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API 20E鉴定系统与传统生化方法用于肠杆菌科细菌鉴定的重新评估:对一种旧产品的新审视。

Reevaluation of the API 20E identification system versus conventional biochemicals for identification of members of the family Enterobacteriaceae: a new look at an old product.

作者信息

O'Hara C M, Rhoden D L, Miller J M

机构信息

Hospital Infections Program, Centers for Disease Control, Atlanta, Georgia 30333.

出版信息

J Clin Microbiol. 1992 Jan;30(1):123-5. doi: 10.1128/jcm.30.1.123-125.1992.

DOI:10.1128/jcm.30.1.123-125.1992
PMID:1734043
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC265006/
Abstract

The API 20E bacterial identification system has been used for 19 years, often as the standard with which other identification systems are compared. Because the accuracy of this system compared with conventional biochemical tests has not been determined in many years, we evaluated the API 20E linear strip by using 291 typical and atypical strains of the family Enterobacteriaceae taken from a culture collection. At 24 h, the API 20E correctly identified by genus and species 229 of 291 (78.7%) of the strains, using Salmonella and Shigella serotyping where indicated. At 48 h, 95.2% were correctly identified by using additional biochemical tests as recommended by the manufacturer. The API 20E misidentified eight (2.7%) strains; these strains were not limited to any particular genus. When 81 of these Enterobacteriaceae strains were arranged into a weighted assortment correlating to the frequency with which they might be found in a clinical laboratory, the API 20E correctly identified 71 (87.7%) at 24 h and 78 (96.3%) at 48 h. This evaluation concluded that the accuracy of the identification of Enterobacteriaceae strains at 24 h (78.7%) may be significantly lower than that of earlier evaluations. However, there is no significant difference in the ability of the API 20E to correctly identify "challenge" type organisms (229 of 291) versus routine hospital isolates (71 of 81) (P greater than 0.05), but the system is not as accurate as the conventional biochemical method of identification.

摘要

API 20E细菌鉴定系统已使用了19年,常被用作与其他鉴定系统进行比较的标准。由于该系统与传统生化试验相比的准确性多年来未得到确定,我们使用从菌种保藏中心获取的291株典型和非典型肠杆菌科菌株对API 20E线性试条进行了评估。在24小时时,API 20E使用沙门菌和志贺菌血清分型法(如适用),正确鉴定出了291株菌株中的229株(78.7%)的属和种。在48小时时,按照制造商推荐使用额外的生化试验,95.2%的菌株被正确鉴定。API 20E错误鉴定了8株(2.7%)菌株;这些菌株不限于任何特定的属。当将这81株肠杆菌科菌株按照它们在临床实验室中可能被发现的频率排列成加权组合时,API 20E在24小时时正确鉴定出71株(87.7%),在48小时时正确鉴定出78株(96.3%)。该评估得出结论,在24小时时对肠杆菌科菌株的鉴定准确性(78.7%)可能显著低于早期评估。然而,API 20E正确鉴定“挑战性”类型生物体(291株中的229株)与常规医院分离株(81株中的71株)的能力没有显著差异(P大于0.05),但该系统不如传统生化鉴定方法准确。

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