Genome expression analysis of Anopheles gambiae: Responses to injury, bacterial challenge, and malaria infection

  1. George Dimopoulos*,
  2. George K. Christophides,
  3. Stephan Meister,
  4. Jörg Schultz,
  5. Kevin P. White§,
  6. Carolina Barillas-Mury, and
  7. Fotis C. Kafatos,
  1. *Department of Biological Sciences, Centre for Molecular Microbiology and Infection, Imperial College of Science, Technology and Medicine, London SW7 2AZ, United Kingdom; European Molecular Biology Laboratory and Cellzome, Meyerhofstrasse 1, 69117 Heidelberg, Germany; §Department of Genetics, Yale University School of Medicine, 333 Cedar Street NSB-386, New Haven, CT 06520; and Colorado State University, Department of Pathology, Fort Collins, CO 80523-1671
  1. Contributed by Fotis C. Kafatos

Abstract

The complex gene expression responses of Anopheles gambiae to microbial and malaria challenges, injury, and oxidative stress (in the mosquito and/or a cultured cell line) were surveyed by using cDNA microarrays constructed from an EST-clone collection. The expression profiles were broadly subdivided into induced and down-regulated gene clusters. Gram+ and Gram bacteria and microbial elicitors up-regulated a diverse set of genes, many belonging to the immunity class, and the response to malaria partially overlapped with this response. Oxidative stress activated a distinctive set of genes, mainly implicated in oxidoreductive processes. Injury up- and down-regulated gene clusters also were distinctive, prominently implicating glycolysis-related genes and citric acid cycle/oxidative phosphorylation/redox-mitochondrial functions, respectively. Cross-comparison of in vivo and in vitro responses indicated the existence of tightly coregulated gene groups that may correspond to gene pathways.

Footnotes

  • To whom reprint requests should be addressed. E-mail: DG-office{at}Embl-Heidelberg.de.

  • Abbreviations:
    EST,
    expressed sequence tag;
    PGN,
    peptidoglycan;
    LPS,
    lipopolysaccharide;
    SOM,
    self-organizing maps;
    TO,
    total of sequenced cluster and nonsequenced clones;
    HO,
    gene clusters showing homology to genes of other organisms
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