Literature DB >> 31123472

Seroepidemiology of Toxocara canis in Children under 14 Years Referring to Laboratories of Sistan and Baluchestan Province in Southeast of Iran.

Mahdi Khoshsima-Shahraki1, Mansour Dabirzadeh1, Hakim Azizi1, Javad Khedri2, Babak Djahed3, Ali Asghar Neshat3.   

Abstract

BACKGROUND: The aim of the present survey was to assess thr seroepidemiologic and parasitological aspects of Toxocara canis infection in children under 14 yr old.
METHODS: Overall, 963 sera were collected from children in the Sistan and Baluchistan Province, Southeast of Iran during the period from Sep 2015 to Jun 2016. IgG antibody against T. canis in the subjects' sera was evaluated using the commercial ELISA kit.
RESULTS: Anti-Toxocara IgG were detected in the serum of 17 (1.7%) of the participants. In the examined children, the highest presence of anti-Toxocara antibodies was 2.1% (9/418) in 6-10-yr olds, which was higher than other age groups (P<0.05). Anti-Toxocara antibodies were significantly higher in males (2.4% or 12/492) than in females (1.1% or 5/471) (P<0.03). Highest serological prevalence of T. canis occurred in tribes (5.5% or 4/69), followed by rural areas (0.9% or 7/757), while in the urban area it was 0.1% (6/163) (P<0.01). A significant association was seen between the serological prevalence of T. canis and laboratory findings such as eosinophilia (P=0.001) and red blood cell count (P=0.02).
CONCLUSION: Seroprevalence of Toxocara infection is high among children living in the poor regions of southeast Iran.

Entities:  

Keywords:  Antibodies; Iran; Seroepidemiology; Toxocara canis; Toxocariasis

Year:  2019        PMID: 31123472      PMCID: PMC6511586     

Source DB:  PubMed          Journal:  Iran J Parasitol        ISSN: 1735-7020            Impact factor:   1.012


Introduction

Toxocariasis is an important parasitic disease caused by the ascarid larvae of Toxocara genus, which are intestinal nematodes (1, 2). Their definitive hosts are domestic dogs and cats. They develop in the intestines and occur mostly in young animals (3). The most common parasitic agents of toxocariasis are Toxocara canis and, less frequently, Toxocara catis (4). Adult female T. canis worms can lay as many as 200,000 eggs per day. Non-embryonated Toxocara eggs are passed through dog feces, become infectious in suitable environments (temperatures of 10–35 °C and high soil humidity), and can remain infective in the soil for many years (5, 6). Human infection can occur through the ingestion of embryonated eggs from contaminated sources (e.g. soil and earthworms), dirty hands, uncooked vegetables, and paratenic hosts (7). The larvae can then penetrate the intestinal wall and migrate for months through different organs until they are overcome by the human inflammatory reaction and finally die (6). Human infection can result in a variety of syndromes with different clinical manifestations. Three commonly described syndromes are visceral larva migrans (VLM) with eosinophilia, pulmonary disorders, hepatomegaly, hyperglobulinemia, pneumonitis, and neurological disorders, ocular larva migrans (OLM) that leads to severe chorioretinitis, uveitis, strabismus, and even blindness, and occult or covert toxocariasis (CT) (1,6). About 76% of the world’s population of stray dogs are infected with toxocariasis. This is an important epidemic factor in nature (5). Although there have been a number of studies on the prevalence of T. canis in stray dogs and soil contamination due to T. canis eggs, there is a gap in our information about the presence of T. canis in children and others study that it may be related to regional climate as humidity, dryness, behaviours and laboratory methods for detection, people’s attitudes toward pets. (4,8,9). Thus, this study, aimed to assess the seroprevalence of toxocariasis infection among children under 14 in rural, urban, and tribal laboratories.

Materials and Methods

Field study area

The present study was performed in Sistan and Baluchistan Province in southeast Iran. It is located between latitudes 25°3′ and 28°31’ north and longitudes 58°48’ and 63°19’ east. This province lies on the border with both Afghanistan and Pakistan. It has a hot and dry climate and is moderately dry in the winter. The average annual rain in Sistan and Baluchistan is reported at around 59 mm and the relative humidity is at ~ 40% (10) (Fig.1).
Fig. 1:

Sistan and Balucheistan Province and its counties (from Wikipedia)

Sistan and Balucheistan Province and its counties (from Wikipedia)

Sample size

Overall, 963 children (471 female and 492 male) under 14 yr in different age groups (1–5 yr old, 6–10 yr old, and 11–14 yr old) were selected from Sep 2015 to Jun 2016 from private, public, and tribal laboratories of Sistan and Baluchestan. The sample size was calculated as 963 using parameters based on a previously published study (11). Data pertaining to each examined participants were collected and recorded in individual files.

Determination of serum antibodies level against Toxocara

For titration of IgG antibody against Toxocara antigens in the laboratory, a blood sample of 4 ml was collected from each child. The collected sample was divided into two tubes—one for blood cell count and the other for measuring anti-Toxocara IgG by ELISA method. The tubes were stored at −20 °C until used. All specimens were tested using a commercial enzyme immunoassay kit (IBL Germany) in accordance with the manufacturer’s instructions.

Statistical analysis

For the analysis of data, descriptive statistics for qualitative data with 95% confidence interval (95% CI) was used to determine the effect of the mentioned risk indicators on the prevalence of infection. A P-value less than 0.05 was considered to be statistically significant. Data were analyzed using Stata, ver. 11.2.

Ethical Approval

The study protocol was performed according to the Helsinki declaration and approved by Ethics Committee of Iranshahr University of Medical Sciences (Permit Number: IR.IRSHUMS.RES.1394.10). Informed written consent was obtained from all patients before they participated in the study.

Results

Out of 963 serum samples from patients, 17 (1.7%) were positive for anti-Toxocara antibodies. Mean antibody titer was 2.2 (± 1.1) in the studied cases. In the examined children, the presence of anti-Toxocara IgG was 2.1% (9/418) in 6-10-yr-old, which was higher than that in the other age groups (P<0.05). Anti-Toxocara antibodies were significantly higher in males (2.4%, 12/492) than in females (1.1%, 5/471) (P<0.03). The influence of different characteristics of participants, such as city of residence (P=0.002), gender (P=0.03), consumption of vegetables (P=0.03), and living place (P=0.01) on the prevalence of toxocariasis antibody was significant (Tables 1–3). A significant association was seen between the serological prevalence of T. canis and laboratory findings such as eosinophilia (P=0.001) and red blood cells count (P=0.02) (Table 4).
Table 1:

Seroepidemiology of Toxocara according to city&area of residents of the participants

CharacteristicsNegative serology N (%)Positive serology N (%)P-value
City of residenceZahedan493(99.4)3(0.6)0.002
Iranshahr189(97.9)4(2.1)
Khash95(97.9)2(2.1)
Nikshahr94(95.9)4(4.1)
Saravan92(95.8)4(4.2)
Area of residentsUrban163(99.9)6(0.1)0.01
Rural757(99.1)7(0.9)
Tribes69(94.5)4(5.5)
Table 3:

Seroepidemiology of Toxocara according to some socio-economic factors

CharacteristicsNegative Serology N (%)Positive Serology N (%)P Value
Dog ExposureYes242(99.2)2(0.8)0.2
No721(98)15(2)
Vegetable ConsumptionOnce A Day399(97.1)12(2.9)0.03
Every Other Day483(99.2)4(0.8)
One Serving A Week81(98.8)1(1.2)
Education Level Of The ParentsIlliterate505(99.9)8(0.1)0.4
Diploma382(98.2)7(1.8)
Academic76(97.4)2(2.6)
Father’s JobRelated To Animals110(97.3)3(2.7)0.6
Employee88(98.9)1(1.1)
Self-Employed/Jobless765(98.3)13(1.7)
Table 4:

Seroprevalence of Toxocara according to the laboratory results

Lab resultsNegative serology N (%)Positive serology N (%)P-value
Eosinophil (%)0≤5338(100)0(0)0.001
≥6625(97.4)17(2.6)
HemoglobinNormal704(98.7)9(1.3)0.5
Low259(97)8(3)
WBC countNormal782(98.2)14(1.8)0.8
high181(98.4)3(1.6)
RBC countNormal811(98.7)11(1.3)0.02
low152(96.2)6(3.8)
PlateletNormal854(98.5)13(1.5)0.3
low109(96.5)4(3.5)
Seroepidemiology of Toxocara according to city&area of residents of the participants Seroepidemiology of Toxocara according to sex & age of the participants Seroepidemiology of Toxocara according to some socio-economic factors Seroprevalence of Toxocara according to the laboratory results

Discussion

Toxocariasis is a global health problem in the general population and children are at the highest risk (2). Additionally, there has been an increase in the number of stray dogs and cats in recent years. This can lead to zoonotic diseases that can even cause death in humans (4). Toxocariasis is between 2.7% and 29.3% in different areas of the country of Iran (8, 12). In our study, the overall seroprevalence of Toxocara infection in patients was 1.7%. There are publications on the prevalence of T. canis among children in different parts of Iran and other countries (in Iran: 2% in Shiraz, 19% in Ahwaz, and 2.7% in Zanjan; among other countries: 48.4% in Brazil, 37.9% in Argentina, and 12.95% in Turkey) (13–16, 3). The difference in the prevalence of toxocariasis could be attributed to cultural habits, food habits, geographical location, climate condition, and temperature (17). The titer of anti-T. canis IgG was 2.2% in our study group and was compatible with previous studies. In a report from the northwestern part of Turkey, including Eskisehir, Bilecik, Kutahya, and Afyon, Dogan studied seroprevalence rate of Toxocara antibody in children and detected that 16.97% and 0.71% were a positive titer of anti-Toxocara antibodies from rural and urban areas respectively (14). It is very difficult to explain the exact differences in anti-Toxocara antibodies in children from different areas. However, a combination of factors, including some forms of cultural habits, method of cooking food, climates and soil condition, vegetative distribution, and humidity level could influence Toxocara antibodies (17, 5). In the current investigation, the Toxocara infection rate was found to be higher in tribal areas than rural and urban areas. In contrast, Sadjjadi and Negri reported higher infection rate in urban areas than in rural areas (18,19). Cultural habits, climate condition, and a closer connection to dogs affect the prevalence of Toxocara infection in different areas (15, 20). The present investigation found that Toxocara infection was significantly higher in males than in females (P<0.03). Gender seemed to be an important factor with regard to a positive serology, as shown in our study (16). In Brazil, higher infection rate of Toxocara reported in male than in female children (3). However, significantly more females were infected than males (21). The difference in findings may be indicative of the incidence of infection relative to differences in gender-specific behavior and type of games (5). The results of this study showed that a higher rate of Toxocara infection was recorded among 6–10-year olds. Our results correspond with another study that reported the maximum infection in children with mean 9.4-year olds in São Paulo Province, Brazil (22). A seroepidemiological study of T. canis infection was conducted in children aged 1.4–14.7 yr and reported that the mean age of onset of infection was 7.3 yr (23). This finding was similar to that of the present study. Toxocariasis is considered to be a common parasitic infection among children under 10 yr of age all over the world that may be due to childlike activities and more contact with the ground (22, 9). Demographic and socioeconomic factors (education level of the parents, the area of residence, and father’s job) may lead to an increase in Toxocara seroprevalence. Dogs are the primary hosts and the main vectors of the Toxocara parasite. Apart from them, consumption of raw vegetables grown in contaminated gardens, raw or undercooked meat from paratenic hosts, and grounds contaminated with embryonated eggs may be other sources of the disease (8). The risk of Toxocara infection is higher among people exposed to dogs and people with low education level (24), which is in agreement with our findings. In this study, we found a significant association between the prevalence of infection with the level of eosinophils and red blood cells. The results of our study are similar to other findings (15), in which the prevalence of infection was significantly associated with high eosinophil levels, while Sarkari et al (16) did not find a significant association between the prevalence of infection with high eosinophil levels. Although blood eosinophilia and a decrease in red blood cells were observed, they were not a consistent characteristic. In the other study, increase in the level of blood eosinophils is reported as one of the most common signals of parasitic infection and decrease in red blood cells, which might indicate a chronic disease (16).

Conclusion

The results of this study give an overview of the data on the prevalence of toxocariasis in southeast Iran. Future studies should consider the effect of toxocariasis on public health, the role of stray dogs and cats in the epidemiology of toxocariasis, and educational programmes for the prevention and control of Toxocara.
Table 2:

Seroepidemiology of Toxocara according to sex & age of the participants

CharacteristicsNegative serology N (%)Positive serology N (%)P-value
GenderMale492(97.6)12(2.4)0.03
Female471(98.9)5(1.1)
Employee88(98.9)1(1.1)
Self-employed/jobless765(98.3)13(1.7)
Age group (yr)1–5353(98.6)5(1.4)0.05
6–10418(97.9)9(2.1)
11–14192(98.5)3(1.5)
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Authors:  S M Sadjjadi; M Khosravi; D Mehrabani; A Orya
Journal:  J Trop Pediatr       Date:  2000-12       Impact factor: 1.165

2.  Seroprevalence of toxocariasis in hypereosinophilic individuals in Ahwaz, south-western Iran.

Authors:  S Maraghi; A Rafiei; R Hajihossein; S M Sadjjadi
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Authors:  Elaine Cristina Negri; Vamilton Alvares Santarém; Guita Rubinsky-Elefant; Rogério Giuffrida
Journal:  Asian Pac J Trop Biomed       Date:  2013-03

4.  Toxocarosis as zoonosis. A review of literature and the prevalence of Toxocara canis antibodies in 511 serum samples.

Authors:  I Theodoridis; S Frydas; M Papazahariadou; M Hatzistilianou; K K Adamama - Moraitou; M Di Gioacchino; M Felaco
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5.  Toxocariasis in children attending a Public Health Service Pneumology Unit in Paraná State, Brazil.

Authors:  Edson V Guilherme; Ariella A Marchioro; Silvana M Araujo; Dina Lúcia Morais Falavigna; Carolina Adami; Gustavo Falavigna-Guilherme; Guita Rubinsky-Elefant; Ana Lucia Falavigna-Guilherme
Journal:  Rev Inst Med Trop Sao Paulo       Date:  2013       Impact factor: 1.846

6.  Toxocara seroprevalence in children from a subtropical city in Argentina.

Authors:  J M Alonso; M V Bojanich; M Chamorro; J O Gorodner
Journal:  Rev Inst Med Trop Sao Paulo       Date:  2000 Jul-Aug       Impact factor: 1.846

7.  Prevalence of Toxocara infection in schoolchildren from the Butantã region, São Paulo, Brazil.

Authors:  Jussara M S Alderete; Cristina M A Jacob; Antonio C Pastorino; Guita R Elefant; Ana P M Castro; Angela B F Fomin; Pedro P Chieffi
Journal:  Mem Inst Oswaldo Cruz       Date:  2003-09-08       Impact factor: 2.743

8.  Laboratory diagnosis of human toxocariasis.

Authors:  J Fillaux; J-F Magnaval
Journal:  Vet Parasitol       Date:  2012-12-20       Impact factor: 2.738

9.  Seroepidemiological survey for Toxocara canis infection in the northwestern part of Turkey.

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10.  Analysis of the course and treatment of toxocariasis in children-a long-term observation.

Authors:  M Wiśniewska-Ligier; T Woźniakowska-Gęsicka; J Sobolewska-Dryjańska; A Markiewicz-Jóźwiak; M Wieczorek
Journal:  Parasitol Res       Date:  2011-12-29       Impact factor: 2.289

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2.  Toxocara infection: seroprevalence and associated risk factors among primary school children in central China.

Authors:  Shuai Wang; Haoran Li; Zhijun Yao; Pengju Li; Dong Wang; Haizhu Zhang; Qing Xie; Zhenchao Zhang; Xiangrui Li
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