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Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources

Received: 15 June 2017    Accepted: 21 July 2017    Published: 16 August 2017
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Abstract

The antibacterial and antimycotic activity of Aframomum melegueta seeds were investigated against Escherichia coli, Staphylococcus aureus, Pseudomonas earuginosa, Salmonella species, Klebsiella species, Bacillus species, Fusarium species, Rhizopus species, Aspergillus species, Penicillium species and Mucor species isolated from spoiled bread and tomatoes using agar well diffusion method. The result showed that the ethanol extract exhibited higher antibacterial activity more than the aqueous extract with Bacillus sp. having the highest zone of inhibition (28mm, 23mm), followed by Salmonella sp. (26mm, 22mm), S. aureus (24mm, 19mm), Klesiella sp. (22mm, 17mm) and E. coli (20mm, 16mm) while P. earuginosa was the least (18mm, 15mm). The antifungal activity showed that Rhizopus sp. was the most inhibited by both ethanol and aqueous extracts respectively (20mm and 16mm), followed Penicillium sp. (17mm and 12mm), Aspergillus sp. (14mm and 11mm) and Fusarium sp. (14mm and 10mm) while Mucor sp. was the least (15mm and 9mm). The minimum inhibitory concentrations (MICs) of the aqueous seed extracts showed that MIC of E. coli, S. aureus, Salmonella sp. and Bacillus sp. was 20mg/mL. MIC for P. earuginosa, Klesiella sp. and Rhizopus sp. was 30mg/mL while Fusarium sp., Aspergillus sp., Penicillium sp. and Mucor sp. have MICs of 50mg/mL. The MICs of the ethanolic extract showed that E. coli and S. aureus have MICs of 10mg/mL, P. earuginosa, Klesiella sp., Penicillium sp. and Rhizopus sp. have 20mg/mL, Fusarium sp., Aspergillus sp. and Mucor sp. have 30mg/mL while Bacillus sp. was the most susceptible with MIC of 5mg/mL. The low MICs are indication of strong antibacterial and antimycotic effects of the extracts. Hence, the extracts could be used in treating infections associated with the test organisms and as well as serve as potential food preservative.

Published in Central African Journal of Public Health (Volume 3, Issue 4)
DOI 10.11648/j.cajph.20170304.12
Page(s) 44-50
Creative Commons

This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Antifungal Activity, Antibacterial Activity, Food Preservation, Foodborne Pathogens, Aframomum melegueta Extracts

References
[1] de-Souza, E. L., Stamford, T. L., Lima, E. D., Trajano, V. N. and Filho, J. M. (2005). Antimicrobial effectiveness of spices: approach for use in food. Brazilian Archives of Biology and Technology International Journal, 48: 549-558.
[2] Rios, J. L. and Recio, M. C. (2005). Medicinal plants and Antimicrobial activity. Journal of Enthopharmacology, 100: 80.
[3] Doherty, V. F., Olaniran, O. O. and Kanife U. C. (2010). Antimicrobial Activities of Aframomum Melegueta (Alligator Pepper). International Journal of Biology, 2 (2): 126-131.
[4] Sofowora, A. (1993). Medicinal plants and Traditional Medicine in Africa. Spectrum Books Limited, Ibadan, Nigeria, p 346.
[5] Edeoga, H. O., Okwu, D. E. and Mbaeble, B. O. (2005). Phytochemical Constituents of some Nigerian Medicinal Plants. African Journal of Biotechnology, 4: 685-688.
[6] Galal, A. M. (1996). Antimicrobial activity of 6-paradol and related Compounds. International Journal of Pharmacognosy, 31: 37-43.
[7] Ikegbunam, M., Maduagwu, U. and Osazuwa, E. (2016). Evaluation of the Antifungal Activity of Aqueous and Alcoholic Extracts of Six Spices. American Journal of Plant Sciences, 7: 118-125.
[8] Okwu, D. E. (2001). A improving Nutritive value of cassava Tapiocmeal with local spices. Journal of Nutraceutical, Functional and medical food, 3: 43-51.
[9] Okwu, D. E. (2004). Phytochemicals and vitamin content of Indigenous spices of South Eastern Nigeria. Journal of Sustain Agricultural environment, 6: 30-34.
[10] Oladunmoye, M. K. and Dada, E. O. (2007). Comparative studies on the Antimicrobial activity of leafs extracts from Aframomum melegueta. Research Journal of Botany, 2 (2): 95-107.
[11] Okigbo, R. N, Ogbonnanya, O. U. (2006). Antifungal effects of two tropical plants extracts Ocimum gratissimum and Afromaomum melegueta on post-harvest yam Discorea spp rot. African Journal of Biotechnology 5 (9): 727-731.
[12] Iwu, M. M. (1999). Handbood of African Medicinal plants. CRC Press, Boca Raton FL, pp 205-210.
[13] Indu, M. N., Hatha, A. A., Abinosh, C., Harsha, U. and Vivekanandan, G. (2006). Antimicrobial activity of some South Indian spices against serotypes of Escherichia coli, Samonella, Listeria monocytogenes and Aeromonas hydrophila. Brazilian Journal of Microbiology, 37: 153 - 158.
[14] Ray, B. (2004). Fundamental food microbiology, 3rd edition. CRC Press, New York.
[15] WHO (2007). Foodborne Disease Outbreak Guidelines. www.who.int/foodsafety/publications/foodborne_disease/FERG_Nov07pdf. Date accessed, June 23, 2013.
[16] Ogodo A. C. and Ekeleme U. G. (2013). In-vitro antibacterial activity of garlic cloves and ginger rhizomes on food-borne pathogens. International Journal of Basic and Applied Sciences, 2 (4): 387-392
[17] Ogodo, A. C. and Ugbogu, O. C. (2016). Public Health significance of aflatoxin in food industry-a review. European Journal of Clinical and Biomedical Sciences, 2 (5): 51-58.
[18] Ronald, M. A. 1994. Principal of Microbiology. USA. 597 – 644.
[19] Okwu, D. E. and Njoku, E. E. (2009). Chemical composition and in-vitro antifungal screening of seed and leaf extracts from Afromaomum melegueta and Monodora myristica against rolfsii of cowpea plant (Vigna ungukulata L. Walp)
[20] Alo, M. N., Anyim, C., Igwe, J. C., Elom, M. and Uchenna, D. S. (2012). Antibacterial activity of water, ethanol and methanol extracts of Ocimum gratissimum, Vernonia amygdalina and Aframomum melegueta. Advances in Applied Science Research, 3 (2): 844-848.
[21] Ekeleme, U. G., Nwachukwu, N. C., Ogodo, A. C., Nnadi, C. J., Onuabuchi, I. A. and Osuocha, K. U. Phytochemical Screening and Antibacterial Activity of Cnidoscolus aconitifolius and Associated Changes in Liver Enzymes in Wistar Rats. Australian Journal of Basic and Applied Sciences, (12): 156-162
[22] Arekemase, O., Kayode, O. and Ajiboye, E. (2011). Antimicrobial Activity and phytochemical analysis of Jatropha curcas plant against some selected microorganisms. International Journal of Biology, 3 (3): 52-55.
[23] Amusa, N. A., Kehinde, I. A. and Ashaye, O. A. (2002). Biodeterioration of Bread fruit in storage and its effects on the Nutrient Composition. African Journal of Biotechnology, 1 (2): 57-60.
[24] Okereke, H. C. and Kanu, I. J. (2004). Identification and characterization of Microorganisms In: Laboratory guide for microbiology, A. Onyeagba, (ed). Crystal Publishers, Okigwe, pp. 95-110.
[25] Holt, J. G., Kieg N. R; Sneath, P. H. A; Staley, J. T. and Williams, S. T. 1994. Bergey s Manual of Determinative Bacteriology (9th edition). The Williams and Wilkins Company Baltimore, U. S. A. Pp 787.
[26] Barnett, J. A., Payne, R. W., Yarrow, D. (2000). Yeasts characteristics and identification, 3rd ed. Cambridge University Press. Cambridge.
[27] Oyeleke, S. B. and Manga, S. B. (2008). Essentials of Laboratory Practical in Microbiology. Tobest Publisher, Minna, Nigeria. Pp 36-75.
[28] Doughari JH, Pukuma MS, De N. (2007). Antibacterial effects of Balanites aegyptiaca L. Drel. and Moringa oleifera Lam. on Salmonella typhi. African Journal of Biotechnology, 6(19): 2212-2215.
[29] Oyemaechi, U. F. Chukwuezi, O. and Ozougwu, V. E. O. (2014). Microbial Agents of Tomato Spoilage in Onitsha Metropolis. Advances in Biological Research 8 (2): 87-93.
[30] Mbajiuka, S. C. and Enya, E. (2014). Isolation of Microorganisms associated with Deterioration of Tomato (Lycopersicon esculentum) and Pawpaw (Carica papaya) Fruits, International Journal of Current Microbiology and Applied Science, 3 (5): 501-512.
[31] Unachukwu M. N. and Nwakanma, C. (2015). The fungi associated with the spoilage of bread in Enugu state. International Journal of Current Microbiology and Applied Sciences, 4 (1): 989-995.
[32] Ravimannan, N., Sevvel, P. and Saarutharshan, S. (2016). Study on fungi associated with spoilage of bread. International Journal of Advanced Research in Biological Sciences, 3 (4): 165-167.
[33] Oyagade, J. O., Awotoye, O. O., Adewunmi, J. T., and Thorpe, H. T., (1999) Antimicrobial activity of some Nigerian medicinal Plants, screening for antibacterial activity. Journal of Bioscience research Communication, 11: 193-197.
[34] Odetunde, S. K. Adekola, I. T. Avungbeto, M. O. and Lawal, A. K. (2015). Antimicrobial effect and phytochemical analysis of Aframomum melegueta on some selected bacteria and fungi. European Journal of Biotechnology and Bioscience, 3 (4): 15-19.
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    Alloysius Chibuike Ogodo, Chioma Blessing Nwaneri, Dawn Ify Agwaranze, Jonathan Ewanfo Inetianbor, Christopher Uchechukwu Okoronkwo. (2017). Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources. Central African Journal of Public Health, 3(4), 44-50. https://doi.org/10.11648/j.cajph.20170304.12

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    Alloysius Chibuike Ogodo; Chioma Blessing Nwaneri; Dawn Ify Agwaranze; Jonathan Ewanfo Inetianbor; Christopher Uchechukwu Okoronkwo. Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources. Cent. Afr. J. Public Health 2017, 3(4), 44-50. doi: 10.11648/j.cajph.20170304.12

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    AMA Style

    Alloysius Chibuike Ogodo, Chioma Blessing Nwaneri, Dawn Ify Agwaranze, Jonathan Ewanfo Inetianbor, Christopher Uchechukwu Okoronkwo. Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources. Cent Afr J Public Health. 2017;3(4):44-50. doi: 10.11648/j.cajph.20170304.12

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  • @article{10.11648/j.cajph.20170304.12,
      author = {Alloysius Chibuike Ogodo and Chioma Blessing Nwaneri and Dawn Ify Agwaranze and Jonathan Ewanfo Inetianbor and Christopher Uchechukwu Okoronkwo},
      title = {Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources},
      journal = {Central African Journal of Public Health},
      volume = {3},
      number = {4},
      pages = {44-50},
      doi = {10.11648/j.cajph.20170304.12},
      url = {https://doi.org/10.11648/j.cajph.20170304.12},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.cajph.20170304.12},
      abstract = {The antibacterial and antimycotic activity of Aframomum melegueta seeds were investigated against Escherichia coli, Staphylococcus aureus, Pseudomonas earuginosa, Salmonella species, Klebsiella species, Bacillus species, Fusarium species, Rhizopus species, Aspergillus species, Penicillium species and Mucor species isolated from spoiled bread and tomatoes using agar well diffusion method. The result showed that the ethanol extract exhibited higher antibacterial activity more than the aqueous extract with Bacillus sp. having the highest zone of inhibition (28mm, 23mm), followed by Salmonella sp. (26mm, 22mm), S. aureus (24mm, 19mm), Klesiella sp. (22mm, 17mm) and E. coli (20mm, 16mm) while P. earuginosa was the least (18mm, 15mm). The antifungal activity showed that Rhizopus sp. was the most inhibited by both ethanol and aqueous extracts respectively (20mm and 16mm), followed Penicillium sp. (17mm and 12mm), Aspergillus sp. (14mm and 11mm) and Fusarium sp. (14mm and 10mm) while Mucor sp. was the least (15mm and 9mm). The minimum inhibitory concentrations (MICs) of the aqueous seed extracts showed that MIC of E. coli, S. aureus, Salmonella sp. and Bacillus sp. was 20mg/mL. MIC for P. earuginosa, Klesiella sp. and Rhizopus sp. was 30mg/mL while Fusarium sp., Aspergillus sp., Penicillium sp. and Mucor sp. have MICs of 50mg/mL. The MICs of the ethanolic extract showed that E. coli and S. aureus have MICs of 10mg/mL, P. earuginosa, Klesiella sp., Penicillium sp. and Rhizopus sp. have 20mg/mL, Fusarium sp., Aspergillus sp. and Mucor sp. have 30mg/mL while Bacillus sp. was the most susceptible with MIC of 5mg/mL. The low MICs are indication of strong antibacterial and antimycotic effects of the extracts. Hence, the extracts could be used in treating infections associated with the test organisms and as well as serve as potential food preservative.},
     year = {2017}
    }
    

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  • TY  - JOUR
    T1  - Antimycotic and Antibacterial Activity of Aframomum melegueta Seed Extracts Against Bacteria and Fungi Species from Food Sources
    AU  - Alloysius Chibuike Ogodo
    AU  - Chioma Blessing Nwaneri
    AU  - Dawn Ify Agwaranze
    AU  - Jonathan Ewanfo Inetianbor
    AU  - Christopher Uchechukwu Okoronkwo
    Y1  - 2017/08/16
    PY  - 2017
    N1  - https://doi.org/10.11648/j.cajph.20170304.12
    DO  - 10.11648/j.cajph.20170304.12
    T2  - Central African Journal of Public Health
    JF  - Central African Journal of Public Health
    JO  - Central African Journal of Public Health
    SP  - 44
    EP  - 50
    PB  - Science Publishing Group
    SN  - 2575-5781
    UR  - https://doi.org/10.11648/j.cajph.20170304.12
    AB  - The antibacterial and antimycotic activity of Aframomum melegueta seeds were investigated against Escherichia coli, Staphylococcus aureus, Pseudomonas earuginosa, Salmonella species, Klebsiella species, Bacillus species, Fusarium species, Rhizopus species, Aspergillus species, Penicillium species and Mucor species isolated from spoiled bread and tomatoes using agar well diffusion method. The result showed that the ethanol extract exhibited higher antibacterial activity more than the aqueous extract with Bacillus sp. having the highest zone of inhibition (28mm, 23mm), followed by Salmonella sp. (26mm, 22mm), S. aureus (24mm, 19mm), Klesiella sp. (22mm, 17mm) and E. coli (20mm, 16mm) while P. earuginosa was the least (18mm, 15mm). The antifungal activity showed that Rhizopus sp. was the most inhibited by both ethanol and aqueous extracts respectively (20mm and 16mm), followed Penicillium sp. (17mm and 12mm), Aspergillus sp. (14mm and 11mm) and Fusarium sp. (14mm and 10mm) while Mucor sp. was the least (15mm and 9mm). The minimum inhibitory concentrations (MICs) of the aqueous seed extracts showed that MIC of E. coli, S. aureus, Salmonella sp. and Bacillus sp. was 20mg/mL. MIC for P. earuginosa, Klesiella sp. and Rhizopus sp. was 30mg/mL while Fusarium sp., Aspergillus sp., Penicillium sp. and Mucor sp. have MICs of 50mg/mL. The MICs of the ethanolic extract showed that E. coli and S. aureus have MICs of 10mg/mL, P. earuginosa, Klesiella sp., Penicillium sp. and Rhizopus sp. have 20mg/mL, Fusarium sp., Aspergillus sp. and Mucor sp. have 30mg/mL while Bacillus sp. was the most susceptible with MIC of 5mg/mL. The low MICs are indication of strong antibacterial and antimycotic effects of the extracts. Hence, the extracts could be used in treating infections associated with the test organisms and as well as serve as potential food preservative.
    VL  - 3
    IS  - 4
    ER  - 

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Author Information
  • Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University Wukari, Wukari, Nigeria

  • Department of Microbiology, School of Biological Sciences, Federal University of Technology Owerri, Owerri, Nigeria

  • Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University Wukari, Wukari, Nigeria

  • Department of Microbiology, Faculty of Pure and Applied Sciences, Federal University Wukari, Wukari, Nigeria

  • Department of Microbiology, Faculty of Biological and Physical Sciences, Abia State University Uturu, Uturu, Nigeria

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