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Asian Jr. of Microbiol. Biotech. Env. Sc. Vol. 14, No. (1) : 2012 : 13-18
© Global Science Publications
INCIDENCE AND ANTIBIOTIC SENSITIVITY OF BACILLUS
CEREUS ISOLATED FROM READY TO EAT FOODS SOLD IN
SOME MARKETS IN PORTHARCOURT, RIVERS STATE, NIGERIA
O. K. AGWA, C.I. UZOIGWE AND E.C. WOKOMA
Department of Microbiology, University of Port Harcourt, Rivers State, Nigeria
Department of Crop and Soil Science, Faculty of Agriculture, University of Port Harcourt, Nigeria
(Received 20 August 2011; Accepted 30 September 2011)
Key words : Antibiotic sensitivity, Bacillus cereus isolates, Microbiological standards, Ready-to-eat indigenous
Abstract - Sixty-four food samples of “cooked rice”, “masa”, “agidi” and “epiti” purchased from local
markets in Obio-Akpor Local Government Area of Port Harcourt, Nigeria were examined
microbiologically. Plate count analysis on mannitol egg-yolk bromothymol blue polymyxin B (MYP) agar
revealed that “cooked rice” had the highest frequency of occurrence of Bacillus cereus isolates (29.51%),
“masa” (26.23%), “agidi” (22.95%) and “epiti” had the least frequency of 21.31%. All Bacillus cereus
isolates tested were found to be susceptible to rifampin (30µg), chloramphenicol (20µg), erythromycin
(30µg), ciprofloxacin (10µg), streptomycin (30µg), gentamycin (10µg) and lincocin (30µg) and 100%
resistance against norfloxapin (30ug), floxapen (30µg) and ampiclox (30µg). The study unveils the
presence of Bacillus cereus in food samples sold in Port Harcourt especially in ‘cooked rice” and “masa”
which may pose serious threat to the health of consumers and should not be ignored.
*Corresponding author - Obioma Agwa, E-mail : o_agwa@yahoo.com
INTRODUCTION
Present economic conditions have resulted in
situations, where food vending has become
increasingly important in most countries;
contributing significant income inflow for
households involved in selling these foods
(Mosupye and vonholy, 1999; FAO/WHO, 2003;
FAO/WHO, 2005 ). Hygiene and sanitation practices
obtained during preparation and marketing of
these foods provide ample opportunities for the
proliferation of these food with food-borne
pathogens (Desai and Varadaraj, 2009). Among the
food- borne pathogens, strains of Bacillus cereus are
of significance because of its ubiquitous nature and
ability to occur in a wide range of foods (Ehling-
schulz, et al., 2004a; Oguntoyinbo and Oni, 2004;
Reyes et al., 2007).
The unique properties of Bacillus cereus includes
heat resistant endospore forming ability, toxin
production in varieties of foods and the psychro-
trophic nature makes the organism a prime cause
of public health hazard (Griffith and Schraft, 2002;
Dierick et al., 2005). Bacilli cause symptoms leading to
illness, relatively mild lasting up to 24h, but could
be severe leading to hospitalisation and in some
cases death. The organism is found in a wide range
of habitat including air, water, dust and soil, from
where spores are introduced into cereal crops,
vegetables, animal hair, fresh water and sediments.
Raw plant foods especially rice, potatoes, beans,
peas, and spices are the most common sources of
Bacillus cereus (Eglezos et al., 2010). The occurrence of
the organism within the environment enables it to
enter the food chain through raw materials and is
a major problem in convenience foods and mass
catering (Beathe and William, 2000; Jensen et al.,
2005; Guinebretiere et al., 2006). Because of the role
of microorganisms in spreading diseases, the need
to assess the safety and quality of foods is very
important, in order to ensure safety of supply,
clean, wholesome and high quality delivery to the
public. When the food hygiene system fails, a
batch of food is contaminated with high level
microbes potential for food borne disease outbreak,
its distribution cannot be controlled, changes in
14 AGWA ET AL.
public health and deterioration and increases
susceptibility rate (Sahota et al., 2008).
In several studies that have been conducted on
the incidence of food-borne pathogens, emphasis
had been on Bacillus cereus (Yusuf et al., 1992; Umoh
and Odoba, 1999; Umar et al., 2006; Desai and
Varadaraj, 2009). The microbiological safety of foods
sold in the market is of major concern because of the
environment in which they are prepared, often in
places that may have poor sanitation, coupled with
use of containers which expose the food to
numerous potential contaminants such as heavy
metals and pesticides. Some of the food samples
have been tested for various microorga-nisms of
public health concern and Bacillus cereus was among
them (Tomlins et al., 2004).
This study was carried out to evaluate the
presence of Bacillus cereus in ready- to -foods
purchased from markets in Port Harcourt and
characterize the organism isolated in terms of
biochemical reaction and antibiotic susceptibility.
MATERIALS AND METHODS
Sampling site and collection
A total of sixty four food samples being sold in
various sales points in urban markets at Mile I,
Mile III, Oil mill, and Rumuokoro areas of Port
Harcourt were enumerated for the viable counts of
Bacillus cereus. The food samples comprised of
Sixteen samples each of “cooked rice”, “masa”,
“agidi” and “epiti”(cereal preparation) were
collected from the food vendors in sterile
disposable polyethylene bags brought to
laboratory for microbiological analysis. Analysis of
samples were performed within 60mins of
collection
Table 1. Ingredients of the food samples analysed
Samples Ingredients
Cooked rice Rice, meat, groundnut oil,
Seasonings(salt, onions, pepper,
tomato paste)
Masa Rice and raw milk
Agidi Powdered corn grain & seasonings
Epiti Powdered corn grain, plantain flour,
palmoil, seasonings.
Enumeration of Bacillus cereus
A homogeneous sample was prepared with 10g of
food sample, aseptically transferred into 90mL of
tryptone broth to give an initial 1:10 dilution.
Aliquots of 0.1mL from 10-5dilutions were surface
plated on sterile dried Mannitol egg-yolk
bromothymol blue polymyxin B (MYP) agar plates.
The plates were incubated at 37C for 24h examined,
then left for another 24h at room temperature and
re-examined. Sixteen presumptive colonies of
Bacillus cereus were randomly selected and counted
based on characteristic colony feature. The colonies
were purified on freshly prepared MYP agar plates.
After incubation, typical colonies of bluish green -
blue colonies with zones of egg yolk precipitate on
the medium were picked, streaked out to obtain
pure cultures and finally maintained on nutrient
agar slopes in the refrigerator (4C). The
presumptive isolates were identified by
morphological characteristics. The morphological
test includes appearance of cell, shape and
pigmentation. Further identification of the
organisms using biochemical characteristics are
Gram’s reaction, position of spores, motility, citrate
utilisation, oxidase, indoleproduction, urease,
voges-proskauer reaction, hydrolysis of starch,
nitrate reduction, gelatine hydrolysis, production
of gasandacid from glucose, sucrose, mannitol and
lactose (Cappuccino and Sherman, 2004).
Antibiotic sensitivity test
All Bacillus cereus isolates were tested for their
sensitivity to antibiotics by means of a disc
diffusion method (Bauer et al., 1966). The organisms
were investigated using antibiotics disc containing
rifampin (10µg), chloramphenicol (20µg),
erythromycin (30µg), ciprofloxacin (10µg),
streptomycin (30µg), gentamycin (10µg) ), floxapen
(30µg), ampiclox (30µg), norfloxapin (30ug),and
lincocin (30µg). The antibiotics disc were
spaciously placed on Mueller - Hinton agar plates
previously seeded with 6h-broth cultures of
Bacillus cereus isolates. The plates were incubated
at 37o
C for18-24h. The different zones of inhibition
were measured to the nearest millimetre and
interpreted as sensitive, moderate sensitive and
resistant based on the interpretation table
recommended by the disc manufacturer (Oxoid,
1998).
RESULTS
The results of Bacillus cereus in some cereal based
ready to eat foods sold in Port Harcourt is depicted
15Incidence and Antibiotic Sensitivity of Bacillus Cereus Isolated from Ready to Eat Foods Sold in
in Fig. 1 and Table 2. Among the various markets
sampled, Oil mill market had the highest microbial
load of the organism, followed by rumuokoro, mile
3 and finally mile 1 market. A total of sixty-four
food samples “cooked rice”, “masa”, “agidi” and
“epiti” were assessed. The average count from the
food samples showed that about 7.2 x 105cfu/mL
were obtained from cooked rice, 6.4 x105cfu/mL
from masa, 5.6 x 105cfu/mL from agidi and 5.3 x
105cfu/mL from epiti. Sixteen presumptive colonies
of Bacillus cereus isolated revealed an irregular edge,
large, flat, rough bluish green to blue colonies with
zones of egg yolk precipitate. Antibiotic sensitivity
test of the isolates determined by the disc diffusion
method in accordance with the instructions of the
antibiotics disc manufacturer are shown in Table 3.
The isolates were highly resistant to ampiclox,
norfloxacin & floxapen, sensitive to erythromycin,
chloramphenicol, streptomycin rifampin and
ciprofloxacin and less sensitive to lincocin and
gentamycin.
Table 2. Cumulative plate count and total percentage
from various food samples
S/No Sample No. of Total % total
tested samples counts
(x106cfu/g)
1 CR 16 72 29.51
2 MS 16 64 26.23
3 AG 16 56 22.95
4 EP 16 52 21.31
Total 64 244 100
Keys: CR = cooked rice, MS = masa,
AG = agidi; EP = epiti
DISCUSSION
The public health significance of Bacillus cereus is of
high concern in view of the organism being
implicated in a number of food poisoning
outbreaks. The isolation of Bacillus cereus from all
the food samples could be explained by the
ubiquitous distribution of this organism and its
ability to form endospores (Kotiranta et al., 2000;
McKillip, 2000). A total of 64 samples (cooked rice,
masa, agidi and epiti) were analysed. From the
results obtained in the study, there were high
contamination levels of Bacillus cereus found in
cooked rice (7.2×105cfu/g) this is not surprising
because the organism is a normal flora of rice
followed by Masa (6.4×105cfu/g), a cereal
preparation from rice which harbour the
organism naturally with total percentage count of
26.23%. Masa was followed by agidi with 5.6 × 105
cfu/g and a total percentage count of 22.95% and
lastly epiti (5.3×105cfu/g) with total percentage
count of 21.31%. The variations in the value of
bacterial count percentages may be attributed to
numerous contaminations potential of the
organism, as most of the food samples were
prepared in places with poor sanitation practices,
poor storage and transport conditions. In most
cases, food vendors do not have adequate bathing
facilities, atimes starts their day without taking a
bath, therefore foods and ingredients are exposed to
repeated contamination from unwashed hands
and materials used for wrapping such as leaves,
newspaper and reusable polyethylene bags.
Purchasing ready-to-eat foods from markets
exposes one to a considerable risk of public health
due to poor hygiene practices (Mosupye and
Vonholy, 1999; Ehirim et al., 2001; FAO/WHO, 2003;
FAO/WHO, 2005). Agidi and epiti which had the
lowest percentage of the isolates could be attributed
to the method of processing the corn grain and
plantain (drying on moderately clean floor and
machine milling) (AOAC, 1995). The limited time &
temperature exposure during agidi preparation is
equally insufficient to destroy Bacillus cereus spores.
Bacillus cereus food poisoning is principally
associated with temperature abuse during the
storage of food. Temperature abuse can result in
spore germination and multiplication of the
vegetative cells leading to hazardous levels of
vegetative cells or toxins in the food at the time of
consumption (Granum, 2001). The extreme
resistance of the spores of this pathogen to heat,
desiccation, sanitizers and irradiation contributes
to their distribution, survival and persistence
within the entire food chain from raw agricultural
commodities to finished retailed products (Eglezos
et al., 2010)
The results of the antibiotic susceptibility of the
isolates are shown in Table 2. The antibiotic
susceptibility was determined by the disc agar
diffusion method in accordance with the instru-
ctions of the antibiotic disc manufacture (Oxoid).
All the Bacillus cereus isolates were susceptible to
Streptomycin (100%) Chloramphenicol (100%),
Rifampin (100%), Erythromycin (100%) and
Ciprofloxacin (100%) Gentamycin (100%) and less
sensitive to Lincocin (82%).
The findings of the present study correspond
16 AGWA ET AL.
with those obtained by other researchers (Umar et
al., 2006; Whong and Kwaga, 2007). Previous works
have shown that antimicrobial susceptibility of
Bacillus cereus were highly susceptible to
streptomycin, chloramphenicol, erythromycin,
ciprofloxacin, and less susceptible to ampicillin,
ampiclox, cotrimazole, cloxacillin (Umar, et al.,
2006). Variations in the percentages may be due to
the differences in the concentrations of antimicro-
bial agents used, differences in the source of
isolates, drug resistance transfer and the overall
wide spread use of the antibiotics in the
environment. The development of drug resistance
may be due to the use of these drugs in medical and
veterinary practice to treat infections and misuse of
the drugs in the society, such practices can lead to
drug resistance strains.The antimicrobial pattern
of resistance of Bacillus cereus from foods is useful
in epidemiological studies but its effectiveness
decreases due to the negligence in utilisation policy
Table 3. Antimicrobial sensitivities of Bacillus cereus isolates from food sample
Antibiotics (conc/µg) Food samples
Zones of inhibition in diameter mm status
CR AG EP MS
Rifampin (10µg) 32(S) 38(S) 32(S) 29(S)
Erythromycin (30µg) 28(S) 23(R) 26(S) 32(S)
Ampiclox (30µg) - - - -
Chloramphenicol (20µg) 40(S) 31(S) 31(S) 30(S)
Norfloxacin (30µg) - - - -
Streptomycin (30µg) 34(S) 40(S) 34(S) 26(S)
Gentamycin (10µg) 20(MS) 30(S) 24(S) 28(S)
Lincocin (30µg) 20(MS) 28(S) 30(S) 20(MS)
Floxapen (30µg) - - - -
Ciprofloxacin (10µg) 27(S) 23(S) 30(S) 27(S)
Bauer et al., (1966)
Keys: CR = Cooked rice ; AG = Agidi ; S = Sensitive ; EP = Epiti ; R = Resistant;
MS = Masa ; MS = Moderately Sensitive
Fig. 1 Distribution of the food samples within the markets analyzed
17Incidence and Antibiotic Sensitivity of Bacillus Cereus Isolated from Ready to Eat Foods Sold in
(Whong and Kwaga, 2007).
The following strategies should be undertaken to
control this pathogen: ensuring adequate
temperature (75o
C) is reached during cooking of
food, hot foods should be kept hot (maintained at a
temperature greater or equal to 63o
C) and cold
foods should be kept cold (maintained at
temperature less than or equal to 5o
C) to prevent
multiplication and toxin production. Training to
help food vendors to comply with regulations and
implement safe food handling practice; improve in
the equipments used to prepare and serve foods
and education campaign to increase consumer’s
awareness about nutrition and safety of foods.
CONCLUSION
Food samples sold in markets are operating in less
than an acceptable and satisfactory environment;
efforts should be made to improve the safety of
street-vended foods. Illness associated with these
food products may be under reported, overlooked
and ignored, a few of the affected seek medical
attention owing to the mild nature and short
duration of symptoms. This must be taken
seriously as might lead to the release of toxins into
the body causing severe damage to the internal
organs and can eventually lead to death. Based on
the result, the effective antibiotic against Bacillus
cereus isolates are streptomycin, chloramphenicol,
rifampin, erythromycin, cipfloxacin and
gentamycin. Food-borne problems pose a serious
threat to human health, the economy of
individuals, families and nations. To ensure the
safety of food, Hazard Analysis and Critical
Control Point (HACCP) must be applied from the
primary producer to final consumption and its
implementation. Their control requires effort on the
part of the Government, food industry (vendors)
and consumers to meet the challenges of the future.
REFERENCES
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confirmation. Microbiological methods, AOAC
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Fundamentals and Frontiers (Eds. Doyle, M.P.,
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poisoning. In: Food borne Diseases, Cliver, D.O. and
Riemann, H.P. (Eds) Academic press, London. pp
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novel duplex PCR system. FEMS Microbiology
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18 AGWA ET AL.
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Food Control. 3 : 150-155.
—❋❋❋—

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Microbiology biotechnology-environment-science

  • 1. Asian Jr. of Microbiol. Biotech. Env. Sc. Vol. 14, No. (1) : 2012 : 13-18 © Global Science Publications INCIDENCE AND ANTIBIOTIC SENSITIVITY OF BACILLUS CEREUS ISOLATED FROM READY TO EAT FOODS SOLD IN SOME MARKETS IN PORTHARCOURT, RIVERS STATE, NIGERIA O. K. AGWA, C.I. UZOIGWE AND E.C. WOKOMA Department of Microbiology, University of Port Harcourt, Rivers State, Nigeria Department of Crop and Soil Science, Faculty of Agriculture, University of Port Harcourt, Nigeria (Received 20 August 2011; Accepted 30 September 2011) Key words : Antibiotic sensitivity, Bacillus cereus isolates, Microbiological standards, Ready-to-eat indigenous Abstract - Sixty-four food samples of “cooked rice”, “masa”, “agidi” and “epiti” purchased from local markets in Obio-Akpor Local Government Area of Port Harcourt, Nigeria were examined microbiologically. Plate count analysis on mannitol egg-yolk bromothymol blue polymyxin B (MYP) agar revealed that “cooked rice” had the highest frequency of occurrence of Bacillus cereus isolates (29.51%), “masa” (26.23%), “agidi” (22.95%) and “epiti” had the least frequency of 21.31%. All Bacillus cereus isolates tested were found to be susceptible to rifampin (30µg), chloramphenicol (20µg), erythromycin (30µg), ciprofloxacin (10µg), streptomycin (30µg), gentamycin (10µg) and lincocin (30µg) and 100% resistance against norfloxapin (30ug), floxapen (30µg) and ampiclox (30µg). The study unveils the presence of Bacillus cereus in food samples sold in Port Harcourt especially in ‘cooked rice” and “masa” which may pose serious threat to the health of consumers and should not be ignored. *Corresponding author - Obioma Agwa, E-mail : o_agwa@yahoo.com INTRODUCTION Present economic conditions have resulted in situations, where food vending has become increasingly important in most countries; contributing significant income inflow for households involved in selling these foods (Mosupye and vonholy, 1999; FAO/WHO, 2003; FAO/WHO, 2005 ). Hygiene and sanitation practices obtained during preparation and marketing of these foods provide ample opportunities for the proliferation of these food with food-borne pathogens (Desai and Varadaraj, 2009). Among the food- borne pathogens, strains of Bacillus cereus are of significance because of its ubiquitous nature and ability to occur in a wide range of foods (Ehling- schulz, et al., 2004a; Oguntoyinbo and Oni, 2004; Reyes et al., 2007). The unique properties of Bacillus cereus includes heat resistant endospore forming ability, toxin production in varieties of foods and the psychro- trophic nature makes the organism a prime cause of public health hazard (Griffith and Schraft, 2002; Dierick et al., 2005). Bacilli cause symptoms leading to illness, relatively mild lasting up to 24h, but could be severe leading to hospitalisation and in some cases death. The organism is found in a wide range of habitat including air, water, dust and soil, from where spores are introduced into cereal crops, vegetables, animal hair, fresh water and sediments. Raw plant foods especially rice, potatoes, beans, peas, and spices are the most common sources of Bacillus cereus (Eglezos et al., 2010). The occurrence of the organism within the environment enables it to enter the food chain through raw materials and is a major problem in convenience foods and mass catering (Beathe and William, 2000; Jensen et al., 2005; Guinebretiere et al., 2006). Because of the role of microorganisms in spreading diseases, the need to assess the safety and quality of foods is very important, in order to ensure safety of supply, clean, wholesome and high quality delivery to the public. When the food hygiene system fails, a batch of food is contaminated with high level microbes potential for food borne disease outbreak, its distribution cannot be controlled, changes in
  • 2. 14 AGWA ET AL. public health and deterioration and increases susceptibility rate (Sahota et al., 2008). In several studies that have been conducted on the incidence of food-borne pathogens, emphasis had been on Bacillus cereus (Yusuf et al., 1992; Umoh and Odoba, 1999; Umar et al., 2006; Desai and Varadaraj, 2009). The microbiological safety of foods sold in the market is of major concern because of the environment in which they are prepared, often in places that may have poor sanitation, coupled with use of containers which expose the food to numerous potential contaminants such as heavy metals and pesticides. Some of the food samples have been tested for various microorga-nisms of public health concern and Bacillus cereus was among them (Tomlins et al., 2004). This study was carried out to evaluate the presence of Bacillus cereus in ready- to -foods purchased from markets in Port Harcourt and characterize the organism isolated in terms of biochemical reaction and antibiotic susceptibility. MATERIALS AND METHODS Sampling site and collection A total of sixty four food samples being sold in various sales points in urban markets at Mile I, Mile III, Oil mill, and Rumuokoro areas of Port Harcourt were enumerated for the viable counts of Bacillus cereus. The food samples comprised of Sixteen samples each of “cooked rice”, “masa”, “agidi” and “epiti”(cereal preparation) were collected from the food vendors in sterile disposable polyethylene bags brought to laboratory for microbiological analysis. Analysis of samples were performed within 60mins of collection Table 1. Ingredients of the food samples analysed Samples Ingredients Cooked rice Rice, meat, groundnut oil, Seasonings(salt, onions, pepper, tomato paste) Masa Rice and raw milk Agidi Powdered corn grain & seasonings Epiti Powdered corn grain, plantain flour, palmoil, seasonings. Enumeration of Bacillus cereus A homogeneous sample was prepared with 10g of food sample, aseptically transferred into 90mL of tryptone broth to give an initial 1:10 dilution. Aliquots of 0.1mL from 10-5dilutions were surface plated on sterile dried Mannitol egg-yolk bromothymol blue polymyxin B (MYP) agar plates. The plates were incubated at 37C for 24h examined, then left for another 24h at room temperature and re-examined. Sixteen presumptive colonies of Bacillus cereus were randomly selected and counted based on characteristic colony feature. The colonies were purified on freshly prepared MYP agar plates. After incubation, typical colonies of bluish green - blue colonies with zones of egg yolk precipitate on the medium were picked, streaked out to obtain pure cultures and finally maintained on nutrient agar slopes in the refrigerator (4C). The presumptive isolates were identified by morphological characteristics. The morphological test includes appearance of cell, shape and pigmentation. Further identification of the organisms using biochemical characteristics are Gram’s reaction, position of spores, motility, citrate utilisation, oxidase, indoleproduction, urease, voges-proskauer reaction, hydrolysis of starch, nitrate reduction, gelatine hydrolysis, production of gasandacid from glucose, sucrose, mannitol and lactose (Cappuccino and Sherman, 2004). Antibiotic sensitivity test All Bacillus cereus isolates were tested for their sensitivity to antibiotics by means of a disc diffusion method (Bauer et al., 1966). The organisms were investigated using antibiotics disc containing rifampin (10µg), chloramphenicol (20µg), erythromycin (30µg), ciprofloxacin (10µg), streptomycin (30µg), gentamycin (10µg) ), floxapen (30µg), ampiclox (30µg), norfloxapin (30ug),and lincocin (30µg). The antibiotics disc were spaciously placed on Mueller - Hinton agar plates previously seeded with 6h-broth cultures of Bacillus cereus isolates. The plates were incubated at 37o C for18-24h. The different zones of inhibition were measured to the nearest millimetre and interpreted as sensitive, moderate sensitive and resistant based on the interpretation table recommended by the disc manufacturer (Oxoid, 1998). RESULTS The results of Bacillus cereus in some cereal based ready to eat foods sold in Port Harcourt is depicted
  • 3. 15Incidence and Antibiotic Sensitivity of Bacillus Cereus Isolated from Ready to Eat Foods Sold in in Fig. 1 and Table 2. Among the various markets sampled, Oil mill market had the highest microbial load of the organism, followed by rumuokoro, mile 3 and finally mile 1 market. A total of sixty-four food samples “cooked rice”, “masa”, “agidi” and “epiti” were assessed. The average count from the food samples showed that about 7.2 x 105cfu/mL were obtained from cooked rice, 6.4 x105cfu/mL from masa, 5.6 x 105cfu/mL from agidi and 5.3 x 105cfu/mL from epiti. Sixteen presumptive colonies of Bacillus cereus isolated revealed an irregular edge, large, flat, rough bluish green to blue colonies with zones of egg yolk precipitate. Antibiotic sensitivity test of the isolates determined by the disc diffusion method in accordance with the instructions of the antibiotics disc manufacturer are shown in Table 3. The isolates were highly resistant to ampiclox, norfloxacin & floxapen, sensitive to erythromycin, chloramphenicol, streptomycin rifampin and ciprofloxacin and less sensitive to lincocin and gentamycin. Table 2. Cumulative plate count and total percentage from various food samples S/No Sample No. of Total % total tested samples counts (x106cfu/g) 1 CR 16 72 29.51 2 MS 16 64 26.23 3 AG 16 56 22.95 4 EP 16 52 21.31 Total 64 244 100 Keys: CR = cooked rice, MS = masa, AG = agidi; EP = epiti DISCUSSION The public health significance of Bacillus cereus is of high concern in view of the organism being implicated in a number of food poisoning outbreaks. The isolation of Bacillus cereus from all the food samples could be explained by the ubiquitous distribution of this organism and its ability to form endospores (Kotiranta et al., 2000; McKillip, 2000). A total of 64 samples (cooked rice, masa, agidi and epiti) were analysed. From the results obtained in the study, there were high contamination levels of Bacillus cereus found in cooked rice (7.2×105cfu/g) this is not surprising because the organism is a normal flora of rice followed by Masa (6.4×105cfu/g), a cereal preparation from rice which harbour the organism naturally with total percentage count of 26.23%. Masa was followed by agidi with 5.6 × 105 cfu/g and a total percentage count of 22.95% and lastly epiti (5.3×105cfu/g) with total percentage count of 21.31%. The variations in the value of bacterial count percentages may be attributed to numerous contaminations potential of the organism, as most of the food samples were prepared in places with poor sanitation practices, poor storage and transport conditions. In most cases, food vendors do not have adequate bathing facilities, atimes starts their day without taking a bath, therefore foods and ingredients are exposed to repeated contamination from unwashed hands and materials used for wrapping such as leaves, newspaper and reusable polyethylene bags. Purchasing ready-to-eat foods from markets exposes one to a considerable risk of public health due to poor hygiene practices (Mosupye and Vonholy, 1999; Ehirim et al., 2001; FAO/WHO, 2003; FAO/WHO, 2005). Agidi and epiti which had the lowest percentage of the isolates could be attributed to the method of processing the corn grain and plantain (drying on moderately clean floor and machine milling) (AOAC, 1995). The limited time & temperature exposure during agidi preparation is equally insufficient to destroy Bacillus cereus spores. Bacillus cereus food poisoning is principally associated with temperature abuse during the storage of food. Temperature abuse can result in spore germination and multiplication of the vegetative cells leading to hazardous levels of vegetative cells or toxins in the food at the time of consumption (Granum, 2001). The extreme resistance of the spores of this pathogen to heat, desiccation, sanitizers and irradiation contributes to their distribution, survival and persistence within the entire food chain from raw agricultural commodities to finished retailed products (Eglezos et al., 2010) The results of the antibiotic susceptibility of the isolates are shown in Table 2. The antibiotic susceptibility was determined by the disc agar diffusion method in accordance with the instru- ctions of the antibiotic disc manufacture (Oxoid). All the Bacillus cereus isolates were susceptible to Streptomycin (100%) Chloramphenicol (100%), Rifampin (100%), Erythromycin (100%) and Ciprofloxacin (100%) Gentamycin (100%) and less sensitive to Lincocin (82%). The findings of the present study correspond
  • 4. 16 AGWA ET AL. with those obtained by other researchers (Umar et al., 2006; Whong and Kwaga, 2007). Previous works have shown that antimicrobial susceptibility of Bacillus cereus were highly susceptible to streptomycin, chloramphenicol, erythromycin, ciprofloxacin, and less susceptible to ampicillin, ampiclox, cotrimazole, cloxacillin (Umar, et al., 2006). Variations in the percentages may be due to the differences in the concentrations of antimicro- bial agents used, differences in the source of isolates, drug resistance transfer and the overall wide spread use of the antibiotics in the environment. The development of drug resistance may be due to the use of these drugs in medical and veterinary practice to treat infections and misuse of the drugs in the society, such practices can lead to drug resistance strains.The antimicrobial pattern of resistance of Bacillus cereus from foods is useful in epidemiological studies but its effectiveness decreases due to the negligence in utilisation policy Table 3. Antimicrobial sensitivities of Bacillus cereus isolates from food sample Antibiotics (conc/µg) Food samples Zones of inhibition in diameter mm status CR AG EP MS Rifampin (10µg) 32(S) 38(S) 32(S) 29(S) Erythromycin (30µg) 28(S) 23(R) 26(S) 32(S) Ampiclox (30µg) - - - - Chloramphenicol (20µg) 40(S) 31(S) 31(S) 30(S) Norfloxacin (30µg) - - - - Streptomycin (30µg) 34(S) 40(S) 34(S) 26(S) Gentamycin (10µg) 20(MS) 30(S) 24(S) 28(S) Lincocin (30µg) 20(MS) 28(S) 30(S) 20(MS) Floxapen (30µg) - - - - Ciprofloxacin (10µg) 27(S) 23(S) 30(S) 27(S) Bauer et al., (1966) Keys: CR = Cooked rice ; AG = Agidi ; S = Sensitive ; EP = Epiti ; R = Resistant; MS = Masa ; MS = Moderately Sensitive Fig. 1 Distribution of the food samples within the markets analyzed
  • 5. 17Incidence and Antibiotic Sensitivity of Bacillus Cereus Isolated from Ready to Eat Foods Sold in (Whong and Kwaga, 2007). The following strategies should be undertaken to control this pathogen: ensuring adequate temperature (75o C) is reached during cooking of food, hot foods should be kept hot (maintained at a temperature greater or equal to 63o C) and cold foods should be kept cold (maintained at temperature less than or equal to 5o C) to prevent multiplication and toxin production. Training to help food vendors to comply with regulations and implement safe food handling practice; improve in the equipments used to prepare and serve foods and education campaign to increase consumer’s awareness about nutrition and safety of foods. CONCLUSION Food samples sold in markets are operating in less than an acceptable and satisfactory environment; efforts should be made to improve the safety of street-vended foods. Illness associated with these food products may be under reported, overlooked and ignored, a few of the affected seek medical attention owing to the mild nature and short duration of symptoms. This must be taken seriously as might lead to the release of toxins into the body causing severe damage to the internal organs and can eventually lead to death. Based on the result, the effective antibiotic against Bacillus cereus isolates are streptomycin, chloramphenicol, rifampin, erythromycin, cipfloxacin and gentamycin. Food-borne problems pose a serious threat to human health, the economy of individuals, families and nations. To ensure the safety of food, Hazard Analysis and Critical Control Point (HACCP) must be applied from the primary producer to final consumption and its implementation. Their control requires effort on the part of the Government, food industry (vendors) and consumers to meet the challenges of the future. REFERENCES AOAC 1995. Bacillus cereus in foods. 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