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本文引用的文献

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The vanB gene confers various levels of self-transferable resistance to vancomycin in enterococci.vanB基因赋予肠球菌对万古霉素不同水平的自身可转移性耐药性。
J Infect Dis. 1993 May;167(5):1220-3. doi: 10.1093/infdis/167.5.1220.
2
The vanB gene of vancomycin-resistant Enterococcus faecalis V583 is structurally related to genes encoding D-Ala:D-Ala ligases and glycopeptide-resistance proteins VanA and VanC.耐万古霉素粪肠球菌V583的vanB基因在结构上与编码D-丙氨酸:D-丙氨酸连接酶以及糖肽抗性蛋白VanA和VanC的基因相关。
Gene. 1993 Feb 14;124(1):143-4. doi: 10.1016/0378-1119(93)90779-3.
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Ability of clinical laboratories to detect antimicrobial agent-resistant enterococci.临床实验室检测耐抗菌药物肠球菌的能力。
J Clin Microbiol. 1993 Jul;31(7):1695-9. doi: 10.1128/jcm.31.7.1695-1699.1993.
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Characterization of glycopeptide-resistant enterococci from U.S. hospitals.美国医院耐糖肽肠球菌的特征分析。
Antimicrob Agents Chemother. 1993 Nov;37(11):2311-7. doi: 10.1128/AAC.37.11.2311.
5
Identification and characterization of multiple species of vancomycin-resistant enterococci, including an evaluation of Vitek software version 7.1.多种耐万古霉素肠球菌的鉴定与特性分析,包括对Vitek 7.1软件版本的评估
J Clin Microbiol. 1993 Oct;31(10):2777-9. doi: 10.1128/jcm.31.10.2777-2779.1993.
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Genetics and mechanisms of glycopeptide resistance in enterococci.肠球菌中糖肽类耐药的遗传学及机制
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Development of a standardized screening method for detection of vancomycin-resistant enterococci.一种用于检测耐万古霉素肠球菌的标准化筛查方法的开发。
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Detection of vancomycin resistance in enterococci by the Alamar MIC system.使用阿拉玛微量肉汤稀释法检测肠球菌对万古霉素的耐药性。
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9
Investigation of the reformulated Remel Synergy Quad plate for detection of high-level aminoglycoside and vancomycin resistance among enterococci.重新配制的Remel Synergy Quad平板用于检测肠球菌中高水平氨基糖苷类和万古霉素耐药性的研究。
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10
Ability of commercial and reference antimicrobial susceptibility testing methods to detect vancomycin resistance in enterococci.商业及参考抗菌药物敏感性检测方法检测肠球菌中万古霉素耐药性的能力。
J Clin Microbiol. 1995 Jun;33(6):1524-7. doi: 10.1128/jcm.33.6.1524-1527.1995.

影响Vitek革兰氏阳性菌药敏系统检测肠球菌中vanB编码的万古霉素耐药性的因素。

Factors influencing the vitek gram-positive susceptibility system's detection of vanB-encoded vancomycin resistance among enterococci.

作者信息

Jett B, Free L, Sahm D F

机构信息

Department of Opthalmology, Dean A. McGee Eye Institute, University of Oklahoma Health Sciences Center, Oklahoma City 73104, USA.

出版信息

J Clin Microbiol. 1996 Mar;34(3):701-6. doi: 10.1128/jcm.34.3.701-706.1996.

DOI:10.1128/jcm.34.3.701-706.1996
PMID:8904441
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC228873/
Abstract

Studies were conducted to identify factors contributing to the inability of the Vitek Gram-Positive Susceptibility system (GPS; bioMerieux, Vitek, Inc., Hazelwood, Mo.) to reliably detect vanB-mediated vancomycin resistance among enterococci. To some extent the accuracy of the GPS depended on a particular strain's level of resistance, as all isolates for which vancomycin MICs were > or = 128 mu g/ml were readily detected but detection of resistance expressed by several strains for which MICs were < or = 64 mu g/ml was sporadic. Factors besides the level of resistance were studied in two vanB strains. For one strain (Enterococcus faecium U8304), the ability of GPS to detect resistance was accurate and consistent, while for the other (Enterococcus faecalis V583), GPS results were inconsistent and unreliable. Using these isolates, we established that growth medium had the most notable effect on the detection of resistance. In the absence of vancomycin, Vitek GPS broth supported growth comparable to that obtained with brain heart infusion broth for both E. faecium U8304 and E. faecalis V583. However, in the presence of vancomycin the growth patterns changed dramatically so that neither VanB strain grew well in Vitek broth, and growth of V583 was barely detectable after 8 h of incubation. In contrast, good growth of both strains was observed in brain heart infusion broth supplemented with vancomycin. Additionally, the same medium effect was observed with other inducibly resistant VanB strains. In conclusion, although Vitek broth can support good enterococcal growth, this medium does not sufficiently support expression of vancomycin resistance by certain strains to allow them to be detected by the Vitek automated system. Furthermore, this observation establishes that the type of growth medium used can substantially influence the expression of vancomycin resistance and indicates that medium-based strategies should be explored for the enhancement of resistance detection among commercial systems.

摘要

开展了多项研究,以确定导致Vitek革兰氏阳性药敏系统(GPS;生物梅里埃公司,Vitek公司,密苏里州黑兹尔伍德)无法可靠检测肠球菌中vanB介导的万古霉素耐药性的因素。在某种程度上,GPS的准确性取决于特定菌株的耐药水平,因为所有万古霉素MIC≥128μg/ml的分离株都能很容易地被检测到,但对于几种MIC≤64μg/ml的菌株所表现出的耐药性检测却是零星的。除耐药水平外,还对两株vanB菌株的其他因素进行了研究。对于一株菌株(屎肠球菌U8304),GPS检测耐药性的能力准确且一致,而对于另一株(粪肠球菌V583),GPS的结果不一致且不可靠。利用这些分离株,我们确定生长培养基对耐药性检测的影响最为显著。在没有万古霉素的情况下,Vitek GPS肉汤支持屎肠球菌U8304和粪肠球菌V583的生长,其生长情况与脑心浸液肉汤相当。然而,在有万古霉素的情况下,生长模式发生了巨大变化,以至于两株VanB菌株在Vitek肉汤中都生长不佳,孵育8小时后V583的生长几乎无法检测到。相比之下,在添加了万古霉素的脑心浸液肉汤中观察到两株菌株都生长良好。此外,在其他诱导型耐药VanB菌株中也观察到了相同的培养基效应。总之,尽管Vitek肉汤可以支持肠球菌良好生长,但这种培养基不能充分支持某些菌株表达万古霉素耐药性,从而无法通过Vitek自动化系统进行检测。此外,这一观察结果表明,所用生长培养基的类型可显著影响万古霉素耐药性的表达,并表明应探索基于培养基策略以提高商业系统中耐药性检测水平。