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埃及多药耐药、广泛耐药和全耐药菌株中氟喹诺酮耐药性的分子检测

Molecular Detection of Fluoroquinolone Resistance among Multidrug-, Extensively Drug-, and Pan-Drug-Resistant Species in Egypt.

作者信息

Ammar Ahmed M, Abd El-Hamid Marwa I, El-Malt Rania M S, Azab Doaa S, Albogami Sarah, Al-Sanea Mohammad M, Soliman Wafaa E, Ghoneim Mohammed M, Bendary Mahmoud M

机构信息

Department of Microbiology, Faculty of Veterinary Medicine, Zagazig University, Zagazig 44519, Egypt.

Animal Health Research Institute-Agriculture Research Center, Zagazig University, Zagazig 44516, Egypt.

出版信息

Antibiotics (Basel). 2021 Nov 3;10(11):1342. doi: 10.3390/antibiotics10111342.

Abstract

In recent times, resistant foodborne pathogens, especially of the species, have created several global crises. These crises have been compounded due to the evolution of multidrug-resistant (MDR) bacterial pathogens and the emergence of extensively drug-resistant (XDR) and pan-drug-resistant (PDR) strains. Therefore, this study aimed to investigate the development of resistance and the existence of both XDR and PDR among isolates. Moreover, we explored the use of the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique for the detection of fluoroquinolone (FQ)-resistant isolates. A total of 120 isolates were identified depending on both phenotypic and genotypic methods. Of note, cefoxitin and imipenem were the most effective drugs against the investigated isolates. Interestingly, the majority of our isolates (75%) were MDR. Unfortunately, both XDR and PDR isolates were detected in our study with prevalence rates of 20.8% and 4.2%, respectively. All FQ-resistant isolates with ciprofloxacin minimum inhibitory concentrations ≥4 µg/mL were confirmed by the genetic detection of chromosomal mutation via substitution of threonine at position 86 to isoleucine (Thr-86-to-Ile) using the PCR-RFLP technique. Herein, PCR-RFLP was a more practical and less expensive method used for the detection of FQ resistant isolates. In conclusion, we introduced a fast genetic method for the identification of FQ-resistant isolates to avoid treatment failure through the proper description of antimicrobials.

摘要

近年来,具有耐药性的食源性病原体,尤其是该物种的病原体,引发了数次全球危机。由于多重耐药(MDR)细菌病原体的进化以及广泛耐药(XDR)和泛耐药(PDR)菌株的出现,这些危机进一步加剧。因此,本研究旨在调查[具体物种]分离株的耐药性发展情况以及XDR和PDR的存在情况。此外,我们探索了使用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)技术检测耐氟喹诺酮(FQ)的[具体物种]分离株。根据表型和基因型方法共鉴定出120株[具体物种]分离株。值得注意的是,头孢西丁和亚胺培南是针对所研究的[具体物种]分离株最有效的药物。有趣的是,我们的大多数分离株(75%)为MDR。不幸的是,在我们的研究中检测到了XDR和PDR分离株,其流行率分别为20.8%和4.2%。所有环丙沙星最低抑菌浓度≥4 µg/mL的耐FQ分离株,通过使用PCR-RFLP技术对86位苏氨酸被异亮氨酸取代(Thr-86-to-Ile)的[具体基因]染色体突变进行基因检测得以确认。在此,PCR-RFLP是一种用于检测耐FQ分离株的更实用且成本更低的方法。总之,我们引入了一种快速的基因方法来鉴定耐FQ分离株,以通过对抗菌药物的恰当描述避免治疗失败。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5d47/8614916/e93f68f453b8/antibiotics-10-01342-g001.jpg

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