http://orcid.org/0000-0003-2868-1314
Figures
Abstract
Escherichia coli and Staphylococcus aureus are important agents of urinary tract infections that can often evolve to severe infections. The rise of antibiotic-resistant strains has driven the search for novel therapies to replace the use or act as adjuvants of antibiotics. In this context, plant-derived compounds have been widely investigated. Cuminaldehyde is suggested as the major antimicrobial compound of the cumin seed essential oil. However, this effect is not fully understood. Herein, we investigated the in silico and in vitro activities of cuminaldehyde, as well as its ability to potentiate ciprofloxacin effects against S. aureus and E. coli. In silico analyses were performed by using different computational tools. The PASS online and SwissADME programmes were used for the prediction of biological activities and oral bioavailability of cuminaldehyde. For analysis of the possible toxic effects and the theoretical pharmacokinetic parameters of the compound, the Osiris, SwissADME and PROTOX programmes were used. Estimations of cuminaldehyde gastrointestinal absorption, blood brain barrier permeability and skin permeation by using SwissADME; and drug likeness and score by using Osiris, were also evaluated The in vitro antimicrobial effects of cuminaldehyde were determined by using microdilution, biofilm formation and time-kill assays. In silico analysis indicated that cuminaldehyde may act as an antimicrobial and as a membrane permeability enhancer. It was suggested to be highly absorbable by the gastrointestinal tract and likely to cross the blood brain barrier. Also, irritative and harmful effects were predicted for cuminaldehyde if swallowed at its LD50. Good oral bioavailability and drug score were also found for this compound. Cuminaldehyde presented antimicrobial and anti-biofilm effects against S. aureus and E. coli.. When co-incubated with ciprofloxacin, it enhanced the antibiotic antimicrobial and anti-biofilm actions. We suggest that cuminaldehyde may be useful as an adjuvant therapy to ciprofloxacin in S. aureus and E. coli-induced infections.
Citation: Monteiro-Neto V, de Souza CD, Gonzaga LF, da Silveira BC, Sousa NCF, Pontes JP, et al. (2020) Cuminaldehyde potentiates the antimicrobial actions of ciprofloxacin against Staphylococcus aureus and Escherichia coli. PLoS ONE 15(5): e0232987. https://doi.org/10.1371/journal.pone.0232987
Editor: Abdelwahab Omri, Laurentian, CANADA
Received: April 11, 2020; Accepted: April 24, 2020; Published: May 14, 2020
Copyright: © 2020 Monteiro-Neto et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This work was supported by Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES; grant number 3325/2013; finance code 001), Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq; grant numbers 309046/2016-5 and 305676/2019-9), Fundação de Amparo à Pesquisa e ao Desenvolvimento Científico e Tecnológico do Maranhão (FAPEMA; grant number 03207/18) and INCT-INOVAMED (grant number 465430/2014-7). J.P.P. and N.C.F.S. are students receiving grants from FAPEMA. L.F.G. is an undergraduate student receiving a grant from CNPq. D.M.S. is an undergraduate student receiving a grant from the Santander Universidades programme. A.R.C.Jr. and N.M.T.O. are PhD students receiving grants from Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) and CAPES, respectively. B.C.d.S. is a MSc student receiving a studentship from Instituto de Pesquisa Pelé Pequeno Príncipe. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Bacteria such as Escherichia coli and Staphylococcus aureus are important agents of urinary tract infections [1–4]. Both bacteria are frequently detected in patients with indwelling urinary tract devices [1, 5–7]. These primary infections often evolve to severe infectious diseases such as sepsis, which presents high morbidity and mortality. E. coli is one of the major pathogens of such infections, causing bacteremia in over 6,000 per 100,000 patients per year [8, 9]. In addition, reports indicate S. aureus is responsible for 21 to 36 cases of bacteremia per 100,000 habitants per year [10, 11] with mortality rates varying from 30 to 70% [12].
The management of such infections mostly relies on antibiotic therapy, with patient survival and recovery largely depending on treatment timing and efficacy. Of note, ciprofloxacin is the most commonly prescribed fluoroquinolone antibiotic for urinary tract infections [13] to which, both S. aureus and E. coli have become resistant [3, 14]. Indeed, the unrestricted and widespread use of antibiotics in the last decades resulted in a rise of multidrug-resistant strains of both E. coli and S. aureus, thus, reducing the chances of a successful treatment of infections caused by these microorganisms. The increased bacterial resistance has driven the search for novel therapeutic approaches that can either replace the use or act as adjuvants of antibiotics [15]. In this context, plant-derived compounds have been widely investigated as antimicrobials and adjuvants to antibiotic therapy [16, 17].
The seeds of Cuminum cyminum L. (Apiaceae), popularly known as cumin, have been largely used in the global cuisine [18]. Its seeds are also used in the folk medicine to treat toothache, dyspepsia, diarrhea, epilepsy, amongst other disease conditions [18, 19]. Recent studies have demonstrated that the essential oil obtained from cumin seeds is antimicrobial against bacteria such as S. aureus and E. coli [20–27]. This activity has been attributed to the high content of cuminaldehyde in the cumin seed essential oil [18, 28, 29]. Recent studies have reported antimicrobial and anti-biofilm actions for this compound in S. aureus and E. coli strains [30–32]. In order to gain additional knowledge on cuminaldehyde properties, we investigated the in silico and in vitro activities of this compound against S. aureus and E. coli. We also assessed the ability of cuminaldehyde to potentiate ciprofloxacin effects on these bacteria.
Materials and methods
In silico analysis
Prediction of biological activities.
To evaluate the biological activities of cuminaldehyde, the Prediction of Activity Spectra for Substances (PASS) Online programme was used. This computational tool calculates the probability of a given organic molecule to present a biological activity by comparing the molecule structure to a database (www.way2drug.com/passonline) composed of other organic molecules with defined biological activities [33, 34]. Thus, the PASS online programme gives the probability of a compound of being active (Pa) or inactive (Pi) on a biological target. For comparison, the biological activity of ciprofloxacin was also analyzed.
Prediction of oral bioavailability.
The SwissADME programme (http://www.swissadme.ch/index.php#) [35] was used to predict the theoretical oral bioavailability of cuminaldehyde. For comparison, ciprofloxacin oral bioavailability was also assessed. Information on the following properties were obtained: total polar surface area (TPSA), partition coefficient (water/oil)—iLogP, molecular weight, number of hydrogen acceptors–nALH and number of hydrogen donors—nDLH of the compound. Then, an analysis based on the "Rule of Five" was performed as previously described [33, 36]. By definition, to present a good estimated oral bioavailability, a molecule needs to meet the requirements for at least three of the analyzed parameters: i) total polar surface area (TPSA) <140 A2, ii) LogP ≤ 5, iii) molecular weight <500 daltons, iv) number of acceptor hydrogen bonds (nALH) ≤ 10, and v) number of donor hydrogen bonds (nDLH) ≤ 5.
Estimation of pharmacokinetic characteristics and toxic effects.
For analysis of the possible toxic effects and the theoretical pharmacokinetic parameters (absorption, distribution, metabolism and excretion) of cuminaldehyde, the Osiris (www.organic-chemistry.org/prog/peo/drugScore.html) [33] and SwissADME (http://www.swissadme.ch/index.php#) [35] programmes were used. These parameters and the toxicity were predicted by comparison of the cuminaldehyde chemical structure with a database containing commercially available drugs and commercially available compounds. Toxic effects were classified as mutagenic, tumorigenic, irritant, and effects on the reproductive system [33].
LD50 values in milligram per kilogram (mg/kg) were estimated by using the PROTOX programme (http://tox.charite.de/protox_II/index.php?site=compound_input) [37] and used to classify cuminaldehyde toxicity as follows: class i- fatal if swallowed at LD50 ≤ 5, class ii- fatal if swallowed when 5<LD50 ≤ 50, class iii- toxic if swallowed when 50 <LD50 ≤ 300, class iv- harmful if swallowed when 300 <LD50 ≤ 2000, class v- harmful if swallowed when 2000 <LD50 ≤ 5000, and class vi- non-toxic when LD50> 5000. Estimations of cuminaldehyde gastrointestinal absorption, permeability through the blood brain barrier and skin permeation (log Kp in centimeters (cm)/s) were assessed by the SwissADME programme (http://www.swissadme.ch/index.php#) [35]. Of note, the more negative the log Kp, the less skin permeant is the molecule.
Additionally, the probability of cuminaldehyde to becoming a commercial drug ("drug-score") was calculated by the Osiris programme (www.organic-chemistry.org/prog/peo/drugScore.html), by combining the values obtained for iLogP, drug-likeness, solubility (Log S; the closer the score is to 0, the higher the solubility) [35], molar mass and toxicity in to a single value. A drug-score value of 0.1 to 1.0 was taken as an index of suitability for commercialization [33].
In vitro assays
Bacterial strains and culture.
The standard strains of S. aureus ATCC 6538 and enteroaggregative E. coli 042 (EAEC 042), and the clinical isolates from urinary tract infections (S. aureus-A (Saa), S. aureus-V (Sav) and E. coli-R (Ecr)) were kindly provided by the bacterial collection sector of the Universidade CEUMA. The bacteria were cultured on Müeller-Hinton (MH; Merck Millipore) agar, at 37°C for 24 h as previously described [38]. The susceptibility profiles of the clinical isolates are depicted in the Table 1 and were determined in an automated VITEK® 2 system (BioMérieux Clinical Diagnostics, USA). Data interpretation was performed as recommended by the Clinical Laboratory Standards Institute—CLSI [39].
Evaluation of minimum inhibitory concentrations (MICs).
Cuminaldehyde (98% purity; Sigma-Aldrich) antimicrobial effects were investigated by the microdilution method [40]. For this, the bacteria previously cultured on MH agar were suspended in saline (~ 1.5 × 108 colony forming units (CFU)/milliliter (ml)). For determining the MICs, 10 μl of the bacterial suspension were incubated in MH broth (190 μl/well; Merck Millipore) containing different concentrations of cuminaldehyde (0.0234–24 mg/ml). Serial dilutions of ciprofloxacin (0.0009–200 μg/ml) were used as positive controls. Sterile dimethyl sulfoxide (DMSO, Sigma-Aldrich; 2% in saline) was used to increase cuminaldehyde solubility and as negative control. Samples were incubated for 24 h at 37°C, and the MICs (the lowest concentration at which no bacterial growth is observed) were evaluated. For this, the absorbances were read at 600 nm.
In parallel, the effects of the sub-inhibitory concentrations (MIC/2-MIC/8) of cuminaldehyde and ciprofloxacin on bacterial viability were assessed and calculated by addition of the PrestoBlue® reagent (1:10; Life Technologies), according to the manufacturer’s instructions. The absorbance was read at 570 nm and 600 nm and cell viability expressed as Δ absorbance in nm.
Effects on biofilm formation.
Biofilm formation was quantified as previously described [38]. For this, 10 μl of each bacterial suspension (prepared as described above) were added per well into a 96-well cell culture plate containing sub-inhibitory concentrations of cuminaldehyde (MIC/2-MIC/8) or ciprofloxacin (MIC/2-MIC/8) in 190 μl of MH broth (Merck Millipore). Vehicle (2% DMSO in saline)-treated bacteria and broth without bacteria were used as negative controls. Samples were incubated at 37°C for 24 h, and then, the wells were washed three times with phosphate-buffered saline (PBS; Sigma-Aldrich). Samples were then, fixed with 200 μl of methanol (100%; Merck Millipore) for 15 min. Following, the methanol was removed and the plate wells allowed to air dry. Biofilm was stained with 5% crystal violet (Sigma-Aldrich) for 10 min at room temperature, and immediately solubilised with methanol (200 μl). The absorbance was read at 570 nm. Biofilm mass results are expressed as absorbance in nm. For analysis of biofilm viability, the PrestoBlue® reagent (1:10; Life Technologies) was used according to the manufacturer’s instructions. The absorbance was read at 570 nm and 600 nm and the results are expressed as Δ absorbance in nm.
Time-kill assay.
An aliquot (200 μl) of each bacterial suspension was added to 2 ml of MH broth (Merck Millipore) containing ciprofloxacin (MIC/2) or cuminaldehyde (MIC/2-MIC/4) alone, or in combination. Vehicle (2% DMSO in saline)-treated bacteria were used as negative control. Cell growth was monitored by plating 10 μl of 10-fold-diluted suspensions from each sample at different time-points (0.15–8 h) in MH agar (Merck Millipore) plates. After 8 h of incubation at 37°C, the colonies were counted and then, the Log10 CFU/ml was calculated. The bactericidal combinatory effects were assessed by variation on Log10 CFU/ml (ΔLC). Synergy was defined as a decrease of ≥ 2 log10 CFU/ml and antagonism as an increase of #x2265; 2 log10 CFU/ml. If ΔLC was between 1 and 2 log10 CFU/ml, the effects were recorded as additive, and as indifferent if ΔLC = ± 1 log10 CFU/ml [40].
Synergy assay with ciprofloxacin on biofilm formation.
The potential of cuminaldehyde to interact with ciprofloxacin was assessed on biofilm formation. Biofilm mass formation was quantified (as described above in the section Effects on biofilm formation). For this, 10 μl of each bacterial suspension were added per well into a 96-well cell culture plate containing cuminaldehyde (MIC/8) and ciprofloxacin (MIC/2) in 190 μl of MH broth (Merck Millipore). Vehicle (2% DMSO in saline)-treated bacteria and broth without bacteria were used as negative controls.
Statistical analysis
All in vitro experiments were performed in triplicate and were obtained from three independent assays. Statistical comparison between groups was performed in the software GraphPad Prism version 5.0 by using one-way and repeated measures analysis of variance followed by the Bonferroni test. P<0.05 were considered significant.
Results
In silico analysis
Identified biological activities.
Analysis of the probable biological activities of cuminaldehyde found that this compound has > 30% (Pa>0.3) probability to present 726 activities. Of those, 198 have moderate probability (Pa>0.5) of occurrence and 69, high probability of occurrence (Pa>0.7). Of the total identified activities, 15 were antimicrobial (Table 2).
For comparison, the biological activities of ciprofloxacin were also evaluated. Forty-seven activities with > 30% probability of occurrence were identified for ciprofloxacin. Of those, only 04 had high probability of occurrence (Pa>0.7). Analysis of all 47 biological activities indicated that 12 of them were antimicrobial (Table 2).
Estimated oral bioavailability and predicted toxicity.
For predicting the oral bioavailibility of cuminaldehyde, its TPSA, iLogP, molecular weight, nALH and nDLH values were analyzed. Table 3 demonstrates that cuminaldehyde fits the criteria to present good estimated oral bioavailability (TPSA = 17.07; LogP of 2.03; molecular weight of 148.20; nALH of 1.0 and nDLH of 0.0). Ciprofloxacin presented a TPSA of 74.57, iLogP of 2.24, molecular weight of 331.34, nDLH of 2.0 and nALH of 5.0 (Table 3).
Table 3 depicts the predicted toxic effects of cuminaldehyde in comparison with those of ciprofloxacin. Cuminaldehyde was suggested to be an irritant, with no mutagenic, tumorigenic, hepatotoxic or harmful effects on reproduction. On the other hand, ciprofloxacin was found to be mutagenic, with no tumorigenic actions and no effects in the liver or the reproductive system. The estimated LD50 was 1,320 and 2,000 mg/kg for cuminaldehyde and ciprofloxacin; respectively (Table 3). Both drugs exhibited a toxicity score of 4.0, indicating they are classified as harmful if swallowed at their LD50 (Table 3).
Information on the estimations of gastrointestinal absorption, permeability through the blood brain barrier and skin permeation (log Kp in centimeters (cm)/s) are shown in Table 3. Both cuminaldehyde and ciprofloxacin were considered to be highly absorbed by the gastrointestinal tract; however, only cuminaldehyde was predicted to cross the blood brain barrier (Table 3). The estimated Log Kp values were of -5.52 and -9.09 cm/s for cuminaldehyde and ciprofloxacin; respectively (Table 3).
Table 3 also indicates the predicted solubility (LogS) of cuminaldehyde in comparison with ciprofloxacin. Both compounds were found to be soluble in water with Log S of -2.81 and -3.32 for cuminaldehyde and ciprofloxacin; respectively. Drug-likeness for cuminaldehyde was estimated at -11.01 and 2.07 for cuminaldehyde and ciprofloxacin; respectively. Both compounds presented similar drug-scores (0.55).
Antimicrobial assays
Analysis of cuminaldehyde antimicrobial activity on S. aureus and E. coli.
Table 4 shows the MIC values detected for cuminaldehyde and ciprofloxacin when assessed against the standard strains S. aureus ATCC 6538 and EAEC 042, and the clinical isolates Saa, Sav and Ecr. Cuminaldehyde presented antimicrobial activity against all tested bacteria, being more effective against EAEC 042 (1.5 mg/ml). All bacteria, except the clinical isolate Ecr, were susceptible to ciprofloxacin (Table 4).
We additionaly investigated the effects of the sub-inhibitory concentrations of cuminaldehyde and ciprofloxacin. Whilst E. coli (EAEC 042 and Ecr; Fig 1D and 1E) viability was reduced (48–62%) by cuminaldehyde at MIC/2-MIC8, no effects were observed for these concentrations when assessed against S. aureus (Fig 1A–1C). Only the clinical isolates Saa and Ecr had their viability reduced by sub-inhibitory concentrations of ciprofloxacin (MIC/2-MIC/8; Fig 1F and 1J). Maximum reductions were of 49% and 30%, for Saa and Ecr; respectively.
Different cuminaldehyde concentrations (MIC/2-MIC/8) were incubated with S. aureus ATCC 6538 (a), EAEC 042 (e) and the clinical isolates Saa, Sav and Ecr (b,c and e), for 24h. For comparison, the effects of sub-inhibitory concentrations of ciprofloxacin were evaluated on S. aureus ATCC 6538 (f), EAEC 042 (i) and the clinical isolates Saa, Sav and Ecr (g,h and j). Vehicle (2% DMSO in saline)-treated bacteria were used as controls. *p<0.05; differs from the control group. Data were obtained from three independent experiments.
Cuminaldehyde effects on biofilm formation by S. aureus and E. coli.
The effects of the sub-inhibitory concentrations of cuminaldehyde on biofilm formation were investigated by analysis of biofilm mass and viability. All tested bacteria, except the clinical isolate Ecr, formed biofilm. Cuminaldehyde reduced the viability of bacterial biofilm when assessed at MIC/2 (Fig 2A–2D). Also, at MIC/4, the compound decreased the viability of both Saa and EAEC 042 (Fig 2B and 2D). On the other hand, only Saa biofilm viability was prevented by ciprofloxacin (MIC/2-MIC/8; Fig 2E–2H).
Different concentrations of cuminaldehyde (MIC/2-MIC/8) were incubated with S. aureus and E. coli, for 24h. Biofilm viability was assessed Cuminaldehyde effects on the viability and mass of the biofilm formed by S. aureus ATCC 6538 (a and e), EAEC 042 (d and h) and the clinical isolates Saa (b and f) and Sav (c and g) were evaluated. For comparison, ciprofloxacin effects on the viability and mass of the biofilm formed by S. aureus ATCC 6538 (i and m), EAEC 042 (l and p) and the clinical isolates Saa (j and n) and Sav (k and o) were also assessed. Vehicle (2% DMSO in saline)-treated bacteria were used as controls. *p<0.05; differs from the control group. Data were obtained from three independent experiments.
Also, cuminaldehyde significantly diminished biofilm mass formation by S. aureus (ATCC 6538, Saa and Sav; Fig 2I–2L). Ciprofloxacin inhibitory effects on biofilm mass were noted in the clinical isolates Saa and Sav (Fig 2N and 2O), but not in S. aureus ATCC 6538 and EAEC 042 strains (Fig 2M–2P).
Effects of the association of sub-inhibitory concentrations of cuminaldehyde and ciprofloxacin on bacterial survival.
Time-kill assays were performed to assess the effects of the association of cuminaldehyde with sub-inhibitory concentrations of ciprofloxacin on S. aureus and E. coli survival. The association of MIC/2 cuminaldehyde and MIC/2 ciprofloxacin was synergistic when assessed against S. aureus. Indeed, their association decreased bacterial population (> 4.0 log10 CFU/ml, > 3.0 log10 CFU/ml and > 4.0 log10 CFU/ml for S. aureus ATCC 6538, Saa and Sav; respectively; Fig 3A–3C). Similarly, the co-incubation of cuminaldehyde (MIC/4) with ciprofloxacin (MIC/2) significantly decreased E. coli survival (> 7.0 log10 CFU/ml.and (> 4.0 log10 CFU/ml, for EAEC 042 and Ecr; respectively; Fig 3D and 3E). No significant effects were observed for cuminaldehyde or ciprofloxacin by themselves, at the tested concentrations.
Cuminaldehyde (MIC/2 or MIC/4) was co-incubated with ciprofloxacin (MIC/2) over 8 h, and their effects were assessed against S. aureus ATCC 6538 (a), Saa (b), Sav (c), EAEC 042 (d) and (e) Ecr. Vehicle (2% DMSO in saline)-treated bacteria, as well those treated with either cuminaldehyde or ciprofloxacin were used as controls. *p<0.05; differs from the ciprofloxacin group. Data was obtained from 3 experiments.
Effects of the association of sub-inhibitory concentrations of cuminaldehyde and ciprofloxacin on biofilm formation.
The effects of the co-incubation of cuminaldehyde (MIC/8) and ciprofloxacin (MIC/2) sub-inhibitory concentrations were analysed (Fig 4A–4D). Data depicted in Fig 4 demonstrates that cuminaldehyde further reduces ciprofloxacin effects on the biofilm mass formation by S. aureus ATCC 6538 and Sav (panels a and c). However, it enhanced the amount of Saa-dependent biofilm formation (Fig 4B), without interfering with EAEC-induced biofilm (Fig 4D).
Cuminaldehyde (MIC/8) was co-incubated with ciprofloxacin (MIC/2), for 24h. The combination was assessed against S. aureus ATCC 6538 (a), EAEC 042 (d) and the clinical isolates Saa (b) and Sav (c). Vehicle (2% DMSO in saline), cumminaldehyde (MIC/8) and ciprofloxacin (MIC/2) effects on the biofilm mass formation were used as controls. *p<0.05; differs from the control group. #p<0.05; differs from the ciprofloxacin group. Data were obtained from three independent experiments.
Discussion
Studies with the essential oil of C. cyminum seeds indicated its antimicrobial potential against a series of bacteria including S. aureus and E. coli [20–27]. Cuminaldehyde has been pointed as the major compound associated with the pharmacological properties of C. cyminum seeds [18, 28].
In our study, the in silico evaluation of the biological activities of cuminaldehyde confirmed its antimicrobial potential. We aimed at gaining further knowledge of the anti-S. aureus and anti-E. coli actions of cuminaldehyde. Therefore, its properties and effects were compared to those of ciprofloxacin which has been commonly used for the treatment of urinary tract infections.
Evaluation of cuminaldehyde oral bioavailability estimated the compound is a good candidate for oral intake with a drug score of 0.55 (which indicates the probability of a compound of becoming a commercial drug), similar to the one observed for ciprofloxacin. However, doses >1,320 mg/kg of the compound would be lethal to mammalians, as cuminaldehyde was classified as harmful if swallowed at this LD50 (toxicity class equal to 4.0). In silico analysis also revealed that, as observed for ciprofloxacin, cuminaldehyde is likely to be absorbed by the gastrointestinal tract. Of note, this compound was suggested to be able to cross the blood brain barrier, meaning its dosing for systemic use should be carefully considered as it may result in unwanted effects in the nervous system.
Prediction of skin permeation (log Kp) indicated that cuminaldehyde is more likely to be absorbable by skin layers than ciprofloxacin. Of note, S. aureus is a common antibiotic-resistant pathogen colonizing skin wounds [41, 42]. Thus, topical cuminaldehyde may be useful as an adjuvant therapy to skin infections in association with topical antimicrobials. In this context, the predicted irritant effects of cuminaldehyde should be considered and a minimum effective dose should be adopted for its topical use.
Recent studies demonstrated cuminaldehyde has antimicrobial effects, presenting a MIC of 0.311 mg/ml and 0.650–4.98 mg/ml for E. coli and S. aureus; respectively [30,32,43]. In our study, cuminaldehyde was antimicrobial against all tested bacteria; however, it was found to be more effective against E. coli. Interestingly, the compound was antimicrobial against the ciprofloxacin-resistant clinical isolate Ecr. Analysis of sub-inhibitory concentrations of cuminaldehyde on bacterial viability reinforced its effectiveness against E. coli. Ciprofloxacin sub-inhibitory concentrations also reduced, although in a smaller degree, Ecr viability (30% viability reduction in ciprofloxacin versus 48% in cuminaldehyde-treated bacteria),
Of importance, compounds with anti-biofilm actions have been investigated as alternative therapies to treat bacterial infections [44–46]. It was previously reported that the essential oil of C. cyminum seeds reduces Streptococcus mutans and S. pyogenes biofilm formation [47]. Similar effects were observed for sub-inhibitory concentrations of the essential oil when assessed against Klebsiella pneumoniae [48]. Recently, cuminaldehyde was shown to impair biofilm formation by E. coli [32]. Herein, cuminaldehyde sub-inhibitory concentrations reduced the viability of all formed biofilms, but only significantly decreased S. aureus biofilm mass formation. By comparison, the sub-inhibitory concentrations of ciprofloxacin were only able to diminish Saa biofilm viability, in addition to Saa and Sav biofilm mass formation. These results indicate that cuminaldehyde presents a broader anti-biofilm activity than ciprofloxacin at the tested concentrations.
Many compounds have been investigated as adjuvants to antibiotic therapy to overcome bacterial resistance [16, 17]. The ability of C. cyminum seed essential oil to potentiate ciprofloxacin antimicrobial effects was shown against K. pneumoniae [48]. Herein, the in silico prediction of the biological activities of cuminaldehyde indicated this compound may act as a membrane permeability enhancer. Therefore, we hypothesized on whether this compound enhances the antimicrobial effects of ciprofloxacin. Our results demonstrate that cuminaldehyde (MIC/2-MIC/4) is synergistic to ciprofloxacin (MIC/2), as their association effectively reduces S. aureus and E. coli survival. A similar effect was seen in S. aureus (ATCC 6538 and Sav) biofilm formation. On the other hand, cuminaldehyde potentiated biofilm mass formation in ciprofloxacin-treated Saa, suggesting the combinatory effects of these drugs on biofilm mass formation may be strain-dependent.
Overall, the evidences gathered herein, suggest that cuminaldehyde may be useful as an adjuvant to ciprofloxacin therapy. As reduced doses of this commercial antibiotic would be used in conjunction with cuminaldehyde to treating S. aureus and E. coli-induced infections, lower pressure on bacterial resistance would probably result from this combined therapy; a hypothesis which remains to be investigated.
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