Functional and Immunological Characterization of a Duffy Binding–Like–γ Domain from Plasmodium falciparum Erythrocyte Membrane Protein–1 Expressed by a Placental Isolate

A recombinant Duffy binding–like (DBL)–γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding...

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Published inThe Journal of infectious diseases Vol. 192; no. 7; pp. 1284 - 1293
Main Authors Chia, Yu-Shan, Badaut, Cyril, Tuikue Ndam, Nicaise G., Khattab, Ayman, Igonet, Sebastien, Fievet, Nadine, Bentley, Graham A., Deloron, Philippe, Klinkert, Mo-Quen
Format Journal Article
LanguageEnglish
Published Chicago, IL The University of Chicago Press 01.10.2005
University of Chicago Press
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ISSN0022-1899
1537-6613
DOI10.1086/432918

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Abstract A recombinant Duffy binding–like (DBL)–γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IEs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3γ domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3γ domain carries preferentially IE-expressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL-γ domain derived from a placental isolate that shows CSA-binding properties
AbstractList A recombinant Duffy binding–like (DBL)–γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IEs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3γ domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3γ domain carries preferentially IE-expressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL-γ domain derived from a placental isolate that shows CSA-binding properties
A recombinant Duffy binding-like (DBL)-γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IBs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3γ domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3γ domain carries preferentially IEexpressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL-γ domain derived from a placental isolate that shows CSA-binding properties.
A recombinant Duffy binding-like (DBL)- gamma domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IEs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3 gamma domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3 gamma domain carries preferentially IE-expressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL- gamma domain derived from a placental isolate that shows CSA-binding properties.A recombinant Duffy binding-like (DBL)- gamma domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IEs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3 gamma domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3 gamma domain carries preferentially IE-expressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL- gamma domain derived from a placental isolate that shows CSA-binding properties.
A recombinant Duffy binding-like (DBL)- gamma domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system and was purified in milligram quantities. The recombinant protein binds specifically to chondroitin sulfate A (CSA) and inhibits CSA binding by placental infected erythrocytes (IEs). Polyclonal antibodies raised against the domain recognized the surfaces of live IEs from CSA-adherent clinical placental isolates. These antibodies also abrogated the in vitro binding of IEs to CSA. The 732 DBL-3 gamma domain was specifically recognized by plasma from pregnant women but not by plasma from control subjects. In addition, the protein was, comparatively, significantly more reactive with plasma from women with infected placentas, strongly suggesting that the 732 DBL-3 gamma domain carries preferentially IE-expressed immunogenic epitopes. High levels of plasma antibodies to the recombinant domain were associated with reduced placental parasite density. This is the first report of a recombinant DBL- gamma domain derived from a placental isolate that shows CSA-binding properties.
Author Chia, Yu-Shan
Tuikue Ndam, Nicaise G.
Badaut, Cyril
Deloron, Philippe
Klinkert, Mo-Quen
Igonet, Sebastien
Bentley, Graham A.
Fievet, Nadine
Khattab, Ayman
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Keywords Infection
Protozoa
Plasmodium falciparum
Apicomplexa
Blood cell
Membrane protein
Microbiology
Red blood cell
Isolate
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Snippet A recombinant Duffy binding–like (DBL)–γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system...
A recombinant Duffy binding-like (DBL)-γ domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell system...
A recombinant Duffy binding-like (DBL)- gamma domain from a previously identified placental isolate, 732, was expressed by use of the baculovirus/insect cell...
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SubjectTerms Amino Acid Sequence
Animals
Antibodies
Antibodies, Protozoan - blood
Baculovirus
Biological and medical sciences
Blood plasma
Cell lines
Cells, Cultured
CHO Cells
Chondroitin Sulfates - metabolism
Cricetinae
Duffy Blood-Group System - metabolism
Female
Fundamental and applied biological sciences. Psychology
Genes
Humans
Infectious diseases
Malaria
Malaria, Falciparum - immunology
Malaria, Falciparum - parasitology
Male
Medical sciences
Microbiology
Molecular Sequence Data
Parasites
Placenta
Placenta - parasitology
Plasmodium falciparum
Plasmodium falciparum - immunology
Plasmodium falciparum - isolation & purification
Pregnancy
Pregnancy Complications, Infectious - immunology
Pregnancy Complications, Infectious - parasitology
Protozoan Proteins - chemistry
Protozoan Proteins - genetics
Protozoan Proteins - immunology
Protozoan Proteins - metabolism
Recombinant proteins
Recombinant Proteins - chemistry
Recombinant Proteins - metabolism
Spodoptera
Sulfates
Title Functional and Immunological Characterization of a Duffy Binding–Like–γ Domain from Plasmodium falciparum Erythrocyte Membrane Protein–1 Expressed by a Placental Isolate
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