Department of Medical Laboratory Science, Nobel College Affiliated to Pokhara University, Kathmandu, Nepal
Department of Medical Microbiology, Nobel College Affiliated to Pokhara University, Kathmandu, Nepal
Abstract
Background and objective: Urinary tract infections (UTIs) are the most common bacterial infections where Escherichia coli (E. coli) and Klebsiella pneumoniae (K. pneumoniae) are the predominating pathogens. These pathogens have a high rate of antibiotic resistance and exhibit the production of extended-spectrum beta-lactamase (ESBL). This study investigated the antibiotic resistance pattern and ESBL production of E. coli and K. pneumoniae isolated from patients with UTIs attending a tertiary care hospital in Nepal by both phenotypic and genotypic techniques.
Materials and methods: A cross-sectional study was performed where 4664 mid-stream urine specimens from suspected UTI cases were cultured. Isolated E. coli and K. pneumoniae were subjected to antibiotic susceptibility testing by Kirby Bauer disc diffusion method. Genotypic detection of blaCTX-M gene was performed using polymerase chain reaction (PCR).
Results: Out of 4664 urine samples processed, 564 (12.1%) were positive for E. coli (475, 10.2%) and K. pneumonia (89, 1.9%). Out of the total 564 studied samples, 267 (47.3%) were MDR isolates (E. coli: 222, 46.7%; K. pneumoniae: 45, 50.6%) and 96 (17%) were positive for ESBL by double disc confirmatory test. Out of 24 ESBL positive E. coli and 6 K. pneumoniae, 19 (79.2%) and 3 (50%) respectively were positive for blaCTX-M gene.
Conclusion: This study indicates high prevalence of MDR and ESBL producing E. coli and K. pneumoniae causing UTIs at an urban hospital setting in Nepal.
July 2024; Vol. 18(2):002. DOI: https://doi.org/10.55010/imcjms.18.014
*Correspondence: Gaurab Pandey, Department of Medical Laboratory Science, Nobel College Affiliated to Pokhara University, Kathmandu, Nepal. Email: [email protected]
Introduction
Urinary tract infection (UTI) is a common bacterial infection encountered in medical practice [1-5]. Escherichia coli and Klebsiella pneumoniae are the two main bacteria frequently linked to urinary tract infections [3,6]. Additionally, these bacteria are also responsible for bloodstream, wound, and respiratory tract infections [7-11]. Antibiotics such as carbapenems, fluoroquinolones, β-lactams, and β-lactam/β-lactamase inhibitors are commonly used to treat urinary tract infections [8,12]. But as of late, many uropathogens have developed resistance to these widely used antimicrobial agents [8,12].
One of the significant classes of β-lactamases known as extended-spectrum β-lactamases (ESBLs) is capable of conferring resistance to a wide range of β-lactam antibiotics. These include the extended spectrum (or third generation) cephalosporins (namely cefotaxime, ceftriaxone, and ceftazidime) and monobactams (aztreonam), but not the cephamycins (namely cefoxitin) and carbapenems (imipenem, meropenem, and etrapenem) [2,13-18]. However, β-lactamase inhibitors such as tazobactam, clavulanic acid, and sulbactam can block these enzymes [14,18-21]. Long-term antibiotic exposure, extended hospital stay, instrumentation or catheterization, are the major risk factors for colonization or infection with ESBL-producing organisms [2,6,7,10,14,16,22,23].
Temoniera (TEM), sulfhydryl reagent variable (SHV), and cefotaximase-Munich (CTX-M) enzymes are the sources of the majority of ESBLs, which are encoded by the blaTEM, blaSHV, and blaCTX-M genes respectively [16,22,24,25]. Recently, CTX-M-type beta-lactamases are reported as the most common resistance factors in clinical settings worldwide [26]. Bacteria that possess the blaCTX-M gene are resistant to a wide range of cephalosporin classes. Therefore, it is important to continuously monitor ESBL producing E. coli and K. pneumoniae causing different types of infections in hospitals and a locality. This study aimed to determine antibiotic resistance pattern, ESBLs production, and blaCTX-M gene in E. coli and K. pneumoniae isolates from urine samples of suspected UTI cases.
Materials and methods
This was a cross-sectional study conducted in the Department of Microbiology at Alka Hospital, Lalitpur, Nepal, from March 2023 to May 2023. The study population comprised of patients with clinically suspected UTIs from all age groups. The study was approved by Institutional Review Committee – Nobel College with the Ref No: BMM IRC 289/2019.
Information on patient demographics (age, sex, and occupation) and relevant clinical history was collected from patients’ records in hospital folders. Mid-stream urine (MSU) sample was collected in a leak-proof, sterile, screw-capped container. Samples held for more than two hours at room temperature and improperly or unlabeled samples, were excluded from the study.
Isolation and Identification of organisms: Urine samples were cultured following standard microbiological guidelines as described elsewhere [27]. Using a sterile calibrated loop (2 mm), the urine samples were streaked directly on MacConkey agar and Blood agar plates. These plates were incubated at 37 °C aerobically and after overnight incubation, they were checked for bacterial growth. Colony count was made, and the positive result was considered for plates showing more than or equal to 105 colony-forming units (CFU)/mL of urine based on Kass, Marple, and Sanford criteria [28]. The isolates were identified based on cultural characteristics in MacConkey agar and Blood agar, Gram staining, catalase test, oxidase test, and other relevant biochemical tests as per standard laboratory methods [29].
Antibiotic susceptibility testing: Antimicrobial susceptibility testing (AST) was done by the Kirby-Bauer disk diffusion technique using Muller Hinton agar [30]. All identified isolates of E. coli and K. pneumoniae were tested for susceptibility against amikacin (30 μg), amoxicillin (10 μg), gentamicin (10 μg), ceftazidime (30 μg), cefotaxime (30 μg), ceftriaxone (30 μg), cotrimoxazole (25 μg), ciprofloxacin (5 μg), nitrofurantoin (300 µg), nalidixic acid (30 μg), norfloxacin (5 μg), meropenem (10 μg), piperacillin/tazobactam (100/10 μg), imipenem (10 μg), tigecycline (15 μg), polymixin B (10 μg) and colistin (10 μg). Results were interpreted based on the Clinical and Laboratory Standards Institute (CLSI) 2016 guidelines [30,31]. The bacterial isolates showing resistance towards three or more different antibiotic classes were considered multidrug-resistant (MDR) [32].
Screening and confirmation of ESBL producers: The screening was done by disc diffusion technique using cefpodoxime (30 µg), cefotaxime (30 µg), ceftazidime (30 µg), ceftriaxone (30 µg), cefotaxime (30 µg), aztreonam (30 µg) discs. For confirmation, combined disc test was performed using ceftazidime (30 µg) alone, and ceftazidime + clavulanic acid (20 µg + 10 µg). A difference of ≥5 mm between the zone diameters of either of cephalosporin disks and their respective cephalosporin/clavulanate disk was taken to be phenotypic confirmation of ESBL production [30].
Amplification and detection of blaCTX-M gene using PCR method: From confirmed ESBL producers, plasmids were extracted using standard alkaline hydrolysis method. These plasmids served as the template for PCR. The blaCTX-M gene amplification was performed by PCR technique using specific primer: 5'-TTTGCGATGTGCAGTACCAGTAA-3' as a forward primer and 5'- CTCCGCTGCCGGTTTTATC-3' as a reverse primer [19]. A final volume of 25 µl was prepared by adding 12.5 µl master mix green go-Taq, 1 μl of forward and reverse primer each, 8.5 µl nuclease-free water, and 2 μl bacterial DNA. Amplification was performed with the following cycling conditions: initial denaturation at 940C for 5 minutes; followed by 30 cycles each of extended denaturation at 950C for 45 seconds, annealing for 620C for 45 seconds, extension at 720C at 30 seconds, and extended extension at 720C for 10 minutes. The PCR products and the DNA marker were visualized by using 2% agarose gel electrophoresis.
Quality Control: E. coli ATCC 25922 and K. pneumoniae ATCC 700603 were used as negative and positive controls, respectively. For PCR already confirmed E. coli strains harboring blaCTX-M were taken as a positive control and nuclease free water as the negative control.
Statistical analysis: The statistical analysis was performed in Statistical Package for Social Sciences (SPSS) version 25.0. Discrete variables were expressed into percentages. Categorical variables were compared using the Chi square test and a p-value <0.05 was considered a statistically significant finding.
Results
Out of 4664 urine samples processed, 564 (12.1%) were positive for E. coli (475, 10.2%) and K. pneumonia (89, 1.9%). Among 564 studied samples, the sex wise distribution of the patients showed that 110 (19.5%) isolates were from male and 454 (80.5%) isolates were from female patients. Most organisms were isolated from the age group 21-40 years. Least organisms were isolated from age group 0 -20 years (Table-1).
Table-1: Age and sex-wise distribution of cases from whom E. coli and K. pneumoniae were isolated
Out of the total 564 studied samples, 267 (47.3%) were MDR isolates (E. coli: 222, 46.7%; K. pneumoniae: 45, 50.6%) and 96 (17%) were positive for ESBL by double disc confirmatory test (Table-2). Out of 222 MDR E. coli, 160 (72.1%) were ESBL positive by screening test while 82 (36.9%) became ESBL positive by confirmatory test. Similarly for K. pneumoniae, the ESBL positivity rate by screening and confirmatory test was 60% and 22.2% respectively. The rate of ESBL positivity among non-MDR isolates of E. coli was 1.6% while none of the non-MDR K. pneumoniae was positive for ESBL (Table-2). There was a significant association between ESBL production and MDR isolates (p<0.001). But the rate of MDR and ESBL positivity was not significantly (p > 0.05) different between E. coli and K. pneumoniae.
Table-2: ESBL positivity in MDR and non-MDR E. coli and K. pneumoniae
Detail rate of ESBL positivity in MDR E. coli and K. pneumoniae isolated from male and female patients is shown in Table-3. Among 222 MDR E. coli isolates, 52 (48.6%) and 170 (46.2%) were from male and female patients respectively. Out of 107 and 368 E. coli isolates from male and female patients, 52 (48.6%) and 170 (46.2%) isolates were MDR respectively. The rate of ESBL producing MDR E. coli from male and female cases was not significantly (p>0.05) different (32.7% vs. 40.6%). Similarly, the rate of ESBL positive K. pneumoniae isolated from male and female patients was not significantly (p>0.5) different (33.3% s. 21.4%).
Table-3: ESBL positivity in MDR E. coli and K. pneumoniae isolated from male and female patients
Age wise distribution of MDR and ESBL producing isolates is shown in Table-4. Rate of MDR E. coli and K. pneumoniae was significantly (p<0.05) higher among the older age groups compared to younger groups. The rate of ESBL producing E. coli and K. pneumoniae was not significantly different among the groups.
Table-4: Age wise distribution of MDR and ESBL producing E. coli and K. pneumoniae
About 40.7% to 67.7% E. coli isolates were resistant to quinolones, amoxicillin+clavulanate, co-trimoxazole and imipenem (Table-5). Except imipenem, the rate of resistance of K. pneumoniae to these antibiotics was between 50%-90%. None of the E. coli and K. pneumoniae was resistant to colistin. Amikacin, meropenem, tigecycline, nitrofurantoin, polymixin-B, and colistin were the most effective antibiotic for ESBL positive E. coli and K. pneumoniae.
Table-5: Antibiotic susceptibility pattern of ESBL producing E. coli and K. pneumoniae
Table-6: Distribution of blaCTX-M gene among ESBL-producing E. coli and K. pneumoniae isolates
Figure-1: Agarose gel electrophoresis of the amplified PCR product for blaCTX-M gene. Lane 1 and 16:100 bp DNA markers; Lane 2 and 17: negative control; Lane 3 and 18: positive control; Lane 4 to 15 and Lane 19 to 30: isolates tested for the presence of blaCTX-M gene (560 bp).
Discussion
The present study sought to determine the rate of ESBL producing E. coli and K. pneumoniae isolates causing urinary tract infections. We found that these organisms had a high level of antibiotic resistance and were the most frequent cause of UTIs. In our series, E. coli and K. pneumoniae was isolated from 12.1% of the 4,664 urine specimens evaluated. This finding is comparable to other reported studies from Nepal [33-35]. Our study sought to determine how common ESBL producing E. coli and K. pneumoniae isolates from urinary tract infections. Of the total E. coli and K. pneumoniae isolates, 17% were ESBL producers. Other studies from Nepal and the region reported variable rates of ESBL producing E. coli and K. pneumoniae in urine and different clinical samples [33-38].
In our study, blaCTX-M gene was present in 79.2% and 50% of E. coli and K. pneumoniae respectively. Others have reported higher prevalence of blaCTX-M gene from 66.6% to 100% in E. coli and K. pneumoniae [19,35,39,40]. Variations in the volume and kind of antibiotic use as well as variations in the time of isolate collection may account for the variations in frequencies and prevalence of these genes.
One of the noteworthy findings in the present study among ESBL producers was the high resistance rate to imipenem (67.7%) which is contrary to that found by Shakya et al [38] and Zeynudin et al [41] who reported the imipenem résistance rate as 0% and 1.90%, respectively. High imipenem resistance can be attributed to the prevalence of carbapenemase β-lactamases as well as a rise in the haphazard use of the antibiotics to treat infections [34]. Furthermore, both of the ESBL isolates in our investigation showed high resistance to amoxicillin+clavulanic acid. The finding is consistent with the findings of Shashwati et al [37]. Multidrug resistance trends can differ between countries or even hospitals within the same nation due to differences in antibiotic prescribing practices during infection and lapses in an efficient infection control program.
The emergence of MDR and ESBL producing E. coli and K. pneumoniae isolates with high antibiotic – resistant rates to commonly used antibiotics and predominance of blaCTX-M-beta lactamase gene poses a serious concern to the clinicians and microbiologists. Regular monitoring of antibiotic susceptibility and associated genes along with rationale use of antibiotics for treating the predominant pathogens like E. coli and K. pneumoniae in healthcare facilities is essential to contain the spread of antibiotic résistance.
Author Contributions
GP: Conceptualization and designing of the study, approval of SOP for the study, supervised the study, and validating the results, manuscript – writing, editing, reviewing and submitting; AK, PK and CT: Writing SOP for the study, sample collection, performing tests, result analysis, and reporting of the results, manuscript writing, literature search.
Conflict of Interest
The authors have no conflicts of interest to declare.
Ethics approval
The ethical approval was granted by Institutional Review Committee – Nobel College with the Ref No: BMM IRC 289/2019.
Funding
The authors did not receive any funding.
References
1. Gharavi MJ, Zarei J, Roshani-Asl P, Yazdanyar Z, Sharif M, Rashidi N.Comprehensive study of antimicrobial susceptibility pattern and extended spectrum beta-lactamase (ESBL) prevalence in bacteria isolated from urine samples. Sci Rep. 2021; 11(1): 578. doi: 10.1038/s41598-020-79791-0.
2. Yadav KK, Adhikari N, khadka R, Pant AD, Shah B. Multidrug resistant Enterobacteriaceae and extended spectrum β-lactamase producing Escherichia coli: a cross-sectional study in National Kidney Center, Nepal. Antimicrob Resist Infect Control. 2015; 4(42): 1-7. doi: 10.1186/s13756-015-0085-0.
3. Subedi K, Lama S, Dahal U, Karki F, Pandey A, Paudyal R. Phenotypic detection of extended spectrum beta lactamase production from E. Coli and K. Pneumoniae in urinary samples among children. Tribhuvan University Journal of Microbiology (TUJM). 2020; 7: 75-82. doi: 10.3126/tujm.v7i0.33801.
4. Tan CW, Chlebicki MP. Urinary tract infections in adults. Singapore Med J. 2016; 57(9): 485. doi: 10.11622/smedj.2016153.
5. Akram M, Shahid M, Khan AU. Etiology and antibiotic resistance patterns of community-acquired urinary tract infections in JNMC Hospital Aligarh, India. Ann Clin Microbiol Antimicrob. 2007; 6(1): 1-7. doi: 10.1186/1476-0711-6-4.
6. Enyinnaya SO, Iregbu KC, Jamal WY, Rotimi VO. Antibiotic susceptibility profiles and detection of genes mediating extended-spectrum β-lactamase (Esbl) production in escherichia coli isolates from National Hospital, Abuja. Niger J Clin Pract. 2022; 25(8): 1216-1220. doi: 10.4103/njcp.njcp_1390_21.
7. Hasibuan M, Suryanto D, Kusumawati RL. Phenotypic and molecular detection of blaCTX-M gene extended-spectrum beta-lactamases in Escherichia coli and Klebsiella pneumoniae of north Sumatera isolates. IOP Conf Ser: Earth Environ Sci.2018; 130(012032): 20-32. doi: 10.1088/1755-1315/130/1/012032.
8. Halabi MK, Lahlou FA, Diawara I, El Adouzi Y, Marnaoui R, Benmessaoud R, et al. Antibiotic resistance pattern of extended spectrum beta lactamase producing Escherichia coli isolated from patients with urinary tract infection in Morocco. Front Cell Infect Microbiol. 2021; 11: 720701. doi: 10.3389/fcimb.2021.720701.
9. Babini GS, Livermore DM. Antimicrobial resistance amongst Klebsiella spp. collected from intensive care units in Southern and Western Europe in 1997–1998. J Antimicrob Chemother. 2000; 45(2): 183-189. doi: 10.1093/jac/45.2.183.
10. Kayastha K, Dhungel B, Karki S, Adhikari B, Banjara MR, Rijal KR, et al. Extended-spectrum β-lactamase-producing Escherichia coli and Klebsiella species in pediatric patients visiting International Friendship Children’s Hospital, Kathmandu, Nepal. Infect Dis (Auckl). 2020; 13: 1178633720909798. doi: 10.1177/1178633720909798.
11. Kaper JB, Nataro JP, Mobley HL. Pathogenic Escherichia coli. Nat Rev Microbiol. 2004; 2(2): 123-140. doi: 10.1038/nrmicro818.
12. Shrestha A, Acharya J, Amatya J, Paudyal R, Rijal N. Detection of beta-lactamases (ESBL and MBL) producing Gram-negative pathogens in National Public Health Laboratory of Nepal. Int J Microbiol. 2022; 2022: 5474388. doi: 10.1155/2022/5474388.
13. Altayb HN, Siddig MAM, El Amin NM, Mukhtar MM. Prevalence of blaCTX-M, blaTEM, and blaSHV genes among extended-spectrum β-lactamases-producing clinical isolates of Enterobacteriaceae in different regions of Sudan. Sudan J Med Sci. 2021; 16(1): 5-16. doi: 10.18502/sjms.v16i1.8933.
14. Somily AM, Habib HA, Absar MM, Arshad MZ, Manneh K, Al Subaie SS, et al. ESBL-producing Escherichia coli and Klebsiella pneumoniae at a tertiary care hospital in Saudi Arabia. J Infect Dev Ctries. 2014; 8(9): 1129-1136. doi: 10.3855/jidc.4292.
15. Higgins O, Chueiri A, O’Connor L, Lahiff S, Burke L, Morris D, et al. Portable differential detection of CTX-M ESBL gene variants, blaCTX-M-1 and blaCTX-M-15, from Escherichia coliisolates and animal fecal samples using loop-primer endonuclease cleavage loop-mediated isothermal amplification. Microbiol Spectr. 2023; 11(1): e03316-22. doi: 10.1128/spectrum.03316-22.
16. El Aila NA, Al Laham NA, Ayesh BM. Prevalence of extended spectrum beta lactamase and molecular detection of blaTEM, blaSHV and blaCTX-M genotypes among Gram negative bacilli isolates from pediatric patient population in Gaza strip. BMC Infect Dis. 2023; 23(1): 99. doi: 10.1186/s12879-023-08017-1.
17. Shilpakar A, Ansari M, Rai KR, Rai G, Rai SK. Prevalence of multidrug-resistant and extended-spectrum beta-lactamase producing Gram-negative isolates from clinical samples in a tertiary care hospital of Nepal. Trop Med Health. 2021; 49(1): 23. doi: 10.1186/s41182-021-00313-3.
18. RamadanAA, Abdelaziz NA, Amin MA, Aziz RK. Novel blaCTX-M variants and genotype-phenotype correlations among clinical isolates of extended spectrum beta lactamase-producing Escherichia coli. Sci Rep. 2019; 9(1): 4224. doi: 10.1038/s41598-019-39730-0.
19. Lohani B, Sharma L, Adhikari H, Sah AK, Khanal AB, Basnet RB, et al.Predominance of CTX-M type extended spectrum β-lactamase (ESBL) producers among clinical isolates of Enterobacteriaceae in a tertiary care hospital, Kathmandu, Nepal. Open Microbiol J. 2019; 13(1): 28-33. doi: 10.2174/1874285801913010028.
20. Paterson DL, Bonomo RA.Extended-spectrum β-lactamases: a clinical update. Clin Microbiol Rev. 2005; 18(4): 657-686. doi: 10.1128/CMR.18.4.657-686.2005.
21. Mansury D, Motamedifar M, Sarvari J, Shirazi B, Khaledi A. Antibiotic susceptibility pattern and identification of extended spectrum β-lactamases (ESBLs) in clinical isolates of Klebsiella pneumoniae from Shiraz, Iran. Iran J Microbiol. 2016; 8(1): 55-61.
22. Nwafia IN,Ohanu ME, Ebede SO, Ozumba UC.Molecular detection and antibiotic resistance pattern of extended-spectrum beta-lactamase producing Escherichia coli in a Tertiary Hospital in Enugu, Nigeria. Ann Clin Microbiol Antimicrob. 2019; 18(1): 41. doi: 10.1186/s12941-019-0342-9.
23. Abrar S, Hussain S, Khan RA, Ain NU, Haider H, Riaz S.Prevalence of extended-spectrum-β-lactamase-producing Enterobacteriaceae: first systematic meta-analysis report from Pakistan. Antimicrob Resist Infect Control. 2018; 7: 26. doi: 10.1186/s13756-018-0309-1.
24. Moghaddam MN, Beidokhti MH, Jamehdar SA, Ghahraman M.Genetic properties of blaCTX-M and blaPER β-lactamase genes in clinical isolates of Enterobacteriaceae by polymerase chain reaction. Iran J Basic Med Sci. 2014; 17(5): 378-383.
25. Castanheira M, Simner PJ, Bradford PA. Extended-spectrum β-lactamases: an update on their characteristics, epidemiology and detection. JAC Antimicrob Resist. 2021; 3(3): dlab092. doi: 10.1093/jacamr/dlab092.
26. D'Andrea MM, Arena F, Pallecchi L, Rossolini GM. CTX-M-type β-lactamases: a successful story of antibiotic resistance. Int J Med Microbiol. 2013; 303(6-7): 305-17. doi: 10.1016/j.ijmm.2013.02.008.
27. Versalovic J. Manual of clinical microbiology, vol. 1. 10th ed. Washington, DC: American Society for Microbiology Press; 2011.
28. Forbes BA, Sahm DF, Weissfeld AS, Bailey WR. Bailey & Scott’s Diagnostic Microbiology. 12th ed. St. Louis: Elsevier Mosby; 2007.
29. Cheesbrough M. District laboratory practice in tropical countries, Part 2, 2nd ed. Tropical Health Technology, Norfolk: Cambridge University press; 2005. doi:10.1017/CBO9780511581304.
30. Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial susceptibility testing (M100S), 26th ed. Wayne P: CLSI; 2016.
31. Humphries RM, Ambler J, Mitchell SL, Castanheira M, Dingle T, Hindler JA, et al. CLSI methods development and standardization working group best practices for evaluation of antimicrobial susceptibility tests. J Clin Microbiol. 2018; 56(4): e01934-17. doi:10.1128/JCM.01934-17.
32. Magiorakos A-P, Srinivasan A, Carey RB, Carmeli Y, Falagas ME, Giske CG, et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect. 2012; 18(3): 268-281. doi:10.1111/j.1469-0691.2011.03570.x.
33. Nepal K, Pant ND, Neupane B, Belbase A, Baidhya R, Shrestha RK, et al. Extended spectrum beta-lactamase and metallo beta-lactamase production among Escherichia coli and Klebsiella pneumoniae isolated from different clinical samples in a tertiary care hospital in Kathmandu, Nepal. Ann Clin Microbiol Antimicrob. 2017; 16(1): 62. doi:10.1186/s12941-017-0236-7.
34. Ghimire A, Acharya B, Tuladhar R. Extended Spectrum β-Lactamase (ESBL) producing multidrug resistant gram-negative bacteria from various clinical specimens of patients visiting a tertiary care hospital. Tribhuvan University Journal of Microbiology (TUJM). 2017; 4(1): 1-8. doi:10.3126/tujm.v4i0.21667.
35. Koirala S, Khadka S, Sapkota S, Sharma S, Khanal S, Thapa A, et al. Prevalence of CTX-M β-lactamases producing multidrug resistant Escherichia coli and Klebsiella pneumoniae among patients attending Bir Hospital, Nepal. Biomed Res Int. 2021; 2021: 9958294. doi:10.1155/2021/9958294.
36. Baral P, Neupane S, Marasini BP, Ghimire KR, Lekhak B, Shrestha B. High prevalence of multidrug resistance in bacterial uropathogens from Kathmandu, Nepal. BMC Res Notes. 2012; 5: 38. doi:10.1186/1756-0500-5-38.
37. Shashwati N, Kiran T, Dhanvijay AG. Study of extended spectrum β-lactamase producing Enterobacteriaceae and antibiotic coresistance in a tertiary care teaching hospital. J Nat Sci Biol Med. 2014; 5(1): 30-35. doi:10.4103/0976-9668.127280.
38. Shakya P, Shrestha D, Maharjan E, Sharma VK, Paudyal R. ESBL production among E. coli and Klebsiella spp. causing urinary tract infection: a hospital based study. Open Microbiol J. 2017; 11:23-30. doi:10.2174/1874285801711010023.
39. Parajuli NP, Maharjan P, Joshi G, Khanal PR. Emerging perils of extended spectrum β-lactamase producing Enterobacteriaceae clinical isolates in a teaching hospital of Nepal. Biomed Res Int. 2016; 2016: 1782835. doi:10.1155/2016/1782835.
40. Chaudhary MK, Jadhav I, Banjara MR. Molecular detection of plasmid mediated blaTEM, blaCTX− M, and blaSHV genes in extended spectrum β-Lactamase (ESBL) Escherichia coli from clinical samples. Ann Clin Microbiol Antimicrob. 2023; 22(1): 33. doi:10.1186/s12941-023-00584-0.
41. Zeynudin A, Pritsch M, Schubert S, Messerer M, Liegl G, Hoelscher M, et al. Prevalence and antibiotic susceptibility pattern of CTX-M type extended-spectrum β-lactamases among clinical isolates of gram-negative bacilli in Jimma, Ethiopia. BMC Infect Dis. 2018; 18(1): 524. doi:10.1186/s12879-018-3436-7.
Cite this article as:
Pandey G, Karki A, Karki P, Thapa C. Extended spectrum beta-lactamase production and blaCTX-M gene in Escherichia coli and Klebsiella pneumoniae causing urinary tract infection at a tertiary care hospital in Nepal. IMC J Med Sci. 2024; 18(2):002. DOI: https://doi.org/10.55010/imcjms.18.014.
