多重耐药肺炎克雷伯菌防御系统的研究进展。

microPublication biology Pub Date : 2025-08-20 eCollection Date: 2025-01-01 DOI:10.17912/micropub.biology.001752
Tosin Yetunde Senbadejo, Samuel Ntiamoah Osei, Abiola Isawumi
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引用次数: 0

摘要

细菌防御机制保护病原体免受宿主免疫、噬菌体和恶劣环境的侵害。本研究调查了来自加纳医院icu的耐多药肺炎克雷伯菌的防御系统,重点关注CRISPR-Cas、限制性修饰(R-M)和毒素-抗毒素(TA)系统。采用PADLOC、defensefinder和TADB3.0对环境菌株(NS2)和临床菌株(PS4)进行基因组测序和分析。NS2携带包括CRISPR-Cas在内的12种防御系统,而PS4则有5种。两者都拥有不同的RM和TA系统。这些菌株对六种抗生素具有耐药性,编码临床重要的防御系统,表明污染物与人类之间的微生物交换,潜在地增加了需要靶向监测的ICU环境中的感染风险。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Snapshot of Defense Systems in Multidrug Resistant <i>Klebsiella pneumoniae</i>.

Snapshot of Defense Systems in Multidrug Resistant Klebsiella pneumoniae.

Bacterial defense mechanisms protect pathogens from host immunity, bacteriophages, and harsh environments. This study investigates defense systems in multidrug-resistant Klebsiella pneumoniae from Ghanaian hospital ICUs, focusing on CRISPR-Cas, restriction-modification (R-M), and toxin-antitoxin (TA) systems. Genomes of environmental (NS2) and clinical (PS4) strains were sequenced and analyzed using PADLOC, defensefinder, and TADB3.0. NS2 carries 12 defense systems, including CRISPR-Cas, while PS4 has five. Both possess diverse RM and TA systems. These strains, resistant to six antibiotic classes, encode clinically significant defense systems, suggesting microbial exchange between fomites and humans, potentially increasing infection risks in ICU environments requiring targeted surveillance.

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