
Whole-genome analysis of Malawian Plasmodium falciparum isolates identifies possible targets of allele-specific immunity to clinical malaria
Author(s) -
Zalak Shah,
Myo Naung,
Kara A Moser,
Matthew Adams,
Andrea G Buchwald,
Ankit Dwivedi,
Amed Ouattara,
Karl B. Seydel,
Don P. Mathanga,
Alyssa E. Barry,
David Serre,
Miriam K. Laufer,
Joana C. Silva,
Shan Takala-Harrison
Publication year - 2021
Publication title -
plos genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.587
H-Index - 233
eISSN - 1553-7404
pISSN - 1553-7390
DOI - 10.1371/journal.pgen.1009576
Subject(s) - biology , plasmodium falciparum , malaria , immunity , genome , genetics , allele , virology , parasite hosting , malaria vaccine , antigen , gene , immune system , immunology , world wide web , computer science
Individuals acquire immunity to clinical malaria after repeated Plasmodium falciparum infections. Immunity to disease is thought to reflect the acquisition of a repertoire of responses to multiple alleles in diverse parasite antigens. In previous studies, we identified polymorphic sites within individual antigens that are associated with parasite immune evasion by examining antigen allele dynamics in individuals followed longitudinally. Here we expand this approach by analyzing genome-wide polymorphisms using whole genome sequence data from 140 parasite isolates representing malaria cases from a longitudinal study in Malawi and identify 25 genes that encode possible targets of naturally acquired immunity that should be validated immunologically and further characterized for their potential as vaccine candidates.