[HTML][HTML] Capsule deletion via a λ-Red knockout system perturbs biofilm formation and fimbriae expression in Klebsiella pneumoniae MGH 78578

TW Huang, I Lam, HY Chang, SF Tsai, BO Palsson… - BMC research …, 2014 - Springer
TW Huang, I Lam, HY Chang, SF Tsai, BO Palsson, P Charusanti
BMC research notes, 2014Springer
Background Klebsiella pneumoniae is a leading cause of hospital-acquired urinary tract
infections and pneumonia worldwide, and is responsible for many cases of pyogenic liver
abscess among diabetic patients in Asia. A defining characteristic of this pathogen is the
presence of a thick, exterior capsule that has been reported to play a role in biofilm formation
and to protect the organism from threats such antibiotics and host immune challenge.
Findings We constructed two knockout mutants of K. pneumoniae to investigate how …
Background
Klebsiella pneumoniae is a leading cause of hospital-acquired urinary tract infections and pneumonia worldwide, and is responsible for many cases of pyogenic liver abscess among diabetic patients in Asia. A defining characteristic of this pathogen is the presence of a thick, exterior capsule that has been reported to play a role in biofilm formation and to protect the organism from threats such antibiotics and host immune challenge.
Findings
We constructed two knockout mutants of K. pneumoniae to investigate how perturbations to capsule biosynthesis alter the cellular phenotype. In the first mutant, we deleted the entire gene cluster responsible for biosynthesis of the extracellular polysaccharide capsule. In the second mutant, we deleted the capsule export subsystem within this cluster. We find that both knockout mutants have lower amounts of capsule but produce greater amounts of biofilm. Moreover, one of the two mutants abolishes fimbriae expression as well.
Conclusions
These results are expected to provide insight into the interaction between capsule biosynthesis, biofilm formation, and fimbriae expression in this organism.
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