Medical Journals

Leishmania Disease Development Depends on the Presence of Apoptotic Promastigotes in the Virulent Inoculum.

Authors:
  • van Zandbergen Ger
  • Bollinger Annalena
  • Wenzel Alexander
  • Kamhawi Shaden
  • Voll Reinhard
  • Klinger Matthias
  • Müller Antje
  • Hölscher Christoph
  • Herrmann Martin
  • Sacks David
  • Solbach Werner
  • Laskay Tamás

From: Institute for Medical Microbiology and Hygiene, University of Lübeck, D-23538 Lübeck, Germany. zandbergen@uni-luebeck.de

Proceedings of the National Academy of Sciences of the United States of America

  • Publish Date: Sep 2006
  • ISSN: 0027-8424
  • Volume: 103
  • Issue: 37
  • Pages: 13837-42
  • Medium: Print
  • Language: English
  • Citation (JAMA): van Zandbergen Ger, Bollinger Annalena, Wenzel Alexander, et al. Leishmania Disease Development Depends on the Presence of Apoptotic Promastigotes in the Virulent Inoculum.. Proc. Natl. Acad. Sci. U.S.A. Sep 2006;103:13837-42

Abstract

The obligate intracellular pathogen Leishmania major survives and multiplies in professional phagocytes. The evasion strategy to circumvent killing by host phagocytes and establish a productive infection is poorly understood. Here we report that the virulent inoculum of Leishmania promastigotes contains a high ratio of annexin A5-binding apoptotic parasites. This subpopulation of parasites is characterized by a round body shape, a swollen kinetoplast, nuclear condensation, and a lack of multiplication and represents dying or already dead parasites. After depleting the apoptotic parasites from a virulent population, Leishmania do not survive in phagocytes in vitro and lose their disease-inducing ability in vivo. TGF-beta induced by apoptotic parasites is likely to mediate the silencing of phagocytes and lead to survival of infectious Leishmania populations. The data demonstrate that apoptotic promastigotes, in an altruistic way, enable the intracellular survival of the viable parasites.

Mesh Headings (Keywords): Animals, Annexin A5, Apoptosis, Down-Regulation, Female, Leishmania major, Leishmaniasis, Mice, Mice, Inbred BALB C, Phagocytes, Transforming Growth Factor alpha, Transforming Growth Factor beta, Up-Regulation, Virulence


Check for Full Text / PubMed Unique Identifier (PMID): 16945916


This abstract is part of PubMed, a service of the U.S. National Library of Medicine. PubMed includes more than 17 million citations from MEDLINE and other life science journals for biomedical articles. See Copyright and Disclaimers.

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The data herein was last updated on July 8th, 2008 and may not reflect the most current and accurate data available from NLM.


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