Signatures of malaria-associated pathology revealed by high-resolution whole-blood transcriptomics in a rodent model of malaria

Sci Rep. 2017 Feb 3:7:41722. doi: 10.1038/srep41722.

Abstract

The influence of parasite genetic factors on immune responses and development of severe pathology of malaria is largely unknown. In this study, we performed genome-wide transcriptomic profiling of mouse whole blood during blood-stage infections of two strains of the rodent malaria parasite Plasmodium chabaudi that differ in virulence. We identified several transcriptomic signatures associated with the virulent infection, including signatures for platelet aggregation, stronger and prolonged anemia and lung inflammation. The first two signatures were detected prior to pathology. The anemia signature indicated deregulation of host erythropoiesis, and the lung inflammation signature was linked to increased neutrophil infiltration, more cell death and greater parasite sequestration in the lungs. This comparative whole-blood transcriptomics profiling of virulent and avirulent malaria shows the validity of this approach to inform severity of the infection and provide insight into pathogenic mechanisms.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cluster Analysis
  • Disease Models, Animal
  • Erythrocytes / parasitology
  • Gene Expression Profiling
  • Host-Parasite Interactions / genetics*
  • Life Cycle Stages
  • Malaria / blood
  • Malaria / genetics*
  • Malaria / parasitology*
  • Mice
  • Mice, Inbred C57BL
  • Neutrophil Infiltration
  • Organ Specificity / genetics
  • Plasmodium / physiology*
  • Plasmodium chabaudi / physiology
  • Platelet Aggregation
  • Transcriptome*
  • Virulence