Abstract:This study investigated the presence of potentially human pathogenic strains of Vibrio spp., Aeromonas spp., Escherichia coli, Salmonella spp. and Staphylococcus aureus in fish commercialized in street markets of São Paulo city, Brazil. Twenty fish of different species were analyzed for foodborne pathogens using conventional methods. High levels of fecal contamination were detected in 25% of samples. S. aureus was isolated from 10% of samples. All were negative for Salmonella. Vibrio species, including Vibrio … Show more
“…In our study, the prevalence of S. aureus in all fish samples tested was 23.8% (19/80). The isolation rates of S. aureus were found to be 10% and 19.6% in fishes reported by Da Silva et al (2010) and Saito et al (2011), respectively. It is possible to say that the incidence rate of S. aureus in fish may be influenced by geographical location, the season, the method of harvest, post-harvest handling and storage (Ray 2004, Hammad et al 2012.…”
Section: Discussionmentioning
confidence: 89%
“…Therefore, S. aureus can be found commonly in various foods including meat (de Boer et al 2009, Jackson et al 2013) and fish (Da Silva et al 2010, Saito et al 2011. It is clear that contamination of food with this pathogen is often related to improper handling and storage conditions, as well as inadequate hygienic conditions and post-production microbial contamination (Ray 2004).…”
A total of 120 samples including 40 freshwaterfish(Oncorhynchus mykiss), 40 seawater fish (Sparus aurata) and 40 ground beef samples were examined for the presence of Staphylococcus aureus. The isolates were identified using biochemical tests and a PCR for the species-specific fragment (Sa442) and thermonuclease gene (nucA). The presence of staphylococcal enterotoxin genes (sea, seb, sec, sed and see), toxin genes (eta, etb, tsst), methicillin resistance gene (mecA) and some phenotypic virulence factors was also tested. Genotypic characterization of the isolates was analyzed by PCR-RFLP of the coa gene. Overall, 36 (30%) meat samples were contaminated with S. aureus. Of the 36 isolates, 3 (8.3%) were found to be positive for enterotoxin genes. Only 1 isolate (5.9%) from ground beef had the sea gene. In addition, 1 (12.5%) of the freshwater fish and 1 (9.1%) of the seawater fish carried both the sea and sed genes. The presence of seb, sec, see, eta, etb and tsst was not detected among the isolates of S. aureus. The amplified coa gene revealed five different clusters. Seven and six distinct RFLP patterns were obtained with AluI and HaeIII digestion, respectively. All isolates were found to be positive for slime, hemolytic and DNase activity while 41.7% of them were beta-lactamase positive. The presence of methicillin resistance was neither detected by PCR nor the disk diffusion method. A total of 94.4% of the isolates were resistant to at least one antimicrobial while 44.4% of them were resistant to at least two or more antimicrobials.
“…In our study, the prevalence of S. aureus in all fish samples tested was 23.8% (19/80). The isolation rates of S. aureus were found to be 10% and 19.6% in fishes reported by Da Silva et al (2010) and Saito et al (2011), respectively. It is possible to say that the incidence rate of S. aureus in fish may be influenced by geographical location, the season, the method of harvest, post-harvest handling and storage (Ray 2004, Hammad et al 2012.…”
Section: Discussionmentioning
confidence: 89%
“…Therefore, S. aureus can be found commonly in various foods including meat (de Boer et al 2009, Jackson et al 2013) and fish (Da Silva et al 2010, Saito et al 2011. It is clear that contamination of food with this pathogen is often related to improper handling and storage conditions, as well as inadequate hygienic conditions and post-production microbial contamination (Ray 2004).…”
A total of 120 samples including 40 freshwaterfish(Oncorhynchus mykiss), 40 seawater fish (Sparus aurata) and 40 ground beef samples were examined for the presence of Staphylococcus aureus. The isolates were identified using biochemical tests and a PCR for the species-specific fragment (Sa442) and thermonuclease gene (nucA). The presence of staphylococcal enterotoxin genes (sea, seb, sec, sed and see), toxin genes (eta, etb, tsst), methicillin resistance gene (mecA) and some phenotypic virulence factors was also tested. Genotypic characterization of the isolates was analyzed by PCR-RFLP of the coa gene. Overall, 36 (30%) meat samples were contaminated with S. aureus. Of the 36 isolates, 3 (8.3%) were found to be positive for enterotoxin genes. Only 1 isolate (5.9%) from ground beef had the sea gene. In addition, 1 (12.5%) of the freshwater fish and 1 (9.1%) of the seawater fish carried both the sea and sed genes. The presence of seb, sec, see, eta, etb and tsst was not detected among the isolates of S. aureus. The amplified coa gene revealed five different clusters. Seven and six distinct RFLP patterns were obtained with AluI and HaeIII digestion, respectively. All isolates were found to be positive for slime, hemolytic and DNase activity while 41.7% of them were beta-lactamase positive. The presence of methicillin resistance was neither detected by PCR nor the disk diffusion method. A total of 94.4% of the isolates were resistant to at least one antimicrobial while 44.4% of them were resistant to at least two or more antimicrobials.
“…parahaemolyticus is an important foodborne pathogen, although in São Paulo outbreaks caused by V. parahaemolyticus have not been reported by the Center for Epidemiologic Surveillance (CVE). In addition, consumption of raw fish in Brazilian cities is popular 39 . Therefore, in this study, V. parahaemolyticus isolated from shellfish were characterized by PCR targeted to 16S rRNA and virulence genes, antibiotic resistance patterns and DNA profiles by PFGE.…”
SUMMARYVibrio parahaemolyticus is a marine bacterium, responsible for gastroenteritis in humans. Most of the clinical isolates produce thermostable direct hemolysin (TDH) and TDH-related hemolysin (TRH) encoded by tdh and trh genes respectively. In this study, twenty-three V. parahaemolyticus, previously isolated from oysters and mussels were analyzed by PCR using specific primers for the 16S rRNA and virulence genes (tdh, trh and tlh) and for resistance to different classes of antibiotics and PFGE. Nineteen isolates were confirmed by PCR as V. parahaemolyticus. The tlh gene was present in 100% of isolates, the tdh gene was identified in two (10.5%) isolates, whereas the gene trh was not detected. Each isolate was resistant to at least one of the nine antimicrobials tested. Additionally, all isolates possessed the bla TEM-116 gene. The presence of this gene in V. parahaemolyticus indicates the possibility of spreading this gene in the environment. Atypical strains of V. parahaemolyticus were also detected in this study.
“…They may play an important role in the fish spoilage and some bacterial species of this family are very pathogenic (Guiraud, 2003;Shabarinath et al, 2007;Lopez Da Silva et al, 2010). Pathogens such as Salmonella spp., Shigella spp.…”
Abstract:Aim of this investigation is to provide the general information about prevalence of members of Enterobacteriaceae in horse mackerel (Trachurus trachurus) sold in open public markets in Istanbul, Turkey. Horse mackerel were randomly selected and collected in warm and cold seasons of the year. Purchased samples were kept in sterile insulated bags with ice and transported to the laboratory for microbiological analyses. Citrobacter spp. showed highest prevalence (45.56%), followed by Proteus mirabilis (22.62%), Proteus vulgaris (9.17%) and Escherichia coli (7.64%). The other isolates were Shigella sonnei (4.28%), Shigella dysenteria (3.36%), Salmonella Typhimurium (1.83%), Salmonella Paratyphi A (1.52%), Klebsiella pneumoniae (1.22%), Klebsiella oxytoca (1.22%), Enterobacter aerogenes (0.91%) and Enterobacter cloacae (0.61%). The percentages of the isolates, obtained in spring and autumn, were also compared. The Citrobacter spp., P. mirabilis and P. vulgaris were the dominantly isolated species, during spring season. P. mirabilis and Citrobacter spp. were also dominant in autumn. However, numbers and percentages of isolated pathogens (E. coli, S. sonnei, S. Dysenteriae, S. Typhimurium and S. Paratyphi A) were much more in autumn than that of spring. Since samples are sold without any chilling treatment in public markets, air temperature might be the reason of higher pathogen isolation in autumn. It is essential to implement cold chain as well as to prevent secondary contamination and to improve quality control.
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