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评价一种检测新德里金属β-内酰胺酶产生肠杆菌科中阿兹台隆和头孢他啶-阿维巴坦协同作用的简单方法。

Evaluation of a simple method for testing aztreonam and ceftazidime-avibactam synergy in New Delhi metallo-beta-lactamase producing Enterobacterales.

机构信息

Department of Microbiology, National Cancer Institute, All India Institute of Medical Sciences (Jhajjar-campus), New Delhi, India.

Department of Microbiology, All India Institute of Medical Sciences, Madurai, India.

出版信息

PLoS One. 2024 May 17;19(5):e0303753. doi: 10.1371/journal.pone.0303753. eCollection 2024.

Abstract

NDM-producing carbapenem-resistant bacterial infections became a challenge for clinicians. Combination therapy of aztreonam and ceftazidime-avibactam is a prudent choice for these infections. However, there is still no recommendation of a practically feasible method for testing aztreonam and ceftazidime-avibactam synergy. We proposed a simple method for testing aztreonam and ceftazidime-avibactam synergy and compared it with reference broth micro-dilution and other methods. Carbapenem-resistant Enterobacterales clinical isolates were screened for the presence of the NDM gene by the Carba R test. NDM harbouring isolates were tested for aztreonam and ceftazidime-avibactam synergy by broth microdilution (reference method), E strip-disc diffusion, double disc diffusion, and disc replacement methods. In the newly proposed method, the MHA medium was supplemented with ceftazidime-avibactam (corresponding to an aztreonam concentration of 4μg/ml). The MHA medium was then inoculated with the standard inoculum (0.5 McFarland) of the test organism. An AZT disc (30 μg) was placed on the supplemented MHA medium, and the medium was incubated overnight at 37°C. Aztreonam zone diameter on the supplemented MHA medium (in the presence of ceftazidime-avibactam) was compared with that from a standard disc diffusion plate (without ceftazidime-avibactam), performed in parallel. Interpretation of synergy was based on the restoration of aztreonam zone diameter (in the presence of ceftazidime-avibactam) crossing the CLSI susceptibility breakpoint, i.e., ≥ 21 mm. Of 37 carbapenem-resistant NDM-producing isolates, 35 (94.6%) were resistant to aztreonam and tested synergy positive by the proposed method. Its sensitivity and specificity were 97.14% and 100%, respectively. Cohen's kappa value showed substantial agreement of the reference method with the proposed method (κ = 0.78) but no other methods. The proposed method is simple, easily interpretable, and showed excellent sensitivity, specificity, and agreement with the reference method. Therefore, the new method is feasible and reliable for testing aztreonam synergy with avibactam in NDM-producing Enterobacterales.

摘要

产 NDM 碳青霉烯酶耐药细菌感染对临床医生来说是一个挑战。联合使用氨曲南和头孢他啶-阿维巴坦是治疗这些感染的谨慎选择。然而,目前仍然没有一种实用可行的方法来检测氨曲南和头孢他啶-阿维巴坦的协同作用。我们提出了一种简单的方法来检测氨曲南和头孢他啶-阿维巴坦的协同作用,并与参考肉汤微量稀释法和其他方法进行了比较。通过 Carba R 检测筛选携带 NDM 基因的碳青霉烯类耐药肠杆菌科临床分离株。用肉汤微量稀释法(参考方法)、E 带药敏纸片扩散法、双纸片扩散法和纸片替换法检测产 NDM 碳青霉烯酶耐药肠杆菌科分离株对氨曲南和头孢他啶-阿维巴坦的协同作用。在新提出的方法中,在 MHA 培养基中添加头孢他啶-阿维巴坦(对应于氨曲南浓度为 4μg/ml)。然后用标准接种物(0.5 McFarland)接种 MHA 培养基。在添加的 MHA 培养基上放置一个 AZT 药敏纸片(30μg),并在 37°C 下孵育过夜。在添加头孢他啶-阿维巴坦的 MHA 培养基上的氨曲南药敏纸片的直径(与没有添加头孢他啶-阿维巴坦的标准药敏纸片进行比较)。协同作用的解释基于在添加头孢他啶-阿维巴坦的情况下,氨曲南药敏纸片的直径(与没有添加头孢他啶-阿维巴坦的标准药敏纸片进行比较)恢复到 CLSI 药敏折点,即≥21mm。在 37 株产 NDM 碳青霉烯酶耐药分离株中,35 株(94.6%)对氨曲南耐药,且该方法检测协同作用阳性。其敏感性和特异性分别为 97.14%和 100%。Cohen's kappa 值显示参考方法与新方法具有高度一致性(κ=0.78),但其他方法没有。该方法简单,易于解释,与参考方法具有良好的敏感性、特异性和一致性。因此,该新方法在检测产 NDM 肠杆菌科中氨曲南与阿维巴坦的协同作用方面是可行和可靠的。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/860c/11101023/cca04f6b84e4/pone.0303753.g001.jpg

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