This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Arakawa, Y.
Right arrow Articles by Goto, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arakawa, Y.
Right arrow Articles by Goto, M.

 Previous Article  |  Next Article 

Journal of Clinical Microbiology, January 2000, p. 40-43, Vol. 38, No. 1
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.

Convenient Test for Screening Metallo-beta -Lactamase-Producing Gram-Negative Bacteria by Using Thiol Compounds

Yoshichika Arakawa,1,* Naohiro Shibata,1 Keigo Shibayama,1 Hiroshi Kurokawa,1 Tetsuya Yagi,1 Hiroshi Fujiwara,1 and Masafumi Goto2

Department of Bacterial and Blood Products, National Institute of Infectious Diseases, Tokyo,1 and Faculty of Pharmaceutical Sciences, Kumamoto University, Kumamoto,2 Japan

Received 28 June 1999/Returned for modification 21 August 1999/Accepted 22 September 1999


    ABSTRACT
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References

A simple disk diffusion test was constructed for detection of IMP-1-type metallo-beta -lactamase-producing gram-negative bacteria. Two Kirby-Bauer disks containing ceftazidime (CAZ) and a filter disk containing a metallo-beta -lactamase inhibitor were used in this test. Several IMP-1 inhibitors such as thiol compounds including 2-mercaptopropionic acid, heavy metal salts, and EDTA were evaluated for this test. Two CAZ disks were placed on a Mueller-Hinton agar plate on which a bacterial suspension was spread according to the method recommended by the National Committee for Clinical Laboratory Standards. The distance between the disks was kept to about 4 to 5 cm, and a filter disk containing a metallo-beta -lactamase inhibitor was placed near one of the CAZ disks within a center-to-center distance of 1.0 to 2.5 cm. For IMP-1-producing strains, the growth-inhibitory zone between the two disks expanded, while no evident change in the shape of the growth-inhibitory zone was observed for CAZ-resistant strains producing serine beta -lactamases such as AmpC or SHV-12. As a result, 2 to 3 µl of undiluted 2-mercaptopropionic acid or mercaptoacetic acid able to block IMP-1 activity gave the most reproducible and clearest results, and CAZ-resistant strains producing AmpC or extended-spectrum beta -lactamases were distinguishable from IMP-1 producers by this test. A similar observation was made with IMP-1-producing clinical isolates such as Serratia marcescens, Klebsiella pneumoniae, Escherichia coli, Enterobacter cloacae, Enterobacter aerogenes, Citrobacter freundii, Proteus vulgaris, Pseudomonas aeruginosa, Pseudomonas putida, Acinetobacter spp., and Alcaligenes xylosoxidans. The specificity and sensitivity of this test were comparable to those of PCR analysis using blaIMP-specific primers. Therefore, this convenient test would be valuable for daily use in clinical laboratories.


    INTRODUCTION
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References

Carbapenem-resistant gram-negative bacterial species such as Serratia marcescens and Pseudomonas aeruginosa have emerged in Japan, and these isolates usually produce IMP-1 metallo-beta -lactamase (7, 9, 13, 15, 17). The blaIMP genes responsible for the IMP-1 production are usually mediated by integrons carried by transferable large plasmids (1). About 4.4% of S. marcescens strains and 1.3% of P. aeruginosa strains have already acquired IMP-1 productivity in Japan (manuscript in preparation), and transmissions of the blaIMP gene cassette have been observed among various gram-negative rods (18). Since IMP-1 producers tend to demonstrate a wide range of resistance to various broad-spectrum beta -lactams including the oxyimino cephalosporins, cephamycins, and carbapenems, early recognition of IMP-1 producers is very important for rigorous infection control (3). The worldwide spread of this kind of organism is becoming a general concern, since several metallo-beta -lactamase-producing gram-negative bacteria have recently been reported outside Japan (5, 11, 19). Indeed, PCR analyses usually give reliable and satisfactory results (18), but this method is of limited practical use for daily application in clinical laboratories because of the cost. Thus, the development of a simple and inexpensive testing method for screening of IMP-1 producers has become necessary.


    MATERIALS AND METHODS
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References

Bacterial strains. Clinically isolated ceftazidime (CAZ)-resistant (MIC, >64 µg/ml) gram-negative bacterial strains were used in the test. Several of these isolates were later found to carry the blaIMP gene by PCR. A well-characterized extended-spectrum beta -lactamase (ESBL) (SHV-12) producer and AmpC hyperproducers were also used as the control strains. A list of the bacterial strains tested in this study is shown in Table 1.

                              
View this table:
[in this window]
[in a new window]
 
TABLE 1.   Strains used in this study

Evaluation of metallo-beta -lactamase inhibitors. CuCl2, FeCl2, EDTA, and thiol compounds including mercaptoacetic acid, 2-mercaptopropionic acid, and mercaptoethanol were used and evaluated for IMP-1 inhibition, because these agents have been reported to block metallo-beta -lactamase (2, 6, 12, 16). A colony of each bacterial strain was suspended and diluted with Mueller-Hinton (MH) broth to 106 CFU/ml and spread on an MH agar plate with a cotton swab according to the protocol recommended by the National Committee for Clinical Laboratory Standards (14). Two commercially supplied Kirby-Bauer (KB) disks, each containing 30 µg of CAZ (Eiken Co. Ltd., Tokyo, Japan), were then placed on the plates. The distance between the two CAZ disks was kept at about 4 to 5 cm, and a filter disk was placed near one of the CAZ disks within a center-to-center distance of 1.0 to 2.5 cm. Two to five microliters of each inhibitor solution was added to the filter disk on the agar, and each agar plate was incubated at 37°C overnight. The concentration and amount of each inhibitor solution added to the filter disk were as follows: for CuCl2, 100 mM (5 µl); for FeCl2, 100 mM (5 µl); for EDTA, 100 mM (5 µl); and for thiol compounds, an undiluted solution (2 to 3 µl).

PCR analysis. CAZ-resistant strains used in this study were tested by PCR analysis to confirm the presence of the blaIMP gene according to the method of Senda et al. (18) by using a new set of PCR primers (5'-ACCGCAGCAGAGTCTTTGCC-3' and 5'-ACAACCAGTTTTGCCTTACC-3').


    RESULTS AND DISCUSSION
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References

Among the metallo-beta -lactamase inhibitors used in this study, 2-mercaptopropionic acid gave the clearest results, because this chemical agent blocked IMP-1 activity very strongly even at a low concentration (6). Mercaptoacetic acid also gave a clear result, but its inhibitory effect was slightly weaker than that of 2-mercaptopropionic acid. By using 2-mercaptopropionic acid, apparent growth-inhibitory zones were observed with all IMP-1-producing strains tested, including S. marcescens MKDM17, Klebsiella pneumoniae MKD115, and P. aeruginosa MKAM12, while no distinct change in the appearance of the growth-inhibitory zone was observed for CAZ-resistant strains producing AmpC or SHV-12 (Fig. 1). Of 3,222 S. marcescens isolates and 2,533 P. aeruginosa isolates, 141 and 88 isolates carrying blaIMP, respectively, demonstrated an expansion of the growth-inhibitory zone by 2-mercaptoacetic acid, and Escherichia coli strains producing Toho-1 or MEN-1 that show resistance to cefotaxime were distinguishable from IMP-1 producers by this method (data not shown). The other IMP-1 producers belonging to the gram-negative bacterial species also showed results similar to those observed with IMP-1-producing S. marcescens and P. aeruginosa strains, as shown in Fig. 2. However, relatively weak and ambiguous growth-inhibitory zones appeared for IMP-1-producing Citrobacter freundii and Enterobacter cloacae, even when two disks containing CAZ and 2-mercaptoacetic acid, respectively, were placed as close together as 1 cm (from center to center) (Fig. 2). This may be due to the hyperproduction of AmpC and/or to a change in membrane permeability in these bacteria. Further study is needed to improve the method for these strains, though IMP-1-producing strains of C. freundii and E. cloacae are still very rare.


View larger version (87K):
[in this window]
[in a new window]
 
FIG. 1.   Inhibitory effects of 2-mercaptopropionic acid (2-MPA) on IMP-1 producers and non-IMP-1 producers. Three CAZ-resistant strains belonging to the gram-negative bacterial species P. aeruginosa, S. marcescens, and K. pneumoniae and producing IMP-1 metallo-beta -lactamase or serine-beta -lactamases (SHV-12 or AmpC) were tested. For each IMP-1 producer, a distinct growth-inhibitory zone appeared between the KB disk containing CAZ and the filter disk containing 2-MPA (left column). No change is evident around the two KB disks containing CAZ with or without 2-MPA for each serine beta -lactamase producer (right column).


View larger version (46K):
[in this window]
[in a new window]
 
FIG. 2.   Appearance of growth-inhibitory zone in IMP-1-producing strains by use of CAZ and 2-mercaptopropionic acid (2-MPA). Various levels of growth inhibition were observed in the IMP-1-producing gram-negative bacterial species tested. Marked growth inhibitions were observed in Acinetobacter sp., Alcaligenes xylosoxidans, Enterobacter aerogenes, E. coli, Proteus vulgaris, and Pseudomonas putida, whereas weak and ambiguous growth inhibitions were observed in C. freundii and E. cloacae.

Heavy metal salts such as CuCl2 and FeCl2 usually formed ring-shaped areas of precipitation around the filter disk and demonstrated their own bactericidal activity, while the growth-inhibitory zone expanded to the disk containing CAZ, as shown in Fig. 3A. The inhibitory effects of both heavy metal salts were similar, but the results were ambiguous in several strains. HgCl2 itself has rather strong bactericidal activity and yielded better results than CuCl2 and FeCl2 in the preliminary tests. However, the use of Hg2+ salt is not recommended from the viewpoint of human health and environmental conservation.



View larger version (4749K):
[in this window]
[in a new window]
 
FIG. 3.   (A) Inhibitory effects of FeCl2 on IMP-1 producers and non-IMP-1 producers. A slight expansion of growth-inhibitory zones between two disks was observed for all three IMP-1 producers (arrowheads). No change in the shape of the growth-inhibitory zone was evident for any serine-beta -lactamase producer. (B) Inhibitory effects of EDTA on IMP-1 producers. Growth-inhibitory zones between two disks appeared for all three IMP-1 producers (arrowheads) when 5 µl of 500 mM EDTA solution was added to the filter.

EDTA also created a growth-inhibitory zone between the two disks, but its appearance and reproducibility were relatively poor in several strains, even when a thick EDTA solution (500 mM) was added to the filter disk (Fig. 3B).

CAZ seemed to be the most suitable substrate for this test, because IMP-1 producers usually demonstrated high-level resistance to CAZ (MIC, >64 µg/ml) in our previous study (17, 18), and a marked inhibitory effect of thiol compounds was usually observed, as shown in Fig. 1 and 2. Indeed, any kind of broad-spectrum beta -lactam disk can be used in this test, but IMP-1 producers usually demonstrate various levels of resistance to imipenem (IPM) (MIC, 4 to >128 µg/ml). However, the inhibitory effect of thiol compounds tends to be ambiguous, especially in strains that demonstrate reduced susceptibility to IPM (MIC, 4 to 8 µg/ml) when the KB disk (IPM) is used (data not shown).

The emergence of gram-negative bacterial species with acquired resistance to various broad-spectrum beta -lactams is becoming a worldwide clinical problem. Strains producing TEM- or SHV-derived ESBLs (4, 10) usually demonstrate high-level resistance to broad-spectrum oxyimino beta -lactams such as CAZ and cefotaxime. Moreover, several K. pneumoniae strains that showed resistance to cephamycins as well as oxyimino cephalosporins were also found to produce AmpC-type beta -lactamases such as MOX-1 (8). In Japan, furthermore, the emergence of carbapenem-resistant gram-negative bacterial strains in species such as S. marcescens or P. aeruginosa is becoming a clinical threat. Some of these isolates produce IMP-1 metallo-beta -lactamase, and these strains tend to demonstrate a wide range of resistance to various broad-spectrum cephalosporins, cephamycins, and carbapenems (7, 9, 15, 17). Recently, gram-negative bacterial strains that were speculated to produce metallo-beta -lactamases very similar to IMP-1 were also isolated in the United Kingdom, Italy, and Singapore (5, 11, 19). Thus, there is a need to develop a simple and specific method to distinguish IMP-1 producers from other bacteria showing a similar antibiotic resistance profile through the production of AmpC, ESBLs, or Toho-1-type beta -lactamases. Indeed, PCR analysis usually gives satisfactory results in the detection of IMP-1 producers (7, 17), but it is not suitable for daily testing in clinical laboratories due to the cost. Therefore, the method described in this study is very helpful for screening IMP-1-producing strains in daily clinical laboratory testing.


    ACKNOWLEDGMENT

This work was supported by a grant (The Research Project for Emerging and Re-Emerging Infectious Diseases: Molecular Analyses of Drug-Resistant Bacteria and Establishment of Rapid Identification Methods, 1997-1999) from the Ministry of Health and Welfare of Japan.


    FOOTNOTES

* Corresponding author. Mailing address: Department of Bacterial and Blood Products, National Institute of Infectious Diseases, 4-7-1 Gakuen, Musashi-Murayama, Tokyo 208-0011, Japan. Phone: 81-42-561-0771, ext. 500. Fax: 81-42-561-7173. E-mail: yarakawa{at}nih.go.jp.


    REFERENCES
Top
Abstract
Introduction
Materials and Methods
Results and Discussion
References

1. Arakawa, Y., M. Murakami, K. Suzuki, H. Ito, R. Wacharotayankun, S. Ohsuka, N. Kato, and M. Ohta. 1995. A novel integron-like element carrying the metallo-beta -lactamase gene blaIMP. Antimicrob. Agents Chemother. 39:1612-1615[Abstract].
2. Bandoh, K., Y. Muto, K. Watanabe, N. Katoh, and K. Ueno. 1991. Biochemical properties and purification of metallo-beta -lactamase from Bacteroides fragilis. Antimicrob. Agents Chemother. 35:371-372[Abstract/Free Full Text].
3. Bush, K. 1998. Metallo-beta -lactamases: a class apart. Clin. Infect. Dis. 27:S48-S53.
4. Bush, K. 1996. Is it important to identify extended-spectrum beta -lactamase-producing isolates? Eur. J. Clin. Microbiol. Infect. Dis. 15:361-364[CrossRef][Medline].
5. Cornaglia, G., M. L. Riccio, A. Mazzariol, L. Lauretti, R. Fontana, and G. M. Rossolini. 1999. Appearance of IMP-1 metallo-beta -lactamase in Europe. Lancet 353:899-900[CrossRef][Medline].
6. Goto, M., T. Takahashi, F. Yamashita, A. Koreeda, H. Mori, M. Ohta, and Y. Arakawa. 1997. Inhibition of the metallo-beta -lactamase produced from Serratia marcescens by thiol compounds. Biol. Pharm. Bull. 20:1136-1140[Medline].
7. Hirakata, Y., K. Izumikawa, T. Yamaguchi, H. Takemura, H. Tanaka, R. Yoshida, J. Matsuda, M. Nakano, K. Tomono, S. Maesaki, M. Kaku, Y. Yamada, S. Kamihira, and S. Kohno. 1998. Rapid detection and evaluation of clinical characteristics of emerging multiple-drug-resistant gram-negative rods carrying the metallo-beta -lactamase gene blaIMP. Antimicrob. Agents Chemother. 42:2006-2011[Abstract/Free Full Text].
8. Horii, T., Y. Arakawa, M. Ohta, S. Ichiyama, R. Wacharotayankun, and N. Kato. 1993. Plasmid-mediated AmpC-type beta -lactamase isolated from Klebsiella pneumoniae confers resistance to broad-spectrum beta -lactams, including moxalactam. Antimicrob. Agents Chemother. 37:984-990[Abstract/Free Full Text].
9. Ito, H., Y. Arakawa, S. Ohsuka, R. Wacharotayankun, N. Kato, and M. Ohta. 1995. Plasmid-mediated dissemination of the metallo-beta -lactamase gene blaIMP among clinically isolated strains of Serratia marcescens. Antimicrob. Agents Chemother. 39:824-829[Abstract].
10. Jacoby, G. A. 1998. Epidemiology of extended-spectrum beta -lactamases. Clin. Infect. Dis. 27:81-83[Medline].
11. Koh, T. H., G. S. Babini, N. Woodford, L. H. Sng, L. M. Hall, and D. M. Livermore. 1999. Carbapenem-hydrolysing IMP-1 beta -lactamase in Klebsiella pneumoniae in Singapore. Lancet 353:2162[CrossRef][Medline].
12. Marumo, K., A. Takeda, Y. Nakamura, and K. Nakaya. 1995. Purification and characterization of metallo beta -lactamase from Serratia marcescens. Microbiol. Immunol. 39:27-33[Medline].
13. Minami, S., M. Akama, H. Araki, Y. Watanabe, H. Narita, S. Iyobe, and S. Mitsuhashi. 1996. Imipenem and cephem resistant Pseudomonas aeruginosa carrying plasmids coding for class B beta -lactamase. J. Antimicrob. Chemother. 37:433-444[Abstract/Free Full Text].
14. National Committee for Clinical Laboratory Standards. 1997. Methods for dilution antimicrobial susceptibility tests for bacteria that grow aerobically, Approved standard M7-A4. National Committee for Clinical Laboratory Standards, Wayne, Pa.
15. Osano, E., Y. Arakawa, R. Wacharotayankun, M. Ohta, T. Horii, H. Ito, F. Yoshimura, and N. Kato. 1994. Molecular characterization of an enterobacterial metallo-beta -lactamase found in a clinical isolate of Serratia marcescens that shows imipenem resistance. Antimicrob. Agents Chemother. 38:71-78[Abstract/Free Full Text].
16. Payne, D. J., R. Cramp, J. H. Bateson, J. Neale, and D. Knowles. 1994. Rapid identification of metallo- and serine beta -lactamases. Antimicrob. Agents Chemother. 38:991-996[Abstract/Free Full Text].
17. Senda, K., Y. Arakawa, K. Nakashima, H. Ito, S. Ichiyama, K. Shimokata, N. Kato, and M. Ohta. 1996. Multifocal outbreaks of metallo-beta -lactamase-producing Pseudomonas aeruginosa resistant to broad-spectrum beta -lactams, including carbapenems. Antimicrob. Agents Chemother. 40:349-353[Abstract].
18. Senda, K., Y. Arakawa, S. Ichiyama, K. Nakashima, H. Ito, S. Ohsuka, K. Shimokata, N. Kato, and M. Ohta. 1996. PCR detection of metallo-beta -lactamase gene (blaIMP) in gram-negative rods resistant to broad-spectrum beta -lactams. J. Clin. Microbiol. 34:2909-2913[Abstract].
19. Woodford, N., M. F. Palepou, G. S. Babini, J. Bates, and D. M. Livermore. 1998. Carbapenemase-producing Pseudomonas aeruginosa in UK. Lancet 352:546-547[Medline].


Journal of Clinical Microbiology, January 2000, p. 40-43, Vol. 38, No. 1
0095-1137/0/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.



This article has been cited by other articles:

  • Zhao, W.-H., Chen, G., Ito, R., Hu, Z.-Q. (2009). Relevance of resistance levels to carbapenems and integron-borne blaIMP-1, blaIMP-7, blaIMP-10 and blaVIM-2 in clinical isolates of Pseudomonas aeruginosa. J Med Microbiol 58: 1080-1085 [Abstract] [Full Text]  
  • Duljasz, W., Gniadkowski, M., Sitter, S., Wojna, A., Jebelean, C. (2009). First Organisms with Acquired Metallo-{beta}-Lactamases (IMP-13, IMP-22, and VIM-2) Reported in Austria. Antimicrob. Agents Chemother. 53: 2221-2222 [Full Text]  
  • Leavitt, A., Chmelnitsky, I., Colodner, R., Ofek, I., Carmeli, Y., Navon-Venezia, S. (2009). Ertapenem Resistance among Extended-Spectrum-{beta}-Lactamase-Producing Klebsiella pneumoniae Isolates. J. Clin. Microbiol. 47: 969-974 [Abstract] [Full Text]  
  • Siarkou, V. I., Vitti, D., Protonotariou, E., Ikonomidis, A., Sofianou, D. (2009). Molecular Epidemiology of Outbreak-Related Pseudomonas aeruginosa Strains Carrying the Novel Variant blaVIM-17 Metallo-{beta}-Lactamase Gene. Antimicrob. Agents Chemother. 53: 1325-1330 [Abstract] [Full Text]  
  • Hu, Z., Zhao, W.-H. (2009). Identification of plasmid- and integron-borne blaIMP-1 and blaIMP-10 in clinical isolates of Serratia marcescens. J Med Microbiol 58: 217-221 [Abstract] [Full Text]  
  • Pavez, M., Neves, P., Dropa, M., Matte, M. H., Grinbaum, R. S., Elmor de Araujo, M. R., Mamizuka, E. M., Lincopan, N. (2008). Emergence of carbapenem-resistant Escherichia coli producing CMY-2-type AmpC {beta}-lactamase in Brazil. J Med Microbiol 57: 1590-1592 [Full Text]  
  • Adams-Haduch, J. M., Paterson, D. L., Sidjabat, H. E., Pasculle, A. W., Potoski, B. A., Muto, C. A., Harrison, L. H., Doi, Y. (2008). Genetic Basis of Multidrug Resistance in Acinetobacter baumannii Clinical Isolates at a Tertiary Medical Center in Pennsylvania. Antimicrob. Agents Chemother. 52: 3837-3843 [Abstract] [Full Text]  
  • Sekiguchi, J.-i., Morita, K., Kitao, T., Watanabe, N., Okazaki, M., Miyoshi-Akiyama, T., Kanamori, M., Kirikae, T. (2008). KHM-1, a Novel Plasmid-Mediated Metallo-{beta}-Lactamase from a Citrobacter freundii Clinical Isolate. Antimicrob. Agents Chemother. 52: 4194-4197 [Abstract] [Full Text]  
  • Nemec, A., Krizova, L., Maixnerova, M., Diancourt, L., van der Reijden, T. J. K., Brisse, S., van den Broek, P., Dijkshoorn, L. (2008). Emergence of carbapenem resistance in Acinetobacter baumannii in the Czech Republic is associated with the spread of multidrug-resistant strains of European clone II. J Antimicrob Chemother 62: 484-489 [Abstract] [Full Text]  
  • Peleg, A. Y., Seifert, H., Paterson, D. L. (2008). Acinetobacter baumannii: Emergence of a Successful Pathogen. Clin. Microbiol. Rev. 21: 538-582 [Abstract] [Full Text]  
  • Picao, R. C., Andrade, S. S., Nicoletti, A. G., Campana, E. H., Moraes, G. C., Mendes, R. E., Gales, A. C. (2008). Metallo-{beta}-Lactamase Detection: Comparative Evaluation of Double-Disk Synergy versus Combined Disk Tests for IMP-, GIM-, SIM-, SPM-, or VIM-Producing Isolates. J. Clin. Microbiol. 46: 2028-2037 [Abstract] [Full Text]  
  • Tan, J., Pitout, J. D. D., Guttman, D. S. (2008). New and Sensitive Assay for Determining Pseudomonas aeruginosa Metallo-Beta-Lactamase Resistance to Imipenem. J. Clin. Microbiol. 46: 1870-1872 [Abstract] [Full Text]  
  • Marchaim, D., Navon-Venezia, S., Schwaber, M. J., Carmeli, Y. (2008). Isolation of Imipenem-Resistant Enterobacter Species: Emergence of KPC-2 Carbapenemase, Molecular Characterization, Epidemiology, and Outcomes. Antimicrob. Agents Chemother. 52: 1413-1418 [Abstract] [Full Text]  
  • Giakkoupi, P., Vourli, S., Polemis, M., Kalapothaki, V., Tzouvelekis, L. S., Vatopoulos, A. C. (2008). Supplementation of Growth Media with Zn2+ Facilitates Detection of VIM-2-Producing Pseudomonas aeruginosa. J. Clin. Microbiol. 46: 1568-1569 [Full Text]  
  • Galani, I., Rekatsina, P. D., Hatzaki, D., Plachouras, D., Souli, M., Giamarellou, H. (2008). Evaluation of different laboratory tests for the detection of metallo-{beta}-lactamase production in Enterobacteriaceae. J Antimicrob Chemother 61: 548-553 [Abstract] [Full Text]  
  • Tokatlidou, D., Tsivitanidou, M., Pournaras, S., Ikonomidis, A., Tsakris, A., Sofianou, D. (2008). Outbreak Caused by a Multidrug-Resistant Klebsiella pneumoniae Clone Carrying blaVIM-12 in a University Hospital. J. Clin. Microbiol. 46: 1005-1008 [Abstract] [Full Text]  
  • Castanheira, M., Sader, H. S., Deshpande, L. M., Fritsche, T. R., Jones, R. N. (2008). Antimicrobial Activities of Tigecycline and Other Broad-Spectrum Antimicrobials Tested against Serine Carbapenemase- and Metallo-{beta}-Lactamase-Producing Enterobacteriaceae: Report from the SENTRY Antimicrobial Surveillance Program. Antimicrob. Agents Chemother. 52: 570-573 [Abstract] [Full Text]  
  • Cagnacci, S., Gualco, L., Roveta, S., Mannelli, S., Borgianni, L., Docquier, J.-D., Dodi, F., Centanaro, M., Debbia, E., Marchese, A., Rossolini, G. M. (2008). Bloodstream infections caused by multidrug-resistant Klebsiella pneumoniae producing the carbapenem-hydrolysing VIM-1 metallo-{beta}-lactamase: first Italian outbreak. J Antimicrob Chemother 61: 296-300 [Abstract] [Full Text]  
  • Pliatsika, V., Afkou, Z., Protonotariou, E., Sofianou, D. (2007). In vitro activity of tigecycline against metallo-{beta}-lactamase-producing Enterobacteriaceae. J Antimicrob Chemother 60: 1406-1407 [Full Text]  
  • Neuwirth, C., Siebor, E., Robin, F., Bonnet, R. (2007). First Occurrence of an IMP Metallo-{beta}-Lactamase in Aeromonas caviae: IMP-19 in an Isolate from France. Antimicrob. Agents Chemother. 51: 4486-4488 [Abstract] [Full Text]  
  • Doi, Y., Ghilardi, A. C. R., Adams, J., de Oliveira Garcia, D., Paterson, D. L. (2007). High Prevalence of Metallo-{beta}-Lactamase and 16S rRNA Methylase Coproduction among Imipenem-Resistant Pseudomonas aeruginosa Isolates in Brazil. Antimicrob. Agents Chemother. 51: 3388-3390 [Abstract] [Full Text]  
  • Kim, S.-Y., Hong, S. G., Moland, E. S., Thomson, K. S. (2007). Convenient Test Using a Combination of Chelating Agents for Detection of Metallo-{beta}-Lactamases in the Clinical Laboratory. J. Clin. Microbiol. 45: 2798-2801 [Abstract] [Full Text]  
  • Queenan, A. M., Bush, K. (2007). Carbapenemases: the Versatile {beta}-Lactamases. Clin. Microbiol. Rev. 20: 440-458 [Abstract] [Full Text]  
  • Andrade, S. S., Picao, R. C., Campana, E. H., Nicoletti, A. G., Pignatari, A. C. C., Gales, A. C. (2007). Influence of Disk Preparation on Detection of Metallo-{beta}-Lactamase-Producing Isolates by the Combined Disk Assay. J. Clin. Microbiol. 45: 2058-2060 [Abstract] [Full Text]  
  • Sekiguchi, J.-I., Asagi, T., Miyoshi-Akiyama, T., Kasai, A., Mizuguchi, Y., Araake, M., Fujino, T., Kikuchi, H., Sasaki, S., Watari, H., Kojima, T., Miki, H., Kanemitsu, K., Kunishima, H., Kikuchi, Y., Kaku, M., Yoshikura, H., Kuratsuji, T., Kirikae, T. (2007). Outbreaks of Multidrug-Resistant Pseudomonas aeruginosa in Community Hospitals in Japan. J. Clin. Microbiol. 45: 979-989 [Abstract] [Full Text]  
  • Aboufaycal, H., Sader, H. S., Rolston, K., Deshpande, L. M., Toleman, M., Bodey, G., Raad, I., Jones, R. N. (2007). blaVIM-2 and blaVIM-7 Carbapenemase-Producing Pseudomonas aeruginosa Isolates Detected in a Tertiary Care Medical Center in the United States: Report from the MYSTIC Program. J. Clin. Microbiol. 45: 614-615 [Abstract] [Full Text]  
  • Wang, J., Bo, R., Xu, L., Mi, Z., Wang, C. (2006). A CARB-like {beta}-lactamase gene from a multiple-drug-resistant Pseudomonas aeruginosa clinical isolate in China.. J Med Microbiol 55: 1609-1610 [Full Text]  
  • Lincopan, N., Leis, R., Vianello, M. A., de Araujo, M. R. E., Ruiz, A. S., Mamizuka, E. M. (2006). Enterobacteria producing extended-spectrum {beta}-lactamases and IMP-1 metallo-{beta}-lactamases isolated from Brazilian hospitals.. J Med Microbiol 55: 1611-1613 [Full Text]  
  • Navon-Venezia, S., Chmelnitsky, I., Leavitt, A., Schwaber, M. J., Schwartz, D., Carmeli, Y. (2006). Plasmid-Mediated Imipenem-Hydrolyzing Enzyme KPC-2 among Multiple Carbapenem-Resistant Escherichia coli Clones in Israel.. Antimicrob. Agents Chemother. 50: 3098-3101 [Abstract] [Full Text]  
  • Zavascki, A. P., Barth, A. L., Goncalves, A. L. S., Moro, A. L. D., Fernandes, J. F., Martins, A. F., Ramos, F., Goldani, L. Z. (2006). The influence of metallo-{beta}-lactamase production on mortality in nosocomial Pseudomonas aeruginosa infections. J Antimicrob Chemother 58: 387-392 [Abstract] [Full Text]  
  • Jacoby, G. A., Walsh, K. E., Walker, V. J. (2006). Identification of Extended-Spectrum, AmpC, and Carbapenem- Hydrolyzing {beta}-Lactamases in Escherichia coli and Klebsiella pneumoniae by Disk Tests.. J. Clin. Microbiol. 44: 1971-1976 [Abstract] [Full Text]  
  • Chen, G.-X., Zhang, R., Zhou, H. W. (2006). Heterogeneity of metallo-{beta}-lactamases in clinical isolates of Chryseobacterium meningosepticum from Hangzhou, China. J Antimicrob Chemother 57: 750-752 [Abstract] [Full Text]  
  • Fiett, J., Baraniak, A., Mrowka, A., Fleischer, M., Drulis-Kawa, Z., Naumiuk, L., Samet, A., Hryniewicz, W., Gniadkowski, M. (2006). Molecular Epidemiology of Acquired-Metallo-{beta}-Lactamase-Producing Bacteria in Poland. Antimicrob. Agents Chemother. 50: 880-886 [Abstract] [Full Text]  
  • Wang, C.-X., Mi, Z.-H. (2006). Imipenem-resistant Pseudomonas aeruginosa producing IMP-1 metallo-{beta}-lactamases and lacking the outer-membrane protein OprD.. J Med Microbiol 55: 353-354 [Full Text]  
  • Wachino, J.-i., Kurokawa, H., Suzuki, S., Yamane, K., Shibata, N., Kimura, K., Ike, Y., Arakawa, Y. (2006). Horizontal Transfer of blaCMY-Bearing Plasmids among Clinical Escherichia coli and Klebsiella pneumoniae Isolates and Emergence of Cefepime-Hydrolyzing CMY-19. Antimicrob. Agents Chemother. 50: 534-541 [Abstract] [Full Text]  
  • Marra, A. R., Pereira, C. A. P., Gales, A. C., Menezes, L. C., Cal, R. G. R., de Souza, J. M. A., Edmond, M. B., Faro, C., Wey, S. B. (2006). Bloodstream Infections with Metallo-{beta}-Lactamase-Producing Pseudomonas aeruginosa: Epidemiology, Microbiology, and Clinical Outcomes. Antimicrob. Agents Chemother. 50: 388-390 [Abstract] [Full Text]  
  • Kassis-Chikhani, N., Decre, D., Gautier, V., Burghoffer, B., Saliba, F., Mathieu, D., Samuel, D., Castaing, D., Petit, J.-C., Dussaix, E., Arlet, G. (2006). First outbreak of multidrug-resistant Klebsiella pneumoniae carrying blaVIM-1 and blaSHV-5 in a French university hospital. J Antimicrob Chemother 57: 142-145 [Abstract] [Full Text]  
  • Dunne, W. M. Jr., Hardin, D. J. (2005). Use of Several Inducer and Substrate Antibiotic Combinations in a Disk Approximation Assay Format To Screen for AmpC Induction in Patient Isolates of Pseudomonas aeruginosa, Enterobacter spp., Citrobacter spp., and Serratia spp.. J. Clin. Microbiol. 43: 5945-5949 [Abstract] [Full Text]  
  • Zavascki, A. P., Gaspareto, P. B., Martins, A. F., Goncalves, A. L., Barth, A. L. (2005). Outbreak of carbapenem-resistant Pseudomonas aeruginosa producing SPM-1 metallo-{beta}-lactamase in a teaching hospital in southern Brazil. J Antimicrob Chemother 56: 1148-1151 [Abstract] [Full Text]  
  • Shiroto, K., Ishii, Y., Kimura, S., Alba, J., Watanabe, K., Matsushima, Y., Yamaguchi, K. (2005). Metallo-{beta}-lactamase IMP-1 in Providencia rettgeri from two different hospitals in Japan. J Med Microbiol 54: 1065-1070 [Abstract] [Full Text]  
  • Vedel, G. (2005). Simple method to determine {beta}-lactam resistance phenotypes in Pseudomonas aeruginosa using the disc agar diffusion test. J Antimicrob Chemother 56: 657-664 [Abstract] [Full Text]  
  • Lolans, K., Queenan, A. M., Bush, K., Sahud, A., Quinn, J. P. (2005). First Nosocomial Outbreak of Pseudomonas aeruginosa Producing an Integron-Borne Metallo-{beta}-Lactamase (VIM-2) in the United States. Antimicrob. Agents Chemother. 49: 3538-3540 [Abstract] [Full Text]  
  • Pitout, J. D. D., Gregson, D. B., Poirel, L., McClure, J.-A., Le, P., Church, D. L. (2005). Detection of Pseudomonas aeruginosa Producing Metallo-{beta}-Lactamases in a Large Centralized Laboratory. J. Clin. Microbiol. 43: 3129-3135 [Abstract] [Full Text]  
  • Yagi, T., Wachino, J.-i., Kurokawa, H., Suzuki, S., Yamane, K., Doi, Y., Shibata, N., Kato, H., Shibayama, K., Arakawa, Y. (2005). Practical Methods Using Boronic Acid Compounds for Identification of Class C {beta}-Lactamase-Producing Klebsiella pneumoniae and Escherichia coli. J. Clin. Microbiol. 43: 2551-2558 [Abstract] [Full Text]  
  • Galani, I., Souli, M., Chryssouli, Z., Orlandou, K., Giamarellou, H. (2005). Characterization of a new integron containing blaVIM-1 and aac(6')-IIc in an Enterobacter cloacae clinical isolate from Greece. J Antimicrob Chemother 55: 634-638 [Abstract] [Full Text]  
  • Walsh, T. R., Toleman, M. A., Poirel, L., Nordmann, P. (2005). Metallo-{beta}-Lactamases: the Quiet before the Storm?. Clin. Microbiol. Rev. 18: 306-325 [Abstract] [Full Text]  
  • Kimura, S., Alba, J., Shiroto, K., Sano, R., Niki, Y., Maesaki, S., Akizawa, K., Kaku, M., Watanuki, Y., Ishii, Y., Yamaguchi, K. (2005). Clonal Diversity of Metallo-{beta}-Lactamase-Possessing Pseudomonas aeruginosa in Geographically Diverse Regions of Japan. J. Clin. Microbiol. 43: 458-461 [Abstract] [Full Text]  
  • Lincopan, N., McCulloch, J. A., Reinert, C., Cassettari, V. C., Gales, A. C., Mamizuka, E. M. (2005). First Isolation of Metallo-{beta}-Lactamase-Producing Multiresistant Klebsiella pneumoniae from a Patient in Brazil. J. Clin. Microbiol. 43: 516-519 [Abstract] [Full Text]  
  • Wang, C.-x., Mi, Z.-h. (2004). IMP-1 metallo-{beta}-lactamase-producing Pseudomonas aeruginosa in a university hospital in the People's Republic of China. J Antimicrob Chemother 54: 1159-1160 [Full Text]  
  • Nishio, H., Komatsu, M., Shibata, N., Shimakawa, K., Sueyoshi, N., Ura, T., Satoh, K., Toyokawa, M., Nakamura, T., Wada, Y., Orita, T., Kofuku, T., Yamasaki, K., Sakamoto, M., Kinoshita, S., Aihara, M., Arakawa, Y. (2004). Metallo-{beta}-Lactamase-Producing Gram-Negative Bacilli: Laboratory-Based Surveillance in Cooperation with 13 Clinical Laboratories in the Kinki Region of Japan. J. Clin. Microbiol. 42: 5256-5263 [Abstract] [Full Text]  
  • Yan, J.-J., Ko, W.-C., Wu, H.-M., Tsai, S.-H., Chuang, C.-L., Wu, J.-J. (2004). Complexity of Klebsiella pneumoniae Isolates Resistant to Both Cephamycins and Extended-Spectrum Cephalosporins at a Teaching Hospital in Taiwan. J. Clin. Microbiol. 42: 5337-5340 [Abstract] [Full Text]  
  • Koh, T. H., Wang, G. C. Y., Sng, L.-H. (2004). Clonal Spread of IMP-1-Producing Pseudomonas aeruginosa in Two Hospitals in Singapore. J. Clin. Microbiol. 42: 5378-5380 [Abstract] [Full Text]  
  • Garrity, J. D., Pauff, J. M., Crowder, M. W. (2004). Probing the Dynamics of a Mobile Loop above the Active Site of L1, a Metallo-{beta}-lactamase from Stenotrophomonas maltophilia, via Site-directed Mutagenesis and Stopped-flow Fluorescence Spectroscopy. J. Biol. Chem. 279: 39663-39670 [Abstract] [Full Text]  
  • Wachino, J.-i., Doi, Y., Yamane, K., Shibata, N., Yagi, T., Kubota, T., Arakawa, Y. (2004). Molecular Characterization of a Cephamycin-Hydrolyzing and Inhibitor-Resistant Class A {beta}-Lactamase, GES-4, Possessing a Single G170S Substitution in the {Omega}-Loop. Antimicrob. Agents Chemother. 48: 2905-2910 [Abstract] [Full Text]  
  • Yu, Y.-S., Yang, Q., Xu, X.-W., Kong, H.-S., Xu, G.-Y., Zhong, B.-Y. (2004). Typing and characterization of carbapenem-resistant Acinetobacter calcoaceticus-baumannii complex in a Chinese hospital. J Med Microbiol 53: 653-656 [Abstract] [Full Text]  
  • Wachino, J.-i., Doi, Y., Yamane, K., Shibata, N., Yagi, T., Kubota, T., Ito, H., Arakawa, Y. (2004). Nosocomial Spread of Ceftazidime-Resistant Klebsiella pneumoniae Strains Producing a Novel Class A {beta}-Lactamase, GES-3, in a Neonatal Intensive Care Unit in Japan. Antimicrob. Agents Chemother. 48: 1960-1967 [Abstract] [Full Text]  
  • Yatsuyanagi, J., Saito, S., Harata, S., Suzuki, N., Ito, Y., Amano, K.-i., Enomoto, K. (2004). Class 1 Integron Containing Metallo-{beta}-Lactamase Gene blaVIM-2 in Pseudomonas aeruginosa Clinical Strains Isolated in Japan. Antimicrob. Agents Chemother. 48: 626-628 [Abstract] [Full Text]  
  • Garrity, J. D., Carenbauer, A. L., Herron, L. R., Crowder, M. W. (2004). Metal Binding Asp-120 in Metallo-{beta}-lactamase L1 from Stenotrophomonas maltophilia Plays a Crucial Role in Catalysis. J. Biol. Chem. 279: 920-927 [Abstract] [Full Text]  
  • Shibata, N., Doi, Y., Yamane, K., Yagi, T., Kurokawa, H., Shibayama, K., Kato, H., Kai, K., Arakawa, Y. (2003). PCR Typing of Genetic Determinants for Metallo-{beta}-Lactamases and Integrases Carried by Gram-Negative Bacteria Isolated in Japan, with Focus on the Class 3 Integron. J. Clin. Microbiol. 41: 5407-5413 [Abstract] [Full Text]  
  • Lee, K., Lim, Y. S., Yong, D., Yum, J. H., Chong, Y. (2003). Evaluation of the Hodge Test and the Imipenem-EDTA Double-Disk Synergy Test for Differentiating Metallo-{beta}-Lactamase-Producing Isolates of Pseudomonas spp. and Acinetobacter spp.. J. Clin. Microbiol. 41: 4623-4629 [Abstract] [Full Text]  
  • Gales, A. C., Menezes, L. C., Silbert, S., Sader, H. S. (2003). Dissemination in distinct Brazilian regions of an epidemic carbapenem-resistant Pseudomonas aeruginosa producing SPM metallo-{beta}-lactamase. J Antimicrob Chemother 52: 699-702 [Abstract] [Full Text]  
  • Yomoda, S., Okubo, T., Takahashi, A., Murakami, M., Iyobe, S. (2003). Presence of Pseudomonas putida Strains Harboring Plasmids Bearing the Metallo-{beta}-Lactamase Gene blaIMP in a Hospital in Japan. J. Clin. Microbiol. 41: 4246-4251 [Abstract] [Full Text]  
  • Yamasaki, K., Komatsu, M., Yamashita, T., Shimakawa, K., Ura, T., Nishio, H., Satoh, K., Washidu, R., Kinoshita, S., Aihara, M. (2003). Production of CTX-M-3 extended-spectrum {beta}-lactamase and IMP-1 metallo {beta}-lactamase by five Gram-negative bacilli: survey of clinical isolates from seven laboratories collected in 1998 and 2000, in the Kinki region of Japan. J Antimicrob Chemother 51: 631-638 [Abstract] [Full Text]  
  • Giakkoupi, P., Petrikkos, G., Tzouvelekis, L. S., Tsonas, S., Legakis, N. J., Vatopoulos, A. C. (2003). Spread of Integron-Associated VIM-Type Metallo-{beta}-Lactamase Genes among Imipenem-Nonsusceptible Pseudomonas aeruginosa Strains in Greek Hospitals. J. Clin. Microbiol. 41: 822-825 [Abstract] [Full Text]  
  • Miriagou, V., Tzelepi, E., Gianneli, D., Tzouvelekis, L. S. (2003). Escherichia coli with a Self-Transferable, Multiresistant Plasmid Coding for Metallo-{beta}-Lactamase VIM-1. Antimicrob. Agents Chemother. 47: 395-397 [Abstract] [Full Text]  
  • Migliavacca, R., Docquier, J.-D., Mugnaioli, C., Amicosante, G., Daturi, R., Lee, K., Rossolini, G. M., Pagani, L. (2002). Simple Microdilution Test for Detection of Metallo-{beta}-Lactamase Production in Pseudomonas aeruginosa. J. Clin. Microbiol. 40: 4388-4390 [Abstract] [Full Text]  
  • Ho, S. E., Subramaniam, G., Palasubramaniam, S., Navaratnam, P. (2002). Carbapenem-Resistant Pseudomonas aeruginosa in Malaysia Producing IMP-7 {beta}-Lactamase. Antimicrob. Agents Chemother. 46: 3286-3287 [Abstract] [Full Text]  
  • Yong, D., Lee, K., Yum, J. H., Shin, H. B., Rossolini, G. M., Chong, Y. (2002). Imipenem-EDTA Disk Method for Differentiation of Metallo-{beta}-Lactamase-Producing Clinical Isolates of Pseudomonas spp. and Acinetobacter spp.. J. Clin. Microbiol. 40: 3798-3801 [Abstract] [Full Text]  
  • Yan, J.-J., Ko, W.-C., Chuang, C.-L., Wu, J.-J. (2002). Metallo-{beta}-lactamase-producing Enterobacteriaceae isolates in a university hospital in Taiwan: prevalence of IMP-8 in Enterobacter cloacae and first identification of VIM-2 in Citrobacter freundii. J Antimicrob Chemother 50: 503-511 [Abstract] [Full Text]  
  • Siemann, S., Evanoff, D. P., Marrone, L., Clarke, A. J., Viswanatha, T., Dmitrienko, G. I. (2002). N-Arylsulfonyl Hydrazones as Inhibitors of IMP-1 Metallo-{beta}-Lactamase. Antimicrob. Agents Chemother. 46: 2450-2457 [Abstract] [Full Text]  
  • Walsh, T. R., Bolmstrom, A., Qwarnstrom, A., Gales, A. (2002). Evaluation of a New Etest for Detecting Metallo-{beta}-Lactamases in Routine Clinical Testing. J. Clin. Microbiol. 40: 2755-2759 [Abstract] [Full Text]  
  • Pellegrino, F. L. P. C., Teixeira, L. M., Carvalho, M. d. G. S., Aranha Nouer, S., Pinto de Oliveira, M., Mello Sampaio, J. L., D'Avila Freitas, A., Ferreira, A. L. P., Amorim, E. d. L. T., Riley, L. W., Moreira, B. M. (2002). Occurrence of a Multidrug-Resistant Pseudomonas aeruginosa Clone in Different Hospitals in Rio de Janeiro, Brazil. J. Clin. Microbiol. 40: 2420-2424 [Abstract] [Full Text]  
  • Gibb, A. P., Tribuddharat, C., Moore, R. A., Louie, T. J., Krulicki, W., Livermore, D. M., Palepou, M.-F. I., Woodford, N. (2002). Nosocomial Outbreak of Carbapenem-Resistant Pseudomonas aeruginosa with a New blaIMP Allele, blaIMP-7. Antimicrob. Agents Chemother. 46: 255-258 [Abstract] [Full Text]  
  • Yan, J.-J., Hsueh, P.-R., Ko, W.-C., Luh, K.-T., Tsai, S.-H., Wu, H.-M., Wu, J.-J. (2001). Metallo-{beta}-Lactamases in Clinical Pseudomonas Isolates in Taiwan and Identification of VIM-3, a Novel Variant of the VIM-2 Enzyme. Antimicrob. Agents Chemother. 45: 2224-2228 [Abstract] [Full Text]  

This Article
Right arrow Abstract Freely available
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrowReprints and Permissions
Right arrow Copyright Information
Right arrow Books from ASM Press
Right arrow MicrobeWorld
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Arakawa, Y.
Right arrow Articles by Goto, M.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Arakawa, Y.
Right arrow Articles by Goto, M.