Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers

A leading cause of lameness in modern broilers is bacterial chondronecrosis with osteomyelitis (BCO). While it is known that the components of BCO are bacterial infection, necrosis, and inflammation, the mechanism behind BCO etiology is not yet fully understood. In numerous species, including chicke...

Full description

Bibliographic Details
Main Authors: Alison Ferver, Elizabeth Greene, Robert Wideman, Sami Dridi
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Veterinary Science
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fvets.2021.640901/full
_version_ 1818331108904796160
author Alison Ferver
Elizabeth Greene
Robert Wideman
Sami Dridi
author_facet Alison Ferver
Elizabeth Greene
Robert Wideman
Sami Dridi
author_sort Alison Ferver
collection DOAJ
description A leading cause of lameness in modern broilers is bacterial chondronecrosis with osteomyelitis (BCO). While it is known that the components of BCO are bacterial infection, necrosis, and inflammation, the mechanism behind BCO etiology is not yet fully understood. In numerous species, including chicken, mitochondrial dysfunction has been shown to have a role in the pathogenicity of numerous diseases. The mitochondria is a known target for intracellular bacterial infections, similar to that of common causative agents in BCO, as well as a known regulator of cellular metabolism, stress response, and certain types of cell death. This study aimed to determine the expression profile of genes involved in mitochondrial biogenesis, dynamics, and function. RNA was isolated form the tibias from BCO-affected and healthy broilers and used to measure target gene expression via real-time qPCR. Mitochondrial biogenesis factors PGC-1α and PGC-1β were both significantly upregulated in BCO along with mitochondrial fission factors OMA1, MTFR1, MTFP1, and MFF1 as well as cellular respiration-related genes FOXO3, FOXO4, and av-UCP. Conversely, genes involved in mitochondrial function, ANT, COXIV, and COX5A showed decreased mRNA levels in BCO-affected tibia. This study is the first to provide evidence of potential mitochondrial dysfunction in BCO bone and warrants further mechanistic investigation into how this dysfunction contributes to BCO etiology.
first_indexed 2024-12-13T13:14:37Z
format Article
id doaj.art-e7eeec3bdb2e4da0809e7cc82adfba5d
institution Directory Open Access Journal
issn 2297-1769
language English
last_indexed 2024-12-13T13:14:37Z
publishDate 2021-02-01
publisher Frontiers Media S.A.
record_format Article
series Frontiers in Veterinary Science
spelling doaj.art-e7eeec3bdb2e4da0809e7cc82adfba5d2022-12-21T23:44:35ZengFrontiers Media S.A.Frontiers in Veterinary Science2297-17692021-02-01810.3389/fvets.2021.640901640901Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected BroilersAlison FerverElizabeth GreeneRobert WidemanSami DridiA leading cause of lameness in modern broilers is bacterial chondronecrosis with osteomyelitis (BCO). While it is known that the components of BCO are bacterial infection, necrosis, and inflammation, the mechanism behind BCO etiology is not yet fully understood. In numerous species, including chicken, mitochondrial dysfunction has been shown to have a role in the pathogenicity of numerous diseases. The mitochondria is a known target for intracellular bacterial infections, similar to that of common causative agents in BCO, as well as a known regulator of cellular metabolism, stress response, and certain types of cell death. This study aimed to determine the expression profile of genes involved in mitochondrial biogenesis, dynamics, and function. RNA was isolated form the tibias from BCO-affected and healthy broilers and used to measure target gene expression via real-time qPCR. Mitochondrial biogenesis factors PGC-1α and PGC-1β were both significantly upregulated in BCO along with mitochondrial fission factors OMA1, MTFR1, MTFP1, and MFF1 as well as cellular respiration-related genes FOXO3, FOXO4, and av-UCP. Conversely, genes involved in mitochondrial function, ANT, COXIV, and COX5A showed decreased mRNA levels in BCO-affected tibia. This study is the first to provide evidence of potential mitochondrial dysfunction in BCO bone and warrants further mechanistic investigation into how this dysfunction contributes to BCO etiology.https://www.frontiersin.org/articles/10.3389/fvets.2021.640901/fullmitochondrial dysfunctionlamenessbroilerschondronecrosisosteomyelitisBCO
spellingShingle Alison Ferver
Elizabeth Greene
Robert Wideman
Sami Dridi
Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
Frontiers in Veterinary Science
mitochondrial dysfunction
lameness
broilers
chondronecrosis
osteomyelitis
BCO
title Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
title_full Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
title_fullStr Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
title_full_unstemmed Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
title_short Evidence of Mitochondrial Dysfunction in Bacterial Chondronecrosis With Osteomyelitis–Affected Broilers
title_sort evidence of mitochondrial dysfunction in bacterial chondronecrosis with osteomyelitis affected broilers
topic mitochondrial dysfunction
lameness
broilers
chondronecrosis
osteomyelitis
BCO
url https://www.frontiersin.org/articles/10.3389/fvets.2021.640901/full
work_keys_str_mv AT alisonferver evidenceofmitochondrialdysfunctioninbacterialchondronecrosiswithosteomyelitisaffectedbroilers
AT elizabethgreene evidenceofmitochondrialdysfunctioninbacterialchondronecrosiswithosteomyelitisaffectedbroilers
AT robertwideman evidenceofmitochondrialdysfunctioninbacterialchondronecrosiswithosteomyelitisaffectedbroilers
AT samidridi evidenceofmitochondrialdysfunctioninbacterialchondronecrosiswithosteomyelitisaffectedbroilers