- Research article
- Open Access
First description of plasmid-mediated quinolone resistance determinants and β-lactamase encoding genes in non-typhoidal Salmonella isolated from humans, one companion animal and food in Romania
Gut Pathogensvolume 7, Article number: 16 (2015)
Gastroenteritis attributable to Salmonella enterica and the continuous increase in antimicrobial resistance of this gut pathogen, which compromises the use of previously effective treatments, is of great concern for public health. This study was conducted in order to investigate the presence of plasmid-mediated quinolone resistance (PMQR) determinants and β-lactamase-encoding genes, in S. enterica, isolated from humans, one companion animal and food. Moreover, the study aimed to identify potential vehicles of transmission of resistant strains to humans, with focus on food products (meat).
A total of 20 S. enterica isolates recovered from food (chicken and pork meat), one companion animal and humans (stool samples), were examined for their serotype, antimicrobial susceptibility and the presence of PMQR and β-lactamase-encoding genes. Moreover, the genetic relatedness of nine Salmonella Infantis and ten Salmonella Enteritidis isolates was analyzed by pulsed-field gel electrophoresis (PFGE).
Among all isolates, 15 (75%) were multidrug-resistant (MDR) and the majority of them proved to be resistant to nalidixic acid and fluoroquinolones (FQs) (ciprofloxacin and levofloxacin). Twelve isolates (60%) harboured at least one PMQR gene [qnrA, qnrB, qnrS, aac (6′)-Ib-cr or qepA] while seven isolates (35%) carried at least one β-lactamase-encoding gene (bla TEM, bla PSE-1, bla SHV or bla CTX-M). Moreover, two or more PMQR or β-lactamase-encoding genes co-existed in a single S. enterica isolate. A number of nine Salmonella Infantis, as well as the majority of Salmonella Enteritidis isolates analyzed by PFGE proved to be closely related.
The study demonstrated the co-existence of PMQR and β-lactamase-encoding genes among the Salmonella isolates recovered and confirmed that multiple mechanisms might be involved in the acquisition and spread of resistance determinants. The close genetic relatedness between the clinical and foodborne S. enterica isolates, suggested that chicken meat might be a possible cause of human salmonellosis in our country, during the study period. Results of this study might improve understanding of the antimicrobial resistance mechanisms and transmission dynamics of Salmonella spp. Here, we report for the first time the presence of PMQR and β-lactamase-encoding genes in S. enterica isolates, recovered from humans, one companion animal and food, in Romania.
Gastroenteritis attributable to Salmonella enterica represents a global public health burden . The main reservoir of S. enterica is the intestinal tract of many animal species and isolates are recovered from food and animal products such as meat from livestock, milk and eggs . In 2013, a total of 85,268 confirmed cases of human salmonellosis were reported in the European Union (EU), among which, a number of 1,404 cases being reported in Romania .
Most of Salmonella infections are self-limiting, however, antimicrobial treatment is required, especially for invasive infections or severe diarrhoea. FQs and extended-spectrum β-lactams (especially extended-spectrum cephalosporins) are often the antimicrobials of choice for treating salmonellosis. Normally, FQs are not recommended in the treatment of infections in paediatric patients, because of their potential to cause arthropathy. However, FQs are still considered one of the last treatment options for life-threatening Salmonella infections, caused by MDR isolates .
Massive usage of antimicrobial agents in livestock production and also in human disease, increased and favored the survival of MDR pathogens and resistant Salmonella isolates recovered from different sources have been frequently reported worldwide [5–14].
The increasing prevalence of MDR among Salmonella spp., not only against the first-line antimicrobials such as ampicillin, chloramphenicol and trimethoprim/sulfamethoxazole, but also, against antimicrobial agents classified by the World Health Organisation (WHO) as critically important for human medicine, such as FQs and third generation cephalosporins (which have been extensively used in human and veterinary medicine), is an important emerging public health problem [15, 16].
The production of β-lactamases is the primary cause of resistance to β-lactams in Gram-negative bacteria and more than 340 β-lactamases have been described and classified. The extended spectrum β-lactamases (ESBLs) belong to class A and many of these enzymes are encoded by genes such as bla TEM, bla PSE, bla PER, bla SHV, bla CTX-M and a few variants of bla OXA . Genes that encode β-lactamases can be located on the bacterial chromosome, plasmids, or transposable elements . The most important high level of resistance to FQs is due to mutations in one or more of the genes that encode the primary and secondary targets of these drugs, the type II topoisomerases (gyrA, gyrB, parC and parE) [8, 11].
Various genes encoding different resistance mechanisms and located on mobile genetic elements, can also decrease susceptibility to quinolones (Qs) and FQs. These are often encoded on plasmids and known as PMQR genes .
Several PMQR mechanisms have been described: the determinant Qnr, which includes genes such as qnrA, qnrB, qnrS, with several variants each, and qnrC and qnrD, that increase resistance to both nalidixic acid and FQs [19, 20]; the cr variant of the common aminoqlycoside acetyltransferase aac(6′)-Ib, which is capable of reducing the activity of certain FQs ; the QepA determinant, an efflux pump that confers decreased susceptibility to hydrophilic FQs; and the multi-resistance efflux pump OqxAB, that is also able to confer resistance to nalidixic acid and ciprofloxacin, among other antimicrobial agents .
Food may act as a vector for the transfer of antimicrobial resistant bacteria and antimicrobial resistance genes to humans . MDR bacteria can spread to humans either via the food supply (e.g., meat, fish, eggs and dairy products), via direct contact with animals or, more indirectly, through environmental pathways . The consequences of antimicrobial resistance are particularly important when pathogens are resistant to antimicrobials that are critically important in the treatment of human disease .
Few new antimicrobial drugs are now in development, mainly represented by Qs (nemonoxacin), FQs such as avarofloxacin, zabofloxacin, finofloxacin or delafloxacin, tetracyclines (omadacyline, eravacycline), as well as a few new β-lactamase inhibitors (avibactam, relebactam) . Therefore, considering that the success rate for drug development is low (at best, only 1 in 5 candidates that enter human testing will be approved for patients), maintaining the efficacy of the currently available antimicrobials is considered to be extremely important . Knowledge regarding mechanisms of resistance and the path of resistant strains, is necessary in order to understand the conditions where resistance is selected and persists.
Until now, in Romania, no study has focused on the occurrence of PMQR determinants and of β-lactamase-encoding genes among S. enterica isolates recovered from food, companion animals and humans.
Therefore, this study was conducted in order to investigate the presence of PMQR determinants and β-lactamase-encoding genes in S. enterica isolated from humans, one companion animal and food. Moreover, the study aimed to identify potential vehicles of transmission of such strains to humans, with focus on food products (especially meat).
Three different serotypes were identified among the recovered S. enterica isolates. The isolates consisted of ten isolates from stool samples of in-patients with diarrhea, nine food isolates (seven chicken meat and two pork meat) and one companion animal isolate, recovered from dog stool. Salmonella Enteritidis was the serotype most frequently detected (ten isolates, mainly recovered from human stool), followed by Salmonella Infantis (nine isolates, predominantly recovered from meat samples) and Salmonella Derby (one isolate) (Table 1).
In total, 14 (70%) of 20 isolates were resistant to nalidixic acid (MIC >64 μg/mL), 12 (60%) were resistant to ciprofloxacin (MIC 1–2 μg/mL), four isolates (20%) had reduced susceptibility to ciprofloxacin (MIC 0.5 μg/mL) and 16 isolates (80%) proved to be resistant to levofloxacin (MIC ≥2 μg/mL (Table 1).
Moreover, based on the β-lactams tested, seven isolates (35%) were resistant to ampicillin (MIC ≥32 μg/mL), 4 (20%) isolates were resistant to cefotaxime (MIC 4 μg/mL), 3 (15%) to piperacillin (MIC ≥128 μg/mL), while all isolates proved to be susceptible to ceftazidime (MIC 0.5–1 μg/mL) (Table 1).
A significant number of isolates were resistant to sulfamethoxazole (ten isolates, 50%; MIC >1,024 μg/mL) and nitrofurantoin (nine isolates, 45%; MIC >512 μg/mL).
A percentage of 15–35% of the isolates were resistant to other commonly used antimicrobials such as gentamicin, amikacin and tobramycin (three isolates, 15%; MIC 2 μg/mL), as well as trimethoprim (five isolates, 25%; MIC >32 μg/mL) and tetracycline (seven isolates, 20%; MIC >64 μg/mL).
The presence of PMQR and β-lactamase-encoding genes
The results regarding the presence of PMQR and β-lactamase encoding genes are presented in Table 1.
Prevalence of PMQR genes
Out of 20 Salmonella isolates, 12 (60%) harboured at least one PMQR gene, the qnr genes (qnrA and qnrS) as well as aac(6′)-Ib-cr gene being the most prevalent ones detected. A number of 6 (30%) isolates contained qnrA, while 5 (25%) isolates contained the qnrS or aac(6′)-Ib-cr genes.
Of the eleven isolates containing a qnr gene, 6 (30%) contained qnrA (three isolates from human stool samples, one isolate from pork meat and two isolates from chicken meat), 4 (20%) isolates harbored qnrB (two isolates from pork meat, one from human stool and the isolate from dog stool), while qnrS gene was detected in 5 (25%) isolates (two from chicken meat and three from human stool).
QepA gene was also detected in 4 (20%) isolates (three from chicken meat and one from dog stool).
All PMQR-bearing isolates were resistant to nalidixic acid and levofloxacin and were also resistant or had reduced susceptibility to ciprofloxacin.
Occurrence of β-lactamase-encoding genes
Of the 20 Salmonella isolates, 7 (35%) carried at least one β-lactamase-encoding gene. Among these, 4 (20%) isolates carried bla PSE-1 gene and 3 (15%) isolates carried bla SHV, bla TEM and bla CTX-M genes. The bla OXA gene was not identified in any of the isolates.
Two chicken meat isolates harbored both bla PSE-1 and bla CTX-M genes (isolate 2 and 9). One human isolate carried bla PSE-1, bla TEM and bla SHV (isolate 15), while the isolate from dog stool (isolate 20) carried bla PSE-1, bla TEM as well as bla CTX-M.
Almost all isolates carrying β-lactamase-encoding genes were also PMQR genes containing isolates, with the exception of a single human isolate.
Genetic relatedness of Salmonella isolates
After digestion by XbaI enzyme, the genetic relatedness of nine Salmonella Infantis and ten Salmonella Enteritidis isolates was evaluated by PFGE. All isolates were typable by applying this method.
Two XbaI-PFGE profiles showing 97% similarity have been identified among nine Salmonella Infantis isolates originating from different sources, including chicken and pork meat, as well as animal (dog) and human stool (Figure 1).
All nine Salmonella Infantis isolates were closely related, differing only by one band (Figure 1). One human isolate (isolate 19) and also the isolate from dog stool (isolate 20) displayed the same PFGE profile as four chicken meat isolates (isolates 1, 2, 4 and 9).
Salmonella Enteritidis isolates recovered from humans and food (chicken meat) revealed four XbaI-PFGE profiles. One isolate from chicken meat (isolate 3) showed indistinguishable band pattern with that of three human isolates (isolates 10, 14 and 18) (Figure 2).
The majority of the isolates proved to be closely related, showing a similarity of 88%, with the exception of one human isolate (isolate 17) (Figure 2).
In this study, 20 S. enterica isolates recovered from food (chicken and pork meat), one companion animal and humans (stool samples) were examined for their serotype, antimicrobial susceptibility and the presence of PMQR and β-lactamase-encoding genes. Moreover, the genetic relatedness of nine Salmonella Infantis and ten Salmonella Enteritidis isolates was analyzed by PFGE.
Three different serotypes were identified among the Salmonella isolates studied: Salmonella Enteritidis, Salmonella Infantis and Salmonella Derby. Salmonella Enteritidis was also the serotype most frequently detected among the human isolates, this being an important serovar causing non-typhoidal gastroenteritis in humans, in Europe .
In 2013, Romania reported a number of 1,404 cases of human salmonellosis (Salmonella Enteritidis being one of the two most commonly reported Salmonella serovars from cases of human infection, in Europe, in 2013) and one of the highest hospitalization proportions in the EU (80–95% of the cases being hospitalized). Interestingly, Romania is also one of the countries that reported the lowest notification rate of salmonellosis (6.5/100.000), which indicates that the surveillance system primarily captures the more severe cases .
In a previous study we reported that 70.87% of a total of 149 Salmonella isolates recovered from chicken and pork meat in Romania were serotyped as S. enterica subsp. enterica serovar Infantis. In this study, 45% of the isolates also belonged to Salmonella Infantis, being mostly recovered from food samples (chicken and pork meat) .
Among all isolates, 15 (75%) were MDR, exhibiting resistance to more than three antimicrobials, while three isolates (15%) proved to be susceptible to all the antimicrobials tested.
Of specific concern is the fact that the majority of the isolates proved to be resistant to Qs (nalidixic acid) and FQs (ciprofloxacin and levofloxacin). Qs and FQs are potent, broad-spectrum antimicrobial agents, commonly used in the treatment of infections in both humans and animals, being also used as prophylactic agents in food producing animals. Moreover FQs are included in the WHO’s list of critically important antimicrobials for human medicine . In current human medical practice, the most commonly prescribed FQs are ciprofloxacin, levofloxacin and moxifloxacin. Despite prescribing guidelines recommending the prudent use of such antimicrobials, resistance continues to rise, as it was proven also in our study. Not only a high percentage of human isolates proved to be resistant to Qs and FQs, which was somehow expected, taking into consideration the extensive use of these agents in human medicine, but high resistance rates were also identified in the case of the meat isolates (Table 1). This could be explained by the fact that enrofloxacin is the second most used antimicrobial in veterinary practice in Romania (after tetracycline) and cross resistance among enrofloxacin, ciprofloxacin and other FQs has been noted .
In our country little information is available regarding antimicrobial susceptibility in Salmonella spp. isolated from food products, notification being mandatory only in poultry and for findings of Salmonella Enteritidis and Salmonella Typhimurium .
Resistance to β-lactams has also been observed in our study, 35% of the isolates being resistant to ampicillin and 15% to piperacillin. A number of four isolates (among which three from humans) proved to be resistant to cefotaxime, a third-generation cephalosporin.
The dramatic increase of the emergence and transmission of strains that are resistant to FQs and cephalosporins is considered to be an important public health concern.
Among the 20 isolates recovered, PMQR genes were found in 12 (60%). The prevalence and diversity of PMQR genes in this study is higher [qnrA, qnrB, qnrS, aac (6′)-Ib-cr and qepA] than reported for Salmonella isolates recovered from humans, animals and food in 13 European countries .
The most prevalent genes detected were represented by the qnr genes (qnrA and qnrS), as well as aac(6′)-Ib-cr gene. Although qnrA gene is more prevalent in E. coli, Klebsiella spp., or other Enterobacteriaceae, it has been rarely found in Salmonella in Europe [29, 30].
In general, PMQR mechanisms have been shown to reduce susceptibility to FQs and are considered to provide only a low level of resistance. However, their presence may stimulate mutations in genes encoding for DNA gyrase and toposiomerase IV .
Qnr determinants have been related to an enhanced facility to develop full resistance to Qs and FQs [32, 33], in agreement with the fact that decreased resistance levels to FQs favor the acquisition of full resistance to these agents . Furthermore, two or more PMQR genes co-existing in a single isolate were frequently detected in our study (Table 1).
Five isolates harboured one of the qnr genes as well as the one that encodes aminoglycoside acetyltransferase, namely aac(6′)-Ib-cr, all being resistant to nalidixic acid, ciprofloxacin and levofloxacin (one isolate displayed intermediate susceptibility to ciprofloxacin). Although the expression of aac(6′)-Ib-cr alone is insufficient to cause complete ciprofloxacin resistance, when combined with the presence of qnr, its expression could result in ciprofloxacin resistance . This might explain the high percentage of nalidixic acid and ciprofloxacin/levofloxacin resistant Salmonella isolates containing qnr and aac(6′)-Ib-cr genes.
Additional analysis would be necessary to reveal other possible resistance mechanisms such as point mutations in the quinolone resistance determining region (QRDR) or even the presence of new undetected PMQR genes.
Out of the 20 Salmonella enterica isolates recovered, 7 (35%) carried at least one β-lactamase-encoding gene (bla TEM, bla PSE-1, bla SHV or bla CTX-M).
Three isolates also produced CTX-M type β-lactamases and proved to be resistant to cefotaxime. The CTX-M type β-lactamases have proved by far the most successful in disseminating in the clinical setting and have overall become the most prevalent ESBLs worldwide .
Of concern, we note that almost all isolates carrying a β-lactamase encoding gene also harboured PMQR genes.
PMQR genes are often carried on plasmids with other antimicrobial resistance genes, notably, genes encoding ESBLs. The carriage of PMQR genes, in association with other resistance genes, has been shown to influence the development of resistance to FQs, even in the absence of FQs drug pressure. Exposure to non-quinolone antimicrobials can favor persistance of PMQR determinants and consequent decreased susceptibility to FQs .
Recently, Vien et al. demonstrated that, after treatment for respiratory disease in Vietnam with non-quinolone antibiotics, there was significant enrichment for the carriage of PMQR genes in the gut flora of patients, even within days of treatment commencing. This was postulated to be due to co-selection of mobile genetic elements carrying multiple antimicrobial-resistance genes .
PFGE is considered to be a highly discriminative subtyping method in epidemiological investigation of many bacterial pathogens .
PFGE results in this study suggested that Salmonella isolates in each analysed serovar were closely related.
Among the Salmonella Infantis isolates, one human isolate (isolate 19) and also the isolate from dog stool (isolate 20) displayed the same PFGE profile as four chicken meat isolates (namely, isolate 1, 2, 4 and 9) (Figure 1). All of these isolates were highly resistant to antimicrobials and carried diverse PMQR and β-lactamase encoding genes. Among these, the human isolate 19, the isolate from dog stool (isolate 20) as well as one isolate from chicken meat (isolate 9), presented almost the same resistance pattern (NAL, CIP, LEV, AMP, PIP, CTX, GEN, AMK, TOB, NIT), with the exception of the chicken meat isolate, which proved to be resistant also to SMX and TET. Furthermore, these three isolates carried common PMQR and β-lactamase encoding genes, such as: bla PSE-1, bla CTX-M and qnrS (Table 1). Isolates carrying the same antimicrobial resistance genes, and also belonging to the same PFGE profile, therefore being closely related, suggest the fact that clonal spread may be responsible for the dissemination of resistance determinants amongst the Salmonella Infantis isolates.
One Salmonella Enteritidis isolate from chicken meat (isolate 3) showed an identical band pattern with that of three Salmonella Enteritidis isolates recovered from human stool (isolates 10, 14 and 18) (Figure 2). Two of these human isolates (isolate 10 and 18) presented an identical resistance pattern (NAL, CIP, LEV, NIT, SMX) and both carried PMQR genes such as qnrA, qnrB, qnrS and aac6′(Ib)-cr (Table 1).
The close genetic relatedness identified between the chicken meat isolates and the Salmonella Infantis and Enteritidis human isolates indicate that chicken meat could be a possible source for infection with these serovars.
Food is generally considered to be the most important vector for the spread of resistance between humans and animals . Foods contaminated with antimicrobial resistant bacteria could be a major threat to public health, as there is the distinct possibility that genes encoding antibiotic resistance determinants, that are carried on mobile genetic elements, may be transferred to other commensal or pathogenic bacteria of human clinical significance .
There is little information regarding the prevalence of antimicrobial resistance in Salmonella spp., isolated from companion animals in many countries and no such related data has been published in Romania.
Taking into consideration the shared environment of humans and companion animals, transfer of resistant bacteria and even antimicrobial resistance genes between companion animals and humans is more likely to occur and has been indicated in some studies [42, 43].
In conclusion, to our knowledge, this is the first study reporting the presence of PMQR and β-lactamase-encoding genes in Salmonella isolates recovered from humans, a companion animal and food and also describing the potential role of chicken meat in human non-typhoidal Salmonella, in Romania.
The study demonstrated the co-existence of PMQR and β-lactamase-encoding genes among the Salmonella isolates recovered and confirmed that multiple mechanisms might be involved in the acquisition and spread of resistance determinants.
The close genetic relatedness between the clinical and foodborne Salmonella isolates suggested that chicken meat might be a possible cause of human salmonellosis in our country, during the study period.
Admittedly, due to the limited number of isolates analysed, we are aware of the fact that the inclusion of more strains, especially isolated from different food sources, would be recommended in future studies, in order to accurately reflect the dissemination of MDR Salmonella isolates from food to humans. Moreover, further studies are needed to estimate the load of non-thypoidal Salmonella clinical cases, attributable to different identified food-originating serovars and to estimate the risk of the consumption of foods contaminated with MDR Salmonella carrying antimicrobial resistance determinants.
Results of this study might improve understanding of the antimicrobial resistance mechanisms and transmission dynamics of Salmonella isolates and highlight the importance of serious monitoring, thus aiding in stimulating the implementation of a continuous, integrated surveillance program at national level.
Salmonella enterica isolates obtained in Romania from different sources, between March and August 2014, were investigated by pheno-and genotyping methods. The repertoire of antimicrobial resistance genes was determined by PCR.
A total of 20 geographically representative S. enterica isolates were recovered from humans (10 isolates from stool samples of in-patients with diarrhea), food isolates (seven chicken meat and two pork meat) and one companion animal (dog stool).
The majority of the isolates were isolated independently, between March and August 2014, at different points in time, from separate food samples or human clinical cases, respectively. Three isolates (one from chicken meat, one from a stool sample and the isolate from dog stool) were epidemiologically linked.
Salmonella spp., were isolated by previously homogenizing the samples (25 g) in buffered peptone water (225 mL) with a laboratory blender (Stomacher 400, England), for approximately 2 min. After incubation for 18–24 h at 37°C, 0.1 mL was inoculated in 10 mL Rappaport–Vassiliadis (RV) green broth (LabM Limited, England) and incubated for 18–24 h at 42°C. Another 1 mL from the culture obtained was inoculated into 10 mL of selenite cysteine (SC) broth (LabM Limited, England) and incubated at 37°C for 18–24 h. From both enrichment broths obtained, 1 mL was streaked onto brilliant green-phenol red-lactose-sucrose (BPLS) agar (Merck, Germany) and xylose lysine deoxycholate (XLD) agar (Oxoid, England). Following the incubation at 37°C for 24 h, presumptive Salmonella colonies were characterized by their biochemical properties through slide agglutination, using standard protocols. The positive colonies where then identified as Salmonella by using the Sensititre Automated Microbiology System Aris 2X (Thermo Scientific, England) following the protocol stated by the producer.
All strains of Salmonella spp., were confirmed by PCR, following the protocol reported in a previous study .
All isolates of S. enterica included in the study were serotyped by serological identification of somatic (O) and flagellar (H) antigens, with commercially available antisera-Salmonella Antisera test group (Denka Seiken Co., England), according to the Kauffman-White serotyping scheme.
Antimicrobial susceptibility testing
MICs were determined by using the reference broth microdilution method, according to the guidelines recommended by the Clinical and Laboratory Standards Institute (CLSI) . The following antimicrobials were tested: ampicillin (AMP), piperacillin (PIP), cefotaxime (CTX), ceftazidime (CAZ), nalidixic acid (NAL), ciprofloxacin (CIP), levofloxacin (LEV), gentamicin (GEN), amikacin (AMK), tobramycin (TOB), nitrofurantoin (NIT), sulfamethoxazole (SMX), trimethoprim (TMP) and tetracycline (TET). The control strain used was E. coli ATCC 25922.
The breakpoints for the interpretation of resistance and susceptibility were determined according to the interpretive standards provided by the CLSI .
Detection of PMQR determinants and of β-lactamase-encoding genes
All isolates were investigated for the presence of qnr (qnrA, qnrB, qnrS), aac (6′)-Ib-cr and qepA determinants and of bla TEM, bla PSE-1, bla OXA, bla SHV and bla CTX-M genes, through PCR amplification, using specific primers, previously reported [35, 45–51] (Table 2).
DNA was extracted from approximately 10–12 single colonies with the Isolate II DNA kit (Bioline, Germany), as specified by the manufacturer. DNA quantities and purities were assessed on a Nanodrop ND-1000 spectrophotometer analyzer (NanoDrop Technologies, Inc., Wilmington, DE, USA). Each sample was adjusted to a concentration of approximately 20 ng/µl in order to perform the PCR.
Single PCR amplifications were performed in a 25 μL reaction mixture containing approximately 10 ng of template DNA and 2.5 pmol of each primer. The amplification protocol followed the steps accordingly: initial denaturation at 94°C for 3 min, followed by 30 cycles of amplification at 94°C for 45 s, annealing at 58°C for 30 s, and extension at 72°C for 30 s (except for the final cycle, which had an extension step of 5 min). The PCR products were analyzed on a 1.5% agarose gel.
Genetic relatedness of Salmonella isolates
In order to determine the genetic relatedness of the S. enterica isolates, nine Salmonella Infantis and ten Salmonella Enteritidis isolates included in the study were analyzed by PFGE, according to PulseNet protocol  and previously described by Usein et al. .
Briefly, chromosomal DNA was digested with XbaI enzyme (Roche) and the DNA macrorestriction fragments were separated by electrophoresis, using a CHEF Mapper electrophoresis system (Bio-Rad, CA, USA), with pulse times of 2.16–63.8 s, during a 19 h run. Salmonella Braenderup H9812 was used as control strain.
The analyses of the gel images were carried out in BioNumerics v6.6.4 (Applied Maths, Kortrijk, Belgium). The comparisons were made by cluster analysis using Dice coefficient and dendrograms were generated using the unweighted-pair group method using average linkages (UPGMA) and a position tolerance of 1.5%.
Different profiles were assigned to XbaI-PFGE types according to differences in the band patterns, which were interpreted according to the criteria proposed by Tenover et al. .
Hendriksen RS, Vieira AR, Karlsmose S, Lo Fo Wong DMA, Jensen AB, Wegener HC et al (2011) Global monitoring of Salmonella serovar distribution from the World Health Organization Global Foodborne Infections Network Country Data Bank: results of quality assured laboratories from 2001 to 2007. Foodborne Pathog Dis 8(8):887–900
Swaminathan B, Gerner-Smidt P, Barrett T (2006) Focus on Salmonella. Foodborne Pathog Dis 3(2):154–156
EFSA/ECDC (2015) The European Union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2013. EFSA J 13(1):3991
Cui S, Li J, Sun Z, Hu C, Jin S, Li F et al (2009) Characterization of Salmonella enterica isolates from infants and toddlers in Wuhan, China. J Antimicrob Chemother 63(1):87–94
Mihaiu L, Lapusan A, Tanasuica R, Sobolu R, Mihaiu R, Oniga O et al (2014) First study of Salmonella in meat in Romania. J Infect Dev Ctries 8:50–58
Clemente L, Manageiro V, Ferreira E, Jones-Dias D, Correia I, Themudo P et al (2013) Occurrence of extended-spectrum β-lactamases among isolates of Salmonella enterica subsp. enterica from food-producing animals and food products, in Portugal. Int J Food Microbiol 167(2):221–228
Dionisi AM, Lucarelli C, Benedetti I, Owczarek S, Luzzi I (2011) Molecular characterisation of multidrug-resistant Salmonella enterica serotype Infantis from humans, animals and the environment in Italy. Int J Antimicrob Agents 38(5):384–389
Kozoderović G, Velhner M, Jelesić Z, Golić N, Lozo J, Kehrenberg C (2012) Prevalence of quinolone resistance and mutations in the topoisomerase genes in Salmonella enterica serotype Enteritidis isolates from Serbia. Int J Antimicrob Agents 40:455–457
Jiang HX, Song L, Liu J, Zhang XH, Ren YN, Zhang WH et al (2014) Multiple transmissible genes encoding fluoroquinolone and third-generation cephalosporin resistance co-located in non-typhoidal Salmonella isolated from food-producing animals in China. Int J Antimicrob Agents 43(3):242–247
Wang Y, Yang B, Wu Y, Zhang Z, Meng X, Xi M et al (2015) Molecular characterization of Salmonella enterica serovar Enteritidis on retail raw poultry in six provinces and two National cities in China. Food Microbiol 46:74–80
Wasyl D, Hoszowski A, Zajac M (2014) Prevalence and characterisation of quinolone resistance mechanisms in Salmonella spp. Vet Microbiol 171:307–314
Toboldt A, Tietze E, Helmuth R, Junker E, Fruth A, Malorny B (2014) Molecular epidemiology of Salmonella enterica serovar Kottbus isolated in Germany from humans, food and animals. Vet Microbiol 170(1–2):97–108
Dan SD, Tabaran A, Mihaiu L, Mihaiu M (2015) Antibiotic susceptibility and prevalence of foodborne pathogens in poultry meat in Romania. J Infect Dev Ctries 9(1):35–41
Afema JA, Mather AE, Sischo WM (2014) Antimicrobial resistance profiles and diversity in Salmonella from humans and cattle, 2004–2011. Zoonoses Public Health. doi:10.1111/zph.12172
Lunguya O, Lejon V, Phoba M-F, Bertrand S, Vanhoof R, Glupczynski Y et al (2013) Antimicrobial resistance in invasive non-typhoid Salmonella from the Democratic Republic of the Congo: emergence of decreased fluoroquinolone susceptibility and extended-spectrum beta lactamases. PLoS Negl Trop Dis 7(3):e2103
WHO (2011) Critically important antimicrobials for human medicine, 3rd revision. World Health Organization, Geneva
Arlet G, Barrett TJ, Butaye P, Cloeckaert A, Mulvey MR, White DG (2006) Salmonella resistant to extended-spectrum cephalosporins: prevalence and epidemiology. Microbes Infect 8(7):1945–1954
Ruiz J, Pons MJ, Gomes C (2012) Transferable mechanisms of quinolone resistance. Int J Antimicrob Agents 40:196–203
Jacoby GA, Walsh KE, Mills DM, Walker VJ, Oh H, Robicsek A et al (2006) qnrB, another plasmid-mediated gene for quinolone resistance. Antimicrob Agents Chemother 50(4):1178–1182
Wang M, Guo Q, Xu X, Wang X, Ye X, Wu S et al (2009) New plasmid-mediated quinolone resistance gene, qnrC, found in a clinical isolate of Proteus mirabilis. Antimicrob Agents Chemother 53(5):1892–1897
Robicsek A, Strahilevitz J, Sahm DF, Jacoby GA, Hooper DC (2006) qnr prevalence in ceftazidime-resistant Enterobacteriaceae isolates from the United States. Antimicrob Agents Chemother 50(8):2872–2874
Poirel L, Cattoir V, Nordmann P (2012) Plasmid-mediated quinolone resistance; interactions between human, animal, and environmental ecologies. Front Microbiol 3:24
Verraes C, Van Boxstael S, Van Meervenne E, Van Coillie E, Butaye P, Catry B et al (2013) Antimicrobial resistance in the food chain: a review. Int J Environ Res Public Health 10(7):2643–2669
Angulo FJ, Nargund VN, Chiller TC (2004) Evidence of an association between use of anti-microbial agents in food animals and anti-microbial resistance among bacteria isolated from humans and the human health consequences of such resistance. J Vet Med B Infect Dis Vet Public Health 51(8–9):374–379
Antibiotics curently in clinical development [Internet]. Available from: http://www.pewtrusts.org/en/multimedia/data-visualizations/2014/antibiotics-currently-in-clinical-development
Barua H, Biswas PK, Talukder KA, Olsen KEP, Christensen JP (2014) Poultry as a possible source of non-typhoidal Salmonella enterica serovars in humans in bangladesh. Vet Microbiol 168(2–4):372–380
Threlfall EJ, Ward LR, Rowe B (1999) Resistance to ciprofioxacin in non-typhoidal Salmonellas from humans in England and Wales—the current situation. Clin Microbiol Infect 5(3):130–134
EFSA (2012) Scientific of EFSA and ECDC: the European union summary report on trends and sources of zoonoses, zoonotic agents and food-borne outbreaks in 2010. EFSA J 10(3):2597
Veldman K, Cavaco LM, Mevius D, Battisti A, Franco A, Botteldoorn N et al (2011) International collaborative study on the occurrence of plasmid-mediated quinolone resistance in Salmonella enterica and Escherichia coli isolated from animals, humans, food and the environment in 13 European countries. J Antimicrob Chemother 66:1278–1286
Strahilevitz J, Jacoby GA, Hooper DC, Robicsek A (2009) Plasmid-mediated quinolone resistance: a multifaceted threat. Clin Microbiol Rev 22(4):664–689
Kim KY, Park JH, Kwak HS, Woo GJ (2011) Characterization of the quinolone resistance mechanism in foodborne Salmonella isolates with high nalidixic acid resistance. Int J Food Microbiol 146(1):52–56
Martínez-Martínez L, Pascual A, Jacoby GA (1998) Quinolone resistance from a transferable plasmid. Lancet 351(9105):797–799
Briales A, Rodríguez-Martínez JM, Velasco C, Díaz de Alba P, Domínguez-Herrera J, Pachón J et al (2011) In vitro effect of qnrA1, qnrB1, and qnrS1 genes on fluoroquinolone activity against isogenic Escherichia coli isolates with mutations in gyrA and parC. Antimicrob Agents Chemother 55(3):1266–1269
Ruiz J, Pons MJ, Gomes C (2012) Transferable mechanisms of quinolone resistance. Int J Antimicrob Agents 40(3):196–203
Robicsek A, Strahilevitz J, Sahm DF, Jacoby G, Hooper DC (2006) qnr prevalence in ceftazidime-resistant Enterobacteriaceae isolates from the United States. Antimicrob Agents Chemother 50(8):2872–2874
D’Andrea MM, Arena F, Pallecchi L, Rossolini GM (2013) CTX-M-type β-lactamases: a successful story of antibiotic resistance. Int J Med Microbiol 303(6–7):305–317
Yang T, Zeng Z, Rao L, Chen X, He D, Lv L et al (2014) The association between occurrence of plasmid-mediated quinolone resistance and ciprofloxacin resistance in Escherichia coli isolates of different origins. Vet Microbiol 170(1–2):89–96
Vien LTM, Minh NNQ, Thuong TC, Khuong HD, Nga TVT, Thompson C et al (2012) The co-selection of fluoroquinolone resistance genes in the gut flora of Vietnamese children. PLoS One 7(8):e42919
Yang B, Wang Q, Cui S, Wang Y, Shi C, Xia X et al (2014) Characterization of extended-spectrum beta-lactamases-producing Salmonella strains isolated from retail foods in Shaanxi and Henan Province, China. Food Microbiol 42:14–18
WHO (2007) Critically important antimicrobials for human medicine: categorization for the development of risk management strategies to contain antimicrobial resistance due to non human antimicrobial use: report of the second WHO Expert Meeting, 29–31 May 2007, Copenhagen
Van TTH, Chin J, Chapman T, Tran LT, Coloe PJ (2008) Safety of raw meat and shellfish in Vietnam: an analysis of Escherichia coli isolations for antibiotic resistance and virulence genes. Int J Food Microbiol 124(3):217–223
Simjee S, White DG, McDermott PF, Wagner DD, Zervos MJ, Donabedian SM et al (2002) Characterization of Tn1546 in vancomycin-resistant Enterococcus faecium isolated from canine urinary tract infections: evidence of gene exchange between human and animal Enterococci. J Clin Microbiol 40(12):4659–4665
Guardabassi L, Schwarz S, Lloyd DH (2004) Pet animals as reservoirs of antimicrobial-resistant bacteria. J Antimicrob Chemother 54(2):321–332
Clinical and Laboratory Standards Institute (2013) M100-S23 performance standards for antimicrobial susceptibility testing; twenty-third informational supplement, pp 44–49
Randall LP, Cooles SW, Osborn MK, Piddock LJV, Woodward MJ (2004) Antibiotic resistance genes, integrons and multiple antibiotic resistance in thirty-five serotypes of Salmonella enterica isolated from humans and animals in the UK. J Antimicrob Chemother 53(2):208–216
Carlson SA, Bolton LF, Briggs CE, Hurd HS, Sharma VK, Fedorka-Cray PJ et al (1999) Detection of multiresistant Salmonella typhimurium DT104 using multiplex and fluorogenic PCR. Mol Cell Probes 13(3):213–222
Gallardo F, Ruiz J, Marco F, Towner KJ, Vila J (1999) Increase in incidence of resistance to ampicillin, chloramphenicol and trimethoprim in clinical isolates of Salmonella serotype Typhimurium with investigation of molecular epidemiology and mechanisms of resistance. J Med Microbiol 48(4):367–374
Hasman H, Mevius D, Veldman K, Olesen I, Aarestrup FM (2005) beta-Lactamases among extended-spectrum beta-lactamase (ESBL)-resistant Salmonella from poultry, poultry products and human patients in The Netherlands. J Antimicrob Chemother 56(1):115–121
Weill F-X, Guesnier F, Guibert V, Timinouni M, Demartin M, Polomack L et al (2006) Multidrug resistance in Salmonella enterica serotype Typhimurium from humans in France (1993 to 2003). J Clin Microbiol 44(3):700–708
Lunn AD, Fàbrega A, Sánchez-Céspedes J, Vila J (2010) Prevalence of mechanisms decreasing quinolone-susceptibility among Salmonella spp. clinical isolates. Int Microbiol 13:15–20
Cattoir V, Weill F-X, Poirel L, Fabre L, Soussy C-J, Nordmann P (2007) Prevalence of qnr genes in Salmonella in France. J Antimicrob Chemother 59(4):751–754
Ribot EM, Fair MA, Gautom R, Cameron DN, Hunter SB, Swaminathan B et al (2006) Standardization of pulsed-field gel electrophoresis protocols for the subtyping of Escherichia coli O157:H7, Salmonella, and Shigella for PulseNet. Foodborne Pathog Dis 3(1):59–67
Usein C-R, Străuţ M, Palade A-M, Tatu-Chiţoiu D, Ciontea SA, Băltoiu MC et al (2010) A multiple typing approach is recommended for the laboratory-based surveillance of salmonellosis in Romania. Roum Arch Microbiol Immunol 69(4):197–203
Tenover FC, Arbeit RD, Goering RV, Mickelsen PA, Murray BE, Persing DH et al (1995) Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J Clin Microbiol 33(9):2233–2239
LC and AT participated in the design and conception of the study, planned and executed experiments, analysed data and wrote the manuscript. MF and SM performed experiments. OO analyzed data. MM had a considerable contribution to the design and conception of this study, analyzed data and revised the manuscript. All authors read and approved the final manuscript.
This article was financially supported by Iuliu Hatieganu University of Medicine and Pharmacy, Cluj-Napoca, by the internal Grant Number: 1491/17/28.01.2014.
Compliance with ethical guidelines
Competing interests The authors declare that they have no competing interests.