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Molecular typing of Australian Scedosporium isolates showing genetic variability and numerous S. aurantiacum

  • Laurence Delhaes
  • , Azian Harun
  • , Sharon C.A. Chen
  • , Quoc Nguyen
  • , Monica Slavin
  • , Christopher H. Heath
  • , Krystyna Maszewska
  • , Catriona Halliday
  • , Vincent Robert
  • , Tania C. Sorrell
  • , Wieland Meyer
  • , Peter Collignon
  • , Richard Benn
  • , Ian Chambers
  • , Nelson Dennis
  • , Deo Dewit
  • , John Ferguson
  • , Iain Gosbell
  • , Thomas Gottlieb
  • , Juliette Holland
  • Alison Kesson, Richard Lawrence, Deborah Marriott, Peter Newton, Pamela Palasanthrian, Robert Pickles, Robert Pritchard, Lex Tierney, Voula Tomasotos, Robert Vaz, Kerry Weeks, Anthony Allworth, Christopher Coulter, Joan Faoagali, Barbara Johnson, David Looke, Joseph McCormack, Graeme Nimmo, Gabrielle O'Kane, E. Geoffrey Playford, Jennifer Robson, David Ellis, Rosemary Handke, Karen Rowlands, David Shaw, Louise Cooley, Erica Cox, Alistair McGregor, Clare Franklin, Cathy Joseph, Tony Korman, Orla Morrissey, Denis Spelman, Bryan Speed, Harsha Sheorey, Peter Boan, John Dyer, Dianne Gardam, Duncan McLennan, Ronan Murray, Todd Pryce

Research output: Contribution to journalArticlepeer-review

48 Citations (Scopus)

Abstract

One hundred clinical isolates from a prospective nationwide study of scedosporiosis in Australia (2003-2005) and 46 additional isolates were genotyped by internal transcribed spacer-restriction fragment length polymorphism (ITS-RFLP) analysis, ITS sequencing, and M13 PCR fingerprinting. ITS-RFLP and PCR fingerprinting identified 3 distinct genetic groups. The first group corresponded to Scedosporium prolificans (n = 83), and the other 2 comprised isolates previously identified as S. apiospermum: one of these corresponded to S. apiospermum (n = 33) and the other to the newly described species S. aurantiacum (n = 30). Intraspecies variation was highest for S. apiospermum (58%), followed by S. prolificans (45%) and S. aurantiacum (28%) as determined by PCR fingerprinting. ITS sequence variation of 2.2% was observed among S. apiospermum isolates. No correlation was found between genotype of strains and their geographic origin, body site from which they were cultured, or colonization versus invasive disease. Twelve S. prolificans isolates from 2 suspected case clusters were examined by amplified fragment length polymorphism analysis. No specific clusters were confirmed.

Original languageEnglish
Pages (from-to)282-290
Number of pages9
JournalEmerging Infectious Diseases
Volume14
Issue number2
DOIs
Publication statusPublished - 1 Feb 2008
Externally publishedYes

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