Daily Johanna P, Le Roch Karine G, Sarr Ousmane, Fang Xuemin, Zhou Yingyao, Ndir Omar, Mboup Soulyemane, Sultan Ali, Winzeler Elizabeth A, Wirth Dyann F
Department of Immunology and Infectious Disease, Harvard School of Public Health, Boston, Massachusetts 02115, USA.
Malar J. 2004 Aug 5;3:30. doi: 10.1186/1475-2875-3-30.
Both host and pathogen factors contribute to disease outcome in Plasmodium falciparum infection. The feasibility of studying the P. falciparum in vivo transcriptome to understand parasite transcriptional response while it resides in the human host is presented.
A custom made oligonucleotide array with probes based on the P. falciparum 3D7 laboratory strain chromosome 2 sequence was used to detect in vivo P. falciparum transcripts. This study analyzed transcripts from total RNA derived from small blood samples of P. falciparum infected patients and compared the in vivo expression profile to the in vitro cultivated 3D7 strain transcriptome.
The data demonstrated that in vivo transcription can be studied from a small blood sample, despite the abundance of human RNA. The in vivo transcriptome is similar to the 3D7 ring stage transcriptome, but there are significant differences in genes encoding a sexual stage antigen and surface proteins.
Whole genome transcription analysis of P. falciparum can be carried out successfully and further studies in selected patient cohorts may provide insight into parasite in vivo biology and defense against host immunity.
宿主和病原体因素均对恶性疟原虫感染的疾病转归产生影响。本文介绍了研究恶性疟原虫在人体宿主体内的转录组以了解寄生虫转录反应的可行性。
使用基于恶性疟原虫3D7实验室株2号染色体序列设计探针的定制寡核苷酸芯片来检测恶性疟原虫的体内转录本。本研究分析了来自恶性疟原虫感染患者少量血液样本的总RNA转录本,并将体内表达谱与体外培养的3D7株转录组进行比较。
数据表明,尽管存在大量人类RNA,但仍可从小血样中研究体内转录情况。体内转录组与3D7环状体期转录组相似,但在编码有性期抗原和表面蛋白的基因方面存在显著差异。
恶性疟原虫的全基因组转录分析能够成功开展,对选定患者队列的进一步研究可能有助于深入了解寄生虫的体内生物学特性及其对宿主免疫的防御机制。