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International Journal of Microbiology
Volume 2018, Article ID 1920198, 12 pages
https://doi.org/10.1155/2018/1920198
Research Article

Antistaphylococcal and Antibiotic Resistance Modulatory Activities of Thirteen Cameroonian Edible Plants against Resistant Phenotypes

Department of Biochemistry, Faculty of Science, University of Dschang, Dschang, Cameroon

Correspondence should be addressed to Victor Kuete; rf.oohay@rotciveteuk

Received 24 March 2018; Accepted 6 June 2018; Published 3 July 2018

Academic Editor: Clemencia Chaves-López

Copyright © 2018 Brice E. N. Wamba et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Abstract

Background. In this study, 18 methanol extracts from Cameroonian edible plants were tested for their antibacterial activities against 26 strains of S. aureus; the role of efflux pumps in the resistance of tested bacteria and the antibiotic resistance-modulating activities against selected multidrug-resistant (MDR) phenotypes were also investigated. Methods. Broth microdilution assay was used to evaluate the antibacterial activity, the role of efflux pumps, and the antibiotic resistance-modulating effects of plant extracts. Results. Extracts from Dacryodes edulis seeds (DES) and Dacryodes edulis bark (DEB) were active against all 26 tested bacterial strains, within the minimal inhibitory concentration (MIC) range of 256–1024 µg/mL. MIC values varied from 64 to 1024 µg/mL against 96.2% of the 26 tested bacteria for Phaseolus vulgaris leaves (PVL), 92.3% for Azadirachta indica bark (AIB), Dacryodes edulis leaves (DEL), and Ricinodendron heudelotii leaves (RHL). The lowest MIC value of 64 µg/mL was obtained with the extract from Cucurbita maxima beans (CMB) against MRSA4 strain and from Uapaca guineensis bark (UGB) against MRSA9 strain. Bacterial efflux pump inhibitor (EPI), carbonyl cyanide m-chlorophenyl hydrazone (CCCP), improved the activity of DES and UGB as well as that of extracts from Hibiscus esculentus leaves (HEL) and Uapaca guineensis leaves (UGL) against resistant S. aureus strains. Antibiotic-modulating effects against more than 70% of the S. aureus strains tested were obtained when RHL (at MIC/2) was combined with CIP, ERY, and KAN (88.89%), CHL (88.89%), TET (77.78%), and STR (88.89%). Conclusion. The present study demonstrated that the 13 tested plants had antistaphylococcal effects and that DES, HEL, UGL, and UGB could be used in combination with EPI to combat resistance to Staphylococcus aureus. Also, it demonstrated that some studied extracts and mostly RHL could be used as antibiotic resistance modulators to fight against resistant strains of S. aureus.

1. Background

Bacterial infections caused by Staphylococcus aureus are globally responsible for 7–10% of deaths annually [1]. It is the most virulent species of the genus Staphylococcus and has emerged as one of the most important human pathogens in the last decades, being one of the main causes of hospital and community infections [2]. This bacterium causes a wide range of clinical infections, ranging from common infections such as skin and soft tissue infections to septicemia, pneumonia, and toxinosis [3, 4]. The fight against S. aureus is hindered by the development of resistance of various strains to antibiotics [59]. The multidrug resistance (MDR) observed in Gram-positive bacteria is mostly attributed to overexpression of efflux pumps and antibiotics-degrading enzymes. This MDR of S. aureus propels the search of new antibacterials with more efficiency and low toxicity. Plant kingdom contains a variety of pharmacologically active secondary metabolites, and some of them have been reported for their antibacterial activities [10, 11]. Their use to combat S. aureus antibiotic resistance is an attractive strategy. In regard to the loss of efficacy of several antibiotics and the scarcity of new antibacterial agents, it is also important to search for substances capable of restoring the activity of antibiotics. Antibacterial screenings of African plants have yielded promising results in the past [1215]. The present study was set up to evaluate the antistaphylococcal potential of 13 Cameroonian food plants: Azadirachta indica A. Juss (Meliaceae), Citrus grandis (L.) Osbeck (Rutaceae), Cucurbita maxima Duch. (Cucurbitaceae), Dacryodes edulis (G. Don) H. J. Lam (Burseraceae), Hibiscus esculentus L. (Malvaceae), Ipomoea batatas (L.) Lam (Convolvulaceae), Irvingia gabonensis (Aubry. Lec. ex O. Rorke) Baill. (Irvingiaceae), Phaseolus vulgaris L. (Fabaceae), Ricinodendron heudelotii (Baill.) Pierre ex Heckel (Euphorbiaceae), Saccharum officinarum L. (Poaceae), Spondias mombin L. (Anacardiaceae), Theobroma cacao L. (Sterculiaceae), and Uapaca guineensis Muell. Arg. (Euphorbiaceae). The study was extended on the role of efflux pumps in resistance to some plant extracts as well as the ability of extracts to potentiate the activity of selected antibiotics.

2. Materials and Methods

2.1. Plant Materials and Extraction

The thirteen edible plants were collected from different localities of Cameroon, namely, Obala (Centre Region), Muyuka (South-West Region), and Dschang (West Region) from March to April 2016. The collected plant samples included the bark of Azadirachta indica A. Juss (Meliaceae), leaves of Citrus grandis (L.) Osbeck (Rutaceae), beans of Cucurbita maxima Duch. (Cucurbitaceae), leaves, bark, and seeds of Dacryodes edulis (G. Don) H. J. Lam (Burseraceae), leaves of Hibiscus esculentus L. (Malvaceae), beans of Ipomoea batatas (L.) Lam (Convolvulaceae), leaves of Irvingia gabonensis (Aubry. Lec. ex O. Rorke) Baill. (Irvingiaceae), leaves of Phaseolus vulgaris L. (Fabaceae), bark and leaves of Ricinodendron heudelotii (Baill.) Pierre ex Heckel (Euphorbiaceae), leaves of Saccharum officinarum L. (Poaceae), leaves of Spondias mombin L. (Anacardiaceae), leaves and beans of Theobroma cacao L. (Sterculiaceae), and leaves and bark of Uapaca guineensis Muell. Arg. (Euphorbiaceae). Plants were identified at the National Herbarium in Yaoundé (Cameroon) where the voucher specimens were conserved under the registration numbers (Table 1). The dried and powdered material (100 g) of each plant was macerated in 300 mL of methanol at room temperature for 48 h and then filtered using Whatman filter paper No. 1. The filtrate obtained was concentrated using a rotary evaporator under reduced pressure to obtain the crude methanol extract, which was kept at 4°C until further use.

Table 1: Information on the studied plants.
2.2. Chemicals

Eight reference antibiotics (RA) purchased from Sigma-Aldrich (St Quentin Fallavier, France) were tested: ampicillin (AMP), cefepime (CEF), chloramphenicol (CHL), ciprofloxacin (CIP), erythromycin (ERY), kanamycin (KAN), streptomycin (STR), and tetracycline (TET); p-iodonitrotetrazolium chloride (INT) (Sigma-Aldrich) was used as bacterial growth revelator; carbonyl cyanide m-chlorophenyl hydrazone (CCCP) and chlorpromazine (CPZ) (Sigma-Aldrich) were used as efflux pump inhibitors (EPIs); and dimethylsulfoxide (DMSO) was used to dissolve the plant extracts.

2.3. Bacteria, Culture Media, and Growth Conditions

The strains of Staphylococcus aureus used included a reference strain obtained from American Type Culture Collection (ATCC; ATCC 25923), 8 methicillin-resistant S. aureus (MRSA) strains (MSSA1, MRSA3, MRSA4, MRSA6, MRSA8, MRSA9, MRSA11, and MRSA12) (obtained from the culture collection of the Laboratory of Microbiology, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Japan, and provided by Dr Jean P. Dzoyem, University of Dschang) [8, 9], and 17 resistant clinical laboratory strains of S. aureus (SA01, SA07, SA18, SA23, SA36, SA39, SA56, SA64, SA68, SA88, SA114, SA116, SA124, SA126, SA127, SA135, and SA139) available in our laboratory collection and previously isolated from patients in Ad-Lucem Hospital in Banka-Bafang (West Region of Cameroon) [54]. Their bacterial features are summarized in Table 2. They were cultured at 37°C overnight on Mueller Hinton agar 24 h prior to any assay. The Mueller Hinton broth (MHB) was used as liquid culture medium for susceptibility tests.

Table 2: Bacterial strains and features.
2.4. Preliminary Phytochemical Screenings

Potential classes of potential antibacterial phytochemicals such as alkaloids (Dragendorff’s and Mayer’s tests: 5 mg plant extract in 10 mL methanol; a portion of 2 mL extract + 1% HCl + steam, 1 mL filtrate + 6 drops of Mayor’s reagents/Wagner’s reagent/Dragendorff’s reagent; cream precipitate/brownish-red precipitate/orange precipitate indicated the presence of respective alkaloids), saponins (frothing test: 0.5 mL filtrate+ 5 mL distilled water; frothing persistence indicated the presence of saponins), steroids and triterpenoids (Liebermann–Burchard test: 5 mg plant extract in 10 mL chloroform, filtered; a 2 mL filtrate + 2 mL acetic anhydride+ conc. H2SO4; blue-green ring or pink-purple indicated the presence of steroids or triterpenoids), phenolics: anthraquinones (5 mg plant extract in 10 mL methanol; a portion of 2 mL + 2 mL ether-chloroform 1 : 1 v/v + 4 mL NaOH 10% (w/v); red color indicated the presence of anthraquinones), flavonoids (5 mg plant extract in 10 mL methanol; a portion of 2 mL + conc. HCl + magnesium; ribbon pink-tomato red color indicated the presence of flavonoids), polyphenols (ferric chloride test: 5 mg plant material in 10 mL methanol; a portion of 2 mL + 2 mL FeCl3; violet-blue or greenish color indicated the presence of phenols), and tannins (5 mg plant extract in 10 mL distilled water; a portion of 2 mL + 2 mL FeCl3; blue-black precipitate indicated the presence of tannins) (Table 3) were investigated according to the described phytochemical methods [11, 55].

Table 3: Extraction yields and phytochemical composition of the plant extracts.
2.5. INT Colorimetric Assay for MIC and Minimal Bactericidal Concentration (MBC) Determinations

The MIC and minimal bactericidal concentration (MBC) determinations on various strains of S. aureus were performed using the rapid INT colorimetric assay [56] with some modifications as previously described [14, 38]. The samples were dissolved in DMSO/MHB. The final concentration of DMSO was lower than 2.5%. The twofold dilutions of the samples were made in a 96-well microplate, and the tested bacterial concentration was 1.5 × 106 colony-forming unit (CFU)/mL. The microplates were incubated at 37°C for 18 h. All assays were performed in triplicate and repeated thrice. Wells containing MHB, 100 µL of inoculum, and DMSO to a final concentration of 2.5% served as negative control. The MIC of each sample was detected after 18 h incubation at 37°C, following addition (40 µL) of 0.2 mg/mL of INT and incubation at 37°C for 30 minutes as the lowest sample concentration that prevented the color change of the medium and exhibited complete inhibition of microbial growth [56]. The MBC was determined by adding 50 µL aliquots of the preparations, which did not show any growth after incubation during MIC assays, to 150 µL of MHB. These preparations were further incubated at 37°C for 48 h. The MBC was regarded as the lowest concentration of samples, which did not produce a color change after addition of INT as mentioned above [57, 58].

2.6. Evaluation of the Role of Efflux Pumps in the Resistance of Selected Bacteria

To evaluate the involvement of efflux pumps in the resistance of selected bacterial strains to some of the active plant extracts, Dacryodes edulis seeds (DES), Hibiscus esculentus leaves (HEL), Uapaca guineensis leaves (UGL), Uapaca guineensis bark (UGB), and CIP (reference drug) were tested in the absence or presence of EPI (CCCP (0.5 µg/mL) or CPZ (25 µg/mL)). MICs of samples alone or in combination with EPI were determined as above, and the increase in activity was determined as the ratio of MIC of sample alone versus sample in combination with EPI. All assays were performed in triplicate and repeated thrice.

2.7. Antibiotic Activity Modulation Assays

To evaluate the antibiotic resistance modulation activity of the most active extracts: Azadirachta indica bark (AIB), Dacryodes edulis seeds (DES), Dacryodes edulis bark (DEB), Dacryodes edulis leaves (DEL), Phaseolus vulgaris leaves (PVL), Ricinodendron heudelotii leaves (RHL), and Uapaca guineensis bark (UGB), a preliminary assay was performed in order to assess the MICs of antibiotics in the absence and presence of these extracts using the broth microdilution method as previously described [14, 38, 56]. S. aureus SA88 was used for the preliminary assay, and the samples were tested at various subinhibitory concentrations (MIC/2, MIC/4, MIC/8, and MIC/16). Results allowed to select DEB, DEL, DES, RHL, and UGB to be tested further against S. aureus ATCC 25923, and 8 resistant strains of S. aureus (MRSA3, MRSA4, MRSA9, MRSA11, MRSA12, SA18, SA36, and SA64) at MIC/2 and MIC/4. Briefly, after serial dilutions of antibiotics, extract was added to each well at its subinhibitory concentrations, the bacterial inoculation was done, and the MIC was determined. Rows receiving antibiotic dilutions without extracts were used for the determination of the MICs of the antibiotics. The modulation factor was defined as the ratio of the MIC of antibiotic alone versus that of antibiotic in the presence of extract. Modulation factor ≥2 was set as the cutoff for biologically significance of antibiotic resistance-modulating effects [59].

3. Results

3.1. Phytochemical Composition of Plant Extracts

The major classes of phytochemicals were screened in the 18 studied plant extracts (Table 3). It appears that all extracts contained polyphenols and tannins. Other classes of phytochemicals were selectively present. Only the extract of the beans of Theobroma cacao contained all the investigated classes of secondary metabolites.

3.2. Antibacterial Activity

The antibacterial activities of the 18 tested extracts and ciprofloxacin against 26 strains of S. aureus are summarized in Table 4. It appears that extracts from Dacryodes edulis seeds (DES) and Dacryodes edulis bark (DEB), within a MIC range of 256–1024 µg/mL, and ciprofloxacin (MIC below 4 µg/mL), were active against all 26 tested bacterial strains. Other extracts were selectively active, and MIC values varied from 64 to 1024 µg/mL against 25/26 (96.2%) tested bacteria for Phaseolus vulgaris leaves (PVL), 24/26 (92.3%) for Azadirachta indica bark (AIB), Dacryodes edulis leaves (DEL), and Ricinodendron heudelotii leaves (RHL), 23/26 (88.5%) for Hibiscus esculentus leaves (HEL), 19/26 (73.1%) for Uapaca guineensis leaves (UGL), 18/26 (69.2%) for Ricinodendron heudelotii bark (RHB) and Uapaca guineensis bark (UGB), 17/26 (61.5%) for Saccharum officinarum leaves (SOL), 16/26 (61.5%) for Ipomoea batatas leaves (IBL) and Theobroma cacao leaves (TCL), 15/26 (57.7%) for Citrus grandis leaves (CGL), 14/26 (53.8%) for Theobroma cacao beans (TCB), 12/26 (46.2%) for Cucurbita maxima beans (CMB), 10/26 (38.5%) for Spondias mombin leaves (SML), and 7/26 (26.9%) for Irvingia gabonensis beans (IGB). The lowest MIC value of 64 µg/mL was obtained with CMB against MRSA4 strain and UGB against MRSA9 strain.

Table 4: MIC and MBC of the plant extracts and ciprofloxacin against Staphylococcus aureus strains.
3.3. Role of Efflux Pumps in the Resistance of Strains of S. aureus

Four extracts (DES, HEL, UGL, and UGB) and CIP (reference drug) were tested in the absence or presence of CCCP (0.5 µg/mL) and CPZ (25 µg/mL) to evaluate the role of efflux pumps in the resistance of 14 tested S. aureus strains. The results are summarized in Tables 5 and 6. It appears that CCCP significantly improved the activity of the 4 tested extracts against the majority of S. aureus strains (Table 5). The increase of activity in the presence of CCCP ranged from 2-fold to >128-fold. The highest increase of activity (>128-fold) was obtained when DES, UGB, and UGL were tested in the presence of CCCP on at least one S. aureus strain. In contrast, in the presence of CPZ, no improvement in the activity of the four extracts was observed (Table 6). This is clear indication that CCCP was the appropriate EPI of the studied S. aureus strains.

Table 5: MIC of extracts and ciprofloxacin in the absence (−) and presence (+) of carbonyl cyanide m-chlorophenyl hydrazone (CCCP) against selected strains of Staphylococcus aureus.
Table 6: MIC of extracts and ciprofloxacin in the absence (−) and presence (+) of chlorpromazine (CPZ) against selected strains of Staphylococcus aureus.
3.4. Antibiotic Resistance Modulation Activity of Extracts

Seven plant extracts, AIB, DES, DEB, DEL, PVL, RHL, and UGB, at their various subinhibitory concentrations (MIC/2, MIC/4, MIC/8, and MIC/16) were first tested in combination with 8 antibiotics: CHL, TET, CIP, AMP, CEF, ERY, STR, and KAN against S. aureus SA88 strain. The results summarized in Table S1 (Supplementary Materials) show that better modulation of the activity of antibiotics was obtained with all extracts at MIC/2 and MIC/4. At their MIC/2, 2-fold or more increase of antibiotic activities was obtained with PVL, AIB, DEB, DES, DEL, UGB, and RHL and 2, 4, 4, 6, 6, 7, and 8 of the 8 tested antibiotics, respectively (Table S1; Supplementary Materials). Consequently, the most active extracts, DEB, DEL, DES, RHL, and UGB, were further tested in combination with the above 8 antibiotics against the reference strains (ATCC 25923) and 8 resistant strains of S. aureus at MIC/2 and MIC/4 (Tables S2S6; Supplementary Materials). Results showed that 2-fold or more antibiotic-modulating effects against more than 70% of the S. aureus strains tested were obtained when DEB was combined with CHL at MIC/2 (77.78%; Table S2; Supplementary Materials), when DEL was combined with CHL and STR at MIC/2 (77.78%; Table S3; Supplementary Materials), when DES was combined with CIP (77.78% at MIC/2), CHL (100% and 88.89 at MIC/2 and MIC/4 resp.), TET (77.78% at MIC/2 and MIC/4), and STR (88.89% and 77.78% at MIC/2 and MIC/4 resp.) (Table S4; Supplementary Materials), when RHL was combined with CIP, ERY, and KAN (88.89% and 77.78% at MIC/2 and MIC/4 resp.), CHL (88.89% at MIC/2 and MIC/4), TET (77.78% at MIC/2 and MIC/4), and STR (88.89% at MIC/2) (Table S5; Supplementary Materials), and when UGB was combined with CHL, KAN, and STR (77.78% at MIC/2 and MIC/4) (Table S6; Supplementary Materials).

4. Discussion

4.1. Phytochemical Composition of Extracts

Polyphenols and tannins were detected in all extracts. The role of several molecules belonging to polyphenols as antibacterials has been demonstrated [10, 11, 38, 61]. Tannins also belong to a class of polyphenols, and its presence in all extracts could in part explain the fact that all the tested extracts were active in at least one strain of the tested bacteria [10]. However, it should be made clear that the presence of a class of secondary metabolite with reported antibacterial effect is not a guarantee of the good activity of a plant. The antibacterial effect depends on the structure and the amount of a particular phytochemical in the plant or possible interactions with other compounds. This could explain why the extract from the beans of Theobroma cacao that contained all the investigated classes of secondary metabolites (Table 3) was not the most active sample (Table 4).

4.2. Antibacterial Potential of Extracts

Resistance of bacteria to antibiotics propels the search of new agents to fight against MDR phenotypes. In the present study, clinical strains of S. aureus used were previously reported as resistant to at least one commonly used antibiotic [8, 9] (Table 2). Several locally isolated strains of S. aureus [54] were used herein, to better adapt the study to our environment. According to established criteria, MIC values in the range of 100–1000 µg/mL are indication that plant extracts bear antimicrobial activities [62]. Also, the antibacterial activity of botanicals is considered significant if MIC values are below 100 µg/mL, moderate if 100 ≤ MICs ≤ 625 µg/mL, and weak if MICs > 625 µg/mL [37, 60]. On these bases, it can be deduced that all the tested plant extracts had antistaphylococcal activities, except Irvingia gabonensis beans (IGB), with MICs above 1000 µg/mL against all tested strains of S. aureus (Table 4). This activity was significant for CMB against MRSA4 strain and UGB against MRSA9 strain (MIC: 64 µg/mL). Most of the recorded MIC values ranged from 512 to 1024 µg/mL, indicating that extracts rather exhibited moderate to low antistaphylococcal effects. However, this activity could be considered important because the clinical strains of S. aureus used were resistant phenotypes while extracts were from edible plants. In effect, it was suggested that if botanicals are food plants, as they are allegedly nontoxic or less toxic than other medicinal plants, their antibacterial activity is significant in a range of 100 ≤ MIC ≤ 512 µg/mL and moderately active in a range of 512 < MIC ≤ 2048 µg/mL [63].

4.3. Role of Efflux Pumps in Susceptibility of S. aureus Strains to the Extracts

Bacterial efflux systems are associated with major human health concerns as they are involved in the resistance of pathogenic bacteria such as S. aureus [6466]. Previously, inhibition of efflux pumps by natural products has been found to improve the activity of antibiotics against S. aureus. For example, inhibition of the TetK efflux pump was reported with the essential oil of Chenopodium ambrosioides and its constituent α-terpinene against S. aureus IS-58 strain [66]. In the present study, two well-known EPIs (CCCP and CPZ) were used to assess the implication of efflux pumps in the resistance of the studied S. aureus strains to plant extracts. CCCP is an inhibitor of the proton-motive force of ATP-binding cassette (ABC) transporters of several Gram-negative and Gram-positive bacteria, including S. aureus [57]. CPZ is capable of reversing or reducing the antibiotic resistance of bacteria including S. aureus [67], due to its indirect effects on ATPase activity that is dependent upon Ca2+ [68]. In the present study, it was found that CCCP contrary to CPZ improved the activity of the four extracts (DES, HEL, UGL, and UGB) (Tables 5 and 6). This indicates that ABC transporters are involved in the resistance of the studied strains of S. aureus and that combination of extracts such as HEL, UGL, and UGB with an inhibitor of ABC transporters could improve the antistaphylococcal fight.

4.4. Antibiotic Modulation Effects of Extracts

The antibiotic resistance-modulating effects of several botanicals and phytochemicals against resistant bacteria have been documented [1215, 59, 69]. It has been suggested that extracts capable of potentiating the activity of antibiotics on more than 70% of bacteria could be potential efflux pump inhibitors [70]. In this study, antibiotic modulation activity of extracts at their MIC/2 on more than 70% tested strains of S. aureus was obtained with the association of DEB and DEL and with 1/8 (12.5%) tested antibiotics (Tables S2 and S3; Supplementary Materials), UGB with 2/8 (25%) antibiotics (Table S6; Supplementary Materials), DES with 4/8 (50%) antibiotics (Table S4; Supplementary Materials), and RHL with 6/8 (75%) antibiotics (Table S5; Supplementary Materials). Hence, the tested extracts and mostly RHL may act as efflux pump inhibitors [70]. The use of CCCP indicated that ABC transporters were the efflux pumps involved in the resistance of the tested bacteria, suggesting that the above extract could be the inhibitors of such pumps. The potential of the R. heudelotii leaf extract (RHL) to reverse antibiotic resistance in Gram-negative MDR bacteria was previously reported [18]. The present study therefore provides more information about the ability of this plant to modulate the activity of antibiotics against resistant strains of S. aureus.

5. Conclusion

In conclusion, the present work provides informative data about the antistaphylococcal potential of 13 Cameroonian food plants. It also indicates that some extracts such as DES, HEL, UGL, and UGB could be used in combination with EPI to combat resistance of Staphylococcus aureus to antibiotics. Finally, this study also demonstrates that some studied extracts and mostly RHL could be used as antibiotic resistance modulators, providing a new weapon against the resistance of S. aureus to antibiotics.

Abbreviations

AIB:Azadirachta indica bark
AMP:Ampicillin
ATCC:American Type Culture Collection
CCCP:Carbonyl cyanide m-chlorophenyl hydrazone
CEF:Cefepime
CFU:Colony-forming unit
CGL:Citrus grandis
CHL:Chloramphenicol
CIP:Ciprofloxacin
CMB:Cucurbita maxima beans
CPZ:Chlorpromazine
DEB:Dacryodes edulis bark
DEL:Dacryodes edulis leaves
DES:Dacryodes edulis seeds
DMSO:Dimethylsulfoxide
EPI:Efflux pump inhibitors
ERY:Erythromycin
HEL:Hibiscus esculentus leaves
IBL:Ipomoea batatas leaves
IGB:Irvingia gabonensis beans
INT:p-Iodonitrotetrazolium chloride
KAN:Kanamycin
MBC:Minimal bactericidal concentration
MDR:Multidrug-resistant
MHB:Mueller Hinton broth
MIC:Minimal inhibitory concentration
MRSA:Methicillin-resistant Staphylococcus aureus
PVL:Phaseolus vulgaris leaves
RA:Reference antibiotics
RHB:Ricinodendron heudelotii bark
RHL:Ricinodendron heudelotii leaves
SA:Staphylococcus aureus
SML:Spondias mombin leaves
SOL:Saccharum officinarum leaves
STR:Streptomycin
TCB:Theobroma cacao beans
TCL:Theobroma cacao leaves
TET:Tetracycline
UGB:Uapaca guineensis bark
UGL:Uapaca guineensis leaves.

Data Availability

The data used to support the findings of this study are included within the article.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

Brice E. N. Wamba, Paul Nayim, Joachim K. Dzotam, and Ornella J. T. Ngalani carried out the study. Armelle T. Mbaveng and Victor Kuete designed the experiments. Armelle T. Mbaveng and Victor Kuete wrote the manuscript. Armelle T. Mbaveng and Victor Kuete supervised the work and provided the bacterial strains. All authors read and approved the final manuscript.

Acknowledgments

The authors are thankful to the Cameroon National Herbarium for identification of plants and also thank Dr. Jean P. Dzoyem (University of Dschang, Cameroon) for providing the MRSA strains of S. aureus.

Supplementary Materials

Preliminary evaluation of antibiotic resistance modulatory activity of extracts against S. aureus SA88 (Table S1); antibiotic resistance modulatory activity of the bark methanol extract from Dacryodes edulis bark (DEB) (Table S2); the leaf methanol extract from Dacryodes edulis leaves (DEL) (Table S3); the seed methanol extract from Dacryodes edulis seeds (DES) (Table S4); the leaf methanol extract from Ricinodendron heudelotii leaves (RHL) (Table S5); and the bark methanol extract from Uapaca guineensis bark (UGB) (Table S6) at their MIC/2 and MIC/4 on selected strains of Staphylococcus aureus. (Supplementary Materials)

References

  1. V. G. Fowler Jr., L. L. Sanders, D. J. Sexton et al., “Outcome of Staphylococcus aureus bacteremia according to compliance with recommendations of infectious diseases specialists: experience with 244 patients,” Clinical Infectious Diseases, vol. 27, no. 3, pp. 478–486, 1998. View at Publisher · View at Google Scholar · View at Scopus
  2. R. Jenkins, N. Burton, and R. Cooper, “Manuka honey inhibits cell division in methicillin-resistant Staphylococcus aureus,” Journal of Antimicrobial Chemotherapy, vol. 66, no. 11, pp. 2536–2542, 2011. View at Publisher · View at Google Scholar · View at Scopus
  3. A. P. Johnson, “Methicillin-resistant Staphylococcus aureus: the European landscape,” Journal of Antimicrobial Chemotherapy, vol. 66, no. S4, pp. iv43–iv48, 2011. View at Publisher · View at Google Scholar · View at Scopus
  4. Y. Taj, F. Essa, F. Aziz, and S. U. Kazmi, “Study on biofilm-forming properties of clinical isolates of Staphylococcus aureus,” Journal of Infection in Developing Countries, vol. 6, no. 5, pp. 403–409, 2012. View at Publisher · View at Google Scholar
  5. A. M. Ojeda-Sana, V. Repetto, and S. Moreno, “Carnosic acid is an efflux pumps modulator by dissipation of the membrane potential in Enterococcus faecalis and Staphylococcus aureus,” World Journal of Microbiology and Biotechnology, vol. 29, no. 1, pp. 137–144, 2012. View at Publisher · View at Google Scholar · View at Scopus
  6. M. Mombeshora and S. Mukanganyama, “Development of an accumulation assay and evaluation of the effects of efflux pump inhibitors on the retention of chlorhexidine digluconate in Pseudomonas aeruginosa and Staphylococcus aureus,” BMC Research Notes, vol. 10, no. 1, p. 328, 2017. View at Publisher · View at Google Scholar · View at Scopus
  7. T. Hirata, R. Wakatabe, J. Nielsen, T. Satoh, S. Nihira, and A. Yamaguchi, “Screening of an inhibitor of the tetracycline efflux pump in a tetracycline-resistant clinical-isolate of Staphylococcus aureus 743,” Biological & Pharmaceutical Bulletin, vol. 21, no. 7, pp. 678–681, 1998. View at Publisher · View at Google Scholar · View at Scopus
  8. A. Paudel, H. Hamamoto, Y. Kobayashi, S. Yokoshima, T. Fukuyama, and K. Sekimizu, “Identification of novel deoxyribofuranosyl indole antimicrobial agents,” Journal of Antibiotics, vol. 65, no. 2, pp. 53–57, 2011. View at Publisher · View at Google Scholar · View at Scopus
  9. J. P. Dzoyem, H. Hamamoto, B. Ngameni, B. T. Ngadjui, and K. Sekimizu, “Antimicrobial action mechanism of flavonoids from Dorstenia species,” Drug Discoveries & Therapeutics, vol. 7, no. 2, pp. 66–72, 2013. View at Publisher · View at Google Scholar · View at Scopus
  10. M. M. Cowan, “Plant products as antimicrobial agents,” Clinical Microbiology Reviews, vol. 12, no. 4, pp. 564–582, 1999. View at Google Scholar
  11. V. Kuete, “Medicinal plant research in Africa,” in Pharmacology and Chemistry, V. Kuete, Ed., Elsevier, Oxford, UK, 2013. View at Google Scholar
  12. A. G. Fankam, V. Kuete, I. K. Voukeng, J. R. Kuiate, and J. M. Pages, “Antibacterial activities of selected Cameroonian spices and their synergistic effects with antibiotics against multidrug-resistant phenotypes,” BMC Complementary and Alternative Medicine, vol. 11, p. 104, 2011. View at Publisher · View at Google Scholar · View at Scopus
  13. J. A. Noumedem, M. Mihasan, S. T. Lacmata, M. Stefan, J. R. Kuiate, and V. Kuete, “Antibacterial activities of the methanol extracts of ten Cameroonian vegetables against Gram-negative multidrug-resistant bacteria,” BMC Complementary and Alternative Medicine, vol. 13, p. 26, 2013. View at Publisher · View at Google Scholar · View at Scopus
  14. D. E. Djeussi, J. A. Noumedem, J. A. Seukep et al., “Antibacterial activities of selected edible plants extracts against multidrug-resistant Gram-negative bacteria,” BMC Complementary and Alternative Medicine, vol. 13, no. 1, p. 164, 2013. View at Publisher · View at Google Scholar · View at Scopus
  15. S. B. Tankeo, P. Tane, and V. Kuete, “In vitro antibacterial and antibiotic-potentiation activities of the methanol extracts from Beilschmiedia acuta, Clausena anisata, Newbouldia laevis and Polyscias fulva against multidrug-resistant Gram-negative bacteria,” BMC Complementary and Alternative Medicine, vol. 15, no. 1, p. 412, 2015. View at Publisher · View at Google Scholar · View at Scopus
  16. H. A. Mohammed and A. F. A. Omer, “Antibacterial activity of Azadirachta indica (Neem) leaf extract against bacterial pathogens in Sudan,” American Journal of Research Communication, vol. 3, pp. 246–251, 2015. View at Google Scholar
  17. S. Maragathavalli, S. Brindha, N. S. Kaviyarasi, B. Annadurai, and S. K. Gangwar, “Antimicrobial activity in leaf extract of neem (Azadirachta indica linn.),” International Journal of Science and Nature, vol. 3, pp. 110–113, 2012. View at Google Scholar
  18. A. G. Fankam, J. R. Kuiate, and V. Kuete, “Antibacterial and antibiotic resistance modulatory activities of leaves and bark extracts of Recinodindron heudelotii (Euphorbiaceae) against multidrug-resistant Gram-negative bacteria,” BMC Complementary and Alternative Medicine, vol. 17, no. 1, p. 168, 2017. View at Publisher · View at Google Scholar · View at Scopus
  19. H. Kim, J. Y. Moon, A. Mosaddik, and S. K. Cho, “Induction of apoptosis in human cervical carcinoma HeLa cells by polymethoxylated flavone-rich Citrus grandis Osbeck (Dangyuja) leaf extract,” Food and Chemical Toxicology, vol. 48, no. 8-9, pp. 2435–2442, 2010. View at Publisher · View at Google Scholar · View at Scopus
  20. Z. Zarina and S. Y. Tan, “Determination of flavonoids in Citrus grandis (Pomelo) peels and their inhibition activity on lipid peroxidation in fish tissue,” International Food Research Journal, vol. 20, no. 1, pp. 313–317, 2013. View at Google Scholar
  21. A. Jabamalairaj, S. Dorairaj, S. A. Yadav, and C. Bathrachalam, “Detection of functional group and antimicrobial activity of leaf extracts of Citrus grandis (L.) against selected clinical pathogens,” Indo American Journal of Pharmaceutical Research, vol. 5, pp. 1642–1648, 2015. View at Google Scholar
  22. P. Saha, U. K. Mazumder, and P. K. Haldar, “Acute and subchronic toxicity of Cucurbita maxima aerial parts,” International Journal of Research in Pharmaceutical and Biomedical Sciences, vol. 2, pp. 634–639, 2011. View at Google Scholar
  23. P. Saha, U. K. Mazumder, P. K. Haldar et al., “Anticancer activity of methanol extract of Cucurbita maxima against Ehrlich as-cites carcinoma,” International Journal of Research in Pharmaceutical Sciences, vol. 2, no. 1, pp. 52–59, 2011. View at Google Scholar
  24. D. K. Kushawaha, S. Chatterji, M. Yadav, and G. Watal, “Antimicrobial potential and preliminary phytochemical evaluation of Cucurbita maxima seeds,” International Journal of Pharma and Bio Sciences, vol. 7, pp. 578–582, 2016. View at Google Scholar
  25. C. Y. Ragasa and K. Lim, “Sterols from Cucurbita maxima,” Philippine Journal of Science, vol. 134, no. 2, pp. 83–87, 2005. View at Google Scholar
  26. N. Muruganantham, S. Solomon, and M. M. Senthamilselvi, “Antimicrobial activity of Cucurbita maxima flowers (Pumpkin),” Journal of Pharmacognosy and Phytochemistry, vol. 5, no. 1, pp. 15–18, 2016. View at Google Scholar
  27. K. K. Ajibesin, E. E. Essien, and S. A. Adesanya, “Antibacterial constituents of the leaves of Dacryodes edulis,” African Journal of Pharmacy and Pharmacology, vol. 5, no. 15, pp. 1782–1786, 2011. View at Publisher · View at Google Scholar · View at Scopus
  28. A. Bouquet, Witch Doctors and Traditional Medicine of Congo (Brazzaville), Mem Works and Documents of the Office of Scientific and Technical Research Overseas, Paris, France, 1969.
  29. P. T. Mpiana, D. S. Tshibangu, O. M. Shetonde, and K. N. Ngbolua, “In vitro antidrepanocytary actvity (anti-sickle cell anemia) of some congolese plants,” Phytomedicine, vol. 14, no. 2-3, pp. 192–195, 2007. View at Publisher · View at Google Scholar · View at Scopus
  30. D. Daly, “Alternative medicinal course taught at the United States Medical School,” Journal of Alternative and Complementary Medicine, vol. 3, no. 4, pp. 406–410, 1997. View at Publisher · View at Google Scholar · View at Scopus
  31. A. J. Uraku, P. M. Ajah, A. N.C. Okala, U. A. Ubiam, and P. N. Onu, “Effects of crude extract of Abelmoshus esculentus on albumin and total bilirubin of diabetic albino rats,” International Journal of Science and Nature, vol. 1, no. 1, pp. 38–41, 2010. View at Google Scholar
  32. I. Dini, G. C. Tenore, and A. Dini, “Saponins in Ipomoea batatas tubers: Isolation, characterization, quantification and antioxidant properties,” Food Chemistry, vol. 113, no. 2, pp. 411–419, 2009. View at Publisher · View at Google Scholar · View at Scopus
  33. M. Nagai, M. Tani, Y. Kishimoto et al., “Sweet potato (Ipomoea batatas L.) leaves suppressed oxidation of low density lipoprotein (LDL) in vitro and in human subjects,” Journal of Clinical Biochemistry and Nutrition, vol. 48, no. 3, pp. 203–208, 2011. View at Publisher · View at Google Scholar · View at Scopus
  34. S. M. Hue, A. N. Boyce, and C. Somasundram, “Antioxidant activity, phenolic and flavonoid contents in the leaves of different varieties of sweet potato (Ipomoea batatas),” Australian Journal of Crop Science, vol. 6, no. 3, pp. 375–380, 2012. View at Google Scholar
  35. H. E. Etta, C. C. Olisaeke, and C. I. Iboh, “Effect of Irvingia gabonensis (AubryLecomte ex O’Rorke) seeds on the liver and gonads of male albino rats,” Journal of Biology, Agriculture and Healthcare, vol. 4, pp. 10–15, 2014. View at Google Scholar
  36. O. Nworie, J. O. Orji, U. O. Ekuma, M. V. Agah, C. S. Okoli, and M. C. Nweke, “Antibacterial activity of the leaf and stem bark of Irvingia gabonensis (Bush Mango) against Escherichia coli and Staphylococcus aureus,” Global Journal of Pharmacology, vol. 10, pp. 13–18, 2016. View at Google Scholar
  37. V. Kuete, “Potential of Cameroonian plants and derived products against microbial infections: a review,” Planta Medica, vol. 76, no. 14, pp. 1479–1491, 2010. View at Publisher · View at Google Scholar · View at Scopus
  38. V. Kuete, G. F. Wabo, B. Ngameni et al., “Antimicrobial activity of the methanolic extract, fractions and compounds from the stem bark of Irvingia gabonensis (Ixonanthaceae),” Journal of Ethnopharmacology, vol. 114, no. 1, pp. 54–60, 2007. View at Publisher · View at Google Scholar · View at Scopus
  39. D. Heimler, P. Vignolini, M. G. Dini, and A. Romani, “Rapid tests to assess the antioxidant activity of Phaseolus vulgaris L. dry beans,” Journal of Agricultural and Food Chemistry, vol. 53, no. 8, pp. 3053–3056, 2005. View at Publisher · View at Google Scholar
  40. D. Madhu and S. Ramica, “Antidepressant activity of aqueous extract of Phaseolus vulgaris (black bean) in rodent models of depression,” International Journal of Nutrition, Pharmacology, Neurological Diseases, vol. 4, no. 2, pp. 118–124, 2014. View at Publisher · View at Google Scholar
  41. M. Pradeepkumar, S. D. Joshi, and V. H. Kulkarni, “Evaluation of antibacterial and antitubercular activity of Phaseolus vulgaris Linn, seeds,” Journal of Applied Pharmaceutical Science, vol. 5, pp. 219–224, 2015. View at Publisher · View at Google Scholar · View at Scopus
  42. S. T. Milan, “Total Phenolic content, flavonoid concentration and antioxidant activity of Marrubium peregrinum L. extracts,” Kragujevac Journal of Science, vol. 33, pp. 63–72, 2011. View at Google Scholar
  43. V. A. Oyono, C. Fokunang, J. P. A. Assam et al., “Acute toxicity studies, antioxidant and in vitro antibacterial activities of extract from the barks of Ricinodendron heudoletti (Euphorbiaceae),” Journal of Pharmacognosy and Phytotherapy, vol. 6, no. 4, pp. 47–53, 2014. View at Publisher · View at Google Scholar · View at Scopus
  44. J. Momeni, R. D. Djoulde, M. T. Akam, and S. F. Kimbu, “Chemical constituents and antibacterial activities of the stem bark extracts of Ricinodendron heudelotii (Euphorbiaceae),” Indian Journal of Pharmaceutical Sciences, vol. 67, pp. 386–399, 2005. View at Google Scholar
  45. C. A. Suresh-Kumar, R. Varadharajan, P. Muthumani, R. Meera, P. Devi, and B. Kameswari, “Psychopharmacological studies on the stem of Saccharum spontaneum,” International Journal of PharmTech Research, vol. 2, no. 1, pp. 319–324, 2010. View at Google Scholar
  46. I. O. Williams, E. O. Onyenweaku, and I. J. Atangwho, “Nutritional and antimicrobial evaluation of Saccharum officinarum consumed in Calabar, Nigeria,” African Journal of Biotechnology, vol. 15, no. 33, pp. 1789–1795, 2016. View at Publisher · View at Google Scholar
  47. A. O. Ayoka, R. O. Akomolafe, O. S. Akinsomisoye, and O. E. Ukponmwan, “Medicinal and economic value of Spondias mombin,” African Journal of Biomedical Research, vol. 11, no. 2, pp. 129–136, 2010. View at Publisher · View at Google Scholar
  48. O. Aromolaran and O. K. Badejo, “Efficacy of fresh leaf extracts of Spondias mombin against some clinical bacterial isolates from typhoid patients,” Asian Pacific Journal of Tropical Disease, vol. 4, no. 6, pp. 442–446, 2014. View at Publisher · View at Google Scholar · View at Scopus
  49. B. Trognitz, X. Scheldeman, K. Hansel-Hohl, A. Kuant, H. Grebe, and M. Hermann, “Genetic population structure of cacao plantings within a young production area in Nicaragua,” PLoS One, vol. 6, no. 1, Article ID e16056, 2011. View at Publisher · View at Google Scholar · View at Scopus
  50. R. X. Santos, D. A. Oliveira, G. A. Sodre, G. Gosmann, M. Brendel, and C. Pungartnik, “Antimicrobial activity of fermented Theobroma cacao pod husk extract,” Genetics and Molecular Research, vol. 13, no. 3, pp. 7725–7735, 2014. View at Publisher · View at Google Scholar · View at Scopus
  51. S. Nidhi, D. Shreyan, D. Abhirup, R. C. Akash, and A. Jayanthi, “Antimicrobial activity and cytotoxicity of Theobroma cacao extracts,” Der Pharmacia Lettre, vol. 7, no. 7, pp. 287–294, 2015. View at Google Scholar
  52. E. J. Ndebia, B. N. Nkeh-Chungag, J. R. Temdie, Y. M. Fodjo, D. T. Ndinteh, and J. T. Mbafor, “Antinociceptive effects of the methanolic extract of Uapaca guineensis (Euphorbiaceae) stilt root bark,” Pharmacologyonline, vol. 3, pp. 153–165, 2007. View at Google Scholar
  53. E. T. Ibibia, O. Peter, and O. S. Olugbemiga, “Evaluation of some Nigerian Savannah plants of antioxydent activity, and total phenols and flavonoid contents,” International Journal of Pharmaceutical Sciences Review and Research, vol. 34, pp. 75–81, 2015. View at Google Scholar
  54. T. J. O. Ngalani, Influence de la Multi-Résistance des Bactéries Entériques aux Antibiotiques Sur l’État Immunologique des Patients Séropositifs au VIH Venus en Consultation à l’Hôpital Adlucem Banka de Bafang, Department of Biochemistry, University of Dschang, Dschang, Cameroon, 2015.
  55. J. Harbone, Phytochemical Methods: a Guide to Modern Techniques of Plant Analysis, Chapman & Hall, London, UK, 1973.
  56. J. N. Eloff, “A sensitive and quick microplate method to determine the minimal inhibitory concentration of plant extracts for bacteria,” Planta Medica, vol. 64, no. 8, pp. 711–713, 1998. View at Publisher · View at Google Scholar · View at Scopus
  57. V. Kuete, F. Nana, B. Ngameni, A. T. Mbaveng, F. Keumedjio, and B. T. Ngadjui, “Antimicrobial activity of the crude extract, fractions and compounds from stem bark of Ficus ovata (Moraceae),” Journal of Ethnopharmacology, vol. 124, no. 3, pp. 556–561, 2009. View at Publisher · View at Google Scholar · View at Scopus
  58. V. Kuete, J. D. Wansi, A. T. Mbaveng et al., “Antimicrobial activity of the methanolic extract and compounds from Teclea afzelii (Rutaceae),” South African Journal of Botany, vol. 74, no. 4, pp. 572–576, 2008. View at Publisher · View at Google Scholar · View at Scopus
  59. J. Kovač, N. Gavari, F. Bucar, and S. Smole Možina, “Antimicrobial and resistance modulatory activity of Alpinia katsumadai seed extract, essential oil and post-distillation extract,” Food Technology and Biotechnology, vol. 52, pp. 248–254, 2014. View at Google Scholar
  60. V. Kuete and T. Efferth, “Cameroonian medicinal plants: pharmacology and derived natural products,” Frontiers in Pharmacology, vol. 1, p. 123, 2010. View at Publisher · View at Google Scholar · View at Scopus
  61. J. Bruneton, Pharmacognosie: Phytochimie, Plantes medicinales, Tec & Doc, Paris, France, 1999.
  62. M. Simões, R. N. Bennett, and E. A. Rosa, “Understanding antimicrobial activities of phytochemicals against multidrug resistant bacteria and biofilms,” Natural Product Reports, vol. 26, no. 6, pp. 746–757, 2009. View at Publisher · View at Google Scholar · View at Scopus
  63. J. D. D. Tamokou, A. T. Mbaveng, and V. Kuete, “Chapter 8-antimicrobial activities of African medicinal spices and vegetables,” in Medicinal Spices and Vegetables from Africa, pp. 207–237, Academic Press, Cambridge, MA, USA, 2017. View at Google Scholar
  64. T. J. Foster, “Antibiotic resistance in Staphylococcus aureus. Current status and future prospects,” FEMS Microbiology Reviews, vol. 41, no. 3, pp. 430–449, 2017. View at Publisher · View at Google Scholar · View at Scopus
  65. M. C. Jennings, M. E. Forman, S. M. Duggan, K. P. C. Minbiole, and W. M. Wuest, “Efflux pumps might not be the major drivers of QAC resistance in methicillin-resistant Staphylococcus aureus,” ChemBioChem, vol. 18, no. 16, pp. 1573–1577, 2017. View at Publisher · View at Google Scholar · View at Scopus
  66. P. W. Limaverde, F. F. Campina, F. A. da Cunha et al., “Inhibition of the TetK efflux-pump by the essential oil of Chenopodium ambrosioides L. and α-terpinene against Staphylococcus aureus IS-58,” Food and Chemical Toxicology, vol. 109, pp. 957–961, 2017. View at Publisher · View at Google Scholar · View at Scopus
  67. M. M. Kristiansen, C. Leandro, D. Ordway et al., “Thioridazine reduces resistance of methicillin-resistant Staphylococcus aureus by inhibiting a reserpine-sensitive efflux pump,” In Vivo, vol. 20, no. 3, pp. 361–366, 2006. View at Google Scholar
  68. A. Martins, L. Machado, S. Costa et al., “Role of calcium in the efflux system of Escherichia coli,” International Journal of Antimicrobial Agents, vol. 37, no. 5, pp. 410–414, 2011. View at Publisher · View at Google Scholar · View at Scopus
  69. F. K. Touani, A. J. Seukep, D. E. Djeussi et al., “Antibiotic-potentiation activities of four Cameroonian dietary plants against multidrug-resistant Gram-negative bacteria expressing efflux pumps,” BMC Complementary and Alternative Medicine, vol. 14, p. 258, 2014. View at Publisher · View at Google Scholar · View at Scopus
  70. L. C. Braga, A. A. Leite, K. G. Xavier et al., “Synergic interaction between pomegranate extract and antibiotics against Staphylococcus aureus,” Canadian Journal of Microbiology, vol. 51, no. 7, pp. 541–547, 2005. View at Publisher · View at Google Scholar · View at Scopus