#Corresponding author: Pathology Department, Singapore General Hospital, 20 College. Road, Academia, Level 7, Diagnostics Tower, , Singapore

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Received 31 January 2011/Returned for modification 2 March 2011/Accepted 15 March 2011

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AAC Accepts, published online ahead of print on 21 October 2013 Antimicrob. Agents Chemother. doi:10.1128/aac.01754-13 Copyright 2013, American Society for Microbiology. All Rights Reserved. 1 Title: Escherichia coli with bla IMP-8 in Singapore 2 Running Title: Escherichia coli with bla IMP-8 in Singapore 3 4 Tse H Koh#, a, Delphine Cao a, Nancy W. S. Tee b, Jeanette W. P. Teo c 5 6 7 #Corresponding author: Pathology Department, Singapore General Hospital, 20 College Road, Academia, Level 7, Diagnostics Tower, 169856, Singapore 8 Email: koh.tse.hsien@sgh.com.sg 9 Tel: +65 6321 4942 10 Fax: +65 6222 6826 11 12 a Pathology Department, Singapore General Hospital, 169856, Singapore 13 14 b Clinical Microbiology Laboratory, KK Women s and Children s Hospital, 229899, Singapore 15 c Department of Laboratory Medicine, National University Hospital, 119074, Singapore 16 17 18

19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 An imipenem-resistant Escherichia coli was isolated from the urine of a local 72 year old female Chinese patient in 2006. The carbapenem minimal inhibitory concentrations (MICs) by Etest (biomérieux SA, Marcy l Etoile, France) were Ertapenem 2 µg/µl, Meropenem 4 µg/µl, and Imipenem >32 µg/µl. A modified Hodge test was weakly positive. The presence of a metallo- -lactamase (MBL) was suspected because of enhancement of the zone of inhibition around ertapanem, imipenem and meropenem antimicrobial susceptibility testing disks with the addition of EDTA (1). A multiplex PCR to carbapenemase genes was positive for bla IMP (2). A 2,847 bp partial integron sequence was amplified using the IntA primer described by Rosser (3) and an in-house primer tnirr (5 -GGC AAG CTT GTG TTC GGT AT-3 ). This sequence (GenBank accession number KF534724) contained inti1, bla IMP-8, an aminoglycoside 6 -N-acetyltrasferase gene (aac(6 )-IId) and tnir (a putative resolvase possibly involved in transposition). This was identical to that of Klebsiella oxytoca (GenBank accession number HQ651093.1) from Fujian in China, except the inti1 partial sequence was not disrupted by IS26, though we have not excluded the possibility that this could have been inserted further downstream in the sense of inti1(4). This structure is carried on a plasmid of approximately 120 kb that was successfully transferred to E. coli J53 Az r by plate mating. This was determined to be Inc A/C by plasmid replicon typing (5). The only other -lactamase gene identified was bla TEM-1. However, the high imipenem MIC relative to the other carbapenems is difficult to explain and it is possible that an undetected mechanism may contribute to the final resistance phenotype. Multilocus sequence typing showed the isolate belonged to ST410 (ST23 complex). This sequence type has been associated with spread of carbapenem-non-susceptible, KPC-2-producing E. coli in Greece (6). 41 42 43 IMP-8 was first described in Klebsiella pneumoniae from Taiwan (7) where it has established itself as the dominant MBL among the Enterobacteriaceae. It is a variant of IMP-2 from

44 45 46 47 which it differs by 2 amino acids. Until recently, the distribution of bla IMP-8 was restricted to Taiwan and China. However recently it has been reported in Pseudomonas mendocina in Portugual (8), Enterobacter cloacae in Argentina (9). K. oxytoca in Spain (10), and K. pneumoniae in Tunisia (11). 48 49 50 51 52 53 54 55 56 Given the close links between Taiwan, China, and Singapore, it is surprising that this is the only IMP-8 producer found so far in Singapore. However these strains may be difficult to detect because of their low ertapenem and meropenem MICs. Taiwanese researchers have reported that only a third of IMP-8 producers had a positive modified Hodge test. Furthermore, meropenem combined disk testing only detected 40% in combination with EDTA, and 2% in combination with dipicolinic acid (12). The phenotype of our isolate was similarly difficult to recognize because the modified Hodge test was weak, like that of an NDM-1 producer, and could easily have been dismissed as negative.

57 58 59 60 61 References 1. Lee, K., Y. Chong, H. B. Shin, Y. A. Kim, D. Yong, Yum, J. H. 2001. Modified Hodge and EDTA-disk synergy tests to screen metallo- -lactamase-producing strains of Pseudomonas and Acinetobacter species. Clin. Microbiol. Infect. 7:88-91. 62 63 64 65 2. Poirel, L., T. R. Walsh, V. Cuvillier, Nordmann, P. 2011. Multiplex PCR for detection of acquired carbapenemase genes. Diagn. Microbiol. Infect. Dis. 70:119-123. 66 67 68 69 3. Rosser, S. J., Young, H. K. 1999. Identification and characterization of class 1 integrons in bacteria from an aquatic environment. J. Antimicrob. Chemother. 44:11-18. 70 71 72 73 74 75 76 77 78 79 80 81 82 83 84 4. Li, B., J. Y. Sun, Q. Z. Liu, L. Z. Han, X. H. Huang, Ni, Y. X. 2011. First report of Klebsiella oxytoca strain coproducing KPC-2 and IMP-8 carbapenemases. Antimicrob. Agents. Chemother. 55:2937-2941. 5. Johnson, T. J., and L. K. Nolan. 2009. Plasmid replicon typing. Methods Mol Biol 551:27-35. 6. Mavroidi, A., V. Miriagou, E. Malli, A. Stefos, G. N. Dalekos, L. S. Tzouvelekis, Petinaki, E. 2012. Emergence of Escherichia coli sequence type 410 (ST410) with KPC-2 -lactamase. Int. J. Antimicrob. Agents 39:247-250. 7. Yan, J. J., W. C. Ko, Wu, J. J. 2001. Identification of a plasmid encoding SHV-12, TEM-1, and a variant of IMP-2 metallo- -lactamase, IMP-8, from a clinical isolate of Klebsiella pneumoniae. Antimicrob. Agents. Chemother. 45:2368-2371.

85 86 87 88 89 90 91 92 93 94 95 96 97 98 99 100 101 102 8. Santos, C., T. Caetano, S. Ferreira, Mendo, S. 2010. First description of bla IMP-8 in a Pseudomonas mendocina isolated at the Hospital Infante D. Pedro, Aveiro, Portugal. Res. Microbiol. 161:305-307. 9. Gomez, S., M. Rapoport, A. Togneri, J. Viegas-Caetano, D. Faccone, A. Corso, A. Petroni, Pasteran, F. 2011. Emergence of metallo- -lactamases in Enterobacteriaceae from Argentina. Diagn. Microbiol. Infect. Dis. 69:94-97. 10. Vergara-Lopez, S., M. C. Dominguez, M. C. Conejo, A. Pascual, Rodriguez- Bano, J. 2013. Wastewater drainage system as an occult reservoir in a protracted clonal outbreak due to metallo- -lactamase-producing Klebsiella oxytoca. Clin. Microbiol. Infect. doi:10.1111/1469-0691.12288. 11. Chouchani, C., R. Marrakchi, I. Henriques, Correia, A. 2013. Occurrence of IMP- 8, IMP-10, and IMP-13 metallo- -lactamases located on class 1 integrons and other extended-spectrum -lactamases in bacterial isolates from Tunisian rivers. Scand. J. Infect Dis. 45:95-103. 103 104 105 106 12. Liao, I. C., H. M. Chen, J. J. Wu, P. F. Tsai, L. R. Wang, Yan J. J. 2011. Metallo- -lactamase-producing Enterobacteriaceae isolates at a Taiwanese hospital: lack of distinctive phenotypes for screening. APMIS. 119:543-550.