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Plasma Metabonomics of Human Adenovirus-infected Patients with Pneumonia and Upper Respiratory Tract Infection.
Wei, Ting-Ting; Xu, Wen; Tu, Bo; Zhang, Wan-Xue; Yang, Xin-Xin; Zhou, Yiguo; Zhang, Shan-Shan; Yang, Jun-Lian; Xie, Ming-Zhu; Du, Juan; Chen, Wei-Wei; Lu, Qing-Bin.
Affiliation
  • Wei TT; Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, 100191, China.
  • Xu W; Department of Infectious Disease, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, 100039, China.
  • Tu B; Department of Infectious Disease, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, 100039, China.
  • Zhang WX; Department of Laboratorial Science and Technology & Vaccine Research Center, School of Public Health, Peking University, Beijing, 100191, China.
  • Yang XX; Department of Infectious Disease, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, 100039, China.
  • Zhou Y; Department of Health Policy and Management, School of Public Health, Peking University, Beijing, 100191, China.
  • Zhang SS; Global Center for Infectious Disease and Policy Research & Global Health and Infectious Diseases Group, Peking University, Beijing, 100191, China.
  • Yang JL; Department of Infectious Disease, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, 100039, China.
  • Xie MZ; Global Center for Infectious Disease and Policy Research & Global Health and Infectious Diseases Group, Peking University, Beijing, 100191, China.
  • Du J; Department of Laboratorial Science and Technology & Vaccine Research Center, School of Public Health, Peking University, Beijing, 100191, China.
  • Chen WW; Department of Infectious Disease, The Fifth Medical Center of Chinese PLA General Hospital, National Clinical Research Center for Infectious Diseases, Beijing, 100039, China.
  • Lu QB; Department of Epidemiology and Biostatistics, School of Public Health, Peking University, Beijing, 100191, China. qingbinlu@bjmu.edu.cn.
Curr Med Sci ; 44(1): 121-133, 2024 Feb.
Article in En | MEDLINE | ID: mdl-38393525
ABSTRACT

OBJECTIVE:

Human adenovirus (HAdV) infection is common and can develop to serious conditions with high mortality, yet the mechanism of HAdV infection remains unclear. In the present study, the serum metabolite profiles of HAdV-7-infected patients with pneumonia or upper respiratory tract infection (URTI) were explored.

METHODS:

In total, 35 patients were enrolled in the study following an outbreak of HAdV-7 in the army, of whom 14 had pneumonia and 21 had URTI. Blood samples were collected at the acute stage and at the recovery stage and were analyzed by untargeted metabolomics.

RESULTS:

Over 90% of the differential metabolites identified between the pneumonia patients and URTI patients were lipids and lipid-like molecules, including glycerophospholipids, fatty acyls, and sphingolipids. The metabolic pathways that were significantly enriched were primarily the lipid metabolism pathways, including sphingolipid metabolism, glycerophospholipid metabolism, and linoleic acid metabolism. The sphingolipid metabolism was identified as a significantly differential pathway between the pneumonia patients and URTI patients and between the acute and recovery stages for the pneumonia patients, but not between the acute and recovery stages for the URTI patients. Ceramide and lactosylceramide, involved in sphingolipid metabolism, were significantly higher in the pneumonia patients than in the URTI patients with good discrimination abilities [area under curve (AUC) 0.742 and 0.716, respectively; combination AUC 0.801].

CONCLUSION:

Our results suggested that HAdV modulated lipid metabolism for both the patients with URTI and pneumonia, especially the sphingolipid metabolism involving ceramide and lactosylceramide, which might thus be a potential intervention target in the treatment of HAdV infection.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Respiratory Tract Infections / Antigens, CD / Adenovirus Infections, Human / Adenoviruses, Human Limits: Humans Language: En Journal: Curr Med Sci Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Pneumonia / Respiratory Tract Infections / Antigens, CD / Adenovirus Infections, Human / Adenoviruses, Human Limits: Humans Language: En Journal: Curr Med Sci Year: 2024 Document type: Article Affiliation country:
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