Background: Obstructive uropathy and urinary tract infection increase the risk of infection and renal scarring. When there is an obstruction in the urinary tract, stasis of urine with multiplication and ascending translocation of bacteria can result in urinary tract infection. These may present as cystitis, pyelonephritis, abscess formation and urosepsis. Treatment requires appropriate antibiotic treatment following urine culture and sensitivity to prevent potentially fatal urosepsis. Objectives: To evaluate the bacteria isolated in the urine culture of patients with obstructive uropathy and determine the common organisms associated with upper and lower urinary tract obstruction. Methods and Methodology: The study was an 8year retrospective evaluation of patients presenting with obstructive uropathy from two hospitals. All patients with upper and urinary tract obstructive uropathy were included. Their laboratory request forms and results of culture and sensitivity were reviewed. The data was extracted from records, coded into Excel, and analyzed using SPSS Version 20. Results: 445 patients with obstructive uropathy had their urine culture reports analyzed in the study population. The ages range from 2years to 108years with a mean age of 58years and a median age of 61years. 397(89.2%) were male, and 48(10.8%) were females. The urine positive culture rate was 70.6%. Gram-negative organisms were the commonest, with Klebsiella sp. 105(23.6%) the most frequently isolated. Escherichia Coli 98(22.0%). Citrobacter sp was the least common pathogen isolated and was not observed in females. Conclusion: Gram-negative organisms are the commonest pathogens cultured from the urine in patients with obstructive uropathy. The positive culture rate was 70.6%. Klebsiella sp. and E. Coli were the most prevalent organisms from the urine in patients with upper and lower urinary tract obstruction.
Stasis of urine in the urinary tract increases the risk of infection and renal scarring 1. Urinary tract obstruction can have long-lasting effects on the physiology of the kidney, including its ability to concentrate urine. 2 Obstructive uropathy is a functional or anatomic obstruction of urine flow at any level of the urinary tract. 2. It is responsible for about 4% of end-stage renal disease. 3 The causes will depend on age. Common causes include posterior urethral valves, pelvic ureteric obstruction, and ureteroceles in children. The usual causes in adult young men include urethral stricture and urinary stones. The aetiological risk factors in the middle-aged and elderly are prostatic enlargement, benign and malignant lesions, bladder tumours and urinary stones. Female causes include bladder tumours, urinary stones and genital malignancies 3, 4. When there is an obstruction in the urinary tract, stasis of urine with multiplication and ascending translocation of bacteria result in urinary tract infection. These may present as cystitis, pyelonephritis, abscess formation and urosepsis. Treatment requires appropriate antibiotic treatment following urine culture and sensitivity. 5, 6, 7, 8
To evaluate the bacteria isolates in the urine culture of patients with obstructive uropathy and determine the common organisms associated with upper and lower urinary tract obstruction.
The study was an 8year retrospective evaluation of patients presenting with obstructive uropathy from two hospitals. The hospital includes the Urology Department, University of Port Harcourt Teaching Hospital, and Rosivylle Clinic and Urology Centre, Port Harcourt, Nigeria, from January 2013 to December 2020. All the patients had obstructive uropathy at some level from the renal calyxes to the tip of the urethra. Included are patients diagnosed with posterior urethral valves, meatal stenosis, pelvi-ureteric obstruction, ureterocele, urinary calculi, urothelial tumours of the ureter, bladder and urethra, bladder outlet obstructions from benign and malignant obstructions, schistosomiasis, and urethral strictures. Their laboratory request forms and results of culture and sensitivity were reviewed. The data was extracted from records, coded into Excel, and analyzed using SPSS Version 20.
Four hundred forty-five patients with obstructive uropathy had their urine culture reports analyzed in the study population. The ages range from 2years to 108years with a mean age of 58years and a median age of 61years. 397(89.2%) were male, and 48(10.8%) were females. The urine positive culture rate was 70.6%. Gram-negative organisms were the commonest, with Klebsiella sp. 105(23.6%) the most frequently isolated. Escherichia Coli 98(22.0%) was next, then Proteus sp. 62(13.9%) and Pseudomonas sp. 46 (10.3%), respectively. Klebsiella was the commonest cultured in females 24(50.0%), while E. Coli was the most frequent in men 89(22.4%). Citrobacter sp was the least common pathogen isolated and was not observed in females.
Obstructive uropathy is a functional or anatomic obstruction of urine flow at any level of the urinary tract. UTI in patients with lower urinary tract symptoms (LUTS) is classified as complicated because stasis is a risk factor for bacteria colonization and mitigates treatment. 9, 10, 11 The combination of sepsis and obstruction have profound effects on the physiological function of the kidney, including its ability to concentrate urine. Obstructive uropathy accounts for up to 4% of end-stage renal diseases. 2 The aetiology depends on the age and sex of the patient.
The age at presentation of the patients with UTI shows a bimodal distribution during childhood and in the sixties 3, 4. In our study, the youngest patient was a two-year-old child with posterior urethral valve, while the oldest was a 108years old with prostate cancer with obstructive LUTS from BPH. Common aetiological factors in the pediatric age group include posterior urethral valves, pelvic ureteric obstruction, and ureterocele. 12 In adult young men, urinary calculi and benign urethral strictures are common causes. In contrast, in the elderly, enlargement of the prostate, both benign and malignant, are often the observed risk factor. 1
The modal age group was the 60-69 gear group with a median age of 61years in our study. (Table 1) The prevalence of bacteriuria among all the patients was 70.6% (Table 1). Considering that majority of the patients were men (89.2%) and that the mean age of the patients was 58.6%, bladder outlet obstruction is expected to be prevalent among these patients.
Oromia Gauguin et al. 13 conducted a prospective study evaluating UTI with BPH aged between 53-80years. They found a positive urine culture rate of 44.7% out of the 94 patients evaluated and observed that E. Coli was the commonest isolated. Akebi et al. 14 in Bida, Nigeria, found the incidence of urinary tract infections in their study population was 62.5%. E. coli 247(67.7%) was also observed to be the most prevalent uropathies followed by Staphylococcus aureus 34 (9.3%), Pseudomonas species 29(7.9%), Klebsiella species 10(2.7%), Proteus species 10(2.7%)
In another West African study, Asafo-Adjei K et al. 15 investigated bladder outlet obstruction at Korle, Accra, Ghana and found a prevalence of UTI of 76.6%. The main risk factor observed in their study was urethral catheterization. Enterobacteriaceae were the most common organisms, and E. coli (62.2%) was the most often seen, followed by Klebsiella sp.(27.0%), Citrobacter sp (8.1%) and Aerobacter spp (2.7%). In their study, Khan R et al. 16 found significant bacteriuria was detected in 19.3% and 55.4% of asymptomatic and symptomatic patients, respectively. The significant risk factors were female sex, diabetes, obstructive uropathy, previous instrumentation, and chronic kidney disease. The most common isolated pathogens were Escherichia coli (52.4%), followed by Klebsiella pneumonia (12.3%) and Citrobacter spp. (9.1%), Enterococcus (6.9%), Proteus spp. (5.3%), Coagulase-negative staphylococcus (5.3%) and staph. aureus (4.0%).
The commonest isolated microbe in urinary tract infection is Escherichia Coli, both in simple, complicated and nosocomial UTIs. The organism is a normal constituent of humans and animals. 17, 18 The distinctive E. coli strains that cause most UTIs have been designated Uropathogenic E. coli. They possess diverse virulence-associated factors that assist them in attaching to, invading, and injuring the host. These include adhesins, toxins, siderophores, protective polysaccharide coatings, invasions, and serum resistance-associated proteins. The presence and numbers of such virulence factors predict in vivo virulence. 19, 20, 21 In our study, E. Coli (22.0%) was the second commonest cultured isolate from the urine of the patients with obstructive uropathy, slightly less prevalent than Klebsiella spp. (23.6%).
Klebsiella spp was the commonest isolated from urine culture in our study. It is closely associated with nosocomial infection and multidrug resistance. This finding is not surprising since most of the patients were referred from other hospitals, and many of them had a history of admission at previous medical facilities. 22, 23
In our study, after Klebsiella sp. and E. Coli, Proteus spp. (13.9%), was the next most commonly cultured organism. Proteus sp. is capable of causing symptomatic infections of the urinary tract, including cystitis and pyelonephritis. It is present in many cases of asymptomatic bacteriuria, particularly in the elderly and among patients with type 2 diabetes. These infections can also cause bacteremia and progress to potentially life-threatening urosepsis. Additionally, Proteus mirabilis infections can cause the formation of urinary urolithiasis. 24, 25, 26
Pseudomonas spp is the fourth most common pathogen in our study and is associated with hospital-acquired catheter-associated UTIs. 27 The virulence of Pseudomonas sp. is multifactorial. It has been attributed to cell-associated factors like alginate, lipopolysaccharide, flagellum, pilus and non-pilus adhesins, and exoenzymes or secretory virulence factors like protease elastase, phospholipase, pyocyanin, exotoxin A, exoenzyme S, hemolysins (rhamnolipids) and siderophores. 28, 29, 30, 31
Finally, Citrobacter spp. are infrequently isolated from urine cultures, and only 3(0.7%) was observed in our study. They are, however, emerging as a common nosocomial multidrug-resistant pathogen, especially in developing countries. UTI caused by Citrobacter spp. have been seen in 12% of patients in 1961, and since then, its prevalence has been increasing. 32 Invasive procedures like catheterization or genitourinary instrumentation seem to assist the organism in colonization and infection of the urinary tract. 33, 34
Irrespective of the causative organisms, obstruction to urine flow leads to stasis and predisposes to infection. The continuous hydrostatic flow of slightly acidic urine is necessary to inhibit ascending colonization of the urinary tract by organisms. 9, 35 This is impaired in obstructive uropathy leading to colonization and urinary tract infection. The virulence of the bacteria is also essential in the ability of microbes to invade the bladder urothelium and establish active infection. 21, 36
All gram-negative organisms can cause urosepsis, with E. Coli most often incriminated, in up to 50.0% of fatal endotoxemia. It is followed by Proteus (15%), Enterobacter (15%), Klebsiella (15%), Pseudomonas aeruginosa (5%), and other gram-positive bacteria (15%). 37, 38 urosepsis is a deadly clinical syndrome characterized by physiologic, biologic, and biochemical abnormalities resulting from dysregulated host response to infection originating from the urinary tract. The associated exaggerated inflammatory response can potentially result in multiple organ dysfunction syndrome and death. 39, 40 The fatality associated with gram-negative endotoxemia underscore the importance of isolation by urine culture, identifying and characterizing the risk by each organism, and effectively treating infections when present, especially before surgical intervention.
Gram-negative organisms are the commonest pathogens cultured from the urine in patients with obstructive uropathy. The positive culture rate was 70.6%. Klebsiella sp. and E. Coli were the most prevalent organisms from the urine in patients with upper and lower urinary tract obstruction.
[1] | Nicolle LE; AMMI Canada Guidelines Committee. Complicated urinary tract infection in adults. Can J Infect Dis Med Microbiol. 2005; 16: 349-360. | ||
In article | View Article PubMed | ||
[2] | Meldrum KK. Pathophysiology of urinary tract obstruction. Wein AJ, Kaposi LR, Partin AW, Peters CA, eds. Campbell-Walsh Urology. 11th ed. Philadelphia, Pa: Elsevier; 2016. 1089-1103. | ||
In article | |||
[3] | Rose JG, Gillen water JY, Wyke AT. The recovery of function of chronically obstructed and infected ureters. Invest Urol. 1975 Sep. 13: 125-130. | ||
In article | |||
[4] | Lemoine L, Dupont C, Capron A, Cerf E, Yilmaz M, Verloop D, Blanckaert K, Senneville E, Alfandari S. Prospective evaluation of the management of urinary tract infections in 134 French nursing homes. Med Mal Infect. 2018 Aug; 48(5): 359-364. | ||
In article | View Article PubMed | ||
[5] | Expert Panel on Pediatric Imaging: Karmazyn BK, Alazraki AL, Anupindi SA, Dempsey ME, Dillman JR, Dorfman SR, Garber MD, Moore SG, Peters CA, Rice HE, Rigsby CK, Safdar NM, Simoneaux SF, Trout AT, Westra SJ, Wootton-Gorges SL, Coley BD. ACR Appropriateness Criteria® Urinary Tract Infection-Child. J Am Coll Radiol. 2017; 14: 362-371. | ||
In article | View Article PubMed | ||
[6] | Yasuda M. Urogenital infections. Nihon Rinsho. 2017; 75: 558-566. | ||
In article | |||
[7] | Abrams P, Hashim H, Tomson C, Macgowan A, Skews R, Warren K. The use of intravesical gentamicin to treat recurrent urinary tract infections in lower urinary tract dysfunction. Neurourol Urodyn. 2017; 36: 2109-2116. | ||
In article | View Article PubMed | ||
[8] | Chernyak S, Salamon C. Intravesical Antibiotic Administration in the Treatment of Recurrent Urinary Tract Infections: Promising Results From a Case Series. Female Pelvic Med Reconstr Surg. 2020; 26: 152-154. | ||
In article | View Article PubMed | ||
[9] | Gomila A, Carratalà J, Eliakim-Raz N, Shaw E, Wiegand I, Vallejo-Torres L, Gorostiza A, Vigo JM, Morris S, Stoddart M, Grier S, Vank C, Cuperus N, Van den Heuvel L, Vuong C, MacGowan A, Leibovici L, Addy I, Pujol M., COMBACTE MAGNET WP5 RESCUING Study Group and Study Sites. Risk factors and prognosis of complicated urinary tract infections caused by Pseudomonas aeruginosa in hospitalized patients: a retrospective multicenter cohort study. Infect Drug Resist. 2018; 11: 2571-2581. | ||
In article | View Article PubMed | ||
[10] | Esposito S, Rinaldi VE, Argentiero A, Farinelli E, Cofini M, D'Alonzo R, Mencacci A, Principi N. Approach to Neonates and Young Infants with Fever without a Source Who Are at Risk for Severe Bacterial Infection. Mediators Inflamm. 2018; 2018: 4869329. | ||
In article | View Article PubMed | ||
[11] | Cruz J, Figueiredo F, Matos AP, Duarte S, Guerra A, Ramalho M. Infectious and Inflammatory Diseases of the Urinary Tract: Role of MR Imaging. Magn Reson Imaging Clin N Am. 2019; 27: 59-75. | ||
In article | View Article PubMed | ||
[12] | Leung AKC, Wong AHC, Leung AAM, Hon KL. Urinary Tract Infection in Children. Recent Pat Inflamm Allergy Drug Discov. 2019; 13: 2-18. | ||
In article | View Article PubMed | ||
[13] | Agbugui JO, Obarisiagbon EO, Osaigbovo II. Bacteriology of Urine Specimens Obtained from Men with Symptomatic Benign Prostatic Hyperplasia. Niger J Surg. 2016; 22: 65-69. | ||
In article | View Article PubMed | ||
[14] | Akobi O A, Inyinbor H E, Akobi E C, Emumwen E G, Ogedengbe S O, Uzoigwe E O et al. Incidence of urinary tract infection among pregnant women attending antenatal clinic at Federal Medical Centre, Bida, Niger- State, North Central Nigeria. Am J Infectious Dis Microbiol. 2014; 2:34-38. | ||
In article | View Article | ||
[15] | Asafo-Adjei K, Mensah J.E, Labi A, Dayie N.T.D and Donkor E.S; Urinary tract infections among bladder outlet obstruction patients in Accra, Ghana: Aetiology, Antibiotic Resistance, and Risk Factors.MDPI Journals/diseases 2018/vol.6/issue 3/10.3390/diseases6030065. | ||
In article | View Article PubMed | ||
[16] | Khan R, Saif Q, Fatima K, Meher R, Shahzad HF, Anwar KS titled clinical and bacteriological profile of UTI in patients attending a North Indian tertiary care centre. J Integr Nephrol Androl 2015; 2: 29-34. | ||
In article | View Article | ||
[17] | Ruiz J, Simon K, Horcajada JP, Velasco M, Barranco M, Roig G, Moreno-Martinez A, Martinez JA, Jimenez de Anta T, Mensa J, Vila J. Differences in virulence factors among clinical isolates of Escherichia coli causing cystitis and pyelonephritis in women and prostatitis in men. Journal of Clinical Microbiology. 2002; 40: 4445-4449. | ||
In article | View Article PubMed | ||
[18] | Zhang L, Foxman B. Molecular epidemiology of Escherichia coli mediated urinary tract infections. Frontiers in Bioscience. 2003; 8: 235-244. | ||
In article | View Article PubMed | ||
[19] | Johnson JR, Kuskowski MA, O'Bryan TT, Colodner R, Raz R. Virulence genotype and phylogenetic origin in relation to antibiotic resistance profile among Escherichia coli urine sample isolates from Israeli women with acute uncomplicated cystitis. Antimicrobial Agents and Chemotherapy. 2005; 49: 26-31. | ||
In article | View Article PubMed | ||
[20] | Sabih A, Leslie SW. Complicated Urinary Tract Infections. [Updated 2022 Feb 14]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK436013. | ||
In article | |||
[21] | Bien J, Sokolova O, Bozko P. Role of Uropathogenic Escherichia coli Virulence Factors in Development of Urinary Tract Infection and Kidney Damage. Int J Nephrol. 2012; 2012:681473. | ||
In article | View Article PubMed | ||
[22] | Broberg CA, Palacios M & Miller VL (2014). Klebsiella: a long way to go towards understanding this enigmatic jet-setter. F1000Prime Rep 6: 64. | ||
In article | View Article PubMed | ||
[23] | Cristea OM, Avrămescu CS, Bălășoiu M, Popescu FD, Popescu F & Amzoiu MO (2017). Urinary tract infection with Klebsiella pneumoniae in Patients with Chronic Kidney Disease. Curr Health Sci J 43(2): 137-148. | ||
In article | |||
[24] | Schaffer JN, Pearson MM. Proteus mirabilis and Urinary Tract Infections. Microbiol Spectr. 2015; 3(5): 10.1128/microbiolspec.UTI-0017-2013. | ||
In article | View Article PubMed | ||
[25] | O'Hara CM, Brenner FW, Miller JM. Classification, identification, and clinical significance of Proteus, Providencia, and Morganella. Clin Microbiol Rev. 2000; 13: 534-546. | ||
In article | View Article PubMed | ||
[26] | Matthews SJ, Lancaster JW. Urinary tract infections in the elderly population. Am J Geriatr Pharmacother. 2011; 9: 286-309. | ||
In article | View Article PubMed | ||
[27] | Jarvis WR, Martone WJ. Predominant pathogens in hospital infections. J Antimicrob Chemother 1992; 29:19-24. | ||
In article | View Article PubMed | ||
[28] | Matheson NR, Potempa J, Travis J. Interaction of a novel form of Pseudomonas aeruginosa alkaline protease (aeruginolysin) with interleukin-6 and interleukin-8. Biol Chem 2006; 387: 911-915. | ||
In article | View Article PubMed | ||
[29] | Yates SP, Jorgensen R, Andersen GR, Merrill AR. Stealth and mimicry by deadly bacterial toxins. Trends Biochem 2006; 31: 123-33. | ||
In article | View Article PubMed | ||
[30] | Zulianello L, Canard C, Kohler T, Caille D, Lacroix JS, Meda P. Rhamnolipids are virulence factors that promote early infiltration of primary human airway epithelia by Pseudomonas aeruginosa. Infect Immun 2006; 74: 3134-3147. | ||
In article | View Article PubMed | ||
[31] | Veesenmeyer JL, Hauser AR, Lisboa T, Rello J. Pseudomonas aeruginosa virulence and therapy: evolving translational strategies. Crit Care Med 2009; 37:1777-86. | ||
In article | View Article PubMed | ||
[32] | Whitby JL, Muir GG. Bacteriological studies of urinary tract infection. Br J Urol. 1961; 33: 130-4. | ||
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In article | |||
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In article | View Article PubMed | ||
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Published with license by Science and Education Publishing, Copyright © 2022 John Edoka Raphael and Kufre Udo
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[1] | Nicolle LE; AMMI Canada Guidelines Committee. Complicated urinary tract infection in adults. Can J Infect Dis Med Microbiol. 2005; 16: 349-360. | ||
In article | View Article PubMed | ||
[2] | Meldrum KK. Pathophysiology of urinary tract obstruction. Wein AJ, Kaposi LR, Partin AW, Peters CA, eds. Campbell-Walsh Urology. 11th ed. Philadelphia, Pa: Elsevier; 2016. 1089-1103. | ||
In article | |||
[3] | Rose JG, Gillen water JY, Wyke AT. The recovery of function of chronically obstructed and infected ureters. Invest Urol. 1975 Sep. 13: 125-130. | ||
In article | |||
[4] | Lemoine L, Dupont C, Capron A, Cerf E, Yilmaz M, Verloop D, Blanckaert K, Senneville E, Alfandari S. Prospective evaluation of the management of urinary tract infections in 134 French nursing homes. Med Mal Infect. 2018 Aug; 48(5): 359-364. | ||
In article | View Article PubMed | ||
[5] | Expert Panel on Pediatric Imaging: Karmazyn BK, Alazraki AL, Anupindi SA, Dempsey ME, Dillman JR, Dorfman SR, Garber MD, Moore SG, Peters CA, Rice HE, Rigsby CK, Safdar NM, Simoneaux SF, Trout AT, Westra SJ, Wootton-Gorges SL, Coley BD. ACR Appropriateness Criteria® Urinary Tract Infection-Child. J Am Coll Radiol. 2017; 14: 362-371. | ||
In article | View Article PubMed | ||
[6] | Yasuda M. Urogenital infections. Nihon Rinsho. 2017; 75: 558-566. | ||
In article | |||
[7] | Abrams P, Hashim H, Tomson C, Macgowan A, Skews R, Warren K. The use of intravesical gentamicin to treat recurrent urinary tract infections in lower urinary tract dysfunction. Neurourol Urodyn. 2017; 36: 2109-2116. | ||
In article | View Article PubMed | ||
[8] | Chernyak S, Salamon C. Intravesical Antibiotic Administration in the Treatment of Recurrent Urinary Tract Infections: Promising Results From a Case Series. Female Pelvic Med Reconstr Surg. 2020; 26: 152-154. | ||
In article | View Article PubMed | ||
[9] | Gomila A, Carratalà J, Eliakim-Raz N, Shaw E, Wiegand I, Vallejo-Torres L, Gorostiza A, Vigo JM, Morris S, Stoddart M, Grier S, Vank C, Cuperus N, Van den Heuvel L, Vuong C, MacGowan A, Leibovici L, Addy I, Pujol M., COMBACTE MAGNET WP5 RESCUING Study Group and Study Sites. Risk factors and prognosis of complicated urinary tract infections caused by Pseudomonas aeruginosa in hospitalized patients: a retrospective multicenter cohort study. Infect Drug Resist. 2018; 11: 2571-2581. | ||
In article | View Article PubMed | ||
[10] | Esposito S, Rinaldi VE, Argentiero A, Farinelli E, Cofini M, D'Alonzo R, Mencacci A, Principi N. Approach to Neonates and Young Infants with Fever without a Source Who Are at Risk for Severe Bacterial Infection. Mediators Inflamm. 2018; 2018: 4869329. | ||
In article | View Article PubMed | ||
[11] | Cruz J, Figueiredo F, Matos AP, Duarte S, Guerra A, Ramalho M. Infectious and Inflammatory Diseases of the Urinary Tract: Role of MR Imaging. Magn Reson Imaging Clin N Am. 2019; 27: 59-75. | ||
In article | View Article PubMed | ||
[12] | Leung AKC, Wong AHC, Leung AAM, Hon KL. Urinary Tract Infection in Children. Recent Pat Inflamm Allergy Drug Discov. 2019; 13: 2-18. | ||
In article | View Article PubMed | ||
[13] | Agbugui JO, Obarisiagbon EO, Osaigbovo II. Bacteriology of Urine Specimens Obtained from Men with Symptomatic Benign Prostatic Hyperplasia. Niger J Surg. 2016; 22: 65-69. | ||
In article | View Article PubMed | ||
[14] | Akobi O A, Inyinbor H E, Akobi E C, Emumwen E G, Ogedengbe S O, Uzoigwe E O et al. Incidence of urinary tract infection among pregnant women attending antenatal clinic at Federal Medical Centre, Bida, Niger- State, North Central Nigeria. Am J Infectious Dis Microbiol. 2014; 2:34-38. | ||
In article | View Article | ||
[15] | Asafo-Adjei K, Mensah J.E, Labi A, Dayie N.T.D and Donkor E.S; Urinary tract infections among bladder outlet obstruction patients in Accra, Ghana: Aetiology, Antibiotic Resistance, and Risk Factors.MDPI Journals/diseases 2018/vol.6/issue 3/10.3390/diseases6030065. | ||
In article | View Article PubMed | ||
[16] | Khan R, Saif Q, Fatima K, Meher R, Shahzad HF, Anwar KS titled clinical and bacteriological profile of UTI in patients attending a North Indian tertiary care centre. J Integr Nephrol Androl 2015; 2: 29-34. | ||
In article | View Article | ||
[17] | Ruiz J, Simon K, Horcajada JP, Velasco M, Barranco M, Roig G, Moreno-Martinez A, Martinez JA, Jimenez de Anta T, Mensa J, Vila J. Differences in virulence factors among clinical isolates of Escherichia coli causing cystitis and pyelonephritis in women and prostatitis in men. Journal of Clinical Microbiology. 2002; 40: 4445-4449. | ||
In article | View Article PubMed | ||
[18] | Zhang L, Foxman B. Molecular epidemiology of Escherichia coli mediated urinary tract infections. Frontiers in Bioscience. 2003; 8: 235-244. | ||
In article | View Article PubMed | ||
[19] | Johnson JR, Kuskowski MA, O'Bryan TT, Colodner R, Raz R. Virulence genotype and phylogenetic origin in relation to antibiotic resistance profile among Escherichia coli urine sample isolates from Israeli women with acute uncomplicated cystitis. Antimicrobial Agents and Chemotherapy. 2005; 49: 26-31. | ||
In article | View Article PubMed | ||
[20] | Sabih A, Leslie SW. Complicated Urinary Tract Infections. [Updated 2022 Feb 14]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from: https://www.ncbi.nlm.nih.gov/books/NBK436013. | ||
In article | |||
[21] | Bien J, Sokolova O, Bozko P. Role of Uropathogenic Escherichia coli Virulence Factors in Development of Urinary Tract Infection and Kidney Damage. Int J Nephrol. 2012; 2012:681473. | ||
In article | View Article PubMed | ||
[22] | Broberg CA, Palacios M & Miller VL (2014). Klebsiella: a long way to go towards understanding this enigmatic jet-setter. F1000Prime Rep 6: 64. | ||
In article | View Article PubMed | ||
[23] | Cristea OM, Avrămescu CS, Bălășoiu M, Popescu FD, Popescu F & Amzoiu MO (2017). Urinary tract infection with Klebsiella pneumoniae in Patients with Chronic Kidney Disease. Curr Health Sci J 43(2): 137-148. | ||
In article | |||
[24] | Schaffer JN, Pearson MM. Proteus mirabilis and Urinary Tract Infections. Microbiol Spectr. 2015; 3(5): 10.1128/microbiolspec.UTI-0017-2013. | ||
In article | View Article PubMed | ||
[25] | O'Hara CM, Brenner FW, Miller JM. Classification, identification, and clinical significance of Proteus, Providencia, and Morganella. Clin Microbiol Rev. 2000; 13: 534-546. | ||
In article | View Article PubMed | ||
[26] | Matthews SJ, Lancaster JW. Urinary tract infections in the elderly population. Am J Geriatr Pharmacother. 2011; 9: 286-309. | ||
In article | View Article PubMed | ||
[27] | Jarvis WR, Martone WJ. Predominant pathogens in hospital infections. J Antimicrob Chemother 1992; 29:19-24. | ||
In article | View Article PubMed | ||
[28] | Matheson NR, Potempa J, Travis J. Interaction of a novel form of Pseudomonas aeruginosa alkaline protease (aeruginolysin) with interleukin-6 and interleukin-8. Biol Chem 2006; 387: 911-915. | ||
In article | View Article PubMed | ||
[29] | Yates SP, Jorgensen R, Andersen GR, Merrill AR. Stealth and mimicry by deadly bacterial toxins. Trends Biochem 2006; 31: 123-33. | ||
In article | View Article PubMed | ||
[30] | Zulianello L, Canard C, Kohler T, Caille D, Lacroix JS, Meda P. Rhamnolipids are virulence factors that promote early infiltration of primary human airway epithelia by Pseudomonas aeruginosa. Infect Immun 2006; 74: 3134-3147. | ||
In article | View Article PubMed | ||
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In article | View Article PubMed | ||
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