Qingyan YE, Yuying ZHANG, Jian SHEN, et al. UHPLC-Q Exactive HRMS-based study on fecal metabolomic characteristics of children with rotavirus enteritis of damp-heat syndrome. [J]. Shanghai Journal of Traditional Chinese Medicine 55(11):18-22(2021)
DOI:
Qingyan YE, Yuying ZHANG, Jian SHEN, et al. UHPLC-Q Exactive HRMS-based study on fecal metabolomic characteristics of children with rotavirus enteritis of damp-heat syndrome. [J]. Shanghai Journal of Traditional Chinese Medicine 55(11):18-22(2021) DOI: 10.16305/j.1007-1334.2021.2008089.
UHPLC-Q Exactive HRMS-based study on fecal metabolomic characteristics of children with rotavirus enteritis of damp-heat syndrome
Objective,2,To explore the fecal metabolomic characteristics of children with rotavirus enteritis of damp-heat syndrome from the perspective of metabolomics.,Methods,2,Fecal samples were collected from 20 children with rotavirus enteritis (RV damp-heat syndrome group) and 20 healthy children, ultra-high performance liquid chromatography coupled with quadrupole-exactive high resolution mass spectrometry (UHPLC-Q Exactive HRMS) was utilized to collect fecal metabolic fingerprints, and orthogonal-partial least squares discriminant analysis (OPLS-DA) pattern recognition approach was introduced for data analysis to identify differential endogenous metabolites.,Results,2,OPLS-DA pattern recognition approach can effectively distinguish RV damp-heat syndrome group from healthy group with high reliability. Eleven differential metabolites were screened out and identified, involving 9 metabolic pathways, such as caffeine metabolism, nicotinate and nicotinamide metabolism, porphyrin and chlorophyll metabolism, unsaturated fatty acid metabolism, arachidonic acid metabolism, arginine and proline metabolism, pyrimidine metabolism, tryptophan metabolism, and glycine, serine and threonine metabolism.,Conclusion,2,There are differential metabolites in fecal samples between children with rotavirus enteritis of damp-heat syndrome and healthy children. The abnormal expression of these metabolic compounds may be an important pathogenesis of rotavirus enteritis of damp-heat syndrome, and it can also be a potential intervention target.
CLARKE E, DESSELBERGER U. Correlates of protection against human rotavirus disease and the factors influencing protection in low-income settings[J]. Mucosal Immunol, 2015, 8(1): 1-17.
TATE J E, BURTON A H, BOSCHI-PINTO C, et al. 2008 estimate of worldwide rotavirus associated mortality in children younger than 5 years before the introduction of universal rotavirus vaccination programmes: a systematic review and meta-analysis[J]. Lancet Infect Dis, 2012, 12(2): 136-141.
CHIOCCHETTI R, POOLE D P, KIMURA H, et al. Evidence that two forms of choline acetyltransferase are differentially expressed in subclasses of enteric neurons[J]. Cell Tissue Res, 2003, 311(1): 11-22.
THERIOT C M, KOENIGSKNECHT M J, CARLSON P E Jr, et al. Antibiotic-induced shifts in the mouse gut microbiome and metabolome increase susceptibility to Clostridium difficile infection[J]. Nat Commun, 2014(5): 3114.
PROBERT C S, JONES P R, RATCLIFFE N M. A novel method for rapidly diagnosing the causes of diarrhoea[J]. Gut, 2004, 53(1): 58-61.
HUA Y L, MA Q, ZHANG X S, et al. Pulsatilla decoction can treat the dampness-heat diarrhea rat model by regulating glycerinphospholipid metabolism based lipidomics approach[J]. Front Pharmacol, 2020(11): 197.