Exploration of the Amino Acid Metabolic Profiling and Pathway in Clonorchis sinensis–Infected Rats Revealed by the Targeted Metabolomic Analysis

华支睾吸虫 华支睾吸虫病 生物 生物化学 代谢途径 缬氨酸 代谢组学 小桶 氨基酸 酪氨酸 苯丙氨酸 新陈代谢 免疫学 基因表达 基因 生物信息学 转录组 蠕虫
作者
Jie Wan,Jian Ding,Xiaoli Zhang,Xinyi Hu,Rui Chen,Su Han
出处
期刊:Vector-borne and Zoonotic Diseases [Mary Ann Liebert]
标识
DOI:10.1089/vbz.2023.0059
摘要

Background: Clonorchiasis remains a serious public health problem. However, the molecular mechanism underlying clonorchiasis remains largely unknown. Amino acid (AA) metabolism plays key roles in protein synthesis and energy sources, and improves immunity in pathological conditions. Therefore, this study aimed to explore the AA profiles of spleen in clonorchiasis and speculate the interaction between the host and parasite. Methods: Here targeted ultrahigh performance liquid chromatography multiple reaction monitoring mass spectrometry was applied to discover the AA profiles in spleen of rats infected with Clonorchis sinensis. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis (KEGG) was performed to characterize the dysregulated metabolic pathways. Results: Pathway analysis revealed that phenylalanine, tyrosine, and tryptophan biosynthesis and β-alanine metabolism were significantly altered in clonorchiasis. There were no significant correlations between 14 significant differential AAs and interleukin (IL)-1β. Although arginine, asparagine, histidine, lysine, methionine, phenylalanine, proline, serine, threonine, tryptophan, tyrosine, and valine were positively correlated with IL-6, IL-10, tumor necrosis factor (TNF)-α as well as aspartate aminotransferase and alanine aminotransferase; β-alanine and 4-hydroxyproline were negatively correlated with IL-6, IL-10, and TNF-α. Conclusion: This study reveals the dysregulation of AA metabolism in clonorchiasis and provides a useful insight of metabolic mechanisms at the molecular level.
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