Multiple drug resistant Enterococcus spp. causes disease and mortality in Zebra fish (Danio rerio)
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https://doi.org/10.56093/ijans.v90i1.98241
Keywords:
Antibiotics, 16S rRNA, Drug resistance, Model fish, Pathogens Present address, 1Professor and Head (uma@tnfu.ac.in), 2, 3Senior researchAbstract
The present report describes the isolation and identification of a multiple drug resistant Enterococcus spp. from diseased zebrafish from a commercial rearing facility in Chennai, Tamil Nadu, India. Zebrafish (Danio rerio) has recently gained great significance as a vertebrate animal model, as its immune system is remarkably similar with that of the humans. However, zebrafish are still susceptible to microbial infection. Gram positive diplococci isolated from kidney was identified as Enterococcus spp. using 16S rRNA gene sequencing analysis. The Enterococcus spp. isolate was either resistant and or intermediately resistant to 14 antibiotics assessed by agar disc diffusion method. This communication is the first report on isolation and confirmation of Enterococcus spp. associated with disease and mortality in zebrafish.
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Abuseliane A F D and H H M. 2011. Pathogenicity of Streptococcus agalactiae isolated from a fish farm in Selangor to juvenile red tilapia (Oreochromis sp.). Journal of Animal and Veterinary Advances 10: 914–19. DOI: https://doi.org/10.3923/javaa.2011.914.919
Austin B and Austin D A. 2012. Bacterial Fish Pathogens: Diseases of Farmed and Wild Fish. Fifth ed. Praxis Publishing Ltd, Chichester, UK. DOI: https://doi.org/10.1007/978-94-007-4884-2
Bauer A W, Kirby W M, Sherris J C and Turck M. 1966. Antibiotic susceptibility testing by a standardized single disk method. American Journal of Clinical Pathology 45(4):493–96. DOI: https://doi.org/10.1093/ajcp/45.4_ts.493
CLSI. 2012. Performance Standards for Antimicrobial Susceptibility Testing; Twenty-Second Informational Supplement. Clinical and Laboratory Standards Institute, Wayne, PA 19087, USA, CLSI document M100-S22.
Collins C H, Lyne P M, Grange J M and Falkinham J O. 2004. Microbiological Methods. 8th ed. Arnold, London, UK.
Heil N. 2009. National Wild Fish Health Survey. Laboratory Procedures Manual, 5th edn. U.S. Fish and Wildlife Service, Warm Springs, GA.
Kanoe M and Abe T. 1988. Enterococcal isolates from environmental sources. Microbios Letters 38: 15–20.
Kimura M A. 1980. Simple method for estimating evolutionary rate of base substitutions through comparative studies of nucleotide sequences. Journal of Molecular Evolution 16: 111–20. DOI: https://doi.org/10.1007/BF01731581
Kusuda R, Kawai K, Salati F, Banner C R and Fryer J L. 1991. Enterococcus seriolicida sp. nov., a fish pathogen. International Journal of Systematic Bacteriology 41(3): 406–09. DOI: https://doi.org/10.1099/00207713-41-3-406
Martins M L, Mourino J L P, Amaral G V, Vieira F N, Dotta G, Jatoba A M B, Pedrotti F S, Jeronimo G T and Buglione-Neto C C. 2008. Haematological changes in Nile tilapia experimentally infected with Enterococcus sp. Brazilian Journal of Biology 68(3): 657–61. DOI: https://doi.org/10.1590/S1519-69842008000300025
Meijer H A and Spaink P H. 2011. Host-pathogen interactions made transparent with the zebrafish model. Current Drug Targets 12(7): 1000–17. DOI: https://doi.org/10.2174/138945011795677809
Nieto J M, Devesa S, Quiroga I and Toranzo A E. 1995. Pathology of Enterococcus spp. infection in farmed turbot, Scophthalmus maximus (L). Journal of Fish Disease 18(1): 21–30. DOI: https://doi.org/10.1111/j.1365-2761.1995.tb01262.x
Osman K M, Al-Maary K S, Mubarak A S, Dawoud T M, Moussa I M, Ibrahim M D, Hessain A M, Orabi A and Fawzy N M. 2017. Characterization and susceptibility of streptococci and enterococci isolated from Nile tilapia (Oreochromis niloticus) showing septicaemia in aquaculture and wild sites in Egypt. BMC Veterinary Research 13(1): 357. DOI: https://doi.org/10.1186/s12917-017-1289-8
Picard F J, Ke D, Boudreau D K, Boissinot M, Huletsky A, Richard D, Ouellette M, Roy P H and Bergeron M G. 2004. Use of tuf sequences for genus-specific PCR detection and phylogenetic analysis of 28 Streptococcal species. Journal of Clinical Microbiology 42(8): 3686–95. DOI: https://doi.org/10.1128/JCM.42.8.3686-3695.2004
Rahman M, Rahman M M, Deb S C, Alam M S, Alam M J and Islam M T. 2017. Molecular identification of multiple antibiotic resistant fish pathogenic Enterococcus faecalis and their control by medicinal herbs. Scientific Reports 7(1): 3747. DOI: https://doi.org/10.1038/s41598-017-03673-1
Tamura K, Stecher G, Peterson D, Filipski A and Kumar S. 2013. MEGA6: Molecular Evolutionary Genetics Analysis version 6.0. Molecular Biology and Evolution 30: 2725–29. DOI: https://doi.org/10.1093/molbev/mst197
Uma A, Stalin N and Rebecca G. 2017. Isolation, molecular identification and antibiotic resistance of Enterococcus faecalis from diseased tilapia. International Journal of Current Microbiology and Applied Science 6(6): 136–46. DOI: https://doi.org/10.20546/ijcmas.2017.606.016
Weisburg W G, Barns S M, Pelletier D A and Lane D J. 1991. 16S ribosomal DNA amplification for phylogenetic study. Journal of Bacteriology 173(2): 697–703. DOI: https://doi.org/10.1128/jb.173.2.697-703.1991
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