Antimicrobial, Anthelmintic, and Antiviral Activity of Plants Traditionally Used for Treating Infectious Disease in the Similipal Biosphere Reserve, Odisha, India.
Journal: 2017/November - Frontiers in Pharmacology
ISSN: 1663-9812
Abstract:
In the present study, we tested in vitro different parts of 35 plants used by tribals of the Similipal Biosphere Reserve (SBR, Mayurbhanj district, India) for the management of infections. From each plant, three extracts were prepared with different solvents (water, ethanol, and acetone) and tested for antimicrobial (E. coli, S. aureus, C. albicans); anthelmintic (C. elegans); and antiviral (enterovirus 71) bioactivity. In total, 35 plant species belonging to 21 families were recorded from tribes of the SBR and periphery. Of the 35 plants, eight plants (23%) showed broad-spectrum in vitro antimicrobial activity (inhibiting all three test strains), while 12 (34%) exhibited narrow spectrum activity against individual pathogens (seven as anti-staphylococcal and five as anti-candidal). Plants such as Alangium salviifolium, Antidesma bunius, Bauhinia racemosa, Careya arborea, Caseria graveolens, Cleistanthus patulus, Colebrookea oppositifolia, Crotalaria pallida, Croton roxburghii, Holarrhena pubescens, Hypericum gaitii, Macaranga peltata, Protium serratum, Rubus ellipticus, and Suregada multiflora showed strong antibacterial effects, whilst Alstonia scholaris, Butea monosperma, C. arborea, C. pallida, Diospyros malbarica, Gmelina arborea, H. pubescens, M. peltata, P. serratum, Pterospermum acerifolium, R. ellipticus, and S. multiflora demonstrated strong antifungal activity. Plants such as A. salviifolium, A. bunius, Aporosa octandra, Barringtonia acutangula, C. graveolens, C. pallida, C. patulus, G. arborea, H. pubescens, H. gaitii, Lannea coromandelica, M. peltata, Melastoma malabathricum, Millettia extensa, Nyctanthes arbor-tristis, P. serratum, P. acerifolium, R. ellipticus, S. multiflora, Symplocos cochinchinensis, Ventilago maderaspatana, and Wrightia arborea inhibit survival of C. elegans and could be a potential source for anthelmintic activity. Additionally, plants such as A. bunius, C. graveolens, C. patulus, C. oppositifolia, H. gaitii, M. extensa, P. serratum, R. ellipticus, and V. maderaspatana showed anti-enteroviral activity. Most of the plants, whose traditional use as anti-infective agents by the tribals was well supported, show in vitro inhibitory activity against an enterovirus, bacteria (E. coil, S. aureus), a fungus (C. albicans), or a nematode (C. elegans).
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Frontiers in Pharmacology. Dec/31/2016; 8
Published online Oct/22/2017

Antimicrobial, Anthelmintic, and Antiviral Activity of Plants Traditionally Used for Treating Infectious Disease in the Similipal Biosphere Reserve, Odisha, India

Abstract

In the present study, we tested in vitro different parts of 35 plants used by tribals of the Similipal Biosphere Reserve (SBR, Mayurbhanj district, India) for the management of infections. From each plant, three extracts were prepared with different solvents (water, ethanol, and acetone) and tested for antimicrobial (E. coli, S. aureus, C. albicans); anthelmintic (C. elegans); and antiviral (enterovirus 71) bioactivity. In total, 35 plant species belonging to 21 families were recorded from tribes of the SBR and periphery. Of the 35 plants, eight plants (23%) showed broad-spectrum in vitro antimicrobial activity (inhibiting all three test strains), while 12 (34%) exhibited narrow spectrum activity against individual pathogens (seven as anti-staphylococcal and five as anti-candidal). Plants such as Alangium salviifolium, Antidesma bunius, Bauhinia racemosa, Careya arborea, Caseria graveolens, Cleistanthus patulus, Colebrookea oppositifolia, Crotalaria pallida, Croton roxburghii, Holarrhena pubescens, Hypericum gaitii, Macaranga peltata, Protium serratum, Rubus ellipticus, and Suregada multiflora showed strong antibacterial effects, whilst Alstonia scholaris, Butea monosperma, C. arborea, C. pallida, Diospyros malbarica, Gmelina arborea, H. pubescens, M. peltata, P. serratum, Pterospermum acerifolium, R. ellipticus, and S. multiflora demonstrated strong antifungal activity. Plants such as A. salviifolium, A. bunius, Aporosa octandra, Barringtonia acutangula, C. graveolens, C. pallida, C. patulus, G. arborea, H. pubescens, H. gaitii, Lannea coromandelica, M. peltata, Melastoma malabathricum, Millettia extensa, Nyctanthes arbor-tristis, P. serratum, P. acerifolium, R. ellipticus, S. multiflora, Symplocos cochinchinensis, Ventilago maderaspatana, and Wrightia arborea inhibit survival of C. elegans and could be a potential source for anthelmintic activity. Additionally, plants such as A. bunius, C. graveolens, C. patulus, C. oppositifolia, H. gaitii, M. extensa, P. serratum, R. ellipticus, and V. maderaspatana showed anti-enteroviral activity. Most of the plants, whose traditional use as anti-infective agents by the tribals was well supported, show in vitro inhibitory activity against an enterovirus, bacteria (E. coil, S. aureus), a fungus (C. albicans), or a nematode (C. elegans).

Introduction

It has been estimated that less than 1–10% of plant species of the world have been studied chemically and pharmacologically for their potential medicinal value (Verpoorte, 2000). For tropical forests that percentage is even much lower (Gurib–Fakim, 2005). Experts estimate that 137 species (plants or animals) are lost every single day (50,000 species in a year) due to rainforest deforestation (http://www.rain-tree.com/facts.htm#.VVhhjRtS-zM). Plants species of tropical forests produce more chemical compounds for defense against pathogens and herbivores due to the high temperatures and scarcity of water during the summer, in addition to competing for space and light which force them to develop a robust means of energy and nutrient utilization along with adequate resources for secondary metabolite production (Fyhrquist, 2007). For these reasons, many tropical plant species contain secondary metabolites with potential medical utility (Wood–Sheldon et al., 1997).

The Similipal Biosphere Reserve (https://en.wikipedia.org/wiki/Simlipal_National_Park#Flora_and_fauna and Panda, 2014) is part of the UNESCO World Network of Biosphere Reserves since 2009, contains a fauna treasure trove of 1,076 plants (1,012 wild and 64 cultivated) from 168 families, including 60 species of pteridophytes, 92 species of orchids and two gymnosperms (Saxena and Brahmam, 1994-1996).

The use of medicinal plants for various ailments is a common practice among the tribal inhabitants of the SBR and is often passed orally from generation to generation. At the current stage, the younger generation of the SBR tribes shows little interest to inherit the traditional knowledge form their elders (Panda, 2014). So, a wealth of information now risks disappearing since it is often kept secret up to an old age by the initiated. Each time a traditional healer dies without passing his knowledge on to the next generation, the tribe and the world lose thousands of years of irreplaceable knowledge about medicinal plants.

Though traditional medicines have been recognized as a part of primary health care, there is a need to evaluate scientifically the crude extracts for clinical usefulness and toxicological risk. Although there are many reports available on antimicrobial properties of medicinal plants used by the tribes of Mayurbhanj, very few systematic surveys exist, and they mostly neglect the scientific validation of this traditional knowledge. Moreover, many surveys do not take full advantage of evidence for clinical efficacy in different diseases. The objective of the present paper is therefore to evaluate the antiviral, antibacterial, antifungal, and anthelmintic activities of medicinal plants used for treating infections by the tribes of the SBR (Mayurbhanj) in a systematic and consistent manner. The results can provide more scientific evidence supporting the clinical application of these plants, and can serve as a starting point for drug discovery. For each type of test, a common causative agent viz. Escherichia coli, Staphylococcus aureus (antibacterial-), Candida albicans (antifungal-), and enterovirus 71 (antiviral activity) was used as target organism, while for anthelmintic testing the model organism Caenorhabditis elegans was used.

Materials and methods

Chemicals and reagents

Acetone (SZBE082SV) of analytical grade was purchased from Sigma-Aldrich Co. (USA). Absolute ethanol (E/0650DF/15) was purchased from Fischer Chemicals (UK). Sterile deionized water was produced by a water purification system (Milli-Q Reagent Water System, MA, USA). Yeast extract and Bacto™ peptone were purchased from Lab M Ltd. (Lancashire, UK). Ammonium chloride, calcium chloride, cholesterol, ciprofloxacin hydrochloride, dextrose, dimethyl sulphoxide (DMSO, molecular biology grade), levamisole hydrochloride, magnesium sulfate, (±)-miconazole nitrate salt, rupintrivir, potassium dihydrogen phosphate, di–sodium hydrogen phosphate, sodium chloride, sodium hydroxide, and sucrose were all purchased from Sigma–Aldrich (MO, USA). MTS (3–[4,5 dimethylthiazol–2–yl]–5–[3–carboxymethyl–phenyl]–2–[4–sulphophenyl]–2H–tetrazolium, inner salt), was purchased from Promega, Leiden, The Netherlands.

Ethnobotanical studies

Study design and sampling procedure

Field trips to the SBR were undertaken (2012–2013) for collecting medicinal plants. Geographic coordinates for each survey site were determined in the field with a global positioning system (GPS) receiver (Garmin Etrex, Olathe, Kansas, USA). Coordinates were recorded as latitude and longitude in decimal degrees. The ethnobotanical studies were performed according to the guidelines of Singh et al. (2013). Traditional knowledge holders (local tribal baidyas (https://en.wikipedia.org/wiki/Baidya) and elders) were included in the design of the study protocol and throughout its implementation. Most of these tribal baidyas are certified and government-recognized traditional knowledge holders (TKH) and belong to Aswin Kumar Vaidya Sangha, in the Mayurbhanj district, Odisha. A semi-structured questionnaire survey provided by SRISTI (Society for Research and Initiatives for Sustainable Technologies and Institutions; http://www.sristi.org/cms/) was employed to document the traditional knowledge. Data were collected in face-to-face interviews with translation where necessary. In total 14 TKH were interviewed. All participants were male with average age of 45. No minors were approached in the present survey. Personal interviews and group discussions with the TKH revealed specific information about the plants, which was further authenticated by crosschecking. Regarding common diseases, the respondents provided information about the frequent occurrence of infection (abscess, burn, wound, skin, eye and ear, sinusitis, diarrhea, dysentery), parasitic disease (different intestinal worms, malaria), bone fracture, gout, fever, jaundice, and snakebite.

Ethical issues

To carry out research activities inside the Similipal Tiger Reserve (national park), permission was obtained from the Principal Chief Conservator of Forests (Odisha) and Field Director, Similipal Tiger Reserve–cum–Regional Chief Conservator of Forests, Baripada, Odisha. However, no permission was required for research activities in the villages near the transition zone of the SBR (http://www.moef.nic.in/division/biosphere-reserves). Ethnopharmacological studies of the type that we conducted fall under the authority of the Indian National Biodiversity Authority, an Autonomous and Statutory Body of the Ministry of Environment, Forest, and Climate Change, Government of India (http://nbaindia.org/link/304/1/1/home.html), and are governed by the Biological Diversity Act, 2002 (http://nbaindia.org/content/25/19/1/act.html).

Participating TKHs were contacted, and the purpose of the research project was explained to them before they gave written informed consent. Each participant of the study agreed to participate voluntarily. Participants were allowed to discontinue the interview at any time. The informed consent form that we used was developed by the National Innovation Foundation and Honey Bee Network and was obtained from the SRISTI website (http://www.sristi.org/cms/). After acceptance of the manuscript for publication, the data will be contributed to the Traditional Knowledge Digital Library (TKDL) of India (http://www.tkdl.res.in/tkdl/langdefault/common/Abouttkdl.asp?GL=Eng).

Botanical identification

In the field work for each plant species, the following data were noted: local name, place, collection method, parts used, preparation methods, and medicinal value. The collected plant species were identified by professional taxonomists of North Orissa University (see acknowledgments) with the help of floras (Saxena and Brahmam, 1994-1996). None of them are endangered or protected species. Identification and voucher specimen deposition of these medicinal plants was done at the Department of Botany, North Orissa University, Baripada, and pictures of selected plants are shown in Figure 1. The information on these plants with their official taxonomic name (according to the plant list- http://www.theplantlist.org), local name, medicinal use, and used part(s), GPS coordinates, origin, and voucher numbers are shown in Table 1.

Figure 1
Photographs of selected plants from Similipal Biosphere Reserve.
Table 1
Ethnomedicinal uses of medicinal plants of SBR and Mayurbhanj district, India.
Voucher No.Taxonomic nameLocal nameFamilyParts usedGPS coordinates and collection provinceMedicinal uses
NOU508/2013Alangium salviifolium (L.f.) WangerinBaghanakhia/AnkulaCornaceaeLeaf21°53′30.9″ N, 86°23′55.0″ E; NawanaWound, infection due to snakebite
NOU100/2012Alstonia scholaris (L.) R. Br.ChatianaApocyanaceaeLeaf21°54′51.4″ N, 86°27′26.1″ E; LulungMouth infection, jaundice
NOU105/2012Anogeissus latifolia (Roxb. ex DC.) Wall. ex Guill. & Perr.Dha/DhauraCombretaceaeBark21°54′51.4″ N, 86°27′26.1″ E; LulungDiarrhea
NOU312/2013Antidesma bunius (L.) Spreng.MuttaPhyllanthaceaeBark, fruit21°55′56.1″ N, 86°27′20.0″ E; MachhakandanaInfection (any), skin, diarrhea
NOU301/2013Aporosa octandra (Buch.-Ham. ex D. Don) VickeryMakaniaPhyllanthaceaeBark, leaf21°53′30.9″ N, 86°23′55.0″ E; NawanaAbscess, infection due to bone fracture
NOU213/2012Barringtonia acutangula (L.) Gaertn.Hinjala/BanasadinaLecythidaceaeLeaf21°56′51.2″ N, 86°33′19.3″ E; SitakundWorm infection, skin infection
NOU302/2013Bauhinia racemosa Lam.AnmataFabaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundInfection (any), skin, diarrhea
NOU207/2012Buchanania lanzan Spreng.CharaAnacardiaceaeBark21°56′51.2″ N, 86°33′19.3″ E; SitakundDiarrhea
NOU290/2012Butea monosperma (Lam.) Taub.PalasaLeguminosaeFlower21°58′32.2″ N, 86°36′35.2″ E; BaldihaDiarrhea, dysentery
NOU315/2013Careya arborea Roxb.KumbhiLecythidaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundSkin infection
NOU315/2013Careya arborea Roxb.KumbhiLecythidaceaeBark21°58′04.3″ N, 86°32′48.1″ E; ChampagadDiarrhea, dysentery
NOU304/2013Casearia graveolens DalzellGirchiSalicaceaeLeaf21°57′27.9″ N, 86°35′26.4″ E; LulungPiscicide, skin infection
NOU301/2013Cleistanthus patulus (Roxb.) Müll. Arg.PhyllanthaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundInfection (any), skin, diarrhea
NOU244/2012Colebrookea oppositifolia Sm.MarangLamiaceaeLeaf21°53′30.9″ N, 86°23′55.0″ E; NawanaSinusitis, malaria, intestinal problems
NOU215/2012Crotalaria pallida AitonFabaceaeFruit21°46′22.5″ N, 86°31′00.6″ E; DebkundIntoxication, antiparasitic
NOU068/2012Croton roxburghii N.P. Balakr.PutuliEuphorbiaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundDiarrhea
NOU062/2012Dillenia pentagyna Roxb.RaiDilleniaceaeLeaf21°56′51.2″ N, 86°33′19.3″ E; SitakundDiarrhea, dysentery
NOU057/2012Diospyros malbarica (Desr.) Kostel.KalikenduEbenaceaeLeaf21°56′51.2″ N, 86°33′19.3″ E; SitakundSkin infection, diarrhea
NOU254/2012Enteda rheedii Spreng.LeguminosaeSeed21°53′30.9″ N, 86°23′55.0″ E; NawanaEye infection
NOU503/2013Glochidion velutinum WightEuphorbiaceaeLeaf21°53′30.9″ N, 86°23′55.0″ E; NawanaInfection due to bone fracture, fever
NOU506/2013Gmelina arborea Roxb.GambhariLamiaceaeLeaf21°58′04.3″N, 86°32′48.1″ E; ChampagadInfection (any), skin, malaria
NOU059/2012Holarrhena pubescens (Buch.-Ham.) Wall. ex G. DonKuruchiApocynaceaeBark21°54′51.4″ N, 86°27′26.1″ E; LulungMalaria, diarrhea, dysentery
NOU059/2012Holarrhena pubescens (Buch.-Ham.) Wall. ex G. DonKuruchiApocynaceaeLeaf21°54′51.4″ N, 86°27′26.1″ E; LulungSkin infection, jaundice
NOU228/2012Hypericum gaitii HainesHypericaceaeLeaf21°47′27.2″ N, 86°24′02.35″ E; NawanaSkin infection, sore throat, fever
NOU310/2013Lannea coromandelica (Houtt.) Merr.JiaAnacardiaceaeBark21°56′51.2″ N, 86°33′19.3″ E; SitakundWorm infection, skin infection
NOU301/2013Macaranga peltata (Roxb.) Müll. Arg.MandaEuphorbiaceaeLeaf21°55′56.1″ N, 86°27′20.0″ E; MachhakandanaSkin infection
NOU232/2012Melastoma malabathricum L.KoraliMelastomataceaeLeaf21°53′30.9″ N, 86°23′55.0″ E; NawanaInfection (any), skin, diarrhea
NOU414/2013Millettia extensa (Benth.) BakerGoraLeguminosaeLeaf21°47′27.2″ N, 86°24′02.35″ E; NawanaSkin infection, cough
NOU208/2012Mimosa rubicaulis Lam.ChurLeguminosaeLeaf21°57′27.9″ N, 86°35′26.4″ E; LulungBurns, wound infections (any)
NOU542/2013Nyctanthes arbor-tristis L.Haragoura/GangasiuliOleaceaeLeaf21°58′32.2″ N, 86°36′35.2″ E; BaldihaInfection (any), skin, diarrhea, malaria, jaundice
NOU314/2013Protium serratum (Wall. ex Colebr.) Engl.RajmoiBurseraceaeFruit21°53′30.9″ N, 86°23′55.0″ E; NawanaTuberculosis, cough
NOU103/2012Pterospermum acerifolium (L.) Willd.MuchkundaSterculiaceaeBark21°58′04.3″ N, 86°32′48.1″ E; ChampagadDiarrhea, dysentery
NOU103/2012Pterospermum acerifolium (L.) Willd.MuchkundaSterculiaceaeFlower21°58′04.3″ N, 86°32′48.1″ E; ChampagadDiarrhea
NOU103/2012Rubus ellipticus Sam.MachaokodiRosaceaeLeaf21°47′27.2″ N, 86°24′02.35″ E; NawanaDiarrhea, malaria
NOU305/2013Suregada multiflora (A. Juss.) Baill.KhakraEuphorbiaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundSkin
NOU305/2013Suregada multiflora (A. Juss.) Baill.KhakraEuphorbiaceaeBark, seed21°46′22.5″ N, 86°31′00.6″ E; DebkundDiarrhea, dysentery
NOU103/2012Symplocos cochinchinensis (Lour.) S.SymplococeaeLeaf21°53′30.9″ N, 86°23′55.0″ E; NawanaSkin
NOU426/2013Ventilago maderaspatana Gaertn.RaktapichulaRhamnaceaeBark, leaf21°53′30.9″ N, 86°23′55.0″ E; NawanaGout, bone fracture, ear, eye infection
NOU306/2013Wrightia arborea (Dennst.) Mabb.Pita karuaApocynaceaeLeaf21°46′22.5″ N, 86°31′00.6″ E; DebkundDiarrhea, skin infection, asthma

Preparation of the extract

Bark, flowers, fruit, leaves, or roots of plants were collected separately during field trips to different places of the SBR. After collection, the healthy leaves were dried at ambient temperature in the absence of sunlight for 7 days to maintain their green color and volatile oils, if present. Other parts such as bark, root, flower, fruits, were dried in an oven (Labotech Solutions, India) at 50°C for 4 days. All the materials were completely dried to prevent growth of fungi, molds, bacteria, or other microorganisms (Panda et al., 2016). The dried raw botanical material was ground to a fine powder and stored in PearlPet plastic jars, 600 gm. One gram of powder was transferred into each of three 15 mL sterile polypropylene tubes with screwcaps, and 10 mL of sterile water, absolute ethanol, or acetone were added, respectively. Extraction was performed at ambient temperature with the aid of repeated vortexing and sonication (4 × 15 min over a 24 h period) in a sonicator water bath (Branson, USA). After 1 day, the tubes were centrifuged for 10 min at 2000 RCF (Hettich Rotanta 46R, C4810, Germany) and the supernatant transferred in 1 mL aliquots to 1.5 mL Eppendorf tubes. After evaporation of the solvent in a Savant SpeedVac Concentrator (SVC 200H, Stratech Scientific, London, UK), the dried residue of 1 mL extract was re-dissolved in 200 μL water (for the aqueous extract) or 200 μL DMSO for the ethanol and acetone extracts. For the antiviral assay, 1 mL of each extract was transferred to a special tube (2D barcoded 2 mL storage tube, Thermo Scientific* Abgene) and the solvent was evaporated as described above. The dry residue was dissolved in DMSO to a final stock concentration of 10 mg/mL. The samples were stored at 4°C until further testing.

Antimicrobial test

Microbial strains

Bacterial strains E. coli (DH10B), S. aureus ATCC 65385 (Rosenbach), and fungal strain C. albicans (SC5314) (American Type Culture Collection, Manassas, Virginia, USA) (Fonzi and Irwin, 1993) were used for the antibacterial and antifungal test, respectively. For bacteria, colonies were inoculated on Mueller-Hinton (MH) agar plates, while for Candida, colonies were inoculated on YPD agar, and after overnight growth both plate types were sealed with parafilm and stored in a cold room (4°C).

Preparation of pre-culture

A single colony of C. albicans, E. coli, or S. aureus was inoculated from an agar plate in 5 mL of YPD medium (1% yeast extract, 2% peptone, and 2% dextrose) for Candida, or MH medium (0.2% beef extract, 1.75% casamino acids, and 0.015% soluble starch) for bacteria, in separate reaction tubes under aseptic conditions. The reaction tubes were incubated overnight while shaking at 200 rpm at 37°C.

Antibacterial activity test (microdilution broth) protocol

Ten μL of the test sample was transferred into the wells of a 96-well plate, as well as the positive control (ciprofloxacin, stock 100 μg/mL) and blank (solvent) controls (DMSO and water). Each well of a microdilution plate was than inoculated with 190 μL of the diluted standardized inoculum (OD = 0.003 at 620 nm). Control wells were prepared with 190 μL MH broth and 10 μL extract to correct of any absorption due to extract components. The microdilution plates were placed in a shaker-incubator at 37°C for 18 h, and then read on a Mithras LB 940 Multimode Microplate Reader (Berthold Technologies GmbH & Co. KG, Bad Wildbad, Germany) at 620 nm with a lamp energy of 13,000 using the MikroWin 2000 software package. The OD was measured at a wavelength of 620 nm and wells with a plant extract were corrected for the absorption contributed by the extract. Tests were typically carried out in duplicate. The relative inhibition (%) of the test sample was calculated by dividing the OD value of the test sample minus that of the non-inoculated extract control by the average OD of the solvent control, and multiplying by 100.

Antifungal test

Antifungal activity was tested against C. albicans in a similar way as for bacteria. Instead of MH broth, YPD broth was used with a smaller quantity of plant extract (to keep the final DMSO concentration below 2%). For antifungal activity, each well of a microdilution plate was inoculated with 196 μL of the diluted yeast suspension and 4 μL of the test solution was added. Control wells were prepared with 196 μL YPD broth and 4 μL extract to correct for any absorption due to extract components, or 4 μL of DMSO or MilliQ (solvent control), or the antifungal miconazole (200 μg/mL) in DMSO (positive control).

Determination of minimum inhibitory concentration (MIC50)

The MIC50 was determined using the 96–well microdilution method as described earlier in section Antibacterial Activity Test (Microdilution Broth) Protocol. The dry weight of each extract was determined on an analytical balance (Sartorius ME235P, Germany). The dry residue was dissolved in 200 μL DMSO (sterile water for aqueous extracts), and a 2–fold serial dilution (up to 32–fold) was prepared in a 96–well conical bottom (V) microplate. Data from dose-response experiments were represented as the percentage of inhibition, and analyzed with Prism™ (GraphPad Prism 5.0 Software Inc., San Diego, CA). The MIC50 for each growth condition was calculated by fitting the data to a non-linear least-squares sigmoid regression curve.

Anthelmintic activity

Culture, maintenance, and synchronization of Caenorhabditis elegans (C. elegans) strains

The N2 wild-type C. elegans strain was grown on Nematode Growth Medium (NGM) in Petri dishes containing a lawn of the bacterium E. coli OP50 (Brenner, 1974). Synchronized populations were obtained by a modified alkaline bleaching method (Lenaerts et al., 2008). Briefly, worm culture plates with eggs and egg-laying adults were washed with M9 buffer and incubated with freshly prepared bleaching solution, followed by three washes with M9. Then, 3.5 mL of worm suspension was added to 1.5 mL of alkaline hypochlorite solution (1 mL of bleach and 0.5 mL of 5 M NaOH). The suspension was shaken for 5 min, and 5.0 mL of a sucrose solution (60% w/v) was added. Then, 1 mL of M9 buffer was gently added to the mixture, followed by centrifugation at 290 RCF (Hettich Rotanta 46R, C4810, Germany) for 3 min. After centrifugation, the eggs were collected and washed five times with M9 buffer were. Eggs in M9 were kept on a rotator at 20°C overnight in the absence of light to hatch into L1 larvae (L1s). After 24 h of incubation, L1s were transferred onto a fresh NGM plate seeded with an E. coli OP50 lawn and grown at 20°C (L2s). “L4” larvae were isolated from those plates after 48 h were washed four times with M9 buffer before being used for assays with plant extracts.

Anthelmintic assay

The anthelmintic assay was carried out in a 96-well microplate (flat-bottom, TPP Techno Plastic Products AG, Switzerland). Synchronized C. elegans (15 μL, ~45 L4 larvae) were added to each well of a 96-well microplate containing 184 μL of E. coli OP50 culture (OD = 0.5 at 620 nm). Subsequently, 1 μL of plant extract was added to each well; DMSO (1 μL) was used in a separate well as a solvent control. After mixing, the 96-well microplate was placed into a WMicroTracker (Phylumtech, Argentina) apparatus and incubated for 16 h at 20°C. The movement of worms in each well was measured every 30 min and recorded by the WMicroTracker. The percentage of the average movement over 16 h of test samples with extract compared to the DMSO control, was used to estimate the relative anthelmintic activity. Levamisole (final concentration 50 μM) was systematically used as a positive control.

Antiviral test

The EV71 BrCr laboratory-adapted strain was used at a low multiplicity of infection (MOI) in a standardized antiviral assay as described earlier (Martínez-Gualda et al., 2017). Briefly, a serial dilution of the extract(s) was prepared in assay medium that was added to an empty microtiter 96-well plate, after which the virus inoculum was added, followed by a suspension of freshly harvested rhabdosarcoma (RD) cells (2 × 104 cells/well). While the cells were settling to the bottom, the virus was allowed to infect them in the presence of extract. The assay plates were incubated at 37°C, 5% CO2 with virus inoculum and compounds until full virus-induced cell death was observed in the untreated, infected controls (3–4 days post-infection). Subsequently, the antiviral effect was quantified using a colorimetric readout with 3- (4,5-dimethylthiazol-2-yl)-5-(3-carboxymethoxyphenyl)-2-(4-sulfophenyl)-2H-tetrazolium/phenazine methosulfate (MTS/PMS method) and the concentration of compound at which 50% inhibition of virus-induced cell death would be observed (EC50) was calculated from the antiviral dose-response curves. A similar assay setup was used to determine the adverse effect of an extract or test compound on uninfected, treated cells for calculation of the CC50 (concentration of sample that reduces overall cell health by 50% as determined by the MTS/PMS method). The final, maximal DMSO concentration that was reached in the assay wells with the highest sample input (1%) was well-tolerated by the cells. Rupintrivir was used as a positive control (Martínez-Gualda et al., 2017). In addition, the selectivity index (SI) was calculated as the ratio of the CC50 for cell growth to the EC50.The Selectivity Surface-SS, was determined from plots (CPE and CC curve) and the Therapeutic Index-TI was calculated as (SS*10logSI) (Supplementary Material).

Results

Ethnomedicinal documentation

The ethnomedicinal uses of 35 plant species belonging to 21 families were recorded from tribes of the SBR and periphery (Table 1). The information on these plants with botanical names (arranged alphabetically), voucher number, local name, taxonomic family, used plant part, origin, and medicinal uses is shown in Table 1. Most of the reported medicinal uses pertained to the treatment of infections such as skin infection (19), diarrhea (17), dysentery (defined as bloody diarrhea) (6), malaria (4), jaundice (3), parasitic (3), wound (3) or other infections of e.g., eye, ear, mouth, or throat, or for bone fractures, snake bites etc. (7) (Figure 2). According to the number of given uses, the most represented families are Euphorbiaceae (5), Apocynaceae (4), Leguminosae (4), Lecythidaceae (3), and Phyllanthaceae (3) (Figure 3).

Figure 2
Frequency of health problems attributed by the tribals of SBR.
Figure 3

Distribution of plant families frequently used by the tribals of SBR compared to frequency of same families found in the broad survey of SBR plants (Girach et al., 1999).

Antimicrobial activity

Antibacterial activity in microdilution broth assays with crude extracts (aqueous, acetone, and ethanol) of different plant parts of different species is presented in Table 2 (percentages of inhibition surpassing 50 are underlined). In total, 285 extracts were tested, of which 86 extract showed high activity while 122 extracts did not show activity (Figure 3). Additionally, 38 extracts had medium—while 39 extracts had low antimicrobial activity (Figure 3). Most activity was detected in ethanol extracts, followed by acetone and aqueous extracts. Of the 35 plants screened, 17 showed activities in at least one extract against E. coli, 34 against S. aureus, and 14 against C. albicans (Figures 4, 5). Among the tested plants, six showed activity against E. coli in the acetone extracts, 10 in the ethanol extracts, and 11 in water extracts. In a few cases, negative values were calculated for the % inhibition. Taken at face value, this could mean that the extract enhanced (rather than inhibited) bacterial growth. This cannot be excluded, but more likely the negative values are due to a combination of experimental variation and an overcorrection for colored compounds in the control samples without bacteria. This may occur when bacteria metabolize some of the colored components in the extract.

Table 2
Antimicrobial activity of selected extracts of plants collected from SBR, India (growth inhibition in % compared to the solvent, OD at 620 nm).
Plant nameParts usedE. coliS. aureusC. albicans
AcetoneWaterEthanolAcetoneWaterEthanolAcetoneWaterEthanol
A. salviifoliumLeaf89585596606–165
A. scholarisLeaf27454898809726662
A. latifoliaBark427346
A. buniusBark14–1911549784152618
A. octandraLeaf774730–2199711318–24
B. acutangulaLeaf3385–2
B. racemosaLeaf118413666564–2113
B. lanzanBark477824
B. monospermaFlower437454
C. arboreaLeaf639956
C. arboreaBark18–2013969295893490
C. graveolensLeaf24784759633845011
C. patulusLeaf11–278810048232112
C. oppositifoliaLeaf24–52298871003311437
C. pallidaFruit12951007746201783
C. roxburghiiLeaf897552
D. pentagynaLeaf688325
D. malbaricaLeaf257982
E. rheediiSeed1347131834241071
G. velutinumLeaf10–8188263–21101226
G. arboreaLeaf18389421–19161374
H. pubescensBark90829897–310094770
H. pubescensLeaf1006696–1–498173227
H. gaitiiLeaf1815209910085201825
L. coromandelicaBark959939
M. peltataLeaf71367711864112533586
M. malabathricumLeaf10072893–3979317110
M. extensaLeaf26112493–2275217814
M. rubicaulisLeaf8781076745564427
N. arbortristisLeaf8–20–393–2–14665
P. serratumFruit–1–3301008362903390
P. acerifoliumBark184826
P. acerifoliumFlower889366
R. ellipticusLeaf7861099951001005988
S. multifloraLeaf13771310585–6891175
S. multifloraBark20862210371–781–2771
S. cochinchinensisLeaf9–1717475818–14523
V. maderaspatanaLeaf3514241061198711222
W. arboreaLeaf918862949925123920
Solvent controlDMSO000000
Water000
Antibiotic–ciprofloxacin97989796105104
Antifungal–miconazole949192

(–) Data absent, % growth inhibition data were rounded to the nearest integer. Underlined values represent above 50 inhibition.

Figure 4
Antimicrobial activity score of different extracts.
Figure 5
Number of SBR plants with at least one extract showing activity (>50%) against tested organism.

Plants that showed more than 75% inhibition with the broth dilution method were further tested by 2-fold serial dilution to evaluate their MIC. The MIC50 of the selected extracts against E. coli, S. aureus, and C. albicans are summarized in Table 3. Most of the test extracts inhibited growth at less than 1,000 μg/mL. The MIC50 value range from (100–1,400 μg/mL), (50–1,370 μg/mL), and (150–780 μg/mL) against E. coli, S. aureus, and C. albicans, respectively.

Table 3

Determination of MIC50 of selected extracts (concentration in μg/mL).

Plant nameParts usedE. coliS. aureusC. albicans
AcetoneWaterEthanolAcetoneWaterEthanolAcetoneWaterEthanol
A. salviifoliumLeaf580750
A. scholarisLeaf1,1701,370870
A. latifoliaBark1,130
A. buniusBark960100
A. octandraLeaf230530500
B. acutangulaLeaf360
B. racemosaLeaf950
B. lanzanBark780
B. monospermaFlower270
C. arboreaLeaf200
C. arboreaBark280800410410-560
C. graveolensLeaf300-
C. patulusLeaf60340
C. oppositifoliaLeaf4001,000340700
C. pallidaFruit1,03010050190
C. roxburghiiLeaf300310
D. pentagynaLeaf580
D. malbaricaLeaf350720
G. velutinumLeaf150-
G. arboreaLeaf520-780
H. pubescensBark260990320100610
H. pubescensLeaf310710300770
H.gaitiiLeaf480860410
L. coromandelicaBark1,000730
M. peltataLeaf430230390560460
M. malabathricumLeaf1301,050680600390480
M. extensaLeaf140210-360-
M. rubicaulisLeaf5602501,700
N. arbortristisLeaf1,280-
P. serratumFruit470310530380-600
P. acerifoliumBark
P. acerifoliumFlower1,40050
R. ellipticusLeaf450200400160240220
S. multifloraLeaf650150630710390
S. multifloraBark250170620260350
V. maderaspatanaLeaf140190150
W. arboreaLeaf170450180170

(–) Data absent; MIC50 value were rounded to the nearest integer.

Except for Entada rheedii, all tested plants showed inhibitory activity against S. aureus at least with one extract (Table 2). There was not much difference in activity across the different extracts of the same plant when tested against S. aureus. Plants such as A. salviifolium, A. scholaris, Antidesma bunius, B. racemosa, C. arborea, C. patulus, C. oppositifolia, H. gaitii, H. pubescens, M. malabathricum, R. ellipticus, and P. serratum have inhibitory activity against S. aureus with all three extracts (acetone, water, and ethanol). Plants such as A. salviifolium, A. octandra, B. acutangula, B. racemosa, C. arborea, C. graveolens, C. pallida, C. roxburghii, D. pentagyna, H. pubescens, L. coromandelica, M. peltata, M. malabathricum, M. rubicaulis, R. ellipticus, S. multiflora, and W. arborea showed broad-spectrum activity by inhibiting both Gram-positive and Gram-negative bacteria.

Plants such as A. scholaris, B. monosperma, C. arborea, C. graveolens, C. pallida, C. roxburghii, H. pubescens, D. malbarica, G. arborea, M. peltata, P. serratum, P. acerifolium, R. ellipticus, and S. multiflora showed activity against C. albicans (Table 2). Like for E. coli, C. albicans also responded differently to extracts of the same plant in different solvents. Ethanol is the best overall extractant (14 plants) followed by acetone (8) and water (3). C. arborea, C. graveolens, C. pallida, C. roxburghii, H. pubescens, M. peltata, R. ellipticus, and S. multiflora were active against all three test strains: E. coli, S. aureus, and C. albicans.

Anthelmintic activity

Table 4 shows the % inhibition (those surpassing 50 are underlined) on C. elegans after treatment with 1 μl of extract. Out of the 35 test plants, 22 plant viz. A. salviifolium, A. bunius, A. octandra, B. acutangula, C. graveolens, C. pallida, C. patulus, G. arborea, H. pubescens, H. gaitii, L. coromandelica, M. peltata, M. malabathricum, M. extensa, N. arbor-tristis, P. serratum, P. acerifolium, R. ellipticus, S. multiflora, S. cochinchinensis, V. maderaspatana, and W. arborea showed promising activity.

Table 4
Anthelmintic activity of selected extracts of plants collected from SBR, India.
Taxonomic nameParts used%, relative movement compared to the solvent
AcetoneWaterEthanol
A. salviifoliumLeaf79 ± 9119 ± 577 ± 10
A. scholarisLeaf73 ± 24
A. latifoliaBark25± 6
A. buniusBark24± 381 ± 1066 ± 6
A. octandraLeaf15± 562 ± 616± 17
B. acutangulaLeaf47± 4
B. racemosaLeaf100 ± 1673 ± 2589 ± 10
B. lanzanBark99 ± 2
B. monospermaFlower96 ± 8
C. arboreaLeaf72 ± 8
C. arboreaBark72 ± 10101 ± 1677 ± 16
C. graveolensLeaf28± 379 ± 583 ± 11
C. patulusLeaf45± 186 ± 669 ± 16
C. oppositifoliaLeaf55 ± 799 ± 883 ± 2
C. pallidaFruit37± 6132 ± 11101 ± 1
C. roxburghiiLeaf86 ± 1
D. pentagynaLeaf110 ± 3
D. malbaricaLeaf83 ± 8
E. rheediiSeed61 ± 6112 ± 3388 ± 4
G. velutinumLeaf72 ± 1086 ± 4116 ± 8
G. arboreaLeaf39± 5126 ± 2034± 9
H. pubescensBark35± 4
H. pubescensLeaf37± 10
H. gaitiiLeaf30± 980 ± 556 ± 2
L. coromandelicaBark16± 8
M. peltataLeaf40± 592 ± 253 ± 4
M. malabathricumLeaf66 ± 1566 ± 1531± 12
M. extensaLeaf43± 488 ± 311± 13
M. rubicaulisLeaf66 ± 17100 ± 272 ± 8
N. arbortristisLeaf35± 479 ± 1136± 8
P. serratumFruit37± 1180 ± 1928± 1
P. acerifoliumBark92 ± 2
P. acerifoliumFlower55 ± 2
R. ellipticusLeaf69 ± 13104 ± 349± 1
S. multifloraLeaf96 ± 8110 ± 662 ± 4
S. multifloraBark82 ± 1182 ± 3736± 3
S. cochinchinensisLeaf108 ± 635 ± 1679 ± 16
V. maderaspatanaLeaf41± 972 ± 2528± 11
W. arboreaLeaf49± 1108 ± 1636± 18
Levamisole48± 353 ± 441± 10

(–) Data absent, all values are listed as mean ± SD; data were rounded to the nearest integer. Underlined values represent above 50 inhibition.

Antiviral activity

The effect of different plant extracts on the inhibition of enterovirus (type 71, BrCr) is presented in Table 5. Of the 35 plants tested, 5 acetone and 5 ethanol extracts, as well as 10 aqueous extracts showed potent inhibitory activity (higher than 50%). These active extracts were subsequently tested for cytotoxicity, and the effective concentration protecting 50 or 90% of the cells (EC50 and EC50) as well as cytotoxic concentration (CC50) are presented in Table 5. Additionally, the Selectivity Index (SI), Selectivity Surface (SS), and Therapeutic Index (TI) were calculated from the dose–response curves (Supplementary Figure 1). Among these plants, A. bunius, C. graveolens, C. patulus, C. oppositifolia, H. gaitii, M. extensa, P. serratum, R. ellipticus, and V. maderaspatana showed the best activity and could be suitable for finding antiviral compounds.

Table 5
Antiviral and cytotoxic activity of selected extracts of plants collected from SBR, India.
Plant nameParts usedExtract testedEC50(μg/ml)EC90(μg/ml)Max. % inhibitionCC50(μg/ml)SISSTI
A. latifoliaBarkAcetone66>1005377100
A. buniusBarkEthanol71 ± 2287 ± 363 ± 698 ± 32 ± 11 ± 21 ± 1
B. racemosaLeafEthanol43 ± 6>10079 ± 1>75>2>3>1
C. graveolensLeafAqueous3 ± 14 ± 1100 ± 0>100>28>18>26
C. patulusLeafAqueous35 ± 15>10085 ± 19>75>2>3>2
C. oppositifoliaLeafAqueous82 ± 17>10063 ± 1>100>1>1>1
G. velutinumLeafAcetone9197026342
H. gaitiiLeafAqueous70 ± 26>10069 ± 6>100>2>3>1
M. peltataLeafAqueous20 ± 181 ± 479 ± 7100 ± 05 ± 011 ± 38 ± 2
M. malabathricumLeafAcetone14 ± 2>7562 ± 420 ± 02 ± 11 ± 0.10.1 ± 0.1
M. malabathricumLeafEthanol46 ± 5>10076 ± 1>75>2>4>1
M. extensaLeafAqueous42 ± 17>10090 ± 14>100>2>4>2
M. rubicaulisLeafAqueous54 ± 1>10081 ± 1>100>2>4>1
P. serratumFruitEthanol15 ± 757 ± 4499 ± 2>100>5>12>10
R. ellipticusLeafAqueous5 ± 58 ± 688 ± 1859 ± 318 ± 1628 ± 1736 ± 33
R. ellipticusLeafEthanol13 ± 615 ± 074 ± 129 ± 43 ± 13 ± 22 ± 1
V. maderaspatanaLeafAqueous74 ± 44>10070 ± 28>100>1>1>1
W. arboreaLeafAcetone125918110
W. arboreaLeafAqueous12 ± 5>7589 ± 1>100>10>11>11
Rupintrivir0.02 ± 0.001μM0.03 ± 0.001μM100 ± 0>10μM

EC50 = 50% Effective Concentration (concentration at which 50% inhibition of virus replication is observed).

EC90 = 90% Effective Concentration (concentration at which 90% inhibition of virus replication is observed).

CC50 = 50% Cytostatic/Cytotoxic Concentration (concentration at which 50% adverse effect is observed on RD cells in parallel with antiviral assay).

SI = Selectivity Index (CC50/EC50).

SS = Selectivity Surface (integrated surface delineated by the EC50 curve, the CC50 curve and the 50% horizontal).

TI = Therapeutic Index (SS*10logSI).

(–) Data absent; all values are listed as mean ± SD; data were rounded to the nearest integer.

Discussion

Since ancient time, plants are well-known as a source of medicine for the treatment of diverse diseases, and they continue to serve as the basis for many pharmaceuticals used today. They are a rich bio-resource for drugs of traditional medicinal systems, modern medicines, nutraceuticals, food supplements, folk medicines, pharmaceuticals, intermediates, and chemicals for synthetic drugs (Hammer et al., 1999). Medicinal uses are well-described in the Indian Ayurveda (Patwardhan, 2005), in Traditional Chinese Medicine (Wan et al., 2016), and in various European historical documents (Ginsburg and Deharo, 2011). However, indigenous knowledge in a particular region is an important component of traditional medicine, which is widely practiced by the tribal communities throughout India. The traditional medicines not only provide valuable clues for finding new drugs, but also help to shift the drug discovery paradigm from “finding new-entity drugs” to “combining existing agents,” and might even guide the combinations between such agents (Wagner and Ulrich–Merzenich, 2009).

From the different test performed in the present study, we conclude that C. arborea, C. graveolens, C. pallida, C. roxburghii, H. pubescens, M. peltata, R. ellipticus, and S. multiflora could be potential sources for broad-spectrum antibiotics as they inhibit all three test strains: E. coli (a model Gram-), S. aureus (a model Gram +), and C. albicans (the most common human pathogenic fungus). Moreover, plants such as A. salviifolium, A. bunius, B. racemosa, C. patulus, C. oppositifolia, H. gaitii, and P. serratum can be a useful source for narrow-spectrum antibiotics against S. aureus, while plants such A. scholaris, B. monosperma, D. malbarica, G. arborea, and P. acerifolium could yield antifungal agents. Thus, the indigenous knowledge by the tribals of the SBR appears to be a promising source for antimicrobial agents.

In this study, 19 plants parts were used traditionally to treat various skin infections, 17 plant parts for diarrhea and six plant parts for dysentery. In the present study, it was experimentally demonstrated that most plants used by tribals of Similipal (Mayurbhanj district), are potential sources of natural antibiotics. According to Williamson et al. (1996), the extraction procedure can be guided by how the plant is used in folk medicine. The tribals of SBR mostly use aqueous extracts (infusion/decoction). We observed that aqueous extracts frequently produce inhibitory effects against both bacterial strains, while they are rarely effective against C. albicans. We also found that some plants show activity in both polar and non-polar solvents, and sometime in all three extracts. This suggests that different active compounds are present, which may show additive or synergistic effects when the complete plant is used for treatment.

The plant extracts were most often active on S. aureus, followed by E. coli and finally C. albicans. Plant extracts typically show stronger inhibition on Gram-positive than Gram-negative bacteria (Desta, 1993). The latter are in general more resistant to the action of antimicrobials compared to the former because of a more complex cell wall (Silhavy et al., 2010).

Like bacterial and fungal infections, parasitic infections pose also major global health problems in humans and animals. Nematode parasites cause serious problems in the livestock industry due to drug resistance in several helminth species (Prichard, 1994; Perry and Randolph, 1999). The traditional practitioners have extensive knowledge about the treatment of parasitic infections. Therefore, we screened for extracts active on C. elegans, which has recently received increased attestation as a model organism for drug discovery (Desalermos et al., 2011). In the present study, of the 83 plant extracts tested, 30 had pronounced anthelmintic activity (>50% activity inhibition). More than half of the extracts show some activity (defined arbitrarily as activity inhibition by more than 25%). This suggests the accuracy of the use of plants by the tribes of the SBR. The plant extracts that inhibited the activity of C. elegans can be promising starting points in the search for anthelmintic drugs.

In addition to antibacterial, antifungal, and anthelmintic properties, the crude extracts were also evaluated for antiviral activity using enterovirus type 71, BrCr strain. The genus Enterovirus is responsible for a wide variety of diseases including meningitis, myocarditis, encephalitis and respiratory diseases (Bruu, 2002). There is currently no effective drug for the treatment of EV71 infections. The EC50 and CC50 were determined for active extracts from the dose–response curves. Considering the Selectivity Index, Selectivity Surface and Therapeutic Index, the crude extracts of A. bunius (bark), C. graveolens (leaf), C. patulus (leaf), C. oppositifolia (leaf), H. gaitii (leaf), M. extensa (leaf), P. serratum (fruit), R. ellipticus (leaf), and V. maderaspatana (leaf) demonstrate potential anti-enteroviral activity.

In the present study for selected extracts, cytotoxic activity was determined by calculating the % of surviving cells across a range of concentrations (1–100 μg/mL). Several plants show significant antiviral effects with no significant cytotoxicity, thus proving safe at least for mammalian cells.

Based on our review of the literature, the antimicrobial activity of A. octandra, C. graveolens, C. patulus, D. pentagyna, G. velutinum, H. gaitii, L. coromandelica, M. extensa, M. rubicaulis, P. serratum, R. ellipticus, S. multiflora, S. cochinchinensis and W. arborea has not been documented so far, while plants such as A. salviifolium (Jain et al., 2010), A. scholaris (Khan et al., 2003; Hussain et al., 2010), A. latifolia (Govindarajan et al., 2006; Patil and Gaikwad, 2010), A. bunius (Lizardo et al., 2015), B. acutangula (Sahoo et al., 2008), B. racemosa (Rashed and Butnariu, 2014), B. lanzan (Pattnaik et al., 2013), B. monosperma (Tiwari et al., 2012; Sahu and Padhy, 2013), C. arborea (Kumar et al., 2006) C. oppositifolia (Mahapatra et al., 2013), C. pallida (Ukil et al., 2016), C. roxburghii (Thatoi et al., 2008; Panda et al., 2010a,b), D. malbarica (Panda et al., 2012), G. arborea (Khan et al., 2003; El–Mahmood et al., 2010), H. pubescens (Chakraborty and Brantner, 1999; Siddiqui et al., 2012), M. malabathricum (Alwash et al., 2014), M. peltata (Bijesh and Sebastian, 2013), N. arbor-tristis (Aggarwal and Goyal, 2013), P. acerifolium (Panda and Dutta, 2012), and V. maderaspatana (Kawde et al., 2014) were reported before to show antimicrobial effects. Likewise, A. salviifolium (Pandey, 2012), B. acutangula (Padmavathi et al., 2011), C. pallida (Panda et al., 2014), G. arborea (Panda et al., 2015), H. pubescens (Satpute et al., 2014), M. malabathricum (Suteky and Dwatmadji, 2011), and N. arbor-tristis (Shruti et al., 2009) were reported earlier for anthelmintic properties, while plants such as A. bunius, A. octandra, C. graveolens, C. patulus, H. gaitii, L. coromandelica, M. peltata, M. extensa, P. serratum, P. acerifolium, R. ellipticus, S. multiflora, S. cochinchinensis, V. maderaspatana, and W. arborea are reported for the first time here to inhibit C. elegans. However, three plants, namely A. scholaris (Singh and Sharma, 2013), B. racemosa (Kumar et al., 2011), and B. monosperma (Prashanth et al., 2001; Sant et al., 2014), were reported earlier for anthelmintic activity, but did not show significant inhibition of C. elegans in the present study. This may be due to differences in test organism, test conditions or concentrations used. Concerning antiviral studies, A. scholaris (Antony et al., 2014) and B. monosperma (Yadava and Tiwari, 2005), were previously reported, while plants such as A. bunius, C. graveolens, C. patulus, C. oppositifolia, H. gaitii, M. extensa, P. serratum, R. ellipticus, and V. maderaspatana showed the highest activity and could be suitable for finding antiviral compounds.

Zhu et al. (2011) published a review on nature-derived drugs, where they analyzed “the ranking of drug-productive plant families based on the ratio of the approved drugs to reported bioactive natural products (including leads of the approved and clinical trials drugs)” and concluded that the top-ranked families that produce high numbers of approved drugs among the plant-derived medicines were Fabaceae, Ephedraceae, Papaveraceae, Asteraceae, Solanaceae, Rubiaceae, and Apocynaceae. Girach and his “co-workers” findings (1999) show that eight families appear in the top 15 on the list of high-use families of Similipal viz. Euphorbiaceae, Caesalpiniaceae, Asteraceae, Lamiaceae, Malvaceae, Mimosaceae, Rubiaceae, and Solanaceae. Most of these families are also confirmed active by bioassay in the present study. Our screening results suggest that the top families with bioactivity for infections are Euphorbiaceae, Leguminosae, Apocyanaceae, Phyllanthaceae, Fabaceae, Anacardiaceae, Lamiaceae, and Lecythidaceae.

Although there are a lot of papers published on medicinal plants from India, they mostly neglect the rich traditional knowledge of the tribal peoples. To the best of our knowledge, this paper is the first systematic bioactivity study of medicinal plants from the SBR based on traditional knowledge of indigenous tribes. However, many previous studies have not determined systematically whether such traditionally used species are more likely to yield useful bioactive compounds. It therefore remains controversial whether traditionally used plants form a good starting point for drug discovery (Fabricant and Farnsworth, 2001; Soejarto et al., 2005) and prospection guided by ethnobotany has fluctuated (Cox and Balick, 1994; Firn, 2003; Newman and Cragg, 2016). One view is that “traditionally used medicinal plants are not necessarily efficacious and there are no robust methods for distinguishing those which are most likely to be bioactive when selecting species for further testing” quoted by Saslis–Lagoudakis et al. (2012). Saslis–Lagoudakis et al. (2012), published a review entitled “phylogenies reveal the predictive power of traditional medicine in bioprospecting,” and conclude that “phylogenetic cross-cultural comparisons can focus screening efforts on a subset of traditionally used plants that are richer in bioactive compounds, and could revitalize the use of traditional knowledge in bioprospecting”. Their study provides unique large-scale evidence that plant bioactivity underlies traditional medicine. Our results agree with this view.

Conclusion

The present study shows the importance of indigenous knowledge of the tribes of the SBR for selecting plants with potential for treating infectious diseases. This knowledge obtained from the tribals and combined with taxonomy, toxicity, and different biological activities demonstrates the value of healing practices and the use of plants by the tribes of the SBR and suggests that bioprospecting of medicinal plants with the help of traditional knowledge of indigenous peoples is useful for the discovery of new drug candidates. However, further scientific studies on isolating the active compounds are essential to discover novel candidate drugs.

Author contributions

Conceived and designed the experiments: SP, ML, and PL. Performed the experiments: SP, LP, ML, and PL. Analyzed the data: SP, PL, and WL. Contributed reagents/materials/analysis tools: SP, PL, JN, and WL. Contributed to the writing of the manuscript: SP and WL.

Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Footnotes

Funding. The author SP was financial supported by receipt of a postdoc fellowship from EMINTE (Erasmus Mundus, EU; http://eminte.eu/).

Acknowledgments

The authors wish to thank the authorities of North Orissa University for providing necessary facilities for the collection, identification, and extraction of plant materials. We are also thankful to the PCCF and Field Director, STR cum RCCF, Baripada, Odisha to provide permission for field visits at SBR (2013-14) Special thanks go to Dr. Anil K. Biswal, Dr. A. K. Bastia, Mr. Kishore K. Mondal (North Orissa University), and Dr. Sanat Das (Ayurveda doctor, Badasahi, Mayurbahnj) for identification of the plant samples. Thanks also to Dr. Gunanidhi Sahoo, Niranjan Patra, Yugal K. Mohanta, Sukumar Bhakta, Himanshu S. Palei, and Santanu K. Jena (North Orissa University), for the collection of plant samples and expert technical help during experiments. The authors are thankful to Yipeng Ma (KU Leuven), who helped in writing the antiviral part and provided critical suggestions for this manuscript. The author SP is also grateful for financial support on receipt of a postdoc fellowship from EMINTE (Erasmus Mundus, EU; http://eminte.eu/). PL is supported by the Flemish IOF (Industrial Research Fund), ML is supported by a CSC fellowship of the Chinese government, and WL largely supported himself. Finally, we wish to thank countless tribal informants, especially Rathu Mohanta and Subash Kumar Mohanta, as they traveled with SP and helped with the collection of plants, provided traditional uses of plants and help in communicating in vernacular languages. We hope that the information produced from these studies will be of use to them and their fellow tribals in the future.

Supplementary material

The Supplementary Material for this article can be found online at: https://www.frontiersin.org/articles/10.3389/fphar.2017.00658/full#supplementary-material

DataSheet1.docxClick here for additional data file.

Abbreviations

ATCCAmerican Type Culture Collection, Manassas, Virginia, USACCCell controlsCC50−50%Cytostatic/Cytotoxic ConcentrationCPECytopathic effectDMSOdimethyl sulphoxideEC5050% Effective ConcentrationEC9090% Effective ConcentrationEV71Enterovirus 71FBSFetal bovine serumLBLuria-Bertani brothMDRMulti–drug resistantMHAMueller–Hinton agarMIC50Minimum inhibitory concentration required to inhibit the growth by 50% of organismsMTS(3–[4,5,dimethylthiazol–2–yl]–5–[3–carboxymethoxy–phenyl]–2–[4– sulfophenyl]–2H–tetrazolium, inner saltNANutrient agarNGMNematode growth mediumODOptical densityRCFRelative Centrifugal ForceSBRSimilipal Biosphere ReserveSISelectivity indexSSSelectivity SurfaceTITherapeutic indexVCVirus controlsYPDYeast extract peptone dextrose medium.

References

  • 1. AggarwalS. G.GoyalS. (2013). Nyctanthes arbor–tristis against pathogenic bacteria. J. Pharmacol. Phytochem.2, 124127.[Google Scholar]
  • 2. AlwashM. S. A.IbrahimN.YaacobW. A.DinL. B. (2014). Antibacterial, antioxidant and cytotoxicity properties of traditionally used Melastoma malabathricum Linn. leaves. Adv. J. Food Sci. Technol.6, 612. [PubMed][Google Scholar]
  • 3. AntonyM.MishraC. S.ThankamaniV. (2014). Evaluation of active fraction from plant extracts of Alstonia scholaris for its in–vitro and in–vivo antiviral activity. Int. J. Pharm Pharma Sci.6, 775781.[Google Scholar]
  • 4. BijeshK.SebastianD. (2013). Isolation and characterization of antibacterial compounds from Macaranga peltata against clinical isolates of Staphylococcus aureus. Int. J. Biol. Pharma Res.4, 11961203.[Google Scholar]
  • 5. BrennerS. (1974). The genetics of Caenorhabditis elegans. Genetics77, 7194. [PubMed][Google Scholar]
  • 6. BruuA.-L. (2002). Enteroviruses: polioviruses, coxsackieviruses, echoviruses and newer enteroviruses, in A Practical Guide to Clinical Virology, 2nd Edn., eds HaaheimL. R.PattisonJ. R.WhitleyR. J. (Chichester, UK: John Wiley & Sons, Ltd). [PubMed][Google Scholar]
  • 7. ChakrabortyA.BrantnerA. H. (1999). Antibacterial steroid alkaloids from the stem bark of Holarrhena antidysenterica. J. Ethnopharmacol.68, 339344. [PubMed][Google Scholar]
  • 8. CoxP. A.BalickM. J. (1994). The ethnobotanical approach to drug discovery. Sci. Am.270, 8287. [PubMed][Google Scholar]
  • 9. DesalermosA.MuhammedM.Glavis–BloomJ.MylonakisE. (2011). Using Caenorhabditis elegans for antimicrobial drug discovery. Expert Opin. Drug Discov.6, 645652. [PubMed][Google Scholar]
  • 10. DestaB. (1993). Ethiopian traditional herbal drugs Part II. Antimicrobial activity of 63 medicinal plants. J. Ethnopharmacol.39, 129139. [PubMed][Google Scholar]
  • 11. El–MahmoodA. M.DoughariJ. H.KimanH. S. (2010). In vitro antimicrobial activity of crude leaf and stem bark extracts of Gmelina arborea (Roxb) against some pathogenic species of Enterobacteriaceae. Afr. J. Pharma Pharmacol.4, 355361.[Google Scholar]
  • 12. FabricantD. S.FarnsworthN. R. (2001). The value of plants used in traditional medicine for drug discovery. Environ. Health Perspect.109, 6975. [PubMed][Google Scholar]
  • 13. FirnR. D. (2003). Bioprospecting – why is it so unrewarding?Biodivers. Conserv.12, 207216. [PubMed][Google Scholar]
  • 14. FonziW. A.IrwinM. Y. (1993). Isogenic strain construction and gene mapping in Candida albicans. Genetics134, 717728. [PubMed][Google Scholar]
  • 15. FyhrquistP. (2007). Traditional Medicinal Uses and Biological Activities of Some Plant Extracts of African Combretum Loefl., Terminalia L. and Pteleopsis Engl. Species (Combretaceae).Academic dissertation, University of Helsinki.
  • 16. GinsburgH.DeharoE. (2011). A call for using natural compounds in the development of new antimalarial treatments–an introduction. Malar. J.10:S1. [PubMed][Google Scholar]
  • 17. GirachR. D.ShaikA. A.SinghS. S.AhmadM. (1999). The medicinal flora of Similipahar forests, Orissa State, India. J. Ethnopharmacol.65, 165172. [PubMed][Google Scholar]
  • 18. GovindarajanR.VijayakumarM.SinghM.RaoC. V.ShirwaikarA.RawatA. K. S.. (2006). Antiulcer and antimicrobial activity of Anogeissus latifolia. J. Ethnophrmacol. 106, 5761. [PubMed][Google Scholar]
  • 19. Gurib–FakimA. (2005). Medicinal plants: traditions of yesterday and drugs of tomorrow. Mol. Aspects Med.27, 193. [PubMed][Google Scholar]
  • 20. HammerK. A.CarsonC. F.RileyT. V. (1999). Antimicrobial activity of essential oils and other plant extracts. J. Appl. Microbiol.86, 985990. [PubMed][Google Scholar]
  • 21. HussainA.ZamanM. K.RamtekeA. M. (2010). Antibacterial activity of trunk bark of Alstonia scholaris. Asian J. Pharmaceut. Clin. Res.3, 4647.[Google Scholar]
  • 22. JainV. C.PatelN. M.ShahD. P.PatelP. K.JoshiB. H. (2010). Antioxidant and antimicrobial activities of Alangium salvifolium (Lf) Wang root. Global J. Pharmacol.4, 1318.[Google Scholar]
  • 23. KawdeA. B.BatraR. J.WeginwarR. G.AkkewarD. M.GondG. S.AparnaY. (2014). Preliminary phytochemical screening and bioevaluation studies of stem bark of Ventilago madersapatana Garten. Int. J. Res. Pharma Chem.4, 7482.[Google Scholar]
  • 24. KhanM. R.OmolosoA. D.KiharaM. (2003). Antibacterial activity of Alstonia scholaris and Leea tetramera. Fitoterapia74, 736740. [PubMed][Google Scholar]
  • 25. KumarR. S.SivakumarT.SundaramR. S.SivakumarP.NethajiR.GuptaM.(2006). Antimicrobial and antioxidant activities of Careya arborea Roxb. stem bark. Iran J. Pharm. Ther.5, 3541.[Google Scholar]
  • 26. KumarT.AlexanderA.DewanganA. D.KhanJ.SharmaM. (2011). Investigation of in–vitro anthelmintic activity of Bauhinia racemosa Linn. J. Appl. Pharm. Sci.1, 7375.[Google Scholar]
  • 27. LenaertsI.WalkerG. A.Van HoorebekeL.GemsD.VanfleterenJ. R. (2008). Dietary restriction of Caenorhabditis elegans by axenic culture reflects nutritional requirement for constituents provided by metabolically active microbes. J. Gerontol. A63, 242252. [PubMed][Google Scholar]
  • 28. LizardoR. C. M.MabesaL. B.DizonE. I.AquinoN. A. (2015). Functional and antimicrobial properties of bignay [Antidesma bunius (L.) Spreng.] extract and its potential as natural preservative in a baked product. Int. Food Res. J.22, 8895.[Google Scholar]
  • 29. MahapatraS. K.MookerjeeM.RoyD. S.KarakP.DasS.DastidarS. G. (2013). Evaluation of antimicrobial potentiality of a flavonoid, isolated from the leaf of the plant Colebrookea Oppositifolia. Int. J. Biol. Pharm. Res.4, 225230.[Google Scholar]
  • 30. Martínez-GualdaB.SunL.Rivero-BucetaE.FloresA.QuesadaE.BalzariniJ.. (2017). Structure-activity relationship studies on a Trp dendrimer with dual activities against HIV and enterovirus A71. Modifications on the amino acid. Antiviral Res.139, 3240. [PubMed][Google Scholar]
  • 31. NewmanD. J.CraggG. M. (2016). Natural products as sources of new drugs from 1981 to 2014. J. Nat. Prod.79, 629661. [PubMed][Google Scholar]
  • 32. PadmavathiD.BharathiR. V.SaralaA. (2011). In vitro anthelmintic activity of ethanolic extracts of Barringtonia acutangula (L.) Geartn. Int. J. Pharm Technol. Res.3, 784786.[Google Scholar]
  • 33. PandaS. K. (2014). Ethno-medicinal uses and screening of plants for antibacterial activity from similipal biosphere reserve. Odisha, India. J. Ethnopharmacol.151, 158175. [PubMed][Google Scholar]
  • 34. PandaS. K.DuttaS. K. (2012). Antibacterial activity from bark extracts of Pterospermum acerifolium (L.) Willd. Int. J. Pharma Sci. Res.2, 584595.[Google Scholar]
  • 35. PandaS. K.BastiaA. K.DuttaS. K. (2010a). Anticandidal activity of Croton roxburghii Balak. Int. J. Curr. Pharma Res.2, 5559.[Google Scholar]
  • 36. PandaS. K.DasD.TripthathyN. K. (2014). Phytochemical investigation and anthelmintic activity of various leaf extracts of Crotalaria pallida Aiton. World J. Pharma Pharmaceut. Sci.4, 336342.[Google Scholar]
  • 37. PandaS. K.DasD.TripthathyN. K. (2015). Phytochemical investigation and anthelmintic activity of various root extracts of Gmelina arborea. Asian J. Plant Sci. Res.5, 5458.[Google Scholar]
  • 38. PandaS. K.DuttaS. K.BastiaA. K. (2010b). Antibacterial activity of Croton roxburghii Balak. against the enteric pathogens. J. Adv. Pharma Technol. Res.1, 388391. [PubMed][Google Scholar]
  • 39. PandaS. K.MohantaY. K.PadhiL.ParkY. H.MohantaT. K.BaeH. (2016). Large scale screening of ethnomedicinal plants for identification of potential antibacterial compounds. Molecules21, 120. [PubMed][Google Scholar]
  • 40. PandaS. K.PatraN.SahooG.BastiaA. K.DuttaS. K. (2012). Anti–diarrheal activities of medicinal plants of Similipal Biosphere Reserve, Odisha, India. Int. J. Med. Arom. Plants2, 123134.[Google Scholar]
  • 41. PandeyR. S. (2012). Anthelmintic activity of Alangium salviifolium bark. J. Nat. Prod. Plant Resour.2, 717720.[Google Scholar]
  • 42. PatilU. H.GaikwadD. K. (2010). Phytochemical profile and Antibacterial activity of stem bark of Anogeissus latifolia. Phrmacogn. J. 17, 7073. [PubMed][Google Scholar]
  • 43. PattnaikA.SarkarR.SharmaA.YadavK. K.KumarA.RoyP.(2013). Pharmacological studies on Buchanania lanzan Spreng.–A focus on wound healing with particular reference to anti–biofilm properties. Asian Pac. J. Trop. Biomed.3, 967974. [PubMed][Google Scholar]
  • 44. PatwardhanB. (2005). Ethnopharmacology and drug discovery. J. Ethnopharmacol.100, 5052. [PubMed][Google Scholar]
  • 45. PerryB. D.RandolphT. F. (1999). Improving the assessment of the economic impact of parasitic diseases and of their control in production animals. Vet. Parasitol.84, 145168. [PubMed][Google Scholar]
  • 46. PrashanthD.AshaM. K.AmitA.PadmajaR. (2001). Anthelmintic activity of Butea monosperma. Fitoterapia72, 421422. [PubMed][Google Scholar]
  • 47. PrichardR. (1994). Anthelmintic resistance. Vet. Parasitol.54, 259268. [PubMed][Google Scholar]
  • 48. RashedK.ButnariuM. (2014). Antimicrobial and antioxidant activities of Bauhinia racemosa Lam. and chemical content. Iran J. Pharm. Res.13, 10731080. [PubMed][Google Scholar]
  • 49. SahooS.PandaP. K.BeheraP. S.MishraS. R.EllaiahP. (2008). Antifungal activity of Barringtonia acutangula against selected human pathogenic fungi. Ind. Drugs45, 2630.[Google Scholar]
  • 50. SahuM. C.PadhyR. N. (2013). In vitro antibacterial potency of Butea monosperma Lam. against 12 clinically isolated multidrug resistant bacteria. Asian Pac. J. Trop. Dis. 3, 217226. [PubMed][Google Scholar]
  • 51. SantA.IngoleA.DhabardeD.KambleM. (2014). Evaluation of anthelmintic activity of flower extract of Butea monosperma var. lutea. J. Pharmacogn. Phytochem.2, 152153.[Google Scholar]
  • 52. Saslis–LagoudakisC. H.SavolainenV.WilliamsonE. M.ForestF.WagstaffS. J.BaralS. R.. (2012). Phylogenies reveal predictive power of traditional medicine in bioprospecting. Proc. Natl. Acad. Sci. U.S.A.109, 1583515840. [PubMed][Google Scholar]
  • 53. SatputeK.BodasK.ShendeV.ChausW.AtulD.AmarG. (2014). Anthelmintic activity of extracts of Holarrhena antidysenterica Wall. World J. Pharma Pharmaceut. Sci.3, 561567.[Google Scholar]
  • 54. SaxenaH. O.BrahmamM. (1994-1996). The Flora of Orissa, Vol. 1–4Bhubaneswar: RRL; CSIR.
  • 55. ShrutiS.GoyalS.ShrivastvaK.SinghP. M.DaveK.SinghN. (2009). In–vitro anthelmintic activity of hydro alcoholic extract of leaves of Nyctanthes arbortristis Linn. J. Global Pharma Technol.1, 101104.[Google Scholar]
  • 56. SiddiquiB. S.AliS. T.RizwaniG. H.BegumS.TauseefS.AhmadA. (2012). Antimicrobial activity of the methanolic bark extract of Holarrhena pubescens (Buch. Ham), its fractions and the pure compound conessine. Nat. Prod. Res.26, 987992. [PubMed][Google Scholar]
  • 57. SilhavyT. J.KahneD.WalkerS. (2010). The bacterial cell envelope. Cold Spring Harb. Perspect Biol.2:a000414. [PubMed][Google Scholar]
  • 58. SinghR. K.SinghK. P.TurnerN. J. (2013). A special note on Prior Informed Consent (PIC). Why are you asking our gyan (knowledge) and padhati (practice)?: Ethics and prior informed consent for research on traditional knowledge systems. Indian J. Tradit. Knowl.12, 547562.[Google Scholar]
  • 59. SinghS. S.SharmaS. K. (2013). Anthelmintic potential of stem bark and roots of Alstonia scholaris (L.) R.Br. World J. Pharma Pharmaceut. Sci.2, 38073817.[Google Scholar]
  • 60. SoejartoD. D.FongH. H. S.TanG. T.ZhangH. J.MaC. Y.FranzblauS. J.. (2005). Ethnobotany/ethnopharmacology and mass bioprospecting: issues on intellectual property and benefit–sharing. J. Ethnopharmacol.100, 1522. [PubMed][Google Scholar]
  • 61. SutekyT.Dwatmadji (2011). Anthelmintic activity of Melastoma malabatricum extract on Haemonchus contortus activity in vitro. Asian J. Pharm. Clin. Res.4, 6870.[Google Scholar]
  • 62. ThatoiH. N.PandaS. K.RathS. K.DuttaS. K. (2008). Antimicrobial activity and ethnomedicinal uses of some medicinal plants from Similipal Biosphere Reserve, Orissa. Asian J. Plant Sci.7, 260267. [PubMed][Google Scholar]
  • 63. TiwariP.JainR.KumarK.MishraR.ChandyA. (2012). Antibacterial activity and physicochemical evaluation of roots of Butea monosperma. Asian Pacific J. Trop. Biomed. 2, S881S883. [PubMed][Google Scholar]
  • 64. UkilS.LaskarS.RoyR. N. (2016). Physicochemical characterization and antibacterial activity of the leaf oil of Crotalaria pallida Aiton. J. Taibah Univ. Sci.10, 490496. [PubMed][Google Scholar]
  • 65. VerpoorteR. (2000). Pharmacognosy in the new millennium: lead finding and biotechnology. J. Pharma Pharmacol.52, 253262. [PubMed][Google Scholar]
  • 66. WagnerH.Ulrich–MerzenichG. (2009). Synergy research: approaching a new generation of phytopharmaceuticals. Phytomedicine16, 97110. [PubMed][Google Scholar]
  • 67. WanH.MoensM.-F.LuytenW.ZhouX.MeiQ.LiuL.. (2016). Extracting relations from traditional Chinese medicine literature via heterogeneous entity networks. J. Am. Med. Informat. Assoc.23, 356365. [PubMed][Google Scholar]
  • 68. WilliamsonE.OkpakoD. T.EvansF. J. (1996). Selection, Preparation and Pharmacological Evaluation of Plant Material. Chichester: John Wiley & Sons.
  • 69. Wood–SheldonJ.BalickM. J.LairdS. A. (1997). Medicinal Plants: Can Utilization and Conservation Coexist?Bronx, NY: The New York Botanical Garden.
  • 70. YadavaR. N.TiwariL. (2005). A potential antiviral flavone glycoside from the seeds of Butea monosperma O. Kuntze. J. Asian Nat. Prod. Res.7, 185188. [PubMed][Google Scholar]
  • 71. ZhuF.QinC.TaoL.LiuX.ShiZ.MaX.. (2011). Clustered patterns of species origins of nature–derived drugs and clues for future bioprospecting. Proc. Natl. Acad. Sci. U.S.A. 108, 1294312948. [PubMed][Google Scholar]
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