Dataset Information

Plasmodium falciparum schizont proteome

ABSTRACT: Proteome of the human malaria parasite Plasmodium falciparum at schizont life cycle stage during blood stage development

INSTRUMENT(S): LTQ FT

ORGANISM(S): Plasmodium Falciparum Palo Alto/uganda

TISSUE(S): Erythrocyte

DISEASE(S): Plasmodium Falciparum Malaria

SUBMITTER: Edwin Lasonder

LAB HEAD: Edwin Lasonder

PROVIDER: PXD008250 | Pride | 2018-02-13

REPOSITORIES: pride

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Publications

Unravelling the immune signature of Plasmodium falciparum transmission-reducing immunity.

Stone Will J R WJR Campo Joseph J JJ Ouédraogo André Lin AL Meerstein-Kessel Lisette L Morlais Isabelle I Da Dari D Cohuet Anna A Nsango Sandrine S Sutherland Colin J CJ van de Vegte-Bolmer Marga M Siebelink-Stoter Rianne R van Gemert Geert-Jan GJ Graumans Wouter W Lanke Kjerstin K Shandling Adam D AD Pablo Jozelyn V JV Teng Andy A AA Jones Sophie S de Jong Roos M RM Fabra-García Amanda A Bradley John J Roeffen Will W Lasonder Edwin E Gremo Giuliana G Schwarzer Evelin E Janse Chris J CJ Singh Susheel K SK Singh Susheel K SK Theisen Michael M Felgner Phil P Marti Matthias M Drakeley Chris C Sauerwein Robert R Bousema Teun T Jore Matthijs M MM

Nature communications 20180208 1

Infection with Plasmodium can elicit antibodies that inhibit parasite survival in the mosquito, when they are ingested in an infectious blood meal. Here, we determine the transmission-reducing activity (TRA) of naturally acquired antibodies from 648 malaria-exposed individuals using lab-based mosquito-feeding assays. Transmission inhibition is significantly associated with antibody responses to Pfs48/45, Pfs230, and to 43 novel gametocyte proteins assessed by protein microarray. In field-based m ...[more]

PMID: 29422648

Similar Datasets

Project description:We used a high-density tiling array to estimate genetic recombination rate among 32 independent recombinant progeny of a P. falciparum genetic cross (7G8 M-CM-^W GB4). We detected 3184 segregating multi-probe single-feature polymorphisms (mSFPs) and 638 recombination events (496 excluding those from subtelomeric regions). These data, in combination with results from 254 previously reported microsatellites, enabled us to construct a high-resolution genetic map. Comparing genetic and physical maps, we obtained an overall recombination rate of 9.6 kb/cM (12.8 kb/cM excluding subtelomeric regions) and identified 54 hotspots, some of which occurred in genes encoding surface antigens or proteins with repetitive motifs that might play a role in genetic recombination in the parasite. Motifs enriched in hotspots were also identified. In agreement with results from a previous cross (HB3 M-BM-4 Dd2), there was positive correlation between sizes of individual chromosomes and their recombination events. These results show that the P. falciparum genome is highly recombinogenic, providing an important genetic basis for parasite survival under various selection pressures. GC-rich repetitive motifs identified in the hotspot sequences may play a role in the high recombination frequency observed. Ten microgram of genomic DNA, extracted and purified from 3D7 (reference), thirty-two P. falciparum independent recombinant progeny of the 7G8 x GB4 cross, and the two parental lines (Hayton, 2008), were hybridized to the PFSANGER GenechipM-BM-. (Affymetrix, Inc., Santa Clara, CA, USA). The scanned image CEL files were first processed using the RMA method, then averaged and compared with reference genome 3D7, and lastly assigned either 7G8 or GB4 alleles based on similarities to the two parental lines. Total of 35 genomic DNA samples (biological replicates: 6 for 3D7, 4 for 7G8, 4 for GB4, and 2 for Pf_WE2). The supplementary file 'GSE25656_QuantNormData_Log2_AllSamples.txt' contains the RMA-normalized data for all of the samples. The supplementary files 'GSE25656_chr*' contain the parental allele assignment of each chromosome and include probe-level annotation.

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