Plasmid Profiles of Multidrug Resistant Uropathogens and Antibacterial Efficacy of Leaf Extracts of Luffa cylindrica

Authors

Harrison Obumseli

Department of Applied Microbiology and Brewing, Faculty of Biosciences, Nnamdi Azikiwe University, Awka (Nigeria)

Ebele Linda Okoye

Department of Applied Microbiology and Brewing, Faculty of Biosciences, Nnamdi Azikiwe University, Awka (Nigeria)

Ugochukwu Chukwuma Okafor

Department of Applied Microbiology and Brewing, Faculty of Biosciences, Nnamdi Azikiwe University, Awka (Nigeria)

Article Information

DOI: 10.51584/IJRIAS.2026.110200086

Subject Category: Public Health

Volume/Issue: 11/2 | Page No: 1006-1024

Publication Timeline

Submitted: 2026-02-09

Accepted: 2026-03-05

Published: 2026-03-14

Abstract

This study analyzes the antibacterial activity of Luffa cylindrica leaf extracts, the plasmid profile and molecular characterization of MDR Uropathogenic bacteria obtained from patients from selected hospitals in Asaba. Two hundred (200) samples of urine were collected, microscopic examinations, cultures, and susceptibility tests were performed. Bacterial isolates that exhibited resistance to three or more classes of antibiotics were defined, for the purpose of this study, as Multidrug-Resistant (MDR) uropathogens. Molecular identification was performed using 16S rRNA sequencing, while plasmid extraction and curing analyses were used to determine the role of plasmid-mediated resistance. Series of quantitative and qualitative tests were conducted in order to assess the phytochemistry of the leaf extracts, and the antibacterial properties of the extracts were characterized using the agar-well diffusion method, along with a determination of the minimum inhibitory concentration (MIC) and minimum bactericidal concentration (MBC). Among the 200 specimens tested, 62 (31%) tested positive in cultures, producing 70 isolates, including Staphylococcus aureus (40%), Escherichia coli (28.6%), Klebsiella pneumonia (18.6%), Proteus mirabilis (7.1%), and Pseudomonas aeruginosa (5.7%). 76% of the isolates were multi-drug resistant (MDR) and Pseudomonas aeruginosa and Proteus mirabilis had 100% resistance. Molecular identification based on 16S rRNA gene sequencing revealed that the isolates were closely related to Escherichia coli, Enterobacter cloacae, and other clinically relevant bacterial species. However, confirmation of uropathogenicity would require further characterization of specific virulence determinants associated with urinary tract infections. All MDR strains had large plasmids (>10 kbp) and in the strains from which plasmids were removed, resistance was decreased, indicating that the resistance was from plasmids. The phytochemical analysis showed that the leaves tested positive for alkaloids, flavonoids, phenols, saponins, tannins, terpenoids, glycosides and steroids. Inhibitory zones of 24-34 mm were produced from ethanolic extracts which also had significant antibacterial activity with Minimum inhibitory concentrations (MICs) of the ethanolic extract ranged from 103.75 ± 4.78 to 310 ± 8.16 mg/mL. Although antibacterial activity was observed, these MIC values are relatively high compared with conventional antibiotics such as ciprofloxacin, suggesting that further purification of active phytochemical constituents may be required to achieve clinically relevant potency. The results suggest that the Luffa cylindrica leaf-extracts have antibacterial qualities and can be used as alternative treatments for resistant strains of uropathogens.

Keywords

Multidrug-resistant uropathogens, Luffa cylindrica, Plasmid-mediated resistance, Phytochemicals

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References

1. Flores-Mireles, A. L., Walker, J. N., Caparon, M., & Hultgren, S. J. (2015). Urinary Tract infections: epidemiology, Mechanisms of Infection and Treatment Options. Nature Reviews Microbiology, 13(5), 269–284. https://doi.org/10.1038/nrmicro3432 [Google Scholar] [Crossref]

2. Mancuso, G., Midiri, A., Gerace, E., Marra, M., Zummo, S., & Biondo, C. (2023). Urinary Tract Infections: The Current Scenario and Future Prospects. Pathogens, 12(4), 623. https://doi.org/10.3390/pathogens12040623 [Google Scholar] [Crossref]

3. Hu, Y., Ma, W., Tang, K., Qi, Q., Xu, W., Hu, R., Liu, S., Zhang, K., Chen, J., & Liang, C. (2025). Global burden of urinary tract infections in older women from 1990 to 2021 with projections to 2040: a trend analysis of the Global Burden of Disease Study 2021. Frontiers in Cellular and Infection Microbiology, 15. https://doi.org/10.3389/fcimb.2025.1577777 [Google Scholar] [Crossref]

4. Sabih, A., & Leslie, S. W. (2024). Complicated urinary tract infections. National Library of Medicine; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK436013/ [Google Scholar] [Crossref]

5. Czajkowski, K., Broś-Konopielko, M., & Teliga-Czajkowska, J. (2021). Urinary tract infection in women. Menopausal Review, 20(1), 40–47. https://doi.org/10.5114/pm.2021.105382 [Google Scholar] [Crossref]

6. Sujith, S., Solomon, A. P., & Bosco, J. (2024). Comprehensive insights into UTIs: from pathophysiology to precision diagnosis and management. Frontiers in Cellular and Infection Microbiology, 14(1). https://doi.org/10.3389/fcimb.2024.1402941 [Google Scholar] [Crossref]

7. Jancel, T., & Dudas, V. (2002). Management of uncomplicated urinary tract infections. Western Journal of Medicine, 176(1), 51–55. https://doi.org/10.1136/ewjm.176.1.51 [Google Scholar] [Crossref]

8. Silago, V., Moremi, N., Mtebe, M., Komba, E., Masoud, S., Mgaya, F. X., Mirambo, M. M., Nyawale, H. A., Mshana, S. E., & Matee, M. I. (2022). Multidrug-Resistant Uropathogens Causing Community Acquired Urinary Tract Infections among Patients Attending Health Facilities in Mwanza and Dar es Salaam, Tanzania. Antibiotics (Basel, Switzerland), 11(12), 1718. https://doi.org/10.3390/antibiotics11121718 [Google Scholar] [Crossref]

9. Muteeb, G., Rehman, T., Shahwan, M., & Aatif, M. (2023). Origin of Antibiotics and Antibiotic Resistance, and Their Impacts on Drug Development: A Narrative Review. Pharmaceuticals, 16(11), 1615. https://pmc.ncbi.nlm.nih.gov/articles/PMC10675245/ [Google Scholar] [Crossref]

10. Talaat, M., Zayed, B., Tolba, S., Abdou, E., Gomaa, M., Itani, D., Hutin, Y., & Hajjeh, R. (2022). Increasing Antimicrobial Resistance in World Health Organization Eastern Mediterranean Region, 2017–2019. Emerging Infectious Diseases, 28(4). https://doi.org/10.3201/eid2804.211975 [Google Scholar] [Crossref]

11. Mahomoodally, M. F. (2013). Traditional Medicines in Africa: An Appraisal of Ten Potent African Medicinal Plants. Evidence-Based Complementary and Alternative Medicine, 2013(617459), 1–14. https://doi.org/10.1155/2013/617459 [Google Scholar] [Crossref]

12. Abdullah, R., Younas, Q., Kaleem, A., Mehwish Iqtedar, Aftab, M., & Saleem, F. (2024). Phytochemical and antimicrobial properties of different plants and in silico investigation of their bioactive compounds in wound healing and rheumatism. Saudi Journal of Biological Sciences, 31(3), 103942–103942. https://doi.org/10.1016/j.sjbs.2024.103942 [Google Scholar] [Crossref]

13. Shenoy, A. (2024). Issue: 7. International Journal of Research and Review (Ijrrjournal.com), 11(7). https://doi.org/10.52403/ijrr.20240738 [Google Scholar] [Crossref]

14. Eme, O. I., & Idike, A. (2015). Census Politics in Nigeria : An Examination of 2006 Population Census. Journal of Policy and Development Studies, 9(3), 47–72. https://doi.org/10.12816/0011166 [Google Scholar] [Crossref]

15. F, A. C., O, A. W., & K, O. A. (2025). A Comparative Satellite-Based Study of Urban Air Pollution Trends in Sub-Saharan Africa: The Case of Asaba and Warri (2019–2024). NIPES Journal of Science and Technology Research, 7(2), 148–168. https://doi.org/10.37933/nipes/7.2.2025.10 [Google Scholar] [Crossref]

16. Khalif, M. A., Hossain, M. K., Rumi, N. A., Rahman, M. S., & Hosen, M. A. (2018). Identification and antibiogram study of bacteria isolated from different street food. Asian Journal of Medical and Biological Research, 4(3), 279–287. https://doi.org/10.3329/ajmbr.v4i3.38467 [Google Scholar] [Crossref]

17. Nix, I. D., Idelevich, E. A., Storck, L. M., Sparbier, K., Drews, O., Kostrzewa, M., & Becker, K. (2020). Detection of Methicillin Resistance in Staphylococcus aureus From Agar Cultures and Directly From Positive Blood Cultures Using MALDI-TOF Mass Spectrometry-Based Direct-on-Target Microdroplet Growth Assay. Frontiers in Microbiology, 11. https://doi.org/10.3389/fmicb.2020.00232 [Google Scholar] [Crossref]

18. Nassar, M. S. M., Hazzah, W. A., & Bakr, W. M. K. (2019). Evaluation of antibiotic susceptibility test results: how guilty a laboratory could be? Journal of the Egyptian Public Health Association, 94(1). https://doi.org/10.1186/s42506-018-0006-1 [Google Scholar] [Crossref]

19. Lesten Eliez Chisomo Chatepa, Bonface Mwamatope, Ibrahim Chikowe, & Kingsley George Masamba. (2024). Effects of solvent extraction on the phytoconstituents and in vitro antioxidant activity properties of leaf extracts of the two selected medicinal plants from Malawi. BMC Complementary Medicine and Therapies, 24(1). https://doi.org/10.1186/s12906-024-04619-7 [Google Scholar] [Crossref]

20. Phytochemical Constituents and Antimicrobial Activities of Ethanolic Extract of Luffa Cylindrica Seed. (2020). Ilorin Journal of Science, 7(2). https://doi.org/10.54908/iljs.2020.07.02.001 [Google Scholar] [Crossref]

21. Patil, M., Luo, C., Ganna Petruk, Jitka Petrlova, Artur Schmidtchen, & Manoj Puthia. (2025). Real-time evaluation of antibacterial efficacy using bioluminescent assays for Pseudomonas aeruginosa and Staphylococcus aureus. Frontiers in Microbiology, 16. https://doi.org/10.3389/fmicb.2025.1569217 [Google Scholar] [Crossref]

22. Shen, Z. (2025). DNA Extraction with Zymo Quick-DNATM Fungal/Bacterial Miniprep Kit v1. https://doi.org/10.17504/protocols.io.dm6gpdw98gzp/v1 [Google Scholar] [Crossref]

23. Chems Eddine Boukhedimi. (2025, May 26). Using statistical tests with SPSS. https://doi.org/10.5281/zenodo.16832344 [Google Scholar] [Crossref]

24. Varney, A. M., Mannix-Fisher, E., Thomas, J. C., & McLean, S. (2024). Evaluation of phenotypic and genotypic methods for the identification and characterization of bacterial isolates recovered from catheter-associated urinary tract infections. Journal of Applied Microbiology, 135(7). https://doi.org/10.1093/jambio/lxae155 [Google Scholar] [Crossref]

25. Nwankwo, U. G., Ezebialu, C. U., Ezeadila, J. O., & Okoli, I. (2020). Macroscopy and Microscopy Urinalysis: A Vital Screening Procedure for Urinary Tract Infections (UTIs) in a Hospital in Awka, Nigeria. Journal of Biology and Life Science, 11(1), 143. https://doi.org/10.5296/jbls.v11i1.16454 [Google Scholar] [Crossref]

26. Bono, M. J., Leslie, S. W., & Reygaert, W. C. (2024). Uncomplicated Urinary Tract Infections. PubMed; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK470195/#__NBK470195_ai__ [Google Scholar] [Crossref]

27. Hertz, M. A., Skjøt-Arkil, H., Heltborg, A., Lorentzen, M. H., Cartuliares, M. B., Rosenvinge, F. S., Nielsen, S. L., Mogensen, C. B., & Johansen, I. S. (2024). Clinical characteristics, factors associated with urinary tract infection and outcome in acutely admitted patients with infection; an exploratory cross-sectional cohort study. Heliyon, 10(12), e32815. https://doi.org/10.1016/j.heliyon.2024.e32815 [Google Scholar] [Crossref]

28. Ripa, F., Pietropaolo, A., Montanari, E., Hameed, B. M. Z., Gauhar, V., & Somani, B. K. (2022). Association of Kidney Stones and Recurrent UTIs: the Chicken and Egg Situation. A Systematic Review of Literature. Current Urology Reports, 23(9), 165–174. https://doi.org/10.1007/s11934-022-01103-y [Google Scholar] [Crossref]

29. Razi, A., Azita Ghiaei, Fahimeh Kamali Dolatabadi, & Haghighi, R. (2024). Unraveling the association of bacteria and urinary stones in patients with urolithiasis: an update review article. Frontiers in Medicine, 11. https://doi.org/10.3389/fmed.2024.1401808 [Google Scholar] [Crossref]

30. Minardi, D., d’Anzeo, G., Cantoro, D., Conti, A., & Muzzonigro, G. (2011). Urinary tract infections in women: etiology and treatment options. International Journal of General Medicine, 4, 333. https://doi.org/10.2147/ijgm.s11767 [Google Scholar] [Crossref]

31. Alshomrani, M. K., Alharbi, A. A., Alshehri, A. A., Arshad, M., Dolgum, S., Alshomrani, M., Alharbi, A. A., Alshehri, A., Arshad, M., & Dolgum, S. (2023). Isolation of Staphylococcus aureus Urinary Tract Infections at a Community-Based Healthcare Center in Riyadh. Cureus, 15(2). https://doi.org/10.7759/cureus.35140 [Google Scholar] [Crossref]

32. Leslie, S. W., Sajjad, H., & Murphy, P. B. (2024, April 20). Renal Calculi, Nephrolithiasis. Nih.gov; StatPearls Publishing. https://www.ncbi.nlm.nih.gov/books/NBK442014/#__NBK442014_ai__ [Google Scholar] [Crossref]

33. Mareș, C., Petca, R.-C., Popescu, R.-I., Petca, A., Geavlete, B. F., & Jinga, V. (2023). Uropathogens’ Antibiotic Resistance Evolution in a Female Population: A Sequential Multi-Year Comparative Analysis. Antibiotics, 12(6), 948. https://doi.org/10.3390/antibiotics12060948 [Google Scholar] [Crossref]

34. Sun, S., Yu, Y., Jo, Y., Han, J. H., Xue, Y., Cho, M., Bae, S.-J., Ryu, D., Park, W., Ha, K.-T., & Zhuang, S. (2025). Impact of extraction techniques on phytochemical composition and bioactivity of natural product mixtures. Frontiers in Pharmacology, 16. https://doi.org/10.3389/fphar.2025.1615338 [Google Scholar] [Crossref]

35. Shama, M., Hridhya, K., & Kulandhaivel, M. (2018). Evaluation of Antimicrobial Activity and Minimum Inhibitory Concentration of Ethanolic Extract of Three Medicinal Plants against Bacteria causing Skin Infection. Journal of Pure and Applied Microbiology, 12(1), 375–379. https://doi.org/10.22207/jpam.12.1.44 [Google Scholar] [Crossref]

36. Elfadadny, A., Ragab, R. F., AlHarbi, M., Badshah, F., Ibáñez-Arancibia, E., Farag, A., Hendawy, A. O., Patricio, Aboubakr, M., Zakai, S. A., & Nageeb, W. M. (2024). Antimicrobial resistance of Pseudomonas aeruginosa: navigating clinical impacts, current resistance trends, and innovations in breaking therapies. Frontiers in Microbiology, 15. https://doi.org/10.3389/fmicb.2024.1374466 [Google Scholar] [Crossref]

37. Wang, M., Yuan, T., Chen, J., Yang, J., Pu, J., Lin, W., Dong, K., Zhang, L., Yuan, J., Zheng, H., Sun, Y., & Xu, J. (2025). A species-level identification pipeline for human gut microbiota based on the V3-V4 regions of 16S rRNA. Frontiers in Microbiology, 16. https://doi.org/10.3389/fmicb.2025.1553124 [Google Scholar] [Crossref]

38. Alharbi, M. S., Soha Abdallah Moursi, Alshammari, A., Aboras, R., Ehab Rakha, Hossain, A., Sami Alshubrumi, Khaled Alnazha, Sajid, A., & Saleem, M. (2025). Multidrug-resistant Pseudomonas aeruginosa : Pathogenesis, resistance mechanisms, and novel therapeutic strategies. Virulence, 16(1), 2580160–2580160. https://doi.org/10.1080/21505594.2025.2580160 [Google Scholar] [Crossref]

39. Okafor, U. C., Umeh, S. O., & Nwozor, C. A. (2018). Comparative analysis of the antimicrobial strenght of three most commonly used antibiotics in Awka metropolis. International Journal of Bioinformatics and Biomedical Engineering, 4(3), 45-49. [Google Scholar] [Crossref]

40. Afriyie, D. K., Adu, L. B., Dzradosi, M., Amponsah, S. K., Ohene-Manu, P., & Manu-Ofei, F. (2018). Comparative in vitro activity of ciprofloxacin and levofloxacin against isolated uropathogens in Ghana: a pilot study. Pan African Medical Journal, 30. https://doi.org/10.11604/pamj.2018.30.194.15457 [Google Scholar] [Crossref]

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