- Research article
- Open Access
Molecular epidemiology of multidrug resistant extended spectrum beta-lactamase producing Klebsiella pneumoniae at a Jamaican hospital, 2000 - 2004
© Christian et al; licensee BioMed Central Ltd. 2010
Received: 10 February 2009
Accepted: 28 January 2010
Published: 28 January 2010
The accurate identification of a pathogen beyond the species level is critical in epidemiological studies and investigations of nosocomial outbreaks of infection. The clonal relatedness of 66 multidrug resistant (MDR) strains of extended spectrum beta-lactamase (ESBL) producing K. pneumoniae isolated from clinical specimens from hospitalized patients at a Jamaican hospital during a 5 year period were determined by pulsed field gel electrophoresis (PFGE).
A total 10 different ESBL producing K. pneumoniae genotypes designated Clones I-X were found. The most frequently occurring strains belonged to Clones I (21/66, 32%), II (15/66, 26%), III (13/66, 20%) and IV (8/66, 12%) which accounted for 86% (57/66) of ESBL producing K. pneumoniae strains over the 5 year period. The remaining 9 (14%) cases of ESBL producing K. pneumoniae were due to strains of Clones V-X. The 4 predominant clones persisted for several years in the hospital.
The clonal and temporal distribution of the MDR ESBL producing K. pneumoniae strains among clinical service areas did not suggest outbreaks of the organism during the period of study. Instead the molecular epidemiology of ESBL producing K. pneumoniae at this hospital was more representative of an endemic persistence of clones of the organism with limited dissemination from patient to patient. Further studies to investigate the factors which determine the emergence and persistence of MDR ESBL producing K. pneumoniae in Jamaican hospitals and their impact on clinical and economic outcomes at such institutions would be useful.
The increasing prevalence of multidrug resistant (MDR) pathogens causing nosocomial infection constitutes a major health problem . Klebsiella pneumoniae ranks among the top ten organisms causing blood stream infection, pneumonia and other invasive infections in hospitalized patients in different countries [2–4]. An increasing prevalence of multidrug resistant strains of K. pneumoniae which possess extended spectrum beta-lactamases (ESBL) enzymes, encoded by plasmid-borne genes which confer resistance to broad spectrum cephalosporins and other antibiotics used to treat serious infection has been widely reported . Multidrug resistance contributes to unfavourable clinical outcomes, impacts the utilization of hospital resources, increases the burden of effective infection control practice and the overall health economic cost [1, 2].
The prevalence of ESBL producing strains of K. pneumoniae differs between countries. In the developing world a recent study from Jamaica reported that almost one-fifth of K. pneumoniae isolates at a tertiary referral teaching hospital were ESBL producers . The presence of ESBL-producing Gram negative bacilli in hospitals in other Caribbean islands also has been reported [6, 7].
This study reports the clonal relationships of MDR ESBL producing K. pneumoniae at a Jamaican hospital.
The majority of the MDR K. pneumoniae isolates were from urine specimens (31/66, 47%), blood (9/66, 13%) and sputum (7/66, 10%). Almost a third (19/66, 29%) were isolated from children admitted to paediatric wards while 15% (10/66) were from intensive care unit (ICU) patients. The remaining 37 strains were isolated from patients admitted to medical (n = 15), surgical (n = 9), special care nursery (n = 5), orthopaedic (n = 5) and obstetrics/gynaecological services (n = 3).
Antibiotic susceptibilities of 66 strains of multidrug resistant (MDR) extended spectrum beta - lactamase (ESBL) producing K. pneumoniae, 2000-2004
All 66 (100%) isolates of MDR K. pneumoniae tested positive for ESBL production in the double- disc synergy test and the E-Test ESBL screen. The E-test ESBL screen showed that all isolates (66/66; 100%) had MIC ceftazidime and cefepime > 32 μg/ml and > 16 μg/ml, respectively. The MICs were subsequently determined by the agar gel dilution method which revealed MICs ranging from 32 - >1024 μg/ml for ceftazidime and 2 - >1024 μg/ml for cefepime indicating ESBL production by all (66/66; 100%) strains.
Temporal distribution of multidrug resistant (MDR) extended spectrum beta-lactamase (ESBL) producing K. pneumoniae clones by hospital service during 2000-2004.
Number of Isolates
I, II, III, IX
Paediatrics, Medicine, Orthopaedics, Obstetrics & Gynaecology
I, II, III, IV
Intensive care unit, Paediatrics, Surgery, Special Care Nursery, Orthopaedics, Obstetrics & Gynaecology
I, II, III, IV
Intensive care unit, Paediatrics, Medicine, Surgery, Special Care Nursery, Orthopaedics
I, II, III, IV, V, VI, VII, VIII, X
Intensive care unit, Paediatrics, Medicine, Surgery, Special Care Nursery
III, IV, VI
The antibiotypes and pulsed field gel electrophoresis (PFGE) clones of the 66 multidrug resistant (MDR) extended spectrum beta-lactamase producing (ESBL) K. pneumoniae strains, 2000-2004
Resistance Profile †
Clones of ESBL K. pneumoniae
NA, Nor, Cip, Lev, Cn, Tob, Min, F, SXT
I, II, III, VIII
NA, Nor, Cip, Lev, Cn, Tob, Min, SXT
NA, Nor, Cip, Lev, Cn, Tob, SXT
Lev, Cn, Tob, Min, F, SXT
I, II, IV
NA, Cn, Tob, F, SXT
NA, Cn, Tob, SXT
I, II, III, IV, VI
I, II, III, IV, VI
Cn, Tob, F, SXT
I, III, IV, IX, X
Cn, Tob, Min, F, SXT
The clonal and temporal distributions of the MDR ESBL producing K. pneumoniae strains among clinical service areas in the hospital do not suggest outbreaks of the organism at that institution during the period studied. Instead the epidemiology of ESBL producing K. pneumoniae at this hospital is more representative of an endemic persistence of clones of the organism with limited dissemination from patient to patient. However, the persistence of related clones over the time period suggests patient to patient transmission or healthcare worker to patient transmission. The emergence and reemergence of Clone I in the ICU during a 6-month period during 2001 is consistent with this concept. Also the results suggest that there has been transmission of some common strains including PFGE Clones I, II and III, over time in the hospital during 2000-2004. This might have been more evident if asymptomatic patients had been screened for MDR K. pneumoniae colonization. The presence of asymptomatically colonized patients may explain the intermittent appearances of certain strains over time in various hospital services. The epidemiology of ESBL producing K. pneumoniae at this hospital proved complex and, as explained by Branger et al , may involve the spread of self-transferable plasmids as well as clonal spread .
Studies conducted in hospitals elsewhere have reported the spread of single clones of MDR K. pneumoniae among patients hospitalized over protracted periods of time [8, 9]. In the present study ESBL producing K. pneumoniae strains belonging to Clone III persisted in the hospital over the 5-year period studied. During 2002 the year in which the largest number of cases, especially of paediatric cases, was seen different genotypes of the organism coexisted in patients on the same wards. This makes it less clear whether or not outbreaks caused by single different strains or involving the 4 endemic clones in the hospital had occurred. The prevalence of ESBL producers at the University Hospital of the West Indies for that year was 18% . The factors contributing to the increasing incidence of ESBL producing K. pneumoniae during 2002 have not been clearly defined at this hospital . A number of risk factors for increased colonization with MDR K. pneumoniae including the use of third generation cephalosporins have been reviewed .
Other interesting observations from the study include the cases of long stay and repeat patients who remained colonized or had repeat infections with the same genotype after long periods of time and those with concomitant infections with different genotypes of ESBL producing K. pneumoniae. Branger et al  reported the case of a patient colonized with the same ESBL producing K. pneumoniae strain for 10 months . Sequential or simultaneous isolation of unrelated strains of ESBL producing K. pneumoniae from individual patients has been reported by others . Weller et al  reported that multiple subvariants of a strain could persist in an infective population without any one subvariant becoming dominant [11, 12].
The previously reported decreased susceptibility to aminoglycosides, fluoroquinolones and trimethoprim/sulfamethoxazole in ESBL producing K. pneumoniae was also observed in this study . The data on antibiotypes provided additional evidence in support of the clonality of the PFGE genotypes. The predominant ESBL producing K. pneumoniae genotypes I, II, III and IV had the quinolone-resistant antibiotype R1. This might have contributed to the endemic persistence of these clones in the hospital . The more susceptible clones were probably not endemic strains at the UHWI and may have been harboured by patients who were already colonized on admission . Notably, the PFGE genotypes V, VII and VIII isolated from ICU patients also had the more resistant antibiotype R1 though found in lower numbers. A number of factors including aggressive antibiotic therapy, prolonged hospitalization and the performance of invasive procedures are well documented contributors to the increased risk of infection with nosocomial strains of MDR K. pneumoniae in patients admitted to the ICU .
Clearly different antibiotic susceptibility patterns distinguish different strains of ESBL producing K. pneumoniae as shown in the current study. However, antibiotic susceptibility testing has relatively limited utility as a typing system in epidemiologic studies not only because of phenotypic variation but also because antibiotic resistance is under extraordinary selective pressure in contemporary hospitals . The selective pressure from antimicrobial therapy may alter the antimicrobial susceptibility profile of an organism, such that related organisms show different resistance profiles . Graffunder et al  found a correlation between the selective pressure of antimicrobial agents identified as risk factors for ESBL producing organisms and the presence of related resistance genes residing on the plasmids . Woodford et al  also suggests that antibiotic pressure may have been a factor for initial colonization of patients and the development of further resistance by the organism .
The limitations of the study are those attending studies involving retrospective data collection, the disproportionately small number of ESBL producing K. pneumoniae strains from some clinical service areas, the long time period over which the isolates were collected, the lack of surveillance cultures to detect asymptomatic, colonized patients with MDR ESBL producing K. pneumoniae and the limited available epidemiologic data to compare with the PFGE typing results. During the extended period of study advances in medical technology, changes in patient population, formulary restrictions and changes in standards of practice or infection control measures may affect the results .
In summary the results showed clonal diversity of MDR ESBL producing K. pneumoniae, elements of its temporal distribution which were suggestive of endemic persistence and dissemination of this organism between patients at this hospital, the extent of which was not fully ascertained. Further studies which investigate the factors which determine the emergence and persistence of ESBL producing K. pneumoniae in Jamaican hospitals and the impact on clinical and economic outcomes at such institutions would be useful.
All clinical isolates (n = 66) of MDR K. pneumoniae from clinical specimens collected from 57 patients admitted to the University Hospital of the West Indies (UHWI), Kingston, Jamaica, a tertiary care referral centre, between June 2000 and April 2004 were stored in tryptose soy broth at -70°C until required. Standard microbiological procedures were followed for the different clinical specimens . Bacterial isolates were identified and the initial antibiotic susceptibility testing was done using the Vitek automated system (Biomerieux, Durham, North Carolina, U.S.A.). The appropriate antibiotic panel for each type of specimen was used as recommended by the manufacturer. The breakpoints for antibiotic susceptibility were determined according to the guidelines of the Clinical and Laboratory Standards Institute (CLSI) . The antibiotics tested included amoxicillin/clavulanic acid, ampicillin, carbenicillin, cefazolin, ceftriaxone, cefuroxime, cephalothin, ceftazidime, ciprofloxacin, gentamicin, levofloxacin, minocycline, nalidixic acid, nitrofurantoin, norfloxacin, ticarcillin/clavulanic acid, tobramycin, trimethoprim/sulfamethoxazole and meropenem. The MDR strains of K. pneumoniae were classified as organisms showing resistance to at least three classes of antibiotics including ceftazidime . Resistance to ceftazidime identified by Vitek was used as the initial screening test for the presence of ESBL which was confirmed by E-test (AB Biodisk, Solna, Sweden) and double-disc synergy test which were performed according to the manufacturer's instructions and CLSI guidelines , respectively. A positive double disc synergy test was defined as enhancement of the zones of inhibition for ceftazidime and cefotaxime in the presence of clavulanic acid.
The MDR ESBL producing K. pneumoniae strains were assigned antibiotypes based on their resistance patterns.
Pulsed Field Gel Electrophoresis
Pulsed-field gel electrophoresis (PFGE) was used to determine the relatedness of the ESBL producing strains of K. pneumoniae. The PFGE was performed as described previously with modifications . Electrophoresis was carried out in 0.5 × TBE buffer using the Chef Mapper XA pulsed field electrophoresis system (Biorad, Hercules, California, U.S.A.). The conditions were 6 V/cm for 21 h at 12°C, with the pulse time ramped linearly from 1 s to 40 s. The molecular size marker included for comparison was Saccharomyces cerevisiae (Biorad, Hercules, California, U.S.A.). Following electrophoresis the gels were stained with ethidium bromide and photographed under ultraviolet light. The banding patterns were compared based on the criteria described by Tenover et al . Isolates were considered indistinguishable if their restriction patterns had the same number of corresponding bands of the same apparent size and closely related for differences of 3 bands. Isolates which differed by 4 or more bands were considered unrelated.
The study was approved by the Ethics Committee in the Faculty of Medical Sciences of the University of the West Indies, Mona.
We thank Mrs Lois Rainford, Mrs Charmaine Parkes and our colleagues in the Bacteriology Section of the Microbiology Department, University of the West Indies for their assistance.
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