This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Honraet, K.
Right arrow Articles by Nelis, H. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Honraet, K.
Right arrow Articles by Nelis, H. J.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, February 2005, p. 770-777, Vol. 43, No. 2
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.2.770-777.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Recurrent Colonization of Successively Implanted Tracheoesophageal Vocal Prostheses by a Member of the Fusarium solani Species Complex

K. Honraet,1 M. M. De Vos,1 R. C. Summerbell,2 I. van Kempen,2 S. De Saeger,3 H. Vermeersch,4 C. Van Peteghem,3 and H. J. Nelis1*

Laboratory for Pharmaceutical Microbiology,1 Laboratory of Food Analysis, University of Ghent,3 Department of Head and Neck Surgery, University Hospital of Ghent, Ghent, Belgium,4 Centraalbureau voor Schimmelcultures, Utrecht, The Netherlands2

Received 29 April 2004/ Returned for modification 28 June 2004/ Accepted 6 October 2004

Tracheoesophageal vocal prostheses (TVP) in laryngectomized patients commonly deteriorate due to overgrowth by yeasts, particularly Candida species. We describe the first case of colonization of such devices by a member of the Fusarium solani species complex in a patient with a history of glottal carcinoma. Three isolates, from three prostheses, were found morphologically consistent with the traditional picture of F. solani. Ribosomal sequence analysis showed that the isolates belonged to a distinct, as yet apparently unnamed phylogenetic species within the F. solani species complex. This species, one of two distinct genetic types (genotype 2) traditionally considered part of the plant-pathogenic subtaxon Fusarium solani f. sp. radicicola, has not previously been identified as an agent of human or animal disease, although it is closely related to a known etiologic agent of mycetoma, an Acremonium-like species recently renamed Fusarium falciforme. Sequence and multisatellite M13 polymorphism analysis revealed no distinctions among the case isolates. Production of cyclosporine was detected for all three case isolates.


* Corresponding author. Mailing address: Laboratory for Pharmaceutical Microbiology, University of Ghent, Harelbekestraat 72, B-9000 Ghent, Belgium. Phone: 32-9-2648091. Fax: 32-9-2648195. E-mail: Hans.Nelis{at}UGent.be.


Journal of Clinical Microbiology, February 2005, p. 770-777, Vol. 43, No. 2
0095-1137/05/$08.00+0     doi:10.1128/JCM.43.2.770-777.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.




This article has been cited by other articles:

  • Baddley, J. W., Mostert, L., Summerbell, R. C., Moser, S. A. (2006). Phaeoacremonium parasiticum Infections Confirmed by {beta}-Tubulin Sequence Analysis of Case Isolates.. J. Clin. Microbiol. 44: 2207-2211 [Abstract] [Full Text]