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本文引用的文献

1
Experience with the MicroSeq D2 large-subunit ribosomal DNA sequencing kit for identification of commonly encountered, clinically important yeast species.使用MicroSeq D2大亚基核糖体DNA测序试剂盒鉴定常见临床重要酵母菌种的经验。
J Clin Microbiol. 2003 Nov;41(11):5099-102. doi: 10.1128/JCM.41.11.5099-5102.2003.
2
Identification of dermatophyte species by 28S ribosomal DNA sequencing with a commercial kit.使用商业试剂盒通过28S核糖体DNA测序鉴定皮肤癣菌种类。
J Clin Microbiol. 2003 Feb;41(2):826-30. doi: 10.1128/JCM.41.2.826-830.2003.
3
Utilization of the internal transcribed spacer regions as molecular targets to detect and identify human fungal pathogens.利用内部转录间隔区作为分子靶点来检测和鉴定人类真菌病原体。
Med Mycol. 2002 Feb;40(1):87-109. doi: 10.1080/mmy.40.1.87.109.
4
Polymorphic internal transcribed spacer region 1 DNA sequences identify medically important yeasts.多态性内部转录间隔区1 DNA序列可鉴定具有医学重要性的酵母。
J Clin Microbiol. 2001 Nov;39(11):4042-51. doi: 10.1128/JCM.39.11.4042-4051.2001.
5
Rapid identification of fungi by using the ITS2 genetic region and an automated fluorescent capillary electrophoresis system.利用ITS2基因区域和自动荧光毛细管电泳系统快速鉴定真菌。
J Clin Microbiol. 1999 Jun;37(6):1846-51. doi: 10.1128/JCM.37.6.1846-1851.1999.
6
Identification of clinically important ascomycetous yeasts based on nucleotide divergence in the 5' end of the large-subunit (26S) ribosomal DNA gene.基于大亚基(26S)核糖体DNA基因5'端核苷酸差异鉴定具有临床重要性的子囊酵母菌。
J Clin Microbiol. 1997 May;35(5):1216-23. doi: 10.1128/jcm.35.5.1216-1223.1997.

使用MicroSeq D2大亚基核糖体DNA测序试剂盒鉴定临床实验室中遇到的丝状真菌的经验。

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

作者信息

Hall Leslie, Wohlfiel Sherri, Roberts Glenn D

机构信息

Division of Clinical Microbiology, Mayo Clinic, Rochester, Minnesota 55905, USA.

出版信息

J Clin Microbiol. 2004 Feb;42(2):622-6. doi: 10.1128/JCM.42.2.622-626.2004.

DOI:10.1128/JCM.42.2.622-626.2004
PMID:14766826
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC344506/
Abstract

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.

摘要

本文介绍了我们使用MicroSeq D2大亚基rDNA测序试剂盒鉴定梅奥诊所真菌学实验室中遇到的丝状真菌的经验。评估中使用了从临床标本中分离出的总共234株丝状真菌。所有菌株均通过在任何培养基或多种培养基组合上宏观和微观观察到的表型特征进行鉴定,这些培养基包括沙氏葡萄糖琼脂、抑制霉菌琼脂、玉米粉琼脂、察氏琼脂、马铃薯葡萄糖琼脂和V8汁琼脂;所有分离株均使用MicroSeq D2大亚基rDNA测序试剂盒进行测序。在234株分离株中,通过核酸测序有158株被正确鉴定到适当的属或属及种。70株(29.9%)分离株(27个属)的序列未包含在MicroSeq文库中。在测序的80株暗色真菌和154株透明真菌中,分别有65株(81.2%)和51.2%的结果与表型鉴定结果一致。使用MicroSeq D2大亚基rDNA测序试剂盒进行核酸测序有望成为一种准确的鉴定系统;然而,相关文库需要纳入更多临床上重要的属和种。