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Journal of Clinical Microbiology, July 2008, p. 2423-2427, Vol. 46, No. 7
0095-1137/08/$08.00+0 doi:10.1128/JCM.00420-08
Copyright © 2008, American Society for Microbiology. All Rights Reserved.

Fanrong Kong,2,
Tania C. Sorrell,2
Hui Wang,1
Yiqun Duan,1 and
Sharon C. A. Chen2*
Research Laboratory for Infectious Skin Diseases, Department of Dermatology, Wuhan First Hospital, Wuhan 430022, People's Republic of China,1 Centre for Infectious Diseases and Microbiology, Westmead Hospital and the University of Sydney, Westmead, New South Wales, Australia2
Received 3 March 2008/ Returned for modification 2 April 2008/ Accepted 12 May 2008
A sensitive rolling-circle amplification (RCA)-based method utilizing species-specific padlock probes targeted to the internal transcribed spacer 2 region of the fungal ribosomal DNA gene complex was developed. The assay was rapid (2 hours) and specific. Of 28 fungal isolates (16 of Candida, six of Aspergillus, and six of Scedosporium spp.), all were all identified correctly.
Published ahead of print on 21 May 2008.
These authors contributed equally to the work.
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