Introduction

Influenza A virus (IAV) is the only influenza virus type that causes pandemic, and it is also responsible for most influenza-related hospitalizations [1]. Within the last 100 years, the world has witnessed four pandemics of novel strains of IAV that caused 500,000–50 million deaths [2]. Effective prophylaxis and antiviral remedies are essential factors for controlling highly contagious diseases. One of the most efficient and common strategies for controlling infection is vaccination. However, because of antigenic drift and antigenic shift, IAV can evade the neutralizing activity of previously established antibodies, causing them to become ineffective against next-year infection [3]. Given this concept, other daily preventive measures appear essential for combating IAV infection. Such preventive measures usually involve recommended procedures such as wearing masks or hand washing [4]. Although hand washing is effective, it only removes viruses from the initial contact site, and it is more operative when other reagents that can disrupt viruses are used concomitantly. Several virucidal agents exist [5]; nevertheless, some of these chemical substances are toxic and corrosive, and they cause environmental pollution, thereby limiting their use as disinfectants for viruses on the human body and surfaces [6]. Several antiviral drugs exist for use. Even if therapeutic efficacy is elicited, the emergence of resistant viral strains is a matter of concern [7]. In addition, the side effects of some medicines have been reported [8]. Owing to the possible insufficient efficacy of currently available vaccines against novel strains, limitations of chemical virucidal agents, and the emergence of drug resistance, safe supportive interventions are required to prevent viral infection and worsening of severity.

The tea plant, Camellia sinensis, is an evergreen tree belonging to the family Theaceae, which is indigenous to China and Southeast Asia. The leaves of C. sinensis contain all the structures and standard enzymes associated with plant cell growth and photosynthesis. The harvested leaf can be treated with various methods to produce three main types of teas: green, black, or Oolong tea. Uniquely, the teas produced from this plant contain relatively large quantities of polyphenols [9, 10]. Tea polyphenols have attracted the researcher’s attention as natural substances and safe therapeutic options for many diseases. It was proven in cell culture that epigallocatechin (EGC), EGC gallate (EGCG), and epicatechin gallate (ECG) present in green tea could inhibit the replication of adenovirus and influenza virus [11,12,13]. Black tea, which comprises 78% of tea consumed worldwide [14], can be synthesized by crushing and rolling the withered leaves of C. sinensis, which are then fully fermented [15]. Black tea is rich in theaflavins (TFs), polyphenols that are produced via the enzymatic oxidation and dimerization of green tea catechins, and their anti-inflammatory [16], anti-microbial [17], and antiviral activities [16, 18, 19] have been reported. In a previous study, highly TF-concentrated tea extract powder TY-1 was produced from raw green tea leaves [20]. Briefly, fresh raw green tea leaves were added to water and green tea leaf extract; then, the leaves were crushed into a paste with a mixer. With this step, polyphenol oxidase, peroxidase, tannase, hydrolase, catechins, caffeine, and other components were released from the plant cells into the water. Then, the raw green tea leaves paste was gently stirred with minimum aeration for 10 min–8 h, which promoted a reaction of various enzymes with components, thus resulting in the conversion of catechins into TFs and gallic acid production. The paste was then heated for sterilization, and the liquid layer was collected. TY-1 powder was produced by filtering and drying this liquid layer. By following this unique procedure, abundant and standardized TFs were obtained. The safety of TY-1 was confirmed by genotoxicity and mutagenicity tests such as the Ames test, micronucleus test, and comet assay. Accordingly, this study examined the virucidal effect of TY-1, which abundantly contains not only TFs but also other polyphenols, on IAV and elucidated its mechanism of action in an effort to introduce the substance as a promising supplement or alternative to the currently available antiviral therapies.

Methods

Virus and cells

IAV subtype H1N1 (A/Puerto Rico/8/1934 strain: ATCC® Catalog No. VR-95TM) was obtained from ATCC (Manassas, VA, USA), then propagated via inoculation into the allantoic cavity of 10-day-old embryonated chicken eggs. Allantoic fluids containing IAV were used as viral solutions unless otherwise stated. To prepare purified IAV, which was used for some studies, sucrose gradient ultracentrifugation was performed as previously mentioned [21]. A Micro BCA protein assay kit (Thermo Fisher Scientific Inc., Waltham, MA, USA) was used to estimate the purified IAV protein concentration. Madin–Darby canine kidney (MDCK) cells were kindly provided by Dr. H. Nagano (Hokkaido Institute of Public Health, Sapporo, Japan). For MDCK cell culture, Dulbecco’s modified Eagle’s minimal essential medium (DMEM; Nissui Pharmaceutical Co., Ltd., Tokyo, Japan) supplemented with 10% fetal bovine serum, 2 mM l-glutamine, 0.15% NaHCO3 (FUJIFILM Wako Pure Chemical Co., Osaka, Japan), 2 μg/mL amphotericin B (Bristol-Myers Squibb Co., New York, NY, USA), and 100 μg/mL kanamycin (Meiji Seika Pharma Co., Ltd., Tokyo, Japan) was used as the growth medium. Following viral inoculation, viral growth medium consisted of DMEM supplemented with 0.2% bovine serum albumin, 0.15% NaHCO3, 0.01% glucose, 2.5 mM HEPES, and 0.0006% trypsin (FUJIFILM Wako Pure Chemical Co.) was used for MDCK cell culture.

Preparation of a TY-1 stock solution and other test solutions

TY-1 powder was provided by Yokoyama Food Co., Ltd. (Sapporo, Japan). The components of TY-1 powder and their corresponding yields were analyzed by Eurofins Food Testing Japan, K.K (Shizuoka, Japan), and those are presented in Table 1. Specifically, the concentrations of TFs were analyzed by high-performance liquid chromatography; those of catechins, caffeine, theanine, and gallic acid were analyzed by liquid chromatography–tandem mass spectrometry method; those of total polyphenol and dietary fiber were analyzed by the Folin–Ciocalteu method and Prosky method, respectively. Chen et al. revealed the chemical structures of TFs and its derivatives [22]. To prepare TY-1 stock solution, 1 g of TY-1 powder was dissolved in 100 mL of phosphate-buffered saline (PBS), followed by centrifugation (9000×g for 10 min). After centrifugation, the water-soluble layer was filtered using a 0.2 μm syringe filter (Sartorius AG, Gottingen, Germany). The obtained solution was kept at − 80 °C until use. Because TY-1 powder contains 50% dextrin, dextrin solution prepared similarly as TY-1 solution was used as the diluent control. The measured pH was 6.8 and 7.1 for the TY-1 and dextrin solutions, respectively. The final concentrations of the TY-1 and dextrin stock solutions were 10 and 5 mg/mL, respectively. A 0.165 mg/mL TFs solution was prepared by dissolving 0.112 mg theaflavin (FUJIFILM Wako Pure Chemical Co), 0.043 mg theaflavin-3′-gallate (FUJIFILM Wako Pure Chemical Co), 0.010 mg theaflavin-3,3′-digallate (FUJIFILM Wako Pure Chemical Co), and 5.000 mg dextrin in 1 mL PBS. A 0.067 mg/mL catechins solution was prepared by dissolving 0.067 mg catechin mixture from green tea (FUJIFILM Wako Pure Chemical Co) and 5.000 mg dextrin in 1 mL PBS. A 0.232 mg/mL TFs + catechins solution was prepared by dissolving 0.112 mg theaflavin, 0.043 mg theaflavin-3′-gallate, 0.010 mg theaflavin-3,3′-digallate, 0.067 mg catechin mixture from green tea, and 5.000 mg dextrin in 1 mL PBS.

Table 1 Composition of 10 mg TY-1 powder
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Evaluation of the virucidal activity of TY-1

The virucidal activity of TY-1 against IAV was investigated as follows. Five concentrations of TY-1 and one concentration of dextrin solution were mixed with the viral solutions. The final concentrations of TY-1 were 0.3, 0.6, 1.3, 2.5, and 5.0 mg/mL in the mixture. The concentration of dextrin used for the mixture was 2.5 mg/mL. Additionally, one concentration each of the catechins solution, TFs solution, and TFs + catechins solution was mixed with the viral solution. In the mixture, the final concentrations of the catechins, TFs, and TFs + catechins were 0.034, 0.083, and 0.116 mg/mL, respectively. The viral titer of the mixtures was adjusted to be approximately 7.45 log10 50% tissue culture infective dose (TCID50)/mL. These mixtures were incubated at 25 °C for different times (10 min, 30 min, 1 h, 3 h, 6 h, 24 h). Following the incubation, the mixtures were inoculated into MDCK cells, and tenfold serial dilutions were performed. Three days later, the viral titers of the test solution-treated viruses were assessed by observing the cytopathic effects on the cells. The viral titer was calculated using the Behrens–Kärber method [23]. The differences in viral titer between the test solution-treated groups and the dextrin solution-treated groups represented the virucidal activity of each test solution. The detection limit of viral titers in each group was determined according to the cytotoxicity of each test solution in MDCK cells in a virus-free condition. As the dextrin, catechins, TFs, TFs + catechins, and 0.3, 0.6, and 1.3 mg/mL TY-1 groups did not exhibit cytotoxicity, the detection limit of the viral titer in these groups was set to 1.25 log10 TCID50/mL, according to our viral titer calculation. However, the 2.5 and 5.0 mg/mL TY-1 groups showed moderate cytotoxicity, and the detection limit in these groups was set to 2.25 log10 TCID50/mL.

Sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE)

The mixtures containing 6.58 log10 TCID50/mL purified IAV and 5.0 mg/mL TY-1 or 2.5 mg/mL dextrin were incubated at 25 °C for 48 h. Then, the mixtures were combined with a one-third volume of 4× SDS sample buffer with and without 2-mercaptoethanol (2-Me; FUJIFILM Wako Pure Chemical Co.). These samples were applied to SDS-PAGE, and then Coomassie brilliant blue (CBB) staining or western blotting (WB) was performed as previously described [24]. For WB to detect IAV hemagglutinin (HA), rabbit anti-H1N1 (A/Puerto Rico/8/34) HA polyclonal antibody (Catalog No. 11684-T62, Sino Biological Inc., Beijing, China) and mouse anti-rabbit IgG peroxidase conjugate (Catalog No. A1949, Clone: RG-96, Sigma-Aldrich, Inc., St. Louis, MO, USA) were used as the primary and secondary antibodies, respectively. For WB to detect IAV neuraminidase (NA), rabbit anti-H1N1 NA (Catalog No. GTX125974, Gentex Inc., Zeeland, MI, USA) and mouse anti-rabbit IgG peroxidase conjugate were used as the primary and secondary antibodies, respectively.

Hemagglutination and NA assays

The mixtures containing 7.25 log10 TCID50/mL purified IAV and 5.0 mg/mL TY-1 or 2.5 mg/mL dextrin were incubated at 25 °C for 48 h. Thereafter, the hemagglutination and NA assays were performed in line with the WHO manual on animal influenza diagnosis and surveillance [25].

Reverse transcription-polymerase chain reaction (RT-PCR)

The mixtures containing 7.25 log10 TCID50/mL purified IAV and 5.0 mg/mL TY-1 or 2.5 mg/mL dextrin were incubated at 25 °C for 48 h. After the incubation, RNA extraction and RT-PCR were performed as previously mentioned [24]. The sequence of primers targeting the IAV M gene used and each PCR condition are presented in Supplementary Table 1.

Transmission electron microscopy (TEM)

The mixtures containing 6.58 log10 TCID50/mL purified IAV and 5.0 mg/mL TY-1 or 2.5 mg/mL dextrin were incubated at 25 °C for 48 h. A two-step protocol [21] was followed in which TEM samples were loaded on a 400-mesh carbon-coated collodion grid (NISSHIN EM Co., Ltd., Tokyo, Japan). On the grids, by using 2% phosphotungstic acid (pH 6.5), the treated viruses were negatively stained for 2 min. Then, the samples were examined using TEM (HT7700; Hitachi High-Tech Co., Tokyo, Japan).

Statistical analysis

Student’s t test was used to determine statistically significant differences between the dextrin and TY-1 groups in each conducted experiment to evaluate viral and hemagglutination titers. One-way analysis of variance (ANOVA), followed by Tukey’s post hoc test were used to determine statistically significant differences among the viral titers of the dextrin, catechins, TFs, TFs + catechins, and TY-1 groups. P values less than 0.05 indicated the existence of significant difference between the selected items.

Results

Virucidal efficacy of TY-1 against IAV

First, the virucidal activities of different concentrations of TY-1 against IAV were evaluated. As a result, all tested concentrations (0.3, 0.6, 1.3, 2.5, 5.0 mg/mL) of TY-1 exhibited statistically significant IAV-inactivating activities within 24 h, and these activities were concentration- and time-dependent. The TY-1 concentration of 5.0 mg/mL displayed statistically significant virucidal activity within 30 min (a 1.33 log10 TCID50/mL reduction of the viral titer compared to the dextrin group). The viral titer in this group was below the detection limit in 6 h (≥ 5.17 log10 TCID50/mL reduction) (Fig. 1a). The 5.0 mg/mL TY-1 contained 0.034 mg/mL catechins and 0.083 mg/mL TFs (Table 1). To evaluate the contribution of catechins and TFs, which are two of the main virucidal components of TY-1, to IAV inactivation, virucidal activity of 5.0 mg/mL TY-1 was compared to that of the 0.034 mg/mL catechins solution, 0.083 mg/mL TFs solution, and 0.116 mg/mL TFs + catechins solution. The viral titers of the dextrin, catechins, TFs, TFs + catechins, and TY-1 groups were 6.88, 6.56, 5.88, 5.88, and ≥ 3.06 log10 TCID50/mL, respectively, within 3 h. Additionally, the viral titers of the dextrin, catechins, TFs, TFs + catechins, and TY-1 groups were 6.13, 5.94, 4.88, 4.38, and ≥ 2.25 log10 TCID50/mL, respectively, within 24 h. With this reaction time, the viral titer of the TFs group was partially lower than that of the dextrin group, but that of the TY-1 group was below the detection limit. Although the viral titer of the catechins group was comparable to that of the dextrin group, that of the TFs + catechins group was slightly but significantly lower than that of the TFs group (Fig. 1b). The 5.0 mg/mL TY-1 treatment, which exhibited the strongest virus-inactivating activity, was further tested against IAV to fully illustrate the mechanism of its virucidal activity.

Fig. 1
figure 1

Evaluation of the virucidal activity of TY-1 at different concentrations and exposure periods. a, b Dextrin (2.5 mg/mL) was used as a solvent control. The results are indicated as the mean ± SD (n > 4 per group). a Student’s t-test was performed to analyze statistical differences between the dextrin group and each TY-1 group: *p < 0.05, **p < 0.001, ***p < 0.001. N.T.: not tested. b One-way analysis of variance (ANOVA) followed by Tukey’s post hoc test were performed to analyze statistical differences among all test solution groups; test solution groups that do not share a common letter were significantly different (*p < 0.05)

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Impact of TY-1 on IAV proteins

The impacts of the TY-1 treatment on the functions and structures of IAV structural proteins were analyzed. Here, purified IAV was used to eliminate the influence of non-viral proteins. After treatment with 5.0 mg/mL TY-1 for 48 h, the viral titers decreased to below the detection limit compared to that in the dextrin group (Fig. 2a). The impact of the TY-1 treatment under the same conditions on the hemagglutination activity of the HA protein was evaluated by a hemagglutination assay. The hemagglutination titer of IAV treated with 5.0 mg/mL TY-1 for 48 h was significantly lower than that of the dextrin group (Fig. 2b). Subsequently, the impacts of TY-1 on the structures of viral proteins were analyzed via SDS-PAGE. As a result, CBB staining showed reduced intensity for some viral protein bands for TY-1-treated IAV. Such changes were observed for the viral HA0 protein detected in the absence of 2-Me and for HA1 and HA2 in the presence of 2-Me, and all changes were tentatively recognized according to their apparent molecular mass. Contrarily, the intensities of bands which were presumed to be the M1 and NP proteins were not affected by TY-1 exposure (Fig. 2c). To further evaluate the impact of TY-1 on viral HA proteins, WB was achieved using a primary antibody that detects the HA protein of IAV. In line with the CBB staining results, TY-1 treatment strongly reduced the intensity of the ~ 60 kDa HA0 protein band. Additionally, the intensities of additional > 75 kDa bands/ladder were stronger under the TY-1 treatment than the dextrin treatment (Fig. 2d-left). While the intensities of the HA1 and HA2 bands were weaker under the TY-1 treatment than the dextrin treatment, the intensities of additional bands/ladder with a higher molecular mass were stronger under the TY-1 treatment than the dextrin treatment (Fig. 2d-right). Meanwhile, the effect of TY-1 on the NA activity and quality of the NA protein were analyzed by NA assay and WB, respectively. TY-1-treated IAV displayed substantially lower NA activity than dextrin-treated IAV (Fig. 3a). Accordingly, the results of WB using an antibody against the NA protein of IAV revealed disappearance of the NA protein band in TY-1-treated IAV, whereas it was clearly identified in dextrin-treated IAV (Fig. 3b).

Fig. 2
figure 2

Evaluation of the effect of TY-1 on influenza A virus (IAV) hemagglutinin (HA) proteins. Dextrin (Dex) and TY-1 were mixed with a solution containing purified IAV and stored at 25 °C for 48 h. a The viral titer of the mixture was evaluated. The results are presented as the mean ± SD (n = 3 per group). b The hemagglutination titer of the mixture was evaluated. The results are presented as the mean ± SD (n = 3 per group). Student’s t test was performed to analyze statistical differences between the dextrin and TY-1 groups: ***p < 0.001. c Coomassie brilliant blue (CBB) staining of the gel from sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS-PAGE). 2-Me: 2-mercaptoethanol, M: Marker. d Results of western blotting (WB) to detect IAV HA proteins. c, d To evaluate the bands of HA0 or HA1/HA2, SDS-PAGE without or with 2-Me was performed, respectively. The results are representatives of three individual experiments

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Fig. 3
figure 3

Evaluation of the effect of TY-1 on influenza A virus (IAV) neuraminidase (NA). Dextrin (Dex) and TY-1 were mixed with a solution containing purified IAV and stored at 25 °C for 48 h. a The NA activity of the mixture was evaluated. The results are indicated as the mean ± SD (n = 3 per group). b Results of western blotting (WB) to detect IAV NA. The results represent two independent experiments

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Impact of TY-1 on the IAV genome

The impact of TY-1 on the IAV genome was explored via RT-PCR, in which primers were designed to amplify three different regions of the IAV M gene and produce amplicons of different lengths. After 48 h of treatment with 5.0 mg/mL TY-1, no PCR products were detected, unlike the results for dextrin-treated IAV (Fig. 4).

Fig. 4
figure 4

Effect of TY-1 on the influenza A virus (IAV) genome. Dextrin (Dex) and TY-1 were mixed with a solution containing purified IAV and stored at 25 °C for 48 h. The viral RNA extracted from the treated viruses was used for reverse transcription-polymerase chain reaction (RT-PCR). RT-PCR was performed using IAV-Primer sets 1, 2, and 3, which amplify 982-, 253-, and 320-bp of the IAV M gene, respectively. The results are representatives of more than two individual experiments. M: marker

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TEM analysis

To analyze whether the TY-1 treatment induced abnormalities of the viral particle structure and a reduction in the particle numbers, TEM observation of IAV particles treated with 5.0 mg/mL TY-1 for 48 h was performed. Although abnormalities of TY-1-treated viral particles were not observed compared to dextrin-treated viral particles, the number of virions drastically decreased under TY-1 treatment compared to those under the effects of dextrin exposure to IAV (Fig. 5a, b).

Fig. 5
figure 5

Transmission electron microscopy (TEM) of TY-1-treated influenza A virus (IAV) virions. Dextrin (a) and TY-1 (b) were mixed with a solution containing purified IAV and stored at 25 °C for 48 h. After treatment, the viral particles were observed using TEM. The results are representative of dextrin- and TY-1-treated viral particles within a single 6.25 μm2 field (upper panel) and 0.52 μm2 field (lower panel), respectively

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Discussion

Natural products have been tested as alternatives to conventional treatments for various diseases in recent decades. Among natural products, medicinal plants can provide safe and effective therapies for many diseases [26, 27]. Among promising plants extracts, tea might be the most extensively consumed beverage globally with a rich historical background [28]. The virucidal activity of TY-1 was concentration- and time-dependent, which was in line with the results of Ohba et al. [29], who reported the effectiveness of TFs against caliciviruses. TY-1 contains not only abundant TF derivatives, catechins, and gallic acid, but also a high amount of other polyphenols. Although TY-1 contains caffeine and theanine (Table 1), the virucidal activity of caffeine against an enveloped virus has not been observed [30], and there have been no reports proving obvious virucidal activity of theanine. Conversely, polyphenols, especially TFs and catechins, are widely reported to have virucidal activities against various types of viruses [12, 29, 31,32,33,34]. Here, our results revealed that TFs partially contributed to the virucidal activity of crude TY-1. Meanwhile, additive IAV inactivation was observed under the TFs + catechins treatment compared to that under TF treatment alone, and the contribution of catechins to IAV inactivation was limited (Fig. 1b). This result suggests that TFs are active compounds in TY-1, but other multiple virucidal polyphenolic compounds, such as catechins, contribute to the comprehensive virucidal activity of TY-1. Since it is expensive to prepare large quantities of pure TFs and other compounds with similar bioactive levels of TY-1, the application of TY-1 might be a more realistic approach to IAV infection control.

The results for the hemagglutination and NA assays and SDS-PAGE in the current study indicated the disruption of both the HA and NA proteins of IAV (Figs. 2 and 3, respectively). Particularly, the target sites of TY-1 in the HA and NA proteins included regions that are involved in hemagglutination activity and NA activity, which may be involved in the virucidal activity of TY-1. The impact of TY-1 on the HA protein is consistent with previous reports in which TF, EGCG, and ECG affected hemagglutination activity of IAV [12, 13, 16]. Similarly, the impact of TY-1 on the NA protein is also consistent with previous reports in which the antiviral activity of TF, EGCG, and ECG on IAV was attributed to NA inhibition [13, 16, 35]. As a result of WB targeting HA protein, the TY-1-induced reduction of the band intensity of HA0, which consists of HA1 and HA2 subunits, seemed to be greater than the reduction of the band intensities of individual HA1 and HA2 subunits. Additionally, TY-1 treatment enhanced the appearance of high molecular mass bands/ladders (Fig. 2d). These bands/ladders are considered HA multimers or HA aggregates. Similar appearances among high molecular mass bands/ladders of the viral spike protein have been observed via another polyphenolic compound treatment [36]. Polyphenols have been reported to interact with proteins in both covalent and non-covalent interactions, which induces the cross-linking of proteins and formation of a high molecular mass complex [37]. Hence, our results suggest that polyphenolic compounds in TY-1 possibly interact with some sites in both HA1 and HA2 subunits, which caused the aggregation of these proteins. Therefore, the reduction of the band intensity of HA0, which has multiple sites of action located in both HA1 and HA2 subunits, may have been greater than those of individual subunits. Conversely, while the NA band almost disappeared after TY-1 treatment, high molecular band/ladders did not appear (Fig. 3b). This result suggests that TY-1 induces not only the aggregation of viral proteins but also their destruction. Discrepancies in the band patterns of TY-1-treated HA and NA proteins can be due to differences in their amino acid sequences and secondary/tertiary structures.

In addition, TEM analysis performed in this study revealed a substantial decrease in the number of IAV particles after TY-1 treatment, suggesting that TY-1 damages the morphology of virions and subsequently inhibits viral adsorption onto and penetration into host cells. It was also found that TY-1 disrupted viral genomes. This result agrees with previous reports that demonstrated other polyphenol-rich plant-derived extracts that induced the viral RNA destruction against multiple virus species [24, 36]. Our findings suggest that the virucidal activity of TY-1 could be attributable to several factors rather than a single mechanism. It has been mentioned that the number of galloyl groups on the chemical structure of TF and catechins appears to be directly related to their antiviral activities [13, 18, 38]. In addition, the hydroxyl groups of TFs are reportedly more important than the galloyl groups for antiviral activity against caliciviruses [29].

TY-1, with which the abundant polyphenol content, may be applicable as an antiviral mouthwash or troche. This idea is supported by previous reports that gargling with green tea and black tea extract decreased the incidence of influenza virus infection [39,40,41]. In addition, Lee et al. [42] found that water and diet comprising green tea components suppressed influenza virus replication in animal experiments. Although our efforts in this study only focused on the direct virucidal activity of TY-1, further studies evaluating the anti-IAV activity of TY-1 in infected cells, animals, and patients are also important to clarify its effectiveness for IAV control measures. These studies may support the idea that the practical use of virucidal supplements developed from TY-1 for the control of IAV infection.

Conclusion

In conclusion, this study revealed the concentration- and time-dependent IAV-inactivating activity of TY-1 enriched with tea-derived TF derivatives and other virucidal polyphenols. Of note, TY-1 disrupted the IAV spike proteins and genome and destroyed viral particles. We anticipate that these findings support the promise of TY-1 as a virucidal supplement that contributes to the control of IAV infection.