Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.

Avoidance of antibody-mediated immune recognition allows parasites to establish chronic infections and enhances opportunities for transmission. The human malaria parasite Plasmodium falciparum possesses a number of multi-copy gene families, including var, rif, stevor and pfmc-2tm, which encode varia...

Full description

Bibliographic Details
Main Authors: Anna Bachmann, Michaela Petter, Ann-Kathrin Tilly, Laura Biller, Karin A Uliczka, Michael F Duffy, Egbert Tannich, Iris Bruchhaus
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2012-01-01
Series:PLoS ONE
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23166704/?tool=EBI
_version_ 1818461432986992640
author Anna Bachmann
Michaela Petter
Ann-Kathrin Tilly
Laura Biller
Karin A Uliczka
Michael F Duffy
Egbert Tannich
Iris Bruchhaus
author_facet Anna Bachmann
Michaela Petter
Ann-Kathrin Tilly
Laura Biller
Karin A Uliczka
Michael F Duffy
Egbert Tannich
Iris Bruchhaus
author_sort Anna Bachmann
collection DOAJ
description Avoidance of antibody-mediated immune recognition allows parasites to establish chronic infections and enhances opportunities for transmission. The human malaria parasite Plasmodium falciparum possesses a number of multi-copy gene families, including var, rif, stevor and pfmc-2tm, which encode variant antigens believed to be expressed on the surfaces of infected erythrocytes. However, most studies of these antigens are based on in vitro analyses of culture-adapted isolates, most commonly the laboratory strain 3D7, and thus may not be representative of the unique challenges encountered by P. falciparum in the human host. To investigate the expression of the var, rif-A, rif-B, stevor and pfmc-2tm family genes under conditions that mimic more closely the natural course of infection, ex vivo clinical P. falciparum isolates were analyzed using a novel quantitative real-time PCR approach. Expression patterns in the clinical isolates at various time points during the first intraerythrocytic developmental cycle in vitro were compared to those of strain 3D7. In the clinical isolates, in contrast to strain 3D7, there was a peak of expression of the multi-copy gene families rif-A, stevor and pfmc-2tm at the young ring stage, in addition to the already known expression peak in trophozoites. Furthermore, most of the variant surface antigen families were overexpressed in the clinical isolates relative to 3D7, with the exception of the pfmc-2tm family, expression of which was higher in 3D7 parasites. Immunofluorescence analyses performed in parallel revealed two stage-dependent localization patterns of RIFIN, STEVOR and PfMC-2TM. Proteins were exported into the infected erythrocyte at the young trophozoite stage, whereas they remained inside the parasite membrane during schizont stage and were subsequently observed in different compartments in the merozoite. These results reveal a complex pattern of expression of P. falciparum multi-copy gene families during clinical progression and are suggestive of diverse functional roles of the respective proteins.
first_indexed 2024-12-14T23:46:03Z
format Article
id doaj.art-0fff85b9b1924253aaf51338c9f5cd9a
institution Directory Open Access Journal
issn 1932-6203
language English
last_indexed 2024-12-14T23:46:03Z
publishDate 2012-01-01
publisher Public Library of Science (PLoS)
record_format Article
series PLoS ONE
spelling doaj.art-0fff85b9b1924253aaf51338c9f5cd9a2022-12-21T22:43:22ZengPublic Library of Science (PLoS)PLoS ONE1932-62032012-01-01711e4954010.1371/journal.pone.0049540Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.Anna BachmannMichaela PetterAnn-Kathrin TillyLaura BillerKarin A UliczkaMichael F DuffyEgbert TannichIris BruchhausAvoidance of antibody-mediated immune recognition allows parasites to establish chronic infections and enhances opportunities for transmission. The human malaria parasite Plasmodium falciparum possesses a number of multi-copy gene families, including var, rif, stevor and pfmc-2tm, which encode variant antigens believed to be expressed on the surfaces of infected erythrocytes. However, most studies of these antigens are based on in vitro analyses of culture-adapted isolates, most commonly the laboratory strain 3D7, and thus may not be representative of the unique challenges encountered by P. falciparum in the human host. To investigate the expression of the var, rif-A, rif-B, stevor and pfmc-2tm family genes under conditions that mimic more closely the natural course of infection, ex vivo clinical P. falciparum isolates were analyzed using a novel quantitative real-time PCR approach. Expression patterns in the clinical isolates at various time points during the first intraerythrocytic developmental cycle in vitro were compared to those of strain 3D7. In the clinical isolates, in contrast to strain 3D7, there was a peak of expression of the multi-copy gene families rif-A, stevor and pfmc-2tm at the young ring stage, in addition to the already known expression peak in trophozoites. Furthermore, most of the variant surface antigen families were overexpressed in the clinical isolates relative to 3D7, with the exception of the pfmc-2tm family, expression of which was higher in 3D7 parasites. Immunofluorescence analyses performed in parallel revealed two stage-dependent localization patterns of RIFIN, STEVOR and PfMC-2TM. Proteins were exported into the infected erythrocyte at the young trophozoite stage, whereas they remained inside the parasite membrane during schizont stage and were subsequently observed in different compartments in the merozoite. These results reveal a complex pattern of expression of P. falciparum multi-copy gene families during clinical progression and are suggestive of diverse functional roles of the respective proteins.https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23166704/?tool=EBI
spellingShingle Anna Bachmann
Michaela Petter
Ann-Kathrin Tilly
Laura Biller
Karin A Uliczka
Michael F Duffy
Egbert Tannich
Iris Bruchhaus
Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
PLoS ONE
title Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
title_full Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
title_fullStr Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
title_full_unstemmed Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
title_short Temporal expression and localization patterns of variant surface antigens in clinical Plasmodium falciparum isolates during erythrocyte schizogony.
title_sort temporal expression and localization patterns of variant surface antigens in clinical plasmodium falciparum isolates during erythrocyte schizogony
url https://www.ncbi.nlm.nih.gov/pmc/articles/pmid/23166704/?tool=EBI
work_keys_str_mv AT annabachmann temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT michaelapetter temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT annkathrintilly temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT laurabiller temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT karinauliczka temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT michaelfduffy temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT egberttannich temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony
AT irisbruchhaus temporalexpressionandlocalizationpatternsofvariantsurfaceantigensinclinicalplasmodiumfalciparumisolatesduringerythrocyteschizogony