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Klebsiella pneumoniae subsp. pneumoniae–bacteriophage combination from the caecal effluent of a healthy woman

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Metagenomic studies on samples from a range of different environments and the potential of bacteriophage (phage) therapy to treat antibiotic-resistant, clinically relevant bacteria have renewed interest in virus-like particles (VLPs). Metagenomic (virome) studies, in particular, have demonstrated that VLPs are the most genetically diverse entities in the biosphere (Reyes et al., 2012). Given their staggering abundance and diversity, coupled to their perceived crucial role in the functioning of ecosystems, it is surprising that VLPs (and by extension, phages) remain the most poorly characterized biological entities (Reyes et al., 2012).

Virome and classical studies examining VLPs in the faeces of adults and infants have demonstrated that there is a vast diversity and abundance of phages associated with the human gut microbiota (Breitbart et al., 2003; Breitbart et al., 2008; Lepage et al., 2008; Reyes et al., 2010; Kim et al., 2011; Minot et al., 2011; Wagner et al., 2013; Hoyles et al., 2014). Similar to the prokaryotic make-up of the human gut microbiota, each individual harbours a unique virome (dsDNA, ssDNA, RNA) that is temporally stable, and whose composition appears to be influenced by diet (Reyes et al., 2010; Minot et al., 2011; Minot et al., 2013). Lepage et al. (2008) reported that mucosal biopsies taken from healthy individuals and Crohn’s patients contained between 4.4 × 107 and 1.7 × 1010 (mean 1.2 × 109) VLPs/biopsy, with Crohn’s patients harbouring significantly more VLPs in their biopsies than healthy individuals. A recent study in which phage populations in human faecal and caecal-effluent samples were estimated using epifluorescence microscopy (EFM) and transmission electron microscopy (TEM) reported the presence of up to 1012 VLPs/g faeces (EFM) and at least 1 × 105 VLPs/ml caecal effluent (TEM) (Hoyles et al., 2014). However, little is known about the host ranges of these VLPs, and their abundance within other regions of the gastrointestinal tract.

Generation of comprehensive gut virome data has been hampered by the lack of available methods for concentrating VLPs within faecal samples and extracting sufficient amounts of DNA from them so sequencing can be performed without the need to amplify the template DNA (Reyes et al., 2012). However, the recent publication of a PEGylation method applied to human faecal samples and demonstration that microgram quantities of DNA can be isolated from faecal VLPs has gone some way to overcome this substantial technical hurdle (Hoyles et al., 2014). When it comes to annotation of virome sequence data, a major stumbling block is the lack of available phage genome sequences against which contigs can be compared, plus the large number of viral genes that are currently not represented in sequence databases. For example, studies of the human faecal virome have reported that between 66% and 98% of the generated sequences have no significant hits with GenBank sequences (Breitbart et al., 2008; Reyes et al., 2010; Minot et al., 2011). There are few, if any, available sequences for human-gut-associated lytic phages so there is a need to isolate and genomically characterize phages from gastrointestinal sources, rather than relying on the assumption that phages found in sewage are primarily of human gut origin. However, sequences of (predicted) prophages from genome sequences of bifidobacteria, lactobacilli, Helicobacter pylori and Escherichia coli (strain Nissle 1917) of gastrointestinal origin are available (Ventura et al., 2005; Villion & Moineau, 2009; Vejborg et al., 2010; Luo et al., 2012).

During a study of the microbiota associated with the caecum of patients with Irritable Bowel Syndrome and healthy controls, attempts were made to isolate bacterium–phage combinations from samples of caecal effluent. Herein, we report the isolation and characterization of a Klebsiella pneumoniae subsp. pneumoniae–phage combination from the caecal effluent of a healthy woman, and the implications of our findings in relation to gastrointestinal microbial ecology and the potential of the human gut as a source of phages with therapeutic uses. Previous studies describing the isolation of lytic phages against K. pneumoniae have reported recovery of these entities from wastewater, seawater, sewage and sewage-contaminated water samples, but never directly from gastrointestinal contents (Souza, Ginoza & Haight, 1972; Kumari, Harjai & Chhibber, 2009; Kumari, Harjai & Chhibber, 2010a; Drulis-Kawa et al., 2011; Hung et al., 2011; Cui et al., 2012; Hsu et al., 2013; Karumidze et al., 2013; Jamal et al., 2015).

Materials and Methods

Ethical approval and patient information

Ethical approval to collect caecal effluent from patients was obtained from St Thomas’ Hospital Research Ethics Committee (06/Q0702/74) covering Guy’s and St Thomas’ Hospitals, and transferred by agreement to London Bridge Hospital. Patients provided written consent to provide samples. The caecal effluent was collected as described by Hoyles et al. (2014) from a 31-year-old female who showed no evidence of colonic abnormalities or disease as based on a routine colonoscopic examination.

Sample processing, and isolation of bacteria and phages from caecal effluent

The sample was transported to the University of Reading under anaerobic conditions (in a gas jar with an anaerobic gas-generating pack; Oxoid Ltd, Hampshire, UK) and on ice, where it was processed within 3 h of collection. The sample was transferred to an anaerobic cabinet (Whitley MG1000 anaerobic workstation; DW Scientific, West Yorkshire, UK; gas composition 80% N2, 10% H2, 10% CO2) and mixed well by shaking. An aliquot (1 ml) of the sample was diluted with 9 ml sterile, anaerobic half-strength peptone water (Oxoid) in a sterile universal bottle containing 2-mm glass beads. A dilution series (10−1 to 10−6) was prepared from the homogenate in sterile, anaerobic half-strength peptone water (Oxoid). Aliquots (20 µl) were plated in triplicate onto fastidious anaerobic agar (BIOTEC laboratories, Ipswich, UK) containing 5% laked horse blood. Bacteria were incubated anaerobically for 5 days at 37 °C, and then enumerated. Ten colonies were selected randomly, streaked to purity, and stored on Microbank cryogenic beads (Prolab Diagnostics, Merseyside, UK) at −70 °C.

The remaining neat caecal effluent (∼25 ml) was processed as described by Hoyles et al. (2014). Briefly, the sample was diluted 1:4 (v/v) with sterile TBT buffer (100 mM Tris/HCl, pH 8.0; 100 mM NaCl; 10 mM MgCl2⋅6H2O filtered through a 0.1 mm pore size filter prior to autoclaving). The sample was homogenized in a stomacher (Stomacher 400 Lab System; Seward, West Sussex, UK) for 2 min at ‘high’ speed, and then placed on ice for 2 h to allow detachment of phages from and settlement of particulate material. The homogenate was centrifuged at 11,180 g for 30 min at 4 °C, and the supernatant passed through a sterile 0.45 µm cellulose acetate filter (Millipore, Billerica, Massachusetts, USA). The filtrate was stored at 4 °C until used in spot assays.

Identification of isolated bacteria

DNA was isolated from bacteria using InstaGene Matrix (Bio-Rad, Deeside, UK) according to the manufacturer’s instructions. Partial (∼600 nt) 16S rRNA gene sequences were obtained for the isolates via the University of Reading’s Biocentre. Nearest relatives of isolates were determined using EzTaxon (Chun et al., 2007). The identity of strain L4-FAA5, tentatively identified as Klebsiella pneumoniae on the basis of its 16S rRNA gene sequence, was confirmed using a species-specific PCR that detects the 16S–23S internal transcribed spacer unit of K. pneumoniae as well as capsular-type-specific, and virulence gene targets (Turton et al., 2010). Malonate and Voges–Proskauer reactions were positive indicating that the isolate was subsp. pneumoniae (rather than subsp. ozaenae) (Turton et al., 2010). Typing was carried out by VNTR analysis at loci A, E, H, J, K and D (Turton et al., 2010) and an additional three loci (N1, N2 and N4). Primers, repeat sizes and flanking sequence sizes for the additional loci were: N1F 5’-CATCAGGTGCAAGATTCCA-3’ and N1R 5’- TGAGCGATTGCTGGCCTA-3’, 116 bp repeat with a 107 bp flanking sequence; N2F 5’-GATGCGGCAAGCACCAC-3’ and N2R 5’-ACGCCCTGACCATTATGC-3’, 57 bp repeat with a 109 bp flanking sequence; and N4F 5’-GTGCGGTGATTGTGATGG-3’ and N4R 5’-CTGACAACGTCGATGTGG-3’, 67 bp repeat with a 119 bp flanking sequence.

Screening of bacteria against filtered caecal effluent

K. pneumoniae strains isolated from the caecum were grown to OD660 ∼ 0.4 in tryptone soya broth (Oxoid Ltd), and used in spot assays as follows. An aliquot of culture (200 µl) was inoculated into 3 ml tryptone soya broth containing 0.3% (w/v) agarose (SeaKem LE agarose; Lonza Rockland) that had been heat-treated by microwaving and dispensed aseptically from a larger volume before cooling to 48 °C. The overlays containing bacteria were poured over 20 ml solid agar plates of autoclaved tryptone soya agar (Oxoid Ltd). Once the agar had solidified, a 10 µl spot of filtered caecal effluent was applied to the overlays, and the plates were incubated overnight at 37 °C in the anaerobic cabinet. Identical plaques were observed on all K. pneumoniae isolates; strain L4-FAA5 was used to propagate and purify an isolated phage in tryptone soya broth or reinforced clostridial and nutrient media (Oxoid Ltd). Neither calcium nor magnesium was added to media during propagations.

The ability of the purified phage to infect a panel of K. pneumoniae subsp. pneumoniae clinical isolates (Table 1) was determined using the spot assay as described above, except that nutrient agar plates were used for the base. Strain L4-FAA5 was used as a positive control.

Table 1:
Description of K. pneumoniae subsp. pneumoniae isolates against which phage KLPN1 was screened.
Straina Capsular type (K PCR result)b rmpA wcaG Source Infected by phage KLPN1
L4-FAA5 K2 + Human caecal effluent Yes
K/5216 K1 (K1 cluster of CC23) + + Liver abscess (Taiwan) No
NCTC 5055 K2 (reference strain) + Human Yesd
NCTC 9660 K5 (reference strain) Cloacae of horse No
PHE1 Rectal swab No
PHE2 Human clinical No
PHE3 Sputum, transplant patient No
PHE4 Urine, spinal injury patient No
PHE5 Human blood No
PHE6 + Urine, incontinent patient No
PHE7 Human clinical No
PHE8 Human blood No
PHE9 Human clinical No
PHE10 Human blood No
PHE11c K2 Blood, patient with urinary tract infection Yesd
PHE12c K2 Urine Yesd
PHE13 K2 Blood and sputum, patient with bacteraemia and pneumonia Yesd
PHE14 K2 + Sputum, patient with bacteraemia Yesd
PHE15 K2 Urine, cardiac patient Yesd
PHE16 K20 + Sputum, transplant patient No
PHE17 K54 + Intensive care unit No
PHE18 K57 Sputum, transplant patient No
DOI: 10.7717/peerj.1061/table-1



No data

Strains with the prefix PHE were submitted for typing by healthcare providers to Public Health England–Colindale. Each isolate represented a distinct strain, with the exception of isolates PHE11 and PHE12.
K PCR can detect K1, K2, K5, K20, K54 and K57 capsular types.
Corresponds to multi-locus sequence type ST14, often seen among multi-drug-resistant isolates producing carbapenemases.
Phage KLPN1 did not exhibit depolymerase activity on these K2 isolates, but it did on L4-FAA5.

Purification of phage particles

A 100-ml culture of strain L4-FAA5 was grown to mid-exponential phase, inoculated with 100 µl of phage stock (∼1010 pfu/ml) and incubated until the medium became clear (∼2 h after infection). The lysate was centrifuged at 4,500 g for 10 min, then passed through a 0.45 µm cellulose acetate filter. PEG 8000 (10%, w/v) and NaCl (6%, w/v) were added to the filtrate, and mixed until all particulates had dissolved. The sample was left at 4 °C for 16 h, then centrifuged at 4,500 g for 30 min. The supernatant was removed and the pellet resuspended in 4 ml TBT buffer. A CsCl block gradient was formed with 5 M and 3 M CsCl, both prepared in TBT buffer and samples were placed on top of this gradient and subjected to centrifugation at 100,000 g for 2 h at 4 °C. The band containing ∼2 ml of TBT buffer and the phages was drawn out of the tube and the purified sample was transferred to dialysis tubing (4,000–6,000 Da cut-off), and dialysed against TBT buffer overnight. The TBT buffer was replaced with fresh TBT buffer, and the sample dialysed for a further 4 h. The purified phage particles were removed from the dialysis tubing and stored at 4 °C.

Transmission electron microscopy

This was done as described by Hoyles et al. (2014).

Extraction of DNA from phage KLPN1 and restriction enzyme profiles

An aliquot (250 µl) of the purified phage particle stock was treated with DNAse (2 U) for 30 min at 37 °C, then heated for 10 min at 80 °C. Two phenol/chloroform extractions were performed, before the DNA was precipitated using 1/10 volume of 3 M sodium acetate (pH 4.8) and 2 volumes of ice-cold ethanol. After air-drying, DNA was resuspended in 100 µl TE buffer. Restriction profiles were obtained for phage KLPN1 using the enzymes EcoRV and HaeIII (SuRE/Cut; Roche Applied Science, Basel, Switzerland): restriction digests contained 3 µl H2O, 1 µl enzyme, 1 µl enzyme buffer and 5 µl DNA, and were incubated for 3 h at 37 °C before being run on a 0.8% (w/v) agarose gel (1 h, 75 V) and stained with ethidium bromide.

Whole-genome sequencing and annotation of the phage genome

DNA (5 µg) was extracted and concentration verified by Nanodrop quantification. Confirmatory molecular identification tests were also conducted on the DNA extract prior to shipment to the contract sequencing facility (Macrogen Inc., Seoul, Korea). Eighty-fold sequencing coverage was obtained using pyrosequencing technology on a 454 FLX instrument. The individual sequence files generated by the 454 FLX instrument were assembled with GSassembler (454 Lifesciences, Branford, Connecticut, USA) to generate a consensus sequence. To ensure correct assembly and resolve any remaining base-conflicts, short segments of the genome were amplified by PCR and the generated amplicons were then subjected to Sanger sequencing (MWG, Ebersberg, Germany). Open reading frames (ORFs) were automatically predicted using Genemark (Besemer & Borodovsky, 1999). General feature format (gff) files were generated for the predicted phage proteome (retaining proteins with a minimum size of 30 amino acids) and visualized using the annotation software Artemis v10.0 (Rutherford et al., 2000). ORF boundaries were verified and, where required, adjusted by manual inspection of Shine–Delgarno sequences. BLASTP (Altschul et al., 1990) was used to provide preliminary functional annotation data, and to carry out a comparative analysis of KLPN1 with previously sequenced Klebsiella phages at the protein level (Altschul et al., 1990). To improve genome annotations/predictions, all proteins encoded by ORFs in the genome sequence of KLPN1 were searched against InterProScan (http://www.ebi.ac.uk/interpro/). HHpred (http://toolkit.tuebingen.mpg.de/hhpred) searches were done to identify domains associated with depolymerase activity.

Screening virome datasets for phage sequences related to KLPN1

Fasta files associated with public virome datasets were downloaded from the METAVIR web server (http://metavir-meb.univ-bpclermont.fr; Roux et al., 2011) on 31 March 2015 (Table S1). Each fasta file was used to create a BLAST database, against which the genome sequence of phage KLPN1 was searched using BLASTN.


Isolation and characterization of bacteria isolated from caecal effluent

On fastidious anaerobe agar, 2.22 × 108 ± 5.30 × 107 (n = 3 replica plating) bacteria were isolated per millilitre of caecal effluent sample (log10 8.35 ± 7.72 bacteria/ml caecal effluent). Ten colonies were randomly selected from one of the triplicate plates used to enumerate the bacteria, and streaked to purity. On the basis of 16S rRNA gene sequence analysis (EzTaxon), isolates represented Klebsiella pneumoniae (n = 5), Bacteroides vulgatus (n = 2), Bacteroides massiliensis (n = 1), a novel member of the order Erysipelotrichales distantly related to [Clostridium] innocuum (n = 1), and Haemophilus parainfluenzae (n = 1).

It is widely accepted that identification of members of the family Enterobacteriaceae is difficult on the basis of 16S rRNA gene sequence data alone; therefore, one of the strains identified as K. pneumoniae, L4-FAA5, was characterized using the PCR-based methods of Turton et al. (2010). The isolate was found to be a strain of K. pneumoniae subsp. pneumoniae, capsular type K2, rmpA+. Its VNTR profile was unique among the clinical isolates tested and on the wider database of clinical isolates held by Public Health England–Colindale.

Screening of filter-sterilized caecal effluent against bacteria to isolate phages

The K. pneumoniae isolates were used in spot assays with the caecum filtrate, which was free of bacteria (as verified by Gram-stained smear and plating on nutrient agar; not shown). Phages infecting these isolates were initially identified in the caecal effluent by spotting 10 µl aliquots of filtered caecal effluent onto TSA overlays containing 200 µl of a given culture in the exponential phase of growth. Plaques identical to those shown in Fig. 1A were observed with all K. pneumoniae isolates in the spot assays, and phages were present at 2 × 105 ± 2.65 × 103 (n = 3) pfu/ml caecal effluent. Clear plaques of 2 mm diameter were visible within 3 h of spotting onto an agar overlay. After prolonged incubation, the area around the plaques developed opaque haloes presumably caused by depolymerase activity, which increased in size over the course of 4 days, although the central clear area of the plaques remained 2 mm in diameter (Fig. 1B). This phenomenon has been observed previously for lytic phages of the families Siphoviridae, Podoviridae and Myoviridae against K. pneumoniae, and is associated with degradation of capsular polysaccharides (Geyer et al., 1983; Verma, Harjai & Chhibber, 2009; Hsu et al., 2013; Lin et al., 2014a; Shang et al., 2015). The non-Klebsiella isolates were not screened against the caecum filtrate for phages.

Appearance of plaques formed on K. pneumoniae subsp. pneumoniae L4-FAA5 by phage KLPN1.

Figure 1: Appearance of plaques formed on K. pneumoniae subsp. pneumoniae L4-FAA5 by phage KLPN1.

(A) Initial isolation of phages from filtered caecal effluent on TSA. (B) Appearance of plaques of pure phage stock after 24 h. (C) Growth of haloes surrounding plaques over the course of the course of 96 h. After 48 h, presumed phage-insensitive mutants can be seen growing in the haloes surrounding the plaques. Images are shown to scale.

Strain L4-FAA5 was used as the host bacterium on which to isolate and propagate one phage (which we named KLPN1) to purity. KLPN1 infected all K. pneumoniae isolates recovered from the filter-sterilized caecal effluent.

The ability of phage KLPN1 to infect a panel of K. pneumoniae subsp. pneumoniae clinical isolates was determined (Table 1), which revealed that all K2 strains tested (including the type strain) were sensitive to this phage, though KLPN1 did not infect any of the other tested strains belonging to other capsular types. VNTR analysis showed that the six K2 isolates in the panel represented five, distinct strains, suggesting a wide susceptibility to the phage among isolates of this capsular type. In addition, it did not exhibit depolymerase activity with any of the clinical K2 isolates.

Characterization of phage KLPN1

Phage KLPN1 is chloroform-resistant. In addition, it displayed stability to prolonged storage in TSB at 4 °C: after 6 and 18 months’ storage, titres for the phage were still 1010 pfu/ml, comparable with the original stock. Transmission electron microscopy revealed the isometric-headed phage to possess a capsid of ∼62.7 ± 2.3 nm (n = 30) in diameter with a long non-contractile tail of ∼164.4 ± 3.0 nm (n = 29), thus indicating that this phage is a member of the family Siphoviridae (Fig. 2). Notably, the base-plate structure was unusual with a distinct central tail fibre [length 33.4 ± 1.7 nm (n = 43)] with apparently three elongated spherical structures [length, 13.2 ± 1.3 nm (n = 43); width, 6.9 ± 0.7 nm (n = 48)] loosely associated with the central regions of the tail fibre. This unique base-plate structures resembles a rosette with three leaves, and can be observed in all five micrographs shown in Fig. 2. A similar structure has been described for Rtp, a lytic phage of Escherichia coli (Wietzorrek et al., 2006), with which KLPN1 shares some sequence identity (discussed below). It is also visible in electron micrographs of phage ϕ28, which infects K. pneumoniae capsular type K28 (Geyer et al., 1983).

Transmission electron micrographs of phage KLPN1.

Figure 2: Transmission electron micrographs of phage KLPN1.

The phage belongs to the family Siphoviridae, and has an unusual base-plate structure, resembling a rosette. The arrows indicate the central tail fibre surrounded by three flexible spherical base-plate structures.

It was straightforward to isolate high-quality DNA from phage KLPN1. Heating an aliquot of CsCl-purified, DNAse-/RNAse-treated sample at 80 °C for 10 min followed by phenol/chloroform/isoamyl alcohol extractions and ethanol precipitation gave large quantities of high-quality DNA that was used for restriction digests (not shown) and genome sequencing. The estimated genome size of KLPN1 based on restriction digests with EcoRV or HaeIII was ∼45 kbp, which was an underestimation of the genome size of 49,037 bp as determined by sequencing (see below).

Sequence analysis of KLPN1

The genome of KLPN1 was 49,037 bp with a G + C content of 50.53%, similar to previously sequenced Klebsiella Siphoviridae phages such as KP36 (Table 2). Initial genome annotation was performed using Genemark (Besemer & Borodovsky, 1999), from which a gff file was generated to allow visualisation of the predicted ORFs in Artemis v10.0 (Rutherford et al., 2000). Each ORF with a minimum amino acid content of 30, a start and stop codon as well as a ribosomal-binding site was retained (Table 3). The genome of KLPN1 was predicted to encompass 73 ORFs divided into four clusters, two rightward and two leftward (Fig. 3, Table 3). Of the 73 predicted ORFs, 23 were assigned a function with the remainder representing hypothetical proteins with no assignable function (Table 3). BLAST analysis of the complete nucleotide sequence indicated that KLPN1 is closely related to the Klebsiella phages KP36 (95% identity across 86% of the genome; Kęsik-Szeloch et al., 2013), F20 (84% identity across 82% of the genome, GenBank accession no. JN672684; Mishra, Choi & Kang, 2012) and phage 1513 (95% identity across 85% of the genome, GenBank accession no. KP658157; Cao et al., 2015). Furthermore, partial identity was observed against Shigella phage Shfl1 as well as enterobacterial phages T1 (Roberts, Martin & Kropinski, 2004) and RTP (Wietzorrek et al., 2006) (GenBank accession numbers HM035024, AY216660 and AM156909, respectively). A comparative analysis of KLPN1 was performed against both known members (KP36, F20) of the genus “Kp36likevirus” (Niu et al., 2014; Table 3, Fig. 3). For completion, KLPN1 was also compared with previously sequenced Klebsiella phages (Table 2). KLPN1 was shown not to share detectable homology with Klebsiella phages belonging to the family Podoviridae or Myoviridae. Based on the amino acid percentage identities presented in Table 3, the genomes of KLPN1 and related phages were divided into functional conserved modules: packaging, phage particle morphogenesis and DNA replication (Fig. 3, Table 3). Sections of the KLPN1 genome were shown to exhibit homology to the Siphoviridae phage phiKO2 genome, although such homology was confined to the tail morphogenesis region and one hypothetical protein (Table 3). Of the 73 predicted ORFs, only three appeared unique to KLPN1: two genes encoding hypothetical proteins located at the 5’ end of the genome and a putative homing endonuclease-gene positioned in the capsid morphogenesis module (Table 3).

Genome structures of the four members of the genus “Kp36likevirus”.

Figure 3: Genome structures of the four members of the genus “Kp36likevirus”.

Phages KLPN1, KP36 and 1513 are virulent to K. pneumoniae, while F20 is virulent to Enterobacter aerogenes (Mishra, Choi & Kang, 2012).
Table 2:
Characteristics of previously sequenced Klebsiella phages.
Phage Family Size (bp) G+C(%) No. of predicted ORFs GenBank accession no. Reference
NTUH-K2044-K1-1 Podoviridae 43,871 54.2 35 NC_025418 Lin et al. (2014a)
F19 Podoviridae 43,766 53.8 51 NC_023567
K11 Podoviridae 41,181 53.2 51 NC_011043
KP34 Podoviridae 43,809 54.1 57 NC_013649 Drulis-Kawa et al. (2011)
KP32 Podoviridae 41,119 52.4 44 NC_013647 Kęsik-Szeloch et al. (2013)
P13 Podoviridae 45,976 51.7 50 Shang et al. (2015)
0507-KN2-1 Myoviridae 159,991 46.7 154 NC_022343 Hsu et al. (2013)
JD001 Myoviridae 48,814 48.5 68 NC_020204 Cui et al. (2012)
KP27 Myoviridae 174,413 41.8 276 NC_020080 Kęsik-Szeloch et al. (2013)
KP15 Myoviridae 174,436 41.8 258 NC_014036 Kęsik-Szeloch et al. (2013)
vB_KleM-RaK2 Myoviridae 345,809 32 534 NC_019526 Šimoliūnas et al. (2012)
K64-1 Myoviridae 346,602 31.72 64 AB897757 Pan et al. (2015)
KP36 Siphoviridae 49,820 50.7 80 NC_019781 Kęsik-Szeloch et al. (2013)
phiKO2 Siphoviridae 51,601 51.5 64 NC_005857 Casjens et al. (2004)
1513 Siphoviridae 49,462 50.61 72 KP658157 Cao et al. (2015)
KLPN1 Siphoviridae 49,037 50.5 73 KR262148 This study
DOI: 10.7717/peerj.1061/table-2
Table 3:
Genomic structure of phage KLPN1.
KLPN1 genome Start Stop Ribosome-binding site Start Strand Predicted product* Representative ORF in phage (% amino acid identity)
KP36 F20 1513 phiKO2
KLPN1_01 516 1079 AAGGAG ATG + Unknown
KLPN1_02 1069 1290 AGGAGG ATG + HP
KLPN1_03 1395 1547 GAGGAA ATG + HP pSf1_0028 (Shigella phage pSf-1) 39 (94)
KLPN1_04 1752 1997 GAAGAtAG TTG + HP (Escherichia phage e4/1c) 38 (98.36)
KLPN1_05 2186 2416 AGGAGGA ATG + HP KP36_04 KP36 04 (74.65) 76 (63.38) 37 (92.11)
KLPN1_06 2487 2699 AGAGGA ATG + HP KP36_06 KP36 06 (82.86) 36 (90)
KLPN1_07 2710 3030 AAGGAGAA ATG + HP KP36_11 KP36 11 (78.3) 70 (65.09) 35 (82.08)
KLPN1_08 3100 3471 GGAGA ATG + HP (Enterobacteria phage F20) 69 (83.74)
KLPN1_09 3481 3783 GAGGtGGccG ATG + HP KP36_15 KP36 15 (91) 68 (56) 33 (85)
KLPN1_10 3783 4028 AAcGGGA ATG + HP KP36_16 KP36 16 (97.53) 67 (83.95) 32 (92.59)
KLPN1_11 4025 4210 GAGGtAAAAG ATG + HP KP36_17 KP36 (signal peptide) 17 (85.25) 66 (78.69) 31 (58.18)
KLPN1_12 4291 4500 AAtcAGGAG ATG + HP (Enterobacteria phage F20) 65 (73.91)
KLPN1_13 4500 4934 GAGGAGA ATG + HP (Enterobacteria phage F20) 19 (33.93) 64 (32.54) 29 (35.58)
KLPN1_14 5004 5750 AAGAGGAA ATG + HP (Enterobacteria phage F20) 20 (50.94) 63 (54.55) 28 (34.84)
KLPN1_15 5827 6099 AGGAG ATG + HP KP36_22 KP36 22 (65.56) 61 (66.67)
KLPN1_16 6096 6668 AAGGtGAtcGAA ATG + HP KP36_23 KP36 23 (96.32) 60 (78.53) 25 (76.44)
KLPN1_17 6738 6974 AAGGAG ATG + HP KP36_24 KP36 24 (92.31) 59a (86.3) 24 (96.15)
KLPN1_18 6962 7195 GGAGAAGG ATG + HP KP36_25 KP36 25 (100) 59 (87.01) 23 (95.45)
KLPN1_19 7324 7518 AAAGGG ATG + HP KP36_26 KP36 26 (96.67) 57 (93.65) 22 (96.88)
KLPN1_20 7512 7718 AAGGGAA ATG + HP KP36_27 KP36 (signal peptide) 27 (96.2) 56 (64.81) 21 (100)
KLPN1_21 7773 8378 GAAGcGGcGtAA ATG + terminase small subunit KP36 28(92.53) 55 (91.95) 20 (90.8)
KLPN1_22 8388 9992 AAGGGccGA ATG + terminase large subunit KP36 (terminase-like family: PF03237) 29 (99.25) 54 (98.13) 19 (99.44)
KLPN1_23 10038 11348 AAAcAAGGttGA ATG + portal protein KP36 (phage portal protein, SPP1 Gp6-like: PF05133) 30 (98.62) 53 (91.78) 18 (99.31)
KLPN1_24 11335 12102 GGAGGcGGA ATG + capsid morphogenesis protein KP36 (phage head morphogenesis domain: IPR006528) 31 (96.44) 52 (90.12) 17 (95.22)
KLPN1_25 12104 12589 GAGGttAG ATG + HP gp40 (Escherichia phage phiEB49) HNH endonuclease (HNH endonuclease: PF13392)
KLPN1_26 12586 13716 GGAGA ATG + capsid protein KP36 32 (99.47) 51 (93.09) 16 (99.47)
KLPN1_27 13768 14286 AGGAGA ATG + HP KP36_33 KP36 33 (96.2) 50 (50.87) 15 (96.84)
KLPN1_28 14400 15359 AGGAG ATG + major capsid protein KP36_34 KP36 34 (98.75) 49 (94.36) 14 (98.43)
KLPN1_29 15451 15756 GGAGcA ATG + HP KP36_35 KP36 35 (100) 48 (86.15) 13 (98.77)
KLPN1_30 15753 16226 AAAAGcGcGGA ATG + HP KP36_36 KP36 36 (100) 47 (92.75) 12 (97.83)
KLPN1_31 16232 16609 GGtAGGtGA ATG + HP KP36_37 KP36 37 (99.2) 46 (94.4) 11 (98.4)
KLPN1_32 16602 17039 AGGGtGGcGA ATG + HP KP36_38 KP36 38 (100) 45 (92.41) 10 (99.05)
KLPN1_33 17029 17463 GAGcGAGG ATG + HP (Enterobacteria phage F20) Tail protein (phage tail protein: PF13554) 39 (76.39) 44 (88.19) 09 (74.19)
KLPN1_34 17450 18136 GGAGGcGA ATG + HP (Enterobacteria phage F20) Tail protein (phage tail protein: PF08813) 43/42 (68.26/42.04) 08 (43.36)
KLPN1_35 18189 18845 AGGAG ATG + HP (Enterobacteria phage F20) Tail protein (phage tail protein: PF08813) 40 (91.67) 42 (82.87) 08 (96.33)
KLPN1_36 18922 19248 AGGAG ATG + Tape measure chaperone protein (domain of unknown function DUF1789: PF08748) 41 (98.15) 41 (57.01) 07 (98.15)
KLPN1_36.1 19239 19562 + Tape measure chaperone protein (phage-related hypothetical protein DUF1799: PF08809) 40 (92.73) 06 (96.36)
KLPN1_38 19620 22565 GAtAAAGtAG TTG + tail length tape-measure protein KP36 (λ phage tail tape-measure protein: PF09718) 43 (91.63) 39 (80.22/68.85) 05 (91.04)
KLPN1_39 22568 22912 AAcGAGGG GTG + minor tail protein KP36 (minor tail protein: PF05939) 44 (88.6) 38 (87.72) 04 (86.84) 16 (28.32)
KLPN1_40 22949 23734 + minor tail protein KP36 (minor tail protein L: TIGR01600) 45 (93.17) 37 (91.27) 03 (92.77) 17 (36.78)
KLPN1_41 23736 24473 GAAAAGcGGAcGG ATG + minor tail protein KP36 (endopeptidase, NlpC/P60 family: PF00877) 46 (93.47) 36 (96.33) 02 (94.69) 18 (42.62)
KLPN1_42 24448 25050 AAGGA ATG + tail assembly protein KP36 (λ tail assembly protein I: PF06805) 47 (94.5) 35 (98) 01 (95.03)
KLPN1_43 25138 28839 AGGAGG ATG + tail fiber protein KP36 (putative phage tail protein: PF13550) 48 (95.86) 34 (88.6) 01a (95.06) 21 (39.75)
KLPN1_44 29027 31297 AAGAGG ATG HP L418_01651 (Klebsiellapneumoniae UCICRE 7) (galactose-binding domain-like: IPR008979) 49 (66.79) 32 (83.49) 71 (70.15)
KLPN1_45 31392 31853 AGGAAcGA ATG single-stranded DNA binding protein KP36 (nucleic-acid binding proteins: SSF50249) 50 (98.04) 31 (82.35) 70 (96.08)
KLPN1_46 31890 32546 AAGGAAA ATG putative recombination protein KP36 (signal peptide) 51 (99.54) 30 (93.12) 69 (98.62)
KLPN1_47 32606 33652 GGAGcAA ATG exodeoxyribonuclease VIII KP36 (PD-(D/E)XK nuclease superfamily: PF12705) 52 (97.7) 29 (93.39) 68 (97.99)
KLPN1_48 34148 35107 GGAGGtAA GTG DNA primase KP36 (bacteriophage T7, Gp4, DNA primase/helicase, N-terminal: IPR013237) 53 (98.7) 28 (88.64) 67 (99.35)
KLPN1_49 35183 35584 GAGGGttAA ATG putative transcriptional regulator KP36 (λ repressor-like, DNA-binding domain: IPR010982) 54 (98.5) 27 (95.49) 66 (99.25)
KLPN1_50 35676 37712 AGGAttG ATG + DNA helicase KP36 (helicase, C-terminal: IPR001650) 55 (98.52) 26 (94.25) 65 (98.82)
KLPN1_51 37709 38116 GGAGGcGAGG GTG + HP KP36_56 KP36 (VRR-NUC domain: IPR014883) 56 (99.08) 25 (86.61) 64 (100)
KLPN1_52 38181 38468 GAAGAAcGGA ATG + HP KP36_57 KP36 (signal peptide) 57 (95.65) 63 (94.87)
KLPN1_53 38471 39202 GcGAGGttAA ATG + DNA adenine methyltransferase KP36 (phage N-6-adenine-methyltransferase: TIGR01712) 58 (97.53) 23 (92.59) 62 (97.94)
KLPN1_54 39204 39440 GcGtAtGcGAA ATG + HP KP36_59 KP36 59 (88.46) 22 (79.49) 61 (89.74)
KLPN1_55 39451 39741 ATG + HP (Enterobacteria phage F20) 60 (98.72) 21 (83.33) 60 (98.72)
KLPN1_56 39741 39989 GGtGAcGA ATG + HP KP36_61 KP36 61 (95.18) 20 (89.02) 59 (96.39)
KLPN1_57 40085 41215 AAttGGGAtAA ATG + HP KP36_62 KP36 (metallo-dependent phosphatase-like: IPR029052) 62 (99.2) 19 (94.15) 58 (99.2)
KLPN1_58 41254 41745 AAGGAAA ATG + 3’-phosphatase, 5’-polynucleotide kinase KP36 (HAD superfamily, subfamily IIIB (acid phosphatase): PF03767) 63 (93.87) 18 (75.46) 57 (95.09)
KLPN1_59 41742 42323 GGAGtAGA ATG + HP KP36_64 KP36 (P-loop containing nucleoside triphosphate hydrolase: IPR027417) 64 (99.48) 17 (88.17) 56 (99.48)
KLPN1_60 42450 42665 AGAGG ATG + holin KP36 65 (83.1) 16 (80.28) 55 (83.1)
KLPN1_61 42667 43149 AGGAGcAAG ATG + endolysin KP36 (lysozyme-like domain: IPR023346) 66 (86.23) 15 (90.57) 54 (98.12)
KLPN1_62 43146 43571 AAGGA ATG + Rz1A protein KP36 67 (96.45) 14 (89.36) 53 (99.29)
KLPN1_63 43641 44102 GAGGtAA ATG HP KP36_68 KP36 68 (98.69) 13 (88.89) 52 (98.69)
KLPN1_64 44106 45674 AGGAGcAAGG ATG HP KP36_69 KP36 (protein of unknown function DUF3987: PF13148) 69 (99.81) 12 (95.79) 51 (99.81)
KLPN1_65 45800 46237 GGAGAAAG ATG HP KP36_70 KP36 70 (97.93) 11 (91.03) 50 (98.62)
KLPN1_66 46238 46420 GAAGAAA ATG HP KP36_71 KP36 71 (93.33) 10 (86.44) 49 (93.33)
KLPN1_67 46417 46620 GGAGtAAAcGGA ATG HP KP36_72 KP36 72 (97.01) 09 (65.67) 48 (92.54)
KLPN1_68 46693 47385 AAAtGGtGGA ATG HP KP36_73 KP36 73 (97.83) 08 (90) 47 (96.96) 42 (56.83)
KLPN1_69 47382 47681 GGcAtAG TTG HP KP36_74 KP36 74 (100) 06 (55.41) 46 (52.7)
KLPN1_70 47688 48065 GAAAcGAGG ATG HP KP36_75 KP36 75 (96) 05 (66.13) 45 (70)
KLPN1_71 48065 48304 GAGAAGGG ATG HP KP36_76 KP36 76 (96.2) 04 (93.1) 44 (97.47)
KLPN1_72 48301 48495 AGGAGAA ATG HP KP36_77 KP36 77 (93.75) 03 (84.81) 43 (95.31)
KLPN1_73 48568 48849 AGAGGG ATG HP KP36_78 KP36 78 (97.47) 02 (84.81) 42 (96.2)
DOI: 10.7717/peerj.1061/table-3


HP, hypothetical protein. Underlined predicted products are from InterProScan (http://www.ebi.ac.uk/interpro/) searches that returned results with the amino acid sequence encoded by each ORF (Table S2).

Based on sequence homology to ORF33 (encoding the host-specificity J protein; InterPro IPR021034) of phage T1, the phage receptor-binding protein of KLPN1 was predicted to be encoded by ORF43. The deduced ORF43 protein was found to exhibit similarity to fibronectin type III domain-containing protein, and potentially encodes the depolymerase whose effect was observed on the phage assay plates (Fig. 1). However, a HHpred search with the protein sequence encoded by this ORF failed to detect any domains associated with enzymes (such as glycanases, deacetylases and lyases) associated with depolymerase activity of Klebsiella lytic phages (Geyer et al., 1983). The protein encoded by ORF34 of phage NTUH-K2044-K1-1 has proven depolymerase activity associated with pectate lyase (Lin et al., 2014a); a HHpred search confirmed the protein encoded by this ORF has a lyase/polygalacturonase domain (1ru4_A pectate lyase, 94.3% probability of true positive, E-value 0.055, P-value 1.6 × 10−6; 1bhe_A PEHA, polygalacturonase, 90.1% probability of true positive, E-value 13, P-value 0.00038). ORF96 of phage 0507-KN2-1 also encodes proven depolymerase activity (Hsu et al., 2013). A HHpred search demonstrated the protein encoded by this ORF has an acetylneuraminidase domain (3gw6_A endo-N-acetylneuraminidase, 99.8% probability of true positive, E-value 1 × 10−19, P-value 2.9 × 10−24). The whole-genome sequence of phage P13 cannot be retrieved from GenBank; however, on the basis of a PSI-BLAST search conducted by Shang et al. (2015), genes 49 and 50 of phage P13 are predicted to encode the exopolysaccharide depolymerase, but no further substrate/functional information is available. HHpred searches of all proteins encoded by KLPN1 showed that ORF34 and ORF35 encode an endo-N-acetylneuraminidase/endosialidase domain (Table 4). Consequently, we predict ORF34 and/or ORF35 encode the depolymerase activity of phage KLPN1. Further work will be required to confirm our hypothesis.

Table 4:
Selected HHpred results for ORF34 and ORF35 of phage KLPN1.
Hit Probability of true positive E-value P-value Score SS Cols ORF amino acids Reference
2k4q_A Major tail protein V; GPV, bacteriophage lambda, viral protein; NMR {Enterobacteria phage lambda} 99.9 1.3 × 10−27 3.6 × 10−32 195.4 7.6 124 99-224 Pell et al. (2009)
3ju4_A Endo-N-acetylneuraminidase; endonf, polysia, high-resolution, glycosidase, hydrolase; HET: SLB; 0.98A {Enterobacteria phage K1F} 81.6 1.4 4.1 × 10−5 42.0 4.1 93 23-123 Schulz et al. (2010)
4hiz_A Endosialidase, PHI92_GP143; sialidase fold, beta-helix, endo-alpha2,8-sialidase, endo-Al sialidase sialic acid polymer; HET: SLB SIA SUC; 1.60A {Enterobacteria phage PHI92} 80.9 4 0.00012 39.1 6.8 65 23-95 Unpublished
2k4q_A Major tail protein V; GPV, bacteriophage lambda, viral protein; NMR {Enterobacteria phage lambda} 99.9 5.3 × 10−28 1.5 × 10−32 195.1 8.6 119 94-214 Pell et al. (2009)
4hiz_A Endosialidase, PHI92_GP143; sialidase fold, beta-helix, endo-alpha2,8-sialidase, endo-Al sialidase sialic acid polymer; HET: SLB SIA SUC; 1.60A {Enterobacteria phage PHI92} 91.4 0.55 1.6 × 10−5 44.1 7.3 65 23-87 Unpublished
3ju4_A Endo-N-acetylneuraminidase; endonf, polysia, high-resolution, glycosidase, hydrolase; HET: SLB; 0.98A {Enterobacteria phage K1F} 90.0 0.59 1.7 × 10−5 43.8 6.2 65 23-87 Schulz et al. (2010)
DOI: 10.7717/peerj.1061/table-4

The proteins encoded by ORF36 and ORF36.1 are predicted to be two chaperones, analogous to gpG and gpGT required for phage λ tail assembly (Xu, Hendrix & Duda, 2013). These ORFs are believed to keep the tail tape measure protein (TMP) soluble and to recruit the major tail protein subunits, both essential processes for tail assembly. ORF36 encodes the short chaperone (gpG), while a programmed -1 translational frameshift facilitates a translational fusion between the products of ORF36 and ORF36.1 so as to form the long chaperone (gpGT) (hence the lack of a ribosome-binding site for ORF36.1) (Fig. 4). A BLASTP search of the predicted 213 aa fusion protein showed it shares 47% identity (E-value 3 × 10−56) with the tape measure chaperone of the Citrobacter Siphoviridae phage Stevie, reported to have a conserved translational frameshift (Shaw et al., 2015; Fig. 4).

ORF36 and ORF36.1 are related by a programmed-1 translational frameshift.

Figure 4: ORF36 and ORF36.1 are related by a programmed-1 translational frameshift.

The frameshift allows translation of a gpGT-like protein (Xu, Hendrix & Duda, 2013). The ORF36/ORF36.1 fusion protein is predicted to contain almost the entire sequence of ORF36. Citrobacter Siphoviridae phage Stevie (GenBank accession number KM236241) has a conserved translational frameshift in its tape measure chaperone (GenBank accession number AIX12284) (Shaw et al., 2015).

The genome sequence of KLPN1 was subjected to BLASTN searches against all publicly available virome sequence data held by METAVIR (51,992,208 sequence reads associated with 70 projects from a range of habitats, including human faeces (Reyes et al., 2010; Kim et al., 2011; Minot et al., 2011; Minot et al., 2013); Table S1). No hits corresponding to KLPN1 were found among these publicly available datasets. However, using InterProScan, the protein sequence encoded by ORF64 was found to belong to the family ‘Protein of unknown function DUF3987’, representing uncharacterized human-gut-microbiome-specific proteins (Ellrott et al., 2010; Table 3).


K. pneumoniae subsp. pneumoniae is an enteric bacterium and important nosocomial and community-acquired opportunistic pathogen, causing pneumonia, and wound, burn, urinary tract and blood infections. There are 79 recognized capsular types of K. pneumoniae subsp. pneumoniae, with capsular types K1, K2, K5, K54 and K57 most frequently associated with invasive disease or pathogenicity; capsular type K20 is much rarer, though there is regional variability in the predominant clinically relevant capsular types (Turton et al., 2010; Pan et al., 2013; Hsu et al., 2013). It has been suggested that the majority of K. pneumoniae-associated liver infections are preceded by colonization of the gastrointestinal tract, and one study has demonstrated familial spread of a virulent clone of K. pneumoniae causing liver disease (Harada et al., 2011; Lin et al., 2012). Using caecal effluent recovered from a healthy woman, we have isolated a capsular type K2 rmpA+ strain (L4-FAA5) of K. pneumoniae subsp. pneumoniae. After K1, K2 strains are most frequently associated with pyogenic liver abscesses and frequently associated with community-acquired pneumonia (Lin et al., 2014b). K1 and K2 strains, along with the rmpA (regulator of mucoid phenotype A) gene, are associated with hypermucoviscosity and virulence. A study examining K1 and K2 strains of K. pneumoniae in 43 Taiwanese patients with liver abscesses showed, using pulsed-field gel electrophoresis (PFGE), that 17 randomly selected pairs of patient faecal or saliva and abscess isolates allowed differentiation of patients based on the PFGE profiles of their isolates. The abscess isolates had PFGE profiles identical, or closely related to, those of faecal or saliva isolates from the same patient (Fung et al., 2012). The similarity between each patient’s faecal and abscess PFGE profiles led Fung et al. (2012) to suggest that the patients’ infections arose from bacteria originating in the gut microbiota. Our isolation of a K. pneumoniae strain with virulence traits from the human caecum supports the assertion that the human gut microbiota is a source of potentially infectious K. pneumoniae. Limited data are available on the carriage and diversity of gut/faecal K. pneumoniae. A study on healthy Chinese adults in Chinese territories and overseas showed between 18.8 and 87.7% faecal carriage of K. pneumoniae, with individuals in Malaysia (64/73) and Taiwan (150/200) showing the highest carriage rates and those in Japan (6/32) showing the lowest (Lin et al., 2012). Isolates were tested with antisera for capsular types K1–K74 and K80–82: K1 and K2 isolates accounted for ∼10% of isolates in all countries, at least one representative of each capsular type was detected in the study and non-typable (11–88%) isolates were reported for 7/8 countries (Lin et al., 2012). The high carriage of K. pneumoniae in Taiwan is thought to contribute to the high incidence of liver abscess disease seen in the country (Fung et al., 2012).

As with other nosocomial opportunistic pathogens, broad-spectrum antibiotic resistance is a feature of K. pneumoniae subsp. pneumoniae and limits treatment options (Cantón et al., 2012). Therefore, identification of alternative treatment therapies or adjuncts to existing therapies for infections associated with this organism is of utmost importance. Phages against K. pneumoniae subsp. pneumoniae have been used to successfully treat K. pneumoniae infections in animal models of sepsis, pneumonia, burn wounds and liver disease, without causing apparent harm to animals (Bogovazova, Voroshilova & Bondarenko, 1991; Malik & Chhibber, 2009; Chhibber, Kaur & Kumari, 2008; Kumari, Harjai & Chhibber, 2009; Kumari, Harjai & Chhibber, 2010b; Hung et al., 2011). The number of known lytic phages that infect K. pneumoniae remains small and their range is limited to a small number of capsular types (though phenotypic information on strains is absent from the majority of publications on K. pneumoniae phages). Given the large number of phages present in faeces and caecal effluent (Hoyles et al., 2014), and because K. pneumoniae subsp. pneumoniae is a member of the human gut microbiota, we were keen to exploit this environment as a source of phages with potential therapeutic applications. We isolated from caecal effluent a phage (named KLPN1) that infects K. pneumoniae subsp. pneumoniae L4-FAA5 and K2 clinical isolates of K. pneumoniae subsp. pneumoniae (Table 1). Phage KLPN1 does not infect non-K2 clinical isolates (Table 1). To the best of our knowledge, this is the first report of the isolation of a bacterium–phage combination from the human caecum.

To date, only eight phages infecting the K2 capsular type of K. pneumoniae have been reported (Bogovazova, Voroshilova & Bondarenko, 1991; Malik & Chhibber, 2009; Kumari, Harjai & Chhibber, 2010b; Hung et al., 2011). Several Podoviridae were isolated on K. pneumoniae B5055 (assumed to be derived from NCTC 5055) and tested as therapeutic agents [Kpn5, Kpn12, Kpn13, Kpn17, Kpn22 (individually and in cocktail) and KØ1] in B5055-induced burn-wound infections in mice (Kumari, Harjai & Chhibber, 2009; Kumari, Harjai & Chhibber, 2010a; Kumari, Harjai & Chhibber, 2010b; Malik & Chhibber, 2009). Phage SS (Podoviridae) was isolated on B5055 and used to treat lobar pneumonia caused by the same strain in mice (Chhibber, Kaur & Kumari, 2008). Phage ϕNK5 (Podoviridae) was isolated from sewage on K. pneumoniae NK-5, isolated from a patient with a primary liver abscess and septicaemia (Hung et al., 2011). The same bacterial strain was used to induce liver abscesses and bacteraemia in mice, which were successfully treated with ϕNK5. None of the aforementioned phages has been tested against a range of clinical K. pneumoniae isolates. Therefore, it is difficult to assess how useful they would be in treatment of a wide range of clinical infections, especially when similar infections can be caused by different capsular types of K. pneumoniae (e.g., Table 1). We can state that KLPN1 has potential for treating K2-associated infections, but note that differences in lytic infection were observed between the caecal isolate and the clinical isolates: KLPN1 infected the caecal isolate and exhibited depolymerase activity that was absent with the clinical K2 isolates. Further investigations may reveal that its infection kinetics differ between K2 strains.

Hung et al. (2011) demonstrated the generation of phage-insensitive mutants after 6 and 12 h co-cultures of NK-5/ϕ NK5, with these mutants lacking the hypermucoviscosity phenotype of NK-5. On solid media, phage-insensitive mutants of K. pneumoniae L4-FAA5 were routinely observed after 48 h incubation with phage KLPN1. Whether mutants are generated more quickly in liquid culture remains to be determined, as does the nature of the mutations that allow them to escape lytic infection with KLPN1. Does solid media act as a spatial refuge (Mills et al., 2013) for sensitive bacteria, delaying the appearance of insensitive mutants?

It is predicted that many members of the human gut microbiota are embedded in biofilms, and phages may contribute to cell lysis in these ecological niches (Mills et al., 2013). The microbiota of the human caecum resides in a highly mucoid biofilm (Randal Bollinger et al., 2007). Phage KLPN1 exhibits depolymerase activity on K. pneumoniae L4-FAA5, which may facilitate the movement of the phage within the caecal biofilm. It has been demonstrated that phages can diffuse within biofilms, be immobilized, amplified and released after a lytic cycle in these environments. They may also potentially interact with their specific binding sites on bacteria, even in the absence of lytic activity (Mills et al., 2013). Further work is needed to understand interactions between K. pneumoniae L4-FAA5 and phage KLPN1 in single- and multi-strain biofilm systems, and to determine whether the “spatial refuge hypothesis” (Mills et al., 2013) holds for the caecal microbiota, preventing the extinction of all sensitive bacteria within the biofilm.

Following whole-genome sequencing and annotation, KLPN1 was found to encompass 73 ORFs and, based on its sequence homology to Klebsiella phages KP36 and F20, it is evident that KLPN1 is a member of the family Siphoviridae, subfamily Tunavirinae, and would become the third member of the genus “Kp36likevirus” (Niu et al., 2014). In addition, based on our sequence analyses phage 1513 (a Siphoviridae that infects a multidrug-resistant K. pneumoniae strain isolated from a patient with pneumonia; Cao et al., 2015) can also be added to this genus, bringing the total number of members to four. This classification would be consistent with the morphological appearance of KLPN1, which has a capsid of 64 nm as well as rosette-like or propeller tail tip, a finding also observed for phages ϕ28, T1 and RTP (Geyer et al., 1983; Wietzorrek et al., 2006). Unsurprisingly, KLPN1 shares no sequence homology with Klebsiella phages belonging to the families Myoviridae or Podoviridae;  however, some similarities to Siphoviridae phage phiKO2 were observed, but these were confined to the tail morphogenesis region and a hypothetical protein. ORF60 and ORF61 are predicted to encode holin (which destroys the cytoplasmic membrane) and endolysin (which degrades peptidoglycan), respectively. These gene products have antibacterial properties that can be used in phage-associated therapies (Viertel, Ritter & Horz, 2014); therefore, further characterization of the proteins encoded by these ORFs is required.


We isolated a K. pneumoniae subsp. pneumoniae–phage combination from the human caecum, and have characterized its lytic properties against a panel of K. pneumoniae subsp. pneumoniae clinical isolates. Phage KLPN1 infects capsular type K2 isolates, and may have applications in treating a range of K2-associated infections. We have, therefore, demonstrated the gut microbiota as a source of clinically relevant phages. Whole-genome sequence analysis of KLPN1 revealed the phage to encode proteins that have potential applications in phage-associated therapies. Characterization of these gene products, or genetically modified variants, is required to determine their usefulness.

Supplemental Information

Supplementary material to be published alongside full paper

Supplementary Table 1. Details of virome datasets against which the genome sequence of phage KLPN1 was searched.

Supplementary Table 2. Genome annotation of phage KLPN1, including InterProScan results.

DOI: 10.7717/peerj.1061/supp-1