Chromosome-based blaOXA-48-like variants in Shewanella species isolates from food-producing animals, fish, and the aquatic environment

Antimicrobial Agents and Chemotherapy

Volumn 61, Issue 2, 2017, Pages

  Ceccarelli, Daniela ^a   Van Essen Zandbergen, Alieda ^a   Veldman, Kees T ^a   Tafro, Nedzib ^b   Haenen, Olga ^a   Mevius, Dik J ^a,c  

^a WAGENINGEN UNIVERSITY   (Netherlands)

^b Dutch Food and Consumer Product Safety Authority (NVWA)   (Netherlands)

^c UTRECHT UNIVERSITY   (Netherlands)

Author keywords

Antibiotic resistance; Carbapenemase; Carbapenems; Fish; Freshwater; Livestock; OXA 48; Shewanella

Indexed keywords

CARBAPENEMASE; ANTIINFECTIVE AGENT; BETA LACTAMASE;

ALLELE; AMINO ACID SUBSTITUTION; ANTIBIOTIC RESISTANCE; ANTIBIOTIC SENSITIVITY; AQUATIC SPECIES; ARTICLE; BACTERIAL GENE; BACTERIUM CONJUGATION; BACTERIUM ISOLATE; BACTERIUM TRANSFORMATION; BLA OXA 48 GENE; BLA OXA 514 GENE; BLA OXA 515 GENE; CHROMOSOMAL LOCALIZATION; CHROMOSOME; DAIRY CATTLE; ENTEROBACTERIACEAE; ESCHERICHIA COLI K 12; GENE; GENETIC VARIABILITY; NONHUMAN; NUCLEOTIDE SEQUENCE; ORNAMENTAL FISH; PIG; PRIORITY JOURNAL; SHEWANELLA; SHEWANELLA XIAMENENSIS; VEAL; WATER TRANSPORT; ANIMAL; BACTERIAL CHROMOSOME; CHICKEN; DRUG EFFECTS; FISH; FOOD CONTROL; GENETICS; ISOLATION AND PURIFICATION; LIVESTOCK; MICROBIOLOGY; NETHERLANDS;

ANIMALS; ANTI-BACTERIAL AGENTS; BETA-LACTAMASES; CHICKENS; CHROMOSOMES, BACTERIAL; DRUG RESISTANCE, BACTERIAL; FISHES; FOOD MICROBIOLOGY; LIVESTOCK; NETHERLANDS; SHEWANELLA; SWINE;

EID: 85010987655     PISSN: 00664804     EISSN: 10986596     Source Type: Journal    
DOI: 10.1128/AAC.01013-16     Document Type: Article

References (23)

1. Queenan AM, Bush K. 2007. Carbapenemases: the versatile β-lactamases. Clin Microbiol Rev 20:440-458. https://doi.org/10.1128/CMR.00001-07.
2. Fischer J, Rodríguez I, Schmoger S, Friese A, Roesler U, Helmuth R, Guerra B. 2013. Salmonella enterica subsp. enterica producing VIM-1 carbapenemase isolated from livestock farms. J Antimicrob Chemother 68:478-480. https://doi.org/10.1093/jac/dks393.
3. Stolle I, Prenger-Berninghoff E, Stamm I, Scheufen S, Hassdenteufel E, Guenther S, Bethe A, Pfeifer Y, Ewers C. 2013. Emergence of OXA-48 carbapenemase-producing Escherichia coli and Klebsiella pneumoniae in dogs. J Antimicrob Chemother 68:2802-2808. https://doi.org/10.1093/jac/dkt259.
4. Morrison BJ, Rubin JE. 2015. Carbapenemase producing bacteria in the food supply escaping detection. PLoS One 10:e0126717. https://doi.org/10.1371/journal.pone.0126717.
5. Woodford N, Wareham DW, Guerra B, Teale C. 2014. Carbapenemase-producing Enterobacteriaceae and non-Enterobacteriaceae from animals and the environment: an emerging public health risk of our own making? J Antimicrob Chemother 69:287-291. https://doi.org/10.1093/jac/dkt392.
6. Tacão M, Correia A, Henriques IS. 2015. Low prevalence of carbapenem-resistant bacteria in river water: resistance is mostly related to intrinsic mechanisms. Microb Drug Resist 21:497-506. https://doi.org/10.1089/mdr.2015.0072.
7. Poirel L, Stephan R, Perreten V, Nordmann P. 2014. The carbapenemase threat in the animal world: the wrong culprit. J Antimicrob Chemother 69:2007-2008. https://doi.org/10.1093/jac/dku054.
8. Guerra B, Fischer J, Helmuth R. 2014. An emerging public health problem: acquired carbapenemase-producing microorganisms are present in food-producing animals, their environment, companion animals and wild birds. Vet Microbiol 171:290-297. https://doi.org/10.1016/j.vetmic.2014.02.001.
9. EFSA Panel on Biological Hazards. 2013. Scientific opinion on carbapenem resistance in food animal ecosystems. EFSA J 11:3501. https://doi.org/10.2903/j.efsa.2013.3501.
10. Gerzova L, Videnska P, Faldynova M, Sedlar K, Provaznik I, Cizek A, Rychlik I. 2014. Characterization of microbiota composition and presence of selected antibiotic resistance genes in carriage water of ornamental fish. PLoS One 9:e103865. https://doi.org/10.1371/journal.pone.0103865.
11. Verner-Jeffreys DW, Welch TJ, Schwarz T, Pond MJ, Woodward MJ, Haig SJ, Rimmer GS, Roberts E, Morrison V, Baker-Austin C. 2009. High prevalence of multidrug-tolerant bacteria and associated antimicrobial resistance genes isolated from ornamental fish and their carriage water. PLoS One 4:e8388. https://doi.org/10.1371/journal.pone.0008388.
12. Central Veterinary Institute of Wageningen University and Research Centre. 2015. MARAN 2015. Monitoring of antimicrobial resistance and antibiotic usage in animals in the Netherlands in 2014. Dutch Working Party on Antibiotic Policy, Rotterdam, The Netherlands. http://www.wur.nl/upload-mm/c/f/3/e751a7fa-4cdd-4bda-951a-25ca4153f84a-NethmapMaran2015.pdf.
13. European Commission. 2013. Commission implementing decision on the monitoring and reporting of antimicrobial resistance in zoonotic and commensal bacteria. C 7145 OJ L 303:26-39. European Commission, Brussels, Belgium. http://eur-lex.europa.eu/legal-content/EN/TXT/?uri=CELEX%3A32013D0652.
14. Poirel L, Héritier C, Tolün V, Nordmann P. 2004. Emergence of oxacillinase-mediated resistance to imipenem in Klebsiella pneumoniae. Antimicrob Agents Chemother 48:15-22. https://doi.org/10.1128/AAC.48.1.15-22.2004.
15. OXA-48-like variant, in Shewanella xiamenensis. PLoS One 7:e48280. https://doi.org/10.1371/journal.pone.0048280.
16. Potron A, Poirel L, Nordmann P. 2011. Origin of OXA-181, an emerging carbapenem-hydrolyzing oxacillinase, as a chromosomal gene in Shewanella xiamenensis. Antimicrob Agents Chemother 55:4405-4407. https://doi.org/10.1128/AAC.00681-11.
17. Antonelli A, Di Palo DM, Galano A, Becciani S, Montagnani C, Pecile P, Galli L, Rossolini GM. 2015. Intestinal carriage of Shewanella xiamenensis simulating carriage of OXA-48-producing Enterobacteriaceae. Diagn Microbiol Infect Dis 82:1-3. https://doi.org/10.1016/j.diagmicrobio.2015.02.008.
18. Hordijk J, Wagenaar JA, Kant A, van Essen-Zandbergen A, Dierikx C, Veldman K, Wit B, Mevius D. 2013. Cross-sectional study on prevalence and molecular characteristics of plasmid mediated ESBL/AmpC-producing Escherichia coli isolated from veal calves at slaughter. PLoS One 8:e65681. https://doi.org/10.1371/journal.pone.0065681.
19. Dierikx C, van Essen-Zandbergen A, Veldman K, Smith H, Mevius D. 2010. Increased detection of extended spectrum beta-lactamase producing Salmonella enterica and Escherichia coli isolates from poultry. Vet Microbiol 145:273-278. https://doi.org/10.1016/j.vetmic.2010.03.019.
20. Poirel L, Bonnin RA, Nordmann P. 2012. Genetic features of the widespread plasmid coding for the carbapenemase OXA-48. Antimicrob Agents Chemother 56:559-562. https://doi.org/10.1128/AAC.05289-11.
21. Evans BA, Amyes SGB. 2014. OXA β-lactamases. Clin Microbiol Rev 27:241-263. https://doi.org/10.1128/CMR.00117-13.
22. Poirel L, Potron A, Nordmann P. 2012. OXA-48-like carbapenemases: the phantom menace. J Antimicrob Chemother 67:1597-1606. https://doi.org/10.1093/jac/dks121.
23. Tacão M, Correia A, Henriques I. 2013. Environmental Shewanella xiamenensis strains that carry blaOXA-48 or blaOXA-204 genes: additional proof for blaOXA-48-like gene origin. Antimicrob Agents Chemother 57:6399-6400. https://doi.org/10.1128/AAC.00771-13.