Hu Mingyang, Zhang Xiyun, Li Jinze, Chen Luotong, He Xiaolin, Sui Tingting
Key Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun, China.
Front Microbiol. 2022 Jul 18;13:940196. doi: 10.3389/fmicb.2022.940196. eCollection 2022.
The fucosyltransferase 2 gene () mediates the synthesis of histoblood group antigens (HBGA) that occur from multiple organs, particularly on the surface of intestinal epithelial cells and body fluids. To date, many studies have demonstrated that the interaction of HBGA with the host microbiota is the cause of pathogenesis of intestinal diseases, making non-secretor a risk factor for inflammatory bowel disease (IBD) due to the lack of HBGA. As HBGA also acts as an attachment site for norovirus (NoV) and rotavirus (RV), the non-secretor becomes a protective factor for both viral infections. In addition, the interaction of norovirus and rotavirus with symbiotic bacteria has been found to play an important role in regulating enteroviral infection in IBD. Given the current incomplete understanding of the complex phenomenon and the underlying pathogenesis of intestinal diseases such as IBD, it has recently been hypothesized that the gene regulates intestinal bacteria through attachment sites, may help to unravel the role of and intestinal flora in the mechanism of intestinal diseases in the future, and provide new ideas for the prevention and treatment of intestinal diseases through more in-depth studies.
岩藻糖基转移酶2基因()介导组织血型抗原(HBGA)的合成,这些抗原存在于多个器官中,尤其是在肠道上皮细胞表面和体液中。迄今为止,许多研究表明,HBGA与宿主微生物群的相互作用是肠道疾病发病机制的原因,由于缺乏HBGA,非分泌者成为炎症性肠病(IBD)的一个危险因素。由于HBGA也是诺如病毒(NoV)和轮状病毒(RV)的附着位点,非分泌者成为这两种病毒感染的保护因素。此外,已发现诺如病毒和轮状病毒与共生细菌的相互作用在调节IBD中的肠道病毒感染中起重要作用。鉴于目前对IBD等肠道疾病的复杂现象和潜在发病机制的理解尚不完整,最近有人提出,该基因通过附着位点调节肠道细菌,这可能有助于在未来阐明该基因和肠道菌群在肠道疾病机制中的作用,并通过更深入的研究为肠道疾病的预防和治疗提供新的思路。