectored vaccine candidate expressing prefusion-stabilized SARS-CoV-2 spike protein brought to phase I/II clinical trials: protection of African green monkeys from COVID-19 disease.

    Nambulli, Sham / Escriou, Nicolas / Rennick, Linda J / Demers, Matthew J / Tilston-Lunel, Natasha L / McElroy, Anita K / Barbeau, Dominique J / Crossland, Nicholas A / Hoehl, Ryan M / Schrauf, Sabrina / White, Alexander G / Borish, H Jacob / Tomko, Jaime A / Frye, Lonnie J / Scanga, Charles A / Flynn, JoAnne L / Martin, Annette / Gerke, Christiane / Hartman, Amy L /
    Duprex, W Paul

    Journal of virology

    2024  , Page(s) e0176223

    Abstract: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged at the end of 2019 and is responsible for the largest human pandemic in 100 years. Thirty-four vaccines are currently approved for use worldwide, and approximately 67% of the world ... ...

    Abstract Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) emerged at the end of 2019 and is responsible for the largest human pandemic in 100 years. Thirty-four vaccines are currently approved for use worldwide, and approximately 67% of the world population has received a complete primary series of one, yet countries are dealing with new waves of infections, variant viruses continue to emerge, and breakthrough infections are frequent secondary to waning immunity. Here, we evaluate a measles virus (MV)-vectored vaccine expressing a stabilized prefusion SARS-CoV-2 spike (S) protein (MV-ATU3-S2PΔF2A; V591) with demonstrated immunogenicity in mouse models (see companion article [J. Brunet, Z. Choucha, M. Gransagne, H. Tabbal, M.-W. Ku et al., J Virol 98:e01693-23, 2024, https://doi.org/10.1128/jvi.01693-23]) in an established African green monkey model of disease. Animals were vaccinated with V591 or the control vaccine (an equivalent MV-vectored vaccine with an irrelevant antigen) intramuscularly using a prime/boost schedule, followed by challenge with an early pandemic isolate of SARS-CoV-2 at 56 days post-vaccination. Pre-challenge, only V591-vaccinated animals developed S-specific antibodies that had virus-neutralizing activity as well as S-specific T cells. Following the challenge, V591-vaccinated animals had lower infectious virus and viral (v) RNA loads in mucosal secretions and stopped shedding virus in these secretions earlier. vRNA loads were lower in these animals in respiratory and gastrointestinal tract tissues at necropsy. This correlated with a lower disease burden in the lungs as quantified by PET/CT at early and late time points post-challenge and by pathological analysis at necropsy.IMPORTANCESevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is responsible for the largest human pandemic in 100 years. Even though vaccines are currently available, countries are dealing with new waves of infections, variant viruses continue to emerge, breakthrough infections are frequent, and vaccine hesitancy persists. This study uses a safe and effective measles vaccine as a platform for vaccination against SARS-CoV-2. The candidate vaccine was used to vaccinate African green monkeys (AGMs). All vaccinated AGMs developed robust antigen-specific immune responses. After challenge, these AGMs produced less virus in mucosal secretions, for a shorter period, and had a reduced disease burden in the lungs compared to control animals. At necropsy, lower levels of viral RNA were detected in tissue samples from vaccinated animals, and the lungs of these animals lacked the histologic hallmarks of SARS-CoV-2 disease observed exclusively in the control AGMs.
    Language English
    Publishing date 2024-04-02
    Publishing country United States
    Document type Journal Article
    ZDB-ID 80174-4
    ISSN 1098-5514 ; 0022-538X
    ISSN (online) 1098-5514
    ISSN 0022-538X
    DOI 10.1128/jvi.01762-23
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  4. Article ; Online: The Potential for Reassortment between Oropouche and Schmallenberg Orthobunyaviruses.

    Tilston-Lunel, Natasha L / Shi, Xiaohong / Elliott, Richard M / Acrani, Gustavo Olszanski

    Viruses

    2017  Volume 9, Issue 8

    Abstract: A number of viruses within ... ...

    Abstract A number of viruses within the
    Language English
    Publishing date 2017-08-11
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2516098-9
    ISSN 1999-4915 ; 1999-4915
    ISSN (online) 1999-4915
    ISSN 1999-4915
    DOI 10.3390/v9080220
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Sustained Replication of Synthetic Canine Distemper Virus Defective Genomes

    Tilston-Lunel, Natasha L / Welch, Stephen R / Nambulli, Sham / de Vries, Rory D / Ho, Gregory W / Wentworth, David E / Shabman, Reed / Nichol, Stuart T / Spiropoulou, Christina F / de Swart, Rik L / Rennick, Linda J / Duprex, W Paul

    mSphere

    2021  Volume 6, Issue 5, Page(s) e0053721

    Abstract: Defective interfering (DI) genomes restrict viral replication and induce type I interferon. Since DI genomes have been proposed as vaccine adjuvants or therapeutic antiviral agents, it is important to understand their generation, delineate their ... ...

    Abstract Defective interfering (DI) genomes restrict viral replication and induce type I interferon. Since DI genomes have been proposed as vaccine adjuvants or therapeutic antiviral agents, it is important to understand their generation, delineate their mechanism of action, develop robust production capacities, assess their safety and
    MeSH term(s) Animals ; Cell Line ; Chlorocebus aethiops ; Defective Viruses ; Distemper Virus, Canine/genetics ; Distemper Virus, Canine/physiology ; Dogs ; Ferrets ; Genome, Viral ; Male ; Raccoons/virology ; Vero Cells ; Virus Replication/genetics ; Virus Replication/physiology
    Language English
    Publishing date 2021-09-22
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ISSN 2379-5042
    ISSN (online) 2379-5042
    DOI 10.1128/mSphere.00537-21
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article: Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses.

    Nambulli, Sham / Xiang, Yufei / Tilston-Lunel, Natasha L / Rennick, Linda J / Sang, Zhe / Klimstra, William B / Reed, Douglas S / Crossland, Nicholas A / Shi, Yi / Duprex, W Paul

    bioRxiv : the preprint server for biology

    2021  

    Abstract: Globally there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian ... ...

    Abstract Globally there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian hamsters that model moderate to severe COVID-19 disease, we demonstrate the high efficacy of PiN-21 to prevent and treat SARS-CoV-2 infection. Intranasal delivery of PiN-21 at 0.6 mg/kg protects infected animals from weight loss and substantially reduces viral burdens in both lower and upper airways compared to control. Aerosol delivery of PiN-21 facilitates deposition throughout the respiratory tract and dose minimization to 0.2 mg/kg. Inhalation treatment quickly reverses animals' weight loss post-infection and decreases lung viral titers by 6 logs leading to drastically mitigated lung pathology and prevents viral pneumonia. Combined with the marked stability and low production cost, this novel therapy may provide a convenient and cost-effective option to mitigate the ongoing pandemic.
    Language English
    Publishing date 2021-02-23
    Publishing country United States
    Document type Preprint
    DOI 10.1101/2021.02.23.432569
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Inhalable Nanobody (PiN-21) prevents and treats SARS-CoV-2 infections in Syrian hamsters at ultra-low doses.

    Nambulli, Sham / Xiang, Yufei / Tilston-Lunel, Natasha L / Rennick, Linda J / Sang, Zhe / Klimstra, William B / Reed, Douglas S / Crossland, Nicholas A / Shi, Yi / Duprex, W Paul

    Science advances

    2021  Volume 7, Issue 22

    Abstract: Globally, there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian ... ...

    Abstract Globally, there is an urgency to develop effective, low-cost therapeutic interventions for coronavirus disease 2019 (COVID-19). We previously generated the stable and ultrapotent homotrimeric Pittsburgh inhalable Nanobody 21 (PiN-21). Using Syrian hamsters that model moderate to severe COVID-19 disease, we demonstrate the high efficacy of PiN-21 to prevent and treat SARS-CoV-2 infection. Intranasal delivery of PiN-21 at 0.6 mg/kg protects infected animals from weight loss and substantially reduces viral burdens in both lower and upper airways compared to control. Aerosol delivery of PiN-21 facilitates deposition throughout the respiratory tract and dose minimization to 0.2 mg/kg. Inhalation treatment quickly reverses animals' weight loss after infection, decreases lung viral titers by 6 logs leading to drastically mitigated lung pathology, and prevents viral pneumonia. Combined with the marked stability and low production cost, this innovative therapy may provide a convenient and cost-effective option to mitigate the ongoing pandemic.
    MeSH term(s) Administration, Inhalation ; Aerosols/administration & dosage ; Animals ; COVID-19/prevention & control ; Disease Models, Animal ; Female ; Male ; Mesocricetus ; Pandemics/prevention & control ; Pneumonia, Viral/drug therapy ; Pneumonia, Viral/prevention & control ; SARS-CoV-2/drug effects ; Single-Domain Antibodies/administration & dosage ; Viral Load/drug effects ; COVID-19 Drug Treatment
    Chemical Substances Aerosols ; Single-Domain Antibodies
    Language English
    Publishing date 2021-05-26
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't
    ZDB-ID 2810933-8
    ISSN 2375-2548 ; 2375-2548
    ISSN (online) 2375-2548
    ISSN 2375-2548
    DOI 10.1126/sciadv.abh0319
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  8. Article ; Online: Rift Valley Fever Virus Infection Causes Acute Encephalitis in the Ferret.

    Barbeau, Dominique J / Albe, Joseph R / Nambulli, Sham / Tilston-Lunel, Natasha L / Hartman, Amy L / Lakdawala, Seema S / Klein, Ed / Duprex, W Paul / McElroy, Anita K

    mSphere

    2020  Volume 5, Issue 5

    Abstract: Rift Valley fever virus (RVFV) is a pathogen of both humans and livestock in Africa and the Middle East. Severe human disease is associated with hepatitis and/or encephalitis. Current pathogenesis studies rely on rodents and nonhuman primates, which have ...

    Abstract Rift Valley fever virus (RVFV) is a pathogen of both humans and livestock in Africa and the Middle East. Severe human disease is associated with hepatitis and/or encephalitis. Current pathogenesis studies rely on rodents and nonhuman primates, which have advantages and disadvantages. We evaluated disease progression in
    MeSH term(s) Acute Disease ; Animals ; Brain/pathology ; Brain/virology ; Disease Models, Animal ; Encephalitis, Viral/virology ; Ferrets/virology ; Male ; Rift Valley Fever/complications ; Rift Valley Fever/physiopathology ; Rift Valley fever virus
    Language English
    Publishing date 2020-10-28
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, Non-U.S. Gov't ; Research Support, U.S. Gov't, Non-P.H.S.
    ISSN 2379-5042
    ISSN (online) 2379-5042
    DOI 10.1128/mSphere.00798-20
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Inhibition of Nipah Virus by Defective Interfering Particles.

    Welch, Stephen R / Tilston, Natasha L / Lo, Michael K / Whitmer, Shannon L M / Harmon, Jessica R / Scholte, Florine E M / Spengler, Jessica R / Duprex, W Paul / Nichol, Stuart T / Spiropoulou, Christina F

    The Journal of infectious diseases

    2020  Volume 221, Issue Suppl 4, Page(s) S460–S470

    Abstract: The error-prone nature of RNA-dependent RNA polymerases drives the diversity of RNA virus populations. Arising within this diversity is a subset of defective viral genomes that retain replication competency, termed defective interfering (DI) genomes. ... ...

    Abstract The error-prone nature of RNA-dependent RNA polymerases drives the diversity of RNA virus populations. Arising within this diversity is a subset of defective viral genomes that retain replication competency, termed defective interfering (DI) genomes. These defects are caused by aberrant viral polymerase reinitiation on the same viral RNA template (deletion DI species) or the nascent RNA strand (copyback DI species). DI genomes have previously been shown to alter the dynamics of a viral population by interfering with normal virus replication and/or by stimulating the innate immune response. In this study, we investigated the ability of artificially produced DI genomes to inhibit Nipah virus (NiV), a highly pathogenic biosafety level 4 paramyxovirus. High multiplicity of infection passaging of both NiV clinical isolates and recombinant NiV in Vero cells generated an extensive DI population from which individual DIs were identified using next-generation sequencing techniques. Assays were established to generate and purify both naturally occurring and in silico-designed DIs as fully encapsidated, infectious virus-like particles termed defective interfering particles (DIPs). We demonstrate that several of these NiV DIP candidates reduced NiV titers by up to 4 logs in vitro. These data represent a proof-of-principle that a therapeutic application of DIPs to combat NiV infections may be an alternative source of antiviral control for this disease.
    MeSH term(s) Animals ; Cell Line ; Chlorocebus aethiops ; Cricetinae ; Defective Viruses ; Genome, Viral ; Mesocricetus ; Nipah Virus/genetics ; Nipah Virus/physiology ; Virus Replication/genetics ; Virus Replication/physiology
    Language English
    Publishing date 2020-02-27
    Publishing country United States
    Document type Journal Article ; Research Support, U.S. Gov't, Non-P.H.S. ; Research Support, U.S. Gov't, P.H.S.
    ZDB-ID 3019-3
    ISSN 1537-6613 ; 0022-1899
    ISSN (online) 1537-6613
    ISSN 0022-1899
    DOI 10.1093/infdis/jiz564
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  10. Article ; Online: The impact of school holidays on the social mixing patterns of school children.

    Eames, Ken T D / Tilston, Natasha L / Edmunds, W John

    Epidemics

    2011  Volume 3, Issue 2, Page(s) 103–108

    Abstract: School holidays are recognised to be of great epidemiological importance for a wide range of infectious diseases; this is postulated to be because the social mixing patterns of school children - a key population group - change significantly during the ... ...

    Abstract School holidays are recognised to be of great epidemiological importance for a wide range of infectious diseases; this is postulated to be because the social mixing patterns of school children - a key population group - change significantly during the holiday period. However, there is little direct quantitative evidence to confirm this belief. Here, we present the results of a prospective survey designed to provide a detailed comparison of social mixing patterns of school children during school terms and during the school holidays. Paired data were collected, with participants recording their social contacts once during term time and once during the holiday period. We found that the daily number of recorded encounters approximately halved during the holidays, and that the number of close contact encounters fell by approximately one third. The holiday period also saw a change in the age structure of children's social contacts, with far fewer contacts of their own age, but an increase in the number of encounters with adults, particularly older adults. A greater amount of mixing between children at different schools was recorded during the holiday. We suggest, therefore, that whilst infections may spread rapidly within schools during term time, in the holiday period there are increased opportunities for transmission to other schools and other age groups.
    MeSH term(s) Adolescent ; Adult ; Age Distribution ; Aged ; Aged, 80 and over ; Child ; Child, Preschool ; Contact Tracing ; Family ; Female ; Holidays ; Humans ; Infant ; Infant, Newborn ; Influenza A Virus, H1N1 Subtype ; Influenza, Human/epidemiology ; Influenza, Human/transmission ; Interpersonal Relations ; Male ; Middle Aged ; Poisson Distribution ; Schools ; Social Behavior ; Social Environment ; Surveys and Questionnaires ; United Kingdom/epidemiology ; Young Adult
    Language English
    Publishing date 2011-04-05
    Publishing country Netherlands
    Document type Comparative Study ; Journal Article ; Research Support, N.I.H., Extramural
    ZDB-ID 2467993-8
    ISSN 1878-0067 ; 1755-4365
    ISSN (online) 1878-0067
    ISSN 1755-4365
    DOI 10.1016/j.epidem.2011.03.003
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