首页> 美国卫生研究院文献>Journal of Clinical Microbiology >Comparison of Effects of Medium Composition and Atmospheric Conditions on Detection of Bilophila wadsworthia β-Lactamase by Cefinase and Cefinase Plus Methods
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Comparison of Effects of Medium Composition and Atmospheric Conditions on Detection of Bilophila wadsworthia β-Lactamase by Cefinase and Cefinase Plus Methods

机译:Cefinase和Cefinase Plus方法检测培养基组成和大气条件对Wadsworthiaβ-内酰胺酶检测的影响

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摘要

The influence of growth medium and incubation conditions on the detection of Bilophila wadsworthia β-lactamase was tested with Cefinase and Cefinase Plus disks. The tests involved aerobic and anaerobic incubation with conventional disk and quantitative tube assays. The production of β-lactamase was correlated with penicillin G, ampicillin, and ampicillin-sulbactam MICs and inhibition zones on penicillin (2-U) disks. The strains were grown on (i) brucella agar (brucella), (ii) brucella agar supplemented with 1% pyruvate (brucella-pyruvate), and (iii) brucella agar supplemented with 1% taurine (brucella-taurine). With the aerobic disk assay, 100, 100, and 7% of strains were positive after 30 min from growth on brucella-pyruvate, brucella, and brucella-taurine plates, respectively; of strains grown on brucella-taurine, 54% remained negative by the Cefinase assay, and 23% remained negative by the Cefinase Plus assay at 2 h. In quantitative assays, the strains became positive after 30 min from brucella-pyruvate plates and after 1 h from brucella plates. The intensities of the reactions were strongest with brucella-pyruvate plates under anaerobic test conditions. Anaerobic incubation enhanced β-lactamase detection of growth on brucella-taurine: at 3 h, 85% of strains were positive in comparison to 38% with aerobic incubation. All β-lactamase-negative strains were susceptible to penicillin G and ampicillin; all β-lactamase-positive strains were resistant to ampicillin and, with the exception of two strains, penicillin G. In conclusion, β-lactamase production correlated with susceptibility to penicillin G and ampicillin. Brucella agar supplemented with 1% pyruvate was the most reliable medium for testing B. wadsworthia β-lactamase, and anaerobic incubation expedited positive results. Brucella agar supplemented with taurine was unsuitable for B. wadsworthia β-lactamase testing. Cefinase and Cefinase Plus results were in agreement, but Cefinase Plus yielded faster reactions.
机译:用Cefinase和Cefinase Plus圆盘测试了生长培养基和孵育条件对Wadsworthia Badophila wadsworthiaβ-内酰胺酶检测的影响。测试包括需氧和厌氧培养,采用常规磁盘和定量管分析法。 β-内酰胺酶的产生与青霉素G,氨苄青霉素和氨苄西林舒巴坦MIC以及青霉素(2-U)盘上的抑制区相关。使菌株在(i)布氏琼脂(brucella),(ii)补充有1%丙酮酸的布鲁氏琼脂(brucella-pyruvate)和(iii)补充有1%牛磺酸的布鲁氏琼脂(brucella-taurine)上生长。用好氧圆盘分析法,在布鲁氏丙酮酸,布鲁氏菌和牛磺酸牛磺酸平板上生长30分钟后,分别有100、100和7%的菌株阳性。在布鲁氏菌素-牛磺酸上生长的菌株中,在2 h时,Cefinase分析显示54%保持阴性,Cefinase Plus分析显示23%保持阴性。在定量测定中,菌株在丙酮酸丙酮酸平板中30分钟后和布鲁氏菌平板1小时后变为阳性。布鲁氏丙酮酸板在厌氧试验条件下反应强度最强。厌氧培养增强了β-内酰胺酶对布鲁氏菌素-牛磺酸生长的检测:在3 h时,85%的菌株呈阳性,而有氧培养则为38%。所有β-内酰胺酶阴性菌株均易受青霉素G和氨苄西林的影响。所有β-内酰胺酶阳性菌株均对氨苄西林耐药,除两个菌株外均对青霉素G耐药。总之,β-内酰胺酶的产生与对青霉素G和氨苄西林的敏感性相关。布鲁氏菌琼脂补充1%丙酮酸是测试B. wadsworthiaβ-内酰胺酶的最可靠培养基,厌氧培养可加快阳性结果。补充牛磺酸的布鲁氏琼脂不适合进行沃兹沃德芽孢杆菌β-内酰胺酶检测。 Cefinase和Cefinase Plus的结果一致,但是Cefinase Plus产生的反应更快。

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