姓 名: | 段屹 | |
地 址: | 安徽省合肥市蜀山区 中国科学技术大学 生命科学与医学部 | |
邮 编: | 230027 | |
电 话: | 0551-63607884 | |
邮 箱: | yduan@ustc.edu.cn |
教育与科研经历 |
2007-09 至 2011-06 | 中国科学技术大学,生物科学,学士 |
2011-08 至 2016-12 | Texas A&M University, Biochemistry,博士 |
2017-03 至 2022-02 | University of California at San Diego,博士后 |
2022-04 至今 | 中国科学技术大学,生命科学与医学部,教授 |
目前研究方向 |
人体肠道内存在着超过1000种,与人体自身细胞数量相当的微生物种群。这一人体“最大的器官”,携带着百倍于人体自身基因数量的“第二套基因组”,在维持机体健康方面发挥着不可或缺的作用。 大量数据表明,肠道菌群失衡与多种人体疾病具备显著相关性。然而,进一步验证其因果性关系,发掘其背后的分子机理并为相关疾病的诊断治疗提供新靶点、新思路的高水平研究,还比较缺乏。深入探究肠道微生物在人体疾病中的作用,精准定位至具体菌株并详细阐明其致病机理,再据此开发以之为靶点的精准治疗手段,有着非常重要的科学价值和临床意义。课题组以此为出发点,旨在更好的揭示肠道微生物对人体疾病的影响,为新一代疾病诊疗突破及药物研发提供方向和思路。 具体研究方向如下: 1. 肠道微生物对代谢性及免疫性疾病的影响及其具体分子机制; 2. 微生物相关生物疗法,尤其是噬菌体疗法。 |
代表性论文 |
1. | Duan Y#, Llorente C#, Lang S, Brandl K, Chu H, Jiang L, et al. (2019). Bacteriophage targeting of gut bacterium attenuates alcoholic liver disease. Nature. 575(7783): 505-511. doi: 10.1038/s41586-019-1742-x. |
2. | Xie S#, Li J#, Lyu F#, Xiong Q#, et al., Duan Y*, Jiang Y*, Zhou H*, Chen P*. (2023). Novel tripeptide RKH derived from Akkermansia muciniphila protects against lethal sepsis. Gut. 14(3):490. doi: 10.1136/gutjnl-2023-329996. |
3. | Xingyao Chen#, Mendes BG#, Alves BS, Duan Y*. (2023). Phage therapy in gut microbiome. Progress in Molecular Biology and Translational Science. doi: 10.1016/bs.pmbts.2023.04.005. |
4. | Mendes BG#, Duan Y#, Schnabl B. (2022). Immune response of an oral Enterococcus faecalis phage cocktail in a mouse model of ethanol-induced liver disease. Viruses. 14(3):490. doi: 10.3390/v14030490. |
5. | Duan Y, Young R, Schnabl B (2022). Bacteriophages and their potential for treatment of gastrointestinal diseases. Nature Reviews Gastroenterology & Hepatology. 19(2):135-144. doi: 10.1038/s41575-021-00536-z. |
6. | Duan Y#, Chu H#, Brandl K, Jiang L, Zeng S, Mendes BG, et al. (2021). CRIg on liver macrophages clears pathobionts and protects against alcoholic liver disease. Nature Communications. 12(1):7172. doi: 10.1038/s41467-021-27385-3. |
7. | Chu H#, Duan Y#, Lang S, Jiang L, Wang Y, Llorente C, et al. (2020). The Candida albicans exotoxin Candidalysin promotes alcohol-associated liver disease. Journal of Hepatology. 72(3):391-400. doi: 10.1016/j.jhep.2019.09.029. |
8. | Gao B#, Duan Y#, Lang S, Barupal D, Wu TC, Valdiviez L, et al. (2020). Functional microbiomics reveals alterations of the gut microbiome and host co-metabolism in patients with alcoholic hepatitis. Hepatology Communications. 4(8):1168-1182. doi: 10.1002/hep4.1537. |
9. | Zeng S, Rosati E, Saggau C, Messner B, Chu H, Duan Y, Hartmann P, et al. (2023). Candida albicans-specific Th17 cell-mediated response contributes to alcohol-associated liver disease. Cell Host Microbe. 31(3):389-404. doi: 10.1016/j.chom.2023.02.001. |
10. | Demir M#, Lang S#, Hartmann P#, Duan Y, Martin A, Miyamoto Y, Bondareva M, et al. (2022). The fecal mycobiome in non-alcoholic fatty liver disease. Journal of Hepatology. 76(4):788-799. doi: 10.1016/j.jhep.2021.11.029. |
11. | Hsu CL, Duan Y, Fouts DE, Schnabl B. (2021). Intestinal virome and therapeutic potential of bacteriophages in liver disease. Journal of Hepatology. 75(6):1465-1475. doi: 10.1016/j.jhep.2021.08.003. |
12. | Zhang Q, Ma C, Duan Y, Heinrich B, Rosato U, Diggs L, et al. (2021). Gut microbiome directs hepatocytes to recruit MDSC and promote cholangiocarcinoma. Cancer Discovery. 11(5):1248-1267. doi: 10.1158/2159-8290.CD-20-0304. |
13. | Jiang L#, Lang S#, Duan Y, Zhang X, Gao B, Chopyk J, et al. (2020). Intestinal virome in patients with alcoholic hepatitis. Hepatology. 72(6):2182-2196. doi: 10.1002/hep.31459. |
14. | Lang S, Duan Y, Liu J, Torralba MG, Kuelbs C, Ventura-Cots M, et al. (2020). Intestinal fungal dysbiosis and systemic immune response to fungi in patients with alcoholic hepatitis. Hepatology. 71(2):522-538. doi: 10.1002/hep.30832. |
15. | Lang S#, Demir M#, Martin A, Jiang L, Zhang X, Duan Y, Gao B, Wisplinghoff H, et al. (2020). Intestinal virome signature associated with severity of nonalcoholic fatty liver disease. Gastroenterology. 159(5):1839-1852. doi: 10.1053/j.gastro.2020.07.005. |
16. | Hendrikx T, Duan Y, Wang Y, Oh JH, Alexander LM, Huang W, et al. (2019). Bacteria engineered to produce IL-22 in intestine induce expression of REG3G to reduce ethanol-induced liver disease in mice. Gut. 68(8):1504-1515. doi: 10.1136/gutjnl-2018-317232. |
17. | Chu H, Duan Y, Yang L, and Schnabl B (2019). Small Metabolites, possible big changes: a microbiota-centered view of non-alcoholic fatty liver disease. Gut. 68(2):359-370. doi: 10.1136/gutjnl-2018-316307. |