Background

Human Salmonella enterica infection poses a significant public-health challenge globally, especially in low-to-middle income countries in sub-Saharan Africa and South Asia where sanitation is poor [1]. The situation is worsened by an increasing rate of emergence and distribution of antibiotic resistant strains [2,3,4].

One surveillance study has demonstrated an obvious increase in overall antimicrobial resistance from 20 to 30% in the early 1990s to as high as 70% in the early 2000s [5]. This report was based on old generic antibiotics which are not currently in use. Chloramphenicol, ampicillin and sulfamethoxazole trimethoprim used to be the drugs of choice for treating Salmonella infection for over a decade [6] . However, because of increased resistance to these first-line drugs, physicians have resorted to ciprofloxacin (a fluoroquinolone) [7]. Since its introduction, there has not been structured surveillance mechanism(s) to identify mutations possibly associated with its resistance in Ghana. Availability of only few new antibiotics, has placed enormous value on investigations into resistance strains of bacteria. The World Health Organisation (WHO) has listed fluoroquinolone–resistant Salmonella spp. as part of the priority pathogens for which new antibiotics are urgently needed [8]. Although phenotypic resistance could be available in some clinical laboratories, there is paucity of data on molecular investigations of fluoroquinolone resistant genes associated with Salmonella infection in Ghana and many African countries.

Fluoroquinolone resistance is mainly due to two mechanisms: chromosomally mediated mutations occurring at the quinolone resistance determining regions (QRDR) of topoisomerase genes (gyrA, gyrB, parC and parE genes) and resistance mediated by plasmids [9]. The latter is further divided into 3 different routes that confer decreased susceptibility to fluoroquinolones: 1) quinolone resistance proteins (encoded by qnr genes (qnrA, qnrB, qnrC, qnrD, qnrS) that shield DNA gyrase from the effect of fluoroquinolones); 2) aac(6′)-Ib-cr resistance mechanism (an aminoglycoside acetyltransferase that modifies fluoroquinolones by acetylating the free nitrogen on the C7 ring of the drug, decreasing binding affinity), and 3) plasmid-mediated resistance by OqxAb and QepA efflux systems [10, 11].

Fluoroquinolones resistance mediated by plasmids have been identified in some developed countries such as United States of America, United Kingdom and France [9, 12, 13]. With the high rate of spread of plasmid-mediated resistance determinants coupled with some factors such as international travels, there is a possibility of fluoroquinolone resistant Salmonella strains circulating in Ghana. More often than not, fluoroquinolone resistance in Salmonella enterica is mediated by gyrA mutations [3, 14], with few reported cases of gyrB mutations [15] and very few cases of topoisomerase IV (parC and parE) genes. Mutation results in a significant reduction of the drug-enzyme binding, and as such the ability for fluoroquinolones to inhibit DNA ligation is totally restricted [16, 17]. Both chromosomal and plasmid-encoded fluoroquinolone resistance are responsible for conferring low-level resistance to fluoroquinolones [18], nonetheless, high level-resistance (with increasing MIC up to 250-fold) has been documented [19].

Fluoroquinolone resistant Salmonella strains with multiple gyr and par mutations have been reported from Cambodia, India and Nepal [20, 21]. In Africa, fluoroquinolone resistant strains of Salmonella are known to circulate in countries such as Kenya, Tanzania, Malawi, South Africa, Zambia, Democratic Republic of Congo and Nigeria [4, 22, 23]. However, meta analysis conducted by Cuypers et al., revealed lower prevalence and spread of these strains in Africa compared to Asia [8].

This study therefore sought to identify resistance associated with mutations in the topoisomerase genes of Salmonella and plasmid-mediated resistant genes associated with fluoroquinolone resistance in Salmonella strains from Ghana.

Methods

Study design and study area

This was a retrospective study of archived isolates (from blood, stool and oropharynx samples) biobanked at Kumasi Centre for Collaborative Research in Tropical Medicine (KCCR), Ghana, between May, 2016 and January, 2018. These isolates were collected as part of a larger study that sought to investigate the burden of severe typhoid in sub-Saharan Africa with six countries in participation (Ghana, Burkina Faso, Democratic Republic of Congo, Ethiopia, Nigeria and Madagascar). Nonetheless, this report focused only on the Ghanaian site. Study population comprised patients that presented with fever at Komfo Anokye Teaching Hospital (KATH) and Agogo Presbyterian Hospital (APH) in the Kumasi Metropolis and Asante-Akim North district, respectively, both located in the middle belt of Ghana. KATH serve as a tertiary hospital in an urban setting whereas APH is a primary health facility in a rural area of Ghana.

Ethics approval

The main study protocol was reviewed and approved by the Committee for Human Research Publications and Ethics (CHRPE) at the School of Medical Sciences, Kwame Nkrumah University of Science and Technology (KNUST) (Approval Number: CHRPE/AP/188/18).

Data collection

Study participants’ biodata such as age and gender were collected from the data department of KCCR. Information regarding the source of isolates, total number of samples received and processed were retrieved from laboratory data.

Laboratory procedures

Bacterial culture

Biobanked isolates were removed from − 80 °C freezer (Thermo Scientific), thawed and sub-cultured unto three standard growth media: Blood Agar (BA – Columbia agar base supplemented with 5% sheep blood), chocolate agar (CA) and macConkey agar (Mac) (BD, Franklin Lakes, New Jersey, USA) under sterile working condition. All the plates were incubated aerobically overnight at 35 °C–37 °C except for CA plates which was incubated in 5% CO2 for microaerophilic condition.

Bacterial identification

Salmonella was identified based on colonial morphology on the various agar, microscopic presentation, latex agglutination test, biochemical tests (including API20E), as well as serotyping (by White-Kauffmann Le-Minor scheme) using commercially available serotyping kit from BD (Franklin Lakes, New Jersey, USA). On both the BA and CA, small, creamy gamma (ɣ) hemolytic colonies consistent with Salmonella sp. was recorded. Gram negative short rods with small colourless non-lactose fermenting colonies on Mac was also documented. Biochemical tests such as triple sugar iron (TSI), urease, citrate tests were performed to aid in Salmonella identification from other enterobacteria based on sugars fermentation, urease production and citrate utilisation, respectively. Isolation and identification of other gram negative and positive bacteria were done according to standard microbiological protocols.

Antibiotic susceptibility testing

We performed antimicrobial susceptibility testing on all biobanked isolates confirmed as Salmonella according to Clinical and Laboratory Standards Institute (CLSI) guidelines [24]. Susceptibility to ampicillin (10 μg), amoxiclav (amoxicillin & clavulanic acid; 20/10 μg), ceftriaxone (30 μg), trimethoprim/sulfamethoxazole (1.25/23.75 μg), ciprofloxacin (5 μg), gentamicin (10 μg), tetracycline (30 μg), chloramphenicol (30 μg), ceftazidime (30 μg), cefotaxime (30 μg) and nalidixic acid (30 μg) was tested on Mueller Hinton agar (BD, USA) using the Kirby-Bauer disc diffusion method. The breakpoints of the various antibiotics used were in line with CLSI 2018. Resistance to fluoroquinolones, defined as isolates with intermediate susceptibility and/or resistance to nalidixic acid (surrogate marker for ciprofloxacin resistance) and/or ciprofloxacin were selected for Minimum Inhibitory Concentration (MIC). Enterobacteria such as E. coli and Klebsiella sp. that were resistant to 3rd generation cephalosporins in this study were further screened to detect the presence of extended spectrum beta-lactamase (ESBL) enzyme using double-disc diffusion method on Mueller Hinton agar according to CLSI guidelines [24]. Again, S. aureus resistant to cefoxitin were regarded as methicillin-resistant Staphylococcus aureus (MRSA).

MIC determination

Minimum inhibitory concentration (MIC) was performed on ciprofloxacin/nalidixic acid intermediate and/or resistant isolates using ciprofloxacin E-test (epsilometer test) according to the manufacturers recommendation (Oxoid, Wesel, Germany) to confirm ciprofloxacin resistance. E-test gives a direct quantification of antimicrobial susceptibility in the form of discrete MIC values. Isolates with ciprofloxacin breakpoint concentration (μg/ml) of ≤0.06 μg/ml was documented as sensitive (S); between 0.12 and 0.5 μg/ml as intermediate (I); and ≥ 1 μg/ml was reported as resistant (R) following the CLSI guidelines.

Quality control

Escherichia coli ATCC 25922 and Salmonella Typhimurium ATCC 14028 were set up together with the test organisms to control media, biochemical tests, potency of antibiotic discs, and ciprofloxacin E-test strip.

Molecular detection of fluoroquinolone resistant genes

DNA extraction

Genomic DNA was extracted from ciprofloxacin and/or nalidixic acid resistant and/or intermediate isolates using spherolyse DNA isolation kit (HainLife Science, Nehren, Germany) according to manufacturer’s instructions. Extracted DNA were used as templates for detection of chromosomally-encoded mutations in the topoisomerase genes and plasmid-mediated fluoroquinolone resistant genes.

Amplification of topoisomerase genes

Detection and amplification of gyrA, gyrB, parC and parE genes by PCR was performed using primers shown in Table 1. Twenty-five microlitres of One Taq Quick-Load 2x Master Mix with standard buffer (New England Biolabs® Inc) was added to 1 μl each of 10 μM forward and reverse primers respectively. Twenty-two microlitres of nuclease-free water was added to the mastermix and finally, 1 μl DNA template to obtain a reaction volume of 50 μl.

Table 1 Sequence of primers for detection of gyrA, gyrB, parC and parE genes
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Amplification using Veriti thermal cycler was conducted using the following PCR cycling condition: an initial denaturation at 94.0 °C for 30 s; 30 cycles of 94.0 °C for 30 s, *60/54/53/52 °C for 1 min and 68.0 °C for 1 min with a final extension of 68.0 °C for 5 min. The reaction was put on hold at 4 °C until attended to.

Note: *60/54/53/52 °C corresponds to annealing temperatures of gyrA, gyrB, parC and parE genes, respectively.

PCR product purification

The products of amplification of gyrA, gyrB, parC and parE genes were purified using DNA clean and concentrator™-25 kit (Zymo research, Irvine, USA) according to manufacturer’s instruction. This was to ensure that ultra-pure PCR products are recovered ahead of Sanger sequencing.

DNA sequencing and analysis of mutation

Sanger sequencing of the purified PCR products was achieved using the aforementioned primers of the topoisomerase genes on an ABI 3730XL DNA Analyzer. Analysis of the DNA sequences was performed by comparing with the reference S. Typhimurium strain LT2 genome (accession number AE006468.2) for gyrA, gyrB, parC and parE genes (accession numbers AAL21173.1, AAL22694.1, AAL22048.1 and AAL22055.1, respectively) at GenBank database using the NCBI (National Centre for Biotechnology Information) BLAST (basic local alignment search tool) program. ExPASy (Expert Protein Analysis System) translate tool, SIB (Swiss Institute of Bioinformatics) was used to translate the nucleotide sequences into amino acid sequences. Global alignment tool EBI (European Bioinformatics Institute) was used to investigate for any mutations using Needleman-Wunsch algorithm (EMBOSS).

Detection of plasmid-mediated quinolonone resistance genes (PMQR)

Polymerase chain reaction (PCR) amplification of fluoroquinolones resistant genes: qnrA, qnrB and qnrS was performed on all Salmonella isolates using the primers [9] in Table 2. Genomic DNA extraction and PCR master-mix preparation were prepared as mentioned before.

Table 2 Primers used for amplification of PMQR genes
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PCR experiments were carried out according to the following cycling conditions for all three genes: initial denaturation - 94 °C for 30s; template denaturation - 94 °C for 30s; annealing - 55 °C for 60s; extension - 68 °C for 60s; final extension - 68 °C for 5mins; and reaction was put on hold at 4 °C until amplicons were collected for agarose gel electrophoresis.

Gel documentation

The amplicons were resolved by agarose gel electrophoresis (1.5% agarose) at 120 V for an hour and band visualisation done with the aid of UV-transilluminator (Vilber Lourmat, Collegien, France). The concentation of agarose used was more suitable for the expected band sizes in this work. The stained gel was captured unto a desktop computer using the infinity® software.

Statistical analysis

Data were entered into Microsoft excel and exported to STATA version 12 (Stata Corp, USA) for analysis. Descriptive statistics was used to summarize the distribution of various variables into tables and graphs. Differences between discrete variables were analysed using Fisher’s exact test.

Results

Socio-demographic characteristics of the study population

Majority (402/1036; 38.8% and 251/364; 69.0%) of the sampled population from the two study sites (APH and KATH) were ≤ 5 years old. The overall mean (±SE) age (in years) of participants was 15.4 ± 0.5. The mean (±SE) age (in years) of recruited patients seeking medical attention at APH and KATH was 18.7 ± 0.6 and 4.5 ± 0.2 respectively. At both sites, there were high proportion of males compared to females.

Distribution of bacteremic pathogens

Of 133 biobanked isolates cultured, 68 (51.1%) and 16 (12%) were identified as Salmonella Typhi and non-typhoidal Salmonella (NTS) respectively (Fig. 1). Other bacteriae identified included Escherichia coli (including ESBL; 11; 8.3%), Staphylococcus aureus (including MRSA; 7; 5.3%) and Klebsiella pneumoniae (5; 3.8%). Salmonella Typhi was predominantly found in APH (56/68; 82.4%) while NTS was high in KATH (9/16; 56.3%).

Fig. 1
figure 1

Distribution of bacteremic isolates from study sites. Biobanked bacterial isolates were cultured and identified using standard microbiological culture methods and biochemical tests

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Salmonella from stool and oropharynx

A total of 13 Salmonella strains were isolated from 418 stool specimens collected from both APH and KATH. Of the 13 strains, 4 (30.8%) and 9 (69.2%) were S. Typhi and NTS, respectively (Table 3). Salmonella was the only pathogen isolated from stool. Five hundred and fifty eight oropharyngeal specimens (OPS) were collected from the two study sites: APH – 401 (71.9%) and KATH – 157 (28.1%). Of the four (4) Salmonella strains isolated from 558 OPS, only 1 (25.0%) was identified as S. Typhi and 3 (75.0%) NTS (Table 3). All the Salmonella strains isolated from stool and OPS were from APH but not KATH.

Table 3 Bacterial isolates from stool and oropharynx
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Serotyping of bacteremic isolates

Serotyping of iNTS revealed that Salmonella Typhimurium (10/16; 62.5%) was the most predominant serovar identified followed by Salmonella Enteritidis (5/16; 31.3%) and finally, 1 (1/16; 6.2%) untypable isolate. Rate of isolation of Salmonella Typhimurium was significantly higher in APH than in KATH (p = 0.011; Table 4), however, Salmonella Enteritidis was isolated from only KATH.

Table 4 Invasive NTS distribution among study population
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Antibiotic resistance profile

Generally, first-line anti-Salmonella drugs (ampicillin, chloramphenicol, trimethoprim/sulfamethoxazole) recorded the highest rate of resistance in both S. Typhi and NTS isolates (between 33.8 and 50.0%). Third-generation cephalosporins (ceftazidime and ceftriaxone) and gentamicin had 100% efficacy rate in all serovars of Salmonella tested. Ciprofloxacin recorded significantly reduced susceptibility (intermediate) in both typhoidal and NTS (14.7 and 37.5%, respectively).

MIC determination for resistant and reduced-susceptible Salmonella strains to fluoroquinolones

Of the 20 ciprofloxacin intermediate/resistant Salmonella isolates tested by MIC, only 5 (breakpoint concentration between 0.12 and 0.5 μg/ml) were intermediate and no resistance recorded (Table 5).

Table 5 MIC of fluoroquinolone resistant and reduced-susceptible Salmonella strains
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Identification of mutations within QRDR

Thirteen isolates were selected (based on MIC values from 0.03 to 0.5 μg/ml) for DNA product purification and subsequent sequencing prior to mutational analysis. Sequence analysis of gyrA gene revealed the presence of 5 different nonsynonymous mutations, with the most frequent mutation (Ile203Ser) occurring in 12 out of 13 isolates tested (Table 6). Gyrase B (gyrB) gene revealed 1 nonsynonymous mutation in 3 out of 13 isolates, substituting amino acid phenylalanine with leucine at codon 601 (Phe601Leu). No mutation was observed in parC and parE genes. In gyrA mutation alone, Serovar Typhi recorded the highest mutation (5/13), followed by Typhimurium (4/13) and Enteritidis (4/13). All three isolates which harboured gyrB mutation were Salmonella Typhi. Again, 3 isolates, all S. Typhi possessed both gyrA and gyrB mutations. Only one S. Enteritidis isolate exhibited Lys154Asn gyrA mutation and 5 S. Typhi isolates had a Glu133Gly mutation in gyrA gene (Table 6). The two isolates with the highest ciprofloxacin MIC (0.5 μg/ml) had common amino acid substitutions resulting in 1 nonsynonymous mutation in gyrA gene (Ile203Ser).

Table 6 Summary of resistance profiles, target gene mutations and prevalence of PMQR genes
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Detection of plasmid-mediated qnr genes

Again, Of the 20 phenotypically resistant and/or intermediate Salmonella isolates to ciprofloxacin and nalidixic acid tested by singleplex PCR reactions, there was no amplification of qnrA and qnrB plasmid-mediated resistant genes. However, 2 isolates were found to harbour qnrS resistant gene of molecular size 550 bp (Fig. 2). Both isolates were non-typhoidal Salmonella strains from the blood (S. Enteritidis) and oropharynx (S. Typhimurium) of 11 and 1 year old children at KATH and APH, respectively. Again, these two isolates recorded the highest MIC value of 0.5 μg/ml (Table 6).

Fig. 2
figure 2

Amplification and detection of qnrS plasmid-mediated fluoroquinolone resistant gene (molecular size 550 bp) by PCR. Lanes 4,8 are positive for qnrS gene (550 bp). Lanes –C, +C are negative and positive controls respectively.L = Molecular ladder of size 100 bp

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Discussion

This study identified five different gyrA mutations and one gyrB nonsynonymous mutation in quinolone-resistant Salmonella enterica from human clinical isolates. Salmonella isolates harbouring plasmid-mediated fluoroquinolone resistant gene qnrS was also identified in this study.

There was high frequency of gyrA gene mutation in this study than the other topoisomerase genes examined. This agrees with findings from Eaves et al., in that mutations occurring at the quinolone resistance determining regions of other topoisomerase genes are more uncommon than those observed in gyrA gene [27]. Thus, there might be other mechanisms of resistance playing an important role, as mutations in all but gyrA gene were rare. In Africa, the most common mutation known to account for ciprofloxacin non-susceptibility in most clinical Salmonella isolates is found in gyrA gene, followed by parC and gyrB genes, with no reported case of parE gene mutation [28]. As observed in this study, both parC and parE gene mutations were completely absent in the study populations, consistent with previous studies [29]. Report by Bae et al., showed a higher frequency (18 out of 27 isolates) of gyrA mutation (Asp87Gly) in nalidixic acid resistant S. Enteritidis from South Korea [30]. However, the present study identified only 2 nalidixic acid resistant S. Enteritidis with the same Asp87Gly gyrA mutation and had ciprofloxacin MIC 0.12 μg/ml. Codons 83 and 87 of gyrA gene are widely known to be a common hotspot for gyrA mutation [31, 32], nevertheless, their frequency was much lower in the current study. Mutations at these codons, especially codon 87, have been shown to be associated with decreased ciprofloxacin susceptibility and nalidixic acid resistance [31].

Other gyrA mutation was detected in 5 S. Typhi isolates which resulted in amino acid substitution from glutamic acid to glycine at codon 133 with MIC of 0.03 μg/ml (4 isolates) and 0.12 μg/ml (only one isolate). With these low MICs, it could be suggested that mutation of Glu133Gly alone could not necessarily lead to quinolone resistance in Salmonella. This agrees with findings from Eibach et al., who detected a Glu133Gly mutation in ciprofloxacin susceptible S. Typhi clinical isolate in Ghana with MIC of 0.06 μg/ml [29]. However, studies in Kenya found 11 S. Typhi reduced ciprofloxacin susceptible isolates with the same gyrA mutation (Glu133Gly) [33].

Studies show that double mutations found in gyrase further reduce binding affinity of the enzyme-DNA complex to fluoroquinolones [34]. This agrees with the current study as 2 S. Typhi isolates identified to have double mutations in gyrA and gyrB genes were MDR and also resistant to the quinolone nalidixic acid.

Gyrase B gene mutation was detected in only 3 S. Typhi isolates which resulted in amino acid substitution from phenylalanine to leucine at codon 601 (Phe601leu). The first gyrB gene mutation (Glu466Asp) reported in Ghana was from S. Typhimurium [15], however, the present study identified gyrB mutation in S. Typhi, for the first time in Ghana. Findings from Tadesse et al., revealed a low proportion (0.2%) of Salmonella gyrB mutation from human and animal sources in Africa [28].

Molecular analysis by PCR detected the presence of quinolone resistance gene qnrS in 2 non-typhoidal Salmonella isolates from the blood and oropharynx in patients attending health care at KATH and APH respectively. The 3 principal genes responsible for plasmid-mediated fluoroquinolone resistance in Salmonella include qnrA, qnrB and qnrS genes [9]. Previous studies in Ghana showed the absence of all three genes [15, 29], indicating a more recent emergence of qnrS resistant gene. Plasmids increase bacterial genetic diversity greatly through acquisition or loss of genes especially, those pertaining to resistance and/or virulence. Detection of qnrS gene in this study might be due to indiscriminate use of over-the-counter antibiotics by humans, without complying to clinicians prescriptions. This could lead to increased selective pressure on the drugs and subsequently contributes to resistance. Again, there could be possibility of zoonotic transmission of these resistant genes [35, 36], as Dekker et al., has already reported on emergence of qnrB resistant gene in poultry population in Ghana [37].

Variant qnrA1 of the qnrA gene family was the first plasmid-mediated fluoroquinolone resistant gene described, however, several studies show that this gene is not commonly found in Salmonella [9, 38, 39]. This might explain why none of the isolates tested in this study was positive for qnrA.

Dekker et al., detected Salmonella Poona plasmid-mediated resistant gene qnrB2 in 3 out of 200 poultry meat samples collected from markets in Ghana [37]. In Africa, evidence-based findings of plasmid-encoded genetic determinants associated with fluoroquinolone resistance in Salmonella strains are generally rare [28]. Few cases of qnrB and qnrS genes have been reported in South Africa [40] and Nigeria [8], respectively. Studies in Europe have reported on the increasing rate of qnrB resistant genes in several European countries (including Spain, Italy and Netherlands) and these were mostly from animal sources (predominantly chicken and turkey) [41]. The most commonly reported qnrB variant is qnrB2 and it is usually harboured in Salmonella serovars Agona, Derby, Enteritidis, Hadar, London and Montevideo [41]. Although qnrB resistant genes are often restricted to animal populations, there is a potential chance of future global transmission to humans, as variant qnrB19 has already been implicated in human S. Typhimurium infection in Netherlands and Italy [42, 43]. Studies in Scotland also revealed the presence of qnrB and qnrS from returning travellers from Egypt and Nigeria [39]. Another study conducted in United States reported on low prevalence of plasmid-mediated fluoroquinolone resistant genes, particularly qnrS [12, 44]. However, this study contrasts findings from some European (like Germany and Poland) and Asian countries, depicting regional differences in the prevalence of plasmid-mediated fluoroquinolone resistant genes [45].

To date, there are 9 variants of qnrS resistant gene (qnrS1 to qnrS9) identified, with qnrS1 being the most predominant [46]. Previous studies showed that qnrS1 alone was capable of conferring reduced susceptibility to ciprofloxacin even in the absence of gyrA mutation [47]. Again, findings from Hopkins et al., in the United States demonstrated that quinolone resistant gene increased ciprofloxacin MIC to 0.38–0.78 μg/ml [13], giving credence to the fact that, qnr genes might confer full resistance in the near future with MIC ≥1 μg/ml if strong surveillance system is not established to control spread of these plasmid-encoded genes.

Other plasmid mediated fluoroquinolone resistant genes not screened in this study include qnrC, qnrD, qnrVC, aac(6′)-lb and plasmid-mediated enhanced efflux pump mechanisms by QepAB and OqxAB [48]. Studies show that the global prevalence of these genes are low [41]. Although qnr genes are usually associated with plasmid-encoded ESBL genes [10, 18], no ESBL gene was identified among the qnrS positive strains in this study.

Resistance of Salmonella to ciprofloxacin and other related fluoroquinolones has serious public health implications because this class of antimicrobials is commonly used to treat invasive forms of Salmonella infections. Mechanisms by these plasmid-mediated genetic determinants lead to low-level resistance that by itself does not exceed clinical breakpoint for susceptibility. However, it facilitates selection of higher level resistance and makes pathogens harbouring PMQR genes difficult to treat [48, 49]. The present study could not examine for the presence of other genetic determinants (such as qnrC, qnrD, qnrVC, aac(6′)-Ib-cr, and qepAB genes) responsible for plasmid-mediated fluoroquinolone resistance. Another limitation to this study was the inability to link the novel mutations (gyrA - Ile203Ser and Lys154Asn; and gyrB – Phe601Leu) to their involvement in reduced ciprofloxacin susceptibility/resistance within the QRDR. A suggested approach is to conduct a conjugational transfer experiment by introducing wild-type allele of the gyrA and gyrB genes into a broad host-range plasmid vector [15].

Conclusion

This study reports for the first time plasmid-mediated fluoroquinolone resistant gene qnrS in Salmonella clinical isolates in Ghana. Nonsynonymous mutations (Asp87Gly, Glu133Gly and Ser83Tyr) which confer Salmonella reduced susceptibility to ciprofloxacin were also detected as reported in several studies [27, 29], with 3 other novel mutations likely to confer Salmonella resistance. We recommend surveillance systems to track the evolution of Salmonella plasmid-mediated resistant genes and to ensure proper use of antibiotics and control of severe infections.