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Journal of Clinical Microbiology, December 2007, p. 4054-4057, Vol. 45, No. 12
0095-1137/07/$08.00+0     doi:10.1128/JCM.00343-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

Clonal Spread of Imipenem-Resistant Acinetobacter baumannii among Different Cities of China

Hua Zhou, Qing Yang, Yun-Song Yu,^* Ze-Qing Wei, and Lan-Juan Li

The Key Laboratory of Infectious Disease of Public Health Ministry, First Affiliated Hospital, College of Medicine, Zhejiang University, No. 79, Qing Chun Road, Hangzhou, Zhejiang 310003, China

Received 13 February 2007/ Returned for modification 1 June 2007/ Accepted 2 October 2007

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A total of 342 imipenem-resistant Acinetobacter baumannii isolates (IRABs) were collected from 16 Chinese cities. Six predominant clones had spread widely, and four clones were detected in distant hospitals. The majority of the IRABs contain bla_OXA-23, with ISAba1 upstream of the gene. These results suggested that clonal spread played an important role in the outbreak of IRABs in China.

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A. baumannii is recognized as an increasingly important opportunistic gram-negative pathogen that is frequently associated with nosocomial outbreaks worldwide (21). Carbapenems are useful agents that could combat many severe Acinetobacter infections. Resistance to carbapenems is now accumulating, largely through clonal spread (13). A few lineages even achieve an epidemic status, reaching multiple hospitals or countries (6). One mechanism of resistance to carbapenems is due to the carbapenem-hydrolyzing β-lactamases of molecular classes B and D (12). Four of the eight clusters of OXA-type carbapenemases were identified in A. baumannii, including clusters OXA-23, OXA-24, OXA-51, and OXA-58 (22). ISAba1 may have an important role in the expression and transfer of OXA-type carbapenemase genes (17, 20).

In this study, we investigated the prevalence of imipenem-resistant A. baumannii isolates (IRABs) in China and characterized the genes of the carbapenemases in IRABs. Three hundred forty-two nonduplicate IRABs were recovered from 16 cities through January 2005 to December 2005 in China (Table 1; Fig. 1). All isolates were identified by the Vitek GNI⁺ card (BioMérieux, Marcy-l'Etoile, France) as members of the Acinetobacter calcoaceticus-A. baumannii complex. Species identification was confirmed by sequence analyses of the 16S-23S rRNA gene spacer region (4).

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TABLE 1. The PFGE clone distribution of 342 clinical isolates among 16 cities

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FIG. 1. The geographic distribution of 16 cities in China. On the left, a map of China shows three autonomous cities (Beijing, Chongqing, and Shanghai) and three provincial cities (Hangzhou [Zhejiang], Guangzhou [Guangdong], and Shenyang [Liaoning]), in which Acinetobacter baumannii isolates were collected. On the right, a map shows the 11 cities, including Hangzhou, in Zhejiang Province.

The MICs of 10 antimicrobial agents were determined by the agar dilution technique by following the standards of Clinical and Laboratory Standards Institute (5); these agents included imipenem (Merck KGaA, Darmstadt, Germany), meropenem (Sumitomo Pharmaceuticals Co., Ltd., Osaka, Japan), piperacillin (Sigma, Deisenhofen, Germany), ceftazidime (Sigma, Deisenhofen, Germany), cefepime (Sino-American Shanghai Squibb Pharmaceuticals Ltd., Shanghai, China), aztreonam (Sigma, Deisenhofen, Germany), amikacin (Sigma, Deisenhofen, Germany), gentamicin (Sigma, Deisenhofen, Germany), ciprofloxacin (Bayer, Leverkusen, Germany), and minocycline (Sigma, Deisenhofen, Germany). The MICs of four other agents, ampicillin-sulbactam, cefoperazone-sulbactam, piperacillin-tazobactam, and polymyxin E, were determined by Etest (AB Biodisk, Solna, Sweden) according to the manufacturer's instructions. The results were interpreted according to CLSI 2006 guidelines (5). Pseudomonas aeruginosa ATCC 27853 was used as a control. All isolates were found to be resistant to imipenem and meropenem. The rates of resistance to ampicillin-sulbactam, cefoperazone-sulbactam, and minocycline were 68.0%, 54.2%, and 75.9%, respectively. The rate of resistance to polymyxin E was 10.8%, the lowest among the tested agents. The rates of resistance to all other tested antimicrobial agents were more than 90%.

To characterize these isolates genetically, the genomic DNA of all the isolates was digested with ApaI and the resultant DNA fragments were subjected to pulsed-field gel electrophoresis (PFGE) as described previously (18). According to the datum-interpreting criteria described by Tenover et al. (19), these A. baumannii isolates belonged to 29 distinct clones (Fig. 2). Among them, six clones were dominant, consisting of 303 strains in total (Table 1).

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FIG. 2. PFGE analysis of the six major clones of A. baumannii. Genomic DNA isolated from the six major A. baumannii clones was digested with ApaI before PFGE analysis. Lane M, ladder used as molecular size marker; lanes A to F, clones A to F, respectively, of A. baumannii.

Crude β-lactamase preparations were extracted by the sonication method (25). pI values were determined by the PhastSystem electrophoresis system (Amersham Pharmacia Biotech, Piscataway, NJ) according to the manufacturer's instructions. pI reference proteins were stained with Coomassie brilliant blue R-250. The pattern was analyzed by Curve Expert software (version 1.3) developed by Daniel Hyams (free software). OXA-23-producing A. baumannii (a collection of our laboratory) was used as the positive control. Metallo-β-lactamase-producing isolates were screened by the imipenem-EDTA double-disk synergy test (10). IMP-4-producing A. baumannii and VIM-2-producing P. aeruginosa were used as the positive controls. All tested isolates had one band at pI 6.64 and were negative by the imipenem-EDTA double-disk synergy test.

bla_IMP-type, bla_VIM-type, bla_SIM-1, bla_OXA-23-like, bla_OXA-24-like, bla_OXA-58-like, and bla_OXA-51-like were analyzed by PCR using primers as described previously (9, 11, 20). PCR mapping was performed using the ISAba1-OXA-23-like primers or the ISAba1-OXA-51-like primers as reported previously (26). The results showed that all the isolates contained bla_OXA-51-like but were negative for the OXA-24-like, OXA-58-like, SIM-1, IMP-type, or VIM-type gene. Three hundred twenty-two isolates contained the bla_OXA-23-like gene. PCR with the ISAba1-OXA-23-like primers generated a PCR product in 314 IRABs, and sequencing analysis showed that the PCR product contained the OXA-23 gene (the GenBank accession number AJ132105), suggesting that a majority of the clones contain the OXA-23 gene with ISAba1 upstream of it. PCR with the ISAba1-OXA-51-like primers generated a PCR product, which contained the OXA-66 gene (the GenBank accession number AY750909) in 13 strains, as revealed by sequencing analysis. There was a 34-bp nucleotide sequence between ISAba1 and bla_OXA-23 and a 7-bp nucleotide sequence between ISAba1 and bla_OXA-66. According to the PCR mapping, the 342 strains belonged to five types (Fig. 3).

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FIG. 3. PCR mapping of blaOXA-51-like, blaOXA-23-like, and ISAba1 in IRABs. According to the PCR mapping results, 342 strains were divided into five types: type I, consisting of 11 strains, contains blaOXA-51-like without the upstream ISAba1; type II, consisting of 9 strains, contains blaOXA-51-like with the upstream ISAba1; type III, consisting of 4 strains, contains both blaOXA-51-like with the upstream ISAba1 and blaOXA-23-like without the upstream ISAba1; type IV, consisting of 314 strains, contains blaOXA-51-like without ISAba1 and blaOXA-23-like with ISAba1; and type V, consisting of 4 strains, contains blaOXA-51-like and blaOXA-23-like without ISAba1 upstream of either gene.

Attempts to transfer bla_OXA-23 by conjugation using the rifampin-resistant Escherichia coli 600 as the recipient failed. Repeated attempts to detect the presence of plasmids capable of hybridizing with the bla_OXA-23 and bla_OXA-66 probes also failed. ApaI-digested PFGE DNAs were transferred to nylon membranes and were hybridized with a v-dCTP (DuPont Corporation)-labeled bla_OXA-23 gene probe. The fragments of the ApaI-digested PFGE DNA of pulsotypes A, B, and C showed hybridization bands at about >220 kb in clone A, about >300 kb in clone B, and about 220 kb in clone C, respectively (data not shown). These results are indicative of a chromosomal location for the bla_OXA-23 gene.

Our study revealed that IRABs have resistance to most antimicrobial agents. Some studies have indicated that colistin may be useful for treating infections caused by carbapenem-resistant pathogens (14). We confirmed that in vitro, the most active agent against these resistant isolates was polymyxin E.

This is the first report to investigate IRABs in China on such a large scale. We found that clones A, B, C, and D were the dominant isolates and had spread widely among hospitals, cities, and even remote areas. Some isolates with the same genetic basis spread in many hospitals in China, suggesting that the spread of isolates plays an important role in the increase of IRABs. So, it is important to monitor and control the spread of A. baumannii having resistance to most β-lactams.

In China, bla_OXA-23 and bla_OXA-51-like were the most popular carbapenemase genotypes. OXA-23-producing IRABs spread widely in the world (1, 2, 7, 9, 16, 23, 24). bla_OXA-51-like genes are the endogenous genes of A. baumannii, and their protein products have weak carbapenem-hydrolyzing activities (3, 8). An insertion of ISAba1 may provide a promoter for the OXA-type carbapenemase genes to increase their expression (20). There were only 15 isolates (4.39%) that lacked ISAba1 upstream of OXA-type carbapenemase coding genes, suggesting that an insertion of ISAbal may be a major factor responsible for the carbapenem resistance.

All isolates belonging to clones B, D, E, and F had a PCR mapping of type IV. In contrast, isolates of clones A and C and sporadic isolates had complex PCR mapping results (Table 2). In the process of the dissemination, the strains may have acquired or lost different gene elements under different antimicrobial pressures (15).

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TABLE 2. The distribution of carbapenemase genes in the major PFGE clones of IRABs

Nucleotide sequence accession numbers. Sequences for the 34 bp between ISAba1 and bla_OXA-23 and the 7 bp between ISAba1 and bla_OXA-66 have been submitted to GenBank under accession numbers DQ923478 (26) and DQ923479, respectively.

 
This work was supported by a research grant from the National Natural Science Foundation of China (no. NSFC30370073), a grant from High Technology Research and Development Program of China (863 program, no. 2006AA02Z413), and a grant from the Program for New Century Excellent Talents in University (no. NCET-04-0552).

 
* Corresponding author. Mailing address: The Key Laboratory of Infectious Disease of Public Health Ministry, First Affiliated Hospital, College of Medicine, Zhejiang University, No. 79, Qing Chun Road, Hangzhou, Zhejiang 310003, China. Phone and fax: 86 571 8723 6421. E-mail: yvys119{at}163.com

Published ahead of print on 17 October 2007.

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Journal of Clinical Microbiology, December 2007, p. 4054-4057, Vol. 45, No. 12
0095-1137/07/$08.00+0     doi:10.1128/JCM.00343-07
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

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• Mendes, R. E., Bell, J. M., Turnidge, J. D., Castanheira, M., Jones, R. N. (2009). Emergence and widespread dissemination of OXA-23, -24/40 and -58 carbapenemases among Acinetobacter spp. in Asia-Pacific nations: report from the SENTRY Surveillance Program. J Antimicrob Chemother 63: 55-59 [Abstract] [Full Text]  

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