Antibiotic Susceptibility Patterns and Prevalence of Some Extended Spectrum Beta-Lactamases Genes in Gram-Negative Bacteria Isolated from Patients Infected with Urinary Tract Infections in Al-Najaf City, Iraq
Majeed, Heba Takleef
Department of Microbiology, Faculty of Science, University of Kufa, Kufa, Iraq
Jaloob Aljanaby, Ahmed Abduljabbar
Department of Microbiology, Faculty of Science, University of Kufa, Kufa, Iraq, Tel: +0096 47816118353, E-mail: Ahmedjaloob@gmail.com, email@example.com
Background: Urinary Tract Infection (UTI) in patients with Chronic Kidney Disease (CKD) caused by multi-drug resistance and Extended Spectrum Beta Lactamase (ESBL)-producing gram-negative bacteria has been increased in different countries. The aim of the present study was to detect the antibiotic susceptibility patterns and the distribution of Bla-TEM, Bla-SHV and Bla-CTX-M genes in gram-negative bacteria isolated from outpatients infected with UTI, with and without CKD in Al-Najaf city, Iraq.
Methods: A total of 120 non-duplicate urine samples were collected from outpatients (37 male and 83 female) infected with UTI in Al-Najaf city, Iraq; 60 samples from patients Without Kidney Disease (WKD) and 60 samples from patients with CKD. The antibiotic susceptibility testing was done according to Kirby-Bauer method. PCR technique was performed to investigate the prevalence of Bla-TEM, Bla-SHV and Bla-CTX-M genes.
Results: A total of 126 different gram-negative bacterial strains were isolated. Escherichia coli (E. coli) was the most prevalent bacterium (49 isolates) followed by Idebsiella pneumonia (K. pneumonia) (35 isolates), Pseudomonas aeruginosa (P. aeruginosa) (18 isolates), Citrobacter freundii (C. freundii) (12 isolates), Enterobocter aerogenes (E. aerogenes) (8 isolates) and Proteus mirabilis (P. mirabilis) (4 isolates). All bacterial isolates from UTI patients with CKD were resistant to antibiotics and carried Bla-TEM, Bla-SHV and Bla-CTX-M genes more than isolates from UTI patients with WKD.
Conclusion: This study demonstrated that all bacterial isolates from UTI patients with CKD were more virulent than isolates from UTI patients with WKD.
Gram-negative bacteria are a common cause of Urinary Tract Infection (UTI), especially in older individuals and in patients infected with Chronic Kidney Disease (CKD). Urinary tract infection is one of the most important recurrent diseases worldwide especially in Middle East countries and the second most common illness in both males and females with prevalence of 1/2, respectively 1,2. Chronic kidney disease is a clinical syndrome characterized by defect in kidney glomerular filtration resulting in decreased clearance of metabolic waste product of the blood 3. About 6 to 40% of patients with CKD are susceptible to infection with UTI caused by Extended-Spectrum β-Lactamase (ESBL)-producing gram-negative bacteria worldwide 4. Annually, about more than 150 million cases are infected with UTI worldwide 5. UTI is often caused by ESBL-producing gram-negative bacteria such as Escherichia coli (E. coli), Klebsiella pneumoniae (K. pneumonia) and Pseudomonas aeruginosa (P. aeruginosa) 6. Almost all these pathogens are Multi-Drug Resistant (MDR) and result in clinical problems because of limited therapeutic options 7,8. Extended-spectrum ß-lactamase antibiotics such as cefotaxime, ceftazidime and ceftriaxone are mostly used to treat this type of infection in most countries 9. Recently, the prevalence of antibiotic resistance in gram-negative bacteria which result in UTI has increased strongly 10,11. Enterobacteriaceae and some other gram-negative pathogens became highly ESBL-producing bacteria. ESßL encoding genes are located on bacterial DNA, plasmids or transposons that can transfer easily between two or more bacteria such as E. coli, K. pneumoniae, Enterobacter cloacae (E. cloacae) and others 12,13.
Since the 1980s, ESβL antibiotics have been widely used for treatment of different infections caused by gram-negative bacteria such as burns infections, wound infections and UTI 14,15. However, bacterial resistance has originated fast due to the production of special enzymes called ESBLs 16. These enzymes are derived from some genes such as Bla-TEM, Bla-SHV and Bla-CTX-M for the narrower spectrum ß-lactamases by mutations that alter the amino acid configuration around the enzyme active site 17. They are typically encoded by plasmids that can be exchanged between bacterial species 18. It is also reported that the predominant types of ESBLs in K. pneumoniae, P. aeruginosa and E. coli and some others type of gram-negative bacteria isolated from urine of patients with UTI are TEM type followed by SHV and CTX-M. Usually, infections caused by ESBL-producing bacteria are associated with increased morbidity and mortality which entails enhanced healthcare costs 19,20.
In Iraq, there are no studies focusing on the relationship between the prevalence of ESLB-genes in gram-negative bacteria causing UTI isolation from urine of outpatients infected with CKD and Without Kidney Disease (WKD). Therefore, the main aim of the present study was to investigate the antibiotic susceptibility patterns and the distribution of Bla-TEM, Bla-SHV and Bla-CTX-M genes in gram-negative bacteria isolated from outpatients infected with UTI, with and without CKD in Al-Najaf city, Iraq.
Materials and Methods :
Patients and study design: This was a case control study carried out in laboratory of University of Kufa, Faculty of Science, Department of Microbiology, Iraq. A total of 120 outpatients (males and females in different age groups) were included in this study who were infected with UTI and were divided in two groups, group one (control) including 60 outpatients infected with UTI WKD and group two (case study) including 60 patients infected with UTI with CKD (diagnosed by specialist physician according to abnormal urinary parameters and an increase in serum creatinine) during the period between July to December 2017.
Urine samples collection: Ten ml of clean and mid-stream of urine samples were collected in sterile containers (Himedia-India) from two groups of outpatients who visited private clinics in Al-Najaf city. All containers were labeled according to gender and age of each patient. Immediately, the urine samples were processed for bacterial cultivation and identification 21.
Isolation and identification of gram-negative bacterial isolates: All urine samples were inoculated by sterile loop (Himedia-India) immediately on blood agar plate and MacConkey agar plate (Oxoid, UK). All agar plates were incubated aerobically at 37oC for 24 hr. Colony Forming Units (CFUs) method was used for growing single and pure bacterial colony; all urine samples containing less than 105 CFUs/ml were excluded 22. All single and pure bacterial colonies were identified according to colony morphology, gram stain, lactose or non-lactose fermenter on MacConkey agar plate, capsule formation and according to standard biochemical tests such as motility, IMVIC, oxidase, catalase and TSI 21. In addition, all bacterial isolates were streaked on CHROM agar medium (Orientation, France). Final identification was done according to Vitek2® system (BioMerieux® -France).
Antibiotic susceptibility test: Antibiotic susceptibility testing was done by Kirby-Bauer disc diffusion method 23. Five to three pure and fresh bacterial colonies were suspended in nutrient broth (Oxoid, UK) and adjusted to 0.5 Mc-Ferland standard tube (1.5×108 CFUs/ml). By using sterile swab (Bioanalyse, Turkey), the suspension was streaked onto the surface of Mueller Hinton agar (Oxoid, UK). By sterile forceps, all antibiotics disc were placed onto the surface of Mueller Hinton agar (Oxoid, UK) and incubated aerobically at 37oC for 24 hr. Clinical and Laboratory Standards Institute 24 was used as a guideline of antibiotic susceptibility and resistance according to bacterial growth zone diameter. Twelve antibiotics used in the current study were obtained from Bioanalyse, Turkey; Amoxicillin 25 µg (AX), Amoxicillin+Clavulanic acid 30 µg (AMC), Cefotaxime 30 µg (CTX), Ceftriaxone 30 µg (CRO), Ceftazidime 30 µg (CAZ), Imipenem 10 µg (IMP), Gentamicin 15 µg (CN), Amikacin 30 µg (AK), Tobramycin 10 µg (µg), Tetracycline 30 UI (TE), Ciprofloxacin 5 µg (CIP) and Levofloxacin 30 µg (LIV). E. coli ATCC25922 was used as a control isolate. MDR, Extensive-Drug Resistance (XDR) and Pan-Drug Resistance (PDR) bacterial isolates were determined as follows; each bacterial isolate was resistant to three deferent antibiotics class considered as MDR, each remained susceptible to one or two antibiotics classes considered as XDR and some resistant to all antibiotics classes considered as PDR 25.
Primary phenotypic detection of ESBL-producing bacterial isolates: This method was done according to Clinical and Laboratory Standards Institute (CLSI, 2006) 25. Standard antimicrobial susceptibility test was performed for each bacterial isolate of three antibiotics; ceftriaxone 30 µg, cefotaxime 30 µg and ceftazidime 30 µg, and any bacterial isolate showing zone of inhibition of ≤25 mm, ≤27 mm and ≤22 mm, respectively was considered as ESBL-producing isolate.
Confirmatory phenotypic detection of ESBL-producing bacteria: Double disc synergy test was done according to Sarojamma and Ramakrishna 26 and Aljanaby and Alhasnawi 2. Bacterial suspension was adjusted according to 0.5 Mc-Ferland standard tube (1.5×108 CFUs/ml). Amoxicillin 10 µg+Clavulanic acid 20 µg was placed in the center of Mueller Hinton agar plate, around three sides of ceftriaxone 30 µg. Cefotaxime 30 µg and ceftazidime 30 µg were placed with distance of 15 mm to center of Amoxicillin 10 µg+Clavulanic acid 20 µg and the plates were incubated at 37oC for 24 hr. Any inhibition zone of any type of 3rd generation cephalosporins antibiotics was increased towards Amoxicillin 10 µg+Clavulanic acid 20 µg which was considered as the positive result of the study.
DNA extraction: This method was preformed according to Aljanaby and Alhasnawi 2 and Aljanaby and Medhat 7. Briefly, five fresh and pure bacterial colonies were suspended in 500 µl of distilled water and heated in water bath (Oxoid, UK) for 30 min and the supernatant was taken as a DNA template after centrifugation at 7500 rpm for 20 min.
PCR primers and thermo cycling conditions: Three primer sequences for three genes and thermo cycle conditions were used in the current study as shown in tables 1 and 2, respectively. Five µl aliquots of PCR product were analyzed by gel electrophoresis with 2% agarose. Gel was stained with ethidium bromide at 2 mg/ml and visualized with UV light.
Statistical analysis: Chi-squared test was used for the comparison between samples using graph-pad prism computer software version 8. A p-value less than 0.05 was considered statistically significant.
Patients: Out of 120 outpatients with UTI, the results indicated that there were 37 males; 18 (15%) WKD, 19 (15.8%) CKD and 83 females; 42 (35%) WKD, 41 (34.1%) with CKD (Figure 1). According to age groups, the results proved that the age group 51-60 years old was the most prevalent range among patients with UTI (48 patients 40%; 22 patients were WKD and 26 patients with CKD) (Table 3).
Total bacterial isolates: A total of 126 different gram-negative bacterial isolates were isolated from 120 urine samples of patients infected with UTI. E. coli was the most prevalent bacteria (49 isolates, 38.9%) followed by K. pneumoniae (35 isolates, 27.8%), P. aeruginosa (18 isolates, 14.3%), Citrobacter freundii (C. freundii) (12 isolates, 12.9%), Enterobacter aerogenes (E. aerogenes) (8 isolates, 6.3%) and Proteus mirabilis (P. mirabilis) (4 isolates, 3.2%) (Figures 2 and 3). The results demonstrated that there were 60 bacterial isolates from WKD patients and 66 isolates from CKD patients (Table 4).
Antibiotics susceptibility testing: According to the results of antibiotics susceptibility test in tables 5 and 6, most bacterial isolates were highly resistant against most antibiotics especially against amoxicillin and third generation cephalosporins, while imipenem provided the best antibacterial effect against most isolates. Most bacterial isolates from urine of CKD patients were highly resistant to antibiotics as compared with isolates from urine of WKD patients. On the other hand, the results proved that there was a high incidence of MDR bacteria isolated from urine of CKD patients (54 isolates, 42.9%) as compared with WKD patients (42 isolates, 33.3%) (Figure 4) (Table 7). All CKD isolates were MDR with percentages between 80 to 95% except E. aerogenes and P. mirabilis which were 50%. E. coli, K. pneumoniae and P. aeruginosa isolated from urine of CKD patients were XDR with percentages of 5, 11.7 and 20%, respectively, and there was one K. pneumoniae isolate with 5.8% which was PDR (Table 7). The results showed that almost CKD isolates were ESBL-producing bacteria (21 isolates, 16.6%) as compared with WKD isolate (6 isolates, 4.7%) (Figure 5) and there was significant increase in CKD and WKD isolates in E. coli and K. pneumoniae with p-value=0.0497 and 0.0153, respectively (Figure 6, Table 8).
Genotypic detection: Out of 126 total isolates, the results proved that all CKD isolates harbored ESBLs-genes more than WKD isolates. Thirty nine CKD isolates (46%) harbored Bla-TEM, 30 isolates (24%) harbored Bla-SHV and 33 isolates (26%) harbored Bla-CTX-M as compared with WKD isolates; 26 isolates (20.6%) harbored Bla-TEM, 19 isolates (15%) harbored Bla-SHV and Bla-CTX-M (Figure 7). K. pneumoniae was the one that mostly carried ESBLs-genes followed by E. coli and C. freundii (Table 9). PCR amplification of genes is shown in figures 8-10.
UTI is one of the most important diseases that infect both males and females especially in age groups between 50 to 70 years old. In the current study, the results proved that out of 120 patients, there were 37 (30.8%) males and 83 (69.2%) females infected with UTI and 51-60 year old group was the most infected one among age groups with percentage of 40%. These results are in agreement with Zhang et al’s 28 and Hsiao et al’s 29 findings when they found a high prevalence of older patients (50 to 75 years old) infected with UTI. On the other hand, females are prone to infection with UTI more than males because of absence of prostatic fluid (Antibacterial activity) and the shortness of the urethra 30,31.
CKD is the continuous defect of renal functions 32. Diagnosis on the basis of abnormal urinary parameters and increase in serum creatinine are associated with increased risk of acute kidney disease and mortality 33. Urinary tract infection affects approximately up to 6 to 40% of CKD, being the main infectious complication among such patient population and one of the most common causes of CKD and mortality 34,35.
In this study, one of the most important results was a high incidence of MDR bacteria (54 isolates, 42.9%) and ESBL- producing gram-negative bacteria (21 isolates, 16.6%) among CKD patients as compared with WKD patients (42 isolates, 33.3% of MDR bacteria and 6 isolates, 26.1% of ESBL-producing gram-negative bacteria) among 126 different gram-negative bacterial isolates. K. pneumoniae, E. coli and C. freundii were the most virulent pathogens isolated from CKD patients. Also, all CKD isolates harbored Bla-TEM, Bla-SHV and Bla-CTX-M genes more than WKD isolates.
Recurrent infection with urinary tract was associated with septic shock or sepsis leading to renal failure or chronic kidney disease 36. On the other hand, some past studies proved that CKD was not a common complication in patients with renal failure 37,38. The risk of UTI in patients with CKD might be increased by host factors such as immunodeficiency and low urinary flow rate 39. Multi-drug resistance of uropathogenic gram-negative bacteria such as K. pneumoniae, E. coli and C. freundii is the leading cause in majority of UTI, including pyelonephritis which may lead to CKD and renal failure in healthy individuals 40. The development of UTI depends on anatomical barriers, host defense strategy and the virulence factors of uropathogenic bacteria that can stay within the urinary tract and act as a reservoir for recurrent UTI and many dangerous complications 41.
The main causative agents responsible for UTI are gram-negative bacteria mostly, E. coli and k. pneumoniae with percentage about 40-60% and 35-25%, respectively, followed by C. freundii, E. aerogenes and P. mirabilis 42-44. K. pneumoniae and virulence strains of E. coli are the most important uropathogenic bacteria causing UTI 2. They are among the most common MDR bacteria causing recurrent UTI 45. Recently, K. pneumonia, E. coli, C. freundii and most gram-negative bacteria have shown their ability to acquire plasmid encoding for ESBL genes such as Bla-TEM, Bla-SHV and Bla-CTX-M and become highly resistant to different antibiotics and wide-spectrum of 3rd generation cephalosporins in hospitals and in community 5,13,46. About more than 200 different types of ESBLs have been discovered worldwide. Most of these genes are found in Enterobacteriaceae family especially in K. penumoniae 47. TEM and SHV are the ESBLs mostly found 48,49. Later, CTX-M was discovered in Germany in 1989 and mostly found in K. pneumoniae, E. coli and in other Enterobacteriaceae family 47,50. In the current study, almost all P. aeruginosa isolates from CKD patients were MDR with high resistance to antibiotics as compared with those isolates from WKD patients, but they harbored small numbers of ESBL genes. Livermore and Subedi et al suggested that P. aeruginosa carries multi-resistance plasmids less than K. pneumoniae and other members of Enterobacteriaceae family and develops resistance to cephalosporins due to mutational and intrinsic and acquired mechanisms 51,52.
Extended spectrum beta lactamases are enzymes not able to hydrolyze carbapenem and cephamycins but able to hydrolyze 3rd and 4th generation cephalosporins. These enzymes present a public health concern due to the high incidence in some members of Enterobacteriaceae family such as E. coli and K. pneumoniae in both hospitals and community 2,5,53. Some high virulence strains of gram-negative bacteria such as E. coli, K. pneumoniae and C. freundii are associated with UTI and if they remain untreated, these strains become capable of adhesion and colonization in the urinary tract of human and migrate to the bladder to cause cystitis and acute pyelonephritis and ultimately cause kidney damage and chronic kidney disease.
This was the first study in Iraq focused on bacterial isolates from urine of UTI patients infected with chronic kidney disease. This study suggested that all bacterial isolates from those patients were highly resistant to antibiotics and were more virulent as compared with the same isolates from urine of UTI patients without kidney disease. The reason may be related to ignoring the treatment of UTI or overusing antibiotics. Therefore, it is advised to be more careful regarding recurrent infection of UTI because this recurrent infection may cause dangerous complications in kidney such as chronic kidney disease or renal failure.
This work was made in and supported by University of Kufa, Faculty of Science, Department of Biology, Al-Najaf City, Iraq.
Conflict of Interest :
There was not any conflict of interest in this work.