Prevalence of Intestinal Parasites and <i>Salmonella typhi</i> among Food Handlers Working in Catering Establishments of Public Institutes Found in Dawuro Zone, South-Western Ethiopia

Kumalo, Abera; Gambura, Eyasu; Dodicho, Terfe; Ahmed, Khawaja Shakeel; Balcha, Tamrat; Beshir, Bahailu; Abraham, Misrak

doi:https://doi.org/10.1155/2021/8889302

Journal of Parasitology Research

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Abstract Introduction Methods Results Discussion Conclusion Abbreviations Data Availability Ethical Approval Consent Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2021 | Article ID 8889302 | https://doi.org/10.1155/2021/8889302

Prevalence of Intestinal Parasites and Salmonella typhi among Food Handlers Working in Catering Establishments of Public Institutes Found in Dawuro Zone, South-Western Ethiopia

Abera Kumalo,¹Eyasu Gambura,²Terfe Dodicho,³Khawaja Shakeel Ahmed,¹Tamrat Balcha,⁴Bahailu Beshir,⁵and Misrak Abraham⁶

Academic Editor: José F. Silveira

Received22 Jul 2020

Revised16 Nov 2020

Accepted04 Jan 2021

Published16 Jan 2021

Abstract

Background. Food borne disease, which is the result of ingestion of foodstuffs contaminated with microorganisms, parasites, or chemicals, encompasses a wide spectrum of illness and public health problem worldwide. Ethiopia is placed on second, third, and fourth position due to the highest burden of ascariasis, hookworm, and trichuriasis, respectively, in sub-Saharan Africa. The present study is aimed at determining the prevalence of Salmonella typhi and intestinal parasites among food handlers working in catering establishments of public institutes found in Dawuro Zone, South-Western Ethiopia. Methods. A cross-sectional study is conducted among food handlers working in catering establishments of public institutions found in Dawuro Zone from March to July 2019. The data was collected by using pretested structured questionnaires. Stool and blood samples were taken from each participant for parasitic examinations concurrently using direct and modified formol ether concentration wet smear techniques and Widal test by slide test and tube serial dilution technique, respectively. The data entered into Epi info version 3.5.1 and then exported into SPSS window version 20.0 for analysis. Logistic regressions were performed to assess the association between binary outcomes and different explanatory variables. value <0.05 was considered statistically significant. Result. The study included 402 (293 females and 109 males) food handlers. Of 402 stool specimens, 20.4% were found to be positive for different parasite species, comprising protozoa (35.9%) and helminths (64.1%). A. lumbricoides was the most prevalent parasite (8.0%), followed by E. histolytica/dispar (4.23%). Twenty-six (6.5%) of food handlers were positive for Widal test. years (AOR: 0.436; 95% CI: 0.203, 0.937), attending no education (AOR: 2.142; 95% CI: 1.048, 4.378), not washing hands after using latrine (AOR: 4.355; 95% CI: 1.771, 10.708), not covering mouth with tissue paper (AOR: 0.530; 95% CI: 0.312, 0.899), no medical checkup (in the last four months) (AOR: 0.278; 95% CI: 0.116, 0.667), and untrimmed fingernails (AOR: 0.382; 95% CI: 0.229, 0.635) were significantly associated with intestinal parasitic or Salmonella typhi infections. Conclusion. The prevalence of intestinal parasitic infection (IPI) and Salmonella among food handlers in the present study is relatively high compared to other different studies conducted in developed and developing countries. Therefore, biannually screening of food handlers for intestinal parasites (IPs) and periodic deworming of infected cases along with provision of food safety measures focusing on personal hygiene and environmental sanitation are recommended to control the parasitic infection in food handlers.

1. Introduction

A food borne disease, which is the result of ingestion of foodstuffs contaminated with microorganisms or chemicals, encompasses a wide spectrum of illnesses and a growing public health problem worldwide (1–3). According to the Ministry of Health (MOH) of Ethiopia, food borne disease implies food that is not handled in clean conditions; hence, the food becomes contaminated by disease causing microorganisms. These microorganisms grow and multiply in the food; hence, people who consume this food may get poisoned or infected by organisms in the food (4). Thus, an estimated 70% of cases of diarrheal diseases are associated with the consumption of contaminated food. Diarrheal diseases are mostly caused by food or waterborne microbial pathogens and remain the leading causes of illness and deaths, with an estimated killing of 1.9 million people annually worldwide. Yet, it is expected that a large number of illnesses remain underreported because only the most serious cases are usually investigated (3, 5).

In worldwide, about one-third of the total population is projected to be infected with intestinal parasites, from which the leading number of people are living in tropical and subtropical parts of the world (6, 7). Centers for Disease Control and Prevention (CDC) estimated that each year, 48 million people get sick, 128,000 are hospitalized, and 3000 die from a foodborne disease (8, 9). About 819 million people are infected with Ascaris lumbricoides (A. lumbricoides), 464.6 million people with Trichuris trichiura (T. trichiura), 438.9 million people with hookworm infection (7, 10), 500 million people with Entamoeba histolytica (E. histolytica), and 2.8 million people are infected with Giardia lamblia (G. lamblia) (7, 11).

In USA, food borne diseases cause an estimated 76 million illnesses, 325,000 hospitalizations, and 5,000 deaths each year. Experts estimate that the yearly cost of all food borne diseases in USA is $5 to $6 billion in direct medical expenses and lost productivity. Salmonella infections alone in USA account for $1 billion yearly in direct and indirect medical costs. Nevertheless, in most developing countries, reliable statistics on food borne diseases are not available due to poor or nonexistent reporting systems (3).

In Ethiopia, the case of intestinal parasitosis is highly common, like that of other developing countries which are found in sub-Saharan Africa. It is assumed that one-third of Ethiopians are infected with A. lumbricoides, one quarter is infected with T. trichiura, and one in eight lives with hookworm. Due to this, Ethiopia is placed in second, third, and fourth position with the highest burden of ascariasis, hookworm, and trichuriasis, respectively, in sub-Saharan Africa (7, 12). According to the different studies, the most prevalent intestinal protozoan parasites in Ethiopia are Giardia lamblia and Entamoeba histolytica/dispar. Helminthic infection includes Ascaris lumbricoides, Trichuris trichuria, and Taenia saginata (9, 13–15). In addition to intestinal parasitosis, Salmonella typhi is also one of the leading causes of food and water borne gastroenteritis in human. Globally, it is one of the important public health concerns with estimated 16 million new cases and 600,000 typhoid fever deaths each year (16, 17).

A food handler is a person with any job that requires him/her to handle unpackaged foods or beverages and involved in preparing, manufacturing, serving, inspecting, or even packaging of food and beverage items and also those who come in contact with eating or cooking utensils or other equipment used in the handling, preparation, service, or sale of food (3, 18). All food handlers are required to use proper hygiene and sanitation methods when working with food (4). According to the world health status review, the health problem of developing nations is primarily interrelated to sanitation issue. Thus, various factors such as the general sanitary standards of the house, the proper use of sanitary facilities like latrines and hand washing lavatories, refuse management systems, and dishwashing facilities affect food safety in food establishments (19–21). Food handling, preparation, and service practices are other important factors in determining the safety of food. Conditions of cooking utensils and food storage systems (time and temperature) as well as food handlers’ knowledge and practices similarly affect food safety directly or indirectly (4, 15, 22–25). The fact that less evidence is obtained in the literature in the current study area regarding the intestinal parasites and Salmonella prevalence as well as associated factors, so the current study is aimed at assessing the prevalence of Salmonella and intestinal parasite among food handlers who are serving in catering establishment of public institutes found in Dawuro Zone, South-Western Ethiopia.

2. Methods

2.1. Study Area, Design, and Period

A cross-sectional study design was conducted from March to July 2019 in three towns found in Dawuro Zone of South-Western Ethiopia, namely, Tarcha, Waka, and Gessa towns. Tarcha is the administrative center of Dawuro Zone which is 476 km away from the capital city, Addis Ababa. Waka and Gessa towns are the district centers of Maraka and Loma districts, Dawuro Zone, which are found to be 460 km and 445 km away from the capital city, Addis Ababa, respectively, in road Sodo to Tarcha.

2.2. Study Population

Sampled food handlers working in catering establishments of public institutions found in Tarcha, Waka, and Gessa towns, Dawuro Zone of South-Western Ethiopia are involved in this study.

2.3. Inclusion Criteria and Exclusion Criteria

Food handlers working in selected food establishment, who have direct contact with food and drinks and who have given an informed consent, were included in the study. Those who had taken antiparasitic drugs and antibiotic within three weeks prior to the study were excluded.

2.4. Sample Size Determination

Sample size that was determined using the formula for single population proportion using the prevalence of intestinal parasite among food handlers was 44.1% (26) from Yebu with a 95% confidence interval, a margin of error of 5%. An initial sample size was 379. By adding 10% nonresponse rate, the final sample size will be 417.

2.5. Sampling Technique

The study participant was 417 food handlers who fulfilled the inclusion criteria that currently working in the food catering establishment of public institutions in Tarcha, Waka, and Gessa towns. Prior to the study, survey study was conducted to know the number and types of the public institution found in each town. Also, the total number of food handlers working in each catering establishment of the public institutes in the respective towns was identified. Then, the total sample size was divided proportionally for the three towns depending on the total number of the food handlers of the public institutes found in each town. Finally, 417 food handlers were included in the study by systematic random sampling until the total sample size met (Figure 1).

2.6. Data and Specimen Collection

The data was collected through face to face interview using pretested structured questionnaires. The structured interview questionnaire was taken 15 minutes with closed-ended questions and predetermined response options which are developed specifically for this study. The questionnaire contains sociodemographic status, knowledge of food handling, practice of food handling, and personal hygiene. The questionnaire was adopted from the World Health Organization (WHO) food safety checklist and other related literatures (9, 20, 23, 27). After interviewing, respondents were asked to collect a small amount of fresh stool sample (2 g or 4 ml if diarrhea) with a clean and tight-lid sample container after orienting on how to collect the stool specimen by attending laboratory technologist. All specimens were immediately transported using cold box to the Microbiology and Parasitology Laboratory of Wolaita Sodo University for analysis.

2.7. Specimen Handling and Processing

Each stool sample was smeared and tested in doubled manner. Parasitological microscopic stool examination was immediately performed by emulsifying uniformly about a matchstick size of stool (2 mg) in a drop of normal saline (0.85% NaCl) on one end of a glass slide, and an iodine wet mount was mainly used to stain the nucleus of the protozoa cysts in the other end of the same slide. Sedimentation technique was performed using the readily modified formalin-ether sedimentation technique. In brief, 1 g of stool was placed in 15 ml conical tube containing 7 ml of 10% formol water, gently emulsified and sieved using 65 mm plastic strainer. The sieved sample was transferred into another conical tube containing 9 ml of 10% formol water and 3 ml of ethyl acetate and centrifuged at 3000 rpm. The supernatant was decanted by inverting the tube, and the last drop allowed to sediment by gravity for 15 min. The sediment was then poured on slide, covered with cover glass (), and examined microscopically under low (10x) with the condenser iris closed sufficiently to give good contrast and high (40x) objective lenses. Eggs and larvae of helminths and cysts and trophozoites of protozoan were assessed by propagule size, shape, cell wall width, and distinctive internal characteristics (9, 28).

2.8. Widal Test

Two milliliters of venous blood was collected by the data collector from food handlers for Widal test. Serum is prepared; allow the whole blood to clot at room temperature for at least one hour or centrifuge the clotted blood for 10 minutes at 2000 rpm. The Widal test was done using S. typhi O and H antigens according to the manufacturer’s instruction. In brief, the test was done by mixing one drop of serum with one drop of O and H antigens separately on glass slide. After rocking the slide back and forth, the mixture was observed for macroscopic agglutination. In addition to slide (screening) test, serial (tube) dilution tests done by using patient serum are made in physiologic saline. An antigen suspension is added to the mixture and incubated for a certain period of time. Finally, the highest dilution giving agglutination reaction (titer) is determined. Widal test is reported by giving the titer for both O and H antibodies. Positive result was reported by the presence of agglutination within one minute, and negative result was reported by the no agglutination (28, 29).

2.9. Methods of Data Processing and Analysis

The coded data was checked, cleaned, and entered into the epidemiological information software (Epi info version 3.5.1) to ensure data accuracy and then exported into SPSS window version 20.0 (SPSS Inc., Chicago, IL) for analysis. Descriptive statistics were manipulated for all variables. Bivariate analysis was first conducted for each potentially explanatory risk factor to see associations to select for multivariate analysis. Variables that had a value <0.25 in bivariate analysis were run in multivariable logistic regression. Multiple logistic regressions were performed to assess the association between binary outcomes and different explanatory variables. The strength of association was interpreted using odds ratio and confidence interval. value <0.05 was considered statistically significant in this study.

2.10. Data Quality Control

Questionnaire was prepared in English and translated to local language (Amharic and Dawuro languages) and retranslated back to English. Data collectors were trained ahead of the actual data collection period. The training was focused on familiarizing interviewers with the questionnaire and giving them the opportunity to practice using it. Well-experienced and trained laboratory technologist was recruited for laboratory examination. Before the actual stool specimen’s examination for the study subjects, pretest was conducted on 5% of stool samples collected from patients attending Tarcha health centers to look the reliability/reproducibility of stool examination procedure by the laboratory technologist with two different microscopes. In addition to slide (screening) test, serial (tube) dilution tests done by using patient serum are made in physiologic saline. An antigen suspension is added to the mixture and incubated for a certain period of time. Finally, the highest dilution giving agglutination reaction (titer) is determined. Widal test is reported by giving the titer for both O and H antibodies.

At time of data collection filled questionnaires was checked for completeness, accuracy, and consistency of information by the supervisor on daily basis, and typing errors were manually edited. Any ambiguity and other problems of data collectors were addressed by communicating with the data collectors before the following week.

3. Results

3.1. Study Population Characteristics

The age and sex distribution of food handlers are presented in Table 1. The study included 402 (293 females and 109 males) food handlers with a response rate of 96.4%. Majority of the food handlers (61.2%) were found in the age group of 20–40 years and had a primary educational level of around 43.8%. Job position in the catering establishment indicates almost more than half had has cooking (60.2%) position, and waiter position indicates 16.4%. The majority (57.5%) of food handlers had served for 1-2 years.

3.2. Etiologic Agents

3.2.1. Intestinal Parasites

Direct microscopic and concentration techniques were used for identifying intestinal parasites from the 402 stool specimens. Of 402 stool specimens, 20.4% were found to be positive for different parasite species, comprising protozoa (35.9%) and helminths (64.1%). A. lumbricoides was the most prevalent parasite (7.9%), followed by E. histolytica/dispar (4.23%) and then G. lamblia (2.74%). Less frequent identified intestinal parasite spp. was S. stercoralis and Taenia species; each accounted for 0.49% and 0.75% of the total isolates. Mixed intestinal parasites (A. lumbricoides, G. lamblia, and Tania species) were detected in 5 (1.2%) of the participants (Table 2).

3.2.2. Salmonella

Out of 402 food handlers screened, Widal test result showed that 26 (6.5%) food handlers were positive for O or/and H antigens of Salmonella typhi.

3.3. Hygienic Practice of Food Handlers

The hygienic practice and knowledge of food handlers are presented in Table 3. In personal hygiene-related practices, more than half of the participants responded keeping ready to eat foods in clean container and covering it properly (348, 86.6%), checking ingredients’ expiry date before using for food preparation (386. 96%), covering mouth with tissue paper, when coughing or sneezing accidentally during food preparation (280, 69.7%), and storing foods which are capable of supporting microorganisms’ growth in the refrigerator (270, 67.2%). However, certified in food preparation and handling is low which accounts 99 (24.6%). In the other part, 250 (62.2%), 291 (72.4%), and 290 (72.1%) food handlers had a habit of hand washing with water only after visiting the latrine, touching dirty materials, and touching body parts, respectively. A few number (19.2% and 25.6%) of food handlers had a habit of medical checkup and habit of covering hair during food preparation, but they are good at shoe wearing habit (294, 73.1%) and trimmed fingernail status (248, 61.7%).

3.4. Knowledge of Food Handlers

With regard to knowledge-related factors, food handlers (74.9%) had little knowledge to use of potable water that decreases the transmission of intestinal parasites/Salmonella typhi. Among food handlers who believed that proper use of latrine (33.1%), cleaning of utensils (37%), cleaning of the kitchen floor (21.6%), proper clothing (34%), and food hygiene and safety training (27%) had a good knowledge that decreases the transmission of intestinal parasites/Salmonella typhi (Table 4).

3.5. Factors Associated with Intestinal Parasitic and Salmonella Infections

As shown in Table 5, different factors were assessed for possible association with intestinal parasitic and Salmonella typhi infection among the study participants. Among the total variables included in the bivariate logistic analysis, eight variables (age (in years), level of education, hand washing practice after visiting the latrine, cover mouth with tissue paper, when coughing or sneezing accidentally during food preparation, store foods which are capable of supporting microorganisms growth in the refrigerator, medical checkup (in the last four months), and fingernail status were associated with IPIs at a value <0.25. All those variables that were associated with IPIs and Salmonella typhi at a value <0.25 in bivariate logistic regression analysis were computed in a multivariate logistic regression analysis. The results of multivariable logistic analysis showed that years (AOR: 0.436; 95% CI: 0.203, 0.937), attending no education (AOR: 2.142; 95% CI: 1.048, 4.378), not washing hands after visiting the latrine (AOR: 4.355; 95% CI: 1.771, 10.708), not covering mouth with tissue paper, when coughing or sneezing accidentally during food preparation (AOR: 0.530; 95% CI: 0.312, 0.899), not storing foods which are capable of supporting microorganisms’ growth in the refrigerator (AOR: 0.465; 95% CI: 0.275, 0.787), without medical checkup (in the last four months) (AOR: 0.278; 95% CI: 0.116, 0.667), and untrimmed fingernails (AOR: 0.382; 95% CI: 0.229, 0.635) were significantly associated with intestinal parasites or Salmonella typhi infections ( value <0.05) (Table 5).

4. Discussion

The spread of disease via food handlers is a public and persistent problem globally. Infection of asymptomatic persons, especially workers dealing with food (food handlers), could become a potential cause of dissemination of variety of pathogens including intestinal parasites and Salmonella (9, 29, 30). Intestinal parasitic infection is one of the problems that affect human health, especially in developing countries. If food handlers are contaminated with parasites which have the potential to be directly transmitted from one person to another, they can transmit contamination to food, dishes, and finally to the people who use them (30). Different studies have been conducted in the field of intestinal parasite prevalence in food handlers. However, published information about food borne pathogens among food handlers in our study area is scarce. Therefore, this study was undertaken to determine the prevalence of Salmonella and intestinal parasites among food handlers working in catering establishments of public institutes found in Dawuro Zone of South-West Ethiopia.

The prevalence of IPIs in the present study was 20.4%. The findings of our study were consistent with the studies done in Haramaya University cafeterias, Eastern Ethiopia, Gondar town, North West Ethiopia, Madda Walabu University, Aksum town, Northern Ethiopia, and Accra, Ghana, with a prevalence of 25.2% (9), 25% (31), 25.3% (32), 14.5% (33), and 15% (34), respectively. On the other hand, the prevalence found in our study is low compared to the previous studies conducted elsewhere in Ethiopia and other parts of the world, like Wolaita Sodo town, Yebu town, Jimma zone, Bahir Dar town, Addis Ababa, Gondar, Abeokuta, Nigeria, and Mekele which reported prevalence of 33.68% (30), 44.1% (26), 41.1% (14), 45.3% (35), 29.1% (36), 97% (37), and 52.4% (25), respectively. The studies done in Sai-Yok, Thailand, and North India reported a prevalence of 10.3% (38) and 1.3 to 7% (39), respectively, which is low compared to our study. Reporting of such variations is large due to the difference in sociodemographic characteristics, geographical location, safe water supply, ignorance of health-promotion practices, food hygiene, and safety training.

In this study, the most frequently isolated intestinal parasite was A. lumbricoides (8.0%) from helminthes and E. histolytica/dispar (4.2%) was the most predominant from protozoan parasites. The findings of our study are in line with other studies conducted in different parts of Ethiopia, like Wolaita Sodo (6.25% and 4.51%) (30), Hawassa (9.6% and 2.2%), (29), and in Gondar (18.11% and 1.6%) (36). But, it was in disagreement with a study reported from Yebu, southwestern Ethiopia, in which A. lumbricoides (17.8%) was the leading parasite from helminths and G. intestinalis (5.9%) predominant from protozoan (26). The study conducted in Mekele, Ethiopia, at different time periods, reported results of 32.3% (40) and 36.6% (15) for A. lumbricoides and E. histolytica/dispar, respectively, which is different from our study, while the study done in Bahir Dar town of Ethiopia, E. histolytica/dispar with 12.76 (14) was predominant compared to A. lumbricoides. The difference in the frequency and type of parasites may be due to differences in geographical location and environmental conditions.

This study also tried to identify S. typhi infection from serum sample of food handlers by using Widal test for “O” or/and “H” antigens of Salmonella typhi. Overall, 26 (6.5%) food handlers were found reactive with Salmonella typhi by “O” or/and “H” antigens. This result is in close agreement with the study conducted among food handlers at the University of Hawassa (8.1%) (29). However, in a study conducted in Bahir Dar, (1.6%) food handlers were found infected with S. typhi (14); in Motta town of North West Ethiopia, the percentage of infection was 2.5% (41), and in Addis Ababa, it was 3.5% (35). The study done by Andargie et al. in Gondar town reported no presence of Salmonella species in food handlers (36). The variation observed could be due to the differences in the socioeconomic conditions, type of diagnostic sensitivity, epidemiological difference, seasonal variation, and the differences in hygiene of the individuals and the working environment.

As shown in Table 5, different factors were assessed for possible association with intestinal parasitic and Salmonella typhi infection among the study participants. The odds ratio of being positive for IPIs or Salmonella typhi infections was 0.436 times higher among food handlers who had age greater than 40 years than those who had age less than 20 years (; AOR: 0.436 95% CI: 0.203, 0.937). Food handlers who had no education were 2.142 times more likely to have increased intestinal parasitic and Salmonella typhi infection as compared to respondents who had secondary and above education (AOR: 2.142; 95% CI: 1.048, 4.378). The findings of our study are supported by earlier studies conducted elsewhere in Ethiopia (9, 31, 33). This may be suggested by due to lack of education among food handlers that makes them more vulnerable to parasitic and enteric infection, as they are short of knowledge about food safety and transmission of parasitic and enteric infection.

The odds ratio of being positive for IPIs or Salmonella typhi infections is 4.355 times higher among food handlers who did not wash their hands after using latrine, compared to those who washed their hands with water and soap (; AOR: 4.355; 95% CI: 1.771, 10.708). This finding is in line with earlier studies conducted elsewhere in Ethiopia (9, 23). This may be due to lack of sanitary materials, level of education, and lack of personal hygiene training.

Not covering mouth with tissue paper during coughing or sneezing accidentally as well as during food preparation and not storing food which are capable of supporting microorganisms’ growth in the refrigerator were identified as significant associated risk factors among food handlers infected by IPs or Salmonella typhi. In this study, the odds ratio of being positive for IPs or Salmonella typhi infections is 0.278 times higher among those food handlers who did not had medical checkup (in the last four months) compared to those who had (; AOR: 0.278; 95% CI: 0.116, 0.667). Earlier studies also suggest that medical checkup of food handlers must be done in every 3, 6, and 9 months (9). Currently, the Ministry of Health of Ethiopia also encourages food handlers to renew their medical certificate in every 3 months (33). The odds ratio of IPs or Salmonella typhi infections is 0.382 times higher among food handlers who had untrimmed fingernails compared to those who had trimmed fingernails (; AOR: 0.382; 95% CI: 0.229, 0.635). Other similar studies also support our findings; untrimmed fingernails can be a risk factor for IPIs among food handlers (9, 14, 33). Untrimmed fingernails could serve as a vehicle for transport of intestinal parasite or enteric bacteria from source to food due to difficulty of cleaning (9, 20). But the present study did not attempt to assess the parasite carriage of the fingernail contents.

In our study, there were some limitations. (1)Due to lack of antigen or molecular tests, Entamoeba histolytica and Entamoeba dispar were not separated(2)The fingernail contents were not investigated for ova/cyst of parasites(3)A specific parasitic diagnostic method was not employed for identification of specific parasites, like string test for Giardia lamblia and adhesive scotch tape for E. vermicular(4)The gold standard test for identification of Salmonella is culture; however, due to lack of laboratory setup in study area, we conducted only screening test of Salmonella by Widal test

5. Conclusion

In conclusion, the prevalence of IPIs among food handlers in our study was 82 (20.4%), which is relatively high in comparison to other different studies conducted in developed and developing countries. A. lumbricoides was the most prevalent parasite (7.9%), followed by E. histolytica/dispar (4.23%) and G. lamblia (2.74%). The study also identified Salmonella typhi infection. The prevalence of Salmonella typhi by Widal test was 26 (6.5%). Since most of the intestinal parasites are transmitted through feco-oral route, food handlers can be an important source of infection to the general population. Among the variables included in the bivariate logistic analysis, eight different variables like (age (in years) level of education, hand washing practice after using latrine, covering mouth with tissue paper when coughing or sneezing accidentally during food preparation, stored food which are capable of supporting microorganisms’ growth in the refrigerator, medical checkup (in the last four months), and fingernail status were identified as significant risk factors which are making food handlers susceptible to intestinal parasites in our study area. Therefore, biannually screening of food handlers for intestinal parasites (IPs) and periodic deworming of infected cases along with provision of food safety measures focusing on personal hygiene, environmental sanitation, and periodical medical checkups are recommended to control the parasitic infection in food handlers.

Abbreviations

AOR:	Adjusted odds ratio
CL:	Confidence level
IPIs:	Intestinal parasitic infections
WHO:	World Health Organization.

Data Availability

All data generated or analyzed during this study are included in this manuscript.

Ethical Approval

Ethical clearance was obtained from Institutional Health Research Ethics Review Committee of Wolaita Sodo University, College of Health Sciences and Medicine.

Written consent was obtained from the participants. Infected individuals were treated freely based on their laboratory findings according to the national standard treatment guideline.

Conflicts of Interest

All the authors declare that they have no conflict of interests, financial, or otherwise.

Authors’ Contributions

AK, EG, BB, TB MA, KS, and TD participated from conceptions of research questions to laboratory sample analysis. AK, TD, EG, KS, and MA participated in the statistical analysis, preparation, and reviewing of the manuscript. All authors read and approved the final manuscript.

Acknowledgments

This research work was partially funded by the Wolaita Sodo University, which is gratefully acknowledged. However, they have no conflict of interest on manuscript editing or writing. We also sincerely acknowledged the study participants and all data collectors.

References

World Health Organization (WHO), “World Health Day: food safety,” 2015.
View at: Google Scholar
L. Eshetu, R. Dabsu, and G. Tadele, “Prevalence of intestinal parasites and its risk factors among food handlers in food services in Nekemte town, West Oromia, Ethiopia,” Research and Reports in Tropical Medicine, vol. Volume 10, pp. 25–30, 2019.
View at: Publisher Site | Google Scholar
F. Kaferstein and M. Abdussalam, Food safety in the 21 st century, Bull World Health Organ, 1999, Report No. 77.
Federal Mistero of Health, “Food Hygiene and Safety Measures,” Tech. Rep., Addis Abeba, 2004.
View at: Google Scholar
J. Schlundt, H. Toyofuku, J. Jansen, and S. A. Herbst, “Emerging food-borne zoonoses,” Revue Scientifique et Technique, vol. 23, no. 2, pp. 513–533, 2004.
View at: Publisher Site | Google Scholar
M.-S. Chan, “The global burden of intestinal nematode infections—fifty years on,” Parasitology Today, vol. 13, no. 11, pp. 438–443, 1997.
View at: Publisher Site | Google Scholar
M. Mama and G. Alemu, “Prevalence and factors associated with intestinal parasitic infections among food handlers of Southern Ethiopia: cross sectional study,” BMC Public Health, vol. 16, p. 105, 2016.
View at: Google Scholar
Centers for Disease Control and Prevention (CDC), “Foodborne illnesses and germs,” 2018, https://www.cdc.gov/ foodsafety/foodborne-germs.html.
View at: Google Scholar
D. Marami, K. Hailu, and M. Tolera, “Prevalence and associated factors of intestinal parasitic infections among asymptomatic food handlers working at Haramaya University cafeterias, eastern Ethiopia,” Annals of Occupational and Environmental Medicine, vol. 30, no. 1, 2018.
View at: Publisher Site | Google Scholar
R. L. Pullan, J. L. Smith, R. Jasrasaria, and S. J. Brooker, “Global numbers of infection and disease burden of soil transmitted helminth infections in 2010,” BMC Parasites & Vectors, vol. 7, no. 1, p. 37, 2014.
View at: Publisher Site | Google Scholar
P. Duc, H. Nguyen-Viet, J. Hattendorf, J. Zinsstag, P. Cam, and P. Odermatt, “Risk factors for Entamoeba histolytica infection in an agricultural community in Hanam province, Vietnam,” Parasit Vectors, vol. 4, pp. 102–111, 2011.
View at: Google Scholar
K. Deribe, K. Meribo, T. Gebre et al., “The burden of neglected tropical diseases in Ethiopia, and opportunities for integrated control and elimination,” Parasites & Vectors, vol. 5, no. 1, p. 240, 2012.
View at: Publisher Site | Google Scholar
H. Girma, G. Beyene, and Z. Mekonnen, “Prevalence of intestinal parasites among food handlers at cafeteria of Jimma University specialized hospital, Southwest Ethiopia,” Asian Pacific Journal of Tropical Disease, vol. 7, no. 8, pp. 930–933, 2017.
View at: Google Scholar
B. Abera, F. Biadegelgen, and B. Bezabih, “Prevalence of Salmonella typhi and intestinal parasites among food handlers in Bahir Dar Town,” Ethiopian Journal of Health Development, vol. 24, no. 1, pp. 46–50, 2010.
View at: Google Scholar
D. Nigusse and A. Kumie, “Food hygiene practices and prevalence of intestinal parasites among food handlers working in Mekelle university student’s cafeteria, Mekelle,” Global Advanced Research Journal of Social Science, vol. 1, no. 4, pp. 065–071, 2012.
View at: Google Scholar
H. Y. Tsen, H. H. Hu, J. S. Lin, C. H. Huang, and T. K. Wang, “Analysis of the Salmonella typhimurium isolates from food-poisoning cases by molecular subtyping methods,” Food microbiology, vol. 17, no. 2, pp. 143–152, 2000.
View at: Publisher Site | Google Scholar
World Health Organization, “Manual for the laboratory identification and antimicrobial susceptibility testing of bacterial pathogens of public health importance in the developing world,” Tech. Rep., Geneva, WHO, 2003.
View at: Google Scholar
“Food handlers job description,” 2016, http://www.ehow.com/about food-handlers job descriptions.html.
View at: Google Scholar
P. C. J. R. C. E. Beaver, Clinical Parasitology. Examination of Specimens for Parasites, B. P. C. JRCE, Ed., Lea and Fabige, Philadelphia, 1984.
Z. Sahlemariam and G. Mekete, “Examination of fingernail contents and stool for ova, cyst and larva of intestinal parasites from food handlers working in student cafeterias in three higher institutions in Jimma,” Ethiopian Journal of Health Sciences, vol. 11, pp. 131–137, 2001.
View at: Google Scholar
E. Tsega and F. T. Nadew, “The threat of amoebic cyst carriers among hospital food handlers,” Ethiopian Medical Journal, vol. 10, pp. 43–53, 1972.
View at: Google Scholar
O. C. Adebukola, A. O. Opeyemi, and A. I. Ayodeji, “Knowledge of food borne infection and food safety practices among local food handlers in Ijebu-Ode local government area of Ogun state,” Journal of Public Health and Epidemiology, vol. 7, no. 9, pp. 268–273, 2015.
View at: Google Scholar
D. Nigusse and A. Kumie, “Food hygiene practices and prevalence of intestinal parasites among food handlers working in Mekelle University students cafeteria,” Mekelle Global Advanced Research Journal of Social Science, vol. 1, no. 4, pp. 65–71, 2012.
View at: Google Scholar
A. Gashe, K. Alemu, and D. Haile, “Factors affecting food handling practices among food handlers of Dangila town food and drink establishments North West Ethiopia,” BMC Public Health, vol. 14, p. 571, 2014.
View at: Google Scholar
K. Zeru and A. Kumie, “Sanitary conditions of food establishments in Mekelle town, Tigray, north Ethiopia,” Ethiopian Journal of Health Development, vol. 21, p. 1, 2007.
View at: Google Scholar
T. Tefera and G. Mebrie, “Prevalence and predictors of intestinal parasites among food handlers in Yebu own, southwest Ethiopia,” PLOS ONE, vol. 9, no. 10, article e110621, 2014.
View at: Publisher Site | Google Scholar
World Health Organization (WHO), “Food safety and HACCP checklist,” 2015, https://ncfreshproducesafety.ces.ncsu.edu/wpcontent/uploads/2014/03/SOPcklistHACCP.pdf?fwd=no.
View at: Google Scholar
M. Cheesbrough, District Laboratory Practice in Tropical Countries, Part 2, Cambridge University Press, New York, 2006.
View at: Publisher Site
M. Desta, “Prevalence of Salmonella and Shigella among food handlers in catering establishments in Hawassa University, Hawassa, Ethiopia,” AAU Electronic libraryFull thesis, pp. 1–42, 2010.
View at: Google Scholar
F. Wadilo, F. Solomon, A. Arota, and Y. Abraham, “Intestinal parasitic infection and associated factors among food handlers in South Ethiopia: a case of Wolaita Sodo town,” Journal of Pharmacy and Alternative Medicine, vol. 12, pp. 5–10, 2016.
View at: Google Scholar
M. Dagnew, M. Tiruneh, F. Moges, and Z. Tekeste, “Survey of nasal carriage of Staphylococcus aureus and intestinal parasites among food handlers working at Gondar University, Northwest Ethiopia,” BMC Public Health, vol. 12, no. 1, p. 837, 2012.
View at: Publisher Site | Google Scholar
K. Ahmed, R. Aman, G. Morka, A. Abebe, and A. Esmael, “Predictors of intestinal parasitic infection among food handlers working in Madda Walabu University, Ethiopia: a cross-sectional study,” Interdisciplinary Perspectives on Infectious Diseases, vol. 2020, no. 8, pp. 1–8, 2020.
View at: Google Scholar
D. Gezehegn, M. Abay, D. Tetemke et al., “Prevalence and factors associated with intestinal parasites among food handlers of food and drinking establishments in Aksum Town, Northern Ethiopia,” BMC Public Health, vol. 17, no. 1, p. 819, 2017.
View at: Publisher Site | Google Scholar
A. O. Forson, I. Arthur, and P. F. Ayeh-Kumi, “The role of family size, employment and education of parents in the prevalence of intestinal parasitic infections in school children in Accra,” PLoS One, vol. 13, no. 2, 2018.
View at: Google Scholar
A. Aklilu, D. Kahase, M. Dessalegn et al., “Prevalence of intestinal parasites, salmonella and shigella among apparently health food handlers of Addis Ababa University student’s cafeteria, Addis Ababa, Ethiopia,” BMC Research Notes, vol. 8, no. 1, p. 17, 2015.
View at: Publisher Site | Google Scholar
G. Andargie, A. Kassu, F. Moges, M. Tiruneh, and K. Huruy, “Prevalence of bacteria and intestinal parasites among food-handlers in Gondar town, northwest Ethiopia,” Journal of Healtrh Population and Nutration, vol. 26, no. 4, pp. 451–455, 2008.
View at: Google Scholar
O. Idowu and S. Rowland, “Oral fecal parasites and personal hygiene of food handlers in Abeokuta, Nigeria,” African Health Sciences, vol. 6, no. 3, pp. 160–164, 2006.
View at: Publisher Site | Google Scholar
T. Kusolsuk, W. Maipanich, S. Nuamtanong et al., “Parasitic and enteric bacterial infections among food handlers in tourist-area restaurants and educational-institution cafeterias, Sai-Yok district, Kanchanaburi province, Thailand,” Journal of Tropical Medicine and Parasitology, vol. 34, no. 2, pp. 49–53, 2011.
View at: Google Scholar
S. Khurana, N. Taneja, R. Thapar, M. Sharma, and N. Malla, “Intestinal bacterial and parasitic infections among food handlers in a tertiary care hospital of North India,” Tropical Gastroenterology, vol. 29, no. 4, pp. 207–209, 2008.
View at: Google Scholar
A. Gebreyesus, K. Adane, L. Negash et al., “Prevalence of Salmonella typhi and intestinal parasites among food handlers in Mekelle University student cafeteria, Mekelle, Ethiopia,” Food Control, vol. 44, pp. 45–48, 2014.
View at: Publisher Site | Google Scholar
T. Yesigat, M. Jemal, and W. Birhan, “Prevalence and associated risk factors of Salmonella, Shigella, and intestinal parasites among food handlers in Motta Town, North West Ethiopia. Canadian,” Journal of Infectious Diseases and Medical Microbiology, vol. 2020, p. 11, 2020.
View at: Google Scholar

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Copyright © 2021 Abera Kumalo et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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