Molecular interactions between Anopheles stephensi midgut cells and Plasmodium berghei: the time bomb theory of ookinete invasion of mosquitoes.

Y S Han, J Thompson, F C Kafatos, C Barillas-Mury
Author Information
  1. Y S Han: Colorado State University, Pathology Department, Fort Collins, CO 80523, USA.

Abstract

We present a detailed analysis of the interactions between Anopheles stephensi midgut epithelial cells and Plasmodium berghei ookinetes during invasion of the mosquito by the parasite. In this mosquito, P. berghei ookinetes invade polarized columnar epithelial cells with microvilli, which do not express high levels of vesicular ATPase. The invaded cells are damaged, protrude towards the midgut lumen and suffer other characteristic changes, including induction of nitric oxide synthase (NOS) expression, a substantial loss of microvilli and genomic DNA fragmentation. Our results indicate that the parasite inflicts extensive damage leading to subsequent death of the invaded cell. Ookinetes were found to be remarkably plastic, to secrete a subtilisin-like serine protease and the GPI-anchored surface protein Pbs21 into the cytoplasm of invaded cells, and to be capable of extensive lateral movement between cells. The epithelial damage inflicted is repaired efficiently by an actin purse-string-mediated restitution mechanism, which allows the epithelium to 'bud off' the damaged cells without losing its integrity. A new model, the time bomb theory of ookinete invasion, is proposed and its implications are discussed.

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Grants

  1. AI5573-01A1/NIAID NIH HHS

MeSH Term

Actins
Animals
Anopheles
Base Sequence
Cell Death
DNA Primers
DNA-Binding Proteins
Digestive System
Epithelial Cells
Models, Biological
Nitric Oxide Synthase
Plasmodium berghei
Proton-Translocating ATPases
Serine Endopeptidases
Trans-Activators
Vacuolar Proton-Translocating ATPases
Virulence
Wound Healing

Chemicals

Actins
DNA Primers
DNA-Binding Proteins
Trans-Activators
Nitric Oxide Synthase
Serine Endopeptidases
Vacuolar Proton-Translocating ATPases
Proton-Translocating ATPases