1999
DOI: 10.1046/j.1439-0507.1999.00514.x
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A polymerase chain reaction ‘PCR’ for a quick diagnosis of aspergillosis

Abstract: A polymerase chain reaction (PCR) was developed from sequencing data generated from a specific target band that is unique for Aspergillus fumigatus DNA digested with EcoR1. The target band was detected through Southern blot hybridization of a non-radioactive probe labelled with DIG-dUTP and DNAs of different aspergilli. The DNA of the target band was purified, concentrated and subjected to sequencing. The size of the sequenced band was approximately 445 bp. One pair of primers was designed and synthesized from… Show more

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Cited by 3 publications
(4 citation statements)
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“…The presence of Aspergillus fumigatus was determined using previously described PCR primers targeting the A. fumigatus alkaline protease gene. , Positive controls used A. fumigatus (ATCC 34506) genomic DNA as the template, and no-template negative controls were included.…”
Section: Methodsmentioning
confidence: 99%
“…The presence of Aspergillus fumigatus was determined using previously described PCR primers targeting the A. fumigatus alkaline protease gene. , Positive controls used A. fumigatus (ATCC 34506) genomic DNA as the template, and no-template negative controls were included.…”
Section: Methodsmentioning
confidence: 99%
“…Aspergillus fumigatus is a species that has been intensively investigated in this respect. [11][12][13]22 The species is also commonly found in indoor air. We examined seven pairs of primers designed for the specific detection of A. fumigatus (sets 21-27, Table 1).…”
Section: Species-specific Primersmentioning
confidence: 99%
“…[8][9][10] For medically important fungi, speciesspecific primers are developed to rapidly screen clinical samples and thus promote early diagnosis. [11][12][13][14] Limited numbers of fungal species are usually included in the initial screening during the development of molecular markers currently in use. Clearly, no experiment could include all the fungal species that could be present, because of the enormous diversity of fungi.…”
Section: Introductionmentioning
confidence: 99%
“…The phenotypic features of pathogenic fungi are poor. To resolve this problem, reliable molecular biological methods for species identification 1–4 and strain typing have been developed 5–9 . In this study, we report a case of pulmonary aspergilloma and the molecular biological analysis of isolates from clinical and pathological specimens.…”
Section: Introductionmentioning
confidence: 99%