Literature DB >> 3709546

Cell surface carbohydrate of Leishmania mexicana amazonensis: differences between infective and non-infective forms.

E M Saraiva, A F Andrade, M E Pereira.   

Abstract

The cell surface carbohydrates of Leishmania mexicana amazonensis (amastigotes and promastigotes, both infective and non-infective forms) were comparatively analyzed by agglutination assay employing 28 highly purified lectins, and by binding assay using 125I-labeled lectins. Among the D-GalNAc binding lectins, Bandeiraea simplicifolia-I, Dolichos biflorus, Phaseolus vulgaris and Glycine max were highly specific for the amastigotes, while that from Maclura aurantiaca selectively agglutinated promastigotes. The lectins from Wistaria floribunda, Phaseolus lunatus (D-GalNAc), Arachis hypogaea (D-Gal) and Triticum vulgaris (D-GlcNAc) were selective for the infective forms (both amastigotes and promastigotes), not reacting with the non-infective ones. Conversely, no parasite agglutination occurred with the L-fucose binding lectins Lotus tetragonolobus and Ulex europaeus-I. Binding studies with 125I-labeled lectins from Wistaria floribunda, Triticum vulgaris and Arachis hypogaea were performed to find whether unagglutinated non-infective promastigotes might have receptors for these lectins, in which case absence of agglutination could be due to a peculiar arrangement of the receptors. These assays essentially confirmed the selectivity, demonstrated in the agglutination assays of these lectins for the infective promastigotes.

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Year:  1986        PMID: 3709546

Source DB:  PubMed          Journal:  Eur J Cell Biol        ISSN: 0171-9335            Impact factor:   4.492


  7 in total

1.  Involvement of the macrophage mannose-6-phosphate receptor in the recognition of Leishmania mexicana amazonensis.

Authors:  E M Saraiva; A F Andrade; W de Souza
Journal:  Parasitol Res       Date:  1987       Impact factor: 2.289

2.  Biological and biochemical characterization of tunicamycin-resistant Leishmania mexicana: mechanism of drug resistance and virulence.

Authors:  J A Kink; K P Chang
Journal:  Infect Immun       Date:  1987-07       Impact factor: 3.441

3.  Population changes in Leishmania chagasi promastigote developmental stages due to serial passage.

Authors:  Soi Meng Lei; Nathan M Romine; Jeffrey K Beetham
Journal:  J Parasitol       Date:  2010-08-13       Impact factor: 1.276

4.  The surface free energy of Leishmania mexicana amazonensis.

Authors:  F C Silva Filho; E M Saraiva; M A Santos; W de Souza
Journal:  Cell Biophys       Date:  1990-10

5.  A comparison of the lectin-binding properties of glycoconjugates from a range of Leishmania species.

Authors:  R J Rossell; A F Stevens; M A Miles; A K Allen
Journal:  Parasitol Res       Date:  1990       Impact factor: 2.289

6.  Virulence attenuation of a UDP-galactose/N-acetylglucosamine beta1,4 galactosyltransferase expressing Leishmania donovani promastigote.

Authors:  S K Bhaumik; M Singh; R Basu; S Bhaumik; K Roychoudhury; K Naskar; S Roy; T De
Journal:  Glycoconj J       Date:  2008-01-16       Impact factor: 2.916

7.  Stimulation of metacyclogenesis in Leishmania (Mundinia) orientalis for mass production of metacyclic promastigotes.

Authors:  Wetpisit Chanmol; Narissara Jariyapan; Kanok Preativatanyou; Chonlada Mano; Pongsri Tippawangkosol; Pradya Somboon; Paul A Bates
Journal:  Front Cell Infect Microbiol       Date:  2022-09-05       Impact factor: 6.073

  7 in total

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