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本文引用的文献

1
A cluster of atypical Yersinia strains with a distinctive 16S rRNA signature.一群具有独特16S rRNA特征的非典型耶尔森菌菌株。
FEMS Microbiol Lett. 1997 Jan 1;146(1):73-8. doi: 10.1111/j.1574-6968.1997.tb10173.x.
2
Genetic diversity among Yersinia enterocolitica strains as revealed by sequence analysis of the 16S rRNA gene.通过16S rRNA基因序列分析揭示的小肠结肠炎耶尔森菌菌株间的遗传多样性。
Contrib Microbiol Immunol. 1995;13:277-80.
3
The phylogeny of the genus Yersinia based on 16S rDNA sequences.基于16S核糖体DNA序列的耶尔森氏菌属系统发育
FEMS Microbiol Lett. 1993 Dec 1;114(2):173-7. doi: 10.1111/j.1574-6968.1993.tb06569.x.
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Evaluation of the four-hour rapid 20E system for identification of members of the family Enterobacteriaceae.用于鉴定肠杆菌科细菌成员的四小时快速20E系统的评估
J Clin Microbiol. 1984 Jul;20(1):51-4. doi: 10.1128/jcm.20.1.51-54.1984.
5
Comparison of the API rapid E four-hour system with the API 20E overnight system for the identification of routine clinical isolates of the family Enterobacteriaceae.用于鉴定肠杆菌科常规临床分离株的API快速E四小时系统与API 20E过夜系统的比较。
J Clin Microbiol. 1985 Apr;21(4):542-5. doi: 10.1128/jcm.21.4.542-545.1985.
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Identification of Yersinia spp. with the API 20E system.使用API 20E系统鉴定耶尔森菌属。
J Clin Microbiol. 1987 Dec;25(12):2398-9. doi: 10.1128/jcm.25.12.2398-2399.1987.
7
Identification of Yersinia species by the API 20E.使用API 20E鉴定耶尔森菌属菌种。
J Clin Microbiol. 1990 Jun;28(6):1443-4. doi: 10.1128/jcm.28.6.1443-1444.1990.
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[Microbiology and epidemiology of Yersinia infections].[耶尔森菌感染的微生物学与流行病学]
Immun Infekt. 1990 Dec;18(6):178-85.
9
Nonradioactive labeling of oligonucleotides in vitro with the hapten digoxigenin by tailing with terminal transferase.通过末端转移酶加尾，在体外使用半抗原地高辛对寡核苷酸进行非放射性标记。
Anal Biochem. 1991 Jan;192(1):222-31. doi: 10.1016/0003-2697(91)90212-c.
10
Description and evaluation of the semiautomated 4-hour ATB 32E method for identification of members of the family Enterobacteriaceae.用于鉴定肠杆菌科细菌成员的半自动4小时ATB 32E方法的描述与评价
J Clin Microbiol. 1991 Jan;29(1):138-41. doi: 10.1128/jcm.29.1.138-141.1991.

耶尔森氏菌属内物种鉴定和区分系统的比较

Comparison of systems for identification and differentiation of species within the genus Yersinia.

作者信息

Neubauer H, Sauer T, Becker H, Aleksic S, Meyer H

机构信息

Institute of Microbiology, Federal Armed Forces Medical Academy, D-80937 Munich, Germany.

出版信息

J Clin Microbiol. 1998 Nov;36(11):3366-8. doi: 10.1128/JCM.36.11.3366-3368.1998.

DOI:10.1128/JCM.36.11.3366-3368.1998
PMID:9774596
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC105332/
Abstract

Of four tested identification systems (API 20E, API Rapid 32 IDE, Micronaut E, and the PCR-based Yersinia enterocolitica Amplification Set), API 20E is still the system of choice for identifying pathogenic Yersinia isolates. It provides the highest sensitivity both at the genus and at the species level and has the best cost-effectiveness correlation.

摘要

在四个经过测试的鉴定系统（API 20E、API Rapid 32 IDE、Micronaut E和基于PCR的小肠结肠炎耶尔森菌扩增试剂盒）中，API 20E仍然是鉴定致病性耶尔森菌分离株的首选系统。它在属水平和种水平上均具有最高的灵敏度，并且具有最佳的性价比关系。