key: cord-0857799-b4rnvxfk
authors: Liang, Jianguo; Chen, Jianping; Tan, Zhiwu; Peng, Jie; Zheng, Xiao; Nishiura, Kenji; Ng, Jenny; Wang, Zhiyu; Wang, Dongmei; Chen, Zhiwei; Liu, Li
title: Extracts of medicinal herb Sanguisorba officinalis inhibit the entry of human immunodeficiency virus type one
date: 2013-12-01
journal: Journal of Food and Drug Analysis
DOI: 10.1016/j.jfda.2013.09.034
sha: 8b71faa49acdaf565c600311c424cdaa4206eb44
doc_id: 857799
cord_uid: b4rnvxfk

Highly active antiretroviral therapy (HAART) has been successful in reducing HIV-1-associated morbidity and mortality since its introduction in 1996. It, however, fails to eradicate HIV-1 infection thoroughly. The high cost of life-long HAART and the emergence of drug resistance among HIV-1-infected individuals have brought renewed pressure for the discovery of novel antivirals and alternative medicines. Traditional Chinese medicine (TCM) is one of the mainstreams of complementary and alternative medicine, and serves as rich resources for new drug development. Despite almost 100 plant-derived compounds are in clinical trials, few target HIV-1 infection. In this study, we discovered that extract of Sanguisorba officinalis (SOE) has anti-HIV-1 activities. Using a cell-based assay and single-cycle luciferase reporter viruses pseudotyped with envelopes from HIV-1 or control viruses, we found that SOE exhibited significant inhibitory ability against both CCR5 and CXCR4 tropic HIV-1 (ADA and HXB2) with respective IC(50) values of 1.91±0.16 μg/ml and 3.70±0.53 μg/ml. Interestingly, SOE also inhibited SIV infection but failed to block vesicular stomatitis virus (VSV), SARS-CoV and influeunza H5N1 pseudoviruses. Furthermore, we showed that SOE had no effects on post-entry events of HIV-1 replication. It blocked entry by acting on viral envelope directly because SOE pre-treatment with the virus but not with cell lines expressing viral receptors showed the maximal inhibitory activity. In addition, SOE was able to inhibit reverse-transcription-inhibitor-resistant viruses (K103N, Y188L, and K103N/Y188L/G190A) and a protease-inhibitor-resistant strain (PI-2840). Our findings demonstrated SOE as a novel and specific entry inhibitor, which shed lights on the discovery of anti-HIV-1 drugs from traditional herbal medicines.

Extracts of the medicinal herb Sanguisorba officinalis inhibit the entry of human immunodeficiency virus-1 1.

Traditional Chinese medicine (TCM) includes various forms of herbal medicine, acupuncture, moxibustion, massage, Qi exercise, meditation, and dietary therapy. TCM was developed in China as a personalized medical practice based on a tradition of more than 5000 years. As a result, thousands of plants have been used as herbal medicines for treating different types of diseases. For example, one of the most famous drugs, artemisinin, was originally extracted from the plant Artemisia annua and is now a standard treatment worldwide for Plasmodium falciparum malaria [1] . During the past decade, the use of TCM has increased globally as one of the mainstreams of complementary and alternative medicine. It also serves as a rich resource for new drug development.

Prior to the availability of highly active antiretroviral therapy (HAART), people with human immunodeficiency virus (HIV)/AIDS often sought herbal therapy in China. This situation continues today because HAART is still not readily accessible or affordable especially in rural areas, where the majority of patients reside. Even in the era of HAART, HIVinfected people who used herbal therapy at a high rate sought more frequent visits to TCM providers and reported helpful improvement with the treatment [2, 3] . In most cases, however, it remains unknown whether the herbs used had any anti-HIV activities, and therefore it is unknown if they were regarded as enhancing patients' immune function, as the treatment of HIV-related symptoms, or as the management of HAART-related side effects [4] . In recent years, studies have demonstrated that evidence-based research on compounds extracted from herbal plants can elucidate their biochemical activity, revealing antitumor activity in some cases and anti-HIV activity in others [5e9] . The study of some herbal compounds has been moved forward into clinical trials [6, 7, 10] . Prior to this study, however, it was unclear if Sanguisorba officinalis had any anti-HIV activity.

Sanguisorba officinalis (also called Great Burnet) is a plant in the family Rosaceae, subfamily Rosoideae. It is easily found in the northern regions of China and has been used as TCM for thousands of years to treat hemostasis and inflammation [11] . Some other functions that have been discovered in recent years include its antioxidant and antitumor properties [12e14] .To the best of our knowledge, we are the first group to study the anti-HIV-1 activities of the extract of S. officinalis (SOE). Our findings have implications for exploring TCM for new antiviral discoveries.

Materials and methods

The stem of S. officinalis was cut into small pieces and immersed in distilled water. The mixture was treated by ultrasound for 1 hour, followed by boiling twice at 100 C for 30 minutes. After filtration, the supernatant was concentrated j o u r n a l o f f o o d a n d d r u g a n a l y s i s 2 1 ( 2 0 1 3 ) s 5 2 es 5 8 by a rotary evaporator under reduced pressure, followed by lyophilization for 48 hours to obtain the aqueous extract powder (SOE). The yield of SOE was 9.9e11.2%. Highperformance liquid chromatography analysis of SOE was conducted on an Ultimate AQ-C18 column (250 mm  4.6 mm, 5 m)(Welch, Shanghai, China). The mobile phase consisted of acetonitrile (A) and 0.2% formic acid (B) in water, using a gradient elution of 5e15% A at 0e10 minutes, 15%e 25% A at 10e25 minutes, 25%e30% A at 25e35 minutes, 30%e 70% A at 35e45 minutes, 70%e95% A at 45e50 minutes, and 95% A at 50e60 minutes. The solvent velocity of flow was 1.0 mL/minute and the column was at room temperature. The detection wavelength was set at 254 nm. The contents of each component were controlled between 1.25% and 1.35% and 1.69% and 1.80%, respectively. The extract powder was dissolved in phosphate buffered saline and passed through 0.45 mm filter for sterilization. SOE was dissolved in dimethyl sulfoxide at a concentration of 40 mg/mL, followed by gentle vortex at room temperature. The supernatants were carefully collected after centrifugation at 3000g for 5 minutes and filtered through a 0.22 mm Millipore syringe filter for experiments.

The cell lines 293T, MDCK, and HEK293T-ACE2 were cultured in Dulbecco's modified Eagle medium with 10% inactivated fetal bovine serum (Invitrogen), 100 units/mL penicillin, and 100 mg/mL streptomycin sulfate (Invitrogen). GHOST(3)-CD4-CCR5/CXCR4 cells were obtained from the US National Institutes of Health (NIH, Bethesda, MA, USA) AIDS Research and Reference Reagent Program and cultured in Dulbecco's modified Eagle medium with 10% fetal bovine serum, 100 units/mL penicillin, 100 mg/mL streptomycin sulfate, 100 mg/mL hygromycin B, 500 mg/mL G418, and 1 mg/mL puromycin (Sigma Aldrich). Single-cycle luciferase HIV ADA , HIV HxB2 , simian immunodeficiency virus (SIV) mac239 , SIV mac1a11 vesicular stomatitis virus (VSV), H5N1 anhui , and severe acute respiratory syndrome coronavirus (SARS-CoV) pseudoviruses were constructed as described previously [9,15e17] . Briefly, pseudoviruses were generated by co-transfection of 293T cells (using polyethylenimine; Polysciences Inc., Warrington, PA, USA) with NL4-3 EeVe Lucþ and envelope protein from different strains of viruses. All non-nucleoside reverse-transcriptase inhibitor (NNRTI) mutant constructs were generated based on a molecular clone backbone NL4-3 EeVe Lucþ, as we previously described [8] . The protease-inhibitor resistant strain (PI-2840) was obtained from NIH (resistant to multiple anti-HIV protease drugs; carrying L10R, M46I, L63P, V82T, and I84V). Cell-free supernatant was collected 48 hours post-transfection and frozen at À80 C. The 50% tissue culture infective dose was calculated as described previously [8] .

GHOST(3)-CD4-CCR5/CXCR4 cells were incubated in the presence or absence of serially diluted SOE at 37 C in 5% CO 2 for 48 hours. Cell viability was then measured using a commercially available kit (CellTiter-Glo Luminescent Cell Viability Assay kit; Promega, USA).

The inhibitory activities of the SOE against viruses were evaluated as described previously [8] . Briefly, a serially diluted drug was tested against virus infection at 50% tissue culture infective dose. GHOST(3)-CD4-CCR5/CXCR4 were used for HIV ADA , HIV HxB2 , SIV mac239 and SIV mac1a11 , whereas MDCK and HEK293T-ACE2 were used for H5N1 and SARS-CoV pseudovirus infection, respectively. The viral infection was determined on Day 3 by measuring the reporter luciferase activity in target cells postinfection using commercially available kits. Antiviral data are reported as the quantity of drug required to inhibit viral production by 50% (EC 50 ).

Different polar solvents were used to obtain subfractions from SOE yielding petroleumeether-partitioned extract (PE), ethylacetate-partitioned extract (EtOAc), n-butanol-partitioned extract (BuOH), and water residues. These subfractions were then concentrated in a vacuum dryer for later testing.

To determine the antiviral activity of SOE, GHOST-CCR5 and GHOST-CXCR4 cells were infected with CCR5-tropic HIV-1 ADA and CXCR4-tropic HIV-1 HxB2 , respectively, in the presence of serial diluted SOE. As a control, VSV pseudovirus was included in parallel experiments. As shown in Fig. 1A and B, SOE displayed an EC50 of 1.91 AE 0.16 mg/mL and 3.70 AE 0.53 mg/mL in the inhibition of HIV-1 replication of both coreceptor tropisms without observed cell toxicity ( Fig. 1C and D) . By contrast, when SOE was tested against VSV pseudovirus infection, no inhibition was observed. Because ADA, HXB2, and VSV pseudoviruses share the same HIV backbone and differ only in the glycoproteins expressed on the viral surface, this result suggests that SOE acts specifically in inhibiting HIV-1 replication at an early stage of viral entry.

To confirm that SOE antagonizes viral entry rather than postentry events, we tested the same panel of viruses but with a modified experimental schedule. Target cells were first coincubated with pseudovirus for 2 hours, washed, and then treated with the presence of 50 mg/mL SOE or 1 mM AZT, which is a potent NNRTI, for 48 hours. As shown in Fig. 2A , with this experimental schedule, SOE does not strongly inhibit HIV-1 anymore, as compared with AZT. This result supports the finding that inhibition of SOE on HIV-1 replication is not due to the blockade at the postentry step (e.g., reverse transcription) but rather at an entry step.

To determine whether SOE inhibits virus entry by directly inactivating HIV-1 or binding to its receptor on target cells, j o u r n a l o f f o o d a n d d r u g a n a l y s i s 2 1 ( 2 0 1 3 ) s 5 2 es 5 8 SOE-virus binding and SOE-cell binding assays were performed. In the SOE-virus binding assay, pseudovirus was pretreated with 50 mg/mL SOE first. In the meantime, dilution solution dimethyl sulfoxide was used as a negative control and entry inhibitor enfuvirtide (T-20) as a positive control. The viruses were then recovered by ultracentrifugation and used to infect target cells. We found that SOE inhibited both ADA and HXB2 pseudovirus infection to a similar degree as T-20, which blocks HIV-1 fusion (Fig. 2B) . Subsequently, the SOE-cell binding assays were performed by pretreating the target GHOST cells with SOE or with the CCR5 antagonist maraviroc (MVC) and CXCR4 antagonist JM2987 as positive controls for 1 hour at 37 C. After washing with phosphate buffered saline, cells were incubated with HIV-1 ADA or HIV-1 HxB2 for 2 hours, washed, and cultured at 37 C for 48 hours [18] . We found that pretreating the target cells with SOE had virtually no antiviral effect, whereas MVC and JM2987 showed strong inhibition against the respective ADA and HXB2 pseudoviruses at 1mM as expected (Fig. 2C ). This demonstrates that SOE inhibits HIV-1 infection by acting on the viral envelope glycoprotein gp160, which mediates viral entry into the host target cells. 

To further confirm that SOE is a HIV-1-specific entry inhibitor, we tested two SIV, one influenza H5N1 and one SARS-CoV pseudoviral strain. A previous study indicated that residue peptides were found to be potent inhibitors of virus entry against both HIV-1 and SIV envelope glycoproteins [19] . Interestingly, SOE inhibited both SIV strains mac239 and mac1A11, but neither influenza H5N1 nor SARS-CoV (Fig. 3) . These results suggest that SOE has a broad and specific reactivity against diverse AIDS viruses.

The rapid emergence of drug-resistant strains of HIV-1 in patients is one of the major obstacles to successful antiretroviral treatment. Therefore, an experiment involving anti-HIV resistant viruses was carried out in which four HIV-1 drug-resistant strains were tested, including three NNRTI resistant viruses (K103N, Y188L, and K103N/Y188L/G190A) and one protease inhibitor resistant virus (PI-2840) [8] . As expected, SOE inhibited all four drug-resistant strains (Fig. 4A) , demonstrating greater breadth of inhibition when compared to nevirapine, which is a United States Food and Drug Administration-approved NNRTI. Consistent with previous findings, nevirapine did not inhibit HIV-1 resistant strains harboring Y188L or K103N/Y188L/G190A mutations (Fig. 4B) . Because viral entry precedes reverse transcription, these results provide further support for SOE as an entry inhibitor against live replicating HIV-1 strains.

To further characterize the anti-HIV activity of aqueous SOE, the extracts were subjected to different polar solvents to obtain PE, EtOAc, BuOH, and water residues. Each fraction was vacuum dried and then screened for anti-HIV-1 activity. The EtOAc and BuUOH subfractions strongly diminished HIV-1 infection of target cell lines similar to SOE (Figs. 1 and  5AeD) . However, the PE subfraction did not show any inhibition of HIV-1. These results indicate that the solubility of SOE is dependent on the polarity of the solvent, which provides direction for future isolation of small molecule HIV-1 entry inhibitors from these subfractions.

In this study, we demonstrated that SOE blocks the entry of both CCR5-tropic and CXCR4-tropic strains of HIV-1. This blockade is HIV-1 specific because SOE does not exhibit any activities against HIV-Lucþ viruses pseudotyped with envelopes of VSV, SARS-CoV, and influenza. Interestingly, SOE acts directly on HIV-1 instead of cellular receptors or coreceptors. It also exhibits potency against replication competent HIV-1 strains resistant to specific drugs targeting protease and reverse transcriptase (RT) activities. Our findings therefore provide scientific evidence for the potential use of SOE in the prevention and treatment of HIV-1 infection and the search for small molecular compounds as specific entry inhibitors. Stopping HIV-1 from entering target cells is a critical strategy for both prevention and treatment [20, 21] . Until now, there have been only two drugs in this category approved by the FDA for clinical use in the market: MVC and T-20. MVC binds to the host CCR5 coreceptor to prevent binding with gp120, whereas T-20 interacts with gp41 to interrupt membrane fusion between HIV-1 and the host target cell plasma membrane. T-20 is part of the repertoire of antiretroviral drugs that have been used in combination therapy to treat HIV-1 infection [22] . Although effective, T-20 has to be administrated by injection, whereas MVC requires the screening of patients to exclude strains of CXCR4-tropism. It is therefore useful to identify new types of HIV-1 entry inhibitors. To this end, it is of great interest to discover that SOE 

is capable of inhibiting entry of both CCR5-and CXCR4-tropic HIV-1 ADA and HXB2 strains, as well as of SIV mac1A11 and SIV mac239 , by binding viral envelope glycoproteins directly. It has previously been shown that despite a significant level of sequence diversity, HIV-1 and SIV share a series of events during virus entry including binding of gp120 to CD4 and chemokine coreceptor, and fusion between viral and cellular membranes [20,23e25] . SOE probably acts upon a highly conserved element of HIV-1 and SIV envelope glycoproteins, an issue that still requires future investigation [23,24,26e28] . Because SIVmac1A11 enters target cells in a CD4-independent way [16] , SOE probably inhibits virus entry through other mechanisms rather than by blocking the CD4 binding site directly. Critically, the proven anti-HIV-1 specificity, together with the lack of antiviral effects against VSV, SARS-CoV, and influenza, also rule out the possibility that SOE simply inactivates the HIV-1 virus by acting on viral lipids like a disinfectant. In support of our findings, several small molecules isolated from plants have been reported to have some moderate inhibitory ability against HIV-1 entry. For example, polyphenols found in green tea probably interrupt membrane fusion between HIV-1 and the host cell plasma membrane [29] . Further investigations, are necessary to reveal the mode of SOE action, which may lead to the identification of a new drug targeting the HIV-1 envelope.

With the enhanced efforts in treatment as prevention, there is also the issue of rapid emergence of drug-resistant strains of HIV-1, especially in developing countries [30] . Although several extracts of herbal medicines have been investigated for their anti-HIV activities, inhibition of anti-HIV drug-resistant strains was rarely studied [7,31e33] . We recently reported that plant-derived calanolide A and their analogues have unique advantages in overcoming the existing drug resistant viruses [8, 9] . Using the same methods as in this study, we showed that SOE inhibited not only RT inhibitor resistant viruses (K103N, Y188L, and K103N/Y188L/G190A) but also a protease inhibitor resistant primary strain (PI-2840). Because RT and protease act after HIV entry, these results are consistent with SOE as a new entry inhibitor. To explore the potential of SOE for treating AIDS patients, a future welldesigned clinical trial should be conducted for in vivo efficacy evaluation. It is also necessary to purify the small molecule compound from SOE with anti-HIV-1 activity.

In conclusion, in this study, we demonstrated that SOE blocks entry by CCR5-tropic and CXCR4-tropic strains of HIV-1. This blockade is HIV-1-specific because SOE does not exhibit any activities against HIV-Lucþ viruses pseudotyped with envelopes of VSV, SARS-CoV, and influenza. Interestingly, SOE acts directly on HIV-1 instead of cellular receptors or coreceptors. It also exhibits potency against replication-competent HIV-1 strains resistant to specific drugs targeting protease and RT activities. Our findings therefore provide evidence for the potential use of SOE in the prevention and treatment of HIV-1 infection, as well as in the search for small molecular compounds as specific entry inhibitors.

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This work was supported by Hong Kong RFCID 11100702, and HKU-UDF/LKSFM MATCHING FUND to AIDS Institute. We thank NIDA grant R13DA035084 for conference support.r e f e r e n c e s