Risk factors associated with prolonged intestinal colonization of ESBL-producing Enterobacteriaceae – a prospective cohort study
Authors Ljungquist O, Schönbeck M, Riesbeck K, Tham J
Received 22 March 2019
Accepted for publication 22 July 2019
Published 26 August 2019 Volume 2019:12 Pages 2637—2648
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 2
Editor who approved publication: Dr Joachim Wink
Oskar Ljungquist,1,2 Marcus Schönbeck,1,2 Kristian Riesbeck,3 Johan Tham1
1Clinical Infection Medicine, Department of Translational Medicine, Faculty of Medicine, Lund University, Malmö SE20502, Sweden; 2Department of Infectious Disease, Helsingborg’s Hospital, Helsingborg, Region Skåne, Sweden; 3Clinical Microbiology, Department of Translational Medicine, Faculty of Medicine, Lund University, Malmö SE20502, Sweden
Correspondence: Oskar Ljungquist
Clinical Infection Medicine, Department of Translational Medicine, Faculty of Medicine, Lund University, Rut Lundskogs gata 3, Malmö SE20502, Sweden
Tel +46 42 406 1000
Email [email protected]
Background: Extended spectrum β-lactamase-producing Enterobacteriaceae (EPE) are responsible for a major part of the widespread antimicrobial resistance (AMR). Increased understanding of risk factors associated with intestinal colonization of EPE is crucial to implement adequate actions against AMR. The aim of this study was to define potential risk factors for prolonged intestinal colonization with EPE. A secondary aim was to analyze if patients were adequately informed about being infected or colonized by antibiotic-resistant bacteria.
Methods: Patients with a positive clinical EPE culture from urine, blood or feces were recruited in a region in the south of Sweden. Selective EPE fecal cultures were obtained at least three months after the initial positive culture. Prolonged intestinal colonization was defined as the prevalence of any EPE in the follow-up fecal sample. Risk factors for prolonged intestinal colonization were evaluated by using a questionnaire and by retrospective review of medical records. A univariate model and a multivariate regression analysis were performed to identify possible risk factors for intestinal EPE colonization.
Results: Out of 143 patients included in the study, 57% remained positive for EPE at the second sampling. In a multivariate regression model, urological intervention, history of EPE infection and travel to Africa and/or Asia within 2 years were found to be significantly associated with prolonged intestinal colonization of EPE. Before being approached by us, 50% of patients displayed inadequate knowledge of EPE infection or colonization.
Conclusion: In this prospective cohort study, urological intervention within 6 months and a history of EPE infection are independently associated with prolonged intestinal colonization with EPE. In contrast, travel to Africa and/or Asia within 2 years is associated with a decreased risk of prolonged intestinal colonization with EPE. There is room for improvement when it comes to patient information regarding EPE to decrease of spread.
Keywords: antibiotic resistance, risk of infection, one health, gram-negative bacteria, antibiotic therapy, patient information
A growing incidence of extended spectrum β-lactamase (ESBL)-producing Enterobacteriaceae (EPE), and consequently a rapidly increasing antimicrobial resistance (AMR) is highly worrying.1,2 It is mainly driven by excessive antimicrobial use in humans and animals in addition to inadequate infection prevention and control practices.3 Humans as well as domestic and wild animals harbor EPE in the intestine, and those bacteria are more often found in the environment as prevalence increases.4 It is crucial to study the pathogenesis, virulence and spread of EPE in order to implement adequate preventive measures.
It has previously been described that E. coli belonging to the phylogenetic group B2 has a greater capacity to colonize the human gut compared to the other groups including A, B1 and D. These strains are associated with carriage of specific virulence genes, such as p-fimbriae and aerobactin.5–7 EPE belonging to phylogroup B2, including the globally disseminated ST131 clone, is highly virulent, and associated with prolonged intestinal carriage of EPE.8–12 It has been suggested that strain-specific virulence factors may impact the persistence of EPE in the intestine.9
The long-term duration of intestinal colonization of EPE is unknown and only a few studies exist that study prolonged colonization.8,10,11,13,14 Most of these studies focus on molecular characterization of EPE, and only a few examine risk factors associated with prolonged colonization. In contrast, numerous investigations on risk factors for acquisition and the short-term loss of EPE have been published.15–23 It is at present unclear whether a failure to detect EPE in fecal cultures from patients previously colonized with EPE reflects an absolute loss of EPE or merely poor sensitivity of detection methods.
International travel to endemic areas is a risk factor for EPE carriage.23 The acquisition rate varies depending on geographical regions visited, and the highest rates are associated with Africa, the Middle East and Asia.24 However, data suggest that travel-associated EPE colonization might be short-lived.25 In addition to international travel and infection with E. coli strains from phylogroup B2, it has previously been demonstrated that immobilization, antibiotic consumption 4 and 12 months prior to colonization, treatment with proton-pump inhibitors and urinary catheter use are independently associated with prolonged intestinal EPE carriage.14,26,27 Previous studies have focused on bacterial characteristics to determine risk factors for intestinal colonization of EPE.8,10 The main goal of this study was to study patient characteristics and putative risk factors for prolonged EPE carriage. Furthermore, we wanted to investigate whether patients were adequately informed about their EPE infection/colonization.
Materials and methods
Study design and data collection
We performed a prospective cohort study in Skåne County, a region in the south of Sweden. Inclusion of patients started in January 2016 and ended in April 2017. Patients 18 years of age or older with a verified culture of EPE in urine, blood, feces or any other location during the inclusion period were eligible for inclusion. Medical records were reviewed using the software Melior (Melior, Siemens Healthcare Services, Upplands Väsby, Sweden) for the following exclusion criteria; alcohol or substance abuse, severe psychiatric disorder, immunosuppressed patients (eg, immunodeficiency, ongoing cancer treatment, neutropenia/leukopenia, treatment with TNF-α-inhibitors), inpatient care, patients with chronic venous catheters, dementia or failure to sign informed consent and newly arrived refugees. These exclusion criteria were established as this study used the same cohort of patients as a prospective randomized clinical trial performed by the same group (not yet published).
Between July 2016 and March 2018, 2148 patients with cultures positive for EPE in the region of Skåne were screened for inclusion. Out of these, 820 adult patients with at least 1 documented positive ESBL-culture from blood, wound, cervix, urine or feces were contacted by mail and asked to submit one fecal sample for microbiological analysis. Prolonged EPE colonization was defined by the group as the prevalence of EPE in the fecal culture obtained with a minimum time period of 3 months from the first positive EPE-culture. Of the 820 adult patients invited to take part in the study, 677 declined to submit a fecal sample. Definition of variables, ie, possible risk factors, was designed prior to data collection. The steering document containing definition of variables is attached in the Supplementary materials.
To assess possible risk factors associated with prolonged intestinal carriage of EPE, medical and personal information was collected by sending out questionnaires to the participants, and by reviewing the patients’ medical records. Some information on potential risk factors relied solely on the answers from the questionnaires, eg, travel habits, social factors, etc. The queries on the questionnaire were tested on a small number of patients before the questionnaires were distributed. Three weeks after sending out the questionnaires, patients who had not responded to the questionnaires were contacted by phone and interviewed according to the same questionnaire. During the period of which the data were collected, three patients were diseased.
The Skåne County is situated in South Sweden with a total population of 1,324,565 (December 2016).28 All samples from primary, secondary as well as tertiary health care suppliers in Skåne County were analyzed at Clinical Microbiology (Laboratory Medicine, Lund, Sweden).
All samples were selectively cultivated for EPE at the Clinical Microbiology laboratory according to standard protocols. Briefly, the sample material was plated on URI-Select four agar plates with vancomycin (BioRad) complemented with two antimicrobial susceptibility discs containing ceftazidime (10 µg/mL, Oxoid) and meropenem (10 µg/mL, Oxoid) followed by incubation at 37°C overnight. Sample material was also plated on chromogenic agar plates ChromID ESBL (BioMerieux) and incubated as above. Colonies of presumptive EPE were subcultivated on horse blood agar (HBA) and typed to bacterial species using matrix-assisted laser desorption/ionization time of flight (MALDI-TOF).
The phenotype of EPE was characterized by susceptibility to cloxacillin (AmpC) or clavulanic acid (ESBL). All EPE were tested for susceptibility against the following antibiotics using the EUCAST methodology and breakpoints; piperacillin-tazobactam, cefotaxime, ceftazidime-avibactam, ceftazidime, ceftolozane-tazobactam, imipenem, meropenem, gentamicin, tobramycin, amikacin, trimethoprim-sulfamethoxazole, ciprofloxacin and, finally, temocillin.
Fisher’s exact test was used to perform univariate analyses. A two-sided exact significance of ≤0.05 was considered significant. These analyses were conducted using dichotomized data. All dichotomized data were analyzed and unevenly distributed variables were excluded for the multiple logistic regression after analyzing the cross-tabulation tables and the Fisher’s exact test. The variable antibiotic use was highly correlated with a history of EPE infection and was thus excluded from the multiple comparisons. The statistical importance of the risk factors was estimated using a binary multiple logistic regression model. Patients willing to submit a fecal sample and not willing to submit a fecal sample were compared with regard to baseline characteristics and risk factors. Due to observed differences regarding resistance against both ciprofloxacin and trimethoprim/sulfamethoxazole and EPE-infected compared to EPE-colonized, statistical weighting with respect to these variables was used. A model of stepwise forward multiple regression was used to determine the most significant risk factors for prolonged intestinal EPE carriage. Figure 1, Tables 1, S1, S3–S5 are based on actual data, whereas Tables 2–4 and S2 are based on weighted data.
Table 1 Baseline characteristics of the study population based on medical records and questionnaires
Table 2 Univariate statistic model of putative risk factors for prolonged intestinal EPE carriage using Fisher’s exact test
Table 3 Multiple logistic regression model of putative risk factors for prolonged intestinal EPE carriage
Table 4 Stepwise forward multiple regression model of potential risk factors for prolonged intestinal EPE carriage
Figure 1 Flow chart of study patient inclusion and questionnaire distribution.Abbreviation: EPE, extended spectrum β-lactamase producing Enterobacteriaceae.
Association between the potential risk factors and prolonged carriage was quantified with odds ratio (OR) with a 95% confidence interval (CI). A P-value of ≤0.05 was considered statistically significant. The statistical analyses were performed using IBM SPSS Statistics for Windows, Version 24.0. Armonk, NY: IBM Corp. Additionally, the statistical analyses were validated by a statistician using the same data.
This study was granted ethical approval from the Regional Ethical Review Board at Lund’s Tingsrätt with reference number 2016-304 and 2018-143. All patients included in the study provided written informed consent and this study was conducted in accordance with the Declaration of Helsinki.
Characteristics of EPE and rate of prolonged colonization
We included a total number of 143 patients in the study, and these individuals carried in total 147 strains of EPE, of which 134 (91%) were E. coli, 12 (8%) were Klebsiella spp. and 1 (1%) was Proteus spp. Out of the 147 strains of EPE, 134 (91%) were characterized as having an ESBL A phenotype (according to the Ambler classification; inhibited by clavulanic acid), 10 (7%) as AmpC (ampicillinase C; inhibited by cloxacillin) and 3 (2%) as having both. Of the 147 strains, 24 (16%) were resistant to ciprofloxacin, 24 (16%) were resistant to trimethoprim/sulfamethoxazole and 71 (48%) were resistant to both antimicrobials. In contrast, 28 (19%) EPE were susceptible to both ciprofloxacin and trimethoprim/sulfamethoxazole. The characteristics of EPE strains are displayed in detail in Table S1.
Eighty-one patients (57%) of the study cohort remained positive for EPE in the follow-up fecal sample (Figure 1). A minority of patients (n=62; 43%) were negative for EPE in feces on follow-up. Of the 81 patients who remained positive for EPE in the follow-up fecal sample, an identical EPE was found as determined by phenotype and species when compared to the original sample. However, 19 patients (23%) had at least one antibiotic that diverged compared to the antibiogram of the original culture.
Baseline characteristics of the study population
Baseline characteristics of the study population based on aggregate of medical record and questionnaires are as outlined in Table 1. Out of the 143 patients included in our study, 92 (64%) were women. The median age was 67 years (range 19–87). The median Charlson comorbidity index was 0 (range 0–7). At the time of inclusion (ie, submission of fecal sample), median duration of known EPE carriage was at least 7 months in both groups. Out of the 143 patients, 106 (74%), 10 (7%) and 27 (19%) had an original culture positive for EPE in urine, blood and rectum, respectively. Furthermore, 116 (81%) of patients had a history of an EPE infection, whereas 27 (19%) patients were merely colonized with EPE. During the last 2 years, 70 (49%) of the 143 patients had been hospitalized and 122 (85%) had received at least one prescription of antibiotics.
The two groups, ie, EPE positive and EPE negative as determined by a follow-up fecal sample, were similar regarding underlying medical conditions. There were no statistical differences in comorbidity as determined by Charlson comorbidity score. Characteristics of the patients’ comorbidity index according to this score are presented in Table S2.
Analyses of putative risk factors for prolonged EPE colonization
In the univariate model, urological intervention within 6 months (P=0.000), an original EPE-positive culture in urine (P=0.009), a history of EPE infection (P=0.007) and travel to Asia and/or Africa within two years (P=0.020) were associated with a follow-up fecal sample positive for EPE. Primary outcome for dichotomized data is presented in Table 2. In the multiple logistic regression model, history of EPE infection (P=0.002, OR 4.12, 95% CI: 1.36–12.51), urological intervention within 6 months (P=0.005, OR 4.53, 95% CI: 1.43–14.38) and one or two medications (P=0.028, OR 0.31, 95% CI: 0.05–0.77) were associated with prolonged intestinal EPE colonization.
Other putative risk factors for prolonged intestinal EPE carriage, ie, age over 70 years, female sex, urinary catheter/intermittent clean catheterization, antibiotic resistance and travel to Africa and/or Asia within two years were not associated with prolonged intestinal EPE colonization. Secondary outcomes from a multiple logistic regression model are displayed in Table 3.
In the stepwise forward multiple regression model, the risk factor one to two medications was no longer of significance. Urological intervention within 6 months (P=0.007, OR 4.32, 95% CI: 1.50–12.42), history of EPE infection (P=0.028, OR 2.82, 95% CI: 1.12–7.10) and travel to Africa and/or Asia within the last 2 years (P=0.04, OR 0.42, 95% CI: 0.18–0.96) remained significant risk factors. The results of the stepwise forward multiple regression model are displayed in Table 4.
Data obtained by the questionnaire
Thus, 140 patients received the questionnaire of which 127 (91%) submitted the form. The remaining 13 study subjects did not submit the questionnaire and could neither be reached by the investigators. The proportion of questions answered is displayed in Table S3.
Out of the 140 patients receiving the questionnaire, 122 (86%) answered the closed question if they had knowledge of EPE before being contacted by the study group. Sixty-one patients (50%) were unaware of prior EPE infection or colonization. When contacted by the research group, 61 patients (50%) had knowledge of EPE infection or colonization. Of the EPE-positive cohort, 37 of 80 (45%) and in the EPE-negative cohort 24 of 61 (39%) were aware of EPE infection or colonization.
Accounting for missing data
Out of 820 patients approached in this study, only 143 (17%) were willing to submit a fecal sample. If the patients who chose not to provide a fecal sample in the study diverged from the patients included in the study, there could be a problem with the external validity of our results. To investigate this, the medical records of the patients (n=677) not willing to submit a fecal sample for the study were reviewed with regard to age, sex and Charlson comorbidity score. Also, the risk factors significantly associated with prolonged colonization with EPE that fell out before weighing were examined – history of EPE infection, urological intervention within 6 months and resistance against both ciprofloxacin and trimethoprim/sulfamethoxazole. These data were compared to the same characteristics of the patients included in our study, and Table S4 shows the background characteristics of the groups. The median age, female sex, median Charlson comorbidity score or percentage of urological intervention within 6 months did not differ in the patients included in our study and the patients not included. Thus, our findings could be generalized to the public. Antibiotic consumption could not, however, be compared since these data relied on the submitted questionnaires. However, there was a difference in the percentage of patients with resistance against both ciprofloxacin and trimethoprim/sulfamethoxazole (P=0.01) and infected compared to colonized (P=0.001) in the two groups. To rectify this, statistical weights were computed with regard to resistance and history of EPE infection. Computed statistical weights are presented in Table S5.
In this prospective cohort study, factors independently associated with prolonged intestinal colonization with EPE were urological intervention within 6 months and a history of EPE infection. Travel to Africa and/or Asia within the last 2 years was also significantly associated with a decreased risk of becoming a long-term carrier. Furthermore, 50% of the patients in this study were not properly informed of infection/colonization of EPE.
Only a few studies exist that investigate why and in whom prolonged EPE colonization occurs.8,10,14 This study adds new information to the knowledge-void that exists in this field of research. The strength of this study is the prospective study design and robust methods of measurement. The statistical method of weighing data allowed for a somewhat sizable cohort of patients affected of EPE to be investigated. Overall, more than 90% submitted the questionnaire, either by sending it in or responding over the telephone, which is a strength in the present study. Furthermore, we show that patients affected by EPE are underinformed by health care givers, something which has not priorly been investigated in a similar setting.
Urological intervention at a maximum 6 months prior to inclusion was associated with prolonged intestinal colonization of EPE. Apart from transrectal prostate biopsy, which is a common cause of nosocomial infection both with and without EPE, it is unlikely that the urological intervention itself is associated with prolonged intestinal colonization with EPE. However, antibiotic prophylaxis is common prior to urological interventions. The recommended prophylaxis according to guidelines in Skåne is one dose of either trimethoprim/sulfamethoxazole or ciprofloxacin prior to the biopsy. It is a well-known fact that quinolones, including ciprofloxacin, are drivers of antibiotic resistance.29 Importantly, EPE isolates from urological patients are less susceptible to ciprofloxacin than isolates from non-urological patients.30 Furthermore, fecal carriage of EPE is common after transrectal prostate biopsy. The presence of EPE after biopsy is associated with fluoroquinolone consumption before biopsy.31 In addition, transrectal prostate biopsy is a common cause of antibiotic-resistant bloodstream infection, and the E. coli clone CTX-M-15 ST131 is a major contributing pathogen in this context.32,33 Hence, administration of antibiotics in relation to urological interventions could explain why we found an association with prolonged intestinal colonization with EPE.
However, a more plausible explanation for the association between urological intervention and prolonged intestinal colonization of EPE is that cystoscopy is routinely performed in patients with recurrent UTIs. In Sweden, a nonendemic country of EPE, repeated urinary cultures with EPE is an indication for urological intervention, to exclude a treatable cause for recurrent UTIs.
We suggest that this at least to a certain extent could explain the association.
When compared to mere colonization, a history of EPE infection was associated with a higher risk for prolonged intestinal colonization with EPE. This is in accordance with a previous study where colonization was associated with clearance of EPE, when compared to clinical samples.18 A study from Sweden revealed that 43% of the patients still being colonized 12 months after EPE infection.9 This colonization rate is higher compared to what Östholm-Balkhed et al and Arcilla and collaborators presented, 11.0% and 11.3%, respectively, found 12 months after EPE-colonization diagnosed after foreign travel.25,34 In addition, Ruppé et al observed an even less frequent prevalence (4.7%) of EPE three months after being colonized/infected abroad.15
Subsequent EPE infection in patients previously colonized with EPE is rare.33 On the other hand, recurrent infection with EPE is common, especially within the first 6 months of the first infection and in patients ≥65 years of age.35 Hence, it is reasonable to assume that more virulent strains to a higher extent possess virulence factors giving them a survival advantage, and the ability to colonize the intestine. Strains merely colonizing the intestine lack important virulence genes needed to trigger infection. This is in accordance with Ny et al who found strains of low pathogenicity in fecal samples in randomly selected Swedish citizens compared to strains causing invasive infection.36
The ST131 clone has managed to disseminate globally due to its ability to frequently colonize the intestine, its enhanced virulence and broader antibiotic resistance compared to other EPE clones.37 Strains originating from this clone are more prone to possess antibiotic resistance against ciprofloxacin and trimethoprim/sulfamethoxazole.38 We did not find any association between EPEs with resistance against ciprofloxacin and trimethoprim/sulfamethoxazole, and prolonged EPE colonization.
Unfortunately, we were not able to conduct any molecular analysis such as whole genome sequencing (WGS) of the EPE isolates. WGS could have given us useful information on EPE characteristics. Furthermore, without WGS, multiple-locus variable number tandem repeat or pulse-field gel electrophoresis, the strain obtained in the fecal culture could not be determined to be exactly the same as the strain in the original culture. In fact, 23% of patients had disconcordant antibiograms when the original culture was compared to the follow-up fecal culture regarding at least one antibiotic. We believe that the main reason for this is that patients can carry many different EPEs, which can be impossible to distinguish when selecting colonies on a blood agar. A previous study, with a longer follow-up time, using MLVA showed that the majority of long-term EPE carriers had either a different ESBL-producing species or a ESBL-producing E. coli with a different MLVA-profile in original culture compared to the follow-up sample.10
Furthermore, the methodology in the Clinical Microbiology laboratory may differ and the probability that the same strain can yield different susceptibility patterns increases as many antibiotics are tested. In addition, there is a slight risk that patients become colonized with new EPE strains, in which the term prolonged intestinal EPE colonization is misused in this context. This risk was estimated low by the study group in this low endemic EPE setting.
We found an association between EPE that were isolated from urine in original cultures, as opposed to any other anatomical location, and prolonged intestinal colonization with EPE in the univariate analysis. This was, however, not confirmed in the multivariate logistic regression model. We believe that these two risk factors, ie, history of EPE infection and EPE present in urine, are closely connected. An EPE-positive urine culture reflects infection or asymptomatic bacteriuria, whereas an EPE-positive rectal culture is a marker of colonization. As previously mentioned, antibiotic consumption is closely connected to a history of EPE infection and the rate of consumption was high in both groups. We did not find any association between previous antibiotic consumption and prolonged intestinal colonization with EPE. This is in accordance with several studies in non-travelers.9,10,14 However, Rogers et al found an association between antibiotic consumption abroad and prolonged colonization of EPE post travel.21
Traveling to high endemic areas of EPE such as Africa, Asia and Middle East is a known risk factor for EPE acquisition. In our study, we found that previous travel to EPE-high endemic areas was associated with a decreased risk of prolonged intestinal carriage of EPE. This is in accordance with ÖstholmBalkhed, who found no risk factors associated with prolonged intestinal colonization with EPE, but found that diarrhea during travel and a new trip during follow-up was associated with a decreased risk of becoming a long-term carrier.25 EPE acquisition during travel may thus be unrelated to specific microbiota profile but could affect the duration of colonization.39
We did not find correlation between a positive EPE fecal sample and abdominal pain or diarrhea, the latter a known risk factor for EPE acquisition.24 Papst et al showed that immobilization is a risk factor for prolonged EPE colonization, a risk factor this study did not address.14 In contrast, Alsterlund et al did not find risk factors associated with prolonged carriage of EPE, but did not perform molecular characterization of the isolates nor multivariable analysis of the data.40
With this study, we also wanted to investigate to what extent patients are informed about their EPE infection or colonization. Surprisingly, 50% of the patients were not adequately informed of their EPE status by their health care supplier. The Public Health Agency of Sweden states that it is mandatory for the responsible physician to provide information regarding infection or colonization with EPE.41 This information is mandatory to prevent EPE from spreading, both in the community and in health care settings, as patients are obliged to disclose their EPE status when seeking health care. Adequate actions are needed by authorities since information is an underestimated but important tool fighting antibiotic resistance.
A limitation with this study is that we used only one follow-up rectal culture, and it is a well-known fact that transient negative samples occur upon EPE-colonization.8,14 It is important to note that we do not consider that a negative follow-up sample as equal to a permanent loss of EPE colonization. It could be argued, however, that a negative EPE fecal sample reflects quantitatively less EPE shedding. This could lead to reduced risk of spreading EPE in the community and hospital setting. If this is associated with a less risk of EPE infection is not answered in this study.
In general, when using questionnaires to collect information, response bias is a matter of concern. This was taken into consideration when composing the questionnaire. Still, some patients could have agreed to be included in the study and answer the questionnaire because they knew their EPE status. This could be addressed by sending specific questionnaires to a sample of the patients who were invited to the study but declined to provide samples for the study.
We discovered that some questions in the questionnaire tended to be misapprehended. Furthermore, some participants did not fulfill the whole questionnaire and sample collecting was not done immediately, which is why lacking memory could affect the answers. This could be countered by interviewing the patients at the time of inclusion.
A major limitation of this study was the low percentage of inclusion in the study, only 17% (143 of 820 patients) of the patients were willing to submit a fecal sample. A reason for this could be lack of information and implications of EPE colonization. Another reason could be a perceived discomfort of submitting a fecal culture to the study group. However, as weighting was performed, our results gained validity.
Results from this study contribute to knowledge about the long-term carriage of EPE. We did not find that patient characteristics such as severe underlying diseases, age, etc., are risk factors associated with prolonged colonization of EPE. Bacterial features such as the ability to trigger an infection over colonization seem to be of greater importance. More information about colonization with EPE is crucial to implement adequate control measures, thus reducing spread of disease. It is particularly important to work preventive in a time of increasing antibiotic resistance. This is the most important reason to continue with well-designed research within this field.
In this prospective cohort study, we have presented that urological intervention within 6 months and a history of EPE infection are independently associated with prolonged intestinal colonization with EPE. Travel to Africa and/or Asia within 2 years is associated with a decreased risk of prolonged intestinal colonization with EPE. We could not find any association between other risk factors including prior antibiotic consumption, comorbidity, international travel, in hospital care, etc., with prolonged intestinal colonization with EPE. These findings ultimately contribute to knowledge about EPE pathogenesis and stimulate further research within this field. Despite the fact that the Public Health Agency of Sweden states that information regarding EPE is mandatory, 50% of the patients in this study were not properly informed about their EPE status.
Special thanks to Associate Professor Fredrik Resman, Professor Svante Twetman, Dr Jonas Tverring, MSc Axel Ström, MSc Fredrik Nilsson, Mrs Lena Hyllebusk and Mrs Anita Eriksson. This work was supported by grants from the Thelma Zoéga and the Stig and Ragna Gorthon foundation.
The authors have no conflict of interest to disclose in this work.
1. World Health Organization. Antimicrobial resistance: global report on surveillance [Internet]. 2014 Available from: https://www.who.int/drugresistance/documents/surveillancereport/en/.
2. European Centre for Disease Prevention and Control. Antimicrobial resistance surveillance in Europe [Internet]. 2016. Available from: https://ecdc.europa.eu/en/publications-data/antimicrobial-resistance-surveillance-europe-2016.
3. Holmes AH, Moore LS, Sundsfjord A, et al. Understanding the mechanisms and drivers of antimicrobial resistance. Lancet. 2016;387(10014):176–187. doi:10.1016/S0140-6736(15)00473-0
4. Jorgensen SB, Soraas AV, Arnesen LS, Leegaard TM, Sundsfjord A, Jenum PA. A comparison of extended spectrum beta-lactamase producing Escherichia coli from clinical, recreational water and wastewater samples associated in time and location. PLoS One. 2017;12(10):e0186576. doi:10.1371/journal.pone.0186576
5. Nowrouzian FL, Adlerberth I, Wold AE. Enhanced persistence in the colonic microbiota of Escherichia coli strains belonging to phylogenetic group B2: role of virulence factors and adherence to colonic cells. Microbes Infect. 2006;8(3):834–840. doi:10.1016/j.micinf.2005.10.011
6. Nowrouzian FL, Wold AE, Adlerberth I. Escherichia coli strains belonging to phylogenetic group B2 have superior capacity to persist in the intestinal microflora of infants. J Infect Dis. 2005;191(7):1078–1083. doi:10.1086/427996
7. Johnson JR, Delavari P, Kuskowski M, Stell AL. Phylogenetic distribution of extraintestinal virulence-associated traits in Escherichia coli. J Infect Dis. 2001;183(1):78–88. doi:10.1086/317656
8. van Duijkeren E, Wielders CCH, Dierikx CM, et al. Long-term carriage of extended-spectrum beta-lactamase-producing Escherichia coli and klebsiella pneumoniae in the general population in The Netherlands. Clin Infect Dis. 2018;66(9):1368–1376. doi:10.1093/cid/cix1015
9. Titelman E, Hasan CM, Iversen A, et al. Faecal carriage of extended-spectrum beta-lactamase-producing Enterobacteriaceae is common 12 months after infection and is related to strain factors. Clin Microbiol Infect. 2014;20(8):O508–O515. doi:10.1111/1469-0691.12742
10. Jorgensen SB, Soraas A, Sundsfjord A, Liestol K, Leegaard TM, Jenum PA. Fecal carriage of extended spectrum beta-lactamase producing Escherichia coli and Klebsiella pneumoniae after urinary tract infection – a three year prospective cohort study. PLoS One. 2017;12(3):e0173510. doi:10.1371/journal.pone.0173510
11. Overdevest I, Haverkate M, Veenemans J, et al. Prolonged colonisation with Escherichia coli O25: ST131 versus other extended-spectrum beta-lactamase-producing E. coli in a long-term care facility with high endemic level of rectal colonisation, the Netherlands, 2013 to 2014. Euro Surveill. 2016;21(42). doi:10.2807/1560-7917.ES.2016.21.42.30376
12. Rodriguez-Revuelta MJ, Lopez-Cerero L, Serrano L, Luna-Lagares S, Pascual A, Rodriguez-Bano J. Duration of colonization by extended-spectrum beta-lactamase-producing Enterobacteriaceae in healthy newborns and associated risk factors: a prospective cohort study. Open Forum Infect Dis. 2018;5(12):ofy312. doi:10.1093/ofid/ofy312
13. Lohr IH, Rettedal S, Natas OB, Naseer U, Oymar K, Sundsfjord A. Long-term faecal carriage in infants and intra-household transmission of CTX-M-15-producing Klebsiella pneumoniae following a nosocomial outbreak. J Antimicrob Chemother. 2013;68(5):1043–1048. doi:10.1093/jac/dks502
14. Papst L, Beovic B, Seme K, Pirs M. Two-year prospective evaluation of colonization with extended-spectrum beta-lactamase-producing Enterobacteriaceae: time course and risk factors. Infect Dis (Lond). 2015;47(9):618–624. doi:10.3109/23744235.2015.1033003
15. Ruppe E, Armand-Lefevre L, Estellat C, et al. High rate of acquisition but short duration of carriage of multidrug-resistant enterobacteriaceae after travel to the tropics. Clin Infect Dis. 2015;61(4):593–600. doi:10.1093/cid/civ333
16. Jallad MA, Naoufal R, Irani J, Azar E. Extended spectrum beta-lactamase carriage state among elderly nursing home residents in Beirut. ScientificWorldJournal. 2015;2015:987580.
17. Lubbert C, Straube L, Stein C, et al. Colonization with extended-spectrum beta-lactamase-producing and carbapenemase-producing Enterobacteriaceae in international travelers returning to Germany. Int J Med Microbiol. 2015;305(1):148–156. doi:10.1016/j.ijmm.2014.12.001
18. Birgand G, Armand-Lefevre L, Lolom I, Ruppe E, Andremont A, Lucet JC. Duration of colonization by extended-spectrum beta-lactamase-producing Enterobacteriaceae after hospital discharge. Am J Infect Control. 2013;41(5):443–447. doi:10.1016/j.ajic.2012.05.015
19. Paltansing S, Vlot JA, Kraakman ME, et al. Extended-spectrum beta-lactamase-producing enterobacteriaceae among travelers from the Netherlands. Emerg Infect Dis. 2013;19(8):1206–1213. doi:10.3201/eid.1908.130257
20. Li B, Zhong Y, Fu XC, et al. Duration of stool colonization in healthy medical students with extended-spectrum-beta-lactamase-producing Escherichia coli. Antimicrob Agents Chemother. 2012;56(8):4558–4559. doi:10.1128/AAC.00171-12
21. Rogers BA, Kennedy KJ, Sidjabat HE, Jones M, Collignon P, Paterson DL. Prolonged carriage of resistant E. coli by returned travellers: clonality, risk factors and bacterial characteristics. Eur J Clin Microbiol Infect Dis. 2012;31(9):2413–2420. doi:10.1007/s10096-012-1584-z
22. Zahar JR, Lanternier F, Mechai F, et al. Duration of colonisation by Enterobacteriaceae producing extended-spectrum beta-lactamase and risk factors for persistent faecal carriage. J Hosp Infect. 2010;75(1):76–78. doi:10.1016/j.jhin.2009.11.010
23. Tangden T, Cars O, Melhus A, Lowdin E. Foreign travel is a major risk factor for colonization with Escherichia coli producing CTX-M-type extended-spectrum beta-lactamases: a prospective study with Swedish volunteers. Antimicrob Agents Chemother. 2010;54(9):3564–3568. doi:10.1128/AAC.00220-10
24. Ruppe E, Andremont A, Armand-Lefevre L. Digestive tract colonization by multidrug-resistant Enterobacteriaceae in travellers: an update. Travel Med Infect Dis. 2018;21:28–35. doi:10.1016/j.tmaid.2017.11.007
25. OstholmBalkhed A, Tarnberg M, Nilsson M, et al. Duration of travel-associated faecal colonisation with ESBL-producing Enterobacteriaceae – a one year follow-up study. PLoS One. 2018;13(10):e0205504. doi:10.1371/journal.pone.0205504
26. Morales Barroso I, Lopez-Cerero L, Navarro MD, Gutierrez-Gutierrez B, Pascual A, Rodriguez-Bano J. Intestinal colonization due to Escherichia coli ST131: risk factors and prevalence. Antimicrob Resist Infect Control. 2018;7:135. doi:10.1186/s13756-018-0427-9
27. Karanika S, Karantanos T, Arvanitis M, Grigoras C, Mylonakis E. Fecal colonization with extended-spectrum beta-lactamase-producing Enterobacteriaceae and risk factors among healthy individuals: a systematic review and metaanalysis. Clin Infect Dis. 2016;63(3):310–318. doi:10.1093/cid/ciw283
28. Statistics Sweden. Population in the country, counties and municipalities on 31/ 12/16 and Population change in 2016 2016. Available from: https://www.scb.se/hitta-statistik/statistik-efter-amne/befolkning/befolkningens-sammansattning/befolkningsstatistik/pong/tabell-och-diagram/helarsstatistik–kommun-lan-och-riket/folkmangd-i-riket-lan-och-kommuner-31-december-och-befolkningsforandringar/.
29. Rodriguez-Bano J, Navarro MD, Romero L, et al. Epidemiology and clinical features of infections caused by extended-spectrum beta-lactamase-producing Escherichia coli in nonhospitalized patients. J Clin Microbiol. 2004;42(3):1089–1094. doi:10.1128/jcm.42.3.1089-1094.2004
30. Bonkat G, Muller G, Braissant O, et al. Increasing prevalence of ciprofloxacin resistance in extended-spectrum-beta-lactamase-producing Escherichia coli urinary isolates. World J Urol. 2013;31(6):1427–1432. doi:10.1007/s00345-013-1031-5
31. Tukenmez Tigen E, Tandogdu Z, Ergonul O, et al. Outcomes of fecal carriage of extended-spectrum beta-lactamase after transrectal ultrasound-guided biopsy of the prostate. Urology. 2014;84(5):1008–1015. doi:10.1016/j.urology.2014.04.060
32. Williamson DA, Roberts SA, Paterson DL, et al. Escherichia coli bloodstream infection after transrectal ultrasound-guided prostate biopsy: implications of fluoroquinolone-resistant sequence type 131 as a major causative pathogen. Clin Infect Dis. 2012;54(10):1406–1412. doi:10.1093/cid/cis194
33. Isendahl J, Giske CG, Hammar U, et al. Temporal dynamics and risk factors for bloodstream infection with extended-spectrum beta-lactamase-producing bacteria in previously colonized individuals: national population-based cohort study.
34. Arcilla MS, van Hattem JM, Haverkate MR, et al. Import and spread of extended-spectrum beta-lactamase-producing Enterobacteriaceae by international travellers (COMBAT study): a prospective, multicentre cohort study. Lancet Infect Dis. 2017;17(1):78–85. doi:10.1016/S1473-3099(16)30319-X
35. Lindblom A, Karami N, Magnusson T, Ahren C. Subsequent infection with extended-spectrum beta-lactamase-producing Enterobacteriaceae in patients with prior infection or fecal colonization. Eur J Clin Microbiol Infect Dis. 2018;37(8):1491–1497. doi:10.1007/s10096-018-3275-x
36. Ny S, Lofmark S, Borjesson S, et al. Community carriage of ESBL-producing Escherichia coli is associated with strains of low pathogenicity: a Swedish nationwide study. J Antimicrob Chemother. 2017;72(2):582–588. doi:10.1093/jac/dkw419
37. Banerjee R, Johnson JR. A new clone sweeps clean: the enigmatic emergence of Escherichia coli sequence type 131. Antimicrob Agents Chemother. 2014;58(9):4997–5004. doi:10.1128/AAC.02824-14
38. Johnson JR, Johnston B, Clabots C, Kuskowski MA, Castanheira M. Escherichia coli sequence type ST131 as the major cause of serious multidrug-resistant E. coli infections in the United States. Clin Infect Dis. 2010;51(3):286–294. doi:10.1086/653932
39. Leo S, Lazarevic V, Gaia N, et al. The intestinal microbiota predisposes to traveler’s diarrhea and to the carriage of multidrug-resistant Enterobacteriaceae after traveling to tropical regions. Gut Microbes. 2019;1–11. doi:10.1080/19490976.2018.1564431
40. Alsterlund R, Axelsson C, Olsson-Liljequist B. Long-term carriage of extended-spectrum beta-lactamase-producing Escherichia coli. Scand J Infect Dis. 2012;44(1):51–54. doi:10.3109/00365548.2011.592987
41. Sweden TPHAo. ESBL-producerande Tarmbakterier Kunskapsunderlag Med Förslag till Handläggning För Att Begränsa Spridningen Av Enterobacteriaceae Med ESBL; 2014. Available from: https://www.folkhalsomyndigheten.se/contentassets/f4df42e7e643414ba3499a9ee1801915/esbl-producerande-tarmbakterier.pdf
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