Research Article

Environmental Distribution and Antibiotic Resistance Patterns of Bacterial Isolates from Open Drainage Systems in Port Harcourt, Southern Nigeria

1 Department of Microbiology, Rivers State University, Nkpolu-Oroworukwo, Port Harcourt, Nigeria
* Corresponding author: ogbonna.david@ust.edu.ng
Published: Jun, 2018
Pages: 4241-4250

Abstract

Bacterial isolates from wastewater and sediments of the Ntanwogba open drainage system in Port Harcourt city was tested for their susceptibility to antibiotics. Wastewater samples were collected twice a week for a period of six months from February through July using standard analytical methods. Results obtained showed that the sediment samples had Escherichia coli with the highest percentage of occurrence of 23.8%, followed by Klebsiella pneumoniae and Proteus mirabilis M18 with 19% each, while Burkholderia multivorans and Pseudomonas fluoresceins had the least occurrence of 4.8% each. Wastewater samples showed that Escherichia coli also had the highest percentage occurrence of 21.2%, followed by Enterobacter asburiae and Plesiomonas shigelloides with 15.2% each, while Pseudomonas fluoresceins had the least occurrence of 6.1%. Antibiotic sensitivity of strains was conducted using the disc diffusion method. The antibiotic sensitivity test carried out on the bacterial isolates showed 100% resistance to Augmentin, Ceftazidime, Cefuroxime, Ceftriaxone, Cloxacillin and Cefi.xime. However, 2.08% were susceptible to Ciprofloxacin, 33.3% to Erythromycin, 77.8% to Gentamicin, 87.5% to Nitrofurantoin and 96.3% to Ofloxacin. Bacillus ginsengisoli was the most resistant, but sensitive to only Ofloxacin, Burkholderia multivorans was the most susceptible bacterial isolate and was susceptible to Ciprofloxacin, Gentamicin, Nitrofurantoin, Ofloxacin. This was followed by Enterobacter asburiae that was sensitive to Gentamicin, Nitrofurantoin, Ofloxacin. While Escherichia coli, Klebsiella pneumoniae, Plesiomonas shigelloides, Proteus mirabilis Ml 8, Proteus mirabilis Ml 9, Pseudomonas fluoresceins and Pseudomonas nitroreducens were all sensitive to Nitrofurantoin and Ofloxacin. The high level of resistance to antimicrobial agents recorded in this study shows that the wastewater effluents and the receiving water bodies could pose a potential health risk to the surrounding communities who depend on these water sources for various domestic activities. Therefore, proper waste water management is fundamental for maintaining public health and protecting the quality of the environment.

References

  1. Abah, S. O. and Ohimain, E.I (2010). Assessment of Dumpsite Perturbation Potential using integrated Risk Based Approach: A case study of Eneka, Nigeria. World Applied Sciences Journal 4: 436-442.
  2. Adeyemo, O. K., Ayodeji, I. O and Aiki-Raji, C. O. (2002). The waste quality and sanitary conditions in a major abattoir (Bodija) in Ibadan, Nigeria. African Journal of Biomedical Research 5: 51-55.
  3. Adieze, I. E., Nnadi, C., Braide, W., Azubuike, C. and Nduka, I. (2015). Antibiotic resistance pattern of bacterial isolates of liquid wastes and waste dump soils of hospitals in Owerri, Nigeria. Nigerian Journal of Microbiology 29: 3002-3011.
  4. Ajayi, A. O. and Akonai, K. A. (2003). Antibiotics sensitivity profile of microorganisms in Lagos lagoon, Nigeria.African Journal of Biotechnology 6: 79-84.
  5. Alom, M. and Khan, M. Z. H. (2014). Environmental and social impact due to urban drainage problems in Dhaka City, Bangladesh.International Journal of Engineering and Advanced Technology (IJEAT) ISSN: 2249-8958
  6. APHA (American Public Health Association; American Water Works Association (AWWA); Water Environmental Federation (WEF) 2012. Standard Methods for the Examination of Water and Wastewater, 22nd ed.
  7. Amisu, K. O., Coker, A. O. and Isokpehi, R. D. (2003). Arcobacterbuizleri strains from poultry abattoir effluent in Nigeria. East African Medical Journal 80: 218-221
  8. CLSI (Clinical and Laboratory Standards Institutes) (2000). Performance standards for antimicrobial disk susceptibility tests. CLSI document M100. (Clinical and Laboratory Standards Institutes), Wayne.
  9. Davison, J. (1999). Genetic exchange between bacteria in the environment. Plasmid 42: 73-91.
  10. Dungeni, M., Van Der Merwe, R. R. and Momba, M. N. B. (2010). Abundance of pathogenic bacteria and viral indicators in chlorinated effluents produced by four wastewater treatment plants in the Gauteng Province, South Africa. Water Africa 36 (5): 607-614.
  11. Frostegard, A., Courtois, A, Ramisse, V, Clere, S, Bernillon, D, Lefall, F, Jeanin, P, Nesme, X. and Simonet, P. (1999). Quantification of bias related to the extraction of DNA directly from soils. Applied Environmental Microbiology 65:5409-5420.
  12. Furuya, E. Y. and Lowy, F. D. (2006). Antimicrobial-resistant bacteria in the community setting. National Review on Microbiology 4: 36-45.
  13. Gobo, A. E., Ubong, I. U. and Ede, P. N. (2008). "Relationship between rainfall trends and flooding in the Niger-Bengue river basins". Journal of Metrology 3:13.
  14. Guo, M., Yuan, Q. and Yang, J. (2013). Microbial selectivity of UV treatment on antibiotic-resistant heterotrophic bacteria in secondary effluents of a municipal wastewater treatment plant. Journal of Water Research 47: 6388-6394.
  15. Hussain, T., Roohi, A., Munir, S., Ahmed, I., Khan, J. and Edel-Hermann, V. (2013). Biochemical characteristics and identification of bacterial strains from drinking water sources of Kohat, Pakistan. International Journal of Microbiology Research 7(6): 1579-1590.
  16. Idris-Nda, A; Aliyu, H K; Dalil, M (2013). The challenges of domestic wastewater management in Nigeria: A case study of Minna, central Nigeria. International Journal of Development and Sustainability 2 (2): 1169-1182
  17. Kresk, M. and Wellington, E. M. H. (1999). Comparison of different methods for the isolation and purification of total community DNA from soil. Journal of Microbiological Methods 39:1-16.
  18. Kurmmerer, K. (2004). Resistance in the environment. Journal of Antimicrobial Chemotherapy 54:311-320.
  19. Lateef, A. (2004). The microbiology of a pharmaceutical effluents and its public health implications. World Journal of Microbiology and Biotechnology 22: 167-171.
  20. Mazhindu, E., T. Gumbo and T. Gondo, 2010. Living with environmental health risks—The case of Addis Ababa. Ecohydrology & Hydrobiology, 10(2): 281-286.
  21. Miller, D. N., Bryant, J. E., Madsen, E. L. and Ghiorse, W. C. (1999). Evaluation and optimization of DNA extraction and purification procedures for soil and sediment samples. Applied and Environmental Microbiology 65: 4715-4724.
  22. Momba, M. N. B., Osode A. N. and Sibewu, M. (2006). The impact of inadequate wastewater treatment on the receiving water bodies – case study: Buffalo City and Nkonkobe Municipalities of the Eastern Cape. Water South Africa 32 (5): 687-692.
  23. Nafarnda, W. D., Ajayi, I. E., Shawulu, J. C, Kawe, M. S., Omeiza, G. K., Sani, N. A., Tenuche, O. Z., Dantong, D. D. and Tags, S. Z. (2012). Bacteriological quality of abattoir effluents discharged into water bodies in Abuja, Nigeria. International Scholarly Research Network.
  24. Ndihokubwayo, J. B, Yahaya, A. A, Desta, A. T, Ki-Zerbo, G. and Odei, E.a.et al. (2013) Antimicrobial resistance in the African region; issues, challenges and actions proposed African Health Monitor 16:27-30.
  25. Nrior, R. R. Douglas, S. I and Ogonjo, M. T. (2017a). Effects of waste water on biodegrability of drilling fluid. International Journal of Development of Sustainability 7(12): 17872-17886.
  26. Nrior, R. R., Daokore-Onukoue, C. and Rufus, A. M. (2017b). Microbiological Evaluation of Key body papers of Niger Delta Shell Seafoods, Blood Clam (Tegillare granosa) and Steamer Clam (Mya arenaria) from upstream and downstream of Andoni River. IOSR Journal of Environmental Science, Toxicology and Food Technology (IOSR-IETFT) 11(10): 40-48
  27. Nrior, R. R., Iyibo, S. N. and Ngerebara, N. N. (2017c). Microbiological Assessment of Niger Delta Shell Sea foods; Periwikle (Tympanotous fuscatus), Oyster (Crassostrea virginica) and Veined rapa whelk (Rapana venosa) from crude oil polluted site. International Journal of Multidisciplinary Current Research 2(7): 01-09.
  28. Odjegwu, O. (1991). Consequences of water pollution by solid wastes and faecal materials in Nigeria. In: Akinyele, I., Omoetu, J. and Innevtore, T (eds). Proceedings of the Third National Conference on Water Pollution. Port Harcourt. Pp. 45-50.
  29. Odeyemi, A.T, Faweya, E.B., Agunbiade, O.R and Ayeni, S.K. (2011). Bacteriological, mineral and radioactive contents of leachate samples from dumpsite of Ekiti State Gov-erment Destitute Center in Ado-Ekiti. Archives of Applied Science Research, 3(4):92-108.
  30. Odeyemi, A. T. (2012). Antibiogram status of bacterial isolates from air around dumpsite of Ekiti State destitute Centre at Itokun, Ado-Ekiti, Microbiology Research 2(2): 12-18
  31. Ogbonna, D. N and Idam, D. Y (2007). Appropriate Sanitation systems for low-income coastal and waterfront communities in the Niger Delta, Nigeria. Journal of Applied Sciences 7(8):1116-1123
  32. Ogbonna, D. N. Amangabra, G. T., and Ekere, T. O. (2007). Urban Solid Waste generation in Port Harcourt Metropolis and its implication for Waste Management. Management of Environmental Quality: An International Journal 18 (1): 71 - 88
How to Cite

Ogbonna, D. N., Nrior, R. R., & Erheriene, B. A. (2018). Environmental Distribution and Antibiotic Resistance Patterns of Bacterial Isolates from Open Drainage Systems in Port Harcourt, Southern Nigeria. Nigerian Journal of Microbiology, 32(1), 4241-4250. https://doi.org/10.67614/njm.2018.bbq4tryx

D. N. Ogbonna, R. R. Nrior, and B. A. Erheriene, "Environmental Distribution and Antibiotic Resistance Patterns of Bacterial Isolates from Open Drainage Systems in Port Harcourt, Southern Nigeria," Nigerian Journal of Microbiology, vol. 32, no. 1, pp. 4241-4250, June 2018. doi: 10.67614/njm.2018.bbq4tryx

Share this article:
Facebook X / Twitter LinkedIn