Open AccessTransposon Mutagenesis Screen of Klebsiella pneumoniae Identifies Multiple Genes Important for Resisting Antimicrobial Activities of Neutrophils in Mice
Author(s) -
Michelle K. Paczosa,
Rebecca J. Silver,
Anne L. McCabe,
Albert Tai,
Colin H. McLeish,
David W. Lazinski,
Joan Mecsas
Publication year - 2020
Publication title -
infection and immunity
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.508
H-Index - 220
eISSN - 1070-6313
pISSN - 0019-9567
DOI - 10.1128/iai.00034-20
Subject(s) - klebsiella pneumoniae , biology , transposon mutagenesis , transposable element , microbiology and biotechnology , mutagenesis , antimicrobial , gene , klebsiella infections , virology , sleeping beauty transposon system , genetics , mutation , escherichia coli , genome
Klebsiella pneumoniae is a Gram-negative bacterial pathogen that causes a range of infections, including pneumonias, urinary tract infections, and septicemia, in otherwise healthy and immunocompromised patients. K. pneumoniae has become an increasing concern due to the rise and spread of antibiotic-resistant and hypervirulent strains. However, its virulence determinants remain understudied. To identify novel K. pneumoniae virulence factors needed to cause pneumonia, a high-throughput screen was performed with an arrayed library of over 13,000 K. pneumoniae transposon insertion mutants in the lungs of wild-type (WT) and neutropenic mice using transposon sequencing (Tn-seq). Insertions in 166 genes resulted in K. pneumoniae mutants that were significantly less fit in the lungs of WT mice than in those of neutropenic mice. Of these, mutants with insertions in 51 genes still had significant defects in neutropenic mice, while mutants with insertions in 52 genes recovered significantly. In vitro screens using a minilibrary of K. pneumoniae transposon mutants identified putative functions for a subset of these genes, including in capsule content and resistance to reactive oxygen and nitrogen species. Lung infections in mice confirmed roles in K. pneumoniae virulence for the Δ dedA , Δ dsbC , Δ gntR , Δ wzm-wzt , Δ yaaA , and Δ ycgE mutants, all of which were defective in either capsule content or growth in reactive oxygen or nitrogen species. The fitness of the Δ dedA , Δ dsbC , Δ gntR , Δ yaaA , and Δ ycgE mutants was higher in neutropenic mouse lungs, indicating that these genes encode proteins that protect K. pneumoniae against neutrophil-related effector functions.