ABSTRACT
Four lytic phages, vB_KpnP_BIS33, vB_KpnP_IL33, and vB_KpnP_PRA33 of the Podoviridae family and vB_KpnM_BIS47 of the Myoviridae family, which act against animal-pathogenic Klebsiella pneumoniae strains, were isolated from sewage plants in Poland. They possess double-stranded DNA genomes of 41,697 bp, 41,335 bp, 40,605 bp, and 147,443 bp, respectively.
GENOME ANNOUNCEMENT
Klebsiella pneumoniae is a facultative anaerobic Gram-negative bacterium that causes a wide range of diseases in humans and in domestic and farm animals. As a pathogen, it can acquire resistance to carbapenems, which are often considered to be drugs of last resort (1). One promising alternative for antibiotic treatment of carbapenem-resistant K. pneumoniae infections might be phage therapy. Lytic bacteriophages (phages) and/or their gene products, such as lysins, can easily be used as therapeutic agents against bacteria, as they are host specific and generally show no side effects.
Four lytic Klebsiella phages, vB_KpnP_BIS33, vB_KpnP_IL33, vB_KpnP_PRA33, and vB_KpnM_BIS47, were isolated by a standard enrichment method (2) using K. pneumoniae strains that had previously been isolated from seals or dogs. Water samples for phage enrichment were collected from sewage plants in Biskupiec (BIS33 and BIS47), Iława (IL33), and Prabuty (PRA33) in Poland. Genomic DNA from the phages was isolated with a modified phenol-chloroform extraction method (3). Sequencing was performed on an Illumina NextSeq500 platform, generating 6 million, 7.1 million, 10 million, and 17.2 million paired-end reads (2 × 150) for PRA33, IL33, BIS47, and BIS33, respectively. Single contigs were obtained for all four genomes by de novo assembling the phage sequences using CLC Genomics Workbench version 8.5.1. Annotation was performed using the myRast (4) and UGENE (5) software packages, with auto-annotation and manual editing, respectively. The upstream sequences of all open reading frames were checked for appropriately spaced ribosome-binding sites with homology to GGAGGT. Promoter sequences were identified by the PHIRE program (6), while tRNA sequences were detected with the tRNAscan-SE (7) and ARAGORN (8) software packages. Table 1 shows the summary report for the four sequenced genomes.
Summary report of the de novo-assembled K. pneumoniae phages from this study
Based on gene predictions, all four phage genomes contain genes for replication, virion structure, and lysis. Coding sequences (CDSs) were identified also for putative homing endonuclease, helicase, DNA ligase, and DNA polymerase. Additionally, CDSs for terminase, head-tail connector protein, collar protein, putative tail tubular proteins, and tail fiber protein were found. Bacteriophages vB_KpnP_BIS33 and vB_KpnP_IL33 possess their own RNA polymerase, suggesting that they are related to phage T7. The CDSs for holin and therapeutically desired endolysin were detected in all four genomes. Lysogenization genes, such as site-specific integrases and repressors, were not identified in any of the four genomes. Additionally, genome annotation of vB_KpnM_BIS47 revealed 18 tRNA genes.
Whole-genome sequence alignments with BLASTn (9) and molecular phylogenetic analyses with the maximum likelihood method (10) demonstrated that phages vB_KpnP_BIS33, vB_KpnP_IL33, and vB_KpnP_PRA33 are closely related to each other. However, they differ in a few CDSs encoding, e.g., putative endonuclease, protein kinase, or, in most cases, hypothetical proteins. Phages vB_KpnP_IL33 and vB_KpnP_PRA33 represent the same clade as bacteriophage KpV289 (GenBank accession no. LN866626) (11). Phages vB_KpnP_BIS33 and vB_KpnM_BIS47 show more than 93% whole-genome sequence identity with phages KpV763 (accession no. KX591654) and KB57 (accession no. KT934943), respectively.
Accession number(s).Nucleotide sequence accession numbers are shown in Table 1.
ACKNOWLEDGMENTS
This study was supported by the National Center for Research and Development (Poland) within project grant LIDER/006/414/L-4/12/NCBR/2013 (to P.G.) and the National Science Center (Poland) within project grant UMO-2016/23/B/NZ6/02537 (to P.G.).
We are grateful to the members of the GERMS-ASM Student Chapter in Gdańsk, Poland, for their excellent technical assistance in water sample collection and phage isolation. We also thank Andrew Kropinski for his invaluable help in genome annotation.
FOOTNOTES
- Received 23 July 2017.
- Accepted 4 October 2017.
- Published 9 November 2017.
- Copyright © 2017 Labudda et al.
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license.
