Whole transcriptome analysis of Mycoplasma bovis-host interactions under in vitro and in vivo conditions

IF 2.7 2区 农林科学 Q3 MICROBIOLOGY Veterinary microbiology Pub Date : 2025-04-01 Epub Date: 2025-02-09 DOI:10.1016/j.vetmic.2025.110426
Aga E. Gelgie , Benti D. Gelalcha , Trevor Freeman , Taylor B. Ault-Seay , Jonathan Beever , Oudessa Kerro Dego
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Abstract

Mycoplasma bovis mastitis is becoming increasingly problematic for dairy cattle farming. M. bovis is inherently resistant to beta-lactam antimicrobials and no effective vaccine is available. The major constraints to developing effective control tools are limited knowledge of M. bovis virulence factors and the underlying pathogenic mechanisms. The objective of this study was to determine virulence-associated genes of M. bovis and host immune response genes expressed during the early stages of host-pathogen interactions. We conducted in vitro infection of mammary epithelial cell (MAC-T) lines and in vivo intramammary infection of dairy cows with M. bovis strain PG45 and evaluated whole transcriptome differential gene expression. A total of 614 and 7161 genes of M. bovis and bovine host cells were differentially expressed, respectively. Insertion sequence (IS) genes that are involved in transposase activity such as ISMbov1, ISMbov2, ISMbov3, and ISMbov9 were significantly upregulated, whereas protein translation-associated genes were significantly downregulated. In MAC-T cells, genes involved in apoptosis pathways and proinflammatory cytokines were significantly upregulated, whereas genes involved in cell cycle, ribosome biogenesis, and steroid biosynthesis were significantly downregulated. Genes encoding formation of neutrophil extracellular traps and proinflammatory cytokines, were significantly upregulated in the mammary gland of M. bovis challenged cows, whereas genes involved in steroid biosynthesis and metabolism were significantly downregulated. Altogether, while our findings shed light on the simultaneous transcriptional changes in M. bovis and the host during infection, further studies are required to understand a complete picture of these interactions that lead to mastitis.
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体外和体内条件下牛支原体与宿主相互作用的全转录组分析
牛支原体乳腺炎正日益成为奶牛养殖的问题。牛支原体对内酰胺类抗菌剂具有固有的耐药性,目前尚无有效的疫苗。开发有效控制工具的主要制约因素是对牛支原体毒力因子和潜在致病机制的了解有限。本研究的目的是确定牛分枝杆菌的毒力相关基因和宿主免疫反应基因在宿主-病原体相互作用的早期阶段表达。我们用牛分枝杆菌PG45菌株体外感染奶牛乳腺上皮细胞(MAC-T)系和体内乳内感染奶牛,并评估了全转录组差异基因的表达。牛分枝杆菌和牛宿主细胞中分别有614个和7161个基因存在差异表达。参与转座酶活性的ISMbov1、ISMbov2、ISMbov3和ISMbov9等插入序列基因显著上调,而蛋白翻译相关基因显著下调。在MAC-T细胞中,参与凋亡途径和促炎细胞因子的基因显著上调,而参与细胞周期、核糖体生物发生和类固醇生物合成的基因显著下调。奶牛乳腺中编码中性粒细胞胞外陷阱和促炎细胞因子的基因显著上调,而涉及类固醇生物合成和代谢的基因显著下调。总之,虽然我们的发现揭示了牛分枝杆菌和宿主在感染期间同时发生的转录变化,但需要进一步的研究来了解导致乳腺炎的这些相互作用的完整图景。
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来源期刊
Veterinary microbiology
Veterinary microbiology 农林科学-兽医学
CiteScore
5.90
自引率
6.10%
发文量
221
审稿时长
52 days
期刊介绍: Veterinary Microbiology is concerned with microbial (bacterial, fungal, viral) diseases of domesticated vertebrate animals (livestock, companion animals, fur-bearing animals, game, poultry, fish) that supply food, other useful products or companionship. In addition, Microbial diseases of wild animals living in captivity, or as members of the feral fauna will also be considered if the infections are of interest because of their interrelation with humans (zoonoses) and/or domestic animals. Studies of antimicrobial resistance are also included, provided that the results represent a substantial advance in knowledge. Authors are strongly encouraged to read - prior to submission - the Editorials (''Scope or cope'' and ''Scope or cope II'') published previously in the journal. The Editors reserve the right to suggest submission to another journal for those papers which they feel would be more appropriate for consideration by that journal. Original research papers of high quality and novelty on aspects of control, host response, molecular biology, pathogenesis, prevention, and treatment of microbial diseases of animals are published. Papers dealing primarily with immunology, epidemiology, molecular biology and antiviral or microbial agents will only be considered if they demonstrate a clear impact on a disease. Papers focusing solely on diagnostic techniques (such as another PCR protocol or ELISA) will not be published - focus should be on a microorganism and not on a particular technique. Papers only reporting microbial sequences, transcriptomics data, or proteomics data will not be considered unless the results represent a substantial advance in knowledge. Drug trial papers will be considered if they have general application or significance. Papers on the identification of microorganisms will also be considered, but detailed taxonomic studies do not fall within the scope of the journal. Case reports will not be published, unless they have general application or contain novel aspects. Papers of geographically limited interest, which repeat what had been established elsewhere will not be considered. The readership of the journal is global.
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