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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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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