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Article

Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria

by
Christiana Adeyinka Odebunmi
1,
Tomi Lois Adetunji
2,*,
Ademola Emmanuel Adetunji
3,
Ahmed Olatunde
4,
Oluwatosin Esther Oluwole
5,
Idowu Ayodeji Adewale
6,
Abdulrasak Opeyemi Ejiwumi
7,
Chinwenwa Esther Iheme
8 and
Taiwo Opeyemi Aremu
8,9
1
Derived Guinea Savannah Research Station, Forestry Research Institute of Nigeria, Oke-Aduin, Ogbomosho P.O. Box 164, Nigeria
2
Unit for Environmental Sciences and Management (UESM), Faculty of Natural and Agricultural Sciences, North-West University, Potchefstroom 2520, South Africa
3
Department of Molecular and Cell Biology, University of Cape Town, Cape Town 7701, South Africa
4
Department of Medical Biochemistry, Abubakar Tafawa Balewa University, Bauchi 740272, Nigeria
5
Division of Epidemiology & Community Health, School of Public Health, University of Minnesota, 1300 S. 2nd Street, Minneapolis, MN 55455, USA
6
Department of Medical Microbiology, University of Ilorin Teaching Hospital, Old Jebba Road, Oke Ose, Ilorin 240001, Nigeria
7
Department of Health Services Management and Policy, College of Public Health, East Tennessee State University, 3rd Floor Sherrod Library, Johnson City, TN 37614, USA
8
Division of Environmental Health Sciences, School of Public Health, University of Minnesota, 420 Delaware Street SE, Minneapolis, MN 55455, USA
9
Department of Pharmaceutical Care & Health Systems (PCHS), College of Pharmacy, University of Minnesota, 308 Harvard Street SE, Minneapolis, MN 55455, USA
*
Author to whom correspondence should be addressed.
Plants 2022, 11(19), 2667; https://doi.org/10.3390/plants11192667
Submission received: 9 September 2022 / Revised: 5 October 2022 / Accepted: 6 October 2022 / Published: 10 October 2022
(This article belongs to the Special Issue Medicinal Plants: Advances in Phytochemistry and Ethnobotany)

Abstract

:
Coronavirus disease 2019 (COVID-19) has extensively spread worldwide with high mortality. Besides vaccination, the United States Food and Drug Administration approved only one oral medication as a treatment. Medicinal plants with antiviral and immunomodulatory properties could be explored as complementary treatments for COVID-19. Ogbomosho is home to such plants traditionally used to treat infectious diseases in Nigeria, making it relevant in complementary medicine. An ethnobotanical survey of medicinal plants used to treat COVID-19 and related ailments, including cough and flu in Ogbomosho South and North Local Government Areas, Nigeria, was conducted using a semi-structured questionnaire. Information was obtained from 56 participants, consisting of different groups of individuals with native knowledge of medicinal plants, and ethnobotanical indices, including the frequency of citation (FC), relative frequency of citation (RFC), and fidelity level (FL) were computed. Twenty-six medicinal plants (17 families) were used to treat COVID-19, 31 (20 families) for cough, and 29 (19 families) for flu. The most cited plant was Zingiber officinale (FC = 10; RFC = 0.18; FL = 18%) for treating COVID-19, Citrus limon (FC = 13; RFC = 0.23; FL = 23%) for cough, and Zingiber officinale (FC = 9; RFC = 0.16; FL = 16%) for flu. Leaves were the most used plant part for treating COVID-19 and flu, while the bark was the most used for cough. Trees and herbs were the most cited plant growth forms. The herbal remedies were mostly prepared by decoction and infusion and were mainly administered orally. Further research should be conducted on the identified species for the scientific validation of their antiviral and immunomodulatory efficacies and safety for use.

1. Introduction

Upper respiratory tract infections (URTIs) are one of the most common diseases in primary care globally [1]. Mainly caused by viruses, the most commonly occurring symptoms of URTIs are sore throat, nasal congestion, runny nose, cough, headache, etc. Whilst these conditions are not usually fatal, the symptoms may significantly affect human efficiency and quality of life [1]. Some poorly managed URTIs can result in complications, including myocarditis, pneumonia, otitis media, etc., accounting for significant morbidity and mortality globally [2]. In December 2019, a novel virus known as the Severe Acute Respiratory Syndrome Coronavirus-2 (SARS-CoV-2), which causes respiratory illness, emerged in Wuhan, China, and has spread to almost all parts of the world [3]. As a result of its massive spread globally, the World Health Organization (WHO) declared the coronavirus disease 2019 (COVID-19) a pandemic on the 11 March 2020 [4,5]. Common symptoms of COVID-19 include headache, fever, fatigue, malaise, and dry cough, while less commonly occurring symptoms include sore throat, nausea, diarrhea, generalized body pain, discoloration of fingers and toes, conjunctivitis, and loss of smell or taste [3,6]. In severe cases, COVID-19 results in life-threatening symptoms such as difficulty in breathing, loss of speech or movement, chest pain, shortness of breath and pressure, typical of acute respiratory distress syndrome (ARDS) [3,7]. The WHO reported 14.9 million deaths linked to the COVID-19 pandemic globally between 1 January 2020 and 31 December 2021 [8].
The Nigerian Federal Ministry of Health confirmed the first national case of COVID-19 in Lagos State on 27 February 2020. Over 256,000 infections have been recorded since the pandemic began while over 3000 COVID-19-related deaths have been reported, making Nigeria one of the 20 countries accounting for over 80% of global mortality resulting from COVID-19 from January 2020 to December 2021 [8].
The increasing spread and mortality resulting from COVID-19 across the globe have led to different interventions, including personal hygiene, quarantine, isolation, and the development of vaccines, to control the spread of the virus [9]. Although an oral medication, Paxlovid, has been developed to treat mild to moderate COVID-19 in vulnerable and severely ill individuals aged 12 and older (weighing at least 40 kg), no other evidence-based oral drugs have been developed to prevent COVID-19 infection. While there may be limited access to Paxlovid in low- and middle-income countries, no evidence-based and cost-saving medications have been adapted for treating or preventing COVID-19 in people living in low-resource countries [10,11]. Besides, no vaccine has been identified to be 100 percent effective against the virus and its emerging variants. Hence, scientists have searched more for safe natural products with antiviral and immunomodulatory activities that can serve as potential prophylactic complementary and/or alternative therapeutics for COVID-19 [12,13].
For ages, medicinal plants have been used by different people worldwide as traditional medical treatments and for the prevention of various ailments, including acute respiratory infections [14]. Medicinal plant use has been recognized in some countries (e.g., Uganda, Ghana, Tanzania, etc.) as the leading primary care medication, and over 80% of people in low and middle-income countries depend directly on it [15,16,17]. Medicinal plants are widely used due to their availability, accessibility, affordability, and perceived safety relative to modern medicine [18]. In many African countries, including Nigeria, herbal medicine is well embraced, as up to 90% of rural dwellers rely on it for their primary health care [16,19]. The efficacy of medicinal plants is attributed to the presence of bioactive compounds that confer several bioactivities with therapeutic properties, such as antiviral, antimicrobial, anti-inflammatory, and immunomodulatory activities, etc. [12].
Since the emergence of COVID-19, the use and demand for some medicinal plants has increased worldwide, particularly those used to treat symptoms (for example, sore throat, flu, and cough) associated with COVID-19 [20]. Ethnobotanical surveys focus on multiplex links between local plants and inhabitants, including cultural beliefs and practices linked to several forms of application [21,22]. These surveys are vital in expressing the importance of plant species, that is, for discovering new therapeutic agents [23]. An ethnobotanical survey of medicinal plants is thus applicable as a vital approach for identifying and selecting plants that can be subjected to further phytochemical and pharmacological screening for developing novel therapeutic agents [24].
In Nigeria, the Yoruba people comprise about 40% of the total population and are largely distributed in the southwestern states (Oyo, Ondo, Osun, Ekiti, Ogun, and Lagos) of Nigeria [25,26]. The southwestern zone of Nigeria is a humid tropical area with rainy and dry seasons; hence, the states in this zone have rich floristic diversity and cultural heritage [25,26]. The major cities and towns in the southwestern states include Ogbomosho, Abeokuta, Ibadan, Ede, Ikire, Osogbo, Ile-Ife, and Lagos [25,26]. The major traditional occupations of the inhabitants of this zone are fishing, pottery, farming, indigenous medical practices, and blacksmithing [25]. The recent study of Ajao et al. [26], which compiled the list of angiosperms in the southwestern zone of Nigeria, identified a total of 493 angiosperm species belonging to 99 families, out of which 418 species are utilized for traditional medicinal purposes. Despite the rich floristic diversity of medicinal species in this zone, studies focusing on the indigenous use and traditional medicinal plant applications are limited [26]. Ogbomosho, one of the major towns in the south-western zone of Nigeria, is endowed with a wide variety of indigenous medicinal plants that local herbalists commonly utilize to treat several ailments, including infectious diseases [27]. The present study aimed to document and provide basic knowledge of medicinal plants used by herb sellers, traditional health practitioners, and other people with indigenous knowledge in the treatment of COVID-19, cough, and flu in Ogbomosho South and North Local Government in Ogbomosho, Oyo State, Nigeria. The ethnobotanical survey of medicinal plants used in the management of COVID-19 in Ogbomosho Local Government Areas of Oyo State, Nigeria, will provide information on the availability, classification, preparation, and therapeutic potential of medicinal plants used in the region for treating COVID-19 and related respiratory ailments, particularly cough and flu.

2. Materials and Methods

2.1. Study Area

The study was conducted between October 2021 and March 2022 in Ogbomosho North and Ogbomosho South Local Government Areas of Oyo State, Nigeria (Figure 1). Ogbomosho lies between latitude 8′08′00″ N and longitude 4′16′00″ E, with an approximate population density of 454,690 [28]. The city is inhabited primarily by the Yoruba ethnic group, and agriculture is the major economy.

2.2. Collection of Data

Ethnobotanical information was obtained from participants using a semi-structured questionnaire. The participants were purposively selected, comprising herb sellers, traditional health practitioners, farmers, and individuals with indigenous knowledge. The questionnaire was prepared in English. However, to facilitate efficient communication, informal discussion with herb sellers and traditional health practitioners was done in Yoruba, the local language in these local government areas. A total of 56 participants were interviewed, and the participants were interviewed individually to maintain confidentiality. Data collected included age, gender, occupation, educational background, residence, local names of the plants used in treating COVID-19 and related ailments, plant part used, method of preparation/extraction, and administration method. The study and data collection were done following the regulations made by the International Society of Ethnobiology (available at https://www.ethnobiology.net, accessed on 30 September 2022).

2.3. Collection and Identification of Medicinal Plants

Plant collection was done with the help of herb sellers and traditional health practitioners, using the plants’ local names (in the Yoruba language). The scientific identification of plants was made at IFE herbarium of the Obafemi Awolowo University, Ile-Ife, Osun State, Nigeria (herbarium code IFE, according to Thiers [29]), and voucher specimens were prepared and deposited at the herbarium. In addition, the currently accepted names of all plants identified were verified on “World Flora Online” (www.worldfloraonline.org, accessed on 1 August 2022).

2.4. Data Analysis

Descriptive statistics were carried out on the participants’ demographic information. The data obtained from the documented plants were analyzed using three ethnobotanical indices: frequency of citation (FC), the relative frequency of citation (RFC), and fidelity level (FL).
Following the methods described by Tardio and Pardo-de-santayana [30], RFC was calculated as:
RCF = FC/N
where FC = Frequency of citation/mention, and N = number of participants in the survey.
Fidelity level was calculated as described by Friedman et al. [31]:
FL = (Ip/Iu) × 100
where Ip = Number of respondents that mentioned a particular plant species used to treat an ailment being considered, and
Iu = Total number of respondents in the survey.

2.5. Ethical Approval

The study was approved by the Committee of Ethics of the Forestry Research Institute of Nigeria, Ibadan, Nigeria, with the ethical approval number CFGO711FRIN06. Informed consent was obtained from the participants prior to data collection.

3. Results and Discussion

3.1. Demographic Information

The interview started with an assessment of the demographic characteristics of the participants (Table 1). Fifty-six participants in the age range of 20 to 61 with indigenous knowledge of medicinal plants were interviewed. Most participants were female (58.9%). Individuals aged 51 and above accounted for about 55.4% of the participants. There were more individuals with primary education, constituting about 46.4% of the participants, followed by individuals with secondary education (33.9%). Most of the participants (48.2%) were herb sellers. The participants who all lived in rural areas were either Yoruba (96.4%) or Igbo (3.6%). It is known that variations in gender, age, and educational status of participants have an important relationship with ethnomedicinal knowledge [32].
The predominance of the female gender in the present study suggests that women have more knowledge of indigenous medicinal plants than their male counterparts in the study area. The current results corroborate the findings of Chukwuma et al. [33], which reported the dominance of female participants with herbal knowledge in an ethnobotanical survey done in Ado-Ekiti, a Southwestern State in Nigeria. Similarly, women were the most involved and informed in the knowledge and utilization of medicinal plants used for preventing and treating COVID-19, for example, in Algeria [32]. Furthermore, the study conducted by Teixidor-Toneu et al. [34] indicated that women have three-fold more knowledge of medicinal plants than men in Morocco. This was attributed to the frequency of cooking by women (since most medicinal plants are widely used in food preparation), women’s specific conditions, and gender-specific culture. In most African countries, rural areas historically collected different native plants’ parts for their diets and family health needs [35].
Generally, the majority (55.4%) of the people with indigenous knowledge in this study were older than age 51. This result is similar to previous reports on the ethnobotanical survey of indigenous medicinal plants in Nigeria [24] and Northern Morocco [36]. The predominance of elderly participants with indigenous knowledge in the present study agrees with previous reports that older people (above age 50) are usually more knowledgeable about the practice of herbal medicine [24]. The results also revealed a gap between the older and younger generations in the knowledge of indigenous plant use in the study area. The erosion of the knowledge of medicinal plant among younger generations has been reported in other parts of the world. For example, in Western and Northwestern Himalaya, the loss of knowledge regarding the use of medicinal plants in the younger generation was reported [37,38]. This valuable knowledge of medicinal plants and their uses erodes in the younger generation is largely due to westernization, higher education level, and habitat destruction of medicinal plants [34,37,38]. Therefore, it is important that indigenous knowledge is documented, preserved, shared with the younger generations, and that plant resources are conserved.
Regarding the level of education, individuals with a tertiary education level constituted the minority (19.64%) of the participants. This result may be attributed to the fact that the practice of traditional medicine or herbalism does not require a degree but is acquired by experience and learning from older generations [36]. Our result is in line with an ethnobotanical survey of local flora used for medicinal purposes conducted in Lagos, Nigeria, which reported that 79% of the participants with indigenous knowledge had only a primary education [39].

3.2. Medicinal Plants Recorded

In total, 26 medicinal plant species belonging to 17 families were used to treat COVID-19, 31 medicinal plants from 20 families were used to treat cough, and 29 plant species belonging to 19 families were used to treat flu (Table 2, Table 3 and Table 4). For COVID-19 treatment, the most represented families in terms of the number of species were Annonaceae, Meliaceae, Rubiaceae, Asteraceae, Zingiberaceae, Rutaceae, and Fabaceae, with 2–3 species in each family. The most representative families for treating cough were the Amaryllidaceae, Poaceae, Zingiberaceae, Anacardiaceae, Rutaceae, Myrtaceae, Fabaceae, and Arecaceae, with 2–3 species per family. For flu-related symptoms, the most representative families were the Annonaceae (three species), followed by Amaryllidaceae, Zingiberaceae, Compositae, Solanaceae, Myrtaceae, and Fabaceae, with two species each (Figure 2). This result is similar to that reported by Benkhaira et al. [36], where Asteraceae and Zingiberaceae were listed as some of the most representative medicinal plant families used for treating and preventing COVID-19 in Northern Morocco. It is also similar to the findings of Lawal et al. [40], where Fabaceae and Poaceae were listed as some of the most represented plant families used for treating coughs in Osun state, Nigeria. The relatively high number of plants and families identified in this study for the treatment of COVID-19, cough, and flu indicates the richness and diversity of the Nigerian flora for various therapeutic purposes. The diverse phytochemicals present in these florae, which are relatively unexplored, can serve as a potential source of drug development for treating different respiratory ailments [41].

3.3. Plant Parts and Growth Forms of Medicinal Plants Used for Treating COVID-19, Cough, and Flu

As participants in the study area reported, diverse plant parts such as bark, bulbs, flower, husk, leaves, rhizomes, and root were used for treating COVID-19, cough, and flu (Figure 3). However, leaves were the most commonly used plant part for treating COVID-19 (39%) and flu (31%), while the bark (20%) was the most commonly used part for treating cough (Figure 3). Several previous studies in Nigeria have also reported that leaves and bark were more utilized in the traditional treatment of different ailments than other plant parts [24,39,40]. The widespread use of leaves for herbal medicine preparation may be attributed to their relatively high abundance, accessibility, and ease of collection [42]. Additionally, the relatively higher photosynthetic and metabolic activities occurring in the aerial parts of most plants (particularly leaves) may have contributed to the build-up of bioactive substances with therapeutic properties [42].
In the study area, the herbal remedies used to treat and prevent COVID-19, cough, and flu were sourced from different growth forms, including trees, shrubs, herbs, grasses, and climbers (Figure 4). However, for the three respiratory infections referenced, a significant number of the medicinal plants were trees (54%, 52%, and 53% for COVID-19, cough, and flu, respectively), followed by herbs (31%, 23%, and 27% for COVID-19, cough, and flu, respectively), and climbers were the lowest growth forms utilized for treating COVID-19, cough, and flu. In terms of sustainability and conservation, harvesting leaves from trees may be more sustainable than other growth forms, given that trees are more resilient due to their sizes [24]. The dominance of woody perennials as sources of herbal remedies may be connected to the rainforest vegetation of the study area. Previous studies [24,43] have reported similar dominance of woody plants in ethnobotanical surveys of plants conducted in the same rainforest zones in Nigeria.

3.4. Method of Preparation and Mode of Administration of Medicinal Plants Species Used for Treating COVID-19, Cough, and Flu

While the participants in the study area identified 10 methods used for preparing the medicinal plant species, the majority of the herbal remedies were formulated by decoction for COVID-19 (81%) and by infusion for cough (28%) and flu (33%) (Figure 5). Several ethnobotanical studies have reported that decoction and infusion are the most cited methods of herbal remedy preparation [32,40,44,45]. Decoction and infusion are the most common forms of herbal remedy preparation in local communities, primarily because of the simplicity of the process [40]. Decoction involves heating the required quantity of the plant part in water for 30 min until about half of the water is lost [46], while the infusion is done by soaking the plant material in pre-warmed or cold water [44]. The herbal preparations in this study were administered orally, by snorting (nasal), and topically. However, the majority of the remedies were administered orally for COVID-19 (88%), cough (94%), and flu (87%) Figure 6. The dominance of oral administration may be explained by the fact that the oral route is simple and rapid and allows for better absorption of bioactive constituents in the medicinal plant [32].

3.5. Ethnobotanical Indices of Medicinal Plants Recorded

Ethnobotanical indices are commonly used to deduce the local importance and relevance of medicinal plants in a given study area [45,47,48]. The indices can be used to rank medicinal plant species based on their acclaimed efficacy, cultural significance, and value. Additionally, these indices are valuable tools that give cues for further scientific investigation of medicinal plant species to discover their therapeutically bioactive constituents and for setting conservation and sustainable use plans [39]. In the present study, RF, RFC, and FL were used to determine the importance of the identified medicinal plant species used for treating and preventing COVID-19, cough, and flu in the study area (Table 2). The top five most cited species for treating COVID-19 were Zingiber officinale (FC = 10; RFC = 0.18; FL = 18%), Curcuma longa (FC = 8; RFC = 0.14; FL = 14%), Azadirachta indica (FC = 8; RFC = 0.14; FL = 14%), Capsicum frutescens (FC = 6; RFC = 0.11; FL = 11%), and Citrus limon (FC = 5; RFC = 0.09; FL = 9%). For cough, the top five cited species were C. limon (FC = 13; RFC = 0.23; FL = 23%), Allium sativum (FC = 12; RFC = 0.21; FL = 21%), Citrus aurantiifolia (FC = 11; RFC = 0.20; FL = 20%), Vitellaria paradoxa (FC = 11; RFC = 0.20; FL = 20%), and Garcinia kola (FC = 8; RFC = 0.14; FL = 14%). The top five most cited species for treating flu were Z. officinale (FC = 9; RFC = 0.16; FL = 16%), Cymbopogon citratus (FC = 7; RFC = 0.13; FL = 13%), A. sativum (FC = 6; RFC = 0.11; FL = 11%), Chromolaena odorata (FC = 6; RFC = 0.11; FL = 11%), and A. indica (FC = 6; RFC = 0.11; FL = 11%) (Figure 7a–c).
While ethnobotanical indices are claimed to be representations of the efficacy of medicinal plants and their potential use for drug development, it should be noted that these indices were not established by pharmacologists and statisticians [49]. Hence, the proof of concept is lacking. Additionally, the medicinal importance of plants and their cultural value cannot be summed up by numbers but are rather better obtained from a critical evaluation of the primary data based on the scope and objectives of the research [39,49].
The study’s most cited medicinal plants for treating COVID-19, including some major phytochemical components of these plants, have been reported to display antiviral and immunomodulatory activities, summarized in Table 5. For example, in an in silico docking study, Rajagopal et al. [50] reported that 8-gingerol and 10-gingerol isolated from Z. officinale were active against COVID-19 with significantly higher Glide scores when compared to hydroxychloroquine. Curcumin, a bioactive compound from C. longa, has been reported to exhibit antiviral activity against different types of enveloped viruses via several mechanisms such as induction of host antiviral responses, direct interaction with viral membrane proteins, and disruption of the viral envelope [13].
In a recent in vivo study, Supriyanto et al. [51] investigated the effect of the methanolic extract of A. indica leaf as an immunomodulator on different immune surveillance cells (CD4+, CD8+, CD25+, and CD62L). The results showed that A. indica demonstrated significant immunomodulatory activities against the cells by increasing pressure molecules and decreasing pro-inflammatory molecules. Capsaicin, the major bioactive component in Capsicum species, including C. frutescens identified in this study, has demonstrated antiviral activity and even structural disruption of viral 3CL-protease of COVID-19. Using molecular dynamics and strategies docking, Gonzalez-Paz et al. [52] evaluated the effect of capsaicin on viral 3CL-protease of COVID-19. The preliminary results from the study suggested that capsaicin can bind to the 3CL-protease of COVID-19, causing structural changes in the viral protease.
C. limon, one of the most cited species used in treating and preventing COVID-19 and cough in this study, is a well-known natural immune-modulator. Using different in silico and computational approaches, Khan et al. [53] investigated the effects of 25 phytochemicals isolated from C. limon against SARS-CoV-2 main protease (Mpro), and their docking scores compared to remdesivir. The results revealed that six flavonoid compounds (diosmetin, quercetin, eriodictoyl, luteolin, spinacetin, and apigenin) exhibited good docking scores against SARS-CoV-2 Mpro without violating any drug-like activity standard parameters. Among these six compounds, diosmetin showed better docking values than the standard antiviral drug (remdesivir).
The promising antiviral and immunomodulatory activities displayed by some of the identified medicinal plants suggest that they are potential candidates for discovering new drugs in the fight against COVID-19 and related respiratory infections. Further in vivo and clinical studies should be done to evaluate their mechanism of action and antagonistic effects against COVID-19.

4. Conclusions

This ethnobotanical survey indicated high usage of medicinal remedies in Ogbomosho North and South Local Government Areas to prevent and treat COVID-19 and related respiratory infections, particularly cough and flu. Most plants documented for COVID-19 are also used to treat other respiratory tract infections, including the common cold. The phytochemical richness and biological activities (e.g., immunomodulatory, antiviral, antimicrobial, etc.) of some of the identified species have been documented. However, further studies on these plants’ phytochemical analysis and pharmacological potentials, particularly those with relatively high ethnobotanical indices, should be conducted. This will help identify bioactive constituents and inform potential drug development to treat respiratory ailments, including COVID-19. Although the increasing global demand for herbal medicine is attributed to the belief that natural products (in this case, medicinal plants) are safe, toxicity studies should be done on the documented species to assess and establish their safety for human use. It is noteworthy that the increasing exploitation of medicinal plants for different uses might endanger the species. Hence, the conservation of these medicinal species should be prioritized for continual and sustainable use.

Author Contributions

Conceptualization, T.L.A.; methodology, C.A.O.; data analysis; C.A.O. and A.E.A.; writing—original draft preparation, C.A.O., T.L.A., A.E.A., A.O. and T.O.A.; writing—review and editing C.A.O., T.L.A., A.E.A., O.E.O., I.A.A., A.O.E., C.E.I. and T.O.A.; funding acquisition, O.E.O., I.A.A., A.O.E., C.E.I., and T.O.A. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was conducted in accordance with the Declaration of Helsinki, and approved by the Ethics Committee) of the Forestry Research Institute of Nigeria, Ibadan, Nigeria, with the ethical approval number CFGO711FRIN06 and approval date (5 May 2022).

Informed Consent Statement

Not applicable.

Data Availability Statement

Not applicable.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Jin, X.; Ren, J.; Li, R.; Gao, Y.; Zhang, H.; Li, J.; Zhang, J.; Wang, X.; Wang, G. Global burden of upper respiratory infections in 204 countries and territories, from 1990 to 2019. E Clin. Med. 2021, 37, 100986. [Google Scholar] [CrossRef]
  2. José, R.J. Respiratory infections: A global burden. Ann. Res. Hosp. 2018, 2, 1–4. [Google Scholar] [CrossRef]
  3. Kyere, K.; Aremu, T.O.; Ajibola, O.A. Availability bias and the COVID-19 pandemic: A case study of Legionella Pneumonia. Cureus 2022, 14, e25846. [Google Scholar] [CrossRef]
  4. Juscamayta-Lopez, T.D.; Valdivia, F.R.; Carhuaricra, D.M. Phylogenomics reveals multiple introductions and early spread of SARS-CoV-2 into Peru. BioRxiv 2020, 10, 5961–5968. [Google Scholar] [CrossRef]
  5. González-Bustamante, B. Evolution and early government responses to COVID-19 in South America. World Dev. 2021, 1, 105180. [Google Scholar] [CrossRef]
  6. Viner, R.M.; Ward, J.L.; Hudson, L.D.; Ashe, M.P.; Hargreaves, D.; Whittaker, E. Systematic review of reviews of symptoms and signs of COVID-19 in children and adolescents. Arch. Dis. Child. 2021, 106, 802–807. [Google Scholar] [CrossRef]
  7. World Health Organisation (WHO). Coronavirus: Symptoms. Available online: https://www.who.int/health-topics/coronavirus#tab%20=%20tab_32021 (accessed on 2 June 2022).
  8. World Health Organization (WHO). 14.9 Million Excess Deaths Associated with the COVID-19 Pandemic in 2020 and 2021. 2022. Available online: https://www.who.int/news/item/05-05-2022-14.9-million-excess-deaths-were-associated-with-the-covid-19-pandemic-in-2020-and-2021 (accessed on 27 May 2022).
  9. Pradhan, D.; Biswasroy, P.; Naik, P.K.; Ghosh, G.; Rath, G. A review of current interventions for COVID-19 prevention. Arch. Med. Res. 2020, 51, 363–374. [Google Scholar] [CrossRef]
  10. U.S. Food & Drug Administration (FDA). Coronavirus (COVID-19) Update: FDA Authorizes First Oral Antiviral for Treatment of COVID-19. FDA. 2021. Published 22 December 2021. Available online: https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19-update-fda-authorizes-first-oral-antiviral-treatment-covid-19 (accessed on 26 June 2022).
  11. Farly, J. FDA Updates on Paxlovid for Health Care Providers. U.S. Food & Drug Administration (FDA). 2022. Published online 4 May 2022. Available online: https://www.fda.gov/drugs/news-events-human-drugs/fda-updates-paxlovid-health-care-providers (accessed on 26 June 2022).
  12. Nugraha, R.V.; Ridwansyah, H.G.; Khairani, A.F.; Atik, N. Traditional herbal medicine candidates as complementary treatments for COVID-19: A review of their mechanisms, pros and cons. Evid. -Based Complement. Altern. Med. 2020, 2560645. [Google Scholar] [CrossRef]
  13. Thimmulappa, R.K.; Mudnakudu-Nagaraju, K.K.; Shivamallu, C.; Subramaniam, K.T.; Radhakrishnan, A.; Bhojraj, S.; Kuppusamy, G. Antiviral and immunomodulatory activity of curcumin: A case for prophylactic therapy for COVID-19. Heliyon 2021, 7, e06350. [Google Scholar] [CrossRef]
  14. Paudyal, V.; Sun, S.; Hussain, R.; Abutaleb, M.H.; Hedima, E.W. Complementary and alternative medicines use in COVID-19: A global perspective on practice, policy and research. Res. Soc. Adm. Pharm. 2022, 18, 2524–2528. [Google Scholar] [CrossRef]
  15. Shrestha, P.M.; Dhillion, S.S. Medicinal plant diversity and use in the highlands of Dolakha district, Nepal. J. Ethnopharmacol. 2003, 86, 81–96. [Google Scholar] [CrossRef]
  16. Hughes, G.D.; Aboyade, O.M.; Okonji, C.O.; Clark, B.; Mabweazara, S.Z. Comparison of the prevalence of non-communicable diseases and traditional herbal medicine use in urban and rural communities in South Africa. Adv. Integr. Med. 2021, 8, 136–143. [Google Scholar] [CrossRef]
  17. Ssenku, J.E.; Okurut, S.A.; Namuli, A.; Kudamba, A.; Tugume, P.; Matovu, P.; Walusansa, A. Medicinal plant use, conservation, and the associated traditional knowledge in rural communities in Eastern Uganda. Trop. Med. Health 2022, 50, 39. [Google Scholar] [CrossRef]
  18. Iwu, M.M.; Duncan, A.R.; Okunji, C.O. New Antimicrobials of Plant Origin. In Perspectives on New Crops and New Uses; Janick, J., Ed.; ASHS Press: Alexandria, VA, USA, 1999; pp. 457–462. ISBN 13: 9780961502706. [Google Scholar]
  19. Okaiyeto, K.; Oguntibeju, O.O. African herbal medicines: Adverse effects and cytotoxic potentials with different therapeutic applications. Int. J. Environ. Res. Public Health 2021, 18, 5988. [Google Scholar] [CrossRef]
  20. Khadka, D.; Dhamala, M.K.; Li, F.; Aryal, P.C.; Magar, P.R.; Bhatta, S. The use of medicinal plants to prevent COVID-19 in Nepal. J. Ethnobiol. Ethnomed. 2021, 17, 26. [Google Scholar] [CrossRef]
  21. Silva, F.S.; Ramos, M.A.; Hanazaki, N.; UPd, A. Dynamics of traditional knowledge of medicinal plants in a rural community in the Brazilian semi-arid region. Rev. Bras. Farmacogn. 2011, 21, 382–391. [Google Scholar] [CrossRef]
  22. Arshad, M.; Ahmad, M.; Ahmed, E.; Saboor, A.; Abbas, A.; Sadiq, S. An ethnobiological study in Kala Chitta hills of Pothwar region, Pakistan: Multinomial logit specification. J. Ethnobiol. Ethnomed. 2014, 10, 13. [Google Scholar] [CrossRef] [Green Version]
  23. Cox, P.A. Will tribal knowledge survive the millennium? Science 2000, 287, 44–45. [Google Scholar] [CrossRef] [Green Version]
  24. Falemara, B.C.; Joshua, V.I.; Ogunkanmi, T.I.; Mbeng, W.O. Ethnomedicinal survey of indigenous medicinal plants in Jos Metropolis, Nigeria. J. Med. Plants Econ. Dev. 2021, 5, 128. [Google Scholar] [CrossRef]
  25. Borokini, T.I.; Lawal, I.O. Traditional medicine practices among the Yoruba people of Nigeria: A historical perspective. J. Med. Plants Stud. 2014, 2, 20–33. [Google Scholar]
  26. Ajao, A.A.; Mukaila, Y.O.; Sabiu, S. Wandering through southwestern Nigeria: An inventory of Yoruba useful angiosperm plants. Heliyon 2021, 8, e08668. [Google Scholar] [CrossRef]
  27. Olorunnisola, O.S.; Adetutu, A.; Afolayan, A.J. An inventory of plants commonly used in the treatment of some disease conditions in Ogbomoso, South West, Nigeria. J. Ethnopharmacol. 2015, 161, 60–68. [Google Scholar] [CrossRef]
  28. Federal Republic of Nigeria, 2006 Population Census. Available online: http://www.nigerianstat.gov.ng/nbsapps/Connections/Pop2006.pdf (accessed on 20 May 2022).
  29. Thiers, B. Index Herbariorum: A global Directory of Public Herbaria and Associated Staff. New York Botanical Garden’s Virtual Herbarium. (continuously updated). Available online: http://sweetgum.nybg.org/ih/ (accessed on 4 October 2022).
  30. Tardìo, J.; Pardo-De-Santayana, M. Cultural importance indices: A comparative analysis based on the useful wild plants of Southern Cantabria (Northern Spain). Econ. Bot. 2008, 62, 24–39. [Google Scholar] [CrossRef]
  31. Friedman, J.; Yaniv, Z.; Dafni, A.; Palewitch, D. A preliminary classification of the healing potential of medicinal plants, based on a rational analysis of an ethnopharmacological field survey among Bedouins in the Negev Desert, Israel. J. Ethnopharmacol. 1986, 16, 275–287. [Google Scholar] [CrossRef]
  32. Brahmi, F.; Iblhoulen, Y.; Issaadi, H.; Elsebai, M.F.; Madani, K.; Boulekbache-Makhlouf, L. Ethnobotanical survey of medicinal plants of bejaia localities from algeria to prevent and treat coronavirus (COVID-19) infection shortened title: Phytomedicine to manage COVID-19 pandemic. Adv. Tradit. Med. 2022, 1–13. [Google Scholar] [CrossRef]
  33. Chukwuma, D.M.; Chukwuma, E.C.; Adekola, O.O. An ethnobotanical survey of Malaria-treating plants in Ado-Ekiti Local Government Area, Ekiti State, Nigeria. Ethnobot. Res. Appl. 2019, 18, 1–10. [Google Scholar] [CrossRef] [Green Version]
  34. Tavilla, G.; Crisafulli, A.; Ranno, V.; Picone, R.M.; Redouan, F.Z.; del Galdo, G.G. First contribution to the ethnobotanical knowledge in the Peloritani Mounts (NE Sicily). Res. J. Ecol. Environ. Sci. 2022, 4, 1–34. [Google Scholar] [CrossRef]
  35. Olatokun, W.M.; Ayanbode, O.F. Use of indigenous knowledge by women in a Nigerian rural community. Indian J. Tradit. Knowl. 2009, 8, 287–295. [Google Scholar]
  36. Benkhaira, N.; Koraichi, S.I.; Fikri-Benbrahim, K. Ethnobotanical survey on plants used by traditional healers to fight against COVID-19 in Fez city, Northern Morocco. Ethnobot. Res. Appl. 2021, 21, 1–18. [Google Scholar] [CrossRef]
  37. Singh, B.; Singh, B.; Kishor, A.; Singh, S.; Bhat, M.N.; Surmal, O.; Musarella, C.M. Exploring plant-based ethnomedicine and quantitative ethnopharmacology: Medicinal plants utilized by the population of Jasrota Hill in Western Himalaya. Sustainability 2020, 12, 7526. [Google Scholar] [CrossRef]
  38. Bhat, M.N.; Singh, B.; Surmal, O.; Singh, B.; Shivgotra, V.; Musarella, C.M. Ethnobotany of the Himalayas: Safeguarding medical practices and traditional uses of Kashmir regions. Biology 2021, 10, 851. [Google Scholar] [CrossRef] [PubMed]
  39. Lawal, I.O.; Rafiu, B.O.; Ale, J.E.; Majebi, O.E.; Aremu, A.O. Ethnobotanical survey of local flora used for medicinal purposes among indigenous people in five areas in Lagos State, Nigeria. Plants 2022, 11, 633. [Google Scholar] [CrossRef] [PubMed]
  40. Lawal, I.O.; Olufade, I.I.; Rafiu, B.O.; Aremu, A.O. Ethnobotanical survey of plants used for treating cough associated with respiratory conditions in Ede South local government area of Osun State, Nigeria. Plants 2020, 9, 647. [Google Scholar] [CrossRef] [PubMed]
  41. Zakariya, A.M.; Adamu, A.; Nuhu, A.; Kiri, I.Z. Assessment of indigenous knowledge on medicinal plants used in the management of malaria in Kafin Hausa, north-western Nigeria. Ethnobot. Res. Appl. 2021, 22, 1–18. [Google Scholar] [CrossRef]
  42. Ahmad, M.; Sultana, S.; Fazl-i-Hadi, S.; Ben Hadda, T.; Rashid, S.; Zafar, M.; Yaseen, G. An ethnobotanical study of medicinal plants in high mountainous region of Chail valley (District Swat-Pakistan). J. Ethnobiol. Ethnomed. 2014, 10, 36. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Tugume, P.; Kakudidi, E.K.; Buyinza, M. Ethnobotanical survey of medicinal plant species used by communities around Mabira Central Forest Reserve, Uganda. J. Ethnobiol. Ethnomed. 2016, 12, 5. [Google Scholar] [CrossRef] [Green Version]
  44. Suroowan, S.; Mahomoodally, M.F. A comparative ethnopharmacological analysis of traditional medicine used against respiratory tract diseases in Mauritius. J. Ethnopharmacol. 2016, 177, 61–80. [Google Scholar] [CrossRef]
  45. Ishtiaq, M.; Maqbool, M.; Ajaib, M.; Ahmed, M.; Hussain, I.; Khanam, H.; Mushtaq, W.; Hussain, T.; Azam, S.; Hayat, B.K.; et al. Ethnomedicinal and folklore inventory of wild plants used by rural communities of valley Samahni, District Bhimber Azad Jammu and Kashmir, Pakistan. PLoS ONE 2021, 16, e0243151. [Google Scholar] [CrossRef]
  46. Nagalingam, A. Drug Delivery Aspects of Herbal Medicines. Jpn Kampo Med. Treat Common Dis. Focus Inflamm. 2017, 17, 143. [Google Scholar]
  47. Hoffman, B.; Gallaher, T. Importance indices in ethnobotany. Ethnobot. Res. Appl. 2007, 5, 201–208. [Google Scholar] [CrossRef] [Green Version]
  48. Weckerle, C.S.; De Boer, H.J.; Puri, R.K.; Van, A.T.; Bussmann, R.W.; Leonti, M. Recommended standards for conducting and reporting ethnopharmacological field studies. J. Ethnopharmacol. 2018, 210, 125–132. [Google Scholar] [CrossRef]
  49. Leonti, M. The relevance of quantitative ethnobotanical indices for ethnopharmacology and ethnobotany. J. Ethnopharmacol. 2022, 288, 115008. [Google Scholar] [CrossRef]
  50. Rajagopal, K.; Byran, G.; Jupudi, S.; Vadivelan, R. Activity of phytochemical constituents of black pepper, ginger, and garlic against coronavirus (COVID-19): An in silico approach. Int. J. Health Allied Sci. 2020, 9, 43–50. [Google Scholar] [CrossRef]
  51. Supriyanto, S.; Widjanarko, S.; Rifa’i, M.; Yunianta, Y. Immunomodulatory activity of methanol leaf extract of neem (Azadirachta Indica Juss.) against suppressor and proinflammatory molecules. J. Trop. Life Sci. 2021, 11, 309–316. [Google Scholar] [CrossRef]
  52. Gonzalez-Paz, L.; Lossada, C.; Moncayo, L.; Romero, F.; Paz, J.; Vera-Villalobos, J.; Pérez, A.; San-Blas, E.; Alvarado, Y. Theoretical molecular docking study of the structural disruption of the viral 3CL-protease of COVID19 induced by binding of capsaicin, piperine and curcumin part 1: A comparative study with chloroquine and hydrochloroquine two antimalaric drugs. Res. Sq. 2020. [Google Scholar] [CrossRef] [Green Version]
  53. Khan, J.; Sakib, S.; Mahmud, S.; Khan, Z.; Islam, M.; Sakib, M.; Simal-Gandara, J. Identification of potential phytochemicals from Citrus limon against main protease of SARS-CoV-2: Molecular docking, molecular dynamic simulations and quantum computations. J. Biomol. Struct. Dyn. 2021, 1–12. [Google Scholar] [CrossRef]
  54. Josling, P. Preventing the common cold with a garlic supplement: A double-blind, placebo-controlled survey. Adv Ther. 2001, 18(4), 189–193. [Google Scholar] [CrossRef] [PubMed]
  55. Li, M.; Yan, Y.X.; Yu, Q.T.; Deng, Y.; Wu, D.T.; Wang, Y.J. Comparison of immunomodulatory effects of fresh garlic and black garlic polysaccharides on RAW 264.7 macrophages. J. Food Sci. 2017, 82, 765–771. [Google Scholar] [CrossRef]
  56. Rouf, R.; Uddin, S.J.; Sarker, D.K.; Islam, M.T.; Ali, E.S.; Shilpi, J.A.; Sarker, S.D. Antiviral potential of garlic (Allium sativum) and its organosulfur compounds: A systematic update of pre-clinical and clinical data. Trends Food Sci. Technol. 2020, 104, 219–234. [Google Scholar] [CrossRef]
  57. Ashfaq, U.A.; Jalil, A.; Qamar, M.T. Antiviral phytochemicals identification from Azadirachta indica leaves against HCV NS3 protease: An in silico approach. Nat. Prod. Res. 2016, 30, 1866–1869. [Google Scholar] [CrossRef]
  58. Olwenyi, O.A.; Asingura, B.; Naluyima, P. In-vitro Immunomodulatory activity of Azadirachta indica A.Juss. Ethanol: Water mixture against HIV associated chronic CD4+ T-cell activation/exhaustion. BMC Complement Med. 2021, 21, 114. [Google Scholar] [CrossRef] [PubMed]
  59. Khurshid, R.; Majeed, S.; Saghir, S.; Saad, M.; Ashraf, H.; Fayyaz, I. Antiviral activity of extract of neem (Azadirachta Indica) leaves: An in vivo study. Pak. J. Med. Health Sci. 2022, 16, 10. [Google Scholar] [CrossRef]
  60. Viveros-Paredes, J.M.; Puebla-Pérez, A.M.; Gutiérrez-Coronado, O.; Macías-Lamas, A.M.; Hernández-Flores, G.; Ortiz-Lazareno, P.C.; Villaseñor-García, M.M. Capsaicin attenuates immunosuppression induced by chronic stress in BALB/C mice. Int. Immunopharmacol. 2021, 93, 107341. [Google Scholar] [CrossRef]
  61. Nudo, L.P.; Catap, E.S. Anti-immunosuppressive effects of Chromolaena odorata (Lf.) King & Robinson (Asteraceae) leaf extract in cyclophosphamide-injected Balb/C mice. Philipp. J. Sci. 2012, 141, 35–43. [Google Scholar]
  62. Boudjeko, T.; Megnekou, R.; Woguia, A.L.; Kegne, F.M.; Ngomoyogoli, J.E.K.; Tchapoum, C.D.N.; Koum, O. Antioxidant and immunomodulatory properties of polysaccharides from Allanblackia floribunda Oliv stem bark and Chromolaena odorata (L.) King and HE Robins leaves. BMC Res. Notes 2015, 8, 759. [Google Scholar] [CrossRef] [Green Version]
  63. Lappas, C.M.; Lappas, N.T. D-Limonene modulates T lymphocyte activity and viability. Cell. Immunol. 2012, 279, 30–41. [Google Scholar] [CrossRef] [PubMed]
  64. Nagy, M.M.; Al-Mahdy, D.A.; Abd El Aziz, O.M.; Kandil, A.M.; Tantawy, M.A.; El Alfy, T.S. Chemical composition and antiviral activity of essential oils from Citrus reshni hort. ex Tanaka (Cleopatra mandarin) cultivated in Egypt. J. Essent. Oil Bear. Plants 2018, 21, 264–272. [Google Scholar] [CrossRef]
  65. Meeran, M.N.; Seenipandi, A.; Javed, H.; Sharma, C.; Hashiesh, H.M.; Goyal, S.N.; Ojha, S. Can limonene be a possible candidate for evaluation as an agent or adjuvant against infection, immunity, and inflammation in COVID-19? Heliyon 2021, 7, e05703. [Google Scholar] [CrossRef]
  66. Diab, K.A. In vitro studies on phytochemical content, antioxidant, anticancer, immunomodulatory, and antigenotoxic activities of lemon, grapefruit, and mandarin citrus peels. Asian Pac. J. Cancer Prev. 2016, 17, 3559–3567. [Google Scholar]
  67. Abd, A.J.; Al-Shammarie, A.M.; Abd, A.H. Antiviral activity of limonin against Newcastle disease virus in vitro. Res. J. Biotechnol. 2019, 14, 320–328. [Google Scholar]
  68. Afolayan, F.I.; Erinwusi, B.; Oyeyemi, O.T. Immunomodulatory activity of curcumin-entrapped poly d, l-lactic-co-glycolic acid nanoparticles in mice. Integr. Med. Res. 2018, 7, 168–175. [Google Scholar] [CrossRef] [PubMed]
  69. Dai, J.; Gu, L.; Su, Y.; Wang, Q.; Zhao, Y.; Chen, X.; Li, K. Inhibition of curcumin on influenza A virus infection and influenzal pneumonia via oxidative stress, TLR2/4, p38/JNK MAPK and NF-κB pathways. Int. Immunopharmacol. 2018, 54, 177–187. [Google Scholar] [CrossRef]
  70. Duran, N.; Kaya, D.A. Chemical composition of essential oils from Origanum onites L. and Cymbopogon citratus, and their synergistic effects with acyclovir against HSV-1. In Proceedings of the 7th International Conference on Advanced Materials and Systems 2018, Bucharest, Romania, 18–20 October 2018; The National Research & Development Institute for Textiles and Leather: București, Romania, 2018; pp. 243–248. [Google Scholar]
  71. Goncalves, E.C.; Assis, P.M.; Junqueira, L.A.; Cola, M.; Santos, A.R.; Raposo, N.R.; Dutra, R.C. Citral inhibits the inflammatory response and hyperalgesia in mice: The role of TLR4, TLR2/Dectin-1, and CB2 cannabinoid receptor/ATP-sensitive K+ channel pathways. J. Nat. Prod. 2020, 83, 1190–1200. [Google Scholar] [CrossRef] [PubMed]
  72. Rosmalena, R.; Elya, B.; Dewi, B.E.; Fithriyah, F.; Desti, H.; Angelina, M.; Seto, D. The antiviral effect of indonesian medicinal plant extracts against dengue virus in vitro and in silico. Pathogens 2019, 8, 85. [Google Scholar] [CrossRef] [Green Version]
  73. Nworu, C.S.; Akah, P.A.; Esimone, C.O.; Okoli, C.O.; Okoye, F.B.C. Immunomodulatory activities of kolaviron, a mixture of three related biflavonoids of Garcinia kola Heckel. Immunopharmacol. Immunotoxicol. 2008, 30, 317–332. [Google Scholar] [CrossRef] [PubMed]
  74. Awogbindin, I.O.; Olaleye, D.O.; Farombi, E.O. Kolaviron improves morbidity and suppresses mortality by mitigating oxido-inflammation in BALB/c mice infected with influenza virus. Viral Immunol. 2015, 28, 367–377. [Google Scholar] [CrossRef]
  75. Farombi, E.O.; Awogbindin, I.O.; Farombi, T.H.; Ikeji, C.N.; Adebisi, A.; Adedara, I.A.; Aruoma, O.I. Possible role of Kolaviron, a Garcinia kola bioflavonoid in inflammation associated COVID-19 infection. Am. J. Biopharmacy Pharm. Sci. 2022, 2, 1–13. [Google Scholar] [CrossRef]
  76. Kudi, A.C.; Myint, S.H. Antiviral activity of some Nigerian medicinal plant extracts. J. Eethnopharmacol. 1999, 68, 289–294. [Google Scholar] [CrossRef]
  77. Foyet, H.S.; Tsala, D.E.; Zogo, E.B.; Carine, A.N.; Heroyne, L.T.; Oben, E.K. Anti-inflammatory and anti-arthritic activity of a methanol extract from Vitellaria paradoxa stem bark. Pharmacogn. Res. 2014, 7, 367–377. [Google Scholar] [CrossRef] [Green Version]
  78. Abdel-Moneim, A.; Morsy, B.M.; Mahmoud, A.M.; Abo-Seif, M.A.; Zanaty, M.I. Beneficial therapeutic effects of Nigella sativa and/or Zingiber officinale in HCV patients in Egypt. EXCLI J. 2013, 11, 43–55. [Google Scholar]
  79. Li, C.; Dong, Z.; Zhang, B.; Huang, Q.; Liu, G.; Fu, X. Structural characterization and immune enhancement activity of a novel polysaccharide from Moringa oleifera leaves. Carbohydr. Polym. 2020, 234, 115897. [Google Scholar] [CrossRef] [PubMed]
  80. Yang, X.; Wei, S.; Lu, X.; Qiao, X.; Simal-Gandara, J.; Capanoglu, E.; Li, N. A neutral polysaccharide with a triple helix structure from ginger: Characterization and immunomodulatory activity. Food Chem. 2021, 350, 129261. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 1. Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 2. Frequency of plant families used for treating COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 2. Frequency of plant families used for treating COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 3. Frequency of plant parts used for treating COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 3. Frequency of plant parts used for treating COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 4. Growth forms of medicinal plants used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 4. Growth forms of medicinal plants used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 5. Methods of preparing medicinal plant species used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 5. Methods of preparing medicinal plant species used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 6. Mode of administration of medicinal plant species used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 6. Mode of administration of medicinal plant species used for the treatment of COVID-19, cough, and flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Figure 7. Relative frequency of citation of top five plant species used for the treatment of (a) COVID-19, (b) cough, and (c) flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Figure 7. Relative frequency of citation of top five plant species used for the treatment of (a) COVID-19, (b) cough, and (c) flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
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Table 1. Demographic information of participants (n = 56) in the study area.
Table 1. Demographic information of participants (n = 56) in the study area.
ParametersGroupNumberPercentage (%)
GenderMale2341.1
Female3358.9
Age (Years)20–3047.14
31–40712.5
41–501425
51 and above3155.4
Local Government AreaOgbomosho South4173.21
Ogbomosho North1626.79
Educational LevelPrimary2646.43
Secondary1933.93
Tertiary1119.64
OccupationHerb seller2748.2
Traditional health practitioner610.7
Farmer11.8
Other2239.3
Table 2. Medicinal plants used to treat and prevent COVID-19 in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Table 2. Medicinal plants used to treat and prevent COVID-19 in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
S/NScientific Name and Voucher Specimen Number Common NameLocal NameFamilyMode of PreparationGrowth FormMode of AdministrationPlant PartPlant SourceMaterialFCRFCFL (%)
1Allium sativum L.
IFE18082
Garlic Ayu Amaryllidaceae Frying Herb Nasal Bulbs CF30.055
2Alstonia boonei De Wild.
IFE18083
Stool weedDoctor igboApocynaceae DecoctionTree OralLeavesCF10.022
3Azadirachta indica A. Juss.
IFE18086
Neem Dongoyaro Meliaceae DecoctionTreeOralLeaves, barkWPF80.1414
4Capsicum frutescens L.
IFE18088
Pepper Ata weweSolanaceae Decoction Herb OralFruit CF60.1111
5Cinnamomum camphora (L.) J. Presl
IFE18091
Camphor Kafura Lauraceae Heating Tree Nasal Bark WPF10.022
6Citrus limon (L.) Osbeck
IFE18093
Lime Oronbo Rutaceae Juice extraction Tree OralFruit CF50.0149
7Clausena anisata (Willd.) Hook.f. ex Benth.
IFE18094
Horsewood Agbasa Rutaceae DecoctionTree OralLeavesWPF10.022
8Curcuma longa L.
IFE18134
Turmeric Ata ile pupaZingiberaceae DecoctionHerb OralRhizomesCD80.1414
9Cymbopogon citratus (DC.) Stapf
IFE18097
Lemon GrassEwe teaPoaceae DecoctionGrass OralLeavesCF10.022
10Drypetes gossweileri S.Moore
IFE18099
Horse radish TreeEpo aganwoPutranjivaceaeDecoctionTree OralBark WPD10.022
11Gymnanthemum amygdalinum (Delile) Sch.Bip. IFE18127Bitter leafEwuro AsteraceaeDecoctionShrub OralLeavesCF20.044
12Momordica charantia L.
IFE18108
Bitter lemonEjinrinCucurbitaceaeDecoctionClimber OralLeavesCF10.022
13Morinda lucida Benth.
IFE18109
Brimstone TreeOruwo Rubiaceae DecoctionTreeOralLeaves, barkWPD30.055
14Neonauclea excelsa (Blume) Merr.
IFE18111
NaucleaEgbeesi Rubiaceae DecoctionTree OralBark WPF10.022
15Nigella sativa L.
IFE18113
Black seed Asofeyeje Ranunculaceae Decoction HerbOralSeedsWPD10.022
16Peperomia pellucida (L.) Kunth
IFE18115
Shiny bushEwe rinrin PiperaceaePulverizing Herb OralLeavesCD10.022
17Pseudocedrela kotschyi Harms
IFE18117
Dry zone cedarEmigbegi Meliaceae DecoctionTree OralLeavesWPF10.022
18Senna alata (L.) Roxb.
IFE18121
Candle bushAsunwon oyinboFabaceae DecoctionTree OralLeavesWPF20.044
19Tetrapleura tetraptera (Schum. and Thonn.) Taub.
IFE18123
Aidan TreeAridan FabaceaeDecoctionTree OralFruit CF30.055
20Tithonia diversifolia (Hemsl.) A.Gray
IFE18124
Tree marigoldSepeleba AsteraceaeDecoctionHerb OralLeavesWPF10.022
21Uvaria afzelii Scott. Elliot
IFE18125
Monkey fingerGbogboniseAnnonaceaeDecoctionTreeOralBark WPD10.022
22Uvaria chamae P. Beauv.
IFE18126
Finger rootEruijuAnnonaceaeDecoctionHerb OralBark CF10.022
23Vitellaria paradoxa C.F Gaertn
IFE18128
Shea butterOriSapotaceae Heating Tree Nasal SeedsWPD60.1111
24Xylopia villosa Chipp
IFE18130
Black palufonEeru awonkaAnnonaceae DecoctionTree OralLeavesWPF10.022
25Zea mays L.
IFE18131
Maize Agbado Poaceae DecoctionGrass OralSeedsCF10.022
26Zingiber officinale Roscoe
IFE18132
GingerAta ileZingiberaceaeDecoction Herb OralRhizomes CF100.1818
Plant source (C—cultivated; WP—wild populations); Material (F—fresh; D—dried); FC—frequency of citation; RFC—relative frequency of citation; FL—fidelity level.
Table 3. Medicinal plants used to treat and prevent cough in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Table 3. Medicinal plants used to treat and prevent cough in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
S/NScientific Name and Voucher Specimen Number Common NameLocal NameFamilyMode of PreparationGrowth FormMode of AdministrationPlant PartPlant SourceMaterialFCRFCFL (%)
1Abrus precatorius L.
IFE18077
Rosary peaOmisinmisinFabaceae DecoctionClimber OralLeavesWPF70.1313
2Aframomum melegueta K. Schum.
IFE18079
Alligator pepperAtaare ZingiberaceaePulverizingHerbOral Seeds, fruitCD50.099
3Allium ascalonicum L.
IFE18080
Spring onionAlubosa eleweAmaryllidaceaeGrating, InfusionHerb OralBulbsCF10.022
4Allium cepa L.
IFE18081
Onion Alubosa Amaryllidaceae Pulverizing Shrub OralBulbs CF30.055
5Allium sativum L.
IFE18082
Garlic Ayu Amaryllidaceae FryingHerb Nasal Bulbs CF120.2121
6Amaranthus spinosus L.
IFE18084
Spinach Igi teteregunAmaranthaceae Decoction Herb OralBark CF20.044
7Capsicum frutescens L.
IFE18088
Hot pepper Ata wewe Solanaceae Pulverizing, Infusion Herb OralSeeds CD20.044
8Citrus aurantiifolia (Christm.) Swingle
IFE18092
Lemon Osan weweRutaceae Juice extractionTree OralFruit CF110.220
9Citrus limon (L.) Osbeck
IFE18093
Lime Orombo Rutaceae Juice extractionTreeOralFruit CF130.2323
10Cocos nucifera L.
IFE18095
CoconutAgbonArecaceaeDecoctionTree OralPod CF20.044
11Crinum jagus (J.Thomps.) Dandy
IFE18096
Poison bulbOgede odoAmaryllidaceaePulverizing, grating, InfusionHerb OralBulbs WPF20.044
12Cymbopogon citratus Stapf
IFE18097
Lemon GrassEwe teaPoaceae DecoctionGrass OralLeavesCF20.044
13Elaeis guineensis Jacq.
IFE18100
Palm TreeOpe Arecaceae Infusion TreeOralSeedsCF20.044
14Eucalyptus globulus Labill
IFE18101
Bluegum EucalyptusEucalyptusMyrtaceaeDecoctionTree OralLeavesWPF20.044
15Ficus asperifolia Hook. ex Miq. IFE18103SandpaperEwe ipinMoraceae Infusion Tree OralLeaves WPD20.044
16Garcinia kola Heckel
IFE18105
Bitter colaOrogbo Clusiaceae Infusion, pulverizingTree OralSeeds CF80.1414
17Gymnanthemum amygdalinum (Delile) Sch.Bip. IFE18127Bitter leafEwuro AsteraceaePulverizing, InfusionShrub OralFlower CF40.077
18Jatropha curcas L. IFE18106Jatropha Lapalapa Euphorbiaceae DecoctionShrub OralFruit WPF40.077
19Mangifera indica L.
IFE18107
MangoMangoro Anacardiaceae Decoction TreeOralBark CF20.044
20Marsdenia latifolia (Benth.) K.Schum. IFE18104Bush buckArokeke, Madunmaro ApocynaceaeMaceration, infusionShrub OralLeaves, bark WPF10.022
21Neonauclea excelsa (Blume) Merr.
IFE18111
NaucleaEgbeesi Rubiaceae Infusion Tree OralRoot WPF50.099
22Olax subscorpioidea Oliv.
IFE18114
Ivory coastIfon OlacaceaePulverizing Tree OralBark WPD20.044
23Psidium guajava L.
IFE18118
Guava GroofaMyrtaceae Decoction Tree OralBark, Leaves CF30.055
24Saccharum officinarum L.
IFE18119
Sugarcane IrekePoaceaePounding, Infusion Grass OralStemCF10.022
25Securidaca longipedunculata Fresen.
IFE18120
Violet TreeIpeta Polygalaceae Pulverizing Tree OralBark WPD30.055
26Spondias mombin L.
IFE18122
Hog plumIyeye Anacardiaceae DecoctionTree OralBark WPF50.099
27Tetrapleura tetraptera (Schum. and Thonn.) Taub.
IFE18123
Aidan TreeAridan/ AidanFabaceaePulverizing, grating, Infusion Tree OralFruit CF10.022
28Vitellaria paradoxa C.F Gaertn
IFE18128
Shea butterOriSapotaceae FryingTree Nasal SeedsWPD110.220
29Xylopia aethiopica A. Rich
IFE18129
African pepperEeru Annonaceae Pulverizing, InfusionTree OralSeeds WPD60.1111
30Zea mays L.
IFE18131
Maize Agbado Poaceae DecoctionGrass OralHusk CF20.044
31Zingiber officinale Roscoe
IFE18132
GingerAta ileZingiberaceaeDecoction, pulverizingHerbOralRhizomes, rootCF30.055
Plant source (C—cultivated; WP—wild populations); Material (F—fresh; D—dried); FC—frequency of citation; RFC—relative frequency of citation; FL—fidelity level.
Table 4. Medicinal plants used to treat and prevent flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
Table 4. Medicinal plants used to treat and prevent flu in Ogbomosho North and South Local Government Areas, Oyo State, Nigeria.
S/NScientific Name and Voucher Specimen Number Common NameLocal NameFamilyMode of PreparationGrowth FormMode of AdministrationPlant PartPlant SourceMaterialFCRFCFL (%)
1Aframomum melegueta K. Schum.
IFE18079
Alligator pepperAtaareZingiberaceaeDecoctionHerb OralSeedsCD20.044
2Allium ascalonicum L.
IFE18080
Spring onionAlubosa eleweAmaryllidaceae Juice extractionHerb OralBulbs CF20.044
3Allium cepa L.
IFE18081
White onionAlubosa funfunAmaryllidaceaeInfusion Shrub OralBulbs CF20.044
4Allium sativum L.
IFE18082
Garlic Ayu Amaryllidaceae Chewing, frying Herb Oral, nasalBulbs CF60.1111
5Annona senegalensis Pers.
IFE18085
Wild soursopEwe aboAnnonaceae Decoction Shrub OralLeaves WPF20.044
6Azadirachta indica A. Juss
IFE18086
Neem Dongoyaro Meliaceae Decoction, infusionTree OralLeaves, barkWPF60.1111
7Capsicum annuum L.
IFE18087
Hot pepper Ata ijoosiSolanaceae Pulverizing Herb OralSeeds CD20.044
8Carica papaya L.
IFE18089
Pawpaw Eso ibepeCaricaceae DecoctionTree OralSeeds CF30.055
9Chromolaena odorata (L.) R.M.King and H.Rob.
IFE18090
Siam weedEwe akintolaAsteraceaePulverizing, infusion Shrub OralLeavesCF,D60.1111
10Cinnamomum camphora (L.) J.Presl
IFE18091
Camphor Kafura Lauraceae Frying Tree Topical Bark WPF10.022
11Citrus limon (L.) Osbeck
IFE18093
Lime Oronbo Rutaceae Juice extraction Tree Topical Fruit CF30.055
12Crinum jagus (J.Thomps.) Dandy
IFE18096
Poison bulbOgede odoAmaryllidaceaePounding HerbOralBulbs WPF20.044
13Cymbopogon citratus (DC.) Stapf
IFE18097
Lemon GrassEwe teaPoaceae Decoction, infusionGrass OralLeavesCF70.1313
14Eucalyptus globulus LabillIFE18101Bluegum EucalyptusEucalyptusMyrtaceaeJuice extraction Tree OralLeavesWPF10.022
15Garcinia kola Heckel
IFE18105
Bitter colaOrogbo Clusiaceae Pulverizing Tree OralSeeds CF50.099
16Gymnanthemum amygdalinum (Delile) Sch.Bip IFE18127Bitter leafEwuro AsteraceaePulverizing, infusion Shrub OralLeaves CF40.077
17Kigelia africana (Lam.) Benth.
IFE18133
Sausage TreePandoro Bignoniaceae Pulverizing, infusion Tree OralBark WPD20.044
18Mangifera indica L.
IFE18107
Mango Mango Anacardiaceae Infusion Tree OralLeaves CF20.044
19Morinda lucida Benth.
IFE18109
Brimstone TreeOruwo Rubiaceae Pulverizing, infusion Tree OralBark WPD20.044
20Musa × paradisiaca L.
IFE18110
Banana OgedeMusaceae Juice extractionHerbOralLeavesCF10.022
21Nicotiana tabacum L.
IFE18112
Tobacco Taba SolanaceaeInfusion Herb OralLeaves CF10.022
22Piper nigrum L.
IFE18116
Black pepperIyere Piperaceae DecoctionClimber OralSeedsCD10.022
23Syzygium aromaticum (L.) Merr. and L.M. Perry
IFE18102
Cloves kannafuruMyrtaceae Infusion, pulverizingTree OralSeeds CD, F10.022
24Tetrapleura tetraptera (Schum. and Thonn.) Taub.
IFE18123
Aidan TreeAridanFabaceae Decoction, infusion, pulverizingTree OralFruitCD, F10.022
25Uvariopsis tripetala (Baker f.) G.E.Schatz IFE18098Pepper fruitAta dudu, ata igbereAnnonaceae DecoctionTree OralSeeds WPD10.022
26Vachellia nilotica (L.) P.J.H.Hurter and Mabb. IFE18078Gum Arabic TreeBooni Fabaceae Pulverizing, infusion Tree OralSeeds WPD, F10.022
27Vitellaria paradoxa C.F.Gaertn
IFE18128
Shea butterOriSapotaceae Frying Tree Topical SeedsWPD10.022
28Xylopia aethiopica A. Rich.
IFE18129
African pepperEeru Annonaceae Pulverizing, infusion, decoction Tree OralSeeds WPD20.044
29Zingiber officinale Roscoe
IFE18132
GingerAta ileZingiberaceaePulverizing, infusion Herb OralRootCF90.1616
Plant source (C—cultivated; WP—wild populations); Material (F—fresh; D—dried); FC—frequency of citation; RFC—relative frequency of citation; FL—fidelity level.
Table 5. Antiviral and immunomodulatory properties of top-cited species used for the treatment of COVID-19, cough, and flu.
Table 5. Antiviral and immunomodulatory properties of top-cited species used for the treatment of COVID-19, cough, and flu.
SpeciesAntiviral ActivitiesImmunomodulatory ActivitiesActive CompoundsMechanism of ActionReferences
Allium sativum L.Clinical study revealed that allicin–garlic capsule prevented common cold in active treatment group than the placebo group.In vitro study showed that polysaccharides isolated from fresh garlic promoted immune functions of RAW 264.7 macrophagesAllicinAntiviral effects of allicin by enhancing immune response. Immunomodulatory effect by promotion of phagocytosis, release of NO, and expressions of several immune-related cytokines.[54,55,56]
Azadirachta indica A.Juss. In vivo study showed that aqueous A. indica leaf extract significantly decreased HCV seropositivity and inhibited the replication of HCV.In vitro study showed that ethanol extract of A. indica downregulated the levels of CD4 + T cell activation, and inhibited SEB induced CD4+ T-cell activation/exhaustionAzadirachtin
3-Deacetyl-3-azadirachtin
Antiviral effects by binding to NS3 protease of HCV.[57,58,59]
Capsicum frutescens L.Molecular dynamics and strategies docking study showed that capsaicin caused structural disruption of viral 3CL-protease of COVID-19.Capsaicin attenuated chronic stress-induced immunosuppression in BALB/c mice.CapsaicinAntiviral effect by binding to 3CL-protease of COVID-19.
Immunomodulatory activity through increased production of Th1 cytokines and decreased production of Th2 cytokines and TGF-β1.
[53,60]
Chromolaena odorata (L.) R.M.King and H.Rob. NREthanolic extract of C. odorata showed immunopotentiating
activities on the innate immunity of Balb/C mice, and reverse a drug-induced immunosuppression.
In another report, soluble polysaccharides (PoS) fraction of C. odorata showed immunostimulatory activity.
PolysaccharidesImmunostimulatory activity of PoS fraction via stimulation of peripheral blood mononuclear cells, and production of IFN-γ.[61,62]
Citrus aurantiifolia (Christm.) SwingleLimonene showed moderate inhibition of the avian influenza A virus (H5N1). Limonene showed immunoregulatory activity in lipopolysaccharides (LPS)-induced pleurisy model.LimoneneAntiviral effects of limonene by the inhibition of viral replication via direct action on the virus. Immunomodulatory effects by the inhibition of NO and the cytokines IFN-γ and IL-4.[63,64,65]
Citrus limon (L.) OsbeckIn vitro study showed that limonin reduced the replication of New-castle disease virus (NDV) in all cell lines.Ethanolic extract of lemon peel increased proliferation of mouse splenocytes signifying immunostimulation activity Limonin Antiviral activity of limoin by downregulation of NDV- haemagglutinin-neuraminidase and matrix genes.
Immunomodulatory effect by augmentation of proliferation of T-lymphocytes.
[66,67]
Curcuma longa L. In vitro study showed that curcumin directly inactivated influenza A virus (IAV) blocked IAV adsorption, and inhibited IAV proliferation.Poly D,L-lactic-co-glycolic acid entrapped curcumin nanoparticle significantly stimulated primary humoral immune response in mice.CurcuminAntiviral effects by Increasing Nrf2, HO-1, NQO1, GSTA3 and IFN-β production; suppression of IAV-induced activation of TLR2/4/7, Akt, p38/JNK MAPK and NF-κB pathways.[68,69]
Cymbopogon citratus (DC.) Stapf In vitro and in silico studies showed that the methanolic extract of C. citratus demonstrated anti-dengue activities. Additionally, E-Citral, Z-Citral, and β-Myrcene from the essential oil of C. citratus showed significant inhibitory effect on herpes simplex virus-1 (HSV-1) replication.Oral citral administration showed marked immunomodulatory effects in lipopolysaccharides (LPS)- induced paw edema in mice.CitralImmunomodulatory effects by the inhibition of oxidative activity, activation of nuclear factor kappa B, peroxisome proliferator-activated receptor (PPAR)-α and γ.[70,71,72]
Garcinia kola HeckelKolaviron, extracted from G. kola seeds impaired IAV-induced mortality and was effective in delaying the clinical symptoms of IAV in BALB/c mice.In vivo and in vitro studies revealed that kolaviron demonstrated immunomodulatory and immunorestorative properties in immunocompetent and immunocompromised animal models.KolavironAntiviral effects by attenuating nitric oxide production and suppression of myeloperoxidase activity, immunomodulatory effect by inhibition of delayed-type hypersensitivity response and enhancement of leukocytes counts.[73,74,75]
Vitellaria paradoxa C.F.Gaertn. Ethanolic extract of V. paradoxa inhibited
50% of human polio virus (Type 1) and
Astrovirus.
Methnolic extract of V. paradoxa displayed significant suppression of inflammation response in carrageenan-induced inflammation in Wistar albino rats.CatechinsInflammation suppression effects by the inhibition of the pro-inflammatory cytokines IL-1, IL-6, and TNF-α.[76,77]
Zingiber officinale Roscoe In a clinical study, ethanolic extract of Z. officinale showed significant decrease in the viral load of patients with hepatitis C virus (HCV). In a recent in silico docking study, 8-gingerol and 10-gingerol isolated from Z. officinale were active against COVID-19 with significantly higher Glide scores when compared to hydroxychloroquine. Neutral ginger polysaccharide fraction (NGP) significantly showed immunomodulatory activity on RAW264.7 cells without cytotoxicity,Gingerol
Neutral ginger polysaccharide
Immunomodulatory effects by the promotion of TNF-α production by macrophage cells.[78,79,80]
NR—Not reported.
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Odebunmi, C.A.; Adetunji, T.L.; Adetunji, A.E.; Olatunde, A.; Oluwole, O.E.; Adewale, I.A.; Ejiwumi, A.O.; Iheme, C.E.; Aremu, T.O. Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria. Plants 2022, 11, 2667. https://doi.org/10.3390/plants11192667

AMA Style

Odebunmi CA, Adetunji TL, Adetunji AE, Olatunde A, Oluwole OE, Adewale IA, Ejiwumi AO, Iheme CE, Aremu TO. Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria. Plants. 2022; 11(19):2667. https://doi.org/10.3390/plants11192667

Chicago/Turabian Style

Odebunmi, Christiana Adeyinka, Tomi Lois Adetunji, Ademola Emmanuel Adetunji, Ahmed Olatunde, Oluwatosin Esther Oluwole, Idowu Ayodeji Adewale, Abdulrasak Opeyemi Ejiwumi, Chinwenwa Esther Iheme, and Taiwo Opeyemi Aremu. 2022. "Ethnobotanical Survey of Medicinal Plants Used in the Treatment of COVID-19 and Related Respiratory Infections in Ogbomosho South and North Local Government Areas, Oyo State, Nigeria" Plants 11, no. 19: 2667. https://doi.org/10.3390/plants11192667

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