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Deciphering Immune Modulation in Chickens Co-Infected with ALV-J and CIAV: A Transcriptomic Approach

机译:破译 ALV-J 和 CIAV 共同感染鸡的免疫调节:一种转录组学方法

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摘要

Viral co-infections pose significant challenges, causing substantial economic losses worldwide in the poultry industry. Among these, avian lLeukosis virus subgroup J (ALV-J) and chicken infectious anemia virus (CIAV) are particularly concerning, as they frequently lead to co-infections in chickens, further compromising their immune defenses, increasing susceptibility to secondary infections and diminishing vaccine efficacy. While our previous studies have examined the pathogenicity and immunosuppressive effects of these co-infections in vitro and in vivo, the key genes and molecular pathways involved remain largely unexplored. This study investigates the synergistic effects of co-infection with ALV-J and CIAV through comprehensive transcriptome analysis using high-throughput sequencing. We identified 1007 differentially expressed mRNAs (DEmRNAs) and 62 differentially expressed miRNAs (DEmiRNAs) associated with the synergistic activation effects of co-infection, along with 331 DEmRNAs and 62 DEmiRNAs linked to specific activation processes. Notably, the immune suppression observed in co-infected chickens may be influenced by the enhanced utilization of reactive oxygen species (ROS) and oxidative stress pathways, which impact host immune responses. Furthermore, co-infection appears to employ distinct immune evasion strategies through the modulation of rRNA metabolism, differing from single infections. These insights provide a deeper understanding of the molecular mechanisms underlying immune suppression during viral co-infections and help develop targeted therapies and improve disease control in poultry, reducing economic losses.
机译:病毒合并感染构成了重大挑战,给全球家禽业造成了巨大的经济损失。其中,禽 lleukosis 病毒亚群 J (ALV-J) 和鸡传染性贫血病毒 (CIAV) 尤其令人担忧,因为它们经常导致鸡的混合感染,进一步损害它们的免疫防御,增加对继发感染的易感性并降低疫苗效力。虽然我们之前的研究已经在体外和体内检查了这些混合感染的致病性和免疫抑制作用,但所涉及的关键基因和分子途径在很大程度上仍未得到探索。本研究通过使用高通量测序进行全面的转录组分析,探讨了 ALV-J 和 CIAV 混合感染的协同效应。我们鉴定了 1007 个差异表达 mRNA (DEmRNA) 和 62 个差异表达 miRNAs (DEmiRNA),以及与共同感染的协同激活作用相关的 331 个 DEmRNAs 和 62 个 DEmiRNA。值得注意的是,在混合感染的鸡中观察到的免疫抑制可能受到活性氧 (ROS) 和氧化应激途径利用增强的影响,这会影响宿主的免疫反应。此外,与单一感染不同,混合感染似乎通过调节 rRNA 代谢采用不同的免疫逃避策略。这些见解有助于更深入地了解病毒混合感染期间免疫抑制的分子机制,并有助于开发靶向疗法并改善家禽的疾病控制,从而减少经济损失。

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