Diverse polysaccharide production and biofilm formation abilities of clinical Klebsiella pneumoniae.

IF 7.8 1区 生物学 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY npj Biofilms and Microbiomes Pub Date : 2024-12-19 DOI:10.1038/s41522-024-00629-y
Robert L Beckman, Elenora Cella, Taj Azarian, Olaya Rendueles, Renee M Fleeman
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Abstract

Klebsiella pneumoniae infections have become a growing threat for human health. The lack of understanding of the relationship between antibiotic resistance, mucoviscosity, and biofilm formation impedes our abilities to effectively predict K. pneumoniae infection outcomes. The Multidrug-Resistant Organism Repository and Surveillance Network offers a unique opportunity into the genetic and phenotypic variabilities in the K. pneumoniae isolates. To this end, we compared the genetic profiles of these isolates with the phenotypic biofilm formation, percent mucoviscosity, and growth rates. There was a significant phenotype-genotype correlation with decreased biofilm formation and an insertion sequence in the transcriptional activator of the type III fimbrial system. Interestingly, the most mucoid strains in the populations were lacking the genetic element regulating the mucoid phenotype and three of these isolates were able to form robust biofilms. The combination of phenotypic, genomic, and image analyses revealed an intricate relation between growth, mucoviscosity and specific virulence-associated genetic determinants.

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临床肺炎克雷伯氏菌的多种多糖生产和生物膜形成能力。
肺炎克雷伯菌感染已成为日益严重的人类健康威胁。缺乏对抗生素耐药性、黏液粘度和生物膜形成之间关系的理解,阻碍了我们有效预测肺炎克雷伯菌感染结果的能力。多药耐药生物库和监测网络为肺炎克雷伯菌分离株的遗传和表型变异提供了独特的机会。为此,我们将这些分离株的遗传谱与表型生物膜形成、黏度百分比和生长速率进行了比较。表型-基因型与生物膜形成减少和III型毛系统转录激活子插入序列存在显著相关性。有趣的是,群体中大多数粘液样菌株缺乏调节粘液样表型的遗传元件,其中三个分离株能够形成坚固的生物膜。表型、基因组和图像分析的结合揭示了生长、黏液粘度和特异性毒力相关遗传决定因素之间的复杂关系。
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来源期刊
npj Biofilms and Microbiomes
npj Biofilms and Microbiomes Immunology and Microbiology-Microbiology
CiteScore
12.10
自引率
3.30%
发文量
91
审稿时长
9 weeks
期刊介绍: npj Biofilms and Microbiomes is a comprehensive platform that promotes research on biofilms and microbiomes across various scientific disciplines. The journal facilitates cross-disciplinary discussions to enhance our understanding of the biology, ecology, and communal functions of biofilms, populations, and communities. It also focuses on applications in the medical, environmental, and engineering domains. The scope of the journal encompasses all aspects of the field, ranging from cell-cell communication and single cell interactions to the microbiomes of humans, animals, plants, and natural and built environments. The journal also welcomes research on the virome, phageome, mycome, and fungome. It publishes both applied science and theoretical work. As an open access and interdisciplinary journal, its primary goal is to publish significant scientific advancements in microbial biofilms and microbiomes. The journal enables discussions that span multiple disciplines and contributes to our understanding of the social behavior of microbial biofilm populations and communities, and their impact on life, human health, and the environment.
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