Research Article Volume 6 Issue 1
1Microbiology and Food Quality Control Laboratory (LAMICODA), Higher School of Biological and Food Techniques (ESTBA), University of Lomé, Lomé, Togo
2Laboratory of Biomedical Sciences, Food and Environmental Health - Research Unit in Biomedical Sciences and Bioactive Substances (LaSBASE-UR-2SB), Higher School of Biological and Food Techniques (ESTBA), University of Lomé, Lomé, Togo
3Department of Biochemistry /Nutrition, Laboratory of Biochemistry applied to Nutrition, Faculty of Sciences, University of Lomé, Lomé, Togo
4Laboratory of Biology, Phytochemistry, Toxicology, Pharmacology and Agrifood (BioPhytToPharmA), Institute African Biomedical, Agrifood, Societal and Environmental Sciences (IASBASE), Lomé-Togo
Correspondence: Gbekley EH, Microbiology and Food Quality Control Laboratory (LAMICODA), Higher School of Biological and Food Techniques (ESTBA), University of Lomé, Lomé, Togo
Received: March 31, 2023 | Published: July 31, 2023
Citation: Alognon A, Poli S, Montant MES, et al. Antifungal activity of African medicinal plants: a review. Open Access J Sci. 2023;6(1):80-84. DOI: 10.15406/oajs.2023.06.00197
In Africa many plants are used as antifungals. However, journals analysing the work of antifungal activities of plants in West Africa in recent years are rare. This study is a synthesis of publications from 2006 to 2021 on plants traditionally used in the fight against antifungal diseases. A systematic search was carried out in the Pub Med and Google Scholar database using the following keywords: vaginitis; West Africa; antifungal activity; medicinal plants; plant extracts; for articles published from 2006 to 2021. These selected articles focus on ethnobotanical studies, in vitro antifungal tests and molecules isolated from these plants. A total of 46 papers were selected from 7 West African countries with 56 plants studied. Nigeria and Ivory coast did more work with 22 and 14 papers respectively and studied more plants with 23 and 17 respectively. 43% of plants show good activity in vitro on strains of Candida albicans in the laboratory with a minimum fungicide concentration and a percentage of inhibition above 50%. The most active extracts are found in Ivory coast with respectively the hexane extracts of Terminalia mantaly with a minimum fungicide concentration= 0.024 mg / mL and the hydroethanolic extract of Terminalia ivorensis with a minimum fungicide concentration of 0.097 mg / mL. It is clear that the traditional West African pharmacopoeia can make an important contribution for the management of vaginitis.
Keywords: vaginitis, West Africa, antifungal activity, plants extracts, medicinal plants
IC50, concentration which inhibits 50% of the growth of germs; MIC, minimum inhibitory concentration, MFC, minimum fungicidal concentration
Candidiasis is the most frequent fungal infection in human pathology.1 Among the different forms of candidiasis, there is vulvovaginal candidiasis which is a frequent reason for consultation in gynecology. Vulvovaginal candidiasis ranks second after bacterial vaginosis. It is estimated that 75% of women have at least one episode of Candida vaginitis in their lifetime, of which 40% to 50% have more than one episode.1 In addition, 5 to 8% of them develop recurrent vulvovaginal candidiasis defined by the occurrence of four episodes per year. The pathogen usually responsible is Candida albicans, a commensal yeast of the vaginal mucosa.2,3 Vulvovaginal candidiasis seems to be favored by a disruption of the vaginal balance and of the local immunity mechanism allowing vaginal colonization by Candida. It is closely linked to the existence of certain factors such as hormonal changes during pregnancy, the use of oral contraceptives and local factors such as lack of hygiene.4 Furthermore, C. albicans is found in 50% of cases via the maternal genital tract.5 In newborns, the incidence of Candida infections is low compared to that of bacterial or viral infections. However, maternal -fetal contamination should not be underestimated because it remains serious and responsible for significant mortality and morbidity in low birth weight premature babies.6 In Cameroon, a study conducted among 397 pregnant women from October 2013 to January 2014 showed a prevalence of 35.52% of cases of vulvovaginal candidiasis.7 In Togo, a study conducted at the University Hospital of Sokode between June 2010 and August 2011 showed that the prevalence of Candida spp is 30.77% of the germs responsible for vaginal infections in pregnant women.8 Another study by Balaka et al. in 2011 in Togo revealed that the prevalence of Candida albicans is 33.3% of the germs responsible for vaginal infections in 918 pregnant women.9 Untreated genital tract infections can lead to complications such as infertility, premature birth, miscarriages and other infectious diseases.10 Indeed, the difficulties of effective and efficient management of vaginitis are felt on the technical, economic and biological levels.
On the technical level, there is a delay in consultation and a lack of technical means. From an economic point of view, the high cost of drugs makes treatment difficult. Biologically, the phenomenon of antibiotic resistance due to repeated use of antibiotics leads to therapeutic failure.11 To remedy these problems, it is necessary to have new sources of drugs. Plants represent an enormous source of chemotherapeutic agents that could be used against bacteria.12 It is therefore necessary to study them for find the solution against this multi-resistance.12 In West Africa, as in the rest of the continent, more than 80% of the population uses traditional medicine for their primary health care.13 Indeed, medicine is of significant use thanks to plants which contain most of the secondary metabolites. Traditional African medicine uses many plants that can be a source of new drugs. Thus, in the West African region, a great deal of scientific research is carried out on medicinal plants identified among populations and traditional health practitioners.14 However, the journals analyzing the work of antifungal activities of plants in West Africa on recent years are rare. Thus, the present study is an analysis of the various pharmacological publications from 2006 to 2021 relating to the plants used empirically for antifungal treatments in West Africa.
A systematic search was carried out in the PubMed and Google Scholar database using the following keywords: Vaginitis; West Africa; antifungal activity; medicinal plants; plant extracts; for articles published from 2006 to 2021 and certain references of these articles. These selected articles relate to ethnobotanical studies, in vitro antifungal tests and molecules isolated from these plants. Articles published before 2006 have been excluded. West Africa, rich in plant biodiversity, includes countries with precarious socio-economic situations. The widespread traditional pharmacopoeia includes a wide variety of medicinal plants.
A total of 46 articles were selected in 7 West African countries from 2006 to 2021 with 56 plants studied. These are Benin, Burkina Faso, Ivory Coast, Ghana, Nigeria, Sierra Leone and Togo. We did not find articles from other countries that met our selection criteria in the selected databases. Nigeria and Ivory coast carried out more work with 22 and 14 articles respectively and studied more plants with 23 and 17 respectively. Medicinal plants are generally identified with populations and traditional healers. Medicinal plants are then subjected to a long process of preclinical experimental studies.14 Extracts from 23 plants out of 56 studied show good in vitro activity on strains of C. albicans in the laboratory with a MFC and a percentage of inhibition beyond 50% (Table 1 & 2). Studies from Ivory coast and Togo have reported the highest numbers of these plants with 12 and 6 respectively Figure 1. So, 32.14% of the plants show good activity. The most active extracts are found in Ivory Coast with respectively the hexane extracts of Terminalia mantaly with MFC = 0.024 mg/ mL15 and the hydroethanolic extract of Terminalia ivorensis with an MFC of 0.097 mg/ mL.16 A few active molecules have nevertheless been isolated from the West African medicinal plants with antifungal activity studied.17 This table indicates West Africa medicinal plants with antifungal activity Table 3. This table shows us some molecules isolated from plants with antifungal activity. Both molecules were isolated from Piper guineense.
Plants |
Extraction solvent: MIC(MFC) (mg/mL) of plants |
IC50 (µg/ml) |
Countries |
References |
Acalypha wilkesiana |
Chloroform: 50 |
|
Nigeria |
|
Acanthospermum hispidum |
Ethanol 70: (25) |
1500 |
Ivory coast |
|
Anogeissus leiocarpa |
Ethanol: 0,195 (0,390) |
|
Ivory coast |
|
Bridelia ferruginea |
Methanol: 10 |
|
Nigeria |
|
Methanol :12,5 |
|
Ivory coast |
||
Calotropis procera |
Ethanol :11 |
|
Nigeria |
|
Carpolobia lutea |
Ethanol: 25 |
|
Nigeria |
|
n-Hexane: 125 |
|
Nigeria |
||
Cassia alata |
Ethanol: 0,312 |
|
Togo |
|
Ethanol: 5, 60 |
|
Nigeria |
||
Clausena anisata |
Ethanol: 5,5 |
|
Ghana |
|
Commelina nudiflora |
Ethanol: 1,20 |
|
Ghana |
|
Croton membranaceus |
Methanol: 0,82 |
|
Ghana |
|
Cymbopogon citratus |
Ethanol: 12,5 |
|
Ghana |
|
Distemonanthus benthamianus |
Methanol: 0,25 (1) |
|
Nigeria |
|
Eclipta prostrata |
Ethanol: (>50) |
6250 |
Ivory coast |
|
Exophiala dermatitidis |
Water: 500 |
|
Nigeria |
|
Euphorbia hirta |
Methanol: 25 |
|
Nigeria |
|
Ficus platyphylla |
Ethanol: 0, 5 (0,5) |
|
Togo |
|
Harrisonia abyssinica |
Ethanol 70: 0,78 (50) |
80 |
Ivory coast |
|
Haematostaphis barteri |
Essential oil: 0,312 |
|
Nigeria |
|
Hunteria eburnea |
Ethanol: (25) |
4000 |
Ivory coast |
|
Khaya senegalensis |
Ethanol: 7,81 |
|
Nigeria |
|
Essential oil: 0,005 |
|
Nigeria |
||
Lannea schimperi, |
Ethanol: 2,99 |
|
Ghana |
|
Piliostigma thonningii |
Dichloromethane: 0, 625 |
|
Togo |
|
Piliostigma reticulatum |
Ethanol: 1,2 |
|
Ghana |
|
Mangifera indica |
Ethanol: 31,25 (62,5) |
|
Nigeria |
|
Mitracarpus scaber |
Hexane-water: (3, 125) |
600 |
Ivory coast |
|
Piper guineense |
Ethanol: 0.039 |
|
Nigeria |
|
Pycnanthus angolensis |
Methanol: 12,5 |
|
Ivory coast |
|
Pteleopsis suberosa |
Water: 43, 49 |
|
Benin |
|
Ricinus communis |
Methanol: 12,5 (200) |
|
Ghana |
|
Saba comorensis |
Butanol: 12,5 |
2 |
Ivory coast |
|
Securinega virosa |
Ethanol: 3,125 (6,250) |
|
Ivory coast |
|
Terminalia ivorensis |
Ethanol 70: (0,097) |
11,40 |
Ivory coast |
|
Terminalia mantaly |
Hexane: (0,024) |
15 |
Ivory coast |
|
Thonningia sanguinea |
Water: (1,56) |
|
Ivory coast |
|
Trema guineensis |
Water: 200 (400) |
14,70 |
Ivory coast |
|
Zanthoxylum zanthoxyloides |
Methanol: 12,5 |
|
Ivory coast |
Table 1 West African plants with antifungal activity
IC50: Concentration which inhibits 50% of the growth of germs; MIC: Minimum Inhibitory Concentration, MFC: Minimum Fungicide Concentration
Plants |
Extraction solvent |
Percentage inhibition (dose in mg/mL) |
Inhibition diameter (dose in mg/mL) |
Countries |
References |
Aframomum melegueta |
Methanol |
8 |
Nigeria |
||
Allium sativum |
Methanol |
22 |
Nigeria |
||
Allium cepa |
Propanol |
12 |
Nigeria |
||
Bridelia ferruginea |
Methanol |
-250 |
50 |
Nigeria |
|
Cajanus cajan |
Ethanol |
Nigeria |
|||
Caloncoba echinata |
Xylen |
Sierra Leonne |
|||
Capsicum annuum, |
Methanol |
8 |
Nigeria |
||
Capsicum chinense |
Methanol |
7 |
Nigeria |
||
Calotropis procera |
Ethanol |
11 |
Nigeria |
||
Cassia alata |
Ethanol |
100 (10) |
Togo |
||
Chromolaena odorata |
Ethanol + water |
75 |
Togo |
||
Cocos nucifera |
Essential oil |
22 |
Nigeria |
||
Croton membranaceus |
Methanol |
7,5(20) |
Ghana |
||
Cymbopogon citratus |
Ethanol |
10 |
Ghana |
||
Jatropha multifida |
Ethanol |
99, 77 |
Togo |
||
Ethanol+ water |
99, 63 |
Togo |
|||
Khaya senegalensis |
Ethanol |
10 |
Nigeria |
||
Mangifera indica |
Ethyl acetate |
7,5 |
Nigeria |
||
Opillia celtidifolia |
Distillated water |
19 |
Burkina -Faso |
||
Ocimum gratissimum |
Essential oil |
44 |
Nigeria |
||
Phyllanthus amarus |
Hexan |
6 |
Nigeria |
||
Piliostigma thonningii |
Dichloromethane |
100 (10) |
Togo |
||
Picralima nitida |
Ethanol |
11(200) |
Nigeria |
||
Sebastiania chamaelea |
Ethanol |
11 |
Benin |
||
Tridax procumbens |
Ethanol + water |
60,44 |
Togo |
||
Vernonia amygdalina |
Ethanol |
21,7 (2000) |
Nigeria |
||
Zingiber officinales |
Methanol |
9 |
Nigeria |
Table 2 Antifungal activity with percentage inhibition and inhibition diameter of West African medicinal plants
Compounds |
Plants |
Extraction solvent |
Countries |
References |
Piperolongumine |
Piper guineense |
Ethanol: 39 |
Nigeria |
|
Piperine |
Piper guineense |
Ethanol: 78 |
Nigeria |
Table 3 Molecules isolated from plants with antifungal activity
After an ethnobotanical survey of populations and traditional healers, medicinal plants are subjected to a process of preclinical experimental studies.14 Tube dilution methods or the agar diffusion method are the two methods used in almost all publications. Fifty-six (56) plants only were the subject of this study. The absence or little work done in other countries could be due to the absence of a research center on vaginitis or the limited financial resources given to research. This is the case of Togo. The most active extracts found in Ivory coast (hexane extracts of Terminalia mantaly with a MFC = 0.024 mg/mL and the hydroethanolic extract of Terminalia ivorensis with a MFC of 0.097 mg/mL) have an activity similar to that of Ketoconazole.16 This confirms the attention in the search for new antifungal molecules. Medicinal plants have many virtues and must be sufficiently explored to effectively fight against vaginitis. A few active molecules have nevertheless been isolated from West African medicinal plants with studied antifungal activity.17 Among these compounds, the majority of the most active are alkaloids. Previous studies have shown that the alkaloids isolated from these plants have great potential for the development of antifungal drugs.17
The present study brings out information on the effectiveness of different medicinal plants used in the treatment of vaginitis in the West African region. Although these herbs are widely used, readily available and affordable compared to conventional drugs, they are not without drawbacks. Some limitations concern the proof of their effectiveness, the lack of dosage and the safety and long-term effect. These limits in the ethnopharmacological strategy show the interest of improving the concept, and the obligation to standardize the processes, whether in the selection of antifungal medicinal plants, or in the strategies of pharmacological explorations. It is obvious that the traditional West African pharmacopoeia can make an important contribution to the discovery of safe, effective, quality and accessible phytomedicines for the management of vaginitis.
We would like to thank all those who have contributed directly or indirectly to the development of this review.
The authors declare that they have no competing interests.
©2023 Alognon, et al. This is an open access article distributed under the terms of the, which permits unrestricted use, distribution, and build upon your work non-commercially.