Genomic analysis of Staphylococcus capitis isolated from blood cultures in neonates at a neonatal intensive care unit in Sweden
Emergence of a genetically distinct, multidrug-resistant Staphylococcus capitis clone (NRCS-A) present in neonatal intensive care units has recently been extensively reported. The aims of the present study were to investigate which clones of S. capitis isolated from blood in a Swedish neonatal intensive care unit (NICU) have been present since 1987 and to investigate whether the NRCS-A clone has disseminated in Sweden. All S. capitis isolates from blood cultures of neonates (≤ 28 days of age) between 1987 and 2017 (n = 46) were whole-genome sequenced, and core genome multilocus sequence typing (cgMLST) was performed. Single-nucleotide polymorphism (SNP)-based phylogenetic relationships between the S. capitis isolates and in silico predictions of presence of genetic traits specific to the NRCS-A clone were identified. Furthermore, antibiotic susceptibility testing, including screening for heterogeneous glycopeptide-intermediate resistance, was performed. Thirty-five isolates clustered closely to the isolates previously determined as belonging to the NRCS-A clone and had fewer than 81 core genome loci differences out of 1063. Twenty-one of these isolates were multidrug resistant. The NRCS-A clone was found in 2001. Six pairs of isolates had differences of fewer than two SNPs. Genetic traits associated with the NRCS-A clone such as nsr, ebh, tarJ, and CRISPR were found in all 35 isolates. The increasing incidence of S. capitis blood cultures of neonates is predominantly represented by the NRSC-A clone at our NICU in Sweden. Furthermore, there were indications of transmission between cases; adherence to basic hygiene procedures and surveillance measures are thus warranted.
KeywordsCoagulase negative staphylococci S. capitis NRCS-A clone Neonatal intensive care unit Whole-genome sequencing
Staphylococcus capitis has been considered a commensal, since it is rarely reported as a pathogen in healthy adults, unless in the presence of cofactors such as foreign bodies or immunosuppression  which could be represented by prosthetic valve endocarditis  or prosthetic joint infections  and bacteraemia in patients with hematological malignancies , respectively.
However, S. capitis has been shown to cause approximately 20% of all cases of neonatal sepsis at neonatal intensive care units (NICUs) [5, 6]. Recently, the emergence of a genetically distinct, multidrug-resistant (MDR), including methicillin-resistant, S. capitis clone has been reported present in NICUs, initially from France but later also from the UK, Belgium, Australia, and New Zealand [7, 8, 9]. This specific clone, named NRCS-A, has been thoroughly investigated, and the genomic features of a prototype strain CR01 described . In addition, this S. capitis clone also displays reduced susceptibility to last-line antistaphylococcal agents such as vancomycin, both as heteroresistance and resistance [5, 7].
We have previously shown that the incidence of neonatal sepsis due to S. capitis has increased from 1987 to 2014 in Örebro County, Sweden, and multilocus sequence typing (MLST) of a limited selection of MDR isolates suggested that these were similar to the isolate CR01 . The dissemination of this clone has been reported from many different countries worldwide [5, 7, 11]. The oldest NRCS-A isolate hitherto described was from Australia in 2000 . However, according to the pulsed-field gel electrophoresis (PFGE) pattern characteristic for the NRCS-A clone, this clone had been found as early as 1994 . Since there are no studies other than ours from Sweden, and limited data from the rest of Scandinavia, the aims of the present study were to investigate which clones of S. capitis isolated from blood in a Swedish single-center NICU have dominated since 1987 and to investigate whether the MDR clone NRCS-A has disseminated in Sweden.
Materials and methods
All S. capitis isolates from blood cultures of neonates (≤ 28 days of age) collected at the Department of Laboratory Medicine, Clinical Microbiology, Örebro University Hospital, Sweden, between 1987 and 2017 (n = 46), were included. Before the implementation of the MALDI-TOF MS (Bruker Daltonik, Bremen, Germany) in January 2014, staphylococci were determined by routine methods such as coagulase test, DNase test, and in selected cases, API32Staph (bioMérieux, Marcy l’Étoile, France). All positive blood cultures from 1980 to 2014 were retrospectively determined to species level by MALDI-TOF MS using Microflex LT and Biotyper 3.1 (Bruker Daltonik) . In addition, S. capitis isolates from blood cultures from neonates from 2015 to 2017 were included. The isolates were stored in a preservation medium of trypticase soy broth with 0.3% yeast extract and 29% horse serum at − 80 °C.
Antibiotic susceptibility testing
Antibiotic susceptibility testing was performed on Mueller-Hinton II agar 3.8% w/v (BD Diagnostic Systems, Sparks, MD, USA) using the standardized disk diffusion method according to the European Committee on Antimicrobial Susceptibility Testing (www.eucast.org) for the following antibiotics: cefoxitin (30 μg), fusidic acid (10 μg), clindamycin (2 μg), erythromycin (15 μg), gentamicin (10 μg), rifampicin (5 μg), trimethoprim-sulfamethoxazole (25 μg), and norfloxacin (10 μg). Isolates resistant to ≥ 3 of the tested antibiotic groups were considered MDR. For vancomycin, minimum inhibitory concentration (MIC) was determined by Etest (bioMérieux).
Screening for heterogeneous glycopeptide-intermediate S. capitis
Detection of heterogeneous glycopeptide-intermediate S. capitis (hGISC) was performed using the VAN4 method, the macromethod Etest (MME), and the glycopeptide resistance detection (GRD) Etest as previously described [3, 5, 12, 13]. However, four droplets of 10 μL each, not 10 mL, were used for the VAN4 test.
Whole-genome sequencing and assembly
DNA extraction was performed using the QIAsymphony DSP Virus/pathogen Midi kit, version 1 (QIAGEN GmbH, Hilden, Germany) on a QIAsymphony (QIAGEN) according to the manufacturer’s description. The protocol was modified to include RNAse treatment as well as Tris-HCl pH 8.0 as elution buffer. The isolates were whole-genome sequenced using the Nextera XT library preparation kit (Illumina Inc., San Diego, CA, USA) on a MiSeq (Illumina) using either v2 2 × 250 bp or v3 2 × 300 paired-end workflow with coverage 40–120×. The reads were trimmed until the average Phred quality was 30 in a window of 20 bases and de novo assembled using Velvet version 1.1.04, using optimized k-mer size within the SeqSphere+ v 4.0.2 software (Ridom GmbH, Münster, Germany). The whole-genome sequence read files have been deposited in the European Nucleotide Archive (ENA) under study accession no. PRJEB32572.
A core genome multilocus sequence typing (cgMLST) target set, based on genome-wide gene-by-gene comparison, was performed using the cgMLST target definer function (version 4.1.6) in SeqSphere+, using default parameters. S. capitis isolate AYP1020 accession number CP007601 (4 April 2018), 2443604 bases, 2262 genes with CDS was used as a reference genome. All publicly available S. capitis genomes from NCBI (accessed 8 August 2018), shown in Supplementary Table 1 (n = 53), in addition to the genomes from the present study (n = 46) were used as query genomes.
SNP-based phylogenetic analysis
Single-nucleotide polymorphism (SNP)-based phylogenetic relationships between the entire set of S. capitis isolates from blood cultures of neonates (n = 46) were determined using the REALPHY online tool v1.12 with default parameters. In brief, phylogenetic trees were constructed using single-nucleotide polymorphisms in homologous sites between the assembled contigs of each isolate and the S. capitis NRCS-A strain CR01 as reference.
For the SNP-based phylogenetic relationships between the NRCS-A isolates, the reads were trimmed and subsequently mapped to the NRCS-A CR01 genome (ENA accession number LN866849) with CLC Genomics Workbench 11.0 (QIAGEN), using default parameters. The alignments were improved by locally realigning the mapped reads. Indels and structural variants were searched and used as guidance for a second local realignment. The positions used for the SNP tree were determined by the basic variant detection with default parameters (minimum coverage 10 and minimum frequency 35%). Phylogenetic trees were constructed in CLC Genomics Workbench using the SNP tree tool with the maximum likelihood algorithm and the nucleotide substitution model Jukes Cantor with a bootstrap analysis of 100 replicates.
In silico prediction of presence of NRCS-A-specific traits
In silico predictions of the presence of genes and other traits specific to the NRCS-A clone according to previous studies were performed [8, 14]. All in silico predictions were performed using CLC Genomics Workbench v 11.0. Presence of the nsr gene coding for nisin resistance was established using in silico PCR with primers previously described . Presence of the ebh gene encoding a cell wall-associated fibronectin-binding protein was determined by mapping the reads of each isolate to AYP1020 Genomic Sequence: NZ_CP007601.1 Range 759600–789017. Presence of tarJ encoding teichoic acid biosynthesis was determined by mapping the reads of each isolate to CR01 genomic accession HG737333.1 product accession CDI72760.1. Presence of clustered regularly interspaced short palindromic repeats (CRISPR) was determined using CRISPRCasFinder ; evidence of 5 (on a 1–5 scale) was interpreted as present.
Genome comparison with other international isolates
SNP-based phylogenetic analysis of isolates from Sweden
Thirty-five out of the 46 isolates were considered to belong to the NRCS-A cluster. Although quite similar, isolate 2010:B was considered a non-NRCS-A isolate because it did not cluster with previously reported NRCS-A isolates (CR01, CR03, CR05, CR07, and CR09) in Fig. 2 and had allelic differences from CR01 in 138 core genome loci as well as 796–848 SNP differences from the other NRCS-A isolates. However, it did harbor the nsr, tarJ, and ebh otherwise unique to NRCS-A isolates (Fig. 1), as previously reported [8, 14]. In general, nsr, ebh, tarJ, and CRISPR were only present in isolates belonging to the NRCS-A cluster (Fig. 1). However, 2016:B did not belong to the NRCS-A cluster but had the nsr gene (97.8% sequence identity to CR01), and ebh was present in five non-NRCS-A isolates (Fig. 1).
The present study showed that the increase of S. capitis among neonates with bacteraemia since 2010 in Region Örebro County, Sweden, is mainly due to the dissemination of the MDR S. capitis NRCS-A clone; however, this clone was probably introduced as early as in or before 2001. The other isolates that did not belong to the NRCS-A cluster were heterogeneous, and the largest cluster contained only three isolates. Moreover, the SNP phylogenetic analysis provided evidence of direct or indirect transmission of the NRCS-A clone between cases.
Although isolates from distant geographical areas were compared, isolates within the NRCS-A cluster differed in a maximum of 81 out of 1063 cgMLST loci. These results are in concordance with previous studies showing that NRCS-A S. capitis is highly conserved and has adapted to the NICU setting . Although the isolates belonging to the NRCS-A clone from Örebro County were highly similar, MDR and non-MDR isolates intermingled within the NRCS-A cluster. The most common MDR profile in the present study was fusidic acid, cefoxitin, and gentamicin resistance, which is in concordance with previous studies [7, 8] where the NICU isolates showed methicillin and aminoglycoside resistance, and either resistance or heteroresistance to vancomycin. None of the S. capitis in the present study were resistant to rifampicin, which was in contrast to previous studies reporting on the antimicrobial susceptibility pattern for the NRCS-A clone [5, 7].
A specific characteristic of the NRCS-A clone is harboring the nsr gene encoding resistance to nisin, a “broad-spectrum” bacteriocin active against various Gram-positive microorganisms, and the presence of this gene is suggested to affect the establishment of the microbiome of the neonate following birth . All isolates considered to belong to the NRCS-A clone carried the nsr gene, and in addition, one isolate not belonging to the clone did carry the nsr gene, which displayed a 97.8% sequence identity to the CR01 strain. That isolate was fully susceptible to all tested antibiotics.
In addition, the NRCS-A isolates in the present study harbored ebh, tarJ, and CRISPR, in concordance with previous studies [8, 14]. However, the ebh gene encoding an extracellular matrix-binding protein, and having been described as a potential virulence factor , was also present in five non-NRCS-A isolates. This is in concordance with the study by Carter et al. , which also found the ebh in one isolate from a separate cluster group. Together, these findings could potentially suggest that this gene is not an NRCS-A-specific trait.
The annual numbers of positive blood cultures from neonates yielding coagulase-negative staphylococci (CoNS) have varied considerably during the study period, ranging from 3 to 25 , and no cases of S. capitis bacteremia were observed in 2012 and 2013. Despite this, there has been an increase in the number of cases with S. capitis. The increase in incidence is predominantly represented by the NRSC-A clone that was introduced in the year 2001, indicating an emergence.
Obvious transmission between children seems to have taken place, since there were six pairs of isolates with a difference of fewer than two SNPs between the pair-wise compared isolates. A limitation is the lack of any clinical data regarding the patients from whom these were isolated, as well as any temporal or spatial association. Despite that, it is highly probable that these cases were the result of direct or indirect transmission. This implies the vital importance of adherence to basic hygiene procedures and surveillance measures when the NRSC-A clone has been established at NICUs.
The results from this study have been presented in part at the 28th European Congress of Clinical Microbiology and Infectious Diseases, Madrid, Spain, 21-24 April 2018.
Open access funding provided by Örebro University. This study was funded by the Örebro County Research Council (OLL-732111).
Compliance with ethical standards
Conflict of interest
The authors declare that they have no conflict of interest.
This study used bacterial isolates from humans. No tissue material or other biological material was stored from the patients, only subcultured bacterial isolates. All information regarding these isolates was anonymized.
Access to data
The whole-genome sequence read files are available from the European Nucleotide Archive (ENA) under study accession no. PRJEB32572.
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