Characterization of Eimeria species in commercial broilers by PCR based on ITS1 regions of rDNA

Coccidiosis is an intestinal disease of chickens caused by various species of protozoan parasites within the genus Eimeria. Diagnosis and genetic characterization of different species of Eimeria are central to the prevention, surveillance, and control of coccidiosis. The aim of this study was to detect different chicken Eimeria species from several areas in Khuzestan, south-west Iran. From February to September 2008, PCR assay as well as parasitological examinations was applied for the identification of field isolates of Eimeria parasites around Ahvaz, center of Khuzestan, southwest Iran. Data were analyzed bythe Kappa statistic test. Eimeria maxima, E. necatrix, E. tenella, E. acervulina and E. mitis were detected in this study. The prevalence of Eimeria spp. was 31.5% [126 and 400] and E. tenella was the most prevalent species in Khuzestan. Based on the Kappa statistical test, a good correlation between the results of PCR and traditional biometrical methods was only observed for E. maxima. The present study is the first on the prevalence of Eimeria species in Khuzestan, based on the molecular findings. We believe that traditional methods are not sufficiently reliable for specific diagnosis of Eimeria species in chickens and PCR based amplification of DNA sequence of parasite, could resolve this problem

Antigenic detection of cryptosporidium parvum in urban and rural dogs in Ahvaz district, southwestern Iran

Cryptosporidium parvum is a zoonotic protozoan parasite with a wide range of vertebrate hosts. The present study was conducted to determine the prevalence of Cryptosporidium parvum in urban and rural dogs of the Ahvaz area. Faecal samples were collected randomly from 93 dogs between May 2005 and September 2007. The studied dogs were divided into two groups [urban and rural] and based on age into three groups [<6 months, 6 months -3 years and >3 years]. The results were analyzed by using Chi-square analysis and Fischer's exact test. Prevalence to Cryptosporidium parvum antigens was 4.3% [4 of 93] by means of ELISA, indicating that this antigen is present in the ecosystem. The infection was more prevalent in rural dogs [6.4%; 3 of 47] in comparison with urban dogs [2.17%; 1 of 46], nevertheless, there were no significant differences between the different groups [P?0.05], but the infection was more prevalent in diarrheic dogs [17.65%; 3 of 17] compared with non-diarrheic dogs [1.3%; 1 of 76], and the difference was significant [P=0.019]. Infection was not significant in the different age groups [P>0.05]. Concurrent detection of cryptosporidium parvum with canine distemper [one sample] and parvovirus [one sample] were shown in the studied dogs. Modified Ziehl-Neelsen staining was also carried out and the prevalence of infection was 2.15% [2 of 93]. The use of ELISA allowed the detection of more positive cases than light microscopy. This study showed that Cryptosporidium parvum can be a risk factor, particularly for those dogs in contact together in the population of urban and rural dogs

[Serological study of Neospora caninum infection in cattle from Ahvaz area, Iran]

In order to investigate the seroprevalence of Neospora caninum infection in cattle in Southwestern Iran, blood samples were collected from Holstein [121 animals] and cross-breed [436 animals] cattle from three farms and seven areas of Ahvaz, respectively. All of the Holstein cattle were >/= 4 years old but cross-breed cattle were from different age groups [< 2.2-4.5-6 and > 6 years old]. Sera were examined by commercial ELISA kit. Anti - N. caninum antibodies were detected in 117 [21%] sera out of 557 tested. A Significant difference was found between Holstein [53.71%] and cross-breed [11.93%] cattle although there were not any significant differences between age groups

Serodiagnosis of sarcocystosis in water buffalo [Bubalus bubalis] by ELISA test and its comparison with digestion method

To compare the ELISA test with digestion method for dignosis sarcocystosis in water buffalo and estimate its sensitivity and specificity. Cross sectional study.Three hundred slaughtered water buffaloes in Ahwaz abattoir.Blood and oesophageal muscles were examined. Oesophageal muscles were examined for sarcocystis by both macroscopic and microscopic [digestion method] examination.Then the ELISA test were designed and compared with digestion method.Finally its sensitivity and specificity were determined. Sensitivity, specificity and 95% confidence intervals were determined by comparing the results obtained by the ELISA assay and digestion method. Me nemar test were used for comparing the percentage of positive cases and their correlation. While specific anti-sarcocytis antibodies were detected in 54.3% of cases macroscpic and microscopic infection were 20% and 57%, respectively. Furthermore, while the positive results of the macroscopic examination significantly differed from those values of the digestion and ELISA methods [P<0.01], no differences were observed between the positive results of the microscopic infection [digestion method] and the ELISA test [P>0.05]. Conclusion: ELISA test providing an effective and reliable means for detecting sarcocystosis in naturally infected water buffaloes. Its simplicity and ease of performance makes it particulary suitable for using in large-scale epidemiological surveys of livestock