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Antimicrobial Activity of Five Herbal Extracts Against Multi Drug Resistant (MDR) Strains of Bacteria and Fungus of Clinical Origin

Rosina Khan, Barira Islam, Mohd Akram and 5 more

Molecules · 2009 · CC BY

doi:10.3390/molecules14020586

Abstract

Antimicrobial activities of the crude ethanolic extracts of five plants were screened against multidrug resistant (MDR) strains of Escherichia coli, Klebsiella pneumoniae and Candida albicans. ATCCstrains of Streptococcus mutans, Staphylococcus aureus, Enterococcus faecalis, Streptococcus bovis, Pseudimonas aeruginosa, Salmonella typhimurium, Escherichia coli, Klebsiella pneumoniae and Candida albicans were also tested. The strains that showed resistance against the maximum number of antibiotics tested were selected for an antibacterial assay. The MDR strains were sensitive to the antimicrobial activity of Acacia nilotica, Syzygium aromaticum and Cinnamum zeylanicum, whereas they exhibited strong resistance to the extracts of Terminalia arjuna and Eucalyptus globulus. Community-acquired infections showed higher sensitivity than the nosocomial infections against these extracts. The most potent antimicrobial plant was A. nilotica (MIC range 9.75-313µg/ml), whereas other crude plant extracts studied in this report were found to exhibit higher MIC values than A. nilotica against community acquired as well as nosocomial infection. This study concludes that A. nilotica, C. zeylanicum and S. aromaticum can be used against multidrug resistant microbes causing nosocomial and community acquired infections.

Full text

From PubMed Central, U.S. National Library of Medicine, as current on Oct 25, 2026. Paragraph numbers are ours, so an answer can point at one.

Introduction

Antibiotics provide the main basis for the therapy of microbial (bacterial and fungal) infections. Since the discovery of these antibiotics and their uses as chemotherapeutic agents there was a belief in the medical fraternity that this would lead to the eventual eradication of infectious diseases. However, overuse of antibiotics has become the major factor for the emergence and dissemination of multi-drug resistant strains of several groups of microorganisms. The worldwide emergence of Escherichia coli, Klebsiella pneumoniae, Haemophilus and many other ß-lactamase producers has become a major therapeutic problem. Multi-drug resistant strains of E. coli and K. pneumoniae are widely distributed in hospitals and are increasingly being isolated from community acquired infections. Candida albicans, also a nosocomial pathogen, has been reported to account for 50-70% cases of invasive candidiasis. Alarmingly, the incidence of nosocomial candidemia has risen sharply in the last decade. All this has resulted in severe consequences including increased cost of medicines and mortality of patients.

Thus, in light of the evidence of rapid global spread of resistant clinical isolates, the need to find new antimicrobial agents is of paramount importance. However, the past record of rapid, widespread emergence of resistance to newly introduced antimicrobial agents indicates that even new families of antimicrobial agents will have a short life expectancy. For this reason, researchers are increasingly turning their attention to herbal products, looking for new leads to develop better drugs against MDR microbe strains.

For thousands of years, natural products have been used in traditional medicine all over the world and predate the introduction of antibiotics and other modern drugs. The antimicrobial efficacy attributed to some plants in treating diseases has been beyond belief. It is estimated that local communities have used about 10% of all flowering plants on Earth to treat various infections, although only 1% have gained recognition by modern scientists. Owing to their popular use as remedies for many infectious diseases, searches for plants containing antimicrobial substances are frequent. Plants are rich in a wide variety of secondary metabolites such as tannins, alkaloids and flavonoids, which have been found in vitro to have antimicrobial properties. A number of phytotherapy manuals have mentioned various medicinal plants for treating infectious diseases due to their availability, fewer side effects and reduced toxicity. There are several reports on the antimicrobial activity of different herbal extracts. Many plants have been found to cure urinary tract infections, gastrointestinal disorders, respiratory diseases and cutaneous infections. Cytotoxic compounds have been isolated from the species of Vismia. Antibacterial activity of the essential oil as well as eugenol purified from Ocimum gratissimum to treat pneumonia, diarrhea and conjunctivitis has also been reported earlier. According to the WHO, medicinal plants would be the best source for obtaining variety of drugs. These evidences contribute to support and quantify the importance of screening natural products. The aim of the present study was to investigate the antibacterial and antifungal activity of ethanolic extracts of Acacia nilotica, Terminalia arjuna, Eucalyptus globulus, Syzygium aromaticum and cinnamomum zeylanicum against multi-drug resistant strains isolated from nosocomial and community acquired infections.

Results and Discussion

In this study, we have tested the ethanolic extracts of five plants for their antimicrobial activity against multi-drug resistant strains. ATCC strains of Gram-negative bacteria, Gram-positive bacteria and yeast species were also used as control sensitive strains. All the plant extracts showed antimicrobial activity against at least four of the types of microorganisms tested, as exhibited by an agar diffusion assay (Table 1). Extracts of A. nilotica, C. zeylanicum and S. aromaticum showed the most potent activity against all the microorganisms studied. E. faecalis, S. aureus, S. bovis and S. mutans were the most susceptible to all the plant extracts tested. On the contrary, S. typhimurium, K. pneumoniae, E. coli, P. aeruginosa and C. albicans strains were found to be sensitive to extracts of A. nilotica, C. zeylanicum and S. aromaticum.

Our data revealed that standard ATCC strains of Gram-positive bacteria were more sensitive than Gram-negative ones towards the plant extracts studied. This data is also supported by previous workers. It has been proposed that the mechanism of the antimicrobial effects involves the inhibition of various cellular processes, followed by an increase in plasma membrane permeability and finally ion leakage from the cells. Amongst the tested Gram-negative bacteria, K. pneumoniae was found to be the most sensitive, while S. typhimurium was the most resistant bacteria. In case of Gram-positive bacteria, E. faecalis was the most sensitive, while S. aureus was the most resistant strain. C. albicans was found to be highly sensitive to the action of A. nilotica (least MIC 4.9 µg/mL) followed by C. zeylanicum and S. aromaticum with the least MIC being 19.5 µg/mL and 156 µg/mL, respectively (Table 2). On the contrary, C. albicans was completely resistant against T. arjuna and E. globulus at the concentrations tested.

In contrast to the previous findings that Gram-negative bacteria are hardly susceptible to the plant extracts in doses less than 2 x 105 µg/mL, our results showed inhibition at concentrations as low as 9.75 µg/mL (A. nilotica). The variation of susceptibility of the tested microorganisms could be attributed to their intrinsic properties that are related to the permeability of their cell surface to the extracts. Due to the emergence of antibiotic resistant pathogens in hospitals and homes, plants are being looked upon as an excellent alternate to combat the further spread of multidrug resistant microorganisms. In this study, amongst the five plants, the crude extracts of A. nilotica, C. zeylanicum and S. aromaticum showed good antimicrobial activity against multidrug resistant strains of K. pneumoniae, E. coli and C. albicans isolated from nosocomial and community acquired infections (Table 3). Extracts of A. nilotica was found to be the most active extract against the nosocomial as well as community acquired isolates. The MIC value of the extract of A. nilotica against different isolates was found to be in the range of 4.9-313 µg/mL.

Our data show that strains isolated from nosocomial infection were more resistant to the extracts than community acquired infection ones. It was also reported earlier that the resistance to antibiotics as well as mortality is almost two times higher in case of nosocomial infections than in community-acquired infections.

Acacia nilotica was found to give the most potent antimicrobial extract (Table 2). It is reported to have antimicrobial, antihyperglycemic and antiplasmodial properties. Cinnamum zeylanicum showed next highest activity, followed by Syzygium aromaticum. These two plants are known to possess antipyretic activity and essential oils from these two species have been shown to possess antibacterial activities. Eugenol, a compound found in S. aromaticum, is reported to have strong antifungal and anti-inflammatory activities, and has been investigated for its potential anticarcinogenic effect. The essential oil from C. zeylanicum shows antioxidant, antibacterial and antifungal activities. Terminalia arjuna, a well known herbal cardiac tonic, is also known to possess antimicrobial activity. Eucalyptus globules, traditionally used to treat diabetes, showed antimicrobial effects only on Gram-positive bacteria (Table 2). T. arjuna contains ellagic acid, ethyl gallate, gallic acid and luteolin that exhibits antimutagenic property. It also possesses a significant antioxidant effect, comparable with vitamin E. Plants of the genus Eucalyptus have been shown to produce a number of phloroglucinol sesquiterpene- or monoterpene-coupled compounds, namely, the macrocarpals and euglobals. Their biological activities such as HIV-RTase inhibition, granulation inhibition and antiviral effects have been reported. Globulol isolated from the fruit of this plant has been shown to be the major source of its antimicrobial activity.

The antimicrobial potency of plants is believed to be due to tannins, saponins, phenolic compounds, essential oils and flavonoids. It is interesting to note that even crude extracts of these plants showed good activity against multidrug resistant strains where modern antibiotic therapy has failed. As per our results, the MIC values for most of the extracts were lower than their MBC/MFC values, suggesting that these extracts inhibited growth of the test microorganisms while being bactericidal/ fungicidal at higher concentrations.

Conclusions

The ethanolic extracts of A. nilotica, C. zeylanicum and S. aromaticum could be a possible source to obtain new and effective herbal medicines to treat infections caused by multi-drug resistant strains of microorganisms from community as well as hospital settings. However, it is necessary to determine the toxicity of the active constituents, their side effects and pharmaco-kinetic properties.

Plant material

Leaves of A. nilotica, E. globulus and bark of T. arjuna were collected from the gardens of AMU, Aligarh, India. C. zeylanicum and S. aromaticum were collected from local market of Aligarh. The taxonomic identity of these plants was confirmed at Department of Botany, AMU, Aligarh, India.

Preparation of plant extracts

Dried leaves of A. nilotica, E. globulus, dried bark T. arjuna, C. zeylanicum and dry buds of S. aromaticum were pulverized or grounded to coarse powder, then suspended in 50% or 90% ethanol for 1 or 7 days. After filtration and evaporation of ethanol, the extracts were oven dried at 60oC. For experiments, each extract was redissolved in ethanol to the desired concentration.

Microbial test strains

Clinical strains of E. coli, K. pneumoniae and C. albicans from nosocomial and community acquired infections were isolated, identified and characterized by conventional biochemical methods. The study includes ESBL producing strains of E.coli and K. pneumoniae from community acquired infections.Other microbial strains investigated were S. mutans ATCC-700610, S. aureus ATCC-29213, E. faecalis ATCC-29212, S. bovis ATCC-9809, P. aeruginosa ATCC-27853, S. typhimurium ATCC-13311, E. coli ATCC-25922, K. pneumoniae ATCC-700603 and C. albicans ATCC- 10231. S. mutans were grown in Brain Heart Infusion (BHI) Broth (Himedia Labs, Mumbai, India), rest of the bacteria were grown in Nutrient Broth (Himedia Labs, Mumbai, India) at 37oC. The yeast, C. albicans were grown in Yeast Peptone Dextrose (YPD) Broth (Himedia Labs, Mumbai, India) at 30oC.

Determination of the strains sensitivity to antibiotics

The susceptibilities of the microbial strains to different antibiotics were tested using disc diffusion method. Antibacterial agents from different classes of antibiotics were used which included cephalothin, ceftazideme, ceftriaxone, cefepime, amoxyclav, aztreonam, piperacillin, amikacin, gentamycin, tobramycin, fluoroquinones, nalidixic acid, ciprofloxacin, nitrofurantoin, tetracycline and chloramphenicol (Himedia Labs, Mumbai, India). For fungal strains the antibiotics used were itraconazole, ketoconazole, nystatin, clotrimazole, fluconazole, amphotericin (Himedia Labs, Mumbai, India).

Agar diffusion assay

The extracts were tested for antimicrobial activity using agar diffusion on solid media. Soyabean Casein Digest Agar (TS) was used for S. mutans, Nutrient Agar for rest of the bacterial strains and YPD Agar for C. albicans. The solid agar was punched with 7mm diameter wells. The inoculums (1.5 x 108 CFU/ml) were spread on to their respective agar plants using sterile swabs and then filled with 100µl extracts. The concentrations of the extracts employed were 0.01 g/ml for A. nilotica and 0.1g/ml for rest of the extracts. The plates were then incubated at 370C for 24h. After incubation, zone of growth inhibition for each extract was measured.

Determination of Minimum Inhibitory Concentration and Minimum Bactericidal/Fungicidal Concentration

Strains with inhibition zones were considered sensitive to the extract, those without such a zone were considered resistant. For MIC, two-fold serial dilutions of the extracts were performed. Each inoculum was prepared in its respective medium and density was adjusted to 0.5 Mcfarland standard (108 CFU/mL) and diluted to 1:100 for the broth microdilution procedure. Microtiter plates were incubated at 37oC and the MIC was recorded after 24 h. The MIC is the lowest concentration of the compound at which the microorganism tested does not demonstrate visible growth. MBC/MFC were determined by sub-culturing the test dilutions on to a fresh solid medium and incubated further for 18-24 h. The highest dilution that yielded no bacterial/fungal growth on solid medium was taken as MBC/MFC.

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