key: cord-0006314-wvw7alsc authors: Dhawan, B. N. title: Anti-Viral Activity of Indian Plants date: 2012-01-18 journal: Proc Natl Acad Sci India Sect B Biol Sci DOI: 10.1007/s40011-011-0016-7 sha: c4ff1a516e796922471882a6831fea0993d2b0d9 doc_id: 6314 cord_uid: wvw7alsc Plants continue to be a major source for new chemical entities to develop novel therapeutic agents. Large number of plants has been shown to be active in vitro against a variety of human pathogenic viruses or their near congeners. In several cases the active compounds have been isolated and characterized. Very few of them, however, have been investigated in detail in vivo or taken to the clinic. Pure compounds like andrographolide, curcumin and glycyrrhizic acid as well as extracts of Azadirachta indica have shown activity against several viruses and should be investigated further for their therapeutic potential. An analysis of available data from several hundred species indicates that antiviral activity is more likely to be found in plants belonging to certain families. It is necessary to screen more plants of these families which are available in India to obtain further leads. Natural products have been, and continue to be, a major source of new chemical entities (NCE) for development of better therapeutic agents against infective and non-infective disorders. The bio-molecules are more stable, clinically more specific and available from renewable source [1] . Plants of Indian origin have provided several novel leads in the past [2] and are likely to yield more NCE in future also. The contribution of natural products to anti-viral chemotherapy, however, has been more modest. Several factors have contributed to this scenario. Viral infections like the common cold are self limited and require only symptomatic treatment. Public health measures like vector control have succeeded in controlling vector transmitted infections. Similarly, development of effective vaccines has played a major role in eliminating diseases like small pox, near eradication of poliomyelitis and treatment of rabies. A major reason for limited input from Indian plants has been the non-availability of strict containment facility needed for such work at most institutions in the country. A large number of plants found in India have, therefore been investigated and found active in Japan, South Korea, US, etc. Data on all such plants also has been included in the present review along with analysis of data generated within the country. Plants active in viruses closely related to human virus [e.g. feline Human Immunodeficiency Virus (HIV) or duck hepatitis] have also been included. Maximum plants have been screened against Ranikhet disease (RNA) virus (RDV) and vaccinia (DNA virus) followed by herpes, HIV and hepatitis. The data in following sections has been arranged in the same order. Most of the studies have used in vitro test systems and crude extracts of various parts of the plants. Pure compounds have been tested in some cases and in vivo procedures have been used in very few cases. In limited number of cases clinical studies also have been done. In several cases the name of the plant or family has been changed now. The name given in the original publication has been retained in the present review to avoid confusion but the names of family have been revised. CSIR Central Drug Research Institute Lucknow (CDRI) has been the pioneer institute to undertake large scale screening of Indian plants for anti-microbial and other biological activities using about 80 in vitro and in vivo tests. The program has used 50% ethanolic extracts of botanically authenticated plant samples. The extracts have been screened in vitro against one RNA virus (Ranikhet disease virus) and one DNA virus (vaccinia virus). Some samples have also been screened against encephalomyocarditis (EMCV), Japanese Encephalitis B (JE) and Semiliki Forest (SFV) viruses. Extracts showing high degree of activity were fractionated according to a standardized protocol to localize activity in one or more fractions. The results of testing 3,789 samples from 3,482 plants belonging to 233 families have been reported in a series of publications [3] [4] [5] [6] [7] [8] [9] [10] [11] [12] [13] [14] . In addition, 967 of these plants were also tested for interferon-like activity against RD and vaccinia viruses [15] . A mid-term review of the work has also been published [16] . Antiviral activity was observed in 242 samples belonging to 96 families. The results have been summarized in Table 1 . The plants have been listed under the appropriate families which have been arranged alphabetically. It also indicates plants where activity has been confirmed further in fractions or those exhibiting anticancer activity also. Some of the active plants have been followed up at CDRI for isolation and characterization of the active constituents. The antiviral activity of (?) odorinol isolated from Aglaia roxburghiana has been reported by Joshi et al. [17] . Subsequently two new triterpinoids also have been isolated and characterized [18] . Lupeol has been identified as the active moiety of hexane fraction of Vicoa indica. It was effective against EMCV, RDV and SFV. Lupeol isolated from same fraction was active against RDV only [19] . Furomolligin isolated from Rubia cardifolia was active against EMCV [20] . The interferon like activity of five plants (Acacia auriculiformis, Cassia fistula, Olex polyama, Senecio tenuifolius and Zingiber capitatum) has been investigated further. The classical fractionation failed to localize activity in a particular fraction. The activity could be localized in each case in non-dialyzable fraction. It was destroyed on treating the fraction with trypsin. These results suggest the presence of an interferon-like or interferon inducing substance in the non-dialyzable fraction [15] . CDRI has also tested plants used as hepato-protective agents in traditional systems of Indian medicine for their anti-hepatitis B virus surface antigen (HB s Ag) activity in serum of patients or carriers. Promising results were obtained with Phyllanthus amarus [21] and Picrorhiza 21. Conyza visicidula Pl V, [5] 22. Eclipta alba Pl R [3] 23. Lagascea molis Pl r, V [6, 15] 24. Laggera pierodanta Pl R [5] 25. Saussurea obvallata Fl R [11] 26. Siegesbeckia orientalis Pl R, r [3, 15] 27. Senecio tenuifolius Pl R, r, v, C [8, 15] 28. 144. Acacia auriculiformis Px, Sb r, v [15] 145. Acacia catechu St R [3] 146. Acacia raddiana Px R [11] 147. Albizzia procera Px r, V, C [5, 15] 148. 157. Eugenia mangifolia Px R [11] 158. Eugenia thwaitesii Px a R [ 12] 159. Syzygium densiflorum Px R [11] 160. Syzygium kurzii Px a S [ 14] 161. Syzygium occidentalis Px R [12] 162. Syzygium samarangense Px R,V [12] 163. Activity against herpes virus has been reported in 49 Indian plants. These have been listed in Table 2 . The activity is distributed widely and the plants belong to 34 families. Most of them have been reported active against herpes-1 virus though a few are active against both herpes-1 and 2. In 12 cases the strain used has not been mentioned. Only four publications have reported in vivo activity. Pure isolated compounds have been tested in 26 cases. Two of the compounds glycyrrhizin and lupeol are active against other human viruses also and this has been indicated at appropriate places in this review. Unfortunately none of them appear to have been followed up further. The results have been published in 43 papers and only 9 of them are from Indian laboratories. Table 2 includes only those plants from foreign publications which are found in India. Large number of papers has been published in recent years reporting anti-HIV activity in numerous natural products, partly because of the large screening program of US National Cancer Institute. Activity has been reported only in 38 Indian plants in 32 papers. These have been shown in Table 3 and belong to 28 families. Data on 41 materials has been reported and 24 of them are pure compounds. Most investigators (26) have studied the activity on HIV-1 and in 10 cases the strain has not been mentioned. HIV-2 has been included in two studies only. Two of the reported plants have been found active against feline immunodeficiency virus (FIV), a close congener of HIV. Most of the publications in this case also are from foreign laboratories and there are only seven Indian publications. There have been claims of usefulness of Ayurvedic and Siddha formulations in treatment of AIDS but no reliable clinical data is available either with these formulations or with the plants listed in Table 3 . Data with Curcuma longa has not been included in this table because curcumin isolated from this plant and its several semi-synthetic and synthetic analogues have been tested. The data has been included in concluding remarks. Large number of medicinal plants has been used for treatment of hepatic disorders in most traditional system of medicine. The parameters generally followed were clearance of jaundice and return of liver function tests to normalcy. Clearance of viraemia in infective hepatitis, the commonest hepatic disorder, became an important parameter after the demonstration of carrier stage and possible induction of malignancy in such persons. One of the earliest demonstrations of viral clearance was provided by the pioneering studies of Thyagarajan et al. [106] with Phyllanthus amarus. This led to screening of large number of plants for activity against the virus. The availability of the duck model for in vivo studies materially facilitated these studies. Protective effect has been reported with 17 Indian plants belonging to 14 families. These have been listed in Table 4 . Most of the plants have been tested against hepatitis B virus by several in vitro procedures. The active compound has been isolated and characterised in nine of these plants. Several hepatoprotective plants have been tested for anti-hepatitis B virus surface antigen (HB s Ag) activity in vitro using serum from patients or asymptomatic carriers harbouring the infection. Neutralizing activity has been reported with extract of Phyllanthus amarus [21] . A purified standardized extract (Picroliv) and a pure compound catalpol isolated from Picrorhiza kurroa were also found active while andrographolide (active constituent of Andrographis paniculata) and silymarin were inactive [22] . Clinical studies have been undertaken with some of the active plants in patients of infective hepatitis. As already reported above [23] efficacy of Picroliv has been demonstrated in Phase III multicentric trials. Beneficial effects have been reported with Phyllanthus amarus and glycyrrhizin also. These and other studies have been reviewed by Handa in a comprehensive publication [114] on hepatoprotective activity of Indian medicinal plants. Interest in respiratory virus has increased following the recent epidemics of SARS and H 1 N 1 infection. Activity has Table 5 . Interest in this group of viruses has continued because of continued occurrence of chicken-pox and measles infection. Only 14 plants have been reported active against a variety of pox viruses. These plants belong to 13 families. Glycyrrhizin from Glycyrrhiza glabra is the only pure compound reported active. Extract from Hibiscus sabdariffa is the only product showing activity against measles. Most of the extracts have been found active against fowl pox. Details of activity have been shown in Table 6 . Activity in several Indian plants has also been reported against a variety of other viruses causing human infection or their close congeners. Table 7 shows such plants belonging to 24 families. In 10 cases pure compounds isolated from plants have been found active. The list includes 12 viruses. The preparations showing activity against chikungunya, Japanese encephalitis and rotavirus are of particular interest due to wide occurrence of these infections in the country and need to be investigated on a priority basis. The broad based biological screening program of CDRI had included tests for several other activities also with the same standardized protocol. An analysis of the results has shown that each particular activity was preferentially observed in certain families. The top 11 families for antiviral activity and three other major activities have been arranged in rank order in Table 8 . It will be observed that rank order is different for different activities even though some families exhibit more than one type of activity. It is evident from the data reviewed above that little effort has been made to study the marine flora around the vast Indian coast line for antiviral compounds. Several Indian mangrove plants (Ceriops decandra, Excocaria agallocha and three species of Rhizophora i.e. lamarckii, mucoranata and spiculata) have been reported to exhibit potent anti-HIV activity [142] highlighting the need of further exploration of this valuable resource. Most of the data reported in this review is from in vitro studies and the leads do not appear to have been followed up. This is partly because of lack of suitable animal models for several infections and partly due to lack of the requirement containment facility in majority of Indian institutions. It is suggested that multi-pronged strategy should be adopted to utilise these leads. There are certain viral infections like Japanese encephalitis, chikungunya or rotavirus which are major national concern. Only few leads are available against them and these need to be followed. Ext crude extracts in different solvents; HSV unspecified strain, 1 or 2 HSV-1 or HSV-2 a Tested in vivo A number of pure compounds have demonstrated activity against several viral infections. These are compounds of varying chemical complexity ranging from simple compounds like curcumin to complicated structures like iridoids glycosides. Adequate attention has not been paid to use them as basic templates to optimise the activity 18. Zizyphus spira-christi Rhamnaceae Ext Newcastle [117] Ext crude extract in different solvents a Tested in vivo b Respiratory synticial virus c Main source of catechin is Acacia catechu [126] d Tested in vitro and in vivo in synthetic or semi-synthetic derivatives. Successful use of this strategy has been made in the case of andrographolide [143] and curcumin [136] , for example. Activity has also been reported in certain compounds which have undergone extensive clinical evaluation in non-viral diseases. Their available safety and dosage regimen data would help in initiating clinical evaluation in viral infection where in vitro or in vivo activity data is available. Andrographolide is a potent hepatoprotective agent [114] besides being active against herpes [30], influenza and H 1 N 1 infections [116] . Dehydroandrographolide succinic acid monoester is active against HIV [143] . Another clinically authenticated hepatoprotective agent Picroliv [23] is also active against several viral infections including hepatitis B [24-26]. Curcumin has received the maximum attention after its activity against HIV was demonstrated. Large number of semi-synthetic or synthetic derivatives have been prepared and tested for anti-HIV activity. Its boron complexes; semi-synthetic reduced curcumin, allyl curcumin and tocopherylcurcumin and synthetic analogues dicafferoyl methane and rosemarinic acid are highly active against HIV in a variety of in vitro protocols. Curcumin is active against herpes simplex 2 in a mouse model and Human papilloma and Epstein Barr viruses in vitro. These activities have been reviewed recently by Krishnaswamy [136] . Its in vitro activity against Friends leukaemia [25], Newcastle and Poliomyelitis viruses [120] has also been reported. Fiore et al. [41] in a recent review have provided reference for activity of glycyrrhizin and its analogues against herpes, hepatitis (including clinical trial), influenza, respiratory syncytial, SARS and vesicular stomatitis viruses. Other investigators have found it active against Japanese encephalitis [137] , poliomyelitis [138] , vaccinia and varicella [130] . It perhaps has the widest spectrum of antiviral activity among the natural products so far investigated. Adequate clinical evaluation is necessary to assess its role in treatment of viral disorders. Azadirachta indica also is a promising plant, even though most of the studies have used its extract. It has a variety of compounds and also has a long history of use in traditional medicine in many countries of the world. The viruses against which the extracts or some of the isolated compounds have shown activity include chikungunya, fowl pox, measles, vaccinia [128] , buffalo pox [127] , Coxsackie [134] and herpes [32] . Detailed studies against some of these viruses, specially herpes and chikungunya are strongly warranted. In conclusion it may be stated that the rich and valuable resource of Indian plants needs to be more extensively exploited to provide new drugs for the treatment of viral disorders. Biodiversity as a source of new chemical entities Plants of Indian origin in drug discovery Screening of Indian plants for biological activity. Part I Screening of Indian plants for biological activity. Part II Srimal RC (1971) Screening of Indian plants for biological activity. Part III Screening of Indian plants for biological activity. Part IV Screening of Indian plants for biological activity. Part V Screening of Indian plants for biological activity. Part VI Screening of Indian plants for biological activity. Part IX Screening of Indian plants for biological activity. Part X Screening of Indian plants for biological activity. Part XII Screening of Indian plants for biological activity. Part XIII Screening of Indian plants for biological activity. Part XIV Screening of Indian plants for biological activity. Part XV Evaluation of plants for antiviral activity Anticancer and antiviral activities in Indian medicinal plants: a review Antiviral activity of (?)-oderinal New cycloarterenol derivatives from Aglaia roxburghiana Antiviral constituents from Vicoa indica Fifty years of extracts of Acacia nilotica for in vitro anti-HIV activity Screening of Tanzanian plants against Plasmodium falciparum and human immunodeficiency virus Virus-cell fusion inhibitory compounds from Ailanthus altissima Swingle Inhibition of viral proteases by Zingiberaceae extracts and flavones isolated from Kaemfaria parviflora HIV-inhibitory diterpinoid from Anisomeles indica Inhibitory effect on HIV-protease of tri-p-coumaroyl-spermidine from Artemisia caruilifolia and related amides Inhibitory effect of Korean medicinal plants and camelliatannin H from Camellia japonica on human immunodeficiency virus type 1 protease A survey of some Indian medicinal plants for anti-human immunodeficiency virus (HIV) activity A new anti-HIV flavonoid glucuronide from Chrysanthemum morifolium Anti-aids agents 54. A potent anti-HIV chalcone and flavonoids from genus Desmos Anti-HIV integrase activity of Thai medicinal plants Screening of selected plant extracts for in vitro inhibitory activity on human immunodeficiency virus Two new compounds and anti-HIV constituents from Illicium verum Guatemalan plant extracts as virucides against HIV-1 infection Bioactive compounds from Lippia javanica and Hoslundia opposita Chemistry and biology of the triterpenes and saponins from the seeds of Mimusops elengi Examination of lectins, polysaccharopeptide, polysaccharide, alkaloid, coumarin and trypsin inhibitors for inhibitory activity against human immunodeficiency virus reverse transcriptase and glycohydrolase HIV inhibition from Thai bitter gourd Studies on anti-HIV activity and cytotoxicity of leaf of Morinda citrifolia Anti-HIV benzylisoquinoline alkaloids and flavonoids from the leaves of Nelumbo nucifera and structure-activity correlations with related alkaloids Isolation and structure of pedilstatin from a republic of Maldives Pedilanthus species Periglaucines A-D, Anti-HBV and -HIV-1 alkaloids from Pericampylus glaucus ) 2-Substituted furans from Polyalthea suberosa Anticholinergic, cytotoxic and anti-HIV1 activities of sesquiterpenes and a flavonoid glycoside from the aerial parts of Polygonum viscosum Anti-HIV-1 activity of compounds isolated from medicinal plant Rhus chinensis A new benzofuranone and anti-HIV constituents from the stem of Rhus chinensis Antiviral activity in vitro of Urtica dioica, Pariteria diffusa M. et. K. and Sambucus nigra L Triterpinoids from Schisandra rubriflora In vitro HIV type-1 reverse transcriptase inhibitory activity from leaf extracts of Scoparia dulcis L Chemistry and pharmacology of genus Sida (Malvaceae)-a review Inhibition of HIV-1 integrase by galloyl glucose from Terminalia chebula and flavonol glycoside gallates from Euphorbia pekinensis Antiviral activity against human immunodeficiency virus (HIV-1) and type 2 (HIV-2) of ethnobotanically selected Ethopian medicinal plants Inhibition of hepatitis-B virus by aqueous extract of Agrimonia eupatoria L Phenolics with antiviral activity from Milletia erythrocalyx and Artocarpus lakoocha Pharmacokinetics, safety and antiviral effects of hypericin, a derivative of St. John's wort plant, in patients with chronic hepatitis-C virus infection In vivo and in vitro anti-hepatitis B virus activity of total phenolics from Oenanthe javanica Effect of Phyllanthus amarus on chronic carriers of hepatitis B virus Herbs of the genus Phyllanthus in the treatment of chronic hepatitis B: observations with three preparations from different geographic sites Antihepatitis-B virus activities of triterpinoid saponin compounds from Potentilla anserine L Evaluation of antiviral activity of compounds isolated from Ranunculus seiboldi and Ranunculus scleratus Inhibition of hepatitis B surface antigen secretion on human hepatoma cells by components from Rubia cardifolia Active compounds from Saussurea lappa Clarks that suppress hepatitis B virus surface antigen gene expression in human hepatoma cills Potential antiviral effects of terminalia chebula, Sanguisorba officinalis Preliminary phytochemical screening and study of antiviral activity and cytotoxicity of Wrightia tinctoria Perspectives of Indian medicinal plants in the management of liver disorders Antiviral activity of diaryheptanoids against influenza virus in vitro Activity of andrographolide and its derivatives against influenza virus in vivo and in vitro The antibacterial, antiviral activities and photochemical screening of some Sudanese medicinal plants New iridoids from the medicinal plant Barleria prionitis with potent activity against respiratory syncitial virus In vitro anti-influenza viral activities of constituents from Caesalpinia sappan Antiviral activity of Phyllanthus amarus and curcumin Inhibitory effect of (?)-catechin on the growth of influenza A/PR/8 in MDCK cells Antivirus effects of extract from Gardenia Immunomodulatory and anti-SARS activities of Houttuynia cordata Studies on the toxicity of Punica granatum L (Punicacaeae) whole fruit extracts Antiviral activity of daphnoretin isolated from Wikstroemia indica Indian Council of Medical Research Novel antiviral agents: a medicinal plants perspective Pharmacological studies for therapeutic potential In vitro antiviral activity of Eugenia jambolana plant extract on buffalo pox virus: conventional and qPCR methods Antiviral activity of glycyrrhizic acid Antiviral effect of Hibiscus sabdariffa and Celosia argentea on measles virus Aegle marmalos) upon human Coxsackie virus B1-B6 In vitro anti-rotavirus activity of some medicinal plants used in Brazil against diarrhea In-vitro' antiviral activity of neem (Azadirachta indica A. Juss) leaf extract against group B Coxsackie viruses 3-Epicabrale hydroxylactone and other triterpinoids from Camellia oil and their inhibitory effects on Epstein-Barr virus activation Turmeric: the salt of orient is the spice of life In vitro antiviral activity of indigenous glycyrrhizin, licorice and glycyrrhizic acid on Japanese encephalitis virus In vitro studies on the effect of glycyrrhizin from Indian Glycyrrhiza glabra Linn on some RNA and DNA viruses Lignans as anti-tumor promoter from the seeds of Hernandia ovigera Anti-tumor promoting activity of bufadienolids from Kalanchoe pinnata and Kalanchoe daigremontiana 9 tubiflora Potential anti-tumor activity of 3-alphahydroxy-D: a-friesdooleanan-2-one from stem bark of Mallotus philippensis In vitro antihuman immunodeficiency virus activity of mangrove plants Dehydroandrographolide succinic acid monoester as an inhibitor against the human immunodeficiency virus