alexa Echinoderm Antimicrobial Peptides to Contrast Human Pathogens | OMICS International
ISSN: 2329-6836
Natural Products Chemistry & Research
Make the best use of Scientific Research and information from our 700+ peer reviewed, Open Access Journals that operates with the help of 50,000+ Editorial Board Members and esteemed reviewers and 1000+ Scientific associations in Medical, Clinical, Pharmaceutical, Engineering, Technology and Management Fields.
Meet Inspiring Speakers and Experts at our 3000+ Global Conferenceseries Events with over 600+ Conferences, 1200+ Symposiums and 1200+ Workshops on
Medical, Pharma, Engineering, Science, Technology and Business

Echinoderm Antimicrobial Peptides to Contrast Human Pathogens

Domenico Schillaci1* and Vincenzo Arizza1,2
1Dip. STEBICEF, Università degli Studi di Palermo, Via Archirafi 18, - 90123 Palermo, Italy
2Istituto Euromediterraneo di Scienza e Biotecnologia - 90139 Palermo, Italy
Corresponding Author : Domenico Schillaci
Dip. STEBICEF, Università degli Studi di Palermo
Via Archirafi 18, - 90123 Palermo, Italy
Tel: +3909123891914
E-mail: [email protected]
Received May 18, 2013; Accepted June 18, 2013; Published June 24, 2013
Citation: Schillaci D, Arizza V (2013) Echinoderm Antimicrobial Peptides to Contrast Human Pathogens. Nat Prod Chem Res 1:109. doi: 10.4172/2329-6836.1000109
Copyright: © 2013 Schillaci D, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Related article at
DownloadPubmed DownloadScholar Google

Visit for more related articles at Natural Products Chemistry & Research

Abstract

Increased attention has been focused in marine invertebrates as a source of bioactive molecules for biomedical applications. Many bioactive molecules are part of the innate immune system. Some more recently isolated compounds, mainly from sea urchin and sea cucumber are antimicrobial peptides (AMP) active against Gram positive, Gram negative and fungi. In this review we described the most recent studies on AMP isolated from echinoderms. The AMP are little peptides <10 kDa with cationic charge and amphipathic structure. Recently, it was demonstrated that in the coelomocyte lysates of Paracentrotus. lividus and Holothuria tubulosa AMP are present with activity against staphylococcal and Pseudomonas aeruginosa antibiofilm. The data show the great potential of application of AMPs in biotechnology for developing novel therapeutic agents and as complements to conventional antibiotic therapy to combat the multi - resistant bacterial strains.

Keywords
Antimicrobial peptides; Therapeutic agents; Antibiotic therapy
Introduction
Echinoderms are an ancient group of marine invertebrates that live in both the intertidal and deep sea benthos composed approximately by 7000 extant species that including sea stars (asteroids), sea urchin (echinoids), sea cucumbers (holothurians), brittle stars (ophiuroids) and sea lilies (crinoids). Because, many species live in near the coastal or estuaries waters overloaded with infectious organisms, such as virus, bacteria, fungi and other parasites, they are exposed to a broad variety of challenges to their self-integrity. To survive in high impact environments have evolved efficient defense strategies.
Echinoderms, similarly to other invertebrates, do not possess a specific immune response. Therefore they ensure the protection of their organism and its homeostasis using natural immunity responses. Among the innate immune system humoral components, antimicrobial peptides (AMPs) are the major defense molecules of innate immunity and are widespread in nature. Indeed they are produced by living organisms of all kingdoms throughout the bacteria and animal including fungi and plants [1-8]. Currently, more than 4000 peptides have been isolated and characterized from tissues and organisms and have been listed in the main databases (Table 1), or in journal publications [9].
Usually, AMPs have small molecular weight with no more 100 amino acids and a molecular weight <10 kDa. They differ considerably in amino acid sequence and structural conformation and most of them are positively charged showing a net positive charge of +2 to +9 due to an excess number of acidic, with a hydrophobic face opposite to hydrophilic one. These chemo-physical characteristics allow these peptides to be soluble in water but react simultaneously with the hydrophobic layer of microbial membranes.
The mode of action of AMPs has rarely been addressed and is therefore not yet understood [10]. It is generally agreed that the AMPs are initially recruited on the microbial surface through electrostatic interaction between cationic portion of the peptides and the negativelycharged microbial cell walls and/or membranes. When, the peptide/ lipid ratio increases, the peptides start forming multimers or selfassociating on top of the membrane. When the peptides reach a high concentration they orientate perpendicularly and insert into the bilayer, thereby interfering with membrane integrity. The microorganisms are then destroyed or via membrane destabilization and/or pore formation [10,11] or through interference with several essential metabolic functions, such as protein, nucleic acid and cell wall syntheses acting on nucleic acids and/or enzymatic proteins, leading to bacterial cell death [10-14]. Moreover, it appears that many AMPs may be multifunctional microbicides, acting simultaneously at the cell membrane and internal sites [11].
In invertebrates, AMPs are ubiquitous distributed, found especially in hemolymph and in tissues such as epidermis, gut and respiratory organs where exposure to pathogenic microorganisms is most likely, expressed constitutively or in response to a pathogen stimulus. The AMPs defend the organisms not only through their ability to kill bacteria, but it was shown that they have antitumor effects, mitogenic activity and, most importantly, participate in immunoregulatory mechanisms by modulating signal transduction and cytokine production and/or release [3,11,12,15-22].
The purpose of this mini-review will be to present the most recent data on antimicrobial peptides isolated and characterized in the phylum Echinoderms. In particular we will focus on their structure, biological functions and in their potential application as antimicrobial and antibiofilm agents to contrast human pathogens.
Antimicrobial Peptides in Echinoderms
Truong et al. [23] discovered, for the first time in echinoderm, the presence of AMPs in the coleomic fluid of the sea cucumber Cucumaria frondosa. Since 2001 the number of molecules has increased steadily. They can be mainly found in coelomocytes, the effector cells of immunity, and occasionally in coelomic fluid. In some cases have been also found in the gastrointestinal organs, in the eggs and in the body wall [24]. Many of AMPs are derived from larger proteins that could be enzymatically digested and produce active fragments. This has been demonstrated by Ghanbari et al. [25]. In fact, by digesting the tissues of sea cucumber Actinopyga lecanora with bromelain, peptides with inhibitory activities against respectively Pseudomonas sp., P. aeruginosa and E. coli were obtained and one papain digested fraction showed antibacterial activity against S. aureus. Aleshina et al. [26], found that among the AMPs isolated in starfish Asterias rubens, two peptides were part of histone molecule H2A. Maltseva and co-workers also found that two other peptides were fragments of actin, while one peptide was a fragment of filamin A.
A fraction at low molecular weight (<5kDa) acid extract of Paracentrotus livudus coelomocytes contained an antimicrobial peptide active against Gram positive and Gram negative pathogens [27]. The peptide belonging to the segment (9-19) of a ß-thymosin, a ubiquitous peptide that possesses several biological effects as such as induction of metalloproteinases, chemotaxis, angiogenesis and inhibition of inflammation [28]. The ß thymosins are a family of highly conserved polar 5-kDa peptides originally thought to be thymic hormones. They are present at high concentrations in almost every cell from vertebrate phyla and have several biological functions due to direct and indirect effects on the actin cytoskeleton. ß-Thymosin is also described as one of the AMP of platelets from animals and human beings [29]. There is little information about the function of thymosins in invertebrates, but their presence has been reported in marine invertebrates [30,31] and in insects where they are up regulated by microbial infections [32].
Cystein Rich Antimicrobial Peptides
Antimicrobial peptides in echinoderms are generally heterogeneous molecules and until a few years ago it was not possible to sort them into classes of molecules. Li [33] discovered in Strongylocentrotus droebachiensis two AMPs called Strongylocins (Table 2). The strongylocin peptides are members of the cysteine-rich AMP family, which have six cysteines with three disulfide bonds involved in peptide conformation, stabilization and resistance to proteases [34] and which are crucial for the antimicrobial activity [35,36]. The strongylocins show different pattern with the other members of the family suggesting that the change in molecular conformation could allow resisting to the proteolysis within the coelomocytes and in the coelomic fluid. Homologues are also present in the sister species S. purpuratus, called SpStrongylocins [37]. Furthermore, in S. purpuratus Li et al. [38] have found other two AMPs called centriocins with a potent activity against Gram-positive and Gram-negative bacteria. These are heterodimeric molecules consisting of two subunits, a heavy chain of (30 amino acids) and a light chain (12 amino acids) linked by an intramolecular disulfide bridge. Novel synthetic peptides sequentially derived from the AMP centrocin 1, were recently tested for their anti-infective and antiinflammatory effects [39].
Antimicrobial Biofilm Peptides
The biofilm is a complex community of microbial cells that are associated with a surface and enclosed in a self-produced biopolymer matrix (Figure 1). The capability to organise a biofilm community is present in almost all Gram-negative and Gram positive bacteria and several of them can be highly pathogenic for animals and human beings. The pathogenic role of bacterial biofilms is well known in human health, because they are responsible for chronic infections and device and biomaterial associated infections [40-42].
Antibiotics can be efficacious against planktonic (free living) pathogens but are quite often poorly effective against the bacteria organized in community which can increase antibiotic resistance by up to 1000 fold [43]. Biofilm structured bacteria develop a multifactorial mechanism of resistance to antibiotics, but the most important factor of tolerance is due to the slow growth and low metabolic activity of bacterial cells in the internal layer of community, so they are intrinsically resistant to conventional antibiotics which target dividing and metabolically active cells.
On the contrary, the prevalent mechanism of action of AMPs is due to their ability to permeabilize and/or to form pores within the cytoplasmic membranes, so they have a high potential to act also on slow-growing or even non growing bacteria that exhibit a reduced susceptibility to many antibiotics and represent a reservoir for recurrent biofilm infections. The AMPs also have a high potential for inhibiting biofilm formation, in fact, they can act at several stages of biofilm formation and with different mechanisms of action: they may minimize initial adhesion of microbial cells to abiotic surfaces by altering the adhesive features of abiotic surfaces, or by binding to microbial surfaces via electrostatic interactions, or may prevent biofilm maturation by killing the early surface colonizers, or by inhibiting quorum sensing (QS), that is the communication system used by many bacteria to build a biofilm. QS is a system composed by small molecules that control collective behaviors, such as bioluminescence, virulence factor production, and biofilm formation [44-47].
As shown in Figure 1, biofilm-formation is generally initiated by the attachment of planktonic cells to a surface through weak van der Waals forces and the colonists are anchored tightly or irreversibly by pili (Figure 1a). To recruit other planktonic cells, the initial cells construct various adhesion sites and the matrix, an extracellular polymeric substance (EPS) (Figure 1b). EPS is composed of extracellular DNA, proteins, lipids, and polysaccharides with various configurations [48]. These components are very important targets for overcoming both biofilms and drug-resistant bacteria [49]. During colonization, some bacteria can communicate through a quorum sensing (QS) system. Subsequently, the grown or developed biofilm provides increased antibiotic-resistance to bacterial colonies through cell division and recruitment (Figure 1c). Later, the developed biofilms are dispersed and the bacteria move to other surfaces, (Figure 1d), where the biofilm formation process occurs again.
The mode of action of antibiotic peptides against biofilm is not fully understood, but it is believed that their major targets are cytoplasmic membrane and intracellular molecules [14,50]. It is also believed that it is very difficult for bacteria to develop resistance to antimicrobial peptides because most kill bacterial cells quickly through their actions on the entire cytoplasmic membrane or can act through complex mechanism [51].
Recently our research group has found novel peptides in P. lividus and in H. tubulosa, with a good activity in preventing biofilm formation of important pathogens involved in human and animal diseases, like staphylococcal or P. aeruginosa strains [27,52]. Sub-MIC concentrations of the 5-kDa peptide fraction of the cytosol from coelomocytes of P.lividus were active to inhibit the formation of young (6 hours old) and mature (24 hours old) staphylococcal biofilm [27].
The synthetic peptides derived from AMP of H. tubulosa were able to inhibit biofilm formation against staphylococcal and Pseudomonas aeruginosa strains [53-55].
The anti-adhesion property of the tested peptides could be also very important against food transmitted pathogens and to contrast the biofilm mode of growth of various organisms involved in food spoilage.
In conclusion, the discovery of novel peptides in Echinoderms represents a good starting point to design new synthetic derivatives with modified chemical-physical properties, with the aim to improve their antimicrobial activity against pathogens and their pharmaceutical potential [46,47].
References























































Tables and Figures at a glance

image   image
Table 1   Table 2

Figures at a glance

image
Figure 1
Select your language of interest to view the total content in your interested language
Post your comment

Share This Article

Relevant Topics

Recommended Conferences

Article Usage

  • Total views: 12093
  • [From(publication date):
    June-2013 - May 26, 2018]
  • Breakdown by view type
  • HTML page views : 8250
  • PDF downloads : 3843
 

Post your comment

captcha   Reload  Can't read the image? click here to refresh

Peer Reviewed Journals
 
Make the best use of Scientific Research and information from our 700 + peer reviewed, Open Access Journals
International Conferences 2018-19
 
Meet Inspiring Speakers and Experts at our 3000+ Global Annual Meetings

Contact Us

Agri & Aquaculture Journals

Dr. Krish

[email protected]

1-702-714-7001Extn: 9040

Biochemistry Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Business & Management Journals

Ronald

[email protected]

1-702-714-7001Extn: 9042

Chemistry Journals

Gabriel Shaw

[email protected]

1-702-714-7001Extn: 9040

Clinical Journals

Datta A

[email protected]

1-702-714-7001Extn: 9037

Engineering Journals

James Franklin

[email protected]

1-702-714-7001Extn: 9042

Food & Nutrition Journals

Katie Wilson

[email protected]

1-702-714-7001Extn: 9042

General Science

Andrea Jason

[email protected]

1-702-714-7001Extn: 9043

Genetics & Molecular Biology Journals

Anna Melissa

[email protected]

1-702-714-7001Extn: 9006

Immunology & Microbiology Journals

David Gorantl

[email protected]

1-702-714-7001Extn: 9014

Materials Science Journals

Rachle Green

[email protected]

1-702-714-7001Extn: 9039

Nursing & Health Care Journals

Stephanie Skinner

[email protected]

1-702-714-7001Extn: 9039

Medical Journals

Nimmi Anna

[email protected]

1-702-714-7001Extn: 9038

Neuroscience & Psychology Journals

Nathan T

[email protected]

1-702-714-7001Extn: 9041

Pharmaceutical Sciences Journals

Ann Jose

[email protected]

1-702-714-7001Extn: 9007

Social & Political Science Journals

Steve Harry

[email protected]

1-702-714-7001Extn: 9042

 
© 2008- 2018 OMICS International - Open Access Publisher. Best viewed in Mozilla Firefox | Google Chrome | Above IE 7.0 version
Leave Your Message 24x7