Research Article Volume 6 Issue 2
1Department of Medical Laboratory Science, Bayero University Kano, Nigeria
2Biology Programme, Abubakar Tafawa Balewa University, Nigeria
Correspondence: Hamza Sule, Department of Medical Laboratory Science, Bayero University Kano, Nigeria, Tel 2348036062021
Received: March 01, 2018 | Published: April 17, 2018
Citation: Sule H, Uba A, Kumurya AS. Antibiotic susceptibility pattern of uropathogens from some selected hospitals in Kano-Nigeria. J Microbiol Exp. 2018;6(2):127-134. DOI: 10.15406/jmen.2018.06.00202
Urinary tract infection (UTI), is a common disease of public health concern that warrants frequent hospital visit by the affected patients worldwide, leading to increased health care expenditure across the globe. Knowledge of the sensitivity or otherwise of its associated pathogens to the commonly used drugs, is of paramount importance. The study was to isolate the common Urinary Tract Pathogens and to determine their pattern of susceptibility to the commonly used anti microbial agents. The study involved 300 urine samples of UTI suspects, of which 114(38%) were positive with different types of uropathogens isolated. The isolated agents were E. coli, Klebsiella puemoniae, Staphylococcus saprophyticus, Staphylococcus aueus, Proteus mirabilis, and Pseudomonas. Various patterns of susceptibilities were observed when interacted with the commonly used antimicrobial agents, Aµgumentin (30µg), Nitrofurontoin (200µg), Amoxycillin (25µg),Tetracyclin (25µg), Gentamycin (10µg), Ofloxacin (5µg), Cotrimoxazole (25µg) and Nalidixic acid (30µg). It was generally observed that ofloxacin and gentamycin were more effective while cotrimoxazole and amoxycilin were the most resisted in vitro, during the study. It is therefore, important to monitor UTI, associated pathogens and their pattern of susceptibility to different antimicrobial agents for better management of cases.
Keywords: urinary tract, susceptibility, antimicrobial agents, uropathogens
Urinary Tract Infection (UTI) is a general term refers to infection/inflammation of any part of the urinary tract caused by microorganisms including bacteria. UTI is one of the most common bacterial infections encountered by clinicians worldwide.1 Moreover, since reporting of antibiotic susceptibility results in suspected cases of UTI, takes at least 48 hours following sampling, conditions are sometimes treated empirically, based on available clinical data, this sometimes leads to antibiotic resistance.2 Among the most common infectious diseases, urinary tract infections are ranked higher by clinicians in developing countries with an estimated annual global incidence of at least 250 million.3,4 Treatment of UTIs cases, is often started empirically and therapy is based on information determined from the previous antimicrobial susceptibility pattern of the urinary pathogens.5 However, a large proportion of uncontrolled antibiotic usage has contributed to the emergence of resistant bacterial infections.6–9 It is known that, the prevalence of antimicrobial resistance among urinary pathogens has been increasing worldwide. Associated resistance (the fact that a bacterium resistant to one antibiotic is often much more likely to be resistant to another) drastically decreases our chances of getting a second empirical attempt right.10
It was found that, one survey results performed in the USA estimated that a UTI episode was associated with an average of 6.1 days with symptoms, 2.4 days of reduced activity and 0.4 days of bed rest, thus generating an estimated annual cost (direct and indirect) of 1.6 billion dollars.11–13 In China, UTIs account for 9.39–50% of nosocomial infections.9 10 Most cases of UTI are caused by Gram-negative bacilli, with Escherichia coli sometimes accounting for over 90% of uncomplicated UTIs.14 Urinary Tract Infection (UTI) has become the most common hospital-acquired infection, accounting for as many as 35 % of nosocomial infections, and it is the second most common cause of bacteraemia in hospitalized patients.15 It accounts for a significant proportion of the work load in clinical microbiology laboratories and enteric bacteria remained the most frequent cause, although the distribution of causative pathogens is changing by locality and by intrinsic and extrinsic factors.15
In pregnancy, cases often begins in week 6 and peaks during weeks 22 to 24 of the pregnancy, and this is due to a number of factors including urethral dilatation, increased bladder volume and decreased bladder tone, along with decreased urethral tone which contributes to increased urinary stasis and ureterovesical reflux, in which up to 70 % of pregnant women develop glycosuria, and this encourages bacterial growth in the urine.16 The objective of the study was to isolate common bacteria responsible for UTI and to determine their susceptibility pattern to commonly used antimicrobial agents in Kano, Nigeria.
Study area and population
Three hundred (300) patients were enrolled in the study, in the three selected hospitals, in Kano metropolis: Murtala Mohammad Specialist Hospital Kano, located at the city center along Sabon titi; Infectious Disease Hospital Kano, located along France Road leading to Katsina Road. And Sir Mohammad Sunusi Hospital Kano, located along Hadejia Road leading to Jigawa State. Most are also traders and some civil servants by occupation. Geographically, Kano metropolis is located within latitude 12oN and 13oN and longitude 8oE and 9oE.
Specimen collection
Universal bottles were used for the collection of the appropriate urine samples for the study. The enrolled patients were educated on the type of urine they should provide (i.e. clean catch midstream urine). The first passed urine may usually contain contaminants, this signifies the reason for the use of mid stream urine. All samples collected were processed immediately. But where delay was anticipated, samples were refrigerated at 8oC before processing.
Specimen processing
Immediately samples were collected, macroscopic examination was carried out for observable features as, colour, turbidity and blood tinge as the case may be. The uncentrifuged urine samples were mixed by rotating the container before inoculating on to Cystein Lactose Electrolyte Deficient Agar (CLED) and Blood Agar by streak method and later incubated at 37oC for 24 hours.17 Media used were from Titan Biotech Ltd, Delhi, India while blood agar was made from to 25 ml of sterile sheep blood to 500 ml nutrient agar according to Cheesbrough.17
Isolation of the uropathogens
Positive plates after 24 hours incubation were subcultured on to MacConkey agar plate to obtain discrete colonies for further characterization and identification.
Identification of the isolates
The discrete colonies obtained on purity plates were used for the identification of the isolates using standard methods and Identification was based on colonial morphology and biochemical characteristics. Colonies produced after 24 hours (on purity plate) were examined for morphological features.18
Characterization of the isolates
In addition to morphological features of the colonies obtained on the purity plates; motility, Gram staining reaction, and biochemical tests were used in characterizing the isolates according to Cheesebrough,17 as follows.
Gram’s staining technique
Discrete colonies were used for the technique as follows:
Results
Dark Purple reaction was considered as gram positive. Pale-dark red reaction was considered as gram negative.
Catalase test
Two ml of 3% hydrogen peroxide solution was pipetted in to three test tubes (for test, positive and negative controls). A sterile wooden stick was used to remove several colonies of the test organisms and immersed into the test tube while a known staphylococcus and streptococcus spp. were immersed into positive and negative controls tubes respectively.
Results
Bubble production in the test and positive control indicated a positive result.
Coagulase test (slide method) for bound coagulase
Tube method (for free coagulase)
Results
Clots or fibrin dots in test and positive control tubes and none in sterile broth tube signified positive test.
Indole test
An overnight broth culture was used for the test of indole production using kovac’s reagent. A clean sterilized test tube was used to transfer the overnight broth culture and about 0.5 ml of kovac’s reagent was added and shacked gently. Results were read immediately. A known E. coli and klebsiella spp. were used as positive and negative controls.
Results
A red ring on top of the test and positive control tubes and absent in the negative control tube, indicated a positive test.
Oxidase test
A clean piece of filter paper was placed in a clean petridish. Three drops of a freshly prepared oxidase reagent was applied. Using a clean wooden stick, colonies of the test organisms were removed and smeared on to the filter paper. Results were read within 10 seconds Pseudomonas and E. coli were used as positive and negative controls.
Results
Blue-purple colour indicated positive test while no blue-purple colour indicated negative test.
Citrate utelization test
The test organisms were streaked on to slope and stab inoculated into the simon’s citrate agar and incubated at 37oC for 24 hours with the cap loosen. Known Klebsiella and Salmonella spp. were used as positive and negative controls respectively.
Results
Bright blue medium after incubation, positive while no change in medium colour showed a negative test.
Urease test
The test organisms were streaked on to urea slope and stab inoculated into the urea agar and incubated at 37°C for 24 hours with the cap loosen. Known proteus and E. coli spp. were used as positive and negative controls respectively.
Results
Change of medium colour to pink was a positive test while if no colour change was a negative test.
Suger test
Kligler iron agar (KIA) were streaked with the test organisms (on the slope) and stab inoculated into the media and incubated at 37oC and results read after 24 hours.
Results
A yellow butt and slope indicated fermentation of both glucose and lactose. A characteristic of both E. coli and Klebsiella pneumonia which were differentiated with motility and indole tests.
Motility test (by hanging drop method)
In each test, using paraffin wax, a ring was made at the center of cover slip. A drop of the overnight broth culture was placed at the center of the ring. A clean grease-free slide was placed on the ring and quickly but gently inverted with the cover slip upper most. The slide was examined using 10x and 40x objective. E. coli and klebsiella species were used as positive and negative controls respectively.
Determination of antimicrobial susceptibility pattern of the bacterial isolates
The susceptibility pattern of the isolates to commonly used antimicrobial agents was determined using National Committee for Clinical Laboratory Standard (NCCLS) modified Kirby–Bauer disc diffusion method, (NCCLS, 2000). Discs of known concentration of antimicrobials, gentamycin 10µg, nitrofurantoin 200µg, nalidixic acid 30µg, tetracycline 25µg, aµgumentin 30µg, cotrimoxazole 25µg, amoxicillin 25µg, and ofloxacin 5µg were placed on plates of Muller Hinton Agar uniformly inoculated with the test organisms. Zone of inhibition around each antibiotic disc was measured using millimeter ruler (Figure 1).18
The data obtained were analyzed using statistical package for social sciences SPSS version 20
Of the total samples analyzed in the study (300), one hundred and fourteen (114), representing (38%) were positive for culture. Different species of uropathogens were isolated with E. coli, as the most prevalent, 58(50.9%), followed by Klebsiella pnuemoniae 27(23.7%), Staphylococcus saprophyticus 11(9.6), Staphylococcus aureus 8(7.0), Proteus mirabilis 8(7.0%), and Pseudomonas aerµginosa having the least frequency of occurrence 2(1.8%) as seen Table 1.
Species isolated |
Frequency of occurrence Percentage (%) |
||||
Escherichia coli |
58 |
50.9 |
|||
Klebsiella pneumoniae |
27 |
23.7 |
|||
Staphylococcus aureus |
8 |
7 |
|||
Staphylococcus saprophyticus |
11 |
9.6 |
|||
Proteus mirabilis |
8 |
7 |
|||
Pseudmonas aeruginosa |
2 |
1.8 |
|||
Total |
114 |
100 |
Table 1 Bacterial isolates obtained from the urine samples 100
The susceptibility pattern of the uropathogens with respect to the used antimicrobial agents has been variable (Table 2). Among the species isolated, E. coli had high sensitivity to ofloxacin (55.1%) and higher resistance to cotrimoxazole (93.1%), (Table 3). Klebsiella peumoniae, was found to be highly sensitive to ofloxacin (77.8%) while mostly resisted cortrimoxazole (81.5%) as seen in Table 4.For Staphylococcus aureus, ofloxacin and gentamicin were found to be the most effective agents with (12.5%) and (25%) resisted respectively (Table 5). Ofloxacin was found sensitive, moderately sensitive and resistant, (63.6%), (27.3%) and (09.1%) to S. saprophyticus isolates respectively (Table 6). Proteus mirabilis on the other hand, exhibited moderate sensitivity to augumentin, amoxycillin and cotrimoxazole with 2(25.0%) 3(37.5%) 1(12.5%) respectively (Table 7). The isolates of Pseudomonas aerµginosa appeared either resistant or moderately sensitive to all the antimicrobials used, (Table 8). The overall susceptibility of the isolates revealed that ofloxacin had the highest in vitro activity against most of the isolates while the second most effective under the same condition was gentamicin. Resistance was mostly observed in cotrimoxazole and amoxycillin.
Aug(%) Nit(%) Amox(%) Tet(%) Gen(%) Oflox(%) Cot(%) Nal(%) |
Uropth E. coli 7(12.1) 25(43.1) 17(29.3) 28(48.3) 32(55.2) 47(81.0) 4(6.9) 19(32.8) |
Kleb. pneu 9(33.3) 12(44.4) 9(33.3) 11(40.7) 15(55.5) 21(77.7) 5(18.5) 10(37.0) |
S. aureus 4(50.0) 5(62.5) 3(37.5) 5(62.5) 6(75.0) 7(87.5) 2(25.0) 4(50.5) |
S. saproph. 7(63.6) 8(72.7) 7(63.6) 7(63.6) 9(81.8) 10(90.9) 5(45.5) 5(45.5) |
P. mirabilis 2(25.0) 4(50.0) 3(37.5) 4(50.0) 5(62.5) 6(75.0) 1(12.5) 4(50.0) |
P. aeruginosa 0(00.0) 1(50.0) 0(00.0) 0(00.0) 1(50.0) 2(100.0) 0(00.0) 0(00.0) |
Table 2 Antibiotic susceptibility pattern of the uropathogens in Kano, Nigeria
Antimicrobials |
Sensitive |
Intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
- |
7(12.1) |
51(87.9) |
58(100) |
Nitrofurontoin (200µg) |
8(13.8) |
17(29.3) |
33(56.9) |
58(100) |
Amoxycillin (25µg) |
2(3.4) |
15(25.9) |
41(70.7) |
58(100) |
Tetracyclin (25µg) |
7(12.1) |
21(36.2) |
30(51.7) |
58(100) |
Gentamicin (10µg) |
10(17.2) |
22(38.0) |
26(44.8) |
58(100) |
Ofloxacin (5µg) |
32(55.1) |
15(25.9) |
11(19.0) |
58(100) |
Cotrimoxazole (25µg) |
- |
4(6.9) |
54(93.1) |
58(100) |
Nalidixic acid (30µg) |
4(6.9) |
15(25.9) |
39(67.2) |
58(100) |
Table 3 Antibiotic susceptibility pattern of the Uropathogenic Eschericia coli isolated N=(58)
Antimicrobials |
Sensitive |
Intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
3(11.1) |
6(22.2) |
6(22.2) |
27(100) |
Nitrofurontoin (200µg) |
3(11.1) |
9(33.3) |
15(55.6) |
27(100) |
Amoxycillin (25µg) |
- |
9(33.3) |
18(66.7) |
27(100) |
Tetracyclin (25µg) |
3(11.1) |
8(29.6) |
16(59.3) |
27(100) |
Gentamicin (10µg) |
7(26.0) |
8(29.6) |
12(44.4) |
27(100) |
Ofloxacin (5µg) |
15(55.6) |
6(22.2) |
6(22.2) |
27(100) |
Cotrimoxazole (25µg) |
- |
5(18.5) |
22(81.5) |
27(100) |
Nalidixic acid (30µg) |
4(14.8) |
6(22.2) |
17(63.0) |
27(100) |
Table 4 Antibiotic susceptibility pattern of the Klebsiella pneumoniae isolated N=(27)
Antimicrobials |
Sensitive |
intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
2(25.0) |
2(25.0) |
4(50.0) |
8(100) |
Nitrofurontoin (200µg) |
1(12.5) |
4(50.0) |
3(37.5) |
8(100) |
Amoxycillin (25µg) |
1(12.5) |
2(25.0) |
5(62.5) |
8(100) |
Tetracyclin (25µg) |
2(25.0) |
3(37.5) |
3(37.5) |
8(100) |
Gentamicin (10µg) |
4(50.0) |
2(25.0) |
2(25.0) |
8(100) |
Ofloxacin (5µg) |
5(62.5) |
2(25.0) |
1(12.5) |
8(100) |
Cotrimoxazole (25µg) |
- |
2(25.0) |
6(75.0) |
8(100) |
Nalidixic acid (30µg) |
- |
4(50.0) |
4(50.0) |
8(100) |
Table 5 Antibiotic susceptibility pattern of the staphylococcus aureus isolated (N=8)
Antimicrobials |
Sensitive |
intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
2(18.2) |
5(45.4) |
5(45.4) |
11(100) |
Nitrofurontoin (200µg) |
2(18.5) |
6(54.5) |
3(27.3) |
11(100) |
Amoxycillin (25µg) |
3(27.2) |
4(36.4) |
4(36.4) |
11(100) |
Tetracyclin (25µg) |
4(36.4) |
3(27.2) |
4(36.4) |
11(100) |
Gentamicin (10µg) |
5(45.4) |
4(36.4) |
2(18.0) |
11(100) |
Ofloxacin (5µg) |
7(63.6) |
3(27.3) |
1(09.1) |
11(100) |
Cotrimoxazole (25µg) |
- |
5(45.5) |
6(54.5) |
11(100) |
Nalidixic acid (30µg) |
1(9.1) |
4(36.4) |
6(54.5) |
11(100) |
Table 6 Antibiotic susceptibility pattern of the S. saprophyticus isolaled (N=11)
Antimicrobials |
Sensitive |
intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
- |
2(25.0) |
6(75.0) |
8(100) |
Nitrofurontoin (200µg) |
1(12.5) |
3(37.5) |
4(50.0) |
8(100) |
Amoxycillin (25µg) |
- |
3(37.5) |
5(62.5) |
8(100) |
Tetracyclin (25µg) |
2(25.0) |
2(25.0) |
4(50.0) |
8(100) |
Gentamicin (10µg) |
3(37.5) |
2(25.0) |
3(37.5) |
8(100) |
Ofloxacin (5µg) |
4(50.0) |
2(25.0) |
2(25.0) |
8(100) |
Cotrimoxazole (25µg) |
- |
1(12.5) |
7(87.5) |
8(100) |
Nalidixic acid (30µg) |
1(12.5) |
3(37.5) |
4(50.0) |
8(100) |
Table 7 Antibiotic susceptibility pattern of the Proteus mirabilis isolated N= (8)
Antimicrobials |
Sensitive |
Intermediate |
Resistance |
N (%) |
Augumentin (30µg) |
- |
2(25.0) |
2(100) |
2(100) |
Nitrofurontoin (200µg) |
- |
1(50.0) |
1(50.0) |
2(100) |
Amoxycillin (25µg) |
- |
- |
2(100) |
2(100) |
Tetracyclin (25µg) |
- |
- |
2(100) |
2(100) |
Gentamicin (10µg) |
- |
1(50.0) |
1(50.0) |
2(100) |
Ofloxacin (5µg) |
- |
2(100) |
- |
2(100) |
Cotrimoxazole (25µg) |
- |
- |
2(100) |
2(100) |
Nalidixic acid (30µg) |
- |
- |
2(100) |
2(100) |
Table 8 Antibiotic susceptibility pattern of the Pseudomonas aeruginosa Isolated N=(2).
The result of the study indicated that, E. coli and Klebsiella pneumonia had the highest prevalence rate (50.9%) and (23.7%) while the only Gram positive bacteria isolated were Staphylococcus aureus and Staphylococcus saphrophyticus (7.0%) and (9.6%) respectively. Similar pattern of uropathogens representation was found Getenet et al.,19 in a study titled: Bacterial Uropathogens in Urinary Tract Infection and Antibiotic Susceptibility Pattern in Jimma University Specialized Hospital, Southwest Ethiopia with (33.3%) and (19.0%) for the highest isolates (E. coli and Klebsiella pneumonia) while Staphylococcus aureus and Staphylococcus saprophyticus were (4.8%) and (14.3%) respectively. While the two studies exhibits similar isolation pattern, the percentage occurrence of the pathogen varied. These isolates percentages variations could be attributable to geographical differences between the two study areas. However a similar study in China,20 revealed a different isolation pattern and species and strains diversity, because, while we had E. coli and Klebsiella pneumoniae as the predominant uropathogens in this study (50. 9%) and (23.7%) respectively their study recorded E. coli and Staphylococcus epidemidis as organisms with highest frequency (50%) and (9%) respectively while Klebsiella pneumonae represented only (5%) of the isolates. They also had more strains of the respective species isolated than found in this study, example, Staphylococcus hominis, Staphylococcus haemolyticus, Staphylococcus cleife and Staphylococcus wameri; Proteus vulgaris; Psedomonas putida; were additional strains isolated among others in their study. According to the results obtained ofloxacin and gentamicin, were the most effective agent against E. coli, with 81% and 55.2% of their isolates, susceptible to the agents respectively. A study in Kenyan, with title, Isolation and antimicrobial susceptibility testing of Escherichia coli causing urinary tract infections by Kebira et al.21 also had the same antimicrobial agents among the most effective against E. coli in vitro. The study also revealed ofloxacin as the most effective agent in vitro with 81.0%, 77.7%, 87.5%, 90.0%, 75.0% and 100% efficacy rates on, E. coli, Klebsiella pneumonia, Staphylococcus aureus, Staphylococcus saprophyticus, Proteus mirabilis, and Pseudomanas aerµginosa respectively. Cotrimoxazole was found the most resisted with only (0.00%) and (6.9%) efficacy rates on Pseudomonas and E. coli, but it was mildly effective against, Proteus mirabilis (12.5%), Klebsiella pneumonia 18.1%, Staphylococcus aureus and Staphylococcus saphyropiticus 25% and 45% respectively. A similar result was obtained in the same study area Aminu Kano Teaching Hospital, Kano, Nigeria, Chedi et al.22 in a seven months retrospective study on urinary tract infection among patients attending the hospital. In their study, fluoroquinolones to which ofloxacin (the most effective agent in our study) belongs proved the most effective class of antimicrobial agents, according to their observation, with (73.5%), (76.9%), (90.9%), 78.9% as percentage efficacy on E. coli, Proteus sp, Klebsiella sp and Pseudomanas sp respectively while almost all the isolates resisted cotrimoxazole with only (4.8%) recorded efficacy against E. coli.
On the species individual bases, eighty one per cent (81%) of E. coli isolates were sensitive to ofloxacin, (55.2%) to gentamicin as the highest efficacious agent while amoxacillin and cotrimoxazole was effective to only (29.3%) and (6.9%) respectively. A North-eastern Nigerian study (Yola, Adamawa state, Nigeria) entitled, Etiology and Antimicrobial Resistance Pattern of Bacterial Agents of Urinary Tract Infections in Students of Tertiary Institutions in Yola Metropolis,23 exhibited concurrent report on sensitivity to these agents, by the uropathogenic E. coli, with, ofloxacin (100%), gentimicin, (94%), amoxicillin (11%), cotrimoxazole, (17%). Klebsiella pneumoniae was found to be sensitive with the following isolates percentages to different antimicrobial agents (33.3%) amoxicillin, (40.7%) tetracyclin, (55.6%) gentamicin, (44.4%) nitrofurantoin, and 77.8% ofloxacin. In the same vein, Samiah HS Al-Mijal24 in Riyadh, Saudi Arabia, had amoxcilin 84% resisted (impying only 16% sensitivity) by the Klebsiella pneumonia isolates, which is even lower than found in this study, nitrofurantoin which was 44.4% in this study also ended up 16% while gentamicin 55.6% in our work had 28%, ofloxacin was substituted by another floroquinolone, levofloxacin and both proved to be effective against the intended uropathogens, 77.8% and 80.0% respectively. These relative differences in some parts of the two studies may be associated with local peculiarities in the respective locations which could also lead to stains variations.
Staphylococcus aureus also showed variable resistant pattern with respect to the used antimicrobials. Resistant rate were found to be, (25%), (37.5%), (75%), and (62.5%) for gentamicin, Tetracyclin, cotrimoxazole, and amoxicillin respectively. This implies highest resistance to cotrimoxazole and amoxicillin. Mulµgeta Kibret and, Bayeh Abera, (2014) reported a concurrent findings in Ethopia, which showed genamicin (16.7%) resisted tetracyclin, (66.7%) resisted, cotrimoxazole (77.8%) resisted while amoxicillin was even (100%) accordingly, the result therefore implies cotrimoxazole and amoxicillin as the most resisted, while gentamicin as one of the most effective as found in this study.
In particular, the resistance to cotrimoxazole are somewhat, much similar, in both cases (75%) and (77.8%) as indicated respectively, meaning that the agent is weakly effective against the intended organisms, but gentamicin which was the second most efficacious in vitro in this study, was also found effective based on their work, with resistance rate of 25% and below, which corresponds to 75% and above sensitivity to the agents. Getenet Beyene et al.19 reported from University Specialized Hospital, Southwest Ethiopia, a higher sensitivity rate than found in this study, by Staphylococcus sapphyropiticus isolates, in which genytamicin, tetracyclin, and nitrofurantoin were 0% resisted (meaning 100% sensitivity) as against 18% , 36.4% and (27.3%) respectively, nalidixic acid had (2%) resisted as against (54.5%) while amoxicillin was (66.7%) as against (36.4%) for them and our study respectively.
The 100% sensitivity to many of the tested agents may suggest a less degree of misuse and abuse of drµgs while higher resistance indicates the contrary in the respective study areas. Acording to the study, Proteus mirabillis exhibited the following susceptibility pattern, amoxicilin (37.5%), tetracyclin (50%), cortrimoxazole (12.5%), oflooxacin (75%) and nitrofurantoin (50%). These indicated highest percentage effectivity by ofloxacin followed by nitrofurantoin and respectively, the same agents were also found as most effective in a study conducted in university of Benin, Orhue,25 ofloxaxacin (64.8%) and nitrofurantoin ( 58.6 %), however, there were some variations in terms of effectiveness of some of the agents used, example, while tetracyclin was active against (50%) of the isolates in our study, it proved active on only (17.9%) of isolates in the Benin study. Similarly, cotrmoxazole was less active in vitro according to our study while it was discovered moderately promising in their work (12.5%) and (42.9%) respectively. In vitro activity of amoxicillin was not encouraging in both studies, because, (37.5%) and (21.4%) of isolates were respectively resisted.
In this study, Pseudomonas was found to be (100%) resistant to nalidixic acid, augumentin and cotrimoxazole while (50%) resistant to gentamicin, on the other hand found (100%) sensitive to ofloxicin, Shah et al.,26 also found (99.2%), (98.8%) and (97.6%) for cortrimoxazole, nalidixic acid and augumentin while gentamicin and ofloxacin were found only (35.3%) and (49%) resisted respectively. The (49%) resistant to ofloxacin could be, because the drug use to be effective, it were over prescribed in the area, which led to the development of resistant strains.27
This study also showed that ofloxacin and gentamicin were the most active antibiotics against uropathogens. Thus it is believed that these antibiotics should be used in the treatment of Urinary tract infection in this region. Moreover, this study has provided epidemiologic data and there is the need for consistent on-going antimicrobial resistance surveillance for important and commonly isolated clinically significant uropathogens to form the basis for developing and implementing measures that can reduce the burden of antimicrobial resistance and prevent a probable impending public health problem.
Government should put more strict rules on the sale of antibiotics and awareness campaign on the significance of consulting doctor before taking medication and completing regimens when prescribed should be made. Ofloxacin and gentamicin should be used to manage Urinary tract infection in Kano, Nigeria.
We acknowledged the Management of the hospitals used in study for the given and for providing enabling environment to carry out the study.
The author declares no conflict of interest.
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