Close

Current Research in Nutrition and Food Science - An open access, peer reviewed international journal covering all aspects of Nutrition and Food Science

lock and key

Sign in to your account.

Account Login

Forgot your password?

Possible Prophylactic and Therapeutic Foods for Prevention and Management Of COVID-19- An Updated Review

Sumia Mohammad Enani*

Department of Food and Nutrition, King Abdul Aziz University, Jeddah, Saudi Arabia.

Corresponding Author Email: senani@kau.edu.sa

DOI : https://dx.doi.org/10.12944/CRNFSJ.8.3.02

Article Publishing History

Received: 14/5/2020

Accepted: 26/9/2020

Plagiarism Check: Yes

Reviewed by: Dr.Pragya Mishra India

Second Review by: Dr.Kamaliya keshav India

Final Approval by: Dr. Nurul Huda

Article Metrics

Views  


PDF Download  PDF Downloads: 1175
Abstract:

Coronavirus disease 2019 (COVID-19), caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), has resulted in an outbreak that is spreading globally. In the absence of a vaccine or effective treatment, improving the body's immune response to combat the virus, or, at least alleviate its health complications, becomes imperative. Potential prophylactic and therapeutic food interventions using black seed, garlic, honey, wasabi and high vit C foods have been proposed in various studies on previous coronaviruses, SARS-CoV and Middle East Respiratory Syndrome Coronavirus (MERS-CoV). Due to the high similarity in the three dimensional structure between SARS-CoV-2 and SARS-CoV, studies that reported antiviral action of certain foods against various viruses including SARS-CoV and MERS-CoV have been discussed in this short review.

Keywords:

Antiviral; Coronavirus; COVID-19; SARS-Cov-2.

Download this article as: 

Copy the following to cite this article:

Enani S. M. Possible Prophylactic and Therapeutic Foods for Prevention and Management Of COVID-19- An Updated Review. Curr Res Nutr Food Sci 2020; 8(3). doi : http://dx.doi.org/10.12944/CRNFSJ.8.3.02


Copy the following to cite this URL:

Enani S. M. Possible Prophylactic and Therapeutic Foods for Prevention and Management Of COVID-19- An Updated Review. Curr Res Nutr Food Sci 2020; 8(3). https://bit.ly/2IJMrVy


Introduction

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a novel single‐stranded positive‐sense RNA β-coronavirus. It is associated with a recent outbreak of coronavirus disease 2019 (COVID-19), which was discovered to be highly contagious, and rapidly spreading, hence forcing the world health organization to declare a global health emergency 1,2. There are no registered medications or vaccines for COVID-19 so far. This raises the demand to seek alternative natural and safe solutions to prevent COVID-19 spread, or at least help to manage active cases.

A recent review has suggested that optimal host nutritional status plays a vital role in the immune system function, and is essential in limiting the impact of emerging viral infections 3, indicating that this acquired through maintaining a balanced diet in addition to supplementations of vitamins and minerals. In particular, this review highlighted the importance of vitamins C and D, zinc and omega-3 fatty acids in enhancing the immune defense 3. Suboptimal status of micronutrients can impair the innate immune system through the impairment of phagocytosis, microbial killing and altering cytokines production 4. It also can affect the adaptive immune system through decreasing the number of lymphocytes and reducing antibody responses 4.

During the past 20 years, two other coronaviruses, severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle-East respiratory syndrome coronavirus (MERS-CoV) have caused deadly types of pneumonia 5,6. Some previous in-vivo, in-vitro and laboratory mechanistic studies discovered some foods that have pharmaceutical components which were found to be affective against these as well as other viruses. These foods might be proposed as (which has an effect if administered after the disease onset) nutrients against Covid-19 as there is a high similarity in the three dimensional genetic structure between SARS-CoV-2 and SARS-CoV 7. In this short review, we will summarize the most important previous findings regarding possible prophylactic and therapeutic nutrient options for the prevention and management of COVID-19, in particular black seed, garlic, honey, wasabi, and vitamin C rich foods.

Black Seed Nigella Sativa

Black seed (Nigella sativa) has been used for decades for medical purposes. Its pharmacological effects are attributed to high content of quinines 8. is widely known as an anti-malarial, anti-inflammatory agent 9 and as a potent antioxidant 10. In animal studies, black seed oil has been shown to provide protective action against murine cytomegalovirus infection in mice through increasing number and activity of macrophages,  and interferon (IFN)-gamma production 11. Black seed oil also showed complete inhibition of virus titers in spleen and liver of mice on the third day of infection, while the titers remained unchanged in the control mice 11. Furthermore, In a study on poultry birds, namely turkeys infected with influenza virus (H9N2), it was noted that feeding with black seeds has enhanced the immune response by increasing the production of IFN-gamma and hemagglutinin-inhibition (HI) titers,  which significantly suppressed the pathogenicity and clinical signs of H9N2 12. Moreover, in laboratory studies, black seed at concentration of 35μM has shown good antiviral effects in Chicken Embryo Rough Cells (CER) infected with Laryngotrachietis Virus (ILTV) 13.

Human studies provided further evidence to the efficacy of black seed against viral infections. Results from a clinical trial indicated that the administration of 450mg of black seed three times daily for 3 months decreased viral load and oxidative stress in patients infected with Hepatitis C virus (HCV), and that the dose was tolerable and safe 14. In addition, a case study on an HIV-positive patient reported that daily administration of 10mls two times daily of black seed concoction for 6 months resulted in both the disappearance of symptoms associated with HIV as measured by absolute count of CD4 cells, and viral load  as measured in (HIV-RNA) copies per ml in blood in a gradual, and duration dependent manner, thus resulting in the patient becoming sero-negative for HIV 15.

Studies indicated that thymoquinone, found at a concentration of 3.5-8.7 mg/g in fixed oil, is one of the most active constituents in black seed oil 8,16. Very recent studies suggested that the modified forms of quinines, chloroquine, and hydroxychloroquine, a derivative of  thymoquinone, were potent inhibitors of SARS coronavirus infection at clinically admissible concentrations through interfering with angiotensin-converting enzyme 2 (ACE2) receptor which is one of cell surface binding sites for S protein of SARS‐CoV that the virus uses for entry into human cells as revealed by docking simulation technique 17,18. This interference was proposed to result in the elevation of vesicular pH, which in turn, inhibits the viral spreading of SARS‐CoV to uninfected cells 17. Therefore, black seed might be a possible prophylactic and therapeutic option for COVID-19.  However, its efficacy still needs to be confirmed by well-designed and controlled clinical trials.

Garlic

Garlic (Allium sativum L.) has been widely used in traditional alternative medicine prescriptions. Various healing, and health enhancing effects of garlic have also been reported in more recent reviews of in-vitro, in-vivo and clinical studies. Reported effects included: , and –viral,  as well as anti-carcinogenic activities that were associated with improvement in respiration and digestion processes during infections, treatment of infectious diseases, and decrease of symptoms of non-communicable diseases 19,20.

Many of the biological effects of garlic are attributed to its organosulfur constitutes, with the strength of its biological activities depending on the number of sulfur atoms 21–24. Allyl disulfide and allyl trisulfide account for more than 50% in content of garlic essential oil 20.

Garlic is considered one of the richest vegetable sources of total phenolic compounds that contribute to its antioxidant action 25,26. Previous reviews reported different antioxidant activities of garlic including radicals trapping, scavenging of hydroxyl radicals, interaction with thiol containing proteins, inhibition of superoxide and nitric oxide production and modification of SH-dependent activities 25–29. This strong antioxidant action has been suggested to attribute to the therapeutic properties of garlic including antimicrobial, anti-carcinogenic and anti-aging properties 30. Sulfer-containing compounds which are present in essential oil extracts of garlic have been reported to exert marked antimicrobial activities against wide range of bacteria and fungi which led to the suggestion of the use of garlic as natural antimicrobial additive in food products 26,31. Garlic’s mechanism of antimicrobial action is suggested to be the ability to inhibit thiol-containing enzymes and other bacterial enzymes such as those involved in the acetyl-CoA-forming system which cause severe damage in the microorganism tissues 31.

In-vitro laboratory studies reported that garlic showed antiviral activities against influenza A and B 32, cytomegalovirus 33,34, rhinovirus 35, HIV 35, herpes simplex virus 1 35 and 2 24, viral pneumonia, and rotavirus 35,36, and were suggested to be strong potent inhibitors of SARS-CoV-2 coronavirus 22. The anticoronavirus suggested mechanism was through the inhibition of ACE2 protein receptor, which leads to loss of the host receptor of the virus,  in addition to attacking the PDB6LU7 protein, which is a main protease of SARS-CoV-2 at the same time 22. These findings suggest that garlic has potential preventive and therapeutic properties against COVID-19, but this needs to be addressed further by clinical trials to obtain conclusive evidence.

Honey

For centuries, honey has been used in traditional medicine to treat many diseases. Its type varies depending on the bees species and the plants on which the bees feed on, which in turn influence its therapeutic value 37. Honey has been reported to possess anti-microbial and healing activities due to its phenolic and flavonoid constitutes 38. Furthermore, honey’s effective wound healing activities were attributed to its antibacterial, anti-inflammatory and cell growth-stimulating properties, as well as immunomodulatory properties and immune-boosting capabilities 39. In an in-vitro study on monocytic cell line, MonoMac-6 (MM6), honey was found to stimulate the immune system through inducing the maximal release of monocyte cytokines 40. Some types of honey exhibit a very high antimicrobial activity and so far, bacteria has not been able to develop resistance to the antibacterial components in these types of honey 41. For example, tualang (Koompassia excelsa) honey possess strong antimicrobial properties against many different microorganisms that are stronger than manuka (L. scoparium) honey in some cases 41.

In addition, anti-viral properties of honey in cell culture studies were reported against Rubella, Varicella Zoster and influenza viruses,  as the incubation of low concentrations of honey with infected cell lines resulted in viral plaque reduction and decreased viability of infected cells 42–44. honey were reported to have antiviral activity against influenza virus in a dose dependent manner, with manuka honey showing  the most potent viral-inhibitory activity 44. Indeed, Manuka honey also was reported to have a potential medicinal value in treating influenza due to its effective virucidal action against the virus at the pre-infection stage, as well as during and after infection by inhibiting viral replication and growth 44. Due to these antiviral mechanisms, honey may be proposed as a potential therapeutic agent against viral infections and their complications, including those caused by COVID-19. Indeed, the National Institute for Health and Care Excellence (NICE) guidelines suggest that honey can be used as a treatment for acute cough caused by upper respiratory tract infection which is currently a core symptom in COVID-19 disease 45. In the light of this, a current ongoing clinical trial has been established to investigate the efficacy of natural honey in treatment of patients infected with COVID-19 compared with current standard care 46.

Wasabi

is a unique traditional cruciferous Brassicaceae crop, that is close to the nasturtiums botanically and that grows on the wet banks of cool mountain streams and springs in Japan 47. Wasabi plant is rich in glucosinolates which become metabolized into isothiocyanates by the action of the myrosinase enzyme which is expressed in the cells of Brassicaceae plants 48. Several bioactive compounds were isolated from the wasabi roots including lignan glycosides, wasabisides and phenolic compounds 49.

Its extract have powerful pharmacological properties due to its isothioocyanate and sinigrin constitutes 50. Phenethyl isothiocyanate has been shown to have immunomodulatory effects on both the innate and specific immune systems of mice 51. Japanese wasabi was reported to have potent anti‐influenza activity as its ethanol extracts highly inhibited virus production of H1N1, H3N2 and B-Shamine influenza viral strains by more than 98%, regardless of the hemagglutinin antigen type in cell cultures 52. The same study reported that wasabi ethanol extract did not exhibit inhibitory effect on intracellular influenza virus synthesis or on the release of the virus from the cell surface as measured by the cytopathic effect of replicating infected cells. However, it suggested that the Japanese wasabi extract inhibited viral adsorption and entrance into cells which possibly occurs in the early phase of infection as measured by influenza virus titer and replication inhibition rate 52. These antiviral effects of wasabi suggests that it could be an alternative preventive, or therapeutic option for COVID-19. However, further controlled studies are needed to confirm its therapeutic value.

Vitamin C Containing Food

Respiratory viruses including influenza, rhino and corona are usually the main cause of common cold which usually results in respiratory symptoms 53–55. Various reviews reported that vitamin C deficiency increased the risk of severe respiratory infections such as pneumonia 56,57. A recent meta-analysis reported that administration of vitamin C lead to a significant reduction in the risk of pneumonia in individuals with low dietary intakes and that vitamin C reduced disease severity and risk of death in older patients with pneumonia especially in individuals with low plasma vitamin C level 58. A recent review concluded that vitamin C level is reduced in leukocytes and urine secretion during common cold episodes and that the administration of high doses of vitamin C during cold episodes reversed this reduction, suggesting that administration of high doses of vitamin C might accelerate the recovery process 56. Furthermore, various clinical trials reported that administration of high doses of vitamin C introduced orally or intravenously in hospitalized patients with acute respiratory infections resulted in returning of plasma vitamin C levels to normal, as well as decreased severity of the respiratory symptoms, and rapid clearance of chest in x-rays 59–61. Moreover, supplementation of Vitamin C has been shown to have both prophylactic and therapeutic values in reducing the duration and severity of upper respiratory tract infections 57,62. The prophylactic effect of vitamin C was reported to be more effective in people under enhanced physical stress 62. In addition, a clinical trial reported that vitamin C supplementation resulted in a greater reduction in “total days indoor” in individuals with low vitamin C dietary intake compared with higher intake suggesting that the therapeutic effect of vitamin C is more profound in individuals with low intake of vitamin C 63.  A recent review recommended that healthy individuals need to increase their daily intake of vitamin C to 200mg during outbreaks such as COVID-19 to protect themselves from the disease, and that sick individuals needs 1–2 g/day to restore normal blood levels 3. These levels are above the Recommended Dietary Allowances (RDA) but still within the US tolerable upper limit for adults 3. According to FoodData Central system of the United States Department of Agriculture, the top 5 foods highest in vitamin C are guavas, bell peppers, kiwi fruits, strawberries and oranges (Table 1) 64

Table 1: The Top 5 Foods Highest in Vitamin C.

Food Vitamin C (mg/cup) Number of cups to obtain 200 mg of vitamin C Number of cups to obtain 1g of vitamin C
Guavas 377 0.5 2.7
Bell peppers 190 1.1 5.3
Kiwi fruit 167 1.2 6.0
Strawberries 98 2.0 10.2
Oranges 96 2.1 10.4
Source 64

 

Since common cold is caused by viruses such as corona virus and vitamin C supplementation has been shown to decrease the duration and severity of common cold, it is worth investigating the prophylactic and therapeutic effects of vitamin C supplementation in the current Covid-19 outbreak.

The discussed prophylactic and therapeutic food intervention for COVID-19 was in accordance to studies on the previous coronaviruses, SARS-CoV and MERS-CoV, and studies that reported antiviral action of these food types. This approach was adopted partly due to the high similarity in the three dimensional structure between SARS-CoV-2 and SARS-CoV 7. The available evidence from previous studies that some components of the discussed food types may interfere with the binding sites of SARS-CoV-2 suggests that the consumption of these foods might protect from getting infected. However, more in-vitro studies that address the influence of discussed foods on all aspects of viral-host interaction, accompanied by longitudinal studies that evaluate the incidence rate of COVID-19 according to the consumption of these food are needed to confirm their prophylactic effect. Clinical studies that investigate the effect on rate of recovery, severity and duration of the disease, duration of lung inflammation and mortality rate in COVID-19 patients are also needed to confirm the therapeutic value of these food types.

Conclusion

Black seed, garlic, wasabi, honey, and vitamin C rich foods contain pharmacologically active components that make them possible prophylactic and therapeutic food interventions for COVID-19 in the absence of clearly indicated medications, and vaccines for this disease. More laboratory, longitudinal and clinical studies are required to confirm these medicinal values.

Acknowledgments

Acknowledgment to Prof. Suhad Bahijri for her help in reviewing the work.

Funding Sources

The author(s) received no financial support for the research, authorship, and/or publication of this article.

Conflict of Interest

The author declares no conflict of interest.

References

  1. WHO. Naming the coronavirus disease (COVID-19) and the virus that causes it. World Heal Organ. 2020:1. https://www.who.int/emergencies/diseases/novel-coronavirus-2019/technical-guidance/naming-the-coronavirus-disease-(covid-2019)-and-the-virus-that-causes-it. Accessed April 27, 2020.
  2. Chen Y, Liu Q, Guo D. Emerging coronaviruses: Genome structure, replication, and pathogenesis. J Med Virol. 2020;92(4):418-423. doi:10.1002/jmv.25681
    CrossRef.
  3. Calder PC, Carr AC, Gombart AF, Eggersdorfer M. Optimal Nutritional Status for a Well-Functioning Immune System Is an Important Factor to Protect against Viral Infections. Nutrients. 2020;12(4):1181. doi:10.3390/nu12041181
    CrossRef.
  4. Gombart AF, Pierre A, Maggini S. A review of micronutrients and the immune system–working in harmony to reduce the risk of infection. Nutrients. 2020;12(1). doi:10.3390/nu12010236
    CrossRef.
  5. Drosten C, Günther S, Preiser W, et al. Identification of a novel coronavirus in patients with severe acute respiratory syndrome. N Engl J Med. 2003;348(20):1967-1976. doi:10.1056/NEJMoa030747
    CrossRef.
  6. Ksiazek TG, Erdman D, Goldsmith CS, et al. A novel coronavirus associated with severe acute respiratory syndrome. N Engl J Med. 2003;348(20):1953-1966. doi:10.1056/NEJMoa030781
    CrossRef.
  7. Chan JF-W, Kok K-H, Zhu Z, et al. Genomic characterization of the 2019 novel human-pathogenic coronavirus isolated from a patient with atypical pneumonia after visiting Wuhan. Emerg Microbes Infect. 2020;9(1):221-236. doi:10.1080/22221751.2020.1719902
    CrossRef.
  8. Gupta B, Ghosh KK, Gupta RC. Thymoquinone. In: Nutraceuticals: Efficacy, Safety and Toxicity. Elsevier Inc.; 2016:541-550. doi:10.1016/B978-0-12-802147-7.00039-5
    CrossRef.
  9. F. Kuhlmann M, Fleckinstein JM. Infectious Diseases – Fourth Edition. Vol 2. 2nd ed. Elsevier Ltd; 2017. doi:10.1016/B978-0-7020-6285-8.00157-X
    CrossRef.
  10. Krishnaveni M, Suresh K, Rajasekar M. Antioxidant and free radical scavenging activity of triphala determined by using different in vitro models. J Med Plants Res. 2013;7(39):2898-2905. doi:10.5897/JMPR2013.5124
  11. Salem ML, Hossain MS. Protective effect of black seed oil from Nigella sativa against murine cytomegalovirus infection. Int J Immunopharmacol. 2000;22(9):729-740. doi:10.1016/S0192-0561(00)00036-9
    CrossRef.
  12. Umar S, Munir MT, Subhan S, et al. WITHDRAWN: Protective and antiviral activities of Nigella sativa against avian influenza (H9N2) in turkeys. J Saudi Soc Agric Sci. September 2016. doi:10.1016/j.jssas.2016.09.004
    CrossRef.
  13. Zaher KS, Ahmed W, Zerizer SN. Observations on the Biological Effects of Black Cumin Seed (Nigella sativa) and Green Tea (Camellia sinensis). Glob Vet. 2008;2(4):198-204. https://www.researchgate.net/publication/239591320_Observations_on_the_Biological_Effects_of_Black_Cumin_Seed_Nigella_sativa_and_Green_Tea_Camellia_sinensis. Accessed April 30, 2020.
  14. Barakat EMF, El Wakeel LM, Hagag RS. Effects of Nigella sativa on outcome of hepatitis C in Egypt. World J Gastroenterol. 2013;19(16):2529-2536. doi:10.3748/wjg.v19.i16.2529
    CrossRef.
  15. Onifade AA, Jewell AP, Adedeji WA. Nigella sativa concoction induced sustained seroreversion in HIV patient. African J Tradit Complement Altern Med. 2013;10(5):332-335.
    CrossRef.
  16. Lutterodt H, Luther M, Slavin M, et al. Fatty acid profile, thymoquinone content, oxidative stability, and antioxidant properties of cold-pressed black cumin seed oils. LWT – Food Sci Technol. 2010;43(9):1409-1413. doi:10.1016/j.lwt.2010.04.009
    CrossRef.
  17. Vincent MJ, Bergeron E, Benjannet S, et al. Chloroquine is a potent inhibitor of SARS coronavirus infection and spread. Virol J. 2005;2(1):69. doi:10.1186/1743-422X-2-69
    CrossRef.
  18. Omar S, Bouziane I, Bouslama Z, Djemel A. In-Silico Identification of Potent Inhibitors of COVID-19 Main Protease (Mpro) and Angiotensin Converting Enzyme 2 (ACE2) from Natural Products: Quercetin, Hispidulin, and Cirsimaritin Exhibited Better Potential Inhibition than Hydroxy-Chloroquine Against. doi:10.26434/CHEMRXIV.12181404.V1
    CrossRef.
  19. Al-Snafi AE. Pharmacological effects of Allium species grown in Iraq. An overview. Int J Pharm Heal care Res. 2013;1(4):132-155. www.ijphr.com. Accessed April 30, 2020.
  20. Bayan L, Koulivand PH, Gorji A. Garlic: a review of potential therapeutic effects. Avicenna J phytomedicine. 2014;4(1):1-14. doi:10.22038/ajp.2014.1741
  21. Dziri S, Casabianca H, Hanchi B, Hosni K. Composition of garlic essential oil ( Allium sativum L.) as influenced by drying method. J Essent Oil Res. 2014;26(2):91-96. doi:10.1080/10412905.2013.868329
    CrossRef.
  22. Thuy BTP, My TTA, Hai NTT, et al. Investigation into SARS-CoV-2 Resistance of Compounds in Garlic Essential Oil. ACS Omega. March 2020. doi:10.1021/acsomega.0c00772
    CrossRef.
  23. Hughes B, Murray B, North J, Lawson L. Antiviral Constituents from Allium sativum. Planta Med. 1989;55(01):114-114. doi:10.1055/s-2006-961894
    CrossRef.
  24. Weber ND, Andersen DO, North JA, Murray BK, Lawson LD, Hughes BG. In vitro virucidal effects of Allium sativum (garlic) extract and compounds. Planta Med. 1992;58(5):417-423. doi:10.1055/s-2006-961504
    CrossRef.
  25. Capasso A. Antioxidant Action and Therapeutic Efficacy of Allium sativum L. Molecules. 2013;18(1):690-700. doi:10.3390/molecules18010690
    CrossRef.
  26. Benkeblia N. Antimicrobial activity of essential oil extracts of various onions (Allium cepa) and garlic (Allium sativum). LWT – Food Sci Technol. 2004;37(2):263-268. doi:10.1016/j.lwt.2003.09.001
    CrossRef.
  27. Borlinghaus J, Albrecht F, Gruhlke M, Nwachukwu I, Slusarenko A. Allicin: Chemistry and Biological Properties. Molecules. 2014;19(8):12591-12618. doi:10.3390/molecules190812591
    CrossRef.
  28. Martins N, Petropoulos S, Ferreira ICFR. Chemical composition and bioactive compounds of garlic (Allium sativum L.) as affected by pre- and post-harvest conditions: A review. Food Chem. 2016;211:41-50. doi:10.1016/j.foodchem.2016.05.029
    CrossRef.
  29. Rahman MS. Allicin and Other Functional Active Components in Garlic: Health Benefits and Bioavailability. Int J Food Prop. 2007;10(2):245-268. doi:10.1080/10942910601113327
    CrossRef.
  30. Huang C-H, Hsu F-Y, Wu Y-H, et al. Analysis of lifespan-promoting effect of garlic extract by an integrated metabolo-proteomics approach. J Nutr Biochem. 2015;26(8):808-817. doi:10.1016/j.jnutbio.2015.02.010
    CrossRef.
  31. Ankri S, Mirelman D. Antimicrobial properties of allicin from garlic. Microbes Infect. 1999;1(2):125-129. doi:10.1016/S1286-4579(99)80003-3
    CrossRef.
  32. Fenwick GR, Hanley AB. Allium species poisoning. Vet Rec. 1985;116(1):28. doi:10.1136/vr.116.1.28
    CrossRef.
  33. Meng Y, Lu D, Guo N, Zhang L, Zhou G. Anti-HCMV effect of garlic components. Virol Sin. 1993;8:147-150.
  34. Guo N, Lu D, Woods GL, et al. Demonstration of the anti-viral activity of garlic extract against human cytomegalovirus in vitro. Chin Med J (Engl). 1993;106(2):93-96.
  35. Tsai Y, Cole LL, Davis LE, Lockwood SJ, Simmons V, Wild GC. Antiviral properties of garlic: in vitro effects on influenza B, herpes simplex and coxsackie viruses. Planta Med. 1985;51(5):460-461. doi:10.1055/s-2007-969553
    CrossRef.
  36. Nagai K. Experimental Studies on the Preventive Effect of Garlic Extract against Infection with Influenza Virus. J Japanese Assoc Infect Dis. 1973;47(9):321-325. doi:10.11150/kansenshogakuzasshi1970.47.321
    CrossRef.
  37. Kek SP, Chin NL, Tan SW, Yusof YA, Chua LS. Molecular identification of honey entomological origin based on bee mitochondrial 16S rRNA and COI gene sequences. Food Control. 2017;78:150-159. doi:10.1016/j.foodcont.2017.02.025
    CrossRef.
  38. Mandal MD, Mandal S. Honey: Its medicinal property and antibacterial activity. Asian Pac J Trop Biomed. 2011;1(2):154-160. doi:10.1016/S2221-1691(11)60016-6
    CrossRef.
  39. Molan P. Why honey is effective as a medicine: 2. The scientific explanation of its effects. Bee World. 2001;82(1):22-40. doi:10.1080/0005772X.2001.11099498
    CrossRef.
  40. Tonks AJ, Cooper RA, Jones KP, Blair S, Parton J, Tonks A. Honey stimulates inflammatory cytokine production from monocytes. Cytokine. 2003;21(5):242-247. doi:10.1016/S1043-4666(03)00092-9
    CrossRef.
  41. Tan HT, Rahman RA, Gan SH, et al. The antibacterial properties of Malaysian tualang honey against wound and enteric microorganisms in comparison to manuka honey. BMC Complement Altern Med. 2009;9(1):34. doi:10.1186/1472-6882-9-34
    CrossRef.
  42. Zeina B, Othman O, Al-Assad S. Effect of honey versus thyme on Rubella virus survival in vitro. J Altern Complement Med. 1996;2(3):345-348. doi:10.1089/acm.1996.2.345
    CrossRef.
  43. Shahzad A, Cohrs RJ. In vitro antiviral activity of honey against varicella zoster virus (VZV): A translational medicine study for potential remedy for shingles. Transl Biomed. 2012;3(2):2. https://www.ncbi.nlm.nih.gov/pubmed/22822475. Accessed May 3, 2020.
  44. Watanabe K, Rahmasari R, Matsunaga A, Haruyama T, Kobayashi N. Anti-influenza Viral Effects of Honey In Vitro: Potent High Activity of Manuka Honey. Arch Med Res. 2014;45(5):359-365. doi:10.1016/j.arcmed.2014.05.006
    CrossRef.
  45. NICE. Cough (acute): antimicrobial prescribing NICE guideline [NG120]. NICE Guidel. 2019. https://www.nice.org.uk/guidance/ng120/chapter/Summary-of-the-evidence. Accessed May 3, 2020.
  46. Efficacy of Natural Honey Treatment in Patients With Novel Coronavirus. https://clinicaltrials.gov/ct2/show/NCT04323345. Published 2020. Accessed May 3, 2020.
  47. Chadwick CI, Lumpkin TA, Elberson LR. The botany, uses and production ofWasabia japonica (Miq.) (Cruciferae) Matsum. Econ Bot. 1993;47(2):113-135. doi:10.1007/BF02862015
    CrossRef.
  48. Kim Y-J, Lee D-H, Ahn J, et al. Pharmacokinetics, Tissue Distribution, and Anti-Lipogenic/Adipogenic Effects of Allyl-Isothiocyanate Metabolites. Alisi A, ed. PLoS One. 2015;10(8):e0132151. doi:10.1371/journal.pone.0132151
    CrossRef.
  49. Kim CS, Subedi L, Kwon OW, et al. Wasabisides A–E, Lignan Glycosides from the Roots of Wasabia japonica. J Nat Prod. 2016;79(10):2652-2657. doi:10.1021/acs.jnatprod.6b00582
    CrossRef.
  50. Depree JA, Howard TM, Savage GP. Flavour and pharmaceutical properties of the volatile sulphur compounds of Wasabi (Wasabia japonica). Food Res Int. 1998;31(5):329-337. doi:10.1016/S0963-9969(98)00105-7
    CrossRef.
  51. Tsou M-F, Tien N, Lu C-C, et al. Phenethyl isothiocyanate promotes immune responses in normal BALB/c mice, inhibits murine leukemia WEHI-3 cells, and stimulates immunomodulations in vivo. Environ Toxicol. 2013;28(3):127-136. doi:10.1002/tox.20705
    CrossRef.
  52. Mochida K, Ogawa T. Anti‐influenza virus activity of extract of Japanese wasabi leaves discarded in summer. J Sci Food Agric. 2008;88(10):1704-1708. doi:10.1002/jsfa.3268
    CrossRef.
  53. Eccles R. Understanding the symptoms of the common cold and influenza. Lancet Infect Dis. 2005;5(11):718-725. doi:10.1016/S1473-3099(05)70270-X
    CrossRef.
  54. Turner R. The common cold. In: Mandell G, Bennet J, Dolin R, eds. Principles and Practice of Infectious Diseases. 7th ed. Philidelphia: Churchill Livingstone; 2010:809-814.
  55. Heikkinen T, Järvinen A. The common cold. Lancet. 2003;361(9351):51-59. doi:10.1016/S0140-6736(03)12162-9
    CrossRef.
  56. Carr AC, Maggini S. Vitamin C and immune function. Nutrients. 2017;9(11):1211. doi:10.3390/nu9111211
    CrossRef.
  57. Hemilä H. Vitamin C and infections. Nutrients. 2017;9(4). doi:10.3390/nu9040339
    CrossRef.
  58. Hemilä H, Louhiala P. Vitamin C for preventing and treating pneumonia. Cochrane Database Syst Rev. 2013;2013(8). doi:10.1002/14651858.CD005532.pub3
    CrossRef.
  59. Hunt C, Chakravorty NK, Annan G, Habibzadeh N, Schorah CJ. The Clinical Effects of Vitamin C Supplementation in Elderly Hospitalised Patients with Acute Respiratory Infections.
  60. Bharara A, Grossman C, Grinnan D, et al. Intravenous Vitamin C Administered as Adjunctive Therapy for Recurrent Acute Respiratory Distress Syndrome. Case Reports Crit Care. 2016;2016:1-4. doi:10.1155/2016/8560871
    CrossRef.
  61. Fowler III AA, Kim C, Lepler L, et al. Intravenous vitamin C as adjunctive therapy for enterovirus/rhinovirus induced acute respiratory distress syndrome. World J Crit Care Med. 2017;6(1):85. doi:10.5492/wjccm.v6.i1.85
    CrossRef.
  62. Hemilä H, Chalker E. Vitamin C for preventing and treating the common cold. Cochrane Database Syst Rev. 2013;2013(1). doi:10.1002/14651858.CD000980.pub4
    CrossRef.
  63. Anderson TW, Reid DB, Beaton GH. Vitamin C and the common cold: a double-blind trial. Can Med Assoc J. 1972;107(6):503-508.
  64. USDA. FoodData Central. US Department of Agriculture. https://fdc.nal.usda.gov/index.html. Published 2019. Accessed May 6, 2020.


Creative Commons License
This work is licensed under a Creative Commons Attribution 4.0 International License.