Extended-Spectrum -Lactamases in the 21st Century: Characterization, Epidemiology, and Detection of This Important Resistance Threat

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1 CLINICAL MICROBIOLOGY REVIEWS, Oct. 2001, p Vol. 14, No /01/$ DOI: /CMR Copyright 2001, American Society for Microbiology. All Rights Reserved. Extended-Spectrum -Lactamases in the 21st Century: Characterization, Epidemiology, and Detection of This Important Resistance Threat PATRICIA A. BRADFORD* Wyeth-Ayerst Research, Pearl River, New York INTRODUCTION AND HISTORY CHARACTERIZATION OF ESBLs Functional and Molecular Grouping Susceptibility and Biochemical Characteristics TYPES OF ESBLs TEM Inhibitor-Resistant -Lactamases SHV CTX-M OXA Other ESBLs ESBL DETECTION METHODS Clinical Microbiology Techniques Molecular Detection Methods Medical Significance of Detection of ESBLs EPIDEMIOLOGY CONCLUSION ACKNOWLEDGMENTS REFERENCES INTRODUCTION AND HISTORY * Mailing address: Wyeth-Ayerst Research, 401 N. Middletown Rd., Pearl River, NY Phone: (845) Fax: (845) bradfop@war.wyeth.com. Emergence of resistance to -lactam antibiotics began even before the first -lactam, penicillin, was developed. The first -lactamase was identified in Escherichia coli prior to the release of penicillin for use in medical practice (1). The age of penicillin saw the rapid emergence of resistance in Staphylococcus aureus due to a plasmid-encoded penicillinase. This -lactamase quickly spread to most clinical isolates of S. aureus as well as other species of staphylococci. Many genera of gram-negative bacteria possess a naturally occurring, chromosomally mediated -lactamase. These enzymes are thought to have evolved from penicillin-binding proteins, with which they show some sequence homology. This development was likely due to the selective pressure exerted by -lactam-producing soil organisms found in the environment (61). The first plasmid-mediated -lactamase in gram-negatives, TEM-1, was described in the early 1960s (48). The TEM-1 enzyme was originally found in a single strain of E. coli isolated from a blood culture from a patient named Temoniera in Greece, hence the designation TEM (96). Being plasmid and transposon mediated has facilitated the spread of TEM-1 to other species of bacteria. Within a few years after its first isolation, the TEM-1 -lactamase spread worldwide and is now found in many different species of members of the family Enterobacteriaceae, Pseudomonas aeruginosa, Haemophilus influenzae, and Neisseria gonorrhoeae. Another common plasmidmediated -lactamase found in Klebsiella pneumoniae and E. coli is SHV-1 (for sulphydryl variable). The SHV-1 -lactamase is chromosomally encoded in the majority of isolates of K. pneumoniae but is usually plasmid mediated in E. coli. Over the last 20 years, many new -lactam antibiotics have been developed that were specifically designed to be resistant to the hydrolytic action of -lactamases. However, with each new class that has been used to treat patients, new -lactamases emerged that caused resistance to that class of drug. Presumably, the selective pressure of the use and overuse of new antibiotics in the treatment of patients has selected for new variants of -lactamase. One of these new classes was the oxyimino-cephalosporins, which became widely used for the treatment of serious infections due to gram-negative bacteria in the 1980s. Not surprisingly, resistance to these expanded-spectrum -lactam antibiotics due to -lactamases emerged quickly. The first of these enzymes capable of hydrolyzing the newer -lactams, SHV-2, was found in a single strain of Klebsiella ozaenae isolated in Germany (81). Because of their increased spectrum of activity, especially against the oxyimino-cephalosporins, these enzymes were called extended-spectrum -lactamases (ESBLs). Today, over 150 different ESBLs have been described. These -lactamases have been found worldwide in many different genera of Enterobacteriaceae and P. aeruginosa. This review will focus on the characterization of ESBLs, the importance of detection of these enzymes, and their epidemiology. 933

2 934 BRADFORD CLIN. MICROBIOL. REV. CHARACTERIZATION OF ESBLs Functional and Molecular Grouping The majority of ESBLs contain a serine at the active site and belong to Ambler s molecular class A (4). Class A enzymes are characterized by an active-site serine, a molecular mass of approximately 29,000 Da, and the preferential hydrolysis of penicillins (95). Class A -lactamases include such enzymes as TEM-1, SHV-1, and the penicillinase found in S. aureus. The molecular classification scheme is still used to characterize -lactamases; however, it does not sufficiently differentiate the many different types of class A enzymes. The classification scheme of Richmond and Sykes was based on the substrate profile and the location of the gene encoding the -lactamase (145). This classification scheme was developed before ESBLs arose, and it did not allow for the differentiation between the original TEM and SHV enzymes and their ESBL derivatives. More recently, a classification scheme was devised by Bush, Jacoby, and Medeiros that uses the biochemical properties of the enzyme plus the molecular structure and nucleotide sequence of the genes to place -lactamases into functional groups (32). Using this scheme, ESBLs are defined as -lactamases capable of hydrolyzing oximino-cephalosporins that are inhibited by clavulanic acid and are placed into functional group 2be (32). Susceptibility and Biochemical Characteristics ESBLs contain a number of mutations that allow them to hydrolyze expanded-spectrum -lactam antibiotics. While TEM- and SHV-type ESBLs retain their ability to hydrolyze penicillins, they are not catalytically as efficient as the parent enzymes (33). In addition, the expansion of the active site that allows the increased activity against expanded-spectrum cephalosporins may also result in the increased susceptibility of ESBLs to -lactamase inhibitors (74). ESBLs are not active against cephamycins, and most strains expressing ESBLs are susceptible to cefoxitin and cefotetan. However, it has been reported that ESBL-producing strains can become resistant to cephamycins due to the loss of an outer membrane porin protein (92, 121, 181). TYPES OF ESBLs Most ESBLs are derivatives of TEM or SHV enzymes (32, 74). There are now 90 TEM-type -lactamases and 25 SHV-type enzymes (for amino acid sequences for TEM, SHV, and OXA extended-spectrum and inhibitor-resistant -lactamases, see With both of these groups of enzymes, a few point mutations at selected loci within the gene give rise to the extended-spectrum phenotype. TEM- and SHV-type ESBLs are most often found in E. coli and K. pneumoniae; however, they have also been found in Proteus spp., Providencia spp., and other genera of Enterobacteriaceae. TEM TEM-1 is the most commonly encountered -lactamase in gram-negative bacteria. Up to 90% of ampicillin resistance in E. coli is due to the production of TEM-1 (85). This enzyme is also responsible for the ampicillin and penicillin resistance that is seen in H. influenzae and N. gonorrhoeae in increasing numbers. TEM-1 is able to hydrolyze penicillins and early cephalosporins such as cephalothin and cephaloridine. TEM-2, the first derivative of TEM-1, had a single amino acid substitution from the original -lactamase (10). This caused a shift in the isoelectric point from a pi of 5.4 to 5.6, but it did not change the substrate profile. TEM-3, originally reported in 1989, was the first TEM-type -lactamase that displayed the ESBL phenotype (157). In the years since that first report, over 90 additional TEM derivatives have been described (for amino acid sequences for TEM, SHV, and OXA extended-spectrum and inhibitor-resistant -lactamases, see /studies/webt.htm). Some of these -lactamases are inhibitorresistant enzymes, but the majority of the new derivatives are ESBLs. As shown in Fig. 1, the amino acid substitutions that occur within the TEM enzyme occur at a limited number of positions. The combinations of these amino acid changes result in various subtle alterations in the ESBL phenotypes, such as the ability to hydrolyze specific oxyimino-cephalosporins such as ceftazidime and cefotaxime, or a change in their isoelectric points, which can range from a pi of 5.2 to 6.5 (Table 1). A number of amino acid residues are especially important for producing the ESBL phenotype when substitutions occur at that position. They include glutamate to lysine at position 104, arginine to either serine or histidine at position 164, glycine to serine at position 238, and glutamate to lysine at position 240 (Fig. 1). In addition to -lactamases TEM-1 through TEM-92 shown in Fig. 1 and Table 1, there has been a report of a naturally occurring TEM-like enzyme, TEM-AQ, that contained a number of amino acid substitutions and one amino acid deletion that have not been noted in other TEM enzymes (127). It is interesting that laboratory mutants of TEM-1 that contain mutations at positions other than the ones described in nature have been constructed (18, 130, 180, 182). It has been suggested that the naturally occurring TEM-type ESBLs are the result of fluctuating selective pressure from several -lactams within a given institution rather than selection with a single agent (18). Although TEM-type -lactamases are most often found in E. coli and K. pneumoniae, they are also found in other species of gram-negative bacteria with increasing frequency. TEM-type ESBLs have been reported in genera of Enterobacteriaceae such as Enterobacter aerogenes, Morganella morganii, Proteus mirabilis, Proteus rettgeri, and Salmonella spp. (19, 91, 101, 120, 128, 166). Furthermore, TEM-type ESBLs have been found in non-enterobacteriaceae gram-negative bacteria. The TEM-42 -lactamase was found in a strain of P. aeruginosa (103). Additionally, a recent report found the TEM-17 -lactamase being expressed from a plasmid in a blood culture isolate of Capnocytophaga ochracea (146). Inhibitor-Resistant -Lactamases Although the inhibitor-resistant -lactamases are not ESBLs, they are often discussed with ESBLs because they are also derivatives of the classical TEM- or SHV-type enzymes. In the early 1990s -lactamases that were resistant to inhibition by clavulanic acid were discovered. Nucleotide sequencing re-

3 VOL. 14, 2001 EXTENDED-SPECTRUM -LACTAMASES 935 Downloaded from FIG. 1. Amino acid substitutions in TEM ESBL derivatives. The amino acids listed within the grey bar are those found in the structural gene of the TEM-1 -lactamase (162). The amino acid numbering is according to the scheme of Ambler et al. (5). Substitutions found in TEM-type ESBL derivatives are shown under the amino acids of TEM-1. TEM-type variants may contain more than one amino acid substitution., TEM-2 is not an ESBL but is included in the figure as a derivative of TEM-1. The Gln39Lys substitution does not contribute to the ESBL phenotype, but a number of ESBLs are derived from TEM-2., TEM-50 and TEM-68 contain amino acid substitutions that are common to both the ESBL and the IRT phenotypes. Only the amino acid substitutions that are common to TEM-type ESBLs are shown in this figure. vealed that these enzymes were variants of the TEM-1 or TEM-2 -lactamase. These enzymes were at first given the designation IRT for inhibitor-resistant TEM -lactamase; however, all have subsequently been renamed with numerical TEM designations. There are at least 19 distinct inhibitorresistant TEM -lactamases (for amino acid sequences for TEM, SHV and OXA extended-spectrum and inhibitor resistant -lactamases, see Inhibitor-resistant TEM -lactamases have been found mainly in clinical isolates of E. coli, but also some strains of K. pneumoniae, Klebsiella oxytoca, P. mirabilis, and Citrobacter freundii (31, 83). Although the inhibitor-resistant TEM variants are resistant to inhibition by clavulanic acid and sulbactam, thereby showing clinical resistance to the -lactam -lactamase inhibitor combinations of amoxicillin-clavulanate, ticarcillin-clavulanate, and ampicillin-sulbactam, they remain susceptible to inhibition by tazobactam and subsequently the combination of piperacillin and tazobactam (23, 37). To date, these -lactamases have primarily been detected in France and a few other locations within Europe (37). In a recent survey of amoxicillin-clavulanate-resistant E. coli in a hospital in France, Leflon-Guibout et al. found that up to 41% of these isolates produced inhibitor-resistant TEM variants (82). Although these enzymes have not yet been reported in isolates originating in the United States, it is likely that they will eventually be detected here as well. As shown in Fig. 2, point mutations that lead to the inhibitor-resistant phenotype occur at a few specific amino acid residues within the structural gene for the TEM enzyme, Met- 69, Arg-244, Arg-275, and Asn-276 (16, 66, 191). The sites of these amino acid substitutions are distinct from those that lead to the ESBL phenotype. Laboratory mutants that contain amino acid substitutions which are common to both the IRT and the ESBL phenotype have been constructed (159). These strains were found to possess either the ESBL or IRT phenotype, but not both. However, the TEM-50 enzyme, which had on November 7, 2018 by guest

4 936 BRADFORD CLIN. MICROBIOL. REV. TABLE 1. Characteristics of TEM-type -lactamases a pi Enzymes Enzyme type Broad spectrum ESBL IRT 5.2 TEM-12, TEM-55, TEM-57, TEM-58 X TEM-30, TEM-31, TEM-35, TEM-36, TEM-37, TEM-38, TEM-41, TEM-45, X TEM-51, TEM-73, TEM TEM-25 X 5.4 TEM-1 X TEM-7, TEM-19, TEM-20, TEM-65 X TEM-32, TEM-33, TEM-34, TEM-39, TEM-40, TEM-44 X 5.42 TEM-29 X 5.55 TEM-5, TEM-17 X 5.59 TEM-9 X 5.6 TEM-2 X TEM-10, TEM-11, TEM-13, TEM-26, TEM-63 X TEM-50 X X TEM-59 X 5.7 TEM-68 X X 5.8 TEM-42 X 5.9 TEM-4, TEM-6, TEM-8, TEM-27, TEM-72 X 6.0 TEM-15, TEM-47, TEM-48, TEM-49, TEM-52, TEM-66, TEM-92 X 6.1 TEM-28, TEM-43 X 6.3 TEM-3, TEM-16, TEM-21, TEM-22 X 6.4 TEM-56, TEM-60 X 6.5 TEM-24, TEM-46, TEM-61 X Not determined TEM-14, TEM-53, TEM-54 X TEM-76, TEM-77, TEM-78, TEM-79, TEM-81, TEM-82, TEM-83, TEM-84 a Amino acid sequences for TEM, SHV, and OXA extended-spectrum and inhibitor-resistant -lactamases may be found at All enzymes listed are naturally occurring mutants. amino acid substitutions common to both the ESBL and inhibitor-resistant TEMs, was recently identified. This enzyme was resistant to inhibition by clavulanate, but it also conferred a slight resistance to the expanded-spectrum cephalosporins (154). This could indicate the possibility of a new group of -lactamases with a complex phenotype sharing some characteristics of ESBLs and inhibitor-resistant enzymes. In addition to the variants of TEM, inhibitor-resistant variants of SHV-1 and the related enzyme OHIO-1 have been detected (22, 137). SHV The SHV-1 -lactamase is most commonly found in K. pneumoniae and is responsible for up to 20% of the plasmid-mediated ampicillin resistance in this species (172). In many strains of K. pneumoniae, bla SHV-1 or a related gene is integrated into the bacterial chromosome (85). Although it has been hypothesized that the gene encoding SHV-1 may exist as part of a transposable element, it has never been proven (75). Unlike the TEM-type -lactamases, there are relatively few derivatives of SHV-1 (Table 2). Furthermore, the changes that have been observed in bla SHV to give rise to the SHV variants occur in fewer positions within the structural gene (Fig. 3). The majority of SHV variants possessing an ESBL phenotype are characterized by the substitution of a serine for glycine at position 238. A number of variants related to SHV-5 also have a substitution of lysine for glutamate at position 240. It is interesting that both the Gly238Ser and Glu240Lys amino acid substitutions mirror those seen in TEM-type ESBLs. The serine residue at position 238 is critical for the efficient hydrolysis of ceftazidime, and the lysine residue is critical for the efficient hydrolysis of cefotaxime (69). To date, the majority of SHV-type derivatives possess the ESBL phenotype. However, one variant, SHV-10, is reported to have an inhibitor-resistant phenotype. This enzyme appears to be derived from SHV-5 and contains one additional amino acid substitution of glycine for serine 130 (137). It is interesting that the inhibitor-resistant phenotype conferred by the Ser140Gly mutation seems to override the strong ESBL phenotype usually seen in enzymes containing the Gly238Ser and the Glu240Lys mutations seen in other SHV-5-type enzymes. The majority of SHV-type ESBLs are found in strains of K. pneumoniae. However, these enzymes have also been found in Citrobacter diversus, E. coli, and P. aeruginosa (27, 51, 108, 139). CTX-M In recent years a new family of plasmid-mediated ESBLs, called CTX-M, that preferentially hydrolyze cefotaxime has arisen. They have mainly been found in strains of Salmonella enterica serovar Typhimurium and E. coli, but have also been described in other species of Enterobacteriaceae (Table 3). They include the CTX-M-type enzymes CTX-M-1 (formerly called MEN-1), CTX-M-2 through CTX-M-10 (9, 11, 12, 13, 21, 29, 58, 59, 64, 148; A. Oliver, J. C. Pérez-Díaz, T. M. Coque, F. Baquero, and R. Cantón, 40th Intersci. Conf. Antmicrob. Agents Chemother., abstr. 1480, 2000) as well as Toho enzymes 1 and 2 (72, 88). These enzymes are not very closely related to TEM or SHV -lactamases in that they show only approximately 40% identity with these two commonly isolated -lactamases (174). Previously, the most closely related enzymes outside this family were thought to be the chromosomally encoded class A cephalosporinases found in K. oxytoca, C. diversus, Proteus vulgaris, X

5 VOL. 14, 2001 EXTENDED-SPECTRUM -LACTAMASES 937 Downloaded from FIG. 2. Amino acid substitutions in TEM IRT derivatives. The amino acids listed within the grey bar are those found in the structural gene of the TEM-1 -lactamase (162). The amino acid numbering is according to the scheme of Ambler et al. (5). Substitutions found in TEM-type IRT derivatives are shown under the amino acids of TEM-1. TEM-type variants may contain more than one amino acid substitution., TEM-50 and TEM-68 contain amino acid substitutions that are common to both the ESBL and the IRT phenotypes. Only the amino acid substitutions that are common to TEM-type IRTs are shown in this figure. pi TABLE 2. Characteristics of SHV-type -lactamases a Enzymes Enzyme type Broad spectrum ESBL Inhibitor resistant 7.0 OHIO-1, LEN-1 X SHV-3, SHV-14 X 7.5 SHV-24 X 7.6 SHV-1, SHV-11 X SHV-2, SHV-2a, SHV-6, SHV-8, X SHV-13, SHV-19, SHV-20, SHV-21, SHV SHV-4, SHV-7 b, SHV-18 X 8.2 SHV-5, SHV-9, SHV-12 X SHV-10 a Amino acid sequences for TEM, SHV, and OXA extended-spectrum and inhibitor-resistant -lactamases may be found at webt.htm. All enzymes listed are naturally occurring mutants. b SHV-7 was reported to have a pi of 7.6 (27), but further examination of this enzyme indicates that the pi is most likely to be 7.8. This enzyme shows an interesting phenomenon in that the isoelectric point varies depending on the day of testing and the purity of the enzyme (unpublished observations). X and Serratia fonticola (73 to 77% homology) (13, 19). However, it was recently reported by Humeniuk et al. that there is a high degree of homology between the chromosomal AmpC enzyme of Kluyvera ascorbata (designated Klu-1 and Klu-2) and the CTX-M-type enzymes, suggesting that the latter probably originated from this species (G. Humeniuk, G. Arlet, R. Labia, P. Grimont, and A. Philippon, Abstr. Reunion Interdis. Chimiother. Anti-infect., abstr. 20/C4, 2000) A phylogenetic study of the CTX-M family of -lactamases showed four major types: the CTX-M-1 type, including CTX-M-1, and CTX-M-3; the CTX-M-2 type, including CTX-M-2, CTX-M-4, CTX-M-5, CTX-M-6, CTX-M-7, and Toho-1; Toho-2; and CTX-M-8, the latter two groups containing only one member to date (21). The evolutionary distances between each of these groupings suggest an early divergence from a common ancestor (21). Kinetic studies have shown that the CTX-M-type -lactamases hydrolyze cephalothin or cephaloridine better than benzylpenicillin and they preferentially hydrolyze cefotaxime over ceftazidime (29, 174). Although there is some hydrolysis of ceftazidime by these enzymes, it is usually not enough to provide clinical resistance to organisms in which they reside. It has on November 7, 2018 by guest

6 938 BRADFORD CLIN. MICROBIOL. REV. FIG. 3. Amino acid substitutions in SHV ESBL derivatives. The amino acids listed within the grey bar are those found in the structural gene of the SHV-1 -lactamase (25). The amino acid numbering is according to the scheme of Ambler et al. (5). Substitutions found in SHV-type ESBL derivatives are shown under the amino acids of SHV-1. SHV-type variants may contain more than one amino acid substitution., SHV-11 is not an ESBL but is included in the figure as a derivative of SHV-1. been suggested that the serine residue at position 237, which is present in all of the CTX-M enzymes, plays an important role in the extended-spectrum activity of the CTX-M-type -lactamases (174). Although it has been shown not to be essential, the Arg-276 residue lies in a position equivalent to Arg-244 in TEM- or SHV-type ESBLs, as suggested by molecular modeling, and may also play a role in the hydrolysis of oxyiminocephalosporins (56). Recent crystallographic data for the Toho-1 enzyme suggested that there was increased flexibility of the interacting 3 strand and loop of this enzyme in comparison to other class A -lactamases. Furthermore, the lack of hydrogen bonds in the vicinity of the loop could account for the extended-spectrum phenotype (71). In addition to the rapid hydrolysis of cefotaxime, another unique feature of these TABLE 3. Characteristics of CTX-M-type ESBLs enzymes is that they are inhibited better by the -lactamase inhibitor tazobactam than by sulbactam and clavulanate (29, 88, 148, 174). Strains expressing CTX-M-type -lactamases have been isolated from many parts of the world, but have most often been associated with focal outbreaks in eastern Europe (29, 57, 64), South America, and Japan (88). There have been a few reports of these enzymes in isolates from patients in western Europe, mostly in isolates from immigrants from the outbreak areas (173). However, Sabeté et al. recently reported that 23 strains of E. coli and Salmonella isolated in Spain expressed the CTX- M-9 -lactamase, suggesting that there may be an endemic focus of this enzyme in western Europe as well (148). Moreover, a CTX-M-3-producing strain of Enterobacter cloacae was -Lactamase Alternative name pi Country of origin Bacterial species Reference(s) CTX-M-1 MEN Germany, Italy E. coli 12, 13 CTX-M Argentina S. enterica a 11, 13 CTX-M Poland C. freundii, E. coli 64 CTX-M Russia S. enterica 57, 59 CTX-M-5 CTX-M Latvia S. enterica 29 CTX-M Greece S. enterica 58, 173 CTX-M-7 CTX-M Greece S. enterica 58, 173 CTX-M Brazil P. mirabilis, E. cloacae, E. aerogenes, 21 C. amalonaticus CTX-M Spain E. coli 148 CTX-M Spain E. coli Oliver et al. b Toho Japan E. coli 72 Toho Japan E. coli 88 a All strains of S. enterica were serovar Typhimurium. b A. Oliver, J. C. Pérez-Díaz, T. M. Coque, F. Baquero, and R. Cantón, 40th Intersci. Conf. Antimicrob. Agents Chemother., abstr. 1480, 2000.

7 VOL. 14, 2001 EXTENDED-SPECTRUM -LACTAMASES 939 TABLE 4. Characteristics of OXA-type ESBLs -Lactamase Derivation pi Amino acid substitutions vs. OXA-10 Country of origin Bacterial species Reference OXA-11 OXA Asn143Ser, Gly157Asp Turkey P. aeruginosa 65 OXA-13 OXA Ile10Thr, Gly20Ser, Asp55N, Asn73Ser, France P. aeruginosa 104 Thr107Ser, Tyr174Phe, Glu229Gly, Ser245Asn, Glu259Ala OXA-14 OXA Gly157Asp Turkey P. aeruginosa 45 OXA-15 OXA-2 8.7, 8.9 doublet NA a Turkey P. aeruginosa 46 OXA-16 OXA Ala124Thr, Gly157Asp Turkey P. aeruginosa 47 OXA-17 OXA Asn73Ser Turkey P. aeruginosa 44 OXA-18 OXA-9, OXA NA France P. aeruginosa 131 OXA-19 OXA Ile10Thr, Gly20Ser, Asp55Asn, France P. aeruginosa 102 Thr107Ser, Gly157Asp, Tyr174Phe, Glu229Gly, Ser245Asn, Glu259Ala OXA-28 OXA Ile10Thr, Gly20Ser, Thr107Ser, Trp154Gly, Gly157Asp, Tyr174Phe, Glu229Gly, Ser245Asn, Glu259Ala France P. aeruginosa 134 a NA, not applicable; these enzymes do not originate from OXA-10. recently isolated in France (50). Several institutions in the areas where outbreaks have occurred reported that the CTX- M-type enzyme is the most frequently isolated ESBL among clinical isolates in their laboratories (148). Interestingly, a number of these enzymes have been found among isolates of Salmonella enterica serovar Typhimurium (11, 29, 57, 58, 173). Large outbreaks of isolates of S. enterica serovar Typhimurium expressing CTX-M -lactamases have occurred in both South America and eastern Europe. These isolates have also been found to express a variety of CTX-Mtype variants. Therefore, it is unlikely that a single origin for the occurrence and propensity of this type of -lactamase among S. enterica serovar Typhimurium can be found. OXA The OXA-type enzymes are another growing family of ES- BLs. These -lactamases differ from the TEM and SHV enzymes in that they belong to molecular class D and functional group 2d (32). The OXA-type -lactamases confer resistance to ampicillin and cephalothin and are characterized by their high hydrolytic activity against oxacillin and cloxacillin and the fact that they are poorly inhibited by clavulanic acid (32). The OXA -lactamase family was originally created as a phenotypic rather than a genotypic group for a few -lactamases that had a specific hydrolysis profile. Therefore, there is as little as 20% sequence homology among some of the members of this family. However, recent additions to this family show some degree of homology to one or more of the existing members of the OXA -lactamase family. While most ESBLs have been found in E. coli, K. pneumoniae, and other Enterobacteriaceae, the OXA-type ESBLs have been found mainly in P. aeruginosa (Table 4). Several of the OXA-type ESBLs have been derived from OXA-10 (OXA- 11, -14, -16, and -17) (44, 45, 65, 104). OXA-14 differs from OXA-10 by only one amino acid residue, OXA-11 and OXA-16 differ by two, and OXA-13 and OXA-19 differ by nine (Table 4). Among the enzymes related to OXA-10, the ESBL variants have one of two amino acid substitutions: an asparagine for serine at position 73, or an aspartate for glycine at position 157. In particular, the Gly157Asp substitution may be necessary for high-level resistance to ceftazidime (44). It appears that either of these mutations may be required to confer the ESBL phenotype on the OXA-type variant. In addition to the OXA-10 group, OXA-15 is a derivative of OXA-2, and OXA-18 is not directly derived from other OXA-type enzymes (closest relative is OXA-9, with 42% homology) (Table 4) (131). The OXA-type ESBLs provide weak resistance to oxyiminocephalosporins when cloned into E. coli, but provide fairly high-level resistance in P. aeruginosa transconjugants (65). In contrast to the majority of the OXA-type ESBLs, which confer resistance to ceftazidime, the OXA-17 -lactamase confers resistance to cefotaxime and ceftriaxone but provides only marginal protection against ceftazidime (44). With respect to -lactamase inhibitors, the original OXA enzymes were characterized by their lack of inhibition by clavulanic acid; however, the OXA-18 -lactamase was reported to be inhibited by this compound (131). One additional OXA-type enzyme has been identified, OXA-21 (184). This enzyme was found in a strain of Acinetobacter baumannii and is the first incidence of an OXA-type enzyme s originating in this organism. Because the clinical isolate of A. baumannii also expressed two other -lactamases, it is unclear whether OXA-21 is an ESBL or an original-spectrum enzyme (184). In addition to the OXA-type ESBLs, a number of recent OXA derivatives that are not ESBLs have also been described. These include OXA-20 (110), OXA-22 (115), OXA-24 (24), OXA-25, -26, and -27 (2), and OXA-30 (155). Many of the newer members of the OXA -lactamase family have been found in bacterial isolates originating in Turkey and in France. It is not certain whether these two countries represent foci of strains harboring these enzymes or if they represent the locale of the investigators studying these -lactamases. Other ESBLs While the majority of ESBLs are derived from TEM or SHV -lactamases and others can be categorized with one of the newer families of ESBLs, a few ESBLs have been reported that are not closely related to any of the established families of -lactamases (Table 5). The PER-1 -lactamase was first discovered in strains of P. aeruginosa isolated from patients in Turkey (113). Later, it was also found among isolates of S.

8 940 BRADFORD CLIN. MICROBIOL. REV. TABLE 5. Characteristics of novel, unrelated ESBLs -Lactamase Closest relative pi Preferred substrate a Country of origin Bacterial species Reference BES-1 Penicllinase from Yersinia 7.5 CTX, CAZ, ATM Brazil S. marcescens 20 enterocolitica FEC CTX Japan E. coli 93 GES-1 Penicillinase from P. mirabilis 5.8 CAZ French Guiana K. pneumoniae 136 CME-1 VEB CAZ Isolated from Chryseobacterium meningosepticum 147 reference strain PER-1 PER CAZ France P. aeruginosa 113 PER-2 PER CAZ Argentina S. enterica serovar Typhimurium 14 SFO-1 AmpA from S. fonticola 7.3 CTX Japan E. cloacae 94 TLA-1 CME CAZ, CTX, ATM Mexico E. coli 153 VEB-1 PER-1, PER CAZ, ATM Vietnam/Thailand E. coli 135 a CTX, cefotaxime; CAZ, ceftazidime; ATM, aztreonam. enterica serovar Typhimurium and A. baumanii (176, 177, 179). The PER-1 -lactamase is widespread across Turkey and is found in up to 60% of ceftazidime-resistant strains of A. baumanii, which represent 46% of total isolates (179). A common plasmid encoding PER-1 was found in multiple nosocomial isolates of S. enterica serovar Typhimurium, suggesting that the strains acquired the resistance plasmids in the hospital setting (176). A related enzyme, PER-2, which has 86% amino acid homology with PER-1, was found among S. enterica serovar Typhimurium strains in Argentina. (14). It is interesting that PER-1 is found almost exclusively in Turkey, while PER-2 has been found almost exclusively in South America. Another enzyme that is somewhat related to PER-1 is the VEB-1 -lactamase (135). VEB-1 was first found in a single isolate of E. coli in a patient from Vietnam, but was subsequently also found in a P. aeruginosa isolate from a patient from Thailand (109). A third related enzyme is CME-1, which was isolated from Chryseobacterium meningosepticum (147). A fourth enzyme in this group is TLA-1, which was identified in an E. coli isolate from a patient in Mexico (153). The PER-1, PER-2, VEB-1, CME-1, and TLA-1 -lactamases are related but show only 40 to 50% homology. These enzymes all confer resistance to oxyimino-cephalosporins, especially ceftazidime, and aztreonam. They also show some homology to the chromosomal cephalosporinases in Bacteroides spp. and may have originated from this genus (147). An unusual feature of SFO-1, which is highly related to a class A -lactamase from Serratia fonticola, is that it is a transferable -lactamase that can be induced to high-level production of -lactamase by imipenem (94). The plasmid carrying the gene encoding the SFO-1 -lactamase also carries the ampr regulatory gene that is necessary for the induction of class C -lactamases. However, unlike class C -lactamases, SFO-1 cannot hydrolyze cephamycins and is inhibited well by clavulanic acid (94). GES-1 is another uncommon ESBL enzyme that is not closely related to any other plasmid-mediated -lactamase but does show 36% homology to a carbenicillinase from Proteus mirabilis (136). A dendrogram of the phylogeny of ESBL sequences is shown in Fig. 4. The TEM and SHV families are tightly clustered and are related to each other. All of the class A ESBLs are more closely related to each other than they are to any of the class D OXA-type enzymes. ESBL DETECTION METHODS The increased prevalence of Enterobacteriaceae producing ESBLs creates a great need for laboratory testing methods that will accurately identify the presence of these enzymes in clinical isolates. Although most ESBLs confer resistance to one or FIG. 4. Phylogeny of ESBLs. Representative sequences of various ESBLs were obtained from GenBank. The PC1 (class A, S. aureus enzyme), IMP-1 (class B, metallo-enzyme), and ACT-1 (class C, AmpC-type enzyme) -lactamases were included for comparison. Signal peptides were identified with SPSScan and removed prior to alignment. Sequences were aligned using Clustal X (168). Trees were constructed with Clustal X, which uses the neighbor-joining method, with a bootstrap value of 1,000. The IMP-1 sequence was used to root the tree. Trees were visualized with TREEVIEW (118).

9 VOL. 14, 2001 EXTENDED-SPECTRUM -LACTAMASES 941 more of the oxyimino- -lactam antibiotics, the -lactamase does not always increase the MICs to high enough levels to be called resistant by the National Committee for Clinical Laboratory Standards (NCCLS) interpretive guidelines (78, 111). The sensitivity and specificity of a susceptibility test to detect ESBLs vary with the cephalosporin tested. A number of investigators have suggested that either dilution tests or disk diffusion susceptibility tests performed with cefpodoxime detected more ESBLs than other cephalosporins such as ceftazidime, cefotaxime, and ceftriaxone (52, 100). However, more recent data suggest that susceptibility testing with cefpodoxime can lead to a high number of false-positives if the current NCCLS interpretive criteria are applied (F. C. Tenover, P. Raney, P. P. Williams, K. L. Brittan, C. D. Steward, S. K. Fridkin, R. P. Gaynes, and J. E. McGowan, Jr., 40th Intersci. Conf. Antimicrob. Agents Chemother., abstr. 1606, 2000). The NCCLS is currently reevaluating the testing procedures and interpretive criteria that should be used for the detection of ESBLs. The failure of either MIC or disk tests alone to accurately detect the presence of an ESBL in all strains of E. coli and K. pneumoniae has been well documented (52, 73). In a recent survey conducted through the World Health Organization, 5.4% of laboratories using disk diffusion tests found an ESBLproducing challenge strain to be susceptible to all cephalosporins (165). In that study, Tenover et al. reported that only 2 of the 130 laboratories surveyed specifically reported the isolate as an ESBL producer (165). It also appears that there is a difference in the ability of various susceptibility-testing methods used for detecting cephalosporin resistance in an ESBLproducing strain. Steward et al. reported the results of a proficiency test assessing the ability of hospital laboratories participating in Project ICARE (Intensive Care Antimicrobial Resistance Epidemiology) to detect specific types of antimicrobial resistance (160). Only 35% of laboratories using the Vitek system reported an ESBL challenge strain of K. pneumoniae as being resistant to ceftazidime and ceftriaxone. In contrast, 100% of the laboratories using the MicroScan system reported the same strain as being resistant. However, only 29% of the laboratories using MicroScan reported the strain as being resistant to ceftriaxone (160). This lack of sensitivity and specificity in traditional susceptibility tests to detect ESBLs has prompted the search for an accurate test to detect the presence of ESBLs in clinical isolates. In the years since ESBLs were first described, a number of different testing methods have been suggested. Clinical Microbiology Techniques Clinical microbiology tests employ a -lactamase inhibitor, usually clavulanate, in combination with an oxyimino-cephalosporin such as ceftazidime or cefotaxime. In these tests, the clavulanate inhibits the ESBL, thereby reducing the level of resistance to the cephalosporin. Several ESBL detection tests that have been proposed are based on the Kirby-Bauer disk diffusion test methodology. One of the first detection tests to be described was the double-disk approximation test described by Jarlier et al. (76). In this test, the organism is swabbed onto a Mueller-Hinton agar plate. A susceptibility disk containing amoxicillin-clavulanate is placed in the center of the plate, and disks containing one of the oxyimino- -lactam antibiotics are placed 30 mm (center to center) from the amoxicillin-clavulanate disk. As shown in Fig. 5, enhancement of the zone of inhibition of the oxyimino- lactam caused by the synergy of the clavulanate in the amoxicillin-clavulanate disk is a positive result (76). This test remains a reliable method for the detection of ESBLs. However, it has been suggested that the sensitivity of this test can be increased by reducing the distance between the disks to 20 mm (169, 171). The use of cefpodoxime as the expanded-spectrum cephalosporin of choice for use in double-disk tests for ESBL detection has been suggested (41). Alternatively, the addition of clavulanate (4 g/ml) to the Mueller-Hinton agar can be used to potentiate the zone of inhibition of one or more disks containing expanded-spectrum cephalosporins (67). A similar test was designed by Jacoby and Han, in which 20 g of sulbactam was added to susceptibility disks containing one of the oxyimino- -lactam antibiotics (73). An increase of 5 mm in the zone of inhibition in a disk containing sulbactam compared to the drug alone was considered a positive test. Although many ESBL-producing strains were detected with this method, a significant number of strains were not. In addition, a number of AmpC-producing strains also showed an enhancement of the zone diameter with the addition of sulbactam (73). Recently, several commercial manufacturers have developed disks that contain an expanded-spectrum cephalosporin plus clavulanate. A differential between results obtained with 10- g disks containing cefpodoxime, ceftazidime, or cefotaxime with or without the addition of 1 g of clavulanate was shown to accurately detect the presence of an ESBL (35, 105). Another method suggested for the detection of ESBLs is the three-dimensional test described by Thomson and Sanders (169). In this test, following inoculation of the test organism onto the surface of a Mueller-Hinton agar plate, a slit is cut into the agar, into which a broth suspension of the test organism is introduced. Subsequently, antibiotic disks are placed on the surface of the plate 3 mm from the slit. Distortion or discontinuity in the expected circular zone of inhibition is considered a positive test (169). This test was determined to be very sensitive in detecting ESBLs, but it is more technically challenging and labor intensive than other methods. All of the tests utilizing one of the variations of a disk diffusion technique require some interpretation and therefore should be performed by clinical microbiologists experienced in reading these tests. It has also been suggested that dilution tests performed with an expanded-spectrum cephalosporin with and without the addition of clavulanic acid or another -lactamase inhibitor be used for the detection of ESBLs in a clinical isolate. In general, these tests look for a reduction in the MIC of the cephalosporin in the presence of a -lactamase inhibitor. However, the question of which cephalosporin to use has not been definitively resolved (170). Currently, the NCCLS recommends an initial screening by testing for growth in a broth medium containing 1 g/ml of one of five expanded-spectrum -lactam antibiotics. A positive result is to be reported as suspicious for the presence of an ESBL (111). This screen is then followed by a phenotypic confirmatory test that consists of determining MICs of either ceftazi-

10 942 BRADFORD CLIN. MICROBIOL. REV. Downloaded from FIG. 5. Double-disk diffusion and Etest ESBL detection tests. (A) The double-disk diffusion ESBL detection test as suggested by Jarlier et al. is shown (76). A disk containing amoxicillin-clavulanate (AMC) is placed in proximity to a disk containing ceftazidime (CAZ) or another oxyimino-cephalosporin. The clavulanate in the amoxicillin-clavulanate disk diffuses through the agar and inhibits the -lactamase surrounding the ceftazidime disk. Enhancement of the zone of the ceftazidime disk on the side facing the amoxicillin-clavulanate disk is interpreted as a positive test. (B) Etest ESBL strip (AB Biodisk, Solna, Sweden). The zone of inhibition is read from two halves of the strip containing ceftazidime alone (TZ) or ceftazidime plus clavulanate (TZL). A reduction in the MIC of ceftazidime of 3 dilutions in the presence of clavulanate is interpreted as a positive test. (C) The Etest ESBL strip is sometimes difficult to interpret with weak enzyme producers such as the strain expressing TEM-12 shown in this panel. The clavulanate from the ceftazidime plus clavulanate half of the strip diffuses into the agar and interferes with the reading of the MICs for the half of the strip containing ceftazidime alone. on November 7, 2018 by guest dime or cefotaxime with and without the presence of clavulanic acid (4 g/ml). A decrease in the MIC of 3 twofold dilutions in the presence of clavulanate is indicative of the presence of an ESBL. If an ESBL is detected, the strain should be reported as nonsusceptible to all expanded-spectrum cephalosporins and aztreonam regardless of the susceptibility testing result (111). Several commercial manufacturers have developed ESBL detection tests that can be used along with MIC test methods already in place in the clinical laboratory. Etest ESBL strips (AB Biodisk, Solna, Sweden) are two-sided strips that contain a gradient of ceftazidime on one end and ceftazidime plus clavulanate on the other end. As shown in Fig. 5, a positive test for an ESBL is a 3-dilution reduction in the MIC of ceftazidime in the presence of clavulanic acid. This test was shown to be more sensitive than the double-disk approximation test in detecting ESBLs in clinical isolates (39). This method is convenient and easy to use, but it is sometimes difficult to read the test when the MICs of ceftazidime are low because the clavulanate sometimes diffuses over to the side that contains ceftazidime alone (Fig. 5) (183). The automated microbial susceptibility test system Vitek

11 VOL. 14, 2001 EXTENDED-SPECTRUM -LACTAMASES 943 TABLE 6. ESBL detection techniques Technique type Test Advantages Disadvantages Reference(s) Clinical microbiology Standard NCCLS interpretive Easy to use, performed in ESBLs not always resistant 78, 111 criteria every lab NCCLS ESBL confirmatory Easy to use and interpret Sensitivity depends on choice of 111 test oxyimino-cephalosporin Double-disk approximation Easy to use, easy to interpret Distance of disk placement for 76, 169, 71 test optimal sensitivity not standardized Three-dimensional test Sensitive, easy to interpret Not specific for ESBLS, labor 169 intensive Etest ESBL strips Easy to use Not always easy to interpret, not as 183 sensitive as double-disk test Vitek ESBL test Easy to use, easy to interpret Reduced sensitivity 149, 164 Molecular detection DNA probes Specific for gene family (e.g., TEM or SHV) PCR Oligotyping PCR-RFLP PCR-SSCP LCR Nucleotide sequencing Easy to perform, specific for gene family (e.g., TEM or SHV) Detects specific TEM variants Easy to perform, can detect specific nucleotide changes Can distinguish between a number of SHV variants Can distinguish between a number of SHV variants The gold standard, can detect all variants Labor intensive, cannot distinguish between ESBLs and non-esbls, cannot distinguish between variants of TEM or SHV Cannot distinguish between ESBLs and non-esbls, cannot distinguish between variants of TEM or SHV Requires specific oligonucleotide probes, labor intensive, cannot detect new variants Nucleotide changes must result in altered restriction site for detection Requires special electrophoresis conditions Requires a large number of oligonucleotide primers Labor intensive, can be technically challenging, can be difficult to interpret manual methods 7, 55, 70 42, 90, , Downloaded from (Biomerieux, Hazlewood, Mo.) has also produced an ESBL test that utilizes either ceftazidime or cefotaxime alone and in combination with clavulanic acid (4 g/ml). A predetermined reduction in growth in wells containing clavulanate compared to those containing drug alone indicates the presence of an ESBL. In a study of Klebsiella spp. and E. coli expressing well-characterized -lactamases, Sanders et al. showed that the Vitek ESBL test was 99% sensitive and specific for the detection of ESBLs (149). Furthermore, updated computer algorithms in the new Vitek system have also been shown to categorize the -lactamases present in many gram-negative clinical isolates based on the phenotype of susceptibility patterns with various -lactam antibiotics (150). While each of these tests has its merit, none of these methods can accurately detect all strains producing ESBLs. Vercauteren et al. showed that the Etest ESBL test with ceftazidime only detected 81% of ESBLs tested in their laboratory, compared to 97 and 91% for the double-disk test and the threedimensional test, respectively (183). Tzelepi et al. have reported that the Vitek ESBL detection test failed to detect the majority of ESBL-producing strains of Enterobacter spp. (171). In a recent survey of detection of ESBLs in clinical isolates, Tenover et al. found that only 18% of laboratories correctly identified challenge organisms as potential ESBL producers using susceptibility to one or more expanded-spectrum -lactam antibiotics as the method of detection (164). Furthermore, a survey in Europe found that 37% of ESBL-producing organisms were mistakenly reported as being susceptible to expanded-spectrum cephalosporins (86). The merits and shortcomings of each of the detection tests are outlined in Table 6. Of the tests that have been developed to date, the double-disk approximation test recommended by Jarlier et al. (76), and the broth-dilution MIC reduction method (NCCLS confirmatory test) (111) are the easiest and most cost-effective methods for use by many clinical laboratories. However, none of the detection tests that are based on the phenotype of the -lactamase produced are 100% sensitive or specific for the accurate detection of ESBLs among clinical isolates of gram-negative bacteria. The need for improved detection of ESBLs in clinical isolates is well recognized (123). It should also be noted that caution must be employed when interpreting ESBL detection tests because there have been reports of false-positive results for ESBL phenotypic screening tests that can occur with strains that do not possess an ESBL. Several groups have reported that the high-level expression of SHV-1 in K. pneumoniae can cause the MIC of ceftazidime to rise to levels at which an ESBL would be suspected (99, 129, 141). In addition, Rasheed et al. reported that the production of SHV-1 in a strain of K. pneumoniae that was also lacking an outer membrane porin protein caused a false-positive in ESBL detection tests that looked at the differential between MICs of oxyimino- -lactam antibiotics with and without clavulanate (139). The presence of an ESBL can also be masked by the expression of an AmpC-type enzyme in the same strain (28). on November 7, 2018 by guest

12 944 BRADFORD CLIN. MICROBIOL. REV. Molecular Detection Methods The tests described above only presumptively identify the presence of an ESBL. The task of identifying which specific ESBL is present in a clinical isolate is more complicated. In the early days of studying ESBLs, determination of the isoelectric point was usually sufficient to identify the ESBL that was present. However, with 90 TEM-type -lactamases, many of which possess identical isoelectric points, determination of the ESBL by isoelectric point is no longer possible. A similar situation is found in the SHV, CTX-M, and OXA families of ESBLs. Early detection of -lactamase genes was performed using DNA probes that were specific for TEM and SHV enzymes (7, 55, 70). However, using DNA probes can sometimes be rather labor intensive. The easiest and most common molecular method used to detect the presence of a -lactamase belonging to a family of enzymes is PCR with oligonucleotide primers that are specific for a -lactamase gene. Oligonucleotide primers can be chosen from sequences available in public databases such as Genbank (GenBank, National Center for Biotechnology Information, These primers are usually chosen to anneal to regions where various point mutations are not known to occur. However, PCR will not discriminate among different variants of TEM or SHV. Several molecular methods that will aid in the detection and differentiation of ESBLs without sequencing have been suggested. The first molecular method for the identification of -lactamase was the oligotyping method developed by Ouellette et al., which was used to discriminate between TEM-1 and TEM-2 (117). This method used oligonucleotide probes that are designed to detect point mutations under stringent hybridization conditions. Subsequently, Mabilat and Courvalin developed additional oligonucleotide probes to detect mutations at six positions within the bla TEM gene (89). Using this method, several new TEM variants were identified within a set of clinical isolates. The probes used in oligotyping tests for TEM -lactamases have been labeled either with a radioisotope or with biotin (89, 167). Another approach for molecular characterization of the TEM -lactamase gene was to add restriction fragment length polymorphism analysis to PCR (PCR-RFLP) (6). In this test, amplified PCR products were subjected to digestion with several restriction endonucleases, and the subsequent fragments were separated by electrophoresis. The sizes of the fragments generated by each restriction enzyme indicate point mutations within the bla TEM structural gene. A number of different tests have been proposed for the detection and identification of SHV derivatives. The simplest of these was suggested by Nüesch-Inderbinen et al. and employs PCR-RFLP (116). Following PCR, the amplified DNA is digested with restriction enzyme NheI, which detects the G- to-a nucleotide change that gives rise to the glycine-to-serine substitution at position 238 that is common to many of the early SHV-type ESBLs. Although this method cannot determine which SHV-type ESBL is present, it can detect the specific mutation at position 238 (116). Another method used to characterize SHV-type ESBLs is PCR single-strand conformational polymorphism (PCR-SSCP) analysis. This method has been used to detect a single base mutation at specific locations within the bla SHV gene (106, 107). In this test, a 475-bp amplimer is generated using oligonucleotide primers that are internal to the coding sequence of the bla SHV gene, digested with restriction enzyme PstI. The fragments are then denatured and separated on a 20% polyacrylamide gel. Genes for SHV-1, -2, -3, -4, -5, and -7 -lactamases can be identified by the electrophoretic pattern of the digested amplimer (106, 107). With the identification of a number of additional SHV-type -lactamase genes, PCR-RFLP was developed to help with the identification of some of the newer SHV variants (38). Following PCR, Chanawong et al. used a variety of restriction endonucleases to detect 12 mutations at 11 positions within the bla SHV structural gene. The combination of PCR-SSCP with PCR-RFLP allows the identification of 17 different SHV genes (38). Another method proposed for the identification of SHV genes is the use of ligase chain reaction (LCR) (80). LCR allows the discrimination of DNA sequences that differ by a single base pair by the use of a thermostable ligase with four oligonucleotide primers that are complimentary to the target sequence and hybridize adjacent to each other. A single base mismatch in the oligonucleotide junction will not be ligated and subsequently amplified. In this LCR test, the target DNA containing the bla SHV gene is denatured in a thermocycler and annealed with biotinylated oligonucleotide primers that detect mutations at four positions. The LCR product is detected by an enzymatic reaction using NADPH-alkaline phosphatase. This method was able to detect seven of the SHV variants. For OXA-10-derived ESBLs, the presence of an OXA-type gene in clinical isolates of P. aeruginosa was first detected using a colony hybridization technique (178). Subsequently, positive isolates were subjected to PCR with specific OXA primers and then digested with restriction endonucleases that would distinguish several groups of related OXA enzymes based on the sizes of the restriction fragments. While this technique does not completely identify which OXA gene is present in a strain, it can distinguish the ESBL OXA-type -lactamases from non- ESBLs that are also related to OXA-10 (178). Nucleotide sequencing remains the standard for determination of the specific -lactamase gene present in a strain. However, this too can give variable results depending on the method used (25). It is possible that some of the variability seen in the sequences for some of the SHV -lactamases was due to compressions and difficulty in reading traditional sequencing autoradiographs, rather than actual differences in the sequence (25). Medical Significance of Detection of ESBLs It is generally thought that patients having infections caused by an ESBL-producing organism are at an increased risk of treatment failure with an expanded-spectrum -lactam antibiotic. Therefore, it is recommended that any organism that is confirmed for ESBL production according to NCCLS criteria be reported as resistant to all expanded-spectrum -lactam antibiotics, regardless of the susceptibility test result (111). While some ESBL-producing strains have overt resistance to expanded-spectrum -lactam antibiotics, many isolates will not be phenotypically resistant according to guidelines such as those previously used by the NCCLS. Therefore, it is important for the clinical microbiology lab to be aware of isolates that