Abstract

Background

The long-standing antimicrobial resistance (AMR) pandemic has proven difficult to resolve and is becoming more complex, especially in the context of increasing forced migration, with little evidence around patterns of AMR in migrant communities. This study aimed to determine the frequency in the carriage of common types of antimicrobial-resistant bacteria between Syrian refugees and the local communities in Türkiye: extended-spectrum β-lactamase (ESBL), methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE).

Methods

We collected nasal swabs and stool samples from the study participants, the local community members, and refugees, between September 2020 and March 2021. We screened clinical samples for the presence of ESBL, MRSA and VRE. Antimicrobial-resistant bacterial isolates were tested by phenotypic analysis to determine the AMR status.

Results

The study included a total of 3960 participants: 1453 individuals in the local community (36.2%) and 2525 Syrian refugees (63.8%). Overall, a significantly greater proportion of refugees (6.7%) carried MRSA compared to the local community (3.2%) (P < 0.001). The ESBL-positivity rate was 17.9% in Syrian refugees and 14.3% in the local community (P = 0.041). Carbapenemase activity was detected in three isolates from Syrian refugees. No VRE was detected in Syrian refugees or the local community.

Conclusions

This large, community-based study on the frequency and the distribution of AMR among Syrian refugees and the local population is the first study in Türkiye.

Introduction

Antimicrobial resistance (AMR) is a major global health problem in both hospitals and community settings. Elevated rates of AMR have been documented in low- and middle-income countries, which can be attributed to healthcare disparities, poor public health infrastructure, hygiene and sanitation measures, access to and consumption of antimicrobials and the quality of drugs. Conditions such as large-scale armed conflicts or disasters can further impact these contributing factors. Evidence shows that an increased movement of people, including both travel and migration, has contributed to the spread of AMR globally.1 However, it is hypothesized that the migration journey alone could also be one of the determinants of AMR among migrants, rather than countries of origin being solely responsible for the importation of drug-resistant organisms. Evidence suggests that, due to conflict situations, migrants may be at higher risk conditions, or they may be acquiring drug-resistant organisms in transit or host countries. Refugees may show particular vulnerability to AMR exposure during and after migration due to factors such as sanitation, hygiene and overcrowding in refugee camps, transit centers and detention facilities, with limited access to health services in host countries.2 However, only limited data exist on the prevalence of AMR carriage or infection among refugees and migrants, particularly for those who have been forcibly displaced. There is a need for robust estimates of the AMR burden in communities receiving a high number of migrants to facilitate the detection, appropriate treatment and prevention of AMR in receiving countries, which may have different AMR profiles.3 Although AMR is among the leading causes of death, the burden of AMR is mostly monitored in resource-limited regions, where data are always more difficult to obtain.4 Therefore, it is important both to improve data quality to conduct surveillence studies, and to ensure sustainable management to develop prevention strategies for AMR.5

Türkiye is a country of origin, transit and destination for migrants since it is a crossroads between Europe and Asia.3 During the initial years of the Syrian crisis, between 2011 and 2016, the Turkish government settled Syrian refugees in conventional refugee camps in the provinces bordering Syria. Currently, only 46 079 (1.26%) of the recorded ∼3.7 million Syrian immigrants in Türkiye are settled in camps. As per government policy, the remaining Syrian refugees (over 98%) are settled in residential neighborhoods throughout the country.3,6 In addition to the Syrian conflict, due to other regional conflicts, there are over 4 million recorded immigrants who have been residing in Türkiye.6 Due to Türkiye’s geopolitical position as a transit route between Europe, Asia and Africa, robust population estimates of AMR carriage in the community are important to inform health policy and public health decision-making. This is necessary to ensure sustainable management, provide equitable services, and reduce the burden of disease in both migrant and local populations. However, no population-based evidence is available on AMR patterns in Türkiye.

This study aimed to examine the frequency and distribution patterns of AMR carriage of common types of antimicrobial-resistant bacteria in the community, including extended-spectrum β-lactamase (ESBL), methicillin-resistant Staphylococcus aureus (MRSA) and vancomycin-resistant enterococci (VRE), among Syrian refugees and the local community members in Türkiye.

Methods

Study design

In this cross-sectional population-based study, we selected seven provinces (Ankara, Gaziantep, Hatay, Istanbul, Izmir, Mersin and Sanliurfa) with the largest Syrian refugee populations (n = 2 309 074; 63.0% of the total refugee population) in Türkiye as a study population. The estimated sample size for each province was calculated using WinPepi electronic epidemiological calculator, version 11.65. A 95% confidence interval (95% CI) estimated AMR carriage prevalence of 50%, a 0.05 margin of error and an additional 10% loss to follow-up were assumed. Inclusion criteria for all study participants were that participants should be residents of the province and aged 5 years or older and have: no symptoms of infection, have never been treated with chemotherapy and have never been diagnosed with cancer. Study participants were enrolled in Family Health Centers (FHCs), where only Turkish citizens received healthcare services, and in Refugee Health Centers (RHCs) where only Syrian refugees received healthcare services. The overall estimated sample size from both FHCs and RHCs was 6116. Each isolate included in the study was obtained from one participant. The workflow for the study is presented in Supplementary figure S1.

The study faced a major obstacle at the initial data collection stage, due to the spread of the SARS-CoV-2 (COVID-19) pandemic. Data collection became unfeasible in the capital city, Ankara, where the national COVID-19 pandemic management center was established. Therefore, Ankara province was removed from the study, leaving a total of six provinces. Culturally sensitive, informed consent was received from all study participants. The study information was provided in a linguistically and culturally appropriate format, in particular to Syrian refugee participants. For that purpose, we employed healthcare professionals who are themselves refugees. In case of need for translation, bilingual trained patient guides helped the study team to support interpretation and data collection.

Collection of demographic data and biological samples

After receiving training on the objectives and methodology of the study, obtaining informed consent, sample collection and shipping to the laboratory, a total of 831 healthcare workers in the centers were involved in the study. All data and samples were collected between 1 September 2020 and 31 March 2021.

Analysis of nasal swab samples

Nasal swabs were incubated on an S. aureus selective medium (mannitol salt agar; HiMedia Laboratories, India). All bacterial isolates were identified by MALDI-TOF MS (Bruker MALDI Biotyper, Germany). Confirmed S. aureus isolates were assessed for methicillin resistance using the disk diffusion method with 30 µg cefoxitin disks (HiMedia Laboratories, India). Controls were S. aureus NCTC 12493, S. aureus NCTC 13552 and S. aureus ATCC 25923 (negative control).

Analysis of stool samples

To identify VRE, stool samples were inoculated onto VRE agar (HiCrome VRE Agar, HiMedia Laboratories). To identify Gram-negative bacilli, stool samples were inoculated onto eosin methylene blue agar. All isolates were identified by MALDI-TOF MS (Bruker MALDI Biotyper, Germany). Antibiotic susceptibility was assessed using the disk diffusion method using the following antibiotics: 30 µg cefepime, 5 µg cefotaxime, 10 µg ceftazidime, 30 µg ceftriaxone, 5 µg ciprofloxacin, 10 µg ertapenem, 10 µg gentamicin, 10 µg imipenem, 10 µg meropenem and 36 µg piperacillin–tazobactam (HiMedia Laboratories, India). Suspected isolates were tested for the production of ESBLs with the combination disk test.7 Isolates resistant to cefoxitin, and cefotaxime or ceftazidime were tested for the production of AmpC β-lactamases (AmpC) using a disk test (Mast Discs Combi, UK). All disc diffusion tests were evaluated according to the European Committee on Antimicrobial Susceptibility Testing (EUCAST).7 Multi-drug resistance (MDR) is defined as combined resistance to third-generation cephalosporins [cefotaxime or ceftazidime or ceftriaxone, fluoroquinolones (ciprofloxacin) and aminoglycosides (gentamycin)]. No VRE was identified.

Statistical analysis

Data were analyzed with SPSS version 15.0 (SPSS Inc., USA) using descriptive statistics (mean and standard deviation, number and percentages).8 Nominal variables were compared using the Chi-square (χ2) test and Fisher’s exact test. 95% CIs were calculated using the Score (Wilson) method with OpenEpi version 3.01.9 Continuous variables were compared using the independent sample Student t-test.

Ethical consideration

A local ethical review of this study has been provided by Health Sciences University, Ankara City Hospital Ethical Review Committee. Additional institutional approval has been received from the MoH (E-19-007). Furthermore, the WHO Ethical Review Committee has also approved the study (ERC.0003212).

Results

Analysis of demographic data

A total of 3960 individuals participated in the study, including 1435 (36.2%) individuals from the local community in Türkiye, and 2525 (63.8%) Syrian refugees. Supplementary table S1 shows the number of participants and the number of biological samples collected from each province. The average age of participants was 35.6 ± 17.1 years for the local community and 30.0 ± 15.0 years for Syrian refugees. Among all, 36.7% of participants claimed they had not used any antibiotics in the last 6 months, and 94.2% of participants claimed that they had not been hospitalized in the last 6 months.

AMR of nasal swab samples

From the 3960 nasal swab samples, 215 (5.4%; 95 CI: 4.8–6.2%) were confirmed to be S. aureus by MALDI-TOF MS. All isolates were confirmed by molecular analysis. No ciprofloxacin-susceptible isolates were identified. Of the 215 S. aureus isolates confirmed by MALDI-TOF MS, 91.6% (n = 197; 95 CI: 87.1–94.6%) exhibited dose-dependent susceptibility to ciprofloxacin. In total, 13.9% (n = 30; 95 CI: 9.9–19.2%) of isolates were resistant to linezolid; of these, 96.6% (n = 29) were from Syrian refugees. Overall, the rate of MRSA was higher among Syrian refugees (6.7%, 95% CI: 5.8–7.7%) than in the local community (3.2%, 95% CI: 2.4–4.2%; P < 0.001) (table 1).

Table 1

MRSA positivity in isolates from the local community and Syrian refugees, by province

ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep28/3547.9 (5.5–11.2)35/4308.1 (5.9–11.1)63/7848.0 (6.3–10.2)0.906
Hatay5/3121.6 (0.7–3.7)14/3553.9 (2.4–6.5)19/6672.8 (1.8–4.4)0.070
Istanbul1/372.7 (0.5–13.8)3/1132.7 (0.9–7.5)4/1502.7 (1.0–6.7)1.000a
Izmir0/30.0 (0.0–56.1)58/8416.9 (5.4–8.8)58/8446.9 (5.4–8.8)1.000a
Mersin4/5160.8 (0.3–2.0)33/5426.1 (4.4–8.4)37/10583.5 (2.5–4.8)<0.001
Sanliurfa8/2133.8 (1.9–7.2)26/24410.7 (7.4–15.2)34/4577.4 (5.4–10.2)0.005
Total46/14353.2 (2.4–4.2)169/25256.7 (5.8–7.7)215/39605.4 (4.8–6.2)<0.001
ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep28/3547.9 (5.5–11.2)35/4308.1 (5.9–11.1)63/7848.0 (6.3–10.2)0.906
Hatay5/3121.6 (0.7–3.7)14/3553.9 (2.4–6.5)19/6672.8 (1.8–4.4)0.070
Istanbul1/372.7 (0.5–13.8)3/1132.7 (0.9–7.5)4/1502.7 (1.0–6.7)1.000a
Izmir0/30.0 (0.0–56.1)58/8416.9 (5.4–8.8)58/8446.9 (5.4–8.8)1.000a
Mersin4/5160.8 (0.3–2.0)33/5426.1 (4.4–8.4)37/10583.5 (2.5–4.8)<0.001
Sanliurfa8/2133.8 (1.9–7.2)26/24410.7 (7.4–15.2)34/4577.4 (5.4–10.2)0.005
Total46/14353.2 (2.4–4.2)169/25256.7 (5.8–7.7)215/39605.4 (4.8–6.2)<0.001

CI: confidence interval.

a

Fisher’s exact test.

Table 1

MRSA positivity in isolates from the local community and Syrian refugees, by province

ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep28/3547.9 (5.5–11.2)35/4308.1 (5.9–11.1)63/7848.0 (6.3–10.2)0.906
Hatay5/3121.6 (0.7–3.7)14/3553.9 (2.4–6.5)19/6672.8 (1.8–4.4)0.070
Istanbul1/372.7 (0.5–13.8)3/1132.7 (0.9–7.5)4/1502.7 (1.0–6.7)1.000a
Izmir0/30.0 (0.0–56.1)58/8416.9 (5.4–8.8)58/8446.9 (5.4–8.8)1.000a
Mersin4/5160.8 (0.3–2.0)33/5426.1 (4.4–8.4)37/10583.5 (2.5–4.8)<0.001
Sanliurfa8/2133.8 (1.9–7.2)26/24410.7 (7.4–15.2)34/4577.4 (5.4–10.2)0.005
Total46/14353.2 (2.4–4.2)169/25256.7 (5.8–7.7)215/39605.4 (4.8–6.2)<0.001
ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep28/3547.9 (5.5–11.2)35/4308.1 (5.9–11.1)63/7848.0 (6.3–10.2)0.906
Hatay5/3121.6 (0.7–3.7)14/3553.9 (2.4–6.5)19/6672.8 (1.8–4.4)0.070
Istanbul1/372.7 (0.5–13.8)3/1132.7 (0.9–7.5)4/1502.7 (1.0–6.7)1.000a
Izmir0/30.0 (0.0–56.1)58/8416.9 (5.4–8.8)58/8446.9 (5.4–8.8)1.000a
Mersin4/5160.8 (0.3–2.0)33/5426.1 (4.4–8.4)37/10583.5 (2.5–4.8)<0.001
Sanliurfa8/2133.8 (1.9–7.2)26/24410.7 (7.4–15.2)34/4577.4 (5.4–10.2)0.005
Total46/14353.2 (2.4–4.2)169/25256.7 (5.8–7.7)215/39605.4 (4.8–6.2)<0.001

CI: confidence interval.

a

Fisher’s exact test.

AMR of stool samples

The presence of VRE and Gram-negative bacteria was investigated in stool samples from 1869 participants. VRE was not isolated from any of the stool samples, whereas 96.7% (n = 1869; 95% CI: 95.8–97.4%) of samples contained Gram-negative bacteria. Owing to the low number of samples containing Acinetobacter spp. (n = 3), Pseudomonas spp. (n = 2) and Stenotrophomonas maltophilia (n = 1), these species were not included in the analysis. Of the Gram-negative isolates, 1729 (92.5%; 95% CI: 91.2–93.6%) were Escherichia coli, 62 (3.3%; 95% CI: 2.6–4.2%) were Klebsiella pneumoniae, 7 were Enterobacter spp., 2 were Klebsiella oxytoca and 1 was Citrobacter freundii. Table 2 shows the results of antibiotic susceptibility testing of E. coli isolates from stool samples. Escherichia coli isolates from Syrian refugees had higher rates of resistance to cephalosporins (cefotaxime and cefepime), piperacillin–tazobactam and gentamicin (see table 2 for P values). Only the rate of ciprofloxacin resistance was higher in the local community than in Syrian refugees (P = 0.049). 6.3% (n = 109; 95% CI: 5.3–7.5%) of E. coli isolates, and 69.3% (n = 43; 95% CI: 57.0–79.4) of K. pneumoniae isolates were ESBL positive, as were one K. oxytoca isolate and two Enterobacter spp. isolates. Additionally, 22.6% (n = 14; 95% CI: 14.0–34.4%) of K. pneumoniae isolates were multi-drug resistant; all of these isolates were ESBL positive. In contrast, only 2.8% (n = 48; 95% CI: 2.1–3.7%) of E. coli isolates were multi-drug resistant; all of these isolates were ESBL-positive. Overall, the study found ESBL-positivity rates of 17.9% (95% CI: 15.6–20.5%) in Syrian refugees and 14.3% (95% CI: 12.0–16.9%) in the local community (P = 0.041). No statistically significant differences in ESBL positivity were found among isolates from different provinces (table 3). Furthermore, no statistically significant relationship was identified between ESBL positivity and antibiotic use or hospitalization in the previous 6 months. Phenotypic analysis identified AmpC in 1.1% (n = 19; 95% CI: 1.1–1.7%) of E. coli isolates and 12.9% (n = 8; 95% CI: 6.7–1.7%) of K. pneumoniae isolates; of the AmpC-positive isolates, 62.9% (n = 17; 95% CI: 44.2–78.5%) were from Syrian refugees. In all, 95.9% (n = 47; 95% CI: 86.3–98.9%) of ESBL-positive E. coli isolates and 100% (n = 43; 95% CI: 91.8–100.0%) of ESBL-positive K. pneumoniae isolates (n = 17; 79.0%; 95% CI: 67.4–87.53%) were multi-drug resistant, with 75.6% (n = 68; 95% CI: 67.8–83.3%) of these from Syrian refugees (table 4).

Table 2

Antibiotic susceptibility of E. coli isolates from the local community and Syrian refugeesa

AntibioticLocal community (n=785)
Syrian refugees (n=944)
Total (n=1729)
P-valueb
Susceptible (%)
R (%)Susceptible (%)
R (%)Susceptible (%)
R (%)
SISISI
Cefepime83.44.112.582.81.815.483.12.814.10.006
Cefotaxime94.51.44.190.12.07.892.11.76.10.003
Ceftazidime66.216.717.164.115.920.065.116.318.70.291
Ceftriaxone83.51.914.582.81.016.283.11.415.50.162
Ciprofloxacin92.61.46.089.47.92.690.92.17.10.049
Ertapenem95.81.82.495.71.13.395.71.42.90.163c
Gentamicin96.83.293.46.695.05.00.001
Imipenem100.00.00.099.70.30.099.80.20.00.256c
Meropenem100.00.00.099.60.40.099.80.20.00.131c
Piperacillin–tazobactam82.217.873.726.377.622.4<0.001
AntibioticLocal community (n=785)
Syrian refugees (n=944)
Total (n=1729)
P-valueb
Susceptible (%)
R (%)Susceptible (%)
R (%)Susceptible (%)
R (%)
SISISI
Cefepime83.44.112.582.81.815.483.12.814.10.006
Cefotaxime94.51.44.190.12.07.892.11.76.10.003
Ceftazidime66.216.717.164.115.920.065.116.318.70.291
Ceftriaxone83.51.914.582.81.016.283.11.415.50.162
Ciprofloxacin92.61.46.089.47.92.690.92.17.10.049
Ertapenem95.81.82.495.71.13.395.71.42.90.163c
Gentamicin96.83.293.46.695.05.00.001
Imipenem100.00.00.099.70.30.099.80.20.00.256c
Meropenem100.00.00.099.60.40.099.80.20.00.131c
Piperacillin–tazobactam82.217.873.726.377.622.4<0.001

I: at increased exposure; R: resistant: S: at standard dose.

a

n =1729.

b

The local community vs. Syrian refugees.

c

Fisher’s exact test.

Table 2

Antibiotic susceptibility of E. coli isolates from the local community and Syrian refugeesa

AntibioticLocal community (n=785)
Syrian refugees (n=944)
Total (n=1729)
P-valueb
Susceptible (%)
R (%)Susceptible (%)
R (%)Susceptible (%)
R (%)
SISISI
Cefepime83.44.112.582.81.815.483.12.814.10.006
Cefotaxime94.51.44.190.12.07.892.11.76.10.003
Ceftazidime66.216.717.164.115.920.065.116.318.70.291
Ceftriaxone83.51.914.582.81.016.283.11.415.50.162
Ciprofloxacin92.61.46.089.47.92.690.92.17.10.049
Ertapenem95.81.82.495.71.13.395.71.42.90.163c
Gentamicin96.83.293.46.695.05.00.001
Imipenem100.00.00.099.70.30.099.80.20.00.256c
Meropenem100.00.00.099.60.40.099.80.20.00.131c
Piperacillin–tazobactam82.217.873.726.377.622.4<0.001
AntibioticLocal community (n=785)
Syrian refugees (n=944)
Total (n=1729)
P-valueb
Susceptible (%)
R (%)Susceptible (%)
R (%)Susceptible (%)
R (%)
SISISI
Cefepime83.44.112.582.81.815.483.12.814.10.006
Cefotaxime94.51.44.190.12.07.892.11.76.10.003
Ceftazidime66.216.717.164.115.920.065.116.318.70.291
Ceftriaxone83.51.914.582.81.016.283.11.415.50.162
Ciprofloxacin92.61.46.089.47.92.690.92.17.10.049
Ertapenem95.81.82.495.71.13.395.71.42.90.163c
Gentamicin96.83.293.46.695.05.00.001
Imipenem100.00.00.099.70.30.099.80.20.00.256c
Meropenem100.00.00.099.60.40.099.80.20.00.131c
Piperacillin–tazobactam82.217.873.726.377.622.4<0.001

I: at increased exposure; R: resistant: S: at standard dose.

a

n =1729.

b

The local community vs. Syrian refugees.

c

Fisher’s exact test.

Table 3

ESBL-positive E. coli positivity in isolates from the local community and Syrian refugees, by province

ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep25/19712.7 (8.7–18.1)59/30219.5 (15.5–24.4)84/49916.8 (13.8–20.4)0.046
Hatay24/19412.4 (8.5–17.8)35/23215.1 (11.1–20.3)59/42613.8 (10.9–17.5)0.419
Istanbul1/916.7 (2.0–43.5)8/4617.4 (9.1–30.7)9/5217.3 (9.4–29.7)1.000a
Izmir1/333.3 (6.2–79.2)11/6915.9 (9.1–26.3)12/7216.7 (9.8–27.0)0.426a
Mersin31/23113.4 (9.6–18.4)10/1099.2 (5.1–16.1)41/34012.1 (9.0–16.0)0.262
Sanliurfa30/15419.5 (14.0–26.5)46/16824.7 (21.2–34.6)76/34022.4 (18.3–27.1)0.977
Total112/78514.3 (12.0–16.9)169/94417.9 (15.6–20.5)281/172916.3 (14.6–18.1)0.041
ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep25/19712.7 (8.7–18.1)59/30219.5 (15.5–24.4)84/49916.8 (13.8–20.4)0.046
Hatay24/19412.4 (8.5–17.8)35/23215.1 (11.1–20.3)59/42613.8 (10.9–17.5)0.419
Istanbul1/916.7 (2.0–43.5)8/4617.4 (9.1–30.7)9/5217.3 (9.4–29.7)1.000a
Izmir1/333.3 (6.2–79.2)11/6915.9 (9.1–26.3)12/7216.7 (9.8–27.0)0.426a
Mersin31/23113.4 (9.6–18.4)10/1099.2 (5.1–16.1)41/34012.1 (9.0–16.0)0.262
Sanliurfa30/15419.5 (14.0–26.5)46/16824.7 (21.2–34.6)76/34022.4 (18.3–27.1)0.977
Total112/78514.3 (12.0–16.9)169/94417.9 (15.6–20.5)281/172916.3 (14.6–18.1)0.041

CI: confidence interval.

a

Fisher’s exact test.

Table 3

ESBL-positive E. coli positivity in isolates from the local community and Syrian refugees, by province

ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep25/19712.7 (8.7–18.1)59/30219.5 (15.5–24.4)84/49916.8 (13.8–20.4)0.046
Hatay24/19412.4 (8.5–17.8)35/23215.1 (11.1–20.3)59/42613.8 (10.9–17.5)0.419
Istanbul1/916.7 (2.0–43.5)8/4617.4 (9.1–30.7)9/5217.3 (9.4–29.7)1.000a
Izmir1/333.3 (6.2–79.2)11/6915.9 (9.1–26.3)12/7216.7 (9.8–27.0)0.426a
Mersin31/23113.4 (9.6–18.4)10/1099.2 (5.1–16.1)41/34012.1 (9.0–16.0)0.262
Sanliurfa30/15419.5 (14.0–26.5)46/16824.7 (21.2–34.6)76/34022.4 (18.3–27.1)0.977
Total112/78514.3 (12.0–16.9)169/94417.9 (15.6–20.5)281/172916.3 (14.6–18.1)0.041
ProvinceLocal community
Syrian refugees
Total
P-value
n/N% (95% CI)n/N% (95% CI)n/N% (95% CI)
Gaziantep25/19712.7 (8.7–18.1)59/30219.5 (15.5–24.4)84/49916.8 (13.8–20.4)0.046
Hatay24/19412.4 (8.5–17.8)35/23215.1 (11.1–20.3)59/42613.8 (10.9–17.5)0.419
Istanbul1/916.7 (2.0–43.5)8/4617.4 (9.1–30.7)9/5217.3 (9.4–29.7)1.000a
Izmir1/333.3 (6.2–79.2)11/6915.9 (9.1–26.3)12/7216.7 (9.8–27.0)0.426a
Mersin31/23113.4 (9.6–18.4)10/1099.2 (5.1–16.1)41/34012.1 (9.0–16.0)0.262
Sanliurfa30/15419.5 (14.0–26.5)46/16824.7 (21.2–34.6)76/34022.4 (18.3–27.1)0.977
Total112/78514.3 (12.0–16.9)169/94417.9 (15.6–20.5)281/172916.3 (14.6–18.1)0.041

CI: confidence interval.

a

Fisher’s exact test.

Table 4

The distribution of variables by MDR in the local community and Syrian refugees

VariableCategoryMDRaTotalMDR % (95% CI)P-value
ParticipantsSyrian127851.5 (0.9–2.7)0.003
Turkish379443.9 (2.9–5.4)
SexFemale288773.2 (2.2–4.6)0.478
Male176602.6 (1.6–4.1)
AgeMean ± SD34.3 ± 16.131.6 ± 16.6N/A (N/A)0.311
Use of antibiotics during the last 6 monthsYes115192.1 (1.2–3.8)0.205
No3310113.3 (2.3–4.5)
Hospitalization in the last 6 monthsYes4478.5 (3.4–20.0)0.046
No4114852.8 (2.0–3.7)
ProvinceGaziantep184993.6 (2.3–5.6)0.519
Hatay154263.5 (2.1–5.7)
Istanbul1521.9 (0.3–10.1)
Izmir1721.4 (0.2–7.5)
Mersin63401.8 (0.8–3.8)
Urfa83402.4 (1.2–4.6)
ESBLPositive4728116.7 (12.8–21.5)<0.001
Negative214480.1 (0.03–0.5)
VariableCategoryMDRaTotalMDR % (95% CI)P-value
ParticipantsSyrian127851.5 (0.9–2.7)0.003
Turkish379443.9 (2.9–5.4)
SexFemale288773.2 (2.2–4.6)0.478
Male176602.6 (1.6–4.1)
AgeMean ± SD34.3 ± 16.131.6 ± 16.6N/A (N/A)0.311
Use of antibiotics during the last 6 monthsYes115192.1 (1.2–3.8)0.205
No3310113.3 (2.3–4.5)
Hospitalization in the last 6 monthsYes4478.5 (3.4–20.0)0.046
No4114852.8 (2.0–3.7)
ProvinceGaziantep184993.6 (2.3–5.6)0.519
Hatay154263.5 (2.1–5.7)
Istanbul1521.9 (0.3–10.1)
Izmir1721.4 (0.2–7.5)
Mersin63401.8 (0.8–3.8)
Urfa83402.4 (1.2–4.6)
ESBLPositive4728116.7 (12.8–21.5)<0.001
Negative214480.1 (0.03–0.5)

CI: confidence interval; ESBL: extended-spectrum beta-lactamases; MDR: multi-drug resistance; SD: standard deviation.

a

MDR: multi-drug resistance is defined as combined resistance to third-generation cephalosporins [cefotaxime or ceftazidime or ceftriaxone, fluoroquinolones (ciprofloxacin) and aminoglycosides (gentamycin)].

Table 4

The distribution of variables by MDR in the local community and Syrian refugees

VariableCategoryMDRaTotalMDR % (95% CI)P-value
ParticipantsSyrian127851.5 (0.9–2.7)0.003
Turkish379443.9 (2.9–5.4)
SexFemale288773.2 (2.2–4.6)0.478
Male176602.6 (1.6–4.1)
AgeMean ± SD34.3 ± 16.131.6 ± 16.6N/A (N/A)0.311
Use of antibiotics during the last 6 monthsYes115192.1 (1.2–3.8)0.205
No3310113.3 (2.3–4.5)
Hospitalization in the last 6 monthsYes4478.5 (3.4–20.0)0.046
No4114852.8 (2.0–3.7)
ProvinceGaziantep184993.6 (2.3–5.6)0.519
Hatay154263.5 (2.1–5.7)
Istanbul1521.9 (0.3–10.1)
Izmir1721.4 (0.2–7.5)
Mersin63401.8 (0.8–3.8)
Urfa83402.4 (1.2–4.6)
ESBLPositive4728116.7 (12.8–21.5)<0.001
Negative214480.1 (0.03–0.5)
VariableCategoryMDRaTotalMDR % (95% CI)P-value
ParticipantsSyrian127851.5 (0.9–2.7)0.003
Turkish379443.9 (2.9–5.4)
SexFemale288773.2 (2.2–4.6)0.478
Male176602.6 (1.6–4.1)
AgeMean ± SD34.3 ± 16.131.6 ± 16.6N/A (N/A)0.311
Use of antibiotics during the last 6 monthsYes115192.1 (1.2–3.8)0.205
No3310113.3 (2.3–4.5)
Hospitalization in the last 6 monthsYes4478.5 (3.4–20.0)0.046
No4114852.8 (2.0–3.7)
ProvinceGaziantep184993.6 (2.3–5.6)0.519
Hatay154263.5 (2.1–5.7)
Istanbul1521.9 (0.3–10.1)
Izmir1721.4 (0.2–7.5)
Mersin63401.8 (0.8–3.8)
Urfa83402.4 (1.2–4.6)
ESBLPositive4728116.7 (12.8–21.5)<0.001
Negative214480.1 (0.03–0.5)

CI: confidence interval; ESBL: extended-spectrum beta-lactamases; MDR: multi-drug resistance; SD: standard deviation.

a

MDR: multi-drug resistance is defined as combined resistance to third-generation cephalosporins [cefotaxime or ceftazidime or ceftriaxone, fluoroquinolones (ciprofloxacin) and aminoglycosides (gentamycin)].

Discussion

Global evidence on AMR in migrants is limited. Linked to the recent influx of migrants to the WHO European Region, the number of studies on this topic is increasing.10 Türkiye hosts a large number of refugees, including Syrians and other nationals from the Global South. This is the first study to compare the prevalence of AMR carriage including Syrian refugees and the local community members in Türkiye. This study found MRSA prevalence rates of 6.7% in Syrian refugees and 3.2% in the local community, and ESBL-positivity rates of 17.9% in Syrian refugees and 14.3% in the local community. The data show that although MRSA was the most common type of AMR detected among both Syrian refugees and Turkish residents, it was significantly more prevalent among Syrian refugees, and ESBL positivity was found to be statistically significantly higher among Syrian refugees. We suggest immigrants and refugees should be screened for MDR at their first admission to the country. This study provides important data in terms of the surrogacy of MDR in Syrian refugees. The microorganisms investigated in the study are important causes of both community-acquired and hospital-acquired infections. As these bacteria can often cause endogenous infections, identifying their carriers is especially important for determining empirical treatment at the local level, developing policies on eliminating AMR, reducing mortality and morbidity due to AMR and supporting antimicrobial governance. Integrating local and national AMR data with the global AMR database is important for global AMR management.11

Studies among Syrian refugees in the WHO European Region have generally used samples from hospitalized patients. A study of migrants in Finland between 2010 and 2017 reported an MRSA carriage rate of 20.9% and an ESBL-positivity rate of 48.8%.12 In our study, these rates were higher. However, the AMR rate we found was lower than an Iraqi study, which reported an MRSA carriage rate of 13.8% in Syrian refugees, with a similar rate in Iraqi citizens (15.4%).13 We suggest that Türkiye’s location between Africa, Asia and Europe influences its AMR pattern: AMR rates in Türkiye are generally lower than in Asian countries but higher than in European countries.12–15

In a study from the Netherlands, the MRSA carriage rate was 9.7% among migrants. In Gram-negative bacteria isolated from migrants, the ESBL-positivity rate was 20%, the quinolone resistance rate was 4.4% and the carbapenem resistance rate was 0.4%.16 Since the present study, instead of infectious agents, investigated bacteria in the nasal and gut flora only, the rate of MRSA carriage was lower than in the other studies. High rates of ESBL positivity were identified in both the local community and Syrian refugees. This finding may relate to the overuse of cephalosporin group antibiotics in Türkiye.17 AMR carriage among Syrian refugees was unknown when they arrived in Türkiye as there is no baseline data available. Further comparative population-based data are needed to analyze AMR rates in these population groups.

Evidence-based data on pre-conflict AMR rates in Syria are very limited. However, the limited available data suggest that the overuse of antibiotics and poor antibiotic stewardship were significant problems.18 The fact that the studies obtained were limited to the cities of Damascus and Aleppo does not allow us to make an evaluation of the country in general. Despite the limited data available, there is evidence that resistance, especially carbapenem resistance, was quite high.18

A 2018 meta-analysis of data on refugees and migrants in Europe suggested that AMR patterns in this population may be affected by factors in transit and destination countries. Although there is evidence transmission may occur between migrants, there is no evidence of transfer from refugees and migrants to the host population.2

The study identified a high number of multi-drug-resistant isolates in both the local community and Syrian refugees. The high carriage frequency for these isolates within the community may be an important causative factor in a future AMR pandemic. Five of the isolates were also resistant to carbapenems; carbapenemase enzymes were detected in three of these: The New Delhi metallo-β-lactamase (NDM) in two and OXA-48 in one. Türkiye is endemic for OXA-48.19 The fact that the OXA-48 carrier had been hospitalized in the previous 6 months suggests that they had acquired the isolate during hospitalization. This finding is consistent with a previous report suggesting that the Middle East may be a reservoir of NDM-producing isolates,20 but more data are needed to explain the origin of these NDM-producing isolates. Overall, the rate of carbapenemase-producing isolates in the present study was similar to those of other studies.13–15 Further studies, especially on AmpC-positive isolates, carbapenem-resistant isolates and MRSA isolates for high-risk clones, will improve the value of this study. However, due to budgetary limitations and COVID-19 restrictions, further studies could not be carried out within the scope of this study.

The present study underlines the importance of analyzing data from all population sub-groups to better understand their AMR patterns and determine how best to prevent and control the spread of resistant organisms across society. The high rate of AMR carriage highlights the need for longitudinal studies, particularly in light of other research on types and rates of resistant bacterial isolates and how this may change over time in people who have lived as refugees for long periods.21 Periodic data collection and analysis may reveal clonal relationships between isolates and allow proactive approaches to monitor and prevent AMR. Such studies may also reveal epidemiological differences between migrant and local populations, and even between migrants from different countries. Therefore, the disease prevalence and carriage of multi-drug-resistant isolates in different population groups should be monitored through a surveillance system that supports international data sharing on AMR. Furthermore, clinical approaches for refugees and migrants should not isolate these groups from society and support their longer-term engagement with health services.22

In a review paper, various aspects of AMR in Syrian refugees were discussed. The paper highlights the importance of AMR as a public health problem, which continues to spread in many countries as Syrian refugees migrate. It is emphasized that global health problems such as AMR need to be addressed with a ‘one-health’ approach. It is also stated that standard management practices should be adopted in the region for refugees to maintain the sustainability of public health measures.23

In the WHO European region, Türkiye is among the countries with the highest use of antibiotics in outpatient settings. Antibiotic usage also changes seasonally.11 In our study, about 63% of the participants claimed that they had used antibiotics in the last 6 months. While it is possible to hypothesize that there is an association between antibiotic use and resistance, we need more evidence for this. However, limiting the use of antibiotics may be one of the strategies to reduce resistance.

The most important limitation we faced was the interruption of data collection due to the COVID-19 pandemic and a major earthquake in the country. Since reliable data on the arrival time of Syrian refugees in Türkiye were unavailable, the study could not consider the time spent in the host country. Participants were limited to people who visited FHCs and RHCs. Another important limitation is the time of the data collection. All Syrian refugees have been in the Turkish community since 2011, first in the refugee camps but after 2014 mostly living outside the camps. So, the year 2020 is considerably late to evaluate and compare the AMR carriage status.

Another limitation was that data were collected from different centers in six provinces. The standardization of study protocols, including collecting epidemiological data, clinical samples and transferring samples, was therefore a challenge. To ensure standardization, structured training was given to healthcare personnel and data collectors in Turkish and Arabic. Another limitation was the time constraint on using enrichment broths for MDR bacteria. During the study period, the study team was also required to work in the COVID-19 pandemic laboratory.

Conclusion

The civil war in Syria and the consequent population dynamics have significantly contributed to the ongoing public health challenges in the WHO European Region. AMR is an important public health problem in the Region, which originates from healthcare disparities, poor living conditions, inadequate hygiene and sanitation, lack of or outdated treatment guidelines and overuse of antimicrobials. The civil war and, consequently, the deterioration in living conditions and public health infrastructure were likely to have exacerbated this problem.

This is the first large-scale study on the carriage of AMR in Türkiye including both refugees and the local populations; as such, it provides an important insight essential for the effective management of AMR in both Türkiye and the region. Our data can inform screening studies and public health policy decision-making, as well as facilitate accessible high-quality healthcare for both migrant and local populations to support the timely detection and treatment of AMR. Phylogenetic analysis of bacterial isolates obtained over time may provide further data on AMR for both Türkiye and countries on migratory routes.

Supplementary data

Supplementary data are available at EURPUB online.

Acknowledgements

We thank Ms. Elif Göksu of the Refugee Health Program, WHO Country Office in Türkiye for supporting the implementation of this project. We also express our deepest gratitude to Drs. Danilo Lo Fo Wong and Saskia Andrea Nahrgang of the Antimicrobial Resistance Team, WHO Regional Office for Europe for reviewing the manuscript. We further acknowledge the valuable contributions of health workers from FHCs and RHCs in Türkiye.

Funding

This study is co-funded by World Health Organization and the Ministry of Health of Türkiye.

Conflicts of interest: None declared.

Key points
  • Antimicrobial resistance (AMR) represents a complex threat to global health, with little evidence of patterns of AMR in migrant communities.

  • This is the first large-scale study into the carriage of AMR in Türkiye, which considers both refugee and local populations.

  • Across 2525 Syrian refugees and 1453 individuals in the local community in Türkiye, a significantly greater proportion of refugees (6.7%) carried methicillin-resistant Staphylococcus aureus compared to the local community (3.2%) (P < 0.001).

  • The extended-spectrum β-lactamase-positivity rate was 17.9% in Syrian refugees and 14.3% in the local community (P = 0.041).

  • The research underscores the importance of better AMR data on both refugee and local populations, the benefit of a surveillance system to support international data sharing on AMR and the need to facilitate access to early high-quality care for refugee communities.

Data availability

Data can be shared upon request.

References

1

Morgan
DJ
,
Okeke
IN
,
Laxminarayan
R
, et al.
Non-prescription antimicrobial use worldwide: a systematic review
.
Lancet Infect Dis
2011
;
11
:
692
701
.

2

Nellums
LB
,
Thompson
H
,
Holmes
A
, et al.
Antimicrobial resistance among migrants in Europe: a systematic review and meta-analysis
.
Lancet Infect Dis
2018
;
18
:
796
811
.

3

Maltezou
HC
,
Theodoridou
M
,
Daikos
GL.
Antimicrobial resistance and the current refugee crisis
.
J Glob Antimicrob Resist
2017
;
10
:
75
9
.

4

Antimicrobial Resistance Collaborators
.
Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis
.
Lancet
2022
;
399
:
629
55
.

5

European Antimicrobial Resistance Collaborators
.
The burden of bacterial antimicrobial resistance in the WHO European region in 2019: a cross-country systematic analysis
.
Lancet Public Health
2022
;
7
:
e897
913
.

6

UNHCR Türkiye: provincial breakdown Syrian Refugees. In:

Türkiye—March 2021
.
Geneva
:
Office of the United Nations High Commissioner for Refugees
,
2021
. https://data2.unhcr.org/en/documents/details/85506 (3 March 2021, date last accessed).

7

The European Committee on Antimicrobial Susceptibility Testing—EUCAST Guidelines for Clinical Break Point. Clinical Breakpoints—Bacteria (v 11.0),

2021
. https://www.eucast.org/clinical_breakpoints (2021, date last accessed).

8

IBM Corp
. Released
2011
.
IBM SPSS Statistics for Windows, Version 20.0
.
Armonk, NY
:
IBM Corp
. 2011.

9

Sullivan
KM
,
Dean
A
,
Soe
MM.
OpenEpi: a web-based epidemiologic and statistical calculator for public health
.
Public Health Rep
2009
;
124
:
471
4
.

10

de Smalen
AW
,
Ghorab
H
,
Abd El Ghany
M
,
Hill-Cawthorne
GA.
Refugees and antimicrobial resistance: a systematic review
.
Travel Med Infect Dis
2017
;
15
:
23
8
.

11

Versporten
A
,
Bolokhovets
G
,
Ghazaryan
L
, et al. ;
WHO/Europe-ESAC Project Group
.
Antibiotic use in Eastern Europe: a cross-national database study in coordination with the WHO Regional Office for Europe
.
Lancet Infect Dis
2014
;
14
:
381
7
.

12

Aro
T
,
Kantele
A.
High rates of methicillin-resistant Staphylococcus aureus among asylum seekers and refugees admitted to Helsinki University Hospital, 2010 to 2017
.
Euro Surveill
2018
;
23
:
1700797
.

13

Rasheed
NA
,
Hussein
NR.
Methicillin-resistant Staphylococcus aureus carriage rate and molecular characterization of the staphylococcal cassette chromosome mec among Syrian refugees in Iraq
.
Int J Infect Dis
2020
;
91
:
218
22
.

14

Ouchar Mahamat
O
,
Tidjani
A
,
Lounnas
M
, et al.
Fecal carriage of extended-spectrum beta-lactamase-producing Enterobacteriaceae in hospital and community settings in Chad
.
Antimicrob Resist Infect Control
2019
;
8
:
169
.

15

Abdallah
HM
,
Alnaiemi
N
,
Reuland
EA
, et al.
Fecal carriage of extended-spectrum beta-lactamase- and carbapenemase-producing Enterobacteriaceae in Egyptian patients with community-onset gastrointestinal complaints: a hospital-based cross-sectional study
.
Antimicrob Resist Infect Control
2017
;
6
:
62
.

16

Ravensbergen
SJ
,
Berends
M
,
Stienstra
Y
,
Ott
A.
High prevalence of MRSA and ESBL among asylum seekers in the Netherlands
.
PLoS One
2017
;
12
:
e0176481
.

17

Robertson
J
,
Iwamoto
K
,
Hoxha
I
, et al.
Antimicrobial medicines consumption in Eastern Europe and Central Asia: an updated cross-national study and assessment of quantitative metrics for policy action
.
Front Pharmacol
2018
;
9
:
1156
69
.

18

Abbara
A
,
Rawson
TM
,
Karah
N
, et al.
A summary and appraisal of existing evidence of antimicrobial resistance in the Syrian conflict
.
Int J Infect Dis
2018
;
75
:
26
33
.

19

Yıldız Suzuk Şimşek
H
,
Bakkaloğlu
Z
,
Numanoğlu Çevik
Y
, et al. ;
Ulusal Karbapenemaz Sürveyans Çalışma Grubu
.
The epidemiology of carbapenemases in Escherichia coli and Klebsiella pneumoniae isolated in 2019 in Türkiye
.
Mikrobiyol Bul
2021
;
55
:
1
16
(in Turkish).

20

Nordmann
P
,
Poirel
L
,
Toleman
MA
,
Walsh
TR.
Does broad-spectrum beta-lactam resistance due to NDM-1 herald the end of the antibiotic era for treatment of infections caused by Gram-negative bacteria?
J Antimicrob Chemother
2011
;
66
:
689
92
.

21

Ravensbergen
SJ
,
Louka
C
,
Ott
A
, et al.
The proportion antimicrob resist infect control
.
Antimicrob Resist Infect Control
2019
;
8
:
6
.

22

Piso
RJ
,
Käch
R
,
Pop
R
, et al.
A cross-sectional study of colonization rates with methicillin-resistant Staphylococcus aureus (MRSA) and extended-spectrum beta-lactamase (ESBL) and carbapenemase-producing Enterobacteriaceae in four Swiss refugee centres
.
PLoS One
2017
;
12
:
e0170251
.

23

Osman
M
,
Rafei
R
,
Ismail
MB
, et al.
Antimicrobial resistance in the protracted Syrian conflict: halting a war in the war
.
Future Microbiol
2021
;
16
:
825
45
.

This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

Supplementary data

Comments

0 Comments
Submit a comment
You have entered an invalid code
Thank you for submitting a comment on this article. Your comment will be reviewed and published at the journal's discretion. Please check for further notifications by email.