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RcAlb-PepII, a synthetic small peptide bioinspired in the 2S albumin from the seed cake of Ricinus communis, is a potent antimicrobial agent against Klebsiella pneumoniae and Candida parapsilosis

Authors :
Jose T.A. Oliveira
Maria Izabel Florindo Guedes
Ilka M. Vasconcelos
Pedro F.N. Souza
Rômulo Farias Carneiro
Maurício Fraga van Tilburg
Daniele O.B. Sousa
Jose L. S. Lopes
Lucas P. Dias
Nadine M.S. Araújo
Source :
Biochimica et biophysica acta. Biomembranes. 1862(2)
Publication Year :
2019

Abstract

Antimicrobial peptides (AMPs) are important constituents of the innate immunity system of all living organisms. They participate in the first line of defense against invading pathogens such as viruses, bacteria, and fungi. In view of the increasing difficulties to treat infectious diseases due to the emergence of antibiotic-resistant bacterial strains, AMPs have great potential to control infectious diseases in humans and animals. In this study, two small peptides, RcAlb-PepI and RcAlb-PepII, were designed based on the primary structure of Rc-2S-Alb, a 2S albumin from the seed cake of Ricinus communis, and their antimicrobial activity assessed. RcAlb-PepII strongly inhibited the growth of Klebsiella pneumoniae and Candida parapsilosis, and induced morphological alterations in their cell surface. C. parapsilosis exposed to RcAlb-PepII presented higher cell membrane permeabilization and elevated content of reactive oxygen species. RcAlb-PepII also degraded and reduced the biofilm formation in C. parapsilosis and in K. pneumonia cells. Experimentally, RcAlb-PepII was not hemolytic and had low toxicity to mammalian cells. These are advantageous characteristics, which suggest that RcAlb-PepII is safe and apparently effective for its intended use and has great potential for the future development of an antimicrobial agent with the ability to kill or inhibit K. pneumoniae and C. parapsilosis cells.

Details

ISSN :
18792642
Volume :
1862
Issue :
2
Database :
OpenAIRE
Journal :
Biochimica et biophysica acta. Biomembranes
Accession number :
edsair.doi.dedup.....dbc506f4d915f8754fbefc85ee6300fd