key: cord-0026460-utg8lsed authors: Roy, Krishna; Islam, Md. Saiful; Paul, Anamika; Ievy, Samina; Talukder, Mithun; Sobur, Md. Abdus; Ballah, Fatimah Muhammad; Khan, Md. Shahidur Rahman; Rahman, Md. Tanvir title: Molecular detection and antibiotyping of multi‐drug resistant Enterococcus faecium from healthy broiler chickens in Bangladesh date: 2021-11-16 journal: Vet Med Sci DOI: 10.1002/vms3.669 sha: fb4e2e0701e4e45bc50729f0485e750adb6a2193 doc_id: 26460 cord_uid: utg8lsed BACKGROUND: Enterococcus faecium is a ubiquitously distributed member of the intestinal microbiota of both humans and animals. Antibiotic resistant E. faecium are a major public health concern. OBJECTIVES: This study aimed to detect multi‐drug resistant (MDR) E. faecium and their antibiotic resistance genes from broiler chickens in Bangladesh. METHODS: A total of 100 faecal samples of healthy broilers were screened by conventional methods and polymerase chain reaction (PCR) to detect E. faecium and their resistance genes. Disk diffusion test was employed to determine antibiotic profiles. RESULTS: By PCR, among 100 samples, 45% [95% confidence interval (CI): 35.62%–54.76%] were positive for E. faecium. Based on antibiogram, all the E. faecium isolates were found resistant to ampicillin, and frequently (93.33%–55.56%) resistant to ceftriaxone, cefotaxime, streptomycin, erythromycin, and imipenem; moderate to lower (26.67%–4.44%) resistance to tetracycline, ciprofloxacin, norfloxacin, chloramphenicol, gentamicin, and vancomycin. Interestingly, 80% (95% CI: 66.18%–89.10%) E. faecium isolates were MDR in nature. In addition, the indices of multiple antibiotic resistance (MAR) ranged from 0.08 to 0.83. By bivariate analysis, high positive significant correlations were observed between resistance profiles of erythromycin and imipenem, ciprofloxacin and norfloxacin, erythromycin and streptomycin, ceftriaxone and cefotaxime, tetracycline and chloramphenicol, and streptomycin and imipenem. Furthermore, the prevalence of resistance genes of E. faecium was 58.33% (tetA), 33.33% (tetB), 35.56% (bla(TEM) ), 60% (CITM), 13.33% (aadA1), and 12% (SHV). CONCLUSIONS: To the best of our knowledge, this is the first study in Bangladesh to detect MDR and MAR E. faecium and their associated resistance genes. The detection of MDR and MAR E. faecium and their corresponding resistance genes from healthy broilers is of public health concern because of their potential to enter into the food chain. broilers is of public health concern because of their potential to enter into the food chain. antibiotic resistance genes, Enterococcus faecium, MAR, MDR, public health INTRODUCTION Members of enterococci, under the family of Enterococcaceae, are deemed symbiotic pathogens which can develop hospital-and community-acquired infections in humans and multifarious types of infections in animals (Tian et al., 2019) . They are ubiquitously present in both humans' and animals' intestinal tracts, in addition to different environmental sources such as water and soil (Kim et al., 2019) . Enterococci are used as faecal indicator organisms to track microbial sources and antibiotic resistance trends in microorganisms. Furthermore, resistance surveillance systems of humans and animals use Enterococcus spp. as important indicator organisms (Tyson et al., 2018) . All age groups of poultry can be affected by Enterococcus spp., but their devastating effects are developed in embryos and young chicks (MSD Manual Veterinary Manual, 2019) . In poultry, Enterococcus spp. can colonize the intestine and cause disease conditions such as osteomyelitis, femoral head necrosis, spondylitis, skeletal disease, and arthritis in poultry. Additionally, Enterococcus faecium cause endocarditis, septicaemia, amyloid arthropathy, and spondylitis (Robbins et al., 2012) . Furthermore, these organisms are directly related to musculoskeletal disease in broiler breeders and broilers (Robbins et al., 2012) . E. faecium along with E. faecalis can cause about 90% of clinical infections and more than 10% of nosocomial infections in humans (Torres et al., 2018) . Importantly, E. faecium are deemed the fourth most dominant among human pathogens globally (Rehman et al., 2018) . In humans, Enterococcus spp. usually develop infections in urinary and respiratory tracts, sites of surgery, skin and soft tissue, and gastrointestinal tracts (Ike, 2017) . The zoonotic pathogens E. faecium can be transmitted from animals to humans and can develop bacteraemia, urinary tract infections, infective endocarditis, wound infections, sepsis, and meningitis (Hammerum, 2012) . Antimicrobial resistance (AMR) shows negative challenges to global public health and endangers all of the one-health components . Low-and middle-developing countries are facing the ominous effects of AMR. AMR will cause a huge number of deaths in the world's human populace if effective and novel antimicrobial agents cannot be introduced in the future (Clifford et al., 2018) . Antibiotic resistance has been promoted in poultry by the haphazard use of antibiotics in their production as growth promoters with treating bacterial infections . These activities in poultry can promote bacteria to be resistant to multiple antibiotics. These resistant bacteria are usually developed in the microbiota of chickens and can easily be spread to the environment via faecal con-tamination (Hafez & Attia, 2020) . Associating in the gut microbiota and environments (litter, surface, air, water, etc.) of poultry, these resistant bacteria can acquire resistance genes and keep persisting them for a long time after discontinuation of the antibiotic treatment (Obeng et al., 2013) . As Enterococcus spp. are naturally gut-oriented pathogens, they can serve as reservoirs of resistance genes. In addition, enterococci show intrinsic resistance to multiple classes of antibiotics which assists them to acquire abilities to be highly resistance against diversified antibiotics and to be transferred horizontally to other bacteria with the help of mobile genetic determinants (Petsaris et al., 2005) . Interestingly, enterococci are resistant to multiple antimicrobial drugs, for example, aminoglycosides, β-lactams, fluoroquinolones, amphenicols, macrolides, tetracyclines, and glycopeptides (Fracalanzza et al., 2007) . The vast resistance characteristics of enterococci can limit therapeutic options especially antibiotic treatment in nosocomial infections in humans and in multiple kinds of diseases in poultry. Therefore, it becomes pivotal to monitor multi-drug resistant (MDR) enterococci which have both animal and public health significance. Globally, there are some studies that describe the detection of E. faecium from broiler chickens (Rehman et al., 2018; Robbins et al., 2012; Šeputienė et al., 2012) , but to the best of our knowledge, there are no data available in Bangladesh that detect antibiotic resistance genes carrying E. faecium from broilers. In addition, the inconveniences in treating enterococci infections are connected with AMR. This study was therefore aimed to detect E. faecium from faecal materials of healthy broiler chickens using a molecular-based approach along with detection of their antibiotic resistance phenotypes and genotypes. As there was no research on molecular detection of Enterococcus spp. in Bangladesh, the sample size was calculated with the 50% assumptive prevalence and the 95% confidence interval (CI). The previously described (Thrusfield, 1995) formula of sample size calculation was as follows: n = Z 2 pq/d 2 , where n = desired sample size, Z = the normal standard deviation (1.96 at 95% CI), p = prevalence (50% or 0.5), q = (1p) = (1-0.5) = 0.5, d = precision (10% or 0.1). So, n = (1.96) 2 × 0.5 × 0.5/ (0.1) 2 = 96.04. Therefore, we collected 100 faecal samples aseptically from broiler chickens. Isolated Enterococcus spp. were subjected to simplex polymerase chain reaction (PCR) to detect E. faecium targeting ddl E. faecium gene (Table 1) . For the PCR, the genomic DNA was extracted from isolated Enterococcus spp. by the boiling method as previously described . In brief, initially, 1 ml previously enriched culture was centrifuged at 5000 rpm for 5 min; subsequently, the supernatant was dis- Van et al., 2008 employed to check the expected band size of the amplified PCR products (Promega). Kirby-Bauer disk diffusion test (Bauer, 1966) three or more classes of antibiotics were recorded as MDR (Sweeney et al., 2018) . Moreover, the multiple antibiotic resistance (MAR) index was calculated by the following formula: MAR = m/n, here 'm' implies the number of antibiotics resistance to a particular E. faecium isolate and 'n' implies the total number of antibiotics used (Krumperman, 1983 ). Simplex PCR was employed to detect resistance genes of E. faecium isolates associate with tetracycline (tetA and tetB), ampicillin (bla TEM and CITM), erythromycin (ereA), imipenem (SHV), and streptomycin (aadA1). The primers and targeted genes are documented in Table 1 Pearson correlation was performed by SPSS to observe the potential association between any of the two antibiotics that were resistant to E. faecium isolates. The statistically significant p-value was fixed at 0.05. Among 100 Table 2 . Of 45 E. faecium isolates, 36 isolates (80%; 95% CI: 66.18%-89.10%) were phenotypically MDR in nature. A total of 18 MDR patterns were observed, of which 22.22% (8/36; 95% CI: 11.72%-38.09%) isolates exhibited the resistance pattern number 9 (E-AMP-S-IMP-CTR-CTX). Two isolates were resistant against 10 antibiotics under eight classes (Patterns 1 and 2) . The ranges of MAR indices of E. faecium isolates were 0.08-0.83. Interestingly, 97.78% (44/45; 95% CI: 88.43%-99.89%) of isolates showed resistance against two or more antibiotics (Table 3) . By PCR, resistance gene tetA and tetB were found to be positive in 58.33% (7/ faecium is a ubiquitously commensal microorganism and is considered as a part of the intestinal microbiota of humans and animals (Dubin & Pamer, 2018) . In addition, enterococci are present in faecal materials of different birds, mammals, reptiles, and even insects (Dubin & Pamer, 2018) . Previously, Banik et al. (2018) isolated Enterococcus spp. from chicken in Bangladesh, but they used only conventional methods and did not carry any molecular approach, for example, PCR assay which was used in our present study. PCR is a robust, sensitive, and rapid method in detecting Enterococcus spp. from any kind of sample and gives higher specificity and sensitivity of the results (Maheux These variations might be lined with the variations in geographical and seasonal distributions, the farm management systems (hygiene, biose-curity, and sanitary), sample size and types, and methodological factors (Islam, Paul, et al., 2021) . The presence of E. faecium in faecal materials of broiler chickens reveals that the droppings of broiler chickens can shed E. faecium to other birds of the farm. In addition, contaminated faecal materials can act as vehicles to contaminate water and broiler feed. Furthermore, the enterococci contamination can be transferred into the production systems via the contaminated faeces, water, or broiler feeds. Broiler meat and its products can be contaminated by enterococci that can be transmitted to the food chain and pose a potential human health concern. Enterococci can grow under extreme temperature up to 72 • C which indicates that consumption of undercooked poultry meat and products has the potential to transmit enterococci to humans (Martinez et al., 2003) . Furthermore, this may reveal a high risk to human health by exposure to colonized birds or by the introduction of poultry meat contaminated with enterococci or by cross-contaminating with ready-toeat foods (Obeng et al., 2013) . Any microorganism resistant to the antibiotic is a threat to human health. Results of phenotypic antibiotic susceptibility test from our present study showed that a high number of E. faecium isolates were resistant to ampicillin, ceftriaxone, cefotaxime, streptomycin, ery- (Bertelloni et al., 2015) . But in contrast, we found that another aminoglycoside-gentamicin was highly sensitive or intermediately sensitive to E. faecium (more than 85% isolates). This variation might have a linkage with the level of concentrations of gentamicin, as enterococci show intrinsic resistance to only a low level of concentrations of aminoglycosides (Lefort et al., 2000) . Previously, Tremblay et al. (2011) also found that high proportion of enterococci was sensitive to gentamicin. However, intrinsic resistance of enterococci either to streptomycin or to gentamicin has not been illustrated properly till now (Bertelloni et al., 2015) . Similarly, enterococci also are naturally resistant to cephalosporins which are lined with the higher resistance to the cephalosporin class of antibiotics -ceftriaxone and cefotaxime -obtained from our present study. Enterococci acquire intrinsic resistance to cephalosporins by a penicillin-binding protein (Pbp5), a transduction system (CroRS), an enzyme to synthesize peptidoglycan precursors (MurAA), and a transmembrane kinase (Ser/Thr) (Kristich et al., 2014) . This trait is well defined for E. faecalis, but for E. faecium, it is not well developed yet. However, gentamicin is vastly used in enterococcal infections with the combination of beta-lactam antibiotics or glycopeptides for obtaining synergistic bactericidal effects (Emaneini et al., 2016) . Interestingly, 55.56% of E. faecium isolates were resistant to imipenem which reveals an alarming condition to both human and animal health facilities. Imipenem is under the carbapenem group of antibiotics which are only exercised for treating severe bacterial infections in humans (Lamb et al., 2002) . E. faecium acquires resistance by two distinct mechanisms: one is incremented via Pbp5 which shows low-affinity to β-lactam antibiotics, and another one is the mutation that occurred in Pbp5 (Joste et al., 2019) . Acquisition of ery-thromycin and tetracycline resistance in enterococci is usually developed by mobile genetic elements (Emaneini et al., 2016) . E. faecium resistance to tetracycline shows importance because of its relatedness with the resistance profiles of other antibiotics (Hammerum, 2012 tetB which codes for a protein that seems to be related to the tetracycline ribosomal protection proteins (Roberts, 1996) . The results of tetA and tetB from tetracycline resistant E. faecium isolates show that the original mechanism of tetracycline resistance generated from broiler chickens is by active efflux system. Resistance gene bla TEM , CITM, and SHV are associated with β-lactam antibiotics. These genes presenting in the organism have abilities to inactivate the antibiotics by hydrolyzing the β-lactam ring (Livermore, 1995) . The gene cassette aadA1 is associated with the resistance to streptomycin which generally presents in class 1 integrons related to transposons Tn21 (Rodríguez et al., 2006) . Through conjugative plasmids, this resistance gene has the ability to be horizontally transferred from E. faecium to other bacteria (Nde & Logue, 2008) . The presence of resistance genes of E. faecium in broiler chickens reveals public health significance as they can be transmitted to humans via the contaminated food supply chain and/or close contact with the animals. In addition, these resistance genes can assist in the emergence of MDR and MAR bacteria in both humans and animals. Infections caused by MDR and MAR bacteria can have serious health repercussions for humans (Urmi et al., 2021) . The abuse and overuse of antibiotics has resulted in the emergence of MDR and MAR enterococci, which has become a severe public health hazard in both humans and animals. MDR and MAR enterococci lessen the treatment option in infections developed by such strains (Obeng et al., 2013) . In the present study, a high proportion of E. faecium isolates (80%) were phenotypically MDR in nature which reveals an alarming situation in poultry as well as humans. Previously, Tremblay et al. (2011) detected 100% MDR E. faecium isolates from broiler chickens in Canada. Furthermore, the index of MAR in E. faecium isolates was risen up to 0.83, which indicates that a high level of antibiotics was haphazardly used in the broiler chickens from where the enterococci were isolated. MDR and MAR in E. faecium might be developed by selective pressure triggered by the misuse, extensive use, and incorrect prescriptions of antibiotics in veterinary practices Tawyabur et al., 2020) . The MDR and MAR E. faecium obtained from our present study have the potential to contaminate the one-health components. They can be transmitted to humans through the food chain or close contact with the broilers and to environments via contaminated water or feed sources. To the best of our knowledge, we detected MDR and MAR E. faecium and their corresponding resistance genes for the first time in Bangladesh from healthy broiler chickens. A high level of E. faecium and their resistance and resistance genes detected in broiler chickens has the potential to enter into the food chain and shows a negative impact on both humans' and animals' health. Furthermore, the presence of MDR enterococci in broilers reveals more potential public health hazards in considering close contact with humans and animals. Though we performed our study with a limited number of broilers, this study has contributed to verify MDR enterococci and their resistance profiles in poultry. We, therefore, suggest that broiler chickens should be kept under strict biosecurity and under regular epidemiological study with a strong one-health approach to prevent the negative effects of enterococci and to minimize the emergence of MDR and MAR E. faecium with their resistance genes in both humans and animals. 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