Sir,Secondary metabolites are small molecules, responsible for various biological activities, acting as antibiotic, antifungal and antiviral agents to protect plants from pathogens. There are large groups of secondary metabolites, which include alkaloids and flavonoids, described mainly by their antimicrobial, and antioxidant potential.

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Pilocarpine is an alkaloid present in the leaves of jaborandi ( Pilocarpus microphyllus), which is utilized as a phytotherapeutic agent in the treatment of glaucoma and xerostomia. Rutin is a flavonoid belonging to the subclass of flavones found in various plant sources, which has shown antioxidant activity, efficacy in the control of Aspegillus oschraceus, anticonvulsivant effects in rats, suppression of cellular immunity, anticarcinogenic activity and antiinflammatory effect. The irrational use of antibiotics and antifungals has resulted in the development of drug resistance. The rapid development of drug resistance and the slow-down in the development of new active drugs, have drawn attention to treatment with drug combinations.

The aim of this study was to evaluate the antibacterial and antifungal activity of rutin and pilocarpine and to determine their possible modifying effect when combined with aminoglycoside antibacterials and the antifungal amphotericin B.The experiments were carried out in Laboratory of Microbiology and Molecular Biology, Department of Biological Chemistry, Regional University of Cariri, Crato, Brazil, with standard and multiresistant strains of Staphylococcus aureus and Escherichia coli: S. Aureus ATCC 12692, S. Aureus 358 (MRSA), E.

Coli ATCC 25922 and E. Coli 27 (EC27).

All strains were maintained on heart infusion agar slants (HIA; Difco, USA), and before the assays, the cells were grown in brain heart infusion broth (BHI; Difco) for 24 h at 37°C. Clinical isolate EC27 was resistant to neomycin and gentamicin (low level) and to amikacin and kanamycin. Aureus 358 (MRSA) showed resistance to methicillin. All strains were obtained from the collection of microorganisms of the Mycology Laboratory, UFPB, Paraiba, Brazil.

Three standard yeast strains were utilized: Candida albicans ATCC 40227, C. Krusei ATCC 6538 and C. Tropicalis ATCC 13803. All these strains were maintained on HIA, and before the assays, the cells were grown in BHI for 24 h at 37°C. The antibiotics tested were the aminoglycosides amikacin, kanamycin, gentamicin and neomycin (Sigma, USA).

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The antifungal agent was amphotericin B (Sigma, USA). The antibiotic and antifungal solutions were prepared following the recommendations of the Clinical and Laboratory Standards Institute – CLSI. The test compounds (pilocarpine and rutin) (obtained from Merck & Company, Germany), was dissolved (10 mg) in 1 ml dimethylsuphoxide (DMSO- Merck, Darmstadt, Germany), giving an initial concentration of 10 mg/ml. Starting with this concentration, a dilution was made to 1024 μg/ml, and further dilutions were made serially 1:2 in culture medium, obtaining concentrations of 512 to 8 μg/ml.

The minimal inhibitory concentration (MIC, μg/ml) was determined in 10 per cent BHI by the broth microdilution method, using a suspension of 10 5 cfu/ml and a drug concentration of 1024-1 μg/ml. To evaluate the test compounds for drug modifying activity when combined with antibiotics and antifungals, a subinhibitory concentration was determined as the MIC/8 values of 16 μg/ml for EC27 and MRSA, and 10 μg/ml for C.

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Krusei and C. The plates were incubated for 24 h at 37 °C, utilizing resarzurin to read bacterial growth and no stain for fungi.The MIC values for rutin and pilocarpine showed no antibacterial or antifungal activity against the strains tested. Pilocarpine, however, increased bacterial sensitivity to the aminoglycosides gentamicin and neomycin, when added concomitantly.

Pilocarpine combined with these aminoglycosides altered synergistically the MIC values against S. Aureus but not E. Neither of the compounds tested showed an antifungal modifying effect ( 1024 μg/ml) with amphotericin B against the Candida strains tested. The MIC values determined in the antifungal and antibacterial assays were equal to that of the negative DMSO control, suggesting that this activity was due to DMSO which is considered toxic only at higher concentration. Rutin has been extensively studied for its various pharmacological properties, such as its anti-candida activity. Missau et al used the direct bioautography method and showed anti-fungal activity against three strains of Candida, with a significant effect against only C. Bolle et al found that this method could result in decomposition of the test substances during the assay.

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Our findings corroborated with that of Pereira et al who showed that rutin, isolated from the plant species Solanum palinacanthum does not inhibit the growth of Staphylococcus aureus. The use of drugs in combination has been extensively studied, mainly because of the emergence of resistant strains.The synergistic effect of pilocarpine indicates a new therapeutic possibility for the treatment of diseases associated with S.

Aureus infection and an alternative for the resistance shown by this microorganism against certain aminoglycosides. Further studies are required to evaluate the toxicity and antibacterial activity of this compound in vivo.

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