BACKGROUND: Toxocara canis is a zoonotic disease that commonly infects canids. Mammals and birds are sometimes infected with this disease as paratenic hosts. It can also cause accidental infection in humans. The increase in the number of stray dogs, the expansion of urban gardens, and the proximity of dogs to humans increase the risk of human infection with Toxocara canis.OBJECTIVES: This study aims to determine the prevalence of Toxocara canis infection in dogs and foxes in Zanjan province, Iran.METHODS: A total of 484 fecal samples of stray dogs (n=355), rescue dogs (n=49), guard dogs (n=50), and foxes (n=30) in Zanjan were randomly collected from June 2021 to February 2022. The microscopic examination was done following formalin-ethyl acetate sedimentation procedures. Finally, the PCR method was used to confirm the presence of Toxocara canis in positive samples.RESULTS: Microscopic study revealed that, out of 484 samples, 21 (4.3%) were positive for Toxocara/ Toxascaris eggs. Between these positive samples of dogs and foxes, only 6 samples from dog feces were confirmed as a Toxocara canis infection by the PCR method.CONCLUSIONS: There is an increase in the prevalence of Toxocara canis infection in stray dogs in Zanjan, Iran. Given the presence of dogs in parks and residential areas, there is a risk of human infection with Toxocara canis, emphasizing the importance of adhering to treatment and prevention protocols in dealing with stray dogs.

BACKGROUND: Brucellosis or Malta fever is one of the most prevalent zoonotic diseases considered as a health and economic concern.OBJECTIVES: The current study aimed to employ several methods to detect Brucella in blood and milk samples of saanen goat and use a safe and definitive method to diagnose this disease.METHODS: In this study, 122 blood samples and 122 milk samples were collected from saanen goats. After culture and serological-based isolation methods (RBPT, Wright, 2ME, and Ring test), DNA was extracted from all the blood and milk samples. PCR was carried out using B4 and B5 primers on all the extracted DNAs in order to detect the B. abortus and B. melitensis; PCR was carried out with Br.a and Br.m primers.RESULTS: The results of all the blood samples were negative, but bacterial growth was observed in three milk samples, which was detected in biotyping, biovar 1 melitenensis. The PCR results for detection of Brucella spp. of nine blood samples and nine milk samples were positive. Using mPCR primers, B. melitensis were identified through all the nine milk and blood samples.CONCLUSIONS: Herein, we found that better bacterial diagnostic system and choosing an appropriate technique for rapid detection, such as PCR and Real Time PCR, in addition to popular awareness and other functions of national veterinary medicine institute could control the diseases and decrease their incidence successfully.

BACKGROUND: Trypanosomosis is a blood parasitic disease with veterinary and cosmopolitan importance due to Trypanosoma evansi (Kinetoplastida: Trypanosomatidae) type A in camels, cattle, buffaloes, and equine and type B in camels. OBJECTIVES: We conducted the present study to discriminate Trypanosoma evansi type A and B infection in one-humped camels (Camelus dromedarius) in Sistan-va-Baluchestan Province, south eastern Iran. METHODS: A total number of 369 blood samples were randomly taken from jugular vein of the examined one-humped camels from different parts of the region. Genomic DNA was extracted and polymerase chain reaction (PCR) was performed to amplify 205bp-fragment-length and 436bp-fragment-length of RoTat 1.2 VSG gene (T. evansi type A) and Minicircle gene (T. evansi type B), respectively. RESULTS: Molecular findings revealed that all the infected camels were affected by T. evansi type A. CONCLUSIONS: Based on the results of the current study, we could conclude that the cause of infection in the examined camels of the region, like other parts of the world, was T. evansi type A.

BACKGROUND: Clostridium perfringens is an important animal pathogen that causes severe loses to the livestock and poultry industries. Therefore, bacterial detection is believed to be of particular importance. OBJECTIVES: The present study aimed to identify Iranian isolates using conventional and molecular methods and to evaluate their toxicity. METHODS: In this work, 23 Clostridium perfringens type B isolates were examined via microbiological and biochemical tests. Subsequently, they were subjected to PCR technique for the final confirmation. After culturing of the isolates in specific medium, the minimum lethal dose test was performed. The most toxigenic isolate and reference strain was prepared the enterotoxaemia anaculture vaccine. Serum neutralization test was performed on the experimental inactive vaccines. RESULTS: The results revealed that etx and cpb gene could be found in all of the isolates, yet cpb2 gene was found in 65.2 % of the isolates. The minimum lethal dose ranges for these bacteria was less than 1/10 to more than 1/900. The results of serum neutralization in Iranian isolate and reference strains were 5 and 10 IU / ml, respectively. CONCLUSIONS: The findings herein implied that strain 1795 with high toxicity could be used in vaccine production. Of course, for use in production, further research on target animals is needed.

BACKGROUND: Polycystic kidney disease is the most prevalent inherited genetic disease in Persian cats, which is caused by mutations in PKD1 and PKD2 genes. Due to the accumulation of fluids inside the cysts and their pressure on the renal parenchym, the patient is prone to developing symptoms of chronic renal failure.OBJECTIVES: The present study aimed to compare ultrasonography and molecular tests in diagnosis of autosomal dominant polycystic kidney disease.METHODS: This study was performed on 97 Persian cats, including 46 male and 51 female cats, with an average age of 6 years (minimum 2 months and maximum 14 years). All the cats were evaluated for the presence of disease using ultrasound and molecular methods.RESULTS: Among 97 females, 32 (33 %) were found to be positive for PKD on the basis of presence of anechoic cysts. In molecular tests, all the cases with cysts in the ultrasonography had mutation in PKD1 gene and 13 cases (13 %) without cysts in ultrasonography were diagnosed to be positive through molecular technique. Among 97 studied cats, 45 (46 %) showed mutated genes. The degree of agreement between the two methods of ultrasonography and PCR was determined by calculating Kapa 0.725 (Cl: 0.592-0.895). The sensitivity and specificity of the ultrasonography were calculated to be 77.11 % and 100 %, respectively.CONCLUSIONS: Imaging and molecular methods were utilized to diagnose the disease. The more frequent use of the molecular methods for the diagnosis of the disease compared to the use of ultrasound could be attributed to the higher sensitivity of the molecular technique, the small size of the cysts, the low number of cysts, the low age of the animal, and the presence of cysts in the medula of the kidney. Therefore, the molecular method could be recommended for screening the disease in the early stages. It can also be employed in breeding programs and the removal of cats with this mutated gene.

BACKGROUND: Neosporosis is a disease caused by the protozoan Neospora caninum, which is characterized by abortion in cattle and neuromuscular paralysis of various organs, particularly the hind limbs of dogs. The diagnosis of neosporosis is often made by serological molecular tests.OBJECTIVES: This study was conducted to investigate the presence of N. caninum oocysts in the feces of dogs. METHODS: A total of 100 fecal samples were collected from indoor and outdoor dogs during 2018-2019 around Tabriz. Information about age, location, and history of antiparasitic treatment of the dogs were recorded in a questionnaire. Primarily, fecal samples were examined microscopically for Neospora ocysts. After breaking the collected oocysts through freeze-thaw and sonication, DNA contents of the oocysts were extracted and analyzed via PCR.RESULTS: In a light microscopic study, oocysts were observed in 45 (45 %) of the fecal samples. In the PCR study, 21 of the 45 cases tested positive for Neospora infection (21 %). All the positive cases of infection were observed in molecular examination in dogs older than one year. The positive cases were observed in 2 % of the domestic dogs, 8 % of the stray dogs, 6 % of the kennel dogs, and 5 % of the rural dogs. Furthermore, 19 % of the infected dogs had no history of antiparasitic treatment; only 2% had a history of antiparasitic treatment. The results of statistical analysis showed that the rate of infection in dogs around Tabriz with Neospora caninum was significantly (P<0.05) related to the animal's living environment and history of antiparasitic treatment. However, this rate was found to have no significant relationships with the age of the animals.CONCLUSIONS: Due to the high rate of infection with Neospora caninum in dogs in Tabriz, it is necessary to apply preventive methods in traditional and industrial farms around this city and use rapid diagnosis methods in them.

BACKGROUND: Ovine theileriosis is an important hemoprotozoal disease of sheep and goats in tropical and subtropical regions which causes high economic loss in the livestock industry. OBJECTIVES: The aim of this study was the differential detection of Theileria species in sheep using PCR method. METHODS: Two hundred blood samples of sheep were investigated in order to differentially diagnose Theileria species. DNA was extracted from blood samples and DNA samples were amplified using specific primers designed for 18S rRNA, TamS1 and TaSp genes. RESULTS: In this study, from 200 examined samples, 42 samples (21%) were infected by Theileria spp. and none of them were infected by Babesia spp. Moreover, from these 42 positive samples, 24 samples (57.1%) were only infected by T. ovis. 12 samples (28.5%) were only infected by T. lestoquardi, 2 samples (4.7%) were only infected by T. annulata and 4 samples (9.5%) were simultaneously infected by T. lestoquardi and T. ovis. The results of nucleotide sequencing showed that PCR product of 18S rRNA from T. lestoquardi has 99 and 95% similarity with T. annulata and T. ovis respectively. T. lestoquardi and T. annulata showed 86% similarity. Also TaSp gene of T. ovis in comparison with T. annulata and T. lestoquardi showed 96 and 86% similarity, respectively. CONCLUSIONS: In the present study could be shown that the two genes (TamS1 and TaSp) from examined three genes could be used for Theileria species specific diagnosis by PCR.

BACKGROUND: Staphylococcus aureus is one of the most important human pathogens that cause infection and also food intoxication by secreting various enterotoxins. Conventional culturing methods to detect S. aureus have some limitations such as being time-consuming due to bacterial growth and low precision and sensitivity in detecting viable but non-cultivable cells. OBJECTIVES: The objective of this study was to detect and quantify enterotoxigenic (A-E) S. aureus in cream pastry products applying PCR coupling with propidium monoazide (PMA) to distinguish dead and live cells. METHODS: One hundred samples were randomly collected from pastry shops in Amol, in a period of 2 months. After preparing dilutions, bacterial pellets were separated and treated with PMA before DNA extraction. Real time PCR was conducted in order to quantify S.aureus cells and enterotoxigenic strains using specific primers. RESULTS: Results of conventional method were close to PMA-qPCR data (P>0.05), but data from qPCR that includes live and dead cells shows more bacterial count than two other methods. Sensitivity of the method applied in the present study, detecting low number of S.aureus cells (less than 10/g) seems considerable. CONCLUSIONS: Findings showed that applying PCR coupling with PMA results in more reliable data than conventional culturing method. Regarding this approach being time-effective, considerably sensitive and specific, it is expected that it be used in food quality control labs in monitoring systems in future.

BACKGROUND: Salmonella are endemic on most large intensive dairy farms and salmonellosis is a common cause of neonatal morbidity and mortality. Disease and mortality usually reflect a variety of management events and environmental stressors that contribute to compromised host immunity and increased pathogen exposure. OBJECTIVES: In this study, PCR method was used to identify Salmonella Enteritidis, Infantis, Dublin and serovars isolated from diarrhea samples and aborted fetuses of Tehran and Alborz provinces dairy Farms. Further observation showed that the isolation of S. Enteritidis and S. Infantis is closely related to the consumption of contaminated poultry meat powder in diet of cows. METHODS: Forty-one Salmonella were isolated from diarrhea and aborted fetus samples in Tehran and Alborz provinces Farms and were confirmed by biochemical assays, then the isolates were identified by serological methods by polyvalent and monovalent Salmonella antisera. DNA of samples was extracted by Boiling method and was tested by PCR. Salmonella serovars were identified according to the presence of specificgenes for Salmonella Enteritidis, Infantis and Dublin.  RESULTS: All samples were tested by PCR were positive. 32 samples were identified as Salmonella Enteritidis (78/04 %), 4 samples were identified as Salmonella Infantis (9/77 %) and 5 samples were identified as Salmonella Dublin (12/19 %). CONCLUSIONS: According to the results, it seems that PCR can be used as a alternative method to the expensive and time consuming biochemical and serological methods for identifying Salmonella serovars. As Salmonella Enteritidis was usually isolated from poultry, isolation from cows may be due to has been used chicken meat powder in diet of the dairy farms.

BACKGROUND: Neospora caninum is one of the most important pathogenic protozoan parasites causing bovine abortion around the world. Objectives: The aim of this study was to detect the presence of Neospora caninum in the brain, cerebellum and medulla oblongata of aborted fetuses in cattle in Arak by means of molecular method. Methods: 38 samples of brain, cerebellum and medulla oblongata from aborted fetuses in dairy cattle of Arak were tested for the presence of Neospora with nested-PCR. Results: Survey findings indicated the presence of DNA in 26.3 % of aborted fetal brains. In the cerebellum and medulla oblongata samples no Neospora caninum  DNA was detected. There was a significant relationship between neosporosis and maternal age (number of calvings), abortion history and the presence of dogs in the herd. Conclusions: The results showed a significant association between the infection and the number of abortions in the examined cows; As a result it seems that neosporosis could be an important factor in epidemic abortions in Arak city’s dairy farms which requires continuous monitoring and implementation of prevention programs in the dairy industry.