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Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus

Newly emergent turkey arthritis reoviruses (TARVs) have been isolated from cases of lameness in male turkeys over 10 weeks of age. In a previous study, experimental inoculation of TARV in one-week-old turkey poults produced lymphocytic tenosynovitis at four weeks post inoculation but without causing...

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Autores principales: Sharafeldin, Tamer A, Mor, Sunil K, Bekele, Aschalew Z, Verma, Harsha, Noll, Sally L, Goyal, Sagar M, Porter, Robert E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337105/
https://www.ncbi.nlm.nih.gov/pubmed/25828424
http://dx.doi.org/10.1186/s13567-015-0144-9
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author Sharafeldin, Tamer A
Mor, Sunil K
Bekele, Aschalew Z
Verma, Harsha
Noll, Sally L
Goyal, Sagar M
Porter, Robert E
author_facet Sharafeldin, Tamer A
Mor, Sunil K
Bekele, Aschalew Z
Verma, Harsha
Noll, Sally L
Goyal, Sagar M
Porter, Robert E
author_sort Sharafeldin, Tamer A
collection PubMed
description Newly emergent turkey arthritis reoviruses (TARVs) have been isolated from cases of lameness in male turkeys over 10 weeks of age. In a previous study, experimental inoculation of TARV in one-week-old turkey poults produced lymphocytic tenosynovitis at four weeks post inoculation but without causing clinical lameness. This study was undertaken to determine if TARV infection at an early age can lead to clinical lameness in birds as they age. One-week-old male turkeys were inoculated orally with a TARV (strain TARV-O’Neil) and monitored for the development of gait defects until 16 weeks of age. At 4, 8, 12 and 16 weeks of age, a subset of birds was euthanized followed by the collection of gastrocnemius tendon, digital flexor tendon, and intestines for virus detection by rRT-PCR and for histologic inflammation scoring. Clinical lameness was first displayed in TARV-infected turkeys at 8 weeks of age and ruptured gastrocnemius tendons with progressive lameness were also seen at 12–16 weeks of age. The virus was detected in gastrocnemius tendon of 4- 8- and 12-week-old turkeys but not in 16-week-old turkeys. Histologic inflammation scores of tendons at each of the four time points were significantly higher in the virus-inoculated group than in the control group (p < 0.01). Lesions began as lymphocytic tenosynovitis with mild synoviocyte hyperplasia at four weeks of age and progressed to fibrosis as the birds aged. These results demonstrate the potential of TARV to infect young turkeys and to produce subclinical tenosynovitis that becomes clinically demonstrable as the turkeys age.
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spelling pubmed-43371052015-02-24 Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus Sharafeldin, Tamer A Mor, Sunil K Bekele, Aschalew Z Verma, Harsha Noll, Sally L Goyal, Sagar M Porter, Robert E Vet Res Research Newly emergent turkey arthritis reoviruses (TARVs) have been isolated from cases of lameness in male turkeys over 10 weeks of age. In a previous study, experimental inoculation of TARV in one-week-old turkey poults produced lymphocytic tenosynovitis at four weeks post inoculation but without causing clinical lameness. This study was undertaken to determine if TARV infection at an early age can lead to clinical lameness in birds as they age. One-week-old male turkeys were inoculated orally with a TARV (strain TARV-O’Neil) and monitored for the development of gait defects until 16 weeks of age. At 4, 8, 12 and 16 weeks of age, a subset of birds was euthanized followed by the collection of gastrocnemius tendon, digital flexor tendon, and intestines for virus detection by rRT-PCR and for histologic inflammation scoring. Clinical lameness was first displayed in TARV-infected turkeys at 8 weeks of age and ruptured gastrocnemius tendons with progressive lameness were also seen at 12–16 weeks of age. The virus was detected in gastrocnemius tendon of 4- 8- and 12-week-old turkeys but not in 16-week-old turkeys. Histologic inflammation scores of tendons at each of the four time points were significantly higher in the virus-inoculated group than in the control group (p < 0.01). Lesions began as lymphocytic tenosynovitis with mild synoviocyte hyperplasia at four weeks of age and progressed to fibrosis as the birds aged. These results demonstrate the potential of TARV to infect young turkeys and to produce subclinical tenosynovitis that becomes clinically demonstrable as the turkeys age. BioMed Central 2015-02-24 2015 /pmc/articles/PMC4337105/ /pubmed/25828424 http://dx.doi.org/10.1186/s13567-015-0144-9 Text en © Sharafeldin et al.; licensee BioMed Central. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Sharafeldin, Tamer A
Mor, Sunil K
Bekele, Aschalew Z
Verma, Harsha
Noll, Sally L
Goyal, Sagar M
Porter, Robert E
Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title_full Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title_fullStr Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title_full_unstemmed Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title_short Experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
title_sort experimentally induced lameness in turkeys inoculated with a newly emergent turkey reovirus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4337105/
https://www.ncbi.nlm.nih.gov/pubmed/25828424
http://dx.doi.org/10.1186/s13567-015-0144-9
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