Abstract
Background: The development of multi-antibiotic resistant bacteria, especially Gram-negative bacteria which are the major cause of hospital-acquired infections worldwide, had been increasing. Escherichia coli and Klebsiella sp. had become more resistant to different classes of antibiotics, and the treatment of infections caused by these bacteria had developed into a challenge in both developed and developing countries. This study had determined the multi-antibiotic resistance (MAR) patterns of Escherichia coli and Klebsiella sp. isolated from clinical inpatient and outpatient samples. Method: The present study had used 50 E. coli and 48 Klebsiella sp. isolates. Antibiotic susceptibility test had been carried out by using disk diffusion method, and the interpretation of results of the zones of inhibition had accorded with Clinical Laboratory Standards Institute (CLSI). The antibiotics used had included the following: streptomycin, ciprofloxacin, erythromycin, nitrofurantoin, amikacin, gentamicin, ofloxacin, cefepime, oxacillin, colistin sulfate, cefotaxime, ceftazidime, pefloxacine, and cloxacillin. Results: E. coli and K. pneumoniae had shown high-resistance patterns. E. coli had exhibited high resistance against cloxacillin (96%), oxacillin (96%), erythromycin (88%), and most especially streptomycin (98%). Similarly, K. pneumoniae had presented a high resistance to streptomycin (88%), cloxacillin (92%), oxacillin (92%), and colistin (92%). E. coli had presented the highest multidrug resistance with a MAR index of 1.00. A total of 17 E. coli isolates had shown resistance to the 14 antibiotics tested. Conclusion: E. coli and Klebsiella sp. in clinical isolates in outpatients and inpatients in Ibadan, Western Nigeria had demonstrated high antimicrobial resistance. Thus, such condition should be considered a major public health concern, and measures must be taken to establish the sources and drivers of this problem.
Keywords: Antibiotics Resistance, Escherichia coli, Klebsiella sp., Nigeria
Introduction
Antibiotic resistance (AR) is a global problem especially in the developing countries; this condition increasingly compromises the outcome of various infections that were until recently, treatable and remain the common infections in Africa.1 AR also threatens public health in both developed and developing countries.2 The development of resistance by bacteria to different antibiotics has resulted in the difficult treatment of infectious diseases. The infections caused by antibiotic resistant bacteria, most especially multi-resistance bacteria, can lead to serious health problems, such as long hospital stay, treatment failure, and death.3 The major factors causing the development of bacterial resistance include the indiscriminate use of antimicrobial agents in human and animal medicine, agriculture, and aquatic farming. Different mechanisms or their combination are used by bacteria in developing resistance to antibiotics; however, a particular mechanism may be dominant and can be identifiable.4 The presence of plasmids that contain one or more resistance genes, with each encoding a single AR phenotype, often causes the development of multiple AR (MAR) in bacteria.5 These AR genes can transfer to other bacteria of the same or different species.
MAR index is an effective, valid, and cost-effective method that is used in source tracking of antibiotic resistant organisms.6 MAR index is calculated as the ratio between the number of antibiotics that an isolate is resistant to and the total number of antibiotics the organism is exposed to. A MAR greater than 0.2 means that the high risk source of contamination is where antibiotics are frequently used.7
Escherichia coli is a Gram-negative, motile facultative anaerobic bacterium which may or may not be encapsulated. This species causes a wide range of infections in humans and is the most common causative agent in urinary tract infections. This bacterium is a commonly isolated in medical microbiology laboratories.1 E. coli is abundant in the human gastro-intestinal tract and also serves as a reservoir or carrier of antibiotic resistant genes.8 E. coli shows increasing resistance to different antibiotics especially to third generation cephalosporins.9
Klebsiella species are Gram-negative, rod shaped, nonmotile, facultative aerobic and anaerobic bacteria. Klebsiella sp. are an emerging threat to human health that causes both endemic and epidemic infections. Most hospital-acquired infections caused by Klebsiella sp. cause a challenge in their treatment because of the development of MAR strains. The resistance of Klebsiella strains to different generations of cephalosporins, especially the third generation, was first reported in 1981; since then, these bacteria have become more resistant to antibiotics.10
This study was carried out to determine the prevalence of multi-antibiotic resistant E. coli and Klebsiella sp. from clinical isolates.
Methodology
Collection of bacterial isolates
Preidentified 98 clinical isolates of Enterobacteriaceae were isolated from blood samples of both outpatients and inpatients from University College Hospital, Ibadan and had been in storage for less than a month. The present study examined 50 Escherichia coli and 48 Klebsiella sp. samples. Nutrient agar slant bottles contained the isolates were stored. The bacterial isolates were then transferred to Microbiology Laboratory of Pure and Applied Biology, Ladoke Akintola University of Technology, Oyo state, Nigeria for further study.
Antibiotic susceptibility test
Antibiotic susceptibility test was carried out by using disc diffusion (Kirby–Bauer) method on Mueller–Hinton agar plates. Bacterial suspension was prepared in 0.5 McFarland turbidity standard for each isolate and was swabbed on already prepared nutrient agar plates. The plates contained the impregnated antibiotics discs (Oxoid, UK), which were incubated at 37 °C for 24 h. The experiment used 14 antibiotics: streptomycin (10 μg), amikacin (30 μg), gentamicin (10 μg), ciprofloxacin (5 μg), pefloxacin (5 μg), ofloxacin (5 μg), erythromycin (15 μg), nitrofurantoin (300 μg), oxacillin (50 μg), cloxacillin (10 μg), colistin sulfate (25 μg), cefepime (5 μg), ceftazidime (30 μg), and cefotaxime (75 μg). Zones of diameter were measured and interpreted as susceptible, intermediate, and resistant in accordance with the recommendation of Clinical and Laboratory Standard Institute.11
Determination of MAR index
Determination of MAR index followed the procedure described by (5), in which the number of antibiotics an isolate is resistant to (a) is divided by the total number of the antibiotics used in the study (b). The calculating formula is shown below:
Statistical analysis
Data analysis used descriptive statistics, frequencies, and bivariate analyses (cross tabulations).
Results
The antibiotic susceptibility profiles of E. coli and Klebsiella strains were classified as “Resistant,” “Intermediate,” and “Susceptible” (Figures 1 and 2, respectively). The test of all the strains against 14 different antibiotics applied the Kirby–Bauer disc diffusion and underwent standardization and evaluation by the methods of the National Committee for the Clinical Laboratory Standards. The percentile distribution was obtained for the prevalence of resistance of isolates to different classes of antibiotics, including penicillin (oxacillin, cloxacillin), aminoglycosides (gentamycin, streptomycin, and amikacin), fluoroquinolones (ciprofloxacin, ofloxacin, and pefloxacin), macrolides (erythromycin), nitrofurantoin, extended spectrum cephalosporins (cefepime, ceftazidime, and cefotaxime), and colistin sulfate (Figures 3 and 4). Comparison focused on the resistance patterns between E. coli and Klebsiella (5). Table 1 shows the MAR indices of both E. coli isolates and Klebsiella.
Figure 1.
Comparison of sensitivity patterns to different antibiotics of E. coli isolated from inpatients and outpatients.
Figure 2.
Comparison of sensitivity patterns to different antibiotics of Klebsiella sp. isolated from inpatients and outpatients.
Figure 3.
Percentage of E. coli resistant to different antibiotics used in this study.
Figure 4.
Percentage of Klebsiella sp. resistant to different antibiotics used in this study.
Figure 5.
Comparison of resistance of E. coli and Klebsiella sp. to different antibiotics.
Table 1.
Frequency of resistance bacterial isolates and the MAR index.
Escherichia coli | Klebsiella spp. |
| |
No of Antibiotics No of Isolates MAR Index | No of Antibiotics No of Isolates MAR Index |
| |
Resistant to | Resistant to |
| |
1 0 - | 1 0 - |
| |
2 0 - | 2 0 - |
| |
3 1 0.21 | 3 0 - |
| |
4 1 0.29 | 4 1 0.29 |
| |
5 0 - | 5 0 - |
| |
6 0 - | 6 1 0.43 |
| |
7 2 0.50 | 7 1 0.50 |
| |
8 5 0.57 | 8 2 0.57 |
| |
9 5 0.64 | 9 3 0.64 |
| |
10 6 0.71 | 10 10 0.71 |
| |
11 6 0.79 | 11 4 0.79 |
| |
12 4 0.86 | 12 7 0.86 |
| |
13 3 0.93 | 13 12 0.93 |
| |
14 17 1.00 | 14 7 1.00 |
| |
Total 50 | 48 |
|
Discussion
The findings in this study reveal the high resistance rates of strains of Escherichia coli and Klebsiella sp. to commonly used antibiotics, such as streptomycin (98%), cloxacillin and oxacillin (96%), and colistin (84%), with relatively lower resistance rates to ciprofloxacin (66%); these findings are similar to those from neighboring countries, namely Kenya12 and Uganda.13 The findings can possibly result from the association of the isolates with AmpC enzymes. E. coli showed the highest resistance toward streptomycin, followed closely by cloxacillin, oxacillin, and erythromycin. However, the clinical isolates exhibited susceptibility to amikacin (36%), followed closely by ofloxacin (26%), cefotaxime (18%), gentamycin, and ciprofloxacin (22%). The susceptibility patterns are similar to those observed by Nahla et al.14 Klebsiella presented the highest resistance toward cefotaxime (93.75%), followed closely by cloxacillin, oxacillin, and colistin sulfate (91.67%). A considerable resistance occurred with streptomycin, similar to that in E. coli and as shown in the work of Kim et al.15 The present work revealed high susceptibility rates toward amikacin (33.37%), which is similar to the result found in E. coli, followed by gentamycin and cefepime (22.92%). This study also revealed that the highest multidrug resistance occurred in E. coli with MAR index of 1.00, and 17 out of 50 isolates (34%) were resistant to all 14 antibiotics. The MAR index of Klebsiella sp. was 0.93, which differs from that of another work5 that reported an index of 0.4; contrary to the low resistance to aminoglycosides reported previously, this work reported resistance of 87.5%, 68.75%, and 58.38% in streptomycin, gentamycin, and amikacin, respectively.
For Klebsiella sp., 7 isolates (14.6%) were resistant to all 14 antibiotics, whereas 12 isolates (25%) were resistant to 13 out of 14 antibiotics tested. These findings are similar to the results of Osundiya et al.5 where 66.7% of the Klebsiella isolates achieved a MAR index greater than 0.2.
The susceptibility of E. coli to fluoroquinolones approximated 80%, and this finding correlates with a review16 that reported an average of 80% susceptibility across different continents. In Khalit et al.17 Klebsiella was resistant to ampicillins and third generation cephalosporins, which corroborates the findings of this research.
Conclusion
These findings have implications for the choice of antibiotics for empirical management of infections and effective hospital infection control. Effective control must be in place to limit the spread of these pathogens. Further work should examine and identify the genes responsible for resistance and/or virulence in these organisms to device preventive and curative alternative therapies in the form of vaccines and antimicrobials, respectively.
References
- 1.Okeke IN, Laxminarayan R, Bhutta ZA, Duse AG, Jenkins P, O'Brien TF. Antimicrobial resistance in developing countries, Part 1: recent trends and current status. The Lancet Inf. Dis. 2005;58:481–493. doi: 10.1016/S1473-3099(05)70189-4. [DOI] [PubMed] [Google Scholar]
- 2.World Health Organization. Ten Threats to Global Health; 2018. https://www.who.int/emergencies/ten-threats-to-global-health-in-2019. Accessed online on March 29, 2019.
- 3. Sangiliyandi G, Yun-Jung C, Jin-Hoi K. Antibacterial Efficacy of Silver Nanoparticles on Endometritis caused by Prevotella melaninogenica and Arcanobacterum pyogenes in Dairy Cattle International Journal of Molecular Science 2018. PMID:29659523 [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Schweizer HP. Efflux as a mechanism of resistance to antimicrobials in Pseudomonas aeruginosa and related bacteria: unanswered questions. Genet. Mol. Res. 2003;2(1):48–62. [PubMed] [Google Scholar]
- 5.Osundiya OO, Oladele RO, Oduyebo OO. Multiple Antibiotic Resistance (MAR) Indices of Pseudomonas and Klebsiella species Isolates in Lagos University Teaching Hospital. Afr. J. Clin. Exper. Microbiol. 2013;14(3):164–168. [Google Scholar]
- 6.Sandhu R, Dahiya S, Sayal P. Evaluation of multiple antibiotic resistance (MAR) index and Doxycline susceptibility of Acinetobacter species among inpatients. Indian J. Microbiol. Res. 2016;3(3):299–304. [Google Scholar]
- 7.Rotchell D, Paul D. Multiple Antibiotic Resistance Index. Fitness and Virulence Potential in Respiratory Pseudomonas aeruginosa from Jamaica. Journal of Medical Microbiology. 2016;65:251–271. doi: 10.1099/jmm.0.000229. [DOI] [PubMed] [Google Scholar]
- 8.Eltai NO, Yassiner HM, Al-Thani AA, Abumadi MA, Ismal A, Ibrahim E et al. Prevalence of antibiotic resistant Escherichia coli isolates from fecal samples of food handlers in Qatar. Antimicrobial Resistant and Infection Control. 2018;71:78–84. doi: 10.1186/s13756-018-0369-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 9.Poirel L, Kieffer N, Liassine N, Thanh D, Nordmann P. Plasmid-mediated carbapenem and colistin resistance in a clinical isolate of Escherichia coli . Lancet Infect Dis. 2016;16:6–22. doi: 10.1016/S1473-3099(16)00006-2. [DOI] [PubMed] [Google Scholar]
- 10.Romanus II, Egwu OA, Ngozi AT, Chidiebuba NA, Chika EP. Extended spectrum beta-lactamase (ESBL) mediated resistance to antibiotics among Klebsiella pneumoniae in Enugu metropolis. Macedonian Journal of Medical Sciences (MJMS) 2009;2(3):196–199. [Google Scholar]
- 11.Clinical and Laboratory Standards Institute (CLSI) Performance Standards for Antimicrobial Susceptibility Testing. 2018; Pp. M100-S24.
- 12.Langata ML, Maingi JM, Musonye HA, Kiiru J, Nyamache AK. Antimicrobial Resistance Genes in Salmonella and Escherichia coli isolates from Chicken Droppings in Nairobi, Kenya. BMC Res Notes. 2019;12:22–4. doi: 10.1186/s13104-019-4068-8. Pp1-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Iramiot JS, Henry K, Joel B, Catherine K, Innocent BR, Benon BA. Multidrug Resistance among Escherichia coli and Klebsiella pneumonia carried in the gut of outpatients from pastoralist communities of Kasese district. Uganda. PLoS one. 2018;13(7):e0200093. doi: 10.1371/journal.pone.0200093. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Nahla OE, Hadi MY, Asmaa AA, Marwan AA, Ahmed I, Emad I et al. Prevalence of antibiotic resistant Escherichia coli isolates from fecal samples of food handlers in Qatar. Antimicrobial Resistance and Infection Control. 2018;7:78. doi: 10.1186/s13756-018-0369-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Kim SH, Wei CI, Tzou YM, An H. Multidrug-resistant Klebsiella pneumonia isolated from farm environments and retail products in Oklahoma. Journal of Food Production. 2005;68(10):2022–2029. doi: 10.4315/0362-028x-68.10.2022. [DOI] [PubMed] [Google Scholar]
- 16.Dong Sup Lee, Seung-Ju Lee, Hyung-Sop Chooe. Community-Acquired Urinary Tract Infection by Escherichia coli in the Era of Antibiotic Resistance. BioMed Research International. 2018;Volume 2018(Article ID 7656752) doi: 10.1155/2018/7656752. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 17.Khalit SK, Vladimir AA, Albert AR, Yuriy ND, Dina RS, Sergey AL et al. Virulene Factors and Antibiotic Resistance of Klebsiella pneumonia Strains Isolated from Neonates with Sepsis. Front Med (Lausanne) 2018;5:225. doi: 10.3389/fmed.2018.00225. 10.3389/fmed.2018.00225 Doi: [DOI] [PMC free article] [PubMed] [Google Scholar]