ORIGINAL RESEARCH article
Prevalence and Characterization of Multi-Drug-Resistant Gram-Negative Bacilli Isolated From Lebanese Poultry: A Nationwide Study
- 1Clinical Microbiology Laboratory, Faculty of Medicine and Medical Sciences, University of Balamand, Beirut, Lebanon
- 2IRD, APHM, MEPHI, IHU-Méditerranée Infection, Aix-Marseille Université, Marseille, France
- 3The Lebanese Ministry of Agriculture, Beirut, Lebanon
Currently, antimicrobial resistance is one of the most prominent public health issues. In fact, there is increasing evidence that animals constitute a reservoir of antimicrobial resistance. In collaboration with the Lebanese Ministry of Agriculture, the aim of this study was to determine the prevalence of intestinal carriage of multi-drug-resistant Gram-negative Bacilli in poultry farms at the national level. Between August and December 2015, 981 fecal swabs were obtained from 49 poultry farms distributed across Lebanon. The swabs were subcultured on MacConkey agar supplemented with cefotaxime (2 μg/ml). Isolated strains were identified using MALDI-TOF mass spectrometry. Multilocus sequence typing analysis was performed for Escherichia coli. Phenotypic detection of extended spectrum β-lactamases (ESBL) and AmpC production was performed using double disk synergy and the ampC disk test, respectively. β-lactamase encoding genes blaCTX-M, blaTEM, blaSHV, blaFOX, blaMOX, blaEBC, blaACC, blaDHA, and blaCMY using PCR amplification. Out of 981 fecal swabs obtained, 203 (20.6%) showed bacterial growth on the selective medium. Of the 235 strains isolated, 217 were identified as E. coli (92%), eight as Klebsiella pneumoniae (3%), three as Proteus mirabilis (1%) and three as Enterobacter cloacae (1%). MLST analysis of E. coli isolates showed the presence of ST156, ST5470, ST354, ST155, and ST3224. The phenotypic tests revealed that 43.5, 28.5, and 20.5% of the strains were ampC, ESBL, and ampC/ESBL producers, respectively. The putative TEM gene was detected in 83% of the isolates, SHV in 20%, CTX-M in 53% and CMY ampC β-lactamase gene in 65%. Our study showed that chicken farms in Lebanon are reservoirs of ESBL and AmpC producing Gram-negative bacilli. The level of antibiotic consumption in the Lebanese veterinary medicine should be evaluated. Future studies should focus on the risk factors associated with the acquisition of multi-drug-resistant organisms in farm animals in Lebanon.
Antibiotic resistance is currently a major topic of interest for researchers and physicians. In particular, the rise of multi-drug resistance in Gram-negative bacteria is now a serious challenge encountered by healthcare professionals (Exner et al., 2017). Resistance in Gram-negative bacteria is mainly mediated via the production of extended spectrum β-lactamases (ESBL), ampC β-lactamases and carbapenemases (Schill et al., 2017). Genes encoding these enzymes are often located on plasmids carrying resistance genes to other commonly used antibiotics in clinical settings (Seiffert et al., 2013). Infections with these multi-drug-resistant organisms (MDROs) will thus pose therapeutic challenges; the antibiotic pipeline is drying up, and no new antimicrobial agents are anticipated in the near future to treat infections caused by MDROs (Bettiol and Harbarth, 2015).
In fact, it has been generally accepted that the main driver for the rapid evolution of bacterial resistance is the uncontrolled usage of antibiotics in human medicine. It is suggested that this theory is also applicable to the veterinary sector (Kempf et al., 2015). The European Centre for Disease Prevention and Control/European Food Safety Authority/European Medicines Agency (ECDC/EFSA/EMA) joint report stated that in 2014, the average antibiotic consumption in animals (152 mg/kg) was higher than in humans (124 mg/kg). Univariate analysis showed a signification correlation between fluoroquinolone consumption and resistance in Escherichia coli in the human and animal sectors, between polymyxins and tetracyclines and E. coli in animals, and for 3rd/4th generation cephalosporins and E. coli in humans (ECDC/EFSA/EMA, 2017). Antibiotics are heavily administered for therapeutic and prophylaxis purposes in veterinary medicine. As growth promoters, this practice is no longer adapted in the European Union, whereas it persists in North America and other countries (Economou and Gousia, 2015). In their study, Chantziaras et al. (2014) found a significant correlation between the use of antibiotics in livestock and the corresponding level of resistance toward these antimicrobials in E. coli strains isolated from pigs, poultry and cattle. During the last years, the prevalence of ESBLs, ampC, and carbapenemase producing Gram-negative bacteria has become extensively reported in food producing animals (Ghodousi et al., 2015; Gonzalez-Torralba et al., 2016; Haenni et al., 2016). In their review paper, Schwarz et al. (2016) showed that studies describing the epidemiology of resistant organisms in livestock targeted mainly swine, cattle and poultry. The prevalence of resistance varied from one country to another (Alonso et al., 2017). Although the extent to which food of animal origin contributes to the zoonotic transmission of multi-drug-resistant organisms, i.e., ESBL and carbapenemase producers, has not yet been well established (Madec et al., 2017), it suggests that sharing the same ESBL genes, plasmids and strains constitutes possible evidence of zoonotic transmission of MDROs from animals to humans (Leverstein-van Hall et al., 2011; Dahms et al., 2014). Furthermore, the increased risk of ESBL fecal carriage in individuals with a high degree of contact with broiler chickens is an indicator of transmission (Huijbers et al., 2014). Enteric-resistant strains in livestock can be easily transferred to humans through direct contact or through the handling/consumption of undercooked/uncooked animal products (Dahms et al., 2014).
In Lebanon, several studies addressing MDROs in hospital settings have been conducted. One study done at the American University of Beirut Medical Center between 2008 and 2011 reported that 1.07 and 2.45% of E. coli and Klebsiella pneumoniae clinical isolates, respectively, were ESBL producers and ertapenem-resistant (Baroud et al., 2013). Another study conducted in the north reported that over the period of 2009–2012, 9% and 28% of the bacteraemia episodes in febrile neutropenic patients were caused by carbapenem and third-generation cephalosporin-resistant Gram-negative bacilli, respectively (Moghnieh et al., 2015). However, very few studies have addressed this issue in the environment. One study showed that Acinetobacter baumannii was detected in 6.9% of water samples, 2.7% of milk samples, 8.0% of meat samples, 14.3% of cheese samples and 7.7% of animal samples (Rafei et al., 2015). Another study in which 115 stool samples were collected from livestock animals from different farms in north Lebanon reported the detection of four VIM-2 producing Pseudomonas aeruginosa, four OXA-23 producing A. baumannii and one OXA-23/OXA-58 co-producing A. baumannii (Al Bayssari et al., 2015a). Furthermore, Al Bayssari et al. (2015b) reported the isolation of an OXA-48 harboring E. coli isolate from fowl in Lebanon. More recently, Diab et al. (2016) detected a relatively high prevalence of CTX-M-15 producing E. coli in Lebanese cattle. In the above-mentioned studies in Lebanese livestock, MLST analysis revealed the presence of sequence types common to both humans and animals (Al Bayssari et al., 2015a; Rafei et al., 2015; Diab et al., 2016), which suggests that Lebanese farms are potent reservoirs of multi-drug-resistant organisms that could be transmitted to humans. In the present study and in collaboration with the Lebanese Ministry of Agriculture, our aim was to determine the national epidemiology of multi-drug-resistant Gram-negative bacilli in Lebanese chicken farms in terms of intestinal carriage.
Materials and Methods
The Ministry of Agriculture in Lebanon granted approval to collect chicken samples from representative farms in the country as per the national norms for animal sampling and manipulation. This sampling was in conformity with the international regulations for animal safety. All of the involved farms officially received authorization from the Ministry of Agriculture, and this was considered, after undergoing an acceptance process, an official and legal document. Therefore, an Institutional Review Board (IRB) approval was obtained for the present study.
Between August and December 2015, 981 rectal swabs were collected from 49 poultry farms distributed over the seven districts of Lebanon. Six to seven farms were visited in each district. The average number of samples taken from each farm was 20 fecal swabs (Table 1). The 20 samples collected were randomly taken from each farm. Technical assistance, i.e., fecal swabs, gloves, costumes, and a portable refrigerator, were provided by the Ministry of Agriculture team. The collected swabs were directly placed in a portable refrigerator, and when they arrived at the University Laboratory, they were stored at -80°C until use. The farms visited were selected by considering their geographical location, presence or absence of a nearby community and the size of the farms (at least 3,000 chickens per breeding site). Eighty percent of the samples were gathered from broiler chickens, while 20% were taken from layers. The mean average age of the broilers and layers was 31 days and 14 months, respectively.
MALDI-TOF MS Identification
Rectal swabs were sub-cultured on a MacConkey agar supplemented with 2 μg/ml of cefotaxime for the preliminary screening of antibiotic-resistant Gram-negative bacilli. After overnight incubation at 37°C, colonies showing different morphologies were picked up from each selective plate and tested separately with MALDI-TOF MS for identification using the Microflex LT spectrometer (Bruker Daltonics, Bremen, Germany) (Seng et al., 2010; Singhal et al., 2015). The spectra obtained for each strain were stored and downloaded into a MALDI Biotyper 3.0 system to create a single main spectrum for each bacterial isolate. Thereafter, a dendrogram was constructed using MALDI Biotyper 3.0 software.
Antibiotic Susceptibility Testing
Using the Kirby–Bauer disk diffusion method, antibiotic susceptibility testing was performed. The results were interpreted according to EUCAST guidelines 2017 (European Committee on Antimicrobial Susceptibility Testing, 2017). Sixteen antimicrobial agents were used including ampicillin, aztreonam, cefotaxime, ceftazidime, cefoxitin, cefepime, amoxicillin-clavulanic acid, piperacillin-tazobactam, meropenem, imipenem, ertapenem, colistin, tigecycline, ciprofloxacin, gentamicin and trimethoprim-sulfamethoxazole (Bio-Rad, Marnes-la-Coquette, France). Phenotypic detection of ESBL was performed using the double-disk synergy test by placing an amoxicillin–clavulanic acid disk in the center between aztreonam, cefepime and ceftazidime. The observation of a “key hole effect” was considered a positive test. On the other hand, ampC β-lactamase detection was performed using the ampC disk test (Black et al., 2005). In brief, a lawn of cefoxitin-susceptible E. coli ATCC 25922 was inoculated on the surface of a Mueller Hinton agar plate. A 30-μg cefoxitin disk was placed on the inoculated surface. A sterile filter paper disk was moistened by adding 20 μl of a 1:1 mixture of saline and 100 × Tris-EDTA (catalog code T-9285; Sigma-Aldrich Corporation, St. Louis, MO, United States). Several colonies of the test isolate were then applied to the disk. The disk was then positioned with its inoculated face in contact with the agar surface. After overnight incubation, a flattening or indentation of the zone of inhibition around the cefoxitin disk was considered a positive result, while an absence of distortion was considered a negative one. Furthermore, for the presumptive detection of carbapenemases, the carba NP test was performed as previously described (Bakour et al., 2015). A bacterium was characterized as being multi-drug-resistant when resistance to at least three classes of antibiotics was observed (Magiorakos et al., 2012).
Molecular Characterization of β-Lactamase Encoding Genes
All of the isolates that showed a key hole effect or had cefoxitin resistance with non-susceptibility to cefepime were subjected to real-time PCR analysis for the detection of SHV, TEM and CTX-M encoding genes (Roschanski et al., 2014). Simplex PCRs for the genes encoding AmpC β-lactamases FOX, MOX, ACC, EBC, DHA, and CMY were conducted for all strains showing non-susceptibility to cefoxitin (Dallenne et al., 2010). Simplex PCR was also used to test the ADC ampC β-lactamase gene in A. baumannii (Liu and Liu, 2015). DNA extraction was performed according to the manufacturer’s instructions using EZ1 DNA extraction kits (Qiagen, Courtaboeuf, France) with the EZ1 Advanced XL biorobot.
Multilocus Sequence Typing
One E. coli strain from each cluster shown in the MSP dendrogram was chosen, and MLST typing was performed based on allelic profiles to determine their evolutionary relationship (Peng and Zong, 2011). Seven housekeeping genes were used: adk, fumC, gyrB, icd, mdh, purA, and recA. Analysis of the genes’ allelic profiles was performed on the MLST1 to determine the sequence type (ST) to which each isolate belongs.
The prevalence, identification, and resistance profiles of isolated strains are all presented as the number (percentage).
Out of 982 collected fecal swabs, 203 (20.6%) showed growth on selective medium. In total, 235 strains were isolated. All 235 isolated Gram-negative bacilli were identified by MALDI TOF mass spectrometry with a score value ≥1.9. The distribution at the species level was as follows: 217 were identified as E. coli (92%), eight as K. pneumoniae (3%), three as Proteus mirabilis (1%), three as Enterobacter cloacae (1%), two as E. albertii, one as E. fergusonii and one as A. baumannii. The MSP dendrogram of the 217 E. coli isolates revealed five clusters at a distance level of 500 (arbitrarily selected) (Figure 1). Cluster 1 was mainly formed by isolates from the Akkar District. Cluster 2 contained two isolates: one from Saida and the other from Baalbek. Cluster 3 was composed of three strains isolated from Jabal Lebnen District. Cluster 4 was mainly composed of isolates from the North Lebanon district, and Cluster 5 contained only one strain from Saida.
Phenotypic Profiles of Resistance
The disk diffusion susceptibility testing results are summarized in Table 2. All of the isolates were susceptible to tigecycline, colistin and carbapenems. Phenotypic identification using the double disk synergy test, ampC disk test and carba NP test revealed that 102 (43.5%) of the isolated strains were ampC β-lactamase producers, 67 (28.5%) were ESBL producers, and 48 (20.5%) were co-producers of ESBL and ampC β-lactamases. Both ESBL and ESBL/ampC production were detected in E. coli, K. pneumoniae, E. fergusonii, and E. cloacae (Table 2), whereas only AmpC production was detected in E. coli, K. pneumoniae, P. mirabilis, E. albertii, and A. baumannii. In addition, 18 E. coli strains (7.5%) did not show a key hole effect and were resistant to cefoxitin but tested negative with the ampC disk test. Moreover, 32% of the isolated strains were co-resistant to gentamicin, ciprofloxacin, and trimethoprim-sulfamethoxazole, whereas 40% were resistant to at least two non-β-lactam antibiotics, 19.5% were resistant to only one non-β-lactam, and 8% were susceptible to all of the non-β-lactam antibiotics tested.
TABLE 2. Resistance profiles and phenotypes of multi-drug-resistant organisms isolated in this study.
Prevalence of MDR-GNB
The distribution of samples showing positive growth on the selective medium was as follows: 54 samples in the North District, 38 in the Akkar District, 37 in Saida, 26 in Bekaa, 24 in Jabal Lebnen, 16 in Baalbek and eight in Nabatieh. The number of positive samples from broilers exceeded the one obtained from Layers (176 vs. 27, respectively). Isolated strains (235) originated from 38 out of the 49 visited farms, i.e., 77.5% of the farms were positive for at least one multi-drug-resistant Gram-negative bacilli. As shown in Figure 2, the highest prevalence was detected in the north-west of the country, with 74 and 44 isolated strains for the North and Akkar Districts, respectively, whereas the lowest prevalence was detected in the north–east and south–east of Lebanon.
FIGURE 2. Prevalence of MDROs in Lebanese poultry farms. Prevalence is expressed as the “number of isolates (percentage).”
PCR Screening of CTX-M, SHV, TEM, and AmpC β-Lactamase Genes
One hundred and twelve isolates suspected to be ESBL producers were subjected to a real-time PCR assay for the detection of SHV, TEM, and CTX-M encoding genes. Of the 112 strains selected, 93 (83%) harbored the TEM gene, 59 (53%) the CTX-M gene and 22 (20%) the SHV gene. Overall, 49% (55) of the ESBL suspected isolates harbored only one gene, 46% (52) harbored at least two genes with the highest concordance being between the TEM and CTX-M genes, and 4% (five) showed the co-existence of all three genes together (Table 3). In parallel, 152 strains including 4 K. pneumoniae, 3 P. mirabilis, 2 E. albertii, and 143 E. coli were positive for blaCMY; whereas fifteen E. coli strains were negative fall ampC β-lactamase genes tested. Furthermore, in A. baumannii the ADC gene was detected.
TABLE 3. Characteristics of the different phenotypes/genotypes of ESBL and ESBL/AmpC producers found in this study.
The MLST typing of the strains, each chosen from the major district-related isolates grouped in each cluster, revealed that they belong to five different STs: ST156 for Cluster 1, ST5470 for Cluster 2, ST354 for Cluster 3, ST155 for Cluster 4 and ST3224 for Cluster 5.
Many years ago, hospitals and health care settings were regarded as the sole source of antimicrobial resistance. However, recent evidence has shown that food producing animals constitute a potent reservoir of multi-drug-resistant organisms (Belmahdi et al., 2016; Bachiri et al., 2017). This was mainly linked to the over-use of antimicrobial agents in veterinary medicine for treatment, growth promotion and prophylaxis (Economou and Gousia, 2015). Although the zoonotic transmission of multi-drug-resistant organisms from animals to humans remains controversial (Olsen et al., 2014), several studies have shown a direct link between direct contact with farm animals and the acquisition of bacterial resistance (Huijbers et al., 2014). One study conducted by Olaitan et al. (2015) demonstrated the zoonotic transmission of a colistin-resistant E. coli strain from a pig to its owner. This owner usually fed his pig without wearing any protective equipment. The two colistin-resistant isolates (in the pig and its owner) belonged to the same sequence type and presented with the same virulence and PFGE pattern (Olaitan et al., 2015).
In Lebanon, very few studies have looked at the prevalence of MDROs in farm animals (Al Bayssari et al., 2015a). Our study is the first epidemiological study in Lebanon quantifying the prevalence of multi-drug-resistant Gram-negative bacilli in chicken farms in terms of intestinal carriage at the national level. The prevalence is similar to the one previously reported from cattle (84%) in Lebanon (Diab et al., 2016). The flock’s size did not influence the prevalence of resistance in each farm (Table 1). On a global level, the prevalence found in our study is approximate to the one reported in Romania (69%) (Maciuca et al., 2015) and Ecuador (60%) (Ortega-Paredes et al., 2016) but is higher than the ones described in Germany (44%) (Kola et al., 2012), Japan (23%) (Kawamura et al., 2014), and Vietnam (3.2%) (Nguyen et al., 2015). Differences in the screening methodologies, sample size used and the level of antibiotic consumption in each country could explain these variations (Rhouma et al., 2016).
Escherichia coli was the most common multi-drug-resistant organism isolated; MALDI-TOF MSP dendrogram and MLST analysis revealed the presence of five clusters from which the representative strains belonged to different STs. Within each cluster, strains isolated from farms of the same district were grouped together; this is especially true for the Akkar and North Lebanon strains. This observation reveals that strains of the same region are closely related. Although PFGE is the standard method for the detection of clones, due to the large number of strains isolated in this study, PFGE typing was not performed; rather, we referred to the MSP dendrogram as a possible rapid tool for strain differentiation according to their geographical and/or phenotypic distribution in epidemiological studies as certain previous studies have suggested (Berrazeg et al., 2013; Khennouchi et al., 2015). With the exception of ST155, none of the sequence types identified in this study were among those frequently reported in chicken such as ST10, ST23, ST48, ST58, ST115, ST117, ST350, and ST648 (Olsen et al., 2014). However, looking at the Warwick E. coli MLST database, we found that the STs detected in our study were previously reported from livestock, cats and dogs, and humans. ST155 has been commonly reported in poultry (Pires-dos-Santos et al., 2013), and it appears to be associated with a zoonotic risk, which has been suggested by some studies (Lazarus et al., 2015). This emphasizes the hypothesis that MDROs in food-producing animals can be transmitted to humans and may be causative agents of infections with therapeutic challenges when high resistance is encountered. It should also be mentioned that clones in animals and humans are not always shared; some studies have shown that E. coli strains in food-producing animals differ from those reported in humans (Randall et al., 2012; Wu et al., 2013). This suggests that only some bacterial clones might be transmitted to the human population.
As our study showed, ESBL producers dominate the Lebanese poultry sector. The prevalence of ampC producers is also elevated (43.5%). ESBL and ampC-producing Gram-negative bacilli were previously reported in clinical and community settings in Lebanon (Dandachi et al., 2016). Molecular characterization revealed that 50% of isolated strains co-harbored at least two β-lactamase genes with the most common being CTX-M and TEM. Moreover, the only AmpC β-lactamase encoding gene was the CMY ampC β-lactamase. This gene was previously reported in poultry (Dierikx et al., 2013; El-Shazly et al., 2017) as well as in food producing animals (Sato et al., 2014; Aguilar-Montes de Oca et al., 2015) and healthy pets (Donati et al., 2014; Liu et al., 2016). As per the phenotypic and genotypic detection of AmpC production, these showed that there are some strains that were negative with the ampC disk test but positive for an ampC β-lactamase gene and vice-versa. Phenotypically false negatives shows the importance of the molecular testing in the detection of AmpC production. On the other hand, in the 15 E. coli strains that were negative for plasmidic ampC β-lactamase genes; one explanation for this might be due to an overexpression of the chromosomal ampC gene mediated by a mutation in the promoter/attenuator region as described in previous studies (Escudero et al., 2010; Haenni et al., 2014). Regarding non-β-lactam co-resistance in ESBL and/or ampC producers, antimicrobial resistance toward gentamicin was relatively high in this study. In fact, 66% of ESBL and/or ampC producing Gram-negative bacilli were gentamicin resistant. This could possibly be linked to the frequent use of this antibiotic in Lebanese farms as several studies have reported (El-Rami et al., 2012; Diab et al., 2016). One study conducted by Abdelnoor et al. (2013) found a significant association between gentamicin resistance in E. coli isolates and the use of this antimicrobial agent as a food additive in poultry in Lebanon. Another study launched a questionnaire-based survey on the most common antibiotics used in Lebanese livestock and found that gentamicin and streptomycin are the most common and heavily used antimicrobial agents (Kassaify et al., 2013). Another thing to mention is that in this study, no carbapenemase producers were detected. There might be two possible explanations for this: the first one is that carbapenemase producers are really scarce in Lebanese chicken farms; the second one is that these isolates were missed due to the medium used for the screening of multi-drug-resistant organisms. As has been reported, OXA-48 carbapenemase producers are frequently found in hospitals and nursing homes and in fowls in Lebanon (Al Bayssari et al., 2015b). OXA-48 carbapenemases do not always confer resistance to third-generation cephalosporins unless there is another mechanism of resistance that co-exists in the same bacterial cell (Poirel et al., 2012). Therefore, Oxacillinase producers could have been missed or under-estimated in our study.
Our study has two main limitations. The first one is that the primers used for blaTEM and blaSHV screening were universal, and thus, the possibility of having non-ESBL variants cannot be ruled out. However, as the strains presented with a typical ESBL phenotype, i.e., the key hole effect and resistance to penicillin, monobactams and third-generation cephalosporins with susceptibility to carbapenems, the TEM-positive strains were considered as ESBL producers and were included in the description of the MDR-GNB prevalence in this study. The second limitation is the low number of isolates subjected to MLST typing. MLST and PFGE analysis remain the gold standard for clone/cluster detection in epidemiological studies regardless of the number of strains (McGregor and Spratt, 2005; Zou et al., 2010).
Our study illustrates the current epidemiology of multi-drug-resistant Gram-negative bacilli in Lebanese chicken farms. ESBL and ampC producers cross-resistant to antibiotics used in human medicine are highly prevalent across the territory. Our study suggests that poultry farms are potent reservoirs of antimicrobial resistance in Lebanon. Although very few studies have reported the detection of carbapenemase producers in Lebanese Livestock (Al Bayssari et al., 2015a,b), it will likely only be a matter of time before these organisms become prevalent in Lebanese animal farms. This is especially true if no strict rules are implemented to control the overuse and misuse of antibiotics for treatment, growth promotion and prophylaxis in Lebanese agriculture. We believe that the prescription of antibiotics often used in human medicine should be reduced or even banned in the veterinary sector.
ID, ES, and ED conducted the phenotypic and molecular work. BE-B was responsible for the collection of the samples. EA, J-MR, and ZD reviewed and edited the manuscript.
This study was funded by the Lebanese Council for Research and the French Government under the “Investissements d’Avenir” (Investments for the Future) program managed by the Agence Nationale de la Recherche (ANR, fr: National Agency for Research) (reference: Méditerranée Infection 10-IAHU-03).
Conflict of Interest Statement
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
We would like to thank Dr. Hervé Chaudet for his assistance in the construction of the MSP dendrogram.
Abdelnoor, A. M., Chokr, S., Fayad, L., and Al-Akl, N. (2013). Review study on external-hospital bacteria as a source of infection and antimicrobial resistance in lebanon. Int. Arab. J. Antimicrob. Agents 3, 1–6.
Aguilar-Montes de Oca, S., Talavera-Rojas, M., Soriano-Vargas, E., Barba-Leon, J., and Vazquez-Navarrete, J. (2015). Determination of extended spectrum beta-lactamases/AmpC beta-lactamases and plasmid-mediated quinolone resistance in Escherichia coli isolates obtained from bovine carcasses in mexico. Trop. Anim. Health Prod. 47, 975–981. doi: 10.1007/s11250-015-0818-3
Al Bayssari, C., Dabboussi, F., Hamze, M., and Rolain, J. M. (2015a). Emergence of carbapenemase-producing Pseudomonas aeruginosa and Acinetobacter baumannii in livestock animals in lebanon. J. Antimicrob. Chemother. 70, 950–951. doi: 10.1093/jac/dku469
Al Bayssari, C., Olaitan, A. O., Dabboussi, F., Hamze, M., and Rolain, J. M. (2015b). Emergence of OXA-48-producing Escherichia coli clone ST38 in fowl. Antimicrob. Agents Chemother. 59, 745–746. doi: 10.1128/AAC.03552-14
Alonso, C. A., Zarazaga, M., Ben Sallem, R., Jouini, A., Ben Slama, K., and Torres, C. (2017). Antibiotic resistance in Escherichia coli in husbandry animals: the African perspective. Lett. Appl. Microbiol. 64, 318–334. doi: 10.1111/lam.12724
Bachiri, T., Bakour, S., Ladjouzi, R., Thongpan, L., Rolain, J. M., and Touati, A. (2017). High rates of CTX-M-15-producing Escherichia coli and Klebsiella pneumoniae in wild boars and barbary macaques in algeria. J. Glob. Antimicrob. Resist. 8, 35–40. doi: 10.1016/j.jgar.2016.10.005
Bakour, S., Garcia, V., Loucif, L., Brunel, J. M., Gharout-Sait, A., Touati, A., et al. (2015). Rapid identification of carbapenemase-producing Enterobacteriaceae, Pseudomonas aeruginosa and Acinetobacter baumannii using a modified Carba NP test. New Microbes New Infect. 7, 89–93. doi: 10.1016/j.nmni.2015.07.001
Baroud, M., Dandache, I., Araj, G. F., Wakim, R., Kanj, S., Kanafani, Z., et al. (2013). Underlying mechanisms of carbapenem resistance in extended-spectrum beta-lactamase-producing Klebsiella pneumoniae and Escherichia coli isolates at a tertiary care centre in lebanon: role of OXA-48 and NDM-1 carbapenemases. Int. J. Antimicrob. Agents 41, 75–79. doi: 10.1016/j.ijantimicag.2012.08.010
Belmahdi, M., Bakour, S., Al Bayssari, C., Touati, A., and Rolain, J. M. (2016). Molecular characterisation of extended-spectrum beta-lactamase- and plasmid AmpC-producing Escherichia coli strains isolated from broilers in bejaia, algeria. J. Glob. Antimicrob. Resist. 6, 108–112. doi: 10.1016/j.jgar.2016.04.006
Berrazeg, M., Diene, S. M., Drissi, M., Kempf, M., Richet, H., Landraud, L., et al. (2013). Biotyping of multidrug-resistant Klebsiella pneumoniae clinical isolates from france and algeria using MALDI-TOF MS. PLoS One 8:e61428. doi: 10.1371/journal.pone.0061428
Black, J. A., Moland, E. S., and Thomson, K. S. (2005). AmpC disk test for detection of plasmid-mediated AmpC disk test for detection of plasmid-mediated AmpC beta-lactamases in Enterobacteriaceae lacking chromosomal AmpC beta-lactamases. J. Clin. Microbiol. 43, 3110–3113. doi: 10.1128/JCM.43.7.3110-3113.2005
Chantziaras, I., Boyen, F., Callens, B., and Dewulf, J. (2014). Correlation between veterinary antimicrobial use and antimicrobial resistance in food-producing animals: a report on seven countries. J. Antimicrob. Chemother. 69, 827–834. doi: 10.1093/jac/dkt443
Dahms, C., Hubner, N. O., Wilke, F., and Kramer, A. (2014). Mini-review: epidemiology and zoonotic potential of multiresistant bacteria and clostridium difficile in livestock and food. GMS Hyg. Infect. Control 9:Doc21. doi: 10.3205/dgkh000241
Dallenne, C., Da Costa, A., Decre, D., Favier, C., and Arlet, G. (2010). Development of a set of multiplex PCR assays for the detection of genes encoding important beta-lactamases in Enterobacteriaceae. J. Antimicrob. Chemother. 65, 490–495. doi: 10.1093/jac/dkp498
Dandachi, I., Salem Sokhn, E., Najem, E., Azar, E., and Daoud, Z. (2016). Carriage of beta-lactamase-producing Enterobacteriaceae among nursing home residents in north lebanon. Int. J. Infect. Dis. 45, 24–31. doi: 10.1016/j.ijid.2016.02.007
Diab, M., Hamze, M., Madec, J. Y., and Haenni, M. (2016). High prevalence of non-ST131 CTX-M-15-producing Escherichia coli in healthy cattle in lebanon. Microb. Drug Resist. 23, 261–266. doi: 10.1089/mdr.2016.0019
Dierikx, C. M., van der Goot, J. A., Smith, H. E., Kant, A., and Mevius, D. J. (2013). Presence of ESBL/AmpC-producing Escherichia coli in the broiler production pyramid: a descriptive study. PLoS One 8:e79005. doi: 10.1371/journal.pone.0079005
Donati, V., Feltrin, F., Hendriksen, R. S., Svendsen, C. A., Cordaro, G., Garcia-Fernandez, A., et al. (2014). Extended-spectrum-beta-lactamases, AmpC beta-lactamases and plasmid mediated quinolone resistance in klebsiella spp. from companion animals in italy. PLoS One 9:e90564. doi: 10.1371/journal.pone.0090564
ECDC/EFSA/EMA (2017). ECDC/EFSA/EMA second joint report on the integrated analysis of the consumption of antimicrobial agents and occurrence of antimicrobial resistance in bacteria from humans and food-producing animals. Sci. Rep. 15:e04872. doi: 10.2903/j.efsa.2017.4872/epdf
El-Shazly, D. A., Nasef, S. A., Mahmoud, F. F., and Jonas, D. (2017). Expanded spectrum beta-lactamase producing Escherichia coli isolated from chickens with colibacillosis in Egypt. Poult. Sci. 96, 2375–2384. doi: 10.3382/ps/pew493
Escudero, E., Vinue, L., Teshager, T., Torres, C., and Moreno, M. A. (2010). Resistance mechanisms and farm-level distribution of fecal Escherichia coli isolates resistant to extended-spectrum cephalosporins in pigs in spain. Res. Vet. Sci. 88, 83–87. doi: 10.1016/j.rvsc.2009.05.021
European Committee on Antimicrobial Susceptibility Testing (2017). Breakpoint Tables for Interpretation of MICs and Zone Diameters, Version 7.1. Available at: http://www.eucast.org/fileadmin/src/media/PDFs/EUCAST_files/Breakpoint_tables/v_7.1_Breakpoint_Tables.pdf
Exner, M., Bhattacharya, S., Christiansen, B., Gebel, J., Goroncy-Bermes, P., Hartemann, P., et al. (2017). Antibiotic resistance: What is so special about multidrug-resistant gram-negative bacteria? GMS Hyg. Infect. Control 12:Doc05. doi: 10.3205/dgkh000290
Ghodousi, A., Bonura, C., Di Noto, A. M., and Mammina, C. (2015). Extended-spectrum ß-lactamase, AmpC-producing, and fluoroquinolone-resistant Escherichia coli in retail broiler chicken meat, Italy. Foodborne Pathog. Dis. 12, 619–625. doi: 10.1089/fpd.2015.1936
Gonzalez-Torralba, A., Oteo, J., Asenjo, A., Bautista, V., Fuentes, E., and Alos, J. I. (2016). Survey of carbapenemase-producing Enterobacteriaceae in companion dogs in madrid, spain. Antimicrob. Agents Chemother. 60, 2499–2501. doi: 10.1128/AAC.02383-15
Haenni, M., Chatre, P., and Madec, J. Y. (2014). Emergence of Escherichia coli producing extended-spectrum AmpC beta-lactamases (ESAC) in animals. Front. Microbiol. 5:53. doi: 10.3389/fmicb.2014.00053
Haenni, M., Saras, E., Ponsin, C., Dahmen, S., Petitjean, M., Hocquet, D., et al. (2016). High prevalence of international ESBL CTX-M-15-producing Enterobacter cloacae ST114 clone in animals. J. Antimicrob. Chemother. 71, 1497–1500. doi: 10.1093/jac/dkw006
Huijbers, P. M., Graat, E. A., Haenen, A. P., van Santen, M. G., van Essen-Zandbergen, A., Mevius, D. J., et al. (2014). Extended-spectrum and AmpC beta-lactamase-producing Escherichia coli in broilers and people living and/or working on broiler farms: prevalence, risk factors and molecular characteristics. J. Antimicrob. Chemother. 69, 2669–2675. doi: 10.1093/jac/dku178
Kassaify, Z., Abi-Khalil, P., and Sleiman, F. (2013). Quantification of antibiotic residues and determination of antimicrobial resistance profiles of microorganisms isolated from bovine milk in lebanon. Food Nutr. Sci. 4, 1–9. doi: 10.4236/fns.2013.47A001
Kawamura, K., Goto, K., Nakane, K., and Arakawa, Y. (2014). Molecular epidemiology of extended-spectrum beta-lactamases and Escherichia coli isolated from retail foods including chicken meat in Japan. Foodborne Pathog. Dis. 11, 104–110. doi: 10.1089/fpd.2013.1608
Kempf, I., Jouy, E., Granier, S. A., Chauvin, C., Sanders, P., Salvat, G., et al. (2015). Comment on “impact of antibiotic use in the swine industry”, by Mary D. Barton [Curr. Opin. Microbiol. 19 (June 2014) 9–15]. Curr. Opin. Microbiol. 26, 137–138. doi: 10.1016/j.mib.2015.06.013
Khennouchi, N. C., Loucif, L., Boutefnouchet, N., Allag, H., and Rolain, J. M. (2015). MALDI-TOF MS as a tool to detect a nosocomial outbreak of extended-spectrum-beta-lactamase- and ArmA methyltransferase-producing Enterobacter cloacae clinical isolates in algeria. Antimicrob. Agents Chemother. 59, 6477–6483. doi: 10.1128/AAC.00615-15
Kola, A., Kohler, C., Pfeifer, Y., Schwab, F., Kuhn, K., Schulz, K., et al. (2012). High prevalence of extended-spectrum-beta-lactamase-producing Enterobacteriaceae in organic and conventional retail chicken meat, Germany. J. Antimicrob. Chemother. 67, 2631–2634. doi: 10.1093/jac/dks295
Lazarus, B., Paterson, D. L., Mollinger, J. L., and Rogers, B. A. (2015). Do human extraintestinal Escherichia coli infections resistant to expanded-spectrum cephalosporins originate from food-producing animals? A systematic review. Clin. Infect. Dis. 60, 439–452. doi: 10.1093/cid/ciu785
Leverstein-van Hall, M. A., Dierikx, C. M., Cohen Stuart, J., Voets, G. M., van den Munckhof, M. P., van Essen-Zandbergen, A., et al. (2011). Dutch patients, retail chicken meat and poultry share the same ESBL genes, plasmids and strains. Clin. Microbiol. Infect. 17, 873–880. doi: 10.1111/j.1469-0691.2011.03497.x
Liu, X., Thungrat, K., and Boothe, D. M. (2016). Occurrence of OXA-48 carbapenemase and other beta-lactamase genes in ESBL-producing multidrug resistant Escherichia coli from dogs and cats in the United States, 2009-2013. Front. Microbiol. 7:1057. doi: 10.3389/fmicb.2016.01057
Maciuca, I. E., Williams, N. J., Tuchilus, C., Dorneanu, O., Guguianu, E., Carp-Carare, C., et al. (2015). High prevalence of Escherichia coli-producing CTX-M-15 extended-spectrum beta-lactamases in poultry and human clinical isolates in romania. Microb. Drug Resist. 21, 651–662. doi: 10.1089/mdr.2014.0248
Madec, J. Y., Haenni, M., Nordmann, P., and Poirel, L. (2017). Extended-spectrum beta-lactamase/AmpC- and carbapenemase-producing Enterobacteriaceae in animals: a threat for humans? Clin. Microbiol. Infect. 23, 826–833. doi: 10.1016/j.cmi.2017.01.013
Magiorakos, A. P., Srinivasan, A., Carey, R. B., Carmeli, Y., Falagas, M. E., Giske, C. G., et al. (2012). Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin. Microbiol. Infect. 18, 268–281. doi: 10.1111/j.1469-0691.2011.03570.x
McGregor, K. F., and Spratt, B. G. (2005). Identity and prevalence of multilocus sequence typing-defined clones of group A streptococci within a hospital setting. J. Clin. Microbiol. 43, 1963–1967. doi: 10.1128/JCM.43.4.1963-1967.2005
Moghnieh, R., Estaitieh, N., Mugharbil, A., Jisr, T., Abdallah, D. I., Ziade, F., et al. (2015). Third generation cephalosporin resistant Enterobacteriaceae and multidrug resistant gram-negative bacteria causing bacteremia in febrile neutropenia adult cancer patients in lebanon, broad spectrum antibiotics use as a major risk factor, and correlation with poor prognosis. Front. Cell Infect. Microbiol. 5:11. doi: 10.3389/fcimb.2015.00011
Nguyen, V. T., Carrique-Mas, J. J., Ngo, T. H., Ho, H. M., Ha, T. T., Campbell, J. I., et al. (2015). Prevalence and risk factors for carriage of antimicrobial-resistant Escherichia coli on household and small-scale chicken farms in the mekong delta of Vietnam. J. Antimicrob. Chemother. 70, 2144–2152. doi: 10.1093/jac/dkv053
Olaitan, A. O., Thongmalayvong, B., Akkhavong, K., Somphavong, S., Paboriboune, P., Khounsy, S., et al. (2015). Clonal transmission of a colistin-resistant Escherichia coli from a domesticated pig to a human in laos. J. Antimicrob. Chemother. 70, 3402–3404.
Olsen, R. H., Bisgaard, M., Lohren, U., Robineau, B., and Christensen, H. (2014). Extended-spectrum beta-lactamase-producing Escherichia coli isolated from poultry: a review of current problems, illustrated with some laboratory findings. Avian Pathol. 43, 199–208. doi: 10.1080/03079457.2014.907866
Ortega-Paredes, D., Barba, P., and Zurita, J. (2016). Colistin-resistant Escherichia coli clinical isolate harbouring the mcr-1 gene in Ecuador. Epidemiol. Infect. 144, 2967–2970. doi: 10.1017/S0950268816001369
Pires-dos-Santos, T., Bisgaard, M., and Christensen, H. (2013). Genetic diversity and virulence profiles of Escherichia coli causing salpingitis and peritonitis in broiler breeders. Vet. Microbiol. 162, 873–880. doi: 10.1016/j.vetmic.2012.11.008
Rafei, R., Hamze, M., Pailhories, H., Eveillard, M., Marsollier, L., Joly-Guillou, M. L., et al. (2015). Extrahuman epidemiology of Acinetobacter baumannii in lebanon. Appl. Environ. Microbiol. 81, 2359–2367. doi: 10.1128/AEM.03824-14
Randall, L., Wu, G., Phillips, N., Coldham, N., Mevius, D., and Teale, C. (2012). Virulence genes in blaCTX-M Escherichia coli isolates from chickens and humans. Res. Vet. Sci. 93, 23–27. doi: 10.1016/j.rvsc.2011.06.016
Rhouma, M., Beaudry, F., and Letellier, A. (2016). Resistance to colistin: What is the fate for this antibiotic in pig production? Int. J. Antimicrob. Agents 48, 119–126. doi: 10.1016/j.ijantimicag.2016.04.008
Roschanski, N., Fischer, J., Guerra, B., and Roesler, U. (2014). Development of a multiplex real-time PCR for the rapid detection of the predominant beta-lactamase genes CTX-M, SHV, TEM and CIT-type AmpCs in Enterobacteriaceae. PLoS One 9:e100956. doi: 10.1371/journal.pone.0100956
Sato, T., Okubo, T., Usui, M., Yokota, S., Izumiyama, S., and Tamura, Y. (2014). Association of veterinary third-generation cephalosporin use with the risk of emergence of extended-spectrum-cephalosporin resistance in Escherichia coli from dairy cattle in Japan. PLoS One 9:e96101. doi: 10.1371/journal.pone.0096101
Schill, F., Abdulmawjood, A., Klein, G., and Reich, F. (2017). Prevalence and characterization of extended-spectrum beta-lactamase (ESBL) and AmpC beta-lactamase producing Enterobacteriaceae in fresh pork meat at processing level in germany. Int. J. Food Microbiol. 257, 58–66. doi: 10.1016/j.ijfoodmicro.2017.06.010
Seiffert, S. N., Hilty, M., Perreten, V., and Endimiani, A. (2013). Extended-spectrum cephalosporin-resistant gram-negative organisms in livestock: an emerging problem for human health? Drug Resist. Updat. 16, 22–45. doi: 10.1016/j.drup.2012.12.001
Seng, P., Rolain, J. M., Fournier, P. E., La Scola, B., Drancourt, M., and Raoult, D. (2010). MALDI-TOF-mass spectrometry applications in clinical microbiology. Future Microbiol. 5, 1733–1754. doi: 10.2217/fmb.10.127
Singhal, N., Kumar, M., Kanaujia, P. K., and Virdi, J. S. (2015). MALDI-TOF mass spectrometry: an emerging technology for microbial identification and diagnosis. Front. Microbiol. 6:791. doi: 10.3389/fmicb.2015.00791
Wu, G., Day, M. J., Mafura, M. T., Nunez-Garcia, J., Fenner, J. J., Sharma, M., et al. (2013). Comparative analysis of ESBL-positive Escherichia coli isolates from animals and humans from the UK, the Netherlands and Germany. PLoS One 8:e75392. doi: 10.1371/journal.pone.0075392
Keywords: ampC, ESBL, E. coli, poultry, carriage
Citation: Dandachi I, Sokhn ES, Dahdouh EA, Azar E, El-Bazzal B, Rolain J-M and Daoud Z (2018) Prevalence and Characterization of Multi-Drug-Resistant Gram-Negative Bacilli Isolated From Lebanese Poultry: A Nationwide Study. Front. Microbiol. 9:550. doi: 10.3389/fmicb.2018.00550
Received: 02 December 2017; Accepted: 12 March 2018;
Published: 23 March 2018.
Edited by:Miklos Fuzi, Semmelweis University, Hungary
Reviewed by:Sebastian Guenther, University of Greifswald, Germany
Djamel Drider, Lille University of Science and Technology, France
Copyright © 2018 Dandachi, Sokhn, Dahdouh, Azar, El-Bazzal, Rolain and Daoud. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Ziad Daoud, email@example.com