High prevalence of Salmonella and IMP-4-producing Enterobacteriaceae in the silver gull on Five Islands, Australia

Journal of Antimicrobial Chemotherapy

Volumn 71, Issue 1, 2016, Pages 63-70

  Dolejska, Monika ^a   Masarikova, Martina ^a   Dobiasova, Hana ^a   Jamborova, Ivana ^a   Karpiskova, Renata ^b   Havlicek, Martin ^c   Carlile, Nicholas ^d   Priddel, David ^d   Cizek, Alois ^a   Literak, Ivan ^a  

^a UNIVERSITY OF VETERINARY AND PHARMACEUTICAL SCIENCES   (Czech Republic)

^b VETERINARY RESEARCH INSTITUTE   (Czech Republic)

^c Small Animal Specialist Hospital   (Australia)

^d OFFICE OF ENVIRONMENT AND HERITAGE   (Australia)

Author keywords

[No Author keywords available]

Indexed keywords

AMOXICILLIN; AMPICILLIN; CARBAPENEMASE; CEFALOTIN; CEFTAZIDIME; CHLORAMPHENICOL; CIPROFLOXACIN; COTRIMOXAZOLE; GENTAMICIN; IMIPENEM; INOSINE PHOSPHATE; INOSINE PHOSPHATE 4; MEROPENEM; NALIDIXIC ACID; STREPTOMYCIN; SULFONAMIDE; TETRACYCLINE; UNCLASSIFIED DRUG; ANTIINFECTIVE AGENT; BACTERIAL PROTEIN; BETA LACTAMASE;

ANTIBIOTIC RESISTANCE; ANTIBIOTIC SENSITIVITY; ARTICLE; AUSTRALIA; BACTERIAL STRAIN; BACTERIOPHAGE TYPING; BACTERIUM CONTAMINATION; BIRD; CARBAPENEMASE PRODUCING ENTEROBACTERIACEAE; CITROBACTER; CITROBACTER FREUNDII; CLONAL VARIATION; ENTEROBACTER AEROGENES; ENTEROBACTER CLOACAE; ESCHERICHIA COLI; GENETIC VARIABILITY; HAFNIA ALVEI; INTEGRON; KLUYVERA; MOLECULAR TYPING; MORGANELLA MORGANII; NONHUMAN; PREVALENCE; PROTEUS MIRABILIS; PROTEUS VULGARIS; PROVIDENCIA; REPLICON; SALMONELLA; SALMONELLA ENTERICA; SALMONELLA ENTERICA SEROVAR TYPHIMURIUM; SILVER GULL; ANIMAL; BIRD DISEASES; CHARADRIIFORMES; CLOACA; ENTEROBACTERIACEAE; ENTEROBACTERIACEAE INFECTIONS; ENZYMOLOGY; GENETICS; GENOTYPE; HUMAN; ISLAND (GEOLOGICAL); ISOLATION AND PURIFICATION; MICROBIAL SENSITIVITY TEST; MICROBIOLOGY; MOLECULAR EPIDEMIOLOGY; NEW SOUTH WALES; VETERINARY;

ANIMALS; ANTI-BACTERIAL AGENTS; BACTERIAL PROTEINS; BETA-LACTAMASES; BIRD DISEASES; BIRDS; CHARADRIIFORMES; CLOACA; ENTEROBACTERIACEAE; ENTEROBACTERIACEAE INFECTIONS; GENOTYPE; HUMANS; ISLANDS; MICROBIAL SENSITIVITY TESTS; MOLECULAR EPIDEMIOLOGY; MOLECULAR TYPING; NEW SOUTH WALES; PREVALENCE;

EID: 84960192289     PISSN: 03057453     EISSN: 14602091     Source Type: Journal    
DOI: 10.1093/jac/dkv306     Document Type: Article

References (35)

1. Cornaglia G, Giamarellou H, Rossolini GM. Metallo-b-lactamases: a last frontier for b-lactams? Lancet Infect Dis 2011; 11: 381-93.
2. Zhao WH, Hu ZQ. IMP-type metallo-b-lactamases in Gram-negative bacilli: distribution, phylogeny, and association with integrons. Crit Rev Microbiol 2011; 37: 214-26.
3. Nordmann P, Naas T, Poirel L. Global spread of carbapenemaseproducing Enterobacteriaceae. Emerg Infect Dis 2011; 17: 1791-8.
4. Hu L, Zhong Q, Shang Y et al. The prevalence of carbapenemase genes and plasmid-mediated quinolone resistance determinants in carbapenemresistant Enterobacteriaceae from five teaching hospitals in central China. Epidemiol Infect 2014; 142: 1972-7.
5. Hong JS, Kim JO, Lee HB. Characteristics of metallo-b-lactamaseproducing Pseudomonas aeruginosa in Korea. Infect Chemother 2015; 47: 33-40.
6. Peirano G, Lascols C, Hackel M et al. Molecular epidemiology of Enterobacteriaceae that produce VIMs and IMPs from the SMART surveillance program. Diagn Microbiol Infect Dis 2014; 78: 277-81.
7. Leung GH, Gray TJ, Cheong EY et al. Persistence of related blaIMP-4 metallo-b-lactamase producing Enterobacteriaceae from clinical and environmental specimens within a burns unit in Australia-a six-year retrospective study. Antimicrob Resist Infect Control 2013; 2: 35.
8. Guerra B, Fischer J, Helmuth R. An emerging public health problem: acquired carbapenemase-producing microorganisms are present in food-producing animals, their environment, companion animals and wild birds. Vet Microbiol 2014; 171: 290-7.
9. Palmgren H, Aspan A, Broman T et al. Salmonella in black-headed gulls (Larus ridibundus); prevalence, genotypes and influence on Salmonella epidemiology. Epidemiol Infect 2006; 134: 635-44.
10. Iveson JB, Shellam GR, Bradshaw SD et al. Salmonella infections in Antarctic fauna and island populations of wildlife exposed to human activities in coastal areas of Australia. Epidemiol Infect 2009; 137: 858-70.
11. Smith GC, Carlile N. Habitat use by silver gulls Larus novaehollandiae in the Sydney-Wollongong region, New South Wales. Wetlands (Australia) 1992; 11: 33-46.
12. Smith GC, Carlile N. Food and feeding ecology of breeding silver gulls (Larus novaehollandiae) in urban Australia. Colonial Waterbirds 1993; 16: 9-17.
13. Grimont P, Weill F. Antigenic Formulae of the Salmonella Serovars. 9th edn. Paris, France: WHO Collaborating Centre for Reference and Research on Salmonella, 2007.
14. Anderson ES, Ward LR, Saxe MJ et al. Bacteriophage-typing designations of Salmonella typhimurium. J Hyg (Lond) 1977; 78: 297-300.
15. Ward LR, de Sa JD, Rowe B. A phage-typing scheme for Salmonella enteritidis. Epidemiol Infect 1987; 99: 291-4.
16. Clinical and Laboratory Standards Institute. Performance Standards for Antimicrobial Susceptibility Testing: Twenty-fourth Informational Supplement M100-S24. CLSI, Wayne, PA, USA, 2014.
17. Dunne MW, Hardin DJ. 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 2005; 43: 5945-9.
18. Giske CG, Gezelius L, Samuelsen Ø et al. A sensitive and specific phenotypic assay for detection of metallo-b-lactamases and KPC in Klebsiella pneumoniae with the use of meropenem disks supplemented with aminophenylboronic acid, dipicolinic acid and cloxacillin. Clin Microbiol Infect 2011; 17: 552-6.
19. Diancourt L, Passet V, Verhoef J et al. Multilocus sequence typing of Klebsiella pneumoniae nosocomial isolates. J Clin Microbiol 2005; 43: 4178-82.
20. Wirth T, Falush D, Lan R et al. Sex and virulence in Escherichia coli: an evolutionary perspective. Mol Microbiol 2006; 60: 1136-51.
21. Clermont O, Bonacorsi S, Bingen E. Rapid and simple determination of the Escherichia coli phylogenetic group. Appl Environ Microbiol 2000; 66: 4555-8.
22. Espedido BA, Partridge SR, Iredell JR. blaIMP-4 in different genetic contexts in Enterobacteriaceae isolates from Australia. Antimicrob Agents Chemother 2008; 52: 2984-7.
23. Maher D, Taylor DE. Host range and transfer efficiency of incompatibility group HI plasmid. Can J Microbiol 1993; 39: 581-7.
24. Carattoli A, Bertini A, Villa L et al. Identification of plasmids by PCR-based replicon typing. J Microbiol Methods 2005; 63: 219-28.
25. Garcia-Fernandez A, Fortini D, Veldman K et al. Characterization of plasmids harbouring qnrS1, qnrB2 and qnrB19 genes in Salmonella. J Antimicrob Chemother 2009; 63: 274-81.
26. Powling J. National Enteric Pathogens Surveillance Scheme, Human Annual Report 1996-2010. Victoria: Microbiological Diagnostic Unit, University of Melbourne, 2010.
27. RabschW, Andrews HL, Kingsley RA et al. Salmonella enterica serotype Typhimurium and its host-adapted variants. Infect Immun 2002; 70: 2249-55.
28. Australian Group on Antimicrobial Resistance. The Evolution of Carbapenemases in Enterobacteriaceae in Australia. Updated 20 October
29. http://www.agargroup.org/files/AGAR_Carbapenemase_evolution% 20Final.pdf.
30. Dahmen S,Metayer V, Gay E et al. Characterization of extended-spectrum b-lactamase (ESBL)-carrying plasmids and clones of Enterobacteriaceae causing cattle mastitis in France. Vet Microbiol 2013; 162: 793-9.
31. Fischer J, Rodriguez I, Baumann B et al. blaCTX-M-15-carrying Escherichia coli and Salmonella isolates from livestock and food in Germany. J Antimicrob Chemother 2014; 69: 2951-8.
32. Izdebski R, Baraniak A, Fiett J et al. Clonal structure, extendedspectrum b-lactamases, and acquired AmpC-type cephalosporinases of Escherichia coli populations colonizing patients in rehabilitation centers in four countries. Antimicrob Agents Chemother 2013; 57: 309-16.
33. Guo S, Wakeham D, Brouwers HJ et al. Human-associated fluoroquinolone-resistant Escherichia coli clonal lineages, including ST354, isolated from canine feces and extraintestinal infections in Australia. Microbes Infect 2015; 17: 266-74.
34. Sidjabat HE, Townell N, Nimmo GR et al. Dominance of IMP-4-producing Enterobacter cloacae amongst carbapenemase-producing Enterobacteriaceae in Australia. Antimicrob Agents Chemother 2015; 59: 4059-66.
35. Lo WU, Cheung YY, Lai E et al. Complete sequence of an IncN plasmid, pIMP-HZ1, carrying blaIMP-4 in a Klebsiella pneumoniae strain associated with medical travel to China. Antimicrob Agents Chemother 2013; 57: 1561-2.