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宿主-寄生虫相互作用过程中贾第虫的转录变化。

Transcriptional changes in Giardia during host-parasite interactions.

机构信息

Department of Cell and Molecular Biology, Uppsala University, Uppsala, Sweden.

出版信息

Int J Parasitol. 2011 Mar;41(3-4):277-85. doi: 10.1016/j.ijpara.2010.09.011. Epub 2010 Nov 11.

Abstract

Giardia intestinalis is one of the major causes of parasite-induced diarrhea. The disease, giardiasis, is caused by trophozoites attaching to the intestinal epithelium, resulting in apoptosis of intestinal epithelial cells, disrupted epithelial barrier function and malabsorption. Microarray studies have detected extensive gene expression changes in intestinal epithelial cells (IECs) during interaction with Giardia trophozoites in vitro. In the present study, we examined this host-parasite interaction further by transcriptional profiling of interacting trophozoites using Giardia microarrays. A total of 200 Giardia transcripts were significantly changed due to the interaction, lasting up to 18 h in complete growth medium. Quantitative reverse transcriptase PCR confirmed the changes in all 12 genes tested using mRNA isolated in separate experiments. Genes encoding proteins previously suggested to be important during host-parasite interactions such as arginine deiminase, enolase and cysteine proteinases were up-regulated early but down-regulated later during the interaction. Cell division and attachment genes were down-regulated in the late time-points of interaction. The most highly up-regulated genes encode oxygen defense proteins and several members of the high cysteine membrane protein (HCMp) and Gly-rich repeat (GRREAT) families. Putative small RNAs were up-regulated, whereas the 5S rRNA was slightly down-regulated during the interaction with IECs. Thus, there are extensive gene expression changes in Giardia trophozoites and IECs during host-parasite interactions which can be important for establishment of infection and the induction of giardiasis.

摘要

肠道贾第虫是引起寄生虫性腹泻的主要原因之一。这种疾病,即贾第虫病,是由滋养体附着在肠上皮引起的,导致肠上皮细胞凋亡、上皮屏障功能紊乱和吸收不良。微阵列研究已经检测到在体外与贾第虫滋养体相互作用时肠上皮细胞(IEC)中广泛的基因表达变化。在本研究中,我们通过使用贾第虫微阵列对相互作用的滋养体进行转录谱分析,进一步研究了这种宿主-寄生虫相互作用。由于相互作用,总共 200 个贾第虫转录本发生了显著变化,在完全生长培养基中持续长达 18 小时。定量逆转录 PCR 证实了在使用单独实验中分离的 mRNA 进行的所有 12 个测试基因的变化。编码先前被认为在宿主-寄生虫相互作用中重要的蛋白质的基因,如精氨酸脱氨酶、烯醇酶和半胱氨酸蛋白酶,在早期被上调,但在相互作用的后期被下调。细胞分裂和附着基因在相互作用的后期下调。上调最明显的基因编码氧防御蛋白和几个高半胱氨酸膜蛋白(HCMp)和富含甘氨酸重复(GRREAT)家族的成员。假定的小 RNA 上调,而在与 IEC 相互作用期间 5S rRNA 略有下调。因此,在宿主-寄生虫相互作用期间,贾第虫滋养体和 IEC 中存在广泛的基因表达变化,这对于建立感染和诱导贾第虫病可能很重要。

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