Abstract
Aim:
The aims of the present study were to assess the prevalence, identification, and antibiogram pattern of Bacillus cereus from 215 samples of different milk and milk products in and around Jammu region.
Materials and Methods:
In the present study, 215 samples of milk, rasgulla, burfi, rasmalai, kalaari, paneer, ice cream, and pastry were collected and analyzed for the isolation of the B. cereus using PEMBA, and antibiogram pattern was observed for all the milk and milk products.
Results:
B. cereus was detected in 61/215 samples with an overall prevalence of 28.37%. Biotyping revealed predominantly 5, 7, and 2 biotypes in raw milk. Burfi and ice cream revealed 2, 3, 5, and 7 biotypes. Rasgulla had 2, 3, and 5 biotypes; paneer and rasmalai had biotypes 2 and 5, while kalaari revealed biotype 5. Antibiogram pattern revealed that isolates were highly sensitive to gentamicin (100%), intermediate to ampicillin (40.98%), tetracycline (31.14%), erythromycin (29.50%), and amoxicillin (26.22%), and high resistance against penicillin G (100%). Adulteration of starch was detected in 16.66 % raw milk samples. All starch positive samples were positive for B. cereus. However, 12 starch negative samples also yielded B. cereus.
Conclusion:
From this study, it was concluded that highest prevalence of B. cereus was found in ice cream. Several isolates of B. cereus showed toxigenic activity, so the presence of B. cereus in milk and milk products may be of public health hazard. The antibiogram pattern of B. cereus isolates showed sensitivity to gentamicin, ciprofloxacin, chloramphenicol, streptomycin, and resistance to penicillin-G and cephalexin. The presence of B. cereus in milk and milk products showed a strong association besides establishing the fact that starch adulteration can be indicative of the presence of B. cereus.
Keywords: Antibiogram, Bacillus cereus, milk, milk products, prevalence
Introduction
Bacillus cereus is a Gram-positive, motile, spore-forming, rod-shaped bacterium. B. cereus is associated with two distinct types of gastrointestinal disorders, the diarrheal and emetic syndrome [1,2]. There are different species of Bacillus, of which the B. cereus is the most important microorganism involved in the spoilage of dairy environment [3]. In general, B. cereus is sensitive to gentamicin, chloramphenicol, vancomycin, and ciprofloxacin, while highly resistant to penicillin G [4-7].
B. cereus is of concern because of its nature and growth in the dairy environment [8]. The isolates of B. cereus from products of dairy origin produce lipase, and other proteases which are thermostable, i.e., have the ability to remain active after pasteurization temperature, which leads to the defects in the final dairy products [3,9]. Since it has the ability to produce toxins and enterotoxins, it poses a concern for the dairy industry as it causes food poisoning. The adherence property of B. cereus to the dairy plant stainless steel surfaces poses a risk to health and serious hygiene issues. There is the loss of both product and equipment due to biofuel production, hence leading to economic loss due to spoilage [8]. Furthermore, the spore-forming and psychotropic nature of certain B. cereus strains ensure the survival and multiplication of bacteria during milk processing. As a result, the dairy industry often reported food poisoning outbreaks due to this organism [8].
India being the largest producer of milk in the world has high per capita milk consumption and also of milk products. The same stands true for Jammu and Kashmir. However, the milk production and processing practices are of low standards and may lead to contaminated milk and milk products which in turn can predispose people to milk-borne infectious agents including B. cereus. Keeping in view the above facts, the objective was framed to study the prevalence, identification, and antibiogram of B. cereus from milk and milk products in and around Jammu region.
Materials and Methods
Ethical approval
No ethical approval was required for the study because no live animal was involved in the study. The samples of different milk and milk products were collected in and around Jammu region.
Media used
In the current study, polymyxin pyruvate egg yolk mannitol bromothymol blue agar (PEMBA), B. cereus agar base, brain heart infusion broth (BHIB), Muller-Hinton agar, sheep blood agar, nitrate broth, motility test medium, and Simmons citrate agar were used.
Bacterial strain
Reference strain of B. cereus (MTCC 1272) obtained from the microbial type culture collection and gene bank (MTCC), Institute of Microbial Technology (IMTECH), Chandigarh, India, was used for standardization of techniques. The strain was maintained by periodic subculturing on a nutrient agar slant.
Sampling
There were a total of 215 samples, of which 30 samples of raw milk were collected in sterile containers from local milk vendors, and 185 samples of milk products comprised of 29 burfi, 28 rasgulla, 28 rasmalai, 25 ice cream, 25 paneer, 25 pastry, and 25 kalaari were collected aseptically from various retail outlets in and around Jammu city. The samples were brought to the laboratory on ice and processed within 2 h of collection.
Isolation and identification of B. cereus
Isolation
PEMBA media were used for isolation of B. cereus. The presumed isolates were purified on nutrient agar slants for further characterization. All presumptive colonies of B. cereus were purified and subjected to morphological and biochemical tests for identification and confirmation as described in Bacteriological Analytical Manual of United States Food and Drug Administration [10] and Bergey’s Manual of Systematic Bacteriology [11].
Biotyping
The isolates were biotyped on the basis of their ability to ferment ammonium salt sugars (ASS), namely, xylose, salicin, and cellobiose as per the scheme proposed by Jha and Narayan [12] (Table-1).
Table-1.
Biotype | Xylose | Salicin | Cellobiose |
---|---|---|---|
1 | - | - | - |
2 | + | - | + |
3 | - | + | - |
4 | + | - | - |
5 | + | + | + |
6 | - | - | + |
7 | - | + | + |
8 | + | + | - |
Antibiogram pattern of B. cereus
All the B. cereus isolates were examined for their antibiogram pattern by disc diffusion technique as described by Bauer et al. [13] against a panel of 10 antibiotics. The results were interpreted as sensitive or resistant based on CLSI interpretive standards HiMedia [14].
Detection of starch/rice flour adulteration [15]
The samples of milk and milk products were subjected to test for detection of starch/rice flour as an adulterant. 3 ml of the test sample (raw milk/milk product) was thoroughly mixed and boiled for 15 min. After cooling to the room temperature, 2-3 drops of 1 % iodine was added drop by drop. A positive test was indicated by the appearance of blue color, which disappeared after boiling and reappeared on cooling.
Results
The present study was carried out to explore the prevalence of B. cereus in milk and milk products collected from Jammu city. B. cereus was isolated and identified on the basis of cultural, morphological, and biochemical characters.
Isolation and identification of B. cereus
On PEMBA medium, typical fimbriate peacock blue-colored colonies (3-5 mm) surrounded by a blue zone of egg yolk hydrolysis against green/greenish-yellow background was presumed as B. cereus. The presumed isolates were purified on nutrient agar slants and were subjected to standard biochemical and other tests for further characterization. After enrichment of each sample in BHIB, inoculums were streaked on PEMBA medium.
All the isolates were identified morphologically and biochemically. All the isolates were Gram-positive, large rods, and sometimes, spores were also observed. Motility test of B. cereus was performed in 18-h-old BHIB which showed characteristic swarming and swimming motility in hanging drop under 40× cavity slide. All the isolates were positive for catalase test, citrate utilization test, Voges–Proskauer test, and nitrate reduction test but negative for oxidase test. The isolates also hydrolyzed starch and produced hemolysis on sheep blood agar. All the isolates produced acid from glucose and mannose but failed to produce acid from mannitol and arabinose.
61 samples were found positive for B. cereus with an overall prevalence of 28.37%. The present study revealed maximum contamination of ice cream, rasgulla, and burfi with B. cereus, followed by pastry, raw milk, rasmalai, paneer, and kalaari (Table-2)
Table-2.
Milk product | Samples tested | Samples positive | % prevalence |
---|---|---|---|
Raw milk | 30 | 8 | 26.66 |
Burfi | 29 | 10 | 34.48 |
Rasgulla | 28 | 11 | 39.28 |
Rasmalai | 28 | 7 | 25 |
Ice cream | 25 | 11 | 44 |
Paneer | 25 | 4 | 16 |
Pastry | 25 | 8 | 32 |
Kalaari | 25 | 2 | 8 |
Total | 215 | 61 | 28.37 |
B. cereus=Bacillus cereus.
Biotyping
The isolates of B. cereus were biotyped as per the scheme proposed by Jha and Narayan [12] by demonstrating their fermentation reaction in ASS, namely, xylose, salicin, and cellobiose. Overall predominant biotypes recovered were biotypes 5 followed by 2, 7, and 3. From rasgulla, biotypes 2, 3, and 5 were recovered. Burfi and ice cream revealed 2, 3, 5, and 7 biotypes, while pastry revealed biotypes 2, 5, and 7. Paneer and rasmalai revealed biotypes 2 and 5 only. In Kalaari, only biotype 5 was present (Table-3).
Table-3.
Samples | Biotype 2 | Biotype 3 | Biotype 5 | Biotype 7 |
---|---|---|---|---|
Raw milk | 2 | - | 3 | 3 |
Burfi | 3 | 2 | 4 | 1 |
Ice cream | 3 | 2 | 3 | 3 |
Rasmalai | 2 | - | 5 | - |
Rasgulla | 6 | 1 | 4 | - |
Paneer | 2 | - | 2 | - |
Pastry | 2 | - | 4 | 2 |
Kalaari | - | - | 2 | - |
Total | 20 | 5 | 27 | 9 |
B. cereus=Bacillus cereus.
Antibiogram pattern of B. cereus
Based on CLSI interpretive standards for Gram-positive and/or aerobic bacteria, the antibiotics to which B. cereus isolates were susceptible included gentamicin, ciprofloxacin, and chloramphenicol followed by streptomycin. On the contrary, all isolates depicted high resistance to penicillin G and cephalexin. Less than 50% resistance was recorded for ampicillin, tetracycline, erythromycin, and amoxicillin (Table-4).
Table-4.
Samples (n) | S (%) | P (%) | C (%) | G (%) | T (%) | Am (%) | CN (%) | E (%) | A (%) | Cip (%) |
---|---|---|---|---|---|---|---|---|---|---|
Milk (8) | 1 (12.5) | 8 (100) | 1 (12.5) | 0 | 2 (25) | 1 (12.5) | 5 (62.50) | 2 (25) | 3 (37.5) | 0 (0) |
Ice cream (11) | 2 (18.18) | 11 (100) | 1 (9.09) | 0 | 5 (45.45) | 3 (27.27) | 11 (100) | 4 (36.36) | 5 (45.45) | 0 (0) |
Burfi (10) | 2 (22.22) | 10 (100) | 0 | 0 | 2 (22.22) | 2 (22.22) | 9 (100) | 3 (33.33) | 4 (44.44) | 1 (10) |
Rasgulla (11) | 1 (10) | 11 (100) | 0 (0) | 0 | 3 (30) | 3 (30) | 10 (100) | 2 (20) | 4 (40) | 0 (0) |
Pastry (8) | 2 (25) | 8 (100) | 2 (25) | 0 | 3 (37.5) | 2 (25) | 8 (100) | 2 (25) | 4 (50) | 1 (12.5) |
Paneer (4) | 0 | 4 (100) | 0 (0) | 0 | 1 (25) | 1 (25) | 3 (75) | 1 (25) | 1 (25) | 0 (0) |
Rasmalai (7) | 1 (14.28) | 7 (100) | 1 (14.2) | 0 | 2 (28.57) | 2 (28.57) | 7 (100) | 3 (42.8) | 4 (57.14) | 0 (0) |
Kalaari (2) | 0 | 2 (100) | 0 (0) | 0 | 1 (50) | 2 (100) | 2 (100) | 1 (50) | 0 (0) | 0 (0) |
Total (61) | 9 (14.75) | 61 (100) | 5 (8.19) | 0 (0) | 19 (31.14) | 16 (26.22) | 55 (90.16) | 18 (29.50) | 25 (40.98) | 2 (3.27) |
n=Number of isolates, S=Streptomycin, P=Penicillin G, C=Chloramphenicol, G=Gentamicin, T=Tetracycline, Am=Amoxicillin, CN=Cephalexin, E=Erythromycin, A=Ampicillin, Cip=Ciprofloxacin, B. cereus=Bacillus cereus
Antibiogram pattern of B. cereus isolates from milk and different milk products
Of eight isolates, two isolates showed intermediate sensitivity to streptomycin and erythromycin, while one isolate showed intermediate sensitivity to tetracycline, amoxicillin, cephalexin, and ampicillin. All the isolates were sensitive to gentamicin and ciprofloxacin while being resistant to penicillin G.
Antibiogram pattern of B. cereus isolates from ice cream
Of eleven isolates, three isolates showed intermediate sensitivity to streptomycin and amoxicillin, and two isolates showed intermediate sensitivity to erythromycin and ampicillin. Five isolates were resistant to tetracycline and ampicillin, while ten isolates were susceptible to chloramphenicol and ciprofloxacin. All the isolates were sensitive to gentamicin but resistant to penicillin G.
Antibiogram pattern of B. cereus isolates from pastry
Of eight isolates, two isolates showed intermediate sensitivity to ampicillin and streptomycin and one isolate to erythromycin. Two isolates showed resistance to streptomycin, chloramphenicol, amoxicillin, and erythromycin. All isolates were susceptible to gentamicin while resistant to cephalexin and penicillin G.
Antibiogram pattern of B. cereus isolates from burfi
Of ten isolates, two isolates showed resistance to streptomycin, tetracycline, and amoxicillin. Three isolates showed resistance to erythromycin and four isolates showed resistance to ampicillin. All the isolates were susceptible to ciprofloxacin, gentamicin, and chloramphenicol. Intermediate sensitivity was shown by two isolates to streptomycin, three isolates to amoxicillin, and one isolate to ampicillin.
Antibiogram pattern of B. cereus isolates from rasmalai
All seven isolates were resistant to penicillin G and cephalexin while susceptible to gentamicin and ciprofloxacin. Only two isolates showed intermediate sensitivity to streptomycin and amoxicillin. One isolate showed resistance to streptomycin and chloramphenicol, and two isolates showed resistance to tetracycline and amoxicillin. Three and four isolates showed resistance to erythromycin and ampicillin, respectively.
Antibiogram pattern of B. cereus isolates from rasgulla
All eleven isolates were susceptible to ciprofloxacin, gentamicin, and chloramphenicol while resistant to penicillin G. Three isolates showed intermediate sensitivity to streptomycin and erythromycin while resistance to tetracycline and amoxicillin.
Antibiogram pattern of B. cereus isolates from Kalaari
Of two isolates, one isolate showed resistance to tetracycline and erythromycin. All the isolates were resistant to penicillin G, amoxicillin, and cephalexin while susceptible to streptomycin, gentamicin, chloramphenicol, ampicillin, and ciprofloxacin.
Antibiogram pattern of B. cereus isolates from paneer
Of four isolates, two isolates showed intermediate sensitivity to ampicillin and one isolate showed intermediate sensitivity to amoxicillin. One isolate showed resistance to tetracycline, amoxicillin, erythromycin, and ampicillin. All the isolates were susceptible to chloramphenicol, streptomycin, gentamicin, and ciprofloxacin.
Starch adulteration in raw milk and milk products
Of 215 samples of raw milk and milk products, 49 samples were found adulterated with the starch (rice flour) showing an overall adulteration of 22.79%.
Maximum starch adulteration among milk and milk products was observed in rasgulla with 10/28 (35.71%) and burfi with 10/29 (34.48%) samples positive followed by pastry and ice cream, 8/25 (32.00%), rasmalai 5/28 (17.85%), and raw milk 5/30 (16.66%). Paneer and kalaari showed the least adulteration with only 2 (8%) and 1 (4%) sample positive, respectively (Table-5).
Table-5.
Sample | Samples tested | Samples adulterated | Total % |
---|---|---|---|
Raw milk | 30 | 5 | 16.66 |
Burfi | 29 | 10 | 34.48 |
Rasgulla | 28 | 10 | 35.71 |
Rasmalai | 28 | 5 | 17.85 |
Ice cream | 25 | 8 | 32 |
Pastry | 25 | 8 | 32 |
Paneer | 25 | 2 | 8 |
Kalaari | 25 | 1 | 4 |
Total | 215 | 49 | 22.79 |
Discussion
Milk and milk products may serve as potential reservoirs for many bacterial pathogens. In the present study, all the 215 samples of milk and milk products were subjected to standard microbiological procedures for the detection of B. cereus. The study revealed 26.66% of raw milk samples contaminated with B. cereus. Sharma et al. [16] reported 66% contamination of milk with B. cereus in Ludhiana which was lower than the results of the current study.
In milk products, the highest prevalence of B. cereus was observed in ice cream (44%), followed by rasgulla (39.28%), burfi (34.48%), pastry (32%), and rasmali (25%). Least prevalence was observed in paneer (16%) and kalaari (8%) samples. These results are in agreement with Hassan et al. [17] who reported a prevalence of 30%, 48%, and 2% in raw milk, ice cream, and yogurt, respectively, in Egypt. In Ludhiana, Sharma et al. [16] reported 44.8 and 44.4% incidence in burfi and milk powder, respectively.
Contamination of milk and milk products by B. cereus has been reported by many workers and established that entry of B. cereus in the raw milk and milk products could be due to many reasons including the adulteration of milk by water and rice flour [18] and use of contaminated utensils [19]. Another possible explanation could be the prolonged holding time under unhygienic conditions at retail outlets, resulting in a higher initial load of B. cereus in raw milk. Recovery of B. cereus from pasteurized milk has also been reported.
The morphological and biochemical characteristics of B. cereus isolates in the present study closely resembled those exhibited by the standard strain. It was interesting to note that majority of the isolates from milk and milk products differed in their response to the fermentation reaction to xylose, salicin, and cellobiose, on the basis of a biotyping scheme for B. cereus as proposed by Jha and Narayan [12]. This scheme was used exclusively for locating the source of contamination of different foods and differentiation of various strains [20,21]; however, to make the scheme more reliable and expressive, the higher number of samples from other possible sources needs to be screened.
In the present study, the biotyping pattern of isolates from the raw milk revealed predominance of biotypes 5, 7, and 2 with 37.5% isolates typed as biotypes 5 and 7 and 25% as biotype 2. Burfi and ice cream revealed 2, 3, 5, and 7 biotypes. Rasgulla harbored biotypes 2, 3, and 5; paneer and rasmalai were contaminated with biotypes 2 and 5, while kalaari revealed biotype 5 only. Previously, Yadav [20] reported a predominance of biotypes 7, 6, and 5 from fried rice and boiled rice; Willayat [21] reported biotypes 7, 6, 5, and 1. Javed [22] reported the predominance of biotypes 1, 7, 5, and 2 in boiled rice and 3, 4, and 2 in the raw milk. In another study [23] in Kashmir region, the presence of biotypes 3, 4, 1, and 6 were reported from the mutton tikka samples and biotypes 6, 7, 5, and 2 from the chutneys. It is documented that biotypes 2, 5, and 7 are frequently associated with starchy foods and the preponderance of these biotypes in milk and milk products in the present study may indicate the adulteration of these products with starchy products.
Keeping in view the above facts, the antibiotic sensitivity of all the B. cereus isolates against a panel of ten commonly used antibiotics was carried out. The antibiotics to which most of the isolates were susceptible included gentamicin (100%), ciprofloxacin (96.73%), and chloramphenicol (91.81%) followed by streptomycin (85.25%). The isolates were resistant to penicillin G (100%) and cephalexin (90.16%). However, <50% resistance was recorded for ampicillin (40.98%), amoxicillin (26.22%), tetracycline (31.14%), and erythromycin (29.50%). These findings are in accordance with the findings of Schlegelova et al. [4], Turnbull et al. [5], Whong and Kwaga [6], and Kursun et al. [7]. Hafeez et al. [23] also reported that the strains of B. cereus isolated from the vendor samples were highly resistant to penicillin G (92.59%). Previous work on the antimicrobial susceptibility of B. cereus revealed higher susceptibility to streptomycin, chloramphenicol, erythromycin, and ciprofloxacin and less susceptible to ampicillin, ampiclox, clotrimazole, and cloxacillin [24]. Variations in the percentages may be due to the differences in the concentrations of antimicrobial agents used, differences in the source of isolates, drug resistance transfer, and overall wide use of the antibiotics. The development of drug resistance against certain antibiotics may be due to the use of these drugs in medical and veterinary practice to treat infections and misuse of the drugs that could have led to drug resistant strains.
Milk and milk products were also subjected to starch adulteration test, and both starch positive as well as starch negative samples were tested for detection of B. cereus by standard procedure. The study revealed 16.66% raw milk samples adulterated with starch. Among milk products, rasgulla was found to be highly adulterated (35.71%) followed by burfi (34.48%), ice cream and pastry (32%), rasmalai (17.85%), paneer (8%), and kalaari (4%). The higher % age of adulteration in rasgulla and burfi may possibly be due to use of the starchy substrate in the manufacture of these products. The lesser % age of adulteration in paneer and kalaari could be because of non-feasibility of adulteration keeping in view the texture, taste, and other factors vital for the acceptability of these products.
In the present study, all the starch positive samples of the milk and milk products revealed the presence of B. cereus which otherwise form the part of the microflora of the rice and rice products, establishing a fact that rice powder may have been adulterant for increasing the physical attributes, texture, and the bulk of the product. However, the starch negative samples of milk and milk products have also revealed positive results for B. cereus and the latter might have entered in the processing line from the water, utensils, or other sources.
The present study unveils the faulty practice of adulteration of milk and milk products with starch, which necessitates stronger monitoring and frequent testing followed by stringent control measures on the part of control authorities. Since all the starch positive samples were confirmed for the presence of B. cereus, starch adulteration may act as an indicator for the presence of B. cereus in milk and milk products.
Conclusion
From the study, it was concluded that the overall prevalence of B. cereus in milk and milk products was 28.37%. The highest prevalence of B. cereus was found in ice cream followed by rasgulla, burfi, pastry, rasmalai, paneer, and kalaari samples. Several isolates of B. cereus showed toxigenic activity, so the presence of B. cereus in milk and milk products may be a public health hazard. The antibiogram pattern of B. cereus isolates showed sensitivity to gentamicin, ciprofloxacin, chloramphenicol, and streptomycin and resistance to penicillin-G and cephalexin. Starch adulteration and B. cereus contamination in milk and milk products showed a strong association besides establishing the fact that starch adulteration can be indicative of the presence of B. cereus. Besides, B. cereus may cause non-gastrointestinal tract syndromes such as meningitis, endocarditis, and septicemia particularly in children and the older people. The effective use of quality control and safety measures during production/manufacture besides creating awareness among food handlers and consumers becomes necessary to ward off the menace of B. cereus and other food poisoning organisms.
Authors’ Contributions
This study was carried out as a part of MVSc study of UY, under the guidance of SKK. SG was actively involved in the whole study, and TA has helped in various ways and designed the manuscript for publication. All the authors have read and approved the final manuscript.
Acknowledgments
The authors are thankful to Dean F.V.Sc and A.H. SKUAST-J for providing all the requirements necessary for this study.
Competing Interests
The authors declare that they have no competing interests.
References
- 1.Jeßberger N, Dietrich R, Bock S, Didier A, Martlbauer E. Bacillus cereusenterotoxins act as major virulence factors and exhibit distinct cytotoxicity to different human cell lines. Toxicon. 2014;77:49–57. doi: 10.1016/j.toxicon.2013.10.028. [DOI] [PubMed] [Google Scholar]
- 2.Li F, Zuo S, Yu P, Zhou B, Wang L, Liu C, Wei H, Xu H. Distribution and expression of the enterotoxin genes ofBacillus cereusin food products from Jiangxi Province, China. Food Control. 2016;67:155–162. [Google Scholar]
- 3.Lucking G, Stoeckel M, Atamer Z, Hinrichs J, Ehling-Schulz M. Characterization of aerobic spore-forming bacteria associated with industrial dairy processing environments and product spoilage. Int. J. Food Microbiol. 2013;166(2):270–279. doi: 10.1016/j.ijfoodmicro.2013.07.004. [DOI] [PubMed] [Google Scholar]
- 4.Schlegelova J, Brychta J, Klimova E, Napravnikova E, Babak V. The prevalence of and resistance to antimicrobial agents ofBacillus cereusisolates from foodstuffs. Vet. Med. Czech Republic. 2003;48:331–338. [Google Scholar]
- 5.Turnbull P.C.B, Sirianni N.M, LeBorn C.I, Samaan M.N, Sutton F.N, Reyes A.E, Peruski L.F. MICs of selected antibiotics forBacillus anthracis Bacillus cereus Bacillus thuringiensisandBacillus mycoidesfrom range of clinical and environmental sources as determined by the Etest. J. Clin. Microbiol. 2004;42:3626–3634. doi: 10.1128/JCM.42.8.3626-3634.2004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Whong C.M.Z, Kwaga J.K.P. Antibiogram ofBacillus cereusisolates from some Nigerian foods. Niger. Food J. 2007;25:178–183. [Google Scholar]
- 7.Kursun O, Guner A, Ozmen G. Prevalence ofBacillus cereusin rabbit meat consumed in Burdur-Turkey, its enterotoxin producing ability and antibiotic susceptibility. Kafkas Univ. Vet. Fakultesi Derg. 2011;17:S31–S35. [Google Scholar]
- 8.Kumari S, Sarkar P.K. Bacillus cereushazard and control in industrial dairy processing environment. Food Control. 2016;69:20–29. [Google Scholar]
- 9.Kumari S, Sarkar P.K. Prevalence and characterization ofBacillus cereusgroup from various marketed dairy products in India. Dairy Sci. Technol. 2014b;94(5):483–497. [Google Scholar]
- 10.Rhodehamel E.J, Harmon S.M. Bacillus cereus. In: Jackson G.J, Merker R.I, Bandler R, editors. Bacteriological Analytical Mannual, Centre for food safety and Applied Nutrition. MD USA: U.S, Food and Drug Administration, College Park; 2001. [Last accessed on 21-07-2017]. Available from: http://www.cfsan.fda.gov/~ebam-14.html . [Google Scholar]
- 11.Clause D, Berkeley R.C.W. In: GenusBacillus. Bergy's Manual of Systemic Bacteriology. Sneath P.H.A, editor. Vol. 2. Baltimore, Md: The Williams and Wilkins Co; 1986. pp. 1105–1139. [Google Scholar]
- 12.Jha N.K, Narayan K.G. Biotyping ofBacillus cereusisolates. J. Food Sci. Technol. 1995;32:231–232. [Google Scholar]
- 13.Bauer A.W, Kerby W.M, Sherris J.C, Truck M. Antibiotic susceptibility testing by a standardized single disc method. Am. J. Pathol. 1966;45:493–496. [PubMed] [Google Scholar]
- 14.Clinical and Laboratory Standards Institute (CLSI) Performance standards for antimicrobial disk susceptibility tests. Vol. 27. Wayne, Pennsylvania, USA: Clinical and Laboratory Standards Institute; 2007. [Google Scholar]
- 15.Altaf M.S, Hussain S.A, Ahmad C.R, Willayat M.M, Imtiyaz A.H, Bhat S. A study on the prevalence ofBacillus Cereusemetic strains in raw milk in and around Srinagar city of J&K. Biomed. Pharmacol. J. 2011;4(1):181–188. [Google Scholar]
- 16.Sharma C.S, Sharma D.K, Gill J.P.S, Aulakh R.S, Sharma J.K. Bacillus cereusfrom foods of animal origin in India and its public health significance. Acta Vet. Scand. 2003;44:118. [Google Scholar]
- 17.Hassan G.M, Mal-Ashmawy M.A, Meshref A.M.S, Afify S.I. Studies on enterotoxigenicBacillus cereusin raw milk and some dairy products. J. Food Saf. 2010;30:569–583. [Google Scholar]
- 18.Lin S, Scraft H, Odumeru J.A, Griffths M.W. Identification of contamination sources ofBacillus cereusin Pasteurized milk. Int. J. Food Microbiol. 1998;43:159–171. doi: 10.1016/s0168-1605(98)00105-6. [DOI] [PubMed] [Google Scholar]
- 19.TeGiffel M.C, Beumer R.R, Bonestroo M.H, Rombouts F.M. Incidence and characterization ofBacillus cereusin two dairy processing plants. Netherl MiIk Dairy J. 1996;50:479–492. [Google Scholar]
- 20.Yadav R. Biotyping and Serotyping ofBacillus cereusIsolated from Rice and Chowmein. Ranchi (Bihar): Phd. Thesis Submitted to Birsa Agricultural University; 1993. [Google Scholar]
- 21.Willayat M.M. Studies onBacillus CereusEnterotoxins and the Pathogenesis”. Ranchi, Bihar: Ph.D. Thesis Submitted to Birsa Agricultural University; 1997. [Google Scholar]
- 22.Javed A.H. Studies on Prevalence of Heat Stable Strains of Bacillus cereus in Milk and Rice“. M.V.Sc Thesis Submitted to SKUAST-Kashmir, J &K; 2001. [Google Scholar]
- 23.Hafeez Y, Iqbal A, Ahmad M. Biotyping ofBacillus cereusfrom the street vended foods in Srinagar area of Kashmir, India. Vet. World. 2012;5(10):590–593. [Google Scholar]
- 24.Umar A.S, Yerima M.B, Uzal U. Antimicrobial sensitivities ofBacillus cereusisolated from food samples sold in Bauchi metropolis toselected antibiotics. Niger. J. Microbiol. 2006;20(1):655–661. [Google Scholar]