Articles

Detection of enterotoxigenic Staphylococcus aureus isolates in domestic dairy products

Abstract

Background and objectives: Staphylococcus aureusis a one of THE most frequent causes of food poisoning (FP) in dairy products. The main etiologic agents of FP are staphylococcal enterotoxins (SE). There are different types of SE; types A (SEA) and B (SEB) are the most clinically important enterotoxins. Traditional dairy products are still produced in small batches and sold by some vendors without a permit from the Ministry of Health. This study focuses on the molecular and serological detection of enterotoxigenic Staphylococcus aureus SEA and SEB genes and its products, respectively from samples of such traditional products.
Materials and Methods: 100 samples from dairy products were produced under sterile conditions via traditional methods and were transported to the laboratory. The samples were cultured and identified by routine bacteriological methods. The isolated bacteria were evaluated by PCR tests for detection of the genes encoding SEA and SEB. Subsequently, the ability of these strains to produce enterotoxin was examined by Sac's culture method and was confirmed by Sigel Radial Immounodiffussion (SRID).
Results: The results indicated that 32% of the dairy products were contaminated by S. aureus (cream 18% , cheese 10%, milk 4%). The PCR results showed that 15.6% of the S. aureus isolates possessed the SEA gene, 9.3% had the SEB gene, and 6.2% possessed both genes. The evaluation of enterotoxin production indicated that 80% of SEA and 33% of SEB genes were expressed.
Conclusion: Enterotoxins SEA and SEB are heat stable and consequently; heating has no effect on dairy products contaminated by entertoxins. Subsequently, gastritis may occur within several hours after consumption. Our findings suggest that PCR is a rapid, sensitive, specific, and inexpensive method for detecting SE and can replace the traditional assays.

Paciorek ML , Kochman M , Piekarska K , Grochowska A , Windyg B. The distribution of enterotoxin and enterotoxin-like genes in Staphylococcus aureus strains isolated from nasal carriers and food samples. Int J of Food Microbiol 2007; 117: 319-323.

Holtfreter S, Bröker BM. Staphylococcal superantigens: Do they play a role in sepsis? Arch. Immunol. Ther. Exp 2005; 53: 13-27.

Heng C , Merlin SB. Purification and some physichemical properties of staphylococcus enterotoxin D. Ame. Chem. Society 1979; 79: 1937-42.

Rossalxn D, B-. Large scale purification of staphylococcal Entertoxins A, B and C by dye ligand affinity chromatography. Appl and Enviro micro. 1990;1: 1067-1072.

Kluytmans JAJW,Wertheim HFL. Nasal carriage of Staphylococcus aureus and prevention of nosocomial infections. Infection 2005; 33: 3-7.

Ruimy R, Angebault C, Djossou F, Dupont C, Epelboin L, Jarraud S, and et al. Are Host Genetics the Predominant Determinant of Persistent Nasal Staphylococcus aureus Carriage in Humans? J Infect Dis. 2010 Aug 2. [Epub ahead of print].

Martin MC, Fueyo JM, Gonzales-Hevia JM, Mendoza MC. Genetic procedure for identification of enterotoxigenic strains of Staphylococcus aureus from three food poisoning outbreaks. J Food Microbiol 2004;94:279-286.

McLauchlin J, Narayanan GL, Mithani V, O’Neill G.The detection of enterotoxins and toxic shock syndrome toxin genes in Staphylococcus aureus by polymerase chain reaction. J Food Prot 2000; 63: 479-488.

Chapaval L, Moon DH , Gomes J E, Duarte F R, and Tsai S M. Use of PCR to detect classical enterotoxin genes and toxic shock syndrome toxin-1 gene in Staphylococcus aureus isolated from crude milk and determination of toxin productivities of S. aureus isolates harboring these genes. J Arq Inst biol 2006; 73:165-169.

Omoe K, Hu DL, Takahashi-Omoe H, Nakane A, Shinagawa K. Comprehensive analysis of classical and newly described staphylococcal superantigenic toxin genes in Staphylococcus aureus isolates. FEMS Microbiol. Lett. 2005; 246: 191-198.

Fueyo JM, Mendoza MC, Alvarez MA, Martin MC.Relationships between toxin gene content and genetic background in nasal carried isolates of Staphylococcus aureus from Asturias, Spain. FEMS Microbiol. Lett.2005; 243: 447-454.

Bania J, Dabrowska A, Korzekwa K, Zarczynska A, Bystron J, Chrzanowska J, Molenda J. The profiles of enterotoxin genes in Staphylococcus aureus from nasal carriers. Lett. Appl. Microbiol 2006; 42: 315-320.

Edwin C, Tatini SR, Maheswaran SK. Specificity and crossreactivity of staphylococcal enterotoxin A monoclonal antibodies with enterotoxins B, C1, D, and E. Appl. Environ. Microbiol 1986; 52: 1253-1257.

Van Belkum A, Molecular diagnostics in medical microbiology: Yesterday, today and tomorrow. Curr. Opin. Pharmacol 2003; 3: 497–501.

Morandi S, Brasca M, Lodi R, Cremonesi P, Castiglioni B. Detection of classical enterotoxins and identification of enterotoxin genes in Staphylococcus aureus from milk and dairy products. Veter Microbiol 2007; 124: 66-72.

Gilmour A ,Harvey J. staphylococci in milk and milk product. J of Appl Microbiology 1990; 1475-1065.

Schantz EJ. Purification and some chemical properties of staphylococcal Enterotoxin A. Biochemistry 1972;11(3): 360-366.

Bradford M M. A rapid and sensitive method for the Quantitation of microgarm Quantities of protein utilizing the principle of protein – dye binding. Analytical biochemistry 1976; 72: 248-254.

Abbar. M. Selected biological properties of enterotoxigenic staphylococci isolated from milk. 20. Sharma NK, Rees CED, Dodd CE. Development of a single-reaction multiplex PCR toxin typing assay for Staphylococcus aureus strains. Applied and Enviro Microbiol 2000; 66 (4): 1347-1353.

BennetRW.Staphylococcus aureus identification characteristics and enterotoxigenicity. J of Food science 1986; 51: 1337-39.

Casman EPRW. BennetAE. Identification of a fourth staphylococcal enterotoxin D. J of Bacteriol 1967;1875-82.

Bradley GS, Teresa K. Staphylococcal enterotoxins: A purring experience in review, Part I. Clin microbiol News Letter 2005; 27 (23): 179-185.

Anvari SH, Sattari M, Forozandehe Moghadam M, Najar Peerayeh SH,Imanee Fouladi AA. Detection of Staphylococcus aureus Enterotoxins A to E from clinical samples by PCR. Res J of Biolo Scie 2008; 3 (8): 826-829.

Jorgensen HJ, Mork T, Hogasen HR, Rovik LM.Enterotoxigenic Staphylococcus aureus in bulk milk in Norway. J Appl Microbiol 2005; 99: 158-167.

Najera-Sanchez G, Maldonado-Rodriguez R, Ruiz Olvera P, Dela Garza L M. Development of two multiplex polymerase chain reactions for the detection of enterotoxigenic strains of Staphylococcus aureus isolated from foods. J Food Protocol 2003; 66: 1055-1062.

Normanno G, Firinu A, Virgilio S, Mula G, Dambro- sio A, Poggiu A, Decastelli L, etal. Coagulase-positive staphylococci and Staphylococcus aureus in food products marketed in Italy. Int J Food Microbiol 2005;98: 73-79.

Imanifooladi, A A, Sattari, M, Najar Peerayeh, SH, Hassan, Z M, Hossainidoust, S R. Detection the Staphylococcus aureus producing enterotoxin isolated from skin infection in hospitalized patients .Pak.J.Bio. Scie 2007; 3: 502-505.

Files
IssueVol 2 No 3 (2010) QRcode
SectionArticles
Keywords
Staphylococcus aureus Enterotoxin Food poisoning Dairy products

Rights and permissions
Creative Commons License This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.
How to Cite
1.
Imani Fooladi A, Tavakoli H, Naderi A. Detection of enterotoxigenic Staphylococcus aureus isolates in domestic dairy products. Iran J Microbiol. 1;2(3):135-140.