Literature DB >> 15157763

A Leishmania donovani gene that confers accelerated recovery from stationary phase growth arrest.

Cornelia Hoyer1, Dorothea Zander, Sandra Fleischer, Markus Schilhabel, Manfred Kroener, Mathias Platzer, Joachim Clos.   

Abstract

We have isolated a gene, LdGF1, from the protozoan parasite Leishmania donovani. Overexpression of this gene confers a strong selective advantage in liquid culture after stationary phase growth arrest. We could show that recombinant L. donovani or Leishmania major, when overexpressing LdGF1, recover faster from a stationary phase growth arrest than control parasite strains. While no advantage of LdGF1 overexpression could be observed in log phase cultures or after a hydroxyurea-induced S-phase growth arrest, recovery from a cell cycle arrest due to serum deprivation was faster in LdGF1-overexpressing strains. This was found to be due to an accelerated release from a G(1) cell cycle arrest. By contrast, in a BALB/c mouse infection system, overexpression of LdGF1 in L. major resulted in reduced virulence. We conclude that increased levels of LdGF1 are beneficiary during recovery from G(1) cell cycle arrest, but pose a disadvantage inside a mammalian host. These results are discussed in the context of the observed loss of virulence during in vitro passage of Leishmania parasites.

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Year:  2004        PMID: 15157763     DOI: 10.1016/j.ijpara.2004.02.006

Source DB:  PubMed          Journal:  Int J Parasitol        ISSN: 0020-7519            Impact factor:   3.981


  6 in total

1.  The co-chaperone SGT of Leishmania donovani is essential for the parasite's viability.

Authors:  Gabi Ommen; Mareike Chrobak; Joachim Clos
Journal:  Cell Stress Chaperones       Date:  2009-12-02       Impact factor: 3.667

2.  Overexpression of a single Leishmania major gene enhances parasite infectivity in vivo and in vitro.

Authors:  Linda Reiling; Mareike Chrobak; Christel Schmetz; Joachim Clos
Journal:  Mol Microbiol       Date:  2010-03-25       Impact factor: 3.501

3.  Stage-specific expression of the mitochondrial co-chaperonin of Leishmania donovani, CPN10.

Authors:  Fanny Beatriz Zamora-Veyl; Manfred Kroemer; Dorothea Zander; Joachim Clos
Journal:  Kinetoplastid Biol Dis       Date:  2005-04-29

4.  The Hsp90-Sti1 interaction is critical for Leishmania donovani proliferation in both life cycle stages.

Authors:  Antje Hombach; Gabi Ommen; Mareike Chrobak; Joachim Clos
Journal:  Cell Microbiol       Date:  2012-11-20       Impact factor: 3.715

5.  A small heat shock protein is essential for thermotolerance and intracellular survival of Leishmania donovani.

Authors:  Antje Hombach; Gabi Ommen; Andrea MacDonald; Joachim Clos
Journal:  J Cell Sci       Date:  2014-09-01       Impact factor: 5.285

6.  Application of CRISPR/Cas9-Based Reverse Genetics in Leishmania braziliensis: Conserved Roles for HSP100 and HSP23.

Authors:  Vanessa Adaui; Constanze Kröber-Boncardo; Christine Brinker; Henner Zirpel; Julie Sellau; Jorge Arévalo; Jean-Claude Dujardin; Joachim Clos
Journal:  Genes (Basel)       Date:  2020-09-30       Impact factor: 4.096

  6 in total

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