DOI QR코드

DOI QR Code

Antimicrobial Resistance Profile of Acinetobacter spp. Isolates from Retail Meat Samples under Campylobacter-Selective Conditions

  • Cha, Min-Hyeok (Laboratory of Food Safety and Evaluation, Department of Biotechnology, Korea University Graduate School) ;
  • Kim, Sun Hee (Division of Biotechnology, College of Life Sciences and Biotechnology, Korea University) ;
  • Kim, Seokhwan (Division of Food Microbiology, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Lee, Woojung (Division of Food Microbiology, National Institute of Food and Drug Safety Evaluation, Ministry of Food and Drug Safety) ;
  • Kwak, Hyo-Sun (Department of Food Science and Biotechnology, Kyung Hee University) ;
  • Chi, Young-Min (Division of Biotechnology, College of Life Sciences and Biotechnology, Korea University) ;
  • Woo, Gun-Jo (Laboratory of Food Safety and Evaluation, Department of Biotechnology, Korea University Graduate School)
  • 투고 : 2021.02.22
  • 심사 : 2021.04.02
  • 발행 : 2021.05.28

초록

Acinetobacter strains are widely present in the environment. Some antimicrobial-resistant strains of this genus have been implicated in infections acquired in hospitals. Genetic similarities have been reported between Acinetobacter strains in nosocomial infections and those isolated from foods. However, the antimicrobial resistance of Acinetobacter strains in foods, such as meat, remains unclear. This study initially aimed to isolate Campylobacter strains; instead, strains of the genus Acinetobacter were isolated from meat products, and their antimicrobial resistance was investigated. In total, 58 Acinetobacter strains were isolated from 381 meat samples. Of these, 32 strains (38.6%) were from beef, 22 (26.5%) from pork, and 4 (4.8%) from duck meat. Antimicrobial susceptibility tests revealed that 12 strains were resistant to more than one antimicrobial agent, whereas two strains were multidrug-resistant; both strains were resistant to colistin. Cephalosporin antimicrobials showed high minimal inhibitory concentration against Acinetobacter strains. Resfinder analysis showed that one colistin-resistant strain carried mcr-4.3; this plasmid type was not confirmed, even when analyzed with PlasmidFinder. Analysis of the contig harboring mcr-4.3 using BLAST confirmed that this contig was related to mcr-4.3 of Acinetobacter baumannii. The increase in antimicrobial resistance in food production environments increases the resistance rate of Acinetobacter strains present in meat, inhibits the isolation of Campylobacter strains, and acts as a medium for the transmission of antimicrobial resistance in the environment. Therefore, further investigations are warranted to prevent the spread of antimicrobial resistance in food products.

키워드

과제정보

This work was supported by a grant from the Ministry of Food and Drug Safety (nos. 15161MFDS645), the Korea National Institute of Health (grant number 2017-NI41004 and 2017ER540601), and the Korea Rural Development Administration (grant number PJ010500). The findings and conclusions of this article are ours and do not necessarily reflect the views of MFDS, NIH, and KRDA.

참고문헌

  1. Fernando DM, Khan IUH, Patidar R, Lapen DR, Talbot G, Topp E, et al. 2016. Isolation and characterization of Acinetobacter baumannii recovered from Campylobacter selective medium. Front. Microbiol. 7: 1871-1871. https://doi.org/10.3389/fmicb.2016.01871
  2. Visca P, Seifert H, Towner KJ. 2011. Acinetobacter infection-an emerging threat to human health. IUBMB Life 63: 1048-1054. https://doi.org/10.1002/iub.534
  3. Maboni G, Seguel M, Lorton A, Sanchez S. 2020. Antimicrobial resistance patterns of Acinetobacter spp. of animal origin reveal high rate of multidrug resistance. Vet. Microbiol. 245: 108702. https://doi.org/10.1016/j.vetmic.2020.108702
  4. Leite GC, Stabler RA, Neves P, Perdigao Neto LV, Ruedas Martins RC, Rizek C, et al. 2019. Genetic and virulence characterization of colistin-resistant and colistin-sensitive A. baumannii clinical isolates. Diagn. Microbiol. Infect. Dis. 95: 99-101. https://doi.org/10.1016/j.diagmicrobio.2019.04.013
  5. Ma F, Shen C, Zheng X, Liu Y, Chen H, Zhong L, et al. 2019. Identification of a novel plasmid carrying mcr-4.3 in an Acinetobacter baumannii strain in China. Antimicrob. Agents Chemother. 63: e00133-19.
  6. Mustapha MM, Li B, Pacey MP, Mettus RT, McElheny CL, Marshall CW, et al. 2018. Phylogenomics of colistin-susceptible and resistant XDR Acinetobacter baumannii. J. Antimicrob. Chemother. 73: 2952-2959. https://doi.org/10.1093/jac/dky290
  7. Cha M-H, Ryu J-G, Chi Y-M, Woo G-J. 2020. Characterization of extended-spectrum β-lactamase-producing Escherichia coli isolated from fresh produce and agricultural environments in Korea. J. Food Protect. 83: 1115-1124. https://doi.org/10.4315/JFP-19-483
  8. Ministry of Food and Drug Safety. 2020. Korean Food Code, pp. 224-225. Cheongju, Korea
  9. La Scola B, Gundi VAKB, Khamis A, Raoult D. 2006. Sequencing of the rpoB gene and flanking spacers for molecular identification of Acinetobacter species. J. Clin. Microbiol. 44: 827-832. https://doi.org/10.1128/JCM.44.3.827-832.2006
  10. Clinical and Laboratory Standards Institute. 2017. Performance Standards for Antimicrobial Susceptibility Testing. CLSI Document M100. Wayne, PA. USA.
  11. Carattoli A, Zankari E, Garcia-Fernandez A, Larsen MV, Lund O, Villa L, et al. 2014. PlasmidFinder and pMLST: in silico detection and typing of plasmids. Antimicrob. Agents Chemother. 58: 3895-3903. https://doi.org/10.1128/AAC.02412-14
  12. Zankari E, Hasman H, Kaas RS, Seyfarth AM, Agerso Y, Lund O, et al. 2013. Genotyping using whole-genome sequencing is a realistic alternative to surveillance based on phenotypic antimicrobial susceptibility testing. J. Antimicrob. Chemother. 68: 771-777. https://doi.org/10.1093/jac/dks496
  13. Aziz RK, Bartels D, Best AA, DeJongh M, Disz T, Edwards RA, et al. 2008. The RAST server: rapid annotations using subsystems technology. BMC Genomics 9: 75. https://doi.org/10.1186/1471-2164-9-75
  14. Siguier P, Perochon J, Lestrade L, Mahillon J, Chandler M. 2006. ISfinder: the reference centre for bacterial insertion sequences. Nucleic Acids Res. 34: D32-D36. https://doi.org/10.1093/nar/gkj014
  15. Clark NM, Zhanel GG, Lynch III JP. 2016. Emergence of antimicrobial resistance among Acinetobacter species: a global threat. Curr. Opin Crit. Care 22: 491-499. https://doi.org/10.1097/MCC.0000000000000337
  16. Choi J-Y, Kim Y, Ko EA, Park YK, Jheong W-H, Ko G, et al. 2012. Acinetobacter species isolates from a range of environments: species survey and observations of antimicrobial resistance. Diagn. Microbiol. Infect. Dis. 74: 177-180. https://doi.org/10.1016/j.diagmicrobio.2012.06.023
  17. Woolhouse M, Ward M, van Bunnik B, Farrar J. 2015. Antimicrobial resistance in humans, livestock and the wider environment. Philos. Trans. R. Soc. Lond., B, Biol. Sci. Philos. T R Soc. B. 370: 20140083. https://doi.org/10.1098/rstb.2014.0083
  18. Carvalheira A, Casquete R, Silva J, Teixeira P. 2017. Prevalence and antimicrobial susceptibility of Acinetobacter spp. isolated from meat. Int. J. Food Microbiol. 243: 58-63. https://doi.org/10.1016/j.ijfoodmicro.2016.12.001
  19. Carvalheira A, Ferreira V, Silva J, Teixeira P. 2016. Enrichment of Acinetobacter spp. from food samples. Food Microbiol. 55: 123-127. https://doi.org/10.1016/j.fm.2015.11.002
  20. de Amorim AMB, dos Santos Nascimento J. 2017. Acinetobacter: an underrated foodborne pathogen? J. Infect. Dev. Countr. 11: 111-114. https://doi.org/10.3855/jidc.8418
  21. Anyanwu MU, Jaja IF, Nwobi OC. 2020. Occurrence and characteristics of mobile colistin resistance (Mcr) gene-containing isolates from the environment: a review. Int. J. Environ. Res. Public Health 17: 1028. https://doi.org/10.3390/ijerph17031028
  22. Bitar I, Medvecky M, Gelbicova T, Jakubu V, Hrabak J, Zemlickova H, et al. 2019. Complete nucleotide sequences of mcr-4.3-carrying plasmids in Acinetobacter baumannii sequence type 345 of human and food origin from the Czech republic, the first case in Europe. Antimicrob. Agents Chemother. 63: e01166-19.
  23. Carattoli A, Villa L, Feudi C, Curcio L, Orsini S, Luppi A, et al. 2017. Novel plasmid-mediated colistin resistance mcr-4 gene in Salmonella and Escherichia coli, Italy 2013, Spain and Belgium, 2015 to 2016. Euro. Surveill. 22: 30589.
  24. Chavda B, Lv J, Hou M, Chavda KD, Kreiswirth BN, Feng Y, et al. 2018. Coidentification of mcr-4.3 and blaNDM-1 in a clinical Enterobacter cloacae isolate from China. Antimicrob. Agents Chemother. 62: e00649-18.
  25. Martins-Sorenson N, Snesrud E, Xavier DE, Cacci LC, Iavarone AT, McGann P, et al. 2020. A novel plasmid-encoded mcr-4.3 gene in a colistin-resistant Acinetobacter baumannii clinical strain. J. Antimicrob. Chemother. 75: 60-64. https://doi.org/10.1093/jac/dkz413