Plasmid Curing of Bacteria Isolated from Upper Respiratory Tract Infections among Patients Attending Specialist Hospital Sokoto
DOI:
https://doi.org/10.47430/ujmr.2493.047Keywords:
Antibiotic resistance, Beta-lactam antibiotics, Plasmid curing, upper respiratory tract infectionAbstract
Study’s Novelty/Excerpt
- This study focuses on curing plasmid-mediated antibiotic resistance in bacteria associated with upper respiratory tract infections in patients at Specialist Hospital Sokoto, an area previously underexplored in this context.
- It uniquely demonstrates the successful reversal of antibiotic resistance in Staphylococcus aureus, Streptococcus pyogenes, and Pseudomonas aeruginosa through plasmid curing experiments, highlighting the significant role of plasmids in resistance mechanisms.
- Additionally, the study underscores the potential for plasmid-mediated resistance to be transferred among bacterial populations, presenting a critical concern for antimicrobial resistance management in the region.
Full Abstract
Presences of resistant plasmids (R-plasmids) in microorganisms make the cells avert the effect of antibiotics and complicates chemotherapy of infections. This study aimed to cure the plasmid of antibiotic-resistant bacteria associated with upper respiratory tract infections among patients attending Specialist Hospital Sokoto by reassessing their susceptibility to antibiotics that were previously resistant. One hundred (100) throat swab samples were collected and analysed. The isolates were isolated and identified using standard methods (Gram staining, biochemical and serological tests). The susceptibility of the isolates to various beta-lactam antibiotics was evaluated, and resistant bacteria were subjected to plasmid curing experiments followed by further susceptibility testing to reassess their susceptibility to the erstwhile resistance. Bacteria isolated were Staphylococcus aureus, Streptococcus pyogenes, and Pseudomonas aeruginosa, with the frequency of occurrence of 20 (57.2%), 9 (25.7%), and 6 (17.1%), respectively. The result of antibiotic susceptibility tests before plasmid curing showed that Staphylococcus aureus, Streptococcus pyogenes, and Pseudomonas aeruginosa resisted Cloxacilline, Cefuroxime, Cloxacillin and Augmentin. Susceptibility results after curing showed that almost all bacteria have reverted to sensitivity to all antibiotics except Cloxacillin and Augmentin. This research implies that the resistance possessed by the bacterial isolates is plasmid-mediated and may easily be transferred to other non-resistant bacteria, which may lead to an alarming rate of antimicrobial resistance in the study area.
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References
Astrid, B. A., Levin, E., Van Houten, M. A., Hasrat, R., Kalkman, G., Biesbroek, G. and Bogaert, D. (2016). Development of upper respiratory tract microbiota in infancy is affected by mode of delivery. EBioMedicine; 9:336-345. https://doi.org/10.1016/j.ebiom.2016.05.031
Atata, R. F., Ibrahim, Y. K., Giwa, A. and Akanbi, A. A. (2013). Antibiotics of Bacterial Isolates from surgical site and hospital environment in a university teaching Hospital in Nigeria. Journal of Medicine and Medical Science; 4: 181-187. http://hdl.handle.net/123456789/3102
Clinical and Laboratory Standards Institute. 2018. Performance standards for antimicrobial susceptibility testing; 27th informational supplement. M100-S28. Clinical and Laboratory Standards Institute, Wayne, PA.
Gambo, S., Mohammad, U-K., Baki A.S., Bello, A. and Gambo, A. (2017). Incidence of Salmonella species isolated from presumptive Typhoid fever patients attending Specialist Hospital Sokoto. Scholarly Journal of Biological Science; 6(2):23-27.
Kho, B. P., Ong, C. M, Tan, F. T. and Wee, C. Y. (2013). Antibiotic prescribing for upper respiratory tract infections in sarawak district hospitals. The Medical Journal of Malaysia; 68: 136-40. https://europepmc.org/article/med/23629559
Kutter, J. S., Spronken, M. I., Fraaij, P. L., Fouchier, R. A. and Herfst, S. (2018). Transmission routes of respiratory viruses among humans. Current opinion in virology, 28, 142-151. https://doi.org/10.1016/j.coviro.2018.01.001
Mawaddah, A., Genden, H. S., Lum, S. G. and Marina, M. B. (2020). Upper respiratory tract sampling in COVID-19. The Malaysian journal of pathology; 42(1), 23-35. http://www.mjpath.org.my/2020/v42n1/sampling-in-COVID-19.pdf
Miriti, D. M., Muthini, J. M. and Nyamache, A. K. (2023). Study of bacterial respiratory infections and antimicrobial susceptibility profile among antibiotics naive outpatients visiting Meru teaching and referral hospital, Meru County, Kenya in 2018. BMC Microbiology; 23(1):172. https://doi.org/10.1186/s12866-023-02905-x.
Patwardhan, R. B., Dhakephalkar, P. K., Chopade, B. A., Dhavale, D. D. and Bhonde, R. R. (2018). Purification and Characterization of an Active Principle, Lawsone, Responsible for the Plasmid Curing Activity of Plumbago zeylanica Root Extracts. Front Microbiol; 9:2618. https://doi.org/10.3389/fmicb.2018.02618.
Peroš-Golubičić, T. and Tekavec-Trkanjec, J. (2015). Upper respiratory tract infections. Textbook of Respiratory and Critical Care Infections. New Delhi: Jaypee Brothers, 16-29. https://doi.org/10.5005/jp/books/12168_2
Shuaibu, A. S., Ibrahim, Y. K., Olayinka, B. O., Atata, R. F., Ungo-kore, H. Y., Olowookere, A. and Shuaibu A. B. (2016). Antiplasmid effect of acridine orange on multiple antibiotics resistant bacteria isolated from a secondary health care institution in Sokoto state. Journal of pharmaceutical and allied sciences; 13:2-7.
Taura, D. W. (2021). Bacterial isolates of the respiratory tract infection and their current sensitivity pattern among patients attending Aminu Kano Teaching Hospital Kano, Nigeria. International Journal of Biomedical and Health Sciences: 7(1):45-51. https://doi.org/10.9734/JAMPS/2017/31291
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