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1.
Med Vet Entomol ; 36(2): 159-167, 2022 06.
Article in English | MEDLINE | ID: mdl-34910823

ABSTRACT

Spiders are often wrongly designated as responsible for cutaneous eruptions. We aim to describe spider bites and the spider species implicated in metropolitan France. A retrospective observational study was conducted for all reported cases of spider bites from 2007 to 2018 extracted from the French Poison Control Centers (PCCs) information system, after exclusion of non-native spiders. We described identification of the spider, level of certainty of the bite, symptoms and severity of cases. 1194 cases of spider bites met the inclusion criteria. The average age of the patients was 36.9 ± 19.8 years. Identification of the species or at least that a spider was implicated was only possible in 346 cases (29.0%). Loxosceles were involved in 53 cases (4.4%), Latrodectus in 46 cases (3.9%) and Cheiracanthium in 35 cases (2.9%). In one third of cases, the involved spider was not known to be present where the bite occurred. Where most of the patients (n = 1111, 93%) reported at least one cutaneous symptom, most of the symptoms were neurological. The bite was considered proven in only 242 cases (20%). Despite the efforts of arachnologists to educate the public, the fear of spiders is still alive in France, where spider bite is rare with low severity and often unproven.


Subject(s)
Spider Bites , Spiders , Animals , France/epidemiology , Phobic Disorders , Retrospective Studies , Spider Bites/epidemiology , Spider Bites/veterinary
2.
Zoonoses Public Health ; 66(2): 254-258, 2019 03.
Article in English | MEDLINE | ID: mdl-30460779

ABSTRACT

Bat rabies cases are attributed in Europe to five different Lyssavirus species of 16 recognized Lyssavirus species causing rabies. One of the most genetically divergent Lyssavirus spp. has been detected in a dead Miniopterus schreibersii bat in France. Brain samples were found positive for the presence of antigen, infectious virus and viral RNA by classical virological methods and molecular methods respectively. The complete genome sequence was determined by next-generation sequencing. The analysis of the complete genome sequence confirmed the presence of Lleida bat lyssavirus (LLEBV) in bats in France with 99.7% of nucleotide identity with the Spanish LLEBV strain (KY006983).


Subject(s)
Chiroptera/virology , Lyssavirus/isolation & purification , RNA, Viral/analysis , Rhabdoviridae Infections/veterinary , Animals , Brain/virology , Genome, Viral , High-Throughput Nucleotide Sequencing , Lyssavirus/genetics , Phylogeny , RNA, Viral/genetics , Rabies/virology , Rhabdoviridae Infections/virology
3.
FEMS Microbiol Lett ; 364(22)2017 Dec 01.
Article in English | MEDLINE | ID: mdl-29069388

ABSTRACT

Usually living as a soil saprophyte, the filamentous fungus Scedosporium boydii may also cause various infections in human. Particularly, it is one of the major causative agents of fungal colonization of the airways in patients with cystic fibrosis (CF). To compete with other microorganisms in the environment, fungi have evolved sophisticated strategies, including the production of secondary metabolites with antimicrobial activity that may also help them to establish successfully within the respiratory tract of receptive hosts. Here, the culture filtrate from a human pathogenic strain of S. boydii was investigated searching for an antibacterial activity, mainly against the major CF bacterial pathogens. A high antibacterial activity against Staphylococcus aureus, including methicillin-resistant strains of this species, was observed. Bio-guided fractionation and analysis of the active fractions by nuclear magnetic resonance or by high-performance liquid chromatography and high-resolution electrospray ionization-mass spectrometry allowed us to identify boydone A as responsible for this antibacterial activity. Together, these results suggest that this six-membered cyclic polyketide could be one of the virulence factors of the fungus. Genes involved in the synthesis of this secreted metabolite are currently being identified in order to confirm the role of this polyketide in pathogenesis.


Subject(s)
Lung Diseases, Fungal/microbiology , Polyketides/pharmacology , Scedosporium/metabolism , Staphylococcus aureus/drug effects , Anti-Bacterial Agents/metabolism , Anti-Bacterial Agents/pharmacology , Chromatography, High Pressure Liquid , Cystic Fibrosis/microbiology , Humans , Liquid-Liquid Extraction , Polyketides/metabolism , Scedosporium/chemistry
4.
Microb Pathog ; 110: 56-65, 2017 Sep.
Article in English | MEDLINE | ID: mdl-28629723

ABSTRACT

Free radicals are often described as chemical compounds characterized by unpaired electrons in their outer orbital rendering them highly reactive species. In mammalians, studies on free radicals were focused on reactive oxygen species (ROS) or reactive nitrogen species (RNS) due to their relative importance in physiological as well as in pathological processes. These cellular compounds are produced by different physiological systems such as the aerobic metabolism and play a major role in cell signaling pathways but also in the host immune defenses against pathogenic microorganisms. ROS and RNS are highly reactive species with potentially harmful effects on any cellular components (lipids, proteins and nucleic acids) when produced with a high level. To maintain ROS and RNS at a non-toxic concentration, enzymatic and non-enzymatic cellular antioxidants coordinate the balance between their production and their degradation. Superoxide dismutases, catalases, glutathione system, thioredoxin system, peroxidase systems, flavohemoglobins and nitrate or nitrite reductases represent the prominent enzymatic antioxidants used to scavenge excess of internal as well as external ROS and RNS. Bacteria, fungi and parasites also display similar enzymatic activities to escape the host oxidative defenses during the immune response against infectious processes. Here we summarize current knowledge on the enzymatic systems that allow microorganisms to fight against ROS and RNS, and shed light on the role that take some of them in microbial infections. Such microbial protective systems are considered as virulence factors, and therefore represent key targets for diagnosis of the infections or development of anti-infectious drugs.


Subject(s)
Antioxidants/metabolism , Microbiological Phenomena , Parasites/physiology , Reactive Nitrogen Species/metabolism , Reactive Oxygen Species/metabolism , Animals , Bacteria/enzymology , Bacteria/pathogenicity , Bacterial Proteins/metabolism , Catalase/metabolism , Fungi/enzymology , Fungi/pathogenicity , Fungi/physiology , Glutathione/metabolism , Hemeproteins/metabolism , Host-Parasite Interactions/immunology , Humans , Metabolic Detoxication, Phase I , Oxidation-Reduction , Parasites/enzymology , Parasites/pathogenicity , Peroxidase/metabolism , Signal Transduction , Superoxide Dismutase/metabolism , Thioredoxins/metabolism , Virulence Factors
5.
Clin Vaccine Immunol ; 22(1): 37-45, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25355796

ABSTRACT

Scedosporium boydii is an opportunistic filamentous fungus which may be responsible for a wide variety of infections in immunocompetent and immunocompromised individuals. This fungus belongs to the Scedosporium apiospermum species complex, which usually ranks second among the filamentous fungi colonizing the airways of patients with cystic fibrosis (CF) and may lead to allergic bronchopulmonary mycoses, sensitization, or respiratory infections. Upon microbial infection, host phagocytic cells release reactive oxygen species (ROS), such as hydrogen peroxide, as part of the antimicrobial response. Catalases are known to protect pathogens against ROS by detoxification of the hydrogen peroxide. Here, we investigated the catalase equipment of Scedosporium boydii, one of the major pathogenic species in the S. apiospermum species complex. Three catalases were identified, and the mycelial catalase A1 was purified to homogeneity by a three-step chromatographic process. This enzyme is a monofunctional tetrameric protein of 460 kDa, consisting of four 82-kDa glycosylated subunits. The potential usefulness of this enzyme in serodiagnosis of S. apiospermum infections was then investigated by an enzyme-linked immunosorbent assay (ELISA), using 64 serum samples from CF patients. Whatever the species involved in the S. apiospermum complex, sera from infected patients were clearly differentiated from sera from patients with an Aspergillus fumigatus infection or those from CF patients without clinical and biological signs of a fungal infection and without any fungus recovered from sputum samples. These results suggest that catalase A1 is a good candidate for the development of an immunoassay for serodiagnosis of infections caused by the S. apiospermum complex in patients with CF.


Subject(s)
Antibodies, Fungal/blood , Antigens, Fungal , Catalase , Cystic Fibrosis/complications , Mycoses/diagnosis , Scedosporium/enzymology , Antigens, Fungal/chemistry , Antigens, Fungal/isolation & purification , Catalase/chemistry , Catalase/isolation & purification , Chromatography, Liquid/methods , Enzyme-Linked Immunosorbent Assay/methods , Humans , Molecular Weight , Mycelium/enzymology , Protein Multimerization , Serologic Tests/methods
6.
PLoS One ; 9(6): e98622, 2014.
Article in English | MEDLINE | ID: mdl-24892287

ABSTRACT

Since bat rabies surveillance was first implemented in France in 1989, 48 autochthonous rabies cases without human contamination have been reported using routine diagnosis methods. In this retrospective study, data on bats submitted for rabies testing were analysed in order to better understand the epidemiology of EBLV-1 in bats in France and to investigate some epidemiological trends. Of the 3176 bats submitted for rabies diagnosis from 1989 to 2013, 1.96% (48/2447 analysed) were diagnosed positive. Among the twelve recognised virus species within the Lyssavirus genus, two species were isolated in France. 47 positive bats were morphologically identified as Eptesicus serotinus and were shown to be infected by both the EBLV-1a and the EBLV-1b lineages. Isolation of BBLV in Myotis nattereri was reported once in the north-east of France in 2012. The phylogenetic characterisation of all 47 French EBLV-1 isolates sampled between 1989 and 2013 and the French BBLV sample against 21 referenced partial nucleoprotein sequences confirmed the low genetic diversity of EBLV-1 despite its extensive geographical range. Statistical analysis performed on the serotine bat data collected from 1989 to 2013 showed seasonal variation of rabies occurrence with a significantly higher proportion of positive samples detected during the autumn compared to the spring and the summer period (34% of positive bats detected in autumn, 15% in summer, 13% in spring and 12% in winter). In this study, we have provided the details of the geographical distribution of EBLV-1a in the south-west of France and the north-south division of EBLV-1b with its subdivisions into three phylogenetic groups: group B1 in the north-west, group B2 in the centre and group B3 in the north-east of France.


Subject(s)
Chiroptera/virology , Rabies/epidemiology , Animals , Female , France , Humans , Male , Phylogeny , RNA, Viral/genetics , Rabies virus/classification , Rabies virus/pathogenicity , Retrospective Studies
7.
Mycopathologia ; 176(5-6): 319-28, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23982284

ABSTRACT

Clinical reports have established that mucormycosis, mainly caused by Rhizopus spp., frequently occurs in patients treated with deferoxamine B (DFO, Desferal(®)) which is misappropriated by these fungi. Siderophore production by twenty mucoralean isolates was therefore investigated using a commercial iron-depleted culture medium. Siderophore production was detected for most of the isolates. Our experiments confirmed that feroxamine B (iron chelate of DFO) promoted in vitro growth of Rhizopus arrhizus. Electrophoretic analysis of somatic extracts revealed iron-regulated proteins of 60 and 32 kDa which were lacking in iron-depleted culture conditions. Using a fluorescent derivative of deferoxamine B, we showed by fluorescence microscopy the entry of the siderophore within the fungal cells, thus suggesting a shuttle mechanism encompassing the uptake of the entire siderophore-ion complex into the cell. This useful tool renders possible a better understanding of iron metabolism in Mucorales which could lead to the development of new diagnostic method or new antifungal therapy using siderophores as imaging contrast agents or active drug vectors.


Subject(s)
Deferoxamine/metabolism , Mucorales/metabolism , Siderophores/metabolism , Culture Media/chemistry , Electrophoresis , Fungal Proteins/analysis , Fungal Proteins/chemistry , Microscopy, Fluorescence , Molecular Weight , Mucorales/growth & development
8.
J Inorg Biochem ; 126: 76-83, 2013 Sep.
Article in English | MEDLINE | ID: mdl-23792913

ABSTRACT

The reaction of nickel(II), copper(II) chlorides and cadmium(II) chloride and bromide with thiophene-2,3-dicarboxaldehyde bis(thiosemicarbazone) (2,3BTSTCH2) leads to a series of new complexes: [Ni(2,3BTSTCH)]Cl, [Cu(2,3BTSTC)], [CdCl2(2,3BTSTCH2)] and [CdBr2(2,3BTSTCH2)]. The crystal structures of the ligand and of [Ni(2,3BTSTCH)]Cl complex have been determined. In this case, we remark an unusual non-symmetrical coordination mode for the two functional groups: one acting as a thione and the second as a deprotonated thiolate. All compounds have been tested for their antifungal activity against human pathogenic fungi: Candida albicans, Candida glabrata and Aspergillus fumigatus, the cadmium complexes exhibit the highest antifungal activity. Cytotoxicity was evaluated using two biological methods: human MRC5 cultured cells and brine shrimp Artemia salina bioassay.


Subject(s)
Antifungal Agents/chemical synthesis , Cadmium Chloride/chemistry , Coordination Complexes/chemical synthesis , Copper/chemistry , Nickel/chemistry , Thiosemicarbazones/chemistry , Animals , Antifungal Agents/pharmacology , Artemia/drug effects , Aspergillus fumigatus/drug effects , Aspergillus fumigatus/growth & development , Candida albicans/drug effects , Candida albicans/growth & development , Candida glabrata/drug effects , Candida glabrata/growth & development , Cell Line , Cell Survival/drug effects , Coordination Complexes/pharmacology , Crystallography, X-Ray , Fibroblasts/cytology , Fibroblasts/drug effects , Humans , Microbial Sensitivity Tests , Molecular Structure
9.
Mini Rev Med Chem ; 13(9): 1311-26, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23701657

ABSTRACT

Naturally occurring hydroxamic acid derivatives are biosynthesized by microorganisms (siderophores) and plants (benzoxazinoids). Recent developments in drug discovery have highlighted the numerous biological and pharmacological properties that the hydroxamic acid function may possess, leading to therapeutic applications. These properties may be explained by its ability to chelate metals via the presence of two oxygen atoms. Their pharmacological activities can be divided into three groups. The first concerns the ability of these hydroxamic acid derivatives to scavenge metals (particularly iron), which leads to antioxidant, antimicrobial and metal detoxification activities. The latter is largely used to treat iron overload in patients. The second group of activities is related to their ability to inhibit metallo-enzymes, which gives them a wide range of pharmacological effects: antimicrobial, anti-inflammatory and antitumor. The third group is linked to the capacity of these compounds to generate nitric oxide, which confers hypotensive activity. However, hydroxamates exhibit relatively low stability in vivo, which can be overcome by the synthesis of appropriately designed analogs. For this purpose, many different strategies have been proposed. In this review, we compare and discuss the various synthetic pathways used to obtain the most complex of them, the N-substituted hydroxamic acids. We conclude that among numerous protocols reported so far, the direct N-substitution of hydroxamic acids, the acylation of the appropriate N-O derivative and the direct oxidation of the corresponding amide allow for the synthesis of a wide range of new biologically active compounds.


Subject(s)
Hydroxamic Acids/pharmacology , Animals , Humans
10.
Vet Microbiol ; 151(3-4): 390-5, 2011 Aug 05.
Article in English | MEDLINE | ID: mdl-21570221

ABSTRACT

Active surveillance of bats in France started in 2004 with an analysis of 18 of the 45 bat species reported in Europe. Rabies antibodies were detected in six indigenous species, mainly in Eptesicus serotinus and Myotis myotis, suggesting previous contact with the EBLV-1 rabies virus. Nineteen of the 177 tested bats were shown serologically positive in seven sites, particularly in central and south-western France. Neither infectious viral particles nor viral genomes were detected in 173 and 308 tested oral swabs, respectively. The presence of neutralising antibodies in female bats (18.6%) was significantly higher than in males (5.6%).


Subject(s)
Chiroptera/virology , Rabies virus/isolation & purification , Rabies/epidemiology , Animals , Antibodies, Neutralizing/blood , Antibodies, Viral/blood , Chiroptera/immunology , Female , France/epidemiology , Male , RNA, Viral/analysis , Rabies/virology
11.
Mycopathologia ; 171(1): 11-21, 2011 Jan.
Article in English | MEDLINE | ID: mdl-20617462

ABSTRACT

Resistance to 5-fluorocytosine (5-FC) has been poorly investigated in the yeast Candida glabrata. This study was conducted on laboratory mutants obtained by exposure of a wild-type isolate to 5-FC. Based on their susceptibility to 5-fluorouracil (5-FU), two of these mutants were selected for further analysis of the molecular mechanisms of 5-FC resistance. One mutant, resistant to both compounds, exhibited a missense mutation in the gene coding the cytosine deaminase and a decrease in the expression level of the gene coding the uridine monophosphate pyrophosphorylase. The other mutant that showed a reduced susceptibility to 5-FC and 5-FU exhibited an overexpression of the genes coding the thymidylate synthase and a cytosine permease, associated with a missense mutation in the last gene. Thus, beside mutations in the FUR1 gene which represent the most common cause of resistance to 5-FC, other mechanisms may also occur in C. glabrata.


Subject(s)
Antifungal Agents/pharmacology , Candida glabrata/drug effects , Drug Resistance, Fungal , Flucytosine/pharmacology , Amino Acid Substitution , Cytosine Deaminase/genetics , DNA Mutational Analysis , Fluorouracil/pharmacology , Gene Expression , Mutation, Missense , Pentosyltransferases/biosynthesis , Thymidylate Synthase/biosynthesis
12.
Med Mycol ; 48 Suppl 1: S98-107, 2010 Nov.
Article in English | MEDLINE | ID: mdl-21067336

ABSTRACT

Scedosporium apiospermum is an emerging pathogen colonizing the airways of patients with cystic fibrosis (CF). While usually responsible for chronic colonization without clinical signs, this fungus may cause severe and often lethal infections in lung transplant recipients. Early diagnosis of its airway colonization and appropriate treatment are required to eradicate the fungus when a lung transplantation is planned. Here we propose an alternative to mycological examination of sputum samples based on extraction of siderophores by chromatography on Amberlite XAD-4, followed by high performance liquid chromatography analysis of the siderophore extract. Improvement of the extraction procedure was performed in a fractional factorial design which revealed the importance of prior ammonium sulfate precipitation of the proteins, alkalinization of the obtained solution and stirring during extraction. In order to verify the specificity of N(α)-methyl coprogen B for S. apiospermum, the method was applied on culture supernatants of different filamentous fungi colonizing the airways of CF patients, including some aspergilli and Exophiala dermatitidis. N(α)-methyl coprogen B was detected exclusively for species of the S. apiospermum complex. Likewise, sputum samples from colonized and non-colonized CF patients were analyzed, and the siderophore was detected exclusively in three out of the five specimens which were found by culture to contain S. apiospermum. Together these results confirmed N(α)-methyl coprogen B as a marker of the airway colonization by species of the S. apiospermum complex.


Subject(s)
Biomarkers/analysis , Cystic Fibrosis/microbiology , Hydroxamic Acids/analysis , Lung Diseases, Fungal/diagnosis , Respiratory System/microbiology , Scedosporium/chemistry , Chromatography, High Pressure Liquid , Humans , Hydroxamic Acids/chemistry , Lung Diseases, Fungal/microbiology , Scedosporium/classification , Scedosporium/isolation & purification , Siderophores/analysis , Siderophores/chemistry , Species Specificity , Spectrometry, Mass, Electrospray Ionization , Sputum/microbiology
13.
Biometals ; 22(6): 1019-29, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19597710

ABSTRACT

Scedosporium apiospermum is an emerging pathogen colonizing the airways of patients with cystic fibrosis and causing severe infections in immunocompromised hosts. In order to improve our knowledge on the pathogenic mechanisms of this fungus, we investigated the production of siderophores. Cultivation on CAS medium and specific assays for different classes of siderophores suggested the secretion of hydroxamates. A maximal production was obtained by cultivation of the fungus at alkaline pH in an iron-restricted liquid culture medium. Siderophores were then extracted from the culture filtrate by liquid/liquid extraction, and separated by reverse phase high performance liquid chromatography. Two siderophores, dimerumic acid and Nα-methyl coprogen B, were identified by electrospray ionization-mass spectrometry and MS-MS fragmentation. Finally, comparison of various strains suggested a higher production of Na-methyl coprogen B by clinical isolates of respiratory origin. Studies are initiated in order to determine the potential usefulness of these siderophores as diagnostic markers of scedosporiosis.


Subject(s)
Diketopiperazines/chemistry , Hydroxamic Acids/chemistry , Siderophores/chemistry , Biomarkers , Chromatography, High Pressure Liquid , Culture Media , Diketopiperazines/isolation & purification , Humans , Hydrogen-Ion Concentration , Hydroxamic Acids/isolation & purification , Hydroxybenzoates/analysis , Indicators and Reagents/analysis , Iron/metabolism , Lung Diseases, Fungal/microbiology , Scedosporium/growth & development , Scedosporium/metabolism , Siderophores/isolation & purification , Siderophores/metabolism , Spectrometry, Mass, Electrospray Ionization
14.
J Enzyme Inhib Med Chem ; 23(5): 617-22, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18821251

ABSTRACT

New 1-[2-azido-2-(2,4-dichlorophenyl)ethyl]-1H/-imidazole were synthesized by nucleophilic substitution of various tertiary alcohols with azide anion in presence of boron trifluoride-diethyl etherate. Their antifungal activity was evaluated against Candida albicans, Candida glabrata, Aspergillus fumigatus and an azole-resistant petite mutant of C. glabrata. Preliminary SAR results are discussed.


Subject(s)
Antifungal Agents/chemical synthesis , Imidazoles/pharmacology , Alcohols , Antifungal Agents/pharmacology , Aspergillus fumigatus/drug effects , Azides , Candida albicans/drug effects , Candida glabrata/drug effects , Imidazoles/chemical synthesis , Structure-Activity Relationship
15.
Antimicrob Agents Chemother ; 52(10): 3701-9, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18694952

ABSTRACT

Unlike the molecular mechanisms that lead to azole drug resistance, the molecular mechanisms that lead to polyene resistance are poorly documented, especially in pathogenic yeasts. We investigated the molecular mechanisms responsible for the reduced susceptibility to polyenes of a clinical isolate of Candida glabrata. Sterol content was analyzed by gas-phase chromatography, and we determined the sequences and levels of expression of several genes involved in ergosterol biosynthesis. We also investigated the effects of the mutation harbored by this isolate on the morphology and ultrastructure of the cell, cell viability, and vitality and susceptibility to cell wall-perturbing agents. The isolate had a lower ergosterol content in its membranes than the wild type, and the lower ergosterol content was found to be associated with a nonsense mutation in the ERG6 gene and induction of the ergosterol biosynthesis pathway. Modifications of the cell wall were also seen, accompanied by increased susceptibility to cell wall-perturbing agents. Finally, this mutation, which resulted in a marked fitness cost, was associated with a higher rate of cell mortality. Wild-type properties were restored by complementation of the isolate with a centromeric plasmid containing a wild-type copy of the ERG6 gene. In conclusion, we have identified the molecular event responsible for decreased susceptibility to polyenes in a clinical isolate of C. glabrata. The nonsense mutation detected in the ERG6 gene of this isolate led to a decrease in ergosterol content. This isolate may constitute a useful tool for analysis of the relevance of protein trafficking in the phenomena of azole resistance and pseudohyphal growth.


Subject(s)
Antifungal Agents/pharmacology , Candida glabrata/drug effects , Candida glabrata/genetics , Codon, Nonsense , Genes, Fungal , Polyenes/pharmacology , Azoles/pharmacology , Base Sequence , Candida glabrata/isolation & purification , Candida glabrata/metabolism , Candidiasis/drug therapy , Candidiasis/microbiology , DNA, Fungal/genetics , Drug Resistance, Fungal/genetics , Ergosterol/metabolism , Guanine/analogs & derivatives , Humans , Molecular Sequence Data
16.
J Enzyme Inhib Med Chem ; 22(5): 563-9, 2007 Oct.
Article in English | MEDLINE | ID: mdl-18035824

ABSTRACT

New 2-(2,4-dihalogenophenyl)-1-(1H-imidazol-1-yl)-3-(isoxazol-5-yl)propan-2-ols and 2-(2,4-dihalogenophenyl)-1-(1H-imidazol-1-yl)-3-(4,5-dihydroisoxazol-5-yl)propan-2-ols were synthesized by 1,3-dipolar cycloaddition between homopropargylic or homoallylic alcohols and in-situ generated nitrile oxide. Their antifungal activity was evaluated against Candida albicans, C. glabrata, Aspergillus fumigatus and an azole-resistant petite mutant of C. glabrata. Preliminary SAR results are discussed.


Subject(s)
Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Aspergillus fumigatus/drug effects , Candida albicans/drug effects , Candida glabrata/drug effects , Isoxazoles , Antifungal Agents/chemistry , Candida glabrata/genetics , Isoxazoles/chemical synthesis , Isoxazoles/chemistry , Isoxazoles/pharmacology , Microbial Sensitivity Tests , Molecular Structure , Mutation
17.
Microbes Infect ; 9(5): 558-65, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17395518

ABSTRACT

A Cu,Zn-superoxide dismutase has been characterized from Scedosporium apiospermum, a fungus which often colonizes the respiratory tract of patients with cystic fibrosis. Enzyme production was stimulated by iron starvation. Purification was achieved from mycelial extract from 7-day-old cultures on Amberlite XAD-16. The purified enzyme presented a relative molecular mass of 16.4 kDa under reducing conditions and was inhibited by potassium cyanide and diethyldithiocarbamate, which are two known inhibitors of Cu,Zn-SODs. Its optimum pH was 7.0 and the enzyme retained full activity after pretreatment at temperatures up to 50 degrees C. Moreover, a 450-bp fragment of the gene encoding the enzyme was amplified by PCR using degenerate primers designed from sequence alignment of four fungal Cu,Zn-SODs. Sequence data from this fragment allowed us to design primers which were used to amplify by walking-PCR the flanking regions of the known fragment. SaSODC gene (890 bp) corresponded to a 154 amino acid polypeptide with a predicted molecular mass of 15.9 kDa. A database search for sequence homology revealed for the deduced amino acid sequence 72 and 83% identity rate with Cu,Zn-SODs from Aspergillus fumigatus and Neurospora crassa, respectively. To our knowledge, this enzyme is the first putative virulence factor of S. apiospermum to be characterized.


Subject(s)
Scedosporium/enzymology , Scedosporium/genetics , Superoxide Dismutase/genetics , Amino Acid Sequence , Cloning, Molecular , Copper/metabolism , Sequence Analysis, DNA , Superoxide Dismutase/metabolism , Zinc/metabolism
18.
J Enzyme Inhib Med Chem ; 21(3): 293-303, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16918077

ABSTRACT

Recent studies reported that an first generation azole (tioconazole) was active against Candida glabrata petite mutants, a fluconazole- and voriconazole- resistant strain of fungi characterized as most azole resistant yeast by an overexpression of the efflux pumps. Therefore, monosubstituted 1-[2-(2,4-dichlorophenyl)ethyl]-1H-imidazoles differing from tioconazole by the nature of the linker and of the aromatic ring in their side-chain were synthesized and evaluated against the mutant and the wild-type strain of C. glabrata. New 2-aryl-1-azolyl-3-thienylbutan-2-ols were then designed and synthesized, and their antifungal activity was evaluated against both strains of C. glabrata and two other major human pathogenic fungi, C. albicans and Aspergillus fumigatus. These new compounds exhibited a broad spectrum activity, as well as good efficiency against the petite mutant, suggesting that they may overcome the increased expression of the efflux pumps usually observed in clinical yeast isolates resistant to current azoles.


Subject(s)
Antifungal Agents/chemical synthesis , Antifungal Agents/pharmacology , Azoles/chemical synthesis , Azoles/pharmacology , Candida glabrata/drug effects , Antifungal Agents/chemistry , Aspergillus fumigatus/drug effects , Azoles/chemistry , Candida albicans/drug effects , Drug Design , Imidazoles/chemical synthesis , Imidazoles/chemistry , Imidazoles/pharmacology , In Vitro Techniques , Microbial Sensitivity Tests , Molecular Structure , Species Specificity , Stereoisomerism , Structure-Activity Relationship
19.
Mycopathologia ; 161(6): 369-75, 2006 Jun.
Article in English | MEDLINE | ID: mdl-16761184

ABSTRACT

An exocellular proteinase synthesized by the geophilic dermatophyte Trichophyton vanbreuseghemii has been purified and characterized. The fungus obtained from soil in Iran was cultivated in modified Czapek-Dox liquid medium containing 0.1% bacteriological peptone and 1% glucose as the nitrogen and carbon sources. Partial purification of the proteinase was accomplished by (NH(4))(2)SO(4) precipitation, followed by ion exchange chromatography. Analysis of the enzyme by SDS-PAGE revealed a single polypeptide chain with an apparent molecular mass of 37 kDa. Proteinase activity was optimum at pH 8, but remained high in the range of pH 7-11. Moreover, the partially purified enzyme presented a keratinolytic activity as evidenced by the keratin azure test. The inhibition profile and the good activity of the enzyme towards the synthetic substrate N-succinyl-Ala-Ala-Pro-Phe-p-nitroanilide suggested that it belonged to the chymotrypsin/subtilisin group of serine proteinases. The keratinolytic properties of T. vanbreuseghemii suggest that this fungus may be an alternative for the recycling of industrial keratinic wastes.


Subject(s)
Serine Endopeptidases/metabolism , Trichophyton/enzymology , Chemical Precipitation , Chromatography, Ion Exchange , Hydrogen-Ion Concentration , Italy , Keratins/metabolism , Molecular Weight , Serine Endopeptidases/chemistry , Serine Endopeptidases/isolation & purification , Soil Microbiology
20.
Antimicrob Agents Chemother ; 49(11): 4608-15, 2005 Nov.
Article in English | MEDLINE | ID: mdl-16251302

ABSTRACT

Azole resistance has been insufficiently investigated in the yeast Candida tropicalis. Here we determined the molecular mechanisms responsible for azole resistance in a clinical isolate of this pathogenic yeast. Antifungal susceptibility testing performed by a disk diffusion method showed resistance or markedly decreased susceptibility to azoles, which was confirmed by determination of MICs. Considering the relationship between azole susceptibility and the respiration reported for other yeast species, the respiratory activity of this isolate was investigated. Flow cytometry using rhodamine 123 and oxygraphy demonstrated an increased respiratory activity, which was not linked to an overexpression or increased number of copies of the mitochondrial genome. Among previously described resistance mechanisms, an increased activity of efflux pumps was investigated by flow cytometry using rhodamine 6G. However, the efflux of rhodamine 6G was lower in the resistant isolate than in susceptible ones. Likewise, real-time reverse transcription-PCR quantification of the expression of C. tropicalis MDR1 (CtMDR1), which encodes an efflux protein belonging to the major facilitator superfamily, did not show overexpression of this gene. In contrast, the resistant isolate overexpressed the CtERG11 gene coding for lanosterol 14alpha-demethylase. This was in agreement with the larger amount of ergosterol found in this isolate. Moreover, sequencing of CtERG11 showed a point mutation leading to a tyrosine substitution in the protein sequence, which might lead to decreased binding affinity for azoles. In conclusion, overexpression of CtERG11 associated with a missense mutation in this gene seemed to be responsible for the acquired azole resistance of this clinical isolate.


Subject(s)
Azoles/pharmacology , Candida/drug effects , Drug Resistance, Fungal/genetics , Base Sequence , Candida/genetics , Candida/metabolism , Cytochrome P-450 Enzyme System/genetics , Genes, MDR , Humans , Microbial Sensitivity Tests , Molecular Sequence Data , Mutation, Missense , Oxidoreductases/genetics , Oxygen Consumption/drug effects , Rhodamines/metabolism , Sterol 14-Demethylase , Sterols/analysis
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