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Journal of Clinical Microbiology, April 2001, p. 1626-1629, Vol. 39, No. 4
Medizinische Klinik, Abteilung II,
Eberhard-Karls-Universität
Tübingen,1 and Institut für
Medizinische Mikrobiologie,2 72076 Tübingen, Germany
Received 13 November 2000/Returned for modification 12 December
2000/Accepted 29 January 2001
Nucleic acid sequence-based amplification (NASBA), an isothermal
amplification technique, was established and evaluated for the
detection of Aspergillus RNA and compared with a previously published, well-defined real-time PCR assay amplifying a region of the
Aspergillus 18S rRNA gene. NASBA showed a lower detection limit of 1 CFU and detected RNA from five different clinically relevant
Aspergillus species, including Aspergillus
fumigatus. All 77 blood samples tested by PCR and NASBA showed
identical results in both assays. Results with the NASBA technique were obtained within 6 h. Thus, the NASBA technique provided a valuable tool for sensitive, specific, fast, and reliable detection of Aspergillus RNA with potential for routine diagnosis,
including the possibility to test the viability of cells.
0095-1137/01/$04.00+0 DOI: 10.1128/JCM.39.4.1626-1629.2001
Copyright © 2001, American Society for Microbiology. All rights reserved.
Nucleic Acid Sequence-Based Amplification of
Aspergillus RNA in Blood Samples
*
Corresponding author. Mailing address: Medizinische
Klinik, Abt. II, Labor Prof. Dr. Med. H. Einsele, Otfried-Mueller-Str. 10, 72076 Tubingen, Germany. Phone: 49-7071-2987355. Fax:
49-7071-293179. E-mail:
juergen.loeffler{at}med.uni-tuebingen.de.
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