Literature DB >> 12654759

In vitro effect on Cryptosporidium parvum of short-term exposure to cathelicidin peptides.

Andrea Giacometti1, Oscar Cirioni, Maria Simona Del Prete, Barbara Skerlavaj, Raffaella Circo, Margherita Zanetti, Giorgio Scalise.   

Abstract

Two laboratory methods, a cell culture system and double fluorogenic staining, were used to study the viability and infective ability of Cryptosporidium parvum sporozoites and oocysts after short-term exposure to four cathelicidin peptides. The compounds, SMAP-29, BMAP-28, PG-1 and Bac7(1-35), exerted a strong cytotoxic effect on sporozoites, but did not affect the viability and function of oocysts consistently. Overall, in the sporozoite series, a percentage of the viable population decreased rapidly to less than detectable levels after 15 and 60 min exposure to the peptides at concentrations of 100 and 10 micro g/mL, respectively. In the oocyst series, no compound produced complete inhibition of parasite growth: 60-85% of the oocyst population was viable after 180 min exposure at 100 micro g/mL. SMAP-29 exerted the highest activity against both sporozoites and oocysts.

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Year:  2003        PMID: 12654759     DOI: 10.1093/jac/dkg149

Source DB:  PubMed          Journal:  J Antimicrob Chemother        ISSN: 0305-7453            Impact factor:   5.790


  13 in total

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Journal:  Infect Immun       Date:  2010-12-28       Impact factor: 3.441

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Journal:  Infect Immun       Date:  2011-11-14       Impact factor: 3.441

3.  Antibodies fused to innate immune molecules reduce initiation of Cryptosporidium parvum infection in mice.

Authors:  Michael Imboden; Michael W Riggs; Deborah A Schaefer; E Jane Homan; Robert D Bremel
Journal:  Antimicrob Agents Chemother       Date:  2010-01-19       Impact factor: 5.191

4.  Differential regulation of beta-defensin gene expression during Cryptosporidium parvum infection.

Authors:  Tarek K Zaalouk; Mona Bajaj-Elliott; John T George; Vincent McDonald
Journal:  Infect Immun       Date:  2004-05       Impact factor: 3.441

5.  The human cathelicidin LL-37 modulates the activities of the P2X7 receptor in a structure-dependent manner.

Authors:  Linda Tomasinsig; Cinzia Pizzirani; Barbara Skerlavaj; Patrizia Pellegatti; Sara Gulinelli; Alessandro Tossi; Francesco Di Virgilio; Margherita Zanetti
Journal:  J Biol Chem       Date:  2008-09-02       Impact factor: 5.157

6.  Cooperative role of macrophages and neutrophils in host Antiprotozoan resistance in mice acutely infected with Cryptosporidium parvum.

Authors:  Dan Takeuchi; Vickie C Jones; Makiko Kobayashi; Fujio Suzuki
Journal:  Infect Immun       Date:  2008-06-02       Impact factor: 3.441

7.  A comparative study on the interactions of SMAP-29 with lipid monolayers.

Authors:  Frances Neville; Andrey Ivankin; Oleg Konovalov; David Gidalevitz
Journal:  Biochim Biophys Acta       Date:  2009-10-02

8.  Intracellular toxicity of proline-rich antimicrobial peptides shuttled into mammalian cells by the cell-penetrating peptide penetratin.

Authors:  Anne Hansen; Ingo Schäfer; Daniel Knappe; Peter Seibel; Ralf Hoffmann
Journal:  Antimicrob Agents Chemother       Date:  2012-07-30       Impact factor: 5.191

9.  Blastocystis Isolate B Exhibits Multiple Modes of Resistance against Antimicrobial Peptide LL-37.

Authors:  John Anthony Yason; Sitara Swarna Rao Ajjampur; Kevin Shyong Wei Tan
Journal:  Infect Immun       Date:  2016-07-21       Impact factor: 3.441

10.  Cathelicidin-like helminth defence molecules (HDMs): absence of cytotoxic, anti-microbial and anti-protozoan activities imply a specific adaptation to immune modulation.

Authors:  Karine Thivierge; Sophie Cotton; Deborah A Schaefer; Michael W Riggs; Joyce To; Maria E Lund; Mark W Robinson; John P Dalton; Sheila M Donnelly
Journal:  PLoS Negl Trop Dis       Date:  2013-07-11
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