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| Status |
Public on Jun 30, 2018 |
| Title |
Transcriptome changes during inducible gametocytogenesis in Plasmodium berghei parasites |
| Organism |
Plasmodium berghei |
| Experiment type |
Expression profiling by high throughput sequencing
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| Summary |
During the malaria infection, Plasmodium parasites invade the host’s red blood cells where they can differentiate into two different life forms. The majority will replicate asexually and infect new erythrocytes. A small percentage, however, will transform into gametocytes – a specialized sexual stage able to survive and develop when taken up by Anopheles mosquito. As the gametocytes ensure the parasite’s transmission to a new host, their generation is an attractive target for new antimalarial interventions. The molecular mechanisms controlling gametocytogenesis, however, remain largely unknown due to the technical challenges: the early gametocytes are morphologically indistinguishable from asexual parasites and present in very low numbers during the infection. Recently, AP2-G - a transcription factor from an apicomplexa-specific apiAP2 family – was described as indispensable for gametocyte commitment in both human malaria parasite Plasmodium falciparum and rodent malaria model Plasmodium berghei. Therefore, we have decided to test whether the overexpression of this factor alone could increase gametocyte production and enable the investigation of uncharacterised, earliest stages of gametocyte development. To this end, we have engineered PBGAMi - a Plasmodium berghei line, in which all parasites were ap2-g deficient by default but able to overexpress it when induced with rapamycin. While the control parasites (PBGAMi R-), as expected, differentiated into asexual forms (schizonts) only, almost all rapamycin-treated parasites (PBGAMi R+) transformed into gametocytes. We used the generated line to perform RNA-seq analysis of the R- and R+ populations at different time points of their development and identify the changes arising between them, mapping the sequence of events leading to the formation of gametocytes.
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| Overall design |
A synchronised population of Plasmodium berghei PBGAMi parasites was either induced with rapamycin (which caused the ap2-g overexpression and gametocyte conversion) or allowed to develop asexually. Parasites from both groups were harvested at different time points post induction and RNA-seq was used to analyse their transcriptome
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| Contributor(s) |
Modrzynska KK, Waters AP, Billker O |
| Citation(s) |
30177743, 36634679 |
| |
| Submission date |
Feb 06, 2018 |
| Last update date |
Jun 28, 2024 |
| Contact name |
Katarzyna Kinga Modrzynska |
| E-mail(s) |
katarzyna.modrzynska@glasgow.ac.uk
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| Phone |
+44 141 330 4599
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| Organization name |
Wellcome Trust Centre for Molecular Parasitology
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| Street address |
B627 Sir Graeme Davies Building, 120 University Place
|
| City |
Glasgow |
| State/province |
Glasgow (City of) |
| ZIP/Postal code |
G12 8TA |
| Country |
United Kingdom |
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| Platforms (1) |
| GPL20293 |
Illumina HiSeq 2500 (Plasmodium berghei) |
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| Samples (32)
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| Relations |
| BioProject |
PRJNA433164 |
| SRA |
SRP132278 |
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