Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.

Many pathogenic bacteria, fungi, and protozoa achieve chronic infection through an immune evasion strategy known as antigenic variation. In the human malaria parasite Plasmodium falciparum, this involves transcriptional switching among members of the var gene family, causing parasites with different...

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Main Authors: Mario Recker, Caroline O Buckee, Andrew Serazin, Sue Kyes, Robert Pinches, Zóe Christodoulou, Amy L Springer, Sunetra Gupta, Chris I Newbold
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-03-01
Series:PLoS Pathogens
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21408201/?tool=EBI
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spelling doaj-69c4427ffae3482883a2ac9c357f4a222021-04-21T17:32:22ZengPublic Library of Science (PLoS)PLoS Pathogens1553-73661553-73742011-03-0173e100130610.1371/journal.ppat.1001306Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.Mario ReckerCaroline O BuckeeAndrew SerazinSue KyesRobert PinchesZóe ChristodoulouAmy L SpringerSunetra GuptaChris I NewboldMany pathogenic bacteria, fungi, and protozoa achieve chronic infection through an immune evasion strategy known as antigenic variation. In the human malaria parasite Plasmodium falciparum, this involves transcriptional switching among members of the var gene family, causing parasites with different antigenic and phenotypic characteristics to appear at different times within a population. Here we use a genome-wide approach to explore this process in vitro within a set of cloned parasite populations. Our analyses reveal a non-random, highly structured switch pathway where an initially dominant transcript switches via a set of switch-intermediates either to a new dominant transcript, or back to the original. We show that this specific pathway can arise through an evolutionary conflict in which the pathogen has to optimise between safeguarding its limited antigenic repertoire and remaining capable of establishing infections in non-naïve individuals. Our results thus demonstrate a crucial role for structured switching during the early phases of infections and provide a unifying theory of antigenic variation in P. falciparum malaria as a balanced process of parasite-intrinsic switching and immune-mediated selection.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21408201/?tool=EBI
collection DOAJ
language English
format Article
sources DOAJ
author Mario Recker
Caroline O Buckee
Andrew Serazin
Sue Kyes
Robert Pinches
Zóe Christodoulou
Amy L Springer
Sunetra Gupta
Chris I Newbold
spellingShingle Mario Recker
Caroline O Buckee
Andrew Serazin
Sue Kyes
Robert Pinches
Zóe Christodoulou
Amy L Springer
Sunetra Gupta
Chris I Newbold
Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
PLoS Pathogens
author_facet Mario Recker
Caroline O Buckee
Andrew Serazin
Sue Kyes
Robert Pinches
Zóe Christodoulou
Amy L Springer
Sunetra Gupta
Chris I Newbold
author_sort Mario Recker
title Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
title_short Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
title_full Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
title_fullStr Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
title_full_unstemmed Antigenic variation in Plasmodium falciparum malaria involves a highly structured switching pattern.
title_sort antigenic variation in plasmodium falciparum malaria involves a highly structured switching pattern.
publisher Public Library of Science (PLoS)
series PLoS Pathogens
issn 1553-7366
1553-7374
publishDate 2011-03-01
description Many pathogenic bacteria, fungi, and protozoa achieve chronic infection through an immune evasion strategy known as antigenic variation. In the human malaria parasite Plasmodium falciparum, this involves transcriptional switching among members of the var gene family, causing parasites with different antigenic and phenotypic characteristics to appear at different times within a population. Here we use a genome-wide approach to explore this process in vitro within a set of cloned parasite populations. Our analyses reveal a non-random, highly structured switch pathway where an initially dominant transcript switches via a set of switch-intermediates either to a new dominant transcript, or back to the original. We show that this specific pathway can arise through an evolutionary conflict in which the pathogen has to optimise between safeguarding its limited antigenic repertoire and remaining capable of establishing infections in non-naïve individuals. Our results thus demonstrate a crucial role for structured switching during the early phases of infections and provide a unifying theory of antigenic variation in P. falciparum malaria as a balanced process of parasite-intrinsic switching and immune-mediated selection.
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/21408201/?tool=EBI
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