Transmission of the malaria parasite Plasmodium falciparum from humans to the mosquito vector requires differentiation of a sub-population of asexual forms replicating within red blood cells into non-dividing male and female gametocytes. The nature of the molecular mechanism underlying this key differentiation event required for malaria transmission is not fully understood.Whole genome sequencing was used to examine the genomic diversity of the gametocyte non-producing 3D7-derived lines F12 and A4. These lines were used in the recent detection of the PF3D7_1222600 locus (encoding PfAP2-G), which acts as a genetic master switch that triggers gametocyte development.The evolutionary changes from the 3D7 parental strain through its derivatives F12 (culture-passage derived cloned line) and A4 (transgenic cloned line) were identified. The genetic differences including the formation of chimeric var genes are presented.A genomics resource is provided for the further study of gametocytogenesis or other phenotypes using these parasite lines.

Original publication

DOI

10.1186/s12936-016-1254-1

Type

Journal article

Journal

Malaria journal

Publication Date

21/04/2016

Volume

15

Pages

229 - 229

Addresses

Faculty of Infectious and Tropical Diseases, London School of Hygiene & Tropical Medicine, London, UK. susana.campino@lshtm.ac.uk.

Keywords

Plasmodium falciparum, Sequence Analysis, DNA, Gametogenesis, Polymorphism, Genetic, Genome, Protozoan