Open Access Open Access  Restricted Access Subscription Access

Prevalence and Multiple Antibiotic Resistance of Vibrio coralliilyticus, along the Southwest Coast of India


Affiliations
1 Department of Marine Biology, Microbiology and Biochemistry, Cochin University of Science and Technology, Fine Arts Avenue, Cochin 682 016, India
2 School of Environmental Sciences, Mahatma Gandhi University, Kottayam 686 560, India
 

Samples from two different estuaries (Cochin and Kumarakom) and a shrimp farm located along the southwest coast of India were analysed for the presence of Vibrio species. V. coralliilyticus, a global marine pathogen had high prevalence in all the three sources. The incidence of V. coralliilyticus was very high in the Cochin estuary (40%) when compared to the shrimp pond (20%) and Kumarakom estuary (19%). The susceptibility of V. coralliilyticus strains to 20 different antibiotics and their plasmid profiles were also checked. All the tested strains exhibited multiple antibiotic resistance, showing resistance towards 5-9 antibiotics tested. Resistance was shown towards amoxycillin, ampicillin, carbenicillin, oxytetracycline, trimethoprim, nitrofurantoin, furazolidone, sulphamethoxasole, erythromycin, while all the strains were sensitive to streptomycin, gentamicin, amikacin, netillin, tetracycline, chloramphenicol, cotrimoxasole, nalidixic acid, norfloxacin and ciprofloxacin. Multiple antibiotic resistance index varied from 0.25 to 0.55. Forty-three per cent of the isolates harboured 1-3 plasmids, with size ranging from 0.5 to 33 kb. Thus the present study demonstrates the high incidence, multiple antibiotic resistance and plasmid profiling of V. coralliilyticus from the southwest coast of India.

Keywords

Antibiotic Resistance, Estuaries, Plasmid Profiling, Shrimp Pond, Vibrio coralliilyticus.
User
Notifications
Font Size

  • Thompson, F., Lida, T. and Swings, J., Biodiversity of vibrios. Microbiol. Mol. Biol. Rev., 2004, 68, 403–422.
  • Ben-Haim, Y., Thompson, F. L., Thompson, C. C., Cnockaert, M. C., Hoste, B., Swings, J. and Rosenberg, E., Vibrio coralliilyticus sp. nov., a temperature-dependent pathogen of the coral Pocillopora damicornis. Int. J. Syst. Evol. Microbiol., 2003, 53, 309– 315.
  • Ben-Haim, Y., Zicherman-Keren, M. and Rosenberg, E., Temperatureregulated bleaching and lysis of the coral Pocillopora damicornis by the novel pathogen Vibrio coralliilyticus. Appl. Environ. Microbiol., 2003, 69, 4236–4242.
  • Sussman, M., Willis, B. L., Victor, S. and Bourne, D. G., Coral pathogens identified for white syndrome (WS) epizootics in the Indo-Pacific. PLoS ONE, 2008, 3, e2393.
  • Jeffries, V. E., Three Vibrio strains pathogenic to larvae of Crassostrea gigas and Ostrea edulis. Aquaculture, 1982, 29, 201– 226.
  • Austin, B., Austin, D., Sutherland, R., Thompson, F. and Swings, J., Pathogenicity of vibrios to rainbow trout (Oncorhynchus mykiss, Walbaum) and Artemia nauplii. Environ. Microbiol., 2005, 7, 1488–1495.
  • De Santos, E. et al., Genomic and proteomic analyses of the coral pathogen Vibrio coralliilyticus reveal a diverse virulence repertoire. ISME J., 2011, 5, 1471–1483.
  • Sambrook, J., Fritsch, E. F. and Maniatis, T., Molecular Cloning: A Laboratory Manual, Cold Spring Harbor Laboratory, Cold Spring Harbor, New York, 1989.
  • Hossain, M. T., Kim, Yu-Ri., Kong and In-Soo, PCR-restriction fragment length polymorphism analysis using groEL gene to differentiate pathogenic Vibrio species. Diagn. Microbiol. Infect. Dis., 2013; doi:10.1016/j.diagmicrobio.2013.10.005.
  • Noguerola, I. and Blanch, A. R., Identification of Vibrio spp. with a set of dichotomous keys. J. Appl. Microbiol., 2008, 105, 175– 185.
  • Bauer, A. W., Kirby, W. M. M., Sheris, J. C. and Turck, M., Antibiotics susceptibility testing by standardized single disk method. Am. J. Clin. Pathol., 1966, 45, 493–496.
  • Krumperman, P. H., Multiple antibiotic resistance indexing of Escherischia coli to identify high risk sources of fecal contamination of food. Appl. Environ. Microbiol., 1983, 46, 165–170.
  • Vizcaino, M. I. et al., Antimicrobial resistance of the coral pathogen Vibrio coralliilyticus and Caribbean sister phylotypes isolated from a diseased octocoral. Microb. Ecol., 2010, 59, 646–657.
  • Kesarcodi-Watson, A., Kaspar, H., Lategan, M. J. and Gibson, L., Two pathogens of Greenshell (TM) mussel larvae, Perna canaliculus: Vibrio splendidus and a V. coralliilyticus/neptunius-like isolate. J. Fish. Dis., 2009, 32, 499–507.
  • Pedersen, K.., The fish pathogen Vibrio anguillarum. Doctoral thesis. The Royal Veterinary and Agricultural University, Denmark, 1999.
  • Vezzulli, L. et al., Vibrio infections triggering mass mortality events in a warming Mediterranean Sea. Environ. Microbiol., 2010, 12, 2007–2019.
  • Pollock, J. F., Wilson, B., Johnson, W. R., Morris, P. J., Willis, B. L. and Burne, D. G., Phylogeny of the coral pathogen Vibrio coralliilyticus. Environ. Microbiol. Rep., 2010, 2, 172–178.
  • Rosenberg, E. and Kushmaro, A., Microbial diseases of corals: pathology and physiology. In Coral Reefs: An Ecosystem in Transition (eds Dubinsky, Z. and Stambler, N.), Springer: New York, 2011, p. 451–464.
  • Sussman, M., Mieog, J. C., Doyle, J., Victor, S., Willis, B. L. and Bourne, D. G., Vibrio zinc-metalloprotease causes photoinactivation of coral endosymbionts and coral tissue lesions. PLoS ONE, 2009, 4, e4511; doi:10.1371/journal.pone.0004511.
  • Ben-Haim, Y. and Rosenberg, E., A novel Vibrio sp. pathogen of the coral Pocillopora damicornis. Mar. Biol., 2002, 141, 47–55.
  • Meron, D. et al., Role of flagella in virulence of the coral pathogen Vibrio coralliilyticus. Appl. Environ. Microbiol., 2009, 75, 5704–5707.
  • Shmidt, A. S., Bruun, M. S., Dalsgaard, I., Pedersen, K. and Larsen, J. L., Occurrence of antimicrobial resistance in fish – pathogenic and environmental bacteria associated with four Danish rainbowtrout farms. Appl. Environ. Microbiol., 2000, 66, 4908–4915.
  • Okoh, A. I. and Igbinosa, E. O., Antibiotic susceptibility profiles of some Vibrio strains isolated from wastewater final effluents in a rural community of the Eastern Cape Province of South Africa, BMC Microbiol., 2010, 10, 143.
  • Hua, L. M. and Apun, K., Antimicrobial susceptibilities of Vibrio parahaemolyticus isolates from tiger shrimps (Penaeus monodon) aquaculture in Kuching, Sarawak. Res. J. Microbiol., 2013, 8, 55– 62.
  • Hsu, C. H., Hwang, S. C. and Liu, J. K., Succession of bacterial drug resistance as an indicator of antibiotic application in aquaculture. J. Fish. Soc. Taiwan, 1992, 19, 55–64.
  • Manjusha, S., Sarita, G. B., Elyas, K. K. and Chandrasekaran, M., Multiple antibiotic resistances of Vibrio isolates from coastal and brackish water areas. Am. J. Biochem. Biotechnol., 2005, 1, 201– 206.
  • Molina-Aja, A., Garcia-Gasca, A., Abreu-Grobois, A., BolanMejia, C., Roque, A. and Gomez-Gill, B., Plasmid profiling and antibiotic resistance of Vibrio strains isolated from cultured penaied shrimp. FEMS Microbiol. Lett., 2002, 213, 7–12.
  • Zhang, R., Wang, Y. and Gu, J. D., Identification of environmental plasmid-bearing Vibrio species isolated from polluted and pristine marine reserves of Hong Kong, and resistance to antibiotics and mercury. Antonie van Leeuwenhoek, 2006, 89, 307–315.
  • Guiney, D. G. and Landa, E., Conjugative transfer of Inc plasmids. In Promicuous Plasmids of Gram-negative Bacteria (ed.Thomas, C. M.), Academic Press, London, 1989, pp. 27–56.
  • Devi, R., Surendran, P. K. and Chakraborty, K., Antibiotic resistance and plasmid profiling of Vibrio parahaemolyticus isolated from shrimp farms along the southwest coast of India. World J. Microbiol. Biotechnol., 2009, 25, 2005–2012.
  • Tiainen, T., Pedersen, K. and Larsen, J. L., Ribotyping and plasmid profiling of Vibrio anguillarum serovar O2 and Vibrio ordalii. J. Appl. Bacteriol., 1995, 79, 384–392.
  • Radu, S. et al., Characterization of Vibrio vulnificus isolated from cockles (Anadara granosa): antimicrobial resistance, plasmid profiles and random amplification of polymorphic DNA analysis. FEMS Microbiol. Lett., 1998, 165, 139–143.
  • Sorum, H., Hvaal, A. B., Heum, M., Daae, F. L. and Wiik, R., Plasmid profiling of Vibrio salmonicida for epidemiological studies of cold-water vibriosis in Atlantic salmon (Salmo salar) and cod (Gadus morhua). Appl. Environ. Microbiol., 1990, 56, 1033– 1037.
  • Pedersen, K., Tiainen, T. and Larsen, J L., Plasmid profiles, restriction fragment length polymorphisms and O-serotypes among Vibrio anguillarum isolates. Epidemiol. Infect., 1996, 117, 471–478.

Abstract Views: 221

PDF Views: 62




  • Prevalence and Multiple Antibiotic Resistance of Vibrio coralliilyticus, along the Southwest Coast of India

Abstract Views: 221  |  PDF Views: 62

Authors

Reshma Silvester
Department of Marine Biology, Microbiology and Biochemistry, Cochin University of Science and Technology, Fine Arts Avenue, Cochin 682 016, India
Deborah Alexander
Department of Marine Biology, Microbiology and Biochemistry, Cochin University of Science and Technology, Fine Arts Avenue, Cochin 682 016, India
Maya George
School of Environmental Sciences, Mahatma Gandhi University, Kottayam 686 560, India
A. A. M. Hatha
Department of Marine Biology, Microbiology and Biochemistry, Cochin University of Science and Technology, Fine Arts Avenue, Cochin 682 016, India

Abstract


Samples from two different estuaries (Cochin and Kumarakom) and a shrimp farm located along the southwest coast of India were analysed for the presence of Vibrio species. V. coralliilyticus, a global marine pathogen had high prevalence in all the three sources. The incidence of V. coralliilyticus was very high in the Cochin estuary (40%) when compared to the shrimp pond (20%) and Kumarakom estuary (19%). The susceptibility of V. coralliilyticus strains to 20 different antibiotics and their plasmid profiles were also checked. All the tested strains exhibited multiple antibiotic resistance, showing resistance towards 5-9 antibiotics tested. Resistance was shown towards amoxycillin, ampicillin, carbenicillin, oxytetracycline, trimethoprim, nitrofurantoin, furazolidone, sulphamethoxasole, erythromycin, while all the strains were sensitive to streptomycin, gentamicin, amikacin, netillin, tetracycline, chloramphenicol, cotrimoxasole, nalidixic acid, norfloxacin and ciprofloxacin. Multiple antibiotic resistance index varied from 0.25 to 0.55. Forty-three per cent of the isolates harboured 1-3 plasmids, with size ranging from 0.5 to 33 kb. Thus the present study demonstrates the high incidence, multiple antibiotic resistance and plasmid profiling of V. coralliilyticus from the southwest coast of India.

Keywords


Antibiotic Resistance, Estuaries, Plasmid Profiling, Shrimp Pond, Vibrio coralliilyticus.

References





DOI: https://doi.org/10.18520/cs%2Fv112%2Fi08%2F1749-1755