Literature DB >> 4039899

Development of infective stage Leishmania promastigotes within phlebotomine sand flies.

D L Sacks, P V Perkins.   

Abstract

Midgut promastigotes were obtained from Phlebotomus papatasi and Lutzomyia longipalpis on days 3-7 after infection with cloned isolates of Leishmania major and Leishmania mexicana amazonensis, respectively, and examined as to their ability to initiate cutaneous infections in BALB/c mice. Sequential development of midgut promastigotes from a noninfective to an infective stage was confirmed for both the New World and Old World species. The generation of infective promastigotes from rapidly dividing avirulent populations occurred as early as day 3 and was well under way by day 4 after infective feed. Optimally infective promastigotes were recovered from midguts shortly after bloodmeal passage, coinciding with the time at which another bloodmeal is sought by the fly.

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Year:  1985        PMID: 4039899     DOI: 10.4269/ajtmh.1985.34.456

Source DB:  PubMed          Journal:  Am J Trop Med Hyg        ISSN: 0002-9637            Impact factor:   2.345


  45 in total

1.  Genomic organisation and expression of a differentially-regulated gene family from Leishmania major.

Authors:  H M Flinn; D F Smith
Journal:  Nucleic Acids Res       Date:  1992-02-25       Impact factor: 16.971

2.  Leishmania disease development depends on the presence of apoptotic promastigotes in the virulent inoculum.

Authors:  Ger van Zandbergen; Annalena Bollinger; Alexander Wenzel; Shaden Kamhawi; Reinhard Voll; Matthias Klinger; Antje Müller; Christoph Hölscher; Martin Herrmann; David Sacks; Werner Solbach; Tamás Laskay
Journal:  Proc Natl Acad Sci U S A       Date:  2006-08-31       Impact factor: 11.205

3.  Sterol methyltransferase is required for optimal mitochondrial function and virulence in Leishmania major.

Authors:  Sumit Mukherjee; Wei Xu; Fong-Fu Hsu; Jigesh Patel; Juyang Huang; Kai Zhang
Journal:  Mol Microbiol       Date:  2018-10-21       Impact factor: 3.501

4.  Cytolytic activity in the genus Leishmania: involvement of a putative pore-forming protein.

Authors:  F S Noronha; F J Ramalho-Pinto; M F Horta
Journal:  Infect Immun       Date:  1996-10       Impact factor: 3.441

5.  Acid phosphatase activity of virulent and avirulent clones of Leishmania donovani promastigotes.

Authors:  K Katakura; A Kobayashi
Journal:  Infect Immun       Date:  1988-11       Impact factor: 3.441

6.  Scanning electron microscopy of Leishmania major in Phlebotomus papatasi.

Authors:  A Warburg; G S Hamada; Y Schlein; D Shire
Journal:  Z Parasitenkd       Date:  1986

7.  The ultrastructure of Leishmania major in the foregut and proboscis of Phlebotomus papatasi.

Authors:  R Killick-Kendrick; K R Wallbanks; D H Molyneux; D R Lavin
Journal:  Parasitol Res       Date:  1988       Impact factor: 2.289

8.  Acquisition of iron from transferrin and lactoferrin by the protozoan Leishmania chagasi.

Authors:  M E Wilson; R W Vorhies; K A Andersen; B E Britigan
Journal:  Infect Immun       Date:  1994-08       Impact factor: 3.441

9.  Ascorbate peroxidase from Leishmania major controls the virulence of infective stage of promastigotes by regulating oxidative stress.

Authors:  Swati Pal; Subhankar Dolai; Rajesh K Yadav; Subrata Adak
Journal:  PLoS One       Date:  2010-06-23       Impact factor: 3.240

10.  Differences in human macrophage receptor usage, lysosomal fusion kinetics and survival between logarithmic and metacyclic Leishmania infantum chagasi promastigotes.

Authors:  Norikiyo Ueno; Carol L Bratt; Nilda E Rodriguez; Mary E Wilson
Journal:  Cell Microbiol       Date:  2009-08-20       Impact factor: 3.715

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