IJESER Federal Polytechnic Wannune | School of Engineering and Environmental Sciences

Isolation, Identification and Antibiotic Susceptibility Profile of Proteus Species Isolated from Patients Attending Saint John's Hospital, Gboko, Benue State

Volume-2, Issue-1

Authors

  1. Tsav E.T,
    Department of Science Laboratory Technology, Federal Polytechnic Wannune, Benue State
  2. Aernan P.T,
    Department of Microbiology, College of Biological Sciences, Joseph Sarwuan Tarka University, Makurdi, Benue State
  3. Agada E.O,
    Department of Microbiology, College of Biological Sciences, Joseph Sarwuan Tarka University, Makurdi, Benue State
  4. Sende M.S,
    Department of Science Laboratory Technology, Federal Polytechnic Wannune, Benue State
  5. Bija M.D
    Department of Science Laboratory Technology, Federal Polytechnic Wannune, Benue State

Abstract

Urinary tract infection (UTI) is one of the most common bacterial infections. It is a broad term that encompasses
asymptomatic bacteriuria and symptomatic infection with bacterial invasion and inflammation of the urinary tract.
This study was carried out to determine the phenotypic characteristics and antibiotic susceptibility pattern of
Proteus species isolated from the urine of patients attending Saint John's Hospital, Gboko, Benue State. Eighty
two (82) midstream urine samples were collected in sterile universal bottles from males and females of all ages.
Blood agar base was prepared according to the manufacturer's instructions. The urine samples were inoculated
onto Blood agar and the inoculated plates were incubated for 24 h at 37°C. The colonies obtained were sub
cultured repeatedly on nutrient agar to obtain pure isolates. The isolates were identified using morphological and
biochemical tests. The antibiotic susceptibility pattern of the isolates was determined using the Kirby-Bauer disc
diffusion method. Thirty-three (33) Proteus isolates were obtained, giving an overall infection rate of 40.24%.
The age group ≥51 years (13.41%, n=11) had the highest rate of infection while the age group 10-20 years (1.22%,
n=1) had the lowest. There was a statistically significant difference in the infection rate between the age groups
examined [χ² = 16.015, df = 4, p = 0.001]. Female subjects (29.27%, n=24) had a higher occurrence rate than male
subjects (10.97%, n=9), and the difference in infection rate between male and female subjects was statistically
significant [χ² = 9.437, df = 1, p = 0.002]. Among the six antibiotics tested, the isolates showed the highest
susceptibility to Ciprofloxacin (27.3%), followed by Cefixime (21.2%), Ofloxacin (15.2%) and Pefloxacin
(15.2%), while susceptibility was lowest to Sparfloxacin (12.1%) and Cefotaxime (9.1%). Resistance was highest
against Ciprofloxacin (40.0%), followed by Cefixime (26.7%), Ofloxacin (20.0%) and Pefloxacin (13.3%); no
isolate was classified as resistant to Sparfloxacin or Cefotaxime. The high resistance rates recorded against the
fluoroquinolones and Cefixime suggest that these drugs have limited efficacy against urinary tract infections,
particularly Proteus species infection, and should be less considered in treatment regimens. The infection rate
recorded in this study indicates a significant level of Proteus-associated urinary tract infection among patients
attending Saint John's Hospital, Gboko, and this signifies a public health hazard. The level of resistance recorded
could be attributed to the abuse of drugs among the study population. Therefore, there is a need for strong
collaboration between physicians and the laboratory in the choice of antibiotics for the treatment of urinary tract
infections.

Keywords

UTI, antibacterial, phenotypic, resistance, susceptibility

References

Andersson, D. I. (2020). Antibiotic resistance: turning evolutionary principles into clinical reality. FEMS
Microbiology Reviews, 44, 171–188.
Ashbolt, N. J., Amézquita, A., Backhaus, T., Borriello, P. and Brandt, K. K. (2013). Human health risk assessment
(HHRA) for environmental development and transfer of antibiotic resistance. Environmental Health
Perspectives, 121, 993–1001.
Ayukekbong, J. A., Ntemgwa, M. and Atabe, A. N. (2017). The threat of antimicrobial resistance in developing
countries: causes and control strategies. Antimicrobial Resistance and Infection Control, 6, 47.
Azami, M., Jaafariz, Z., Masoumi, M., Shohani, M., Badfar, G., Mahmudi, L. and Abbasalizadeh, S. (2019). The
etiology and prevalence of urinary tract infection and asymptomatic bacteriuria in pregnant women in
Iran: A systematic review and meta-analysis. BMC Urology, 19, 43.
Baur, D., Gladstone, B. P. and Burkert, F. (2017). Effect of antibiotic stewardship on the incidence of infection
and colonisation with antibiotic-resistant bacteria and Clostridium difficile infection: a systematic review
and meta-analysis. Lancet Infectious Diseases, 17(9), 990–1001.
Bengtsson-Palme, J. and Larsson, D. J. (2016). Concentrations of antibiotics predicted to select for resistant
bacteria: proposed limits for environmental regulation. Environment International, 86, 140–149.
Boyle, D. P. and Zembower, T. R. (2015). Epidemiology and management of emerging drug-resistant Gram
negative bacteria: extended-spectrum β-lactamases and beyond. Urologic Clinics of North America,
42(4), 493–505.
Brites, D. and Gagneux, S. (2015). Co-evolution of Mycobacterium tuberculosis and Homo sapiens.
Immunological Reviews, 264(1), 6–24.
Cabello, F. C., Godfrey, H. P., Buschmann, A. H. and Dölz, H. J. (2016). Aquaculture as yet another
environmental gateway to the development and globalisation of antimicrobial resistance. Lancet
Infectious Diseases, 16, e127–e133.
Cantón, R., Horcajada, J. P., Oliver, A., Garbajosa, P. R. and Vila, J. (2013). Inappropriate use of antibiotics in
hospitals: the complex relationship between antibiotic use and antimicrobial resistance. Enfermedades
Infecciosas y Microbiología Clínica, 31, 3–11.
Charani, E., Castro-Sanchez, E. and Sevdalis, N. (2013). Understanding the determinants of antibiotic prescribing
within hospitals: the role of "prescribing etiquette". Clinical Infectious Diseases, 57(2), 188–196.
Cheesbrough, M. (2006). District Laboratory Practice in Tropical Countries, Part 2. Cambridge University Press,
UK. p. 434.
Clinical and Laboratory Standards Institute (CLSI) (2024). Performance Standards for Antimicrobial
Susceptibility Testing (M100, 34th ed.). CLSI, Wayne, PA.
Folliero, G., Gandra, S. and Laxminarayan, R. (2020). Poverty and prevalence of antibiotic resistance in invasive
isolates. International Journal of Infectious Diseases, 52, 59–61.
Kabujo, M., Lavasani, Z., Norouzirad, R., Najibpour, R., Mohamadpour, M., Nikpoor, A. R., Raeisi, M. and
ZareMarzouni, H. (2016). Prevalence of urinary tract infection among pregnant women and its
complications in their newborns during the birth in the hospitals of Dezful City, Iran, 2012-2013. Iranian
Red Crescent Medical Journal, 17, e26946.
Khanal, B. E., Said, H. S. and Abdelmegeed, E. S. (2016). Incidence of virulence determinants among
enterococcal clinical isolates in Egypt and its association with biofilm formation. Microbial Drug
Resistance, 25(6), 880–889.
Muhammad, M. H., El-Badawy, O., Hadiya, S., Daef, E. A., Suh, S. J. and Boothe, D. M. (2019). Patterns of
fluoroquinolone resistance in Enterobacteriaceae isolated from the Assiut University Hospitals, Egypt:
A comparative study. Microbial Drug Resistance, 25(4), 509–519.
Nwachukwu, G., Owusu, M., Owusu-Ofori, A., Osei, I., Sarpong, N. and Sylverken, A. (2018). Chromosomal
and plasmid-mediated fluoroquinolone resistance in human Salmonella enterica infection in Ghana.
BMC Infectious Diseases, 19(1), 898.
Odoki, M. K., Kwaga, J. K. P., Hendriksen, R. S., Okolocha, E. C. and Thakur, S. (2015). Genetic relatedness of
multidrug resistant Escherichia coli isolated from humans, chickens and poultry environments.
Antimicrobial Resistance and Infection Control, 10, 58.
Oluwafemi, M. Z., Sayed, M., Hassuna, N. A., Mahmoud, M. S. and Abdelwahab, S. F. (2018). Multi-drug
resistant Enterococcus faecalis among Egyptian patients with urinary tract infection. Journal of
Chemotherapy, 29(2), 74–82.
Onoh, R., Costa, J. and Vaz-Carneiro, A. (2013). Biomarkers as point-of-care tests to guide prescription of
antibiotics in patients with acute respiratory infections in primary care. Cochrane Database of Systematic
Reviews, 11, CD010130.
Ranjan, D. W. K. (2018). Patient information: Food poisoning (foodborne illness) (Beyond the Basics). In:
UpToDate, Basow, D. S. (Ed).
Tibyange, C. C., Chukwueze, C. M., Enebe, N. O., Enebe, J. T. and Ezeah, G. (2015). Epidemiology of pathogens
causing urinary tract infections in rural communities of Enugu State, Nigeria. International Journal of
Tropical Disease and Health, 43(23), 21–30.