Development and validation of a pentaplex PCR assay for rapid detection of blaCTX-M, blaOXA–1, blaCMY, blaNDM and the PBP3 insert in Enterobacterales

IF 1.4 4区 医学 Q4 IMMUNOLOGY
Yamuna Devi Bakthavatchalam , Fizaa Abdullah , Devishree Srinivasan , Sangeetha Nithiyanandam , Ayyanraj Neeravi , Poojah Shah , Nivedhana Subburaju , Subha Vajjiravelu Jaganathan , Rema Devi , Gita Nataraj , Binesh Lal Yesudason , Kamini Walia , Balaji Veeraraghavan
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引用次数: 0

Abstract

Background

There is a high diversity of beta-lactamases in gram negative pathogens, making them difficult to treat. In the presence of OXA-1 and ampC, PTZ is no longer clinically relevant when treating Enterobacterales expressing ESBLs. Further, MBL infections are often treated with the combination of ceftazidime/avibactam with aztreonam. . It has recently been reported that NDM-expressing E. coli isolates co-harboring PBP3 insert develops resistance to this triple combination.

Methods

A pentaplex PCR is developed and validated to simultaneously detect blaCTX-M, blaOXA-1, blaCMY, blaNDM, and the PBP3 insert in whole genome sequenced E. coli and K. pneumoniae isolates. In addition, the isolates chosen for pentaplex PCR evaluation were tested for their minimum inhibitory concentrations (MICs) against piperacillin/tazobactam, cefoperazone/sulbactam (C/S), ertapenem, imipenem, meropenem, ceftazidime/avibactam, aztreonam/avibactam, cefepime/taniborbactam, and cefiderocol.

Results

The developed pentaplex PCR showed 100 % reproducibility with the antimicrobial resistance profile generated from whole genome sequenced data. PTZ and C/S are not effective against ESBL and/or OXA-1 expressing E. coli and K. pneumoniae isolates and do not offer any activity against CMY co-producers. Further, the combined effect of CMY, NDM and PBP3 inserts impacts aztreonam/avibactam activity and reduces the susceptibility to 40 % in E. coli isolates. While, aztreonam/avibactam showed potent activity against NDM-expressing K. pneumoniae isolates. Importantly, cefepime/taniborbactam and cefiderocol showed limited activity against NDM-expressing E. coli and K. pneumoniae isolates.

Conclusion

The pentaplex PCR was effective in detecting four beta-lactamases (blaCTX-M, blaOXA-1, blaCMY, blaNDM) as well as PBP3 inserts. It is expected that using pentaplex PCR as a diagnostic test for resistance detection in clinical practice will improve patient outcomes by providing prompt and targeted treatment.

开发并验证用于快速检测肠杆菌中 blaCTX-M、blaOXA-1、blaCMY、blaNDM 和 PBP3 插入物的五重 PCR 法。
背景:革兰氏阴性病原体中的β-内酰胺酶种类繁多,因此难以治疗。由于存在 OXA-1 和 ampC,在治疗表达 ESBLs 的肠杆菌时,PTZ 不再具有临床意义。此外,MBL 感染通常使用头孢唑肟/阿维菌素和阿曲南来联合治疗。最近有报道称,表达 NDM 的大肠杆菌分离物中同时存在 NDM,并对这种三联疗法产生耐药性:方法:开发并验证了五重 PCR,用于检测全基因组测序分离物中的 blaCTX-M、blaOXA-1、blaCMY、blaNDM 和 PBP3 插入物。此外,还检测了被选作五重 PCR 评估的分离株对哌拉西林/他唑巴坦、头孢哌酮/舒巴坦(C/S)、厄他培南、亚胺培南、美罗培南、头孢唑肟/阿维巴坦、阿曲南/阿维巴坦、头孢吡肟/他尼巴坦和头孢克肟的最低抑菌浓度(MICs):所开发的五联 PCR 与全基因组测序数据生成的抗菌药物耐药性图谱具有 100% 的重现性。PTZ 和 C/S 对表达 ESBL 和/或 OXA-1 的大肠杆菌和肺炎双球菌分离物无效,对 CMY 协同产生者也没有任何活性。此外,CMY、NDM 和 PBP3 插入物的共同作用会影响阿曲南药/阿维菌素的活性,并将大肠杆菌分离物的易感性降低至 40%。同时,唑曲南/阿维巴坦对表达 NDM 的肺炎克氏菌分离物显示出强大的活性。重要的是,头孢吡肟/他尼巴坦和头孢克肟对表达 NDM 的大肠杆菌和肺炎双球菌分离物的活性有限:五重 PCR 能有效检测四种 beta-内酰胺酶(blaCTX-M、blaOXA-1、blaCMY 和 blaNDM)以及 PBP3 插入物。预计在临床实践中使用五重 PCR 作为耐药性检测诊断试验将能提供及时和有针对性的治疗,从而改善患者的预后。
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来源期刊
CiteScore
2.20
自引率
0.00%
发文量
154
审稿时长
73 days
期刊介绍: Manuscripts of high standard in the form of original research, multicentric studies, meta analysis, are accepted. Current reports can be submitted as brief communications. Case reports must include review of current literature, clinical details, outcome and follow up. Letters to the editor must be a comment on or pertain to a manuscript already published in the IJMM or in relation to preliminary communication of a larger study. Review articles, Special Articles or Guest Editorials are accepted on invitation.
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