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Journal ArticleDOI

Thaulin-1: The first antimicrobial peptide isolated from the skin of a Patagonian frog Pleurodema thaul (Anura: Leptodactylidae: Leiuperinae) with activity against Escherichia coli.

TL;DR: Patagonia's biodiversity has been explored from many points of view, however, skin secretions of native amphibians have not been evaluated for antimicrobial peptide research until now and the first peptides described for amphibians of the Pleurodema genus are described.
About: This article is published in Gene.The article was published on 2017-03-20 and is currently open access. It has received 21 citations till now. The article focuses on the topics: Antimicrobial peptides & Pleurodema.

Summary (1 min read)

Introduction

  • The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form.
  • B IPCSH – CONICET, Consejo Nacional de Investigaciones Científicas y Técnicas, Bvd. Brown 2915.

INTRODUCCTION

  • During the last decades there has been a rapid increase in the number of antimicrobial peptides (AMPs) described, with more than 1017 active peptides derived from amphibians (antimicrobial peptide database, APD).
  • Figure 1. (A) Pleurodema thaul distribution from the International Union for Conservation of Nature (IUCN).
  • (B) Collection site area (photo by S. Polcowñuk, used with permission).

RESULTS AND DISCUSSION

  • Preproregions (signal peptide and acidic region boxed white and black respectively) and variable domain (boxed gray) that correspond to mature peptide are AC CE PT ED M AN US CR IP T signaled.
  • It is noteworthy that the highest similarity belongs to membrane proteins described in Gram-negative microorganisms.
  • Synthetic purified and quantified thaulin-1 and Gly-thaulin- 1 peptides showed identical minimal inhibitory concentration (MIC) and minimal bactericidal concentration (MBC) values (Table 4), demonstrating that the mechanism of action is mainly bactericide, not involving a significant inhibitory stage.

CONCLUSIONS

  • This work reports the first four peptides identified from the skin of the Patagonian frog P. thaul.
  • Sequences were analyzed using the Lasergene sequence analysis software (DNASTAR, Inc.).
  • All tests were performed in triplicate and according to CLSI (2012).
  • Cultures of BMDM were supplemented with the different concentrations of the test compounds for 24h.
  • Peptides were tested at different concentrations (15.62–500 µg/mL) according to Bignami [Bignami, 1993] with modifications.

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Citations
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Journal ArticleDOI
TL;DR: A review of the application of surface plasmon resonance and dual polarization interferometry-based biosensors to the study of biomembrane-based systems using both planar mono- or bilayers or liposomes is presented.
Abstract: The molecular analysis of biomolecular-membrane interactions is central to understanding most cellular systems but has emerged as a complex technical challenge given the complexities of membrane structure and composition across all living cells. We present a review of the application of surface plasmon resonance and dual polarization interferometry-based biosensors to the study of biomembrane-based systems using both planar mono- or bilayers or liposomes. We first describe the optical principals and instrumentation of surface plasmon resonance, including both linear and extraordinary transmission modes and dual polarization interferometry. We then describe the wide range of model membrane systems that have been developed for deposition on the chips surfaces that include planar, polymer cushioned, tethered bilayers, and liposomes. This is followed by a description of the different chemical immobilization or physisorption techniques. The application of this broad range of engineered membrane surfaces to bio...

51 citations

Journal ArticleDOI
TL;DR: Ocellatin-PT3 may be promising as a template for the development of novel antimicrobial peptides against P. aeruginosa, and was capable of preventing the proliferation of 48-h mature biofilms at concentrations ranging from 4 to 8× the MIC.
Abstract: Aim To test ocellatin peptides (ocellatins-PT2-PT6) for antibacterial and antibiofilm activities and synergy with antibiotics against Pseudomonas aeruginosa. Materials & methods Normal- and checkerboard-broth microdilution methods were used. Biofilm studies included microtiter plate-based assays and microscopic analysis by confocal laser scanning microscopy and atomic force microscopy. Results Ocellatins were more active against multidrug-resistant isolates of P. aeruginosa than against susceptible strains. Ocellatin-PT3 showed synergy with ciprofloxacin and ceftazidime against multidrug-resistant isolates and was capable of preventing the proliferation of 48-h mature biofilms at concentrations ranging from 4 to 8× the MIC. Treated biofilms had low viability and were slightly more disaggregated. Conclusion Ocellatin-PT3 may be promising as a template for the development of novel antimicrobial peptides against P. aeruginosa. [Formula: see text].

39 citations

Journal ArticleDOI
TL;DR: The biocompatibility of the derivatives was confirmed by the low hemolytic rate (<5%), non-toxic on Artemia salina (LD50%>3000 ppm), and significant index (1-34%) of antioxidant activity, and the results demonstrated that chitosan and its derivatives are promising biomaterials.

27 citations

Journal ArticleDOI
TL;DR: It is concluded that amphibian AAMPs represent an untapped potential source of biologically active agents and merit far greater research interest.
Abstract: Anionic antimicrobial peptides (AAMPs) with net charges ranging from -1 to -8 have been identified in frogs, toads, newts and salamanders across Africa, South America and China. Most of these peptides show antibacterial activity and a number of them are multifunctional, variously showing antifungal activity, anticancer action, neuropeptide function and the ability to potentiate conventional antibiotics. Antimicrobial mechanisms proposed for these AAMPs, include toroidal pore formation and the Shai-Huang-Matsazuki model of membrane interaction along with pH dependent amyloidogenesis and membranolysis via tilted peptide formation. The potential for therapeutic and biotechnical application of these AAMPs has been demonstrated, including the development of amyloid-based nanomaterials and antiviral agents. It is concluded that amphibian AAMPs represent an untapped potential source of biologically active agents and merit far greater research interest.

25 citations


Cites background from "Thaulin-1: The first antimicrobial ..."

  • ...Thaulin-4 DDGEEAE SEAANPE ENTVGG Pleurodema thaul [36]...

    [...]

  • ...He-1 NT NT NT [35] Thaulin-4 NT NT NT [36] Octacidin + NT NT NT [37] Pleurain-C1 + + NT NT [38] Pleurain-C2 NT NT NT NT [38] Brevinin-1-AJ3 NT NT NT NT [39]...

    [...]

  • ...Most recently, thaulin-4, which also has a net charge -8, was isolated from the Chilean four-eyed frog, Pleurodema thaul, which is widely distributed in Argentina and Chile [36]....

    [...]

Journal ArticleDOI
TL;DR: An overview of recent developments in antimicrobial peptides (AMPs), summarizing structural diversity, potential new applications, activity targets and microbial killing responses in general is provided.
Abstract: This review article provides an overview of recent developments in antimicrobial peptides (AMPs), summarizing structural diversity, potential new applications, activity targets and microbial killing responses in general. The use of artificial and natural AMPs as templates for rational design of peptidomimetics are also discussed and some strategies are put forward to curtail cytotoxic effects against eukaryotic cells. Considering the heat-resistant nature, chemical and proteolytic stability of AMPs, we attempt to summarize their molecular targets, examine how these macromolecules may contribute to potential environmental risks vis-a-vis the activities of the peptides. We further point out the evolutional characteristics of the macromolecules and indicate how they can be useful in designing target-specific peptides. Methods are suggested that may help to assess toxic mechanisms of AMPs and possible solutions are discussed to promote the development and application of AMPs in medicine. Even if there is wide exposure to the environment like in the hospital settings, AMPs may instead contribute to prevent healthcare-associated infections so long as ecotoxicological aspects are considered.

24 citations


Cites background from "Thaulin-1: The first antimicrobial ..."

  • ...Summarily, majority of AMPs from sources other than bacteria kill mostly Gram positive bacteria except for a few like G3KL, Thaulin-1 from Pleurodema thaul [87], BnPRP1, MjPen-II from Marsupenaeus japonicus [15] and Scolopendin from Scolopendra subspinipes mutilans [88] which are able to kill Gram negative and/or other microorganisms....

    [...]

References
More filters
Journal ArticleDOI
TL;DR: The phospholipid class-specific changes in membrane acyl chain composition induced by PC depletion are discussed, which identify PC as key player in a novel regulatory mechanism balancing the proportions of bilayer and non-bilayer lipids in yeast.

94 citations


"Thaulin-1: The first antimicrobial ..." refers background in this paper

  • ...Phosphatidylcholine (PC) is commonly present in membranes of eukaryotic organisms [de Kroon, 2007] while, despite variations among species, bacterial membranes tend to contain more lipids with anionic head groups [Epand and Epand, 2009] AC CE PT ED M AN US CR IP T The latter group is effectively…...

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Journal ArticleDOI
TL;DR: Dermaseptins and magainins are two classes of cationic, amphipathic α-helical peptides that have been identified in the skin extracts of frogs Phyllomedusa sauvagei and Xenopus laevis and it is believed that these two peptides are appropriate candidates in the evaluation of newer and safer microbicides spermicides in the future.
Abstract: Sexually transmitted infections (STIs) and human immunodeficiency virus (HIV), the causative agents of acquired immunodeficiency syndrome (AIDS), are two great concerns in the reproductive health of women. Thus, the challenge is to find products with a double activity, on the one hand having antimicrobial/antiviral properties with a role in the reduction of STI, and on the other hand having spermicidal action to be used as a contraceptive. In the absence of an effective microbicide along with the disadvantages of the most commonly used spermicidal contraceptive worldwide, nonoxynol-9, new emphasis has been focused on the development of more potential intravaginal microbicidal agents. Topical microbicides spermicides would ideally provide a female-controlled method of self-protection against HIV as well as preventing pregnancies. Nonoxynol-9, the only recommended microbicide spermicide, damages cervicovaginal epithelium because of its membrane-disruptive properties. Clearly, there is an urgent need to identify new compounds with dual potential microbicidal properties; antimicrobial peptides should be candidates for such investigations. Dermaseptins and magainins are two classes of cationic, amphipathic α-helical peptides that have been identified in the skin extracts of frogs Phyllomedusa sauvagei and Xenopus laevis. Regarding their contraceptive activities and their effect against various STI-causing pathogens, we believe that these two peptides are appropriate candidates in the evaluation of newer and safer microbicides spermicides in the future.

88 citations


Additional excerpts

  • ...…2015], insecticidal [Smith et AC CE PT ED M AN US CR IP T al., 2011], chemotactic [Craik et al., 2010] antioxidant [Guo et al., 2014], spermicidal [Zairi et al., 2009], wound healing [Mangoni et al. 2016]; protease inhibition [Miller et al., 1989] and neuropeptide function [Pukala et al., 2006]…...

    [...]

Journal ArticleDOI
TL;DR: The influences of peptide self‐assembly on the activity and mode of action, and some specific features it introduces to the AMPs, such as particular responsiveness, improved cell selectivity and stability and sustained release are discussed.
Abstract: Antimicrobial peptides (AMPs) are considered as potential antibiotic substitutes because of their potent activities. Previous studies mainly focused on the effects of peptide charges and secondary structures, but the self-assembly of AMPs was neglected. As more and more researchers notice the roles of peptide self-assembly in AMPs, it has been considered as another important property. In this review, we will discuss the influences of peptide self-assembly on the activity and mode of action, and some specific features it introduces to the AMPs, such as particular responsiveness, improved cell selectivity and stability and sustained release. In addition, some methods to design self-assembling AMPs are primarily discussed. With further understanding about the self-assembling regularity, design of particular self-assembling AMPs will be very helpful for their applications, especially in the fields of drug delivery and biomedical engineering. Copyright © 2015 European Peptide Society and John Wiley & Sons, Ltd.

86 citations


"Thaulin-1: The first antimicrobial ..." refers background in this paper

  • ...The role of peptide self-assembly is considered as another important property that influences on the activity and mode of action of peptides such as particular responsiveness, sustained release, improved selectivity and stability [Tian et al., 2015]....

    [...]

Journal ArticleDOI
13 May 2015-PLOS ONE
TL;DR: Fluorescence microscopic studies indicated that the FITC-labeled K4R2-Nal2-S1 preferentially binds cancer cells and causes apoptotic cell death, and a significant inhibition in human lung tumor growth was observed in the xenograft mice treated with K4r2- Nal2 -S1.
Abstract: We describe a strategy to boost anticancer activity and reduce normal cell toxicity of short antimicrobial peptides by adding positive charge amino acids and non-nature bulky amino acid β-naphthylalanine residues to their termini. Among the designed peptides, K4R2-Nal2-S1 displayed better salt resistance and less toxicity to hRBCs and human fibroblast than Nal2-S1 and K6-Nal2-S1. Fluorescence microscopic studies indicated that the FITC-labeled K4R2-Nal2-S1 preferentially binds cancer cells and causes apoptotic cell death. Moreover, a significant inhibition in human lung tumor growth was observed in the xenograft mice treated with K4R2-Nal2-S1. Our strategy provides new opportunities in the development of highly effective and selective antimicrobial and anticancer peptide-based therapeutics.

84 citations


"Thaulin-1: The first antimicrobial ..." refers background in this paper

  • ...…multiple potential applications have been identified for AMPs such as anticancer [Oelkrug et al., 2015; Wu et al., 2014; Gaspar et al., 2013; Chu et al., 2015], insecticidal [Smith et AC CE PT ED M AN US CR IP T al., 2011], chemotactic [Craik et al., 2010] antioxidant [Guo et al., 2014],…...

    [...]

Journal ArticleDOI
TL;DR: Waddell's method of estimating protein concentration by the difference between spectrophotometric absorptions has been reexamined and is probably as accurate a measure of total protein as measurement by nitrogen analysis, with the advantage of being nondestructive.

84 citations

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Frequently Asked Questions (2)
Q1. What contributions have the authors mentioned in the paper "Thaulin-1: the first antimicrobial peptide isolated from the skin of a patagonian frog pleurodema thaul (anura: leptodactylidae: leiuperinae) with activity against escherichia coli" ?

Please cite this article as: Mariela M. Marani, Luis O. Perez, Alyne Rodrigues de Araujo, Alexandra Plácido, Carla F. Sousa, Patrick Veras Quelemes, Mayara Oliveira, Ana G. Gomes-Alves, Mariana Pueta, Paula Gameiro, Ana M. Tomás, Cristina Delerue-Matos, Peter Eaton, Silvia A. Camperi, Néstor G. Basso, Jose Roberto de Souza de Almeida Leite, Thaulin-1: The first antimicrobial peptide isolated from the skin of a Patagonian frog Pleurodema thaul ( Anura: Leptodactylidae: Leiuperinae ) with activity against Escherichia coli. The address for the corresponding author was captured as affiliation for all authors. 

Further work will be performed to explore this application.