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1.
Int J Mol Sci ; 13(1): 726-736, 2012.
Article in English | MEDLINE | ID: mdl-22312282

ABSTRACT

In this study we pursued a diagnostic target in Aspergillus fumigatus (AF) by using qualitative Realtime PCR combined with proprietary DNA primers and a hydrolysis probe specific for this fungal target. Qualitative Realtime PCR is a diagnostic tool that utilizes Realtime PCR technology and detects the presence or absence target specific DNA within a predetermined detection range. Respiratory tissue and fluids from experimentally infected guinea pigs were tested by extracting DNA from the samples which were amplified and detected using AF specific DNA primers and probe. This study included qualitative evaluations of all specimens for the presence of the DNA of AF. The findings in the tissues after AF infection were compared to the numbers of spores in aerosolized samples used to inoculate the animals. Results demonstrated that the specific probe and primer set could detect the presence or absence of AF DNA in the sample. The qualitative detection limit of the assay ranged from 6 × 10(4) copies to 6 copies. Since blood cultures are rarely positive for Aspergillosis, our data indicate that qualitative Realtime PCR, in combination with the appropriate DNA primers and probe can serve as an effective diagnostic tool in the early detection of fungal infections.


Subject(s)
Aspergillus fumigatus/genetics , Bronchoalveolar Lavage Fluid/microbiology , Lung/microbiology , Animals , Aspergillus fumigatus/isolation & purification , DNA Primers/genetics , DNA Primers/metabolism , DNA, Fungal/analysis , Guinea Pigs , Lung/pathology , Male , Real-Time Polymerase Chain Reaction
2.
Int J Mol Sci ; 11(2): 647-55, 2010 Feb 05.
Article in English | MEDLINE | ID: mdl-20386658

ABSTRACT

Drywall from China has been reported to release sulfur producing products which are corrosive to metals, result in noxious odors, and represent a significant health risk. It has been reported that these emissions produce medical symptoms such as respiratory or asthma type problems, sinusitis, gastrointestinal disorders, and vision problems in home owners and their household pets. We report here a method of identifying a causative agent for these emissions by sampling affected gypsum wallboard and subjecting those samples to Real Time Polymerase Chain Reaction [RT-PCR] studies. Specific DNA probes and primers have been designed and patented that detect a specific iron and sulfur reducing bacterium (i.e., Thiobacillus ferrooxidans). One hundred percent of affected drywall samples obtained from homes located in the southeastern United States tested positive for the presence of T. ferrooxidans. All negative controls consisting of unaffected wallboard and internal controls, Geotrichum sp., tested negative within our limits of detection.


Subject(s)
Iron/metabolism , Sulfur/metabolism , Thiobacillus/isolation & purification , Wood/microbiology , DNA Probes/metabolism , DNA, Bacterial/analysis , Iron/chemistry , Oxidation-Reduction , Real-Time Polymerase Chain Reaction , Sulfur/chemistry , Thiobacillus/genetics , Thiobacillus/metabolism
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