Beckman Robert L, Cella Elenora, Azarian Taj, Rendueles Olaya, Fleeman Renee M
Burnett School of Biomedical Sciences, College of Medicine, University of Central Florida, Orlando, FL, USA.
Laboratoire de Microbiologie et Génétique Moléculaires (LMGM), UMR5100, Centre de Biologie Intégrative (CBI), Université de Toulouse, CNRS, Université Toulouse III - Paul Sabatier (UT3), Toulouse, France.
NPJ Biofilms Microbiomes. 2024 Dec 19;10(1):151. doi: 10.1038/s41522-024-00629-y.
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.
肺炎克雷伯菌感染对人类健康构成的威胁日益增大。对抗生素耐药性、黏液黏稠度和生物膜形成之间关系的认识不足,阻碍了我们有效预测肺炎克雷伯菌感染结果的能力。多重耐药生物库与监测网络为了解肺炎克雷伯菌分离株的遗传和表型变异性提供了独特的机会。为此,我们将这些分离株的基因图谱与表型生物膜形成、黏液黏稠度百分比和生长速率进行了比较。生物膜形成减少与III型菌毛系统转录激活因子中的插入序列之间存在显著的表型-基因型相关性。有趣的是,群体中黏液性最强的菌株缺乏调节黏液表型的遗传元件,其中三株分离株能够形成强大的生物膜。表型、基因组和图像分析的结合揭示了生长、黏液黏稠度与特定毒力相关遗传决定因素之间的复杂关系。