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Green Tea Catechins: Their Use in Treating and Preventing Infectious Diseases

Wanda C. Reygaert

BioMed Research International · 2018 · Review

doi:10.1155/2018/9105261

Abstract

Green tea is one of the most popular drinks consumed worldwide. Produced mainly in Asian countries from the leaves of the Camellia sinensis plant, the potential health benefits have been widely studied. Recently, researchers have studied the ability of green tea to eradicate infectious agents and the ability to actually prevent infections. The important components in green tea that show antimicrobial properties are the catechins. The four main catechins that occur in green tea are (-)-epicatechin (EC), (-)-epicatechin-3-gallate (ECG), (-)-epigallocatechin (EGC), and (-)-epigallocatechin-3-gallate (EGCG). Of these catechins, EGCG and EGC are found in the highest amounts in green tea and have been the subject of most of the studies. These catechins have been shown to demonstrate a variety of antimicrobial properties, both to organisms affected and in mechanisms used. Consumption of green tea has been shown to distribute these compounds and/or their metabolites throughout the body, which allows for not only the possibility of treatment of infections but also the prevention of infections.

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From PubMed Central, U.S. National Library of Medicine, as current on Oct 21, 2026. Paragraph numbers are ours, so an answer can point at one.

1. Introduction

Infectious diseases are a leading cause of morbidity and mortality worldwide. HIV/AIDS and malaria are among the top ten infectious diseases in the world; and the most common types of infections are respiratory tract and diarrheal diseases. With the advent of antimicrobial agents in the mid-1900s came the hope that eradication of infectious diseases was close. Unfortunately, the microorganisms involved were able to become resistant to the antimicrobial agents, and that only made it harder to fight these organisms. The CDC has estimated that each year more than two million people in the US suffer from antibiotic-resistant infections and that as many as 23,000 people die each year from these infections. This results in not only increased morbidity and mortality, but also increased healthcare costs, which can be a huge financial burden for many countries. A recent analysis of the medical costs from healthcare-associated infections (those infections acquired in a healthcare facility) alone estimated that the annual costs of these infections in the US are between 28 and 45 billion dollars. Antimicrobial resistance issues continue to impact these costs. One study found that the cost of antimicrobial resistance associated illnesses in the US could be as high as 55 billion dollars (20 billion dollars for healthcare costs and 35 billion dollars for lost productivity) annually. To help in the fight against infectious diseases, researchers are looking at the possibilities of using natural plant products, which could turn out to provide a tremendous cost savings in healthcare. One of the plants that is currently being widely studied is the tea plant, looking especially at green tea.

Tea is one of the most commonly consumed beverages in the world, and green tea is becoming increasingly popular, accounting for around 20% of total global tea production. Tea is produced from the Camellia sinensis plant and is grown in over 30 countries. The best areas for growing tea plants are in specific tropical and subtropical regions. There are four main tea types produced: white, green, Oolong, and black tea. The type of tea is determined by how the tea leaves are processed, specifically by drying and fermentation methods. White tea is processed the least and uses very young leaves and leaf buds. Green tea is produced from more mature leaves with no fermentation. Oolong tea is produced by partially fermenting the leaves and black tea by fully fermenting the leaves. Green tea is most commonly consumed in China, Japan, and Korea. Black tea is most commonly consumed in the US and the UK.

Green tea has been shown to have anticarcinogenic, anti-inflammatory, antimicrobial, and antioxidant properties and is beneficial in cardiovascular disease (CVD), diabetes and obesity, and neurologic and oral health. The anticarcinogenic properties include controlling cell proliferation, apoptosis and angiogenesis in tumor cells. Inflammation is a component of many conditions and diseases including aging, arthritis, cancer, CVD, diabetes, and obesity. The general anti-inflammatory properties of green tea include the ability to decrease the denaturation of proteins and increase the production of anti-inflammatory cytokines. Oxidative stress results from the damaging effects of reactive oxygen species (ROS). The antioxidant properties of green tea include the ability to limit the amount of free radicals by binding to ROS, upregulating basal levels of antioxidant enzymes, and increasing the activity of these antioxidant enzymes. The effects of green tea on CVD include the anti-inflammatory and antioxidant effects. In addition, the consumption of green tea has been shown to inhibit atherosclerosis, reduce total lipid levels, and improve the ratio of LDL to HDL. Diabetes and obesity are closely associated with a spectrum of disorders known as metabolic syndrome (MetS) which includes increased waist diameter, elevated plasma triglycerides, decreased HDL, increased fasting blood glucose, and elevated blood pressure. Type 2 diabetes is also associated with insulin resistance and sometimes decreased insulin production. Green tea has been shown to increase insulin receptor sensitivity and stimulate glucose-induced insulin secretion. Obesity is a result of an increase in fat mass which is caused by increase in the size of fat cells. Green tea has been shown to inhibit digestive enzymes and absorption of fat, which leads to decreased body waist circumference, intra-abdominal fat, plasma total and LDL cholesterol, triglycerides, and blood pressure. The challenges of inflammation and oxidative stress can lead to DNA damage, protein misfolding, and loss of ATP production in mitochondria. This can result in cell death and loss of cognitive functions in the brain. The anti-inflammatory and antioxidant properties of green tea also protect neurons, and green tea metabolites have been shown to cross the blood brain barrier. Green tea has been shown to be antimicrobial against most oral bacteria. In addition, it has been shown to improve oral health by increasing the activity of oral peroxidases, preventing the development and progression of periodontitis, and reducing dentin erosion and tooth loss, and it has a role in improving bad breath.

2. Green Tea Composition

The components in green tea that are the most medically relevant are the polyphenols. The most pertinent polyphenols are the flavonoids; and the most pertinent flavonoids are the catechins. The catechins comprise 80-90% of the flavonoids and around 40% of the water-soluble solids in green tea. Green tea contains more catechins than the other teas, mainly because of the way it is processed after harvesting. The amount of catechins in green tea can also be affected by where the tea is grown, the growth conditions, when it is harvested, how the leaves are processed, and the brewing temperature and length of time of brewing. These factors lead to a huge variation in catechin content among the varieties and brands of green tea consumed.

The four main catechins found in green tea are-epicatechin (EC),-epigallocatechin (EGC),-epicatechin-3-gallate (ECG), and-epigallocatechin-3-gallate (EGCG). The most abundant catechin is EGCG (~60%), and the next most abundant is EGC (~20%), then ECG (~14%), and EC (~6%). EGCG is the most studied in association with health, but EGC and ECG have been studied as well. As mentioned above, there can be a wide variation in the amount of catechins in any particular green tea beverage, although standardized extracts are available for use as supplements.

In order to be effective in the body these catechins need to be bioavailable after consumption. Once in the body, the catechins undergo metabolic processing in the liver and small intestine and colon. This processing produces glucuronide and sulfate conjugates or methyl epicatechins. Native forms of ECG and EGCG and metabolites of EC and EGC can be detected and measured in blood plasma. No forms of ECG and EGCG can be detected in urine, only metabolites of EC and EGC. Catechins are generally most stable in solution at a pH range of 4-6. It is now known that human serum albumin acts as a stabilizer, binding to the catechins and then transporting them. Various studies in humans have found that the peak concentrations of catechins and their metabolites occur in blood plasma between 1.5 and 2 hours after ingestion and in urine between 4 and 6 hours after ingestion. The levels of these peak concentrations are affected by an individual's metabolism and of course by the amount of catechins in the ingested type of green tea. Commonly, the levels found in the body are directly proportional to the amount of catechins consumed. Tables 1 and 2 show examples of blood plasma and urine concentration studies in humans.

3. Antimicrobial Properties

The antimicrobial effects of green tea catechins (GTCs) on microorganisms have been studied for many years. Green tea has been shown to combat these organisms in various ways, directly and indirectly, and has been shown to work synergistically with some antibiotic agents. Other known health benefits of green tea such as the anti-inflammatory and antioxidant effects may also contribute to the antimicrobial effects. Studies conducted on Escherichia coli found that exposure to green tea polyphenols (GTPs) resulted in major gene expression changes for 17 genes, with upregulation occurring in nine genes and downregulation in eight genes. Table 3 shows a summary of the antimicrobial effects of green tea on bacteria.

4. Effects on the Bacteria Cell Membrane

One of the major properties of GTCs is the ability to bind to bacterial cell membranes. This binding can lead to interference in various bacterial processes and can damage the cell membrane resulting in increased permeability and leading to cell lysis. Because EGCG is negatively charged it can combine with the positively charged bacterial cell membrane, especially in gram positive bacteria. The lipopolysaccharide (LPS) on the outer membrane of gram negative bacteria makes them more resistant to binding by GTCs. Studies with E. coli and Pseudomonas aeruginosa have shown that EGCG binding to the bacterial cell membrane can result in generation of H2O2 which is involved in damage to the cell membrane. Studies with Staphylococcus aureus have shown that this assault on the cell membrane causes a major cell wall stress response, resulting in upregulation of peptidoglycan biosynthesis genes and an alteration in cell wall structure. In methicillin-resistant Staphylococcus aureus (MRSA) strains, this change in peptidoglycan biosynthesis genes results in the production of PBP2 (penicillin-binding protein 2), which is what confers resistance to β-lactam drugs. Production of PBP2 is also inhibited by EGCG. An important result of green tea binding is the loss of bacterial ability to bind to host cells. Studies using human and mammalian cells lines have shown that various bacteria such as Fusobacterium nucleatum, Staphylococcus epidermidis, and Helicobacter pylori have significantly decreased adherence to these cells. Other important results are the loss of the ability for quorum sensing and biofilm formation of P. aeruginosa, F. nucleatum, and Streptococcus mutans. Damage to the cell membrane also results in loss of function to transmembrane transporter proteins which are responsible for secretion of toxins and efflux of substances such as antimicrobial agents.

5. Effects on Other Bacterial Cell Functions

There are a wide variety of other effects that GTCs have on bacterial functions. An important one which can affect most bacteria is the ability of GTCs to inhibit bacterial fatty acid biosynthesis by inhibiting enzymes involved in the biosynthetic pathway. Because this is an essential pathway for most bacteria, researchers are looking at targeting this pathway in antimicrobial drug development. Fatty acids are important for building cell membranes, as an energy source, and are involved in the production of toxic bacterial metabolites. Another target is the folate biosynthesis pathway. The enzyme dihydrofolate reductase (DHFR) is essential in this pathway, and is known to be a target for certain sulfa drugs. EGCG has also been shown to inhibit DHFR activity. Other important effects against enzymes include inhibition of bacterial DNA gyrase, inhibition of bacterial ATP synthase activity, and inhibition of bacterial protein tyrosine phosphatase and cysteine proteases. Some specific bacterial effects include reducing bacterial H2S production and inhibiting hemolytic activity of F. nucleatum, inhibiting the ability of Listeria monocytogenes to escape from the macrophage phagosome by inhibiting activity of listeriolysin O, and inhibiting the ability of E. coli to transfer plasmid content via conjugation.

6. Synergism

Since GTCs are known to have antimicrobial action, researchers have begun assessing the potential synergism of these catechins with other known antimicrobial agents. Green tea catechins have now been shown to act in synergy with imipenem against MRSA; with metronidazole against Porphyromonas gingivalis; with azithromycin, cefepime, ciprofloxacin, chloramphenicol, doxycycline, erythromycin, nalidixic acid, piperacillin, or tobramycin against E. coli; with ampicillin, Cefalotin, doxycycline, erythromycin, penicillin, or tetracycline against Enterobacter aerogenes; with chloramphenicol or tetracycline against Pseudomonas aeruginosa; and with aztreonam, ceftazidime, ciprofloxacin, gentamicin, meropenem, or tetracycline against Acinetobacter baumannii. The ability of GTCs to inhibit the function of bacterial efflux pumps (as mentioned previously) also plays a role in at least an additive antimicrobial effect for GTCs and many antimicrobial drugs, especially in gram negative bacteria that possess RND-type efflux pumps. Table 4 lists antimicrobial agents that have shown synergy with GTCs and the targets of these drugs.

7. Effects on Other Microorganisms

Green tea catechins have also been shown to be effective against a number of viruses, parasites, fungi, and even prions. The main antiviral effects include inhibiting the virus from binding to and entering host cells (adenovirus, enterovirus, HBV, HCV, HIV, HSV, influenza, and rotavirus); inhibiting viral RNA and DNA synthesis and viral gene transcription (enterovirus, EBV, HBV, HCV, and HIV); and destroying and functionally altering various viral molecules (adenovirus, HSV, and influenza). Studies performed with adult healthcare workers to determine if green tea supplements could prevent infection with viruses causing influenza showed significantly fewer instances of influenza symptoms and a reduced incidence of laboratory-confirmed influenza cases versus the control group.

The main effect of GTCs on various parasite infections is a decrease in parasite numbers and growth. Other effects noted were fragmentation of parasite DNA and reduced fatty acid synthesis in the parasites. Studies with parasites include Plasmodium falciparum, Babesia spp., Trypanosoma brucei, Trypanosoma cruzi, and Leishmania braziliensis.

Fungi that have been affected by GTCs include Aspergillus niger, Candida spp., Penicillium sp., Microsporum canis, Trichophyton mentagrophytes, and Trichophyton rubrum. Research testing for synergistic effects found that EGCG showed synergism with amphotericin B, fluconazole, and miconazole in Candida spp.; and in Candida tropicalis strains that were resistant to fluconazole, EGCG, and fluconazole together induced apoptosis in the yeast cells.

Prions are proteins that are considered to be infective agents because the abnormally structured (β-sheet) forms are able to induce normally structured (α-helix) forms to change shape. In the abnormal shape, protein function is lost and protein aggregation occurs in cells. Unlike other infectious agents, prions cannot be destroyed using autoclaving; the proteins have to be degraded to be noninfectious. Research using yeast cells found that EGCG could inhibit the β-sheet prions from changing the α-helical forms and could induce reversal of the β-sheet forms back to α-helical forms.

8. Antimicrobial Scope

There is a large amount of research that has assessed the antimicrobial effects of green tea catechins on a wide variety of microorganisms, including many gram negative and gram positive bacteria, some viruses, fungi, and prions. One of the most clinically important bacteria that has been researched is S. aureus, especially MRSA strains. The most studied gram negative bacteria is E. coli which is known for causing the majority of urinary tract infections. There are several recently published manuscripts that contain extensive information on which organisms are affected by green tea catechins.

9. Prevention of Infection

Since it has been shown that GTCs have multiple types of antimicrobial abilities against so many organisms, it would be expected that green tea catechins could also prevent infections. One study was mentioned previously describing how green tea reduced the number of colds and influenza incidents. Another study involving adults showed that consuming green tea supplements twice daily for 3 months resulted in 32% fewer instances of cold or influenza symptoms and nearly 23% fewer illnesses of 2 or more days duration. A study involving children found that, in school-aged children who consumed green tea on a regular basis, the number of incidents of influenza A or B was inversely associated with the number of cups of green tea consumed per day or per week. Another study with Japanese nursey school children who gargled with green tea (or placebos) at least once each day found that there were up to 3 times fewer instances of illnesses with fevers in the green tea gargling group. Two other studies with adults found that gargling with a green tea extract (GTE) solution resulted in at least half as many cases of influenza in the GTE gargling groups compared with the control groups.

10. Conclusions

The research into the effects of green tea on human health has shown that it can be an important dietary factor in the prevention and treatment of various diseases such as arthritis, cancer, CVD, diabetes and obesity, infections, and in neurologic and oral health. Studies that were originally performed in animals and cell lines have become more frequently performed using humans. This type of research is vital if we are to fully discover what benefits GTCs can have in health issues. The more researchers that become involved in this, the clearer the answers. The studies on antimicrobial effects are providing very promising data, especially if GTCs prove to have synergistic abilities with many of the currently used antimicrobial agents and perhaps with drugs used to treat other diseases. The emergence of various multidrug-resistant bacteria, along with a dearth of effective antimicrobial drugs, makes the potential of green tea an extremely timely issue. There are also many areas across the globe where the cost of drugs is currently beyond the earning power of most of the population. Green tea is relatively inexpensive and fairly easy to obtain for most people. It could prove to be an answer for improving health on a global scale.

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    Lee M. J., Wang Z. Y., Li H. Analysis of plasma and urinary tea polyphenols in human subjects. Cancer Epidemiology, Biomarkers & Prevention. 1995;4(4):393-399.

    Not in our library

  57. 57.

    Lee M. J., Maliakal P., Chen L., et al. Pharmacokinetics of tea catechins after ingestion of green tea and (-)-epigallocatechin-3-gallate by humans: formation of different metabolites and individual variability. Cancer Epidemiology, Biomarkers & Prevention. 2002;11(10):1025-1032.

    Not in our library

  58. 58.

    Nakagawa K., Okuda S., Miyazawa T. Dose-dependent incorporation of tea catechins, (-)-epigallocatechin-3-gallate and (-)-epigallocatechin, into human plasma. Bioscience, Biotechnology, and Biochemistry. 1997;61(12):1981-1985.

    Not in our library10.1271/bbb.61.1981

  59. 59.

    Ullmann U., Haller J., Decourt J. P., et al. A single ascending dose study of epigallocatechin gallate in healthy volunteers. Journal of International Medical Research. 2003;31(2):88-101.

    Not in our library10.1177/147323000303100205

  60. 60.

    Ullmann U., Haller J., Decourt J. D., Girault J., Spitzer V., Weber P. Plasma-kinetic characteristics of purified and isolated green tea catechin epigallocatechin gallate (EGCG) after 10 days repeated dosing in healthy volunteers. International Journal for Vitamin and Nutrition Research. 2004;74(4):269-278.

    Not in our library10.1024/0300-9831.74.4.269

  61. 61.

    Yang C. S., Chen L., Lee M. J., Balentine D., Kuo M. C., Schantz S. P. Blood and urine levels of tea catechins after ingestion of different amounts of green tea by human volunteers. Cancer Epidemiology Biomarkers & Prevention. 1998;7(4):351-354.

    Not in our library

  62. 62.

    Rhodes L. E., Darby G., Massey K. A., et al. Oral green tea catechin metabolites are incorporated into human skin and protect against UV radiation-induced cutaneous inflammation in association with reduced production of pro-inflammatory eicosanoid 12-hydroxyeicosatetraenoic acid. British Journal of Nutrition. 2013;110(5):891-900.

    Not in our library10.1017/s0007114512006071

  63. 63.

    Jeon J., Kim J. H., Lee C. K. The antimicrobial activity of (-)-epigallocatechin-3-gallate and green tea extracts against Pseudomonas aeruginosa and Escherichia coli isolated from skin wounds. Annals of Dermatology. 2014;26(5):564-569.

    Not in our library10.5021/ad.2014.26.5.564

  64. 64.

    Steinmann J., Buer J., Pietschmann T., Steinmann E. Anti-infective properties of epigallocatechin-3-gallate (EGCG), a component of green tea. British Journal of Pharmacology. 2013;168(5):1059-1073.

    Not in our library10.1111/bph.12009

  65. 65.

    Nakayama M., Shimatani K., Ozawa T., et al. Mechanism for the antibacterial action of epigallocatechin gallate (EGCg) on Bacillus subtilis. Bioscience, Biotechnology, and Biochemistry. 2015;79(5):845-854.

    Not in our library10.1080/09168451.2014.993356

  66. 66.

    Ben Lagha A., Haas B., Grenier D. Tea polyphenols inhibit the growth and virulence properties of Fusobacterium nucleatum. Scientific Reports. 2017;7.

    Not in our library10.1038/srep44815

  67. 67.

    Lee K.-M., Yeo M., Choue J.-S., et al. Protective mechanism of epigallocatechin-3-gallate against Helicobocter pylori-induced gastric epithelial cytotoxicity via the blockage of TLR-4 signaling. Helicobacter. 2004;9(6):632-642.

    Not in our library10.1111/j.1083-4389.2004.00281.x

  68. 68.

    Xu X., Zhou X. D., Wu C. D. The tea catechin epigallocatechin gallate suppresses cariogenic virulence factors of Streptococcus mutans. Antimicrobial Agents and Chemotherapy. 2011;55(3):1229-1236.

    Not in our library10.1128/aac.01016-10

  69. 69.

    Kanagaratnam R., Sheikh R., Alharbi F., Kwon D. H. An efflux pump (MexAB-OprM) of Pseudomonas aeruginosa is associated with antibacterial activity of Epigallocatechin-3-gallate (EGCG). Phytomedicine. 2017;36:194-200.

    Not in our library10.1016/j.phymed.2017.10.010

  70. 70.

    Lee S., Razqan G. S. A., Kwon D. H. Antibacterial activity of epigallocatechin-3-gallate (EGCG) and its synergism with β-lactam antibiotics sensitizing carbapenem-associated multidrug resistant clinical isolates of Acinetobacter baumannii. Phytomedicine. 2017;24:49-55.

    Not in our library10.1016/j.phymed.2016.11.007

  71. 71.

    Gradišar H., Pristovšek P., Plaper A., Jerala R. Green tea catechins inhibit bacterial DNA gyrase by interaction with its ATP binding site. Journal of Medicinal Chemistry. 2007;50(2):264-271.

    Not in our library10.1021/jm060817o

  72. 72.

    Kohda C., Yanagawa Y., Shimamura T. Epigallocatechin gallate inhibits intracellular survival of Listeria monocytogenes in macrophages. Biochemical and Biophysical Research Communications. 2008;365(2):310-315.

    Not in our library10.1016/j.bbrc.2007.10.190

  73. 73.

    Wang Y., Ma S. Recent advances in inhibitors of bacterial fatty acid synthesis type II (FASII) system enzymes as potential antibacterial agents. ChemMedChem. 2013;8(10):1589-1608.

    Not in our library10.1002/cmdc.201300209

  74. 74.

    Xiong L. G., Chen Y. J., Tong J. W., et al. Tea polyphenol epigallocatechin gallate inhibits Escherichia coli by increasing endogenous oxidative stress. Food Chemistry. 2017;217:196-204.

    Not in our library10.1016/j.foodchem.2016.08.098

  75. 75.

    Cho Y. S., Schiller N. L., Kahng H. Y., Oh K. H. Cellular responses and proteomic analysis of Escherichia coli exposed to green tea polyphenols. Current Microbiology. 2007;55(6):501-506.

    Not in our library10.1007/s00284-007-9021-8

  76. 76.

    Sirk T. W., Brown E. F., Friedman M., Sum A. K. Molecular binding of catechins to biomembranes: relationship to biological activity. Journal of Agricultural and Food Chemistry. 2009;57(15):6720-6728.

    Not in our library10.1021/jf900951w

  77. 77.

    Sirk T. W., Brown E. F., Sum A. K., Friedman M. Molecular dynamics study on the biophysical interactions of seven green tea catechins with lipid bilayers of cell membranes. Journal of Agricultural and Food Chemistry. 2008;56(17):7750-7758.

    Not in our library10.1021/jf8013298

  78. 78.

    Levinger O., Bikels-Goshen T., Landau E., Fichman M., Shapira R. Epigallocatechin gallate induces upregulation of the two-component VraSR system by evoking a cell wall stress response in Staphylococcus aureus. Applied and Environmental Microbiology. 2012;78(22):7954-7959.

    Not in our library10.1128/aem.02253-12

  79. 79.

    Stapleton P. D., Shah S., Ehlert K., Hara Y., Taylor P. W. The β-lactam-resistance modifier (-)-epicatechin gallate alters the architecture of the cell wall of Staphylococcus aureas. Microbiology. 2007;153(7):2093-2103.

    Not in our library10.1099/mic.0.2007/007807-0

  80. 80.

    Sharma A., Gupta S., Sarethy I. P., Dang S., Gabrani R. Green tea extract: Possible mechanism and antibacterial activity on skin pathogens. Food Chemistry. 2012;135(2):672-675.

    Not in our library10.1016/j.foodchem.2012.04.143

  81. 81.

    Stenvang M., Dueholm M. S., Vad B. S., et al. Epigallocatechin gallate remodels overexpressed functional amyloids in pseudomonas aeruginosa and increases biofilm susceptibility to antibiotic treatment. The Journal of Biological Chemistry. 2016;291(51):26540-26553.

    Not in our library10.1074/jbc.m116.739953

  82. 82.

    Spina M., Cuccioloni M., Mozzicafreddo M., et al. Mechanism of inhibition of wt-dihydrofolate reductase from E. coli by tea epigallocatechin-gallate. Proteins: Structure, Function, and Genetics. 2008;72(1):240-251.

    Not in our library10.1002/prot.21914

  83. 83.

    Chinnam N., Dadi P. K., Sabri S. A., Ahmad M., Kabir M. A., Ahmad Z. Dietary bioflavonoids inhibit Escherichia coli ATP synthase in a differential manner. International Journal of Biological Macromolecules. 2010;46(5):478-486.

    Not in our library10.1016/j.ijbiomac.2010.03.009

  84. 84.

    Zhao W.-H., Hu Z.-Q., Hara Y., Shimamura T. Inhibition by epigallocatechin gallate (EGCg) of conjugative R plasmid transfer in Escherichia coli. Journal of Infection and Chemotherapy. 2001;7(3):195-197.

    Not in our library10.1007/s101560100035

  85. 85.

    Aboulmagd E., Al-Mohamme H. I., Al-Badry S. Synergism and Postantibiotic Effect of Green Tea Extract and Imipenem Against Methicillin-resistant Staphylococcus aureus. Journal of Microbiology. 2011;1(3):89-96.

    Not in our library10.3923/mj.2011.89.96

  86. 86.

    Fournier-Larente J., Morin M.-P., Grenier D. Green tea catechins potentiate the effect of antibiotics and modulate adherence and gene expression in Porphyromonas gingivalis. Archives of Oral Biolog. 2016;65:35-43.

    Not in our library10.1016/j.archoralbio.2016.01.014

  87. 87.

    Haghjoo B., Lee L. H., Habiba U., Tahir H., Olabi M., Chu T. The synergistic effects of green tea polyphenols and antibiotics against potential pathogens. Advances in Bioscience and Biotechnology. 2013;04(11):959-967.

    Not in our library10.4236/abb.2013.411127

  88. 88.
    Effects of green tea on Escherichia coli as a uropathogen · 2015
    Not checked
  89. 89.

    Passat D. N. Interactions of Black and Green Tea Water Extracts with Antibiotics Activity in Local Urinary Isolated Escherichia coli. Journal of Al-Nahrain University Science. 2012;15(3):134-142.

    Not in our library10.22401/jnus.15.3.19

  90. 90.

    Fink R. C., Roschek B., Alberte R. S. HIV type-1 entry inhibitors with a new mode of action. Antiviral Chemistry & Chemotherapy. 2009;19(6):243-255.

    Not in our library10.1177/095632020901900604

  91. 91.

    Hauber I., Hohenberg H., Holstermann B., Hunstein W., Hauber J. The main green tea polyphenol epigallocatechin-3-gallate counteracts semen-mediated enhancement of HIV infection. Proceedings of the National Acadamy of Sciences of the United States of America. 2009;106(22):9033-9038.

    Not in our library10.1073/pnas.0811827106

  92. 92.

    Lin Y., Wu Y., Tseng C., et al. Green Tea Phenolic Epicatechins Inhibit Hepatitis C Virus Replication via Cycloxygenase-2 and Attenuate Virus-Induced Inflammation. PLoS ONE. 2013;8(1):p. e54466.

    Not in our library10.1371/journal.pone.0054466

  93. 93.

    Liu S., Li H., Chen L., et al. (-)-epigallocatechin-3-gallate inhibition of epstein-barr virus spontaneous lytic infection involves ERK1/2 and PI3-K/Akt signaling in EBV-positive cells. Carcinogenesis. 2013;34(3):627-637.

    Not in our library10.1093/carcin/bgs364

  94. 94.

    Pang J.-Y., Zhao K.-J., Wang J.-B., Ma Z.-J., Xiao X.-H. Green tea polyphenol, epigallocatechin-3-gallate, possesses the antiviral activity necessary to fight against the hepatitis B virus replication in vitro. Journal of Zhejiang University SCIENCE B. 2014;15(6):533-539.

    Not in our library10.1631/jzus.b1300307

  95. 95.

    Yang J., Li L., Tan S., et al. A natural theaflavins preparation inhibits HIV-1 infection by targeting the entry step: Potential applications for preventing HIV-1 infection. Fitoterapia. 2012;83(2):348-355.

    Not in our library10.1016/j.fitote.2011.11.016

  96. 96.
    A Review of the Antiviral Role of Green Tea Catechins · 2017
    No notice
  97. 97.

    Matsumoto K., Yamada H., Takuma N., Niino H., Sagesaka Y. M. Effects of green tea catechins and theanine on preventing influenza infection among healthcare workers: a randomized controlled trial. BMC Complementary and Alternative Medicine. 2011;11(15).

    Not in our library10.1186/1472-6882-11-15

  98. 98.

    Aboulaila M., Yokoyama N., Igarashi I. Inhibitory effects of (-)-Epigallocatechin-3-gallate from green tea on the growth of Babesia parasites. Parasitology. 2010;137(5):785-791.

    Not in our library10.1017/s0031182009991594

  99. 99.

    Güida M. C., Esteva M. I., Camino A., Flawiá M. M., Torres H. N., Paveto C. Trypanosoma cruzi: in vitro and in vivo antiproliferative effects of epigallocatechin gallate (EGCg). Experimental Parasitology emphasizes. 2007;117(2):188-194.

    Not in our library10.1016/j.exppara.2007.04.015

  100. 100.

    Inacio J. D. F., Gervazoni L., Canto-Cavalheiro M. M., Almeida-Amaral E. E. The Effect of (-)-Epigallocatechin 3-O - Gallate In Vitro and In Vivo in Leishmania braziliensis: Involvement of Reactive Oxygen Species as a Mechanism of Action. PLOS Neglected Tropical Diseases. 2014;8(8).

    Not in our library10.1371/journal.pntd.0003093

  101. 101.

    Thipubon P., Uthaipibull C., Kamchonwongpaisan S., Tipsuwan W., Srichairatanakool S. Inhibitory effect of novel iron chelator, 1-(N-acetyl-6-aminohexyl)-3-hydroxy-2-methylpyridin-4-one (CM1) and green tea extract on growth of Plasmodium falciparum. Malaria Journal. 2015;14(1, article no. 382).

    Not in our library10.1186/s12936-015-0910-1

  102. 102.

    Vigueira P. A., Ray S. S., Martin B. A., Ligon M. M., Paul K. S. Effects of the green tea catechin (-)-epigallocatechin gallate on Trypanosoma brucei. International Journal for Parasitology: Drugs and Drug Resistance. 2012;2:225-229.

    Not in our library10.1016/j.ijpddr.2012.09.001

  103. 103.

    Da Silva C. R., De Andrade Neto J. B., De Sousa Campos R., et al. Synergistic effect of the flavonoid catechin, quercetin, or epigallocatechin gallate with fluconazole induces apoptosis in Candida tropicalis resistant to fluconazole. Antimicrobial Agents and Chemotherapy. 2014;58(3):1468-1478.

    Not in our library10.1128/aac.00651-13

  104. 104.

    Muthu M., Gopal J., Min S. X., Chun S. Green Tea Versus Traditional Korean Teas: Antibacterial/Antifungal or Both? Applied Biochemistry and Biotechnology. 2016;180(4):780-790.

    Not in our library10.1007/s12010-016-2132-6

  105. 105.

    Ning Y., Ling J., Wu C. D. Synergistic effects of tea catechin epigallocatechin gallate and antimycotics against oral Candida species. Archives of Oral Biolog. 2015;60(10):1565-1570.

    Not in our library10.1016/j.archoralbio.2015.07.001

  106. 106.

    Park B. J., Taguchi H., Kamei K., Matsuzawa T., Hyon S.-H., Park J.-C. In vitro antifungal activity of epigallocatechin 3-O-gallate against clinical isolates of dermatophytes. Yonsei Medical Journal. 2011;52(3):535-538.

    Not in our library10.3349/ymj.2011.52.3.535

  107. 107.

    Thomas A., Thakur S., Habib R., Marwah N. Comparison of Antimicrobial Efficacy of Green Tea, Garlic with Lime, and Sodium Fluoride Mouth Rinses against Streptococcus mutans, Lactobacilli species, and Candida albicans in Children: A Randomized Double-blind Controlled Clinical Trial. International Journal of Clinical Pediatric Dentistry. 2017;10(3):234-239.

    Not in our library10.5005/jp-journals-10005-1442

  108. 108.

    Roberts B. E., Duennwald M. L., Wang H., et al. A synergistic small-molecule combination directly eradicates diverse prion strain structures. Nature Chemical Biology. 2009;5(12):936-946.

    Not in our library10.1038/nchembio.246

  109. 109.

    Farooqui A., Khan A., Borghetto I., Kazmi S. U., Rubino S., Paglietti B. Synergistic antimicrobial activity of Camellia sinensis and Juglans regia against multidrug-resistant bacteria. PLoS ONE. 2015;10(2).

    Not in our library10.1371/journal.pone.0118431

  110. 110.

    Rowe C. A., Nantz M. P., Bukowski J. F., Percival S. S. Specific formulation of Camellia sinensis prevents cold and flu symptoms and enhances gamma, delta T cell function: a randomized, double-blind, placebo-controlled study. Journal of the American College of Nutrition. 2007;26(5):445-452.

    Not in our library10.1080/07315724.2007.10719634

  111. 111.

    Park M., Yamada H., Matsushita K., et al. Green tea consumption is inversely associated with the incidence of influenza infection among schoolchildren in a tea plantation area of Japan. Journal of Nutrition. 2011;141(10):1862-1870.

    Not in our library10.3945/jn.110.137547

  112. 112.

    Noda T., Ojima T., Hayasaka S., Murata C., Hagihara A. Gargling for oral hygiene and the development of fever in childhood: A population study in Japan. Journal of Epidemiology. 2012;22(1):45-49.

    Not in our library10.2188/jea.je20100181

  113. 113.

    Yamada H., Takuma N., Daimon T., Hara Y. Gargling with tea catechin extracts for the prevention of influenza infection in elderly nursing home residents: a prospective clinical study. The Journal of Alternative and Complementary Medicine. 2006;12(7):669-672.

    Not in our library10.1089/acm.2006.12.669

  114. 114.

    Yamada H., Daimon T., Matsuda K., et al. A randomized controlled study on the effects of gargling with tea catechin extracts on the prevention of influenza in healthy adults. Japanese Journal of Clinical Pharmacology and Therapeutics. 2007;38(5):323-330.

    Not in our library

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