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Pyrosequencing-based analysis reveals a novel capsular gene cluster in a KPC-producing Klebsiella pneumoniae clinical isolate identified in Brazil

Pablo Ivan Pereira Ramos1, Renata Cristina Picão24, Eliana Carolina Vespero3, Marsileni Pelisson3, Luiz Fernando Goda Zuleta1, Luiz Gonzaga P Almeida1, Alexandra L Gerber1, Ana Tereza R Vasconcelos1, Ana Cristina Gales4 and Marisa Fabiana Nicolás1*

Author affiliations

1 Laboratório Nacional de Computação Científica (LNCC), Petrópolis, Rio de Janeiro, Brazil

2 Instituto de Microbiologia Paulo de Góes, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil

3 Departamento de Patologia Clínica, Análises Clínicas e Toxicologia, Universidade Estadual de Londrina, Londrina, Brazil

4 Laboratório ALERTA, Divisão de Doenças Infecciosas, Universidade Federal de São Paulo, São Paulo, Brazil

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Citation and License

BMC Microbiology 2012, 12:173  doi:10.1186/1471-2180-12-173


The electronic version of this article is the complete one and can be found online at: http://www.biomedcentral.com/1471-2180/12/173


Received:8 February 2012
Accepted:23 May 2012
Published:11 August 2012

© 2012 Ramos et al.; licensee BioMed Central Ltd.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background

An important virulence factor of Klebsiella pneumoniae is the production of capsular polysaccharide (CPS), a thick mucus layer that allows for evasion of the host's defense and creates a barrier against antibacterial peptides. CPS production is driven mostly by the expression of genes located in a locus called cps, and the resulting structure is used to distinguish between different serotypes (K types). In this study, we report the unique genetic organization of the cps cluster from K. pneumoniae Kp13, a clinical isolate recovered during a large outbreak of nosocomial infections that occurred in a Brazilian teaching hospital.

Results

A pyrosequencing-based approach showed that the cps region of Kp13 (cpsKp13) is 26.4 kbp in length and contains genes common, although not universal, to other strains, such as the rmlBADC operon that codes for L-rhamnose synthesis. cpsKp13 also presents some unique features, like the inversion of the wzy gene and a unique repertoire of glycosyltransferases. In silico comparison of cpsKp13 RFLP pattern with 102 previously published cps PCR-RFLP patterns showed that cpsKp13 is distinct from the C patterns of all other K serotypes. Furthermore, in vitro serotyping showed only a weak reaction with capsular types K9 and K34. We confirm that K9 cps shares common genes with cpsKp13 such as the rmlBADC operon, but lacks features like uge and Kp13-specific glycosyltransferases, while K34 capsules contain three of the five sugars that potentially form the Kp13 CPS.

Conclusions

We report the first description of a cps cluster from a Brazilian clinical isolate of a KPC-producing K. pneumoniae. The gathered data including K-serotyping support that Kp13’s K-antigen belongs to a novel capsular serotype. The CPS of Kp13 probably includes L-rhamnose and D-galacturonate in its structure, among other residues. Because genes involved in L-rhamnose biosynthesis are absent in humans, this pathway may represent potential targets for the development of antimicrobial agents. Studying the capsular serotypes of clinical isolates is of great importance for further development of vaccines and/or novel therapeutic agents. The distribution of K-types among multidrug-resistant isolates is unknown, but our findings may encourage scientists to perform K-antigen typing of KPC-producing strains worldwide.

Keywords:
Capsular gene cluster; Capsular polysaccharide; K-antigen; KPC-producing K. pneumoniae; Molecular serotyping; Monosaccharide biosynthesis pathways

Background

Klebsiella pneumoniae is a Gram-negative, rod-shaped bacterium frequently associated with nosocomial and community-acquired infections [1]. Over the past decade, healthcare practitioners have observed the rapid evolution of antimicrobial resistance among K. pneumoniae clinical isolates worldwide. The emergence and subsequent global spread of strains producing Klebsiella pneumoniae carbapenemase (KPC) represents a significant threat to public health [2]. The gene encoding this β-lactam resistance factor is frequently carried along with genes conferring resistance to multiple classes of antimicrobial agents. As a result, the therapeutic options to treat infections caused by KPC-producing K. pneumoniae are generally scarce and in some instances limited to polymyxins [2].

The development of an effective response against K. pneumoniae infections depends on the integrity of the immune system. Indeed, many authors have provided evidence that activation of the inflammatory response is required to clear such infections [3-5]. Unfortunately, most patients infected by multidrug-resistant K. pneumoniae have serious underlying conditions and/or a compromised immune status [1,6]. Capsule production is believed to be one of the most important virulence factors for this species. The polysaccharide matrix found on its cell surface may prevent desiccation, confer adherence to host cells and protect it against both non-specific and specific host immunity [7]. However, there are differences in the degree of virulence conferred by different Klebsiella capsule types, possibly depending on the mannose and/or rhamnose content of the CPS [1]. The K. pneumoniae capsule is generally composed of acidic polysaccharides, including uronic acid repeats and, in several instances, mannose, rhamnose, galactose, pyruvate and fucose residues [8]. The genes involved in the biosynthesis, transport and assembly of K. pneumoniae and E. coli group 1 capsules are found at a locus called cps, which is organized similarly in the two species [9]. The biosynthetic process of both types of capsules is also related between the two bacteria. Briefly, CPS synthesis initially takes place on the cytoplasmic side of the inner membrane with the assembly of individual sugar repeat residues which are linked by the sequential activities of specific glycosyltransferases (GTs) [10]. These are then flipped across the inner membrane by the action of the Wzx protein and undergo polymerization by the Wzy protein [11]. Polymerization control and translocation of the nascent polymer to the cell surface occurs with the coordinated action of Wza, Wzb and Wzc proteins [12].

To date, a variety of cps gene clusters have been characterized in Klebsiella spp., mostly from isolates recovered in the USA, Asia and Europe [13-15]. To our knowledge, there have been no studies on the cps organization of K. pneumoniae isolates from Brazil, KPC-producing or otherwise. Here, we report the unique cps organization of a KPC-producing K. pneumoniae isolate showing multidrug resistance. This bacterium was responsible for a large nosocomial outbreak in a teaching hospital located in Southern Brazil (Ana C. Gales, personal communication).

Results and Discussion

General features of the cpsKp13 gene cluster

The cpsKp13 gene cluster is 26.4 kbp in length and contains 20 open reading frames (ORFs) from galF to wzy (Figure 1, Table 1). The average GC content of these genes is 42%, which is lower than the average GC content of the entire Kp13 genome (57.5%, data not shown). Comparable GC content has been reported for twelve other K. pneumoniae cps clusters [15].

thumbnailFigure 1. Overall organization of thecpscluster ofK. pneumoniaeKp13. The cpsKp13 spans galF to wzy. ORFs are represented by arrows (gray for those encoding glycosyltransferases and double-headed for possible mobile elements). Rectangles above the ORFs represent distinct variably conserved regions of the cps cluster as discussed in the text. A plot of the GC content of the region using a 100-bp sliding window is shown below. The dashed horizontal line represents the mean GC content of the entire Kp13 chromosome.

Table 1. General features of the 20 coding sequences identified in the Kp13cpsgene cluster

The cpsKp13 has a genomic organization similar to other K. pneumoniae cps clusters, and it can be divided into three regions as shown in Figure 1. The 5’ end or region 1 (from galF to wbaP) contains conserved genes responsible for polymer assembly and translocation [12]. The central region or region 2 contains genes encoding serotype-specific GTs and gnd. The 3’ end or region 3 is more variable among different capsular types, with some containing the manCB operon that encodes GDP-D-mannose, like serotypes K1 and K5 [15]. Similarly to serotypes K9 and K52, the 3’ end of the cpsKp13 gene cluster contains the rmlBADC operon for the synthesis of dTDP-L-rhamnose instead of the manCB operon [15]. The genes wzx and wzy are also found in the 3’ region of the Kp13 cps cluster. This region is succeeded by defective IS elements and a prophage fragment (Figure 1). The discussed conservation of region 1 and variability of region 2 can be readily observable on a comparison of the cps loci of different K-types deposited in NCBI (Figure 2).

thumbnailFigure 2. Comparison of sequencedK. pneumoniae cpsloci. For each cps cluster, a two-way comparison with the clusters immediately above and/or below is presented. The K-type of each compared cluster is shown in red, followed by the strain/isolate identification and its NCBI accession number in parentheses. The blue segments connecting each cluster represent variably conserved (60–100% identity) regions among them (from a BLASTN comparison with e-value ≤ 10-4). Predicted glycosyltransferases are colored in orange, wzy and gnd homologs in yellow and purple, respectively. N.T., new K-type; N.D., K-type not determined.

The cpsKp13 monosaccharide biosynthesis pathways: UDP-D-glucuronate, UDP-D-galacturonate and L-rhamnose

As in other bacteria that produce group-1 capsules, galF delimits the 5’ region of cpsKp13. This gene shows 100% identity to the galF sequence present in K. pneumoniae NK8 [GenBank:BAI43699], which codes for a UTP-glucose-1-phosphate uridylyltransferase (EC 2.7.7.9, Figure 3). This enzyme belongs to the nucleotidyltransferase family and catalyzes the reaction UTP + α-D-glucose 1-phosphate ↔ diphosphate + UDP-D-glucose. This enzyme is important because UDP-D-glucose serves as a precursor for the biosynthesis of bacterial lipopolysaccharides and capsular polysaccharides. It is also possible that the galF product interacts with the product of galU, thus elevating UDP-D-glucose concentration in the cell and providing more material for the synthesis of capsular polysaccharides [11]. In fact, a galU homolog found in Kp13 outside the cps region (KP04702) shows 94% identity (BLASTP) to GalU from Shigella flexneri [Swiss-Prot:P0AEP6]. Immediately downstream of the rmlBADC operon, the gene ugd is found (Figure 1). It encodes a UDP-glucose 6-dehydrogenase (EC 1.1.1.22). As depicted in Figure 3, this enzyme converts UDP-D-glucose to UDP-D-glucuronate, a common constituent of bacterial capsules [7]. As with other sequences located in the 3’ region of the cpsKp13 gene cluster, this coding sequence exhibits remarkable amino acid conservation. It is 100% identical to Ugd from K. pneumoniae strains NK8 [GenBank:BAI43716] and VGH404 serotype K5 [GenBank:BAI43755] (Table 1), both studied by Shu et al. [15]. Uge catalyzes the conversion of UDP-D-glucuronate to UDP-D-galacturonate (Figure 3), which is also present in both bacterial capsules and LPS. In fact, Kp13 has two copies of this gene, uge-1 (KP03793) and uge-2 (KP03786). A NAD-dependent epimerase domain (Pfam accession no. PF01370) is predicted to occupy amino acids 4 to 230 in both Uge sequences. Two copies of uge are also found in the genome of K. pneumoniae subsp. rhinoscleromatis (which produces a K3 capsule), one in the cps cluster and an inverted adjacent copy in the cluster for LPS synthesis [16]. As the K3 CPS contains D-galacturonate in its composition, uge was considered the last gene of its cps cluster [16] instead of ugd as usually regarded [15,17]. In Kp13 uge-1 should also be considered within the cps since the genes necessary to the flippase and polymerase activities, wzx and wzy respectively, are located downstream (Figure 1); therefore, D-galacturonate could also form the Kp13 CPS composition. The effects of a uge null mutation on colonization and virulence were studied in K. pneumoniae 52145, which is a highly virulent strain able to colonize different surfaces [18]. A uge deletion reduced colonization and rendered the strain completely avirulent in an experimental model of pneumonia [18]. This suggests that the uge-1 and/or uge-2 mutation in Kp13 could have important, measurable effects on colonization and virulence.

thumbnailFigure 3. Amino- and polyketide sugar production inK. pneumoniaeKp13. Pathways leading to UDP-D-galacturonate, UDP-D-galactose and dTDP-L-rhamnose are shown, as these residues could be present in the capsular structure of Kp13. Enzymes coded by genes present in the cpsKp13 cluster are underlined.

In the cpsKp13 cluster, genes encoding enzymes that participate on the synthesis of dTDP-L-rhamnose from glucose 1-phosphate are found immediately downstream of the gnd gene (Figure 1). The rmlBADC genes were found in three capsular serotypes studied by Shu et al. [15]: K9, K14 and K52. In serotypes K9 and K52, these genes are also found downstream of gnd. The lengths of the products encoded by rmlA, rmlB, rmlC and rmlD are shown in Table 1, along with the best BLAST hits for these genes. The gene rmlA codes for a glucose-1-phosphate thymidylyltransferase (EC 2.7.7.24), which catalyzes the first reaction of L-rhamnose synthesis: dTTP + α-D-glucose 1-phosphate → diphosphate + dTDP-D-glucose (Figure 3). The second reaction is performed by dTDP-D-glucose 4,6-dehydratase (EC 4.2.1.46, Figure 3), the product of rmlB, which catalyzes the dehydration of dTDP-D-glucose to dTDP-4-keto 6-deoxy-D-glucose. Epimerization at the C3’ and C5’ positions of this molecule is performed by dTDP-4-dehydrorhamnose 3,5-epimerase (rmlC, EC 5.1.3.13, Figure 3), producing dTDP-4-oxo-L-rhamnose. Finally, dTDP-4-dehydrorhamnose reductase (EC 1.1.1.133, Figure 3), encoded by rmlD, catalyzes the reduction of dTDP-4-oxo-L-rhamnose to dTDP-L-rhamnose, which can be subsequently linked to the capsular polymer by a specific rhamnosyltransferase. All three conserved regions (the Y-X3-K loop, the Wierenga motif G-X2-G-X2-G and the STDYVF sequence) discussed by Giraud and Naismith [19] are present in Kp13’s RmlD.

Whereas the chemical composition of the Kp13 capsule remains to be determined, the pyrosequencing-based genomic analysis of cpsKp13 allowed the identification of sugar metabolic pathways. Genes encoding enzymes for the biosynthesis of sugar nucleotide precursors in the Kp13 capsule, such as UDP-D-glucose, UDP-D-glucuronate, UDP-D-galacturonate and dTDP-L-rhamnose, are found in the cps cluster. Thus, the capsule of Kp13 may contain any of these sugar nucleotide precursors. In particular, the presence of two genes in the cps cluster encoding possible rhamnosyltransferases suggests that L-rhamnose makes up part of the Kp13 capsule (see discussion below). On the other hand, galE (KP02995) was identified outside the cps region, and it encodes a UDP-glucose 4-epimerase with roles in the amino sugar and nucleotide sugar pathways producing UDP-D-galactose from UDP-D-glucose (Figure 3). The presence of this gene suggests that the capsule composition of Kp13 could also include UDP-D-galactose derivatives. Neither the manA, manB and manC genes of the cps cluster nor other genes of the mannose and fucose biosynthesis pathways were identified in the Kp13 genome. This suggests that the CPS of Kp13 does not contain GDP-D-mannose or GDP-L-fucose derivatives.

Proteins involved in translocation, surface assembly and polymerization: Wzi, Wza, Wzb, Wzc, Wzx and Wzy

The deduced amino acid sequences of the wzi and wza genes found in cpsKp13 show 98% and 97% identity, respectively, with homologs from K. pneumoniae VGH484 (Table 1), and both proteins were predicted to localize in the outer membrane (PSORTb scores: Wzi, 9.52; Wza, 9.92). Moreover, a signal peptide was predicted for the wzi gene product. Analysis of the secondary structure of the Kp13 Wzi protein using PSIPRED showed that it is rich in β-sheet regions (data not shown), an observation that has been experimentally confirmed for a Wzi homolog in E. coli [GenBank:AAD21561.1] [20] which shares 98% identity with that of Kp13. Also, Rahn et al. [20] established the importance of the Wzi outer membrane protein for capsule synthesis by showing that wzi mutants have lower amounts of cell-associated capsular polysaccharide.

The wza product of Kp13 has 92% identity with Wza from E. coli [GenBank:AAD21562.1], which has been shown to be an integral lipoprotein with exposed regions on the cell surface. The E. coli protein forms a ring-like structure responsible for polymer translocation through the outer membrane [12]. Wzc and Wzb are a tyrosine autokinase and its cognate acid phosphatase, respectively, and they are ubiquitously found in group 1 capsule clusters [12,21]. The Kp13 Wzc protein was predicted to have two transmembrane regions, like its counterpart in the K. pneumoniae strain Chedid, with which it shares 72% amino acid identity [Swiss-Prot:Q48452]. The inner membrane is the probable location of Kp13’ Wzc (PSORTb score 9.99), in agreement with its role in capsule synthesis. Wzc is involved in the translocation of capsular polysaccharide from the periplasm to the cellular surface through formation of a complex with Wza [22]. Wzc undergoes autophosphorylation of its tyrosine-rich C-terminal residues (of the last 17 residues in Kp13 Wzc, eight are Tyr) potentially modulating the opening and closing of the translocation channel [12]. The Wzb protein (EC 3.1.3.48) of Kp13 is probably located in the cytoplasm (PSORTb score: 9.26). Wzb catalyzes the removal of a phosphate group from phosphorylated Wzc and is necessary for continued polymerization of the repeat units [12]. Sequence conservation of the Wzy and Wzx proteins is usually low [23]. The localization of wzx and wzy in Kp13 is different from that observed in various K-serotypes by Shu et al. [15], in which the genes usually mapped upstream of gnd. In Kp13, both genes are located downstream of gnd, in region 3 of the cps cluster, and wzy is transcribed in the opposite direction relative to other cps genes. Wzx is an inner membrane protein that transfers the polysaccharide units, assembled in the cytoplasm, into the periplasm, thus acting as a flippase [12]. The Wzx protein from cpsKp13 has 10 predicted transmembrane segments and is 411 aa long, which is in agreement with a previous study of this protein in E. coli that predicted 10–12 transmembrane segments [23]. BLASTP against the NCBI database shows that the best hit (64% identity) is a putative Wzx protein from E. coli TA271 (NCBI accession no. ZP_07523140, Table 1). A polysaccharide biosynthesis domain (Pfam accession no. PF01943), common to Wzx proteins, was found spanning amino acids 8 to 275 of Kp13 Wzx.

Wzy from Kp13 is 348 aa long and also had 10 predicted transmembrane segments, similar to the Wzy proteins of other Enterobacteriaceae that have 10–11 transmembrane segments [24]. This protein is believed to be a polysaccharide polymerase, although experimental evidence for this activity has not yet been reported due to the technical difficulty of working with Wzy in vitro [12]. NCBI BLASTP searches show that the best hit (35% identity) for Wzy is a conserved protein from Thermoanaerobacter wiegelii [GenBank:ACF14522.1] (Table 1).

It is remarkable that the wzy gene from isolate Kp13 is transcribed in the opposite direction compared to other genes of the cps cluster, a characteristic that to our knowledge has not been reported for previously studied cps clusters, as can be observed in Figure 2, where the position of wzy within different K. pneumoniae cps loci is highlighted.

Downstream wzy, we have identified an 862-bp region showing 70% identity to an IS element of the IS3 family [GenBank:CP002438.1]. No terminal inverted repeats or target site duplications were found in this element. Although three ORFs identified within this putative IS showed significant identity to distinct transposases, these structures do not seem to encode functional enzymes. The occurrence of mutations leading to premature stop codons and/or frameshifts might have rendered this transposase non-functional. Alternatively, this chimeric structure could have resulted from homologous recombination events with other transposase-encoding genes. Upstream wzy, there is a 1539-bp ORF whose deduced amino acid sequence shows 31% identity to a defective tail fiber protein of a Mu-like prophage identified in Dickeya dadantii [GenBank:ADM97620]. Notably, other prophage genes were absent. The location of wzy between two defective mobile genetic elements suggests that this gene may have been incorporated into Kp13’s cps via an ancient horizontal gene transfer event. Subsequently, these mobile genetic elements may have been truncated in order to assure that wzy would be permanently present in the cpsKp13 region, which is desirable because capsule assembly is a Wzy-dependent process.

The conserved gene gnd, found in the central region of cpsKp13, encodes a 468 aa protein (6-phosphogluconate dehydrogenase, EC 1.1.1.44, Figure 3) that catalyzes the conversion of 6-phospho-D-gluconate to D-ribulose 5-phosphate during the third step of the pentose phosphate pathway. This gene was found in all of the cps gene clusters studied by Shu et al. [15] and shows a high degree of conservation among them, which would be expected from an evolutionary standpoint due to the central role of this metabolic pathway. At the protein sequence level, the best hit (99% identity) for Kp13’s gnd product is an ortholog from strain VGH484, serotype K9 [GenBank:BAI43786.1] (Table 1).

Kp13’s cps gene cluster has five GTs: WbaP, Orf8, Orf9, Orf10 and Orf19

The products of wbaP, orf8, orf9, orf10 and orf19 are GTs, enzymes specialized on the polymerization of sugar molecules into existing molecules, which can be carbohydrates, lipids or proteins. Because of the variety of modifications catalyzed by GTs it is difficult, based on sequence analysis alone, to define the exact outcome of each reaction [25], even though they may play an important part on the diversity of capsular structures encountered in K. pneumoniae. The number of GTs in K. pneumoniae’s cps cluster is variable, ranging from three (serotypes K1 and K2) to six as reported by Shu et al. [15]. Kp13 has a total of five GTs, four of these located contiguously (wbaP, orf8, orf9 and orf10) and one of them found on the 3’ end of the cluster (orf19). All the GTs found on Kp13’s cps gene cluster have been predicted to belong to the family 2 GTs, comprising enzymes that use an inverting catalytic mechanism which modifies the anomeric configuration of the transferred sugar [26]. wbaP (formerly rfbP) is the first GT on Kp13’s cps gene cluster and encodes a 482 aa long UDP-Gal::undecaprenolphosphate Gal-1-P transferase, which catalyzes the initial transfer of galactose-1-phosphate to an undecaprenol phosphate acceptor, thus initiating the capsule polymer synthesis. This protein was predicted to be located in the cytoplasmic membrane (PSORTb score: 10.0) and may contain five transmembrane-spanning regions. A conserved WbaP phosphotransferase domain (IPR017472, e-value 7.5e-194) is also found ranging from amino acids 21 to 482. NCBI BLASTP searches showed identity of up to 80% with WbaP from other K. pneumoniae and E. coli. The protein presents two conserved DxD motifs, which are widespread in GTs and are thought to be involved in metal/nucleotide binding and catalysis [27,28]: DED, ranging from amino acids 356–358 and DVD, 442–444 aa. The latter has been found in all but one of 12 different capsular serotypes studied by Shu et al. [15]. orf8 (KP03804) encodes a 302 aa uncharacterized GT whose amino acid sequence shows 67% identity (Table 1) with putative rhamnosyltransferases from K. pneumoniae strain A1517 showing a unique capsular serotype [GenBank:BAF75773.1] [14]. The GT encoded by orf9 (KP03803) is predicted to be 298 aa long, with a best hit on NCBI BLASTP with a putative dTDP-rhamnosyltransferase from D. dadantii [GenBank:ADM97617.1] (63% identity, Table 1). D. dadantii is a distantly related plant pathogen of the Enterobacteriaceae family. Interestingly, there is little similarity between orf9 and other K. pneumoniae sequences. The highest identity match (31%) is with a putative rhamnosyltransferase from strain VGH484 [GenBank:BAI43783.1]. The presence of the rmlBADC genes (previously discussed) together with the possible rhamnosyltransferases provides appealing evidence that L-rhamnose makes part of Kp13’s capsular structure. orf10, the third gene encoding a putative GT located in region 2 of the Kp13 cps cluster, is predicted to code for a 253 aa long protein with a conserved domain of unknown function spanning amino acids 36 to 193 (Pfam accession no. PF04765). As with orf9, the best hit (57% identity, Table 1) is also with a sequence encoding a putative GT from D. dadantii [GenBank:ADM97619.1]. There was no similarity between the orf10 (KP03802) product and other published Klebsiella sequences.

Finally, the last GT from cpsKp13, termed orf19, is located on the 3’ end of the cps cluster and encodes a predicted 330 aa product. This protein has similarity with several uncharacterized GTs family 2 from different Enterobacteriaceae, including E. coli TA271 [GenBank:EGI36158.1] (58% identity), D. dadantii [GenBank:ADM97622.1] (38%) and Cronobacter sakazakii [GenBank:ABX51890.1] (34%). Only a general domain of the GTs family 2 was found in this protein, spanning amino acids 7 to 145 (Pfam accession no. PF00535).

In silico serotyping

Using molecular serotyping for the cps cluster, Brisse et al. [29] showed that very distinct PCR-RFLP patterns (C patterns) were obtained for most of the K serotypes, indicating that differences in antigenic specificity among serotypes are due to differences in cps gene content. Thus, we have also applied in silico molecular serotyping to determine the capsular serotype of isolate Kp13. For this approach, the sequence between the primers published by Brisse et al. [29] was used to search in silico for restriction sites of the HincII endonuclease. This sequence spanned 12,031 bp from wzi to gnd, and the in silico restriction analysis identified 12 restriction sites, corresponding to 11 restriction fragments (Table 2). The fragments, ranging in size from 368 to 1,777 bp, were selected for analysis as suggested by Brisse et al. [29] (Table 2). The cpsKp13 RFLP pattern was compared to 102 previously published C patterns [29]. None of the reference patterns matched the one displayed by Kp13 (see Additional file 1). The similarity score for Kp13 was greater than 10.4 (MST cutoff value score ≥ 0.75), thus providing additional evidence that Kp13 K-type is a new serotype.

Additional file 1. Cluster analysis of 103 RFLP patterns after MST analysis. MST distances between serotypes are represented as alignment scores, with 0.75 used as the scale-adjusted threshold for distinguishing two serotypes. K. pneumoniae Kp13 is labeled as KP13, while the other serotypes follow the C-pattern nomenclature from Brisse et al. [29].

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Table 2. In silico HincII restriction pattern obtained for the 12,031 bp sequence spanningwzitogndin the Kp13cpsgene cluster

In vitro K-serotyping

Kp13 showed a weak positive reaction with both K9 and K34 antisera that could not be resolved by modifying antiserum dilution or quellung reaction. This result is not surprising since cross-reactions with the type-specific antisera is commonly observed among K. pneumoniae clinical isolates due to the activity of common genetic elements among distinct cps clusters [30]. In fact, the rmlBADC genes are also present in the cps cluster displayed by serotype K9 [15], and its CPS is composed of D-glucuronate, D-galactose and L-rhamnose residues [31]. Given the gene content of cpsKp13 and the presence of galE on the Kp13 genome, these residues could all be synthesized by this isolate, hence cross-reactions were not unexpected. From the comparison of cpsKp13 and cpsVGH484 (K9, Figure 2) it is clear that they have common genes, but the Kp13 cps also has distinguishing features like its repertoire of GTs, the presence of uge-1 and a different cluster organization (e.g. the positions of wzy and wzx). In the same line of evidence, the CPS of serotype K34 is composed of L-rhamnose, D-glucose and D-galacturonate residues [32], all of which also potentially present in the Kp13 CPS as discussed earlier, and D-galacturonate being produced by the epimerase activity from the uge-1 product. No cps sequences from K34 isolates were found on public databases. Nevertheless, our results indicate that Kp13 possess a unique serotype since it showed a distinct RFLP pattern compared to those 102 patterns, including representatives of serotypes K9 and K34, previously described [29]. It has also been observed that cps-PCR genotyping seems to be a more sensitive and specific way for detecting novel serotypes [14], and our pyrosequencing-based approach together with the careful scrutinization of each CDS in the cluster and the in vitro results supports the finding that Kp13 synthesizes a novel CPS.

Regulation of cps gene expression in Kp13

The transcriptional regulation of cps genes is thought to be under the control of three promoters, P1, P2 and P3, which are located upstream of galF, wzi and rmlB, respectively [13,15]. As previously shown for other strains by Shu et al. [15], in the cpsKp13 cluster the transcripts driven by P1 and P2 should consist of galF/orf2 and wzi to gnd, respectively (Figure 4). Regulatory elements have been identified within the promoters P1 and P2 of the cpsKp13 cluster. Promoter P1 contains the regulatory RcsAB box operator (5-TAAGATTATTCTCA-3’) that is essential for the induction of Rcs-regulated promoters by way of its interaction with the regulators RcsB and RcsA [33]. Predicted rcsB and rcsA genes are present in the Kp13 genome, encoded, respectively, by predicted coding sequences KP00953 and KP04844.

thumbnailFigure 4. Model of regulation in theK. pneumoniaeKp13cpscluster. Only selected genes are shown. The promoters are depicted as upside-down triangles, and the JUMPStart element is shown as a hexagon. The rectangles under each cluster represent transcriptional units, and the stems are possible Rho-independent attenuators. P3 could either drive the transcription of rmlB through orf19 or there could be other promoters (P4, P5 or P6). The possible transcriptional units are depicted.

The JUMPStart element was found within promoter P2 (Figure 4). This element was identified upstream of a number of bacterial cps clusters [15,34]. The 8-bp ops element (5’-GGCGGTAG-3’) is located within JUMPStart and has been reported to function as a binding site for the RfaH activator protein [35]. Indeed, rfaH is found elsewhere in the Kp13 genome (KP31625), and its deduced amino acid sequence displays 80% identity with an ortholog from E. coli K12 [Swiss-Prot:P0AFW0]. A possible stem-loop structure (Figure 4) related to the Rho-independent transcription attenuator is located in the intergenic region between wzc and wbaP of the cpsKp13 cluster, as predicted by the ARNold web server [36] with a calculated free energy of −8.49 kcal/mol. Similar features have also been identified in other cps clusters from K. pneumoniae[9,15]. Additionally, a second putative stem-loop structure (Figure 4) was predicted downstream of orf10 (ΔG = −8.20 kcal/mol). Further studies are necessary to confirm the implications of this finding; a stem-loop in this position has not been previously described. The transcription of cpsKp13 region 3 may occur from different promoters. For instance, the P3 promoter upstream rmlB may transcribe a polycistronic mRNA from this gene up to orf19 or, alternatively, each individual promoter predicted in this region may drive the transcription of a limited number of genes (Figure 4).

Notably, wzy is located between defective mobile elements and is transcribed in the opposite direction of other genes in the cps cluster (Figure 1). Thus, it should have its own promoter (possibly P7). A putative −10 box was found, separated by 15 bp from its −35 counterpart, but no obvious RBS could be identified. This observation raises the question of how Kp13 coordinates expression of wzy, since this protein is also essential for the formation of CPS.

Deviations from the −10 and −35 consensus sequences significantly modify the strength of each promoter [37], so the number of promoters could in fact be different from that proposed here. Still, their roles in cps cluster regulation deserve further experimental study, and our sequence-based bioinformatic approach provides candidates for follow-up.

Conclusions

In this study, we report a unique cps cluster organization in Kp13, a multidrug-resistant, KPC-producing K. pneumoniae strain that caused a large outbreak in a Brazilian teaching hospital. The Kp13 cps cluster contains all of the genes necessary for capsule biosynthesis. Based on the sugar metabolic pathways identified in cpsKp13 and in other genomic regions, we have predicted that the capsule composition of Kp13 may include D-glucose, D-glucuronate, D-galacturonate, D-galactose and L-rhamnose residues.

Methods

Ethics statement

This study was approved by the Ethics Committee of the Universidade Estadual de Londrina (UEL) under reference number CAAE: 3356.0.000.268-09. Clinical assessment and blood sampling were performed after diagnostic routine procedures in the intensive care unit of the Hospital Universitário-UEL, with written informed consent of the patient.

Bacterial strain

Between February and May 2009, a teaching hospital located in Southern Brazil experienced its first outbreak of nosocomial infections due to KPC-producing K. pneumoniae. The KPC-producing K. pneumoniae isolate Kp13 was recovered from the blood culture of a patient admitted to the intensive care unit with diabetes mellitus and cranial encephalic trauma. Automated bacterial identification was conducted with a MicroScan WalkAway apparatus (Dade Behring, Sacramento, CA, USA). Kp13 was phenotypically detected as a carbapenemase producer by the modified Hodge [38], and the specific blaKPC-2 gene was identified by PCR and amplicon sequencing using previously described primers and cycling conditions [39].

Kp13 was identified as K. pneumoniae subsp. pneumoniae by showing that its rpoB gene has 99% identity to rpoB of K. pneumoniae subsp. pneumoniae strain MGH 78578 [GenBank:ABR79724.1].

DNA sequencing, assembly and sequence analysis

Genome sequencing of Kp13 was performed at the Unidade Genômica Computacional - UGC/LNCC Facility (http://www.labinfo.lncc.br/index.php/ugc webcite) located in Petrópolis, Rio de Janeiro, Brazil, using the Genome FLX sequencer (454 Life Science/Roche). Both shotgun and 3 kb paired-end libraries were constructed, and sequencing was carried out using FLX-Titanium chemistry. A paired-end (PE) library analysis was applied to determine the orientation and relative position of contigs produced by de novo shotgun sequencing. The data consisted of a total of 1,336,815 whole-genome shotgun reads and 558,997 paired-end reads.

Assembly of the sequence data into contigs and scaffolds was performed using the GS De Novo Assembler software provided by 454 Life Sciences/Roche (v 2.5). The high-quality reads were assembled into 151 contigs and 15 scaffolds, comprising 5.9 Mb of sequence. For the cpsKp13 region from galF to wzy, 99.9% of the bases had Phred-like quality ≥ 60. The SABIA annotation pipeline [40] was used to predict protein-coding genes and non-coding RNA genes. With the aim of detecting complete cpsKp13 genes, functional annotation of the ORFs was performed by searching the NCBI non-redundant protein database using BLASTX, followed by manual curation.

Protein subcellular localizations and signal peptides were predicted using PSORTb 3.0 [41] with default parameters for Gram-negative bacteria. A score of 7.5 was considered to be the cutoff for identification of protein localization. Transmembrane regions were analyzed using TMHMM [42]. Protein secondary structures were predicted using the PSIPRED web server [43], available at http://bioinf.cs.ucl.ac.uk/psipred webcite. Prediction of promoters was performed using the in-house SABIA platform as well as the BPROM program (http://linux1.softberry.com webcite), which searches for promoters under the control of the sigma factor 70. Ribosome binding sites search was performed using the RBS finder software that is included in the SABIA platform. EasyFig [44] was used to generate the structural comparison of cpsKp13 and other sequenced cps loci.

In silico serotyping

An in silico serotyping approach was applied using the Molecular Serotyping Tool (MST) [45]. MST is a program for computer-assisted molecular identification of restriction fragment length polymorphisms (RFLP) patterns, in which the concepts of similarity and alignment between RFLP patterns were adapted from Needleman and Wunsch's dynamic programming algorithm. By analogy, RFLP patterns represented by ordered fragment sizes can be aligned, and their similarity can be calculated as the sum of penalties for edit operations (insertions, deletions or substitutions) that transform one pattern into another [45]. MST, available at http://www.cebio.org/mst webcite, was originally designed for the identification of RFLP patterns from Escherichia coli and the Shigella O-antigen gene clusters [46,47]. At present, identification of K. pneumoniae serotypes can also be achieved because the RFLP patterns of the amplified capsular antigen gene clusters of all known Klebsiella serotypes were published by Brisse et al. [29].The RFLP of Kp13 was determined and compared to those already described. All scores were used to build a distance matrix in a PHYLIP compatible format [48]. The distance matrix was used to reconstruct a phylogeny by the UPGMA method with the NEIGHBOR program, available in the PHYLIP package. The tree generated by UPGMA was visualized with the graphical viewer FIGTREE (http://tree.bio.ed.ac.uk/software/figtree/ webcite). To improve the analysis of the UPGMA tree, the two-time-scales were applied. The MST distance cutoff that is able to distinguish between two serotypes is 1.5, and the scale-adjusted measure should be interpreted as 0.75.

In vitro K-serotyping

Isolate Kp13 was sent to the International Escherichia and Klebsiella Reference Center (WHO), Statens Serum Institut, Copenhagen, Denmark, for serotyping. Briefly, K-typing was done by counter-current immunoelectrophoresis (CCIE) against antiserum pools as previously described [49]. Then, Kp13 was tested against with the specific K-antisera of the reacting pool. The presence of a visible capsule by wet-mount microscopy with Indian Ink, quellung reaction, was also carried out with specific antisera since a cross-reaction had occurred.

Nucleotide sequence accession numbers

The cpsKp13 sequence and annotations are available from Genbank (http://www.ncbi.nlm.nih.gov/Genbank webcite) under accession number [GenBank:JN377737]. The GenBank accession numbers for other sequences discussed in the manuscript are [GenBank:JN377738] (galE), [GenBank:JN377739] (galU), [GenBank:JN377740] (rfaH), [GenBank:JN377741] (rcsB) and [GenBank:JN377742] (rcsA).

Competing interests

The authors declare that there are no competing interests.

Authors’ contributions

ECV and MP provided the Kp13 isolate and performed bacterial identification. ALG, MFN and ATRV conceived the pyrosequencing strategy. Annotation and bioinformatics analyses were performed by LGPA, LFGZ, PIPR, RCP, ACG and MFN. The manuscript was prepared by PIPR, RCP, ACG and MFN. All authors read and approved the final manuscript.

Acknowledgements

The authors thank Dr. Roney S. Coimbra, Dr. Fabiano S. Pais and Dr. Angela Volpini for performing the in silico serotyping. We thank Eva Møller Nielsen from the Serum Institut for their technical assistance with K-serotyping. We thank Alex Sandro Mundstein and Oberdan de Lima Cunha for carrying out the automatic genome annotation at the SABIA platform. PIPR had a Masters scholarship from Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES), Brazil. ACG would like to thank the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq), Brazil (Process number: 307816/2009-5). MFN thanks the CNPq, Brazil (Process number: 309370/2009-4) and the Fundação Carlos Chagas Filho de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ), Brazil (Process number: E-26/102.214/2009). Finally, we thank the anonymous reviewers whose comments and suggestions greatly improved our manuscript.

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