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Ghana Medical Journal logoLink to Ghana Medical Journal
. 2018 Jun;52(2):88–93. doi: 10.4314/gmj.v52i2.5

Parasitic contamination of commonly consumed vegetables in two markets in Ghana

Catherine Kudah 1,, Simon Sovoe 1, Frank Baiden 1,2
PMCID: PMC6326541  PMID: 30662081

Summary

Introduction

Fresh vegetables are an important source of vital nutrients. Poor farming practices and improper washing put consumers at risk of parasitic infections. This study explored the presence of parasitic contamination of commonly-consumed vegetables procured from two markets in Ghana. It also explored the decontamination effects of washing vegetables with different concentrations of saline solution.

Method

Vegetables were procured from two major open markets in Koforidua, Ghana. Vegetables were thoroughly washed twice using 0.0%, 0.45%, 0.9%, 1.5% concentrations of saline solutions. The deposits were examined under the light microscope for the presence of parasites. Smears were made from sediments, stained and observed with Fluorescence microscope to detect any spores or oocysts of Microsporidium sp., and Cryptosporidium sp.

Result

Three hundred and sixty of five types of vegetables were procured. Two hundred and seven (57.5%, 95% Confidence Interval 52.2% – 62.7%) were found to be contaminated with at least one type of parasite. The extent of vegetable contamination was 97.2% (90.3–99.7) of spring onions, 70.8% (58.9–81.0) of lettuce and 50.0% (38.0–62.0) of tomatoes. The commonest parasites were Strongyloides stercoralis (36.4%, 31.4–41.6), Balantidium coli (13.6%, 10.2–17.6) and Cryptosporidium oocyst (11.1%, 8.1–14.8). Parasite recovering rates were 57.5% (52.2–62.7) and 42.2% (37.1–47.5) after first and second washings respectively.

Conclusion

The level of parasite contamination is high and consumption of raw vegetables procured from these markets carry a high risk of parasite infection. Washing vegetables twice with saline was not effective for parasite removal. Improved approaches for washing vegetables before consumption are needed.

Funding

Ensign College-Students Research Award Program of Bob and Lynette Gay

Keywords: Parasites, contamination, vegetables, market, Ghana

Introduction

Fresh vegetables are a major source of vital nutrients. Consumption is promoted for the vitamins, minerals, dietary fiber, and antioxidants it provides. Traditional practices in the cultivation, manuring and harvesting of vegetables in many parts of sub-Saharan Africa remains an area of concern. The use of sewage and other form of liquid waste during cultivation are potential source of contamination with the eggs and larvae of parasitic infections. Human infection occurs through consumption of raw vegetables.1, 2

Epidemiological studies have indicated that in areas of the world where helminthic diseases are endemic and where raw untreated waste water is used to irrigate vegetables generally eaten uncooked, the consumption of such waste irrigated vegetables may lead to parasitic infestation.3 Bad hygienic practice during transport, processing and preparation by handlers including consumers could also contribute to vegetable contaminations. Other factors which affect the susceptibility of the public to foodborne diseases include food consumption patterns, such as the increase in the number of people eating meals prepared in restaurants, canteens and fast food outlets as well as from street food vendors who do not always observe optimal food safety.

In developing countries, the diarrhea diseases of food or hydrous origin have been reported to kill about 2.2million people annually.4 It is common in Ghana to see farmers cultivate vegetables near gutters and other waste water disposal routes.

The consumption of raw vegetables has been implicated in a number of outbreaks of diarrheal diseases. Outbreaks associated with diseases like giardiasis, amoebiasis, cyclosporiasis and cryptosporidiosis have been reported with high levels of morbidity and mortality in parts of the country.2

This study explored the presence of parasitic contamination of commonly-consumed vegetables procured from two markets in Ghana and examined the extent to which washing with different concentrations of saline solutions is able to remove the contaminants.

Methods

Study sites

Koforidua in the Eastern Region of Ghana is a major centre for the trade in vegetables. Many outlining areas in the municipality are under small and large-scale vegetable cultivation. The produce from these farms are transported to the main markets in Koforidua for sale. Traders, most of whom come from Accra buy bulk quantities of these vegetable for retail in markets in Accra. This study involved analysis of vegetables procured from the Central and Agartha markets in Koforidua. Fresh-delivered vegetables were conveniently picked by traditional buying methods from sellers who were told the purchased vegetables will be analyzed without any identifiers as to the persons from whom they were purchased.

Laboratory preparation

Each vegetable type was transported to the laboratory in plastic bags. First, the edible part was separated from non-edibles parts according to household practice. About 150–200g of cabbage was weighed and chopped; carrot and spring onion were chopped; the leafy part of lettuce were separated; and tomatoes were washed with 150 ml of different concentrations of saline concentrations (0.0%, 0.45%, 0.9%, 1.5%NaCl) prepared after being autoclaved. The washing water was left for 12 hours for it to sediment after using gauze to remove visible particles, the top water was discarded, and the remaining water was centrifuged at 1500 rpm for five minutes.

Each particular vegetable in a given level of concentration was washed twice i.e. first and second wash. The processing for analysis (saline preparation, autoclaving and staining) followed standard guidelines as described in laboratory standard operation manuals which was adapted from “District Laboratory Practice In Tropical Medicine”.5 Personal safety precautions were taken during every procedure.

The supernatant was removed and the residue carefully collected in the test tube by tapping the bottom of the tube and transferring unto labeled clean slides for examination purposes. A drop of the sediment was applied on the center of a clean grease-free labeled slide. A clean cover slip was placed gently to avoid air bubbles and over flooding. The preparation was examined under a light microscope using X10 and X40 objectives (OLYMPUS CX21). The sediment was mixed with a drop of Lugol's Iodine solution and examined as in simple smear for the purpose of parasite confirmation. Two (2) slides were prepared for each sediment.

Sediment smears were stained for the purpose of Fluorescence microscopy to detect any oocysts and spores of Microsporidium sp., and Cryptosporidium sp. Two slides were prepared for each sediment for fluorescence staining.6 A thin smear of the sediment was done, air dried and fixed with methanol for 3 minutes. The slides were stained with Auramine O-phenol for 20 minutes, after which the slides were washed with distilled water, and then differentiated in 0.5 % hydrochloric acid-ethanol solution for 3 minutes. The slides were rinsed in distilled water and counter stained with 0.5% potassium per manganate for 30 seconds. The slides were rinsed with water; air dried, and examined microscopically using 40x objective lens of fluorescence microscope (ZEISS). Pictorial guide from “District Laboratory Practice in Tropical Medicine” were used. Parasites were recorded as either present or not. The parasites were counted as well.5

Data Analysis

Data was recorded on specially-designed study record forms. This was subsequently entered into Excel worksheet. Frequencies were run on all variables to check for errors and inconsistency. These were corrected through checking with the original entry on the record forms. It was exported into STATA version 14.0 (StataCorp Lp). Chi square tests were done to test for associations between presence of parasite and (market type, vegetable types and the different saline concentrations). The 95% confidence intervals were constructed around the identified levels of contamination.

Ethical approval for the study was obtained from the Institutional Review Board of the Ensign College of Public Health.

Results

A total of 360 samples of salad vegetables which included tomatoes (72), carrot (72), lettuce (72), cabbage (72), spring onion (72) were bought from two major market sites between January and March 2017.

They were examined for parasitological contamination at the Regional Hospital Laboratory, Koforidua. The period of sample collection coincided with the dry season in Eastern Region of Ghana. Two hundred and seven (57.5%, 95% Confidence Interval 52.2% – 62.7%) samples were identified to be contaminated with at least one type of parasite.

These include 97.2% (90.3–99.7) of spring onions, 70.8% (58.9–81.0) of lettuce, 50.0% (38.0–62.0) of tomatoes, 43.1% (31.4–55.3) of cabbage and 26.4% (16.7–38.1) of carrot. The types of parasites identified were Strongyloides stercoralis larvae (36.4%, 31.4–41.6), Balantidium coli (13.6%, 10.2–17.6), Cryptosporidium sp. oocyst (11.1%, 8.1–14.8), flagellates (7.8%, 5.2–11.0) and Fasciola egg (7.2%, 4.8–10.4) (Table 1).

Table 1.

Types of vegetable and parasite contaminants

Vegetable Type Number
Examined
Strongyloides
stercoralis
n(%)
Balantidium coli
n (%)
Fasciola egg
n (%)
Flagellate
n (%)
Cryptosporidium
oocyst n (%)
Cabbage 72 8 (11.1) 21 (29.2) 0 (0) 10 (13.9) 12 (16.7)
Lettuce 72 39 (54.2) 3 (4.2) 26 (36.1) 0 (0) 15 (20.8)
Carrot 72 14 (19.4) 2 (2.8) 0 (0) 3 (4.2) 4 (5.6)
Spring onion 72 70 (97.2) 1 (1.4) 0 (0) 0 (0) 8 (11.1)
Tomatoes 72 0 (0) 22 (30.6) 0 (0) 15 (20.8) 1 (1.4)
Total 360 131 (36.4) 49 (13.6) 26 (7.2) 28 (7.8) 40 (11.1)

n = number of vegetable type contaminated

No oocyst of Microsporidium sp. was detected during the fluorescence microscopy. Only oocyst of Cryptosporidium sp. was detected. Strongyloides stercoralis larvae were detected in all the vegetable types except tomatoes. Fasciola egg was found only in lettuce. Some amount of Cryptosporidium sp. oocyst and Balantidium coli were found in all the vegetable types. Flagellates were recovered from cabbage, carrot, tomatoes and not in lettuce and spring onion (Table 1).

The parasitic contamination rate among the different vegetable types; tomatoes, cabbage, lettuce, spring onion and carrot were reasonably high. The test of association between the vegetable types and parasitic contamination was very significant different (p value < 0.001). Test of association (Chi-square) between different saline concentration that were used for the washing of vegetables and parasitic contamination showed no significant difference (p value =0.623).

The study showed that parasitic contamination was higher for vegetables from Agartha market (67.8%) than from the main market (47.2%).

There was however, a significant difference (p<0.001) for test of association between parasite detected and market type (Table 2).

Table 2.

Parasitic contamination per market, vegetable type and effect of washing with different concentrations of saline solutions

Variables (n= 360) Total Positive (% with 95% CI) chi-square p-value
Market 15.5612 < 0.001
Agartha 180 122 (67.8%, 60.4–74.5)
Main Market 180 85 (47.2%, 39.8–54.8)
Vegetable Type 88.0477 < 0.001
Cabbage 72 31 (43.1%, 31.4–55.3)
Lettuce 72 51 (70.8%, 58.9–81.0)
Carrot 72 19 (26.4%, 16.7–38.1)
Spring Onion 72 70 (97.2%, 90.3–99.7)
Tomatoes 72 36 (50.0%, 38.0–62.0)
Saline Concentration after first wash (g/dl) 1.7619 0.623
0 90 50 (55.6%, 44.7–66.0)
0.45 90 57 (63.3%, 52.5–73.2)
0.9 90 49 (54.4%, 43.6–65.0)
1.5 90 49 (54.4%, 43.6–65.0)
Total 360 207 (57.5%, 52.2–62.7)
Saline Concentration after second wash (g/dl) 3.9170 0.271
0 90 40 (44.4%, 34.0–55.3)
0.45 90 43 (47.8%, 37.1–58.6)
0.9 90 37 (41.1%, 30.8–52.0)
1.5 90 32 (35.6%, 25.7–46.3)
Total 360 152 (42.2%, 37.1–47.5)

Discussion

The study aimed to estimate parasitic contamination of commonly consumed salad vegetables sold in two major market sites in Koforidua, New Juaben Municipal. The overall prevalence was 57.5%. The highest contaminated vegetable being 97.2% of spring onion, followed by 70.8% of lettuce, 50.0% of tomatoes, and 43.1% of cabbage and the least being 26.4% of carrot.

The overall parasitic recovering rate among all the vegetable types in this study was consistent with previous report from Jimma Town, Southwest Ethiopia (57.8%).7 In similar studies done in Ghana, Accra, a much lower recovering rate of 36.0% was observed.2 Other lower prevalence rates were detected in Alexandria, Egypt6, in Ardabil, Iran8, and Nigeria3 where the contamination rates were (31.7%), (29%), and (36%) respectively. Much lower rates of contamination were detected in Riyadh, Saudi Arabia (16.2%) 9, and Turkey (6.3%).10 Higher prevalence rate were detected in Kenya (65.5%)11, Tripoli, Libya (68%)12 and in Khorramabad, Iran (79%).13

This variation in contamination rates of the vegetables may in part, be due to the differences in shape and surface of vegetables. Green leafy vegetables such as lettuce has uneven surfaces that probably facilitate sticking of parasitic eggs, cysts, and oocysts more readily, either at the farm or when washed with contaminated water. However, vegetables with smooth surface such as carrot had the lowest prevalence rates. The differences in the prevalence rate may also have been due to different sample size, sampling method, laboratory investigation methods used and cross contamination during transportation, or handling of vegetables in the market.6

The most contaminated vegetable type identified was spring onion and the least being carrot. However, in similar study in Accra, lettuce was found to be the most contaminated (61%) while tomatoes was the least (18%).2 Other works done in Benha, Egypt, and Saudi Arabia, identified lettuce as the most contaminated vegetable where prevalence were 45.5% and 27.8% respectively. This difference may be due to pre harvest factors such as contaminated water mostly used for irrigation and soil contaminate with human feces.14, 15

The most frequent occurring parasite was Strongyloides stercoralis larvae (36.4%) and the least occurring was Fasciola egg (7.2%), flagellate was (7.8%), Balantidium coli was 13.6%, and Cryptosporidium sp. was 11.1%. Strongyloides stercoralis was also detected as the most occurring parasite (43%) in Duedu's work2 and 45.8% was detected in south western Nigeria while as a much lower prevalence rate of 1.1% was detected by Aziz and others and 16.5% in Jos, Nigeria.16,17 Strongyloides stercoralis has been noted to be widely distributed in areas of poor sanitation. Infection may have occurred due to soil and water being contaminated by human defecation. The differences in the rates may have been due to different geographical locations as well.

Balantidium coli was the second highest parasite detected in this study. A much lower prevalence of 8.19% and 0.8% were however detected in Ilorin, Nigeria and south western Nigeria respectively.16, 18 High contamination is possibly due to pig and human fecal matter contaminating the water supply used for irrigation.

Cryptosporidium sp. oocyst (11.11%) compared to similar study in Alexandria (29.3%), was lower.6 But much lower rates were detected in south Ethiopia and Norway with the prevalence of 4.72% and 6 % respectively.1, 19 Presence of Cryptosporidium sp. oocyst may be due to use of contaminated water used for irrigation.

Fasciola egg was identified as 7.2% in this study. Lower recovery rates of 5% was detected in similar studies in Iran8 and higher rate of 14.5% in Riyadh.9 Some Fasciola sp. are known to be zoonotic.20, 21

Other parasites like flagellates which were fast moving were recovered from almost all the vegetable types in this study.

Washing vegetables the second time recovered 42.2% parasites. This may be an indication that two wash alone is not enough to remove all the parasites from the vegetables. Duedu et al. (2014) has shown that, washing vegetables with just water was not enough to remove any contaminating parasites. He, however, recorded that using saline, phosphate buffered saline and tap water recovered 52%, 34% and 14% parasites respectively and use of saline was more effective in recovering of parasites.

Parasitic contamination was higher in Agartha market (67.8%) than the main market (47.2%). This might have been associated with mode of display of vegetable, exposure to dust and flies. Houseflies have been reported as a transport host for transmission of Cryptosporidium sp.2224

Several factors may have contributed to such differences the parasitic prevalence such as geographical area, category of samples examined, methods used for detection of the parasites, type of water used for irrigation, and processing of such vegetables which are different from country to another.

Conclusion

The level of parasitic contamination of vegetables in the two markets surveyed is high. This calls for public education on the rigor required to wash these vegetables before they are consumed. The sources of contamination of these vegetables need to be investigated to enable interventions at farm level to reduce levels of contamination.

Acknowledgement

This research was supported by Ensign College-Students Research Award Program of Bob and Lynette Gay. We appreciate the support of the medical laboratory scientists of the Eastern Regional Hospital Laboratory.

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