Comparative analysis of the antimicrobial resistance and virulence traits in ESBL-producing-Klebsiella pneumoniae ST307 strains colonizing the gastrointestinal tract and causing a fatal bloodstream infection in a leukemia patient

IF 2.6 4区 医学 Q3 INFECTIOUS DISEASES Infection Genetics and Evolution Pub Date : 2024-04-21 DOI:10.1016/j.meegid.2024.105598
Luana Boff , Humberlânia de Sousa Duarte , Gabriela Bergiante Kraychete , Gabriel Taddeucci-Rocha , Bianca Diniz Oliveira , Rodolpho Mattos Albano , Ana Paula D'Alincourt Carvalho-Assef , Silvana Vargas Superti , Ianick Souto Martins , Renata Cristina Picão
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Abstract

Klebsiella pneumoniae is an opportunistic pathogen that can colonize the gastrointestinal tract (GIT) of humans. The mechanisms underlying the successful translocation of this pathogen to cause extra-intestinal infections remain unknown, although virulence and antimicrobial resistance traits likely play significant roles in the establishment of infections. We investigated K. pneumoniae strains isolated from GIT colonization (strains Kp_FZcol-1, Kp_FZcol-2 and Kp_FZcro-1) and from a fatal bloodstream infection (strain Kp_HM-1) in a leukemia patient. All strains belonged to ST307, carried a transferable IncF plasmid containing the blaCTX-M-15 gene (pKPN3–307 TypeA-like plasmid) and showed a multidrug-resistance phenotype. Phylogenetic analysis demonstrated that Kp_HM-1 was more closely related to Kp_FZcro-1 than to the other colonizing strains. The Kp_FZcol-2 genome showed 81 % coverage with the Kp_HM-1 246,730 bp plasmid (pKp_HM-1), lacking most of its putative virulence genes. Searching public genomes with similar coverage, we observed the occurrence of this deletion in K. pneumoniae ST307 strains recovered from human colonization and infection in different countries. Our findings suggest that strains lacking the putative virulence genes found in the pKPN3–307 TypeA plasmid are still able to colonize and infect humans, highlighting the need to further investigate the role of these genes for the adaptation of K. pneumoniae ST307 in distinct human body sites.

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产ESBL肺炎克雷伯氏菌ST307菌株的抗菌药耐药性和毒力特征比较分析,这些菌株在胃肠道定植并导致一名白血病患者发生致命性血流感染
肺炎克雷伯氏菌是一种可在人类胃肠道(GIT)定植的机会性病原体。虽然毒性和抗菌药耐药性特征可能在感染的形成过程中发挥了重要作用,但这种病原体成功转移到肠道外引起感染的机制仍不清楚。我们研究了从胃肠道定植(菌株 Kp_FZcol-1、Kp_FZcol-2 和 Kp_FZcro-1)和白血病患者致命血流感染(菌株 Kp_HM-1)中分离出的肺炎克氏菌菌株。所有菌株都属于 ST307,携带含有 blaCTX-M-15 基因的可转移 IncF 质粒(pKPN3-307 TypeA-like 质粒),并表现出多重耐药表型。系统发育分析表明,Kp_HM-1 与 Kp_FZcro-1 的亲缘关系比与其他定殖菌株的亲缘关系更近。Kp_FZcol-2基因组与Kp_HM-1 246 730 bp质粒(pKp_HM-1)的覆盖率为81%,但缺少其大部分推测的毒力基因。通过搜索具有类似覆盖率的公共基因组,我们发现在不同国家从人类定植和感染中恢复的肺炎克菌 ST307 株系中也出现了这种缺失。我们的研究结果表明,pKPN3-307 TypeA 质粒中缺乏推测毒力基因的菌株仍然能够定殖和感染人类,这突出表明有必要进一步研究这些基因对肺炎克菌 ST307 在不同人体部位的适应性所起的作用。
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来源期刊
Infection Genetics and Evolution
Infection Genetics and Evolution 医学-传染病学
CiteScore
8.40
自引率
0.00%
发文量
215
审稿时长
82 days
期刊介绍: (aka Journal of Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases -- MEEGID) Infectious diseases constitute one of the main challenges to medical science in the coming century. The impressive development of molecular megatechnologies and of bioinformatics have greatly increased our knowledge of the evolution, transmission and pathogenicity of infectious diseases. Research has shown that host susceptibility to many infectious diseases has a genetic basis. Furthermore, much is now known on the molecular epidemiology, evolution and virulence of pathogenic agents, as well as their resistance to drugs, vaccines, and antibiotics. Equally, research on the genetics of disease vectors has greatly improved our understanding of their systematics, has increased our capacity to identify target populations for control or intervention, and has provided detailed information on the mechanisms of insecticide resistance. However, the genetics and evolutionary biology of hosts, pathogens and vectors have tended to develop as three separate fields of research. This artificial compartmentalisation is of concern due to our growing appreciation of the strong co-evolutionary interactions among hosts, pathogens and vectors. Infection, Genetics and Evolution and its companion congress [MEEGID](http://www.meegidconference.com/) (for Molecular Epidemiology and Evolutionary Genetics of Infectious Diseases) are the main forum acting for the cross-fertilization between evolutionary science and biomedical research on infectious diseases. Infection, Genetics and Evolution is the only journal that welcomes articles dealing with the genetics and evolutionary biology of hosts, pathogens and vectors, and coevolution processes among them in relation to infection and disease manifestation. All infectious models enter the scope of the journal, including pathogens of humans, animals and plants, either parasites, fungi, bacteria, viruses or prions. The journal welcomes articles dealing with genetics, population genetics, genomics, postgenomics, gene expression, evolutionary biology, population dynamics, mathematical modeling and bioinformatics. We also provide many author benefits, such as free PDFs, a liberal copyright policy, special discounts on Elsevier publications and much more. Please click here for more information on our author services .
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