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Antimicrob Agents Chemother. 2008 August; 52(8): 2818–2824.
Published online 2008 May 27. doi:  10.1128/AAC.00171-08
PMCID: PMC2493136

Molecular Characterization and Epidemiology of Extended-Spectrum- β-Lactamase-Producing Escherichia coli and Klebsiella pneumoniae Isolates Causing Health Care-Associated Infection in Thailand, Where the CTX-M Family Is Endemic[down-pointing small open triangle]


Extended-spectrum β-lactamase (ESBL)-producing Escherichia coli and Klebsiella pneumoniae have rapidly spread worldwide and pose a serious threat for health care-associated (HA) infection. We conducted molecular detection and characterization of ESBL-related bla genes, including blaTEM, blaSHV, blaCTX-M, blaVEB, blaOXA, blaPER, and blaGES, among 362 isolates of ESBL-producing E. coli (n = 235) and ESBL-producing K. pneumoniae (n = 127) collected from patients who met the definition of HA infection at two major university hospitals in Thailand from December 2004 to May 2005. The prevalence of ESBL-producing E. coli and ESBL-producing K. pneumoniae, patient demographics and the susceptibilities of these bacteria to various antimicrobial agents were described. A total of 87.3% of isolates carried several bla genes. The prevalence of blaCTX-M was strikingly high: 99.6% for ESBL-producing E. coli (CTX-M-14, -15, -27, -40, and -55) and 99.2% for ESBL-producing K. pneumoniae (CTX-M-3, -14, -15, -27, and -55). ISEcp1 was found in the upstream region of blaCTX-M in most isolates. Up to 77.0% and 71.7% of ESBL-producing E. coli and ESBL-producing K. pneumoniae, respectively, carried blaTEM; all of them encoded TEM-1. ESBL-producing K. pneumoniae carried blaSHV at 87.4% (SHV-1, -2a, -11, -12, -27, -71, and -75) but only at 3.8% for ESBL-producing E. coli (SHV-11 and -12). bla genes encoding VEB-1 and OXA-10 were found in both ESBL-producing E. coli (8.5% and 8.1%, respectively) and ESBL-producing K. pneumoniae (10.2% and 11.8%, respectively). None of the isolates were positive for blaPER and blaGES. Pulsed-field gel electrophoresis analysis demonstrated that there was no major clonal relationship among these ESBL producers. This is the first study to report CTX-M-3, CTX-M-27, CTX-M-40, SHV-27, SHV-71, and SHV-75 in Thailand and to show that CTX-M ESBL is highly endemic in the country.

Extended-spectrum β-lactamases (ESBLs) have spread threateningly in many regions of the world and presently comprise over 300 variants ( A typical characteristic of ESBLs is their ability to hydrolyze oxyiminocephalosporins and aztreonam while being inhibited by β-lactamase inhibitors (8, 30). ESBL-producing organisms have achieved notoriety for causing nosocomial infections (7, 30). Based on multivariable analysis, it was shown that exposure to oxyiminocephalosporins and transfer from another hospital were among identified risk factors associated with infection due to ESBL producers in Thailand (2). Therefore, health care interactions appeared to play a role in the acquisition of ESBL producers.

The first ESBL, SHV-2, was reported from a strain of Klebsiella ozaenae in 1983 (21). Thereafter, the number of ESBL variants occurring through amino acid mutations has progressively increased while demonstrating geographic variations (38). SHV-type ESBLs are mostly derivatives of a non-ESBL SHV-1 and quickly invaded several continents (7, 29). The majority of plasmid-mediated β-lactamases, namely, TEM-1 or, less frequently, TEM-2, are broad-spectrum β-lactamases, which, in contrast to ESBLs, do not hydrolyze oxyiminocephalosporins or aztreonam. Several TEM-1 derivatives, however, confer ESBL properties and are prevalent in North America (30). The CTX-M family, first described in 1992 (3), is known to be the most dominant non-TEM, non-SHV ESBL among Enterobacteriaceae and is recognized as a rapidly growing family of ESBLs that selectively prefer to hydrolyze cefotaxime rather than ceftazidime (6). However, variants of CTX-M with increased hydrolyzing activity against ceftazidime have emerged (20, 31, 32). The insertion sequence (IS) element ISEcp1 is commonly present in the upstream region of the CTX-M gene and is likely responsible for the transposition process of the gene (34). Other ESBL enzymes are less often encountered. VEB-1 ESBL was identified among Enterobacteriaceae and Pseudomonas aeruginosa isolates and was previously reported from Thailand (14, 15). Among members of the OXA family, a class D β-lactamase originating in P. aeruginosa, derivatives of OXA-2 and -10 show activity considered to be ESBL like. The PER and GES families, both first identified in P. aeruginosa, are also among β-lactamase families exhibiting ESBL-like activities. Nevertheless, epidemiologic data on these less common ESBLs are very limited. Several surveillance studies revealed a relatively high prevalence of ESBL-producing organisms in the Asia-Pacific area (4, 17). In particular, CTX-M ESBL is believed to be the dominant type in East Asia, since it has appeared or caused outbreaks in many countries (6, 22). In Thailand, however, studies pertaining to molecular characterization of ESBL-conferring bla genes and the epidemiology of ESBL producers, especially among health care-associated (HA) infections, are rare. We report here the first extensive phenotypic and genetic studies of ESBL-producing Escherichia coli and Klebsiella pneumoniae causing HA infections in Thailand, as well as patient demographics, the epidemiology of ESBL genes, and molecular typing of isolates by pulsed-field gel electrophoresis.


Study setting, patient demographics, and clinical specimens.

This study included all clinical specimens submitted for bacterial culture at the microbiology laboratories of two major university hospitals in Thailand, the 2,400-bed Siriraj hospital (Bangkok) and the 500-bed Thammasart hospital (Pratumthani province, north of Bangkok) from December 2004 to May 2005. ESBL producers are not limited to causing nosocomial infections; community-onset infections have also been reported in Thailand (1, 20). Most community-onset cases, however, have been related to health care. In this study, we focused on patients who had HA infections. An HA infection was previously defined (2) as an infection that met one of the following criteria: (i) it occurred more than 48 h after admission to a hospital, (ii) it occurred 48 h or less after admission in a patient who had been hospitalized during the 30 days prior to admission to our hospitals, or (iii) it occurred in a patient who was transferred from another hospital or nursing home. All patients who had infections due to ESBL-producing E. coli or ESBL-producing K. pneumoniae and met the definition of HA infection were reviewed for their demographics, including age, sex, the hospital unit where they had received medical service, and the types of clinical specimens. The χ2 test was used where appropriate to compare discrete variables, which were considered statistically significant at a P value of <0.05. This study was approved by the ethics committees of both institutions.

Bacterial isolates, antimicrobial susceptibility testing, and detection of ESBL.

Bacteria recovered from clinical specimens were identified by standard biochemical methods. The production of ESBL was tested for all E. coli and K. pneumoniae isolates by using the combination disk method based on the inhibitory effect of clavulanic acid according to the Clinical and Laboratory Standards Institute (CLSI) criteria (13). Consecutive nonduplicate clinical isolates of ESBL-producing E. coli and ESBL-producing K. pneumoniae were collected for further investigation. The MIC50 and MIC90 values of six antimicrobial agents (ceftazidime, cefotaxime, ceftriaxone, imipenem, ertapenem, and meropenem) for ESBL-producing isolates were determined by the Etest method (AB Biodisk, Solna, Sweden). All isolates were also tested against non-β-lactam agents, including tetracycline, amikacin, gentamicin, cotrimoxazole, and ciprofloxacin, by the standard disk diffusion method, and the results were interpreted based on the CLSI guidelines (13). Isolates shown to be resistant to at least three different classes of antimicrobial agents were determined to be multidrug resistant (MDR). All antimicrobial disks used for susceptibility testing were obtained from BD BBL Sensi-Disc (Becton Dickinson, Sparks, MD). E. coli ATCC 25922 and K. pneumoniae ATCC 700603 were used for quality control processes as recommended by CLSI (13).

DNA manipulation, PCR, and nucleotide sequencing.

Because most ESBL genes were shown to be plasmid mediated, plasmid DNA was extracted and purified using the Nucleospin Plasmid kit (Macherey-Nagel, Düren, Germany). PCR amplification of bla genes, including blaTEM, blaSHV, blaCTX-M, blaVEB, blaOXA, blaPER, and blaGES, was performed with Taq DNA polymerase (Invitrogen, Carlsbad, CA) using primers listed in Table Table1.1. PCR detection of blaOXA was focused on the blaOXA-2 and blaOXA-10 groups, whose derivatives have shown ESBL characteristics. The PCRs were conducted in a GeneAmp PCR system 9600 (Perkin-Elmer, Norwalk, CT) under the conditions specified in the reference sources (Table (Table1).1). Detection of IS elements in the upstream region of blaCTX-M was performed for all isolates carrying blaCTX-M by PCR using primers and conditions described previously (20, 34). All PCR amplicons were verified by gel electrophoresis on a 2.0% (wt/vol) SeaKem LE agarose gel (FMC BioProducts, Rockland, ME). The gels were stained with ethidium bromide (0.5 μg/ml). Purifications of PCR amplicons were carried out by using a Nucleospin Extract II kit (Macherey-Nagel). PCR products of bla genes and IS elements were subjected to bidirectional nucleotide sequencing using PCR primers to determine their molecular types. DNA sequences were analyzed with the 3100 Genetic Analyzer (Applied Biosystems, Foster City, CA) according to the manufacturer's recommendations.

Primers used for PCR amplification of bla genes and IS element

Conjugation assay.

To demonstrate that bla genes detected by PCR were located on plasmids, a resistance transfer experiment using a conjugation assay (broth mating) was performed for selected isolates that carried at least four bla genes as described previously (16). E. coli JM109 was used as the recipient. Transconjugants were selected on MacConkey agar (Oxoid, Basingstoke, United Kingdom) supplemented with cefotaxime (2 mg/liter). Antimicrobial susceptibility, a confirmatory test for ESBL phenotype, PCR detection, and DNA sequencing of bla genes were performed for transconjugants by the procedures mentioned above.

Pulsed-field gel electrophoresis (PFGE).

For molecular typing, chromosomal DNA of ESBL-producing E. coli and ESBL-producing K. pneumoniae were obtained for comparison by PFGE analysis using a CHEF Mapper XA apparatus (Bio-Rad Laboratories, Hercules, CA). Agarose plugs containing bacterial DNA were prepared and processed for PFGE as described elsewhere (19). Restriction analysis of chromosomal DNA with XbaI (New England BioLabs, Beverly, MA) was performed, and separation of DNA was carried out by using 1% pulsed-field gel agarose (Bio-Rad Laboratories, La Jolla, CA). DNA banding patterns were compared using Fingerprinting II Software, version 3.0 (Bio-Rad Laboratories, Hercules, CA). The unweighted pair group method using arithmetic averages was used to generate a dendrogram with the position tolerances set at 1.5%. The Dice coefficients were used for band similarity measurements to determine DNA relatedness. Isolates were considered to be clonally related if the Dice coefficient correlation was over 80%, which corresponds to the “possibly related” category according to the criteria suggested by Tenover et al. (36).


Prevalence of ESBL-producing E. coli and ESBL-producing K. pneumoniae and patient demographics.

During the study period, a total of 2,777 patients were identified as having infections due to E. coli (n = 1,776) or K. pneumoniae (n = 1,001) at both major tertiary-care centers. Among these patients, 235 and 127 had infections due to ESBL-producing E. coli and ESBL-producing K. pneumoniae, respectively, and met the criteria for HA infection. Thus, the prevalences of ESBL-producing E. coli and ESBL-producing K. pneumoniae causing HA infections were 13.2% and 12.7%, respectively. Patient demographics are shown in Table Table2.2. Female patients predominated, particularly for ESBL-producing E. coli infection. A majority of patients were over 60 years old. Most patients had been hospitalized in medical or surgical units. ESBL-producing K. pneumoniae was more dominant among patients admitted to intensive-care units, while ESBL-producing E. coli was more common in outpatient departments. For both ESBL-producing E. coli and ESBL-producing K. pneumoniae, a majority of isolates were recovered from urine specimens.

Demographics of and specimen types from patients who had HA infections due to ESBL-producing E. coli or K. pneumoniae

Susceptibility of ESBL-producing E. coli and ESBL-producing K. pneumoniae to antimicrobial agents.

The MIC50s/MIC90s (μg/ml) of ceftazidime, ceftriaxone, cefotaxime, imipenem, ertapenem, and meropenem for ESBL-producing E. coli were 32/256, >256/>256, 256/>256, 0.25/0.38, 0.094/0.38, and 0.047/0.094, respectively, and those for ESBL-producing K. pneumoniae were 128/>256, 256/>256, 128/>256, 0.25/0.38, 0.094/0.38, and 0.047/0.125, respectively. All isolates demonstrated high MICs of oxyiminocephalosporin while they remained in the susceptible range for carbapenems. The rates of resistance to non-β-lactam agents, including tetracycline, amikacin, gentamicin, cotrimoxazole, and ciprofloxacin, for ESBL-producing E. coli were 87.5%, 12.5%, 66.3%, 72.7%, and 78.1%, respectively, and for ESBL-producing K. pneumoniae they were 85.7%, 28.6%, 76.4%, 72.1%, and 76.6%, respectively. Up to 72.3% and 81.9% of ESBL-producing E. coli and ESBL-producing K. pneumoniae, respectively, expressed the MDR phenotype.

Molecular characterization of ESBL genes.

All ESBL-producing isolates were subjected to PCR experiments to detect ESBL genes, including blaTEM, blaSHV, blaCTX-M, blaVEB, blaOXA (OXA-2 and OXA-10 groups), blaPER, and blaGES. Only blaTEM, blaSHV, blaCTX-M, blaVEB, and blaOXA-10 groups were detected in 77.0%, 3.8%, 99.6%, 8.5%, and 8.1% of ESBL-producing E. coli and 71.7%, 87.4%, 99.2%, 10.2%, and 11.8% of ESBL-producing K. pneumoniae, respectively (Tables (Tables33 and and4).4). None of the blaOXA-2 group, blaPER, and blaGES were present in all isolates. Three hundred and sixteen out of 362 isolates (87.3%) carried several bla genes (up to five genes). blaCTX-M was most prevalent in both ESBL-producing E. coli and ESBL-producing K. pneumoniae. Among ESBL-producing E. coli isolates, blaCTX-M encoding CTX-M-14, -15, -27, -40, and -55 was found in 43.6%, 37.2%, 1.3%, 0.4%, and 17.5% of isolates, respectively. Among ESBL-producing K. pneumoniae isolates, blaCTX-M encoding CTX-M-3, -14, -15, -27, and -55 was found in 3.2%, 52.4%, 38.9%, 0.8%, and 4.7% of isolates, respectively. ISEcp1 was present in the upstream region of blaCTX-M in 357 isolates (99.2%). Upon sequencing of the blaCTX-M upstream DNA, IS10, IS26, and IS903 were also found interrupting ISEcp1 in two, nine, and five isolates, respectively. The structural analysis of ISEcp1-carrying blaCTX-M upstream DNA is shown in Table Table5.5. blaSHV genes from ESBL-producing E. coli encoded SHV-11 and -12 at 1.2% and 2.6%, respectively, while those from ESBL-producing K. pneumoniae encoded SHV-1, -2a, -11, -12, -27, -71, and -75 at 20.5%, 3.1%, 24.4%, 34.6%, 1.6%, 1.6%, and 1.6%, respectively. All PCR products of blaTEM, blaVEB, and blaOXA-10 groups encoded TEM-1, VEB-1, and OXA-10, respectively. TEM-1, SHV-1, SHV-11, and OXA-10 are not classified as ESBLs. Based on the conjugation assay of selected isolates, all bla genes detected were able to be transferred to transconjugants, suggesting that they were plasmid mediated.

Molecular characterization of bla genes among ESBL-producing E. coli isolates (n = 235)
Molecular characterization of bla genes among ESBL-producing K. pneumoniae (n = 127)
Analysis of the blaCTX-M upstream DNA region

Antimicrobial susceptibilities of CTX-M-producing isolates.

Based on amino acid sequence similarities, CTX-M-3, -15, and -55 are classified in the CTX-M-1 subgroup, while CTX-M-14 and -27 are members of the CTX-M-9 subgroup. Therefore, CTX-M-producing isolates identified in this series mainly produced ESBLs in either the CTX-M-1 or -9 subgroup. Analyses of MIC90s and susceptibility patterns of these two subgroups are shown in Table Table6.6. Without other bla genes, the CTX-M-1 subgroup exhibited a level of resistance to ceftazidime fourfold-higher than what appeared for the CTX-M-9 subgroup. The MIC90 of ceftazidime among the CTX-M-9 subgroup was elevated but remained in the susceptible range. Nevertheless, when other bla genes were present, the CTX-M-9 subgroup showed a significant increase in the MIC90 of ceftazidime to a level similar to that of the CTX-M-1 subgroup. Both subgroups demonstrated no significant difference in MICs of other β-lactam agents. Interestingly, isolates carrying the CTX-M-1 subgroup alone significantly exhibited reduced susceptibilities to tetracycline and cotrimoxazole compared to the CTX-M-9 subgroup (P < 0.05). In addition, when other bla genes were detected, the susceptibilities to ciprofloxacin and, for the CTX-M-9 subgroup only, tetracycline and cotrimoxazole were significantly decreased.

Antimicrobial susceptibilities of isolates carrying blaCTX-M in the CTX-M-1 and CTX-M-9 subgroups

PFGE typing.

To study the clonal relationships of ESBL-producing isolates, molecular typing by PFGE was analyzed for both ESBL-producing E. coli and ESBL-producing K. pneumoniae. Chromosomal DNAs of 229 ESBL-producing E. coli and 127 ESBL-producing K. pneumoniae isolates were available for PFGE typing. Banding patterns were not obtained from six ESBL-producing E. coli isolates because their DNAs were consistently autodigested. The results showed that there were few isolates demonstrating DNA relatedness, and only isolates producing the same type of CTX-M exhibited such genetic relationships (see the supplemental material). Therefore, based on CTX-M types, all clusters according to PFGE profiles of ESBL-producing E. coli and ESBL-producing K. pneumoniae are shown in Table Table7.7. Clonality was determined if isolates showed over 80% similarity of PFGE patterns. In addition, there were some clusters among both ESBL-producing E. coli and ESBL-producing K. pneumoniae that exhibited over 60%, but less than 80%, similar banding patterns, suggesting that these clusters may be distantly related. Upon a retrospective chart review, all of these related isolates occurred sporadically and randomly within different hospital units and were recovered from a variety of specimen sources. A majority of isolates showed unique, unrelated PFGE profiles (Table (Table7)7) and were unlikely to be considered the cause of an epidemic.

PFGE profiles of ESBL-producing E. coli and K. pneumoniae based on CTX-M type


The spread of ESBL-producing bacteria has been strikingly rapid worldwide, indicating that continuous monitoring systems and effective infection control measures are absolutely required. Therapeutic options for infections due to ESBL producers have also become increasingly limited. Health care interactions including the use of antibiotics, particularly oxyiminocephalosporins, and hospital transfer are among well-defined risk factors for acquisition of ESBL-producing bacteria (1, 2, 24). However, epidemiologic data and characterization of ESBL-producing isolates causing HA infection in Thailand are still rarely documented. Our results showed that a majority of patients were elderly and those who had urinary tract infections. It was not surprised that females had a higher prevalence of infection due to ESBL producers than males, since females are more vulnerable to urinary tract infection. ESBL-producing K. pneumoniae appeared to be an important cause of infection among patients in intensive-care units. All isolates remained susceptible to carbapenems. Besides high MICs of oxyiminocephalosporins, a majority of isolates were also resistant to non-β-lactam agents, especially tetracycline, gentamicin, cotrimoxazole, and ciprofloxacin, resulting in a very high percentage of MDR isolates. ESBL-producing K. pneumoniae generally appeared to be more resistant and showed an MDR phenotype at a higher rate than ESBL-producing E. coli.

Among 362 ESBL-producing isolates, 87.3% carried several bla genes, which can probably account for a high-level β-lactam-resistant phenotype. Although CTX-M types of ESBLs have been known for their rapid spread in Europe and Asia (6, 25), it was remarkable that in this study, 99.6% of ESBL-producing E. coli and 99.2% of ESBL-producing K. pneumoniae isolates carried blaCTX-M. We therefore report the highest prevalence, to our knowledge, of blaCTX-M among ESBL-producing E. coli and ESBL-producing K. pneumoniae and demonstrate that CTX-M-type ESBL is highly endemic in Thailand. Interestingly, a survey at a university hospital in northeastern Thailand from 1994 to 1996 revealed that, among 32 isolates of ESBL-producing E. coli and ESBL-producing K. pneumoniae, blaSHV was most predominant while blaCTX-M was not detected (11). The first detection of blaCTX-M in Thailand was later documented from a study of 48 Enterobacteriaceae isolates recovered during 1998 and 1999 at this hospital, where the prevalence of blaCTX-M was 52% (CTX-M-9 only) and subsequently increased to 65% among 52 isolates collected in 2003 (CTX-M-15, 44%; CTX-M-14, 11%; and CTX-M-9, 10%) (12). A survey in a neighboring country, Vietnam, during 2000 and 2001 demonstrated a low prevalence of ESBL-producing E. coli (4.4%) and ESBL-producing K. pneumoniae (3.0%) (9). In that series, CTX-M ESBLs were present in 18.7% of ESBL-producing E. coli and 61.5% of ESBL-producing K. pneumoniae, and CTX-M-14 was the only predominant type in which CTX-M-15 was not detected. Therefore, these surveys indicated not only geographic variations, but also increasing trends in the prevalence of CTX-M ESBLs.

In our study, a majority of ESBL-producing E. coli isolates possessed CTX-M-14, -15, and -55, while only CTX-M-14 and -15 were predominant among ESBL-producing K. pneumoniae. CTX-M-55, a member of the CTX-M-1 subgroup, is a novel ceftazidime-resistant CTX-M recently reported by our group for its emergence in Thailand (20). This is also the first study to report CTX-M-27 and -40 in ESBL-producing E. coli and CTX-M-3 and -27 in ESBL-producing K. pneumoniae from Thailand. The fact that isolates carrying a gene of the CTX-M-1 subgroup significantly reduced susceptibility to tetracycline and cotrimoxazole and that the presence of other bla genes did not further increase the resistance rate may suggest that these resistance genes are often associated or cotransferred with blaCTX-M. On the other hand, resistance to tetracycline and cotrimoxazole increased at a significant rate among CTX-M-9 subgroup-producing isolates only when other bla genes were present. Thus, these resistance genes are probably related to a gene in the CTX-M-9 subgroup at a greater distance. Further studies are needed to characterize plasmids that bla and other resistance genes are located on to gain a better understanding of their genetic relationships. ISEcp1, a member of the IS1380 family, is often located in the upstream region preceding blaCTX-M, particularly in the CTX-M-1, -2, and -9 subgroups, and it probably plays a role in gene transfer or in providing a promoter for blaCTX-M (18, 23, 33). ISEcp1 was detected in most blaCTX-M-carrying isolates in this study, supporting the rationale previously proposed that this IS element mainly mediated the dissemination of the gene. In addition, other IS elements, including IS10, IS26, and IS903, which was previously noted elsewhere to perhaps be involved in the mobilization of the blaCTX-M gene (6, 23, 34), were also found in some isolates. No IS element was detected in four blaCTX-M-carrying isolates after several repetitions of the PCR experiment. There may be two reasons for this: (i) the IS element is located far upstream of blaCTX-M, beyond the region covered by the primers used for PCR, or (ii) blaCTX-M mobilization may occur via an integron associated with a nearby gene on the transposable element, i.e., it did not require its own IS. The evidence that ISEcp1s of different strains were found at various distances upstream from blaCTX-M is likely due to different insertion events and may support the first reason. It is noteworthy that four isolates of CTX-M-15-producing E. coli carried IS26 within ISEcp1, a characteristic reported to be a useful marker for isolates causing epidemics in the United Kingdom (39).

Other ESBL genes were less often encountered. Only 3.8% of ESBL-producing E. coli isolates carried blaSHV, while 87.4% of ESBL-producing K. pneumoniae isolates carried blaSHV. SHV-12 was the only SHV-type ESBL found among ESBL-producing E. coli. Among blaSHV-carrying ESBL-producing K. pneumoniae, 51.4% of the genes encoded non-ESBL SHV-1 or -11 while the rest produced SHV-type ESBLs, including SHV-2a, -12, -27, -71, and -75. It is noteworthy that this study reported the detection of SHV-27-, -71-, and -75-producing isolates for the first time in Thailand. blaVEB-1 was found associated with blaOXA-10 in 32 out of 33 isolates, supporting the previous rationale that both genes are colocalized on the same class 1 integron (14, 26). The plasmid- or integron-mediated transfer was believed to cause the spread of blaVEB-1 among enterobacterial isolates in Thailand (14), but its prevalence has rarely been studied. We report that blaVEB-1 was detected in an average of 9.1% of ESBL-producing E. coli and ESBL-producing K. pneumoniae isolates, which was less than a Vietnam report of 17.8% (9). OXA-10 is not an ESBL, while its derivatives, including OXA-11, -14, and -16, confer the ESBL phenotype by amino acid substitutions (7). Therefore, isolates in this series did not produce OXA-type ESBLs. The two bla genes encoding GES and PER β-lactamases were not detected in this study. The PFGE typing of ESBL-producing isolates showed various DNA banding profiles. Only a small number of isolates showed clonal relationships (>80% similarity) or were more distantly related (>60 to 80% similarity). A retrospective review of medical records suggested that these isolates did not significantly share patient demographics and occurrence periods. Generally, there was no significant difference in patient demographics and isolate characteristics between two hospitals studied. This clearly indicated that most ESBL-producing isolates were sporadic and that multiple clones were widespread in Thailand.

In summary, we report the first extensive study regarding the prevalence and molecular characterization of ESBL genes and the epidemiology of ESBL-producing E. coli and ESBL-producing K. pneumoniae isolates causing HA infection in Thailand. This study clearly indicated that CTX-M, mainly CTX-M-14 and -15, and CTX-M-55 for ESBL-producing E. coli only, was highly endemic in Thailand. Most ESBL producers were resistant to oxyiminocephalosporins and other non-β-lactam agents at high levels and exhibited a high rate of the MDR phenotype. The spread of ESBL-producing bacteria appeared to be polyclonal, and none of the major epidemic strains were identified.

Supplementary Material

[Supplemental material]


This study was financially supported by the Siriraj Research Fund foundation.

We thank the Divisions of Medical Records at both institutes for their assistance in obtaining patient information.


[down-pointing small open triangle]Published ahead of print on 27 May 2008.

Supplemental material for this article may be found at


1. Apisarnthanarak, A., P. Kiratisin, P. Saifon, R. Kitphati, S. Dejsirilert, and L. M. Mundy. 2007. Clinical and molecular epidemiology of community-onset, extended-spectrum beta-lactamase-producing Escherichia coli infections in Thailand: a case-case-control study. Am. J. Infect. Control. 35:606-612. [PubMed]
2. Apisarnthanarak, A., P. Kiratisin, P. Saifon, R. Kitphati, S. Dejsirilert, and L. M. Mundy. 2007. Risk factors for and outcomes of healthcare-associated infection due to extended-spectrum beta-lactamase-producing Escherichia coli or Klebsiella pneumoniae in Thailand. Infect. Control. Hosp. Epidemiol. 28:873-876. [PubMed]
3. Bauernfeind, A., J. M. Casellas, M. Goldberg, M. Holley, R. Jungwirth, P. Mangold, T. Rohnisch, S. Schweighart, and R. Wilhelm. 1992. A new plasmidic cefotaximase from patients infected with Salmonella typhimurium. Infection 20:158-163. [PubMed]
4. Bell, J. M., J. D. Turnidge, A. C. Gales, M. A. Pfaller, R. N. Jones, and the Sentry APAC Study Group. 2002. Prevalence of extended spectrum beta-lactamase (ESBL)-producing clinical isolates in the Asia-Pacific region and South Africa: regional results from SENTRY Antimicrobial Surveillance Program (1998-99). Diagn. Microbiol. Infect. Dis. 42:193-198. [PubMed]
5. Bert, F., C. Branger, and N. Lambert-Zechovsky. 2002. Identification of PSE and OXA beta-lactamase genes in Pseudomonas aeruginosa using PCR-restriction fragment length polymorphism. J. Antimicrob. Chemother. 50:11-18. [PubMed]
6. Bonnet, R. 2004. Growing group of extended-spectrum beta-lactamases: the CTX-M enzymes. Antimicrob. Agents Chemother. 48:1-14. [PMC free article] [PubMed]
7. Bradford, P. A. 2001. Extended-spectrum β-lactamases in the 21st century: characterization, epidemiology, and detection of this important resistance threat. Clin. Microbiol. Rev. 14:933-951. [PMC free article] [PubMed]
8. Bush, K., G. A. Jacoby, and A. A. Medeiros. 1995. A functional classification scheme for beta-lactamases and its correlation with molecular structure. Antimicrob. Agents Chemother. 39:1211-1233. [PMC free article] [PubMed]
9. Cao, V., T. Lambert, D. Q. Nhu, H. K. Loan, N. K. Hoang, G. Arlet, and P. Courvalin. 2002. Distribution of extended-spectrum beta-lactamases in clinical isolates of Enterobacteriaceae in Vietnam. Antimicrob. Agents Chemother. 46:3739-3743. [PMC free article] [PubMed]
10. Celenza, G., C. Pellegrini, M. Caccamo, B. Segatore, G. Amicosante, and M. Perilli. 2006. Spread of bla(CTX-M-type) and bla(PER-2) beta-lactamase genes in clinical isolates from Bolivian hospitals. J. Antimicrob. Chemother. 57:975-978. [PubMed]
11. Chanawong, A., F. H. M'Zali, J. Heritage, A. Lutitanond, and P. M. Hawkey. 2001. SHV-12, SHV-5, SHV-2a and VEB-1 extended-spectrum β-lactamases in Gram-negative bacteria isolated in a university hospital in Thailand. J. Antimicrob. Chemother. 48:839-852. [PubMed]
12. Chanawong, A., A. Lulitanond, W. Kaewkes, V. Lulitanond, S. Srigulbutr, and P. Homchampa. 2007. CTX-M extended-spectrum beta-lactamases among clinical isolates of Enterobacteriaceae in a Thai university hospital. Southeast Asian J. Trop. Med. Public Health 38:493-500. [PubMed]
13. Clinical and Laboratory Standards Institute. 2005. Performance standards for antimicrobial susceptibility testing; 15th informational supplement. CLSI document M100-S15. Clinical and Laboratory Standards Institute, Wayne, PA.
14. Girlich, D., L. Poirel, A. Leelaporn, A. Karim, C. Tribuddharat, M. Fennewald, and P. Nordmann. 2001. Molecular epidemiology of the integron-located VEB-1 extended-spectrum β-lactamase in nosocomial enterobacterial isolates in Bangkok, Thailand. J. Clin. Microbiol. 39:175-182. [PMC free article] [PubMed]
15. Girlich, D., T. Naas, A. Leelaporn, L. Poirel, M. Fennewald, and P. Nordmann. 2002. Nosocomial spread of the integron-located VEB-1-like cassette encoding an extended-spectrum beta-lactamase in Pseudomonas aeruginosa in Thailand. Clin. Infect. Dis. 34:603-611. [PubMed]
16. Gray, K. J., L. K. Wilson, A. Phiri, J. E. Corkill, N. French, and C. A. Hart. 2006. Identification and characterization of ceftriaxone resistance and extended-spectrum β-lactamases in Malawian bacteraemic Enterobacteriaceae. J. Antimicrob. Chemother. 57:661-665. [PubMed]
17. Hirakata, Y., J. Matsuda, Y. Miyazaki, S. Kamihira, S. Kawakami, Y. Miyazawa, Y. Ono, N. Nakazaki, Y. Hirata, M. Inoue, J. D. Turnidge, J. M. Bell, R. N. Jones, S. Kohno, and the SENTRY Asia-Pacific Participants. 2005. Regional variation in the prevalence of extended-spectrum beta-lactamase-producing clinical isolates in the Asia-Pacific region (SENTRY 1998-2002). Diagn. Microbiol. Infect. Dis. 52:323-329. [PubMed]
18. Karim, A., L. Poirel, S. Nagarajan, and P. Nordmann. 2001. Plasmid-mediated extended-spectrum beta-lactamase (CTX-M-3 like) from India and gene association with insertion sequence ISEcp1. FEMS Microbiol. Lett. 201:237-241. [PubMed]
19. Kaufmann, M. E. 1998. Pulsed-field gel electrophoresis. Methods Mol. Med. 15:17-31.
20. Kiratisin, P., A. Apisarnthanarak, P. Saifon, C. Laesripa, R. Kitphati, and L. M. Mundy. 2007. The emergence of a novel ceftazidime-resistant CTX-M extended-spectrum beta-lactamase, CTX-M-55, in both community-onset and hospital-acquired infections in Thailand. Diagn. Microbiol. Infect. Dis. 58:349-355. [PubMed]
21. Knothe, H., P. Shah, V. Krcmery, M. Antal, and S. Mitsuhashi. 1983. Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens. Infection 11:315-317. [PubMed]
22. Komatsu, M., N. Ikeda, M. Aihara, Y. Nakamachi, S. Kinoshita, K. Yamasaki, and K. Shimakawa. 2001. Hospital outbreak of MEN-1-derived extended spectrum beta-lactamase-producing Klebsiella pneumoniae. J. Infect. Chemother. 7:94-101. [PubMed]
23. Lartigue, M. F., L. Poirel, and P. Nordmann. 2004. Diversity of genetic environment of blaCTX-M genes. FEMS Microbiol. Lett. 234:201-207. [PubMed]
24. Lautenbach, E., J. B. Patel, W. B. Bilker, P. H. Edelstein, and N. O. Fishman. 2001. Extended-spectrum beta-lactamase-producing Escherichia coli and Klebsiella pneumoniae: risk factors for infection and impact of resistance on outcomes. Clin. Infect. Dis. 32:1162-1171. [PubMed]
25. Livermore, D. M., R. Canton, M. Gniadkowski, P. Nordmann, G. M. Rossolini, G. Arlet, J. Ayala, T. M. Coque, I. Kern-Zdanowicz, F. Luzzaro, L. Poirel, and N. Woodford. 2007. CTX-M: changing the face of ESBLs in Europe. J. Antimicrob. Chemother. 59:165-174. [PubMed]
26. Naas, T., L. Poirel, A. Karim, and P. Nordmann. 1999. Molecular characterization of In50, a class 1 integron encoding the gene for the extended-spectrum β-lactamase VEB-1 in Pseudomonas aeruginosa. FEMS Microbiol. Lett. 176:411-419. [PubMed]
27. Pai, H., S. Lyu, J. H. Lee, J. Kim, Y. Kwon, J. W. Kim, and K. W. Choe. 1999. Survey of extended-spectrum beta-lactamases in clinical isolates of Escherichia coli and Klebsiella pneumoniae: prevalence of TEM-52 in Korea. J. Clin. Microbiol. 37:1758-1763. [PMC free article] [PubMed]
28. Pasterán, F., M. Rapoport, A. Petroni, D. Faccone, A. Corso, M. Galas, M. Vázquez, A. Procopio, M. Tokumoto, and V. Cagnoni. 2006. Emergence of PER-2 and VEB-1a in Acinetobacter baumannii strains in the Americas. Antimicrob. Agents Chemother. 50:3222-3224. [PMC free article] [PubMed]
29. Paterson, D. L., K. M. Hujer, A. M. Hujer, B. Yeiser, M. D. Bonomo, L. B. Rice, and R. A. Bonomo. 2003. Extended-spectrum beta-lactamases in Klebsiella pneumoniae bloodstream isolates from seven countries: dominance and widespread prevalence of SHV- and CTX-M-type beta-lactamases. Antimicrob. Agents Chemother. 47:3554-3560. [PMC free article] [PubMed]
30. Paterson, D. L., and R. A. Bonomo. 2005. Extended-spectrum β-lactamases: a clinical update. Clin. Microbiol. Rev. 18:657-686. [PMC free article] [PubMed]
31. Poirel, L., T. Naas, I. Le Thomas, A. Karim, E. Bingen, and P. Nordmann. 2001. CTX-M-type extended-spectrum beta-lactamase that hydrolyzes ceftazidime through a single amino acid substitution in the omega loop. Antimicrob. Agents Chemother. 45:3355-3361. [PMC free article] [PubMed]
32. Poirel, L., M. Gniadkowski, and P. Nordmann. 2002. Biochemical analysis of the ceftazidime-hydrolysing extended-spectrum beta-lactamase CTX-M-15 and of its structurally related beta-lactamase CTX-M-3. J. Antimicrob. Chemother. 50:1031-1034. [PubMed]
33. Poirel, L., J. W. Decousser, and P. Nordmann. 2003. Insertion sequence ISEcp1B is involved in expression and mobilization of a blaCTX-M beta-lactamase gene. Antimicrob. Agents Chemother. 47:2938-2945. [PMC free article] [PubMed]
34. Saladin, M., V. T. Cao, T. Lambert, J. L. Donay, J. L. Herrmann, Z. Ould-Hocine, C. Verdet, F. Delisle, A. Philippon, and G. Arlet. 2002. Diversity of CTX-M beta-lactamases and their promoter regions from Enterobacteriaceae isolated in three Parisian hospitals. FEMS Microbiol. Lett. 209:161-168. [PubMed]
35. Sturenburg, E., A. Kuhn, D. Mack, and R. Laufs. 2004. A novel extended-spectrum beta-lactamase CTX-M-23 with a P167T substitution in the active-site omega loop associated with ceftazidime resistance. J. Antimicrob. Chemother. 54:406-409. [PubMed]
36. Tenover, F. C., R. D. Arbeit, R. V. Goering, P. A. Mickelsen, B. E. Murray, D. H. Persing, and B. Swaminathan. 1995. Interpreting chromosomal DNA restriction patterns produced by pulsed-field gel electrophoresis: criteria for bacterial strain typing. J. Clin. Microbiol. 33:2233-2239. [PMC free article] [PubMed]
37. Vourli, S., P. Giakkoupi, V. Miriagou, E. Tzelepi, A. C. Vatopoulos, and L. S. Tzouvelekis. 2004. Novel GES/IBC extended-spectrum beta-lactamase variants with carbapenemase activity in clinical enterobacteria. FEMS Microbiol. Lett. 234:209-213. [PubMed]
38. Winokur, P. L., R. Canton, J. M. Casellas, and N. Legakis. 2001. Variations in the prevalence of strains expressing an extended-spectrum beta-lactamase phenotype and characterization of isolates from Europe, the Americas, and the Western Pacific region. Clin. Infect. Dis. 32:S94-S103. [PubMed]
39. Woodford, N., M. E. Ward, M. E. Kaufmann, J. Turton, E. J. Fagan, D. James, A. P. Johnson, R. Pike, M. Warner, T. Cheasty, A. Pearson, S. Harry, J. B. Leach, A. Loughrey, J. A. Lowes, R. E. Warren, and D. M. Livermore. 2004. Community and hospital spread of Escherichia coli producing CTX-M extended-spectrum beta-lactamases in the UK. J. Antimicrob. Chemother. 54:735-743. [PubMed]
40. Yan, J. J., S. H. Tsai, C. L. Chuang, and J. J. Wu. 2006. OXA-type beta-lactamases among extended-spectrum cephalosporin-resistant Pseudomonas aeruginosa isolates in a university hospital in southern Taiwan. J. Microbiol. Immunol. Infect. 39:130-134. [PubMed]

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