Received Date: October 12, 2020; Accepted Date: October 27, 2020; Published Date: November 02, 2020
Citation: Alemu A, Addis M, Degefu H (2020) Identification, Antimicrobial Resistance Pattern and Community Knowledge, Attitude and Practices of Salmonella in Mizan Town, Ethiopia: Cross Sectional Study. Health Sci J. 14 No. 7: 779.
Salmonella is the leading cause of foodborne diseases worldwide. A crosssectional study was conducted between the periods of March and October 2019 at municipal abattoir and butcher houses of Mizan town, Ethiopia with the objectives to determine the prevalence, antimicrobial resistance pattern, risk factors and assess public awareness of Salmonella. A total of 320 samples consisting of 240 from abattoir and 80 from butcher houses were collected and examined for the presence of Salmonella using the procedures outlined by the International Organization for Standardization. The overall prevalence of Salmonella was found to be 13.4% (43/320). Out of a total isolates, 30/240 (12.5%) were isolated from abattoir source, of which 21/175 (12%) from carcass swab, 4/25 (16%) from abattoir personnel hand swab and 5/40 (12.5%) from abattoir materials swab while 13.3/80 (16.2%) from butcher houses source, of which 5/30 (16.6%) from butcher personnel hand swab and 8/50 (16%) from butcher materials swab. However, there was no statistically significant difference (P>0.05) in the prevalence of salmonella among sample source and type. Out of the total 43 isolates, 42(97.67%) were multiple antimicrobial resistant and the highest level of resistance was observed for ertrymycin (100). Multivariable logistic regression result showed that, materials which were not cleaned and people who didn’t know contamination as risk were the major risk factors for the occurrence of Salmonella among abattoir and butcher houses in the study area.Besides, the knowledge, attitude and practices of beef meat handlers were founded to be poor. Thus, urgent intervention program is essential to minimize the risk associated with consumption of beef meat contaminated with Salmonella and prudent use of antimicrobialsis recommended.
Abattoir; Antimicrobial; Butcher; Beef meat; Prevalence; Salmonella; Mizan
Salmonella is considered the most prevalent foodborne pathogen worldwide and has long been recognized as an important zoonotic microorganism of economic significance in animals and humans. Consumption of raw or unsafe food, crosscontamination, improper food storage, poor personal hygiene practices, inadequate cooling and reheating of food items, and a prolonged time lapse between preparing and consuming food items were mentioned as contributing factors to an outbreak of salmonellosis in humans . The ubiquity of Salmonella isolates creates a persistent contamination hazard in all raw foods and also in animal-origin food products, which are often implicated in sporadic cases and outbreaks of human salmonellosis .
Besides, antibiotic-resistant Salmonella infections of both human and animal is a concern, particularly in developing countries where the risk of infection is high because of unhygienic living conditions, close contact and sharing of houses between animals and humans [2,3].
In the study area there is much less information on the knowledge, attitudes and practices (KAP) around meat safety; the gender and social determinants of meat safety; or the relation between hazards in meat and health outcomes in consumers of meat in the country. In line with the aforementioned limitations in the study area the prevalence of Salmonella species andtheirantimicrobial resistance patternas well as the knowledge, attitude and practice of the community was not yet known. Therefore, this study was designed with the objectives to determine the prevalence and antimicrobial resistance pattern of Salmonella isolates from slaughtered cattle, personnel and materials in the abattoir and butcher houses, to observe risk factors associated for the occurrence of Salmonellaand to assess the knowledge, attitude and practice of meat value chain: abattoir workers and butchers on meat hygiene and safety.
Study period and area
The study was conducted between the periods of March and December 2019 in Bench Maji zone, at Mizan municipal abattoir and Butcher houses.
Study population and sampling
The study populations were all apparently healthy local indigenous zebu cattle which were brought to the abattoir for slaughtering. We were using systematic random sampling procedure to select our study animals to take swab sample from carcasses. Samples were also taken from cattle meat handlers (abattoir workers, butchers) and materials in contact with meat.
Sample size determination
For isolation and prevalence of Salmonella from carcass, sample size was calculated according to Thrusfield using 95% confidence level and 5% precision. The 12.5% expected prevalence  of Salmonella from carcass in agro ecologically similar study area, in Southwest, Ethiopia was used.
For questionnaire survey, observation, personnel hand swab and material samples, the sample size was determined purposively based on the willingness of the interviewees, ease for follow up, the total number of persons engaged and the availability of materials to be sampled in the abattoir and butcher houses. Accordingly, 145 samples were taken.
A cross-sectional study involving microbiological analysis, questionnaire survey and observational survey was employed.
Sampling technique and sample collection
A total of 320 samples consisting of 240 from Abattoir and 80 from Butcher houses were sampled. Systematic random sampling technique was used for carcass swabs and purposive sampling technique was used for personnel and materials swabs. Swabs from carcass were taken from the abdomen (flank), thorax (lateral), crutch, and breast (lateral) while both the right and left hands were swabbed for personnel hand swabs and all surfaces of the materials were swabbed thoroughly. All samples were labeled legibly with permanent marker identifying type/ source of sample and date of sampling. Finally, by using ice boxes with ice packs the samples were transported to Mizan Regional Veterinary Laboratory, South West Ethiopia.
Isolation and identification of Salmonella
Isolation and Identification of Salmonella organisms were carried out according to [6,7]. Accordingly, Non-selective preenrichment, Selective enrichment, Plating on selective media and Biochemical confirmation were used.
The swabs were directly inoculated into 10 ml buffered peptone water (BPW) in screw capped bottles and incubated at 37°C for 16-18 hrs. Each 25 ml of the swab content was inoculated into 225 ml of BPW and homogenized for two minutes with stomacher. After mixing thoroughly, the samples were incubated at 37°C for 16-18 hours .
From the pre-enrichment broth after incubation and thoroughly shaking, 0.1 ml of the broth was transferred into a tube containing 10 ml of Rappaport-Vassiliadis medium (RV broth). Then 1 ml of the pre-enrichment broth was transferred into a tube containing 10 ml of Selenite broth (SB broth). The inoculated RV broth was incubated at 41.5°C ± 1°C for 24 ± 3 hours and the inoculated SB broth at 37°C ± 1°C for 24 ± 3 hours .
Plating and identification
Xylose lysine desoxycholate (XLD) agar plate was used for plating and identification purpose. A loop-full of inoculum each from the RV and SB broth was transferred and streaked separately onto the surface of XLD agar. The plates were incubated at 37°C ± 1°C for 24 ± 3 hours. The plates were examined for the presence of suspected Salmonella colonies, which on XLD agar were pink with a darker center and a lightly transparent zone of reddish color due to the color change of the indicator whereas lactose positive Salmonellae were yellow with or without blackening. Presumptive colonies were transferred to nonselective solid media for further confirmatory tests. Confirmation was done by using biochemical test according to .
Triple sugar iron agar
A loopful culture of pure growth from nutrient agar was stabbed into the butt and streaked on the slant and incubated for 24 hours at 37°C. Typical Salmonella cultures showed alkaline (red) slants and acid (yellow) butts with gas production (bubbles) and formation of hydrogen sulfide (blackening of the agar) .
The isolates were inoculated into the urea to determine urease production. The inoculated tubes were incubated at 37°C for up to 96 hours. Then an observation was made at an interval of 4, 24, 48 and 96 hours. Urease positive cultures changed the color of the indicator to red.
Citrate utilization test
The colonies were cultured on the prepared Simmon’s citrate agar medium, incubated at 37°C for 48 hours and observations were recorded. Opacity and change in color of bromothymol from green to blue indicated a positive reaction.
Lysine decarboxylation medium
Lysine decarboxylation broth was inoculated with the loopful culture of the test organism and one was kept uninoculated control. Both tubes were incubated for 24 hours at 37°C. Turbidity and a purple color after incubation indicated a positive reaction. A yellow color indicated a negative reaction.
Peptone water was prepared and the ingredients were dissolved in distilled water, dispensed in test tubes and sterilized by autoclaving at 121°C for 15 minutes. The tubes of the medium were inoculated with test isolates using sterile platinum loop and incubated at 37°C aerobically for up to 96 hours. Finally, 0.5 ml of Kovac’s reagent was added to each of the inoculated and un-inoculated controls. The tubes were shaken gently and the results were recorded. Positive results were indicated by the development of red colour in the alcoholic layer of the reagent and no colour in the control tube.
Antimicrobial resistance pattern tests
The antimicrobial resistances testing of the isolates were performed by using the disc-diffusion method according to the recommendations of the National Committee for Clinical Laboratory Standards . Four to five well-isolated colonies from nutrient agar plates were transferred into tubes containing 5 ml of Tryptone soya broth (Oxoid, England). The broth culture was incubated at 37ºC for 4 hours until it achieved the 0.5 McFarland turbidity standards. Sterile cotton swab was dipped into the suspension, rotated several times, pressing firmly on the inside wall of the tube above the level to remove excess inoculums and swabbed uniformly over the surface of Muller Hinton agar plate (Oxiod, England). The plates were held at room temperature for 30 min to allow drying.
The resistance of the isolates were tested for the following antibiotic discs: Ampicillin (AMP) 2 μg, Oxicillin (OX) 5 μg, Gentamicin (HLG) 120 μg, Kanamycin (K) 5 μg, Ox tetracycline (O) 30 μg, Erythromycin (E) 5 μg, Neomycin (N) 30 μg and Penicillin G (P) 1 μg were placed at least 15 mm apart from the edge of the plates to prevent overlapping of the inhibition zones. The plates were incubated at 37ºC for 24 h. The diameter of the zones of inhibitions was compared with recorded diameters of the control organism E. coli ATCC 25922 and classified as resistant, intermediate, or susceptible according to the interpretive standards of the Clinical Laboratory Standards Institute .
Descriptive statistics such as frequency, percentage, and/or proportion were used for prevalence, antimicrobial resistance test, questionnaire survey and observation results. Chi-squire test was used to assess significant differences of Salmonella status between sample source and types while Binary Logistic regression (odds ratio) was used to assess the association of possible risk factors for the occurrence of Salmonellausing statistical package for social science (SPSS) version 20 software. The results with less than P-value of 0.05 were considered statistically significant.
The study was approved by the Research Ethics Committee and the letter of clearance was obtained from Jimma University College of Agriculture and veterinary Medicine, and Bench Maji zone administration office. The data was collected after written informed consent was made with all study participants. All the rights of privacy and confidentiality of participants were protected.
Over all occurrence of Salmonella
The overall prevalence of Salmonella in this study was found to be 13.4% (43/320) with prevalence of 12.5% in abattoir and 16.2% in butcher houses. Statistical analysis of the data showed that there was no statistically significant difference (P>0.05) on the prevalence of Salmonella between abattoir and butcher houses sources (Table 1).
Table 1 Proportion of Salmonella isolates from Abattoir and Butcher Houses.
|Source of samples||Number Examined||Prevalence (%)||χ2||P-value|
|Butcher house||80||13 (16.2)|
Occurrence of Salmonella isolates among sample types
The specific prevalence of Salmonella was found to be 12% in carcass swab, 16% in abattoir personnel hand swab, 12.5% in abattoir materials swab, 16.6% in butcher men hand swab and 16% in butcher materials swab.-The lowest prevalence was observed from carcasses samples among the others. The prevalence of Salmonella retrieval was not statistically significant (P>0.05) among the sample types (Table 2).
Table 2 Prevalence and Association of Salmonella Recovery between Sample Types.
|Sample type||Total Observation||Frequency of Positivity||Prevalence||χ2||P-value|
|Abattoir personnel hand swab||25||4||16%|
|Abattoir materials swab||40||5||12.5%|
|Butcher men hand swab||30||5||16.66%|
|Butcher materials swab||50||8||16%|
Antimicrobial resistance pattern test
Out of the total 43 isolates subjected to antimicrobial resistance test to 8 different antimicrobials, the highest level of resistance was observed for erythromycin (100%) followed by ampicillin (83.7%), oxacillin (72.09%) and neomycin (67.44%). All isolates were found to be susceptible to gentamycin (Table 3).
Table 3 Antimicrobial Resistance Pattern of Salmonella from Abattoir and Butcher Houses.
|Antimicrobials||Disc concentration (µg)||Number of isolates|
|Resistant (%)||Intermediate (%)||Susceptible (%)|
|Oxy tetracycline (O)||30||12(27.9)||-||31(72.09)|
|Penicillin G (P)||1||19(44.18)||17(39.53)||7(16.27)|
Out of the total isolates, 42/43 (97.67%) were resistance to at least one antimicrobial agents tested (Table 4).
Table 4 Multiple Antimicrobial Resistance Patterns of Salmonella
|No. Isolates with same pattern||Antimicrobial resistance pattern||No. of antimicrobials developed resistance|
|6||ERY,AMP ,KAN, PEN||4|
|3||N, ERY ,PEN ,KAN, AMP,OXY||6|
OXY: Ox tetracycline; ERY: Erythromycin; KAN: Kanamycin; AMP: Ampicillin; OX: Oxicillin; PEN: Penicillin; N: Neomycin
Occurrence of Salmonella among risk factors
Out of 145 purposive samples expected to be potential risk factors (abattoir worker=25, abattoir materials=40, butchers=30 and butcher house materials=50), a total of 22 (15.1%) Salmonella was isolated. The specific prevalence of Salmonella was found to be 16% (4/25), 12.5% (5/40), 16.6% (5/30) and 16% (8/50) respectively in abattoir workers, abattoir materials, butchers and butcher house materials.
The association of Salmonella recovery in personnel and materials with the possible risk factors by Univariable logistic regression reveled that; those personnel who were not educated (Illiterates) have 4.23 times more likely the chance of contaminating carcass than the other categories of educational status (95% CL: 0.966- 18.528:p=0.046), people who did not wash their hands during meat processing have 18.9 times more likely the chance of contaminating meat with Salmonella comparing with those who wash their hands at least before or after contact with meat/ equipment (95% CL: 2.292-155.82: p=0.006).
With regarding to cleaning equipment, those materials which have not been cleaned regularly have 3 times more likely the chance of contaminating meat than equipment that regularly washed (95% CL: 1.181-7.788 with p=0.021).While abattoir workers and butchers who did not knew contamination as risk have 22.7 times more likely the chance of cross contaminating carcasses in comparison to those who knew contamination as risk (95% CL: 7.367-70.180 with p=0.000) and also workers who used jewelry materials on their hands during meat processing have chance of 4.3 times more likely to contaminate meat comparing with those who did not used (95% CI 1.680-11.250 with p=0.002).
Job related training and personal hygiene were not significantly associated with the occurrence of Salmonella (p>0.05; table 5). All significantly associated variables (p<0.25) in univariable logistic regression analysis were taken to multivariable logistic regression analysis to control confounders.
Table 5 Univariable and Multivariable Logistic Regression analysis of the association of risk factors for the occurrence of salmonella among Abattoir and Butcher houses.
|Risk factors||Categories||Frequency||Positive No. (%)||Univariable||P-value||Multivariable||P-value|
|OR (95% CI)||OR (95% CI)|
|> grade 12||18||3(16.6)||**||**|
|Hand washing||before& after||28||2(7.1)||**||**|
|Manner of cleaning equipment||water&detergent||63||2(3.1)||**||**|
|Manner of hand washing||water&detergent||78||1(1.28)||**||**|
|Job related training||No||119||13(10)||0.39(0.14-1.08)||0.072||0.33(0.03-3.2)||0.346|
|Job related medical test||No||128||16(12)||0.10(0.033-0.3)||0.000||0.11(0.01-1.03)||0.054|
|Using protective clothes||No||80||15(18)||0.24(0.09-0.6)||0.007||0.74(0.09-5.8)||0.778|
nation as risk
CI=Confidence interval; OR=odd ratio; **=Reference point
In multivariable logistic regression analysis the occurrence of Salmonella isolates in abattoir and butcher houses were more likely higher in materials which were not cleaned (OR=12.56; 95% CI: 0.986-160.13%; P=0.048) and people who didn’t know contamination as risk (OR=11.586; 95% CI: 1.65-80.98%; P=0.014) than other manners of cleaning equipment categories and in those who know contamination as risk respectively (Table 5).
Questionnaire and observational survey
For questionnaire survey analysis, a total of 145respondents used, of which 60 from Abattoir workers and 85 from Butchers houses. Twenty two (36.66%) of the workers use unclean knives while 37 (61.66%) of them keep equipment in unhygienic places.Whilst 43 of the respondents responded that unclean hand and equipment as major causes of carcass contamination, sixteen considered falling on the ground as a major source of contamination.
Washing the hands before and after work is practiced by only four of the interviewees and thirty eight did not regularly put on clean protective clothing at work. Only seven of them responded that the faeces, skin and dirty water could possibly cause carcass contamination. Most (65%) interviewees consider that keeping hygiene is the role of the management while some (35%) of them think the role of management is setting standards for hygiene in abattoir and workers role is maintaining standards for hygiene in the slaughterhouse.
Direct observations revealed the absence of hot water, sterilizer, carcass retention room and all processes were achieved in a single floor of the abattoir. During slaughtering equipments were placed on unclean surfaces. Knives were placed on the floor, in their (workers) mouth, on the skin of killed and in the anus of a slaughtered animals. The protective clothes were unclean, blood tinged and frequently in contact with carcasses (Table 6).
Table 6 The Knowledge, Attitude and Practice of Abattoir Workers.
|beyond grade 12||7||11.66|
|Placement in the abattoir||Slaughteringa||25||41.66|
|Washing the intestine||8||16.66|
|Job related training||Yes||12||20|
|Job related medical test||Yes||6||10|
|Know contamination as risk||Yes||39||65|
|Hand washing||Before & after||4||6.66|
|Knives are clean||Yes||38||63.33|
|Unhygienic equipment placing||Yes||37||61.66|
a=Cutting the throat, flaying eviscerating, splitting the carcass and carcass washing
Among the 85 butchers, 71 acquired meat selling skills from observations and fourteen of them from informal training. Forty one of the butchers did not use protective clothes and forty four of them wash their hands with only water after work. All reported that they use a single knife for cutting meat and edible offal. Twenty had worn jewelries and sixty two handled money while selling meat. Forty eight of the butchers cleaned their shop and equipment every day at end of the selling process by using water and soap (Table 7).
Table 7 The knowledge, attitude and practice of Butcher house workers.
|Beyond grade 12||11||12.94|
|Received job related training||Yes||14||16.47|
|Received job related medical test||Yes||11||12.94|
|Hand washing||Before and after||9||10.58|
|Manner of hand washing||Using detergent and water||23||27.05|
|Rinsing with water only||44||51.76|
|Butcher with bare hand||62||72.94|
|Cleaning equipment at the end of work using water &saop||Yes||48||56.47|
|Separate for d/t organs &meat||28||32.94|
In the present study, the overall prevalence of Salmonella was 13.4% (43/320). This finding agrees with previous studies undertaken in different parts of Ethiopia which was 14.8% at Dessie and 12.5% at Wolaitasodo.
Resistance to multiple antimicrobials (97.67%) which was observed in current study was in line with the reports of Asrat,  who revealed 95.45%.
The occurrence of Salmonella in the study area was directly or indirectly associated with the risk factors since Salmonella is cross contaminant of foods mainly meat. The current finding is in agreement with the studies conducted in Ethiopia, which showed that people and equipments were found to be significantly associated with carcass contamination by Salmonella.
The majority 37(61.66 %) of the abattoir workers proposed unclean hand and equipment as the major causes of carcass contamination but few responded that the faces, skin and dirty water can cause carcass contamination. Besides, most consider that keeping hygiene is the role of the management while some of them think the role of management is setting standards for hygiene in abattoir and workers role is maintaining standards for hygiene in the slaughterhouse.
The hygienic practices at the butcheries were unhygienic. Most of the butchers (72.9%) handle money with bare hands while processing meat and do not put appropriate protective clothes. Similarly, Molla  and Yismaw et al  reported 91.7% and 95% of the butchers in handle money while processing meat. In addition, other study indicates that, handling of foods with bare hands may also result in cross contamination, hence introduction of microbes on safe food.
This study revealed that high prevalence of Salmonella, presence of poor personal hygiene, resistance of Salmonella to most antimicrobials, low level of public awareness about contamination of beef meat with Salmonella and the associated risk factors for the occurrence of Salmonella in the study area. Consequently, beef meat provided to the consumers in the town was found to be poor quality and risk full for human health calling for urgent intervention.
AA: Study conduction, data collection, analysis, reference search, and manuscript writing; MA: Study conduction, reference search, manuscript writing, and editing. HD: analysis, reference search, and manuscript writing. All authors have read and approved the final manuscript.
The authors are grateful to College of Agriculture and Veterinary Medicine, Jimma University for providing financial assistance to conduct the research work. We would also like to thank abattoir and butchers houses workers at Mizan town for providing time while appropriate sample collection.
The authors declare that they have no competing interest.