Stephen Lu, Lucas C de Sousa-Paula, Jose M C Ribeiro, Lucas Tirloni
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Dimensional and differential expression analyses revealed four primary transcriptional profiles corresponding to unfed, slow-feeding, transitory (from slow- to rapid-feeding), and rapid-feeding stages. Additionally, comparing the current dataset with previously deposited transcriptome from other tick species allowed the identification of commonly expressed transcripts across different feeding stages.</p><p><strong>Conclusion: </strong>Our findings provide a detailed temporal resolution of numerous metabolic pathways in the midgut of A. americanum adult females throughout the feeding process, highlighting the dynamic transcriptional regulation of the tick's midgut as feeding progresses. Furthermore, we identified conserved transcripts across three different tick species that exhibit similar expression patterns. 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引用次数: 0
摘要
背景:雌性蜱会在宿主身上停留多日,以完成一次血食。伴随着这一漫长的进食期,蜱的体型和体重会显著增加,同时蜱的中肠也会发生显著变化。虽然中肠在血液储存和处理方面的作用已得到公认,但它在病原体的获取、存活和增殖方面也发挥着至关重要的作用。尽管如此,我们对蜱中肠生物学的总体了解仍然有限:我们的转录组分析确定了 15,599 个假定 DNA 编码序列 (CDS),并将其分为 26 个功能组。维度和差异表达分析揭示了四种主要的转录谱,分别对应未进食、慢速进食、过渡阶段(从慢速进食到快速进食)和快速进食阶段。此外,将目前的数据集与以前保存的其他蜱物种的转录组进行比较,可以确定不同摄食阶段的常见表达转录本:我们的研究结果提供了雌性成年蜱中肠在整个摄食过程中许多代谢途径的详细时间分辨率,突出了蜱中肠在摄食过程中的动态转录调控。此外,我们还发现了三个不同蜱物种中表现出相似表达模式的保守转录本。这些知识不仅加深了我们对蜱中肠生理过程的了解,还为开发针对多种蜱的控制方法开辟了潜在的途径。
Exploring the longitudinal expression dynamics of midguts in adult female Amblyomma americanum ticks.
Background: Female ticks remain attached to their host for multiple days to complete a blood meal. This prolonged feeding period is accompanied by a significant increase in the tick's size and body weight, paralleled by noteworthy changes to the tick midgut. While the midgut is recognized for its established role in blood storage and processing, its importance extends to playing a crucial role in the acquisition, survival, and proliferation of pathogens. Despite this, our overall understanding of tick midgut biology is limited.
Results: Our transcriptome analysis identified 15,599 putative DNA coding sequences (CDS), which were classified into 26 functional groups. Dimensional and differential expression analyses revealed four primary transcriptional profiles corresponding to unfed, slow-feeding, transitory (from slow- to rapid-feeding), and rapid-feeding stages. Additionally, comparing the current dataset with previously deposited transcriptome from other tick species allowed the identification of commonly expressed transcripts across different feeding stages.
Conclusion: Our findings provide a detailed temporal resolution of numerous metabolic pathways in the midgut of A. americanum adult females throughout the feeding process, highlighting the dynamic transcriptional regulation of the tick's midgut as feeding progresses. Furthermore, we identified conserved transcripts across three different tick species that exhibit similar expression patterns. This knowledge not only enhances our understanding of the physiological processes within the tick midgut but also opens up potential avenues for developing control methods that target multiple tick species.
期刊介绍:
BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics.
BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.