Abstract

Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems. Biofilms attach to the surfaces of either living or nonliving objects and protect bacteria against antibiotics and a host's immune system. Here, a novel type of biofilm (the "R-biofilm") is reported. These biofilms were formed by clinically isolated Klebsiella pneumoniae strains following double-stranded-DNA breaks (DSBs), while undamaged bacteria did not form classic biofilms even in the later stages of growth. R-biofilms had a fixed ring-like or discoid shape with good ductility and could protect many living bacterial cells within. We show that extracellular proteins and DNAs released, probably by dead bacteria, were the core structural materials of R-biofilms. We anticipate that novel signaling pathways besides the bacterial SOS response are involved in R-biofilm formation. The observations in this study suggest a limitation to the use of the currently popular Cas9-mediated bactericidal tools to eliminate certain bacteria because the resulting DSBs may lead to the formation of these protective R-biofilms.IMPORTANCE Many pathogenic bacteria can form biofilm matrices that consist of complex molecules such as polysaccharides, proteins, and DNA. These biofilms help the bacteria to infect and colonize a host. Such biofilms may attach and develop on the surfaces of indwelling medical devices or other supportive environments. This study found that following double-strand breaks in their DNA, Klebsiella pneumoniae cells can form a novel type of biofilm with ring-like or discoid morphology. This biofilm structure, named the "R-biofilm," helps protect the bacteria against adverse conditions such as exposure to ethanol, hydrogen peroxide, and UV radiation.

Highlights

  • Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems

  • We found a previously unreported type of biofilm when we adopted the above-described strategy to kill K. pneumoniae, while the bacteria did not form classical biofilms even in the later stages of growth

  • Considering that the DNA break sites may be repaired by error-prone DNA polymerases using homologous recombination from another unbroken copy on the genome during replication, we first tested the bactericidal efficiency of the designed CRISPR-Cas9 system

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Summary

Introduction

Biofilms usually form when the density of bacteria increases during the middle to late periods of growth in culture, commonly induced by quorum-sensing systems. We designed a CRISPRCas9 bactericidal plasmid (pB16Kp) with an arabinose-inducible Cas9 protein, and a guide RNA (gRNA) targeting the 16S rRNA sequence (N20-TGAAATGCGTAGAGATCTGG-) in the genome of K. pneumoniae strain 355, aiming to cause multiple fatal breaks in the cellular DNA (Fig. 1A).

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