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Review

Aromatic Herbs, Medicinal Plant-Derived Essential Oils, and Phytochemical Extracts as Potential Therapies for Coronaviruses: Future Perspectives

by
Mohamed Nadjib Boukhatem
1,* and
William N. Setzer
2,3
1
Département de Biologie et Physiologie Cellulaire, Faculté des Sciences de la Nature et de la Vie, Université - Saad Dahlab - Blida 1, BP 270, Blida 09000, Algeria
2
Department of Chemistry, University of Alabama in Huntsville, Huntsville, AL 35899, USA
3
Aromatic Plant Research Center, 230 N 1200 E, Suite 100, Lehi, UT 84043, USA
*
Author to whom correspondence should be addressed.
Plants 2020, 9(6), 800; https://doi.org/10.3390/plants9060800
Submission received: 28 April 2020 / Revised: 29 May 2020 / Accepted: 24 June 2020 / Published: 26 June 2020
(This article belongs to the Special Issue Medicinal Plants)

Abstract

:
After its recent discovery in patients with serious pneumonia in Wuhan (China), the 2019 novel coronavirus (2019-nCoV), named also Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has spread quickly. Unfortunately, no drug or vaccine for treating human this coronavirus infection is available yet. Numerous options for controlling or preventing emerging 2019-nCoV infections may be predicted, including vaccines, interferon therapies, and small-molecule drugs. However, new interventions are likely to require months to years to develop. In addition, most of the existing antiviral treatments frequently lead to the development of viral resistance combined with the problem of side effects, viral re-emergence, and viral dormancy. The pharmaceutical industry is progressively targeting phytochemical extracts, medicinal plants, and aromatic herbs with the aim of identifying lead compounds, focusing principally on appropriate alternative antiviral drugs. Spices, herbal medicines, essential oils (EOs), and distilled natural products provide a rich source of compounds for the discovery and production of novel antiviral drugs. The determination of the antiviral mechanisms of these natural products has revealed how they interfere with the viral life cycle, i.e., during viral entry, replication, assembly, or discharge, as well as virus-specific host targets. Presently, there are no appropriate or approved drugs against CoVs, but some potential natural treatments and cures have been proposed. Given the perseverance of the 2019-nCoV outbreak, this review paper will illustrate several of the potent antiviral chemical constituents extracted from medicinal and aromatic plants, natural products, and herbal medicines with recognized in vitro and in vivo effects, along with their structure–effect relationships. As this review shows, numerous potentially valuable aromatic herbs and phytochemicals are awaiting assessment and exploitation for therapeutic use against genetically and functionally different virus families, including coronaviruses.

Graphical Abstract

1. Introduction

Viruses are responsible for several infections and diseases comprising cancer, while complex disorders such as Alzheimer’s illness and type 1 diabetes have also been linked to virus-related infections [1]. In addition, due to increased foreign travel and rapid urbanization, infectious outbreaks caused by emerging and re-emerging pathogens, including viruses, pose a serious danger to community health care, principally if antiviral treatment and protective vaccines are not available. Up to the present time, several viruses persist without potent immunization, and only limited virucidal molecules are approved for clinical use in humans [2].
In 1937, coronaviruses were identified from poultry and were considered extremely important pathogenic viruses in livestock, causing periodic cold or mild human digestive infections [3]. A new human coronavirus (CoV) became notably popular in spring 2003 because of an outbreak in South-East Asia and Canada [4].
At the time, the suspect virus was quickly recognized as the Severe Acute Respiratory Syndrome-Coronavirus (SARS-CoV) but did not bear a resemblance to the human CoVs. SARS-CoV worried the world because it sickened more than 7500 persons and killed more than 700 of them [5]. It was not until the SARS epidemic of 2002–2003 that research and investigation for particular anti-coronavirus vaccines or therapies started [6].
A novel coronavirus has caused severe mortality associated with a respiratory contagious disease. The virus is named Middle East Respiratory Syndrome Coronavirus (MERS-CoV). This novel MERS-CoV was first observed in different countries including Saudi Arabia [7]. A novel coronavirus with human-to-human contagion and causing a particularly serious illness, occurring in Wuhan, China, was confirmed towards the end of December 2019 [8]. The virus was named SARS-CoV-2 and the disease it causes was named Coronavirus Disease 2019 (abbreviated “COVID-19”).
Early on, several of the patients at the epidemic center in Wuhan, Hubei Province (China), had some connection with a vast market of seafood and animals, implying the animal-to-person transmission. Afterward, an increasing number of patients apparently had no access to animal marketplaces, implying transmission from person to person [9]. The coronavirus group comprises numerous species (Figure 1) and induces respiratory tract and gastrointestinal infections in vertebrates; however, some CoVs such as SARS, MERS, and SARS-CoV-2 have been shown to be especially dangerous to humans [10]. Coronaviruses comprise an extensive collection of viruses, which commonly infect humans as well as numerous other mammalian species such as cattle, farm animals, household pets, and bats [11]. Infrequently, coronaviruses could infect humans from animals and subsequently expand among persons, as was observed for MERS-CoV, SARS-CoV, and now with SARS-CoV-2 [12].
There are no effective or approved therapies for CoV diseases, and protective vaccines are still being investigated. Therefore, it is necessary to discover potent antivirals for protection from and management of CoV infection in humans [13]. The novelty of the 2019 novel coronavirus (2019-nCoV) means that there are numerous uncertainties surrounding its behavior; consequently, it is too early to conclude whether herbal and medicinal plants, spices, or isolated compounds and molecules could be used as prophylactic/preventive drugs or as appropriate therapeutic compounds against COVID-19. Nevertheless, due to the high similarity of SARS-CoV-2 with the previously reported MERS-CoV and SARS-CoV viruses, previous research articles on phytomedicine and herbal compounds, which have been demonstrated to have anti-coronavirus properties, may be an appreciated guide to searching and discovering antiviral phytochemical extracts which may be effective against SARS-CoV-2 virus [14,15,16,17,18,19,20,21,22,23,24,25,26,27,28,29,30,31,32,33,34].
Published patent applications and academic investigations on the most relevant compounds and methods for the treatment of coronaviruses are reviewed, focusing on those strategies that attack one particular phase of the development cycle of coronaviruses, because they have greater potential as lead structural templates for further development.
In this review article, we summarize the antiviral properties from numerous phytochemical extracts, aromatic herbs, and medicinal plants against different CoV. These medicinal plants and phytochemical extracts offer an important source for innovative and effective antiviral drug discovery, allowing inexpensive and relatively safe drug development.

2. COVID-19 Is Now Officially a Pandemic

The coronavirus 2019-nCoV has infected numerous people in China and spread to other regions in a short period. On 30 January, 2020, the World Health Organization (WHO) confirmed that the epidemic of 2019-nCoV is a global health crisis and delivered initial suggestions [34,35]. On 2 February 2020, and according to China’s National Health Commission’s report, 14,488 clinical infections were found in China, comprising 304 deaths.
As we write this and according to the WHO, COVID-19 threatens 200 nations and regions across the planet and two multinational transports: the luxury ship Diamond Princess harbored in Yokohama, Japan, and the cruise ship MS Zaandam from Holland America [36]. The COVID-19 viral infection resulted in the deaths of more than 182,000 individuals and is now officially considered to be a pandemic. This viral infection is considered to be the first pandemic due to a coronavirus. In addition, it is the first time the WHO has called an infectious outbreak a pandemic since the H1N1 “swine flu” in 2009. Furthermore, different American, Asian, and European countries are now each recording more than 800,000 cases of COVID-19, caused by the 2019-nCoV that has infected more than 5,000,000 people worldwide. In the past three weeks, the number of affected countries has tripled, and the number of human cases of COVID-19 outside China has increased 15-fold. The WHO is profoundly worried, both with the disturbing degrees of seriousness of the infection and the dissemination of the disease and with the disturbing degrees of indecision and complacency of many world leaders in reaction to the epidemic. Therefore, COVID-19 is now recognized as a pandemic. In the previous pandemic, according to the WHO, the H1N1 influenza virus infected more than 18,000 people in more than 214 territories and nations.

3. An Overview of COVID-19

The entire medical picture of COVID-19 is not completely known. Recorded illnesses have oscillated from very minor (even those with no clinical symptoms) to serious, including deadly infection. Although clinical reports have shown that most infections with COVID-19 are mild to date, a recent investigation [37] from China indicates that severe illness occurs in 16% of cases. Older individuals and different age groups with serious chronic medical conditions such as respiratory disease, cardiovascular disease, and diabetes tend to be at higher risk of contracting extreme COVID-19 [38,39,40]. As individuals, practicing prevention measures and good hygiene as well as applying actions of social distancing, including avoiding crowded places, remain to be very essential [34,41].
The pandemic is persisting, and discovering innovative prevention and medicinal medicines or vaccinations as early as possible is vital and necessary. In addition, effective measures for early identification, exclusion, and diagnosis of individual patients, as well as reducing exposure and dissemination by social contact and activities must be implemented.
Although successful vaccinations and antiviral medicines are the most potent means of combating or avoiding virus diseases and contaminations, there are no cures yet for 2019-nCoV infection. The creation and production of such medications may take several months or years, thereby indicating the need for finding alternative rapid treatment or control strategies.

4. Antiviral Activity of Herbal Medicines and Phytochemicals against Coronaviruses

To this end, aromatic herbs, herbal teas, culinary spices, and medicinal plants used in ethnobotanical treatments may represent highly useful sources. During the 2003 SARS outbreak [16], the efficacy and performance of herbal therapy and phytomedicine for preventing viral infections was illustrated.
As such, different countries, including Algeria, are encouraging the use of herbal and medicinal plants in fighting SARS-CoV-2 infection [15,16,17,21,22,24,25,26,29,30].
After the outbreak of SARS-CoV, first described in early 2003, researchers and scientists have been dynamically trying to explore different antiviral extracts, drugs, and molecules against SARS-CoV. This had led a group of experts to screen more than 200 medicinal plants, culinary spices, and aromatic herbs for their antiviral properties against this SARS-CoV strain [42]. In fact, after the outbreak of SARS, many groups started to search for anti-coronavirus agents, including some natural compounds and phytochemical extracts that exist in traditional herbal medicines [18,21,23,31]. Table 1 presents several studies reporting the inhibitory effect of medicinal plants or isolated compounds on different strains of human coronavirus.
Among these, four extracts exhibited moderate to potent inhibition effects against SARS-CoV: Lycoris radiata (red spider lily), Pyrrosia lingua (a fern) (Figure 2a), Artemisia annua (sweet wormwood) (Figure 2b), and Lindera aggregata, which is an aromatic evergreen shrub, member of the laurel family. The antiviral effects of these extracts were dose-dependent and ranged from low to high concentrations of the extracts, depending in the herbal extract considered. In particular, L. radiata exhibited the most potent antiviral activity against the virus strain [23].
These data are in accordance with those of two other research teams, which confirmed that an active compound contained in licorice roots, i.e., glycyrrhizin (Figure 3a), exerts an anti-SARS-CoV effect by stopping viral replication [18,62]. In another investigation, glycyrrhizin (Glycyrrhiza glabra, Fabaceae family) (Figure 2b) also displayed antiviral property when tested for its in vitro antiviral activity on 10 different clinical strains of SARS-CoV.
Baicalin (Figure 4a), a constituent of the plant Baikal skullcap (Scuttelaria baicalensis) (Figure 4b), was been examined in this research under the same conditions and also revealed antiviral potential against SARS-CoV [15]. Baicalin has also been shown to inhibit the replication of the HIV-1 virus in vitro in previous publications [24,65]. Nevertheless, it should be noted that in vitro findings may not correlate with in vivo clinical efficacy. This is because the oral quantity of these molecules in humans may not attain a blood serum dose comparable to that tested in vitro dose.
Lycorine (Figure 5) is a toxic crystalline alkaloid found in various Amaryllidaceae species, such as the cultivated bush lily (Clivia miniata), surprise lilies (Lycoris), and daffodils (Narcissus). It has also demonstrated a potent antiviral effect against SARS-CoV. Several previous investigations suggest that lycorine seems to have broad antiviral properties and has been reported to have an inhibitory action on the Herpes simplex virus (HSV, type I) [67] and Poliomyelitis virus [68].
Other medicinal herbs and plants and culinary spices that have been described to have antiviral properties against SARS-CoV are Japanese honeysuckle (Lonicera japonica Thunb.) (Figure 6), the commonly known Eucalyptus tree, and Korean ginseng (Panax ginseng) (Figure 7), the last one through its active secondary metabolite ginsenoside-Rb1 [31].
One hundred British Columbian aromatic and medicinal herbs were evaluated for antiviral effect against seven viruses [29]. Twelve phytochemical extracts were shown to possess antiviral properties at the doses used. The phytochemical extracts of Saskatoon or Pacific serviceberry (Amelanchier alnifolia) and Nootka or wild rose (Rosa nutkana) (Figure 8) were the most effective against an enteric coronavirus. Respiratory syncytial virus (RSV) was totally blocked by a root extract of tall cinquefoil (Potentilla arguta) (Figure 9) and a branch tip extract of red elderberry (Sambucus racemosa) (Figure 10).
Bioflavonoids derived from herbal medicines have been tested for antiviral properties [75]. The black tea flavonoid theaflavin (Figure 11) has been a well-known antioxidant with free radical-scavenging ability and has been able to neutralize infections of bovine coronavirus [76].

5. Mode of Antiviral Action

Many investigations and studies of plant extracts and pure molecules have been carried out with different strains of coronavirus. Proteins involved in coronaviral replication and the conductance of ion channels and proteases were the main targets [78]. Several researchers have discovered plant formulations that inhibit in vivo and in vitro viral replication [79,80].
Evidence from the above-mentioned publications and reports and numerous other international investigations reveal that many phytochemical extracts and medicinal plant constituents have displayed antiviral properties against coronaviruses [29], and their principal mode of action seems to be through the inhibition of viral replication [19]. Otherwise, molecules that have an antiviral activity work like a disinfectant or antiseptic and do not necessitate repetition to inactivate a virus [81]. Resistance to antiviral compounds is probably caused by mutations created in the viral genome in the course of replication [82].
It has been experimentally verified that saikosaponins (a, b2, c, and d) (Figure 12), which are naturally produced triterpene glycosides isolated from herbal medicines such as Chinese thoroughwax (Bupleurum spp., belonging to the family Apiaceae), parsley tree (Heteromorpha spp., belonging to the family Apiaceae), and Figwort (Scrophularia scorodonia, belonging to the family Scrophulariaceae), have antiviral activity against HCoV-22E9, a species of CoV that infects humans and animals and together with human coronavirus OC43 is one of the common-cold viruses [17]. Such natural molecules effectively suppress and deter the early process of infection by HCoV-229E, including viral penetration and attachment, after co-challenge with the virus.
Natural antagonists of SARS-CoV enzymes, e.g., nsP13 helicase and 3CL protease, have been described, including myricetin (Figure 13) (a flavonoid polyphenolic molecule with antioxidant effects detected in fruits and vegetables), scutellarein (Figure 14) (a flavone occurring in the roots, stems, and flowers of Scutellaria lateriflora, a perennial member of the Lamiaceae, and other Scutellaria species, as well as Asplenium belangeri), and phenolic compounds from dyer’s woad (Isatis indigotica) (Figure 15) and Japanese nutmeg-yew (Torreya nucifera) (Figure 16) [26,51,55].
Many natural anti-CoV phytomedicines include an aqueous extract of fish mint (Houttuynia ordata) (Figure 17), which has been demonstrated to mediate several antiviral mechanisms against SARS-CoV, e.g., inhibition of viral RNA-dependent RNA polymerase and suppression of the function of the viral 3CL protease [53].
Herbal preparations have been used as traditional medicines to ameliorate several illnesses. Some plant extracts were revealed to inhibit virus replication [88]. While medicinal plants, aromatic herbs, and volatile oils are known for their antibacterial and antifungal properties, there are currently insufficient scientific data to assess nontoxic and effective means to use them as antiviral treatments
The strongest options for efficacious antiviral chemotherapeutics are certain compounds that function on different viral biosynthetic pathways. In the viral replication cycle, they suppress different processes, and therefore little or no viral progeny is created. These medications may work at small doses, which do not damage the host cell. They will deter viruses from multiplying, eventually curing the contaminated cells. Regrettably, replicating viruses can develop resistance to these particular medications. Virucidal medications, on the other hand, interact with the membrane shell of enveloped viruses and solubilize viral structural glycoproteins [17,53,55]. The complex metabolism of natural bioactives is at the basis of numerous therapeutic agents and has contributed to the development of new antivirals. Compared with pesticides, herbal antiviral medicines have been understudied. However, some scientific trials have begun to evaluate their effectiveness more specifically. Medicinal plants and their isolated components have shown antiviral effects against certain coronaviruses [29], and the mechanism of action (Table 2) of these traditional supplements is mainly by viral replication suppression [17,19,23,26,48].

6. Phytomedicine and Clinical Trials for Coronavirus Infections

Chinese medicinal plants may provide additional solutions for COVID-19 prevention in high-risk communities, based on previous documents and demonstration of SARS protection in humans, but additional labor-intensive studies are required to validate the potential preventive impact of Chinese traditional medicine.
A Cochrane Review investigating the results of alternative therapies used during the SARS epidemic suggested a combination of herbal and conventional medicine did not lower the mortality rate but concluded that it may improve the quality of life, reduce chances of deep lung infiltration, and lower the dose of medications like corticosteroids [28]. A total of 640 persons with SARS participated in the investigation, which included 12 Chinese herbs. In combination with Western drugs, there was no statistical evidence of Chinese herbs reducing mortality over Western medicines alone. However, two plants demonstrated the ability to improve symptoms, five plants enhanced corticosteroid absorption through penetration of the lung, four herbs minimized corticosteroid dosages, three herbs enhanced the quality of life of patients with SARS, and one herb shortened the duration hospitalization.
China is currently conducting more than 80 preclinical studies on prospective COVID-19 therapies as well, including a few trials using traditional Chinese herbs [100]. There are about 15 experiments identified in China’s database, with more than 2000 estimated participants involved in studies on a number of traditional Chinese therapies. One of largest studies is testing shuanghuanglian, a Chinese herbal medication that includes substances from the dried fruit lianqiao (Forsythiae fructus), which has reportedly been used to treat infections for more than two millennia. The study involves 400 patients, including an experimental group receiving a normal treatment rather than a placebo therapy.
According to recent research [101], herbal medicines, like herbs and oils, may have a part to play in counteracting COVID-19. Research investigating the use of Indian medications as a therapy for manifestations of COVID-19 has been reported. The research presents the molecular morphology of the virus, potential modes of action inside the target cells, genomic similarity between COVID-19 and SARS, syndrome similarity between COVID-19, SARS, MERS, and typical flu, existing diagnosis, current clinical studies, and conventional Indian herbal medicines that may be produced as treatments directly aimed at COVID-19.
Luo et al. [102] have reviewed historical and clinical research on traditional Chinese medicines to avoid and alleviate infections in order to provide support to health agencies in China for the treatment of COVID-19, SARS, and H1N1 influenza. They traced back the use of traditional Chinese medicines to circumvent infectious epidemics and pandemics to ancient times.
Based on these findings, three investigations followed focusing on Chinese medicine for the prevention of SARS. None one of the participants in these studies who received herbal remedies became infected with SARS. Based on those data, 23 territories in China released COVID-19 prevention strategies using appropriate herbal medicines used in Chinese medicine:
  • Radix astragali (dried root of Astragalus membranaceus (Fisch.) (Figure 18) Bunge and Astragalus mongholicus Bunge (Fabaceae)) is a popular traditional Chinese medicine, and its active compounds may help fortify the immune system and decrease inflammation. Astragalus is occasionally also administrated as an injection in hospitals [102].
  • Radix glycyrrhizae (dried roots and rhizomes of Glycyrrhiza glabra) or liquorice root is one of the 50 important plants used in phytomedicine [102].
  • Radix saposhnikoviae, Saposhnikovia divaricate, recognized as fángfēng meaning “defend against the wind” in Chinese, is the single species in the genus Saposhnikovia [102].
  • Atractylodis macrocephalae rhizome (Figure 19) is hailed as “the most essential Qi herb (vital energy in Chinese medicine) that tonifies and enhances the spleen”. It is the dried rhizome of Atractylodes lancea (Thunb.), Atractylodes chinensis Koidz, or any other nearby plant like Japonica atractylodes [32].
  • Lonicera japonica Flos, member of the family Caprifoliaceae, is among the most widely used traditional medicines. It includes bioactive components such as caffeic acid derivatives, essential oils (EOs), flavonoids, iridoid glycosides, and terpenoids and it has anti-inflammatory, antimicrobial, anticancer, antioxidant, and immune-modulating properties [102].
  • Golden Bell (Fructus forsythia) has long been recognized as a cure-all for patients who are especially vulnerable to skin infection. The plant has demonstrated broad-spectrum antibacterial activity and some suppression of influenza virus, leptospira, as well as other viruses. The plant also exhibits antipyretic and anti-inflammatory properties [32].
It has been reported that China has widely used traditional Chinese aromatic herbs and medicinal plants for the treatment of SARS successfully in several cases [102]. Nevertheless, there is no considerable confirmation yet on the clinical efficacy of these treatments in COVID-19 patients. In a study, 135 COVID-19 patients already received antiretroviral therapy in a previous clinical trial (135 received both immunotherapy and Kaletra®), while 59 received antibacterial therapy, and 36 were treated with anti-inflammatory agents (corticosteroids). In comparison, 124 patients were treated with Chinese traditional medicine [105].
The Chinese herbals used to treat COVID-19 mainly included glycyrrhiza (G. glabra), ephedra (Ephedra sinica), bitter almond (Prunus dulcis var. amara), gypsum, reed root (Phragmites communis), Amomum, and Trichosanthes (family Cucurbitaceae), and their principal function is to relieve cough and to improve immunity. This research recommended that patients should receive Kaletra® (a combination of antiviral drugs lopinavir and ritonavir) very early and should also be treated by an association of Western and Chinese medicines, since Kaletra® and traditional Chinese medicinal plants play a significant action in the management of viral pneumonia. Further scientific research is required to discover the mechanism of Kaletra® and traditional Chinese medicinal plants in COVID-19 treatment.

7. Future Prospects

It is necessary to continue the development of efficacious antiviral chemotherapeutics that are cost-effective and with minimal side effects and which can also be used in combination with other drugs to improve the therapy of coronavirus-infected subjects. As protective vaccines and active antiviral drugs are not available for the treatment of several viruses, eliminating these viral infections seems hard and problematic. However, natural products serve as a tremendous source of biodiversity for developing innovative antivirals, with new structure–activity relationships, and potent medical and therapeutic approaches against viral infections.
A main problem surrounding antiviral drugs targeting specific viral proteins or genes is the capacity of a virus to rapidly mutate during replication, as observed for HIV and HSV [106], oseltamivir-resistant influenza viruses [107], and acyclovir- and nucleoside/nucleotide analog-resistant hepatitis B viruses [108]. There are several aspects that should be taken into account when assessing the antiviral activity of preparations of medicinal herbs, such as the extraction techniques used, since the highest level of antiviral activity is attained with acetone extracts or methanol fractions [109]. It is therefore appropriate, at the outset of a prospective study on aromatic herbal medicines, to identify the correct methodology for the preparation of the extracts, the parts of the plants to be used, the suitable season(s) for the collection of the materials, and the details of the application modality [110].
Although most research studies in this area are in their initial stages, additional research on the identification of active substances, the description of underlying mechanisms, as well as the analysis of efficiency and probable in vivo applications is recommended in order to assist the exploration of potent antiviral chemotherapeutics. Additional research should also investigate the possibility of combining these treatments with other natural ingredients or with standard medicines, as a multiple-target solution may help diminish the infection potential of drug-resistant virus strains. We trust that natural remedies, such as aromatic herbs, essential oils derived from medicinal plants, and pure oil compounds, will continue to play an important role and participate in the development and advancement of anti-coronavirus drugs.

8. Conclusions

Many viral infections are still lethal and/or are not yet treatable, even though some can be kept under control with life-prolonging agents, which, however, are expensive and outside the reach of most people. Thus, the discovery and development of safe, effective, and low-cost antiviral molecules is among the top universal urgencies of drug research.
Therefore, scientists and researchers from divergent medical fields are studying aromatic herbs and ethnomedicinal plants, with an eye to their applicability as antiviral drugs. Widespread research on ethnopharmacology and phytomedicine for the last 50 years resulted in the discovery of antivirals from natural products. Various traditional aromatic herbs and medicinal plants have been described as having strong and potent antiviral properties. Volatile oils, aqueous and organic extracts have, in general, demonstrated similar successful properties.
Considering the significant number of traditional medicinal plants that have provided good outcomes, it would seem reasonable to assume that these products contain different types of antiviral compounds. A characterization of secondary metabolites will reveal further health benefits. Therefore, the common usage of many traditional medicines for the prevention of viral infections is warranted. Eventually, the discovery and development of new antiviral agents from medicinal plants and herbs to control the threats presented by certain pathogenic viruses, such as the 2019-nCoV, is critical.

Author Contributions

Conceptualization, M.N.B.; investigation, M.N.B.; writing—original draft preparation, M.N.B. and W.N.S.; writing—review and editing, M.N.B. and W.N.S. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Conflicts of Interest

The authors declare no conflict of interest.

Abbreviations

ACE2: Angiotensin-Converting Enzyme 2; BCV: Bovine Coronavirus; CDC: US Centers for Disease Control and Prevention; CoV: Coronavirus; COVID-19: Coronavirus Disease 2019; EC50: half maximal effective concentration; EOs: Essential Oils; H1N1: Hemagglutinin Type 1 and Neuraminidase Type 1; HIV: Human Immunodeficiency Virus; HSV: Herpes Simplex Virus; IBV: Infectious Bronchitis Virus; IC50: Median Inhibitory Concentration; MERS-CoV: Middle East Respiratory Syndrome Coronavirus; nsP13: non-structural protein 13; RNA: RiboNucleic Acid; RSV: Respiratory Syncytial Virus; SARS-CoV: Severe Acute Respiratory Syndrome-Coronavirus; WHO: World Health Organization.

References

  1. Vehik, K.; Dabelea, D. The changing epidemiology of type 1 diabetes: Why is it going through the roof? Diab. Metabol. Res. Rev. 2011, 27, 3–13. [Google Scholar] [CrossRef]
  2. De Clercq, E.; Li, G. Approved antiviral drugs over the past 50 years. Clin. Microbiol. Rev. 2016, 29, 695–747. [Google Scholar] [CrossRef] [Green Version]
  3. Wang, W.; Lin, X.D.; Guo, W.P.; Zhou, R.H.; Wang, M.R.; Wang, C.Q.; Holmes, E.C. Discovery, diversity and evolution of novel coronaviruses sampled from rodents in China. Virology 2015, 474, 19–27. [Google Scholar] [CrossRef] [Green Version]
  4. Drosten, C.; Günther, S.; Preiser, W.; Van Der Werf, S.; Brodt, H.R.; Becker, S.; Berger, A. Identification of a novel coronavirus in patients with severe acute respiratory syndrome. N. Engl. J. Med. 2003, 348, 1967–1976. [Google Scholar] [CrossRef]
  5. Liang, G.; Chen, Q.; Xu, J.; Liu, Y.; Lim, W.; Peiris, J.S.M.; Di, B. Laboratory diagnosis of four recent sporadic cases of community-acquired SARS, Guangdong Province, China. Emerg. Infect. Dis. 2004, 10, 1774. [Google Scholar] [CrossRef]
  6. Hilgenfeld, R.; Peiris, M. From SARS to MERS: 10 years of research on highly pathogenic human coronaviruses. Antivir. Res. 2013, 100, 286–295. [Google Scholar] [CrossRef] [PubMed]
  7. Zaki, A.M.; Van Boheemen, S.; Bestebroer, T.M.; Osterhaus, A.D.; Fouchier, R.A. Isolation of a novel coronavirus from a man with pneumonia in Saudi Arabia. N. Engl. J. Med. 2012, 367, 1814–1820. [Google Scholar] [CrossRef] [PubMed]
  8. Paraskevis, D.; Kostaki, E.G.; Magiorkinis, G.; Panayiotakopoulos, G.; Sourvinos, G.; Tsiodras, S. Full-genome evolutionary analysis of the novel corona virus (2019-nCoV) rejects the hypothesis of emergence as a result of a recent recombination event. Infect. Genet. Evol. 2020, 79, 104212. [Google Scholar] [CrossRef] [PubMed]
  9. Roosa, K.; Lee, Y.; Luo, R.; Kirpich, A.; Rothenberg, R.; Hyman, J.M.; Chowell, G. Real-time forecasts of the COVID-19 epidemic in China from February 5 to 24 February 2020. Infect. Dis. Model. 2020, 5, 256–263. [Google Scholar] [PubMed]
  10. Guo, Y.R.; Cao, Q.D.; Hong, Z.S.; Tan, Y.Y.; Chen, S.D.; Jin, H.J.; Yan, Y. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak–an update on the status. Milit. Med. Res. 2020, 7, 1–10. [Google Scholar] [CrossRef] [Green Version]
  11. Hu, B.; Ge, X.; Wang, L.F.; Shi, Z. Bat origin of human coronaviruses. Virol. J. 2015, 12, 221. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  12. Yang, Y.; Peng, F.; Wang, R.; Guan, K.; Jiang, T.; Xu, G.; Chang, C. The deadly coronaviruses: The 2003 SARS pandemic and the 2020 novel coronavirus epidemic in China. J. Autoimmun. 2020, 109, 102434. [Google Scholar] [CrossRef] [PubMed]
  13. Zhou, Y.; Hou, Y.; Shen, J.; Huang, Y.; Martin, W.; Cheng, F. Network-based drug repurposing for novel coronavirus 2019-nCoV/SARS-CoV-2. Cell. Discov. 2020, 6, 1–18. [Google Scholar] [CrossRef] [Green Version]
  14. Chang, F.R.; Yen, C.T.; Ei-Shazly, M.; Lin, W.H.; Yen, M.H.; Lin, K.H.; Wu, Y.C. Anti-human coronavirus (anti-HCoV) triterpenoids from the leaves of Euphorbia neriifolia. Nat. Prod Comm. 2012, 7, 1934578X1200701103. [Google Scholar] [CrossRef] [Green Version]
  15. Chen, F.; Chan, K.H.; Jiang, Y.; Kao, R.Y.T.; Lu, H.T.; Fan, K.W.; Guan, Y. In vitro susceptibility of 10 clinical isolates of SARS coronavirus to selected antiviral compounds. J. Clin. Virol. 2004, 31, 69–75. [Google Scholar] [CrossRef] [PubMed]
  16. Chen, Z.; Nakamura, T. Statistical evidence for the usefulness of Chinese medicine in the treatment of SARS. Phytother. Res. 2004, 18, 592–594. [Google Scholar] [CrossRef]
  17. Cheng, P.W.; Ng, L.T.; Chiang, L.C.; Lin, C.C. Antiviral effects of saikosaponins on human coronavirus 229E in vitro. Clin. Experim. Pharmacol. Physiol. 2006, 33, 612–616. [Google Scholar] [CrossRef]
  18. Hoever, G.; Baltina, L.; Michaelis, M.; Kondratenko, R.; Baltina, L.; Tolstikov, G.A.; Cinatl, J. Antiviral Activity of Glycyrrhizic Acid Derivatives against SARS− Coronavirus. J. Med. Chem. 2005, 48, 1256–1259. [Google Scholar] [CrossRef]
  19. Jassim, S.A.A.; Naji, M.A. Novel antiviral agents: A medicinal plant perspective. J. Appl. Microbiol. 2003, 95, 412–427. [Google Scholar] [CrossRef] [Green Version]
  20. Kim, H.Y.; Shin, H.S.; Park, H.; Kim, Y.C.; Yun, Y.G.; Park, S.; Kim, K. In vitro inhibition of coronavirus replications by the traditionally used medicinal herbal extracts, Cimicifuga rhizoma, Meliae cortex, Coptidis rhizoma, and Phellodendron cortex. J. Clin. Virol. 2008, 41, 122–128. [Google Scholar] [CrossRef]
  21. Kim, H.Y.; Eo, E.Y.; Park, H.; Kim, Y.C.; Park, S.; Shin, H.J.; Kim, K. Medicinal herbal extracts of Sophorae radix, Acanthopanacis cortex, Sanguisorbae radix and Torilis fructus inhibit coronavirus replication in vitro. Antivir. Therap. 2010, 15, 697–709. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  22. Kim, D.E.; Min, J.S.; Jang, M.S.; Lee, J.Y.; Shin, Y.S.; Park, C.M.; Kwon, S. Natural Bis-Benzylisoquinoline Alkaloids-Tetrandrine, Fangchinoline, and Cepharanthine, Inhibit Human Coronavirus OC43 Infection of MRC-5 Human Lung Cells. Biomolecules 2019, 9, 696. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  23. Li, S.Y.; Chen, C.; Zhang, H.Q.; Guo, H.Y.; Wang, H.; Wang, L.; Li, R.S. Identification of natural compounds with antiviral activities against SARS-associated coronavirus. Antivir. Res. 2005, 67, 18–23. [Google Scholar] [CrossRef] [PubMed]
  24. Li, B.Q.; Fu, T.; Dongyan, Y.; Mikovits, J.A.; Ruscetti, F.W.; Wang, J.M. Flavonoid baicalin inhibits HIV-1 infection at the level of viral entry. Biochem. Biophys. Res. Commun. 2000, 276, 534–538. [Google Scholar] [CrossRef] [PubMed]
  25. Li, X.Q.; Song, Y.N.; Wang, S.J.; Rahman, K.; Zhu, J.Y.; Zhang, H. Saikosaponins: A review of pharmacological effects. J. Asian Nat. Prod. Res. 2018, 20, 399–411. [Google Scholar] [CrossRef]
  26. Lin, C.W.; Tsai, F.J.; Tsai, C.H.; Lai, C.C.; Wan, L.; Ho, T.Y.; Chao, P.D.L. Anti-SARS coronavirus 3C-like protease effects of Isatis indigotica root and plant-derived phenolic compounds. Antivir. Res. 2005, 68, 36–42. [Google Scholar] [CrossRef]
  27. Lin, L.T.; Hsu, W.C.; Lin, C.C. Antiviral natural products and herbal medicines. J. Trad. Complement. Med. 2014, 4, 24–35. [Google Scholar] [CrossRef] [Green Version]
  28. Liu, X.; Zhang, M.; He, L.; Li, Y. Chinese herbs combined with Western medicine for severe acute respiratory syndrome (SARS). Cochr. Database. Syst. Rev. 2012, 10, 1–44. [Google Scholar] [CrossRef]
  29. McCutcheon, A.R.; Roberts, T.E.; Gibbons, E.; Ellis, S.M.; Babiuk, L.A.; Hancock, R.E.W.; Towers, G.H.N. Antiviral screening of British Columbian medicinal plants. J. Ethnopharmacol. 1995, 49, 101–110. [Google Scholar] [CrossRef]
  30. Tsai, Y.C.; Lee, C.L.; Yen, H.R.; Chang, Y.S.; Lin, Y.P.; Huang, S.H.; Lin, C.W. Antiviral Action of Tryptanthrin Isolated from Strobilanthes cusia Leaf against Human Coronavirus NL63. Biomolecules 2020, 10, 366. [Google Scholar] [CrossRef] [Green Version]
  31. Wu, C.Y.; Jan, J.T.; Ma, S.H.; Kuo, C.J.; Juan, H.F.; Cheng, Y.S.E.; Liang, F.S. Small molecules targeting severe acute respiratory syndrome human coronavirus. Proc. Nat. Acad. Sci. USA 2004, 101, 10012–10017. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  32. Yang, Y.; Islam, M.S.; Wang, J.; Li, Y.; Chen, X. Traditional Chinese medicine in the treatment of patients infected with 2019-new coronavirus (SARS-CoV-2): A review and perspective. Int. J. Biol. Sci. 2020, 16, 1708. [Google Scholar] [CrossRef] [PubMed]
  33. Boukhatem, M.N. Effective Antiviral Activity of Essential Oils and their Characteristics Terpenes against Coronaviruses: An Update. J. Pharmacol. Clin. Toxicol. 2020, 8, 1138. [Google Scholar]
  34. Boukhatem, M.N. Novel Coronavirus Disease 2019 (COVID-19) Outbreak in Algeria: A New Challenge for Prevention. J. Community Med. Health Care 2020, 5, 1035. [Google Scholar]
  35. World Health Organization (WHO). Statement on the Second Meeting of the International Health Regulations Emergency Committee Regarding the Outbreak of Novel Coronavirus (2019-nCoV). Available online: www.who.int/news-room/detail/30-01-2020-statement-on-the-second-meeting-of-the-international-health-regulations-(2005)-emergency-committee-regarding-the-outbreak-of-novel-coronavirus-(2019-ncov) (accessed on 2 February 2020).
  36. COVID-19 Coronavirus Pandemic. Available online: www.worldometers.info/coronavirus/ (accessed on 23 May 2020).
  37. Guan, W.J.; Ni, Z.Y.; Hu, Y.; Liang, W.H.; Ou, C.Q.; He, J.X.; Du, B. Clinical characteristics of coronavirus disease 2019 in China. N. Engl. J. Med. 2020, 382, 1708–1720. [Google Scholar] [CrossRef] [PubMed]
  38. Zheng, Y.Y.; Ma, Y.T.; Zhang, J.Y.; Xie, X. COVID-19 and the cardiovascular system. Nat. Rev. Cardiol. 2020, 17, 259–260. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  39. The Novel Coronavirus Pneumonia Emergency Response Epidemiology Team. The epidemiological characteristics of an outbreak of 2019 novel coronavirus diseases (COVID-19)—China, 2020. China CDC Wkly. 2020, 2, 113–122. [Google Scholar]
  40. Liu, Y.; Yan, L.M.; Wan, L.; Xiang, T.X.; Le, A.; Liu, J.M.; Zhang, W. Viral dynamics in mild and severe cases of COVID-19. Lancet. Infect. Dis. 2020, 20, 656–657. [Google Scholar] [CrossRef] [Green Version]
  41. Dalton, C.; Corbett, S.; Katelaris, A. Pre-emptive low cost social distancing and enhanced hygiene implemented before local COVID-19 transmission could decrease the number and severity of cases. Med. J. Aust. 2020, 212, 1. [Google Scholar] [CrossRef]
  42. CDC SARS Response Timeline. Available online: www.cdc.gov/about/history/sars/timeline.htm (accessed on 18 March 2020).
  43. Yang, Q.Y.; Tian, X.Y.; Fang, W.S. Bioactive coumarins from Boenninghausenia sessilicarpa. J. Asian Nat. Prod. Res. 2007, 9, 59–65. [Google Scholar] [CrossRef]
  44. Wen, C.C.; Shyur, L.F.; Jan, J.T.; Liang, P.H.; Kuo, C.J.; Arulselvan, P.; Yang, N.S. Traditional Chinese medicine herbal extracts of Cibotium barometz, Gentiana scabra, Dioscorea batatas, Cassia tora, and Taxillus chinensis inhibit SARS-CoV replication. J. Tradit. Complement. Med. 2011, 1, 41–50. [Google Scholar] [CrossRef] [Green Version]
  45. Thabti, I.; Albert, Q.; Philippot, S.; Dupire, F.; Westerhuis, B.; Fontanay, S.; Varbanov, M. Advances on Antiviral Activity of Morus spp. Plant Extracts: Human Coronavirus and Virus-Related Respiratory Tract Infections in the Spotlight. Molecules 2020, 25, 1876. [Google Scholar] [CrossRef] [PubMed]
  46. Shen, Y.C.; Wang, L.T.; Khalil, A.T.; Chiang, L.C.; Cheng, P.W. Bioactive pyranoxanthones from the roots of Calophyllum blancoi. Chem. Pharm. Bull. 2005, 53, 244–247. [Google Scholar] [CrossRef] [Green Version]
  47. Michaelis, M.; Doerr, H.W.; Cinatl, J., Jr. Investigation of the influence of EPs® 7630, a herbal drug preparation from Pelargonium sidoides, on replication of a broad panel of respiratory viruses. Phytomedicine 2011, 18, 384–386. [Google Scholar] [CrossRef] [PubMed]
  48. Yi, L.; Li, Z.; Yuan, K.; Qu, X.; Chen, J.; Wang, G.; Chen, L. Small molecules blocking the entry of severe acute respiratory syndrome coronavirus into host cells. J. Virol. 2004, 78, 11334–11339. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  49. Loizzo, M.R.; Saab, A.M.; Tundis, R.; Statti, G.A.; Menichini, F.; Lampronti, I.; Doerr, H.W. Phytochemical analysis and in vitro antiviral activities of the essential oils of seven Lebanon species. Chem. Biodiv. 2008, 5, 461–470. [Google Scholar] [CrossRef] [PubMed]
  50. Zhuang, M.; Jiang, H.; Suzuki, Y.; Li, X.; Xiao, P.; Tanaka, T.; Qin, C. Procyanidins and butanol extract of Cinnamomi Cortex inhibit SARS-CoV infection. Antivir. Res. 2009, 82, 73–81. [Google Scholar] [CrossRef]
  51. Yu, M.S.; Lee, J.; Lee, J.M.; Kim, Y.; Chin, Y.W.; Jee, J.G.; Jeong, Y.J. Identification of marketing and scutellarein as novel chemical inhibitors of the SARS coronavirus helicase, nsP13. Bioorg. Med. Chem. Lett. 2012, 22, 4049–4054. [Google Scholar] [CrossRef]
  52. Luo, W.; Su, X.; Gong, S.; Qin, Y.; Liu, W.; Li, J.; Xu, Q. Anti-SARS coronavirus 3C-like protease effects of Rheum palmatum L. extracts. Biosci. Trends. 2009, 3, 124–126. [Google Scholar]
  53. Lau, K.M.; Lee, K.M.; Koon, C.M.; Cheung, C.S.F.; Lau, C.P.; Ho, H.M.; Tsui, S.K.W. Immunomodulatory and anti-SARS activities of Houttuynia cordata. J. Ethnopharmacol. 2008, 118, 79–85. [Google Scholar] [CrossRef]
  54. Park, J.Y.; Kim, J.H.; Kim, Y.M.; Jeong, H.J.; Kim, D.W.; Park, K.H.; Ryu, Y.B. Tanshinones as selective and slow-binding inhibitors for SARS-CoV cysteine proteases. Bioorg. Med. Chem. 2012, 20, 5928–5935. [Google Scholar] [CrossRef] [PubMed]
  55. Ryu, Y.B.; Jeong, H.J.; Kim, J.H.; Kim, Y.M.; Park, J.Y.; Kim, D.; Rho, M.C. Biflavonoids from Torreya nucifera displaying SARS-CoV 3CLpro inhibition. Bioorg. Med. Chem. 2010, 18, 7940–7947. [Google Scholar] [CrossRef] [PubMed]
  56. Park, J.Y.; Yuk, H.J.; Ryu, H.W.; Lim, S.H.; Kim, K.S.; Park, K.H.; Lee, W.S. Evaluation of polyphenols from Broussonetia papyrifera as coronavirus protease inhibitors. J. Enzym. Inhib. Med. Chem. 2017, 32, 504–512. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  57. Kim, D.W.; Seo, K.H.; Curtis-Long, M.J.; Oh, K.Y.; Oh, J.W.; Cho, J.K.; Park, K.H. Phenolic phytochemical displaying SARS-CoV papain-like protease inhibition from the seeds of Psoralea corylifolia. J. Enzym. Inhib. Med. Chem. 2014, 29, 59–63. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  58. Weng, J.R.; Lin, C.S.; Lai, H.C.; Lin, Y.P.; Wang, C.Y.; Tsai, Y.C.; Lin, C.W. Antiviral activity of Sambucus FormosanaNakai ethanol extract and related phenolic acid constituents against human coronavirus NL63. Virus. Res. 2019, 273, 197767. [Google Scholar] [CrossRef] [PubMed]
  59. O’Keefe, B.R.; Giomarelli, B.; Barnard, D.L.; Shenoy, S.R.; Chan, P.K.; McMahon, J.B.; McCray, P.B. Broad-spectrum in vitro activity and in vivo efficacy of the antiviral protein griffithsin against emerging viruses of the family Coronaviridae. J. Virol. 2010, 84, 2511–2521. [Google Scholar] [CrossRef] [Green Version]
  60. Pyrrosia Lingua. Available online: https://www.flickr.com/photos/harumkoh/17118611672/ (accessed on 16 June 2020).
  61. Artemisia annua. Available online: https://www.flickr.com/photos/47108884@N07/4738072658 (accessed on 16 June 2020).
  62. Cinatl, J.; Morgenstern, B.; Bauer, G.; Chandra, P.; Rabenau, H.; Doerr, H.W. Glycyrrhizin, an active component of liquorice roots, and replication of SARS-associated coronavirus. Lancet 2003, 361, 2045–2046. [Google Scholar] [CrossRef] [Green Version]
  63. Graebin, C.S. The pharmacological activities of glycyrrhizinic acid (“glycyrrhizin”) and glycyrrhetinic acid. In Sweeteners, 1st ed.; Mérillon, J.M., Ramawat, K.G., Eds.; Springer International Publishing: Gewerbestrasse, Switzerland, 2018; pp. 245–261. [Google Scholar]
  64. Glycyrrhiza Glabra Linn. Available online: https://www.flickr.com/photos/valdelobos/4657830744 (accessed on 16 June 2020).
  65. Kitamura, K.; Honda, M.; Yoshizaki, H.; Yamamoto, S.; Nakane, H.; Fukushima, M.; Tokunaga, T. Baicalin, an inhibitor of HIV-1 production in vitro. Antivir. Res. 1998, 37, 131–140. [Google Scholar] [CrossRef]
  66. Scutellaria Baicalensis. Available online: https://www.flickr.com/photos/tanaka_juuyoh/2718717267 (accessed on 16 June 2020).
  67. Renard-Nozaki, J.; Kim, T.; Imakura, Y.; Kihara, M.; Kobayashi, S. Effect of alkaloids isolated from Amaryllidaceae on herpes simplex virus. Res. Virol. 1989, 140, 115–128. [Google Scholar] [CrossRef]
  68. Ieven, M.; Vlietinick, A.J.; Berghe, D.V.; Totte, J.; Dommisse, R.; Esmans, E.; Alderweireldt, F. Plant antiviral agents. III. Isolation of alkaloids from Clivia miniata Regel (Amaryl-lidaceae). J. Nat. Prod. 1982, 45, 564–573. [Google Scholar] [CrossRef]
  69. Çitoğlu, G.S.; Acıkara, Ö.B.; Yılmaz, B.S.; Özbek, H. Evaluation of analgesic, anti-inflammatory and hepatoprotective effects of lycorine from Sternbergia fisheriana (Herbert) Rupr. Fitoterapia 2012, 83, 81–87. [Google Scholar] [CrossRef] [PubMed]
  70. Lonicera japonica ‘Japanese Honeysuckle’. Available online: https://www.flickr.com/photos/89906643@N06/9892035994/ (accessed on 27 April 2020).
  71. Ginseng (Panax ginseng). Available online: https://www.flickr.com/photos/eekim/4145898809 (accessed on 16 June 2020).
  72. Wild Rose-Rosa nutkana. Available online: https://www.flickr.com/photos/nordique/7188593733 (accessed on 22 April 2020).
  73. Potentilla arguta. Available online: https://www.flickr.com/photos/glaciernps/23703091762 (accessed on 16 June 2020).
  74. Red elderberry. Available online: https://www.flickr.com/photos/brewbooks/217464248 (accessed on 16 June 2020).
  75. Tsuchiya, Y.; Shimizu, M.; Hiyama, Y.; Itoh, K.; Hashimoto, Y.; Nakayama, M.; Morita, N. Antiviral activity of natural occurring flavonoids in vitro. Chem. Pharmac. Bull. 1985, 33, 3881–3886. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  76. Clark, K.J.; Grant, P.G.; Sarr, A.B.; Belakere, J.R.; Swaggerty, C.L.; Phillips, T.D.; Woode, G.N. An in vitro study of theaflavins extracted from black tea to neutralize bovine rotavirus and bovine coronavirus infections. Veterin. Microbiol. 1998, 63, 147–157. [Google Scholar] [CrossRef]
  77. Yang, G.Y.; Liu, Z.; Seril, D.N.; Liao, J.; Ding, W.; Kim, S.; Yang, C.S. Black tea constituents, theaflavins, inhibit 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK)-induced lung tumorigenesis in A/J mice. Carcinogenesis 1997, 18, 2361–2365. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  78. Parthasarathy, K.; Ng, L.; Lin, X.; Liu, D.X.; Pervushin, K.; Gong, X.; Torres, J. Structural flexibility of the pentameric SARS coronavirus envelope protein ion channel. Biophys. J. 2008, 95, L39–L41. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  79. Notka, F.; Meier, G.; Wagner, R. Concerted inhibitory activities of Phyllanthus amarus on HIV replication in vitro and ex vivo. Antivir. Res. 2004, 64, 93–102. [Google Scholar] [CrossRef]
  80. Ganesan, S.; Faris, A.N.; Comstock, A.T.; Wang, Q.; Nanua, S.; Hershenson, M.B.; Sajjan, U.S. Quercetin inhibits rhinovirus replication in vitro and in vivo. Antivir. Res. 2012, 94, 258–271. [Google Scholar] [CrossRef]
  81. Reichling, J.; Koch, C.; Stahl-Biskup, E.; Sojka, C.; Schnitzler, P. Virucidal activity of a β-triketone-rich essential oil of Leptospermum scoparium (manuka oil) against HSV-1 and HSV-2 in cell culture. Planta Med. 2005, 71, 1123–1127. [Google Scholar] [CrossRef]
  82. Schnitzler, P.; Koch, C.; Reichling, J. Susceptibility of drug-resistant clinical herpes simplex virus type 1 strains to essential oils of ginger, thyme, hyssop, and sandalwood. Antimicrob. Agents. Chemother. 2007, 51, 1859–1862. [Google Scholar] [CrossRef] [Green Version]
  83. Jang, J.H.; Lee, S.H.; Jung, K.; Yoo, H.; Park, G. Inhibitory Effects of Myricetin on Lipo- polysaccharide-Induced Neuroinflammation. Brain Sci. 2020, 10, 32. [Google Scholar] [CrossRef] [Green Version]
  84. Lin, Y.; Ren, N.; Li, S.; Chen, M.; Pu, P. Novel anti-obesity effect of scutellarein and potential underlying mechanism of actions. Biomed. Pharmacother. 2019, 117, 109042. [Google Scholar] [CrossRef] [PubMed]
  85. Woad Root (Ban Lan Gen), Isatis Indigotica-Radix Isatidis. Available online: https://www.flickr.com/photos/nhq9801/9216111022/in/photostream/ (accessed on 16 June 2020).
  86. Hughes, K. A Plant a Day: Japanese Nutmeg-Yew (Torreya nucifera, T. spp.). Available online: https://www.flickr.com/photos/138014579@N08/35706702426 (accessed on 16 June 2020).
  87. Houttuynia cordata. Available online: https://www.flickr.com/photos/dakiny/34949957600 (accessed on 16 June 2020).
  88. Zhu, H.; Zhang, Y.; Ye, G.; Li, Z.; Zhou, P.; Huang, C. In vivo and in vitro antiviral activities of calycosin-7-O-beta-D-glucopyranoside against coxsackie virus B3. Biol. Pharm. Bull. 2009, 32, 68–73. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  89. Chen, C.N.; Lin, C.P.; Huang, K.K.; Chen, W.C.; Hsieh, H.P.; Liang, P.H.; Hsu, J.T.A. Inhibition of SARS-CoV 3C-like protease activity by theaflavin-3, 3′-digallate (TF3). Evid Based Complement Alternat Med. 2005, 2, 209–215. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  90. Yuan, S.L.; Piao, X.S.; Li, D.F.; Kim, S.W.; Lee, H.S.; Guo, P.F. Effects of dietary Astragalus polysaccharide on growth performance and immune function in weaned pigs. Anim. Sci. 2006, 82, 501–507. [Google Scholar] [CrossRef]
  91. Wen, C.C.; Kuo, Y.H.; Jan, J.T.; Liang, P.H.; Wang, S.Y.; Liu, H.G.; Hou, C.C. Specific plant terpenoids and lignoids possess potent antiviral activities against severe acute respiratory syndrome coronavirus. J. Med. Chem. 2007, 50, 4087–4095. [Google Scholar] [CrossRef] [Green Version]
  92. Ho, T.Y.; Wu, S.L.; Chen, J.C.; Li, C.C.; Hsiang, C.Y. Emodin blocks the SARS coronavirus spike protein and angiotensin-converting enzyme 2 interaction. Antivir. Res. 2007, 74, 92–101. [Google Scholar] [CrossRef]
  93. Kumar, V.; Tan, K.P.; Wang, Y.M.; Lin, S.W.; Liang, P.H. Identification, synthesis and evaluation of SARS-CoV and MERS-CoV 3C-like protease inhibitors. Bioorg. Med. Chem. 2016, 24, 3035–3042. [Google Scholar] [CrossRef]
  94. Speranza, L.; Franceschelli, S.; Pesce, M.; Reale, M.; Menghini, L.; Vinciguerra, I.; Grilli, A. Antiinflammatory effects in THP-1 cells treated with verbascoside. Phytother. Res. 2010, 24, 1398–1404. [Google Scholar] [CrossRef]
  95. Chu, X.; Ci, X.; Wei, M.; Yang, X.; Cao, Q.; Guan, M.; Deng, X. Licochalcone a inhibits lipopolysaccharide-induced inflammatory response in vitro and in vivo. J. Agr. Food. Chem. 2012, 60, 3947–3954. [Google Scholar] [CrossRef]
  96. Sun, Q.; Chen, L.; Gao, M.; Jiang, W.; Shao, F.; Li, J.; Yu, B. Ruscogenin inhibits lipopolysaccharide-induced acute lung injury in mice: Involvement of tissue factor, inducible NO synthase and nuclear factor (NF)-κB. Int. Immunopharmacol. 2012, 12, 88–93. [Google Scholar] [CrossRef]
  97. Chen, C.; Zuckerman, D.M.; Brantley, S.; Sharpe, M.; Childress, K.; Hoiczyk, E.; Pendleton, A.R. Sambucus nigra extracts inhibit infectious bronchitis virus at an early point during replication. BMC Veter. Res. 2014, 10, 24. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  98. Chen, H.; Muhammad, I.; Zhang, Y.; Ren, Y.; Zhang, R.; Huang, X.; Abbas, G. Antiviral Activity Against Infectious Bronchitis Virus and Bioactive Components of Hypericum perforatum L. Front. Pharmacol. 2019, 10, 1272. [Google Scholar] [CrossRef] [PubMed]
  99. Shen, L.; Niu, J.; Wang, C.; Huang, B.; Wang, W.; Zhu, N.; Tan, W. High-throughput screening and identification of potent broad-spectrum inhibitors of coronaviruses. J. Virol. 2019, 93, e00023-19. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  100. Maxmen, A. More than 80 clinical trials launch to test coronavirus treatments. Nature 2020, 578, 347. [Google Scholar] [CrossRef] [Green Version]
  101. Vellingiri, B.; Jayaramayya, K.; Iyer, M.; Narayanasamy, A.; Govindasamy, V.; Giridharan, B.; Rajagopalan, K. COVID-19: A promising cure for the global panic. Sci. Total. Environ. 2020, 138277. [Google Scholar] [CrossRef]
  102. Luo, H.; Tang, Q.L.; Shang, Y.X.; Liang, S.B.; Yang, M.; Robinson, N.; Liu, J.P. Can Chinese medicine be used for prevention of corona virus disease 2019 (COVID-19)? A review of historical classics, research evidence and current prevention programs. Chinese. J. Integr. Med. 2020, 26, 1–8. [Google Scholar]
  103. Astragalus Membranaceus. Available online: https://www.flickr.com/photos/jennyhsu47/4539175733 (accessed on 16 June 2020).
  104. Rhizoma Atractylodes macrocephalae. Available online: https://www.flickr.com/photos/jennyhsu47/4539818092 (accessed on 16 June 2020).
  105. Wan, S.; Xiang, Y.; Fang, W.; Zheng, Y.; Li, B.; Hu, Y.; Huang, X. Clinical Features and Treatment of COVID-19 Patients in Northeast Chongqing. J. Med. Virol. 2020, 7, 797–806. [Google Scholar] [CrossRef]
  106. McMahon, M.A.; Siliciano, J.D.; Lai, J.; Liu, J.O.; Stivers, J.T.; Siliciano, R.F.; Kohli, R.M. The antiherpetic drug acyclovir inhibits HIV replication and selects the V75I reverse transcriptase multidrug resistance mutation. J. Biol. Chem. 2008, 283, 31289–31293. [Google Scholar] [CrossRef] [Green Version]
  107. Collins, P.J.; Haire, L.F.; Lin, Y.P.; Liu, J.; Russell, R.J.; Walker, P.A.; Gamblin, S.J. Crystal structures of oseltamivir-resistant influenza virus neuraminidase mutants. Nature 2008, 453, 1258–1261. [Google Scholar] [CrossRef]
  108. Delaney, W.E., IV; Borroto-Esoda, K. Therapy of chronic hepatitis B: Trends and developments. Curr. Opinion. Pharmacol. 2008, 8, 532–540. [Google Scholar] [CrossRef]
  109. Asres, K.; Bucar, F.; Kartnig, T.; Witvrouw, M.; Pannecouque, C.; De Clercq, E. Antiviral activity against human immunodeficiency virus type 1 (HIV-1) and type 2 (HIV-2) of ethnobotanically selected Ethiopian medicinal plants. Phytother. Res. 2001, 15, 62–69. [Google Scholar] [CrossRef]
  110. Hudson, J.B. Antiviral Compounds from Plants; CRC Press: Boston, MA, USA, 1990. [Google Scholar]
Figure 1. The taxonomy of the order Nidovirales. https://epomedicine.com/medical-students/coronavirus-disease-covid-2019/; (CSSE; FT research; Updated: 17 March 2020, 10:00 GMT). SARS, Severe Acute Respiratory Syndrome, MERS, Middle East Respiratory Syndrome Coronavirus, nCov, novel coronavirus. α: Alpha; β: Beta; γ: Gamma; δ: Delta.
Figure 1. The taxonomy of the order Nidovirales. https://epomedicine.com/medical-students/coronavirus-disease-covid-2019/; (CSSE; FT research; Updated: 17 March 2020, 10:00 GMT). SARS, Severe Acute Respiratory Syndrome, MERS, Middle East Respiratory Syndrome Coronavirus, nCov, novel coronavirus. α: Alpha; β: Beta; γ: Gamma; δ: Delta.
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Figure 2. Aromatic plants tested against SARS-CoV: (a) Pyrrosia lingua [60]; (b) Artemisia annua [61].
Figure 2. Aromatic plants tested against SARS-CoV: (a) Pyrrosia lingua [60]; (b) Artemisia annua [61].
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Figure 3. (a) Structure of glycyrrhizic acid (glycyrrhizin; glycyrrhizinic acid) [63]; (b) Glycyrrhiza glabra. [64].
Figure 3. (a) Structure of glycyrrhizic acid (glycyrrhizin; glycyrrhizinic acid) [63]; (b) Glycyrrhiza glabra. [64].
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Figure 4. (a) Baicalin structural formula: baicalin is a flavone (flavonoid) found in several species of the genus Scutellaria, including (b) Scutellaria baicalensis root [66].
Figure 4. (a) Baicalin structural formula: baicalin is a flavone (flavonoid) found in several species of the genus Scutellaria, including (b) Scutellaria baicalensis root [66].
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Figure 5. Lycorine chemical structure. It is a toxic alkaloid found in various Amaryllidaceae species (other names: galanthidine, amaryllis, narcissine) [69].
Figure 5. Lycorine chemical structure. It is a toxic alkaloid found in various Amaryllidaceae species (other names: galanthidine, amaryllis, narcissine) [69].
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Figure 6. Flowers of honeysuckle (Lonicera japonica Thunb) [70].
Figure 6. Flowers of honeysuckle (Lonicera japonica Thunb) [70].
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Figure 7. Korean ginseng (Panax ginseng) [71].
Figure 7. Korean ginseng (Panax ginseng) [71].
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Figure 8. Nookta Rose (Rosa nutkana) [72].
Figure 8. Nookta Rose (Rosa nutkana) [72].
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Figure 9. Potentilla arguta [73].
Figure 9. Potentilla arguta [73].
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Figure 10. Sambucus racemosa (red elderberry) [74].
Figure 10. Sambucus racemosa (red elderberry) [74].
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Figure 11. Theaflavin chemical structure. Theaflavin is an effective inhibitor of influenza A (H1N1) neuraminidase [77].
Figure 11. Theaflavin chemical structure. Theaflavin is an effective inhibitor of influenza A (H1N1) neuraminidase [77].
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Figure 12. Chemical structures of saikosaponins a, c, and d [25].
Figure 12. Chemical structures of saikosaponins a, c, and d [25].
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Figure 13. Myricetin chemical structure. Myricetin is a widespread plant-derived flavonoid with wide-ranging beneficial biological activities such as antioxidant, anticancer, and anti-inflammatory activities [83].
Figure 13. Myricetin chemical structure. Myricetin is a widespread plant-derived flavonoid with wide-ranging beneficial biological activities such as antioxidant, anticancer, and anti-inflammatory activities [83].
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Figure 14. Scutellarein chemical structure [84].
Figure 14. Scutellarein chemical structure [84].
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Figure 15. Isatis indigotica Fort. (Fam. Brassicaceae) [85].
Figure 15. Isatis indigotica Fort. (Fam. Brassicaceae) [85].
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Figure 16. Japanese nutmeg-yew (Torreya nucifera) [86].
Figure 16. Japanese nutmeg-yew (Torreya nucifera) [86].
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Figure 17. Houttuynia cordata [87].
Figure 17. Houttuynia cordata [87].
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Figure 18. Astragali radix [103].
Figure 18. Astragali radix [103].
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Figure 19. Rhizoma Atractylodes macrocephalae [104].
Figure 19. Rhizoma Atractylodes macrocephalae [104].
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Table 1. Studies describing the antiviral potential of different medicinal plants or isolated pure compounds against different strains of coronavirus (Cov). SARS, Severe Acute Respiratory Syndrome.
Table 1. Studies describing the antiviral potential of different medicinal plants or isolated pure compounds against different strains of coronavirus (Cov). SARS, Severe Acute Respiratory Syndrome.
Coronavirus StrainsPlant Species or Isolated CompoundReferences
SARS-CoVLycoris radiataLi et al. [23]
Artemisia annua
Pyrrosia lingua
Lindera aggregata
Isatis indigotica
Lin et al. [26]
Boenninghausenia sessilicarpaYang et al. [43]
Lonicera japonica
Eucalyptus spp.
Panax ginseng
Wu et al. [31]
Bovine coronavirus (BCV)Amelanchier alnifolia
Cardamine angulata
Rosa nutkana
Verbascum Thapsus
McCutcheon et al. [29]
SARS-CoV (Hong Kong strain)Dioscorea batatas
Cassia tora
Taxillus chinensis
Wen et al. [44]
10 strains of SARS-CoV
in fRhK4 cell line
Glycyrrhizin (Glycyrrhiza uralensis)
Baicalin (Scutellaria baicalensis)
Chen et al. [15]
HCoV-229EMulberry (Morus alba var. alba, Morus alba var. rosa, and Morus rubra)Thabti et al. [45]
Calophyllum blancoiShen et al. [46]
Pelargonium sidoidesMichaelis et al. [47]
Saikosaponins (Bupleurum spp., Heteromorpha spp., Scrophularia scorodonia)Cheng et al. [17]
SARS-CoV BJ01Galla chinensisYi et al. [48]
SARS-CoV FFM1Glycyrrhizin and glycyrrhetinic acid found in: Glycyrrhiza radixHoever et al. [18]
Laurus nobilis Essential oil
fGentiana scabra
Loizzo et al. [49]
SARS-CoV PUMC01 F5Cinnamomum sp.Zhuang et al. [50]
SARS-CoV helicase non-structural protein 13 (nsP13)Scutettaria baicalensisYu et al. [51]
SARS-CoV 3CLproRheum palmatumLuo et al. [52]
Houttuynia cordataLau et al. [53]
SARS-CoV CLproSalvia miltiorrhizaPark et al. [54]
Torreya nuciferaRyu et al. [55]
SARS-CoV PLproBroussonetia papyriferaPark et al. [56]
Psoralea corylifoliaKim et al. [57]
HCoV-NL63Strobilanthes cusia leafTsai et al. [30]
Sambucus formosanaWeng et al. [58]
HCoV-OC43
HCoV-299E
HCoV-NL63
Griffithsin (Griffithsia sp.)O’Keefe et al. [59]
Table 2. List of medicinal plants or isolated active compounds inhibiting Coronaviruses.
Table 2. List of medicinal plants or isolated active compounds inhibiting Coronaviruses.
Medicinal Plants (Phytochemicals or Compounds)Common NameAntiviral MechanismIC50 or EC50 ValueReferences
Rosa nutkanaNootka Rose or wild RoseInhibition or reduction of the activity of enteric coronavirus—unidentified mechanisms.-McCutcheon et al. [29]
Amelanchier alnifoliaSaskatoon or pacific serviceberry or western serviceberry-
Luteolin Blocking the viral entry of HIV-luc/SARS pseudo-type virus.9.02 μMYi et al. [48]
Lycoris radiataRed spider lilyInhibition or reduction of viral attachment and penetration.2.4 ± 0.2 μg/mLLi et al. [23]
Artemisia annuaSweet wormwood34.5 ± 2.6 μg/mL
Pyrrosia linguaTongue Fern43.2 ± 14.1 μg/mL
Lindera aggregataSpicewood88.2 ± 7.7 μg/mL
Isatis indigotica
(Beta-sitosterol)
Chinese Woad or dyer’s woadInhibition of nsP13 helicase and 3CL-like protease.1.210 μMLin et al. [26]
Black tea (Theaflavin) Inhibition of 3C-like protease of SARS-CoV.9.5 μMChen et al. [89]
Bupleurum marginatumMargined Chinese ThoroughwaxInterfering with early stages of viral replication, such as the penetration of the virus into the target cells.
Some flavonoids are metabolized within the body into phenolate ions, inhibiting viral polymerase function, and connecting with viral nucleic acid or viral cuspid proteins. That tends to lead to viral replication being inhibited or reduced.
-Cheng et al. [17]
Astragalus membranaceusMongolian milkvetch or Chinese astragalusImmunomodulatory effects by increasing the number of lymphocytes and the proportion of CD4+ lymphocytes.-Yuan et al. [90]
Saikosaponins B2 Inhibition of viral attachment and penetration steps of HCoV-22E9.1.7 ± 0.1 μM/LCheng et al. [17]
Curcumin Inhibition of 3CL protease.40 μMWen et al. [91]
Rheum officinaleChinese rhubarbInhibition of the interaction between SARS-CoV S protein and angiotensin-converting enzyme 2 (ACE2).1 to 10 μg/mLHo et al. [92]
Polygonum multiflorumTuber fleeceflower
Houttuynia cordataFish mint or Chameleon-plantInhibition of 3CL-like protease and viral polymerase, and RNA-dependent RNA polymerase (RdRp) which are key enzymes involved with virus functions.
Stimulate the proliferation of splenic lymphocytes which are necessary immune cells for fighting infection.
Increase the proportion of CD4+ and CD8+ T cells necessary to fight viral infection.
-Lau et al. [53]
Kumar et al. [93]
Torreya nucifera (Amentoflavone)Japanese nutmeg-yew or Japanese torreyaInhibition of nsP13 helicase and 3CL protease.8.3 μMRyu et al. [55]
Verbascum Thapsus
(Verbascoside)
Great Mullein or Common mulleinActive ingredients decrease inflammation during respiratory infection.-Speranza et al. [94]
Herbal extracts (Gentiana scabra, Dioscorea batatas, Cassia tora, Taxillus chinensis, Cibotium barometz) Inhibition of 3CL-like protease.39 μg/mL and 44 μg/mL (two extracts of Cibotium barometz)Wen et al. [44]
Glycyrrhiza glabra
(Licorice Root)
Liquorice or SweetwoodIn vivo anti-inflammatory effect in the lungs by a glycoside known as LicoA.-Chu et al. [95]
Ruscus aculeatusButcher’s broom, knee holly or piaranthusIn vivo protection of lungs from inflammatory injury by the active ingredient (Ruscogenin, steroid sapogenin).
Decreases of cerebral ischemia-induced blood–brain barrier dysfunction.
Anti-inflammatory and anti-thrombotic properties.
-Sun et al. [96]
Myricetin 3CL protease inhibition of SARS-CoV.-Yu et al. [51]
Sambucus nigra
Blue elder, common elder or ElderberryInhibition of chicken coronavirus strain if given at an early stage of infection.-Chen et al. [97]
Psoralea corylifolia (Bavachinin)BabchiInhibitions of papain-like protease (PLpro).38.4 ± 2.4 μMKim et al. [57]
Hypericum perforatumPerforate St John’s wort or common Saint John’s wortInhibition of mRNA expression in Avian coronavirus infectious bronchitis virus (IBV). Chen et al. [98]
Sambucus formosanaBlue elder, common elder or elderberryInhibition of chicken coronavirus strain and coronavirus NL63 by interfering with the viral envelopes, rendering them non-infectious.-Weng et al. [58]
Lycorine Inhibition of cell division of different strains of coronaviruses (HCoV-OC43, HCoV-NL63, MERS-CoV, and MHV-A59).0.15–0.31 μM.Shen et al. [99]

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Boukhatem, M.N.; Setzer, W.N. Aromatic Herbs, Medicinal Plant-Derived Essential Oils, and Phytochemical Extracts as Potential Therapies for Coronaviruses: Future Perspectives. Plants 2020, 9, 800. https://doi.org/10.3390/plants9060800

AMA Style

Boukhatem MN, Setzer WN. Aromatic Herbs, Medicinal Plant-Derived Essential Oils, and Phytochemical Extracts as Potential Therapies for Coronaviruses: Future Perspectives. Plants. 2020; 9(6):800. https://doi.org/10.3390/plants9060800

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Boukhatem, Mohamed Nadjib, and William N. Setzer. 2020. "Aromatic Herbs, Medicinal Plant-Derived Essential Oils, and Phytochemical Extracts as Potential Therapies for Coronaviruses: Future Perspectives" Plants 9, no. 6: 800. https://doi.org/10.3390/plants9060800

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