Single nucleotide polymorphism of Notch1 gene rs3124599 allele is associated with the severity of CVA6-related HFMD in the Chinese Han population

• Published in: BMC infectious diseases Vol. 24; no. 1; pp. 750 - 9
• Main Authors: Li, Zijie, Ji, Wangquan, Dai, Bowen, Chen, Shouhang, Wang, Fang, Duan, Guangcai, Jin, Yuefei
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 29.07.2024; BioMed Central; BMC
• Subjects: Age composition; Alleles; Analysis; Asian People - genetics; Blood; Blood levels; Care and treatment; Chi-square test; Child; Child, Preschool; China - epidemiology; Confidence intervals; Correlation; Coxsackievirus infections; Cytokines; Development and progression; Disease; East Asian People; Enterovirus A, Human - genetics; Ethylenediaminetetraacetic acid; Female; Gene Frequency; Gene polymorphism; Genes; Genetic aspects; Genetic Predisposition to Disease; Genetic transcription; Genotype; Genotype & phenotype; Genotypes; Genotyping; Hand, Foot and Mouth Disease - genetics; Hand, Foot and Mouth Disease - virology; Hand, foot, and mouth disease; Health aspects; Humans; Infant; Leukocytes; Male; Medical research; Medicine, Experimental; Monocytes; Notch protein; Notch1; Notch1 protein; Nucleic acids; Nucleotides; Pathogenesis; Peripheral blood; Phenols; Polymerase chain reaction; Polymorphism; Polymorphism, Single Nucleotide; Population; Population genetics; Population studies; Real time; Receptor, Notch1 - genetics; Restriction fragment length polymorphism; RNA; rs3124599; Severity of Illness Index; Signal transduction; Single nucleotide polymorphisms; Single-nucleotide polymorphism; SNP; Statistical analysis; China; Beijing China; United States > US; rs3124599; SNP; Hand, foot, and mouth disease; Notch1
• ISSN: 1471-2334; 1471-2334
• DOI: 10.1186/s12879-024-09640-2

There is evidence suggesting that Notch1 signaling pathway contributes to the development of hand, foot, and mouth disease (HFMD); however, the role of Notch1 gene polymorphisms in the severity of coxsackievirus A6 (CVA6)-related HFMD remains unclear. This study aimed to investigate the correlation between Notch1 gene polymorphisms and the severity of CVA6-related HFMD. A total of 196 patients (Chinese Han population) diagnosed with CVA6-related HFMD through nucleic acid testing were included in this study. Among them, 97 patients were classified as severe cases, while 99 cases were categorized as mild. The mRNA levels of Notch1 in the peripheral blood leukocytes of HFMD patients were detected by quantitative real-time polymerase chain reaction (qRT-PCR), and the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique was utilized for genotyping of rs3124599, rs3124603, and rs3124591. The frequencies of rs3124599 alleles were G (39.0%) and A (61.0%), while the frequencies of rs3124599 genotypes were GG (12.2%), GA (53.6%), and AA (34.2%), respectively. In the recessive model, the frequency of rs3124599 AA genotypes significantly increased in severe patients, compared to mild patients (P < 0.05). Due to the low frequency of alleles for rs3124591 and rs3124603 in patients, as well as the absence of any difference in their distribution between the two groups (P > 0.05), no additional statistical analysis was performed. After adjusting for age and sex, patients with rs3124599 AA genotype had a significantly higher risk of severe HFMD in comparison to G allele carriers (GA/GG), with an odds ratio (95% confidence interval) of 2.010 (1.094, 3.691). Meanwhile, the mRNA levels of Notch1 were found to be significantly higher in severe patients compared to mild patients (P < 0.05), and a positive correlation was observed between Notch1 mRNA levels and the peripheral blood monocyte count (r = 0.42, P < 0.001). Additionally, there were significant differences observed in Notch1 mRNA levels and peripheral blood monocyte counts between patients with the AA genotype of rs3124599 and those with the GA genotype or G allele carriers (P < 0.05). In the Chinese Han population, there is a strong correlation between the Notch1 rs3124599 allele and the severity of CVA6-related HFMD. This correlation may be attributed to genetic polymorphism of rs3124599 regulating Notch1 transcription levels. These findings reveal the important role of Notch1 gene polymorphism in CVA6 infection, establishing a scientific foundation for the precise control of severe HFMD.