African Health Sciences Makerere University Medical School ISSN: 1680-6905 EISSN: 1729-0503 Vol. 9, Num. 4, 2009, pp. 264-269

African Health Sciences, Vol. 9, No. 4, December, 2009, pp. 264-269

Antibacterial agents from the leaves of Crinum purpurascens herb (Amaryllidaceae)

Nkanwen ERS¹, *Gatsing D², Ngamga D¹, Fodouop SPC², Tane P ¹

¹ Department of Chemistry, Faculty of Science, University of Dschang, Dschang, Cameroon
² Department of Biochemistry, Faculty of Science, University of Dschang, Dschang, Cameroon
*Corresponding author: Dr Donatien Gatsing, Department of Biochemistry, Faculty of Science, University of Dschang , P.O. Box 67 , Dschang, Cameroon Tel: +237 77516740 E-mail: gatsingd@yahoo.com

Code Number: hs09063

Abstract

Background: Typhoid fevers and urogenital infections continue to be serious health problems in developing countries. In our search for therapeutic agents from natural sources with potential for the treatment of typhoid fevers and urogenital infections, extract and compounds were obtained from Crinum purpurascens and tested.
Methods: Two alkaloids (4,5-ethano-9,10-methylenedioxy-7-phenanthridone or hippadine (1) and 4,5-ethano-9-hydroxy-10-methoxy-7-phenanthridone or pratorimine (2)) and one steroid (â-D -glucopyranoside of sitosterol (3)) were isolated from the CH₂Cl₂/MeOH (1:1) leaf extract of Crinum purpurascens and screened for antibacterial activity using both agar diffusion and broth dilution techniques.
Results: For the CH₂Cl₂/MeOH extract, the MIC values obtained were 3 mg/ml (against P. aeruginosa), 4 mg/ml (against E. coli, K. pneumoniae and S. aureus) and 6 mg/ml (against S. typhi and S. paratyphi B), whereas the MBC values varied between 7 and 12 mg/ml. For compound 1, the MIC values varied between 200 and 250 µg/ml, whereas the MBC value was 300 µg/ml against all the bacteria strains used. Compound 2 did not show any antimicrobial activity against these bacteria strains. For compound 3, the MIC values varied between 250 and 300 µg/ml, whereas the MBC values were 300 µg/ml (against S. typhi and S. paratyphi B) and > 300 µg/ml (against the other bacteria strains).
Conclusion: These data suggest that C. purpurascens leaf extract contains antibacterial agents which could be used in the treatment of typhoid fevers and urogenital infections.

Keywords: Crinum purpurascens., alkaloids, steroid, antimicrobial activity,.

Introduction

Crinum purpurascens herb (Amaryllidaceae), known in English as starry crinum (Morton), is a herbaceous plant of about 90 cm height, with bulbs and leaves, growing in humid regions of Africa ¹. It is often grown for ornamental purposes ². However, in Cameroonian folk medicine the macerated leaves are used as anti-poison or as antidote of mystical poisoning ¹. Also, an infusion of the leaves of Crinum purpurascens is used for the treatment of some microbial infections. Biologically active compounds have been detected within species of the genus Crinum; extracts and compounds obtained from some species of Crinum have been reported to exhibit antitumour, antifungal, antiparasitic and insecticidal activities ².

Typhoid, paratyphoid A and paratyphoid B fevers are caused by Salmonella typhi, Salmonella paratyphi A and Salmonella paratyphi B, respectively ³. Typhoid fever continues to be a marked public health problem in developing countries in general and in sub-Saharan Africa in particular, where it is endemic ⁴. Non specific urogenital infections are caused by a variety of bacteria whose habitat is not limited to the urogenital tract only. These bacteria are generally commensals which become pathogenic in debilitated persons or following a modification of their habitat ⁵. Among the bacteria causing non specific urogenital infections are Escherichia coli ⁶, Klebsiella pneumoniae, Pseudomonas aeruginosa ⁷ and Staphylococcus aureus ⁵. Cases of resistance to the currently used antibiotics have been encountered with some strains of these bacteria ^5,8.

In a continuation of our search for therapeutic agents from natural sources with potential for the treatment of typhoid fevers and urogenital infections ^{3,4,9,10,11,12,13,14}, two alkaloids (4,5-ethano-9,10-methylenedioxy-7-phenanthridone or hippadine (1) and 4,5-ethano-9-hydroxy-10-methoxy-7-phenanthridone or pratorimine (2)) and one steroid (â-D -glucopyranoside of sitosterol (3)) were obtained from the extract of the leaves of Crinum purpurascens through bioassay-guided fractionation. C. purpurascens was selected based on the claims of some traditional healers and users consulted in the area of collection, and on the results of the preliminary tests. The extract and the above three compounds were tested for their antimicrobial activity. Compounds 1 and 2 were isolated for the first time from C. pratense by Ghosal et al. ¹⁵

Materials and Methods

Plant material

The leaves of Crinum purpurascens Herb. were collected in the West province of Cameroon, in the month of May 2006. The authentification was carried out at the Cameroon National Herbarium in Yaoundé, where a voucher specimen (N° 97/SRF/CAM) is deposited.

Test bacteria and culture media

The bacteria strains, including Salmonella typhi, Salmonella paratyphi B, Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae and Staphylococcus aureus, were obtained from the Medical Bacteriology Laboratory of the pasteur Centre, Yaoundé, Cameroon. The culture media used, namely Salmonella-Shigella agar (used for the isolation of the Salmonella species and for the screening of contaminants when preparing the inoculums), Mueller Hinton agar, selenite broth and tryptose phosphate broth (used for antibacterial tests), were obtained from International Diagnostics Group PLC, UK.

Extraction and isolation

The leaves of C. purpurascens were chopped, dried, ground (600 g of powder) and extracted with a cold mixture of methylene chloride/methanol (1:1) for 3 days. Filtration and concentration on a rotavapor afforded 91 g (15.16%) of extract. This extract was dissolved in distilled water, followed by acidification with H₂SO₄ (pH 3-4) and filtration. The residue was then further extracted with n-butanol to obtain n-butanol extract (14 g). The acidic filtrate was extracted with ethyl acetate to produce two phases which were separated by decantation to obtain a neutral extract and an acidic extract. The acidic extract obtained was basified with 10% NH₄OH (pH 8-10) and further extracted with ethyl acetate to produce an aqueous phase and an organic extract. The organic extract was conserved while the aqueous phase was further extracted with a mixture of ethyl acetate/methanol (2:3) to yield an aqueous and another organic phase which was then added to the previous organic phase conserved which constituted the alkaloid-containing fraction (9 g).

Vacuum liquid chromatography of the neutral fraction on alumina gel (activity III) using a gradient of methanol in methylene chloride (100:0; 98:2; 95:5; 90:10; 80:20; 70:30; 60:40; 40:60; 20:80 and 0:100) gave forty-seven fractions (10 ml each), which were concentrated and combined on the basis of TLC profiles. Compound 1 (34 mg; colourless solid) was obtained from the residue of fraction 2 (0.1 g) under further recrystallisation in pure methanol. The residue obtained from fractions 3-7 (0.2 g) was purified on a silica gel (60 g) column eluted with CH₂Cl₂ (5 ml for each fraction) to yield compound 2 (17 mg; colourless solid).

Vacuum liquid chromatography of n-butanol fraction (14 g) on silica gel using a gradient of MeOH in CH₂cl₂ (100: 0; 98:2; 96:4; 90: 10; 85:15; 80:20; 60:40; 20:80 and 0:100) gave one hundred and forty fractions (100 ml each), which were concentrated and combined on the basis of TLC profiles. Chlorophyll was removed from fraction 67-91 (obtained with CH₂Cl₂/MeOH (85:15 and 80:20) by gel permeation through Sephadex LH-20 (70 g), (Hex/CH₂Cl₂/MeOH (7:4:2) 10 ml for each elution). The remaining residue of the fraction 67-91 previous was purified on a silica gel (150 g) column using a gradient of EtOAc in n-hexane (50 ml for each fraction) to yield compound 3 (23 mg, colourless solid). The structure of compounds 1 and 2 were successfully determined using a combination of one dimensional NMR techniques (¹H and ¹³C), homo and heteronuclear two-dimensional NMR techniques (¹H-¹H COSY, HMBC, HMQC spectra), and other spectroscopy methods (IR and mass spectra). Compound 3 was identified by comparative co-chromatography with authentic sample available in our laboratory.

Antimicrobial bioassay

The antibacterial activity was determined using both agar diffusion and broth dilution techniques as previously described by Gatsing et al. ³.

Agar diffusion susceptibility testing was done using both the well and the disc methods. The well method was used to test the CH₂Cl₂/MeOH (1:1) extract, whereas the disc method was used to test the isolated pure compounds, chloramphenicol and ciprofloxacin. On each plate containing the appropriate agar medium already inoculated with the test organism (100 µl of the bacteria suspension in the broth, at the concentration of 5.10⁵ cfu/ml), equidistant wells (of 6 mm diameter) were bored using a cork borer. The bottom of each well was sealed with a drop of molten agar. The wells were filled with 100 µl of the solution (40 mg/ml) of the extract dissolved in DMSO. For the disc method, a disc of blotting paper was impregnated with 10 µl of a 20 mg/ml solution of each pure compound dissolved in DMSO. Thus, the disc potency was 200 µg for each compound. Ciprofloxacin (5 µg) and chloramphenicol (30 µg) were used as the standard drugs for urogenital infection bacteria and typhoid fever bacteria, respectively. After drying, the disc was placed on a plate of sensitivity testing agar inoculated with the appropriate test organism. The petridishes were left at room temperature (25 ± 2 °C) for about 45 min to allow the extract or the compounds to diffuse from the well/disc into the medium. They were then incubated at 37 °C for 24 h, after which the zones of no growth were noted and their diameters recorded as the zones of inhibition.

For the broth dilution susceptibility testing, the solutions (maximum concentration) of the extract and pure compounds were prepared in DMSO, diluted following an arithmetic progression by the amount of 1 (for the extract) and 25 (for the compounds), and 0.5 ml of each dilution was introduced into a test tube containing 4.4 ml of selenite broth or tryptose phosphate broth; then 0.1 ml of bacteria suspension (5.10⁵ cfu/ml) was added and the mixture was homogenized. The total volume of the mixture was 5 ml, with the extract concentrations in the tube ranging from 20 to 1 mg/ml, those of the test-compounds ranging from 300 to 25 µg/ml, and those of the standard drugs, i.e. ciprofloxacin and chloramphenicol, ranging from 20 to 1 µg/ml. After 24 h of incubation at 37 °C, the MIC was reported as the lowest concentration of antimicrobial that prevented visible growth. The MBC was determined by sub-culturing the last tube showing visible growth and all the tubes in which there was no growth on already prepared plates containing Mueller Hinton agar medium. The plates were then incubated at 37 °C for 24 h and the lowest concentration showing no growth was taken as the MBC.

Results

The CH₂Cl₂/MeOH extract was initially tested against Escherichia coli, Pseudomonas aeruginosa, Klebsiella pneumoniae, Staphylococcus aureus, Salmonella typhi and Salmonella paratyphi B. This extract showed a remarkable activity against P. aeruginosa, K. pneumoniae, S. aureus, E. coli, S. typhi and S. paratyphi B, as shown by the diameters of zones of inhibition. Thereafter the CH₂Cl₂/MeOH extract was fractionated and purified to yield mainly two alkaloids (4,5-ethano-9,10-methylenedioxy-7-phenanthridone or hippadine (1) and 4,5-ethano-9-hydroxy-10-methoxy-7-phenanthridone or pratorimine (2)) and one steroid (â-D -glucopyranoside of sitosterol (3)) which were also tested against all the six bacteria strains. The data obtained from the diffusion sensitvity test showed that compound 1 (at 200 µg) was active against all except P. aeruginosa and K. pneumoniae, whereas compound 3 was active against all the six bacteria strains. Compound 2 did not show any antimicrobial activity against the bacteria strains used (Table 1).

The antimicrobial activity of the extract and pure compounds was further studied using broth dilution technique in order to determine the MIC and MBC values (Table 2). For the CH₂Cl₂/MeOH extract, the MIC values were 3 mg/ml (against P. aeruginosa), 4 mg/ml (against E. coli, K. pneumoniae and S. aureus) and 6 mg/ml (against S. typhi and S. paratyphi B), whereas the MBC values varied between 7 and 12 mg/ml. For compound 1, the MIC values were 200 µg/ml (against K. pneumoniae and S. aureus) and 250 µg/ml (against E. coli, P. aeruginosa, S. typhi and S. paratyphi B), whereas the MBC value was 300 µg/ml against all the bacteria strains used. Compound 2 still did not show any antimicrobial activity against the bacteria strains tested. For compound 3, the MIC values were 250 µg/ml (against K. pneumoniae, S. typhi and S. paratyphi B) and 300 µg/ml (against E. coli, P. aeruginosa and S. aureus), whereas the MBC values were 300 µg/ml (against S. typhi and S. paratyphi B) and > 300 µg/ml (against E. coli, P. aeruginosa, K. pneumoniae and S. aureus).

Discussion

Among the three compounds isolated from C. purpurascens CH₂Cl₂/MeOH leaf extract, 1 and 3 were the only compounds found to exhibit antimicrobial activity against the bacteria used. Compound 2 did not show any antimicrobial activity against these bacteria strains. From the structures of 1 and 2, it can be seen that compound 2 differs from 1 only by the opening of methylenedioxy cycle (in C₉ and C₁₀) which yields the methoxy group in C₁₀ and hydroxyl group in C_9. Therefore, the activity of compound 1 may be attributed to the methylenedioxy (-O-CH₂-O-) cycle in its structure.

Antimicrobial substances are considered as bactericidal agents when the ratio MBC/MIC ≤ 4 and bacteriostatic agents when the ratio MBC/MIC > 4 ^3,4,13,14,16. For the extract, compounds 1 and 3, the ratio MBC/MIC ≤ 4 (Table 2), suggesting that they may be classified as bactericidal agents. Besides, the compounds 1 and 3 showed activity against both Gram-negative rods (e.g. K. pneumoniae, P. aeruginosa, E. coli, S. typhi and S. paratyphi B) and Gram-positive cocci (e.g. S. aureus), indicating that these substances may be large spectrum antibacterials.

Compounds 1 and 3 were, however, about 150 times less active than ciprofloxacin and about 100 times less active than chloramphenicol (Table 2).

Conclusion

All these results suggest that the C. purpurascens CH₂Cl₂/MeOH leaf extract, compounds 1 and 3 have antibacterial properties, and could be developed into remedies for the treatment of typhoid fevers and urogenital infections. Also, the activity of compound 1 may be attributed to the methylenedioxy (-O-CH₂-O-) cycle in its structure. However, in vivo antityphoid properties and the toxicity of these extract and compounds should be evaluated in a further study to ascertain the therapeutic efficacy and the safety of these natural products.

Acknowledgement

We acknowledge the international foundation for Science (IFS) and the Organisation for the Prohibition of Chemical Weapons (OPCW) for their support (grant N° F/3974 1 to D. Ngamga). We also wish to express our gratitude to Dr (Mrs) Fonkoua M. Marie-Christine, Medical Microbiology Laboratory, Pasteur Centre, Yaounde, Cameroon, for her co-operation.

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