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本文引用的文献

1
Evaluation of API An-IDENT and RapID ANA II systems for identification of Actinomyces species from clinical specimens.评估API An-IDENT和RapID ANA II系统用于从临床标本中鉴定放线菌属菌种的能力。
J Clin Microbiol. 1995 Feb;33(2):329-30. doi: 10.1128/jcm.33.2.329-330.1995.
2
Rapid enzymatic characterization of clinically encountered anaerobic bacteria with the API ZYM system.使用API ZYM系统对临床分离的厌氧菌进行快速酶学鉴定
Eur J Clin Microbiol. 1984 Aug;3(4):294-300. doi: 10.1007/BF01977476.
3
Comparison of the PRAS II, AN-Ident, and RapID-ANA systems for identification of anaerobic bacteria.PRAS II、AN-Ident和RapID-ANA系统用于鉴定厌氧细菌的比较。
J Clin Microbiol. 1985 Jul;22(1):32-5. doi: 10.1128/jcm.22.1.32-35.1985.
4
Evaluation of the AnIdent system for the identification of anaerobic bacteria.用于鉴定厌氧细菌的AnIdent系统的评估
Diagn Microbiol Infect Dis. 1986 May;5(1):9-15. doi: 10.1016/0732-8893(86)90086-6.
5
Anaerobic bacteria. Their role in infection and their management.厌氧菌。它们在感染中的作用及其治疗。
Postgrad Med. 1987 Jun;81(8):141-7. doi: 10.1080/00325481.1987.11699866.
6
Comparison of Minitek Anaerobe II, API An-Ident, and RapID ANA systems for identification of Clostridium difficile.用于艰难梭菌鉴定的Minitek厌氧II型系统、API An-Ident系统和RapID ANA系统的比较
Am J Clin Pathol. 1986 Jun;85(6):716-8. doi: 10.1093/ajcp/85.6.716.
7
Clinical evaluation of the Vitek ANI card for identification of anaerobic bacteria.用于鉴定厌氧菌的Vitek ANI卡的临床评估
J Clin Microbiol. 1988 Feb;26(2):225-30. doi: 10.1128/jcm.26.2.225-230.1988.
8
Evaluation of the new RapID-ANA II system for the identification of clinical anaerobic isolates.新型RapID-ANA II系统用于临床厌氧菌分离株鉴定的评估
J Clin Microbiol. 1991 May;29(5):874-8. doi: 10.1128/jcm.29.5.874-878.1991.
9
Clinical evaluation of the RapID-ANA II panel for identification of anaerobic bacteria.用于鉴定厌氧菌的RapID-ANA II鉴定板的临床评估
J Clin Microbiol. 1991 Mar;29(3):457-62. doi: 10.1128/jcm.29.3.457-462.1991.
10
Fluorogenic and chromogenic substrates used in bacterial diagnostics.用于细菌诊断的荧光和显色底物。
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BBL 晶体厌氧菌鉴定系统的评估

Evaluation of the BBL Crystal Anaerobe identification system.

作者信息

Cavallaro J J, Wiggs L S, Miller J M

机构信息

Diagnostic Microbiology Section, Hospital Infections Program, Centers for Disease Control and Prevention, Atlanta, Georgia 30333, USA.

出版信息

J Clin Microbiol. 1997 Dec;35(12):3186-91. doi: 10.1128/jcm.35.12.3186-3191.1997.

DOI:10.1128/jcm.35.12.3186-3191.1997
PMID:9399517
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC230145/
Abstract

The BBL Crystal Anaerobe (ANR) identification system was evaluated, and the results were compared with those from conventional anaerobic methods. We tested 322 clinically significant anaerobic bacteria according to the manufacturer's instructions. The system identified correctly 286 of 322 (88.8%) of the anaerobic bacteria tested. Of these, 263 of 322 (81.7%) were identified correctly on initial testing and 49 were identified correctly only to the genus level; on repeat testing, 23 of 49 (46.9%) were identified correctly to both the genus and the species levels. A total of 26 (8.5%) were misidentified at the species level, and 10 (3.1%) were not identified. Performance characteristics for individual strains varied. The system correctly identified all tested strains of Campylobacter, Desulfomonas, Desulfovibrio, Leptotrichia, Mobiluncus, Peptostreptococcus, Porphyromonas, Provetella, Propionibacterium, Tisierella, and Veillonella and 36 of 37 (97.3%) Actinomyces strains, 42 of 46 (91.3%) B. fragilis group strains, 79 of 103 (76.7%) Clostridium strains, (however, the system failed to identify any of the 7 C. innocuum and 9 C. tetani strains tested), and 8 of 15 (53.3%) Bacteroides strains. This system was easy to use, did not involve the addition of reagents, and was faster than conventional anaerobic procedures. It would be a useful addition to the anaerobe laboratory of most hospitals.

摘要

对BBL Crystal厌氧菌(ANR)鉴定系统进行了评估,并将结果与传统厌氧方法的结果进行了比较。我们按照制造商的说明对322株具有临床意义的厌氧菌进行了测试。该系统正确鉴定了322株测试厌氧菌中的286株(88.8%)。其中,322株中的263株(81.7%)在初次测试时被正确鉴定,49株仅在属水平上被正确鉴定;在重复测试中,49株中的23株(46.9%)在属和种水平上均被正确鉴定。共有26株(8.5%)在种水平上被错误鉴定,10株(3.1%)未被鉴定。各菌株的性能特征有所不同。该系统正确鉴定了所有测试的弯曲杆菌、脱硫单胞菌、脱硫弧菌、纤毛菌、动弯杆菌、消化链球菌、卟啉单胞菌、普氏菌、丙酸杆菌、蒂西埃拉菌和韦荣球菌菌株,以及37株放线菌中的36株(97.3%)、46株脆弱拟杆菌群菌株中的42株(91.3%)、103株梭菌中的79株(76.7%)(然而,该系统未能鉴定所测试的7株无害梭菌和9株破伤风梭菌中的任何一株),以及15株拟杆菌中的8株(53.3%)。该系统使用方便,无需添加试剂,且比传统厌氧程序更快。它将是大多数医院厌氧菌实验室的一个有用补充。