Literature DB >> 10601638

SMAP-29: a potent antibacterial and antifungal peptide from sheep leukocytes.

B Skerlavaj1, M Benincasa, A Risso, M Zanetti, R Gennaro.   

Abstract

SMAP-29 is a cathelicidin-derived peptide deduced from sheep myeloid mRNA. The C-terminally amidated form of this peptide was chemically synthesized and shown to exert a potent antimicrobial activity. Antibiotic-resistant clinical isolates highly susceptible to this peptide include MRSA and VREF isolates, that are a major worldwide problem, and mucoid Pseudomonas aeruginosa associated with chronic respiratory inflammation in CF patients. In addition, SMAP-29 is also active against fungi, including Cryptococcus neoformans isolated from immunocompromised patients. SMAP-29 causes significant morphological alterations of the bacterial surfaces, as shown by scanning electron microscopy, and is also hemolytic against human, but not sheep erythrocytes. Its potent antimicrobial activity suggests that this peptide is an excellent candidate as a lead compound for the development of novel antiinfective agents.

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Year:  1999        PMID: 10601638     DOI: 10.1016/s0014-5793(99)01600-2

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  41 in total

1.  Congeners of SMAP29 kill ovine pathogens and induce ultrastructural damage in bacterial cells.

Authors:  V C Kalfa; H P Jia; R A Kunkle; P B McCray; B F Tack; K A Brogden
Journal:  Antimicrob Agents Chemother       Date:  2001-11       Impact factor: 5.191

2.  Communication: Antimicrobial Activity of SMAP28 with a Targeting Domain for Porphyromonas gingivalis.

Authors:  Carol L Bratt; Karl G Kohlgraf; Katie Yohnke; Colleen Kummet; Deborah V Dawson; Kim A Brogden
Journal:  Probiotics Antimicrob Proteins       Date:  2010-03-01       Impact factor: 4.609

3.  Damage of the bacterial cell envelope by antimicrobial peptides gramicidin S and PGLa as revealed by transmission and scanning electron microscopy.

Authors:  Mareike Hartmann; Marina Berditsch; Jacques Hawecker; Mohammad Fotouhi Ardakani; Dagmar Gerthsen; Anne S Ulrich
Journal:  Antimicrob Agents Chemother       Date:  2010-06-07       Impact factor: 5.191

Review 4.  Antimicrobial peptide killing of African trypanosomes.

Authors:  J M Harrington
Journal:  Parasite Immunol       Date:  2011-08       Impact factor: 2.280

5.  Antimicrobial activity and bacterial-membrane interaction of ovine-derived cathelicidins.

Authors:  Rachel C Anderson; Robert E W Hancock; Pak-Lam Yu
Journal:  Antimicrob Agents Chemother       Date:  2004-02       Impact factor: 5.191

6.  Art-175 is a highly efficient antibacterial against multidrug-resistant strains and persisters of Pseudomonas aeruginosa.

Authors:  Yves Briers; Maarten Walmagh; Barbara Grymonprez; Manfred Biebl; Jean-Paul Pirnay; Valerie Defraine; Jan Michiels; William Cenens; Abram Aertsen; Stefan Miller; Rob Lavigne
Journal:  Antimicrob Agents Chemother       Date:  2014-04-21       Impact factor: 5.191

Review 7.  Will new generations of modified antimicrobial peptides improve their potential as pharmaceuticals?

Authors:  Nicole K Brogden; Kim A Brogden
Journal:  Int J Antimicrob Agents       Date:  2011-07-05       Impact factor: 5.283

Review 8.  Properties and mechanisms of action of naturally occurring antifungal peptides.

Authors:  Nicole L van der Weerden; Mark R Bleackley; Marilyn A Anderson
Journal:  Cell Mol Life Sci       Date:  2013-02-05       Impact factor: 9.261

9.  Activity of cathelicidin peptides against Chlamydia spp.

Authors:  Manuela Donati; Korinne Di Leo; Monica Benincasa; Francesca Cavrini; Silvia Accardo; Alessandra Moroni; Renato Gennaro; Roberto Cevenini
Journal:  Antimicrob Agents Chemother       Date:  2005-03       Impact factor: 5.191

10.  Susceptibilities of oral bacteria and yeast to mammalian cathelicidins.

Authors:  J M Guthmiller; K G Vargas; R Srikantha; L L Schomberg; P L Weistroffer; P B McCray; B F Tack
Journal:  Antimicrob Agents Chemother       Date:  2001-11       Impact factor: 5.191

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