Mobile colistin resistance: Prevalence, mechanisms, and current detection methods

N. Q. Truong, L. Thuy, S. Egorova, Lidiia A. Kaftyreva, Hoang Quoc Cuong
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Abstract

Colistin is considered the last-line antibiotic against multidrug-resistant Gram-negative bacterial infections. The global dissemination of Mobile colistin resistance mcr-harboring bacteria is threatening public health. Such isolates have been detected in various reservoirs including animals, food products, the environment, and humans. From these reservoirs, the isolates are approximate: 53% from animals; 39% from humans; 5% from the environment; and 3% from food. Bacterial distributions were: E.coli 91%; Salmonella 7%; and Klebsiella 2%. Among the 10 mcr variants, mcr-1 and mcr-9 are the most prevalent (up to 95% and 64.53%, respectively, in different studies) while other variants account for 5%. The coexistence of mcr and other antibiotic resistance genes in single isolates is a significant concern; mcr variants carried by different plasmid types increase antibiotic resistance and transfer of mcr genes to other bacteria. The hypothesis that the food chain is intimately involved in mcr gene transfer is supported by the presence of mcr-harboring isolates in animals and foods relative to humans. Cheaper, quicker, and more effective diagnostic tools for detecting colistin-resistant bacterial phenotypes and genotypes are essential and urgent. Currently, high quality tests include RPNP (99.3% specificity, 96.7% sensitivity) and MRPNP (95.4% specificity, ~100% sensitivity). LBJMR, CHROM agar, COL-APSE, and Super Polymyxin are now the best media to screen the bacteria, with near 100% selectivity. Multiplex PCR is a suitable method to quickly and accurately detect mcr genes in E. coli and Salmonella . Multi-drug resistant Gram-negative bacteria remain a global burden and need to have continuous and effective surveillance.
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移动粘菌素耐药性:流行、机制和当前的检测方法
粘菌素被认为是对抗多重耐药革兰氏阴性细菌感染的最后一线抗生素。移动粘菌素耐药细菌的全球传播威胁着公众健康。这些分离株已在包括动物、食品、环境和人类在内的各种宿主中发现。在这些水库中,分离株大致为:53%来自动物;39%来自人类;5%来自环境;3%来自食物。细菌分布:大肠杆菌91%;沙门氏菌7%;克雷伯氏菌2%。在这10种mcr变异中,以mcr-1和mcr-9最为常见(在不同的研究中分别高达95%和64.53%),其他变异占5%。mcr和其他抗生素耐药基因在单一分离株中的共存是一个重大问题;不同类型的质粒携带的MCR变异增加了抗生素耐药性和MCR基因向其他细菌的转移。在动物和相对于人类的食物中存在携带mcr的分离株,支持了食物链密切参与mcr基因转移的假设。检测耐粘菌素细菌表型和基因型的更便宜、更快和更有效的诊断工具是必要和紧迫的。目前,高质量的检测包括RPNP(特异性99.3%,敏感性96.7%)和MRPNP(特异性95.4%,敏感性~100%)。LBJMR、CHROM琼脂、COL-APSE和Super Polymyxin现在是筛选细菌的最佳培养基,选择性接近100%。多重PCR是快速、准确检测大肠杆菌和沙门氏菌中mcr基因的有效方法。多重耐药革兰氏阴性菌仍然是全球负担,需要持续有效地监测。
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