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1.
Mycopathologia ; 185(4): 613-627, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32710392

ABSTRACT

Emmonsia crescens is known as an environmental pathogen causing adiaspiromycosis in small rodents. As the generic name Emmonsia is no longer available for this species, its taxonomic position is re-evaluated. The intraspecific variation of Emmonsia crescens was analyzed using molecular, morphological, and physiological data, and the relationship between frequency of adiaspiromycosis and body temperature of host animals was explored. A North American and a pan-global lineage could be discerned, each with subclusters at low genetic distance. European strains produced the classical type of very large adiaspores, while in the North American lineage adiaspores relatively small, resembling the broad-based budding cells of Blastomyces. Members of the closely related genus Emergomyces may exhibit large, broad-based in addition to small, narrow-based budding cells. We conclude that the morphology of the pathogenic phase in these fungi differs gradationally between species and even populations, and is therefore less suitable as a diagnostic criterion for generic delimitation. Two Emmonsia species are reclassified in Emergomyces.


Subject(s)
Body Temperature , Chrysosporium , Lung Diseases, Fungal , Animals , Chrysosporium/classification , Chrysosporium/pathogenicity , Lung Diseases, Fungal/veterinary
2.
J Clin Microbiol ; 56(1)2018 01.
Article in English | MEDLINE | ID: mdl-29070656

ABSTRACT

Magnusiomyces capitatus and Saprochaete clavata are members of the clade of arthroconidial yeasts that represent emerging opportunistic pulmonary pathogens in immunocompromised patients. Given that standard ribosomal DNA (rDNA) identification often provides confusing results, in this study, we analyzed 34 isolates with the goal of finding new genetic markers for classification using multilocus sequencing and amplified fragment length polymorphism (AFLP). The interspecific similarity obtained using rDNA markers (the internal transcribed spacer [ITS] and large subunit regions) was in the range of 96 to 99%, whereas that obtained using protein-coding loci (Rbp2, Act, and Tef1α) was lower at 89.4 to 95.2%. Ultimately, Rbp2 was selected as the best marker for species distinction. On the basis of cloned ITS data, some strains proved to be misidentified in comparison with the identities obtained with phenotypic characters, protein sequences, and AFLP profiles, indicating that different copies of the ribosomal operon were present in a single species. Antifungal susceptibility testing revealed that voriconazole had the lowest MIC against M. capitatus, while amphotericin B had the lowest MIC against S. clavata Both species exhibited in vitro resistance to fluconazole and micafungin.


Subject(s)
Lung Diseases, Fungal/diagnosis , Pathology, Molecular/methods , Saccharomycetales/genetics , Amplified Fragment Length Polymorphism Analysis/methods , Antifungal Agents/pharmacology , Bacterial Proteins/genetics , Cluster Analysis , DNA, Fungal/genetics , DNA, Ribosomal/genetics , Drug Resistance, Bacterial , Genetic Markers/genetics , Humans , Lung Diseases, Fungal/microbiology , Microbial Sensitivity Tests , Multilocus Sequence Typing , Saccharomycetales/drug effects , Saccharomycetales/physiology , Species Specificity
3.
Microb Pathog ; 125: 43-47, 2018 Dec.
Article in English | MEDLINE | ID: mdl-30194974

ABSTRACT

Chromoblastomycosis is one of the most prevalent implantation fungal infections caused by melanized fungi, affecting individuals with certain risk factors with high morbidity due to its recalcitrant nature. It is difficult to identify the etiological agents and thus a suitable reproductive molecular identification method applicable in developing countries has been investigated. We report the identification of four different fungal causative agents of chromoblastomycosis by reverse line blotting hybridization (RLB) based on biotin-labeled PCR products and amine labeled probes to hybridize. Sixty five reference strains, including type strains, i.e. Fonsecaea pedrosoi, F. monophora, F. nubica, and Phialophora verrucosa, obtained from the CBS-KNAW were included in this study. Internal transcribed spacer 1 (ITS1) regions of relevant species were aligned and adjusted using BIONUMERICS v. 4.61 in order to design four specific probes to identify informative nucleotide polymorphisms. The final identification of these species by RLB assay was concordant with ITS sequencing and showed 100% specificity with no cross hybridization, able to identify all tested strains. The time and cost were less compare to other routine identification methods such as sequencing. This assay allows sensitive and specific simultaneous detection and identification of a different fungal species.


Subject(s)
Ascomycota/classification , Ascomycota/isolation & purification , Chromoblastomycosis/diagnosis , Molecular Diagnostic Techniques/methods , Nucleic Acid Hybridization/methods , Polymerase Chain Reaction/methods , Ascomycota/genetics , Chromoblastomycosis/microbiology , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Humans , Oligonucleotide Probes/genetics , Sensitivity and Specificity , Sequence Analysis, DNA
4.
Med Mycol ; 56(6): 695-702, 2018 Aug 01.
Article in English | MEDLINE | ID: mdl-29228273

ABSTRACT

Detection of species of Exophiala and Scedosporium in the respiratory tracts of cystic fibrosis (CF) patients remains controversial because of highly variable results. The results of our study suggested a significantly higher prevalence and more complex colonization than previously estimated. Approximately 17% (27/162) of clinical sputum samples were found to be positive for Exophiala dermatitidis and 30% (49/162) were positive for Scedosporium apiospermum / S. boydii species complex determined by reverse line blot (RLB) hybridization. In contrast, only 14.2% (23/162) and 1.2% (2/162) of clinical sputa were positive for E. dermatitidis and S. apiospermum / S. boydii species complex when tested by culture, respectively. Molecular detection methods, such as loop-mediated isothermal amplification (LAMP) or reverse line blot (RLB) hybridization, have the potential to become powerful alternatives to selective culture, providing a more realistic understanding on the prevalence of E. dermatitidis and S. apiospermum / S. boydii species complex in the respiratory tract of CF patients.


Subject(s)
Cystic Fibrosis/complications , Exophiala/isolation & purification , Mycoses/complications , Mycoses/diagnosis , Scedosporium/isolation & purification , Sputum/microbiology , Exophiala/genetics , Humans , Nucleic Acid Amplification Techniques , Reproducibility of Results , Respiratory System/microbiology , Scedosporium/genetics , Sensitivity and Specificity , Tubulin/genetics
5.
Mycoses ; 60(6): 358-365, 2017 Jun.
Article in English | MEDLINE | ID: mdl-28111800

ABSTRACT

The opportunistic black yeast are particularly known through the genus Exophiala, characterised by annellidic budding cells. However, this phenotype is polyphyletic within the order Chaetothyriales. Seventeen generic names are available in the family Herpotrichiellaceae, one of which is Exophiala. Future taxonomy will be based on molecular phylogeny; each multi-species clade may qualify for one of these names. This paper focuses on the genus Nadsoniella, which is the oldest valid name in the Herpotrichiellaceae. Despite its exophiala-like phenotype, the type species of Nadsoniella clusters in the jeanselmei-clade, competing with the sympodial genus Rhinocladiella. In contrast, Exophiala competes with morphologically pronounced genera Thysanorea and Veronaea. Replacing the current phenotypic system for phylogenetic nomenclature requires highly stable phylogenies, which currently are not available.


Subject(s)
Exophiala/classification , Phylogeny , DNA, Fungal/genetics , Exophiala/genetics , Exophiala/isolation & purification , Humans , Mitosporic Fungi/classification , Mitosporic Fungi/genetics , Mitosporic Fungi/isolation & purification , Nucleic Acid Amplification Techniques , Sequence Alignment , Sequence Analysis, DNA
6.
Mycopathologia ; 182(7-8): 739-745, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28260132

ABSTRACT

A 37-year-old male living in Oman was seen by his physician with complaints of cough, body aches with bilateral lower limb weakness and on and off fever. He was diagnosed with HIV infection and culture from blood and bone marrow grew Talaromyces marneffei. He had travelled to Malaysia on several occasions. Treatment with liposomal amphotericin B resulted in complete cure. This case is reported for its rarity and unusual presentation to alert clinicians and microbiologists to consider T. marneffei as an etiology in high risk individuals. Our case is the first recorded diagnosis of T. marneffei in Oman.


Subject(s)
Communicable Diseases, Imported/diagnosis , Communicable Diseases, Imported/pathology , HIV Infections/complications , Mycoses/diagnosis , Mycoses/pathology , Talaromyces/isolation & purification , Adult , Communicable Diseases, Imported/microbiology , Humans , Malaysia , Male , Mycoses/microbiology , Oman , Travel
7.
Antimicrob Agents Chemother ; 60(4): 2346-51, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26833164

ABSTRACT

Primary central nervous system phaeohyphomycosis is a fatal fungal infection due mainly to the neurotropic melanized fungiCladophialophora bantiana,Rhinocladiella mackenziei, andExophiala dermatitidis.Despite the combination of surgery with antifungal treatment, the prognosis continues to be poor, with mortality rates ranging from 50 to 70%. Therefore, a search for a more-appropriate therapeutic approach is urgently needed. Ourin vitrostudies showed that with the combination of amphotericin B and flucytosine against these species, the median fractional inhibitory concentration (FIC) indices for strains ranged from 0.25 to 0.38, indicating synergy. By use of Bliss independence analysis, a significant degree of synergy was confirmed for all strains, with the sum ΔE ranging from 90.2 to 698.61%. No antagonism was observed. These results indicate that amphotericin B, in combination with flucytosine, may have a role in the treatment of primary cerebral infections caused by melanized fungi belonging to the orderChaetothyriales Furtherin vivostudies and clinical investigations to elucidate and confirm these observations are warranted.


Subject(s)
Amphotericin B/pharmacology , Antifungal Agents/pharmacology , Exophiala/drug effects , Flucytosine/pharmacology , Saccharomycetales/drug effects , Cerebral Phaeohyphomycosis/microbiology , Cerebral Phaeohyphomycosis/pathology , Culture Media/chemistry , Drug Combinations , Drug Synergism , Exophiala/growth & development , Exophiala/isolation & purification , Exophiala/pathogenicity , Factor Analysis, Statistical , Humans , Microbial Sensitivity Tests , Saccharomycetales/growth & development , Saccharomycetales/isolation & purification , Saccharomycetales/pathogenicity
8.
Transpl Infect Dis ; 18(5): 674-680, 2016 Oct.
Article in English | MEDLINE | ID: mdl-27385317

ABSTRACT

BACKGROUND: Solid organ transplant (SOT) recipients are at risk of infections of the central nervous system. However, the incidence and clinical course of bacterial meningitis in SOT recipients are unclear. We studied occurrence, disease course, and prognosis of bacterial meningitis in SOT recipients in the Netherlands. METHODS: All patients with a medical history of solid organ transplantation were selected from our nationwide prospective cohort study on community-acquired bacterial meningitis in patients >16 years old, performed from March 1, 2006 to October 31, 2014. Data on patient history, symptoms and signs on admission, treatment, and outcome were collected prospectively. For transplant recipients, additional information was collected retrospectively. RESULTS: We identified 6 SOT recipients, all receiving renal transplants. The annual incidence of bacterial meningitis was 7-fold higher (95% confidence interval [CI] 2.94-17.02, P < 0.001) for renal transplant recipients as compared with the general population (9.56 [95% CI 3.98-22.96] vs. 1.35 [95% CI 1.28-1.43] per 100,000 patients per year). One of the 6 patients (17%) presented with the classic presentation of bacterial meningitis (fever, neck stiffness, and change in mental status). Seizures were common, occurring in 33% of patients. Streptococcus pneumoniae and Listeria monocytogenes were identified in 2 patients each, and Escherichia coli and Pseudomonas aeruginosa were both identified once. Four of 6 patients (67%) had an unfavorable functional outcome. CONCLUSION: Bacterial meningitis is a rare but devastating complication of solid organ transplantation. SOT recipients are at high risk for developing meningitis, and recognition of this condition may be difficult, owing to atypical clinical manifestation.


Subject(s)
Community-Acquired Infections/epidemiology , Kidney Transplantation/adverse effects , Meningitis, Bacterial/epidemiology , Transplant Recipients/statistics & numerical data , Adult , Aged , Community-Acquired Infections/complications , Community-Acquired Infections/etiology , Community-Acquired Infections/microbiology , Escherichia coli/isolation & purification , Female , Humans , Incidence , Listeria monocytogenes/isolation & purification , Male , Meningitis, Bacterial/complications , Meningitis, Bacterial/etiology , Meningitis, Bacterial/microbiology , Middle Aged , Netherlands/epidemiology , Prognosis , Prospective Studies , Pseudomonas aeruginosa/isolation & purification , Retrospective Studies , Risk Factors , Streptococcus pneumoniae/isolation & purification
9.
Eur J Clin Microbiol Infect Dis ; 34(1): 115-122, 2015 Jan.
Article in English | MEDLINE | ID: mdl-25079513

ABSTRACT

The diagnosis of invasive pneumococcal pneumonia is based mainly on bacteraemia. Episodes without bacteraemia, but with a positive urinary antigen test (UAT), are considered non-invasive. We determined differences in outcome between patients with bacteraemic and non-bacteraemic/UAT-positive pneumococcal community-acquired pneumonia (CAP). Adult patients with clinical and radiological evidence of CAP with blood cultures and UAT tests performed at presentation in three Dutch laboratories between June 2008 and May 2010 were included. Clinical characteristics were retrospectively extracted from hospital records. Overall, 168 patients had non-bacteraemic/UAT-positive pneumococcal CAP and 123 had bacteraemic pneumococcal CAP. The day-30 mortality was 9% and 13% for non-bacteraemic/UAT-positive and bacteraemic pneumococcal CAP patients, respectively [risk difference -4%, 95% confidence interval (CI) -11% to +3%, p = 0.28]. In a multivariable logistic regression model, age ≥ 65 years, admission to the intensive care unit/coronary care unit (ICU/CCU) and presence of an immunocompromising condition were associated with day-30 mortality. A non-significant association with mortality was found for bacteraemia [odds ratio (OR) 2.21, 95% CI 0.94-5.21, p = 0.07). No such trend was found for UAT positivity. The median lengths of hospital stay were 8 [interquartile range (IQR) 5-14] and 10 (IQR 6-18) days for non-bacteraemic/UAT-positive and bacteraemic pneumococcal CAP patients, respectively (p = 0.05). As compared to non-bacteraemic/UAT-positive pneumococcal CAP, bacteraemic pneumococcal CAP has a stronger association with day-30 mortality.


Subject(s)
Antigens, Bacterial/urine , Community-Acquired Infections/pathology , Pneumonia, Pneumococcal/pathology , Adolescent , Adult , Aged , Aged, 80 and over , Bacteremia/microbiology , Bacteremia/mortality , Bacteremia/pathology , Community-Acquired Infections/microbiology , Female , Humans , Male , Pneumonia, Pneumococcal/complications , Pneumonia, Pneumococcal/mortality , Retrospective Studies , Survival Analysis , Young Adult
10.
Med Mycol ; 53(2): 99-106, 2015 Feb 01.
Article in English | MEDLINE | ID: mdl-25431472

ABSTRACT

Mucormycosis caused, in part, by representatives of the genus Cunninghamella is a severe infection with high mortality in patients with impaired immunity. Several species have been described in the literature as etiologic agents. A DNA barcoding study using ITS rDNA and tef-1α provided concordance of molecular data with conventional characters. The currently accepted Cunninghamella species were well supported in phylogenetic trees of both markers except for C. septata with ITS that clustered in the C. echinulata clade. Sequence variability was distinctly higher for the ITS than for tef-1α. Intraspecific ITS variability of some of the species exceeded that between some closely related species, but the marker remained applicable for species identification. The most variable species for both markers was C. echinulata. Cunninghamella bertholletiae is the main pathogenic species; infections by C. blakesleeana, C. echinulata, and C. elegans are highly exceptional.


Subject(s)
Cunninghamella/classification , Cunninghamella/genetics , DNA Barcoding, Taxonomic , Cluster Analysis , Cunninghamella/isolation & purification , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Humans , Molecular Sequence Data , Mucormycosis/microbiology , Peptide Elongation Factor 1/genetics , Phylogeny , Sequence Analysis, DNA
11.
Euro Surveill ; 20(31)2015 Aug 06.
Article in English | MEDLINE | ID: mdl-26290429

ABSTRACT

Although the disease burden of listeriosis on population level is low, on individual level the impact is high, largely due to severe illness and a high case fatality. Identification of risk factors supports and specifies public health actions needed for prevention. We performed a case­control study to determine host- and food-related risk factors for non-perinatal listeriosis in the Netherlands. Patients with non-perinatal listeriosis reported between July 2008 and December 2013 were compared with controls from a periodic control survey who completed a questionnaire in the same period. Higher age, male sex, underlying disease, especially cancer and kidney disease, and use of immunosuppressive medicine were strong risk factors for acquiring non-perinatal listeriosis. Analysis of the food consumption in the group of cases and controls with underlying diseases did not reveal any high-risk food products. Information and advice should continue to be given to persons at risk of severe listeriosis. Univariate analyses indicate that patients using gastric acid inhibitors are at risk. It is worth adding these patients to the group of susceptible persons.


Subject(s)
Food Contamination , Food Microbiology , Listeria monocytogenes/isolation & purification , Listeriosis/diagnosis , Adult , Age Factors , Aged , Aged, 80 and over , Case-Control Studies , Feeding Behavior , Female , Humans , Listeriosis/epidemiology , Listeriosis/microbiology , Male , Middle Aged , Netherlands/epidemiology , Risk Factors , Sex Distribution , Surveys and Questionnaires , Young Adult
12.
Mycopathologia ; 180(1-2): 7-17, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26093392

ABSTRACT

Ochroconis bacilliformis, O. phaeophora and O. robusta, three novel species of the melanized genus Ochroconis (Sympoventuriaceae, Venturiales), are described, illustrated and distinguished phenotypically and molecularly from previously described species in the genus Ochroconis. Their potential significance for infection of cold-blooded vertebrates is discussed.


Subject(s)
Ascomycota/classification , Ascomycota/isolation & purification , Mycoses/microbiology , Mycoses/veterinary , Animals , Ascomycota/cytology , Ascomycota/genetics , Cluster Analysis , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Genes, rRNA , Microbiological Techniques , Microscopy , Molecular Sequence Data , Phylogeny , RNA, Fungal/genetics , RNA, Ribosomal/genetics , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA , Vertebrates
13.
Antimicrob Agents Chemother ; 58(10): 5877-85, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25070092

ABSTRACT

Scedosporium species show decreased susceptibility to the majority of systemic antifungal drugs. Acquired resistance is likely to disseminate differentially with the mode of exchange of genetic material between lineages. Inter- and intraspecific diversities of Scedosporium species were analyzed for three partitions (rDNA internal transcribed spacer gene [ITS], partial ß-tubulin gene, and amplified fragment length polymorphism profiles), with the aim to establish distribution of resistance between species, populations, and strains. Heterogeneity of and recombination between lineages were determined, and distances between clusters were calculated using a centroid approach. Clinical, geographic, and antifungal data were plotted on diversity networks. Scedosporium minutisporum, Scedosporium desertorum, and Scedosporium aurantiacum were distinguished unambiguously in all partitions and had differential antifungal susceptibility profiles (ASP). Pseudallescheria fusoidea and Pseudallescheria ellipsoidea were indistinguishable from Scedosporium boydii. Pseudallescheria angusta took an intermediate position between Scedosporium apiospermum and S. boydii. Scedosporium boydii and S. apiospermum had identical ASP. Differences in (multi)resistance were linked to individual strains. S. apiospermum and S. boydii showed limited interbreeding and were recognized as valid, sympatric species. The S. apiospermum/S. boydii group, comprising the main clinically relevant Scedosporium species, consists of separate lineages and is interpreted as a complex undergoing sympatric evolution with incomplete lineage sorting. In routine diagnostics, the lineages in S. apiospermum/S. boydii are indicated with the umbrella descriptor "S. apiospermum complex"; individual species can be identified with rDNA ITS with 96.3% confidence. Voriconazole is recommended as the first-line treatment; resistance against this compound is rare.


Subject(s)
Antifungal Agents/pharmacology , Scedosporium/drug effects , Pseudallescheria/drug effects , Voriconazole/pharmacology
14.
J Clin Microbiol ; 52(10): 3531-5, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25009046

ABSTRACT

In this study, we developed rapid and sensitive assays for the detection of Cladophialophora carrionii, a common agent of human chromoblastomycosis. The isothermal techniques evaluated were rolling-circle amplification (RCA), multiplex ligation-dependent probe amplification (MLPA), and loop-mediated isothermal amplification (LAMP). The probes for RCA and MLPA were designed with target sequences in the rDNA internal transcribed spacer gene (ITS) region, and LAMP primers were designed using the elongation factor 1α gene (EF1); these probes and primers specifically amplified DNA of isolates of the species. The three techniques were sufficiently specific and sensitive for discriminating target DNA of C. carrionii from that of related Cladophialophora species and other agents of chromoblastomycosis. RCA, MLPA, and LAMP are advantageous in their reliability and ease of operation compared to standard PCR and conventional methods.


Subject(s)
Ascomycota/isolation & purification , Chromoblastomycosis/diagnosis , Chromoblastomycosis/microbiology , Molecular Diagnostic Techniques/methods , Nucleic Acid Amplification Techniques/methods , Ascomycota/genetics , DNA Primers/genetics , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal Spacer/genetics , Humans , Molecular Sequence Data , Oligonucleotide Probes/genetics , Peptide Elongation Factor 1 , Sensitivity and Specificity , Sequence Analysis, DNA , Time Factors
15.
Eur J Clin Microbiol Infect Dis ; 33(2): 279-84, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24019162

ABSTRACT

Generally accepted laboratory methods that have been used for decades do not reliably distinguish between H. influenzae and H. haemolyticus isolates. H. haemolyticus strains are often incorrectly identified as nontypeable Haemophilus influenzae (NTHi). To distinguish H. influenzae from H. haemolyticus we have created a new database on the matrix-assisted laser desorption ionization time-of-flight mass spectrometry (MALDI-TOF MS) bio-typer 2 and compared the results with routine determination of Haemophilus (growth requirement for X and V factor), and multilocus sequence typing (MLST). In total we have tested 277 isolates, 244 H. influenzae and 33 H. haemolyticus. Using MLST as the gold standard, the agreement of MALDI-TOF MS was 99.6 %. MALDI-TOF MS allows reliable and rapid discrimination between H. influenzae and H. haemolyticus.


Subject(s)
Bacteriological Techniques/methods , Haemophilus/chemistry , Haemophilus/isolation & purification , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods , Haemophilus Infections/diagnosis , Humans
16.
Epidemiol Infect ; 142(9): 1996-9, 2014 Sep.
Article in English | MEDLINE | ID: mdl-24229845

ABSTRACT

Analysis of the Dutch national invasive pneumococcal disease (IPD) surveillance data by sex reveals an increase in the incidence of serotype-1 disease in young female adults in The Netherlands after the introduction of the 7-valent pneumococcal conjugate vaccine (PCV7) in the national immunization schedule. This has led to an overall increase in IPD in women aged 20-45 years, which was not observed in men of the same age. No other differences in serotype shifts possibly induced by the introduction of PCV7 were observed between the sexes in this age group. Serotype 1 is a naturally fluctuating serotype in Europe and it has been associated with disease in young healthy adults before. It remains uncertain whether or not there is an association between the observed increase in serotype-1 disease in young female adults and the implementation of PCV7 in The Netherlands.


Subject(s)
Pneumococcal Infections/microbiology , Streptococcus pneumoniae/classification , Adult , Female , Humans , Incidence , Male , Middle Aged , Netherlands/epidemiology , Pneumococcal Infections/epidemiology , Serotyping , Young Adult
17.
J Clin Microbiol ; 51(3): 931-7, 2013 Mar.
Article in English | MEDLINE | ID: mdl-23303502

ABSTRACT

The species diversity and identification of black fungi belonging to Cyphellophora and Phialophora, which colonize and infect human skin and nails, were studied using amplified fragment length polymorphism (AFLP). A total of 76 Cyphellophora and Phialophora isolates were evaluated, and their delimitation was compared to earlier studies using multilocus sequencing. The results of the AFLP analysis and sequencing were in complete agreement with each other. Seven species-specific padlock probes for the most prevalent species were designed on the basis of the ribosomal DNA internal transcribed spacer region, and identification of the respective species could easily be achieved with the aid of rolling circle amplification.


Subject(s)
Amplified Fragment Length Polymorphism Analysis/methods , Ascomycota/classification , Ascomycota/genetics , Molecular Typing/methods , Mycological Typing Techniques/methods , Phialophora/classification , Phialophora/genetics , Ascomycota/isolation & purification , DNA Primers/genetics , DNA, Ribosomal Spacer/genetics , Phialophora/isolation & purification
18.
Clin Oral Investig ; 17(3): 739-50, 2013 Apr.
Article in English | MEDLINE | ID: mdl-22707232

ABSTRACT

OBJECTIVES: The aim of this randomized controlled clinical trial was to evaluate the 4-year clinical performance of a self-adhesive resin cement, RelyX Unicem (3M ESPE), used for cementation of ceramic inlays. In addition, the influence of selectively acid-etching enamel prior to luting on the clinical performance of the restorations was assessed. METHODS: Sixty-two IPS Empress 2 inlays/onlays were placed in 31 patients by two experienced clinicians. The restorations were luted with RelyX Unicem with (=experimental group: E) or without (=control group: NE) prior enamel etching with phosphoric acid. At baseline, 6 months, and 1, 2, and 4 years after placement, the restorations were assessed by two calibrated investigators using modified USPHS criteria. Ten selected samples of each group were investigated under SEM regarding morphological changes at the cement-inlay interface. RESULTS: The recall rate at 4 years was 97%. Two restorations (1 E, 1 NE) were lost, and one (E) had to be replaced due to inlay and tooth fracture resulting in a survival rate of 95%. No significant differences between the experimental and control group were noticed regarding all criteria (McNemar, p < 0.05). An obvious deterioration in marginal integrity was observed after 4 years as only 5% (E = 7%; NE = 3%) of the restorations exhibited an excellent marginal adaptation. In 90% of the restorations small, still clinically acceptable marginal deficiencies were observed. SEM of the luting gap showed an increased wear of the RelyX Unicem cement over the 4-year period. CONCLUSIONS: The self-adhesive luting cement RelyX Unicem can be recommended for bonding of ceramic inlays/onlays. Additional selective enamel etching does not improve the clinical performance of the restorations within the 4-year period. CLINICAL RELEVANCE: The self-adhesive resin composite RelyX Unicem showed acceptable clinical performance after 4 years of clinical service.


Subject(s)
Acid Etching, Dental , Cementation , Dental Cements , Dentin-Bonding Agents , Inlays , Adolescent , Adult , Dental Marginal Adaptation , Dental Porcelain , Dental Prosthesis Retention , Female , Humans , Kaplan-Meier Estimate , Male , Microscopy, Electron, Scanning , Middle Aged , Resin Cements , Statistics, Nonparametric , Young Adult
19.
Persoonia ; 30: 48-56, 2013 Jun.
Article in English | MEDLINE | ID: mdl-24027346

ABSTRACT

Mucormycosis usually presents as a progressive infection with significant angio-invasion. Mucormycosis due to Mucor irregularis (formerly Rhizomucor variabilis var. variabilis), however, is exceptional in causing chronic cutaneous infection in immunocompetent humans, ultimately leading to severe morbidity if left untreated. More than 90 % of the cases known to date were reported from Asia, mainly from China. The nearest neighbour of M. irregularis is the saprobic species M. hiemalis. The aim of this study was to evaluate the taxonomic position, epidemiology, and intra- and inter-species diversity of M. irregularis based on 21 strains (clinical n = 17) by multilocus analysis using ITS, LSU, RPB1 and RPB2 genes, compared to results of cluster analysis with amplified fragment length polymorphism (AFLP) data. By combining MLST and AFLP analyses, M. irregularis was found to be monophyletic with high bootstrap support, and consisted of five subgroups, which were not concordant in all partitions. It was thus confirmed that M. irregularis is a single species at 96.1-100 % ITS similarity and low recombination rates between populations. Some geographic structuring was noted with some localised populations, which may be explained by limited air-dispersal. The natural habitat of the species is likely to be in soil and decomposing plant material.

20.
J Clin Microbiol ; 50(9): 2987-94, 2012 Sep.
Article in English | MEDLINE | ID: mdl-22760037

ABSTRACT

The first yellow-grain fungal mycetoma, in a 60-year-old man from Central Sudan, is reported. Morphological and phylogenetic analysis of the ribosomal small subunit (SSU), large subunit (LSU), internal transcribed spacer (ITS), ß-tubulin (BT2), actin (ACT1), and elongation factor (TEF1) genes revealed that the isolate deviated from any known agent of mycetoma; it clustered in the genus Pleurostoma (anamorph genus, Pleurostomophora) in the order Calosphaeriales. The novel species, here named Pleurostomophora ochracea, is characterized by phenotypic features. The species proved to be highly susceptible to itraconazole, ketoconazole, posaconazole, and voriconazole, but not to fluconazole. The fungus was inhibited by caspofungin at 8 µg/ml, while no inhibition was found with 5-flucytosine (MIC > 64 µg/ml). Compared to other members of the genus Pleurostomophora, P. ochracea is slow growing, with a relatively high optimum growth temperature (36 to 37°C). This is the first case of a yellow-grain fungal mycetoma; yellow grains are otherwise of bacterial nature. Our case emphasizes that identification of mycetoma agents by the color of the grain only is not sufficient and may lead to inappropriate therapy.


Subject(s)
Ascomycota/isolation & purification , Mycetoma/microbiology , Mycetoma/pathology , Antifungal Agents/pharmacology , Ascomycota/cytology , Ascomycota/drug effects , Ascomycota/growth & development , Cluster Analysis , DNA, Fungal/chemistry , DNA, Fungal/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , DNA, Ribosomal Spacer/chemistry , DNA, Ribosomal Spacer/genetics , Fungal Proteins/genetics , Genes, rRNA , Humans , Male , Microbial Sensitivity Tests , Microscopy , Middle Aged , Molecular Sequence Data , Phylogeny , RNA, Fungal/genetics , RNA, Ribosomal, 18S/genetics , Sequence Analysis, DNA , Sudan , Temperature
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