Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed

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Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed. / Subramani, Ramesh; Quadt, Katharina; Jeppesen, Anine Engholm; Hempel, Casper; Petersen, Jens Emil Vang; Hassenkam, Tue; Hviid, Lars; Barfod, Lea Klingenberg.

In: mBio, Vol. 6, No. 5, e01456-15, 2015.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Subramani, R, Quadt, K, Jeppesen, AE, Hempel, C, Petersen, JEV, Hassenkam, T, Hviid, L & Barfod, LK 2015, 'Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed', mBio, vol. 6, no. 5, e01456-15. https://doi.org/10.1128/mBio.01456-15

APA

Subramani, R., Quadt, K., Jeppesen, A. E., Hempel, C., Petersen, J. E. V., Hassenkam, T., Hviid, L., & Barfod, L. K. (2015). Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed. mBio, 6(5), [e01456-15]. https://doi.org/10.1128/mBio.01456-15

Vancouver

Subramani R, Quadt K, Jeppesen AE, Hempel C, Petersen JEV, Hassenkam T et al. Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed. mBio. 2015;6(5). e01456-15. https://doi.org/10.1128/mBio.01456-15

Author

Subramani, Ramesh ; Quadt, Katharina ; Jeppesen, Anine Engholm ; Hempel, Casper ; Petersen, Jens Emil Vang ; Hassenkam, Tue ; Hviid, Lars ; Barfod, Lea Klingenberg. / Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed. In: mBio. 2015 ; Vol. 6, No. 5.

Bibtex

@article{8cfe34230c32428d8c7ff34f1ff6ba0a,
title = "Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed",
abstract = "UNLABELLED: Members of the clonally variant Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family mediate adhesion of infected erythrocytes (IEs) to vascular receptors. PfEMP1 expression is normally confined to nanoscale knob protrusions on the IE surface membrane. To investigate the relationship between the densities of these IE surface knobs and the PfEMP1 variant expressed, we used specific antibody panning to generate three sublines of the P. falciparum clone IT4, which expresses the PfEMP1 variants IT4VAR04, IT4VAR32b, and IT4VAR60. The knob density in each subline was then determined by atomic force microscopy (AFM) and scanning electron microscopy (SEM) and compared to PfEMP1 and knob-associated histidine-rich protein (KAHRP) expression. Selection for uniform expression of IT4VAR04 produced little change in knob density, compared to unselected IEs. In contrast, selection for IT4VAR32b expression increased knob density approximately 3-fold, whereas IEs selected for IT4VAR60 expression were essentially knobless. When IT4VAR60(+) IEs were subsequently selected to express IT4VAR04 or IT4VAR32b, they again displayed low and high knob densities, respectively. All sublines expressed KAHRP regardless of the PfEMP1 expressed. Our study documents for the first time that knob density is related to the PfEMP1 variant expressed. This may reflect topological requirements to ensure optimal adhesive properties of the IEs.IMPORTANCE: Infections with Plasmodium falciparum malaria parasites are still responsible for many deaths, especially among children and pregnant women. New interventions are needed to reduce severe illness and deaths caused by this malaria parasite. Thus, a better understanding of the mechanisms behind the pathogenesis is essential. A main reason why Plasmodium falciparum malaria is more severe than disease caused by other malaria species is its ability to express variant antigens on the infected erythrocyte surface. These antigens are presented on membrane protrusions known as knobs. This study set out to investigate the interplay between different variant antigens on the surface of P. falciparum-infected erythrocytes and the density of the knobs on which the antigens are expressed. Such a direct analysis of this relationship has not been reported before but adds to the important understanding of the complexity of malaria antigen presentation.",
author = "Ramesh Subramani and Katharina Quadt and Jeppesen, {Anine Engholm} and Casper Hempel and Petersen, {Jens Emil Vang} and Tue Hassenkam and Lars Hviid and Barfod, {Lea Klingenberg}",
note = "Copyright {\textcopyright} 2015 Subramani et al.",
year = "2015",
doi = "10.1128/mBio.01456-15",
language = "English",
volume = "6",
journal = "mBio",
issn = "2161-2129",
publisher = "American Society for Microbiology",
number = "5",

}

RIS

TY - JOUR

T1 - Plasmodium falciparum-infected erythrocyte knob density is linked to the PfEMP1 variant expressed

AU - Subramani, Ramesh

AU - Quadt, Katharina

AU - Jeppesen, Anine Engholm

AU - Hempel, Casper

AU - Petersen, Jens Emil Vang

AU - Hassenkam, Tue

AU - Hviid, Lars

AU - Barfod, Lea Klingenberg

N1 - Copyright © 2015 Subramani et al.

PY - 2015

Y1 - 2015

N2 - UNLABELLED: Members of the clonally variant Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family mediate adhesion of infected erythrocytes (IEs) to vascular receptors. PfEMP1 expression is normally confined to nanoscale knob protrusions on the IE surface membrane. To investigate the relationship between the densities of these IE surface knobs and the PfEMP1 variant expressed, we used specific antibody panning to generate three sublines of the P. falciparum clone IT4, which expresses the PfEMP1 variants IT4VAR04, IT4VAR32b, and IT4VAR60. The knob density in each subline was then determined by atomic force microscopy (AFM) and scanning electron microscopy (SEM) and compared to PfEMP1 and knob-associated histidine-rich protein (KAHRP) expression. Selection for uniform expression of IT4VAR04 produced little change in knob density, compared to unselected IEs. In contrast, selection for IT4VAR32b expression increased knob density approximately 3-fold, whereas IEs selected for IT4VAR60 expression were essentially knobless. When IT4VAR60(+) IEs were subsequently selected to express IT4VAR04 or IT4VAR32b, they again displayed low and high knob densities, respectively. All sublines expressed KAHRP regardless of the PfEMP1 expressed. Our study documents for the first time that knob density is related to the PfEMP1 variant expressed. This may reflect topological requirements to ensure optimal adhesive properties of the IEs.IMPORTANCE: Infections with Plasmodium falciparum malaria parasites are still responsible for many deaths, especially among children and pregnant women. New interventions are needed to reduce severe illness and deaths caused by this malaria parasite. Thus, a better understanding of the mechanisms behind the pathogenesis is essential. A main reason why Plasmodium falciparum malaria is more severe than disease caused by other malaria species is its ability to express variant antigens on the infected erythrocyte surface. These antigens are presented on membrane protrusions known as knobs. This study set out to investigate the interplay between different variant antigens on the surface of P. falciparum-infected erythrocytes and the density of the knobs on which the antigens are expressed. Such a direct analysis of this relationship has not been reported before but adds to the important understanding of the complexity of malaria antigen presentation.

AB - UNLABELLED: Members of the clonally variant Plasmodium falciparum erythrocyte membrane protein 1 (PfEMP1) family mediate adhesion of infected erythrocytes (IEs) to vascular receptors. PfEMP1 expression is normally confined to nanoscale knob protrusions on the IE surface membrane. To investigate the relationship between the densities of these IE surface knobs and the PfEMP1 variant expressed, we used specific antibody panning to generate three sublines of the P. falciparum clone IT4, which expresses the PfEMP1 variants IT4VAR04, IT4VAR32b, and IT4VAR60. The knob density in each subline was then determined by atomic force microscopy (AFM) and scanning electron microscopy (SEM) and compared to PfEMP1 and knob-associated histidine-rich protein (KAHRP) expression. Selection for uniform expression of IT4VAR04 produced little change in knob density, compared to unselected IEs. In contrast, selection for IT4VAR32b expression increased knob density approximately 3-fold, whereas IEs selected for IT4VAR60 expression were essentially knobless. When IT4VAR60(+) IEs were subsequently selected to express IT4VAR04 or IT4VAR32b, they again displayed low and high knob densities, respectively. All sublines expressed KAHRP regardless of the PfEMP1 expressed. Our study documents for the first time that knob density is related to the PfEMP1 variant expressed. This may reflect topological requirements to ensure optimal adhesive properties of the IEs.IMPORTANCE: Infections with Plasmodium falciparum malaria parasites are still responsible for many deaths, especially among children and pregnant women. New interventions are needed to reduce severe illness and deaths caused by this malaria parasite. Thus, a better understanding of the mechanisms behind the pathogenesis is essential. A main reason why Plasmodium falciparum malaria is more severe than disease caused by other malaria species is its ability to express variant antigens on the infected erythrocyte surface. These antigens are presented on membrane protrusions known as knobs. This study set out to investigate the interplay between different variant antigens on the surface of P. falciparum-infected erythrocytes and the density of the knobs on which the antigens are expressed. Such a direct analysis of this relationship has not been reported before but adds to the important understanding of the complexity of malaria antigen presentation.

U2 - 10.1128/mBio.01456-15

DO - 10.1128/mBio.01456-15

M3 - Journal article

C2 - 26443460

VL - 6

JO - mBio

JF - mBio

SN - 2161-2129

IS - 5

M1 - e01456-15

ER -

ID: 145536915