肺炎克雷伯菌不同碳青霉烯酶和嗜苷酸盐的产生对头孢克肟敏感性的影响

IF 4.1 2区 医学 Q2 MICROBIOLOGY
Chengcheng Yang, Liang Wang, Jingnan Lv, Yicheng Wen, Qizhao Gao, Feinan Qian, Xiangxiang Tian, Jie Zhu, Zhichen Zhu, Liang Chen, Hong Du
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引用次数: 0

摘要

革兰氏阴性菌对嗜苷类抗生素头孢克洛的耐药机制主要归因于碳青霉烯酶和嗜苷类物质的吸收途径,但具体因素及其关系仍有待全面阐明。在此,我们构建了携带不同碳青霉烯酶和敲除嗜苷基因的耐头孢克洛菌(CRKP)菌株,以研究各种碳青霉烯酶和嗜苷基因在头孢克洛耐药性产生过程中的作用。抗菌药敏感性测试表明,blaNDM 和 blaKPC 能显著提高肺炎克雷伯氏菌(KP)对头孢克洛的最低抑菌浓度(MIC),而 blaOXA-48 的增幅不大。值得注意的是,与表达 KPC 的 KP 相比,表达 NDM 的 KP 表现出更高的头孢羟氨苄 MIC,尽管单独表达 NDM 并不会诱导头孢羟氨苄耐药性。实验室进化实验表明,将 pNDM 与苷元吸收受体基因 cirA 的突变相结合,以及将 pKPC 与双组分系统基因 envZ 的突变相结合,可使 KP 达到较高的头孢羟氨苄耐药性水平。虽然 pOXA 与双组分系统基因 baeS 的突变结合不会诱导头孢克洛抗性,但会显著降低易感性。此外,嗜苷酸盐也会影响头孢羟氨苄耐药性的产生。缺乏肠杆菌素的菌株对头孢羟氨苄的敏感性增加,而缺乏yersiniabactin和salmochelin的菌株对头孢羟氨苄的敏感性没有明显变化。总之,碳青霉烯酶基因的表达促进了头孢克洛耐药性的产生,但仅有碳青霉烯酶基因的表达是不够的。CRKP 中的头孢羟氨苄耐药性通常涉及某些基因的异常表达和其他因素,如苷酸吸收受体基因和双组分系统基因突变。肠杆菌素苷酸合成基因 entB 也可能导致耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of different carbapenemase and siderophore production on cefiderocol susceptibility in Klebsiella pneumoniae.

The resistance mechanism of Gram-negative bacteria to the siderophore antibiotic cefiderocol is primarily attributed to carbapenemase and siderophore uptake pathways; however, specific factors and their relationships remain to be fully elucidated. Here, we constructed cefiderocol-resistant Klebsiella pneumoniae (CRKP) strains carrying different carbapenemases and knocked out siderophore genes to investigate the roles of various carbapenemases and siderophores in the development of cefiderocol resistance. Antimicrobial susceptibility testing revealed that both blaNDM and blaKPC significantly increased the minimum inhibitory concentration (MIC) of Klebsiella pneumoniae (KP) to cefiderocol, while blaOXA-48 showed a modest increase. Notably, KP expressing NDM exhibited a higher cefiderocol MIC compared to KP expressing KPC, although expression of NDM alone did not induce cefiderocol resistance. Laboratory evolutionary experiments demonstrated that combining pNDM with mutations in the siderophore uptake receptor gene cirA and pKPC with a mutation in the two-component system gene envZ led to KP reaching a high level of cefiderocol resistance. Although combining pOXA with mutations in the two-component system gene baeS did not induce cefiderocol resistance, it significantly reduced susceptibility. Moreover, siderophores could influence the development of cefiderocol resistance. Strains deficient in enterobactin exhibited increased susceptibility to cefiderocol, while deficiencies in yersiniabactin and salmochelin showed no significant alterations. In conclusion, carbapenemase gene expression facilitates cefiderocol resistance, but its presence alone is insufficient. Cefiderocol resistance in CRKP typically involves abnormal expression of certain genes and other factors, such as mutations in siderophore uptake receptor genes and two-component system genes. The enterobactin siderophore synthesis gene entB may also contribute to resistance.

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来源期刊
CiteScore
10.00
自引率
8.20%
发文量
762
审稿时长
3 months
期刊介绍: Antimicrobial Agents and Chemotherapy (AAC) features interdisciplinary studies that build our understanding of the underlying mechanisms and therapeutic applications of antimicrobial and antiparasitic agents and chemotherapy.
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