Modeling parasite, microbiota and host interactions to develop a better understanding of goblet cell biology

对寄生虫、微生物群和宿主相互作用进行建模，以更好地了解杯状细胞生物学

• 批准号: RGPIN-2019-06739
• 负责人: Khan, Waliul
• 金额: $ 2.4万
• 依托单位: McMaster University
• 依托单位国家: 加拿大
• 项目类别: Discovery Grants Program - Individual
• 财政年份: 2022
• 资助国家: 加拿大
• 起止时间: 2022-01-01 至 2023-12-31
• 项目状态: 已结题
• 来源: https://www.nserc-crsng.gc.ca/ase-oro/Details-Detailles_eng.asp?id=761972
• 关键词: Modeling; parasite; microbiota; host; interactions

Enteric parasites are probably the most important parasites in terms of their widespread prevalence and have major socio-economic impact in both developing and developed countries including Canada by affecting animal well--being, productivity, and agriculture. A better understanding of the host-parasite interactions will lead to improved strategies for control of these parasites. Mucins produced in the gastrointestinal (GI) tract by goblet cells are considered to have a protective role in host in a number of parasite infections, including those by nematode parasites. The GI tract also harbours trillions of commensal microbes, mainly bacteria. GI microbes can regulate mucin production by activating different signaling cascades and secretory elements. Due to the co-existence of nematode parasite and microbes within the infected GI tract, it is very likely that interactions between nematode and microbiota play an important role in goblet cell biology and mucin production. The overall objectives of this research program are to understand intestinal goblet cell biology and the mechanism of mucin production in relation to host-parasitic interactions. Built on exciting new preliminary data that shows that gut microbial composition is altered in mice infected with nematode parasite, Trichuris muris, and transfer of microbiota from T. muris-infected mice into germ free (GF) mice up-regulates goblet cells numbers, in this application, I propose to further explore the interactions between microbiota and nematode parasites in goblet cell biology and in mucin production. I hypothesize that nematode infection-induced altered gut microbiota modulates the response of local goblet cells as well as mucin production. The changed composition of the microbiota, in concert with the nematode thus acts jointly to modulate goblet cell function in relation to innate defense. By employing T. muris model, GF mice, intestinal organoids and mucin producing epithelial cell line this hypothesis will be addressed through three aims. In the first aim we will determine the role of nematode infection-induced altered gut microbiota in regulating goblet cell responses and mucin production in relation to innate defense. In the second aim we will determine the contributions of Nod proteins and TLRs in modulation of mucin production by nematode-induced altered microbiota and in the final aim we will elucidate the transcription program by which nematode-induced altered microbiota modulates goblet cell responses. This research will generate novel data on the interactions between enteric parasite and the resident gut microbiota in modulation of goblet cell function in relation to innate defense. Furthermore, given the impact of parasite infection in Canada, affecting livestock, companion animals, and eco-systems this research will contribute in understanding host-parasite interactions which may ultimately lead to improved strategies to tackle infection with nematode parasites.

就其广泛流行而言，肠道寄生虫可能是最重要的寄生虫，并通过影响动物福利、生产力和农业，在包括加拿大在内的发展中国家和发达国家产生重大的社会经济影响。更好地了解宿主-寄生虫的相互作用将导致改进控制这些寄生虫的策略。由杯状细胞在胃肠道(GI)产生的粘蛋白被认为在包括线虫在内的许多寄生虫感染中对宿主具有保护作用。胃肠道还藏有数以万亿计的共生微生物，主要是细菌。胃肠道微生物可以通过激活不同的信号级联和分泌元件来调节粘蛋白的产生。由于线虫寄生虫和微生物在感染的胃肠道中共存，线虫和微生物群之间的相互作用很可能在杯状细胞生物学和粘蛋白产生中发挥重要作用。这项研究计划的总体目标是了解肠道杯状细胞生物学和与宿主-寄生虫相互作用相关的粘蛋白产生机制。基于令人兴奋的新的初步数据，表明感染线虫寄生虫的小鼠肠道微生物组成发生了改变，从感染线虫的小鼠转移到无菌(GF)小鼠的微生物群上调了杯状细胞的数量，在这一应用中，我建议进一步探索微生物群和线虫寄生虫在杯状细胞生物学和粘蛋白生产中的相互作用。我推测，线虫感染引起的肠道微生物区系改变调节了当地杯状细胞的反应和粘蛋白的产生。因此，微生物群的变化组成与线虫共同作用，调节与先天防御有关的杯状细胞功能。通过使用T.Muris模型、GF小鼠、肠道器官和产生粘蛋白的上皮细胞系，这一假说将通过三个目标得到解决。在第一个目标中，我们将确定线虫感染诱导的肠道微生物区系改变在调节杯状细胞反应和粘蛋白产生中的作用，这与天然防御有关。在第二个目的中，我们将确定Nod蛋白和TLRs在线虫诱导的改变的微生物群调节粘蛋白产生中的作用，在最终目的中，我们将阐明线虫诱导的改变的微生物群调控杯状细胞反应的转录程序。这项研究将产生关于肠道寄生虫和肠道微生物群之间相互作用的新数据，这些微生物群调节与天然防御相关的杯状细胞功能。此外，鉴于寄生虫感染在加拿大的影响，影响到牲畜、同伴动物和生态系统，这项研究将有助于了解宿主与寄生虫的相互作用，最终可能导致改进应对线虫寄生虫感染的战略。