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  1. Article ; Online: The diagnosis of proventricular dilatation disease: use of a Western blot assay to detect antibodies against avian Borna virus.

    Villanueva, Itamar / Gray, Patricia / Mirhosseini, Negin / Payne, Susan / Hoppes, Sharman / Honkavuori, Kirsi S / Briese, Thomas / Turner, Debra / Tizard, Ian

    Veterinary microbiology

    2010  Volume 143, Issue 2-4, Page(s) 196–201

    Abstract: Avian Borna virus (ABV) has recently been shown to be the causal agent of proventricular dilatation disease (PDD) a lethal neurologic disease of captive psittacines and other birds. An immunoblot assay was used to detect the presence of antibodies ... ...

    Abstract Avian Borna virus (ABV) has recently been shown to be the causal agent of proventricular dilatation disease (PDD) a lethal neurologic disease of captive psittacines and other birds. An immunoblot assay was used to detect the presence of antibodies against avian Borna virus in the serum of affected birds. A lysate from ABV-infected duck embryo fibroblasts served as a source of antigen. The assay was used to test for the presence of antibodies to ABV in 117 birds. Thirty of these birds had biopsy or necropsy-confirmed proventricular dilatation disease (PDD), while the remaining 87 birds were apparently healthy or were suffering from diseases other than PDD. Sera from 27 of the 30 PDD cases (90%) contained antibodies to ABV. Seventy-three (84%) of the apparently "healthy" birds were seronegative. Additionally, sera from seven macaws and one parrot trapped in the Peruvian Amazon were seronegative. Positive sera recognized the bornaviral nucleoprotein (N-protein). While the presence of antibodies to ABV largely corresponded with the development of clinical PDD, 14 apparently healthy normal birds possessed detectable antibodies to ABV. The existence of a carrier state was confirmed when 13 of 15 apparently healthy cockatiels were shown by PCR to have detectable ABV RNA in their feces. Western blot assays may be of significant assistance in diagnosing proventricular dilatation disease. Many apparently healthy birds may however be seronegative while, at the same time, shedding ABV in their feces.
    MeSH term(s) Animals ; Antibodies, Viral/blood ; Bird Diseases/blood ; Bird Diseases/immunology ; Bird Diseases/virology ; Blotting, Western/veterinary ; Borna Disease/blood ; Borna Disease/diagnosis ; Borna disease virus/immunology ; Psittaciformes ; Sensitivity and Specificity ; Serologic Tests/veterinary
    Chemical Substances Antibodies, Viral
    Language English
    Publishing date 2010-07-14
    Publishing country Netherlands
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 753154-0
    ISSN 1873-2542 ; 0378-1135
    ISSN (online) 1873-2542
    ISSN 0378-1135
    DOI 10.1016/j.vetmic.2009.11.041
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article ; Online: Facile Discovery of a Diverse Panel of Anti-Ebola Virus Antibodies by Immune Repertoire Mining.

    Wang, Bo / Kluwe, Christien A / Lungu, Oana I / DeKosky, Brandon J / Kerr, Scott A / Johnson, Erik L / Jung, Jiwon / Rezigh, Alec B / Carroll, Sean M / Reyes, Ann N / Bentz, Janelle R / Villanueva, Itamar / Altman, Amy L / Davey, Robert A / Ellington, Andrew D / Georgiou, George

    Scientific reports

    2015  Volume 5, Page(s) 13926

    Abstract: The ongoing evolution of Ebolaviruses poses significant challenges to the development of immunodiagnostics for detecting emergent viral variants. There is a critical need for the discovery of monoclonal antibodies with distinct affinities and ... ...

    Abstract The ongoing evolution of Ebolaviruses poses significant challenges to the development of immunodiagnostics for detecting emergent viral variants. There is a critical need for the discovery of monoclonal antibodies with distinct affinities and specificities for different Ebolaviruses. We developed an efficient technology for the rapid discovery of a plethora of antigen-specific monoclonal antibodies from immunized animals by mining the VH:VL paired antibody repertoire encoded by highly expanded B cells in the draining popliteal lymph node (PLN). This approach requires neither screening nor selection for antigen-binding. Specifically we show that mouse immunization with Ebola VLPs gives rise to a highly polarized antibody repertoire in CD138(+) antibody-secreting cells within the PLN. All highly expanded antibody clones (7/7 distinct clones/animal) were expressed recombinantly, and shown to recognize the VLPs used for immunization. Using this approach we obtained diverse panels of antibodies including: (i) antibodies with high affinity towards GP; (ii) antibodies which bound Ebola VLP Kissidougou-C15, the strain circulating in the recent West African outbreak; (iii) non-GP binding antibodies that recognize wild type Sudan or Bundibugyo viruses that have 39% and 37% sequence divergence from Ebola virus, respectively and (iv) antibodies to the Reston virus GP for which no antibodies have been reported.
    MeSH term(s) Animals ; Antibodies, Viral/genetics ; Antibodies, Viral/immunology ; Antibody Formation/genetics ; Antibody Formation/immunology ; B-Lymphocytes/immunology ; B-Lymphocytes/metabolism ; Cross Reactions ; Disease Models, Animal ; Ebolavirus/immunology ; Epitopes/genetics ; Epitopes/immunology ; Hemorrhagic Fever, Ebola/genetics ; Hemorrhagic Fever, Ebola/immunology ; Humans ; Immunization ; Immunoglobulin G/genetics ; Immunoglobulin G/immunology ; Immunoglobulin Heavy Chains/genetics ; Immunoglobulin Heavy Chains/immunology ; Immunoglobulin Light Chains/genetics ; Immunoglobulin Light Chains/immunology ; Immunoglobulin Variable Region/genetics ; Immunoglobulin Variable Region/immunology ; Lymph Nodes/immunology ; Mice ; Phenotype ; Protein Binding/immunology
    Chemical Substances Antibodies, Viral ; Epitopes ; Immunoglobulin G ; Immunoglobulin Heavy Chains ; Immunoglobulin Light Chains ; Immunoglobulin Variable Region
    Language English
    Publishing date 2015-09-10
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Research Support, U.S. Gov't, Non-P.H.S.
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep13926
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  3. Article: The diagnosis of proventricular dilatation disease: Use of a Western blot assay to detect antibodies against avian Borna virus

    Villanueva, Itamar / Gray, Patricia / Mirhosseini, Negin / Payne, Susan / Hoppes, Sharman / Honkavuori, Kirsi S / Briese, Thomas / Turner, Debra / Tizard, Ian

    Veterinary microbiology. 2010 July 14, v. 143, no. 2-4

    2010  

    Abstract: Avian Borna virus (ABV) has recently been shown to be the causal agent of proventricular dilatation disease (PDD) a lethal neurologic disease of captive psittacines and other birds. An immunoblot assay was used to detect the presence of antibodies ... ...

    Abstract Avian Borna virus (ABV) has recently been shown to be the causal agent of proventricular dilatation disease (PDD) a lethal neurologic disease of captive psittacines and other birds. An immunoblot assay was used to detect the presence of antibodies against avian Borna virus in the serum of affected birds. A lysate from ABV-infected duck embryo fibroblasts served as a source of antigen. The assay was used to test for the presence of antibodies to ABV in 117 birds. Thirty of these birds had biopsy or necropsy-confirmed proventricular dilatation disease (PDD), while the remaining 87 birds were apparently healthy or were suffering from diseases other than PDD. Sera from 27 of the 30 PDD cases (90%) contained antibodies to ABV. Seventy-three (84%) of the apparently “healthy” birds were seronegative. Additionally, sera from seven macaws and one parrot trapped in the Peruvian Amazon were seronegative. Positive sera recognized the bornaviral nucleoprotein (N-protein). While the presence of antibodies to ABV largely corresponded with the development of clinical PDD, 14 apparently healthy normal birds possessed detectable antibodies to ABV. The existence of a carrier state was confirmed when 13 of 15 apparently healthy cockatiels were shown by PCR to have detectable ABV RNA in their feces. Western blot assays may be of significant assistance in diagnosing proventricular dilatation disease. Many apparently healthy birds may however be seronegative while, at the same time, shedding ABV in their feces.
    Keywords Psittacidae ; parrots ; aviary birds ; bird diseases ; Borna disease ; Borna disease virus ; disease detection ; Western blotting ; antibody detection ; bioassays ; blood serum ; hematologic tests ; validity ; disease diagnosis ; central nervous system diseases ; etiology ; disease transmission ; carrier state
    Language English
    Dates of publication 2010-0714
    Size p. 196-201.
    Publishing place Amsterdam; New York: Elsevier
    Document type Article
    ZDB-ID 753154-0
    ISSN 1873-2542 ; 0378-1135
    ISSN (online) 1873-2542
    ISSN 0378-1135
    DOI 10.1016/j.vetmic.2009.11.041
    Database NAL-Catalogue (AGRICOLA)

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  4. Article ; Online: Corrigendum: Facile Discovery of a Diverse Panel of Anti-Ebola Virus Antibodies by Immune Repertoire Mining.

    Wang, Bo / Kluwe, Christien A / Lungu, Oana I / DeKosky, Brandon J / Kerr, Scott A / Johnson, Erik L / Tanno, Hidetaka / Lee, Chang-Han / Jung, Jiwon / Rezigh, Alec B / Carroll, Sean M / Reyes, Ann N / Bentz, Janelle R / Villanueva, Itamar / Altman, Amy L / Davey, Robert A / Ellington, Andrew D / Georgiou, George

    Scientific reports

    2016  Volume 6, Page(s) 27229

    Language English
    Publishing date 2016-06-10
    Publishing country England
    Document type Journal Article
    ZDB-ID 2615211-3
    ISSN 2045-2322 ; 2045-2322
    ISSN (online) 2045-2322
    ISSN 2045-2322
    DOI 10.1038/srep27229
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Use of avian bornavirus isolates to induce proventricular dilatation disease in conures.

    Gray, Patricia / Hoppes, Sharman / Suchodolski, Paulette / Mirhosseini, Negin / Payne, Susan / Villanueva, Itamar / Shivaprasad, H L / Honkavuori, Kirsi S / Lipkin, W Ian / Briese, Thomas / Reddy, Sanjay M / Tizard, Ian

    Emerging infectious diseases

    2010  Volume 16, Issue 3, Page(s) 473–479

    Abstract: Avian bornavirus (ABV) is a newly discovered member of the family Bornaviridae that has been associated with the development of a lethal neurologic syndrome in birds, termed proventricular dilatation disease (PDD). We successfully isolated and ... ...

    Abstract Avian bornavirus (ABV) is a newly discovered member of the family Bornaviridae that has been associated with the development of a lethal neurologic syndrome in birds, termed proventricular dilatation disease (PDD). We successfully isolated and characterized ABV from the brains of 8 birds with confirmed PDD. One isolate was passed 6 times in duck embryo fibroblasts, and the infected cells were then injected intramuscularly into 2 healthy Patagonian conures (Cyanoliseus patagonis). Clinical PDD developed in both birds by 66 days postinfection. PDD was confirmed by necropsy and histopathologic examination. Reverse transcription-PCR showed that the inoculated ABV was in the brains of the 2 infected birds. A control bird that received uninfected tissue culture cells remained healthy until it was euthanized at 77 days. Necropsy and histopathologic examinations showed no abnormalities; PCR did not indicate ABV in its brain tissues.
    MeSH term(s) Animals ; Bird Diseases/virology ; Bornaviridae/isolation & purification ; Bornaviridae/pathogenicity ; Cells, Cultured ; Dilatation, Pathologic ; Ducks/embryology ; Fibroblasts/virology ; Parrots/virology ; Proventriculus/pathology ; Proventriculus/physiopathology ; Proventriculus/virology
    Language English
    Publishing date 2010-03
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 1380686-5
    ISSN 1080-6059 ; 1080-6040
    ISSN (online) 1080-6059
    ISSN 1080-6040
    DOI 10.3201/eid1603.091257
    Database MEDical Literature Analysis and Retrieval System OnLINE

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