Cargando…
An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection
BACKGROUND: The development of a mouse model as an in vivo pathogenicity screening tool for Brachyspira spp. has advanced the study of these economically important pathogens in recent years. However, none of the murine models published to date have been used to characterize the clinical signs of dis...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568335/ https://www.ncbi.nlm.nih.gov/pubmed/28830508 http://dx.doi.org/10.1186/s12917-017-1166-5 |
_version_ | 1783258841453953024 |
---|---|
author | Ek, Courtney E. Nosach, Roman Fernando, Champika Huang, Yanyun Perez, Jason Byron D.S. Costa, Matheus O. Ekanayake, Samantha Hill, Janet E. Harding, John C.S. |
author_facet | Ek, Courtney E. Nosach, Roman Fernando, Champika Huang, Yanyun Perez, Jason Byron D.S. Costa, Matheus O. Ekanayake, Samantha Hill, Janet E. Harding, John C.S. |
author_sort | Ek, Courtney E. |
collection | PubMed |
description | BACKGROUND: The development of a mouse model as an in vivo pathogenicity screening tool for Brachyspira spp. has advanced the study of these economically important pathogens in recent years. However, none of the murine models published to date have been used to characterize the clinical signs of disease in mice, instead focusing on pathology following oral inoculation with various Brachyspira spp. The experiments described herein explore modifications of published models to characterize faecal consistency, faecal shedding and pathology in mice challenged with “Brachyspira hampsonii” clade II (Bhamp). METHODS AND RESULTS: In Experiment 1, 24 CF-1 mice were randomly allocated to one of three inoculation groups: sham (Ctrl), Bhamp, or B. hyodysenteriae (Bhyo; positive control). Half of each group was fed normal mouse chow (RMH) while the other received a low-zinc diet (TD85420). In Experiment 2, eight CF-1 mice and nine C3H/HeN mice were divided into Ctrl or Bhamp inoculation groups, and all fed TD85420. In Experiment 1, mice fed TD85420 demonstrated more severe mucoid faeces (P = 0.001; Kruskal Wallis) and faecal shedding for a significantly greater number of days (P = 0.005; Kruskal Wallis). Mean faecal scores of Bhamp inoculated mice trended higher than Ctrl (P = 0.06; Wilcoxon rank-sum) as did those of Bhyo mice (P = 0.0; Wilcoxon rank-sum). In Experiment 2, mean faecal scores of inoculated CF-1 mice were significantly greater than in C3H mice (P = 0.049; Kruskal Wallis) but no group differences in faecal shedding were observed. In both experiments, mice clustered based on the severity of colonic and caecal histopathology but high lesion scores were not always concurrent with high fecal scores. CONCLUSION: In our laboratory, CF-1 mice and the lower-zinc TD85420 diet provide a superior murine challenge model of “Brachyspira hampsonii” clade II. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-017-1166-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5568335 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55683352017-08-29 An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection Ek, Courtney E. Nosach, Roman Fernando, Champika Huang, Yanyun Perez, Jason Byron D.S. Costa, Matheus O. Ekanayake, Samantha Hill, Janet E. Harding, John C.S. BMC Vet Res Research Article BACKGROUND: The development of a mouse model as an in vivo pathogenicity screening tool for Brachyspira spp. has advanced the study of these economically important pathogens in recent years. However, none of the murine models published to date have been used to characterize the clinical signs of disease in mice, instead focusing on pathology following oral inoculation with various Brachyspira spp. The experiments described herein explore modifications of published models to characterize faecal consistency, faecal shedding and pathology in mice challenged with “Brachyspira hampsonii” clade II (Bhamp). METHODS AND RESULTS: In Experiment 1, 24 CF-1 mice were randomly allocated to one of three inoculation groups: sham (Ctrl), Bhamp, or B. hyodysenteriae (Bhyo; positive control). Half of each group was fed normal mouse chow (RMH) while the other received a low-zinc diet (TD85420). In Experiment 2, eight CF-1 mice and nine C3H/HeN mice were divided into Ctrl or Bhamp inoculation groups, and all fed TD85420. In Experiment 1, mice fed TD85420 demonstrated more severe mucoid faeces (P = 0.001; Kruskal Wallis) and faecal shedding for a significantly greater number of days (P = 0.005; Kruskal Wallis). Mean faecal scores of Bhamp inoculated mice trended higher than Ctrl (P = 0.06; Wilcoxon rank-sum) as did those of Bhyo mice (P = 0.0; Wilcoxon rank-sum). In Experiment 2, mean faecal scores of inoculated CF-1 mice were significantly greater than in C3H mice (P = 0.049; Kruskal Wallis) but no group differences in faecal shedding were observed. In both experiments, mice clustered based on the severity of colonic and caecal histopathology but high lesion scores were not always concurrent with high fecal scores. CONCLUSION: In our laboratory, CF-1 mice and the lower-zinc TD85420 diet provide a superior murine challenge model of “Brachyspira hampsonii” clade II. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12917-017-1166-5) contains supplementary material, which is available to authorized users. BioMed Central 2017-08-22 /pmc/articles/PMC5568335/ /pubmed/28830508 http://dx.doi.org/10.1186/s12917-017-1166-5 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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 Article Ek, Courtney E. Nosach, Roman Fernando, Champika Huang, Yanyun Perez, Jason Byron D.S. Costa, Matheus O. Ekanayake, Samantha Hill, Janet E. Harding, John C.S. An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title | An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title_full | An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title_fullStr | An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title_full_unstemmed | An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title_short | An optimized swine dysentery murine model to characterize shedding and clinical disease associated with “Brachyspira hampsonii” infection |
title_sort | optimized swine dysentery murine model to characterize shedding and clinical disease associated with “brachyspira hampsonii” infection |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5568335/ https://www.ncbi.nlm.nih.gov/pubmed/28830508 http://dx.doi.org/10.1186/s12917-017-1166-5 |
work_keys_str_mv | AT ekcourtneye anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT nosachroman anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT fernandochampika anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT huangyanyun anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT perezjasonbyronds anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT costamatheuso anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT ekanayakesamantha anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT hilljanete anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT hardingjohncs anoptimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT ekcourtneye optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT nosachroman optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT fernandochampika optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT huangyanyun optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT perezjasonbyronds optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT costamatheuso optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT ekanayakesamantha optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT hilljanete optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection AT hardingjohncs optimizedswinedysenterymurinemodeltocharacterizesheddingandclinicaldiseaseassociatedwithbrachyspirahampsoniiinfection |