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1.
Eur J Clin Microbiol Infect Dis ; 33(7): 1081-7, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24535571

ABSTRACT

Proteases are essential for the proliferation and growth of bacteria, and are also known to contribute to bacterial virulence. This makes them interesting candidates as diagnostic and therapeutic targets for infectious diseases. In this review, the authors discuss the most recent developments and potential applications for bacterial proteases in the diagnosis and treatment of bacterial infections. Current and future bacterial protease targets are described and their limitations outlined.


Subject(s)
Anti-Bacterial Agents/pharmacology , Bacteria/enzymology , Enzyme Inhibitors/pharmacology , Peptide Hydrolases , Virulence Factors , Anti-Bacterial Agents/isolation & purification , Enzyme Inhibitors/isolation & purification , Humans , Peptide Hydrolases/metabolism , Virulence Factors/metabolism
2.
Antonie Van Leeuwenhoek ; 105(1): 221-8, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24198119

ABSTRACT

Toxin-antitoxin modules are necessary for the mode of action of several antibiotics. One of the most studied toxin-antitoxin modules is the quorum sensing-dependent MazEF system in Escherichia coli. The quorum sensing factor in this system is called the extracellular death factor (EDF), a linear pentapeptide with the sequence NNWNN. In spite of the extensive research on the mazEF system and the involvement of the quorum sensing factor EDF, the effect of EDF itself on bacteria has not yet been studied. In this research, we determined the effect of EDF and variants on cell growth in the Gram-negative bacterium E. coli and the Gram-positive Bacillus globigii. By aligning the zwf gene (from where EDF originates) of different bacterial species, we found 27 new theoretical variants of the peptide. By evaluating growth curves and light microscopy we found that three EDF variants reduced bacterial cell size in B. globigii, but not in E. coli. The D-peptides did not affect cell size, indicating that the effect is stereospecific. Peptides wherein tryptophan was substituted by alanine also did not affect cell size, which indicates that the effect seen is mediated by an intracellular target.


Subject(s)
Bacillus/cytology , Bacillus/metabolism , Oligopeptides/metabolism , Amino Acid Sequence , Bacillus/chemistry , Bacillus/genetics , Escherichia coli/chemistry , Escherichia coli/genetics , Escherichia coli/metabolism , Molecular Sequence Data , Oligopeptides/chemistry , Oligopeptides/genetics , Quorum Sensing , Sequence Alignment
3.
Ned Tijdschr Tandheelkd ; 120(3): 164-7, 2013 Mar.
Article in Dutch | MEDLINE | ID: mdl-23600182

ABSTRACT

The currently available methods for the identification of micro-organisms in a clinical sample are time consuming, complex or lack sensitivity and specificity. Consequently, no tests are available for rapid microbiological diagnostics in dental clinics so far. Based on the fact that bacteria posess unique enzymes for processing dextrorotary amino acids, a rapid method has been developed to detect metabolically active bacteria. Using dextrorotary amino acid containing substrates, Porphyromonas gingivalis could be detected in clinical samples with a specificity of 96-100% within 10 minutes. This new method opens the door for the development of a rapid oral diagnostic microbiological test.


Subject(s)
Bacteriological Techniques/methods , Peptide Hydrolases/analysis , Porphyromonas gingivalis/isolation & purification , Colony Count, Microbial , Humans , Periodontitis/diagnosis , Periodontitis/microbiology , Sensitivity and Specificity , Time Factors
4.
J Periodontal Res ; 47(5): 616-25, 2012 Oct.
Article in English | MEDLINE | ID: mdl-22458637

ABSTRACT

BACKGROUND AND OBJECTIVE: The aim of the study was to compare the detection of Porphyromonas gingivalis using a fluorescence resonance energy transfer (FRET) technology with commonly used diagnostic methods in salivary and subgingival plaque samples from subjects with dental implants. P. gingivalis was considered as a marker for a pathogenic microbiota. MATERIAL AND METHODS: Ninety-seven adult subjects were recruited, including periodontally healthy controls with no dental implants, implant controls with no peri-implant disease and patients with peri-implant disease. Saliva and subgingival/submucosal plaque samples were collected from all subjects and were analyzed using culture, real-time PCR and FRET technology employing P. gingivalis-specific substrates. RESULTS: It was found that the P. gingivalis-specific substrates were highly suitable for detecting the presence of P. gingivalis in saliva and in subgingival plaque samples, showing comparable specificity to culture and real-time PCR. CONCLUSION: We applied the FRET technology to detect P. gingivalis in implant patients with or without an implant condition and in controls without implants. The technique seems suitable for detection of P. gingivalis in both plaque and saliva samples. However, with all three techniques, P. gingivalis was not very specific for peri-implantitis cases. Future work includes fine-tuning the FRET technology and also includes the development of a chair-side application.


Subject(s)
Bacteroidaceae Infections/microbiology , Dental Implants/microbiology , Fluorescence Resonance Energy Transfer/methods , Peri-Implantitis/microbiology , Porphyromonas gingivalis/isolation & purification , Adult , Aged , Aged, 80 and over , Bacterial Load , Bacteriological Techniques/statistics & numerical data , Chromogenic Compounds , Dental Plaque/microbiology , Feasibility Studies , Female , Fluorescence Resonance Energy Transfer/statistics & numerical data , Gingival Hemorrhage/microbiology , Gingival Recession/microbiology , Humans , Male , Middle Aged , Periodontal Pocket/microbiology , Real-Time Polymerase Chain Reaction/statistics & numerical data , Saliva/microbiology , Sensitivity and Specificity , Stomatitis/microbiology
5.
Folia Microbiol (Praha) ; 56(2): 95-102, 2011 Mar.
Article in English | MEDLINE | ID: mdl-21468758

ABSTRACT

We determined the role of Yersinia pestis virulence markers in an animal model of pneumonic plague. Eleven strains of Y. pestis were characterized using PCR assays to detect the presence of known virulence genes both encoded by the three plasmids as well as chromosomal markers. The virulence of all Y. pestis strains was compared in a mouse model for pneumonic plague. The presence of all known virulence genes correlated completely with virulence in the Balb/c mouse model. Strains which lacked HmsF initially exhibited visible signs of disease whereas all other strains (except wild-type strains) did not exhibit any disease signs. Forty-eight hours post-infection, mice which had received HmsF(-) strains regained body mass and were able to control infection; those infected with strains possessing a full complement of virulence genes suffered from fatal disease. The bacterial loads observed in the lung and other tissues reflected the observed clinical signs as did the cytokine changes measured in these animals. We can conclude that all known virulence genes are required for the establishment of pneumonic plague in mammalian animal models, the role of HmsF being of particular importance in disease progression.


Subject(s)
Plague/microbiology , Plague/pathology , Virulence Factors/metabolism , Yersinia pestis/pathogenicity , Animals , Bacterial Load , Bacterial Outer Membrane Proteins/genetics , Bacterial Outer Membrane Proteins/metabolism , Body Weight , Cytokines/metabolism , DNA, Bacterial/genetics , Disease Models, Animal , Genes, Bacterial , Lung/microbiology , Mice , Mice, Inbred BALB C , Plague/mortality , Plasmids/analysis , Polymerase Chain Reaction , Rodent Diseases/microbiology , Rodent Diseases/mortality , Rodent Diseases/pathology , Survival Analysis , Virulence , Virulence Factors/genetics , Yersinia pestis/genetics
6.
Gene Ther ; 11(18): 1391-8, 2004 Sep.
Article in English | MEDLINE | ID: mdl-15229633

ABSTRACT

As small molecule drugs for Duchenne muscular dystrophy (DMD), antisense oligonucleotides (AONs) have been shown to restore the disrupted reading frame of DMD transcripts by inducing specific exon skipping. This allows the synthesis of largely functional Becker muscular dystrophy (BMD)-like dystrophins and potential conversion of severe DMD into milder BMD phenotypes. Thus far we have used 2'-O-methyl phosphorothioate (2OMePS) AONs. Here, we assessed the skipping efficiencies of different AON analogs containing morpholino-phosphorodiamidate, locked nucleic acid (LNA) or peptide nucleic acid (PNA) backbones. In contrast to PNAs and morpholinos, LNAs have not yet been tested as splice modulators. Compared to the most effective 2OMePS AON directed at exon 46, the LNA induced higher skipping levels in myotubes from a human control (85 versus 20%) and an exon 45 deletion DMD patient (98 versus 75%). The morpholino-induced skipping levels were only 5-6%, whereas the PNA appeared to be ineffective. Further comparative analysis of LNA and 2OMePS AONs containing up to three mismatches revealed that LNAs, while inducing higher skipping efficiencies, show much less sequence specificity. This limitation increases the risk of adverse effects elsewhere in the human genome. Awaiting further improvements in oligochemistry, we thus consider 2OMePS AONs currently the most favorable compounds, at least for targeted DMD exon 46 skipping.


Subject(s)
Genetic Therapy/methods , Muscle Cells/metabolism , Muscular Dystrophy, Duchenne/therapy , Oligonucleotides, Antisense/genetics , Base Sequence , Case-Control Studies , Cells, Cultured , Dystrophin/genetics , Electrophoretic Mobility Shift Assay , Exons , Gene Dosage , Humans , Molecular Sequence Data , Muscle Fibers, Skeletal/metabolism , Muscular Dystrophy, Duchenne/metabolism , Oligonucleotides , Oligonucleotides, Antisense/administration & dosage , Sequence Alignment
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