Experience with the MicroSeq D2 large-subunit ribosomal DNA sequencing kit for identification of filamentous fungi encountered in the clinical laboratory

被引:64
作者
Hall, L [1 ]
Wohlfiel, S [1 ]
Roberts, GD [1 ]
机构
[1] Mayo Clin, Div Clin Microbiol, Rochester, MN 55905 USA
关键词
D O I
10.1128/JCM.42.2.622-626.2004
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Described herein is our experience with the MicroSeq D2 large-subunit rDNA sequencing kit for the identification of filamentous fungi encountered in the mycology laboratory at the Mayo Clinic. A total of 234 filamentous fungi recovered from clinical specimens were used in the evaluation. All were identified by using phenotypic characteristics as observed macroscopically and microscopically on any medium or a combination of media, which included Sabouraud's dextrose, inhibitory mold, cornmeal, Czapek-Dox, potato dextrose, and V8 juice agars; all isolates were sequenced using the MicroSeq D2 large-subunit rDNA sequencing kit. Of the of 234 isolates, 158 were correctly identified to the appropriate genus or genus and species by using nucleic acid sequencing. Sequences for 70 (29.9%) of the isolates (27 genera) were not included in the MicroSeq library. Of the 80 dematiaceous and 154 hyaline fungi sequenced, 65 and 51.2%, respectively, gave results concordant with those determined by phenotypic identification. Nucleic acid sequencing using the MicroSeq D2 large-subunit rDNA sequencing kit offers promise of being an accurate identification system; however, the associated library needs to include more of the clinically important genera and species.
引用
收藏
页码:622 / 626
页数:5
相关论文
共 6 条
[1]   Polymorphic internal transcribed spacer region 1 DNA sequences identify medically important yeasts [J].
Chen, YC ;
Eisner, JD ;
Kattar, MM ;
Rassoulian-Barrett, SL ;
Lafe, K ;
Bui, U ;
Limaye, AP ;
Cookson, BT .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (11) :4042-4051
[2]   Experience with the MicroSeq d2 large-subunit ribosomal DNA sequencing kit for identification of commonly encountered, clinically important yeast species [J].
Hall, L ;
Wohlfiel, S ;
Roberts, GD .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (11) :5099-5102
[3]  
Iwen PC, 2002, MED MYCOL, V40, P87, DOI 10.1080/mmy.40.1.87.109
[4]   Identification of clinically important ascomycetous yeasts based on nucleotide divergence in the 5' end of the large-subunit (26S) ribosomal DNA gene [J].
Kurtzman, CP ;
Robnett, CJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 1997, 35 (05) :1216-1223
[5]   Identification of dermatophyte species by 28S ribosomal DNA sequencing with a commercial kit [J].
Ninet, B ;
Jan, I ;
Bontems, O ;
Léchenne, B ;
Jousson, O ;
Panizzon, R ;
Lew, D ;
Monod, M .
JOURNAL OF CLINICAL MICROBIOLOGY, 2003, 41 (02) :826-830
[6]   Rapid identification of fungi by using the ITS2 genetic region and an automated fluorescent capillary electrophoresis system [J].
Turenne, CY ;
Sanche, SE ;
Hoban, DJ ;
Karlowsky, JA ;
Kabani, AM .
JOURNAL OF CLINICAL MICROBIOLOGY, 1999, 37 (06) :1846-1851