Bacteriophages of Klebsiella spp., their diversity and potential therapeutic uses

Department of Biosciences, Nottingham Trent University, Nottingham, United Kingdom
Life Sciences, University of Westminster, London, United Kingdom
DOI
10.7287/peerj.preprints.27890v1
Subject Areas
Microbiology, Virology, Infectious Diseases
Keywords
antimicrobial resistance, phage therapy, Klebsiella oxytoca, Klebsiella pneumoniae
Copyright
© 2019 Herridge et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ Preprints) and either DOI or URL of the article must be cited.
Cite this article
Herridge WP, Shibu P, O'Shea J, Brook TC, Hoyles L. 2019. Bacteriophages of Klebsiella spp., their diversity and potential therapeutic uses. PeerJ Preprints 7:e27890v1

Abstract

Klebsiella spp. are commensals of the human microbiota, and a leading cause of opportunistic nosocomial infections. The incidence of multi-drug resistant (MDR) strains of Klebsiella pneumoniae causing serious infections is increasing, and K. oxytoca is an emerging pathogen. Alternative strategies to tackle infections caused by these bacteria are required as strains become resistant to last-resort antibiotics such as colistin. Bacteriophages (phages) are viruses that can infect and kill bacteria. They and their gene products are now being considered as alternatives or adjuncts to antimicrobial therapies. Several in vitro and in vivo studies have shown the potential for lytic phages to combat MDR K. pneumoniae infections. Ready access to cheap sequencing technologies has led to a large increase in the number of genomes available for Klebsiella-infecting phages, with these phages heterogeneous at the whole-genome level. This review summarises our current knowledge on phages of Klebsiella spp. and highlights technological and biological issues relevant to the development of phage-based therapies targeting these bacteria.

Author Comment

This is a preprint submission to PeerJ Preprints.

Supplemental Information

Supplementary Material

The compressed file includes newick-format files used to generate figures, the fasta file used to generate Figure 1 and the list of tables used to generate the supplementary figure.

DOI: 10.7287/peerj.preprints.27890v1/supp-1