Background
Enterobacter cloacae are commensal bacteria of the human gut that can inactivate third-generation cephalosporins through overproduction of chromosomally encoded AmpC beta-lactamases, especially during treatment with these antibiotics. Therefore, recommended treatment of infections with these bacteria includes trimethoprim/sulfamethoxazole, fluoroquinolones or carbapenem antibiotics.
The
E. cloacae complex comprises five species:
E. cloacae,
Enterobacter asburiae,
Enterobacter hormaechei,
Enterobacter kobei, and
Enterobacter ludwigii.
E. cloacae and
E. hormaechei are the most frequently isolated human isolates [
1]. Classification beyond genus level is difficult, and therefore often not performed. Aminoglycoside resistance in
Enterobacter species is usually attributable to aminoglycoside-modifying enzymes that are often plasmid-encoded but can also be associated with transposable elements [
1]. Colistin resistance is mostly caused by chromosomal mutations, most likely inducing changes in the negatively charged surface lipopolysaccharides [
2]. Recently, plasmid-mediated resistance encoded by different
mcr genes has been described [
3].
Antibiotics may create a selective pressure leading to detectable carriage with Enterobacter species, especially in hospitalized patients (endogenous selection). Although such new detections are often considered acquisition, they do not represent true acquisition events. An increased incidence of healthcare-associated infections or carriage with E. cloacae can, therefore, result from endogenous selection, but also from clonal transmission, either or not facilitated by selective antibiotic pressure. Bacterial typing is required to disentangle the relative importance of both acquisition routes.
Selective decontamination of the digestive tract (SDD) is an infection prevention measure consisting of mouthpaste and intragastric suspension containing tobramycin, colistin and amphotericin B, and intravenous cefotaxime during the first days of ICU admission. Selective oropharyngeal decontamination (SOD) only includes the mouthpaste, with the same topical antibiotics. Based on studies in which SDD and SOD were associated with lower ICU mortality, SOD or SDD became standard-of-care in Dutch ICUs [
4]. The effect of SDD and SOD on the emergence of colistin resistance among Gram negative bacteria is unknown. In longitudinal studies in Dutch ICUs using SDD this risk was low [
5], but outbreaks with colistin-resistant bacteria during SDD have been reported as well [
6].
A high incidence of carriage and infection with colistin-resistant E. cloacae complex isolates in patients admitted in the intensive care unit (ICU) in a Dutch hospital was noted in June 2014. It was hypothesized that the use of SDD in this ICU since 1990 had contributed to this high incidence, either due to repeated events of endogenous selection or due to incidental introduction of colistin-non-susceptible strains followed by clonal transmission. A detailed retrospective and prospective investigation was performed to investigate the epidemiology of antibiotic-resistant E. cloacae complex isolates.
Methods
Setting
The hospital is a 540-bed secondary care hospital with two ICUs (16 and 6 beds) on physically separated locations. There is intensive exchange of employees and patients between both ICUs. SDD consisting of mouthpaste (500 mg 4 times daily) and intragastric suspension (8 ml 4 times daily) (tobramycin, colistin, and amphotericin B) and intravenous cefotaxime 1000 mg 4 times daily for the first 3 days of ICU admission, was used routinely for patients with an expected length of invasive ventilation of > 24 h and patients receiving enteral tube feeding for an expected length of ICU stay of > 48 h, since 1990. As part of the SDD strategy, screening was performed on admission and twice weekly using throat and rectum swabs. This standard of care was interrupted only between 2004 and 2006 as part of a multicentre trial evaluating the effects of SDD, in which SOD was used for 6 months and neither SDD nor SOD were used for another 6 months [
4].
Data collection
Demographic data, patient location data and data on antibiotic use were extracted from the electronic hospital information system. Data was collected from 1 May 2005 to 1 November 2014. Data on antibiotic prescriptions are available from 1 November 2005, and data on patient location from 1 January 2007. Microbiological data was extracted from the electronic laboratory system, and data were available from 1 May 2005 onwards. Colistin susceptibility was documented since November 2009 and presence of ESBL since January 2011.
Microbiological methods
Species identification and susceptibility testing of clinical isolates was performed using Vitek 2 (bioMérieux, Marcy-l’Étoile, France). Isolates with elevated MIC for meropenem and/or imipenem were sent to a reference laboratory to test for presence of carbapenemases. Pulsed-field gel electrophoresis (PFGE) had been performed on 96 Enterobacter isolates from 62 patients and 8 environmental samples as screening (data not shown).
For isolates selected for whole-genome sequencing (WGS, as described below) species identification was performed by MALDI-TOF (Microflex, Bruker, Germany), antibiotic susceptibility testing was performed by Vitek 2, colistin resistance was additionally determined by Etest (bioMérieux, Marcy-l’Étoile, France), and presence of ESBL by cefepime-clavulanate ESBL Etest (bioMérieux, Marcy-l’Étoile, France), both on Mueller Hinton 2 agar.
Definitions
Multi-resistant
Enterobacter species (MREb) was defined as
Enterobacter isolates with ESBL production and/or tobramycin non-susceptible (MIC> 4 mg/L; EUCAST 2013 [
7]) and/or colistin resistant (MIC> 2 mg/L; EUCAST 2013). Furthermore,
Enterobacter isolates were classified on resistance profile as I) tobramycin non-susceptible
Enterobacter spp., II) colistin resistant
Enterobacter spp., or III) ESBL producing
Enterobacter spp.
Selection of isolates for whole genome sequencing (WGS)
First, from each patient from whom Enterobacter spp. isolates had been stored, isolates in each of the following groups were selected for WGS a) isolates for which PFGE had been performed before, b) blood culture isolates, c) cerebrospinal fluid (CSF) isolates, d) colistin-resistant isolates, e) isolates from ICU. When multiple isolates for one individual patient were available in one of the groups, the final selection per patient was based on 1) location (ICU, ward, outpatient), 2) highest MIC for colistin, tobramycin and ESBL positivity, 3) the most invasive isolate (culture site: blood, CSF, broncho-alveolar lavage, fluid/punctate, wound, urine, sputum, catheter tip, throat, rectum, nose, faeces), 4) culture date (first).
From one patient both colistin-susceptible (n = 2) and resistant E. cloacae complex isolates (n = 1) were selected for WGS. For one patient isolates collected 4 years apart were selected (colistin susceptible, tobramycin susceptible).
As control isolates, which were considered not be linked to the local hospital epidemiology, we included 23 Enterobacter isolates; 17 cultured between 2002 and 2014 in another Dutch hospital in the same region, one from Curacao, an island in the Caribbean Sea, and six unrelated isolates.
To test whether colistin resistance had been induced in susceptible isolates that were prevalent in the geographic area, 15 susceptible isolates were also included. These included seven isolates from patients admitted in the same period, six isolates from general practice patients and two isolates from a different hospital in the same city. None of these patients had documented carriage with MREb.
Whole genome sequencing
Isolates were cultured overnight at 37 °C on blood agar plates. Subsequently one colony was transferred to Lysogeny Broth and incubated overnight at 37 °C. From this culture DNA was isolated using the Ultra Clean Microbial DNA isolation kit (Mo Bio Laboratories, Inc., Carlsbad, CA). Library preparation used the Illumina Nextera XT DNA Sample Preparation kit and sequencing was performed on an Illumina NextSeq with the mid-output 2 × 150 bp kit using paired-ends (Illumina, San Diego, CA).
Comparative genomics analysis
In total, genomic DNA of 172
Enterobacter cloacae complex isolates were sequenced. Sequence reads were first quality-filtered using seqtk with option “trimfq -q 0.01” (version 1.0-r31) [
8] and then assembled using SPAdes (version 3.7.0) [
9]. Genomes with lengths ranging between 3 Mb and 8 Mb were selected for further analysis, which resulted in a total of 150 genomes. Assembled contigs were annotated using prokka (version 1.12-beta) [
10]. Proteins among these strains were first aligned against each other using BLAST+ (version 2.2.31) [
11], where length of aligned part must be longer than the half length of both query and reference sequences. Resulting alignment file was used as an input to orthAgogue (version 1.0.3) [
12] to find orthologous proteins and orthologous proteins were clustered using mcl (version 12–135) [
13]. Genes that are present in all strains (core genes) were concatenated to create a core genome. Next, recombination regions in the core genome were identified using gubbins (version 1.4.9) [
14]. Subsequently, all gene sequences in identified recombination regions were discarded and final recombination-filtered core genomes were used to build a phylogenetic tree using FastTree2 (version 2.1.8) with the GTR model and with 100 bootstrap samples [
15].
Statistical analyses
Incidence of acquisition in ICU was calculated per year as number of patients with a positive culture according to one of the classifications, per 1000 patient days at risk. Acquisition was defined as growth of Enterobacter spp. from a microbiological culture on ICU-day 3 or thereafter, with a preceding negative culture. Admissions < 48 h were not included in this analysis as these were not considered at risk for acquisition according to this definition. Patient days at risk are the sum of all uncolonized days in ICU of all patients until ICU-discharge or until the day of the first culture with Enterobacter spp. Prevalence is calculated as the percentage of colonized patient days divided by the total number of patient days. Sensitivity and specificity of determination of colistin resistance using Vitek were calculated with Etest as reference standard. Data analysis was performed using SPSS version 22 and R version 3.1.2.
Discussion
This study demonstrates a persistently stable low-level endemicity of Enterobacter species resistant to colistin and/or tobramycin in a Dutch ICU that used SDD since 1999. The incidence of acquisition of resistant E. cloacae was 4.61 and 1.86 per 1000 admission days for ICU 1 and 2 respectively, and the mean prevalence was 7 and 3%, respectively. Although 69% of the resistant isolates were resistant to colistin, susceptibility to either one of the preferred antibiotics for infections caused by Enterobacter species, such as co-trimoxazole, ciprofloxacin or meropenem, was 99%. Carbapenemase production was demonstrated in one resistant E. cloacae isolate, which appeared to be introduced from abroad. Therefore, resistance in these Enterobacter species did not reduce antibiotic treatment options. WGS revealed two large clusters spanning a prolonged time period, strongly suggesting incidental clonal transmission, sufficient to maintain low-level endemicity, which probably is higher than in most other Dutch ICUs.
Evaluation of long-term trends in antibiotic resistance in ICU isolates in June 2014 led to the recognition of the presence of colistin-resistant Enterobacter species, and initiated the formation of an outbreak management team, including medical microbiologists, infection prevention specialists, intensivists, ICU nurses, infectiologists, and facilitary services. A variety of measures were taken including reinforcement of existing infection prevention measures, including hand hygiene precautions and isolation protocols, replacement of dated equipment, daily infection prevention audits and renovation of some spaces. On 1 September 2014 SDD was replaced by SOD.
The investigation described here started in January 2015 (after all measures had been implemented). The focus of investigation was on the ICU where screening cultures had been obtained routinely as part of SDD. As such, the likelihood of detecting such isolates outside the ICUs is lower. Yet, from 2007 onwards, up to 81 patients had not been admitted to ICU before their first positive culture with resistant E. cloacae, suggesting that transmission was not limited to the ICUs.
In this study, colistin susceptibility testing as performed by Vitek appeared adequate in distinguishing resistant from susceptible isolates using Etest as a comparator. It should be noted that gradient tests have recently been tested to generally underestimate MICs, resulting in false susceptible results [
16]
, thus misclassification in our study cannot be ruled out. Yet, there were only a limited number of isolates with an MIC in the intermediate range.
The possible effects of colistin use in SDD could not be disentangled, as SDD was administered to all eligible patients admitted to the ICU, precluding a comparison with control patients. The conversion rate from carriage of colistin-susceptible to resistant
E. cloacae (0.20 and 0.13 conversions per 1000 patient days) is lower than previously reported in ICUs using SDD [
5], even though we might have overestimated true conversion in these patients as susceptible isolates of these patients were not routinely stored. Previously, estimated conversion rates for colistin in
Enterobacter spp.,
Escherichia coli or
Klebsiella spp
. during SDD in rectal isolates were 1.0 and 0.7 per 1000 patient days in two cohorts [
5]. For respiratory isolates conversion rates in
Acinetobacter spp.,
Pseudomonas spp.,
Enterobacter spp.,
E. coli or
Klebsiella spp
. during SDD were 0.7 per 1000 patient days. In that study 1 of 17 and 3 of 9 conversions in intestinal colonization, and 4 of 12 conversions in respiratory colonization (standard care, SOD and SDD combined) were in
Enterobacter species [
5].
WGS provided essential information for interpreting the molecular epidemiology of
Enterobacter spp. in these ICUs. Plasmids do not belong to the core genome, and are not taken into account in the analysis of WGS. Plasmid-based colistin resistance genes (
mcr-1 to 4) were not detected in any of the sequenced isolates (data not shown). The relatively low correlation between clustering and presence of ESBL may have resulted from horizontal transfer of plasmids encoding ESBLs. There is limited data on the number of expected SNPs in clonal transmission. In a set of presumed outbreak isolates based on identical PFGE patterns from two patients isolates had less than 22 SNPs, while isolates from a third patient were distinct with a distance greater than 150 SNPs [
17]. It was concluded that the third patient was unlikely to have been associated with a transmission event involving one of the other two patients. We found two clusters with up to 126 SNPs.