Skip to main content

Ethnobotanical and antimicrobial study of some selected medicinal plants used in Khyber Pakhtunkhwa (KPK) as a potential source to cure infectious diseases



Present investigation deals with antimicrobial screening of ten medicinally important plants used by the inhabitants of district Haripur, Khyber Pakhtunkhwa (KPK) for different infectious diseases.


Aqueous, n-hexane and ethanolic extracts of each plant were tested for their antimicrobial activity against both Gram positive and Gram negative strains of bacteria, as well as strain of yeast. Agar well diffusion and broth dilution methods were used to determine the antimicrobial activity of different plant extracts.


The results indicated that all plants exhibited antimicrobial activity against one or more test pathogens. Interestingly, extracts of three plants showed strong and broad spectrum activity as compared to rest of the extracts which demonstrated the moderate activity. On the whole ethanolic extracts exhibited maximum antimicrobial effect than their corresponding aqueous and n-hexane extracts, when compared with standard antibiotics i.e., Streptomycin and Tetracycline. Among various extracts, only ethanloic extract of Azadirachta indica and aqueous and ethanolic extracts of Eucalyptus globulus and Bergenia ciliata and ethanolic extract of Punica granatum were found to have potentially promising activity against test microorganisms.


Different plant extracts show promising antimicrobial activity justifying their usage in traditional medicines. This study will be continued to identify more plants with potential antimicrobial components.

Peer Review reports


There is an increase interest to explore the secret of traditional herbal remedies based on information collected from local residents and traditional practioners in different parts of the world [1, 2]. Chemical and biological investigations of folk medicinal plants with the reputation of being curative have provided the world with many of clinical drugs of today [3]. It has been reported that at least 119 compounds derived from 91 plant species can be regarded as important drugs currently in use and that 77% of them were derived from traditional medicines [4]. The search for new antibacterial agents, in particular, has increased in the last decade mainly because of the increase in bacterial infections especially in countries with poor populations and more so because of bacterial resistance to current antibiotics [5]. Bacterial infections have also been implicated in complication of chronic conditions, especially transplants, cancer, and AIDS because of weakened immunity [6, 7].

Studies also claimed that some plants, which are already used as traditional medicine, possess antimicrobial properties against bacteria, fungi, and viruses [8, 9] and preparation from such plants considered to be effective against diseases of microbial etiology like small pox, tuberculosis, typhoid and diphtheria etc. [1012]. Since most of the infectious diseases are commonly treated with antibiotics and some antibiotics like Penicillin is added to items such as chewing gums, mouthwashes and toothpastes. Due to this indiscriminate use of antimicrobial drugs, have lead to the problem of drug resistance [13, 14]. Furthermore, the evolution of new strains of disease causing agents is of great concerns to the global health community [15]. In addition to this problem, antibiotic are sometimes associated with adverse effects on host which include, hypersensitivity, depletion of guts and mucosal microorganism, immune suppression and allergic reaction. Furthermore, antibiotics can also be responsible to kill the useful microflora with in the human body [1620]. It was also found that production of synthetic drugs results into the pollution of natural resources and ultimately leads to activation of antibiotic resistant genes in bacterial population in the environment [21]. All these factors associated with the use of synthetic drugs, has always been one of the driving force that encourage the researchers to search for the safe and economic alternatives from bio resource. One approach is to screen the local medicinal plants for possible antimicrobial properties.

In countries where the infectious diseases are prevalent, there is a need to develop some medicine of plant origin against persisting infectious diseases, which may be comparable to modern medicines and antibiotics. Medicinal plants used in the traditional medicines offer a great reservoir for the discovery of new plants having antimicrobial properties comparable to antibiotics used in modern medicines. Since almost all the antimicrobial agents are being imported and by considering the availability of medicinal plants in these countries, a lot of foreign exchange may be saved. In addition the cost of treatment is steadily increasing and it is becoming unaffordable by common user. Therefore, development of therapeutic agents from our own indigenous resources will be of great help.

In traditional medicines some of the indigenous medicinal plants including Calotropis procera, Artemisia spp. Neolitsea chinensis, Melia azedarach, Azadirachta indica, Eucalyptus globulus, Punica granatum, and Nigella sativa have been claimed to exert curative effect in the diseases caused by bacterial species. These plants are available in different regions of Pakistan (KPK, North of Punjab and Azad Jammu and Kashmir). All these plants are used in traditional medicines by traditional healer, local inhabitants and herbal practioners in different regions of the country to cure a variety of diseases [22].

The main objective of the present study is to evaluate in vitro antimicrobial effects of different medicinal plants based on the information collected from the local residents for the isolation and development of new broad spectrum antimicrobial compounds.


Ethnobotanical survey and collection of plant material and its processing

Periodic surveys were made in the remote areas of district Haripur, KPK, Pakistan during spring and summer. Information regarding the medicinal uses of different plants was collected through interviews with local people and traditional practitioners. Each interview followed a semi-structured questionnaire designed to obtain the following information: local names, parts of plant utilized and their medicinal uses. The sample from each plant was pressed, dried and mounted on herbarium sheets for identification. The plant identification and verification was carried in the Herbarium of Quaid-i-Azam University Islamabad, Pakistan and National Herbarium, National Agriculture and Research Council, Islamabad, Pakistan. The voucher specimen for each plant was submitted in the herbarium of Quaid-i-Azam University, Islamabad, Pakistan.

Preparation of extracts

Preparation of extracts and antimicrobial assays were conducted in Drugs Control and Traditional Medicine Division, National Institute of Health, Islamabad, Pakistan. The plant material was collected, washed (rhizome and bark) to scrap off the sand or mud. The bark and rhizomes were then cut into smaller pieces and then allowed to dry in shad for 25–30 days. Similarly, all the plant material collected was dried in shade, powdered in an electric grinder. Dried plant material (bark, rhizomes, leaves, seeds and fruits) were divided in lots of 25 g each for extraction. 25 g of ground plant material was extracted successively with distilled H2O in Soxhelt extraction apparatus. All these extracts were collected separately and dried in EYELA vacuum rotary evaporator under reduce pressure at 70°C. To evaporate the last traces of H2O a water bath is used as a heating source. Here other two portions of ground material (25 g each) were macerated each with absolute ethanol and n-hexane (250 ml) for 8–10 days with regular stirring after 24 hrs. All these extracts were then filtered through Whatmann filter paper No.1. The filtrates were evaporated to a thick residue at 30°C and reduce pressure using EYELA vacuum rotary evaporator. The last traces of ethanolic extracts were evaporated on water bath. However, n-hexane extracts were just evaporated to a thick residue. The powdered aqueous and ethanolic extracts were then dissolved in their respective solvents in a proportion of 50 mg/ml. The concentration of reference antibiotics i.e., Streptomycin and Tetracycline was 100 μg/ml.

Microbial strains tested

The following strains of bacteria were used: Bacillus subtilis ATCC # 6633, Staphylococcus aureus ATCC # 6538 (Gram positive strains), Escherichia coli ATCC # 10536, Klebsiella pneumoniae ATCC # 10031, Salmonella typhi ATCC # 19430, and Shigella dysentriae ATCC # 11835 (Gram negative strains). The yeast strain used in this study was Sacchromyces cerevisiae ATCC # 9763. The tested strains were obtained from Microbiology Laboratory, Drugs Control and Traditional Medicine Division, National Institute of Health, Islamabad, Pakistan. The microorganisms were grown overnight at 37°C in 2% Nutrient Agar (Merk Germany) at pH 7 except yeast which was grown at 30°C. Their sensitivity to the reference antibiotics was checked. Streptomycin and Tetracycline (Sigma, USA) were used for this purpose.

Preparation of inocula

The inocula were prepared by inoculating a loop of each bacterial strain from a 24 hrs old culture into a sterile nutrient broth aseptically. The culture was allowed to grow for 24 hrs in a shaking incubator at 37°C. The overnight culture is taken and checked until the visible turbidity is equal or greater than that of 0.5 McFarland standards (Pro-Lab Diagnostics) at 560 nm using UV-Visible spectrophotometer (IRMECO UV–VIS U2020, Germany). Sterilized nutrient broth is used as blank. If the absorbance is higher, then the culture is diluted with sterilized nutrient broth and absorbance is noted again. The standardized cultures were used for further analysis.

Determination of antimicrobial activity

The antibacterial tests were performed using agar well diffusion method [23]. Agar plates were prepared by using sterile Mueller-Hinton (MH) agar (Bio Lab). Bacterial cultures of standardized cultures were prepared by adding the seed culture in the autoclaved agar medium followed by pouring into petri plates. The wells were made with 8 mm sterile cork borer. 50 μl of each extract (50 mg/ml) was added in the pre labelled wells together with water, n-hexane and ethanol as negative control and Streptomycin and Tetracycline as positive control. Both reference antibiotics were used in the concentration of 100 μg/ml. The diffusion of extracts was allowed for 1 hr at room temperature on a sterile bench. The plates were then sealed with Parafilm X and incubated for 24 hrs at 37°C. However, in case of S. cerevisieae the plats were incubated for 48 hr at 30°C. The plates were observed for the presence of inhibition of bacterial growth and that was indicated by clear zone of inhibition of bacterial growth around the wells. The size of zone of inhibition was measured in milli meters (mm). Minimum Inhibitory Concentration (MIC) was determined as described by Sahin et al. [24] with little modification. Briefly the sterile broth media (5 ml) was added in to sterile screw cap test tubes followed by the addition of 50 μl diluted microbial suspension in the test tubes. Initially, 1000 μl of each plant extract (50 mg/ml) was added to the corresponding tube. The dilutions for each extract were performed at a final concentration of 2.0, 4.0, 6.0, 8.0 and 10.0 mg/ml. For each dilution 1000 μl of extract was added to corresponding microbial strain and each extract was assayed twice. The extracts in simple broth were used as negative control to ensure medium sterility while the microbial suspensions served as positive control to control the adequacy of the broth for bacterial growth. The test tubes were put on shaker at 37°C for 24−48 hrs to check the microbial growth. After 48 hrs the growth of microbial strains was measured as a function of turbidity. The dilution that showed no turbidity after 24−48 hr was regarded as MIC of the respective plant extract.

Results and discussions

The medicinal plants find an extensive use in traditional system of medicines all over Pakistan especially in the rural areas to cure various health problems. The main reason for the popularity of herbal medicines are i) these plants are near to nature, hence more effective than allopathic medicines ii) they are easily accessible iii) are cheaper mode of treatment and iv) show fewer side effects or adverse reactions as compared to modern synthetic drugs. In the present study the efforts were made to investigate the antimicrobial activity of those plant species which are used to treat various infectious diseases like syphilis, leprosy, tuberculosis, pneumonia, whooping cough and urinary tract infections [2]. Long before the invention of synthetic antimicrobial drugs, herbal drugs were used to treat such diseases. More than 100 plants in the indigenous system of medicine possessing antibacterial activity have been evaluated [25].

In the present study a total of ten plant species belonging to eight different families were screened for antimicrobial activity. These plants are used by local inhabitants, traditional healers and herbal practitioners in different sites of the visited areas to treat various ailments. Most of these plant species and their parts used to cure various diseases are taken individually. All these plants were collected from different localities of KPK. The common/local names, botanical names, their families, voucher number, plant part used, and their medicinal uses have been described in Table 1. The plants have been listed in alphabetical order according to their families along with respective voucher number. For antimicrobial activity the extracts of each plant were prepared in three fractions namely, aqueous, n-hexane and ethanolic. The antimicrobial activity of each extract was monitored in concentration of 50 mg/ml. The activity of each plant extract was then compared against the standards i.e., Streptomycin and Tetracycline (100 μg/ml). The samples were run in triplicate to get a complete picture of effectiveness of extracts against each microorganism used in the present study. The effectiveness was measured in the form of zone of inhibition.

Table 1 Plant species utilized in this study with their medicinal activities

The extracts were tested against Gram positive and Gram negative strains of bacteria and the yeast by agar diffusion method, measuring inhibition zone. This method gives the maximum growth conditions for all organisms and avoids the problems of sterilizing plant extracts prior to testing [35]. Table 2 represents the antimicrobial activity (zone of inhibition) of different plant extracts against respective microbial strains.

Table 2 Antimicrobial activities (in terms of inhibition zone in mm) where bacterial growth was inhibited by plant extracts

The MIC values of the different extracts from various plant species against all tested microorganisms were observed (Table 3). In this case, only those extracts which inhibited the growth of microbial strains in agar well diffusion method were subjected to MIC evaluation. The MIC values of all extracts correlated to the screening test results. It was found that K. pneumonia and S. cerevisiae were the most susceptible microorganisms with the lowest MIC values of aqueous and ethanolic extracts of E. globulus (less than 2 mg/ml). The ethanolic extract of E. globulus displayed the same MIC values against B. subtilis, and S. aureus. However, n-hexane extract of E. globulus exhibited the least activity against S. aureus (more than 10 mg/ml). Similar trend was found in the S. dysentriae when it was subjected to aqueous and ethanloic extract of B. ciliata. The ethanolic extracts of B. ciliata also exhibited the lowest MIC values against E. coli and S. aureus. On the other hand, ethanloic extract of A. maritima is least effective against S. cerevisiae i.e., more than 10 mg/ml. Same behaviour was found in the ethanolic extracts of C. toona against S. aureus and E. coli. Similarly E. coli and S. dysentriae were least susceptible to aqueous extract of P. granatum. Rest of the tested plant extracts exhibited the activity between the concentrations of 2–10 mg/ml (Table 3).

Table 3 Minimum Inhibitory Concentration (MIC) values (mg/ml) of different plant extracts against tested microorganisms

The results obtained in the present study revealed that absolute ethanolic extract of C. procera showed broad spectrum activity against all the test microorganisms except K. pneumoniae. S. dysentriae was the most susceptible microorganism to ethanolic extract with MIC value of 6.0 mg/ml while the growth of other microorganisms was inhibited at MIC value of about 8.0 mg/ml. The antimicrobial activity found in the present investigation is in agreement with the findings of [36] who determined the antimicrobial activity of leaves and latex of C. procera against a wide range of microorganisms. The aqueous and ethanolic extract of latex of C. procera was also found to be effective against B. subtilis, S. aureus, E. coli, and K. pneumoniae. It was found that the chloroform, ethyl acetate, n-hexane, methanol and aqueous extracts of another species of Calotropis i.e., C. gigantia (L.) R. Br. inhibited the growth of different strains of carcinogenic bacteria [37]. It was found that ethanolic extract of aerial parts of A. maritima exhibited moderate and broad spectrum activity against all the test microorganisms used in the present study with MIC value ranged from 6.0 mg/ml (S. cerevisiae) to more than 10.0 mg/ml for E. coli. However, both n-hexane and aqueous extracts of A. maritima did not show any activity. This positive response of ethanolic extract of A. maritima on different strains of Gram positive and Gram negative strains of bacteria is in accordance with the results evaluated by [38]. However, it was found that 50% ethanolic extract of aerial parts of A. maritima did not exhibit any activity against S. aureus, B. subtilis, E. coli, and S. typhi. This difference in activity might be due to the percentage of ethanolic extract used to measure the antimicrobial activity. The present results are also in agreement with the findings of [5] who found that ethanolic extract of leaves of A. nilagirica possesses promising activity against the several clinical pathogens.

Present study reveals that ethanolic extract of the bark of N. chinensis has exhibited good and broad spectrum activity against various pathogenic organisms used in the present study except K. pneumonia while n-hexane extract exhibited narrow spectrum activity against E. coli, S. typhi (Gram negative) bacteria and S. cerevisiae (Table 2). However, its aqueous extract did not show any activity against any of the tested microorganism. B. subtilis and E. coli were the most susceptible to ethanolic extract of N. chinensis bark (MIC value 4.0 mg/ml). On the other hand S. cerevisiae was the least susceptible (MIC value more than 10.0 mg/ml) to n-hexan extract. Other finding supporting the present results is of [39] who reported that 50% ethanolic extract of another species of the same genus i.e., N. sebifer a responded positively against B. subtilis, S. aureus, E. coli, and S. typhi. The narrow spectrum activity of n-hexane extract of N. chinensis against E. coli and S. dysentriae (Gram negative) bacteria only (Table 2) might be due to solubility of some active constituents in n-hexane which eventually showed this activity.

The A. indica is widely used as an insecticidal by the local residents of the visited areas. The ethanolic extract of leaves inhibited the growth of all microorganisms used in the present investigation. The most sensitive microorganisms were B. subtilis, E. coli and S. typhi with MIC value of 2.0 mg/ml and minimum activity was recorded against S. aureus and S. dysentriae (6.0 mg/ml). On the other hand the aqueous and n-hexane extracts were totally ineffective. C. toona is locally used as an alternative of A. indica, but the ethanolic extract of C. toona leaves is effective against only B. subtilis, S. aureus, E. coli and S. cerevisiae while found ineffective against all the other test microorganisms used in the study (Table 2). Similarly, the aqueous and n-hexane extracts did not show any activity. The results indicated that as for as antimicrobial activity is concerned, the ethanolic extracts of A. indica leaves exhibited the strongest antimicrobial activity as compared to C. toona though both plants are used for the same purposes in different localities. In case of M. azedarach the activity was found only in aqueous extract against S. aureus while the ethanolic and n-hexane extracts were totally ineffective in the present investigation (Table 2). The present study strengthens the findings of [16] who showed that absolute ethanolic extracts of bark and leaves of A. indica collectively had good activity against S. cerevicea and B. subtilis. However, [40] could not find any such activity who subjected the ethanolic extract of A. indica in various concentrations i.e., 100%, 75%, 50%, 25% and 10% against Bascillus spp and E. coli. The suppressed activity might be due to the negligible amount of active constituents at the time of collection as compared to present findings. The chloroform extract of A. indica was also found to be effective against S. aureus, Streptococcus pyogens, E. coli and Pseudomonas aureginosa[41]. The methanol extract of A. indica was also reported to be effective against Vibrio cholerae which is a causative agent of cholera [42].

The leaves of E. globulus are used as expectorant, stimulant, antiseptic, carminative, whereas the volatile oil is said to be antimalarial and disinfectant. The aqueous and ethanolic extracts of E. globulus leaves exhibited the strongest and the broad spectrum activity against all the test microorganisms where the MIC values are even less than 2.0 mg/ml against different tested pathogens (Table 3). Present study revealed that n-hexane extract of E. globulus also has mild antimicrobial activity against all the test microorganisms. These results supported the findings of [43] who tested the antibacterial activity of E. maidenni against K. pneumoniae. This broad spectrum activity in the present study is also in accordance with the results of [44] who analysed the essential oil composition of 12 species of Eucalyptus and tested against E. coli, S. aureus and S. cerevisiae. It was found that essential oil obtained from E. globules and E. camaldulensis is effective against E. coli and S. aureus[45].

The present study revealed that the aqueous and ethanolic extracts of P. granatum rind have a good deal of antimicrobial activity. Both the extracts exhibited broad spectrum activity, although ethanolic extract has stronger effect than aqueous fraction (Table 3), while n-hexane extract did not inhibit the growth of any organism (Table 2). This study supported the findings of [46] who found that petroleum ether extract of P. granatum had exhibited significant antibacterial activity against S. dysentreae and E. coli. It was recorded [47] that boiling water extract of P. granatum exhibited marked activity against S. typhi. The various results supporting these finding are of [48, 49]. The work of [50] also supporting these findings. The methanolic extract of fruit peels of P. granatum was also effective against Listeria monocytogenes, S. aureus, E. coli and Yersinia enterocolitica[51].

The present study revealed that ethanolic extract of N. sativa seeds was effective against all tested microorganisms except S. cerevisiae, the yeast. On the other hand, n-hexane extract of N. sativa seeds was ineffective against all the tested microorganisms in the present study. The work of [52] showed the same behaviour of 90% ethanolic extract of N. sativa seeds against S. typhi, S. dysentriae, Vibrio cholera and S. aureus. Diethyl ether extract of N. sativa seeds was found to be effective against S. aureus, E. coli and Pseudomonas aeruginosa[53]. The ethanolic extract was also found to be effective against Proteus vulgaris and Pseudomonas aeruginosa[16]. The aqueous and ethanolic extracts of B. ciliata rhizome exhibited marked and broad spectrum antimicrobial activity against all the test microorganisms used in the present study (Table 2). The highest activity was recorded in the aqueous extract against E. coli and S. dysentriae. Similar trend was found in the ethanolic extract against S. aureus and S. dysentriae (Table 3). The present findings are in agreement with the results of [54] who found that various extracts of roots and leaves of B. ciliata had promising activity against B. subtilis, Bacilliusm egaterium and Pseudomonas aeruginosa.

In the present study it was found that the absolute ethanolic extract of A. maritima, ethanolic extract of leaves A. indica, aqueous and ethanolic extracts of E. globules and B. ciliata rhizome, and ethanolic extracts of P. granatum rind inhibited the growth of all microorganisms used in the present investigation (Table 2). Furthermore, the inhibition zone (value) showed by the positive control was significantly smaller compared to those displayed by aqueous and ethanolic extracts of E. globulus, ethanolic extracts of P. granatum rind, aqueous and ethanolic extracts B. ciliata against tested microorganisms. Similar trend was recorded for MIC values of these extract (Table 3). This suggests that the bacterial species are more susceptible to these extracts compared with the other extracts from different plant parts investigated in the present study. The variations of the present results with the previous findings are not unexpected as phyto-constituents are known to vary with ecological factors [55] seasonal variation [56], the type of the solvent, and presence of different chemicals [41] which may or may not be effective against the test microorganisms. The antimicrobial components also change with the age of the plants [57]. Sometimes the compositions of the chemicals change with the orientation of the plant parts. The environmental factors like excessive rain fall or drought enhance the quality of active compounds or diminish it [58].

It has been evaluated that sixteen plant extracts out of a total of thirty (53%) of different plant parts did not exhibit antimicrobial activity against one or more test microorganism used in the study (Table 2). Out of thirty plants extracts ten plant extracts (40%) i.e., the ethanolic extracts of C. procera, A. maritima, N. chinensis, A. indica, C. toona, and that of N. sativa inhibited the growth of both Gram positive and Gram negative strains of bacteria i.e., showed broad spectrum activity. Similarly, the aqueous and ethanolic extracts of E. globulus, P. granatum and B. ciliata also exhibited the stronger and broad spectrum activity. Two plants extract (6.5%) i.e., n-hexane fractions of N. chinensis and aqueous extract of M. azedarach leaves were found to have narrow spectrum activity. Figure 1 indicates the pattern of antimicrobial activity form different plant extracts against various microorganisms used in the study. In general, ethanolic extract exhibited the highest degree of antimicrobial activity as compared to aqueous and n-hexane extract fractions (Figure 2). This suggests that ethanol is the better solvent to extract active constituents from the plant material than the other solvents used. The Streptomycin and Tetracycline were used as the reference antibiotics in this study. Both have exhibited the antimicrobial activity against all the test microorganisms used in the present investigation. It was found that Tetracycline showed slightly stronger activity against the test microorganisms than Streptomycin. On the other hand all the three solvents remained ineffective in their contact form as they were used as control in each experiment. An interesting finding in the present study is that as for as solvent is concerned the ethanolic extract exhibited the maximum activity as compared to aqueous and n-hexane fractions.

Figure 1

Antimicrobial activity of total plant extracts.

Figure 2

Efficiency of three different solvents used for the extraction of different plant parts to study antimicrobial activity.

The present study shows that plants possess antimicrobial activity which in the extracted form can be utilized successfully to treat infectious diseases and protect the host from microbial infections. In this regards the plants used in the traditional system of medicine, offer a great reservoir for the discovery of not only antimicrobial drugs but some other drugs as well. Many biological and pharmaceutical groups have already begun to perform the laboratory work in a meaningful way on herbal remedies like the development of analytical methodology from common herbal remedies [59, 60] and the toxicological evaluation of phytomedicine compounds [61, 62].


The results obtained in the present investigation have very promising antimicrobial activities and they can be used in the treatment of infectious diseases. The results obtained in the present study justify the use of these medicinal plants to cure various infectious diseases in the rural areas of Pakistan. Furthermore, it is desirable to make in depth studies of these plants for the isolation and characterization of antimicrobial compounds to adjudicate the veracity of the claim.


  1. 1.

    Mathabe MC, Nikolova RV, Lall N, Nyazema NZ: Antibacterial activities of medicinal plants used for the treatment of diarrhoea in Limpopo Province. S Afri J Ethnopharmocol. 2006, 105: 286-293. 10.1016/j.jep.2006.01.029.

    CAS  Article  Google Scholar 

  2. 2.

    Abbasi AM, Khan MA, Ahmad M, Jahan S, Sultana S: Ethnopharmacological application of medicinal plants to cure skin diseases and in folk cosmetics among the tribal communities of North-West Frontier Province, Pakistan. J Ethnopharmocol. 2010, 128: 322-335. 10.1016/j.jep.2010.01.052.

    Article  Google Scholar 

  3. 3.

    Izzo AA, Ernst E: Interaction between herbal medicines and prescribed drugs. Drugs. 2009, 69: 1777-1798. 10.2165/11317010-000000000-00000.

    CAS  Article  PubMed  Google Scholar 

  4. 4.

    Cragg GM, Newman DJ, Snader KM: Natural Products in Drug Discovery and Development. J Nat Prod. 1997, 60: 52-60. 10.1021/np9604893.

    CAS  Article  PubMed  Google Scholar 

  5. 5.

    Ahameethunisa AR, Hopper W: Antibacterial activity of Artemisia nilagirica leaf extracts against clinical and phytopathogenic bacteria. BMC Compl Alter Med. 2010, 10: 6-10.1186/1472-6882-10-6.

    Article  Google Scholar 

  6. 6.

    Panghal M, Arya V, Yadav S, Kumar S, Yadav JP: Indigenous knowledge of medicinal plants used by Saperas community of Khetawas, Jhajjar District, Haryana, India. J Ethnobiol Ethnomed. 2010, 6: 4-10.1186/1746-4269-6-4.

    Article  PubMed  PubMed Central  Google Scholar 

  7. 7.

    Voravuthikunchai SP, Phongpaichit S, Subhadhirasakul S: Evaluation of antibacterial activities of medicinal plants widely used among AIDS patients in Thailand. Pharma Biol. 2005, 43: 701-706. 10.1080/13880200500385194.

    Article  Google Scholar 

  8. 8.

    Bibi Y, Nisa S, Chaudhary FM, Zia M: Antibacterial activity of some selected medicinal plants of Pakistan. BMC Comp Alter Med. 2011, 11: 52-10.1186/1472-6882-11-52.

    Article  Google Scholar 

  9. 9.

    Rojas JJ, Ochoa VJ, Ocampo SA, Munoz JF: Screening for antimicrobial activity of ten medicinal plants used in Colombian folkloric medicine: A possible alternative in the treatment of non-nosocomial infections. BMC Comp Altern Med. 2006, 6: 1-6. 10.1186/1472-6882-6-1.

    Article  Google Scholar 

  10. 10.

    Arndt W, Mitnik C, Denzler KL, White S, Waters R, Jacobs BL, Rochon Y, Olson VA, Damon IK, Langland JO: In vitro characterization of a nineteenth-century therapy for smallpox. PloS ONE. 2012, 7: e32610-10.1371/journal.pone.0032610.

    CAS  Article  PubMed  PubMed Central  Google Scholar 

  11. 11.

    Gupta R, Thakur B, Singh P, Singh HB, Sharma VD, Katoch VM, Chauhan SV: Anti-tuberculosis activity of selected medicinal plants against multi-drug resistant Mycobacterium tuberculosis isolates. Indian J Med Res. 2010, 131: 809-813.

    PubMed  Google Scholar 

  12. 12.

    Evans CE, Banso A, Samuel OA: Efficacy of some nupe medicinal plants against Salmonella typhi: an in vitro study. J Ethnophormocol. 2002, 80: 21-24. 10.1016/S0378-8741(01)00378-6.

    Article  Google Scholar 

  13. 13.

    Bidault P, Chandad F, Grenier D: Risk of bacterial resistance associated with systemic antibiotic therapy in periodontology. J Canadian Dent Asso. 2007, 73: 721-725.

    Google Scholar 

  14. 14.

    Hancock EW: Mechanisms of action of newer antibiotics for Gram-positive pathogens. Lancet Infect Dis. 2005, 5: 209-218. 10.1016/S1473-3099(05)70051-7.

    CAS  Article  PubMed  Google Scholar 

  15. 15.

    Frey FM, Meyers R: Antibacterial activity of traditional medicinal plants used by Haudenosaunee peoples of New York State. BMC Comp Alter Med. 2010, 6: 10-64.

    Google Scholar 

  16. 16.

    Ahmad I, Mehmood Z, Mohammad F: Screening of some Indian medicinal plants for their antimicrobial properties. J Ethnopharmacol. 1998, 62: 183-193. 10.1016/S0378-8741(98)00055-5.

    CAS  Article  PubMed  Google Scholar 

  17. 17.

    Walsh C: Where will new antibiotics come from?. Nat Reviews Micro. 2003, 1: 65-70. 10.1038/nrmicro727.

    CAS  Article  Google Scholar 

  18. 18.

    Koehn FE, Carter GT: The evolving role of natural products in drug discovery. Nat Rev Drug Discov. 2005, 4: 206-220. 10.1038/nrd1657.

    CAS  Article  PubMed  Google Scholar 

  19. 19.

    Rafii F, Sutherland JB, Cerniglia CE: Effect of treatment with antimicrobial agents on the human colonic microflora. Ther Clin Risk Manag. 2008, 4: 1343-1358.

    CAS  PubMed  PubMed Central  Google Scholar 

  20. 20.

    Rashid M-U, Weintraub A, Nord CE: Effect of new antimicrobial agenst on the eclological balance of human microflora. Anaerob. 2012, 18: 249-253. 10.1016/j.anaerobe.2011.11.005.

    CAS  Article  Google Scholar 

  21. 21.

    Krintiansson E, Fick J, Janzon A, Grabic R, Rutgersson C, Weijdegård B, Söderstrom H, Larsson DGJ: Pyrosequencing of antibiotic-contaminated river sediments reveals high levels of resistance and gene transfer elements. PLoS One. 2011, 6: e17038-10.1371/journal.pone.0017038.

    Article  Google Scholar 

  22. 22.

    Abbasi AM, Khan MA, Ahmad M, Zafar M: Medicinal plant biodiversity of lesser Himalayas-Pakistan. New York: Springer

  23. 23.

    Perez C, Paul M, Bazerque P: Antibiotic assay by agar-well diffusion method. Acta Bio et Med Exp. 1999, 15: 13-115.

    Google Scholar 

  24. 24.

    Sahin F, Karaman I, Güllüce E, Öğütçü H, Şengül M, Adigüzel A, Öztürk S, Kotan R: Evaluation of antimicrobial activities of Satureja hortensis L. J Ethnopharmacol. 2003, 87: 61-65. 10.1016/S0378-8741(03)00110-7.

    CAS  Article  PubMed  Google Scholar 

  25. 25.

    Dastur JF: Medicinal plants of India and Pakistan. 1985, Bombay: DB Taraporevala

    Google Scholar 

  26. 26.

    Qureshi RA, Sultana KN, Ashraf M, Khan AG: Ethnobotanical studies of medicinal plants of Gilgit district and surrounding areas. Ethnobot Res Appl. 2006, 5: 115-122.

    Article  Google Scholar 

  27. 27.

    Hayat MQ, Khan MA, Ashraf M, Jabeen S: Ethnobotany of the genus Artemisia L. (Asteraceae) in Pakistan. Ethnobot Res Appl. 2009, 7: 147-162.

    Article  Google Scholar 

  28. 28.

    Adnan SM, Khan AA, Latif A, Shinwari ZK: Threats to the sustainability of Ethno-Medicinal uses in Northern Pakistan (a case study of Miandam Valley, district Swat, NWFP Province, Pakistan). Lyonia. 2006, 11: 91-100.

    Google Scholar 

  29. 29.

    Gul F, Shinwari ZK, Afzal I: Screening of indigenous knowledge of herbal remedies for skin diseases among local communities of North West Punjab, Pakistan. Pak J Bot. 2012, 44: 1609-1616.

    Google Scholar 

  30. 30.

    Akhter N, Rashid A, Murad W, Bergmeier E: Diversity and use of ethno-medicinal plants in the region of Swat, North Pakistan. J Ethnobiol Ethnomed. 2013, 9: 25-10.1186/1746-4269-9-25.

    Article  Google Scholar 

  31. 31.

    Shah GM, Khan MA: Check list of medicinal plants of Siran Valley Mansehra-Pakistan. Ethnobot Leaflets. 2006, 10: 63-71.

    Google Scholar 

  32. 32.

    Abbasi AM, Khan MA, Khan N, Shah MH: Ethnobotanical survey of medicinally important wild edible fruits species used by tribal communities of Lesser Himalayas-Pakistan. J Ethnopharmacol. 2013, 148: 528-536. 10.1016/j.jep.2013.04.050.

    Article  PubMed  Google Scholar 

  33. 33.

    Qureshi RA, Ghufran MA, Gilani SA, Yousaf Z, Abbas G, Batool A: Indigenous medicinal plants used by local women in southern himalayan regions of Pakistan. Pak J Bot. 2009, 41: 19-25.

    Google Scholar 

  34. 34.

    Khan SM, Page S, Ahmad H, Shaheen H, Ullah Z, Ahmad M, Harper DM: Medicinal flora and ethnoecological knowledge in the Naran Valley, Western Himalaya, Pakistan. J Ethnobiol Ethnomed. 2013, 9: 4-10.1186/1746-4269-9-4.

    Article  PubMed  PubMed Central  Google Scholar 

  35. 35.

    Le G, Wondergem APA, Verpoorte R, Pousset JL: Anti-infectious phytotherapies of the tree-savannah of senegal (West-Africa) II. Antimicrobial activity of 33 species. J Ethnopharmocol. 1989, 28: 25-31.

    Google Scholar 

  36. 36.

    Kareem SO, Akpan I, Ojo OP: Antimicrobial activities of Calotropis procera on selected pathogenic microorganisms. Afr J Biomed Res. 2008, 11: 105-110.

    Google Scholar 

  37. 37.

    Ishnava KB, Chauhan JB, Garg AA, Thakkar AM: Antibacterial and phytochemical studies on Calotropis gigantia (L.) R. Br. latex against selected cariogenic bacteria. Saudi J Bio Sci. 2012, 9: 187-191.

    Google Scholar 

  38. 38.

    Mehrotra S, Rawat AKS, Shome U: Antimicrobial activity of the essential oils of some Indian Artemisia species. Fitoterapia. 1993, 64: 65-68.

    CAS  Google Scholar 

  39. 39.

    Naqvi SBS, Sheikh D, Sheikh R: Screening of plants for antibacterial activity. Pak J Sci Ind Res. 1985, 28: 269-275.

    Google Scholar 

  40. 40.

    Parasad G, Pandey S, Gupta KK: Antibacterial activity of certain indigenous and drug plants against certain bacterial species. Hamdard Medicus. 1999, 42: 53-57.

    Google Scholar 

  41. 41.

    Thaker AM, Anjaria JV: Antimicrobial and infected wound healing response of some traditional drugs. Indian J Pharmacol. 1986, 18: 171-174.

    Google Scholar 

  42. 42.

    Thakurta P, Bhowmik P, Mukerjee S, Hajra TK, Patra A, Bag PK: Antibacterial, antisecretory and antihemorrhagic activity of Azadirachta indica used to treat cholera and diarrhea in India. J Ethnopharmocol. 2007, 111: 607-612. 10.1016/j.jep.2007.01.022.

    Article  Google Scholar 

  43. 43.

    Gundidza MS, Mavi C: A skin irritant principle from Euphorbia confinals Var. J Planta Medica. 1993, 59: 704-708.

    Article  Google Scholar 

  44. 44.

    Chaudhry NMA, Tariq P: Anti-microbial activity of Cinnamomum cassia against diverse microbial flora with its nutritional and medicinal impacts. Pak J Bot. 2006, 38: 169-174.

    Google Scholar 

  45. 45.

    Ghalem BR, Mohamed B: Antibacterial activity of leaf essential oils of Eucalyptus globulus and Eucalyptus camaldulensis. Afri J Pharm Pharmacol. 2008, 2: 211-215.

    Google Scholar 

  46. 46.

    Miranda D, Pereira L, Sirsat SM, Antarkar DS, Vaidya AB: In vitro action of Dadima (Punica granatum Linn.) against microorganisms involved in human gastrointestinal infections isolation and identification of tannins. J Res Ayurveda Siddha. 1993, 14: 154-164.

    Google Scholar 

  47. 47.

    Pérez C, Anesini C: In vitro antibacterial activity of Argentinian folk medicinal plants against Salmonella typhi. J Ethnopharmocol. 1994, 9: 41-46.

    Article  Google Scholar 

  48. 48.

    Ahmad I, Beg AZ: Antimicrobial and phytochemical studies on 45 Indian medicinal plants against multi-drug resistant human pathogens. J Ethnopharmacol. 2001, 74: 113-133. 10.1016/S0378-8741(00)00335-4.

    CAS  Article  PubMed  Google Scholar 

  49. 49.

    Nimri LF, Meqdam MM, Alkofahi A: Antibacterial activity of Jordanian medicinal plants. Pharmaceu Bio. 1999, 37: 196-201. 10.1076/phbi.

    Article  Google Scholar 

  50. 50.

    Jain P, Bansal D, Bhasin PA: Antimicrobial activity and phytochemical screening of five wild plants against Escherichia coli, Bacillus subtilis and Staphylococcus aureus. J Pharm Res. 2010, 3: 1260-1262.

    CAS  Google Scholar 

  51. 51.

    Al-Zoreky NS: Antimicrobial activity of pomegranate (Punica granatum L.) fruit peels. Inter J Food Microb. 2009, 134: 244-248. 10.1016/j.ijfoodmicro.2009.07.002.

    CAS  Article  Google Scholar 

  52. 52.

    Rizvi HA, Yasmeen A, Badar Y: Screening of higher plants for antibacterial activity. Pak J Sci Ind Res. 1987, 25: 147-152.

    Google Scholar 

  53. 53.

    Hanafy MS, Hatem ME: Studies on the antimicrobial activity of Nigella sativa seed (black cumin). J Ethnopharmacol. 1991, 34: 275-280. 10.1016/0378-8741(91)90047-H.

    CAS  Article  PubMed  Google Scholar 

  54. 54.

    Islam MU, Azhar I, Mazhar F, Usmanghani K, Ahmad A, Gill MA, Shahab UD: Evaluation of antibacterial activity of Bergenia ciliata. Pak J Pharm Sci. 2002, 15: 21-27.

    Google Scholar 

  55. 55.

    Dhar ML, Dhar MM, Dhawan BN, Mehrotra BN, Ray C: Screening of Indian plants for biological activity: Part I. Indian J Exp Bio. 1968, 6: 232-247.

    CAS  Google Scholar 

  56. 56.

    Rafique M, Chaudry FM: Seasonal variation in the composition of essential oil of Eucalyptus camaldulensis from Pakistan. Pak J Sci Ind Res. 1999, 42: 282-285.

    CAS  Google Scholar 

  57. 57.

    Mangla M, Kamal R: Steroidal sapogenins and glycoalkaloids from berries of Solanum pseudocapsicum L. at different stages of growth. Indian J Exp Bio. 1989, 27: 370-371.

    CAS  Google Scholar 

  58. 58.

    Vlachos V, Critchley AT, Holy AV: Antimicrobial activity of extracts from selected Southern African marine macro-algae. South Afri J Sci. 1997, 93: 328-332.

    CAS  Google Scholar 

  59. 59.

    Assob JCN, Kamga HLF, Nsagha DS, Njunda AL, Nde PF, Asongalem EA, Njouendou AJ, Sandjon B, Penlap VB: Antimicrobial and toxicological activities of five medicinal plant species from Cameroon Traditional Medicine. BMC Compl Alter Med. 2011, 11: 70-10.1186/1472-6882-11-70.

    Article  Google Scholar 

  60. 60.

    Yuan X, Chapman RL, Wu Z: Analytical methods for heavy metals in herbal medicines. Phytochemanaly. 2011, 22: 198-189.

    Google Scholar 

  61. 61.

    Maruo VM, Bernardi MM, Spinosa HS: Toxicological evaluations of long-term consumption of Solanum lycocarpum St. Hill fruits in male and female adult rats. Phytomedicine. 2003, 10: 48-52. 10.1078/094471103321648656.

    CAS  Article  PubMed  Google Scholar 

  62. 62.

    Wintola OAA, Sunmonu TO, Afolayan AJ: Toxicological evaluation of aqueous extract of Aloe ferox Mill.inloperamide-induced constipated rats. Human Exp Toxicol. 2011, 30: 425-431. 10.1177/0960327110372647.

    CAS  Article  Google Scholar 

Pre-publication history

  1. The pre-publication history for this paper can be accessed here:

Download references


The authors would like to thank the microbiology section, Drugs Control and Traditional Medicine Division for providing facilities to conduct the respective studies.

Author information



Corresponding author

Correspondence to Nadeem Khan.

Additional information

Competing interests

The authors declare that there are no conflicts of interest.

Authors’ contributions

NK has carried out the main experimental work, AMA, AN, GD and GMS have participated in sampling and ethnobotanical data collection, while MMS and MHS critically evaluated the manuscript. All authors read and approved the final manuscript.

Authors’ original submitted files for images

Below are the links to the authors’ original submitted files for images.

Authors’ original file for figure 1

Authors’ original file for figure 2

Rights and permissions

This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( applies to the data made available in this article, unless otherwise stated.

Reprints and Permissions

About this article

Cite this article

Khan, N., Abbasi, A.M., Dastagir, G. et al. Ethnobotanical and antimicrobial study of some selected medicinal plants used in Khyber Pakhtunkhwa (KPK) as a potential source to cure infectious diseases. BMC Complement Altern Med 14, 122 (2014).

Download citation


  • Ethnobotanical
  • Antimicrobial
  • Medicinal plants
  • Infectious diseases
  • Pakistan