Background
Milk and dairy products are important source of vital nutrients for human beings [
1,
2]. The unique composition and properties make milk an excellent medium for bacterial growth and source of bacterial infection [
3]. Milk-borne pathogenic bacteria pose a serious threat to human health, and constitute about 90% of all dairy- related diseases [
4].
Staphylococcus aureus, Salmonella spp., Listeria monocytogenes,
Escherichia coli O157:H7 and
Campylobacter are the main microbiological hazards associated with raw milk consumption [
3]. Microbiological status of raw milk is affected by several factors including a health status of the animal, farm management practices, environmental hygiene and poor temperature control [
5].
In some countries with low socio-economic status, income growth and urbanization has led to almost doubled consumption of milk and dairy products [
1,
2]. In Ethiopia, as the dairy industry is developing towards a market-oriented system, majority of milk vendors and cafeterias collect unpasteurized milk from different dairy farms to sell it to consumers [
6]. A survey conducted in central Ethiopia reported that 31.8% of farmers consumed raw milk [
7]. In the milk market value chain, milk handled in unhygienic way can be easily contaminated by milk-borne bacterial pathogens and serve as a suitable vehicle for disease transmission, causing a significant public health threat to consumers [
6‐
8]. A study documented that hygienic practices during milking, handling and storing of milk were substandard resulting in poor quality milk products and safety problems [
9]. A study conducted in northern Ethiopia reported milk contamination rate varying from 45 to 75% [
10]. `.
In Tigray region, where less than 1% of the milk produced for commercial purpose is pasteurized and in situation where there is no set standard and regulation to control the safety and quality of milk produced for commercial purpose, the risk of milk contamination is high. Despite this fact, there are few studies that examined the health hazards of raw milk consumption in the study area, other than those conducted in localized areas with a small sample size. This study is expected to fill the gap in information on the magnitude and type of hazards associated with raw milk consumption and outline measures that are needed to be taken by milk producers, vendors and regulators to ensure the safety and quality milk in the milk supply value chain.
Therefore, the objective of this study was to assess the prevalence of milk-borne bacterial hazards and associated factors in commercially marketed raw milk in the Tigray regional state, Ethiopia.
Methods
Study design and setting
This study used a cross-sectional study design to assess the magnitude of milk-borne bacterial pathogens and associated factors in the study area during February to May 2017.
Study area
Tigray regional state is located in the northernmost part of Ethiopia. The region has a total population of 6.2 million, 85% of which live in the rural areas and about 83% of the populations were farmers [
11]. This study was carried out in the three big cities of the regional state; Mekelle, Wukro and Adigrat. Mekelle is the capital city of the region and Adigrat is the zonal capital for the eastern zone of the Tigray region [
11].
Source and study population
The source populations were all dairy farmers, milk vendors, and cafeterias who sold milk in different forms in the three selected cities. The study populations were all dairy farmers, milk vendors, and cafeterias who sold milk in different forms in the selected lowest administrative units (Kebelles) in Mekelle, Wukro and Adigrat cities during the study period.
Sample size determination and sampling procedure
Sample size was estimated using a single population proportion formula with the following assumption: Confidence level = 95%, prevalence = 0.75 [
10], margin of error = 0.05. Thus, the total sample size was calculated as 288 study subjects and milk samples. We allocated the sample size using proportional to population size of the randomly selected ten
Kebelles from Mekelle and four
Kebelles from each of the two other study sites. In all the selected
Kebelles, systematic random sampling was used to select dairy farmers, milk vendors or cafeterias.
Questionnaire survey
The instrument used for this study was developed by modifying from other studies [
7‐
10,
12,
13]. The investigators used a pre-tested structured questionnaire and administered it through face-to-face interviews with dairy farmers, milk vendors, and cafeteria owners after obtaining written informed consent from each study subject. Checklist was also used to assess the farm hygiene status. Data were collected on socio-demographic factors, milking, milk handling and storage practices. Data collectors were trained on the objective of the study, content, and method of administration of the tool. Data were collected by BSc level health professionals under close supervision.
Milk sample collection and laboratory examination
A total of 315 milk samples were collected from all enrolled dairy farmers (96), milk vendors (51), and cafeterias (168) by conducting house-to-house visits. About 30 mL of bulk milk samples were collected aseptically from the containers used for storage of milk, put into a sterile universal bottle and placed in a cool box packed with ice packs. Milk samples were transported from the field to the laboratory within four hours of collection and stored at 4 °C in a refrigerator until testing.
Laboratory tests for bacterial isolation and identification
To determine the bacteriological quality of the raw cow milk, total bacterial count (TBC), staphylococcus spp. count (SC) and coliform count (CC) were performed. Plate Count agar (HiMedia, India), the Baired-Parker Agar Base (Oxoid, UK) enriched with Egg Yolk Tellurite Emulsion (Damstadt, Germany) and the Violet Red Bile agar (MiMedia, India) were used for each procedure, respectively. Peptone water was used as a diluent for serial ten-fold dilutions.
The enumeration of total viable bacteria, staphylococcus spp. and coliform bacteria were performed following standard procedures [
14,
15]. To describe briefly, for each sample a tenfold serial dilution, up to 10
− 6 dilutions were prepared using peptone water. From each dilution, 1 ml was put in the center of the respective agar plates using micropipette and spread evenly to the whole plate using sterile bent glass rod. For each serial dilution, duplicate agar plates were employed. The inoculated agar plates were incubated at 37 °C for 24–48 h. Agar plates with 30–300 colonies were counted using colony counter as per the recommendation [
14,
15]. For identification of bacteria to species level, colony morphology and different primary and secondary biochemical testes were employed. The detailed laboratory procedures used for isolation and identification of the bacteria is described elsewhere [
5,
6,
14‐
19].
Data management and analysis
The investigators entered the data into Epidata software and exported it to SPSS version 20 for analysis. Bacterial counts data were transformed to logarithm of colony forming units per milliliter of sample (log CFU/ml) and the results were presented as mean ± standard error (SE), median with interquartile range (IQR) and percentage (%). Bacterial contamination level in cow milk was graded according to the Standard European Union (EU) microbiological limits (TBC ≤1 × 10
5 CFU/mL, SC < 10
5 CFU/mL and CC ≤10
2 CFU/mL) [
20]. Descriptive statistics were calculated using simple frequencies, percentages, and mean. Bivariate and multivariable logistic regressions were used to identify factors associated with milk-borne bacterial hazards by controlling the confounding effect of selected variables. Statistical significance was determined by
p values, crude odds ratio (COR) and adjusted odds ratio (AOR) with their corresponding 95% confidence intervals.
Ethical considerations
Ethical clearance was obtained from the Ethical Review Board of the College of Health Sciences, Mekelle University. All the study subjects in this study were adults above 20 years old. The investigators administered written informed consent to all study subjects after provision of information on the study. The autonomy of study participants was ensured and all collected data were kept confidential.
Discussion
This study reported a higher prevalence of bacterial contamination of milk (52%). The prevalence of milk-borne bacterial contamination of milk is similar to a report from Adigrat city where milk contamination rate was 45% in farm settings, 60% in milk vendor shops and 75% in cafeterias [
10]. In terms of
S. aureus contamination level, it was lower than the prevalence of
S. aureus (19.6%) reported in Central Oromia [
21] and Tigray region (38.7%), Ethiopia [
6]. Similarly, this study recorded lower contamination level comparing to a report from Côte d’Ivoire where 76.5% of the samples showed the presence of one or more of the three pathogens (
E. coli, S. aureus, and
Enterococcus) [
22]. Moreover, higher rate of contamination of milk was reported from another study in India [
23]
. Possible reasons for this high level of milk contamination in the study area could be attributed to the use of un-pasteurized milk for commercial purposes, sub-optimal hygiene practices, inadequate cooling and lack of standard facilities for milking, storage, and transportation of milk. There is considerable evidence that microbial contamination in the milk market value chain can originate from a diseased cow, unhygienic milking practice, poor personal hygiene, unsanitary utensils and/or milking equipment, poor storage conditions, and lack pure water supply [
24,
25]. A study reported that in developing countries like Ethiopia, there are inadequate hygienic practices throughout the dairy production system and standard milking protocols do not exist which is evidenced by the presence of many dairy farmers that do not disinfect teats prior to milking and inadequate washing of hands before milking [
26,
27].
From the total cultured milk samples, 47.9 and 40.6% were isolates of coliform and
S. aureus, respectively. Coliform counts are important indicators that are used to measure the level of microbial quality and hygiene in milk handling [
28,
29]. Previous studies have also indicated that coliform and staphylococcus are the most frequent bacterial contaminants of milk and this was attributed to their abundant availability both in the animal body and in the environment [
29,
30]. In this study, more than 31% of the dairy farms have been using rivers, ponds or wells as their source of water and this might have contributed to the high coliform contamination of milk in our study. Contamination of
S. aureus can arise from various sources as the bacteria is commonly found on the various body parts of warm blooded animals and it can be isolated from faeces, soil and fresh water [
25]. Moreover,
S. aureus can be carried in
approximately 20–50% healthy individuals in their nasal cavity [
31].
The high bacterial contamination rate of milk in our study implies that milk can pose health risks to consumers. If milk is not handled properly and in hygienic condition, it will support the growth of pathogenic micro-organisms leading to transmission of zoonotic and foodborne diseases that can compromise the health of the population. Therefore, to prevent contamination of milk by pathogenic micro-organism, improving animal health, environmental hygiene, dairy farming practices, milk handling, transportation and storage practices are required [
28,
32].
Among the socio-demographic factors evaluated for association with milk contamination, type of business was significantly associated with higher level of milk contamination. The proportion of milk contamination was significantly lower in milk collected from dairy producers (33.3, 95% CI: 24.5–43.2) compared to milk from vendors and cafeterias. This is consistent with the findings of Merhawit et al. [
10] and Oliver et al. [
33] where the bacteriological quality of milk deteriorated along the milk supply chain due to the proliferation of the microorganisms initially present in the milk or/and due to cross contamination [
4]. As there was increasing trend of milk contamination from farmers to points of sale, milk vendors and cafeterias should use appropriate and clean containers, timely delivery of milk, cold chain during transportation, and refrigeration of milk during storage.
Throughout the developing world, over 80% of the milk consumed is unregulated, and in Ethiopia less than 1% of the milk consumed is pasteurized [
34,
35]. It is reported that the contamination of milk is high in countries where there is traditional farming systems and market is unregulated. Increased contamination level of milk along the milk market chain indicates that food safety is becoming an important public health agenda particularly in milk produced for commercial purpose. When milk is produced for commercial purpose with inadequate hygienic practices, milk contaminated with pathogenic micro-organisms can end-up with mass distribution, mass outbreaks affecting more people and cause a greater economic impact. Therefore, focus needs to be placed on setting food safety standards particularly for milk produced for commercial purpose [
4]. Generally, the implementation of good hygienic practice and sanitation, introduction of quality and safety standards as well as the use of an effective cold chain and pasteurization technologies are the key measures to improve the microbial quality and safety of the milk.
This study was conducted in a large milk-shed area using adequate sample size. As limitation, this study didn’t comprehensively examine all important bacterial contaminants of milk and factors responsible for milk contamination. Moreover, residual confounding and social desirability bias might have occurred during variables measurement.
Conclusions
The following conclusions are made from this study:
The level of milk contamination in this study was high indicating the presence of significant health risks to the consumer. Milk collected from milk vendors and cafeterias was significantly associated with higher level of milk contamination compared to milk sampled from dairy farms.
Therefore, considering the study findings, the following recommendations are made.
Milk vendors and cafeteria owners should apply good hygienic and sanitation practices during handling of milk; use appropriate, clean containers, and cold chain during transportation; and refrigeration of milk during storage. Governmental bodies should set quality and safety standards for milk produced for commercial purpose to improve microbial quality and safety of milk. Further research is required to assess contamination of milk by other important pathogens particularly Salmonella spp., Campylobacter spp., L. monocytogenes spp.
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