Investigation of Host Metabolism by Utilizing LC-MS based Metabolomics/Lipidomics Approaches

A special issue of Metabolites (ISSN 2218-1989). This special issue belongs to the section "Microbiology and Ecological Metabolomics".

Deadline for manuscript submissions: closed (31 January 2024) | Viewed by 1468

Special Issue Editors


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Guest Editor
The Department of Microbiology, School of Clinical Medicine, Faculty of Medicine, The University of Hong Kong, Hong Kong 999077, China
Interests: lipidomics/metabolomics; functional lipids/metabolites discovery; key host factors associated with pathogenic infections; antiviral/-bacterial approach development

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Guest Editor
School of Chinese Medicine, Hong Kong Baptist University, Hong Kong 999077, China
Interests: functional metabolomics; precision oncology; microbial metabolism; systems pharmacology

Special Issue Information

Dear Colleagues,

Metabolomics and lipidomics are scientific studies aiming to comprehensively characterize the metabolome/lipidome within cells, biofluids, tissues, or organisms. Mass spectrometry (MS), a powerful analytical tool, is frequently used to perform metabolomics/lipidomics studies that could provide the sensitive and reproducible detection of hundreds to thousands of metabolites/lipids. Within the context of system biology, metabolomics/lipidomics are strongly related to the study of biological phenotypes. Many thousands of metabolites/lipid species exist in cells, and they consist of biological metabolic networks via numerous metabolism pathways. These networks can also change in response to cellular environment alterations, such as the phenotype change during disease development. Measuring such alterations and understanding the pathways involved is crucial to fully understanding cellular metabolism and potential mechanisms of disease.

In most cases of infectious diseases, metabolic processes are intimately connected to the mechanisms of disease pathogenesis and the resulting pathology and pathophysiology. For example, viruses are obligate intracellular parasites that depend on the metabolic network of the host cell to provide the energy and macromolecule subunits necessary for their replication.

Lipidomics/metabolomics studies can uncover virus-utilized host signaling pathways and identify the functional enzymes, lipids, or metabolites in these host pathways, which are associated with the virus life cycle and affect virus fitness. During the last decade, many metabolomics and lipidomics studies on multiple pathogens including virus and bacteria have been performed, especially during the COVID-19 pandemic.

This Special Issue is devoted to metabolomics/lipidomics studies in the context of infectious diseases. Covered topics will include (not exclusively) metabolomics/lipidomics of the host response upon pathogen infections (e.g., virus, bacteria, or fungi) such as lipid/metabolic profile characterization post infections, key host factor identification, antipathogenic lipids/metabolites discovery and validation, antipathogenic drug candidates (host enzyme inhibitor, natural product, active compounds) development, host–pathogen interactions, and potential mechanism upon pathogen infections.

Dr. Bingpeng Yan
Prof. Dr. Haitao Lyu
Guest Editors

Manuscript Submission Information

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Keywords

  • metabolomics
  • lipidomics
  • LC-MS
  • pathogen–host interaction
  • viral infection
  • bacterial infection
  • host factor/target

Published Papers (1 paper)

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Research

17 pages, 4514 KiB  
Article
Time-Course Lipidomics of Ornithine-Induced Severe Acute Pancreatitis Model Reveals the Free Fatty Acids Centered Lipids Dysregulation Characteristics
by Jinxi Yang, Manjiangcuo Wang, Qi Qiu, Yan Huang, Yiqin Wang, Qianlun Pu, Na Jiang, Rui Wang, Li Wen, Xiaoying Zhang, Chenxia Han and Dan Du
Metabolites 2023, 13(9), 993; https://doi.org/10.3390/metabo13090993 - 05 Sep 2023
Viewed by 906
Abstract
The relationship between the type and intensities of lipids of blood and pancreas and the pathological changes in the pancreas during severe acute pancreatitis (SAP) remains unclear. In our study, we employed a rat model of SAP induced through intraperitoneal ornithine injections. We [...] Read more.
The relationship between the type and intensities of lipids of blood and pancreas and the pathological changes in the pancreas during severe acute pancreatitis (SAP) remains unclear. In our study, we employed a rat model of SAP induced through intraperitoneal ornithine injections. We collected serum and pancreas samples at various time points (0–144 h) for histopathological and biochemical assessments, followed by lipidomic analyses using LC-MS/MS or in situ mass spectrometry imaging (MSI) To discern changes over time or at specific points, we employed time-course and univariate analyses for lipid screening, respectively. Our findings indicated that the peak inflammation in the Orn-SAP model occurred within the 24–30 h timeframe, with evident necrosis emerging from 24 h onwards, followed by regeneration starting at 48 h. Time-course analysis revealed an overall decrease in glycerophospholipids (PEs, PCs, LPEs, LPCs), while CEs exhibited an increase within the pancreas. Univariate analysis unveiled a significant reduction in serum TAGs containing 46–51 carbon atoms at 24 h, and CERs in the pancreas significantly increased at 30 h, compared with 0 h. Moreover, a substantial rise in TAGs containing 56–58 carbon atoms was observed at 144 h, both in serum and pancreas. MSI demonstrated the CERs containing saturated mono-acyl chains of 16 and 18 carbon atoms influenced pancreatic regeneration. Tracing the origin of FFAs hydrolyzed from pancreatic glycerophospholipids and serum TAGs during the early stages of inflammation, as well as FFAs utilized for CEs and CERs synthesis during the repair phase, may yield valuable strategies for diagnosing and managing SAP. Full article
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