Abstract
The 2019 novel coronavirus, SARS-CoV-2, producing the disease COVID-19 is a pathogenic virus that targets mostly the human respiratory system and also other organs. SARS-CoV-2 is a new strain that has not been previously identified in humans, however there have been previous outbreaks of different versions of the beta coronavirus including severe acute respiratory syndrome (SARS-CoV1) from 2002 to 2003 and the most recent Middle East respiratory syndrome (MERS-CoV) which was first identified in 2012. All of the above have been recognised as major pathogens that are a great threat to public health and global economies. Currently, no specific treatment for SARS-CoV-2 infection has been identified; however, certain drugs have shown apparent efficacy in viral inhibition of the disease. Natural substances such as herbs and mushrooms have previously demonstrated both great antiviral and anti-inflammatory activity. Thus, the possibilities of natural substances as effective treatments against COVID-19 may seem promising. One of the potential candidates against the SARS-CoV-2 virus may be Inonotus obliquus (IO), also known as chaga mushroom. IO commonly grows in Asia, Europe and North America and is widely used as a raw material in various medical conditions. In this review, we have evaluated the most effective herbs and mushrooms, in terms of the antiviral and anti-inflammatory effects which have been assessed in laboratory conditions.
1. COVID-19 SARS-CoV-2 Infection
The novel coronavirus, SARS-CoV-2, causes severe acute respiratory syndrome and has quickly become a serious threat to public health [1]. Since the initial cases were reported in Wuhan, China, the virus has quickly spread globally, affecting more than 200 countries. As to date, over 20,046,642 cases have been identified with more than 734,525 deaths being reported [2]. Coronaviruses are enveloped positive-sense single-stranded RNA viruses, that primarily target the human respiratory system. The viruses have been shown to cause disease in both animals and humans [3]. Coronaviruses have either a round or elliptical form with an approximate diameter of 60–140 nm [4]. Coronaviruses belong to the Coronaviridae family, of which there are four subgroups: alpha (α), beta (ß), gamma (γ) and delta (δ). Of these subgroups, ß-coronaviruses tend to cause the most severe disease and fatalities in human populations [5]. Over the past two decades, two highly pathogenic ß-coronaviruses have been identified in humans, including severe acute respiratory syndrome (SARS-CoV-1) from 2002 to 2003, and the most recent Middle East respiratory syndrome (MERS-CoV) which was first identified in 2012 [6]. Based on its genomic structure and phylogenetic relationships, the novel coronavirus SARS-CoV-2 has also been identified as a ß-coronavirus. The coronavirus genome is comprised of approximately 30,000 nucleotides and is enclosed in a lipid envelope. A typical coronavirus contains around six open reading frames (ORFs) within its genome. Two-thirds of viral RNA, mainly located in the ORF 1a/b, encode for 16 non-structure proteins. The rest of the virus genome encodes for structural and accessory proteins associated with the virus [7]. Four main structural proteins are encoded by ORFs 10 and 11, these include a spike (S) protein, an envelope (E) protein, a membrane (M) protein, as well as the nucleocapsid (N) protein [8]. The N protein is bound to the virus single-positive strand RNA and allows the virus to hijack host cells. The N protein also coats the viral RNA genome and has also been shown to play an important role in viral replication and transcription. The M protein is thought to act as a central organiser for coronavirus assembly and is also the most abundant protein on the viral surface. The E protein is a membrane protein composed of approximately 76 to 109 amino-acids, and the protein plays an important role in virus–host cell interaction and virus assembly [9]. Despite displaying similarities with the other human ß-coronaviruses, SARS-CoV-2 possesses many differences in its genomic and phenotypic structure which greatly influences the pathogenesis of SARS-CoV-2 [8,10].
Coronaviruses have been described as zoonotic infections, with alpha and beta coronaviruses found primarily in mammals such as bats whereas gamma and delta are more common in pigs and birds. Additionally, investigations into the previous coronavirus outbreaks found that SARS-CoV1 was transmitted from bats to humans and MERS-CoV from dromedary camels to humans [5]. Much like its predecessors, SARS-CoV-2 has also proven to be successful in making its transmission from an animal host to humans. Many efforts have been made in order to identify the reservoir host or the intermediate host for the novel coronavirus. Despite the fact the exact origin of SARS-CoV-2 is yet to be identified, genomic analysis of SARS-CoV-2 has shown 88% similarity between two severe acute respiratory syndromes (SARS)-like coronaviruses derived from bats, thus demonstrating that SARS-CoV-2 could have evolved from a coronavirus of bat origin [3,10,11]. However, there have also been other reports linking SARS-CoV-2 to snakes and even pangolins [3].
The primary mode of human to human transmission of SARS-CoV-2 has been identified to be through respiratory droplets [12]. Once the virus has gained entry into a human host, reports have shown that SARS-CoV-2 infects cells using receptor-mediated endocytosis via the membrane-bound aminopeptidase angiotensin-converting enzyme II receptor (ACE2). Studies have shown that the primary target for this novel virus seems to be the lung alveolar epithelial cells, which ultimately results in the manifestation of respiratory symptoms [11]. Additionally, a recent study has shown that SARS-CoV-2 exhibits a 10-fold higher affinity for the ACE2 receptor, thus explaining its high transmission rate compared to that of both SARS-CoV1 [13].
COVID-19 symptoms appear after an incubation period of around 2–14 days. The duration from the onset of symptoms to death has ranged from 6 to 41 days. However, this duration is dependent on both the age of the patient and the status of their immune system [11]. Patients over 70 years of age seem to be more susceptible to this virus, probably as a result of a weaker immune system [14]. SARS-CoV-2 infection has been associated with many symptoms and clinical signs. However, based on hospitalised data, patients mainly exhibited symptoms of acute respiratory distress syndrome, associated with pyrexia, cough, fever and fatigue [14]. Additionally, one study found that approximately 80% of patients reported being asymptomatic or with mild symptoms (n = 19). The remaining 20% of cases, however, were more critical and severe [15]. COVID-19 has shown similar clinical presentations to that of its predecessors; however, in contrast to SARS-CoV and MERS-CoV, COVID-19 seems to have a lower fatality rate [3]. Despite there being limited information regarding the innate immune response of patients with COVID-19, most studies have shown that patients often develop lymphopenia [16]. A recent study investigating 99 patient cases in Wuhan demonstrated an increase in neutrophils (38%), lymphopenia (35%), increased IL-6 (52%) as well as an increase in C- reactive protein in 84% of cases [16]. Moreover, this increase in neutrophils and a decrease in lymphocytes have proven to directly correlate with both disease severity and fatality [16]. In addition, patients who had severe SARS-CoV-2 infection also presented with high levels of pro-inflammatory cytokines such as IL-7, IL-10, IL-2, G-CSF, MCP-1, MIP-1A and TNFα. These findings correlate with the clinical profile of SARS-CoV-1 and MERS-CoV, thus suggesting that lymphopenia and the presence of a cytokine storm contributed to the pathogenesis of SARS-CoV-2 [17].
Due to the increasing number of human casualties, research has focused on understanding the nature of the disease in order to develop effective treatments. Currently, no specific treatment has been identified for COVID-19. The race to develop a preventive vaccine is still ongoing, with many still in the early stages of clinical trials. Therefore, there is a dire need to develop an effective antiviral with enhanced efficacy for the prophylaxis and treatment of coronavirus infection. Various medications have now been identified and developed as a means for controlling and suppressing inflammatory crises such as steroids, nonsteroidal anti-inflammatory drugs and immunosuppressants [18]. In practice, the goal is to develop a drug with the minimum effective dose, which has increased efficacy. However, developing such medications often means that they are associated with adverse side effects such as ulceration, gastric irritation, angioedema, hepatic failure, headache, haemolytic anaemia, hyperglycaemia and immunodeficiency-related problems, as well as others [18]. Therefore, the use of natural medicinal products that are generally considered safe as a form of alternative therapy to increase the pharmacological response with the lowest degree of unwanted side effects is now being considered [18]. There have been many reports regarding the use of natural substances isolated from medicinal plants as effective treatments against viral infections. Lin et al. (2014) summarised the antiviral capabilities of herbal medicines against several viral pathogens such as coronavirus, coxsackie virus, hepatitis B virus, hepatitis C virus, herpes simplex virus (HSV), human immunodeficiency virus (HIV), influenza virus and respiratory syncytial virus (RSV). In regard to coronaviruses, this review highlighted that naturally occurring triterpene glycosides, known as saikosaponins, isolated from medicinal plants such as Bupleurum spp., Heteromorpha spp. and Scrophularia exhibited great antiviral activity against human coronaviruses (Table 1). These naturally occurring compounds were able to effectively prevent early stages of coronavirus infection by affecting viral attachment and cell penetration. Moreover, many natural compounds such as myricetin, scutellarein and phenolic compounds from Isatis indigotica and Torreya nucifera have been identified as natural inhibitors against the number of coronavirus enzymes, including nsP13 helicase and 3CL protease [19]. The water extract from Houttuynia cordata has also been identified as another anti-coronavirus natural medicine, as it has been observed to both inhibit the viral 3CL protease and block the viral RNA-dependent RNA polymerase activity, thus displaying various antiviral mechanisms against SARS-CoV1 [20]. Based on the data presented, this mini-review aims to review the antiviral and the anti-inflammatory effects of natural herbs and mushrooms against viral infections (Table 2) as well as to provide an insight into the possibilities of using such natural as effective treatments against COVID-19.
Table 1.
Antiviral effects of several natural products against coronavirus.
Table 2.
The list of introduced medicinal herbs and mushrooms. (+ stands for the level activity, representing mild, moderate, severe and very severe respectively).
2. The Potential Use of Mushrooms and Herbs against SARS-CoV-2 Infection
Currently, no specific treatment for COVID-19 has been recognised; however, certain drugs have shown apparent efficacy in viral inhibition of the disease [15]. Using an artificial intelligence (AI) programme, a group of researchers found potential therapeutic candidates that could inhibit clathrin-mediated endocytosis and thus inhibit viral infection. Such drugs could be used as potential therapeutics against COVID-19 [21]. However, in the cases of such commercial medications, there is always an increased risk of the potential development of drug resistance, especially in the case of specific viral enzyme inhibitors. Therefore, there is an urgent need to discover novel antivirals that are cost-effective and exhibit enhanced efficacy for the management and control of viral infections when vaccines and standard therapies are unsuccessful [19]. Natural substances such as mushrooms and herbs have previously shown both great antiviral and anti-inflammatory activity and thus serve as excellent sources of novel antiviral treatments, hence the possibilities of natural substances as effective novel treatments against COVID-19 may seem promising [22].
5. Conclusions
Developing viruses such as Ebola virus (EBOV), Lassa virus (LASV), avian influenza virus H5N1 (AIV) and the more recent SARS-COV-2 virus are seen as global health concerns. Despite many advancements in science, no effective vaccine or specific therapy has been approved for humans against these viruses, and so there is an urgent need to develop therapeutic treatments against these threats [68]. Traditional Chinese medicine holds an exclusive position among the variety of traditional medicines because of its thousand-year history. The extracts described in this review have been proven to possess great antiviral activities, with a general consensus of low toxicity. In addition, compared to commercial pharmaceuticals, such medicinal herbs are readily available and much cheaper. With the current pandemic, many scientists have rushed to the development of a potential vaccine and therapeutic agent that is effective against COVID-19; however, herbal agents should not be overlooked. The data presented in this review show the promising effects many herbs and mushrooms have against a variety of viral infections. This review has highlighted the therapeutic potential of Inonotus obliquus as a natural antiviral treatment against SARS-COV-2. Earlier studies into this mushroom have laid the groundwork into the antiviral capabilities of Inonotus obliquus, however further research into characterising the bioactive ingredients, understanding the underlying mechanisms as well as assessing the efficacy and potential application in vivo should be encouraged in order to develop an effective antiviral treatment against COVID-19. Until the present time, there has not been much research regarding the potential of natural agents against COVID-19, thus opening the research into this field may unlock the potential such extracts may have against SARS-CoV-2.
Author Contributions
M.N. has written the review article, and F.S. and D.A. have edited the manuscript. All authors have read and agreed to the published version of the manuscript.
Funding
This research received no external funding.
Acknowledgments
First and foremost, we express our deepest gratitude to the doctors and nurses who work on the front line, battling each day against this COVID-19 pandemic. We thank the medical teams who, with each shift, risk their own lives to save those of their patients.
Conflicts of Interest
The authors declare no conflict of interest.
References
- Shereen, M.; Khan, S.; Kazmi, A.; Bashir, N.; Siddique, R. COVID-19 infection: Origin, transmission, and characteristics of human coronaviruses. J. Adv. Res. 2020, 24. [Google Scholar] [CrossRef] [PubMed]
- Worldometer. COVID-19 Coronavirus Pandemic; Worldometer: USA, 2020. [Google Scholar]
- Wang, L.-S.; Wang, Y.-R.; Ye, D.-W.; Liu, Q.-Q. A review of the 2019 Novel Coronavirus (COVID-19) based on current evidence. Int. J. Antimicrob. Agents 2020. [Google Scholar] [CrossRef] [PubMed]
- Cascella, M.; Rajnik, M.; Cuomo, A.; Dulebohn, S.C.; di Napoli, R. Features, Evaluation and Treatment Coronavirus (COVID-19). In StatPearls; StatPearls Publishing: Treasure Island, FL, USA, 2020. [Google Scholar]
- Velavan, T.P.; Meyer, C.G. The COVID-19 epidemic. Trop. Med. Int. Health 2020, 25, 278–280. [Google Scholar] [CrossRef] [PubMed]
- Milne-Price, S.; Miazgowicz, K.; Munster, V. The emergence of the Middle East Respiratory Syndrome coronavirus (MERS-CoV). Pathog. Dis. 2014, 71. [Google Scholar] [CrossRef] [PubMed]
- Guo, Y.R.; Cao, Q.D.; Hong, Z.S.; Tan, Y.Y.; Chen, S.D.; Jin, H.J.; Tan, K.S.; Wang, D.Y.; Yan, Y. The origin, transmission and clinical therapies on coronavirus disease 2019 (COVID-19) outbreak—An update on the status. Mil. Med. Res. 2020, 7, 11. [Google Scholar] [CrossRef] [PubMed]
- Mousavizadeh, L.; Ghasemi, S. Genotype and phenotype of COVID-19: Their roles in pathogenesis. J. Microbiol. Immunol. Infect. 2020. [Google Scholar] [CrossRef] [PubMed]
- Boopathi, S.; Poma, A.B.; Kolandaivel, P. Novel 2019 coronavirus structure, mechanism of action, antiviral drug promises and rule out against its treatment. J. Biomol. Struct. Dyn. 2020, 1–10. [Google Scholar] [CrossRef] [PubMed]
- Wrobel, A.G.; Benton, D.J.; Xu, P.; Roustan, C.; Martin, S.R.; Rosenthal, P.B.; Skehle, J.J.; Gamblin, S.J. SARS-CoV-2 and bat RaTG13 spike glycoprotein structures inform on virus evolution and furin-cleavage effects. Nat. Struct. Mol. Biol. 2020, 27, 763–767. [Google Scholar] [CrossRef]
- Rothan, H.A.; Byrareddy, S.N. The epidemiology and pathogenesis of coronavirus disease (COVID-19) outbreak. J. Autoimmun. 2020. [Google Scholar] [CrossRef]
- Rothe, C.; Schunk, M.; Sothmann, P.; Bretzel, G.; Froeschl, G.; Wallrauch, C.; Zimmer, T.; Thiel, V.; Janke, C.; Guggemos, W.; et al. Transmission of 2019-nCoV Infection from an Asymptomatic Contact in Germany. N. Engl. J. Med. 2020. [Google Scholar] [CrossRef]
- Wrapp, D.; Nianshuang, W.; Corbett, K.; Goldsmith, J.; Hsieh, C.-L.; Abiona, O.; Graham, B.; Mclellan, J. Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation. Science 2020, 367, eabb2507. [Google Scholar] [CrossRef] [PubMed]
- Chen, N.; Zhou, M.; Dong, X.; Qu, J.; Gong, F.; Han, Y.; Qiu, Y.; Wang, J.; Wei, Y.; Xia, J.A.; et al. Epidemiological and clinical characteristics of 99 cases of 2019 novel coronavirus pneumonia in Wuhan, China: A descriptive study. Lancet 2020, 395, 507–513. [Google Scholar] [CrossRef]
- Huang, C.; Wang, Y.; Li, X.; Ren, L.; Zhao, J.; Hu, Y.; Zhang, L.; Fan, G.; Xu, J.; Gu, X.; et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China. Lancet 2020, 395. [Google Scholar] [CrossRef]
- Zhou, P.; Yang, X.; Wang, X.-G.; Hu, B.; Zhang, L.; Zhang, W.; Si, H.-R.; Zhu, Y.; Li, B.; Huang, C.-L.; et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin. Nature 2020, 579. [Google Scholar] [CrossRef] [PubMed]
- Prompetchara, E.; Ketloy, C.; Palaga, T. Immune responses in COVID-19 and potential vaccines: Lessons learned from SARS and MERS epidemic. Asian Pac. J. Allergy Immunol. 2020, 38. [Google Scholar] [CrossRef]
- Bagad, A.S.; Joseph, J.A.; Bhaskaran, N.; Agarwal, A. Comparative Evaluation of Anti-Inflammatory Activity of Curcuminoids, Turmerones, and Aqueous Extract of Curcuma longa. Adv. Pharmacol. Sci. 2013, 2013, 805756. [Google Scholar] [PubMed]
- Lin, L.T.; Hsu, W.C.; Lin, C.C. Antiviral natural products and herbal medicines. J. Tradit. Complement Med. 2014, 4, 24–35. [Google Scholar] [CrossRef]
- Lau, K.M.; Lee, K.M.; Koon, C.M.; Cheung, C.S.F.; Lau, C.P.; Ho, H.M.; Lee, M.Y.-H.; Au, S.W.-N.; Cheng, C.H.-K.; Lau, C.B.-S.; et al. Immunomodulatory and anti-SARS activities of Houttuynia cordata. J. Ethnop. 2008, 118, 79–85. [Google Scholar] [CrossRef]
- Stebbing, J.; Phelan, A.; Griffin, I.; Tucker, C.; Oechsle, O.; Smith, D.; Richardson, P. COVID-19: Combining antiviral and anti-inflammatory treatments. Lancet Infect. Dis. 2020, 20. [Google Scholar] [CrossRef]
- Lindequist, U.; Niedermeyer, T.H.J.; Julich, W.D. The pharmacological potential of mushrooms. Evid. Based Complement. Alternat. Med. 2005, 2, 285–299. [Google Scholar] [CrossRef]
- Jassim, S.A.A.; Naji, M.A. Novel antiviral agents: A medicinal plant perspective. J. Appl. Microbiol. 2003, 95, 412–427. [Google Scholar] [CrossRef] [PubMed]
- Chen, Y.; Zhang, X.; Guo, Q.; Cao, L.; Qin, Q.; Li, C.; Zhao, M.; Wang, W. Plant morphology, physiological characteristics, accumulation of secondary metabolites and antioxidant activities of Prunella vulgaris L. under UV solar exclusion. Biol. Res. 2019, 52, 17. [Google Scholar] [CrossRef]
- Wang, S.J.; Wang, X.H.; Dai, Y.Y.; Ma, M.H.; Rahman, K.; Nian, H.; Zhang, H. Prunella vulgaris: A Comprehensive Review of Chemical Constituents, Pharmacological Effects and Clinical Applications. Curr. Pharm. Des. 2019, 25, 359–369. [Google Scholar] [CrossRef] [PubMed]
- Bai, Y.; Xia, B.; Xie, W.; Zhou, Y.; Xie, J.; Li, H.; Liao, D.; Lin, L.; Li, C. Phytochemistry and pharmacological activities of the genus Prunella. Food Chem. 2016, 204, 483–496. [Google Scholar] [CrossRef]
- Fisher, R. The English Names of Our Commonest Wild Flowers; T. Buncle & Co.: Arbroath, UK, 1932. [Google Scholar]
- Zhang, X.; Ao, Z.; Bello, A.; Ran, X.; Liu, S.; Wigle, J.; Kobinger, G.; Yao, X. Characterization of the inhibitory effect of an extract of Prunella vulgaris on Ebola virus glycoprotein (GP)-mediated virus entry and infection. Antivir. Res. 2016, 127, 20–31. [Google Scholar] [CrossRef] [PubMed]
- Chiu, L.; Zhu, W.; Ooi, V. A polysaccharide fraction from medicinal herb Prunella vulgaris downregulates the expression of herpes simplex virus antigen in Vero cells. J. Ethnopharmacol. 2004, 93, 63–68. [Google Scholar] [CrossRef]
- Zhang, Y.; But, P.; Ooi, V.; Xu, H.-X.; Delaney, G.; Lee, S.; Lee, S. Chemical properties, mode of action, and in vivo anti-herpes activities of a lignin-carbohydrate complex from Prunella vulgaris. Antivir. Res. 2007, 75, 242–249. [Google Scholar] [CrossRef]
- Audet, J.; Wong, G.; Wang, H.; Lu, G.; Gao, G.F.; Kobinger, G.; Qiu, X. Molecular characterization of the monoclonal antibodies composing ZMAb: A protective cocktail against Ebola virus. Sci. Rep. 2014, 4, 6881. [Google Scholar] [CrossRef]
- Qiu, X.; Alimonti, J.; Melito, P.; Fernando, L.; Stroeher, U.; Jones, S. Characterization of Zaire ebolavirus glycoprotein-specific monoclonal antibodies. Clin. Immunol. 2011, 141, 218–227. [Google Scholar] [CrossRef]
- Qiu, X.; Wong, G.; Audet, J.; Bello, A.; Fernando, L.; Alimonti, J.B.; Fausther-Bovendo, H.; Wei, H.; Aviles, J.; Hiatt, E.; et al. Reversion of advanced Ebola virus disease in nonhuman primates with ZMapp. Nature 2014, 514, 47–53. [Google Scholar] [CrossRef]
- Fang, Y.; Zhang, L.; Feng, J.; Lin, W.; Cai, Q.; Peng, J. Spica Prunellae extract suppresses the growth of human colon carcinoma cells by targeting multiple oncogenes via activating miR-34a. Oncol. Rep. 2017, 38, 1895–1901. [Google Scholar] [CrossRef] [PubMed]
- Ma, F.-W.; Kong, S.-Y.; Tan, H.-S.; Wu, R.; Xia, B.; Zhou, Y.; Xu, H.-X. Structural characterization and antiviral effect of a novel polysaccharide PSP-2B from Prunellae Spica. Carbohydr. Polym. 2016, 152, 699–709. [Google Scholar] [CrossRef] [PubMed]
- EL-Saber Batiha, G.; Beshbishy, A.M.; Wasef, L.W.; Elewa, Y.H.A.; Al-Sagan, A.A.; Abd El-Hack, M.E.; Taha, A.E.; Abd-Elhakim, Y.M.; Devkota, H.P. Chemical Constituents and Pharmacological Activities of Garlic (Allium sativum L.): A Review. Nutrients 2020, 12, 872. [Google Scholar] [CrossRef] [PubMed]
- Goncagul, G.; Ayaz, E. Antimicrobial effect of garlic (Allium sativum). Recent Pat. Antiinfect Drug. Discov. 2010, 5, 91–93. [Google Scholar] [CrossRef]
- Weber, N.; Andersen, D.; North, J.; Murray, B.; Lawson, L.; Hughes, B. In Vitro Virucidal Effects of Allium sativum (Garlic) Extract and Compounds. Planta Med. 1992, 58, 417–423. [Google Scholar] [CrossRef]
- Bayan, L.; Koulivand, P.H.; Gorji, A. Garlic: A review of potential therapeutic effects. Avicenna J. Phytomed. 2014, 4, 1–14. [Google Scholar]
- Tatarintsev, A.V.; Vrzhets, P.; Ershov, D.; Shchegolev, A.A.; Turgiev, A.; Karamov, E.; Kornilaeva, G.; Makarova, T.; Fedorov, N.; Varfolomeev, S. The ajoene blockade of integrin-dependent processes in an HIV-infected cell system. Vestn. Ross. Akad. Meditsinskikh Nauk/Ross. Akad. Meditsinskikh Nauk 1992, 6–10. [Google Scholar]
- Mao, Q.-Q.; Xu, X.-Y.; Cao, S.-Y.; Gan, R.-Y.; Corke, H.; Beta, T.; Li, H.-B. Bioactive Compounds and Bioactivities of Ginger (Zingiber officinale Roscoe). Foods 2019, 8, 185. [Google Scholar] [CrossRef]
- Aboubakr, H.; Nauertz, A.; Luong, N.; Agrawal, S.; El-Sohaimy, S.; Youssef, M.; Goyal, S. In Vitro Antiviral Activity of Clove and Ginger Aqueous Extracts against Feline Calicivirus, a Surrogate for Human Norovirus. J. Food Prot. 2016, 79, 1001–1012. [Google Scholar] [CrossRef]
- Chang, J.; Wang, K.; Yeh, C.; Shieh, D.; Chiang, L.-C. Fresh ginger (Zingiber officinale) has anti-viral activity against human respiratory syncytial virus in human respiratory tract cell lines. J. Ethnopharmacol. 2012, 145, 146–151. [Google Scholar] [CrossRef]
- Seo, S.H.; Webster, R. Tumor Necrosis Factor Alpha Exerts Powerful Anti-Influenza Virus Effects in Lung Epithelial Cells. J. Virol. 2002, 76, 1071–1076. [Google Scholar] [CrossRef] [PubMed]
- Rasool, A.; Khan, M.-U.-R.; Ali, M.; Anjum, A.; Ahmed, I.; Aslam, A.; Rafique, G.; Masood, S.; Nawaz, M. Anti-Avian influenza virus H9N2 activity of aqueous extracts of Zingiber officinalis (Ginger) & Allium sativum (Garlic) in chick embryos. Pak. J. Pharm. Sci. 2017, 30, 1341–1344. [Google Scholar] [PubMed]
- Money, N.P. Are mushrooms medicinal? Fungal. Biol. 2016, 120, 449–453. [Google Scholar] [CrossRef]
- Vilček, J.; Le, J. Interferon γ. In Encyclopedia of Immunology, 2nd ed.; Delves, P.J., Ed.; Elsevier: Oxford, UK, 1998. [Google Scholar]
- Ren, G.; Xu, L.; Lu, T.; Yin, J. Structural characterization and antiviral activity of lentinan from Lentinus edodes mycelia against infectious hematopoietic necrosis virus. Int. J. Biol. Macromol. 2018, 115. [Google Scholar] [CrossRef] [PubMed]
- He, Y.; Li, X.; Hao, C.; Zeng, P.; Zhang, M.; Liu, Y.; Chang, Y.; Zhang, L. Grifola frondosa polysaccharide: A review of antitumor and other biological activity studies in China. Discov. Med. 2018, 25, 159–176. [Google Scholar] [PubMed]
- Gu, C.-Q.; Li, J.W.; Chao, F.; Jin, M.; Wang, X.-W.; Shen, Z.-Q. Isolation, identification and function of a novel anti-HSV-1 protein from Grifola frondosa. Antivir. Res. 2007, 75, 250–257. [Google Scholar] [CrossRef]
- Gu, C.-Q.; Li, J.W.; Chao, F.-H. Inhibition of hepatitis B virus by D-fraction from Grifola frondosa: Synergistic effect of combination with interferon-α in HepG2 2.2.15. Antivir. Res. 2006, 72, 162–165. [Google Scholar] [CrossRef]
- Nanba, H.; Kodama, N.; Schar, D.; Turner, D. Effects of Maitake (Grifola frondosa) glucan in HIV-infected patients. Mycoscience 2000, 41, 293–295. [Google Scholar] [CrossRef]
- Abu-serie, M.M.; Habashy, N.H.; Attia, W.E. In vitro evaluation of the synergistic antioxidant and anti-inflammatory activities of the combined extracts from Malaysian Ganoderma lucidum and Egyptian Chlorella vulgaris. BMC Complement. Altern. Med. 2018, 18, 154. [Google Scholar] [CrossRef]
- Hyun, K.; Jeong, S.; Lee, D.; Park, J.; Lee, J. Isolation and characterization of a novel platelet aggregation inhibitory peptide from the medicinal mushroom, Inonotus obliquus. Peptides 2006, 27, 1173–1178. [Google Scholar] [CrossRef]
- Pan, H.-H.; Yu, X.-T.; Li, T.; Wu, H.-L.; Jiao, C.-W.; Cai, M.-H.; Li, X.-M.; Xie, Y.-Z.; Wang, Y.; Peng, T. Aqueous Extract from a Chaga Medicinal Mushroom, Inonotus obliquus (Higher Basidiomyetes), Prevents Herpes Simplex Virus Entry Through Inhibition of Viral-Induced Membrane Fusion. Int. J. Med. Mushrooms 2013, 15, 29–38. [Google Scholar] [CrossRef] [PubMed]
- Shibnev, V.A.; Mishin, D.V.; Garaev, T.M.; Finogenova, N.P.; Botikov, A.G.; Deryabin, P.G. Antiviral activity of Inonotus obliquus fungus extract towards infection caused by hepatitis C virus in cell cultures. Bull. Exp. Biol. Med. 2011, 151, 612–614. [Google Scholar] [CrossRef] [PubMed]
- Lemieszek, M.; Langner, E.; Kaczor, J.; Kandefer-Szerszeń, M.; Sanecka, B.; Mazurkiewicz, W.; Rzeski, W. Anticancer Effects of Fraction Isolated from Fruiting Bodies of Chaga Medicinal Mushroom, Inonotus obliquus (Pers.:Fr.) Pilát (Aphyllophoromycetideae): In Vitro Studies. Int. J. Med. Mushrooms 2011, 13, 131–143. [Google Scholar] [CrossRef] [PubMed]
- Glamoclija, J.; Ciric, A.; Nikolic, M.; Fernandes, A.; Barros, L.; Calhelha, R.; Ferreira, I.; Soković, M.; van Griensven, L. Chemical characterization and biological activity of Chaga (Inonotus obliquus), a medicinal “mushroom”. J. Ethnopharmacol. 2015, 162. [Google Scholar] [CrossRef] [PubMed]
- Filippova, E.I.; Mazurkova, N.A.; Kabanov, A.S.; Teplyakova, T.V.; Ibragimova, Z.B.; Makarevich, E.V.; Mazurkov, O.Y.; Shishkina, L.N. Antiviral properties of aqueous extracts isolated from higher basidiomycetes as respect to pandemic influenza virus a(IIIIII)2009. Biol. Sci. 2013. [Google Scholar] [CrossRef]
- Moro, C.; Palacios, I.; Lozano, M.; D’arrigo, M.; Guillamón, E.; Villares, A.; Martínez, J.A.; García-Lafuente, A. Anti-inflammatory activity of methanolic extracts from edible mushrooms in LPS activated RAW 264.7 macrophages. Food Chem. 2012, 130, 350–355. [Google Scholar] [CrossRef]
- Najafzadeh, M.; Reynolds, P.D.; Baumgartner, A. Chaga mushroom extract inhibits oxidative DNA damage in lymphocytes of patients with inflammatory bowel disease. Biofactors 2007, 31, 191–200. [Google Scholar] [CrossRef]
- Van, Q.; Nayak, B.; Reimer, M.; Jones, P.; Fulcher, R.; Rempel, C.B. Anti-inflammatory effect of Inonotus obliquus, Polygala senega L., and Viburnum trilobum in a cell screening assay. J. Ethnopharmacol. 2009, 125, 487–493. [Google Scholar] [CrossRef]
- Chen, Y.-F.; Zheng, J.-J.; Qu, C.; Xiao, Y.; Li, F.-F.; Jin, Q.-X.; Li, H.-H.; Meng, F.-P.; Jin, G.-H.; Jin, D. Inonotus obliquus polysaccharide ameliorates dextran sulphate sodium induced colitis involving modulation of Th1/Th2 and Th17/Treg balance. Artif. Cells Nanomed. Biotechnol. 2019, 47, 757–766. [Google Scholar] [CrossRef]
- Lee, I.-K.; Kim, Y.-S.; Jang, Y.-W.; Jung, J.-Y.; Yun, B.-S. New antioxidant polyphenols from the medicinal mushroom Inonotus obliquus. Bioorganic Med. Chem. Lett. 2008, 17, 6678–6681. [Google Scholar] [CrossRef]
- Ma, L.; Chen, H.; Dong, P.; Lu, X. Anti-inflammatory and anticancer activities of extracts and compounds from the mushroom Inonotus obliquus. Food Chem. 2013, 139, 503–508. [Google Scholar] [CrossRef] [PubMed]
- Shibnev, V.A.; Garaev, T.M.; Finogenova, M.P.; Kalnina, L.B.; Nosik, D.N. Antiviral activity of aqueous extracts of the birch fungus Inonotus obliquus on the human immunodeficiency virus. Vopr. Virusol. 2015, 60, 35–38. [Google Scholar] [PubMed]
- Aras, A.; Gohar Khalid, S.; Jabeen, S.; Farooqi, A.; Xu, B. Regulation of cancer cell signaling pathways by mushrooms and their bioactive molecules: Overview of the journey from benchtop to clinical trials. Food Chem. Toxicol. Int. J. Publ. Br. Ind. Biol. Res. Assoc. 2018. [Google Scholar] [CrossRef] [PubMed]
- Li, B.Y.; Hu, Y.; Li, J.; Shi, K.; Shen, Y.F.; Zhu, B.; Wang, G.X. Ursolic acid from Prunella vulgaris L. efficiently inhibits IHNV infection in vitro and in vivo. Virus Res. 2019, 273, 197741. [Google Scholar] [CrossRef] [PubMed]
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