Toxoplasmosis is one of the most important diseases in humans and animals that causes by Toxoplasma gondii parasite. Reservoir and final host is cat and intermediate host is warm blood animals. For example, domestic animals such as sheep, cattle and goat (Dubey, 1988).
Toxoplasmosis prevalence in humans and animals is different on base of age, geographical area, nutrition habitat and keeping of cat at farm. In this subject toxoplasmosis prevalence depends to increasing the age, consumption of the raw or half- cooked meat and living in warm and humid areas. Toxoplasmosis in pregnant mother may be cause blindness, mental retardation or other nervous disease and abortion that concomitant with immune system deficiency (Dubey, 1988).
Toxoplasmosis in animals such as sheep is a widespread disease in which the major economic losses are abortion, death of the fetus and neonatal death of the fetus and neonatal death (Buxton et al., 1991). The first study on T. gondii in sheep was carried out by Olafson and Monlux in 1942 (Dubey, 1988). Data colleted from serological studies in many countries throughout the world have shown different prevalence rate (0-100%) of toxoplasmosis in sheep.
Bandpei area in Babol city is one of the important areas in animal husbandry industry in Mazandaran province, north of Iran. Thus, the main objective of this study was to detect the seroprevalence study of T. gondii infection in sheep in Bandpei region by using the Indirect Fluorescent Antibodies (I FA).
MATERIALS AND METHODS
This descriptive-cross sectional study is carried-out to determine anti Toxoplasma antibodies in 285 sheep in Bandpei area Babol, northen Iran, from September through December 2004. Two to three milliliter blood sample from each sheep have been taken and after 5 min centrifugation with 2000 rpm; serum kept in sterile tubes in -70°
C. Then all of samples survived with IFA method. At first all of samples screening test with 1:50 titer and positive sample detected. Followed by positive sample survived with 1:100, 1:200, 1:400 and 1:800 titer. The statistical analysis was performed by using chi-square and t-test (p<0.05) was considered as statistical significant.
Eigtynine cases out of 285 sheep (31.2%) survived that were positive and 196
cases (68.8%) were negative. Fifty sheep were male and the remain were female
(Table 1).After diagnosis of positive cases from negative
cases, for determination of antibody titer a several dilution of 1:100, 1:200,
1:400 and 1:800 were applied that repeated by serial dilution titer.
||Total number and percentage of Toxoplasmosis in sheep in Bandpei,
Babol, northen Iran
||Toxoplasmosis antibody titer in sheep of Bandpei, Babol city,
northen Iran, 2004
The results of 80 positive cases in the final assay, the most valuable antibody
titer was 1:800 (10.1%) and the lowest valuable titers 1:200 (50.6%) (Fig.
Many studies have been carried-out in different countries through the world aimed at detection of the prevalence of T. gondii in animals and to confirm its signification as an infection source for man by means of various serological tests including IHA. LAT and IFA as well as isolation procedures (Sevgili and Babure, 2005).
Results of this research showed that 31.2% sheep of Bandpei with serological test by IFA method was positive. The infection rate of toxoplasmosis in sheep in the UK, Australia and New Zealand were reported 33 and 14%, respectively (Blewett and Watson, 1983).
Due to estimation of Mc Colgan and Buxton (1986) the annually damages of toxoplasmosis in sheep around the world is 6-12 million US Dollars. This concerned to abortion, deerews of milk prevention and economical damages (Mc Colgan and Buxton, 1986).
Some of researches about toxoplasmos in other area of Iran, e.g., Saveh central Iran showed 25.5% of infection rate in sheep (Chegini and Assmar, 2002). The decreasing of sera titer may be due to different climate conditions and sheep keeping in comparison with the present study area.
Another study by Hashemi Fesharaki (1996). domestic animals by latex agglutination
(LAT) and Indirect Haemaglotian Antibodies (IHA) method showed 24.5% of positive
cases. Perhaps decreasing positive rate in Hashemi Fesharaki (1996) research
in comparison with this research in short, IFA is more sensitive and specific
test than IHA and LAT.
This work was supported by a grant from Islamic Azad University, Babol Branch, Iran.