ANTIBACTERIAL EFFICACY OF BACTERIOPHAGES AGAINST VIBRIO CHOLERAE
DOI:
https://doi.org/10.34016/pjbt.2024.21.02.961Keywords:
Cholera, Bacteriophages, MDR bacteria, Phage therapyAbstract
This study investigates the use of bacteriophages as an alternative antibacterial approach to combat antibiotic-resistant Vibrio cholerae, a major public health concern. Vibrio cholerae strains were identified through culture on TCBS agar, microscopy, and biochemical tests (catalase, oxidase, indole, and citrate). Antibiotic susceptibility was assessed using the Kirby-Bauer disk diffusion method across five antibiotics: tetracycline, norfloxacin, ampicillin, ciprofloxacin, and erythromycin. Results showed resistance to ampicillin, tetracycline, and erythromycin, while strains remained susceptible to norfloxacin and ciprofloxacin Five bacteriophages against Vibrio cholerae were isolated from 50 wastewater samples, and only two (F1 and F2) showed lytic activity, forming clear plaques. These two lytic phages were further purified and characterized for stability across different temperatures, pH levels, and host range. The isolated phages were tested for host range against six Vibrio cholerae strains, with F1 lysing five strains and F2 lysing three, and demonstrated stability across temperatures (20°C to 55°C) and pH levels (4 to 9). They remained active across a wider temperature and pH range demonstrating their potential for therapeutic use. The study shows that these phages are highly specific, targeting only Vibrio cholerae strains from various sources without affecting other bacterial species. This specificity makes them safer for therapeutic use, as they are less likely to disrupt the body’s natural bacterial flora. Further genomic studies are recommended to characterize the genetic makeup of these phages, optimizing their application in cholera treatment. This study provides critical insights into the potential of bacteriophages as an alternative treatment for antibiotic-resistant Vibrio cholerae.
Metrics
References
Fleischmann, S., Herrig, I., Wesp, J., Stiedl, J., Reifferscheid, G., Strauch, E., ... & Brennholt, N. (2022). Prevalence and distribution of potentially human pathogenic Vibrio spp. on German North and Baltic Sea coasts. Frontiers in Cellular and Infection Microbiology, 12, 846819. DOI: https://doi.org/10.3389/fcimb.2022.846819
Hu, D., Liu, B., Feng, L., Ding, P., Guo, X., Wang, M., & Wang, L. (2016). Origins of the current seventh cholera pandemic. Proceedings of the National Academy of Sciences, 113(48), E7730-E7739. DOI: https://doi.org/10.1073/pnas.1608732113
Zahid, M. S. H., Udden, S. N., Faruque, A. S. G., Calderwood, S. B., Mekalanos, J. J., & Faruque, S. M. (2008). Effect of phage on the infectivity of Vibrio cholerae and emergence of genetic variants. Infection and immunity, 76(11), 5266-5273. DOI: https://doi.org/10.1128/IAI.00578-08
Shaw, S., Samanta, P., Chowdhury, G., Ghosh, D., Dey, T. K., Deb, A. K., & Mukhopadhyay, A. K. (2022). Altered molecular attributes and antimicrobial resistance patterns of Vibrio cholerae O1 El Tor strains isolated from the cholera endemic regions of India. Journal of Applied Microbiology, 133(6), 3605-3616 DOI: https://doi.org/10.1111/jam.15794
Deen, J., Mengel, M. A., & Clemens, J. D. (2020). Epidemiology of cholera. Vaccine, 38, A31-A40. DOI: https://doi.org/10.1016/j.vaccine.2019.07.078
Abed, S. Y., Alsakini, A. H., Rasool, K. H., Mohammed, S. Q., & Kaabi, S. A. G. (2022). Formulation of a Novel Phage Cocktail against Vibrio cholerae O1. Research Journal of Pharmacy and Technology, 15(6), 2605-2608. DOI: https://doi.org/10.52711/0974-360X.2022.00435
Mittal, M., Tripathi, S., Saini, A., & Mani, I. (2023). Phage for treatment of Vibrio cholerae infection. Progress in Molecular Biology and Translational Science, 201, 21-39. DOI: https://doi.org/10.1016/bs.pmbts.2023.03.021
Shrivastava, S. R., Shrivastava, P. S., & Ramasamy, J. (2018). Responding to the challenge of antibiotic resistance: World Health Organization. Journal of Research in Medical Sciences, 23(1), 21. DOI: https://doi.org/10.4103/1735-1995.228593
Shah, M.M., Bundi, M., Kathiiko, C., Guyo, S., Galata, A., Miringu, G., Ichinose, Y., & Yoshida, L. (2023). Antibiotic-Resistant Vibrio cholerae O1 and Its SXT Elements Associated with Two Cholera Epidemics in Kenya in 2007 to 2010 and 2015 to 2016. Microbiolgy Spectrum, 1;11(3):e04140-22 DOI: https://doi.org/10.1128/spectrum.04140-22
Das, B., Verma, J., Kumar, P., Ghosh, A., & Ramamurthy, T. (2020). Antibiotic resistance in Vibrio cholerae: understanding the ecology of resistance genes and mechanisms. Vaccine, 38, A83-A92. DOI: https://doi.org/10.1016/j.vaccine.2019.06.031
Jaiswal, A., Koley, H., Ghosh, A., Palit, A., & Sarkar, B. (2013). Efficacy of cocktail phage therapy in treating Vibrio cholerae infection in rabbit model. Microbes and Infection, 15(2), 152-156. DOI: https://doi.org/10.1016/j.micinf.2012.11.002
Hsueh, B. Y., & Waters, C. M. (2019). Combating cholera. F1000Research, 8 DOI: https://doi.org/10.12688/f1000research.18093.1
Cai, L., Tian, Y., Li, Z., Yang, Y., Ai, C., & Zhang, R. (2023).
A broad-host-range lytic phage vB_VhaS-R18L as a candidate against vibriosis. Frontiers in Microbiology, 14, 1191157.
Naser, I. B., Hoque, M. M., Abdullah, A., Bari, S. M. N., Ghosh, A. N., & Faruque, S. M. (2017). Environmental bacteriophages active on biofilms and planktonic forms of toxigenic Vibrio cholerae: Potential relevance in cholera epidemiology. PLoS ONE, 12(7), e0180838. DOI: https://doi.org/10.1371/journal.pone.0180838
O'Hara, B. J., Alam, M., & Ng, W.-L. (2022). The Vibrio cholerae Seventh Pandemic Islands act in tandem to defend against a circulating phage. PLoS Genetics, 18(8), e1010250. DOI: https://doi.org/10.1371/journal.pgen.1010250
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2024 Rafiq Ahmad, Muhammad Fayaz Khan, Hifza Rehman, Samia Gul, Daniyal Akram, Afshan Saleem, Sidra Fareed
This work is licensed under a Creative Commons Attribution 4.0 International License.