Research Article | Open Access

Nooralden Abdulkarem Jasim Al-Tulaibawi

Department of Clinical Laboratories Sciences, College of Pharmacy, University of Misan, Misan, Iraq.
J Pure Appl Microbiol, 2019, 13 (2): 847-853 | Article Number: 5549 | © The Author(s). 2019 

Received: 02/03/2019| Accepted: 08/04/2019 | Published: 06/05/2019

Urinary tract infections and their complications causing serious health problems especially in diabetic patients in Misan province, it is essential to determine the causative agent for appropriate treatment of this disease. One hundred and fifty urine samples were taken from adult patients with diabetes. The microbial growth appeared in 106 (70.6%) samples. Axenic culture was 83% versus 17% mixed growth. UTI prevalence was 65% with females comparing 35% of males and it was 56.6% in age group 35-49 years. Furthermore, UTIs were more incident in patients without antibiotics use and diabetic period 5-10 years (82% and 64%) respectively. Escherichia coli was identified as the most common causative agent of UTIs (52.9%), followed by Klebsiella pneumoniae and Enterococcus faecalis (9,1% and 6.6%, respectively). Streptococcus agalactiae and Klebsiella aerugenes were (4.2%, for each). Moreover, Pseudomonas aeruginosa, Klebsiella oxytoca and Staphylococcus haemolyticus were 2.48% for each. Additionally, the frequency of Proteus mirablis, Staphylococcus aureus, Streptococcus pyogenes, Serratia marcessens, Staphylococcus epidermidis and Staphylococcus warnerii was 1.65% for each, while Acinetobacter baumani and Bacillus subtilis were 0.82% for each. Most bacterial isolates had a high sensitivity to imipenem (78.8%) followed by amikacin (61.9%), but low sensitivity to ceftriaxone, tetracycline and Co-trimaxazole (36.4%, 29.7% and 26.3%, respectively) whereas, highly resistance to ampiclox and nitrofurantoin (98.3% and 87.3%, respectively). High rate of multidrug resistance observed among bacterial isolates.


UTIs; diabetes; bacteria; antibiotic susceptibility; imipenem.


Urinary tract infections (UTIs) are one of the most common infectious diseases encountered in medical practice affecting humans of all ages1. Globally, UTIs incidence was estimated about 150 million persons per year2.

Diabetes mellitus is a group of chronic metabolic disorders characterized by increased blood glucose level resulting from defects in secretion, action of insulin or both3. The chronic hyperglycemia is associated with long term damage, dysfunction and failure of different organs especially the eyes, urinary system, nerves and cardiovascular system3. Over time, diabetic patients may develop cystopathy, nephropathy and renal papillary necrosis complications that predispose them to UTIs4. Higher severity of UTI can be cause many complications, ranging from dysuria to pyelonephritis5. Moreover, diabetic patients encounter further urinary urgency and incontinence during night6. Further more, those patients frequently suffer from bacterial cystitis with higher prevalence in diabetic women including higher prevalence of both asymptomatic bacteriuria and symptomatic UTI added to recurrent complications comparing with healthy women7,8.

In diabetic and non- diabetic patients, about 80% of UTIs cases were caused by gram-negative bacteria mainly Escherichia coli, Klebsiella spp., Pseudomonas aeruginosa and Proteus spp., while only 15% were caused by gram- positive including Enterococcus spp., Staphylococcus spp. and Streptococcus spp.9-11.

Susceptibility to antibiotics is usually variable among species and strains, therefore, the resistance to different antibiotics making it difficult to treat in some infections12. The widespread and indiscriminate use of broad-spectrum antibiotics led to the emergence of multi-drug resistant bacteria13.

Briefly, this study was designed to determine the prevalence of causative microbial agents of urinary tract infections in diabetic adult patients and their susceptibility to antibiotics.


Study design
A descriptive study was conducted at the Microbiology Laboratory, Department of Clinical Laboratories Sciences, College of Pharmacy, University of Misan, Misan city, South of Iraq over the period from May to August in 2018. This study was approved by Ethical Committees of College of Pharmacy of Misan University with written consent withdrawn from all the patients.

Sample collection
One hundred and fifty midstream urine samples were obtained from 150 diabetic adult outpatients between 20-64 years old attending to the Microbiological Examinations Unit at Al-Sadar Teaching Hospital in Misan city with written consent. The urine samples were collected by sterilized disposable containers (BIOZEK, Netherlands) after necessary precautions14. Samples were brought to the laboratory within one hour. Questionnaires had completed covering the information pertaining to sex, age, period of diabetes and antibiotics used.

Urine culture
A 0.1 ml of urine sample was inoculated separately onto Blood agar (LAB, UK) and MacConkey agar (LAB, UK) plates, and incubated aerobically at 37°C for 24 h. The grown colonies were calculated colony forming unit (CFU) per ml. The plates containing more than 10 CFU/ml were selected as a significant growth, then gram stain for initial identification15. All grown colonies from primary cultures were subcultured onto Nutrient agar (LAB, UK) plates for the following confirm assays.

The confirm diagnosis for bacterial isolates was accomplished by analytical profile index (API) system (API 20E, API 20 STREP and API STAPH) add to motility, catalase, coagulase and oxidase tests described by Cheesbrough12.

Antibiotic susceptibility testing
Antimicrobial susceptibility patterns for bacterial isolates were performed by the standard disc diffusion method employing Muller-Hinton (LAB, UK) plates based on the guidelines of Clinical Laboratory Standards Institute16 using the following antibiotics disc: Amikacin (AK) 30 µg, Ampiclox (APX) 30µg, Ceftriaxone (CTR) 30 µg, Ciprofloxacin (CIP) 30µg, Co-trimoxazole (SXT) 25µg, Gentamicin (CN) 10µg, Imipenem (IMP) 10 µg, Nitrofurantoin (F) 300µg, Tetracycline (TE) 30µg (Titan, Biotech., India ) and Cefexime (CFX ) 5µg (Oxoid, UK). The inhibition zones of bacterial isolates for antibiotics were measured in mm by applying ordinary ruler.

Statistical analysis
Statistical analysis was achieved with the Chi-square test by Statistical Package for Social Sciences (SPSS) version 18. P-value less than 0.05 was considered as statistically significant and P-value less than 0.01 considered as highly significant.


Growth and Gram’s staining
Out of 150 urine samples examined in this study, only 106 (70.6%) samples yielded growth with a significant difference (P ≤ 0.01). Axenic culture was appeared in 88 (83%) samples than mixed growth at P ≤ 0.01, as in Table 1. Gram-negative bacteria were 85 (70.2%), while Gram-positive were 36 (29.8%) at P ≤ 0.01 as in Table 2.

Table (1):
Growth of uropathogens isolated from urine samples in adult diabetic Patients

Microbial Culture Number  (%)
Axenic Growth 88(83)*
Mixed Growth 18(17)
Total growth 106 (70.6)
No growth 44(29.4)
Total samples 150(100)

*: P ≤ 0.01.

Table (2):
Gram-staining of microbial isolates from urinesamples in adult diabetic patients

Gram’s Staining
Number (%)
Gram- Positive
Gram- Negative
Total isolates

*: P ≤ 0.01.

Prevalence of UTIs in diabetic patients according to some factors
A total of 150 urine samples enrolled in this study, 84(56%) were of females and 66(44%) were of males. Out of 106 positive cultures, the prevalence of UTIs was high in females 69 (65%) than males with a significant difference at P ≤ 0.01. Furthermore, UTIs were more incidence in patients without antibiotics use and period of diabetes 5-10 years (82% and 64%, respectively), while it was 56.6% in age group 35-49 years without signification, as in Table 3.

Table (3):
Prevalence of UTIs in diabetic patients according to some factors



Sex n(%) Age Group (year)

n (%)

Diabetes period (year) n(%) Antibiotics use n(%)
106 (100) Male Female 20-34 35-49 50-64 < 5 5-10 > 10 Yes No
37(35) 69(65)** 15(14.2) 60(56.6) 31(29.2 25(23.6) 68(64.1)** 13(12.3) 19(16) 87(82)**

*n: Number of the patients with positive culture  **: P ≤ 0.01.

A total of 121 microbial isolates were obtained, Escherichia coli was the most common causative agent of UTIs with 64 isolates, followed by Klebsiella pneumonia, and Enterococcus faecalis (11 and 8, respectively). Streptococcus agalactiae and Klebsiella aerugenes were 5 for each. Moreover, Klebsiella oxytoca, Pseudomonas aeruginosa, Staphylococcus haemolyticus and Candida albicans were 3 for each. Nevertheless, the frequency of Proteus mirablis, Staphylococcus aureus, Streptococcus pyogenes, Serratia marcessens, Staphylococcus epidermidis and Staphylococcus warnerri was 2 for each, while Acinetobacter baumani and Bacillus subtilis were 1 for each.

Antimicrobial susceptibility pattern
Antibiotic susceptibility test for urinary bacterial isolates118 showed highly sensitive to imipenem (78.8%) with significance differences at P ≤ 0.01, and Amikacin (61.9%) at P£0.05. Furthermore, they were 56.5%, 50% and 44.9% for cefexime, ciprofloxacin and gentamicin respectively, but without signification. Moreover, they were low sensitivity to ceftriaxone, tetracycline and Co-trimaxazole (36.9%, 29.7% and 26.3%, respectively). On the other hand, they were a highly resistance to ampiclox and nitrofurantoin (98.3% and 87.3%, respectively) at P ≤ 0.01, as in Table 4. E. coli (64) appeared sensitive to imipenem and amikacin (89% and 76.6%, respectively) at P£ 0.01. K. pneumoniae11 was sensitive to amikacin (72.7%) at P ≤ 0.01, followed by imipenem, cefexime and ciprofloxacin (54.5%, for each), but without signification. K. aerugenes5 was sensitive to imipenem (80%) at P ≤ 0.01, while it was 60% for amikacin, ciprofloxacin, gentamicin and ceftrixone at P£0.05. S. agalactiae5 was sensitive to imipenem (100%), amikacin and ciprofloxacin (80%, for each) at P ≤ 0.01, followed by cefixime, gentamicin and tetracycline (60%, for each) at P£0.05. K. oxytoca3 was sensitive to imipenem, amikacin, cefexime, and ceftriaxone (66.7% for each) at P ≤ 0.01. S. haemolyticus3 was sensitive to imipenem (100%), cefixime and ciprofloxacin (66.7%, for each) at P£ 0.01. S.pyogenes and S. warnerii (2, for each) were sensitive to imipenem and cefexime (100%, for each). Serratia marssecens2 was sensitive to cefexime and ciprofloxacin (100%, for each). S. epidermidis2 was sensitive to imipenem (100%). Finally, B. subtilis1 was sensitive to imipenem, amikacin, cefexime, ciprofloxacin, gentamicin, ceftriaxone and tetracycline (100%, for each). While A. baumanii1 was 100% sensitive for imipenem and amikacin.

Table (4):
Antibiotic sensitivity profile of bacterial species isolated from adult diabetic patients with UTI

Antibiotic sensitivity n(%) *n Bacterial species
0(0) 9(14) 25(39) 21(32.8) 27(42.2) 34(53.1) 37(57.8) 35(54.7) 49(76.6) 57(89) 64 Escherichia coli
0(0) 3(27.2) 3(27.2) 2(18.2) 4(36.3) 6(54.5) 3(27.2) 6(54.5) 8(72.7) 6(54.5) 11 Klebsiella pneumoniae
0(0) 0(0) 0(0) 2(25) 3(37.5) 3(37.5) 2(25) 3(37.5) 3(37.5) 4(50) 8 Enterococcus faecalis
0(0) 1(20) 1(20) 2(40) 3(60) 3(60) 3(60) 3(60) 3(60) 4(80) 5 Klebsiella aerugenes
2(40) 0(0) 1(20) 3(60) 2(40) 4(80) 3(60) 3(60) 4(80) 5(100) 5 Streptococcus agalactiae
0(0) 0(0) 0(0) 1(33.3) 2(66.7) 1(33.3) 1(33.3) 2(66.7) 2(66.7) 2(66.7) 3 Klebsiella


0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 1(33.3) 0(0) 1(33.3) 3 Pseudomonas aeruginosa
0(0) 0(0) 0(0) 0(0) 0(0) 2(66.7) 1(33.3) 2(66.7) 1(33.3) 3(100) 3 Staphylococcus haemolyticus
0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 1(50) 0(0) 1(50) 2 Proteus mirablis
0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 1(50) 0(0) 1(50) 2 Staphylococcus aureus
0(0) 0(0) 0(0) 0(0) 0(0) 1(50) 1(50) 2(100 0(0) 2(100) 2 Streptococcus pyogenes
0(0) 0(0) 0(0) 1(50) 0(0) 1(50) 0(0) 1(50) 0(0) 2(100) 2 Staphylococcus epidermidis
0(0) 1(50) 0(0) 1(50) 0(0) 1(50) 0(0) 2(100) 0(0) 2(100) 2 Staphylococcus warnerii
0(0) 1(50) 1(50) 1(50) 1(50) 2(100) 1(50) 2(100) 1(50) 1(50) 2 Serratia


0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 0(0) 1(100) 1(100) 1 Acinetobacterbaumanii
0(0) 0(0) 0(0) 1(100) 1(100) 1(100) 1(100) 1(100) 1(100) 1(100) 1 Bacillus subtilis
2(1.7) 15(12.7) 31(26.3) 35(29.7) 43(36.4) 59(50) 53(44.9) 65(56.5) 73(61.9)*** 93(78.8)** 118 Total

*n: Number of isolates, **:P ≤ 0.01, ***:P ≤ 0.05.
IMP: Imipenem, AK: Amikacin, CFX: Cefixime, CN: Gentamicin, CIP: Ciprofloxacin, CTR: Ceftriaxone, TE: Tetracycline, SXT: Co-trimoxazole, F: Nitrofurantoin, APX: Ampiclox


The present study showed that axenic culture was 83% versus to mixed growth, this result in agreement with Abd Al Abbas and Jasim17 founding 82% of samples gave axenic growth. Axenic refer to pure colonies from the primary culture, as in Table 1. Furthermore, this study showed that a large proportion of uropathogens were gram-negative comparing to gram-positive isolates as in Table 2. This result is consistent with previous studies10,18,19.

Table (3) shows the prevalence of UTI according to some factors. The results revealed a high prevalence of UTI in females (65%), in agreement with other previously reported studies9-11,19. Females are more prone to have UTI than males because the urethra is shorter and closer to the anus adding to a sexual intercourse20. Nevertheless, this study showed that the occurrence of UTI in diabetes was more frequently in the age group (35-49 years), followed by the age group(50-64 years) in agreement with study done by Adeyeba et al.21. Generally, engagement in sexual activity and increasing age of diabetics make them vulnerable to urinary tract infection22. Moreover, UTI occurrence was more frequent in patients without antibiotics use and diabetic period (5-10 years). Indiscriminate and uncontrolled use of antibiotics for long period with chronic glucosuria encouraging the microbial growth and thereby increase the risk of UTIs23,24.

The present study showed that E. coli was the most common bacteria with 64 isolates (52.9%), followed by Klebsiella spp. 19(15.7%) isolates then E. faecalis 8(6.6%) isolates and S. agalactiae 5(4.1%) isolates. Several studies reported that E. coli and Klebsiella spp. were the most frequent uropathogens in diabetic patients, while the other species were different10,18,19,25. Relatively, UTIs occur when gastro-intestinal bacteria can be entering to the urethra and then colonization, once these bacteria gain access to the urinary bladder they may multiply and transmitting up through ureters to kidneys14. E. coli is normally habitat in the intestinal tract, it is most predominant bacterium causing UTI in both diabetic and non- diabetic patients11,25,26. E. coli have numerous virulence factors which enable to colonize the urethra such as P-fimbria to bind the epithelium, other factors contribute in its pathogenicity like a and b-hemolysins, colicins and cytotoxic necrotizing factor27. Klebsiella spp. are opportunistic pathogens and they are the etiological agents for urinary tract infection in both community- acquired and hospital- acquired infections. Capsule production, siderophore activity and biofilm formation are an important virulence factors in pathogenesis of Klebsiella28. Enterococcus faecalis is also opportunistic bacterium and it’s the causative agent for UTI in the general population26. This bacterium has many virulence factors playing an important role in its pathogenicity such as aggregation substance, Enterococal surface protein and hemolysins29. On the other hand, S. agalactiae has been isolated from patient with poorly glucosuria10. Although, the bacterium form a part of urogenital flora, but became opportunistic, particularly in patient with poor immunity.

Table (4) showed that the uropathogenic bacteria were highly sensitive to imipenem (78.8%), followed by Amikacin (61.9%). These results are consistent with other previous studies18,19,25. In contrast, all bacterial species appeared a complete resistance to ampiclox (100%) with the exception of S. agalactiae (60%). This is due to the acquisition of mec A gene by plasmid transferring30,31. On the other hand, many bacterial species appeared resistant to three or more antibiotics which may be due to plasmid carrying drug resistant genes, a biofilm formation inside the urinary bladder increases the chance of multi-drug resistance bacteria to colonize the urinary tract and thus to infection32,33. Furthermore, MDR efflux – system contributes to the emergence of multi- drug resistance strains, especially in gram – negative bacteria34,35. Additionally, the exposure of bacterial pathogens to high concentration of antibiotics for long times creates severe selection pressure leading to emergence of resistance36.


The prevalence of UTIs was higher in females comparing of males, and the age group (35-49) years in adult diabetic patients. Escherichia coli was identified as the most common causative agent of UTIs in diabetes in Misan province. Although, the high rate of multi – drug resistance among bacterial isolates, but imipenem is a very effective antibiotic.




Data Availability
All datasets generated or analyzed during this study are included in the manuscript.

Ethics Statement
This article does not contain any studies with human participants or animals performed by any of the authors.

Conflict of Interest

The authors declare that there is no conflicts of interest.

  1. Kunin C.M. Chemoprophylaxis and suppressive therapy in the management of urinary tract infections. J. Antimicrob. Chemoth.,1994; 33(suppl-A): 51-62.
  2. Gupta K., Sahm D.F. Mayfield D. & Stamm W.E. Antimicrobial resistance among uropathogens that cause community-acquired urinary tract infections in women: A nationwide analysis. Clin. infect.dis.,2001; 33(1): 89-94.
  3. American Diabetes Association: Diagnosis and classification of diabetes Mellitus. Diabetes Care2014; 38: S81-S90.
  4. Nitzan O., Elias M., Chazan B. & Saliba W. Urinary tract infections in patients with type 2 diabetes mellitus: Review of prevalence, diagnosis, and management. Diab., metabol. synd. and obesit.: targets and therap., 2015; 8: 129-136.
  5. Saleem M. and Daniel B. Prevalence of Urinary Tract Infection among Patients with Diabetes in Bangalore City. Int. J. Emerg. Sci 2011; 2(1): 133-142.
  6. Bonadio M, Costarelli S, Morelli G & Tartaglia T. The influence of diabetes mellitus on the spectrum of uropathogens and the antimicrobial resistance in elderly adult patients with urinary tract infection. BMC infec. dis., 2006; 6(54): 1-7.
  7. Geerlings S.E., Stolk R.P., Camps M.J., Netten P.M., Collet T.J., Hoepelman A.I. & Group, D.W. B. U. S. Risk factors for symptomatic urinary tract infection in women with diabetes. Diabetes Care, 2000; 12(23): 1737-1741.
  8. Geerlings S.E., Stolk R.P., Camps M.J., Netten P.M., Hoekstra J.B., Bouter K.P., et al.. Asymptomatic bacteriuria may be considered a complication in women with diabetes. Diabetes mellitus women asymptomatic bacteriuria utrecht study group. Diabetes care, 2000; 6(23): 744-749.
  9. Rangari A.A. , Sharma S., Tyagi N., Singh P., Singh G. & Thakur R. Antibiotic susceptibility pattern of bacterial uropathogens isolated from patients at a tertiary care hospital in western uttar pradesh of india. J. Curr. Microbiol. Appl. Sci, 2015; 10(4): 646-657.
  10. Tektook N.K., Al-Lehibi K.I. & Al-Husseinei R.K. Prevalence some pathogenic bacteria causing uti in diabetic patients in/specialized center for endocrinology and diabetes of baghdad city–iraq. Med. J. Babylon, 2017; 14(2): 260-266.
  11. Alhamdany M.H.A. 2018. Antibiotic susceptibility of bacteria isolated from patients with diabetes mellitus and recurrent urinary tract infections in babylon province, iraq. Med. J. Babyl., 2018; 15(1):63-68.
  12. Cheesbrough M. District Laboratory Practice in Tropical Countries ; p.434. 2ndEd. Cambridge University Press, 2006.
  13. Weber J.T. & Courvalin P. An emptying quiver: Antimicrobial drugs and resistance. Emerg. Infect. Dis., 2005; 11(6): 791-793.
  14. Tille P.M. Bailey and Scott’s: Diagnostic Microbiology, p 1001. 13thEd. Mosby Inc., an affiliate of Elsevier Inc., 2014.
  15. Sham D, Weissfeld A & Forbes B. Bailey & Scott’s diagnostic microbiology. pp60-80.12th Ed. Mosby Inc., an affiliate of Elsevier Inc, 2014.
  16. CLSI editor. Clinical and Laboratory Standards Insitute. Performance Standards for Anti-microbial Susceptebility Testing; 2012: Twenty-second Informational Supplement M100-S22. Wayne, PA, USA.
  17. Abd Al-Abbas M.J. and Jasim N.A. Molecular study of urinary tract infection bacteria and their relationship to the present of Oxalobacter-formigenes in stool of kidney stone patients.Am. Sci. Res. J. Engine. Tech. Sci. 2016; 1(26): 230-249.
  18. Yadav K & Prakash S. Antimicrobial resistance pattern of uropathogens causing urinary tract infection (uti) among diabetics. Biomed. Res. Intern., 2016; 1: 07-15.
  19. Almazini M. Incidence and sensitivity of bacterial uropathogens among diabetic patients. Eur. J. Exper. Biol.,2016; 6(3): 8-12.
  20. Kunin C.M. Urinary tract infections in females. Clin. Infect. Dis. 1994; 1(18): 1-12.
  21. Adeyeba O.A., Adesiji Y.O., Omosigho P.O. Bacterial Urinary Tract Infections in Patients with Diabetes Mellitus Int. Trop. J. Med. 2007; 3(2): 89-92.
  22. Kumar Jha P., Baral, R. & Khanal B. Prevalence of uropathogens in diabetic patients and their susceptibility pattern at a tertiary care center in nepal-a retrospective study. Int. J. Bio. Lab. Sci., 2014; 3(2): 29-34.
  23. F nfst ck R., Nicolle L.E., Hanefeld M. & Naber K.G. Urinary tract infection in patients with diabetes mellitus. Clin. nephro., 2012; 77(1): 40-48.
  24. Wang M.C., Tseng C.C., Wu A.B., Lin W.H., Teng C.H., Yan J. & Wu J.J. Bacterial characteristics and glycemic control in diabetic patients with escherichia coli urinary tract infection. J. Microbiol., Immuno.Infect., 2013; 46(1): 24-29.
  25. Rashmi B. & Venkatesha D. Antibiogram of urinary pathogens in patients with diabetes mellitus-experience from a tertiary care hospital. Int. J. Curr. Microbiol. App. Sci, 2017; 6: 4830-4837.
  26. Acharya D., Bogati B., Shrestha G. & Gyawali P. Diabetes mellitus and urinary tract infection: Spectrum of uropathogens and their antibiotic sensitivity. J. Manmohan Memorial Inst. of Health Sci., 2015; 1(4): 24-28.
  27. Kausar Y., Chunchanur S.K., Nadagir S.D., Halesh L. & Chandrasekhar M. Virulence factors, serotypes and antimicrobial suspectibility pattern of Escherichia coli in urinary tract infections. Al Ameen. J. Med. Sci., 2009; 2(1): 47-51.
  28. Clegg S. & Murphy C.N. Epidemiology and virulence of klebsiella pneumoniae. Microbio. spect., 2016; 4(1): 1-17.
  29. Upadhyaya P.G., Ravikumar K. & Umapathy B. Review of virulence factors of Enterococcus: An emerging nosocomial pathogen. Indian j. med. microbiol., 2009; 27(4): 301.
  30. Ito T., Katayama Y., Asada K., Mori N., Tsutsumimoto K., Tiensasitorn C. & Hiramatsu K. Structural comparison of three types of staphylococcal cassette chromosome mec integrated in the chromosome in methicillin-resistant staphylococcus aureus. Antimicrob. agents and chemo., 2001; 45(5): 1323-1336.
  31. Abd Al-Abbas M.J. Antimicrobial susceptibility of enterococcus faecalis and a novel plano-microbium isolate of bacterimia. Int. J.Med. and Med. Sci., 2012; 4(2): 19-27.
  32. Stamm W.E. Urinary tract infections, pyelonephritis, and prostatitis. Harrison’s Principles of In. Med. 17th ed New York, NY: McGraw-Hill, 2008; 1820-1827.
  33. Shalini J.M., Rashid M. & Joshi H. Study of antibiotic sensitivity pattern in urinary tract infection at a tertiary hospital. NJIRM, 2011; 2(3): 43-46.
  34. Sulavik M.C., Houseweart C., Cramer C., Jiwani N, Murgolo N., Greene J, et al.. Antibiotic susceptibility profiles ofEscherichia coli strains lacking multidrug efflux pump genes. Antimicrob. agents and chemother., 2001; 45(4): 1126-1136.
  35. Hirsch E.B. & Tam V.H. Impact of multidrug-resistant Pseudomonas aeruginosa infection on patient outcomes. Expert rev. pharma.& outcomes res., 2010; 10(4): 441-451.
  36. Brisson-Noel A., Arthur M. & Courvalin P. Evidence for natural gene transfer from gram-positive cocci to Escherichia coli. J. bacterio., 1988; 170(4): 1739-1745.

Article Metrics

Article View: 2817

Share This Article

© The Author(s) 2019. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.