Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/60801
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dc.contributor.authorAssen, Awol Men
dc.contributor.authorGroves, Peter Jen
dc.contributor.authorEtherington, Ashleyen
dc.contributor.authorGerber, Priscilla Fen
dc.contributor.authorSexton, Margareten
dc.contributor.authorWilliamson, Sarahen
dc.contributor.authorWalkden-Brown, Stephenen
dc.date.accessioned2024-06-17T07:12:15Z-
dc.date.available2024-06-17T07:12:15Z-
dc.date.issued2022-09-
dc.identifier.citationAvian diseases, 66(3), p. 299-307en
dc.identifier.issn1938-4351en
dc.identifier.issn0005-2086en
dc.identifier.urihttps://hdl.handle.net/1959.11/60801-
dc.description.abstract<p>Aplicacion de campo del monitoreo por qPCR del virus de la laringotraque ´ ´ıtis infecciosa en el polvo de casetas av´ıcolas y su funcion en el control de un brote importante ´ El muestreo a nivel de poblacion basado en la detecci ´ on por qPCR del virus de la laringotraque ´ ´ıtis infecciosa (ILTV) en el polvo de instalaciones av´ıcolas se puede utilizar para evaluar los resultados de la vacunacion contra esta enfermedad despu ´ es de la administraci ´ on´ masiva en el agua de bebida. Se reporta la aplicacion de campo de este enfoque para evaluar el ´ exito de la administraci ´ on de vacunas y su ´ uso en el control de brotes por laringotraque´ıtis infecciosa en pollos de engorde. En el Estudio 1, se recolectaron muestras de polvo de 26 parvadas de pollos de engorda a los 0, 4, 7, 14 y 21 d´ıas despues de la vacunaci ´ on en el agua de bebida (DPV) a los 7 a 13 d ´ ´ıas de edad con las vacunas de laringotraque´ıtis vivas atenuadas Serva o A20. Inesperadamente, se detecto ADN del virus de laringotraque ´ ´ıtis en muestras de polvo recolectadas antes de la vacunacion en 22/26 parvadas. La tipificaci ´ on revel ´ o que el virus detectado era diferente ´ del virus de la vacuna. Para determinar si el ADN del virus de laringotraque´ıtis detectado proced´ıa de una infeccion activa o del ´ remanente de un virus no infeccioso, se implemento el Estudio 2 en 14 parvadas adicionales con muestras de polvo recolectadas a los 0, ´ 7, 14 y 21 d´ıas despues de la vacunaci ´ on y de hisopos traqueales recolectados de 15 aves/parvada a los cero y 21 d ´ ´ıas despues de la ´ vacunacion. Los resultados indicaron que hab ´ ´ıa infeccion activa con el virus de laringotraque ´ ´ıtis en esas parvadas antes de la vacunacion. Este enfoque contribuy ´ o a un programa de control estatal que result ´ o en la erradicaci ´ on de laringotraque ´ ´ıtis del sur de Australia, como lo confirmaron los resultados negativos de las pruebas del mismo virus para muestras de polvo de 50 parvadas y la ausencia de laringotraque´ıtis infecciosa cl´ınica. Estos hallazgos muestran que la infeccion por el virus de la laringotraque ´ ´ıtis antes de la vacunacion es com ´ un en situaciones de brotes y que las muestras de polvo deben recolectarse a los cero y 7 d ´ ´ıas despues de la ´ vacunacion para una interpretaci ´ on significativa de los resultados de la vacunaci ´ on y el estado de esta enfermedad. Las pruebas de polvo ´ comparativamente de bajo costo durante un brote, junto con la informacion de tipificaci ´ on, ayudaron mucho con la toma de decisiones ´ y con las estrategias de control durante un brote importante, incluida la confirmacion de la ausencia de infecci ´ on en las etapas finales.</p>en
dc.languageenen
dc.publisherAmerican Association of Avian Pathologists, Incen
dc.relation.ispartofAvian diseasesen
dc.titleField Application of qPCR Monitoring of Infectious Laryngotracheitis Virus in Settled Chicken House Dust and Its Role in Control of a Major Outbreaken
dc.typeJournal Articleen
dc.identifier.doi10.1637/aviandiseases-D-22-00022en
local.contributor.firstnameAwol Men
local.contributor.firstnamePeter Jen
local.contributor.firstnameAshleyen
local.contributor.firstnamePriscilla Fen
local.contributor.firstnameMargareten
local.contributor.firstnameSarahen
local.contributor.firstnameStephenen
local.profile.schoolSchool of Environmental and Rural Scienceen
local.profile.schoolSchool of Environmental and Rural Scienceen
local.profile.emailpgerber2@une.edu.auen
local.profile.emailswalkden@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.publisher.placeUnited States of Americaen
local.format.startpage299en
local.format.endpage307en
local.peerreviewedYesen
local.identifier.volume66en
local.identifier.issue3en
local.contributor.lastnameAssenen
local.contributor.lastnameGrovesen
local.contributor.lastnameEtheringtonen
local.contributor.lastnameGerberen
local.contributor.lastnameSextonen
local.contributor.lastnameWilliamsonen
local.contributor.lastnameWalkden-Brownen
dc.identifier.staffune-id:pgerber2en
dc.identifier.staffune-id:swalkdenen
local.profile.orcid0000-0002-8343-8299en
local.profile.orcid0000-0002-0638-5533en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:1959.11/60801en
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
dc.identifier.academiclevelAcademicen
local.abstract.english<p>Population-level sampling based on qPCR detection of infectious laryngotracheitis virus (ILTV) in poultry dust can be used to assess ILT vaccination outcomes following mass administration in drinking water. We report on the field application of this approach to assess the success of vaccine administration and its use in ILT outbreak control in meat chickens. In Study 1, dust samples were collected from 26 meat chicken flocks at 0, 4, 7, 14, and 21 days post drinking water vaccination (DPV) given between 7 to 13 days of age with the Serva or A20 live attenuated ILT vaccines. Unexpectedly, ILTV DNA was detected in dust samples collected prior to vaccination in 22/26 flocks. Typing revealed that the detected ILTV was different from the vaccine virus. To determine whether the detected ILTV DNA was from active infection or carryover of a noninfectious virus, Study 2 was implemented in 14 additional flocks with dust samples collected at 0, 7, 14, and 21 DPV and tracheal swabs collected from 15 birds/flock at 0 and 21 DPV. The results indicated that there was active infection with ILTV in those flocks before vaccination. This approach contributed to a statewide control program resulting in the eradication of ILT from South Australia as confirmed by negative ILTV test results for dust samples from 50 flocks and the absence of clinical ILT. These findings show that ILTV infection prior to vaccination is common in outbreak situations and that dust samples must be collected at 0 and 7 DPV for meaningful interpretation of vaccination outcomes and ILTV status. Comparatively low-cost dust testing during an outbreak, coupled with typing information, greatly assisted with decision making and control strategies during a major outbreak, including confirmation of the absence of infection in the final stages.</p>en
local.title.maintitleField Application of qPCR Monitoring of Infectious Laryngotracheitis Virus in Settled Chicken House Dust and Its Role in Control of a Major Outbreaken
local.relation.fundingsourcenoteThis study was funded by AgriFutures Australia grant number PRJ010639.en
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorAssen, Awol Men
local.search.authorGroves, Peter Jen
local.search.authorEtherington, Ashleyen
local.search.authorGerber, Priscilla Fen
local.search.authorSexton, Margareten
local.search.authorWilliamson, Sarahen
local.search.authorWalkden-Brown, Stephenen
local.open.fileurlhttps://rune.une.edu.au/web/retrieve/0f13612d-d828-40f7-b419-0fab9997d5aben
local.uneassociationYesen
local.atsiresearchNoen
local.sensitive.culturalNoen
local.year.published2022en
local.fileurl.openhttps://rune.une.edu.au/web/retrieve/0f13612d-d828-40f7-b419-0fab9997d5aben
local.fileurl.closedpublishedhttps://rune.une.edu.au/web/retrieve/0f13612d-d828-40f7-b419-0fab9997d5aben
local.subject.for20203009 Veterinary sciencesen
local.profile.affiliationtypeUNE Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeUNE Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeExternal Affiliationen
local.profile.affiliationtypeUNE Affiliationen
local.date.moved2024-06-18en
Appears in Collections:Journal Article
School of Environmental and Rural Science
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