Latin American Plants against Microorganisms: History
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Please note this is an old version of this entry, which may differ significantly from the current revision.
Contributor:
Sofía Isabel Cuevas-Cianca
,
Cristian Romero-Castillo
,
José Luis Gálvez-Romero
,
Eugenio Sánchez-Arreola
,
Zaida Nelly Juárez
,
Luis Ricardo Hernández

Antimicrobial resistance is a severe and developing clinical issue that has reduced the therapeutic effectiveness of conventional antibiotics and narrowed the treatment choices for bacterial infections. Antibiotic-resistant bacteria are generally difficult to treat due to reduced membrane penetration, efflux pump overexpression, target site shifting, inactive subpopulations, biofilm growth, and enzymatic destruction. Resistant bacteria are strains resistant to several medicines, resulting in increased infections.

  • Latin American plants
  • microorganisms
  • bacteria
  • fungi
  • virus

1. Introduction

Infectious diseases are a significant source of public health issues. Despite breakthroughs in creating and manufacturing antivirals and antibiotics, bacteria, viruses, and other microorganisms continue to kill millions of people each year.
Antimicrobial resistance is a severe and developing clinical issue that has reduced the therapeutic effectiveness of conventional antibiotics and narrowed the treatment choices for bacterial infections. Antibiotic-resistant bacteria are generally difficult to treat due to reduced membrane penetration, efflux pump overexpression, target site shifting, inactive subpopulations, biofilm growth, and enzymatic destruction. Resistant bacteria are strains resistant to several medicines, resulting in increased infections [1].
Many bacteria may infect and live in their hosts for extended periods. This might be related to host immunosuppression, pathogen immune evasion, and/or inadequate drug clearance. Bacteria that are resistant or tolerant to antibiotics can survive treatment. Persistent bacteria are a transiently antibiotic-tolerant subset of bacterial cells that grow slowly or cease developing but can resume proliferation after exposure to fatal stress. Persistent cell production creates phenotypic variation within a bacterial population, significantly enhancing the odds of effectively responding to environmental change. The existence of resistant cells can lead to the emergence and recurrence of chronic bacterial infections and an increased risk of antibiotic resistance [2].
Emerging viral infections, on the other hand, continue to be a severe concern for worldwide public health. In 1997, it was revealed that a highly virulent avian influenza A (H5N1) virus may be transferred directly from poultry to people, in contrast to previously known human-to-human and livestock-to-human modes of transmission, raising severe fears about a probable influenza pandemic. Several additional avian influenza A virus subtypes (H7N9, H9N2, and H7N3) have also been linked to human sickness, increasing concerns that all influenza A virus subtypes circulating in domestic poultry and cattle in the wild might transmit to people and cause pandemics.
The most recent viral pneumonia epidemic, which began in mid-December 2019 (COVID-19) in Wuhan, China, and has spread swiftly throughout the world, is a stark reminder of the vulnerability to new viral illnesses. Tens of thousands of people are currently infected with SARS-CoV-2 [3].
In the case of fungus, it is believed that roughly 5 million species are extensively ubiquitous in the environment, of which approximately 300 can cause infections in people. However, only 20–25 are commonly seen in the clinic and are the cause of sick patients. Patients with HIV, organ transplant recipients, or those undergoing chemotherapy are examples of such people. The most frequent fungal diseases are Candida spp., Cryptococcus spp., Aspergillus spp., and Pneumocystis spp., which cause around 2 million illnesses and 1 million deaths yearly [4].

2. Plant Antimicrobials

2.1. Antimicrobial Resistance

As COVID-19 rages, the antimicrobial resistance (AMR) epidemic continues in the background. AMR causes recurrent microbe (viruses, bacteria, and fungi) infections that lengthen hospital stays and result in preventable deaths. It is estimated that 4.95 million people died due to AMR in 2019 and that by 2050, there will be 10 million annual deaths due to antimicrobial resistance. Two factors primarily cause antimicrobial resistance. The first is the overuse of antimicrobials, which exposes microbes to them regularly, increasing their chances of developing resistance. The second issue is that few new antimicrobial drugs are being developed to replace ineffective ones due to rising drug resistance [5][6].
Compared to non-resistant forms, resistant bacteria are two times more likely to develop into a serious health problem and are three times more likely to lead to death [7][8]. Resistance to first-line antibiotics, such as fluoroquinolones and lactam antibiotics, is responsible for more than two-thirds of AMR-related deaths (carbapenems, cephalosporins, and penicillins). People with low incomes are disproportionately affected by AMR because they have limited access to more expensive second-line antibiotics that may be effective when first-line drugs fail. Physicians should avoid inappropriate antibiotic therapy when, for example, the illness has a viral origin [5][9][10].
There are different mechanisms of resistance to antibiotics (Figure 1). Bacteria produce enzymes that can destroy or alter the structure of the drug, causing the drug to lose its activity during enzymatic inactivation. Drug-inactivating enzymes are classified into three types: hydrolase (primarily lactamase), passivating enzymes (aminoglycoside-inactivating enzyme, chloramphenicol acetyltransferase, and erythromycin esterase), and modifying enzymes (aminoglycoside-modifying enzyme). Similarly, changing the target to which the drug is directed ensures that the antibiotic binds appropriately to the bacteria. This mechanism is primarily seen in Gram-positive bacteria with drug resistance and polymyxin resistance. Changes in outer membrane permeability that result in channel alteration or decreased expression make the bacteria less sensitive. In the drug efflux pump, when the drug is removed from the bacterial cytoplasm, the concentration is much lower than is required for it to exhibit activity, resulting in drug resistance. This process requires energy and works with various antibiotics [6][11][12][13].
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Figure 1. Antibiotic resistance mechanisms [6][11][12][13]. Created with BioRender.com.

2.2. Natural Products and Plant Extracts with Antimicrobial Activity against MDR Strains

Multidrug resistance (MDR) is a major cause of human suffering because it undermines doctor–patient trust, resulting in massive economic losses. In this world of microbe–man cohabitation, the survival of the human species will be compromised in the absence of health-giving microbes, and there will be no way to avoid the emergence of MDR superbugs. Throughout history, the isolation and identification of biologically active compounds and molecules from nature have resulted in the discovery of new therapeutics, advancing the health and pharmaceutical industries. Phytochemicals are used in the research and development of the pharmaceutical industry as a source of new molecules, leading to the development of novel drugs [14][15].
As shown in Table 1, several classes and subclasses of secondary metabolites (Figure 2) have been isolated from plants with antimicrobial activity, each with a different mechanism of action. This table shows that, depending on the compound class, they share the same kind of mechanism of action.
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Figure 2. Structures of plant antimicrobial compounds found in medicinal plants from Latin America, from Table 1.
Regarding essential oils, the essential oil of rosemary (Rosmarinus officinalis) was found to have antibacterial activity against three types of MDR acne-causing bacteria: Staphylococcus aureus, Staphylococcus epidermidis, and Cutibacterium acnes [16]. Similarly, volatile oils extracted from cinnamon (Cinnamomum verum) and tree basil (Ocimum gratissimum) had potent bactericidal activity against MDR A. baumannii bacteria [17].
Terminalia bellirica fruits were studied, and it was discovered that the aqueous and methanol extracts had antibacterial activity against all strains of MRSA (Methicillin-resistant Staphylococcus aureus), MDR Acinetobacter spp., and MDR P. aeruginosa [18].
The aqueous, hexane, and ethanol extracts of Punica granatum peel demonstrated antibacterial activity against MDR pathogens such as P. aeruginosa and A. baumannii. Valoneic acid dilactone (aqueous fractions), Hexoside (ethanol fractions), and Coumaric acid (hexane fractions) were discovered to be bioactive compounds [17]. Ethanolic extracts of Azadirachta indica, Allium sativum, and Syzygium cumini were found to have anti-MDR-Candida spp. activity. According to a phytochemical analysis of ethanolic plant extracts, all the plants studied contained alkaloids, flavonoids, glycosides, phenols, tannins, and saponins [19].
ESKAPE (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumannii, Pseudomonas aeruginosa, and Enterobacter species) MDR pathogens were tested using various extracts. Three ethanolic extracts from Adiantum capillus-veneris, Artemisia absinthium, and Martynia annua were found to inhibit the growth of MDR strains of ESKAPE pathogens [20].
Aside from the plant extracts mentioned above, various plant compounds (Figure 3) with anti-MDR bacteria activity have already been identified. Table 2 lists these compounds, as well as the biological effects they have on specific strains.
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Figure 3. Structures of promising plant-derived compounds merit combating drug-resistant pathogenic microbes, from Table 2.
Because of the severe problem of MDR properties in microbes, the discovery of alternative drugs from natural products should be one of the primary goals of current research. Understanding the nature of pathogenic microbes, recognizing biofilm formation and architectural scheme, and employing cross-disciplinary techniques are thus critical for discovering new potent and novel drugs.
Table 1. Antimicrobial mechanisms of plant compounds present in Latin American medicinal plants.
Class Subclass Examples Source of the Compound Mechanism References
Phenolics Simple phenols Eugenol (1) Syzygium aromaticum Membrane disruption. [21][22]
Resveratrol (2) Vitis vinifera Binds reversibly to ATP synthase. [21][23]
Phenolic acids Methyl gallate (3) Euphorbia hyssopifolia Inhibits DNA gyrase or ATPase. [21][24]
Quinones Emodin (4) Rheum rhabarbarum Destroys the integrity of the cell wall and cell membrane. [21][25]
Flavonoids Chrysin (5) Passiflora caerulea Binds to adhesins. [26][27]
Flavones Abyssinone V (6) Erythrina abyssinica Complexes with the cell wall, inactivate enzymes and inhibit HIV reverse transcriptase. [26]
Acacetin (7) Robinia pseudoacacia - [21]
Flavonols Quercetin (10) Brickellia cavanillesii Disrupts bacterial cell walls and cell membranes, disrupt nucleic acid synthesis, inhibit biofilm formation, and reduce expression of virulence factors. [27][28]
Tannins Ellagitannin (9) Punica granatum Binds to proteins, bind to adhesins, enzyme inhibition, substrate deprivation, complex with the cell wall, membrane disruption, metal ion complexation. [26]
Coumarins Warfarin (13) Melilotus officinalis Interacts with eukaryotic DNA (antiviral activity). [26]
Terpenoids   Capsaicin (11) Capsicum annuum Membrane disruption. [26]
  Carvacrol (12) Xylopia aromatica Membrane disruption. [21][29]
  Thymol (8) Induces the permeability and depolarization of the cytoplasmic membrane. [21][30]
Alkaloids   Caffeine (14) Coffea arabica Inhibits biofilm development. [21][31]
  Berberine (15) Argemone mexicana Damages bacterial cells by destroying cellular proteins. [21][32]
Lectins and polypeptides   Fabatin (16) Vicia faba Blocks viral fusion or adsorption and forms disulfide bridges. [26]
Table 2. Different compounds derived from plants with promising activity to combat drug-resistant pathogens (based on [33]).
Name of the Compound Source of the Compound Biological Effect on MDR Bacteria References
9,12,15-Octadecatrienoic acid (17) Ocimum basilicum Used in contesting E. coli, S. aureus, K. pneumonia, P. aeruginosa, and P. mirabilis. [33]
Furanone (18) Vanilla planifolia Interferes in the quorum sensing system of P. aeruginosa. [34]
Plumbagin (19) Plumbago indica Has antibacterial properties by binding to the ATP cassette transporter. [35][36]
Arjunolic acid (20) Cercidium microphyllum Inhibits E. coli, B. subtilis, and S. sonnei. [37]
1,8-Cineole (21) Eucalyptus globulus Has antibacterial (methicillin-resistant S. aureus), antibiofilm, and anti-quorum sensing activities. [38][39]
Leucoanthocyanidin (22) Umbellularia californica Has a cidal effect against B. cereus ATCC14579, S. pyogens ATCC10782, and MRSA ATCC-BAA-1683. [40]
Quercetin (10) Citrus sinensis Inhibits the proton motive force (PMF) of S. aureus and inhibits P. aeruginosa (POA1), E. coli O157H7, and V. harveyi BB120. [41]
Warfarin (13) Dipteryx odorata Inhibits S. viridans, S. mutans and S. aureus. [15]
α-Pinene (23) Callistemon viminalis Suppresses the growth of B. cereus, S. typhi, P. aeruginosa, B. subtilis, E. coli, and P. vulgaris. [42]
p-Cymen-8-ol (24) Senecio nutans Interferes with the membrane permeability of V. cholerae. [43]
Luteolin (25) Guazuma ulmifolia Has a cidal effect against M. tuberculosis. [44]
Allicin (26) Allium sativum Interferes with the metabolic systems of H. pylori, S. epidermidis, B. cepacia, P. aeruginosa, and S. aureus. [45]
Thymol (8) Lippia sidoides Has activity against L. monocytogen, S. typhimurium, and E. coli O157:H7. [45][46]
Dehydroabietic acid (27) Pinus elliottii Has a cidal effect against E. faecalis, S. haemolyticus, S. capitis, and MDR-S. epidermidis. [47]
Pogostone (28) Pogostemon cablin Is effective against both gram-negative and gram-positive bacteria. [48]
Apigenin (29) Mentha pulegium Interferes with the growth of B. cereus, E. coli, and S. aureus. [49]
Isosakuranetin (30) Hyptis albida Inhibits S. aureus and B. subitilis. [50]
Guaijaverin (31) Psidium guajava Significantly inhibits the adherence of S. mutans. [51][52]
Zingerone (32) Zingiber officinale Inhibits biofilm formation and attenuation of motility properties in P. aeruginosa. [53][54][55]

2.3. Pathogenic Fungi for Human

Fungi are eukaryotic organisms widely distributed across the planet, with more than 700,000 species classified [56]; however, it is estimated that there may be more than 1 million species in existence [57]. Despite these data, the number of fungi that can affect other species is minimal, with less than 0.1% being of medical importance to humans, and less than 50 species being identified as pathogenic fungi. In recent years, fungi adapted to modified ecosystems have significantly impacted human health, as they tend to infect plants and their metabolism, negatively affecting the food web [58][59].
Mycoses are usually superficial, cutaneous, systemic, or opportunistic. A worldwide risk factor is immunosuppression; however, the microbiome imbalance caused by antibiotics must be considered, as it can lead to an even more severe infection [60][61]. It is widely thought that most mycoses are opportunistic. It is extremely important to take into account that mycosis can be considered dangerous due to the entry of several fungi, with cosmopolitan genera such as Candida, Cryptococcus, and Aspergillus being prevalent [62][63][64], while creating invasive fungal infections (IFIs) that cause high mortality rates worldwide [59][65][66].

2.4. Mechanism of Action and Drug-Resistance of Pathogenic Fungi

Pathogenic fungi create complex signaling cascades that depend on the host and environment [67]. A 2017 review points out the importance of recognizing the pathways involved in fungal pathogenicity and identifying opportunity areas to create better antibiotics [68], even if knowing these factors would make it impossible to create efficient vaccines [69][70]. However, current antifungal drugs have different mechanisms of action (Table 3); the most common mechanisms are directed against the fungal cell wall or membrane, specifically against ergosterol or (1,3)-β-d-glucan biosynthesis, except for pyrimidines and orotomides that target crucial molecules in nucleic acid metabolism [71][72][73][74].
Table 3. Mechanisms of action of families of antifungal drugs.
Family of Antifungal Drugs Mechanism of Action References
Azoles
(fluconazole)		 Inhibit fungal cell cytochrome P-450-3-A, disrupting ergosterol synthesis and intoxicating the cell with sterol intermediates. [71][72][73]
Polyene
(anfotericine B)		 Binds to ergosterol and generates pores in the membrane, causing oxidative damage and cell death. [71][72]
Echinocandins
(micafungin)		 Inhibit the enzyme 1,3-β-D-glucan synthase, which weakens the cell wall, causing osmotic instability. [71][72]
Allylamines
(terbinafine)		 Block the enzyme squalene epoxidase, reducing ergosterol levels and increasing squalene. This increases the permeability of the cell. membrane, causing a decrease in fungal growth. [71]
Pyrimidines
(flucytosine)		 Bind to cytosine permease, already in the nucleus, and generate fluorardilic acid, which is incorporated into the RNA, rendering it useless. [71][73]
Orotomides
(olorofim)		 Inhibit dihydroorotate dehydrogenase synthesis, preventing the synthesis of DNA and RNA. [75][76]
Fosmanogepix Inhibits the enzyme Gwt1, responsible for glycosylphosphatidylinositol synthesis. [74]
Just as bacteria generate drug resistance, so do fungi; this drug resistance can be described from a clinical point of view, referring to the worsening of an infection despite receiving adequate drug treatment. On the other hand, in the laboratory context, resistance is evaluated through a Minimum Inhibitory Concentration (MIC) assay to determine the growth of the pathogen at different concentrations of antibiotics [67][68][77]. It is necessary to point out the concept of drug tolerance, which is considered as the fungus persistence on the substrate; however, its growth is slow due to multifactorial causes [78][79].

2.5. Latin American Plants with Antifungal Effects

Fungi drug resistance has created a worldwide clinical challenge, and treatment alternatives have been considered, such as including two or more antifungals for one treatment; however, this does not make a significant difference [80]. This is why alternatives should be considered, such as using plant-derived compounds that can act via bypassing common metabolic pathways in fungal pathology. Table 4 summarizes the medicinal plant extracts with antifungal properties.
Table 4. Extracts of Latin American plants with activity against pathogenic fungi.
Species Extract Fungi References
Achyrocline satureioides Ethanolic Fusarium verticillioides [81]
Achyrocline tomentosa Ethanolic Fusarium verticillioides [81]
Aloysia citriodora Ethanolic Fusarium verticillioides [81]
Annona cherimola Ethanolic Fusarium oxysporum [82]
Annona muricata L. Ethanolic Candida albicans [83]
Aristolochia argentina Griseb. Ethanolic Fusarium verticillioides [81][84]
Asclepias curassavica Hexanic, Methanolic Candida albicans [85]
Baccharis artemisioides Ethanolic Fusarium verticillioides [81]
Baccharis flabellata Ethanolic Fusarium verticillioides [81]
Baccharis salicifolia Ethanolic Fusarium verticillioides [81]
Bixa orellana Ethanolic Candida albicans [86]
Curcuma zedoaria Acetone, Hexanic Candida albicans [87][88]
Dalea elegans Ethanolic Fusarium verticillioides [81]
Echinacea angustifolia Ethanolic Cryptococcus neoformans [89]
Echinacea atrorubens Ethanolic Cryptococcus neoformans [90]
Echinacea pallida Ethanolic Candida albicans [90]
Echinacea purpurea Ethanolic Saccharomyces cerevisiae [89]
Eupatorium buniifolium Methanolic Trichophyton mentagrophytes [91]
Euphorbia hyssopifolia Methanolic Aspergillus niger [92]
Flourensia oolepis Ethanolic Fusarium verticillioides [81]
Gaillardia megapotamica Ethanolic Fusarium verticillioides [81]
Galphimia glauca Hexanic, Methanolic Trichophyton mentagrophytes [85][93]
Grindelia pulchella Ethanolic Fusarium verticillioides [81]
Heterothalamus alienus Ethanolic Fusarium verticillioides [81]
Hibiscus sabdariffa Methanolic Candida albicans [94]
Kageneckia lanceolata Ethanolic Fusarium verticillioides [81]
Larrea cuneifolia Ethanolic Lenzites elegans [95]
Larrea divaricata Ethanolic Penicillium notatum; Candida spp. [95][96]
Lepechinia floribunda Ethanolic Fusarium verticillioides [81]
Lippia turbinata Ethanolic Fusarium verticillioides [81]
Loeselia mexicana Ethanolic Trichophyton mentagrophytes [97]
Lygodium venustum Ethanolic Candida albicans [98]
Lysiloma acapulcensis Hexanic Trichophyton mentagrophytes [99]
Miconia mexicana Methanolic Candida albicans [99]
Microliabum candidum Ethanolic Fusarium verticillioides [81]
Minthostachys verticillata Ethanolic Fusarium verticillioides [81]
Morrenia brachystephana Ethanolic Fusarium verticillioides [81]
Otholobium higuerilla Ethanolic Fusarium verticillioides [81]
Passiflora caerulea Methanolic Aspergillus flavus [100]
Pimenta dioica Essential oil Fusarium oxysporum [101]
Polygonum acuminatum Dichloromethane Cryptococcus neoformans [102]
Salix alba Methanolic Aspergillus ornatus [103]
Salvia cuspidata Ethanolic Fusarium verticillioides [81]
Sebastiania commersoniana Ethanolic Candida spp. [104]
Senecio vira-vira Ethanolic Fusarium verticillioides [81]
Smilax domingensis Ethanolic Candida albicans [105]
Syzygium aromaticum Essential oil Candida spp. [106]
Terminalia triflora Methanolic Trichophyton mentagrophytes [91]
Thalictrum decipiens Ethanolic Fusarium verticillioides [81]
Tithonia diversifolia Aquous Fusarium oxysporum [107]
Trichocline reptans Ethanolic Fusarium verticillioides [81]
Vernonia mollisima Ethanolic Fusarium verticillioides [81]
Vernonia nudiflora Ethanolic Fusarium verticillioides [81]
Vitis vinifera Aqueous Candida spp. [108]
Zanthoxylum coco Ethanolic Fusarium verticillioides [81]
Zinnia peruviana Ethanolic Fusarium oxysporum [95]
Zuccagnia punctata Ethanolic Aspergillus niger [95]
Zuccagnia punctata Dichloromethane Candida albicans [109]

2.6. Medicinal Plant Antiviral Activity against Human-Infecting Viruses

In 2018, over 4400 virus species were classified into 122 families and 7535 [110] subfamilies. Human-infecting viruses include RNA viruses, DNA viruses, retroviruses, bare viruses, and virions, with RNA viruses being the most prevalent. Numerous medicinal plants contain compounds that inhibit the replication of viruses or enhance the immune system. Alkaloids, terpenes, flavonoids, numerous glucosides, and proteins have been recognized as phytochemicals; their metabolites include apigenin (29), kaempferol (34), and luteolin (25), in addition to the triterpenoids oleanolic acid (35) and ursolic acid (36) [111].

2.6.1. Biological Mechanisms of Antiviral Activity

Plant biocompounds may function similarly to conventional antiviral medications by inhibiting viral replication polymerase, protease, integrase, fusion molecules, and cell membrane binding. For example, the exposure of non-enveloped norovirus to 0.5% of carvacrol (12) results in the degradation of its capsid [112]. Some polysaccharides may also deter viruses from attaching to cells, while thiophenes, terpenoids, and polyacetylenes can interact with the membrane of infected cells [113]. Lignans, phenolic compounds, terpenoids, flavonoids, alkaloids, and furocoumarins can all inhibit viral replication. Biocompounds of Allium sativum are among the most studied; they have antiviral activity against human, animal, and plant infections. Multiple of these metabolites can strengthen the immune system’s response to infections. This biocompound interacts in vivo with thiols such as glutathione and L-cysteine to produce S-allyl-mercapto-glutathione (SAMG) and S-allyl-mercapto-cysteine (SAMC), which can degrade viral protein. In addition, it contains lectins, flavonoids (kaempferol (34), quercetin (10), and myricetin (37)), polysaccharides (fructan), steroids, saponins, fatty acids (lauric (38) and linoleic acid (39)), diverse enzymes, vitamins (A, B1, and C), allixin (40), minerals (Ca, Cu, Fe, K, Mg, Zn, and Se), and amino acids [114].
Table 5 summarizes the medicinal plant extracts and their possible mechanisms of action (Figure 4), while Table 6 discusses the medicinal plant biocompounds with antiviral properties (Figure 5, Figure 6 and Figure 7).
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Figure 4. Various biocompounds’ potential antiviral mechanisms of action. Created with BioRender.com.
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Figure 5. Antiviral biological compounds (Table 6).
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Figure 6. Antiviral biological compounds (Table 6).
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Figure 7. Antiviral biological compounds (Table 6).

2.6.2. Antiviral-Active Extracts for Respiratory Infections

The leading cause of morbidity in humans is viral respiratory tract infections, with rhinovirus, influenza, respiratory syncytial virus (RSV), and human coronavirus having the most significant impact.
Several extracts of medicinal plants exhibit antiviral activity in vitro; the ethanolic, ethyl acetate, and hexane extracts of Echinacea pallida var. angustifolia root inhibit rhinovirus replication [115]. The Echinacea purpurea ethanolic extract inhibits the invasion of HcoV-299E (coronavirus) into cells [116]. The ethanolic extract of Sambucus formosana Nakai seeds inhibits the binding of HCoV-NL63 (coronavirus) [117]. Aqueous extracts of Plantago asiatica and Clerodendrum trichotomun inhibit RSV (respiratory syncytial virus) replication [118].

2.6.3. Extracts and Biocompounds with Activity against Human Herpes Viruses

Several medicinal plant extracts have in vitro anti-herpes simplex activity: the hexane, dichloromethane, and methanolic extracts of Clinacanthus mutans and C. siamensis inhibit the formation of HS-1 and HS-2 viral plaques [119]. Caffeic acid and chlorogenic acid are inhibitors of HS replication [120]. Polygonum minus methanolic extract inhibits HS adhesion [121]. Aloe vera glycerol extract prevents HS-2 replication [122]. Lysimachia mauritiana ethanolic extract inhibits varicella-zoster virus replication [88].
Alkaloids, glycosides, taxol derivatives, terpenes, flavonoids, ellagitannin, catechin, phenolic acids, triterpenoids, monoterpenoids, and steroids have been identified as active against Herpes simplex types 1 and 2 [123].
Carvacrol (12), extracted from the essential oil of Mexican oregano (Lippia graveolens), demonstrates antiviral activity against RNA and DNA viruses (primarily herpes viruses) [124].
Coumarins imperatorin (41) and phellopterin (42), isolated from Angelica archeangelica L., exhibit antiviral activity against herpes simplex virus type 1 and, most likely, Coxsackievirus B3 [125].
Eugenin (43) is a biocompound extracted from Geum japonicum and Syzygium aromaticum. Eugenin (43) inhibits the DNA polymerase of the Herpes simplex virus, which appears to be its mechanism of action. Also, it inhibits Herpes simplex virus activity in both Vero cells and mice [126].
The monoterpene aldehydes citral a (45), citral b (46), and citronellal (44) are the biocompounds found to have anti-herpes virus activity in Melissa officinalis essential oil [127]. Moreover, rosmarinic acid (47) from the hydroalcoholic leaf extract of M. officinalis demonstrates anti-herpes simplex type 2 activity [128]. The potential mechanism of action is to prevent virus entry into cells [129].

2.6.4. Activity against Epstein-Barr Virus

Epstein–Barr (EBV) is a herpes virus that affects 90 percent of the world’s population and is linked to numerous immunological and neoplastic diseases.
Epigallocatechin-3-gallate (48), a catechin derived from Camellia sinensis, inhibits the spontaneous lytic infection of infected cells and blocks their transcription and protein expression via the ERK1/2 (extracellular-regulated kinase 12) and PI3-K/Akt (phosphatidylinositol-3-kinase) pathways [130].
The compounds sesamol (49) and resveratrol (2), along with sesame and sunflower essential oils, inhibit the early antigen activation in vitro of the Epstein–Barr virus [131].
Konoshima et al. [132] found that monoterpenylmagnolol (52) and β-eudesmol (50), extracted from Magnolia officinalis, inhibit replication (EBV) in Raji cells.
Berberine (15) is an alkaloid derived from several medicinal plants (Cortidis rhizome, Coptis chinensis, and Barnerini vulgaris) that inhibits cell proliferation and induces apoptosis in Epstein–Barr virus-infected cells via the inhibition of p-STAT3 and the overexpression of EBNA1 [133].
Curcumin (33) is highly effective at reducing TPA-, butyrate-, and TGF-b-induced levels of BZLF1 mRNA and TPA-induced luciferase mRNA, indicating that it inhibits three main EBV pathways [134].
Apigenin (29) inhibits the expression of the EBV lytic proteins Zta, Rta, EAD, and DNase in B and epithelial cells. In addition, it decreases the number of EBV-reactivating cells detectable via immunofluorescence analysis. Additionally, apigenin (29) has been found to significantly reduce EBV virus production [135].
Glycyrrhizic acid (56) (18-GL or GL) possesses a wide range of antiviral activities, pharmacological effects, and sites of action. In vitro, GL (56) inhibits Epstein–Barr virus (EBV) infection by interfering with an early stage in the EBV replication cycle (possibly attachment or penetration) [136].
The flavonoid luteolin (25) inhibits EBV reactivation significantly. In EBV-positive epithelial and B cell lines, 25 inhibits the expression of EBV-lytic gene-encoded proteins. In addition, it decreases the number of EBV-reactivating cells detected via immunofluorescence and virion production. Moreover, 25 decreases the activities of the promoters of the immediate–early genes Zta (Zp) and Rta (Rp). It inhibits the activity of Sp1-luc, indicating that the disruption of Sp1 binding is involved in the mechanism of inhibition [137].

2.6.5. Anti-Cytomegalovirus Activities

Human cytomegalovirus (hCMV) is a pervasive herpesvirus that causes a latent infection that persists throughout the host’s lifetime and can be reactivated when immunity is compromised.
Genistein (55) and baicalein (57) are antiviral flavonoids against HCMV. The primary mode of action of genistein’s antiviral activity against HCMV is to inhibit the function of immediate–early proteins. Baicalein’s antiviral activity against HCMV works primarily by inhibiting the kinase activity of EGFR to prevent viral entry [138].
Supplementation with piceatannol (58) inhibits the lytic changes caused by hCMV infection. In addition, piceatannol dose-dependently inhibits the expression of hCMV immediate–early (IE) and early (E) proteins and the replication of hCMV DNA [139].
Resveratrol (2) inhibits human cytomegalovirus DNA replication to undetectable levels during the second (late) phase of virus-induced phosphatidylinositol-3-kinase signaling and transcription factor activation [140].
Allitridin (59), a compound extracted from A. sativum, reduces the amount of viral DNA in cytomegalovirus-infected cells by inhibiting the transcription of the IE gene [141].

2.6.6. Anti-HIV Activity of Extracts and Biocompounds

Among the extracts that inhibit in vitro HIV activity or replication is an aqueous extract of Salvia miltiorrhiza that inhibits HIV-1 integrase [142]. Rhaphiolepsis indica methanolic extract inhibits its replication [143]. Acacia arabica’s n-butanol fraction inhibits the activity of viral proteases and Tat [144]. The Phyllanthus amarus ethanolic and aqueous extracts inhibit its replication [145]. The Olea europaea aqueous extract inhibits cell–cell infection [146]. Hyssopus officinalis L. aqueous extract inhibits its replication [147]. The reverse transcriptase is inhibited by the methanolic extract of Terminalia sericea [148], the n-hexane fraction of Phyllanthus emblica and Cassia occidentalis, and the pine cone extract of Pinus yunnanensis [149]; floral extracts of Calendula officinalis inhibit HIV-1 reverse transcriptase activity [150]. Cassine xylocarpa’s lupane-type pentacyclic triterpenoid also possesses anti-HIV activity [151].

2.6.7. Antiviral Activity of Extracts and Biocompounds against Hepatitis B and C Viruses

The secondary metabolites and extracts listed below have demonstrated in vitro activity against HBV (Hepatitis virus B): isochlorogenic acid A (61), obtained from Laggera alata, inhibits replication and decreases the stability of its core protein [152]. Amide alkaloids from Piper longum [153] and dehydrocheilanthifoline (60), isolated from Corydalis saxifolia, inhibit its replication [154]. Saikosaponins (Bupleurum species) inhibit the replication and expression of its surface antigen [155]; the ethanolic extract of Polygonum cuspidatum inhibits its surface antigen expression [156]; and curcumin (33) (Curcuma longa) decreases the expression of the PGC-1a coactivator, required for its transcription [157]. Glycyrrhizinic acid (56) (Glycyrrhiza glabra), artemisinin (62) (Artemisia annua), and LPRP-Et-97,543 compound (Liriope platyphylla) all inhibit its viral production [158]. On the other hand, epigallocatechin-3-gallate (48) (Camellia sinensis) inhibits its viral replication [159].
Concerning the hepatitis C virus, flavonolignans (Silybum marianum) possess antiviral and antioxidant properties [160], while curcumin (33) (Curcuma longa) inhibits its viral replication via the Akt-SREBP-1 pathway [161]. Epigallocatechin-3-gallate (48) [162] and ladanein (77) [163] inhibit viral entry; griffithsin inhibits viral cell–cell transmission [164], tellimagrandin I (78) (Rosa rugosa) inhibits viral invasion [158], chebulagic acid (64) and punicalagin (65) (Terminalia chebula) inhibit the viral particles necessary for their fusion and cell–cell transmission [165], saikosaponin B2 (79) (Bupleurum kaoi) prevents viral binding, and chalepine (66) and pseudan IX (80) (Ruta angustifolia) decrease viral protein synthesis and RNA replication [158][166].
Betulinic acid (67) and betulin (68), derived from Betula alba L., exhibit anti-hepatitis C virus activity. Shikov et al. (2011) [167] suggested that 68 can induce TNF-α expression and thereby enhance the Th1-type immune cell response in patients with chronic hepatitis C virus.

2.6.8. Anti-Influenza Activity of Extracts and Biomolecules

Moradi (2019) [168] reported that ethanolic and polyphenolic extracts of Punica granatum inhibit influenza replication and virions. Geranium sanguineum polyphenolic, methanolic, and ethanolic extracts have antiviral properties [169]. Glycyrrhizin (56) from Glycyrrhiza glabra induces the apoptosis of H5N1-infected cells [170]; polyphenols from Chenomeles sinensis inhibit the binding of its hemagglutinins [171]; and the Sambucus nigra fruit inhibits viral entry and modulates cytokine release. It has been shown in other studies to inhibit hemagglutins and the replication of influenza viruses: A/Shangdong 9/93 (H3N2), A/Beijing 32/92 (H3N2), A/Texas 36/91 (HlNl), A/Singapore 6/86 (HlNl), type B/Panama 45/90, B/Yamagata 16/88, and B/Ann Arbor [172].
The Phyllanthus embolica aqueous extract inhibits hemagglutinin and viruses in infected cells [173]. Catechin derived from Camellia sinensis inhibits both RNA synthesis and neuraminidase activity [174].
Arctigenin (69) and arcitiin (70), extracted from the fruits of Arctium lappa L., exhibit potent anti-influenza A virus activity in vitro [175].
Echinacea extract is active against influenza A/B viruses (H3N2, H1N1, H5N1, H7N7, and S-OIV), Respiratory Syncytial Virus, and Herpes Simplex [176]. On the other hand, it also induces the production of IL-6 and IL-8 (CXCL8) and other cytokines with antiviral properties [177]. In a clinical trial, it was demonstrated to be as effective as oseltamivir in reducing influenza symptoms if administered at the onset of the disease [178].
On the other hand, the monoterpene aldehydes citral a (45) and citral b (46), from Melissa officinalis, exhibit synergistic activity with oseltamivir against the H9N2 influenza virus [179].
Wyde et al. [180] found that polyphenolic polymers derived from the Euphorbiaceae shrub are active in vitro against parainfluenza virus type 3, Respiratory Syncytial Virus, and influenza viruses.

2.6.9. Extracts In Vitro Possess Anti-Papillomavirus Activity

Their growth is inhibited by polyphenon E (71) (poly E) and epigallocatechin gallate (48) from Camellia sinensis [181]. Artemisinin (62) (Artemisia absintium) inhibits the expression of HPV-39, induces apoptosis, and reduces the proliferation of infected cells in ME-180 cells [182]. Curcumin (33) (Curcuma longa L.) has been utilized to boost immunity against HPV. Hamamelis virginiana tannins inhibit HPV-16, Ficus religiosa aqueous extract induces the apoptosis of HPV-16 and 18 infected cervical cells, and the Phyllanthus emblica fruit inhibits HPV-16 and 18 carcinogenic gene expression. The chloroplast leaf extract of Bryophyllum pinnatum inhibits HPV-18 transcription in cervical cancer cells, whereas the soluble extract of Pinellia pedatisecta inhibits HPV-E6 expression in multiple cell lines [183].

2.6.10. In Vitro Activity of Extracts against Dengue and Chikungunya Viruses

Coumarin (72) and the ether extract of Alternanthera philoxeroides [184], as well as aqueous and chloroform extracts of Carioca papaya [185], inhibit dengue virus. Sambucus nigra methanolic extract protects against dengue serotype 2 [186].
Vernonia amygdalina ethyl acetate extract reduces the Chikungunya viral burden [187]. Chikungunya helicases and proteases are inhibited by aqueous extracts of Picrorhiza kurrooa, Ocimum tenuiflorum, and Terminalia chebula [188].

2.6.11. Antiviral Activity of In Vitro Extracted Compounds against SARS-CoV

The following organisms were evaluated for their anti-SARS-CoV-1 activity: Lycoris radiate, Artemisia annua, Pyrrosia lingua, Lindera aggregata, Isatis indigotica (inhibition of 3CL protease) [189], Rheum officinale Bail, Polygonum multiforum Thunb. (inhibit ACE2 protein interaction with spike protein) [190], Gentiana scabana, Dioscorea batatas, Casssia tora, Taxillus chinensis, Cibotium barometz (inhibit 3CL protease) [191], and ethanolic extracts of Anthemis hyalina, Nigella sativa, and Citrus sinensis (increase IL-8, modify TRPA, TRPM, and TRPV gene expression) [192]. Some purified secondary metabolites that show activity against SARS-CoV are as follows: aloe-emodin (73), β-sitosterol (63), hesperetin (74), indigo (75), and sinigrin (76) (obtained from Isatis indigotica) [193], amentoflavone (53), apigenin (29), luteolin (25), quercetin (10) (obtained from Torreya nucifera), which inhibit 3CL protease [194], and lycorine (54) (obtained from Lycoris radiata) [189].
In the case of SARS-CoV-2 (which causes COVID-19), the following secondary metabolites (Figure 8) may be advantageous [195]:
Plants 12 03997 g008
Figure 8. Natural products reported to have anti-SARS-CoV-2 activity.
  • To inhibit the binding of the spike protein to the ACE-2 receptor: caffeic acid (51), emodin (82), glycyrrhizin (56), luteolin (25), and tetra-O-galloyl-β-D-glucose (81).
  • To prevent virus transcription: cepharanthin (83), fangquinoline (84), forystoside A (85), tetrandin (87), coumaroyltyramine (86), cryptoansionone (88), kaempferol (34), moupinamide (89), N-cis-feruloyltyramine (90), quercetin (10), tanshinone IIa (91), and tryptanthrine (92).
  • To inhibit viral translation: tryptanthrine (92).
  • To inhibit the cellular discharge of virions: emodin (82) and kaempferol (34).
Table 5. Antiviral extracts derived from plants.
Plant Extract Virus Possible Antiviral Mechanism References
Echinacea pallida var. angustifolia Hexane Rhinovirus Impedes replication. [115]
Echinacea purpurea Ethanolic Coronavirus HcoV-299E Prevents the invasion of cells. [116]
Sambucus formosana Nakai Ethanolic HCoV-NL63 (coronavirus) Prevents bonding. [117]
Plantago asiatica Aqueous extract Respiratory syncytial virus Replication inhibition. [118]
Clerodendrum trichotomun Aqueous extract Respiratory syncytial virus Replication inhibition. [118]
Clinacanthus mutans
Clinacanthus siamensis		 Hexane, dichloromethane, and methanolic Herpes simplex-1 and 2 Inhibit viral plaques. [119]
Polygonum minus Methanolic Herpes simplex-1 and 2 Inhibits adhesion. [121]
Aloe vera Glycerol Herpes simplex 2 Impedes replication. [122]
Lysimachia mauritania Ethanolic extract Varicella-zoster Impedes replication. [88]
Sesamum indicum
Helianthus annuus		 Sesame essential oil and Sunflower essential oil Epstein-Barr Virus Inhibit precocious antigen activation. [131]
Salvia miltiorrhiza Aqueous extract HIV-1 Interferes with integrase activation. [142]
Rhaphiolepsis indica Methanolic extract HIV-1 Impedes replication. [143]
Acacia arabica N-butanol fraction HIV-1 Inhibits viral proteases and Tat activity. [144]
Phyllanthus amarus Schum. Ethanolic and aqueous extract HIV-1 Impedes replication. [145]
Olea europaea Aqueous extract HIV-1 Prevents infections between cells. [146]
Hyssopus officinalis L. Aqueous extract HIV-1 Inhibits replication. [147]
Polygonum cuspidatum Ethanolic extract Hepatitis virus B Inhibits surface antigen expression. [156]
Punica granatum Ethanolic and polyphenolic extracts Influenza virus Inhibits influenza replication and virions. [168]
Geranium sanguineum Polyphenolic, methanolic, and ethanolic Influenza virus No study. [169]
Chenomeles sinensis Polyphenols Influenza virus Inhibits the attachment of its hemagglutinins. [171]
Sambucus nigra Aqueous extract Influenza virus Modulates cytokine release and inhibits viral entrance. [172]
Phyllanthus emblica Aqueous extract Influenza virus Prevents hemagglutinins and viruses from infecting infected cells. [173]
Echinacea purpurea Aqueous extract Influenza A/B viruses H3N2, H1N1, H5N1, H7N7, and S-OIV Induces IL-6 and IL-8 production. [176]
Euphorbiacea shrub Polyphenolic polymers Influenza No study. [180]
Ficus religiosa Aqueous extract Papillomavirus HPV-16 apoptosis is induced. [183]
Bryophyllum pinnatum Chloroplast extract Papillomavirus Suppresses HPV-18 transcription. [183]
Pinellia pedatisecta Soluble extract Papillomavirus Inhibits the HPV-E6 expression in multiple cell lines. [183]
Carioca papaya Aqueous and chloroplast extract Chikungunya Stops the dengue virus. [185]
Sambucus nigra Methanolic extract Dengue serotype 2 Defends against infection. [186]
Vernonia amygdalina Ethyl acetate extract Chikungunya Minimizes the viral burden. [187]
Picrorhiza kurrooa
Ocimum tenuiflorum
Terminalia chebula		 Aqueous extracts Chikungunya Block helicases and proteases. [188]
Lycoris radiate, Artemisia annua, Pyrrosia lingua, Lindera aggregata, and Isatis indigotica Different extracts SARS-CoV-1 Obstruct 3CL protease. [189]
Rheum officinale Bail, Polygonum multiforum Thunb Different extracts SARS-CoV-1 Inhibit the interaction between ACE2 and spike proteins. [190]
Gentiana scabana, Dioscorea batatas, Casssia tora, Taxillus chinensis, and Cibotium barometz Different extracts SARS-CoV-1 Prevent 3CL protease. [191]
Anthemis hyalina, Nigella sativa, and Citrus sinensis Ethanolic extracts SARS-CoV-1 Increase IL-8 and modulate gene expression of TRPA, TRPM, and TRPV. [192]
Table 6. Antiviral biological compounds.
Secondary Metabolite Class Biocompound (Species) Virus Potential Antiviral Mechanism Reference
Menthane monoterpenoids Carvacrol (12) (Lippia graveolens) Herpes viruses No study. [124]
Furocoumarin Imperatorin (41) and phellopterin (42) (Angelica archangelica) Herpes simplex virus type 1
Coxsackievirus B3		 No study. [125]
Chromone Eugenin (43) (Geum japonicum,
Syzygium aromaticum)		 Herpes simplex virus Prevents DNA polymerase. [126]
Cinnamic acid derivative Rosmarinic acid (47)
(M. officinalis)		 Herpes simplex type 2 Prevents virus entry into cells. [128]
Flavan-3-ol Epigallocatechin-3-gallate (48) (Camellia sinensis) Epstein–Barr Virus Blocks transcription and protein expression via ERK1/2 (extracellular-regulated-kinase 12) and PI3-K/Akt (phosphatidylinositol-3-kinase) pathways. [130]
Phenol, Monomeric stilbene Sesamol (49), resveratrol (2) (Sesamum indicum) Epstein–Barr Virus Inhibit early antigen activation. [131]
Isoquinoline alkaloid Berberine (15) (Barnerini vulgaris) Epstein–Barr Virus Inhibits cell proliferation and induces apoptosis in Epstein–Barr virus-infected cells by inhibiting p-STAT3. [133]
Linear diarylheptanoid Curcumin (33) (Curcuma longa) Epstein–Barr Virus Inhibits TPA-, butyrate-, and TGF-b induced levels of BZLF1 mRNA [134]
Flavone Apigenin (29) (purchased from Sigma-Aldrich Co., St. Louis, MO, USA) Epstein–Barr Virus Inhibits lytic proteins Zta, Rta, EAD, and DNase in B and epithelial cells and reduces the production of EBV viruses. [135]
Oleanane triterpenoid Glycyrrhizic acid (56) (Glycyrrhiza radix) Epstein–Barr Virus Interferes with the initial phase of EBV replication. [136]
Flavone Luteolin (25) (purchased from Sigma-Aldrich Co.) Epstein–Barr Virus Inhibits the expression of proteins encoded by the EBV lytic gene. [137]
Isoflavone Genistein (55) (purchased from Sigma-Aldrich) Cytomegalovirus Inhibits immediate-early (ie) protein function. [138]
Flavone Baicalein (57) (purchased from Sigma-Aldrich) Cytomegalovirus Inhibits EGFR’s kinase activity to prevent viral entry. [138]
Monomeric stilbene Piceatannol (58) (purchased from Sigma-Aldrich) Cytomegalovirus Inhibits the lytic modifications and expression of hCMV early (E) and immediate–-early (IE) proteins. [139]
Monomeric stilbene Resveratrol (2) (purchased from Sigma-Aldrich) Cytomegalovirus Reduces DNA replication. [140]
Sulfide Allitridin (59) (A. sativum) Cytomegalovirus Inhibits the IE genes’ transcription. [141]
Neolignan Monoterpenylmagnolol (52) and β-eudesmol (50) (Magnolia officinalis) Epstein–Barr Virus Impede replication. [132]
Cinnamic acid derivative Isochlorogenic acid A (61) (Laggera alata) Hepatitis virus B Impedes replication. [152]
Alkaloid Amide alkaloids (Piper longum) Hepatitis virus B Inhibit replication and surface antigen expression. [153]
Saponin Saikosaponins (Bupleurum species) Hepatitis virus B Inhibit replication and surface antigen expression. [155]
Protoberberine alkaloid Dehydrocheilanthifoline (60) (Corydalis saxifolia) Hepatitis virus B Prevents reproduction. [154]
Linear diarylheptanoid Curcumin (33) (Curcuma longa) Hepatitis virus B Decreases
Transcription.		 [157]
Oleanane triterpenoid Glycyrrhizinic acid (56) (Glycyrrhiza glabra) Hepatitis virus B Prevents viral reproduction. [158][196]
Sesquiterpene lactone Artemisinin (62) (Artemisia annua) Hepatitis virus B Prevents viral reproduction. [158][196]
Isoflavonoid LPRP-Et-97543 (93) (Liriope platyphylla) Hepatitis virus B Prevents viral reproduction. [158][196]
Flavan-3-ol Epigallocatechin-3-gallate (48) (Camellia sinensis) Hepatitis virus B Prevents viral reproduction. [159]
Lignan Flavonolignans (Silybum marianum) Hepatitis C virus No study. [160]
Linear diarylheptanoid Curcumin (33) (Curcuma longa) Hepatitis C virus Inhibits viral replication by blocking Akt-SREBP-1. [161]
Flavan-3-ol Epigallocatechin-3-gallate (48) (Camellia sinensis) Hepatitis C virus Inhibits viral introduction. [162]
Flavone Ladanein (77) (Marrubium peregrinum) Hepatitis C virus Inhibits viral introduction. [163]
Peptide Recombinant Griffithsin (Nicotiana benthamiana) Hepatitis C virus Inhibits viral cell–cell transmission. [164]
Gallotannin Tellimagrandin I (78) (Rosae rugosae) Hepatitis C virus Prevents viral penetration. [158]
Benzopyran tannin and phenol Chebulagic acid (64) and punicalagin (65) (Terminalia chebula Retz) Hepatitis C virus Inhibit fusion and cell–cell transmission. [165]
Oleanane triterpenoid Saikosaponin B2 (79) (Bupleurum kaoi) Hepatitis C virus Prevents viral attachment. [158]
Furocoumarin, Quinoline alkaloid Chalepine (66), pseudan IX (80) (Ruta angustifolia) Hepatitis C virus Reduce viral protein synthesis and viral RNA replication. [158]
Lupane triterpenoids Betulinic acid (67) and betulin (68) (Betula alba L) Hepatitis C virus Induce expression of TNF-α. [167]
Oleanane triterpenoid Glycyrrhizin (56) (Glycyrrhiza glabra) Influenza virus Initiates cell death in H5N1-infected cells. [170]
Catechin Catechins (Camellia sinensis) Influenza virus Inhibit both RNA synthesis and neuraminidase activity. [174]
Dibenzylbutyrolactone lignans Arctigenin (69) and arcitiin (70) (Arctium lappa) Influenza virus Anti-influenza A virus in vitro activity. [175]
Monoterpenaldehydes Citral a (45) and citral b (46) (Melissa officinalis) H9N2 influenza virus Have synergistic activity with oseltamivir. [179]
Flavan-3-ols Polyphenon E (poly E) (71) and epigallocatechin gallate (48) (Camellia sinensis) Papillomavirus Impede growth. [181]
Sesquiterpene lactone Artemisinin (62) (Artemisia absintium) Papillomavirus In ME-180 cells, this compound inhibits the expression of HPV-39, induces apoptosis, and reduces the proliferation of infected cells. [182]
Tannin Tannins (Hamamelis virginiana) Papillomavirus Inhibit HPV-16 [183]
Benzopyrone Coumarin (33) (Alternanthera philoxeroides) Chikungunya Stops the dengue virus. [184]
Anthraquinone, Stigmastane steroid, Flavanone, Anthranilic acid alkaloid, Glucosinolate Emodin (82), β-sistosterol (63), hesperetin (74), indigo (75), and sinigrin (76) (Isatis indigotica) SARS-CoV-1 Block the 3CL protease. [193]
Flavones, Flavonol Amentoflavone (53), apigenin (29), luteolin (25), quercetin (10) (Torreya nucifera) SARS-CoV-1 Block the 3CL protease. [194]
Indolizidine alkaloid Lycorine (54) (Lycoris radiata) SARS-CoV-1 Block 3CL protease. [189]
Cinammic acid derivative, Anthraquinone,
Oleanane triterpenoid, Flavonoid, Gallotannin		 Caffeic acid (51), emodin (82), glycyrrhizin (56), luteolin (25), and tetra-O-galloyl-β-D-glucose (81) SARS-CoV-2 Inhibit the spike protein’s interaction with the ACE-2 receptor. [195]

2.6.12. Molecules with Antiviral Activity Identified In Silico

Computational models enable to simulate the interaction between the biocompound and the virus’s target molecule [197]. Quercetin-7-O-glucoside inhibits influenza virus RNA polymerase. Quercetagetin, a flavonoid with activity against HVC through the inhibition of RNA bound to NS5B non-structural polymerase [198], naringenin, and quercetin, could inhibit hepatitis C virus proteases [199], and β-amyrin could inhibit hepatitis D virus proteases [200].
Luteolin could block SARS-CoV-2 entrance into cells [201]; isothymol and curcumin can block angiotensin-converting enzyme receptor (ACE2) activity [202]; gingerol binds to the spike protein; and quercetin with proteases [203], enterodiol, taxifolin, eriodictyol, leucopelargonidin, morin, and myricetin were found to exhibit remarkable binding affinities against the major protease (Mpro) and potato-like protease (PLpro) [204].

This entry is adapted from the peer-reviewed paper 10.3390/plants12233997

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