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Toxocariasis and Ingestion of Raw Cow Liver in Patients with Eosinophilia

Toxocariasis and Ingestion of Raw Cow Liver in Patients with Eosinophilia

Article information

Korean J Parasito. 2008;46(3):139-143
Publication date (electronic) : 2008 September 20
doi : https://doi.org/10.3347/kjp.2008.46.3.139
1Department of Radiology and Center for Imaging Science, Korea.
2Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
3Department of Laboratory Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul 135-710, Korea.
4Department of Parasitology, College of Medicine, Hallym University, Chuncheon 200-702, Korea.
Corresponding author (jhlim@skku.edu)
Received 2008 June 24; Accepted 2008 August 13.

Abstract

Ingestion of raw animal liver has been suggested as a possible mode of infection of human toxocariasis. We evaluated the relationship between toxocariasis and the ingestion of raw meat in patients with eosinophilia of unknown etiology. The study population consisted of 120 patients presenting with peripheral blood eosinophilia (> 500 cells/µl or > 10% of the white blood cell count). They were divided into 2 groups: 104 seropositive patients based on a Toxocara excretory-secretory IgG ELISA and 16 seronegative patients. While 25.0% of seronegative patients had a recent history of eating raw cow liver, 87.5% of seropositive patients had this history. Multivariate statistical analysis showed that a recent history of eating raw cow liver was related to an increased risk of toxocariasis. Collectively, it is proposed that raw cow liver is a significant infection source of toxocariasis in the patients with eosinophilia of unknown etiology.

INTRODUCTION

Toxocara canis is a common round worm found in the small intestines of dogs; however, T. canis can also infect other animals. Infection of dogs as well as other animals takes place by ingestion of soil contaminated with eggs in dooryards and parks. The infected larvae reach the liver and are dormant in the liver parenchyme. They move slowly from place-to-place within the liver, or migrate to the lungs and other tissues, which is called as visceral larva migrans [1,2]. These encapsulated larvae in animal tissues do not grow into adult worms, but are capable of transmitting to other animals that eat the infected tissues harboring encapsulated larvae. This mode of transmission among carnivorous vertebrates has been established with experimental studies [1,3-5]. A large variety of non-canine animals can be infected with T. canis. Known paratenic hosts include mice, rats, chickens, pigeons, lambs, pigs, and cows. Animals are infected by ingestion of embryonated eggs in contaminated soil or of encapsulated larvae in the tissues of paratenic hosts.

Like animals, human infections may take place in 2 ways: 1) ingestion of embryonated eggs, and 2) transfer (ingestion) of encapsulated larvae of T. canis in the tissues of a paratenic host [2]. In certain ethnic groups, some adults tend to eat uncooked animal tissues which contain encapsulated infective larvae. After swallowing, the encapsulated larvae are liberated after hatching in the small intestine, penetrate the intestinal wall, get into the portal vein, and then reach the liver and lungs. They again become encapsulated and remain alive for a certain period. Uncooked livers of cow [3,6-8], pig [9], lamb [10], and chicken [11,12] have been reported as sources of human infections. However, epidemiologic data on the role of ingesting raw liver of animals in the transmission of T. canis from animals-to-humans is limited [8]. In order to evaluate the relationship between toxocariasis and the ingestion of raw meat, we conducted a prospective study.

MATERIALS AND METHODS

Patients

Between March 2006 and April 2007, 146 patients registered in the allergic clinic in Samsung Medical Center, Sungkyunkwan University School of Medicine, for evaluation of eosinophilia of unknown etiology. Eosinophilia was defined as > 500 cells/µl in the peripheral blood or ≥ 10% of the total white blood cell count [13]. Among the 146 patients, 120 agreed to participate in this study. One interviewer gave the patients a questionnaire. We told the patients on the possibility of toxocariasis through ingestion of uncooked animal tissues or breeding dogs in the house or garden. The study protocol was approved by the Institutional Review Board and we obtained an informed consent from each patient. There were 97 males and 23 females (age range, 21-76 yr; median age, 53 yr, mean age, 53.4 yr) enrolled in the study.

Questionnaire

One trained interviewer used a structured questionnaire to collect data regarding each patient's social characteristics, including a history of eating raw liver or meat of cows or other animals, raw blood of animals, and raw freshwater fish. The questionnaire contained the time and frequency, the number of occasions and the amount they ate, and the species of animals. The questionnaire also included a question whether patients had a recent history (within a year) of keeping dogs. The study coordinator and physicians made every effort to keep the interviewer blind to the clinical information of the patients. After a thorough review of the questionnaire filled up by the interviewer, an experienced physician without knowledge of any other information concerning the patient determined whether or not he or she had a significant history of eating raw tissues of animals or freshwater fish. The patient was considered to have a significant recent history of eating raw tissues if he or she met all of the following criteria: 1) one or more definite experiences of eating raw tissues of animals or fish, 2) the amount consumed was more than a single mouthful, and 3) the time of ingestion was within 1 yr.

Diagnosis of toxocariasis

ELISA kit (Bordier Affinity Products SA, Crissier, Switzerland) was used for the serologic diagnosis of human toxocariasis, which detects human IgG antibodies to Toxocara excretory-secretory (ES) antigens. This kit has been reported to have a 91% sensitivity and a 86% specificity [14]. The titers for positive results were variable, according to the daily reference control. Although some cross reactions may occur in other human helminthiases, such as trichinosis, fascioliasis, and strongyloidiasis, the titers in these helminthiases are lower than those in positive control sera in patients with toxocariasis [14]. All patients underwent ELISA for parasite infections not uncommon in Korea, i.e., Clonorchis sinensis, Paragonimus westermani, sparganosis, and cysticercosis.

Statistical analysis

We evaluated the relationships of patients with positive results in Toxocara ELISA and their recent histories of eating raw livers of cows or other animals, raw meat of animals, raw blood of animals, and a history of eating raw freshwater fish, a history of keeping dogs, and serologic results of other parasites with multivariate statistical analysis. Odd ratios (ORs) of results of Toxocara ELISA, together with their corresponding 95% confidence intervals (CIs), in relation to 7 variables were derived using a multiple logistic regression analysis. A P value of < 0.05 was considered a significant difference. Data analyses were performed with a commercially available software program (SPSS for Windows, version 11.0; SPSS, Chicago, Illinois, USA).

RESULTS

One hundred four (86.7%) of the 120 patients showed positive results in Toxocara ELISA tests. Among them, 92.3% were confidently diagnosed as toxocariasis because they had no other possible causes to increase the eosinophil count. Twenty-four patients were diagnosed as other parasitic infections, as they showed positive ELISA results for C. sinensis (n = 12), P. westermani (2), sparganosis (4), and cysticercosis (6). Among the seropositive patients for toxocariasis, 87.5% had a recent history of consuming raw cow liver, whereas only 25.0% of seronegative patients had such a history. In 28 patients who ate raw cow livers frequently (4 times or more per year), the seropositive rate was 96.4%. In 45 patients who ate raw cow livers within 6 months prior to the interview, the seropositive rate was 95.6%. Twenty-one patients ate raw livers of animals other than the cow, such as pig (n = 7), dog (4), goat (3), chicken (3), rabbit (2), duck (1), and goose (1). Among these patients, 95.2% had a history of eating raw cow liver. Nineteen patients drank raw blood of animals, such as deer (n = 16), goat (2), duck (2), cow (1), pig (1), or mud turtle (1).

Table 1 presents the distribution of seropositive and seronegative patients in Toxocara ELISA. According to multivariate analyses, a recent history of eating raw cow liver was related to an increased risk of toxocariasis. Recent histories of eating raw liver of other animals, raw meat of animals, raw blood of animals, and raw freshwater fish, keeping dogs, and serologic results for other parasites were not related to an increased risk of toxocariasis.

Distribution of 104 seropositive and 16 seronegative patients for Toxocara ELISA

DISCUSSION

Chops of raw cow liver are one of the popular dishes in some restaurants or buffets in Korea. Chops of raw cow liver are usually served along with usual cooked or barbecued meat. Some people believe that raw liver and meat are good for health, particularly for eyesight. In our study population, patients had a history of eating raw cow liver within 1 yr and some people ate chops of raw cow liver frequently whenever they go to meat restaurants. Not infrequently, some people eat raw liver of pigs, dogs, chickens, goat, duck, goose, or rabbits. Because of this eating habit, there are many patients with subclinical toxocariasis. Usually, they are checked by clinicians because of eosinophilia [8], or sometimes after small nodular lesions are incidentally found in the liver, lungs, or both on sonography or computed tomography [7].

The results of our study suggest that the ingestion of raw cow liver substantially increase the risk of toxocariasis. The seropositive rate in patients who ate raw cow liver was more than 3 times higher than in patients who did not eat raw cow liver. Patients who ate raw cow liver frequently or more recently showed very high seropositive rates. It appears that the seropositive rate is higher in people who had history of eating raw cow liver frequently and recently.

In spite of being seropositive for toxocariasis, some patients denied a history of ingestion of cow livers. Ingestion of raw livers of pigs, lambs, and chicken has been reported as route of human infections [9-12]. We attempted to establish a role of eating habit of raw animal livers other than cow livers in toxocariasis. There were 21 seropositive patients who had a history of eating raw livers of other animals, but they all had a history of eating cow livers as well. Therefore, we could not verify the relation between toxocariasis and ingestion of raw livers of other animals.

Several patients who denied a history of ingestion of cow livers were keeping dogs (3 in the house and the other 4 in gardens). Infection might take place by ingestion of eggs of T. canis, which were laid by their own dogs and then embryonated in their surroundings. In our study, however, the history of keeping dogs was not statistically significant in infection of T. canis. Among these 7 patients, 3 were not only keeping dogs but also ate raw meat of animals within 1 yr. In other 2 patients who were seropositive without history of raw cow liver ingestion, infection might have taken place by eating raw cow meat. They have eaten raw meat of animals without history of keeping dogs. There have been several case reports that toxocariasis probably took place by ingestion of raw meat of animals [15,16]. In animal experiments, Toxocara larvae were recovered in the lungs, liver, kidneys, brain, and also in muscles [3,17]. Tahira et al. [18] suggested the possibility of zoonotic risk of toxocariasis through eating animal meat. In our study, many adults who ate raw cow liver also ate raw cow meat. We could not make a differentiation of the patients infected through ingestion of raw cow liver from those infected through ingestion of raw cow meat.

We did not determine the route of toxocariasis in 4 patients. We cannot exclude the possibility of toxocariasis by other Toxocara spp., such as T. cati and T. leonina [19]. There may be some cross reaction of human IgG antibodies to Toxocara ES antigens to other helminthiases, such as trichinosis, fascioliasis, and strongyloidiasis [20].

The toxocariasis seropositive rate in general population is variable depending on countries; specifically, 18% in rural areas in China [21], 20% in Malaysia [22], 26% in Iran [23], 6-36% in the Czech Republic [24], 2-5% and 14-37% in urban and rural areas in the Midi-Pyrenees area in France, respectively [25], 5% in Switzerland [26], and 5% in a rural area of Korea [27]. Because dogs and cats are popular pets, there is widespread contamination of environment with infective eggs, and therefore toxocariasis is a worldwide disease, irrespective of developed or underdeveloped countries. Higher rates of seroprevalence have been reported in Indonesia (68%) and Nepal (81%) [28,29]. It was suggested that a high seroprevalence among healthy adults of Taiwanese aboriginal populations (46%) was due to their habit of eating raw liver or meat [9]. The population enrolled in this study consisted of patients with eosinophilia of unknown etiology. Thus, they showed very high rates of seropositivity for toxocariasis and a history of eating raw cow liver. Further studies on the relationship between toxocariasis and ingestion of raw food in general population with lower seropositive rate are needed.

This study had some limitations. This study was cross-sectional and thus temporal associations cannot be inferred. A bias arising from recall data based on the patient's ability to recall past history of eating raw tissue of animals cannot be avoided. We first expected the ingestion of raw liver of other animals and raw meat of animals as possible risk factors. However, only the ingestion of raw cow liver increased the risk of toxocariasis in our multivariate statistics. The two ingestion histories could not be demonstrated as risk factors because of the small numbers of cases and substantial overlapping histories of ingesting raw cow livers. Another limitation is that we did not count the amount of animal tissues ingested in determining the seropositivity of the enrolled patients. Finally, the results of this study could be different from the general people. Only a minority of Koreans eat raw cow liver. When we designed this study, we worried about a very low toxocariasis seropositive rate in general population. Therefore, we selected patients with eosinophilia.

With the limitations of our study in mind, we suggest that ingestion of raw cow liver increase the risk of toxocariasis. Ingestion of uncooked livers of paratenic hosts may also be a potential source of human toxocariasis, at least in patients with eosinophilia.

ACKNOWLEDGEMENTS

This work was supported by the Samsung Biomedical Research Institute grants, Seoul, Korea (No. SBRI C-A6-424-2).

References

1. Glickman LT, Schantz PM. Epidemiology and pathogenesis of zoonotic toxocariasis. Epidemiol Rev 1981. 3230–250. 7030762.
2. Gillespie SH, Hawkey PM. Medical Parasitology 1995. 1st edth ed. New York, USA: Oxford University Perss Inc; 177–183.
3. Lee KT, Min HK, Chung PR, Chang JK. Studies on the inducing possibility of human visceral larva migrans associated with eating habit of raw liver of domestic animals. Korean J Parasitol 1976. 1451–60.
4. Pahari TK, Sasmal NK. Experimental infection of mice with Toxocara canis larvae obtained from Japanese quails. Int J Parasitol 1990. 20263–264. 2332284.
5. Pahari TK, Sasmal NK. Experimental infection of Japanese quail with Toxocara canis larvae through earthworms. Vet Parasitol 1991. 39337–340. 1957494.
6. Fitzgerald PR, Mansfield ME. Visceral larva migrans (Toxocara canis) in calves. Am J Vet Res 1970. 31561–565. 5462751.
7. Chang S, Lim JH, Choi D, Park CK, Kwon NH, Cho SY, Choi DC. Hepatic visceral larva migrans of Toxocara canis: CT and sonographic findings. AJR Am J Roentgenol 2006. 187W622–W629. 17114516.
8. Kwon NH, Oh MJ, Lee SP, Lee BJ, Choi DC. The prevalence and diagnostic value of toxocariasis in unknown eosinophilia. Ann Hematol 2006. 85233–238. 16463154.
9. Fan CK, Lan HS, Hung CC, Chung WC, Liao CW, Du WY, Su KE. Seroepidemiology of Toxocara canis infection among mountain aboriginal adults in Taiwan. Am J Trop Med Hyg 2004. 71216–221. 15306714.
10. Salem G, Schantz P. Toxocaral visceral larva migrans after ingestion of raw lamb liver. Clin Infect Dis 1992. 15743–744. 1420700.
11. Nagakura K, Tachibana H, Kaneda Y, Kato Y. Toxocariasis possibly caused by ingesting raw chicken. J Infect Dis 1989. 160735–736. 2794572.
12. Morimatsu Y, Akao N, Akiyoshi H, Kawazu T, Okabe Y, Aizawa H. A familial case of visceral larva migrans after ingestion of raw chicken livers: appearance of specific antibody in bronchoalveolar lavage fluid of the patients. Am J Trop Med Hyg 2006. 75303–306. 16896137.
13. van Assendelft OW. Reference values for the total and differential leukocyte count. Blood Cells 1985. 1177–96. 4074894.
14. Jacquier P, Gottstein B, Stingelin Y, Eckert J. Immunodiagnosis of toxocarosis in humans: evaluation of a new enzyme-linked immunosorbent assay kit. J Clin Microbiol 1991. 291831–1835. 1774303.
15. Schantz PM. Toxocara larva migrans now. Am J Trop Med Hyg 1989. 4121–34. 2679161.
16. Stürchler D, Weiss N, Gassner M. Transmission of toxocariasis. J Infect Dis 1990. 162571.
17. Dubey JP. Migration of Toxocara cati larvae in mice. Trop Geogr Med 1968. 20172–176. 5690282.
18. Taira K, Saeed I, Permin A, Kapel CM. Zoonotic risk of Toxocara canis infection through consumption of pig or poultry viscera. Vet Parasitol 2004. 121115–124. 15110409.
19. Min HK. An epidemiological study on zoonoses in Korea. Korean J Parasitol 1981. 1960–75.
20. Watthanakulpanich D, Smith HV, Hobbs G, Whalley AJ, Billington D. Application of Toxocara canis excretory-secretory antigens and IgG subclass antibodies (IgG1-4) in serodiagnostic assays of human toxocariasis. Acta Trop 2008. 10690–95. 18343348.
21. Luo ZJ, Wang GX, Yang CI, Luo CH, Cheng SW, Liao L. Detection of circulating antigens and antibodies in Toxocara canis infection among children in Chengdu, China. J Parasitol 1999. 85252–256. 10219304.
22. Hakim SL, Mak JW, Lam PL. ELISA seropositivity for Toxocara canis antibodies in Malaysia, 1989-1991. Med J Malaysia 1993. 48303–307. 8183143.
23. Sadjjadi SM, Khosravi M, Mehrabani D, Orya A. Seroprevalence of Toxocara infection in school children in Shiraz, southern Iran. J Trop Pediatr 2000. 46327–330. 11191141.
24. Uhlíková M, Hübner J. Seroprevalence of Toxocara canis infection in Czech Republic. Cent Eur J Public Health 1998. 6195–198. 9787920.
25. Pelloux H, Faure O. Toxocariasis in adults. Rev Med Interne 2004. 25201–206. 15049281.
26. Speiser F, Gottstein B. A collaborative study on larval excretory/secretory antigens of Toxocara canis for the immunodiagnosis of human toxocariasis with ELISA. Acta Trop 1984. 41361–372. 6084948.
27. Park HY, Lee SU, Huh S, Kong Y, Magnaval JF. A seroepidemiological survey for toxocariasis in apparently healthy residents in Gangwon-do, Korea. Korean J Parasitol 2002. 40113–117. 12325440.
28. Rai SK, Uga S, Ono K, Nakanishi M, Shrestha HG, Matsumura T. Seroepidemiological study of Toxocara infection in Nepal. Southeast Asian J Trop Med Public Health 1996. 27286–290. 9279991.
29. Uga S, Ono K, Kataoka N, Hasan H. Seroepidemiology of five major zoonotic parasite infections in inhabitants of Sidoarjo, East Java, Indonesia. Southeast Asian J Trop Med Public Health 1996. 27556–561. 9185269.

Article information Continued

Table 1.

Distribution of 104 seropositive and 16 seronegative patients for Toxocara ELISA

History Positive rate (%) for Toxocara ELISA Negative rate (%) for Toxocara ELISA P valuea OR (95% CI)b
Ingesting raw cow liver
 Ever 87.5 25.0 < 0.001 34.861 (5.971-203.513)
 Never 12.5 75.0
Ingesting raw liver of other animals
 Ever 19.2 6.3 0.974 1.040 (0.098-11.002)
 Never 80.8 93.8
Ingesting raw meat of animals
 Ever 77.9 31.3 0.388 1.979 (0.419-9.340)
 Never 22.1 68.8
Ingesting raw blood of animals
 Ever 17.3 6.3 0.997 1.004 (0.087-11.597)
 Never 82.7 93.8
Ingesting raw freshwater fish
 Ever 28.8 12.5 0.489 2.023 (0.275-14.901)
 Never 71.2 87.5
Keeping a dog
 Ever 34.6 18.8 0.082 5.260 (0.811-34.115)
 Never 65.4 81.3
Serologic tests for other parasites
 Positive 21.2 12.5 0.054 7.281 (0.970-54.678)
 Negative 78.8 87.5
a

Multivariate statistical results by using multiple logistic regression analysis.

b

OR, odds ratio; 95% CI, 95% confidence interval.