Extended spectrum beta-lactamase and fluoroquinolone resistance genes among Escherichia coli and Salmonella isolates from children with diarrhea, Burkina Faso

Background The emergence and spread of multidrug-resistant gram-negative bacteria (MDR) has become a major public health concern worldwide. This resistance is caused by enzymes-mediated genes (i.e., extended spectrum beta-lactamases) that are common in certain Enterobacterioceae species. However, the distribution of these genes is poorly documented in Burkina Faso. This study aims to determine the prevalence and distribution of the resistant genes coding for broad spectrum beta-lactamases and quinolones in rural Burkina Faso. Methods Multiplex PCR assays were carried out to detect ESBL-encoding genes, including blaOXA, blaTEM, blaCTX-M, blaSHV. The assays also assessed the presence of quinolone resistance gene namely qnrA, qnrB and qnrS in the quinolone-resistance DEC and Salmonella strains. Results The Extended-Spectrum Beta-Lactamases (ESBL) resistance phenotype was reported in all the E. coli isolates (5/5). Cross-resistance phenotype to quinolones (CRQ) was shown by one Salmonella strain (1/9) and three E. coli (3/5). Cross-resistance phenotypes to fluoroquinolones (CRFQ) were harboured by one Salmonella (1/9) and carbapenemase phenotypes were detected in two E. coli strains (2/5). Whilst the blaOXA genes were detected in 100% (5/5) of E. coli isolates and in 33.33% (3/9) Salmonella isolates. One strain of E. coli (1/5) harbored the blaCTX−M gene and the qnrB gene simultaneously. Conclusions This study identified β-lactam (bla) and quinolone resistance (qnr) genes in multidrug-resistant E. coli and Salmonella spp. in rural Burkina Faso. Our finding which highlighted the enterobacteriaceae strains resistance to β-lactams and quinolones are of high interest for adequate management of antimicrobial resistant genes outbreak in Burkina Faso.


Background
Diarrheal disease is the second leading cause of death among children aged below 5 years [1]. These diseases are especially common in developing countries with poor hygiene and sanitation and with limited access to safe drinking water [2,3]. In our previous study, the overall prevalence of gastrointestinal infections was 19.7% in children group [4]. These infections are due to bacteria such as Escherichia coli and Salmonella which remain major contributors to acute enteric infection in children. However, the emergence and spread of multidrug-resistant gram-negative bacteria (MDR) has become a major public health concern worldwide [5]. Extended-spectrum beta-lactamases (ESBL) producing Enterobacteriaceae isolates, particularly in Escherichia coli, have been frequently reported in recent years at global scale [6][7][8]. Indeed, ESBL-producing Enterobacteriaceae (ESBL-PE) are associated with high morbidity and mortality rates, prolonged hospital stays and increased costs of healthcare [9,10]. Some studies have shown that ESBL are responsible for producing antibiotic-resistant bacteria strains [11,12]. The spread of the strains is likely to limit the effectiveness of antimicrobials used to treat the patients suffering from pathogen bacteria such as Escherichia coli and Salmonella [13][14][15][16]. These ESBL-producing bacteria often show resistance to several antimicrobials such as third and fourth generation cephalosporins as well as quinolones and aminoglycosides [17][18][19]. Although inhibited by clavulanic acid, ESBL enzymes have the ability to hydrolyze third generation cephalosporins and aztreonam [9].
The first ESBL strain which was a Klebsiella ozaenae resistant to oxyimino-cephalosporins was discovered in Germany [20]. In addition to β-lactams, fluoroquinolone resistance due to Qnr genes is emerging and this may pose a challenge in treatment of typhoid in future. These genes belong to the family of repeat pentapeptides that are capable of binding to DNA gyrase and topoisomerase IV, and thus protecting them from inhibitory activities of quinolones [21]. The resistance to quinolones (qnrA) mediated by plasmids in an isolate of Klebsiella pneumoniae was first reported in 1998 from the United States [22]. The excessive use of antibiotics, in particular βlactams, leads to the selection of ESBL producing strains [23]. However, in developing countries, E. coli identification and microbial drug resistance tests have been limited by phenotypic methods.
Although several antibiotic resistance gene studies have been carried out in Burkina Faso, these studies have been solely conducted in Ouagadougou and Bobo-Dioulasso's hospitals [24][25][26]. Therefore, the objective of the present study was to determine the prevalence and distribution of resistance gene coding for broad spectrum beta-lactamases and quinolones in two remote rural health centres (Boromo and Gourcy). The main economic activities in these communities are subsistence farming, animal husbandry and commercial activities [4]. Abuse of antibiotics use in animal husbandry has been highlighted in the country with prevalences of antimicrobial residues of 31% and 51.72% in meat and raw milk, respectively [27,28]. Although antimicrobial use for animals is under veterinary prescription control in Burkina Faso, farmers still use unprescribed antimicrobials as growth promoters or treatment for cattle, poultry and swine [29,30]. However, there are similarities between the antibiotics employed in agriculture and veterinary and those prescribed for humans in terms of types and mode of actions [31]. Therefore, consumption of contaminated animal-derived food products by residual antibiotics may pose serious public health concerns. In rural settings of Burkina Faso and in many parts of Africa where there is no enough healthcare facilities [32,33], a high rate of ESBL producing Enterobacteriaceae contaminations is expected among children which might lead to high infantine mortality rates.

Antimicrobial susceptibility test and ESBL production
Antibiotic susceptibility was determined on Mueller-Hinton agar using the standard disc diffusion procedure as described by the European Committee of Antimicrobial Susceptibility Testing (EUCAST) [38]. Nineteen antibiotics belonging to 7 different families were tested as shown in Table 1 (Bio-Rad, France). The diameters of the antibiotic sensitivity halos were recorded according to the EUCAST recommendations. Intermediate (I) susceptibility of pathovars was classified as resistant (R). A double synergy test was used for ESBL-producing strains testing. This consisted of placing discs (2-3 cm diameter) of ceftriaxone and cefotaxime around an amoxicillin-clavulanic acid disc on the bacterial plate.

Molecular identification of resistance genes
DNA extraction was performed using heating method [39]. A loopful of bacterial growth from Mueller Hinton agar (Liofilchem, Italy) plate was suspended in 1 ml of sterilized water. The mixture was boiled for 10 min at 100°C and centrifuged for 10 min at 12,000 rpm at + 4°C. Supernatant was then collected and used in the PCR reactions as DNA matrices. Multiplex PCR assays were performed to assess ESBL-encoding genes, including bla OXA , bla TEM , bla CTX−M , bla SHV and the presence of quinolone resistance genes including qnrA, qnrB, qnrS from the quinolone-resistant DEC and Salmonella strains. Primers (GeneCust, France) used for these amplifications are described in Table 2. The PCR assays were carried out in a 25 ml reaction mixture, which consisted of 2.5 µl of the supernatant added to 22.5 µl reaction mixture. This mixture contained 5U of Taq DNA polymerase (Accu Power, South Korea), deoxyribonucleic triphosphate (10 mM), buffer GC (10X), MgCl 2 (25 mM) and PCR primers (10 µM). Thermocycling conditions were as follows: 5 min at + 94°C, followed by 35 amplification cycles at + 94°C for 30 s, + 59 ± 4°C for 60 s and + 72°C for 60 s with a final extension of + 72°C for 10 min on a thermal cycler (AB Applied Biosystems). Following PCR, the reaction products were separated using electrophoresis in 1.5% agarose gel (weight/volume), stained with Redsaf solution (Prolabo, France) and visualized under UV light (Gel Logic 200) [39].

Antimicrobial resistance
At least, 5 diarrheagenic E. coli and 9 Salmonella strains were identified from our previous studies in 2019 and 2018 respectively. The strains of E. coli identified exhibited a strong resistance to beta-lactams with 100% resistant to amoxicillin-clavulanic acid and amoxicillin, 80% resistant to piperacillin, 60% resistant to cefotaxime, ceftriaxone, aztreonam, cefixime, cefepime and piperacillintazobactam. These strains were less resistant to quinolones, 60% resistant to nalidixic acid and no resistant to ciprofloxacin (Fig. 2). By contrast, the Salmonella strains exhibited 100 and 89% resistance to amoxicillin and amoxicillin-clavulanic acid, respectively. Likewise, the resistance of Salmonella to cefixime and cefepime, ceftriaxone and cefotaxime were 67 and 56%, respectively. Salmonella isolates harboured low resistance to quinolones (22% to nalidixic acid and 11% to ciprofloxacin) (Fig. 2).

Associated resistance phenotypes
The distribution of the associated resistance phenotypes is shown in Table 3. Extended-Spectrum Beta-Lactamases (ESBL) resistance phenotype was reported in all E. coli isolates (5/5). Cross-resistance phenotype to quinolones (CRQ) was shown by one Salmonella strain (1/9) and three E. coli (3/5). The Cross-resistance phenotypes to fluoroquinolones (CRFQ) were harboured by one Salmonella (1/9) and carbapenemase phenotypes were detected in two E. coli strains.

Characterization of β-lactamase and quinolones genes
Molecular characterization of E. coli and Salmonella isolates revealed that they harboured several ß-lactamase-    Table 2. The genes bla TEM , bla SHV , qnrA and qnrS were not found in this study.

Discussion
The current study was undertaken to screen the ESBL and fluoroquinolone resistance genes among E. coli and Salmonella isolated in children with diarrhea in two   These findings were consistent with previous studies in developing countries which showed a resistant rate greater than 50% [40]. This high resistance is likely due to the extensive and excessive clinical use of antibiotics.
Our study showed that all the E. coli isolates (5/5) were ESBL producers in agreement with 95.60% reported in Togo [41]. The presence of ESBL-producing bacteria in hospitals is a major challenge that affects both developed and developing countries [26]. It is known that β-Lactams (mainly extended-past spectrum cephalosporins and carbapenems) and fluoroquinolones constitute the main therapeutic choices to treat infections caused by Enterobacteriaceae. Although carbapenems are the most effective against Gram-positive and Gram-negative bacteria presenting a broad spectrum of antibacterial activity [42], our findings revealed a strong resistance to beta-lactams and moderate rates of resistance to quinolones in E. coli and Salmonella isolated. Indeed, Cross-resistance phenotypes to quinolones (CRQ), Cross-resistance phenotypes to fluoroquinolones (CRFQ) and carbapenemase phenotypes were associated with different rates to our Salmonella and E. coli strains. In agreement with our results, resistance to these compounds has been reported increasingly in several countries [11,43,44], limiting dramatically treatment options. Therefore, older agents, such aspolymyxins and fosfomycin, which were rarely implemented in the past because of efficacy and/or toxicity concerns, together with the newer tige-cycline, have become last-resort choices [42].
According to the existing data, this study is the first of kind on rural samples of Burkina Faso. However, it has been shown that fecal carriage of ESBL-PE isolates is one of the main drivers for their dissemination in hospital and community settings worldwide [45]. Because of this mode of diffusion, the ESBLs constitute a significant threat for the countries of West Africa wherè the weak socio-economic conditions result in poor hygienic conditions, promoting the spread of resistance. Indeed, most of the farms in Burkina Faso are mainly traditional with unhygienic practices [27]. Furtheremore, our previous study reported that the people in households mainly use well water as a source of drinking [34].
The present study showed that the bla OXA genes were the most common ß-lactamase-producing genes (57.14%), followed by bla CTX−M (7.14%). These findings contrast with those previously reported in Burkina Faso [8,26]. Otherwise, a spread of bla CTX−M , particularly CTX-M-15 in community and hospital settings has been reported [32,45,46]. This difference could be explained by the weakness of the number of multiresistant strains of enterobacteria tested in our study. On the other hand, we noted the simultaneous presence of the bla CTX−M and bla OXA genes in the same strain of E. coli. Our finding confirms the frequent association between bla CTX−M −15 and bla OXA−1 genes in ESBL-PE isolates which has been reported [45,[47][48][49]. This coexistence could reduce the therapeutic options for treatment with βlactam antibiotics. Thus, combined production of CTX-M and OXA enzymes by E. coli and K. pneumoniae improved resistance to b-lactamase inhibitors, presumably explaining their non-susceptibility to amoxicillin/clavulanate [45,49,50]. The genes bla TEM and bla SHV were not identified in the present study. In contrast, these genes have been previously reported in three major hospitals of Ouagadougou [26]. A future study based on more multiresistant strains producing ESBL would shed more light on the existence and prevalence of these genes among rural dwellings.
We also reported the prevalence of plasmid-mediated quinolone resistance in Salmonella and E. coli. Only a single isolate of E. coli (20%) was positive for the qnrB gene which is lower than 67.21% reported in Togo [41] and higher than 3.17% reported in Niger [51]. No Salmonella strain was positive for the qnr genes in the present study. In France, a study revealed 0.2% of qnrA in single isolate of Salmonella [52]. These results may indicate a low dissemination rate of qnr genes among human Salmonella and E. coli isolates. Morever, the E. coli strain that harbored qnrB gene was also positive to ESBL and carbapenemase phenotypes. Indeed, qnr are genes that confer resistance to nalidixic acid and reduced susceptibility to fluoroquinolones [53] and there is frequent association of genes coding for expandedspectrum b-lactamases (ESBLs) and these genes [52].
The main limitation of the present study consists of the low number of isolates which makes generalizability difficult. Further studies consisting of larger sample size than the number of multidrug-resistant isolates considered in the present study would be necessary. Despite this, the results of this study alert us to (i) the emergence and spread of antibiotic resistance in young children, (ii) the existence of bla and qnr genes in rural areas of Burkina Faso. In addition, the absence of these genes in certain investigated strains maybe due to other mechanisms of resistance to beta-lactams and quinolones.

Conclusions
This study characterized some bla and qnr genes circulating in rural settings that are characterized by their easy transfer between bacteria. The results should contribute to the establishment of a surveillance system for antibiotic resistance in Burkina Faso. Indeed, the data gathered is of paramount importance since it may contribute to design strategies to curtail the emergence and spread of ESBL-producing Enterobacteriaceae among children in rural Burkina Faso and devise innovative therapeutic approaches against multidrug-resistant strains. The intestinal carriage of ESBL-PE is a significant challenge for public health, and highlights the urgent necessity to improve sanitation and implement antibiotic stewardship in developing countries.