Browse the corpus

Members of the bacterial genus Pseudomonas, especially P. aeruginosa, are among the major nosocomial pathogens because of their ubiquitous nature and ability to colonize and survive in hospital reservoirs and because of their role in causing infections in immunocompromised and critically ill patients (1). P. aeruginosa shows a high level of intrinsic resistance to antimicrobial drugs and an ability to become even more drug resistant. These characteristics are caused by selective pressure of mutations in chromosomal genes that lead to ampC hyperexpression, repression or inactivation of oprD, and overexpression of efflux pumps (2). In addition, P. aeruginosa is able to acquire other drug-resistance determinants by horizontal transfer of mobile genetic elements coding for class B carbapenemases (also called metallo-β-lactamases [MBLs]), which hydrolyze all β-lactams except aztreonam (3).

nactivation of oprD, and overexpression of efflux pumps (2). In addition, P. aeruginosa is able to acquire other drug-resistance determinants by horizontal transfer of mobile genetic elements coding for class B carbapenemases (also called metallo-β-lactamases [MBLs]), which hydrolyze all β-lactams except aztreonam (3). Because they can be disseminated horizontally through transfer of resistance determinants, MBLs have become a serious concern in hospitals worldwide over the past decade. Such acquired MBLs include the IMP and VIM types SPM-1, GIM-1, SIM-1, AIM-1, KHM-1, NDM-1, and SID-1 (4,5). MBL genes are normally encoded in class 1 integrons along with other resistance determinants, such as the aminoglycoside-modifying enzymes. The integrons are frequently located in plasmids or transposons, the dissemination of which contributes to the global spread of this resistance mechanism (6,7). The versatility and ability of P. aeruginosa to combine different resistance mechanisms has led to emergence of strains that are resistant to multiple antimicrobial drugs, which severely limits therapeutic options for treating infections (8,9). Interim definitions defining multidrug-resistant (MDR), extensively drug-resistant (XDR), and pandrug-resistant bacteria, including P. aeruginosa, have been recently reported (10).

nce of strains that are resistant to multiple antimicrobial drugs, which severely limits therapeutic options for treating infections (8,9). Interim definitions defining multidrug-resistant (MDR), extensively drug-resistant (XDR), and pandrug-resistant bacteria, including P. aeruginosa, have been recently reported (10). Although the prevalence of P. aeruginosa strains producing carbapenemases in Spain was considered low (0.4% of carbapenem-resistant isolates) (11) compared with prevalence in other countries in Europe, such as Italy (12.6% of carbapenem-resistant isolates) (12), detection of these isolates is no longer sporadic (13,14). Recent evidence from multicenter studies indicates an ≈10-fold increase in prevalence of these isolates in the past 5 years (15). During 2007 and 2008, a polyclonal outbreak of VIM-2–producing P. aeruginosa was detected in a hospital in Spain. At the same time, another outbreak in the hematology department of a hospital in Spain was caused by a P. aeruginosa ST235 clone, which produced GES-1 and GES-5, 2 extended-spectrum β-lactamases (16). We have observed a sharp increase in infections with drug-resistant P. aeruginosa that produces carbapenemase. Thus, we conducted a study to determine the clinical and molecular epidemiologic characteristics of drug-resistant P. aeruginosa isolates detected at a major hospital during 2007–2010.

ctrum β-lactamases (16). We have observed a sharp increase in infections with drug-resistant P. aeruginosa that produces carbapenemase. Thus, we conducted a study to determine the clinical and molecular epidemiologic characteristics of drug-resistant P. aeruginosa isolates detected at a major hospital during 2007–2010. Materials and Methods Study Population We conducted a retrospective study of all non–cystic fibrosis adult patients who were colonized or infected with P. aeruginosa isolates during January 2007–December 2010 at the Hospital Universitario 12 de Octubre in Madrid. This hospital is a 1,300-bed tertiary-care facility serving a population of 600,000 persons (≈42,000 admissions/year). We classified resistance patterns in P. aeruginosa according to recently published proposed interim definitions (10). An isolate was defined as MDR if it was resistant to >1 drug in >3 categories of drugs and XDR if it was resistant to >1 drug in <2 drug categories. The drugs on which our categorization was based included antipseudomonal cephalosporins (ceftazidime [CAZ], cefepime [FEP]), carbapenems (imipenem [IMP], meropenem [MER]), piperacillin/tazobactam (PIP-TZ), aztreonem, fluoroquinolones (ciprofloxacin [CIP]), and aminoglycosides (gentamicin [GEN], tobramycin [TOB], amikacin [AMK]).

on which our categorization was based included antipseudomonal cephalosporins (ceftazidime [CAZ], cefepime [FEP]), carbapenems (imipenem [IMP], meropenem [MER]), piperacillin/tazobactam (PIP-TZ), aztreonem, fluoroquinolones (ciprofloxacin [CIP]), and aminoglycosides (gentamicin [GEN], tobramycin [TOB], amikacin [AMK]). Unique (nonduplicate) clinical isolates from colonized or infected patients were collected during the study. A case was defined as nosocomial if infection or colonization was detected in a person >48 hours after admission or if a person had documented evidence of hospitalization within the previous 12 months. Colonization was defined as isolation of P. aeruginosa from >1 clinical specimens in the absence of clinical signs consistent with infection. Medical charts were reviewed and demographic, clinical, and microbiological data were collected. Antimicrobial Drug Susceptibility Testing Identification and antimicrobial drug susceptibility testing of P. aeruginosa isolates included in this study were performed by using semi-automated microdilution panels (Soria, Melguizo, Spain) (17). The antimicrobial drugs tested were PIP-TZ, CAZ, FEP, ATM, IMP, MER, CIP, GEN, TOB, AMK and colistin. Break points were applied according to Clinical and Laboratory Standards Institute (CLSI) guidelines (18).

-5 extended-spectrum β-lactamase/class A carbapenemase producers (16). Overall, the percentage of MBL-producing MDR or XDR Pseudomonas spp. isolates during the study was 63.9%. Moreover, if one considers the clone producing GES-1-GES-5, the overall prevalence of isolates producing acquired carbapenemases reaches 79.8%. To investigate the genetic content of integrons from clone B isolates, we conducted PCR mapping of blaVIM-2 and blaIMP-22 genes for 4 strains. The structure of integrons from isolates producing VIM-2 was IntlI-VIM2-aac6'Ib-qacEΔ1 (Figure 2) in all isolates. IMP-22 was also found to be encoded in a class 1 integron, but we were unable to amplify the fragment between blaIMP-22 and qacEΔ1 by PCR, perhaps because of the large size of this DNA fragment. Figure 2 Structure of the class I integron detected in 4 representative isolates of the Pseudomonas spp. epidemic multidrug-resistant sequence type 175 clone, Spain. PA, P. aeruginosa. *Dotted line indicates undetermined part not amplified by PCR.

cluded in this study were performed by using semi-automated microdilution panels (Soria, Melguizo, Spain) (17). The antimicrobial drugs tested were PIP-TZ, CAZ, FEP, ATM, IMP, MER, CIP, GEN, TOB, AMK and colistin. Break points were applied according to Clinical and Laboratory Standards Institute (CLSI) guidelines (18). Genotyping Analysis Epidemiologic relatedness of isolates was studied by using pulsed-field gel electrophoresis (PFGE) and multilocus sequence typing (MLST). PFGE was conducted by macrorestriction of chromosomal DNA with SpeI and separation of restriction fragments by using a CHEF DRIII PFGE system (Bio-Rad Laboratories, Hercules, CA, USA). Migration of DNA fragments was normalized by using an appropriate mass marker, and computer-assisted analysis of PFGE patterns was conducted by using Bionumerics software (Applied Maths, St-Martens-Latem, Belgium). PFGE types were defined on the basis of DNA banding patterns in accordance with criteria defined by Tenover et al. (19). MLST was performed on selected isolates according to published protocols (20). Standard DNA amplification and sequencing of 7 housekeeping genes (acsA, aroE, guaA, mutL, nuoD, ppsA, and trpE) were performed. Isolates were assigned a sequence type (ST) number according to the allelic profiles available in the MLST database (http://pubmlst.org/paeruginosa).

es according to published protocols (20). Standard DNA amplification and sequencing of 7 housekeeping genes (acsA, aroE, guaA, mutL, nuoD, ppsA, and trpE) were performed. Isolates were assigned a sequence type (ST) number according to the allelic profiles available in the MLST database (http://pubmlst.org/paeruginosa). Characterization of Acquired MBLs and Integron Analysis The presence of horizontally acquired β-lactamases was determined by using phenotypic and genetic approaches. Phenotypic tests included analysis with Etest MBL strips (AB Biodisk, Solna, Sweden) for detection of class B carbapenemases. On the basis of positive results from preliminary phenotypic tests, the potential presence of genes encoding acquired metallo-β-lactamases was explored by using PCR amplification and DNA sequence analysis. Described primers and conditions were used to amplify genes encoding VIM and IMP type β-lactamases (11,13). After PCR amplification, sequencing reactions were performed by using the BigDye Terminator Kit (PE Applied Biosystems, Foster City, CA, USA), and sequences were analyzed by using an ABI prism 3100 DNA Sequencer (PE Applied Biosystems). Resulting sequences were compared with those available in GenBank (www.ncbi.nih.gov/BLAST). Integrons harboring MBL-encoding genes were characterized by PCR and DNA sequencing by using specific primers to amplify the IntI1 and qacEΔ1 markers, the DNA region located between intI1 and qacEΔ1, and the corresponding MBL-encoding gene (11,13).

were compared with those available in GenBank (www.ncbi.nih.gov/BLAST). Integrons harboring MBL-encoding genes were characterized by PCR and DNA sequencing by using specific primers to amplify the IntI1 and qacEΔ1 markers, the DNA region located between intI1 and qacEΔ1, and the corresponding MBL-encoding gene (11,13). Statistical Analysis Univariate analysis was performed by using the t test for continuous variables and the χ2 or Fisher exact tests for categorical variables. A p value <0.05 was considered significant. Data were stored and analyzed by using SPSS version 17.0 for Windows software (Analytical Software, St. Paul, MN USA). Results General Characteristics During the 4-year study, of 2,145 patients who were infected or colonized with Pseudomonas spp., 183 harbored MDR or XDR isolates: 13 (2.8%) of 460 in 2007, 32 (6.2%) of 517 in 2008, 38 (7.4%) of 514 in 2009, and 100 of (15.3%) 654 in 2010. The estimated annual incidence of MDR Pseudomonas–infected persons increased from 0.04/1,000 bed-days in 2007 to 0.34/1,000 bed-days in 2010 (Figure 1). Of 183 isolates, 177 were identified as P. aeruginosa and 6 as P. putida. Figure 1 Annual incidence of infections/colonizations by multidrug-resistant (MDR) Pseudomonas spp. and temporal distribution of human cases according to clonal type, Spain.

Results General Characteristics During the 4-year study, of 2,145 patients who were infected or colonized with Pseudomonas spp., 183 harbored MDR or XDR isolates: 13 (2.8%) of 460 in 2007, 32 (6.2%) of 517 in 2008, 38 (7.4%) of 514 in 2009, and 100 of (15.3%) 654 in 2010. The estimated annual incidence of MDR Pseudomonas–infected persons increased from 0.04/1,000 bed-days in 2007 to 0.34/1,000 bed-days in 2010 (Figure 1). Of 183 isolates, 177 were identified as P. aeruginosa and 6 as P. putida. Figure 1 Annual incidence of infections/colonizations by multidrug-resistant (MDR) Pseudomonas spp. and temporal distribution of human cases according to clonal type, Spain. The mean ± SD age of patients was 65.1 ± 15.7 years, and 70.5% were men. Most (95%) cases were nosocomially acquired. The main clinical wards in which drug-resistant bacteria were isolated were internal medicine (57 cases, 31.1%), surgery (32, 17.5%), intensive care (24, 13.1%), pulmonology (21, 11.5%), and hematology (15, (8.2%). Of 183 patients, 143 (78.1%) were considered infected, including 36 (19.7%) with lower respiratory tract infection, 30 (16.4%) with urinary tract infection, 28 (15.3%) with bacteremia, and 22 (12%) with intraabdominal infection. A total of 42 (23%) patients died during hospitalization (Table).

d hematology (15, (8.2%). Of 183 patients, 143 (78.1%) were considered infected, including 36 (19.7%) with lower respiratory tract infection, 30 (16.4%) with urinary tract infection, 28 (15.3%) with bacteremia, and 22 (12%) with intraabdominal infection. A total of 42 (23%) patients died during hospitalization (Table). Molecular Typing of an MDR P. aeruginosa Clone Genotyping analysis of clinical isolates by PFGE showed that 104 isolates belonged to a single major clone (clone B), 29 belonged to a second clone (clone A), and 2 belonged to 2 clones (clones C and D). The remaining isolates, including the 6 P. putida isolates, showed unique PFGE patterns. MLST analysis was performed on 9 isolates in clone B to determine their relationship to other strains that had been described. All isolates that we examined exhibited the same allelic profile (acsA [28], aroE [22], guaA [5], mutL [3], nuoD [3], ppsA [14], and trpE [19]), and were identified as ST175 according to the MLST database. MLST analysis of isolates in clone A had already been performed, and these isolates were classified as ST235 (16).

All isolates that we examined exhibited the same allelic profile (acsA [28], aroE [22], guaA [5], mutL [3], nuoD [3], ppsA [14], and trpE [19]), and were identified as ST175 according to the MLST database. MLST analysis of isolates in clone A had already been performed, and these isolates were classified as ST235 (16). Clone B was initially isolated in February 2008 from a patient admitted to the pulmonology ward with a diagnosis of lower tract respiratory infection. Subsequently, 4 additional clone B isolates were detected in 2008, 23 in 2009, and 76 in 2010 (Figure 1). Twelve patients infected or colonized with this clone were referred to Hospital Universitario 12 de Octubre from 4 other hospitals in Madrid and from a fifth hospital in the Canary Islands. From 5 of these patients, the MDR P. aeruginosa isolate was recovered at the time of admission to Hospital Universitario 12 de Octubre.

e patients infected or colonized with this clone were referred to Hospital Universitario 12 de Octubre from 4 other hospitals in Madrid and from a fifth hospital in the Canary Islands. From 5 of these patients, the MDR P. aeruginosa isolate was recovered at the time of admission to Hospital Universitario 12 de Octubre. Comparison of clinical characteristics for patients infected or colonized with clone B and other MDR P. aeruginosa clones did not show major differences, but patients infected with clone B were slightly older (mean age 67.5 vs. 61.9 years; p = 0.016) and they were more frequently admitted to the internal medicine (37.5% vs. 22.8%; p = 0.033) and pulmonology wards (16.3% vs. 5.1%; p = 0.018). Patients infected with clone B had more frequent underlying respiratory disease such as chronic obstructive pulmonary disease (36.5% vs. 22.8%; p = 0.046) (Table) than patients infected with other clones. We also found similar differences between patients infected with clone A and those infected with other MDR Pseudomonas spp. clones as reported (16).

d more frequent underlying respiratory disease such as chronic obstructive pulmonary disease (36.5% vs. 22.8%; p = 0.046) (Table) than patients infected with other clones. We also found similar differences between patients infected with clone A and those infected with other MDR Pseudomonas spp. clones as reported (16). Antimicrobial Drug Susceptibility Antimicrobial drug–resistance patterns of 183 Pseudomonas spp. isolates were CAZ (100% resistant), FEP (100%), IMP (100%), MER (100%), GEN (97.3%), TOB (96.7%), and CIP (94%), and resistance to PIP-TZ (50.3%), AMK (42.1%), and ATM (41%) was more variable (Table A1). When break points recommended by the European Committee on Susceptibility Testing (EUCAST; www.eucast.org) were applied, the percentage of PIP-TZ–resistant and ATM-resistant isolates increased to 98.4% and 97.8%, respectively. There were no differences in MIC ranges for the other drugs tested when either CLSI or EUCAST break points were applied. All isolates were susceptible to COL. Resistance profiles of MDR isolates in clone B were CAZ (100% resistant), FEP (100%), IMP (100%), MER (100%), CIP (100%), GEN (100%), and TOB (100%), and some isolates were also resistant to ATM (13.5%) and AMK (25%). The percentage of isolates resistant to PIP/TZ according to break points recommended by CLSI and EUCAST were 20.2% and 97.1%, respectively (Table A1).

ere CAZ (100% resistant), FEP (100%), IMP (100%), MER (100%), CIP (100%), GEN (100%), and TOB (100%), and some isolates were also resistant to ATM (13.5%) and AMK (25%). The percentage of isolates resistant to PIP/TZ according to break points recommended by CLSI and EUCAST were 20.2% and 97.1%, respectively (Table A1). Resistance profiles of isolates in clone A were CAZ (100% resistant), FEP (100%), IMP (100%), MER (100%), CIP (96.5%), GEN (100%), TOB (89.6%), AMK (86.2%) and ATM (86.2%). As a result, this clone was classified as XDR, as were clones C and D (Table A1). Detection of MBL Genes All isolates in clone B were positive by phenotypic methods for MBL. PCR analysis and sequencing identified MBL VIM-2 in 103 isolates and IMP-22 in 1 isolate (Table A1). VIM-2 was also detected in isolates in clone C, in 4 unique clones of P. aeruginosa, and in 5 of 6 isolates of P. putida. In 1 P. putida isolate, VIM-1 and VIM-2 MBLs were detected. A VIM-1-type MBL was also found in 1 clone of P. aeruginosa (Table A1). No MBL genes were detected among isolates in clone A, which demonstrated that these isolates were GES-1/GES-5 extended-spectrum β-lactamase/class A carbapenemase producers (16). Overall, the percentage of MBL-producing MDR or XDR Pseudomonas spp. isolates during the study was 63.9%. Moreover, if one considers the clone producing GES-1-GES-5, the overall prevalence of isolates producing acquired carbapenemases reaches 79.8%.

To investigate the genetic content of integrons from clone B isolates, we conducted PCR mapping of blaVIM-2 and blaIMP-22 genes for 4 strains. The structure of integrons from isolates producing VIM-2 was IntlI-VIM2-aac6'Ib-qacEΔ1 (Figure 2) in all isolates. IMP-22 was also found to be encoded in a class 1 integron, but we were unable to amplify the fragment between blaIMP-22 and qacEΔ1 by PCR, perhaps because of the large size of this DNA fragment. Figure 2 Structure of the class I integron detected in 4 representative isolates of the Pseudomonas spp. epidemic multidrug-resistant sequence type 175 clone, Spain. PA, P. aeruginosa. *Dotted line indicates undetermined part not amplified by PCR. Discussion Outbreaks by MBL-producing P. aeruginosa have been documented in hospitals in several countries, and VIM-is the most dominant MBL variant in Spain and worldwide (14,21–27). We report a large outbreak of VIM-2–producing MDR P. aeruginosa. The predominant clone belonged to ST175, a strain that was first detected on February 2008, and it has become increasingly common in Hospital Universitario 12 de Octubre, affecting 104 patients. This MDR P. aeruginosa clone was found in in several wards of the hospital, although it was more frequently associated with patients in the internal medicine and pulmonology wards.

was first detected on February 2008, and it has become increasingly common in Hospital Universitario 12 de Octubre, affecting 104 patients. This MDR P. aeruginosa clone was found in in several wards of the hospital, although it was more frequently associated with patients in the internal medicine and pulmonology wards. The spread of the ST175 clone should be considered an emerging pandemic. It was first identified in 2005 in the United Kingdom and Canada (http://pubmlst.org/paeruginosa) and has been reported in Hungary, the Czech Republic, Poland, Spain, the Unites States, and China (15,28–31). Our study also identified this clone in patients referred to Hospital Universitario 12 de Octubre from 5 other hospitals in Spain, supporting the notion that this clone has disseminated nationwide (28). ST175 has been associated with multidrug-resistant isolates and acquisition of different β-lactamases, mostly located on mobile elements such as integrons (15,31,32).

referred to Hospital Universitario 12 de Octubre from 5 other hospitals in Spain, supporting the notion that this clone has disseminated nationwide (28). ST175 has been associated with multidrug-resistant isolates and acquisition of different β-lactamases, mostly located on mobile elements such as integrons (15,31,32). In our study, all MDR P. aeruginosa isolates belonging to ST175 producedVIM-2 type MBLs, except for 1 that produced IMP-22. PCR mapping showed that VIM-2 was inserted in a class 1 integron with an aminoglycoside-modifying enzyme (aac6′-1b). The IMP-type MBLs are most common among Pseudomonas spp. isolates in Asia, although they have been reported less frequently in some countries in Europe such as Italy and Austria (33,34). We report a lineage of ST175 MDR P. aeruginosa that produces IMP-22, which adds this MBL to the list of acquired β-lactamases associated with this epidemic clone. A thorough understanding of the genetic mechanism involved and horizontal and longitudinal dissemination is necessary, particularly for those carrying integron- and plasmid-borne MBLs, given their additional capacity for intraspecies and interspecies spread of multidrug resistance. Although the origin of the ST175-VIM-2 MDR P. aeruginosa strain is unknown, this clone emerged in Hospital Universitario 12 de Octubre in February 2008, seven months after the first detection of VIM-2 type MBLs in a strain of P. putida. This species and other Pseudomonas species might play a major role as potential reservoirs for MDR determinants by enhancing their transfer to P. aeruginosa clones (3).

e emerged in Hospital Universitario 12 de Octubre in February 2008, seven months after the first detection of VIM-2 type MBLs in a strain of P. putida. This species and other Pseudomonas species might play a major role as potential reservoirs for MDR determinants by enhancing their transfer to P. aeruginosa clones (3). The ST175 clone was able to persist in Hospital Universitario 12 de Octubre for >34 months and has disseminated widely in spite of control measures that have been implemented, such as strict isolation of patients, active surveillance of patients at the time of entry into intensive care units, and environment investigation of possible sources of colonization. The spread of this clone among patients admitted to different sections of the hospital and high selective pressure for antimicrobial drug resistance may encourage its persistence. The design and implementation of infection control strategies in these hyperendemic situations is challenging. We recently faced a similar situation in Hospital Universitario 12 de Octubre with a large outbreak of MDR Acinetobacter baumannii that persisted for >30 months but that was finally controlled (35). This study also detected emergence of multiple strains of Pseudomonas spp. that produced VIM-2- and VIM-1-type MBLs, including >6 P. aeruginosa and 6 P. putida clones. The polyclonal nature of MBL-based resistance might have major epidemiologic implications because sporadically isolated strains may eventually spread in the hospital environment or act as a reservoir for horizontal transfer of resistance determinants.

VIM-1-type MBLs, including >6 P. aeruginosa and 6 P. putida clones. The polyclonal nature of MBL-based resistance might have major epidemiologic implications because sporadically isolated strains may eventually spread in the hospital environment or act as a reservoir for horizontal transfer of resistance determinants. The emergence of MBL-producing MDR P. aeruginosa is a major health problem because it leaves the clinician with almost no therapeutic options for treating nosocomial infections caused by P. aeruginosa. Our results showed that isolates belonging to ST175 had susceptibility only to PIP/TZ (79.8%), ATM (86.5%), AK (75%), and colistin (100%). The difference in PIP/TZ susceptibility depending on the break point criteria applied is remarkable. When the EUCAST susceptibility testing criteria were applied, only 2.9% isolates were susceptible to PIP/TZ compared with ≈80% when criteria recommended by CLSI were applied. A recent report concluded that in P. aeruginosa bacteremia caused by isolates with reduced PIP/TZ susceptibility (32/4 µg/mL or 64/4 µg/mL), empirically prescribed PIP/TZ therapy was associated with increased patient deaths (36). In our study, most isolates had PIP/TZ susceptibility in this range. Fortunately, the 2012 CLSI PIP/TZ break point (37), which was implemented during the review of this report, has been reported as 16/4 µg/mL, thus agreeing with the break point established by EUCAST. Confluence of susceptibility testing criteria among agency standards are useful for optimizing strategies to treat severe MDR P. aeruginosa infections.

/TZ break point (37), which was implemented during the review of this report, has been reported as 16/4 µg/mL, thus agreeing with the break point established by EUCAST. Confluence of susceptibility testing criteria among agency standards are useful for optimizing strategies to treat severe MDR P. aeruginosa infections. In summary, we report a large outbreak of infections caused by a VIM-2–producing ST175 MDR P. aeruginosa strain that was responsible for 76% of infections or colonizations by MDR P. aeruginosa in 2010 at Hospital Universitario 12 de Octubre, and >50% of infections or colonizations during the study period. This epidemic clone is also circulating in other hospitals in Spain and other countries. The underlying reasons for the widespread success of this clone still need to be fully elucidated fully, including the potential for an enhanced ability to acquire MDR determinants that facilitate persistence under conditions of antimicrobial drug selective pressure encountered in the hospital environment (21,22). Deciphering the epidemiologic and molecular aspects driving the emergence and spread of such strains is crucial to the implementation of efficient measures to control their dissemination. Suggested citation for this article: Viedma E, Juan C, Villa J, Barrado L, Orellana MÁ, Sanz F, et al. VIM-2–producing multidrug-resistant Pseudomonas aeruginosa clone ST175, Spain. Emerg Infect Dis [serial on the Internet]. 2012 Aug [date cited]. http://dx.doi.org/10.3201/eid1808.111234 Acknowledgment We thank Tobin Hellyer for reviewing the manuscript.

Suggested citation for this article: Viedma E, Juan C, Villa J, Barrado L, Orellana MÁ, Sanz F, et al. VIM-2–producing multidrug-resistant Pseudomonas aeruginosa clone ST175, Spain. Emerg Infect Dis [serial on the Internet]. 2012 Aug [date cited]. http://dx.doi.org/10.3201/eid1808.111234 Acknowledgment We thank Tobin Hellyer for reviewing the manuscript. This study was supported by Spanish Network for the Research in Infectious Diseases (RD06/0008) from the Instituto de Salud Carlos III, Spain.

Suggested citation for this article: Viedma E, Juan C, Villa J, Barrado L, Orellana MÁ, Sanz F, et al. VIM-2–producing multidrug-resistant Pseudomonas aeruginosa clone ST175, Spain. Emerg Infect Dis [serial on the Internet]. 2012 Aug [date cited]. http://dx.doi.org/10.3201/eid1808.111234 Acknowledgment We thank Tobin Hellyer for reviewing the manuscript. This study was supported by Spanish Network for the Research in Infectious Diseases (RD06/0008) from the Instituto de Salud Carlos III, Spain. Table A1 Clonal distribution, type of carbapenemase, and drug resistance patterns of MDR Pseudomonas isolates, Spain, January 2007–December 2010 * Isolate No. isolates/y Carbapenemase type (no. isolates) ST No. (%) resistant isolates 2007 2008 2009 2010 PIP/TZ CAZ FEP IMP MER ATM GEN TOB AMK CIP All MDR isolates (183) 13 32 38 100 VIM-1, VIM-2, IMP-22, GES1–5 (146) NA 92 (50.3)/ 180 (98.4) 183 (100) 183 (100) 183 (100) 183 (100) 75 (41.0)/ 179 (97.8)† 178 (97.3) 177 (96.7) 77 (42.1) 172 (94) P. aeruginosa (clonal types) B (104) 0 5 23 76 VIM-2 (103), IMP-22 (1) 175, 175 21 (20.2)/ 101 (97.1)† 104 (100) 104 (100) 104 (100) 104 (100) 14 (13.5)/ 100 (95.2)† 104 (100) 104 (100) 26 (25) 104 (100) A (29)‡ 8 16 4 1 GES 1/5 (29) 235 29 (100) 29 (100) 29 (100) 29 (100) 29 (100) 25 (86.2) 29 (100) 26 (89.6) 25 (86.2) 28 (96.5) C (2) 0 0 1 1 VIM-2 (2) NA 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) D (2) 0 0 0 2 Noncarbapenemase (2) NA 2 (100) 2 (100) 2 (100) 2 (100) 2 (100) 0 2 (100) 2 (100) 2 (100) 2 (100) Unique clones (40) 4 10 8 18 Noncarbapenemase (35) NA 31 (88.6)/ 35 (100)† 35 (100) 35 (100) 35 (100) 35 (100) 26 (74.3) 30 (85.7) 32 (65.7) 17 (48.3) 25 (71.4) 0 1 0 0 PA_5 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 1 0 PA_10 VIM-2 NA 0 0 0 0 0 0 0 0 1 0 PA_12 VIM-1 NA 4 (80)/ 5 (100)† 5 (100) 5 (100) 5 (100) 5 (100) 4 (80) 5 (100) 5 (100) 3 (60) 5 (100) 0 0 1 0 PA_13 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 0 0 1 PA_28 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 P. putida (clonal types) Unique clones (6) 1 1 2 2 0 NA 0 0 0 0 0 0 0 0 0 0 1 0 0 0 PP_1 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 1 0 0 PP_11 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 0 1 0 PP_14 VIM-2 NA 3 (50)/ 6 (100)† 6 (100) 6 (100) 6 (100) 6 (100) 4 (66.6) 6 (100) 6 (100) 2 (33.3) 6 (100) 0 0 1 0 PP_19 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 0 1 0 PP25_VIM-1/VIM-2 NA 0 0 0 0 0 0 0 0 0 0 0 0 1 0 PP_27 VIM-2 NA 0 0 0 0 0 0 0 0 0 0 *MDR, multidrug resistant; ST, sequence type; PIP/TZ, piperacillin-tazobactam; CAZ, ceftazidime; FEP, cefepime; IMP, imipenem; MER, meropenem; ATM, aztreonam; GEN, gentamicin; TOB, tobramycin; AMK, amikacin; CIP, ciprofloxacin; NA, not available. None of the isolates showed resistance to colistin.

A 0 0 0 0 0 0 0 0 0 0 *MDR, multidrug resistant; ST, sequence type; PIP/TZ, piperacillin-tazobactam; CAZ, ceftazidime; FEP, cefepime; IMP, imipenem; MER, meropenem; ATM, aztreonam; GEN, gentamicin; TOB, tobramycin; AMK, amikacin; CIP, ciprofloxacin; NA, not available. None of the isolates showed resistance to colistin. †Percentage drug-resistant isolates when the European Committee on Susceptibility Testing break point was applied. ‡Viedma et al. (16).

A 0 0 0 0 0 0 0 0 0 0 *MDR, multidrug resistant; ST, sequence type; PIP/TZ, piperacillin-tazobactam; CAZ, ceftazidime; FEP, cefepime; IMP, imipenem; MER, meropenem; ATM, aztreonam; GEN, gentamicin; TOB, tobramycin; AMK, amikacin; CIP, ciprofloxacin; NA, not available. None of the isolates showed resistance to colistin. †Percentage drug-resistant isolates when the European Committee on Susceptibility Testing break point was applied. ‡Viedma et al. (16). Table Characteristics of 183 patients colonized or infected with clone B or nonclone B multidrug-resistant Pseudomonas isolates, Spain, January 2007–December 2010* Characteristic Patients with clone B, n = 104 Patients with non–clone B, n = 79 p value Mean ± SD age, y 67.5 ± 15.4 61.9 ± 15.7 0.016 Male 74 (71.1) 55 (69.6) 0.822 Hospital location Surgical ward 15 (14.4) 17 (21.5) 0.211 Intensive care unit 11 (10.6) 13 (16.4) 0.243 Internal medicine ward 39 (37.5) 18 (22.8) 0.033 Hematology ward 4 (3.8) 11 (13.9) 0.014 Pulmonology ward 17 (16.3) 4 (5.1) 0.018 Hospitalization within previous 3 mo 48 (46.1) 37 (46.8) 0.927 Surgical procedure 29 (27.9) 32 (40.5) 0.073 Transplant 4 (3.8) 8 (10.1) 0.089 Hematologic malignancy 8 (7.7) 11(13.9) 0.171 Solid tumor 21 (20.2) 13 (16.4) 0.520 Diabetes mellitus 29 (27.9) 21 (26.9) 0.845 Chronic obstructive pulmonary disease 38 (36.5) 18 (22.8) 0.046 Central catheter 83 (79.8) 59 (76.7) 0.410 Urinary catheter 60(57.7) 44(55.7) 0.441 Infections 82 (78.8) 61 (77.2) 0.791 Respiratory tract 25 (24) 11 (13.9) 0.088 Intraabdominal 7 (6.7) 15 (19) 0.012 Wound 4 (3.8) 8 (10.1) 0.089 Urinary tract 19 (18.3) 11 (13.9) 0.432 Bacteremia 12 (11.5) 16 (20.2) 0.105 Died during hospitalization 20 (19.2) 22 (27.8) 0.170 *Values are no. (%) unless otherwise indicated.

ections 82 (78.8) 61 (77.2) 0.791 Respiratory tract 25 (24) 11 (13.9) 0.088 Intraabdominal 7 (6.7) 15 (19) 0.012 Wound 4 (3.8) 8 (10.1) 0.089 Urinary tract 19 (18.3) 11 (13.9) 0.432 Bacteremia 12 (11.5) 16 (20.2) 0.105 Died during hospitalization 20 (19.2) 22 (27.8) 0.170 *Values are no. (%) unless otherwise indicated. Dr Viedma is a clinical microbiologist at Hospital Universitario 12 de Octubre, Madrid, Spain. Her research interest is the molecular epidemiology of multidrug-resistant microorganisms.