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Brazilian Journal of Microbiology

Print version ISSN 1517-8382

Braz. J. Microbiol. vol.44 no.2 São Paulo  2013

http://dx.doi.org/10.1590/S1517-83822013000200008 

FOOD
RESEARCH PAPER

 

Enterotoxigenicity of Staphylococcus aureus isolated from traditional and commercial dairy products marketed in Iran

 

 

Ebrahim Rahimi

Department of Food Hygiene, College of Veterinary Medicine, Islamic Azad University, Shahrekord Branch, Shahrekord, Iran

Send correspondence to

 

 


ABSTRACT

This study was conducted to determine the prevalence rate, enterotoxigenecity, and antimicrobial resistance of S. aureus isolated from dairy products in Iran. From September 2010 to July 2011, a total of 347 samples from various dairy products, traditional and commercial, were collected from randomly selected retail stores. Overall, 20 samples (5.8%) were found to be contaminated with S. aureus. The highest prevalence of S. aureus was found in traditional cheese (11.1%), followed by traditional ice-cream (5.9%), cream (5.6%), and butter (5.3%). The ability to synthesize classical staphylococcal enterotoxins (SEA-E) was determined in 7 of 20 (35%) isolates by using ELISA. SE type C was the most common enterotoxin found in the isolated S. aureus (42.9%), followed by SE type A (28.6%), SEA+SEC and SE type D (14.3%). Of the 20 isolates, 16 (80.0%) were positive for one or more entrotoxin genes and 8 different genotypes were observed. Susceptibilities of the isolates were determined for 14 antimicrobial drugs using the disk diffusion assay. Most of the isolates (95.0%) were resistant to one or more two antimicrobial agent and 45.0% of the isolates were resistant to three or more of drugs. Resistance to ampicillin was the most common finding (55.0%), followed by tetracycline (40.0%) and penicillin G (30.0%). The results of this study showed the wide spread of enterotoxigenic and multidrug-resistant S. aureus strains in traditional dairy products in Iran and highlighted their public health hazards.

Key words: antimicrobial resistance, dairy products, SE genes, staphylococcal enterotoxins, Staphylococcus aureus.


 

 

Introduction

Staphylococci are ubiquitous in nature; although the primary reservoir is on the skin and mucous membranes of mammals and birds. The presence of Staphylococcus aureus (S. aureus) in products for human consumption is important to the food industry as some strains are the cause of foodborne intoxication (Pelisser et al., 2009). The genus Staphylococci includes over 30 species; whit 18 of these species and subspecies are of potential hazard in food poisoning as they produce either coagulase, heat stable nuclease or enterotoxins. The coagulase positive species are S. aureus subsp. aureus which is the most common enterotoxigenic species (Le Loir et al., 2003, Loncarevic et al., 2005). S. aureus is a common pathogen associated with serious community and hospital acquired diseases and has for long been considered as a major problem of public health (Pesavento et al., 2007).

The pathogenicity of S. aureus and its ability to cause diseases is attributed to a number of virulence factors such as the heat stable enterotoxins (Sandel and McKillip, 2004). S. aureus produces 15 enterotoxins (Atichou et al., 2004). The five classical enterotoxins (SE, type A, B, C, D and E) were known to be responsible for 95% of staphylococcal food poisoning (SFP) cases, the rest of cases were due to the new types of SEs (SEG-SEO) (Jay et al., 2005). However, the role of newly identified enterotoxins in food poisoning is not fully clarified, and the development of methods for the detection of these novel se genes is of critical importance for food poisoning investigations.

SFP is a mild intoxication occurring after the ingestion of food containing from 20 ng to 1 µg of staphylococcal enterotoxin (SE) which is enough to induce symptoms in human beings (Normanno et al., 2007). SFP symptoms appear 1-6 h after ingestion of contaminated food, depending on individual susceptibility and toxic dose ingested. They include nausea, abdominal cramps, diarrhoea and a characteristic projectile vomiting. Clinical signs of SFP generally disappear within 24-48 h. Deaths occur rarely and specifically in the very young or elderly (Jay et al., 2005).

Pasteurization kills S. aureus cells, and fermentation or ripening of cheese may prevent growth of S. aureus in raw milk cheese. However, once formed the thermostable SEs generally retain their biological activity (Becker et al., 2007, Le Loir et al., 2003).

Currently, there is limited information regarding the prevalence and antimicrobial susceptibility patterns of S. aureus in milk and dairy products in Iran. The aims of this study were to determine the prevalence rate, enterotoxigenecity, and antimicrobial resistance of S. aureus in commercial and traditional cheese, yoghurt, ice cream, butter, cream, kashk and dough in Iran. Although, governmental regulation of milk pasteurization and sanitation in dairy processing plants has been in existence in Iran for many years, direct sale of unpasteurized milk and dairy products from producers to the consumer is common in many regions including Isfahan, Chaharmahal va Bakhtyari, and Khuzestan provinces.

 

Materials and Methods

Sample collection

A total of 347 samples of various traditional and commercial dairy products including cheese (n = 90), ice-cream (n = 85), butter (n = 57), cream (n = 36), yoghurt (n = 30), kashk (n = 24), and Iranian dough (n = 25) from different brands were obtained from randomly selected retail stores located in 25 major cities of Isfahan, Chaharmahal va Bakhtyari, and Khuzestan provinces From September 2010 to July 2011. Kashk and doogh are two popular dairy products in Iran that are available both as traditional and commercial products. Kashk is prepared by prolonged boiling yogurt and doogh which is also called yogurt soda is prepared by beating unflavored yogurt until smooth, and then diluting with water to a consistency similar to whole milk. Traditional dairy products in Iran are produced in small productive centers mostly located in urban areas and distributed unpacked. These products may be produced from unpasteurized milk. All samples were immediately transferred to the food microbiology laboratory, Islamic Azad University of Shahrekord Branch, in portable insulated cold-boxes. The samples were analyzed on the day they were collected.

Isolation of S. aureus

A 10 g portion of each food product was added to 90 g of sterile phosphate buffered saline (137 mM NaCl, 10 mM phosphate, 2.7 mM KCl, pH is 7.4) and stomached for 30-90 s. Then microbiological processing of the samples for the isolation of S. aureus was performed using Baird-Parker agar (Difco) following a standard procedure. Decimal dilutions of sample suspensions were spread plated on the agar plates in duplicate following incubation for 24-48 h at 35 ºC and then finally examined for colonies with typical appearance of S. aureus. To identify S. aureus, Gram stain, catalase, coagulase, and Voges-Proskaver (VP) tests were conducted on suspected colonies (Huong et al., 2010).

Detection of classical staphylococcal enterotoxins (SEs)

To detect SEs, the isolates were cultured overnight aerobically in10 mL nutrient broth (Merck, Germany) at 37 ºC. Bacterial culture supernatants were collected by centrifugation at 4,000 x g for 10 min and used for detection of SEA, SEB, SEC, SED, and SEE using an enzyme linked immunosorbent assay (ELISA) detection kit (RIDASCREEN® SET A, B, C, D, E Art. No: R4101, R-Biopharm AG, Germany). The assay was performed according to the manufacturer's recommendation and as described elsewhere (Rahimi and Ghasemian Safai, 2010). The mean lower detection limit of the assay was 0.1 mg/mL. All experiments were performed in duplicate.

Detection of sea, seb, sec, sed, see, seg, seh, sei, and sej

Purification of DNA was achieved using a Genomic DNA purification kit (Fermentas, GmbH, Germany) according to the manufacturer's instruction and the total DNA was measured at 260 nm optical density according to the method described by Sambrook and Russell (2001). After DNA isolation, amplification of selected enterotoxin genes (sea, seb, sec, sed, see, seg, seh, sei, and sej) was achieved using 9 primer sets in the one reaction mixture. The sequences of the primers used for gene amplification are presented in Table 1. All oligonucleotide primers were obtained from a commercial source (Cinna Gen, Iran). Polymerase chain reaction (PCR) assays for the detection of S. aureus enterotoxin genes were performed according to the methods described previously (Rall et al., 2008, Zouharova and Rysanek, 2008). Briefly, amplification reactions were performed in a 25 µL mixture containing1UTaq polymerase (Fermentas, GmbH, Germany), 200 µM of each dNTP (Fermentas, GmbH, Germany), 2.5 µL PCR buffer 10x (Fermentas, GmbH, Germany), 1.0 µM MgCl2 (Fermentas, GmbH, Germany), 10 pmol of each primers, and 3 µL DNA. The final volume was adjusted to 25 µL by adding sterile ultrapure water (Rall et al., 2008). Amplification reactions were carried out using a DNA thermal cycler (Master Cycle Gradiant, Eppendrof, Germany) with the following program: one cycle of 5 min at 94 ºC, 30 cycles each consisting of 45 s at 94 ºC, 1 min and 30 s at 65 ºC, 1 min at 72 ºC and a final extension step of 8 min at 72 ºC. The PCR products were stained with 1% solution of ethidium bromide and visualized under UV light after gel electrophoresis on 1.5% agarose. S. aureus ATCC 19095, ATCC 23235 and ATCC 700699 were used as the positive controls and DNase free water was used as the negative control.

Antimicrobial susceptibility testing

One colonia from each S. aureus-positive sample was selected for susceptibility tests. Antimicrobial susceptibility testing was performed by the Kirby-Bauer disc diffusion method using Mueller-Hinton agar (HiMedia Laboratories, Mumbai, India) supplemented with 5% defibrinated sheep blood, according to the Clinical Laboratory Standards Institute (2006). The following antimicrobial impregnated disks (HiMedia Laboratories, Mumbai, India) were used: penicillin G (10 IU), cephalotin (30 µg), chloramphenicol (30 µg), clindamycin (15 µg), ciprofloxacin (30 µg), erythromycin (15 µg), tetracycline (30 µg), oxacillin (15 µg), gentamycin (10 µg), ampicillin (10 µg), enrofloxacin (10 µg), trimethoprim-sulfamethoxazole (25 µg), methicillin (5µg), and vancomycin (30 µg). After incubation at 37 ºC for 48 h, the susceptibility of the S. aureus isolates to each antimicrobial agent was measured and the results were interpreted in accordance with interpretive criteria provided by CLSI (2006).

Statistical analysis

Data were transferred to Microsoft Excel spreadsheet (Microsoft Corp., Redmond, WA, USA) for analysis. Using SPSS 16.0 statistical software (SPSS Inc., Chicago, IL, USA), chi-square test and fisher's exact two-tailed test analysis was performed and differences were considered significant at values of p < 0.05.

 

Results

In the present study, a total of 347 samples of various commercial and traditional milk and dairy products were tested for enterotoxigenic S. aureus (Table 2). Using cultural techniques, 20 of 347 samples (5.8%) were positive for S. aureus.No S. aureus was isolated from commercial cheese, ice cream, butter and cream samples and all yogurt, doogh, and kashk samples were negative for S. aureus.In contrast, 10 cheese (11.1%), 5 ice cream (5.9%), 2 cream (5.6%) and 3 butter (5.3%) samples were contaminated with S. aureus. In this study, total S. aureus counts determined were between 1x102 and 1x106 cfu/g in samples. In 3 (6.0%) of traditional cheese, and 1 (3.7%) butter samples, CPS counts were above 105 cfu/g (Table 2).

The ability to synthesize classical enterotoxins was found in 7 of 20 (35.0%) isolates by using ELISA technique. Two isolates produced SEA (28.6%), 3 isolates produced SEC (42.9%), 1 isolates produced SEA+SEC (14.3%), and 1 isolates produced SEA + SED (14.3%) (Table 2). No SEB and SEE were identified in dairy product samples. Type A enterotoxin was found in 1 butter and 1 ice-cream samples. Type C and type A+C enterotoxin was detected in only 4 traditional cheeses. Type A + D enterotoxin was found in 1 butter (Table 2). No SEs was identified in cream samples.

Table 3 shows the results of PCR assays for the detection of genes encoding the SEA-SEJ toxins. Of the 20 strains of S. aureus tested, 16 (80.0%) were positive for one or more SE genes and 9 different genotypes were observed.

Five strains possessed only one type of toxin gene and the reimaining isolates harbored more than one toxin genes. The most commonly detected genes were seg + sei (20.0%), sej (15.0%), sec + sej (15.0%), sei + seh (10.0%), sea + sed + sej (5.0%), sea + sej + sei (5.0%), and sea + sec + seh (5.0%). No see or seb gene was detected in any of the isolates.

On comparing the data relative to the strains isolated from chesses, ice cream, butter, and cream, 8 of the 10 (80.0%) strains isolated from cheese samples were se gene positive in which the sec genes were found more frequently. Three of the 5 (60.0%) S. aureus isolated from ice-cream and all of the S. aureus isolated from butter and cream samples were se gene positive.

The resistance pattern of S. aureus isolates to 14 antimicrobial agents tested in this study is shown in Table 4. Most of the isolates (95.0%; n = 19) were resistant to one or more antimicrobial agent. Three isolates (15.0%) were resistant to single antibiotic and 7 isolates (35.0%) showed resistance to 2 antimicrobial agents. Multiresistance which was defined as resistance to 3 or more of antimicrobial agents tested was found in 45.0% of S. aureus isolates.

 

 

Results and Discussion

In the present study, 20 of the 220 traditional (9.1%) dairy product samples were positive for S. aureus.No S. aureus was isolated from 127 commercial dairy products and the difference was statistically significant (p < 0.05). The high occurrence of S. aureus in traditional dairy products could be due to environmental contamination with infected animal wastes or unsanitary food production and storage practices. However, this could be also due to the use of unpasteurized milk because the shedding of bacteria from the infected mammary glands of dairy animals is most likely the primary source of S. aureus contamination of milk and dairy products. While commercials products are produced with pasteurized milk under sanitary condition.

S. aureus count was determined about 103 cfu/g in 20 samples period. In 3 of sheep cheese, and 1 butter samples, S. aureus counts were above 105 cfu/g (Table 2). The prevalence of S. aureus in traditional cheese, ice cream, cream and butter was 11.1%, 5.9%, 5.6%, and 5.3%, respectively, which is comparable with those reported by Manfreda et al (2005), Ertas et al. (2010), Bostan et al. (2006), and Pelisser et al. (2009). Necidová et al. (2009) reported, S. aureus count higher than 105 cfu/g is unsuitable for the production of cheese. Staphylococcal counts should reach approximately 106 cfu/g to produce enterotoxin (Necidová et al., 2009, Pelisser et al., 2009).

In this study, 35.0% of isolated S. aureus strains produced classical enterotoxins. This result is in agreement with those reported by other investigators (Morandi et al., 2007, Normanno et al., 2005). Most of the isolated strains produced SEA, SED, and SEC. Our data show that SEs and se genes are in close correlation with the S. aureus strain origin. For example, a higher ratio of strains isolated from traditional sheep and goat cheeses produced mainly SEC, while the strains isolated from other dairy products made from cow milk produced SEA and SED. These results are in agreement with the data reported from other countries (Akineden et al., 2008, Loncarevic et al., 2005, Morandi et al., 2005, Rall et al., 2008, Scherrer et al., 2004). Of the 20 strains of S. aureus tested, 17 (85.0%) were positive for one or more SE genes and 8 different genotypes were observed. Five strains possessed one type of toxin gene, while the reimaining 12 harbored more than one toxin genes. The most commonly detected genes were seg + sei, sej, sec + sej, sei + seh, sea + sed + sej, sea + sej + sei, and sea + sec + seh. Similar results were presented by Normanno et al. (2005), Manfreda et al. (2005), and Tkacikova et al. (2003). In contrast, the incidence of S. aureus and their SEs was reported relatively high by several authors (Fotta et al., 2000, Holeckova et al., 2002) when compared with our results. Variation in the results reported in other studies may be a result of different sampling techniques employed, seasonal effects, and/or laboratory methodologies employed in different studies.

S. aureus strains are known to be frequently resistant to antibiotic therapy due to their capacity to produce an exopolysaccharide barrier and because of their location within microabscesses, which limit the action of drugs (Gündogan et al., 2006). The resistance pattern of S. aureus isolates to 12 antimicrobial agents tested in this study is shown in Table 3. Most of the 20 S. aureus isolates (95.0%) were resistant to one or more antimicrobial agent. Resistance to ampicillin was the most common finding, followed by resistance to tetracycline, penicillin G, oxacillin, eritromycin, trimethoprim-sulfametoxazole, enrofloxacin, gentamycin, chloramphenicol, clindamycin, and ciprofloxacin. All isolates tested for antibiotic sensitivity were susceptible to methicillin cephalotin and vancomycin. These results are comparable to those reported by other investigators (Gündogan et al., 2006, Normanno et al., 2007, Peles et al., 2007, Pereira et al., 2009, Pesavento et al., 2007). The results of antimicrobial resistance found in this study are correlated to antibiotics that are being used to treat infection in food animals in Iran. A national monitoring program for antibiotic resistance, including both human and food isolates, is needed In Iran.

National legislation of S. aureus in milk and dairy products which is 102 cfu/g. S. aureus in about 9% of traditional dairy products found to be above which shows the importance of some traditional dairy products as potential sources of S. aureus infection in people who consume traditional dairy products. We recommend that coordinated actions are needed to reduce or eliminate the risks posed by this organism at a number of stages in the food chain. These include Good Agricultural Practice, Good Manufacturing Practice and Hazard Analysis of Critical Control Points at every stages of the meat supply chain, from the farm, to the retailer, and those involved with the handling and processing of raw milk products in the home environment.

 

Acknowledgments

The authors would like to thank Hassan Momtaz, Manochehr Momeni and Majed Riahi for the sincere help in performing technical parts of the project.

 

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Send correspondence to:
E. Rahimi
Department of Food Hygiene, College of Veterinary Medicine, Islamic Azad University
Shahrekord Branch, Shahrekord, Iran
E-mail: ebrahimrahimi55@yahoo.com; rahimi@iaushk.ac.ir

Submitted: October 5
Approved: July 23, 2012

 

 

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