Identification of three podoviruses infecting Klebsiella encoding capsule depolymerases that digest specific capsular types.
Yi-Jiun PanTzu-Lung LinYi-Yin ChenPeng-Hsuan LaiYun-Ting TsaiChun-Ru HsuPei-Fang HsiehYi-Tsung LinJin-Town WangPublished in: Microbial biotechnology (2019)
Klebsiella pneumoniae is an important human pathogen causing opportunistic nosocomial and community-acquired infections. A major public health concern regarding K. pneumoniae is the increasing incidence of multidrug-resistant strains. Here, we isolated three novel Klebsiella bacteriophages, KN1-1, KN3-1 and KN4-1, which infect KN1, KN3 and K56, and KN4 types respectively. We determined their genome sequences and conducted a comparative analysis that revealed a variable region containing capsule depolymerase-encoding genes. Recombinant depolymerase proteins were produced, and their enzymatic activity and specificity were evaluated. We identified four capsule depolymerases in these phages that could only digest the capsule types of their respective hosts. Our results demonstrate that the activities of these capsule depolymerases were correlated with the host range of each phage; thus, the capsule depolymerases are host specificity determinants. By generating a capsule mutant, we demonstrate that capsule was essential for phage adsorption and infection. Further, capsule depolymerases can enhance bacterial susceptibility to serum killing. The discovery of these phages and depolymerases lays the foundation for the typing of KN1, KN3, KN4 and K56 Klebsiella and could be useful alternative therapeutics for the treatment of K. pneumoniae infections.
Keyphrases
- multidrug resistant
- klebsiella pneumoniae
- public health
- escherichia coli
- healthcare
- endothelial cells
- small molecule
- pseudomonas aeruginosa
- risk factors
- nitric oxide
- genome wide
- high throughput
- candida albicans
- replacement therapy
- bioinformatics analysis
- structural basis
- dna methylation
- smoking cessation
- aqueous solution