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Revista do Instituto de Medicina Tropical de São Paulo

On-line version ISSN 1678-9946

Rev. Inst. Med. trop. S. Paulo vol.52 no.3 São Paulo May/June 2010

http://dx.doi.org/10.1590/S0036-46652010000300003 

BACTERIOLOGY

 

Antibacterial effect (in vitro) of Moringa oleifera and Annona muricata against Gram positive and Gram negative bacteria

 

Efeito antibacteriano (in vitro) de Moringa oleifera (moringa) e Annona muricata (graviola) frente a bactérias Gram-negativas e Gram-positiva

 

 

Gustavo Hitzschky Fernandes VieraI; Jozeanne Alves MourãoI; Ângela Maria ÂngeloI; Renata Albuquerque CostaII;Regine Helena Silva dos Fernandes VieiraIII

ILaboratory of Microbiology. State University of Vale do Acaraú, Sobral, Ceará, Brazil
IIDoctoral Student in Fisheries Engineering, Federal University of Ceará, Fortaleza, Ceará, Brazil. PROPAG
IIIInstitute of Sea Science (LABOMAR). UFC, Fortaleza, Ceará, Brazil

Correspondence to

 

 


SUMMARY

Antibacterial effects of aqueous and ethanolic extracts of seeds of moringa (Moringa oleifera) and pods of soursop (Annona muricata) in the concentration of 1:5 and 1:10 in volumes 50, 100, 150 and 200 µL were examined against Staphylococcus aureus, Vibrio cholerae, Escherichia coli (isolated from the organism and the aquatic environment) and Salmonella Enteritidis. Antibacterial activity (inhibition halo > 13 mm) against S. aureus, V. cholerae and E. coli isolated from the whiteleg shrimp, Litopenaeus vannmaei, was detected in aqueous and ethanolic extracts of moringa. E. coli isolated from tilapiafish, Oreochromis niloticus, was sensitive to the ethanolic extract of moringa. The aqueous extracts of soursop showed an antibacterial effect against S. aureus and V. cholerae, but the antibacterial activity by the ethanol extracts of this plant was not demonstrated.

Keywords: Antibacterial effect; Moringa oleifera; Annona muricata.

RESUMO

Para avaliação do efeito bactericida frente à Staphylococcus aureus, Vibrio cholerae, Escherichia coli (isolada de pescados e ambiente aquático) e Salmonella Enteretidis, foram testados extratos aquosos e etanólicos de sementes de moringa (Moringa oleifera) e casca de graviola (Annona muricata) na concentração de 1:5 e 1:10, nos volumes de 50, 100, 150 e 200 µL. Os resultados mostraram efeito antibacteriano (halo de inibição > 13mm) dos extratos aquosos e etanólicos de moringa frente a S. aureus, V. cholerae e E. coli isoladas de camarão cinza Litopenaeus vannmaei. A cepa de E. coli isolada do pescado Oreochromis niloticus apresentou sensibilidade frente ao extrato etanólico de moringa. Os extratos aquosos de graviola apresentaram efeito bactericida frente a S. aureus e V. cholerae, entretanto, os extratos etanólicos dessa planta não mostraram atividade antibacteriana.


 

 

INTRODUCTION

Multiresistant bacterial strains are a growing public health concern worldwide4,12,22 justifying investments in the search for alternative forms of treatment of infections. As a result, a number of medicinal plants used in indigenous medicine have been tested and found to possess bactericidal properties11,30,32,35,43.

The moringa plant (Moringa oleifera) has been the object of much research due to its multiple uses and well-known bactericidal potential9,37,17,38. According to BEZERRA et al.8, the moringa tree is native to northeastern India. It is rich in nutrients and, apart from a range of industrial and medicinal applications, is used to purify water for human consumption. Not surprisingly, as explained by MAKKAR & BECKER29, the moringa is of economic importance in the production of several commodities, such as oils, foods, condiments and medicines.

Likewise, the soursop (Annona muricata) is employed for a number of medicinal purposes6. It is found in most of tropical America and, though not native to Brazil, is grown extensively in the northern and northeastern regions of the country36. CAVALCANTE et al.10 has shown that the semiarid climate of northeastern Brazil offers the ideal combination of temperature, moisture, sunlight and soil composition for soursop cultivation.

The objective of this study was to evaluate the bactericidal effect of moringa and soursop extracts upon four bacterial species commonly associated with food intoxication: Staphylococcus aureus, Vibrio cholerae, Escherichia coli and Salmonella spp.

 

MATERIALS AND METHODS

Origin of strains: The controls used in the experiment were standard strains of S. aureus ATCC25923, V. cholerae classic 569B and Samonella Enteritidis obtained from the Environment and Seafood Microbiology Laboratory of the Marine Sciences Institute (LABOMAR, Federal University of Ceará). E. coli strains were isolated from water samples from a local lake (Lagoa da Fazenda, Sobral, Ceará) and river (Rio Acaraú, Sobral, Ceará) and from aquiculture livestock (Tilapia, Oreochromis niloticus, and Pacific white shrimp, Litopenaeus vannamei). E. coli was isolated with the method described by FENG et al.15 including testing with indole, methyl red, acetoin (Voges-Proskauer), citrate and H2S, and confirmation by lactose fermentation. All strains were stored in tryptone soy agar (TSA/Difco) until the moment of testing.

Preparation of extracts: To prepare the moringa extracts, 30g of moringa seeds were homogenized with 150 mL distilled water or 150 mL ethanol p.a. in a magnetic stirrer for 30 minutes. The water-based and ethanol-based homogenates were then paper-filtered and spread on Petri dishes in the amounts 50, 100, 150 and 200 µL. Similarly, to prepare the soursop extracts, 10g of soursop peel was homogenized in 100 mL distilled water or 100 mL ethanol p.a. in a magnetic stirrer for 30 minutes, after which the water-based and ethanol-based homogenates were spread on Petri dishes in the amounts 50, 100, 150 and 200 µL. All moringa and soursop samples were obtained from the Center for Nutrition and Food Production of the Vale do Acaraú State University (NUNPRA/UVA), and specimens were deposited in the herbarium of the same institution under entry numbers 5823, 5824, 5825 and 5826.

Evaluation of bactericidal effects: The bactericidal effect of the extracts was evaluated with the modified Kirby-Bauer disk diffusion method7. The strains were inoculated in TSA and incubated at 35 ºC for 24 hours. Cultures were then adjusted to a concentration of 108 CFU/mL by making a suspension in 0.85% saline solution match the 0.5 McFarland turbidity standard21. Using a sterilized swab, aliquots from each tube were spread on dishes with Muller-Hinton agar (Difco), extract was added and incubated at 35 ºC for 24 hours. Disks soaked with sterile distilled water and ethanol p.a. were used as negative control. Extracts producing halos of bacterial growth inhibition greater than 13 mm were considered effective34.

 

RESULTS AND DISCUSSION

Water-based moringa extracts efficiently inhibited (halo > 13 mm) the growth of S. aureus, V. cholerae and E. coli isolated from shrimp samples, especially at 150 and 200 µL/dish. Similar strains isolated from tilapia and shrimp samples were inhibited by ethanol-based moringa extracts at all the volumes tested (Table 1).

 

 

Likewise, all volumes of soupsop extract were bactericidal to S. aureus and V. cholerae. The greatest halos (16 and 23 mm) were observed at 200 µ L/dish (Table 2).

 

 

In the present study moringa extracts were found to be more bactericidal than soursop extracts (Fig. 1). Nevertheless, in an investigation of the active substances contained in moringa seeds, EILERT et al.13 satisfactorily inhibited the growth of Mycobacterium phlei with 40 µM extract/L and that of Bacillus subtilis with 56 µM extract/L, compared to the greater volumes used in our study (10g/100 mL).

 

 

JAHN et al.24 identified the bactericidal substances in moringa seeds as pterygospermin, moringine and the glycosides 4-(α-L-rhamnosyloxy)-benzylisothiocyanate and 4-(α-L-rhamnosyloxy)-phenylacetonitrile. These substances have been shown to inhibit mainly Bacillus subtilis, Mycobacterium phei, Serratia marcescens, E. coli, Pseudomonas aeruginosa, Shigella and Streptococcus. According to GALLÃO et al.16,, moringa seeds consist of mostly proteins (approximately 40%), followed by lipids (18.8%), starch (6.02%), oligosaccharides (3.31%) and soluble sugars (3.14%).

The lack of bactericidal effects in our ethanol-based soursop extracts matches findings published by LIMA et al.27, who reported S. aureus, E. coli and Salmonella to be resistant to all soursop extracts based on 95% ethanol. On the other hand, bioactivity of water-based soursop extracts against S. aureus and V. cholerae may be related to the chemical structure of the active substances. In an investigation of the bactericidal properties of eight species of annonaceae, TAKAHASHI et al.39 isolated and confirmed the ability of trachylobanoic acid to inhibit B. subtilis and S. aureus. Annonaceae contain other bioactive substances, including a range of acetogenins with a wide spectrum of action, including antibiotic effects. Structurally, annonaceous acetogenins are series of C-35/C-37 natural products derived from C-32/C-34 fatty acids and combined with a 2-propanol unit2.

Three of the four extracts tested in this study (the water- and ethanol-based moringa extracts and the water-based soursop extract) inhibited the growth of two Gram-negative bacterial cultures (V. cholerae and E. coli) and one Gram-positive (S. aureus) bacterial culture. According to KOSTOVA & DINCHEV25, the observation of both Gram-negative and Gram-positive effects in the same plant extract may be explained by the presence of a wide spectrum of bactericidal substances, or by the action of toxins produced by the plant.

As shown by GONÇALVES et al.18 and NASCIMENTO et al.31, S. aureus has been inhibited by extracts prepared from a variety of phanerogams. Likewise, VIEIRA et al.42 found S. aureus to be sensitive to guava leaf extracts in a study testing medicinal plants against bacteria causing diarrhea in children.

The susceptibility of V. cholerae to vegetable extracts was also tested by THAKURTA et al.40 who found serotypes O1, O139, non-O1 and non-O139 to be inhibited by extracts of the neem tree (Azadirachta indica). Moreover, AKINSINDE & OLUKOYA1 observed vibriocidal effects of medicinal plants from Nigeria, and in a study testing the bactericidal effect in vitro of 14 plant species upon V. cholerae, GUEVARA et al.19 proposed using extracts of pomegranate peel (Punica granatum), the most efficient of the samples, as an alternative treatment for cholera.

The susceptibility of E. coli strains to moringa extracts in our study is supported by a study by JABEEN et al.23, in which moringa seed extracts were observed to produce halos of bacterial inhibition measuring 18-20.5 cm.

In contrast with the extracts used by HEINRICH et al.20, our water-based extracts of soursop peel did not inhibit E. coli effectively (halos < 13 mm).

Also, while MADSEN et al.28 observed Salmonella Enteritidis cultures to be susceptible to water treated with moringa seed extract, in our own study none of the extracts was capable of inhibiting this species (Table 1). Salmonella has however been shown to be susceptible to medicinal plant extracts before, as in the studies by AL-BAYATI & AL-MOLA3 and by EJA et al.14.

The fact that the only strains resistant to all our extracts (Salmonella and E. coli, sampled at the lake "Lagoa da Fazenda") were Gram-negative, may be related to cell wall structure. According to TORTORA et al.41, the cell wall of Gram-negative bacteria acts as a barrier to a number of substances, including antibiotics. This would also explain why medicinal plants tend to be more effective against Gram-positive than Gram-negative cultures5,26,33.

The results of the present study confirm the importance of laboratory-testing medicinal plants used in indigenous medicine in search of new substances capable of inhibiting S. aureus, classic V. cholerae and E. coli.

 

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Correspondence to:
Renata Albuquerque Costa
Laboratório de Microbiologia Ambiental e do Pescado, Instituto de Ciências do Mar
Av. Abolição 3207
60165-081 Fortaleza, Ceará, Brasil
Phone + 55 85 3366 7027. Fax: + 55 85 3366 7002
E-mail: renata.albuq@gmail.com

Received: 10 August 2009
Accepted: 29 April 2010

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