幽门螺杆菌感染小鼠模型的应用进展
PDF下载 (2270)朱 媚,马郁荃,谷海瀛.幽门螺杆菌感染小鼠模型的应用进展[J].宁波大学学报(理工版),2021,34(3):91-95.DOI:
ZHU Mei,MA Yuquan,GU Haiying.Progress in application of mouse models of Helicobacter pylori infection[J].Journal of Ningbo University(Natural Science & Engineering Edition),2021,34(3):91-95.DOI:
| Title: | Progress in application of mouse models of Helicobacter pylori infection |
| 作者: | 朱 媚, 马郁荃, 谷海瀛 |
| Author(s): | ZHU Mei, MA Yuquan, GU Haiying |
| 关键词: | 幽门螺杆菌; 动物模型; 小鼠; 胃炎; 胃癌 |
| Keywords: | Helicobacter pylori; animal models; mice; gastritis; gastric cancer |
| 分类号: | R378.99 |
| 文献标识码: | A |
| 摘要: | 幽门螺杆菌动物模型是幽门螺杆菌感染导致人类胃炎、消化性溃疡、胃癌等致病机制研究的基础, 也是幽门螺杆菌感染和胃肠外疾病相关性研究的重要工具. 近年来幽门螺杆菌感染动物模型得到了广泛的应用和发展, 制备感染模型常用的动物有小鼠、蒙古沙鼠、豚鼠、悉生乳猪和恒河猴等, 其中幽门螺杆菌悉尼菌株感染的小鼠模型使用最广泛. 本文对幽门螺杆菌感染小鼠模型应用的最新进展做一综述. |
| Abstract: | Animal models of Helicobacter pylori are the basis for the study of pathogenic mechanisms of Helicobacter pylori infection in humans such as gastritis, peptic ulcer, and gastric cancer. They are also important tools for studying the correlation between Helicobacter pylori infection and extra gastric diseases. In recent years, animal models of Helicobacter pylori infection have been widely used and developed. The commonly used animals for infection models include mice, Mongolian gerbils, guinea pigs, gnotobiotic piglets and rhesus monkeys. Mice infected with Helicobacter pylori Sydney Strain are the most widely used models among them. In this article, the latest progress in the application of mouse models is reviewed. |
| 参考文献 /References: | [1] Gu H. Role of flagella in the pathogenesis of Helicobacter pylori[J]. Current Microbiology, 2017, 74 (7):863-869. [2] Kato M, Ota H, Okuda M, et al. Guidelines for the management of Helicobacter pylori infection in Japan: 2016 Revised Edition[J]. Helicobacter, 2019, 24(4): e12597. [3] Malfertheiner P, Megraud F, O’Morain C A, et al. Management of Helicobacter pylori infection: The Maastricht V/Florence consensus report[J]. Gut, 2017, 66 (1):6-30. [4] Zamani M, Ebrahimtabar F, Zamani V, et al. Systematic review with meta-analysis: The worldwide prevalence of Helicobacter pylori infection[J]. Alimentary Pharmacology & Therapeutics, 2018, 47(7):868-876. [5] Krakowka S, Morgan D R, Kraft W G, et al. Establishment of gastric Campylobacter pylori infection in the neonatal gnotobiotic piglet[J]. Infection and Immunity, 1987, 55(11):2789-2796. [6] Lee A. Animal models for host-pathogen interaction studies[J]. British Medical Bulletin, 1998, 54(1):163-173. [7] Dubois A, Berg D E, Incecik E T, et al. Transient and persistent experimental infection of nonhuman primates with Helicobacter pylori: Implications for human disease[J]. Infection & Immunity, 1996, 64(8):2885-2891. [8] Sjunnesson H, Stureg?rd E, Hynes S, et al. Five month persistence of Helicobacter pylori infection in guinea pigs[J]. APMIS, 2003, 111(6):634-642. [9] Solnick J V, Eaton K A, Peek R M. Animal models of Helicobacter pylori infection[M]//Backert S, Yamaoka Y. Helicobacter pylori Research. Japan: Springer Japan, 2016:273-297. [10] Kusters J G, van Vliet A H M, Kuipers E J. Pathogenesis of Helicobacter pylori infection[J]. Clinical Microbiology Reviews, 2006, 19(3):449-490. [11] Lee A, O’Rourke J, De Ungria M C, et al. A standardized mouse model of Helicobacter pylori infection: Introdu- cing the Sydney strain[J]. Gastroenterology, 1997, 112(4): 1386-1397. [12] Pritchard D M, Przemeck S M C. Review article: How useful are the rodent animal models of gastric adenocarcinoma?[J]. Alimentary Pharmacology & Thera- peutics, 2004, 19(8):841-859. [13] Kim D H, Kim S W, Song Y J, et al. Long-term evaluation of mice model infected with Helicobacter pylori: Focus on gastric pathology including gastric cancer[J]. Alimentary Pharmacology & Therapeutics, 2003, 18(S1):14-23. [14] Kuzushita N, Rogers A B, Monti N A, et al. p27kip1 deficiency confers susceptibility to gastric carcinogenesis in Helicobacter pylori-infected mice[J]. Gastroenterology, 2005, 129(5):1544-1556. [15] Fox J G, Rogers A B, Whary M T, et al. Accelerated progression of gastritis to dysplasia in the pyloric antrum of TFF2-/- C57BL6 × Sv129 Helicobacter pylori-infected mice[J]. The American Journal of Pathology, 2007, 171 (5):1520-1528. [16] Neumeyer V, Vieth M, Gerhard M, et al. Mutated Rnf43 aggravates Helicobacter Pylori-induced gastric Pathology [J]. Cancers, 2019, 11(3):372. [17] Nam K T, Oh S-Y, Ahn B, et al. Decreased Helicobacter pylori associated gastric carcinogenesis in mice lacking inducible nitric oxide synthase[J]. Gut, 2004, 53(9): 1250-1255. [18] Fukuda T, Asou E, Nogi K, et al. Association between Helicobacter pylori infection and platelet count in mice[J]. Experimental Animals, 2018, 67(4):487-492. [19] Burns M, Muthupalani S, Ge Z, et al. Helicobacter pylori infection induces anemia, depletes serum iron storage, and alters local iron-related and adult brain gene expression in male INS-GAS mice[J]. PLoS One, 2015, 10(11):e0142630. [20] Arismendi S A C, Salinas I A G, Pérez C M V, et al. Study of Helicobacter pylori infection on lung using an animal model[J]. Microbial Pathogenesis, 2018, 123:410-418. [21] Arismendi S A C, Salinas I A G, Pérez C M V, et al. Inflammatory response induced by Helicobacter pylori infection in lung[J]. Microbial Pathogenesis, 2020, 142:104103. [22] Baudron C R, Chambonnier L, Buissionnière A, et al. An eighteen-month Helicobacter infection does not induce amyloid plaques or neuroinflammation in brains of wild type C57BL/6J mice[J]. Journal of Alzheimer’s Disease, 2015, 45(4):1045-1050. [23] Beydoun M A, Beydoun H A, Elbejjani M, et al. Helicobacter pylori seropositivity and its association with incident all-cause and Alzheimer’s disease dementia in large national surveys[J]. , 2018, 14(9):1148-1158. [24] Hathroubi S, Servetas S L, Windham I, et al. Helicobacter pylori biofilm formation and its potential role in pathogenesis[J]. Microbiology and Molecular Biology Reviews, 2018, 82(2):e00001-18. [25] Attaran B, Falsafi T, Moghaddam A N, et al. Study of biofilm formation in C57BL/6J mice by clinical isolates of Helicobacter pylori[J]. Saudi Journal of Gastroen- terology, 2016, 22(2):161-168. [26] Muthupalani S, Ge Z, Joy J, et al. Muc5ac null mice are predisposed to spontaneous gastric antro-pyloric hyperplasia and adenomas coupled with attenuated H. pylori-induced corpus mucous metaplasia[J]. Laboratory Investigation, 2019, 99(12):1887-1905. [27] Suarez G, Romero-Gallo J, Piazuelo M B, et al. Nod1 imprints inflammatory and carcinogenic responses toward the gastric pathogen Helicobacter pylori[J]. Cancer Research, 2019, 79(7):1600-1611. |
| 备注/Memo: | 收稿日期:2020-12-06.宁波大学学报(理工版)网址:http://journallg.nbu.edu.cn/ 基金项目:浙江省自然科学基金重点项目(LZ14H200001). 第一作者:朱媚(1979-),女,湖北石首人,在读硕士研究生,主要研究方向:临床检验诊断学.E-mail:364846095@qq.com *通信作者:谷海瀛(1966-),男,吉林长春人,博士/教授,主要研究方向:临床微生物学.E-mail:guhaiying@nbu.edu.cn 宁波大学学报(理工版)网址:http://journallg.nbu.edu.cn/ |