Wailla Rafaela Barroso Mendes, Karla Fabiane Lopes de Melo, Francisco Canindé Ferreira de Luna, Carolina Ramos Dos Santos, Edna Cristina Dos Santos Franco, Arnaldo Jorge Martins Filho, Pedro Fernando da Costa Vasconcelos, Samir Mansour Moraes Casseb
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The research aims to understand the immune response to ZIKV in the context of sexual transmission.</p><p><strong>Methods: </strong>The study utilized hamsters of the species Mesocricetus auratus, divided into four groups: three infected with ZIKV and one control group. The animals were euthanized according to ethical guidelines, and renal tissues were collected. Total RNA was extracted and quantified, and both viral load and cytokine mRNA levels were measured using RT-qPCR. The study targeted cytokines such as TNF-A, RIG-I, RANTES, MDA5, IFN-A, and IFN-B. Statistical analysis was performed using Jamovi v 1.6.</p><p><strong>Results: </strong>The study found that the viral load peaked between 3 and 5 days postinfection and then significantly decreased. The expression of cytokine mRNAs showed distinct patterns, with peaks and declines at various time points post-infection. These patterns differed between male and female subgroups. Pearson correlation analysis revealed negative correlations between mRNA expression and days post-infection in most groups.</p><p><strong>Conclusion: </strong>The study concludes that ZIKV infection in hamsters induces a robust inflammatory response in the kidneys, with dynamic cytokine expression profiles that could serve as markers for monitoring infection and related pathologies. 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引用次数: 0
摘要
背景:正黄病毒寨卡病毒(ZIKV)是黄病毒科的一员,由于其感染神经祖细胞的能力,与严重的神经问题,特别是小头畸形有关。本研究探讨了猪中囊绦虫感染寨卡病毒时参与炎症反应的细胞因子mRNA的表达。这项研究旨在了解寨卡病毒在性传播背景下的免疫反应。方法:以金中纹仓鼠为研究对象,随机分为4组:3组感染寨卡病毒,1组对照组。根据道德准则对这些动物实施安乐死,并收集肾脏组织。提取总RNA并定量,RT-qPCR检测病毒载量和细胞因子mRNA水平。本研究针对TNF-A、RIG-I、RANTES、MDA5、IFN-A、IFN-B等细胞因子。采用Jamovi v 1.6进行统计学分析。结果:研究发现,病毒载量在感染后3 ~ 5天达到高峰,然后显著下降。细胞因子mrna的表达表现出不同的模式,在感染后的不同时间点有高峰和下降。这些模式在男性和女性亚群之间有所不同。Pearson相关分析显示,大多数组mRNA表达量与感染后天数呈负相关。结论:本研究表明,ZIKV感染仓鼠可引起肾脏强烈的炎症反应,其动态细胞因子表达谱可作为监测感染和相关病理的标志物。性别特异性免疫反应突出了寨卡病毒发病机制的复杂性,提示了寨卡病毒相关并发症的潜在治疗靶点。
Analysis of Cytokine mRNA Expression During Zika Virus Infection In Mesocricetus auratus.
Background: The Orthoflavivirus zikaense (ZIKV), a member of the Flaviviridae family, has been associated with severe neurological issues, particularly microcephaly, due to its ability to infect neural progenitor cells. This study investigates the mRNA expression of cytokines involved in the inflammatory response during ZIKV infection in Mesocricetus auratus. The research aims to understand the immune response to ZIKV in the context of sexual transmission.
Methods: The study utilized hamsters of the species Mesocricetus auratus, divided into four groups: three infected with ZIKV and one control group. The animals were euthanized according to ethical guidelines, and renal tissues were collected. Total RNA was extracted and quantified, and both viral load and cytokine mRNA levels were measured using RT-qPCR. The study targeted cytokines such as TNF-A, RIG-I, RANTES, MDA5, IFN-A, and IFN-B. Statistical analysis was performed using Jamovi v 1.6.
Results: The study found that the viral load peaked between 3 and 5 days postinfection and then significantly decreased. The expression of cytokine mRNAs showed distinct patterns, with peaks and declines at various time points post-infection. These patterns differed between male and female subgroups. Pearson correlation analysis revealed negative correlations between mRNA expression and days post-infection in most groups.
Conclusion: The study concludes that ZIKV infection in hamsters induces a robust inflammatory response in the kidneys, with dynamic cytokine expression profiles that could serve as markers for monitoring infection and related pathologies. Genderspecific immune responses highlight the complexity of ZIKV pathogenesis, suggesting potential therapeutic targets for Zika-related complications.
期刊介绍:
Current Molecular Medicine is an interdisciplinary journal focused on providing the readership with current and comprehensive reviews/ mini-reviews, original research articles, short communications/letters and drug clinical trial studies on fundamental molecular mechanisms of disease pathogenesis, the development of molecular-diagnosis and/or novel approaches to rational treatment. The reviews should be of significant interest to basic researchers and clinical investigators in molecular medicine. Periodically the journal invites guest editors to devote an issue on a basic research area that shows promise to advance our understanding of the molecular mechanism(s) of a disease or has potential for clinical applications.