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        Prevalence and antimicrobial resistance of Salmonella spp. in raw retail frozen imported freshwater fish to Eastern Province of Saudi Arabia

        2014-03-23 06:56:35NasreldinElhadi

        Nasreldin Elhadi

        Department of Clinical Laboratory Science, College of Applied Medical Sciences, University of Dammam, P. O. Box 2435, 31441 Dammam, Kingdom of Saudi Arabia

        Prevalence and antimicrobial resistance of Salmonella spp. in raw retail frozen imported freshwater fish to Eastern Province of Saudi Arabia

        Nasreldin Elhadi

        Department of Clinical Laboratory Science, College of Applied Medical Sciences, University of Dammam, P. O. Box 2435, 31441 Dammam, Kingdom of Saudi Arabia

        PEER REVIEW

        Peer reviewer

        Dr. Weaam N. E. Ebrahim, Assistant Professor, Dept. of Pharmacognosy and Medicinal Plants, Faculty of Pharmacy, Mansoura University, 35516 Mansoura, Egypt.

        Tel: 002-011-43665566

        E-mail: weaamnabil@mans.edu.eg

        Comments

        This is a good research work in which author determined the proportion of imported frozen fish contaminated with Salmonella spp. among retail food stores and supermarkets in the Eastern Province of Saudi Arabia. The results add valuable informations to the formulation of food safety and food hygiene measures.

        Details on Page 237

        Objective:To determine the proportion of imported frozen fish contaminated with Salmonella among retail food stores and supermarkets in the Eastern Province of Saudi Arabia.

        Salmonella, Antibiogram, Frozen fish, Food safety

        1. Introduction

        Capture fisheries and aquaculture supplied the world with about 148 million tonnes of fish in 2010 (with a total value of USD 217.5 billion, of which about 128 million tonnes was utilized as food for people, and preliminary data for 2011 indicate increased production of 154 million tonnes, of which 131 million tonnes was destined as food[1]. There is a global trade in aquaculture products which has considerably increased in recent decades, and the expansion of aquaculture production, particularly from Asia, has the potential to meet most of the growing global demand for fish and fishery products[2]. According to Food and Agriculture Organization (FAO), aquaculture supplies about 50% of the global demand for fish and fishery products with about 90% of the aquaculture productscoming from Asian region[3]. Fishery products have been recognized as a major carrier of food-borne pathogens[4,5]. Pathogenic bacteria associated with fish and fishery product can be categorized into three general groups: (1) indigenous bacteria that belong to the natural microflora of fish (Clostridium botulinum, pathogenicVibriospp.,Aeromonas hydrophila); (2) enteric bacteria (nonindigenous bacteria) that are present due to fecal contamination (Salmonellaspp.,Shigellaspp., pathogenicEscherichia coli,Staphylococcus aureus); and (3) bacterial contamination during processing, storage or preparation for consumption (Bacillus cereus, Listeria monocytogenes, Staphylococcus aureus, Clostridium perfringens, Salmonellaspp.)[6].

        Salmonellais a member of Enterobacteriaceae, Gramnegative, facultative anaerobe, motile, with peritrichous flagella, non-spore forming rods that responsible of causing salmonellosis. In humans, these pathogenic bacteria caused enteric fever (typhi or paratyphi) and acute gastroenteritis[7].

        In Saudi Arabia, data regarding the presence of medically significantSalmonellaspp. in imported frozen freshwater fish are limited or not available. Thus, present study was conducted to determine the prevalence and antibiotic resistance ofSalmonellaspp. in imported frozen freshwater fish imp in Eastern Province of Saudi Arabia.

        2. Materials and methods

        2.1. Sample collection

        Starting from December 2012 till March 2013, a total of 223 frozen freshwater fishes (Catfish, Carfu, Mirgal, Milkfish, Mackerel, Tilapia and Rohu) were purchased from different supermarkets and grocery stores. The samples originated from five countries, namely, Thailand, India, Bahrain, Myanmar and Vietnam, respectively. All fish samples during collection were placed in sterile polypropylene bag, placed in polystyrene box containing crushed ice and the temperatures was between 4 °C and 8 °C during transportation. The samples were transported to the laboratory and examined on the same day for the presence ofSalmonellaspp.

        2.2. Isolation and biochemical identification

        The isolation ofSalmonellawas determined by using the methods described in Bacteriological Analytical Manual (BAM, 2011)[8]. The fish samples were gently removed from coolers and processed in aseptic condition. The gills, intestines parts and skin parts were removed by using sterile knifes and forceps and placed on sterile tray and chopped thoroughly with sterile knife. About 25 g of samples (fish gills, intestines parts and skin) were placed into a stomacher bag containing 225 mL of buffered peptone water and homogenized using a stomacher (Seward Stomacher 400 circulator, UK) for 2 min and incubated for 18-24 h at 37 °C. From this nonselective pre-enrichment, 0.1 mL and 1.0 mL were, respectively, transferred into 10 mL of Rappaport-Vassiliadis broth and 10 mL of selenite cystine broth, and incubated for 18-24 h at 42 °C (Rappaport-Vassiliadis) and at 37 °C (selenite cystine). A drop from each selective enrichment broth was streaked onto selective Hektoen agar, Rambach agar and CHROMagarSalmonellaagar (CHROMagar, Paris, France) plates and incubated for 24-48 h at 37 °C. Suspected colonies on selective agar plates were purified and bio-typed by using biochemical tests and API 20E strips (BioMerieux, Marcy, France).Salmonella entericasubsp. enterica serovar enteritidis American Type Culture Collection 13076 was used as a reference strain for CHROMagar, biochemical tests and API 20E strips.

        2.3. Antibiotic susceptibility testing

        Antimicrobial susceptibility was determined by the disk diffusion method on Muller-Hinton agar, as described by Kirby-Bauer, in accordance with the guidelines of the Clinical and Laboratory Standards Institute. The isolates were tested against 18 antibiotics which included: amikacin 30 μg, amoxicillin-clavulanic acid 30 μg, ampicillin 10 μg, cefotaxime 30 μg, ceftazidime 30 μg, ceftriaxone 30 μg, chloramphenicol 30 μg, ciprofloxacin 5 μg, kanamycin 30 μg, nalidixic acid 30 μg, nitrofurantoin 300 μg, norfloxacin 10 μg, piperacillin 100 μg, polymyxin B 300 units, tetracycline 30 μg, ticarcillin 75 μg, tobramycin 10 μg, trimethoprim/ sulfamethoxazole (1.25 μg/23.75 μg). The antibiotics discs were obtained from Oxoid (Baringstoke, Hampshire, United Kingdom). Cultures were grown overnight in tryptic soy broth and incubated at 37 °C. The overnight cultures were diluted to a turbidity of 0.5 on McFarland scale. The cultures were streaked on Mueller Hinton Agar (Oxoid, Baringstoke, Hampshire, United Kingdom) plates using a cotton swab. After 30 min, 3-4 antibiotic discs were placed on the plates and were incubated at 37 °C for 18-24 h. After the incubation period, the diameter of inhibition zones was measured and compared with interpretive chart proposed by the ‘Performance Standards for Antimicrobial Disk Susceptibility Tests’ and which were classified as resistant (CLSI, 2010)[9].Escherichia coliAmerican Type Culture Collection 25922 was used as a reference strain for antimicrobial disk control.

        2.4. Statistical analysis

        Overall prevalence rates for specific fish types werecalculated using the Kruskal-Wallis test. The distribution of antibiotic resistance was compared for the three groups of resistance, intermediate and susceptible. The distribution of antibiotic resistance for each fish type was used to calculate two measures of diversity, dominance and entropy, widely used in ecology. The dominance measure ranges from 0 in which all antibiotics (in this case) are equally present, to 1, in which one antibiotic dominates. The entropy measures ranges from 0 in which only one antibiotic is present (no diversity) to high values, showing that different antibiotics are present. The calculations were done using PAST software version 2.04[10].

        3. Results

        The prevalence and contamination rates of imported frozen fish withSalmonellaare presented in Table 1. Out of 223 samples examined, 140Salmonellaspp. isolates were isolated.Salmonellaspp. were detected in 89 fish samples with prevalence rate of 39.9%. The prevalence of positive samples were reported for the freshwater fish of catfish (60.0%,n=12), carfu (27.7%,n=5), mirgal (35.0%,n=7), milkfish (52.0%,n=13), mackerel (31.4%,n=11), tilapia imported from Thailand (64.0%,n=16), tilapia imported from India (28.0%,n=14), rohu imported from Thailand (26.6%,n=4) and rohu imported from Myanmar (46.6 %,n=7) as shown in Table 1.

        Table 1 Prevalence of Salmonella spp. in raw retail frozen imported fish to Eastern Province of Saudi Arabia.

        All isolates (140) ofSalmonellaspp. isolated from at least seven different types of frozen freshwater fish imported from five different countries were tested for their susceptibility to 18 selected antimicrobial agents. Most ofSalmonellaisolates showed resistance to tetracycline (90.71%,n=127) followed by ampicillin (70%,n=98) and amoxicillin-clavulanic acid (45%,n=63) as presented in Table 2. The highest antibiograms ofSalmonellaexhibited resistance to tetracycline, ampicillin and amoxicillin-clavulanic acid were isolated from catfish, tilapia (India), tilapia (Thailand), rohu, milkfish and mirgal, respectively. The lowest antibiograms ofSalmonellaexhibited resistance to tetracycline, ampicillin and amoxicillin-clavulanic acid were isolated from mackerel and carfu imported Bahrain and Thailand, respectively. As Table 2 shows, the highest value of dominance is for number of resistance isolates, for those ones, tetracycline predominates.

        Table 2 Antibiogram of Salmonella spp. isolated from raw retail frozen imported fish to Eastern Province of Saudi Arabia.

        The highest value of antimicrobial diversity is for number of susceptibility, for those ones, none of antibiotics predominates. Partly because of the absence of resistance in many of the antibiotics, comparison of the three groups (resistant, intermediate and susceptible) using the Kruskal-Wallis test did not yield any statistical significance between them (H=2.898,P=0.392 9).

        4. Discussion

        In this study,Salmonellaspp. were isolated from at least seven different types of frozen fish (pangas, carfu, mirgal, milkfish, mackerel, tilapia and rohu) imported from five different countries (Thailand, India, Bahrain, Vietnam and Myanmar) to Eastern Province of Saudi Arabia. The overall prevalence ofSalmonellaspp. contamination of frozen imported fish (39.9%) observed in this study is significantly very high.Salmonellacontaminates in fish and fishery products have also been reported from other countries and areas such as India, Mexico, Thailand, Hong Kong, Spain and Turkey[11-14]. The highestSalmonellaincidence in fishery products was determined in Central Pacific and African countries while it was lower in Europe and includingRussia and North America[15]. In this study, the highest numbers ofSalmonellastrains were isolated from catfish (imported from Thailand), tilapia (imported from India), tilapia (imported from Thailand), milkfish (imported from Vietnam), rohu (imported from Mynmar), mackerel (imported from Bahrain) and mirgal (imported from Thailand), while the lowest number ofSalmonellastrains were isolated from carfu and rohu (imported from Thailand).

        In the Asia-Pacific region, cultured fishes are fed by both commercial and homemade feeds (fresh feed material or farm feed material). According to FAO, homemade feeds are used to reduce cost of production[16]. Homemade feed is usually made from chicken viscera, kitchen refuse, chicken bone and other food waste materials[17]. Such feeds can be a source of pathogenic bacteria such asSalmonellaspp. which can be transmitted to catfish and tilapia and ultimately to consumers[18]. In a recent study in Malaysia, Budiatiet al. reported that feeds, such as chicken offals and spoiled eggs, can posed a potential source ofSalmonellaspp. and the high risks associated with the dissemination of antibiotic resistance genes among bacteria associated with catfish, tilapia and environment of aquaculture systems[19]. In this study, number ofSalmonellaisolates resistant to tetracycline (90.71%) followed by ampicillin (70%) and amoxicillinclavulanic acid (45%), and this could indicate and reflect the wide spread use of excessive antibiotics in fish farming. The increase and spread of antimicrobial-resistantSalmonellahas been associated with extensive use of antimicrobial agents, not only in human and veterinary medicine, but also in livestock production for disease prevention or as growth promoters in the animal husbandry and aquaculture which lead to development of resistance among environmental species[20-22]. This increase of antimicrobial-resistantSalmonellaphenomenon could limit the therapeutic options for clinical cases that require antimicrobial treatment[23].

        The main finding in the study is that there were high rates ofSalmonellacontamination of a wide variety of imported freshwater frozen fish to Eastern Province of Saudi Arabia, and this highlights a lack of applications of adequate hygiene forSalmonellacontrol in the fisheries production in some countries. Thus, to ensure the safety of imported fish and fisheries products for human consumption, the study recommends the surveillance of foodborneSalmonellathrough all imported frozen fish and fisheries products should be adopted and considered seriously by food control authorities in the study region.

        Conflict of interest statement

        We declare that we have no conflict of interest.

        Acknowledgements

        The author thanks the participating laboratory specialists Lauro Bartolome, Abdulrahim Osman and Bader Sager for constructive collaboration. This research was funded by the Deanship of Scientific Research, University of Dammam (Grant No. 2012139).

        Comments

        Background

        This study was conducted in order to determine the proportion of imported frozen fish contaminated withSalmonellaamong retail food stores and supermarkets in the Eastern Province of Saudi Arabia.

        Research frontiers

        Salmonellais a member of Enterobacteriaceae, Gramnegative, facultative anaerobe, motile, with peritrichous flagella, non-spore forming rods that responsible of causing salmonellosis. In humans, these pathogenic bacteria caused enteric fever (typhi or paratyphi) and acute gastroenteritis.

        Related reports

        There is a global trade in aquaculture products which has considerably increased in recent decades and the expansion of aquaculture production, particularly from Asia, has the potential to meet most of the growing global demand for fish and fishery products. According to FAO, aquaculture supplies about 50% of the global demand for fish and fishery products with about 90% of the aquaculture products coming from the Asian region.

        Innovations and breakthroughs

        The obtained results of this study shows that these raw retail imported frozen freshwater fish are contaminated with potentially pathogenicSalmonellaspp., and the study recommends and suggests that there is a need for adequate consumer measures.

        Applications

        In Saudi Arabia, data regarding the presence of medically significantSalmonellaspp. in imported frozen freshwater fish are limited or not available. Thus, present study was conducted to determine the prevalence and antibiotic resistance ofSalmonellaspp. in imported frozen freshwater fish imported in Eastern Province of Saudi Arabia.

        Peer review

        This is a good research work in which author determinedthe proportion of imported frozen fish contaminated withSalmonellaspp. among retail food stores and supermarkets in the Eastern Province of Saudi Arabia. The results add valuable informations to the formulation of food safety and food hygiene measures.

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        [6] Lyhs U. Microbiological methods. In: Rehbein H, Oehlenschl?ger J, editors. Fishery products: quality, safety and authenticity. 1st ed. Oxford: Wiley Blackwell; 2009, p. 318-348.

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        [9] Clinical And Laboratory Standards Institute. Performance standards for antimicrobial disk susceptibility tests, informal supplement, M100S20. Wayne: Clinical and Laboratory Standards Institute; 2010.

        [10] Hammer O, Harper DA, Ryan PD. Past: paleontological statistics software package for education and data analysis. Palaeontologia Electronica 2001; 4(1): 9.

        [11] Huss HH, Ababouch L, Gram L. Assessment and management of seafood safety and quality. Rome: Food and Agriculture Organization of the United Nations; 2004. [Online] Available from: http://www.best-bfq.org/downloads/QA-Program/FAOAssessment-and-magmt-of-seafood-quality-and-safety-FT-paper-444.pdf. [Accessed on 28th October, 2013]

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        [14] Pamuk S, Gurler Z, Yildirim Y, Siriken B. Detection of microbiological auality of common Carp (Cyprinus carpio) sold in public Baazar in Afyonkarahisar. J Anim Vet Adv 2011; 10(8): 1012-1018.

        [15] New MB, Csavas I. Aquafeeds in Asia: a regional overview. In: New MB, Tacon AG, Csavas I, editors. Farm-made aquafeeds. Rome: FAO Fisheries Technical Paper. No. 343.

        [16] Food and Agriculture Organization of the United Nations. FAO expert workshop on the application of biosecurity measures to control Salmonella Contamination in Sustainable aquaculture. Rome: Food and Agriculture Organization of the United Nations; 2010. [Online] Available from: http://www.fao.org/docrep/013/ i1547e/i1547e00.pdf. [Accessed on 28th October, 2013]

        [17] New MB, Tacon AGJ, Csavas I, editors. Farm-made aquafeeds. Proceedings of the regional expert consultation on farm-made aquafeeds; 1992 Dec 14-18; Bangkok, Thailand. Bangkok: FAO Regional Office for Asia and the Pacific; 1993.

        [18] Lunestad BT, Nesse L, Lassen J, Svihus B, Nesbakken T, Fossum K, et al. Salmonella infish feed; occurrence and implications for fish and human health in Norway. Aquaculture 2007; 265: 1-8.

        [19] Budiati T, Rusul G, Wan-Abdullah WN, Atrip YM, Ahmad R, Thong KL. Prevalence, antibiotic resistance and plasmid profiling of Salmonella in catfish (Clarias gariepinus) and tilapia (Tilapia mossambica) obtained from wet markets and ponds in Malaysia. Aquaculture 2013; 372-375: 127-132.

        [20] Romero J, Feijoó CG, Navarrete P. Antibiotics in aquaculture: Use, abuse and alternatives. In: Carvalho E, editor. Health and environment in aquaculture. Santiago: InTech Publisher; 2012.

        [21] Angkititrakul S, Chomvarin C, Chaita T, Kanistanon K, Waethewutajarn S. Epidemiology of antimicrobial resistance in Salmonella isolated from pork, chicken meat and humans in Thailand. Southeast Asian J Trop Med Public Health 2005; 36(6): 1510-1515.

        [22] Little CL, Richardson JF, Owen RJ, de Pinna E, Threlfall EJ. Campylobacter and Salmonella in raw red meats in the United Kingdom: prevalence, characterization and antimicrobial resistance pattern, 2003-2005. Food Microbiol 2008; 25(3): 538-543.

        [23] Cruchaga S, Echeita A, Aladue?a A, García-Pe?a J, Frias N, Usera MA. Antimicrobial resistance in Salmonellae from humans, food and animals in Spain in 1998. J Antimicrob Chemother 2001; 47(3): 315-321.

        10.1016/S2221-1691(14)60237-9

        *Corresponding author: Dr. Nasreldin Elhadi,Department of Clinical Laboratory Science, College of Applied Medical Sciences, University of Dammam, P. O. Box 2435, 31441 Dammam, Kingdom of Saudi Arabia.

        Tel: +966 13 333 1250

        Fax: +966 13 8572872

        E-mail: nmohammed@ud.edu.sa

        Foundation Project: Supported by the Deanship of Scientific Research, University of Dammam (Grant No. 2012139).

        Article history:

        Received 12 Nov 2013

        Received in revised form 26 Nov, 2nd revised form 9 Dec, 3rd revised form 14 Dec 2013

        Accepted 24 Dec 2013

        Available online 28 Feb 2014

        Methods:A total of 223 frozen freshwater fish purchased from different supermarkets and grocery stores were analyzed for the presence of foodborne pathogen Salmonella. The isolation of Salmonella was determined and confirmed by using the methods of US Food and Drug Administration’s Bacteriological Analytical Manual, CHROMagar Salmonella plus, biochemical tests and API 20E strips. Antimicrobial susceptibilities of Salmonella isolates were determined by the disk diffusion method on Muller-Hinton agar, as described by Kirby-Bauer, in accordance with the guidelines of the Clinical and Laboratory Standards Institute.

        Results:Out of the total 223 fish samples (20 of catfish, 18 of carfu, 20 of mirgal, 25 of milkfish, 35 of mackerel, 75 of tilapia, and 30 of rohu), 89 (39.9%) were tested positive for Salmonella. The prevalence of positive samples were reported for the freshwater fish of pangas (60.0%, n=12), carfu (27.7%, n=5), mirgal (35.0%, n=7), milkfish (52.0%, n=13), mackerel (31.4 %, n=11), tilapia imported from Thailand (64.0%, n=16), tilapia imported from India (28.0%, n=14), rohu imported from Thailand (26.6%, n=4) and rohu imported from Myanmar (46.6%, n=7). A total of 140 isolates of Salmonella spp. were yielded from at least seven different types of frozen freshwater fish imported from 5 different countries and were tested for their susceptibility to 16 selected antimicrobial agents. The highest antibiotic resistance was observed to tetracycline (90.71%) followed by ampicillin (70%) and amoxicillin-clavulanic acid (45%).

        Conclusions:The obtained results of this study shows that these raw retail imported frozen freshwater fish are contaminated with potentially pathogenic Salmonella spp. And the study recommend and suggest that there is a need for adequate consumer measures.

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