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宿主内导致多药耐药性增加的肺炎克雷伯菌克隆的逐步进化。

Stepwise Evolution of a Klebsiella pneumoniae Clone within a Host Leading to Increased Multidrug Resistance.

机构信息

Department of Clinical Chemistry and Laboratory Medicine, Kyushu University Hospitalgrid.411248.a, Fukuoka, Japan.

Department of Bacteriology, Graduate School of Medical Sciences, Kyushu Universitygrid.411248.agrid.177174.3, Fukuoka, Japan.

出版信息

mSphere. 2021 Dec 22;6(6):e0073421. doi: 10.1128/mSphere.00734-21. Epub 2021 Nov 24.

DOI:10.1128/mSphere.00734-21
PMID:34817239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8612250/
Abstract

Five -positive Klebsiella pneumoniae isolates (KpWEA1, KpWEA2, KpWEA3, KpWEA4-1, and KpWEA4-2) were consecutively obtained from a patient with relapsed acute myeloid leukemia who was continuously administered antimicrobials. Compared with KpWEA1 and KpWEA2, KpWEA3 showed decreased susceptibility to antimicrobials, and KpWEA4-1 and KpWEA4-2 (isolated from a single specimen) showed further-elevated multidrug-resistance (MDR) phenotypes. This study aims to clarify the clonality of the five isolates and their evolutionary processes leading to MDR by comparison of these complete genomes. The genome comparison revealed KpWEA1 was the antecedent of the other four isolates, and KpWEA4-1 and KpWEA4-2 independently emerged from KpWEA3. Increasing levels of MDR were acquired by gradual accumulation of genetic alterations related to outer membrane protein expression: the loss of OmpK35 and upregulation of AcrAB-TolC occurred in KpWEA3 due to overexpression caused by a mutation in ; then OmpK36 was lost in KpWEA4-1 and KpWEA4-2 by different mechanisms. KpWEA4-2 further acquired colistin resistance by the deletion of . In addition, we found that and , which encode repressors of hexuronate metabolism-related genes, were disrupted in different ways in KpWEA4-1 and KpWEA4-2. The two isolates also possessed different amino acid substitutions in AtpG, which occurred at very close positions. These genetic alterations related to metabolisms may compensate for the deleterious effects of major porin loss. Thus, our present study reveals the evolutionary process of a K. pneumoniae clone leading to MDR and also suggests specific survival strategies in the bacteria that acquired MDR by the genome evolution. Within-host evolution is a survival strategy that can occur in many pathogens and is often associated with the emergence of novel antimicrobial-resistant (AMR) bacteria. To analyze this process, suitable sets of clinical isolates are required. Here, we analyzed five Klebsiella pneumoniae isolates which were consecutively isolated from a patient and showed a gradual increase in the AMR level. By genome sequencing and other analyses, we show that the first isolate was the antecedent of the later isolates and that they gained increased levels of antimicrobial resistance leading to multidrug resistance (MDR) by stepwise changes in the expression of outer membrane proteins. The isolates showing higher levels of MDR lost major porins but still colonized the patient's gut, suggesting that the deleterious effects of porin loss were compensated for by the mutations in hexuronate metabolism-related genes and , which were commonly detected in the MDR isolates.

摘要

从一位患有复发性急性髓系白血病并持续接受抗生素治疗的患者中连续分离到五株产 5 型肺炎克雷伯菌(KpWEA1、KpWEA2、KpWEA3、KpWEA4-1 和 KpWEA4-2)。与 KpWEA1 和 KpWEA2 相比,KpWEA3 对抗生素的敏感性降低,而 KpWEA4-1 和 KpWEA4-2(从单个标本中分离)表现出进一步升高的多药耐药(MDR)表型。本研究旨在通过比较这些完整基因组,阐明这五个分离株的克隆性及其导致 MDR 的进化过程。基因组比较表明,KpWEA1 是其他四个分离株的前身,KpWEA4-1 和 KpWEA4-2 分别独立于 KpWEA3 出现。通过与外膜蛋白表达相关的遗传改变的逐渐积累,获得了更高水平的 MDR:KpWEA3 由于突变导致过度表达而失去了 OmpK35 并上调了 AcrAB-TolC;然后,KpWEA4-1 和 KpWEA4-2 通过不同的机制失去了 OmpK36。KpWEA4-2 通过 删除进一步获得了多粘菌素耐药性。此外,我们发现, 在 KpWEA4-1 和 KpWEA4-2 中以不同方式发生突变,分别破坏了编码六碳糖代谢相关基因的抑制剂的基因。这两个分离株在 AtpG 中也具有不同的氨基酸取代,这些取代发生在非常接近的位置。这些与代谢相关的遗传改变可能补偿了主要孔蛋白缺失的有害影响。因此,本研究揭示了导致 MDR 的肺炎克雷伯菌克隆的进化过程,并表明在通过基因组进化获得 MDR 的细菌中存在特定的生存策略。 宿主内进化是一种可以在许多病原体中发生的生存策略,通常与新型抗微生物药物耐药(AMR)细菌的出现有关。为了分析这个过程,需要合适的临床分离株集。在这里,我们分析了从一位患者中连续分离到的五株肺炎克雷伯菌,它们的 AMR 水平逐渐升高。通过基因组测序和其他分析,我们表明,第一个分离株是后来分离株的前身,它们通过外膜蛋白表达的逐步变化获得了更高水平的抗菌药物耐药性,导致了多药耐药性(MDR)。表现出更高 MDR 水平的分离株失去了主要的孔蛋白,但仍定植在患者的肠道中,这表明六碳糖代谢相关基因和 的突变共同检测到,在 MDR 分离株中,孔蛋白缺失的有害影响得到了补偿。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/e535d30d2311/msphere.00734-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/f4f0c7c7f61e/msphere.00734-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/49b6338e4310/msphere.00734-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/0e5aaf7931fc/msphere.00734-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/a508d98acce7/msphere.00734-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/e535d30d2311/msphere.00734-21-f005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/f4f0c7c7f61e/msphere.00734-21-f001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/49b6338e4310/msphere.00734-21-f002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/0e5aaf7931fc/msphere.00734-21-f003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/a508d98acce7/msphere.00734-21-f004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/615e/8612250/e535d30d2311/msphere.00734-21-f005.jpg

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