RNA-seq reveals downregulated osteochondral genes potentially related to tibia bacterial chondronecrosis with osteomyelitis in broilers.

IF 2.9 Q2 Biochemistry, Genetics and Molecular Biology
Haniel Cedraz de Oliveira, Adriana Mércia Guaratini Ibelli, Simone Eliza Facioni Guimarães, Mauricio Egídio Cantão, Jane de Oliveira Peixoto, Luiz Lehmann Coutinho, Mônica Corrêa Ledur
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引用次数: 2

Abstract

Background: Bacterial chondronecrosis with osteomyelitis (BCO) develops in the growth plate (GP) of the proximal femur and tibia and is initiated by damage to the less mineralized chondrocytes followed by colonization of opportunistic bacteria. This condition affects approximately 1% of all birds housed, being considered one of the major causes of lameness in fast growing broilers. Although several studies have been previously performed aiming to understand its pathogenesis, the molecular mechanisms involved with BCO remains to be elucidated. Therefore, this study aimed to generate a profile of global differential gene expression involved with BCO in the tibia of commercial broilers, through RNA sequencing analysis to identity genes and molecular pathways involved with BCO in chickens.

Results: Our data showed 192 differentially expressed (DE) genes: 63 upregulated and 129 downregulated in the GP of the tibia proximal epiphysis of BCO-affected broilers. Using all DE genes, six Biological Processes (BP) were associated with bone development (connective tissue development, cartilage development, skeletal system development, organ morphogenesis, system development and skeletal system morphogenesis). The analyses of the upregulated genes did not indicate any significant BP (FDR < 0.05). However, with the downregulated genes, the same BP were identified when using all DE genes in the analysis, with a total of 26 coding genes explaining BCO in the tibia: ACAN, ALDH1A2, CDH7, CHAD, CHADL, COL11A1, COMP, CSGALNACT1, CYR61, FRZB, GAL3ST1, HAPLN1, IHH, KIF26B, LECT1, LPPR1, PDE6B, RBP4A, SERINC5, SFRP1, SOX8, SOX9, TENM2, THBS1, UCHL1 and WFIKKN2. In addition, seven transcription factors were also associated to BCO: NFATC2, MAFB, HIF1A-ARNT, EWSR1-FLI1, NFIC, TCF3 and NF-KAPPAB.

Conclusions: Our data show that osteochondral downregulated genes are potential molecular causes of BCO in broilers, and the bacterial process seems to be, in fact, a secondary condition. Sixteen genes responsible for bone and cartilage formation were downregulated in BCO-affected broilers being strong candidate genes to trigger this disorder.

Abstract Image

Abstract Image

RNA-seq揭示了肉仔鸡胫骨细菌性软骨坏死伴骨髓炎可能与下调的骨软骨基因相关。
背景:细菌性软骨坏死伴骨髓炎(BCO)发生于股骨和胫骨近端生长板(GP),是由矿化程度较低的软骨细胞受损引发的,随后是机会性细菌的定植。这种情况影响了大约1%的家禽,被认为是快速生长肉鸡跛脚的主要原因之一。虽然之前已经进行了一些旨在了解其发病机制的研究,但与BCO相关的分子机制仍有待阐明。因此,本研究旨在通过RNA测序分析,确定鸡BCO相关基因和分子通路,建立商品肉鸡胫骨BCO相关基因的全球差异表达图谱。结果:我们的数据显示,bco感染肉鸡胫骨近端骨骺GP中有192个差异表达(DE)基因,其中63个表达上调,129个表达下调。使用所有DE基因,6个生物过程(BP)与骨发育相关(结缔组织发育、软骨发育、骨骼系统发育、器官形态发生、系统发育和骨骼系统形态发生)。结论:我们的数据表明,骨软骨下调基因是肉鸡BCO的潜在分子原因,细菌过程实际上似乎是次要条件。在bco感染的肉鸡中,16个负责骨和软骨形成的基因被下调,这是引发这种疾病的强有力的候选基因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Genetics
BMC Genetics 生物-遗传学
CiteScore
4.30
自引率
0.00%
发文量
77
审稿时长
4-8 weeks
期刊介绍: BMC Genetics is an open access, peer-reviewed journal that considers articles on all aspects of inheritance and variation in individuals and among populations.
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