Abstract
Background:
Toxocariasis is a disease caused by Toxocara nematodes and occurs from consuming their eggs. The main hosts of these worms are dogs and cats. The disease in humans becomes a visceral larva migrans (VLM). This descriptive cross-sectional study was conducted to determine the prevalence of toxocariasis in children aged 6–14 years.
Methods:
This cross-sectional descriptive study was conducted from Jun 1 2016 to Dec 1 2017 in Sanandaj, west of Iran. A total of 182 serum samples were collected from children age 6 to14 yr referred to medical diagnostic laboratories. Demographic data (age, sex, and parents’ literacy status), clinical signs (cough, headache, fever, abdominal pain), and the history of contact with dogs and cats was collected by a questionnaire. The presence of anti-Toxocara IgG antibody was detected by T. canis IgG ELISA (IBL, Germany) kit.
Results:
Of 182 subjects, 97 (53.3%) were male and 85 (46.7%) female. The average age was 9.2 years. Antibodies against T. canis were positive in three cases (1.65%) of all the studied subjects.
Conclusions:
The results showed a low prevalence of toxocariasis in children studied.
Keywords: Children, Toxocara, Toxocariasis, Iran
Introduction
Toxocariasis is caused by a series of nematode species (called ascarids or Toxocara spp.) that routinely infect dogs and cats. T. canis (dog roundworm) is the main cause of the disease in humans. Human toxocariasis is most prevalent helminthozoonosis diseases caused by T. canis and T. cati, due to the migration larvae through human organism.
The Toxocara eggs pass out of the body of the definitive host in the excreta feces, the embryonation of eggs occurs in the soil (1). Stray dogs are considered as the most important causes of outbreaks in the environment; in the process of they disperse feces in the city’s parks, on the streets, or playgrounds, and in private gardens (2). Humans become an accidental host because of ingesting the eggs containing the larval stage of the Toxocara. Young children (aged 6–14 yr) have a higher chance of being exposed to the parasite eggs due to play and behavioral habits, usually by touching contaminated hands to the mouth or direct and close contact with the soil and dogs (3–5). Humans are infected by ingesting the eggs from contaminated soil, food, or water; and by eating undercooked meat of paratenic hosts like chicken, cow, and sheep (6, 7). The eggs hatch in the duodenum and the larvae penetrate the intestinal wall, then they are carried by the circulation system to a wide variety of tissues (liver, heart, lungs, brain, muscle, and eyes). Toxocara larvae tend to accumulate in an organ, especially in the CNS, causing a chronic disease (2).
The signs and symptoms vary with regard to the number of migrating juveniles and the involved organs. There are three clinical manifestation of Toxocara infection in humans as follows: 1) visceral toxocariasis or visceral larva migrans (VLM); 2) ocular toxocariasis or ocular larva migrans (OLM); 3) nervous toxocariasis or nervous larva migrans (NLM); and 4) covert or common toxocariasis (CT), is usually manifested as mild and non-specific. VLM symptoms usually include fever, cough, wheezing, hepatomegaly, splenomegaly, fatigue, malnutrition, anorexia, and abdominal pain. Toxocariasis is related to asthma, pulmonary inflammation, and eosinophilia in children. In addition, some of the complications of toxocariasis in the central nervous system have been reported as convulsions and mental and growth retardation (3, 8, 9). The migration of Toxocara larva to the eye (OLM) causes reduced visual acuity, strabismus, and, in some cases, blindness in one or both eyes due to granulomatous lesions in the retina. OLM in most cases occur in children aged 5– 10 yr (10). Serological techniques are reliable methods to detect larval antigens. Until now ELISA with Toxocara excretory–secretory antigens (TES-ELISA) is the most reliable methods to detect Toxocara-specific antibodies (11).
The prevalence of toxocariasis was reported in different countries as follows: Bolivia 27%, Brazil 8.7–38.8%, Chile 2.2%, Colombia 47.5%, Cuba 5.2%, Puerto Rico 6.5%, Venezuela 66.6%, Peru 32.4%, Ecuador 30%, Argentina 10.6–36.9%, Korea 50.5%, Spain 1%, and Denmark 2.4% (12–15). Based on previous data, the average seroprevalence of Toxocara infection from 2000 to 2010 among Iranian children was 15.8% (16).
Various factors, such as the presence of stray dogs in the city and the easy entry of dogs into parks may bring the spread of Toxocara eggs. One of the main problems for controlling and eradicating toxocariasis is the lack of accurate statistics for its prevalence. Therefore, this study was conducted to determine the prevalence of toxocariasis in children aged 6–14 yr in Sanandaj, Iran in 2017.
Materials and Methods
This cross-sectional descriptive study was conducted from Jun 1 2016 to Dec 1 2017 in Sanandaj. Sanandaj is the capital town of Kurdistan province in Iran with geographical coordinates of 35°20′ north, 47°18′ east of Greenwich meridian, and 15° west of Tehran meridian (Fig. 1) (17).
Fig. 1:
Geographical location of Sanandaj city in west of Iran
During Jun to Dec 2017, 182 serum samples were collected from children aged between 6 and 14 yr who referred to medical diagnostic laboratories. Samples were kept at −20 °C until the test was performed. Demographic data and history of contact with dogs were obtained by questionnaire.
The presence of anti-Toxocara IgG antibody of T. canis was detected by using IgG ELISA kit (IBL, Germany) and performed according to the manufacturer’s instructions.
STATA version 12.0 (Stata Corp, College Station, Texas USA) was used to analyze the data of the study. At first, the prevalence of contamination was assessed in general and then in terms of the variables considered. For all estimated values, a 95% confidence interval was also calculated.
Ethical approval
The present study was performed in accordance with the ethical standards of the Declaration of Helsinki. It was approved by the Ethics Committee of the Kurdistan University of Medical Sciences (Grant No. 1395/190).
Results
Of 182 samples, 97 (53.3%) were male and 85 (46.7%) female. The mean and standard deviation of the participants in the study were 9.2 and 2.6 yr, respectively. Three cases (95% CI = 0.349: 95% CI, P = 0.0165) showed antibodies against T. canis. Of them, two were female (95% CI-057/05%, P = 0.0235), and one was male (95% CI-0317 / 0– 95%, P = 0.0103). The mean and standard deviation of the age of the positive cases were 8 and 1 yr, respectively. Of these, 2 showed a history of contact with dogs. Abdominal pain was present in all three positive cases. Cough and headache was reported in the 2 positive cases.
Discussion
The average seroprevalence of toxocariasis in Iranian children is 15.8%. In this study, the prevalence rate was 1.64%. The seroprevalence of toxocariasis is similar to the results in urban area in Zanjan (1.6%) (18), Isfahan (1.39%) (19) and Ahwaz (2%) (16, 20). However, higher prevalences were reported in Sistan and Baluchestan (3.8%), Shiraz (25.6%) (21), East Azerbaijan (29.46%) (22), Hamedan (8.8%) (23), Sari (25%) (24), Lorestan (4.4%) (25) and Mahidasht (46.8%) (26).
Dogs are definitive hosts of T. canis and are a major factor in the spread of eggs in the environment. In another study conducted by the authors, the contamination rate in stray dogs in Sanandaj was 6.3% in 2017 (unpublished data). Otherwise, the average infection rate in dogs in Iran was 26.8% (16, 20). Therefore, a low prevalence in children in this study is related to the rate of infection in stray dogs within the geographical region of Sanandaj.
In this study, out of 3 positive cases, 2 cases were girls and 2 cases had a history of contact with dogs. There was no significant relationship between age, sex, history of contact with dogs, and the level of education of the parents. Abdominal pain was reported in all positive cases, cough and headache were reported in 2 out of the 3 positive cases. Fever was not seen in any of the positive cases.
Cultural differences such as the absence shepherds and domestic dogs can be attributed to the low prevalence in children who live in Sanandaj when compared with other areas.
Conclusion
This study shows a low prevalence of toxocariasis in children in Sanandaj at 2017.
Ethical considerations
Ethical issues (Including plagiarism, informed consent, misconduct, data fabrication and/or falsification, double publication and/or submission, redundancy, etc.) have been completely observed by the authors.
Acknowledgements
This article is based on a research project approved by the Deputy of Research and Technology of Kurdistan University of Medical Sciences at IR.MUK.REC.1395/190. The researchers found themselves obliged to thank the Mrs. Khorush Javan for her collaboration in doing experiments. This study was funded by Vice-chancellor for Research and Technology, Kurdistan University of Medical Sciences (Grant No. 1395/190).
Footnotes
Conflict of interest
The authors declare that there is no conflict of interest.
References
- 1.Overgaauw PA. Aspects of Toxocara epidemiology: toxocarosis in dogs and cats. Crit Rev Microbiol. 1997;23(3):233–251 [DOI] [PubMed] [Google Scholar]
- 2.Despommier D. Toxocariasis: Clinical aspects, epidemiology, medical ecology, and molecular aspects. Clin Microbiol Rev. 2003;16(2):265–272. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Macpherson CN. The epidemiology and public health importance of toxocariasis: A zoonosis of global importance. Int J Parasitol. 2013;43(12–13):999–1008. [DOI] [PubMed] [Google Scholar]
- 4.Nunez CR, Martinez GDM, Arteaga SY, et al. Prevalence and risk factors associated with Toxocara canis infection in children. Scientific World Journal. 2013;572089. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Baboolal S, Rawlins SC. Seroprevalence of toxocariasis in schoolchildren in Trinidad. Trans R Soc Trop Med Hyg. 2002;96(2):139–143. [DOI] [PubMed] [Google Scholar]
- 6.Strube C, Heuer L, Janecek E. Toxocara spp. Infections in paratenic hosts. Vet Parasitol. 2013;193(4):375–389. [DOI] [PubMed] [Google Scholar]
- 7.Magnaval JF, Glickman LT, Dorchies P, et al. Highlights of human toxocariasis. Korean J Parasitol. 2001;39(1):1–11. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 8.Deutz A, Fuchs K, Auer H, et al. Toxocarainfestations in austria: A study on the risk of infection of farmers, slaughterhouse staff, hunters and veterinarians. Parasitol Res. 2005;97(5):390–394. [DOI] [PubMed] [Google Scholar]
- 9.Del Brutto OH. Parasitic infections of the central nervous system. CNS Infections. 2017:181–197. [Google Scholar]
- 10.Good B, Holland CV, Taylor MR, et al. Ocular toxocariasis in schoolchildren. Clin Infect Dis. 2004;39(2):173–178. [DOI] [PubMed] [Google Scholar]
- 11.Noordin R, Smith HV, Mohamad S, et al. Comparison of IGG-ELISA and IGG4-ELISA for Toxocara serodiagnosis. Acta Trop. 2005;93(1):57–62. [DOI] [PubMed] [Google Scholar]
- 12.Hotez PJ, Bottazzi ME, Franco-Paredes C, et al. The neglected tropical diseases of latin america and the caribbean: A review of disease burden and distribution and a roadmap for control and elimination. PLoS Negl Trop Dis. 2008;2(9):e300. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Seo M, Yoon SC. A seroepidemiological survey of toxocariasis among eosinophilia patients in Chungcheongnam-do. Korean J Parasitol. 2012;50(3):249–251. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Portus M, Riera C, Prats G. A serological survey of toxocariasis in patients and healthy donors in Barcelona (spain). Eur J Epidemiol. 1989;5(2):224–227. [DOI] [PubMed] [Google Scholar]
- 15.Stensvold CR, Skov J, Moller LN, et al. Seroprevalence of human toxocariasis in Denmark. Clin Vaccine Immunol. 2009;16(9):1372–1373. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Abdi J, Darabi M, Sayehmiri K. Epidemiological situation of toxocariasis in Iran: Meta-analysis and systematic review. Pak J Biol Sci. 2012;15(22):1052–1055. [DOI] [PubMed] [Google Scholar]
- 17.Tabari H, Somee BS, Zadeh MR. Testing for long-term trends in climatic variables in Iran. Atmospheric Research. 2011;100(1):132–140. [Google Scholar]
- 18.Nourian A, Amiri M, Ataeian A, et al. Seroepidemiological study for toxocariasis among children in Zanjan-northwest of Iran. Pak J Biol Sci. 2008;11(14):1844–7. [DOI] [PubMed] [Google Scholar]
- 19.Hosseini-Safa A, Mousavi SM, Badorani MBB, et al. Seroepidemiology of toxocariasis in children (5–15 yr old) referred to the pediatric clinic of Imam Hossein Hospital, Isfahan, Iran. Iran J Parasitol. 2015;10(4):632–7. [PMC free article] [PubMed] [Google Scholar]
- 20.Zibaei M, Sadjjadi S. Trend of toxocariasis in iran: A review on human and animal dimensions. Iran J Vet Res. 2017;18(4):233–242. [PMC free article] [PubMed] [Google Scholar]
- 21.Sadjjadi SM, Khosravi M, Mehrabani D, et al. Seroprevalence of toxocara infection in school children in Shiraz, southern Iran. J Trop Pediatr. 2000;46(6):327–330. [DOI] [PubMed] [Google Scholar]
- 22.Garedaghi Y. Seroprevalence of toxocariasis in children in east-Azerbaijan Province, Iran. Cukurova Med J. 2013;38(4):581–586. [Google Scholar]
- 23.Fallah M, Azimi A, Taherkhani H. Seroprevalence of toxocariasis in children aged 1–9 years in western Islamic Republic of Iran, 2003. East Mediterr Health J. 2007;13(5):1073–1077. [DOI] [PubMed] [Google Scholar]
- 24.Sharif M, Daryani A, Barzegar G, et al. Seroprevalence of toxocariasis in schoolchildren in northern Iran. Pak J Biol Sci. 2010;13(4):180–184. [DOI] [PubMed] [Google Scholar]
- 25.Mahmoudvand H, Taee N, Ebrahimzadeh F, et al. Seroprevalence and risk factors of Toxocara canis infection in children (2–15 years old) referred to health centers of Lorestan province, Iran. J Pediatr Infect Dis. 2018;13:20–24. [Google Scholar]
- 26.Akhlaghi L, Ourmazdi H, Sarafnia A, et al. An investigation on the toxocariasis seroprevalence in children (2–12 years old) from mahidasht area of Kermanshah Province (2003–2004). RJMS. 2006;13(52):41–48. [Google Scholar]

