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1.
PLoS One ; 8(6): e66257, 2013.
Article in English | MEDLINE | ID: mdl-23776646

ABSTRACT

Plants produce many compounds that are biologically active, either as part of their normal program of growth and development or in response to pathogen attack or stress. Traditionally, Anadenanthera colubrina, Commiphora leptophloeos and Myracrodruon urundeuva have been used by communities in the Brazilian Caatinga to treat several infectious diseases. The ability to impair bacterial adhesion represents an ideal strategy to combat bacterial pathogenesis, because of its importance in the early stages of the infectious process; thus, the search for anti-adherent compounds in plants is a very promising alternative. This study investigated the ability of stem-bark extracts from these three species to control the growth and prevent biofilm formation of Pseudomonas aeruginosa, an important opportunistic pathogen that adheres to surfaces and forms protective biofilms. A kinetic study (0-72 h) demonstrated that the growth of extract-treated bacteria was inhibited up to 9 h after incubation, suggesting a bacteriostatic activity. Transmission electron microscopy and fluorescence microscopy showed both viable and nonviable cells, indicating bacterial membrane damage; crystal violet assay and scanning electron microscopy demonstrated that treatment strongly inhibited biofilm formation during 6 and 24 h and that matrix production remained impaired even after growth was restored, at 24 and 48 h of incubation. Herein, we propose that the identified (condensed and hydrolyzable) tannins are able to inhibit biofilm formation via bacteriostatic properties, damaging the bacterial membrane and hindering matrix production. Our findings demonstrate the importance of this abundant class of Natural Products in higher plants against one of the most challenging issues in the hospital setting: biofilm resilience.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacterial Adhesion/drug effects , Biofilms/drug effects , Pseudomonas aeruginosa/drug effects , Tannins/pharmacology
2.
Ticks Tick Borne Dis ; 4(5): 366-76, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23583751

ABSTRACT

Rhipicephalus (Boophilus) microplus is constantly challenged during its life cycle by microorganisms present in their hosts or in the environment. Tick eggs may be especially vulnerable to environmental conditions because they are exposed to a rich and diverse microflora in the soil. Despite being oviposited in such hostile sites, tick eggs remain viable, suggesting that the egg surface has defense mechanisms against opportunistic and/or pathogenic organisms. R. microplus engorged females deposit a superficial wax layer onto their eggs during oviposition. This egg wax is essential for preventing desiccation as well as acting as a barrier against attack by microorganisms. In this study, we report the detection of anti-biofilm activity of R. microplus egg wax against Pseudomonas aeruginosa PA14. Genes involved in the functions of production and maintenance of the biofilm extracellular matrix, pelA and cdrA, respectively, were markedly downregulated by a tick egg-wax extract. Moreover, this extract strongly inhibited fliC gene expression. Instead of a compact extracellular matrix, P. aeruginosa PA14 treated with egg-wax extract produces a fragile one. Also, the colony morphology of cells treated with egg-wax extract appears much paler and brownish, instead of the bright purple characteristic of normal colonies. Swarming motility was also inhibited by treatment with the egg-wax extract. The inhibition of P. aeruginosa biofilm does not seem to depend on inhibition of the quorum sensing system since mRNA levels of the 3 regulators of this system were not inhibited by egg-wax extract.


Subject(s)
Anti-Bacterial Agents/pharmacology , Biofilms/drug effects , Gene Expression Regulation, Bacterial/drug effects , Ovum/chemistry , Pseudomonas aeruginosa/drug effects , Rhipicephalus/chemistry , Adhesins, Bacterial/drug effects , Adhesins, Bacterial/genetics , Animals , Anti-Bacterial Agents/isolation & purification , Bacterial Proteins/drug effects , Bacterial Proteins/genetics , Cattle , Down-Regulation , Extracellular Matrix/drug effects , Extracellular Matrix/metabolism , Female , Microscopy, Electron, Scanning , Ovum/microbiology , Oxidative Stress , Pseudomonas aeruginosa/cytology , Pseudomonas aeruginosa/physiology , RNA, Bacterial/genetics , Rhipicephalus/microbiology , Virulence
3.
Environ Microbiol ; 15(7): 2008-18, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23419060

ABSTRACT

The cattle tick Rhipicephalus (Boophilus) microplus lays eggs in the soil near the roots of grass, or in similar highly moist environments that are prone to biofilm formation. Tick eggs have a protective wax coating that may be a source of nutrients for microorganisms. However, as the eggs remain viable and show no visible signs of microbial colonization, we hypothesized that the coating might have anti-biofilm properties. We show here that the coating inhibits biofilm formation by both Gram-negative and Gram-positive bacteria, though by different mechanisms. We have identified the anti-biofilm molecule as N-(3-sulfooxy-25-cholest-5-en-26-oyl)-L-isoleucine (boophiline), and we show that it inhibits the expression of fliC (flagellin) and cdrA (biofilm scaffold), whose products are necessary for biofilm formation in Pseudomonas aeruginosa. Boophiline is a novel biofilm inhibitor being also effective against Staphylococcus epidermidis biofilm. In our study we show evidences of the boophiline mode of action in the protection of arthropod eggs against biofilm colonization.


Subject(s)
Bacteria/drug effects , Biofilms/drug effects , Cholestenes/pharmacology , Isoleucine/analogs & derivatives , Rhipicephalus/chemistry , Rhipicephalus/microbiology , Animals , Anti-Bacterial Agents/isolation & purification , Anti-Bacterial Agents/pharmacology , Cholestenes/isolation & purification , Gene Expression Regulation, Bacterial/drug effects , Isoleucine/isolation & purification , Isoleucine/pharmacology , Ovum/chemistry , Ovum/microbiology , Pseudomonas aeruginosa/drug effects
4.
Int J Parasitol ; 42(7): 635-45, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22584130

ABSTRACT

The cattle tick, Rhipicephalus (Boophilus) microplus, is a haematophagous arthropod responsible for considerable losses in the livestock industry. Immunological control with vaccines is a promising alternative to replace chemical acaricides. Due to their importance in parasite physiology, cysteine endopeptidases are potential targets. In a previous study, native Vitellin Degrading Cysteine Endopeptidase (VTDCE) was successfully tested as a vaccine antigen for bovines against R. microplus. In this work, nucleotide and amino acid VTDCE sequences were obtained from cDNA databanks, based on data from Edman sequencing and mass spectrometry. Subsequently, cloning and expression, purification, immunological and biochemical characterisation of the recombinant protein were performed to determine the biological importance of VTDCE. By Western blot, polyclonal antibodies produced against recombinant VTDCE recognised native VTDCE. Interestingly, molecular analysis showed that the VTDCE sequence has similarity to antimicrobial peptides. Indeed, experimental results revealed that VTDCE has an antimicrobial activity which is independent of endopeptidase activity. We believe that this is the first known study to show that an arthropod enzyme has antimicrobial activity.


Subject(s)
Cathepsins/metabolism , Rhipicephalus/enzymology , Rhipicephalus/physiology , Amino Acid Sequence , Animals , Anti-Infective Agents/metabolism , Base Sequence , Cathepsins/chemistry , Cathepsins/genetics , Cloning, Molecular , DNA, Complementary/genetics , Female , Gene Expression , Mass Spectrometry , Molecular Sequence Data , Peptides/metabolism , Recombinant Proteins/isolation & purification , Recombinant Proteins/metabolism , Rhipicephalus/genetics , Rhipicephalus/immunology , Sequence Analysis, DNA , Sequence Analysis, Protein
5.
Bioorg Med Chem ; 16(2): 771-82, 2008 Jan 15.
Article in English | MEDLINE | ID: mdl-17967541

ABSTRACT

A series of new piperazine derivatives of ursolic acid was synthesized and tested against Plasmodium falciparum strains. They were also tested on their cytotoxicity effects upon MRC-5 cells. Seven new piperazinyl analogues showed significant activity in the nanomolar range (IC(50)=78-167nM) against Plasmodium falciparum CQ-resistant strain FcB1. A possible mechanism of interaction implicating binding of these compounds to beta-hematin was supported by in vitro tests. Moreover, the importance of the hydrophilic framework attached at the terminal nitrogen atom of the bis-(3-aminopropyl)piperazine joined to the triterpene ring was also explored through molecular dynamic simulations.


Subject(s)
Antimalarials , Piperazines , Plasmodium falciparum/drug effects , Triterpenes , Animals , Antimalarials/chemical synthesis , Antimalarials/chemistry , Antimalarials/pharmacokinetics , Antimalarials/pharmacology , Combinatorial Chemistry Techniques , Ilex paraguariensis/chemistry , Inhibitory Concentration 50 , Molecular Structure , Parasitic Sensitivity Tests , Piperazines/chemical synthesis , Piperazines/chemistry , Piperazines/pharmacokinetics , Piperazines/pharmacology , Plants, Medicinal/chemistry , Structure-Activity Relationship , Triterpenes/chemical synthesis , Triterpenes/chemistry , Triterpenes/pharmacokinetics , Triterpenes/pharmacology , Ursolic Acid
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