NDM-1 in Traveler, Canada | CDC EID - Volume 17, Number 2–February 2011

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Volume 17, Number 2–February 2011
Dispatch
New Delhi Metallo-β-Lactamase from Traveler Returning to Canada1


Gisele Peirano, Jasmine Ahmed-Bentley, Neil Woodford, and Johann D. Pitout Comments to Author
Author affiliations: Calgary Laboratory Services, Calgary, Alberta, Canada (G. Peirano, J.D. Pitout); University of Calgary, Calgary (G. Peirano, J.D. Pitout); DynaLife Diagnostic Laboratories Services, Edmonton, Alberta, Canada (J. Ahmed-Bentley); and Health Protection Agency, London, UK (N. Woodford)

Suggested citation for this article

Abstract
An Escherichia coli isolate with New Delhi metallo-β-lactamase was isolated from a patient with pyelonephritis and prostatitis who returned to Canada after recent hospitalization in India. The patient was successfully treated with ertapenem and fosfomycin. This patient highlights the role of international travel in the spread of antimicrobial drug resistance and blaNDM-1.

The Enterobacteriaceae, particularly Escherichia coli and Klebsiella pneumoniae, are among the most common causes of serious hospital- and community-acquired bacterial infections in humans. Resistance to antimicrobial agents in these species has become increasingly prevalent. Of special concern is the development of resistance to the carbapenems; this development is caused by bacterial carbapenemases. These drugs are often the last line of effective therapy for treating infections caused by multidrug-resistant Enterobacteriaceae. Three types of β-lactamases inactivate the carbapenems: K. pneumoniae carbapenemases, metallo-β-lactamases (MBLs), and oxacillinases. The 2 most reported MBLs are the VIM and IMP types, which until recently have been mostly associated with Pseudomonas aeruginosa and Acinetobacter spp., although VIM-2 has spread among Enterobacteriaceae in Greece and, to a lesser extent, Italy (1).

Recently, a new type of MBL, New Delhi metallo-β-lactamase (NDM-1), in bacteria (K. pneumoniae and E. coli) recovered from a patient from Sweden who was hospitalized in New Delhi, India, was described (2).We characterized a carbapenem-resistant E. coli isolate from the urine of a patient with pyelonephritis and prostatitis who returned to Canada after recent hospitalization while visiting India.
The Study

A 32-year-old man was admitted to the medical ward of a hospital in Mysore, southwestern India, during 2010, with hyperglycemia and upper urinary tract infection (UTI). His underlying diabetes mellitus was stabilized, but his UTI did not improve after 5 days of ciprofloxacin. He was transferred to a hospital in Alberta, Canada. Prostatitis with pyelonephritis was diagnosed, and the patient was treated with ertapenem, 2 g/day. Culture of a clean-catch urine sample taken before the ertapenem was started yielded E. coli MH01 at >105 CFU/mL urine. The patient improved clinically, and a urine culture taken after 7 days of therapy showed no bacterial growth. The patient received 1 dose of 3 g fosfomycin after completing the ertapenem.

Antimicrobial drug susceptibility was determined with the VITEK 2 instrument (Vitek AMS; bioMérieux Vitek Systems, Hazelwood, MO, USA). MICs of the following drugs were determined: amoxicillin/clavulanic acid, piperacillin/tazobactam, cefoxitin, ceftriaxone, ceftazidime, aztreonam, meropenem, ertapenem, amikacin, gentamicin, tobramycin, ciprofloxacin, and trimethoprim/sulfamethoxazole. Additional susceptibility tests for imipenem, meropenem, ertapenem, tigecycline, and colistin were performed by using Etest (AB BioDisk, Solna, Sweden) according to the manufacture's instructions. Results were interpreted by using Clinical and Laboratory Standards Institute (CLSI) criteria for broth dilution (3). Fosfomycin susceptibility was determined by using CLSI disk methods (3).

The sample with E. coli was screened for MBLs with the MBL Etest according to the manufacturer's instructions. Isoelectric focusing was performed on freeze–thaw extracts on polyacrylamide gels as described (4). PCR amplification for blaVIM, blaIMP, blaNDM, blaCTX-Ms, blaOXAs, blaTEMs, and blaSHV was conducted on the isolate by using a GeneAmp 9700 ThermoCycler instrument (Applied Biosystems, Norwalk, CT, USA) and PCR conditions and primers as described (4–6). The blaCTX-M was sequenced by using PCR conditions and primers as described (4), and the blaNDM was sequenced by using the following primers and conditions: NDM-F1: 5′-CAGCGCAGCTTGTCG-3′, NDM-R1: 5′-TCGCGAAGCTGAGCA-3′. The PCR program consisted of an initial denaturation step at 95°C for 5 min; followed by 30 cycles of DNA denaturation at 95°C for 1 min, primer annealing at 52°C for 1 min, and primer extension at 72°C for 1 min; followed by a final extension at 72°C for 5 min.

The qnrA, qnrS, and qnrB genes were amplified in MH01 by using multiplex PCR (7). The aac(6′)-Ib and qepA genes were amplified in a separate PCR by using primers and conditions as described (8,9). The variant aac(6′)-Ib-cr was further identified by digestion with BstF5I (New England Biolabs, Ipswich, MA, USA).

Multilocus sequencing typing (MLST) was performed on MH01 by using 7 conserved housekeeping genes (adk, fumC, gyrB, icd, mdh, purA, and recA). The MLST protocol, including allelic type and sequence type assignment methods, is detailed at http://mlst.ucc.ie/mlst/dbs/Ecoli.

MH01 was assigned to 1 of the 4 main E. coli phylogenetic groups (A, B1, B2, D) by using a multiplex PCR-based method (10). Plasmid sizes were determined by using protocols and conditions described (11) and assigned to plasmid families by PCR-based replicon typing (12). Conjugation experiment was performed by mating-out assays with a selection agar containing different β-lactams (IMP 2 μg/mL, ceftazidime 4 μg/mL respectively) and by using E. coli C600N as recipient.

When we used Vitek 2, E. coli MH01 was resistant to amoxicillin/clavulanic acid, piperacillin/tazobactam, cefoxitin, ceftriaxone, ceftazidime, aztreonam, meropenem, ertapenem, amikacin, gentamicin, tobramycin, ciprofloxacin, and trimethoprim/sulfamethoxazole. The MICs detected by Etest were meropenem 32 μg/mL, imipenem 32 μg/mL, ertapenem >32 μg/mL, tigecycline 0.5 μg/mL, and colistin 0.125 μg/ml. The zone size for fosfomycin was 26 mm. MH01 was susceptible only to tigecycline and fosfomycin; CLSI has not published colistin MICs for Enterobacteriaceae.

E. coli MH01 was positive for MBL production by MBL Etest. Isoelectric focusing showed that E. coli MH01 produces 2 β-lactamases with isoelectric points of 5.2 and 8.9; PCR with sequencing identified these enzymes as NDM-1 and CTX-M-15, respectively. The isolate was positive for aac(6′)-Ib (but not aac(6′)-Ib-cr) and belonged to MLST clone 101 and phylogenetic group B1. E. coli MH01 harbored 4 plasmids of 75 kb, 165 kb, 300 kb, and 400 kb. E. coli (MH01A) transconjugant with an MBL phenotype was obtained, and plasmid analysis showed that it harbored a 75-kb plasmid. PCR confirmed that the transconjugant contained blaNDM that was untypeable by PCR-based replicon typing. The blaCTX-M-15 was identified on the 165-kb plasmid that belonged to incompatibility groups IncA/C and IncFII. These results were similar to those obtained by Poirel et al. (13).
Conclusions

Kumarasamy et al. (5) recently provided evidence that NDM-producing Enterobacteriaceae (mostly K. pneumoniae and E. coli) are widespread in the Indian subcontinent. They also found that many patients in the United Kingdom infected with bacteria that produce NDM-1 had been hospitalized on the Indian subcontinent. The patients sought care for a variety of hospital- and community-associated infections; UTIs were the most common clinical infections. NDM-producing Enterobacteriaceae also have recently been isolated from patients residing in the United States (14), Netherlands (15), and Australia (5); all patients had received medical care while visiting India.

Our findings add Canada to the growing list of countries from which these bacteria have been isolated. An E. coli isolate with NDM-1 and belonging to the same sequence type has been reported from Australia from a patient previously hospitalized in Bangladesh (13). Isolation of the same clone in 2 patients in different countries without any obvious contact underscores the probable acquisition of these bacteria during receipt of medical care in the subcontinent and suggests that E. coli ST101 with NDM-1 may be widespread throughout the region. The recent pandemic caused by E. coli clone ST131, which produces CTX-M types of β-lactamases, highlights the ability of certain clones to spread rapidly. E. coli ST101 with NDM-1 may have the potential to cause a similar pandemic.

The worldwide spread of Enterobacteriaceae-producing NDMs has serious implications for the empiric treatment of hospital- and community-associated infections because of the multiresistant nature of these bacteria, which severely limits treatment options. Worse, few antimicrobial drugs being developed have activity against gram-negative bacteria. If the emerging public health threat of international travel in the spread of antimicrobial resistance is ignored, the medical community may face carbapenem-resistant Enterobacteriaceae that cause common infections such as UTIs.

This study was supported by research grants from the Calgary Laboratory Services (no. 73-4063).

Dr Pitout is a professor at the University of Calgary, Alberta, Canada, and a medical microbiologist in the Division of Microbiology, Calgary Laboratory Services, Calgary. His major research and teaching interests are antimicrobial drug resistance mechanisms, especially newer types of β-lactamases in gram-negative bacteria, and the application of antimicrobial drug susceptibility testing in the clinical laboratory.

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Suggested Citation for this Article

Peirano G, Ahmed-Bentley J, Woodford N, Pitout JDD. New Delhi metallo-β-lactamase from traveler returning to Canada. Emerg Infect Dis [serial on the Internet]. 2011 Feb [date cited]. http://www.cdc.gov/EID/content/17/2/242.htm


DOI: 10.3201/eid1702.101313

Comments to the Authors

Please use the form below to submit correspondence to the authors or contact them at the following address:

Johann D. Pitout, Calgary Laboratory Services, #9, 3535 Research Rd NW, Calgary, AB T2L 2K8, Canada; email: johann.pitout@cls.ab.ca

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