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The diagnosis and treatment of invasive mould infections in haematology patients

Histological appearances of many moulds overlap and there is a need for a method to allow identification in tissue specimens.  Two methods for extracting fungal DNA from wax tissue sections, based on the TaKaRa DEXPAT <sup>TM</sup> kit and QIAamp<sup><span style='font-family:Symbol'>Ò </sup>DNA Mini Kit, were optimised and compared.  DNA was amplified by PCR using pan-fungal primers, and detected by Southern blot hybridisation with a probe specific for <i>Aspergillus fumigatus </i>and <i>A. flavus.  </i>The TaKaRa DEXPAT <sup>TM </sup> kit based method, with additional steps using lyticase and ethanol precipitation, was superior and was used to test sequential wax tissue specimens from 56 patients with IFI.  PCR products not hybridising with the probe were identified by sequencing.  The species was confirmed in all tissue culture positive cases (23 <i>A. fumigatus </i>or <i>A. flavus, </i>one <i>Chaetomium globosum</i> and one <i>Scedosporium apiospermum).  </i>Of culture negative cases, a diagnosis of <i>A. fumigatus</i> or <i>A. flavus</i> was established in 25 and emerging moulds in two (one probable <i>Alternaria </i>species and one unidentified).  Overall, emerging moulds were identified in 4 cases (7%) with a trend toward a temporal increase in these infections.  This method provides a valuable diagnostic tool for both patient management and future antifungal and epidemiological trials. Reasons for therapeutic failure in IFI are unclear.  Amphoterican B susceptibility of isolates cultured from tissue biopsies from patients who had received a median of 12 days therapy, were tested using a method  based on the NCCLS M38-A broth microdilution method.  The difficulty in treating IFI does not appear to be due to susceptibility of the isolates, but may be due to poor penetration of antifungal agents into infected tissue.

Identiferoai:union.ndltd.org:bl.uk/oai:ethos.bl.uk:425016
Date January 2006
CreatorsPaterson, Pamela J.
PublisherUniversity of Aberdeen
Source SetsEthos UK
Detected LanguageEnglish
TypeElectronic Thesis or Dissertation

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