Cited by 44Malaria Research and ControlHemoglobinopathies and Related DisordersBlood groups and transfusion

Two DBLγ subtypes are commonly expressed by placental isolates of Plasmodium falciparum

Fried, Michal, Duffy, Patrick E·2002·Molecular and Biochemical Parasitology

Abstract

Adhesion to chondroitin sulfate A (CSA), a distinguishing feature of malaria parasites obtained from the human placenta, might be mediated by the Duffy-binding-like (DBL) gamma domain of the variant surface antigen Plasmodium falciparum erythrocyte membrane protein-1 (PfEMP1). We studied transcription of var genes (that encode PfEMP1) in placental parasites by amplifying and sequencing DBLgamma fragments from genomic DNA and cDNA of field isolates collected in western Kenya. We amplified DBLgamma fragments with divergent sequences from individual isolates by using various sequence-specific or degenerate primers. Transcripts detected with degenerate primers clustered phylogenetically within two DBLgamma subtypes with homology to chr5_1.gen_150 or FCR3.varCSA. Interestingly, the DBLalpha encoded by chr5_1.gen_150 was recently found to be commonly expressed by placental isolates from Malawi (Mol. Biochem. Parasitol. 185 (2002) 1207). The findings are consistent with earlier serologic evidence that surface antigens of placental parasites have conserved features, and suggest that vaccines based on DBLgamma may only need to target a limited number of variants.

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Crossref · 10.1016/s0166-6851(02)00103-2

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  • var1csa does not show enhanced transcription in placental or CSA-selected parasites and is transcribed by parasites from nonpregnant females and children.

    “The most extensively studied of these genes (var1csa) does not show enhanced transcription in placental or CSA-selected parasites (22, 23) and is transcribed by parasites from nonpregnant females and children (24, 25).”

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Authors
Fried, M., & Duffy, P. E.
Affiliations
Center for Infectious Disease Research (US)
Corresponding author
Fried, Michal
Venue
Molecular and Biochemical Parasitology
Publisher
Elsevier BV
Published
2002-07
Volume
122
Issue
2
Pages
201-210
ISSN
0166-6851 (ISSN-L)
OpenAlex
W2040878871
Cited by
44
References
2
Citations by year
2019: 2 · 2016: 1 · 2014: 1 · 2012: 1
FWCI
9.16
Type
journal article
Language
en
Open access
closed
Locations
  • Molecular and Biochemical Parasitology (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Institutes of Health (7r01ai043680-04)
  • National Institute of Allergy and Infectious Diseases (R01 AI 43680, R01 AI48654)
Topics
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Malaria Research and Control
  • Health Sciences › Medicine › Genetics › Hemoglobinopathies and Related Disorders
  • Health Sciences › Medicine › Hematology › Blood groups and transfusion
Keywords
Plasmodium falciparum, placental malaria, PfEMP1, var genes, erythrocyte membrane protein 1, vaccine targets, gene expression
MeSH terms
Adolescent, Adult, Amino Acid Sequence, Animals, Duffy Blood-Group System, Erythrocytes, Female, Humans, Middle Aged, Molecular Sequence Data, Placenta, Plasmodium falciparum, Pregnancy, Transcription, Genetic, Pregnancy Complications, Parasitic, Protozoan Proteins, Polymerase Chain Reaction, Malaria, Falciparum, Sequence Analysis, DNA, Protein Structure, Tertiary, DNA Primers, Reverse Transcriptase Polymerase Chain Reaction

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