Method for rapid synchronization of different growth cycles of Plasmodium falciparum in vitro and application in differential gene expression profile of 3D7 after dihydroartemisinin treatment.
10.19540/j.cnki.cjcmm.20191031.401
- Author:
Zhong-Yuan ZHENG
1
;
Li-Na CHEN
2
;
Ting YANG
1
;
Hui LIU
3
;
Shui-Qing QU
3
;
Yuan-Min YANG
2
;
Yu-Jie LI
2
;
Shu-Qiu ZHANG
4
Author Information
1. School of Pharmacy, Shanxi Medical University Taiyuan 030001, China Artemisinin Research Center, China Academy of Chinese Medical Sciences Beijing 100700, China.
2. Artemisinin Research Center, China Academy of Chinese Medical Sciences Beijing 100700, China Institute of Chinese Materia Medica, China Academy of Chinese Medical Sciences Beijing 100700, China.
3. Artemisinin Research Center, China Academy of Chinese Medical Sciences Beijing 100700, China School of Traditional Chinese Medicine, Guangdong Pharmaceutical University Guangdong 510006, China.
4. School of Pharmacy, Shanxi Medical University Taiyuan 030001, China.
- Publication Type:Journal Article
- Keywords:
Plasmodium falciparum;
RNA-seq;
in vitro culture;
malaria;
synchronization
- MeSH:
Animals;
Antimalarials;
Artemisinins;
Erythrocytes;
Plasmodium falciparum;
Transcriptome
- From:
China Journal of Chinese Materia Medica
2020;45(10):2454-2463
- CountryChina
- Language:Chinese
-
Abstract:
Plasmodium culture in vitro is often used as an antimalarial drug evaluation model, but the lifecycle of P. falciparum culture in vitro tends to be disordered, which affects the research and evaluation of antimalarial drug mechanism in vitro. By combining magnetic bead separation method with sorbitol synchronization method, a synchronization method was constructed to quickly acquire different lifecycles of P. falciparum and obtain large amounts of parasite with a narrow synchronization window in a short period. Furthermore, the dihydroartemisinin(DHA) was used to treat the early trophozoite phase of P. falciparum 3 D7 for 4 h. Then mRNA was extracted and RNA-seq was conducted to analyze the differential expression of mRNA after drug treatment and obtain the differential gene expression profile. Differential expression of up-regulated genes and down-regulated genes was analyzed according to the screening criteria of |log_2FC|>1 and P<0.05. There, 262 genes were up-regulated and 77 genes were down-regulated. GO functional enrichment analysis of all the differentially expressed genes showed that the enrichment items mainly included cell membrane components, transporter activity, serine/threonine kinase activity, Maurer's clefts(MCs), rhoptry, antigen variation and immune evasion. The enrichment of KEGG pathway included malaria, fatty acid metabolism and peroxisome. Protein-protein interaction(PPI) analysis showed that the down-regulated genes in the modules with high degree of association included rhoptry, myosin complex, transporter and other genes related to the important life activities of malaria invasion and immune escape; the up-regulated genes were mainly related to various toxic exportins of malaria, such as PfSBP1 of MCs. qRT-PCR was used to verify the expression level of some genes, and most of the results were the same as the sequencing results. SBP1 was significantly up-regulated, while some antigenic protein expression levels were down-regulated. Above all, key molecules of DHA therapy were mainly involved in the parasites' rhoptry, transporter, antigenic variation, plasmodium exportin. These results offer us many hints to guide the further studies on mechanism of artemisinin and provide a new way for development of new antimalarial drugs.
