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1.
Med Mycol ; 48(2): 335-45, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20141373

ABSTRACT

Anamorphic members of the ascomycete family Trichocomaceae including Aspergillus, Penicillium, Paecilomyces, Geosmithia and Sagenomella have been reported from infections in canines. Six clinical isolates (five associated with infections in canines and one from a human source) demonstrated simple phialides producing conidia in long chains and were investigated for their potential relationship to Sagenomella chlamydospora, a known agent of canine disseminated mycosis. Phylogenetic analyses of internal transcribed spacer (ITS) and small subunit (SSU) region sequences revealed that all of the canine-associated isolates were distinct from Sagenomella species. The new anamorphic genus and species Phialosimplex caninus is described to accommodate the clinical isolates. Sagenomella chlamydospora and Sagenomella sclerotialis are transferred to the new genus as Phialosimplex chlamydosporus comb. nov. and Phialosimplex sclerotialis comb. nov.


Subject(s)
Dog Diseases/microbiology , Eurotiales/isolation & purification , Mycoses/veterinary , Animals , DNA, Fungal/genetics , DNA, Intergenic/genetics , Dogs , Eurotiales/cytology , Eurotiales/genetics , Mycoses/microbiology , Phylogeny
2.
J Clin Virol ; 47(3): 229-33, 2010 Mar.
Article in English | MEDLINE | ID: mdl-20080438

ABSTRACT

BACKGROUND: Rapid influenza diagnostic tests (RIDTs) are used in various settings as a first-line screen of patient specimens. During the initial outbreak of the 2009 novel influenza A/H1N1 virus, the Nebraska Public Health Laboratory (NPHL) adopted a testing algorithm, attempting to maximize the usefulness of RIDTs. However, it became apparent that a high percentage of the positive specimens received from off-site facilities were negative for influenza viruses by the confirmatory test, the Luminex xTAG Respiratory Viral Panel (RVP) molecular assay. OBJECTIVES: To explore the cause of discrepancies between RIDTs results obtained from on-site facility testing versus confirmatory testing performed at NPHL. STUDY DESIGN: Specimens (n=336) tested with RIDTs at off-site facilities and screened for high-probability of containing H1N1 were sent to the NPHL for confirmatory testing by RVP. RESULTS: Of 336 specimens analyzed, 104 were negative for influenza A or B by both RIDT and RVP; 127 were positive by both tests; 102 were positive by RIDT only; and 3 were positive by RVP only. Using the RVP assay as the gold standard, overall RIDT characteristics in this screened population were: sensitivity=97.7% (95%CI: 92.5, 99.3); specificity=48.1% (95%CI: 40.4, 55.8); positive predictive value=54.3% (95%CI: 47.0, 61.4); and negative predicative value=97.1% (95%CI: 90.6, 99.1). CONCLUSIONS: The results show that the confirmation of RIDT-positive results varied widely by testing site. Possible explanations for the discrepancies in performance characteristics include testing a narrowly defined sample population, test facility characteristics, facility work load, and seasonal timing.


Subject(s)
Diagnostic Tests, Routine/methods , Disease Outbreaks , Influenza, Human/diagnosis , Mass Screening/methods , Adolescent , Adult , Aged , Aged, 80 and over , Child , Child, Preschool , Female , Humans , Infant , Male , Middle Aged , Nebraska/epidemiology , Predictive Value of Tests , Sensitivity and Specificity , Young Adult
3.
J Clin Microbiol ; 45(2): 636-40, 2007 Feb.
Article in English | MEDLINE | ID: mdl-17122018

ABSTRACT

A case of primary cutaneous zygomycosis caused by Mucor circinelloides is described. Histopathology showed typical hyphae along with chlamydospores. The isolate was identified by molecular and phenotypic methods. The utility of sequence analysis of the internal transcribed spacer region is highlighted; however, further studies are needed to assess species genetic heterogeneity.


Subject(s)
Dermatomycoses/microbiology , Mucor/classification , Mucor/isolation & purification , Mucormycosis/microbiology , Aged, 80 and over , DNA, Fungal/analysis , DNA, Fungal/isolation & purification , Dermatomycoses/diagnosis , Humans , Male , Molecular Sequence Data , Mucor/genetics , Mucor/ultrastructure , Mucormycosis/diagnosis , Mycological Typing Techniques , Phenotype , Polymerase Chain Reaction/methods , Sequence Analysis, DNA
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