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采用Etest法检测亨氏巴尔通体的药敏情况。

Antimicrobial susceptibility of Bartonella henselae using Etest methodology.

作者信息

Pendle S, Ginn A, Iredell J

机构信息

Centre for Infectious Diseases and Microbiology, University of Sydney, Westmead Hospital, NSW, Australia.

出版信息

J Antimicrob Chemother. 2006 Apr;57(4):761-3. doi: 10.1093/jac/dki485. Epub 2006 Feb 7.

Abstract

OBJECTIVES

Bartonella henselae is a fastidious slow growing pathogen which is seldom cultured in the laboratory. Previous descriptions of antimicrobial susceptibility have been largely limited to feline isolates and/or laboratory reference strains, with no accounting for genotypic or phenotypic diversity.

METHODS

An optimal method of antimicrobial susceptibility testing by Etest was established to compare the antimicrobial susceptibilities of 12 different isolates of B. henselae, 5 human and 7 feline, which have previously been well characterized by 16S rRNA sequencing, multi-locus sequence typing (MLST), phase variation and passage number.

RESULTS

No difference in susceptibility could be attributed to differences in genotype, source of the isolate or passage number. Where comparisons were drawn with previously published results, these were found to be concordant.

CONCLUSIONS

We conclude that antibiotic susceptibility can be determined by a simple Etest method for B. henselae isolates. This method is reproducible among diverse strains, and is sufficiently predictable that generalizations can be confidently made about optimal antibiotic choices.

摘要

目的

汉赛巴尔通体是一种苛求的生长缓慢的病原体,在实验室中很少培养。以往关于抗菌药敏性的描述主要局限于猫源分离株和/或实验室参考菌株,未考虑基因型或表型多样性。

方法

建立了一种通过Etest进行抗菌药敏试验的优化方法,以比较12株不同的汉赛巴尔通体分离株(5株人源和7株猫源)的抗菌药敏性,这些分离株此前已通过16S rRNA测序、多位点序列分型(MLST)、相变和传代次数进行了充分表征。

结果

药敏性的差异不能归因于基因型、分离株来源或传代次数的差异。与先前发表的结果进行比较时,发现结果一致。

结论

我们得出结论,对于汉赛巴尔通体分离株,可以通过简单的Etest方法确定抗生素敏感性。该方法在不同菌株中具有可重复性,并且具有足够的可预测性,因此可以自信地对最佳抗生素选择进行概括。

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