Abstract
The Asteraceae family is the largest family of flowering plants, comprising over 25,000 species grouped into 16,000 genera and distributed around the world. This research aimed to evaluate the antibacterial effectiveness of 12 native plants from the Asteraceae family. Their efficacy was tested against 11 bacterial strains using the liquid microdilution technique to determine the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). MIC values ranged from 0.125 to 4 mg/mL, and MBC values ranged from 0.25 to 4 mg/mL, against six bacterial strains. These results describe the potential antibacterial activity attributes of Asteraceae species.
1. Introduction
Asteraceae is the world’s largest flowering plant family, with 1700 genera structured into 17 tribes [1]. In total, 26,000 different plant species are represented in the global distribution [2], 750 of which are native to Madagascar [3]. These plants flowers and leaves have been shown to have antibacterial, antifungal, antiviral, and anti-inflammatory activities [4]. For this reason, many different species in this family are used in traditional medicine. Plants in this study such as eleven species of Helichrysum and one species of Catatia are used in Malagasy traditional medicine. The aims of this study were to demonstrate that these plants from Asteraceae had antibacterial activity and could be a source of antibacterial agents. To reach that goal, the antibacterial activities of these plant extracts against 11 strains were evaluated using the microdilution method.
2. Materials and Methods
The plant materials used consisted of the aerial parts of Helichrysum bojeranum, Helichrysum chermezonii, Helichrysum cordifolium, Helichrysum cryptomerioides, Helichrysum dubardii, Helichrysum faradifani, Helichrysum fulvescens, Helichrysum gymnocephalum, Helichrysum hirtum, Helichrysum microcephalum, Helichrysum mutisiaefolium, and Catatia cordata. These plants were collected and identified by researchers at the Department of Enthobotany and Botany of the National Centre for the Application of Pharmaceutical Research (CNARP), Madagascar (Figure S1 in Supplementary Material). The voucher specimens were deposited at the herbarium of the aforementioned department. The harvested aerial parts were dried in a ventilated room at 30 °C and then ground into powder.
The aerial parts were extracted via maceration with methanol for 24 h at room temperature until exhaustion.
The broth microdilution method was used to determine the MIC (minimum inhibitory concentration) values in 96-well plates [5]. All methanolic extracts were assessed against five Gram-positive (Bacillus cereus LMG6910, Bacillus megaterium ATCC8145, Listeria monocytogenes ATCC19114TM, Staphylococcus aureus ATCC11632, and Streptococcus pneumoniae ATCC6301) and six Gram-negative (Enterobacter cloacae ATCC13047, Escherichia coli ATCC8739, Klebsella oxytoca ATCC8721, Proteus mirabilis ATCC35659, Pseudomonas aeruginosa ATCC10145, and Salmonella enteritidis ATCC3710) bacteria. All extracts were two-fold serially diluted using Muller–Hinton broth in the wells of the microtitration plates (from 4 to 0.0019 mg/mL), and the bacterial suspensions were then added (1.5 × 107 bacteria/mL), followed by overnight incubation at 37 °C. The MIC value was obtained by identifying the lowest concentration of the test sample that inhibited visible bacterial growth. The MBC value corresponded to the lowest concentration of the test sample that can kill bacteria, so no bacterial growth would be observed on the agar.
3. Results
The Asteraceae family is the most diverse and globally present of all flowering plant families. Their extracts have been proven in studies to have an effect on bacterial growth [6]. Table 1 shows the MICs and MBCs of each plant’s extract. Extracts of H. microcephalum and H. dubardii were ineffective against all strains tested. Extracts of H. bojeranum, H. cordifolium, H. chermezonii, H. faradifani, H. fulvescens, H. gymnocephalum, H. hirtum, H. mutisiaefolium, and C. cordata were active against two Gram-negative strains (E. cloacae and P. mirabilis) and four Gram-positive strains (L. monocytogenes, B. cereus, B. megaterium, and S. pneumoniae), but they are inactive against other strains such as S. aureus, E. coli, P. aeruginosa, K. oxytoca, and S. enteritidis. These MICs against Gram-positive strains were between 0.125 and 4 mg/mL, but their MBC ranged from 0.25 to 4 mg/mL. According to Marmonier [7], if the MBC/MIC is ≤4, the extract is bactericidal, and if the MBC/MIC is >4 is bacteriostatic. Thus, extracts of H. bojeranum, H. faradifani, H. fulvescens, and H. gymnocephalum have bactericidal activity against two Gram-negative strains and four Gram-positive strains. E. cloacae was sensitive to H. chermezonii extract with bacteriostatic action. H. cordifolium extract is bactericidal against three Gram-positive strains (L. monocytogenes, S. pneumoniae, and B. megaterium), although it reveals bacteriostatic activity against P. mirabilis. Also, H. hirtum extract is bactericidal against four strains (two Gram-positive strains: B. cereus and L. monocytogenes; and two Gram-negative strains: E. cloacae and P. mirabilis) and shows bacteriostatic activity against B. megaterium. H. mutisiaefolium extract was found to be bactericidal against L. monocytogenes, a Gram-positive strain. C. cordata extract revealed bacteriostatic activity against L. monocytogenes and bactericidal activity against five strains (B. cereus, B. megaterium, S. pneumonia, E. cloacae, and P. mirabilis).
Table 1.
Minimal inhibitory concentration (I) and minimum bactericidal concentration (B) of extracts from some Asteraceae species on six microorganisms.
4. Discussion
This research conducted by Boubekeur et al. [8] on the aqueous extract of Helichrysum stoechas prepared via maceration; its MIC on K. pneumonia is only 1.250 to 5 mg/mL and is inactive against E. coli, S. aureus, and B. cereus. Bactericidal activity against B. cereus and L. monocytogenes was reported in wild edible Asteraceae from Mediterranean flora (Reichardia picroides, Hymenonema graecum, Sonchus oleraceus, Scolymus hispanicus, Hedypnois cretica, Picris echioides, Urospermum picroides, and Taraxacum sp., with MIC values varying from 0.075 to 0.3 mg/mL) [9], the same as our extracts (C. cordata, H. bojeranum, H. faradifani, H. fulvescens, H. gymnocephalum, and H. hirtum, with MIC values ranging from 1 to 4 mg/mL) that have bactericidal activity against these strains, with B. cereus and L. monocytogenes. However, according to Kuete and Efferth [10], a scale for antibacterial activity is given for plant extracts. It is said that extracts are significantly active if their MIC values are ≤100 μg/mL, moderately active if 100 < MIC ≤ 625 μg /mL, and weakly active if the MIC is >625 μg/mL. Therefore, H. cordifolium, H. faradifani, and C. cordata are moderately active on L. monocytogenes. The other extracts are weakly active on the strains tested. Nevertheless, it should be stated that plants show contrasting antibacterial activities due to differences in species, producing areas, harvest seasons, parts used, and extraction methods. Compared to chemical antibacterial agents, herbal products show low efficiency for bacteriostasis and sterilization, as well as poor antibacterial specificity.
5. Conclusions
The results show the Helichrysum and Catatia species, among the Asteraceae family, endemic to Madagascar have antibacterial activity. Even with the weak activities of most of the extracts studied, there is still a need to isolate and identify more small molecular compounds with potent bioactivity within those extracts. Undeniably, medicinal phytochemicals will play an important role in future discoveries of new drugs; nonetheless, only a small percentage of them have been studied.
Supplementary Materials
The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/ECM2023-16410/s1, Figure S1: Species collection sites.
Author Contributions
Conceptualization, N.R. and R.R.; methodology, V.R.; validation, V.R. and R.R.; investigation, A.R. and R.R.; resources, N.R. and R.R.; data curation, A.R.; writing—original draft preparation, A.R., N.R. and R.R.; visualization, A.R.; supervision, N.R.; project administration, N.R. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Institutional Review Board Statement
Not applicable.
Informed Consent Statement
Not applicable.
Data Availability Statement
Data will be provided on request.
Acknowledgments
We would like to thank Rakotonandrasana S, Rakotondrafara A., and Rakotoarisoa M. for support with plant collection and identification. Thanks to Andrianary E. for the collection map conception.
Conflicts of Interest
The authors declare no conflicts of interest.
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