Table of Contents
ISRN Microbiology
Volume 2014, Article ID 715310, 3 pages
Research Article

Emergence of blaTEM Type Extended-Spectrum β-Lactamase Producing Salmonella spp. in the Urban Area of Bangladesh

International Centre for Diarrheal Disease Research, Bangladesh (icddr,b), Dhaka 1212, Bangladesh

Received 23 January 2014; Accepted 25 February 2014; Published 10 March 2014

Academic Editors: G. Koraimann and F. Navarro-Garcia

Copyright © 2014 Dilruba Ahmed et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. O. Lunguya, V. Lejon, M. F. Phoba et al., “Antimicrobial resistance in invasive non-typhoid Salmonella from the Democratic Republic of the Congo: emergence of decreased fluoroquinolone susceptibility and extended-spectrum beta lactamases,” PLoS Neglected Tropical Diseases, vol. 7, no. 3, article e2103, 2013. View at Google Scholar
  2. H. X. Jiang, L. Song, J. Liu et al., “Multiple transmissible genes encoding fluoroquinolone and third-generation cephalosporin resistance co-located in non-typhoidal Salmonella isolated from food-producing animals in China,” International Journal of Antimicrobial Agents, 2013. View at Publisher · View at Google Scholar
  3. M. Sjölund-Karlsson, R. Rickert, C. Matar et al., “Salmonella isolates with decreased susceptibility to extended-spectrum cephalosporins in the United States,” Foodborne Pathogens and Disease, vol. 7, no. 12, pp. 1503–1509, 2010. View at Publisher · View at Google Scholar · View at Scopus
  4. I. Olesen, H. Hasman, and F. M. Aarestrup, “Prevalence of β-lactamases among ampicillin-resistant Escherichia coli and Salmonella isolated from food animals in Denmark,” Microbial Drug Resistance, vol. 10, no. 4, pp. 334–340, 2004. View at Google Scholar · View at Scopus
  5. J. D. D. Pitout, A. Hossain, and N. D. Hanson, “Phenotypic and molecular detection of CTX-M-β-lactamases produced by Escherichia coli and Klebsiella spp,” Journal of Clinical Microbiology, vol. 42, no. 12, pp. 5715–5721, 2004. View at Publisher · View at Google Scholar · View at Scopus
  6. P. L. Winokur, D. L. Vonstein, L. J. Hoffman, E. K. Uhlenhopp, and G. V. Doern, “Evidence for transfer of CMY-2 AmpC β-lactamase plasmids between Escherichia coli and Salmonella isolates from food animals and humans,” Antimicrobial Agents and Chemotherapy, vol. 45, no. 10, pp. 2716–2722, 2001. View at Publisher · View at Google Scholar · View at Scopus
  7. F. González and M. Araque, “Association of transferable quinolone resistance determinant qnrB19 with extended-spectrum β-lactamases in Salmonella Give and Salmonella Heidelberg in Venezuela,” International Journal of Microbiology, vol. 2013, Article ID 628185, 6 pages, 2013. View at Publisher · View at Google Scholar
  8. H. Knothe, P. Shah, V. Krcmery, M. Antal, and S. Mitsuhashi, “Transferable resistance to cefotaxime, cefoxitin, cefamandole and cefuroxime in clinical isolates of Klebsiella pneumoniae and Serratia marcescens,” Infection, vol. 11, no. 6, pp. 315–317, 1983. View at Google Scholar · View at Scopus
  9. J. S. Lewis II, M. Herrera, B. Wickes, J. E. Patterson, and J. H. Jorgensen, “First report of the emergence of CTX-M-type extended-spectrum β-lactamases (ESBLs) as the predominant ESBL isolated in a US health care system,” Antimicrobial Agents and Chemotherapy, vol. 51, no. 11, pp. 4015–4021, 2007. View at Publisher · View at Google Scholar · View at Scopus
  10. D. Ahmed, A. Hoque, R. Mazumder et al., “Salmonella entericsa serovar Typhi strain producing extended-spectrum beta-lactamases in Dhaka, Bangladesh,” Journal Medical Microbiology, vol. 61, no. 7, pp. 1032–1033, 2012. View at Google Scholar