首页> 美国卫生研究院文献>Canadian Journal of Comparative Medicine >Comparison of Agar Dilution and E-test for antimicrobial susceptibility testing of Campylobacter coli isolates recovered from 80 Ontario swine farms
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Comparison of Agar Dilution and E-test for antimicrobial susceptibility testing of Campylobacter coli isolates recovered from 80 Ontario swine farms

机译:从80个安大略省养猪场回收的弯曲杆菌分离株的琼脂稀释法和E-test药敏试验的比较

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摘要

The primary aim of this study was to evaluate the level of agreement of the E-test for in vitro antimicrobial susceptibility testing of Campylobacter coli using the agar dilution technique, which is the approved method. A convenience sample of 80 Ontario swine farms was chosen for this study; each farm was visited from January to June 2004. A total of 233 isolates of C. coli were tested for susceptibility to 10 antimicrobials by agar dilution and the E-test. Performance of the tests was evaluated using 7 quality control strains: Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 29213, Campylobacter jejuni ATCC 33560, and Campylobacter coli ATCC 33559 for the E-test and E. coli ATCC 25922, Pseudomonas aeruginosa ATCC 27853, and C. jejuni ATCC 33560 for the agar dilution test. Weighted Cohen’s kappa and prevalence-adjusted bias-adjusted kappa (PABAK) tests were used for statistical analysis. The E-test and agar dilution test results had a strong agreement when resistance to streptomycin and tetracycline were evaluated (weighted kappa: 0.68 and 0.66, respectively). However, marked disagreement was detected when testing susceptibility to nalidixic acid and ampicillin (0.15 and 0.22, respectively). Almost perfect agreement was detected by PABAK when testing susceptibility to gentamicin (0.99). Agreement was found to be moderate for ciprofloxacin, azithromycin, clindamycin, erythromycin, and chloramphenicol. Although the level of agreement between the E-test and agar dilution depended on the antimicrobial being tested, the E-test always detected a lower proportion of resistant isolates compared to agar dilution.
机译:这项研究的主要目的是使用琼脂稀释技术评估E-test对弯曲杆菌的体外抗菌药敏试验的一致性水平,这是公认的方法。本研究选择了80个安大略省养猪场的便利样本。从2004年1月至6月对每个农场进行了访问。通过琼脂稀释和E检验对总共233株大肠杆菌进行了10种抗微生物药敏感性测试。使用7种质量控制菌株评估了测试的性能:大肠杆菌ATCC 25922,金黄色葡萄球菌ATCC 29213,空肠弯曲杆菌ATCC 33560和大肠杆菌弯曲杆菌ATCC 33559进行了E检验,大肠杆菌ATCC 25922,铜绿假单胞菌ATCC 27853和空肠弯曲杆菌ATCC 33560用于琼脂稀释试验。加权Cohen的Kappa和患病率调整的偏倚调整的Kappa(PABAK)测试用于统计分析。当评估对链霉素和四环素的抗药性时,E检验和琼脂稀释试验结果具有很强的一致性(加权κ:分别为0.68和0.66)。但是,在测试对萘啶酸和氨苄西林的敏感性(分别为0.15和0.22)时,发现存在明显分歧。当测试对庆大霉素的敏感性时,PABAK检测到几乎完美的一致性(0.99)。已发现对于环丙沙星,阿奇霉素,克林霉素,红霉素和氯霉素而言适中。尽管E-检验和琼脂稀释度之间的一致性水平取决于所测试的抗微生物剂,但E-检验始终检测到比琼脂稀释度低的抗性菌株。

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