Int J Pharm Pharm Sci, Vol 6, Issue 10, ??-??Original Article



1Jawaharlal Nehru Tropical Botanic Garden and Research Institute (JNTBGRI), Palode, Thiruvananthapuram, Kerala, India, 2Agroprocessing and Natural Products Division, National Institute for Interdisciplinary Science and Technology (NIIST), Council of Scientific and Industrial Research (CSIR), Thiruvananthapuram 695019, Kerala, India.

Received: 22 Aug 2014 Revised and Accepted: 20 Sep 2014


Objective: The main objective of the present study was to investigate the antimicrobial activity of the methanol extract of the roots of four Thottea species.

Methods: The root extracts of four Thottea species were subjected to antimicrobial assay by Minimum Inhibitory Concentration (MIC) and Agar Disc diffusion Assay against various medically important pathogens.

Results: It is evident from the study that. Significant antibacterial activity was recorded by Thottea sivarajanii and highest activity was recorded against Pseudomonas aeruginosa and Staphylococcus epidermis (64 µg/ml). Out of the four extracts tested for antifungal activity, Thottea barberi and Thottea ponmudiana recorded significant antifungal activity and the highest activity was recorded by T. barberi against Trichophyton rubrum (16 µg/ml).

Conclusion: Results offer a scientific basis for the traditional use of Thottea species in the treatment of microbial infections, showing that the plant extract has an enormous potential as a prospective alternative drug against microbial pathogens. The present study lays the basis for future studies, to validate the possible use of Thottea species as a candidate in the treatment of microbial infections.

Keywords: Antimicrobial activity, Thottea species, MIC, Methanol extract.


Infectious diseases are still a major threat to public health, despite the tremendous progress made in human medicine. Their impact is particularly large in developing countries due to the relative unavailability of medicines and the emergence of widespread drug resistance [1]. Contrary to synthetic drugs, antimicrobials of plant origin are not associated with many side effects and have an enormous therapeutic potential to treat many infectious diseases [2]. Plants and plant products have been used extensively to treat various ailments. Numerous studies have been carried out to extract various natural products for screening antimicrobial activity [3]. It has been estimated that between 60-90% of the population in developing countries use traditional and herbal medicines exclusively and consider them to be a normal part of primary healthcare [4]. The Indian subcontinent is unique in its richness of plant wealth. Over 15000 species of higher plants occur in India, of which 9000 are economically useful. The therapeutic potentials of a large number of plants are yet to be explored [5]. Plant-based antimicrobials and anti bacterials represent a vast untapped source for medicines and hence have enormous therapeutic potential. Therefore, interest in higher plant extracts exhibiting antimicrobial activity has increased in recent years [6-8].

The genus Thottea belongs to the family Aristolochiaceae. This small genus of shrubby understory species is occurring in tropical forests of India and South East Asia [9]. The genus consists of about 35 species distributed in India, Sri Lanka, Bangladesh, China, Myanmar, Thailand and Malaysia [10-11]. Twelve species are reported from India [12] of which eight are distributed in the southern Western Ghats [13-14]. Various therapeutic properties were attributed to some species of Thottea. T. siliquosa is credited with alexiteric properties [15]. The roots of T. duchartrei are crushed and applied externally for abscess, inflammation and poisonous bites by the Kani and Malapandaram tribes of Kerala. The Malappandaram tribe used the root of T. duchartrei against malaria [16]. The root powder of T. duchartrei is given in hot water as an antidote to poison and externally applied on swellings [17]. Tribal communities in Pathanamthitta district, Kerala are using the fresh roots of T. dinhoui for the treatment of dysentery [18]. The pounded leaves of T. dependens are used for skin complaints in peninsular Malaysia. The decoction of the roots and rhizomes is used to treat cough, bronchitis and asthma. Rhizomes of T. parviflora and the crushed stem and leaves of T. tomentosa are also used to cure cough. The crushed leaf of T. tomentosa is used in peninsular Malaysia as antivenom against snake bite. In Java, T. tomentosa is used as an emmenagogue and for treating boils. The stem and root are diuretic and the juice is given for cough [19]. Rhizome of T. grandiflora is an excellent tonic. The decoction of the rhizome of T. rhizantha is used to treat gonorrhoea by natives of Sarawak. The decoction of T. parviflora and T. tomentosa are used as a diuretic and also for the treatment of prostatitis by the people of Thailand. T. grandiflora and T. corymbosa are also diuretic [20].

The species selected for the present study are Thottea barberi (Gamble) Ding Hou., T. ponmudiana Sivar., T. siliquosa (Lam.) Ding Hou. and T. sivarajanii Santhosh, Shanavas and Binu. Its roots are pungently aromatic. Among the candidate species, T. siliquosa is used in Ayurvedic System of Medicine and also by various tribal communities of Kerala, India for treating a number of ailments, while the rest of the species are under exploited. Paste prepared from the root of T. siliquosa is applied externally for headache and also against spider, scorpion and snake poison. Decoction of root is administered internally for chest pain and cough [21].

The Paniyar community is using the fruits of T. siliquosa to cure stomach ache [22]. The Malappandaram tribe is using the root juice and paste of T. siliquosa as an anti inflamatory drug, against fever, intestinal colic, diarrhoea and dysentery [23]. They also used the root juice mixed with coconut water for diarrhea [24]. The Mannan tribes as well as Uralis of Idukki district are using the root of T. siliquosa to reduce pain during pregnancy by applying a paste over the abdomen [25]. In Ayurveda the roots of T. siliquosa are used against cholera, diarrhoea and dysentery. Ointment made using the plant with oil is said to be beneficial for carbuncles, chronic ulcers, psora or invertebrate ulcers [26]. Roots are powdered and given with warm water as an antidote to venomous bites. Leaves crushed and boiled with coconut oil is applied to cure itches [27]. T. siliquosa is one of the main components in a medicinal preparation developed for inducing apoptosis [28].

However, these species were so far not subjected to a comprehensive antimicrobial screening. The present study was aimed to investigate the comparative antimicrobial activity of methanol extracts of the roots of four Thottea species.


Plant Material

The roots of the four Thottea species viz. Thottea barberi, T. ponmudiana, T. siliquosa, and T. sivarajanii were collected from its natural habitats from Kerala, India viz. Chemunji (Thiruvananthapuram), Ponmudi (Thiruvananthapuram), Palode (Thiruvananthapuram) and Thariode (Wayanad). The taxonomic identity of all the species was certified by the concerned taxonomist and also confirmed by matching with the authentic live and herbarium specimens at Jawaharlal Nehru Tropical Botanic Garden and Research Institute (JNTBGRI), Thiruvananthapuram, Kerala, India.

Voucher Specimen

Anilkumar 40639, Chemunji, Thiruvananthapuram (TBGT); Anilkumar 40623, Ponmudi, Thiruvananthapuram (TBGT); Anilkumar 40606, Palode, Thiruvananthapuram (TBGT); Anilkumar 40628, Thariode, Wayanad, (TBGT).

Preparation of the extracts

The methanolic extracts of the dried root of the four Thottea species were filtered and then concentrated under reduced pressure in a rotary evaporator. The dry extracts were stored at -20°C for further studies. The extracts were dissolved in 5% dimethyl sulphoxide (DMSO) for the experiments.

Antimicrobial activity

Microorganisms and media

The following bacteria were used as test organisms in this study: Gram positive bacteria: Bacillus subtilis MTCC 2756, Staphylococcus aureus MTCC 902, S. epidermidis MTCC 435 and S. simulans MTCC 3610; Gram negative bacteria: Escherichia coli MTCC 2622, Klebsiella pneumoniae MTCC 109, Proteus mirabilis MTCC 425, Vibrio cholerae MTCC 3905, Pseudomonas aeruginosa MTCC 2642 and Salmonella typhi MTCC 3216. Bacterial cultures were maintained on Müller Hinton agar substrates (Hi-media, Mumbai, India). Fungal pathogens used in the present study were Aspergillus flavus MTCC 183, Candida tropicalis MTCC 184, Candida albicans MTCC 277, Trichophyton rubrum MTCC 296 and Fusarium oxysporum MTCC 284. All cultures were stored at 4°C and subcultured every 15 days.

The sensitivity of microorganisms to methanol extracts of the investigated species was tested by determining the Minimal Inhibitory Concentration (MIC). Bacterial inoculi were obtained from bacterial cultures incubated for 24 hours at 37°C on Mueller-Hinton agar substrate and brought up by dilution according to the 0.5 McFarland standards to approximately 108 CFU/ml and then further diluted to approximately 106 CFU/ml according to the procedure recommended by NCCLS.

Minimal Inhibitory Concentration (MIC)

The Minimal Inhibitory Concentration (MIC) was determined by the broth microdilution method using 96-well micro-titer plates [29]. A series of dilutions with concentrations ranging from 1 to 2000 µg/ml for extracts was used in the experiment against every microorganism tested. The starting solutions of extracts were obtained by measuring of a certain quantity of extract and dissolving it in DMSO. Two-fold dilutions of extracts were prepared in Mueller-Hinton broth for bacterial cultures and SD broth for fungal cultures. The MIC was determined with resazurin. Resazurin is an oxidation-reduction indicator used for the evaluation of microbial growth. It is a blue non-fluorescent dye that becomes pink and fluorescent when reduced to resorufin by oxidoreductases within viable cells. The boundary dilution without any changing color of resazurin was defined as the MIC for the tested microorganism at the given concentration. As a positive control of growth inhibition, ciprofloxacin was used. A DMSO solution was used as a negative control for the influence of the solvents. All experiments were performed in triplicate.

Antimicrobial assay by agar diffusion

Agar disc diffusion technique was used to determine the antibacterial activity of oils using Mueller Hinton agar medium [30]. The test cultures maintained in nutrient agar slant at 4°C were sub-cultured in nutrient broth to obtain the working cultures approximately containing 1×106CFU/ml. The methanol extract (50 µg/ml) were incorporated in a 6 mm sterile disc. Mueller Hinton agar plates were swabbed with each bacterial strain and the test discs were placed. Ciprofloxacin discs (5 μg/disc) were used as positive control. Plates were incubated overnight at 37°C. Clear, distinct zone of inhibition was visualized surrounding the discs. The determinations were done in duplicates. After 24 hours of incubation, the plates were examined if there was any inhibition zone. The diameters of the inhibition zones produced by each of the concentrations of the solutions were measured in millimeters and interpreted using the CLSI zone diameter interpretative standards.

Antifungal activity

MIC of the extract was determined using potato dextrose agar media against the standard fungicide bavistin by the poisoned food technique [31] against Aspergillus flavus, Fusarium oxysporum, and Trichophyton rubrum. A stock solution of 2000 µg/ml of the test extracts was prepared, which was further diluted with methanol to give the required concentrations 1000 to 1 µg/ml. One tube was used as solvent control. For Candida albicans and C. tropicalis, the broth dilution method was adopted using potato dextrose broth against the standard fungicide fluconazole. All experiments were done in triplicate for each treatment against each fungus.

Agar disc diffusion method

In vitro antifungal activity of the extracts was measured using agar disc diffusion assay against the test bacteria and fungi. The sterile discs were impregnated with MIC concentration of test compounds. The fluconazole (10 µg/disc) was used as positive reference standards. The antimicrobial activity was evaluated by measuring the zone of growth inhibition surrounding the discs. All the assays were carried out in triplicate.

Statistical analysis

Statistical analyses were performed with the EXCEL and SPSS software packages. To determine the statistical significance of antioxidant activity, student’s t-test was used. All values were expressed as mean ± SD of three parallel measurements.


The antimicrobial activities of the extracts of four Thottea species are shown in Table 1-4. Significant antibacterial activity was recorded by T. sivarajanii (Table 1 and 2) and highest activity was recorded against Pseudomonas aeruginosa and Staphylococcus epidermidis (64 µg/ml). T. ponmudiana recorded poor antibacterial activity (Table 1).

Antifungal activity of the extracts of the four species is shown in Table 3 and 4. Out of the four extracts tested, T. barberi and T. ponmudiana recorded significant antifungal activity and the highest activity was recorded by T. barberi against Trichophyton rubrum (16 µg/ml).

Emergence of multiple drug resistance in human pathogenic organisms has given momentum to search new antimicrobial substances from alternative sources. There have been several mechanisms proposed for the antibacterial activity of potent drugs including plant extracts [32]. In many cases phytochemicals can be more effective than chemically synthesized pure compounds because they are a complex mixture of compounds. Their complexity enables them to interact with multiple molecular targets and thus it becomes more difficult for targeting microorganisms to develop resistance because of multiple response sites [33].

Some of the test extracts (T. sivarajanii, T. barberi and T. siliquosa) in the current work exhibited considerable antibacterial activity. Some of the test bacteria (S. epidermis, P. mirabilis and V. cholerae) also exhibited resistance to a few extracts (T. barberi, T. ponmudiana, and T. siliquosa) at test concentration. Gram-negative bacteria are frequently reported to have developed multidrug resistance to many of the currently available antibiotics [34]. Therefore, it is not surprising to learn that Gram-negative bacteria are the least responding bacterial strains to some of the tested extracts.

Table 1: MIC values of the methanol extract of Thottea species against bacteria

Test bacteria MIC (µg/ml)
T. barb T. ponm T. sili T. siva ciprofloxacin
B. subtilis 125 - 250 - 2
S. aureus 1000 - 125 - 2
E. coli 500 - 500 125 2
P. aeruginosa 250 - 125 64 4
S. epidermidis - - - 64 4
P. mirabilis - - - 125 8
V. cholerae - - - 250 4
K. pneumonia 500 2000 250 250 4
S. simulans 125 2000 - 125 8
S. typhi - 1000 - 1000 1

Values represent mean of three replications. -no MIC up to 2000 µg/ml

Table 2: Disc diffusion values of the methanol extract Thottea species against bacteria

 Test bacteria Diameter of zone of inhibition (mm)
T. barb T. ponm T. sili T. siva ciprofloxacin
B. subtilis 15.00 - 11.52 - 30.00
S. aureus 9.12 - 12.72 - 31.00
E. coli 11.00 - 9.00 14.00 32.12
P. aeruginosa 9.72 - 11.15 17.00 29.72
S. epidermis - - - 19.12 28.51
P. mirabilis - - - 13.72 28.12
V. cholerae - - - 12.52 24.72
K. pneumonia 8.00 7.52 12.77 11.12 27.51
S. simulans 13.12 8.00 - 12.72 29.58
S. typhi - 10.77 - 12.1 33.72

Values represent mean of three replications. –no zone of inhibition.

Table 3: MIC values of the methanol extract of Thottea species against fungi

Test fungi MIC (µg/ml)
T. barb T. ponm T. sili T. siva fluconazole
A. flavus - - - - 1
C. tropicalis  32 32 64 125 0.5
C. albicans 64 64 250 250 1
T. rubrum  16 32 16 34 1
F. oxysporum - - - - 8

Values represent mean of three replications. -no MIC up to 2000 µg/ml.

Table 4: Disc diffusion values of the methanol extract Thottea species against fungi

Test fungi Diameter of zone of inhibition (mm)
T. barb T. ponm T. sili T. siva fluconazole
A. flavus - - - - 23.72
C. tropicalis  13.12 16.00 15.00 14.12 25.00
C. albicans 16.72 18.72 14.00 10.00 20.00
T. rubrum  21.00 17.52 22.52 18.52 25.12
F. oxysporum - - - - 22.52

Values represent mean of three replications. –no zone of inhibition


The demonstration of antibacterial activity against gram-positive bacteria is an indication that the selected Thottea species are potential sources for the production of drugs with a broad spectrum of activity.

The results of the study also supports the traditional application of the plant and suggest that plant extracts possess compounds with antibacterial properties which can be used as antibacterial agents in novel drugs for the treatment of several ailments and infections. Further pharmacological evaluations, toxicological studies and possible isolation of the therapeutic antibacterial compounds from these species are the future challenges.


The authors are thankful to the Director, NIIST, Thiruvananthapuram and the Director, JNTBGRI, Palode, Thiruvananthapuram for providing facilities to carry out the work.


  1. Okeke IN, Laxminarayan R, Bhutta ZA, Duse AG, Jenkins P, O’Brien TF, et al. Antimicrobial resistance in developing countries. part i: recent trends and current status. Lancet Infect Dis 2005;5:481–93.
  2. Iwu MW, Duncan AR, Okunji CO. New antimicrobials of plant origin. In: Janick J. Editor. Perspectives on new crops and new uses. JASHS Press: Alexandria, Va, USA; 1999. p. 457–62.
  3. Prabhakar T, Kumar P, Bhogavalli, Narasimha RVB, Reddy S, Gangula, et alIn vitro studies on antimicrobial screening of leaf extracts of Sapindus saponaria against common dental pathogens. Plant Sci Feed 2012;2(2):15–8.
  4. Alli AI, Ehinmidu JO, Ibrahim YKE. Preliminary phytochemical screening and antimicrobial activities of some medicinal plants used in ebiraland. Bayero J Pure Appl Sci 2011;4(1):10–6.
  5. Trivedi PC. Ethnobotany. Aavishkar Publishers and Distributors, Jaipur, India; 2002. p. 1-12.
  6. Bagchi AK. Alternative medicine-old wine in a new bottle. J Indian Med Assoc 2000;98:332–3.
  7. Mishra K, Mishra A, Bhargava A, Pandey AK. Antimicrobial activity of essential oils from the leaves of Cinnamomum spp. Natl Acad Sci Lett 2008;31:341–5.
  8. Maurya A, Chauhan P, Mishra A, Pandey AK. Surface functionalization of TiO2 with plant extracts and their combined antimicrobial activities against E. faecalis and E. coli. J Res Updates Polym Sci 2012;1:43–51.
  9. Neinhuis C, Wake S, Hilu KW, Muller K, Borsch T. Phylogeny of Aristolochiaceae based on parsimony, likelihood and Bayesian analysis of trnL-trnF sequences. Plant Syst Evol 2005;250:7-26.
  10. Hou D. Aristolochiaceae. In: Van CGGJ, De Wilde WJJO, editors. Flora of Malesiana. Kulwar Academic Publishers, London; 1984;1(10):53-108.
  11. Mabberly DJ. Mabberly’s Plant Book: A portable dictionary of plants, their classification and uses. 3rd ed. Cambridge University, Cambridge; 2008.
  12. Karthikeyan S, Sanjappa M, Moorthy S. Flowering plants of India, dicotyledons (Acanthaceae–Avicenniaceae). Botanical Survey of India, Kolkata; 2009. p. 156-7.
  13. Nayar TS, Beegam AR, Mohanan N, Rajkumar G. Flowering plants of Kerala –A handbook. Tropical Botanic Garden and Research Institute, Palode. Thiruvananthapuram; 2006. p. 81.
  14. Nayar TS, Beegam AR, Mohanan N, Rajkumar G. Flowering plants of Western Ghats of India – dicots. Jawaharlal Nehru Tropical Botanic Garden and Research Institute, Palode. Thiruvananthapuram; 2014. p. 113,
  15. Kirtikar KR, Basu BD. Indian medicinal plants. Reprint ed. Bishen Singh Mahendra Pal Singh, Dehra Dun; 2003. p. 2118.
  16. Nair GM, Rajasekharan S, George V. Final scientific and technical report on pilot participatory programme on conservation and sustainable use of medicinal and aromatic plants. Tropical Botanic Garden and Research Institute, Thiruvananthapuram; 2004. Appendix VII. p. 6, 17.
  17. Anilkumar N, Sivadasan M, Ravi N. Flora of Pathanamthitta district (Western Ghats, Kerala, India). Daya Publishing House, New Delhi; 2005. p. 415-6.
  18. Binu S. An enumeration of medicinal plants used by the tribals in Pathanamthitta district of Kerala, India–part –VI. J Econ Taxon Bot 2013;37(2):274-9.
  19. Anonymous. The Wealth of India–Raw Materials. Reprint ed. National Institute of Science Communication and Information Resources, CSIR, New Delhi; 2010. p. 318.
  20. Burkill IH. A dictionary of the economic products of the Malay Peninsula. Revised ed. Ministry of Agriculture and Co-operatives, Kuala Lumpur, Malaysia; 1966. p. 2156-7.
  21. Radhakrishnan K, Pandurangan AG, Pushpangadan P, Sasidharan A. Less known ethnomedicinal plants of kerala state and their conservation. Ethnobotany 1996;8:82-4.
  22. Nazarudeen A, Seeni S, Koshy KC, Pushpangadan P. Folk plants of food, medicine, adornment and repellent used by the Paniyar community in North Kerala. In: Maheswari JK, editor. Ethnobotany of South Asia. Scientific Publishers, Jodhpur, India; 1996. p. 295-305.
  23. Nair GM, Rajasekharan S, George V. Final scientific and technical report on pilot participatory programme on conservation and sustainable use of medicinal and aromatic plants. Tropical Botanic Garden and Research Institute, Thiruvananthapuram; 2004. p. 7.
  24. Augustine J, Sivadasan M. Ethnomedicinal plants of periyar tiger reserve, kerala, india. Ethnobot 2004;16:44-9.
  25. Ajesh TP. Ethnogynaecological studies of the tribes in Idukki district, Kerala, India. Ph. D Thesis, Gandhigram Deemed University, Tami Nadu; 2014.
  26. Yoganarasimhan SN, Subramaniyan K, Razi BA. Flora of Chikmagalur district, Karnataka, India. International Book distributors, Dehradun; 1981. p. 273.
  27. Subramanian KN. Flora of Thenmala. International Book Distributors, Dehradun; 1995. p. 302.
  28. Subbaiah V. Natural product based apoptosis inducers. Phyto Myco Research Corporation, Greenville, NC, US. [Internet]; 2005.
  29. CLSI (Clinical and Laboratory Standards Institute). Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically. CLSI documents M27-S3. 940, West Valley Road, Suite 1400, Wayne, Pennsylvania, 19087-1898 USA; 2006.
  30. CLSI (Clinical and Laboratory Standards Institute). Performance standards for antimicrobial disk susceptibility tests; approved standard-11th ed. CLSI documents M02-A11. West Valley Road, Suite 2500, Wayne, PA 19087, USA; 2012.
  31. Rollas S, Kalyoncuoglu N, Sur-Altiner D, Yegenglu Y. 5-(4-Aminophenyl)-4-substituted 2,4-dihydro-3H-1,2,4-triazole-3-thiones: synthesis, antibacterial and antifungal activities. Pharmazie 1993;48:308-9.
  32. Mishra A, Kumar S, Bhargava A, Sharma B, Pandey AK. Studies on in vitro antioxidant and antistaphylococcal activities of some important medicinal plants. Cell Mol Biol 2011;57:16–25.
  33. Wink M. Evolution of toxins and antinutritional factors in plants with special emphasis on Leguminosae. In: Acamovic T, Stewart CS, Pennycott TW, editors. Poisonous plants and related toxins. CABI Publishing, Wallingford, UK; 2004. p. 1–25.
  34. Mishra AK, Singh BK, Pandey AK. In vitro antibacterial activity and phytochemicals of (Tejpat) leaf extracts and oil. Rev Infect 2010;1:134–9.

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Antimicrobial activity, Thottea species, MIC, Methanol extract.



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International Journal of Pharmacy and Pharmaceutical Sciences
Vol 6, Issue 10, 2014 Page: 444-447

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Authors & Affiliations

Anilkumar Es

Mathew Dan
Jawaharlal Nehru Tropical Botanic Garden and Research Institute

Nishanth Kumar S
Interdisciplinary Science and Technology

Dileep Kumar B S
Interdisciplinary Science and Technology

Latha P G
Jawaharlal Nehru Tropical Botanic Garden and Research Institute

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