Detection of Bacteriophages Specific to Vibrio parahaemolyticus in Marine Water Samples, Surat Thani, Thailand
Keywords:
Vibrio parahaemolyticus, shrimp pond water, estuarine water, seawater, environmental parameter, bacteriophageAbstract
Vibrio parahaemolyticus is a halophilic bacterium commonly found in estuarine and marine water. It is a seafood-borne pathogen that causes acute gastroenteritis worldwide. V. parahaemolyticus bacteriophage is a virus that infects V. parahaemolyticus bacteria. The application of a bacteriophage that can eliminate pathogenic bacteria may decrease the severity of outbreaks. The objectives of this study were to determine water quality and isolate V. parahaemolyticus bacteriophage from various marine water environments. Ten marine water samples from Surat Thani province were examined, consisting of shrimp pond water (6 samples), estuarine water (1 sample), and seawater (3 samples). Each water sample was tested for physical quality using environmental parameters. Results revealed that temperature, pH, dissolved oxygen (DO), oxidation-reduction potential (ORP), and salinity were in the ranges of 25.6°C – 30.6°C, 7.26 – 8.64, 0.00 – 4.45 mg/L, (-)30 – 181 mV, and 1.0 – 30 ppt, respectively. Total viable bacterial counts on plate count agar (PCA) were in the ranges of 1.2x103 – 7.2x103 CFU/ml, 1.2x104 CFU/ml, and 1.8x106 – 2.5x106 CFU/ml for the six shrimp pond water, one estuary, and three seawater samples, respectively. Green colonies on Thiosulfate Citrate Bile Salts Sucrose (TCBS) agar that were considered to be presumptive V. parahaemolyticus were enumerated; 2.2x102 CFU/ml was found in one shrimp pond water sample (P3). The results of environmental parameters and biological indicators were within the standard ranges prescribed by the guidelines of good practice for advanced shrimp culture, Department of Fisheries, Thailand. No bacteriophage specific to the shrimp pathogen V. parahaemolyticus was isolated from tested water samples using the double agar layer method. This preliminary study may benefit further alternative applications of bacteriophages to reduce the number of specific bacterial host cells in marine environments.
References
Chonsin K. Virulence factors of foodborne pathogenic Vibrio parahaemolyticus. J Med Health Sci 2020; 27(1): 160-72. (Thai)
Chobkatanyoo A. Food poisoning. Annual Epidemiological Surveillance Report. 2011: 105-7.
Manatsathit S, Dupont HL, Farthing M, Kositchaiwat C, Leetakusolvong S, Ramakrishna BS, et al. Guideline for the management of acute diarrhea in adults. J Gastroenterol Hepatol 2002; 17(S1): S54-71.
Chen Y, Chen X, Yu F, Wu M, Wang R, Zheng S, et al. Serology, virulence, antimicrobial susceptibility and molecular characteristics of clinical Vibrio parahaemolyticus strains circulating in southeastern China from 2009 to 2013. Clin Microbiol Infect 2016; 22(258): e9-16.
Kitiyodom S, Khemtong S, Wongtavatchai J, Chuanchuen R. Characterization of antibiotic resistance in Vibrio spp. isolated from farmed marine shrimps (Penaeus monodon). FEMS Microbiol Ecol 2010; 72(2): 219-27.
Thitamadee S, Prachumwat A, Srisala J, Jaroenlak P, Salachan PV, Sritunyalucksana K, et al. Review of current disease threats for cultivated penaeid shrimp in Asia. Aquaculture 2016; 452: 69-87.
Lee CT, Chen IT, Yang YT, Ko TP, Huang YT, Huang JY, et al. The opportunistic marine pathogen Vibrio parahaemolyticus becomes virulent by acquiring a plasmid that expresses a deadly toxin. Proc Natl Acad Sci USA 2015; 112(34): 10798-803.
Changkaew K, Utrarachkij F, Siripanichgon K, Nakajima C, Suthienkul O, Suzuki Y. Characterization of antibiotic resistance in Escherichia coli isolated from shrimps and their environment. J Food Protect 2014; 77(8): 1394-401.
Holmstrom K, Graslund S, Wahlstrom A, Poungshompoo S, Bengtsson BE, Kautsky N. Antibiotic use in shrimp farming and implications for environmental impacts and human health. Int J Food Sci Technol 2003; 38(3): 255-66.
Le TX, Munekage Y, Kato S. Antibiotic resistance in bacteria from shrimp farming in mangrove areas. Sci Total Environ 2005; 349(1-3): 95-105.
Koytrup L. Occurrence and distribution of pathogenic and non-pathogenic vibrios in external and internal parts of aquacultured white shrimp, Phang-nga province. [M.Sc. Thesis in Public Health]. Nakhon Pathom: Faculty of Graduate studies, Mahidol University; 2009.
Teiwvilai N. Distribution of pathogenic and non-pathogenic vibrios in water from shrimp growing and waste ponds in Phang-nga province, Thailand. [M.Sc. Thesis in Public Health]. Nakhon Pathom: Faculty of Graduate studies, Mahidol University; 2009.
Vinod MG, Shiv MM, Umesha KR, Rajeeva BC, Krohne G, Karunasagar I, et al. Isolation of Vibrio harveyi bacteriophage with a potential for biocontrol of luminous vibriosis in hatchery environments. Aquaculture 2006; 255(1-4): 117-24.
Suthienkul O. Enumeration of total viable bacteria in food and drinking water. In: Hirunpetcharat C, editor. Public Health Microbiology and Immunology Laboratory Methods. Bangkok: Department of Microbiology, Faculty of Public Health, Mahidol University; 2009. (Thai)
Suthienkul O. The determination of Vibrio cholerae, Vibrio parahaemolyticus, and Vibrio vulnificus from seafood by standard methods for microbiology. Bangkok; Department of Microbiology, Faculty of Public Health, Mahidol University; 2010. (Thai)
Suthienkul O. Bacteriophage typing of Vibrio fluvialis. Southeast Asian J Trop Med Public Health 1993; 24(3): 449-54.
Department of Fisheries. Guidelines of good practice for advanced shrimp culture. Available from https://www.fisheries.go.th/if-suratthani/web2/images/download/vannamei.pdf, accessed May 11, 2020. (Thai)
Wei Y, Jiao Y, An D, Li D, Li W, Wei Q. Review of dissolved oxygen detection technology: from laboratory analysis to online intelligent detection. Sensors 2019; 19: 3995.
Cheng W, Liu CH, Kuo CM. Effects of dissolved oxygen on hemolymph parameters of freshwater giant prawn, Macrobrachium rosenbergii (de Man). Aquaculture 2003; 220: 843-56.
Alfiansah YR, Hassenruck C, Kunzmann A, Taslihan A, Harder J, Gardes A. Bacterial abundance and community composition in pond water from shrimp aquaculture systems with different stocking densities. Front Microbiol 2018; 9: 2457.
Yin Y, Liu D, Yang S, Almeida A, Guo Q, et al. Bacteriophage potential against Vibrio parahaemolyticus biofilms. Food Control 2019; 98: 156-63.
Buranapratheprat A, Yanagi T, Matsumura S. Seasonal variation in water column conditions in the upper Gulf of Thailand. Cont Shelf Res 2008; 28(17): 2509-22.
Department of Marine and Coastal Resources. The 2018 marine and coastal resources and coastal erosion situations of Thailand. Available from https://www.dmcr.go.th/detailLib/4933, accessed May 30, 2020. (Thai)
Liu B, Liu H, Pan Y, Xie J, Zhao Y. Comparison of the effects of environmental parameters on the growth variability of Vibrio parahaemolyticus coupled with strain sources and genotypes analyses. Front Microbiol 2016; 7: 994.
Zhang L, Mai K, Tan B, Ai Q, Qi C, Xu W, et al. Effects of dietary administration of probiotic Halomonas sp. B12 on the intestinal microflora, immunological parameters, and midgut histological structure of shrimp, Fenneropenaeus chinensis. J World Aquacult Soc 2009; 40(1): 58-66.
Suantika G, Aditiawati P, Astuti DI, Khotimah ZF. The use of indigenous probiotic Halomonas aquamarina and Shewanella algae for white shrimp (Litopenaeus vannamei Boone) hatchery productivity in zero water discharge system. J Aquac Res Dev 2013; 4(5): 1000194.
Alagappan KM, Deivasigamani B, Somasundaram ST, Kumaran S. Occurrence of Vibrio parahaemolyticus and its specific phages from shrimp ponds in east coast of India. Curr Microbiol 2010; 61(4): 235-40.
Parveen S, Hettiarachchi KA, Bowers JC, Jones JL, Tamplin ML, McKay R, et al. Seasonal distribution of total and pathogenic Vibrio parahaemolyticus in Chesapeake Bay oysters and waters. Int J Food Microbiol 2008; 128: 354-61.
Baross JA, Liston J, Morita R. Incidence of Vibrio parahaemolyticus bacteriophages and other Vibrio bacteriophages in marine samples. Appl Environ Microbiol 1978; 36(3): 492-9.
Tipluy P. Isolation and characterization of Vibrio cholerae and their phages in water samples from Chao Phraya River before, during, and after flooding disaster, Bangkok 2011. [M.Sc. Thesis in Public Health]. Nakhon Pathom: Faculty of Graduate studies, Mahidol University; 2013.
Kongrueng J, Mitraparp-arthorn P, Bangpanwimon K, Robins W, Vuddhakul V, Mekalanos J. Isolation of Bdellovibrio and like organisms and potential to reduce acute hepatopancreatic necrosis disease caused by Vibrio parahaemolyticus. Dis Aquat Organ 2017; 124: 223-32.
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