生物
滑膜支原体
转录组
基因
小桶
RNA序列
遗传学
支原体
基因表达
基因组
微生物学
核糖核酸
DNA微阵列
下调和上调
跨膜蛋白
抄写(语言学)
RNA提取
逆转录酶
微阵列
基因表达谱
抑制消减杂交
分子生物学
非翻译区
软体动物
基因表达调控
膜蛋白
深度测序
细胞生物学
GenBank公司
微阵列分析技术
作者
Duoduo Si,Shijun Bao,Lei Guo,Fan Yang,Shenghu null He,Jidong Li
标识
DOI:10.1186/s12864-026-12748-1
摘要
Mycoplasma synoviae infection in chickens is associated with development of synovitis and arthritis, leading to a decline in poultry production and significant economic repercussions. However, the mechanism of this infection remains imperfectly known. Prokaryotic transcriptome sequencing was used to identify differentially expressed genes (DEGs) in M. synoviae when exposed to mixed cultures of chicken macrophages and chicken embryo fibroblast cells, as well as M. synoviae cultured in vitro. Of 416 DEGs, 262 are upregulated and 122 are downregulated. Ten DEGs were randomly selected and subjected to verification through quantitative reverse transcriptase PCR. The upregulated DEGs exhibited significant enrichment in various Gene Ontology (GO) terms, notably transmembrane transport, transporter activity, and membrane protein complex. Additionally, these DEGs were enriched in Kyoto Encyclopedia of Genes and Genomes (KEGG) pathways, including ABC transporters, quorum sensing, aminoacyl-tRNA biosynthesis, DNA replication, and the bacterial secretion system. The 5’ untranslated region, transcription starting point and noncoding small RNA (sRNA) were also revealed, thirty-one upregulated genes were predicted to interact with sRNA NZ_CP011096_predRNA9. These findings revealed the expression of M. synoviae transcripts when exposed, which beneficial for the treatment of M. synoviae’s target proteins study, will also help to enhance understanding of mechanisms underlying M. synoviae infection.
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