Clinical and pathological findings were described in stillborn kids affected with congenital goiter in a goat flock of Beetle breed in Garmsar Iran.The observations involved seven stillborn kids with goiter, including one case with triplet fetuses and two cases with twine fetuses. The thyroid glands were clearly visible, enlarged, and palpable in all the dead kids. The fetuses had a large swelling in the cranio-ventral neck region. Upon cutting skin in each fetus, the swelling revealed the extremely enlarged thyroid gland with two almost symmetrical lobes with both lobes approximately 15 × 8 × 5 cm in size.Histopathological hyperplastic goiter was observed in four kids and colloid goiter was diagnosed in three.Twins or triplets were observed to be predisposed to congenital goitre. All the stillborn kids were twins or triplets. On the other hand, single-born kids survived and showed a normal growth rate.

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: Ovine pulmonary adenocarcinoma, also known as jaagsiekte, is a chronic, contagious, and transmissible lung cancer. It is prevalent in ovine spp while rarely occurring in caprine with long incubation period. The disease is mostly observed in older animals (over 2 years old).OBJECTIVES: The present study aims to determine the prevalence of the disease based on histopathological diagnosis and investigate its correlation with age and sex in the slaughtered local sheep in Garmsar (Semnan province).METHODS: Herein, the lungs of 9030 slaughtered sheep are morphopatthologically examined for the presence of ovine pulmonary adenocarcinoma.RESULTS: Based on the morphopathological examination, ovine pulmonary adenocarcinoma was observed in the lungs of 438  (4.87 %) out of 9030 sheep. That said, 250 indicated the classical form, as firm, white to grayish coalescing masses mostly in the cranio-ventral lobes; this form is associated with wet cut surface and frothy fluid in the airways. The remaining 188 sheep showed the atypical form, as small, clear demarcated nodules mostly in diaphragmatic lobes associated with dry cut surface and minor fluid in the airways. Almost similar histopathological changes were seen in the two forms. An acinar or papillary growth of neoplastic cells in the alveoli and polypoid proliferation of bronchiolar epithelium were observed in both forms. However, there were variable amounts of connective tissue, and infiltration of lymphocytes and plasma cells in the interstitial tissue of the affected alveoli and no metastatic lesion in the lymph nodes. The peribronchial and peribronchiolar lymphoid aggregates were consistent features in most of the cases studied.CONCLUSIONS: The findings of the present study, as the first report of ovine pulmonary adenocarcinoma in sheep from Garmsa county, revealed the higher prevalence of this disease compared to that reported in previous reports in the country. Moreover, according to the obtained results, atypical and classical forms represented different stages of a single disease spectrum.

BACKGROUND: Oxidative stress is believed to be one of the major causes of tissue damage in aquatic animals exposed to heavy metals. It leads to certain changes in the antioxidant and enzyme system. Given the fact that research on the effect of sub-acute toxicity of silver nitrate in shrimps is not very developed, the present study can be conducive to formulating the international standards of contamination of shrimps with silver nitrate.OBJECTIVES: The present study aimed to evaluate the toxic effects of silver nitrate on the changes in the antioxidant and enzyme systems of hepatopancreas, muscle and gills of Litopenaeus vannamei.METHODS: After acclimatization of shrimps, they were exposed to silver nitrate with concentrations of 0.0084, 0.021, 0.042 and 0.063 mg/L for 21 days. At the end of the experimental period, gill, muscle and hepatopancreas were sampled, and the changes in the antioxidant system (SOD, GPx and GST) and metabolic enzymes (ALT, ALP, AST and LDH) were examined.RESULTS: There was no significant difference in terms of SOD and GST activity in the gill and muscle of the exposed shrimps (P>0.05). However, GPx in treatment 4 increased significantly in gill and muscle while it saw a decrease in hepatopancreas (P<0.05). In hepatopancreas, GST significantly increased in treatments 3 and 4 (P<0.05) whereas SOD did not show any significant changes compared with other treatments (P>0.05). The metabolic enzymes of the muscle did not show any significant differences in any of the treatments (P>0.05), but in gill, the level of ALT in treatment 4 decreased significantly while the levels of AST and LDH in treatment 3 and 4 significantly increased (P<0.05). In hepatopancreas, the activity of ALT in treatments 2 and 4, AST in treatments 3 and 4, and ALP in all treatment except treatment 1 saw significant reduction. Nevertheless, LDH in treatments 3 and 4 had a significant rise (P<0.05).CONCLUSIONS: A significant increase in GST and LDH as well as a significant decrease in GPx and ALT, AST and ALP enzymes in the hepatopancreas revealed that the antioxidant and enzyme system of shrimps is further disturbed with the rise in silver nitrate concentration in the hepatopancreas compared to the gill and muscle.

BACKGROUND: Major histocompatibility complex (MHC) encodes for highly variable molecules, most of which are responsible for foreign antigen recognition and activation of immune responses in the host. LEI0258 microsatellite, located in the poultry MHC region, is a suitable genetic marker for determining MHC haplotypes and genetic diversity in poultry.OBJECTIVES: Considering the fact that there is no report on the frequency and types of MHC alleles and population genetic analysis in Ross 308 poultry in Iran, the present study aimed to investigate the diversity of MHC haplotypes of Ross 308 broilers by LEI0258 microsatellite.METHODS: A total of 216 blood samples were collected from two productive herds of Ross 308 broilers. After extracting DNA of the blood samples and amplifying LEI0258 microsatellite alleles, genotyping of MHC haplotypes was performed using agarose gel electrophoresis and fragment analysis techniques.RESULTS: A total of seven alleles and 21 genotypes were identified for LEI0258 microsatellite in these two groups. the highest and the lowest frequencies belonged respectively to allele 385 bp (42.86 %) and allele 300 bp (4.33 %). Heterozygous 207/385 was found to be the dominant genotype in both populations. According to the similarity matrix analysis, there was an 84.56 % similarity between the two groups.CONCLUSIONS: The results obtained in this study revealed a high level of heterozygosity (85.71 % and 91.35 %) and deviation from Hardy–Weinberg equilibrium (P<0.0001) in these two Ross populations. Ross 308 broiler chickens had lower allelic diversity and higher genetic similarity compared to the native ones. These findings provided additional information on the use of MHC as a candidate gene marker in genetic improvement and resource conservation in broiler populations.

In bovine tuberculosis caused by Mycobacterium bovis, cattle are known as the main host, and sheep are relatively resistant. Sheep become infected only when there is very close contact between cattle and sheep or when the mycobacterium is abundant in the environment. In the present study, a case of generalized tuberculosis was reported in the sheep of the Sanandaj slaughterhouse.The examined animal carcass was transferred from the slaughterhouse to the University of Kurdistan microbiology laboratory and was dissected under complete health safety conditions. In the carcass examination, necropsy lesions (generalized tubercular granulomas) were visible in different organs and mediastinal lymph nodes, bronchioles, mesentery, and liver portal system. These lesions were seen in the lymph nodes of different body parts, including the lung, liver, digestive system, reproductive system, bladder, and different muscles, including the peritoneal muscle, diaphragm muscle, and abdominal muscles.Diagnostic tests included clinical observations, Ziehl-Neelsen staining for Mycobacterium bacteria, and polymerase chain reaction (PCR) molecular technique. In Ziehl-Neelsen staining, Mycobacterium acid-fast bacilli were seen in red color on the pale blue background of the slide. Also, the product of 499 base pairs was amplified in the specific PCR reaction, which confirmed Mycobacterium bovis.The present report shows that Mycobacterium bovis strains present in the region can be transmitted to sheep and cause disease with severe clinical symptoms. This report is critical, particularly for mixed cattle and sheep farming. Since cattle and sheep are kept together in many breeding farms in Kurdistan province, special attention was paid to the possibility of transmission of bovine tuberculosis to sheep and humans.

BACKGROUND: Meat is one of society's most important nutritional needs, the price of which is higher than other food groups. In recent years, the use of meat products has increased due to human lifestyle changes. Fraud in meat products occurs for various reasons, including the economic value of meat. Therefore, it is crucial to use fast and accurate methods of identifying these frauds.OBJECTIVES: The purpose of this study is to determine the unauthorized tissue by a histological method as well as to determine the unauthorized species used in meat products of factories in Hamadan province.METHODS: In the summer of 2021, fifty samples were collected from active production units of the Hamedan province that were available in the Hamadan city market and transferred to the laboratory for histological laboratory and animal species determination by PCR test. For the histology test based on the national standard 6103, the samples were subjected to fixation, passage (dehydration, clearing, impregnation with molten paraffin), blocking, sectioning, and H&amp;E staining. PCR method was used to determine the type of animal species used in the production of the collected samples.RESULTS: The results confirmed the presence of unauthorized tissues, including bone, cartilage (articular and respiratory cartilage), skin, and glandular organ in meat products. Also, PCR test results showed that chicken meat was found in 100% of the samples labeled with beef.CONCLUSIONS: The presence of illegal tissue and the use of chicken meat in products labeled as beef meat is evident in the sausages produced in Hamadan province.

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: Yersiniosis is known as one of the most prevalent bacterial diseases in fish, which causes high mortality and economic losses in cultured fish farms every year. OBJECTIVES: The present study was conducted to investigate the changes in hematological indices and gut histopathology in Caspian roach (Rutilus caspicus) exposed to Yersinia ruckeri. METHODS: 60 Caspian roach broodstock with an average weight of 63.4 ± 2.1 g were divided into three groups (with two replicates for each group), including one treatment, one positive control, and one negative control groups. The treatment group was intraperitoneally injected with Yersinia ruckeri bacterium at a dosage of 3.8 × 107 cell/fish. The positive group just received normal saline (0.9 % NaCl) via intraperitoneal injection. No injection was performed in the negative control group. RESULTS: Symptoms appeared on the fourth day after exposure and 20 % of the fish in the treatment group died 5 days after the challenge. Cumulative mortality reached 53 % on day 9 after the challenge.  According to hematological analysis, the challenge with Yersinia ruckeri led to a significant increase in white blood cell counts (WBC) compared to the control groups. Moreover, 10 days following exposure, the treatment group experienced hypochromic macrocytic anemia. Gut histopathology was characterized with necrosis and detachment of intestinal epithelial cell and inflammatory cells infiltration in the treatment group. CONCLUSIONS: Based on the obtained results herein, Yersinia rackeri can cause acute disease in Caspian roach; therefore, preventing and controlling this disease is essential for these fish in infected regions.

BACKGROUND: Calf pneumonia is one of the most common diseases in dairy and beef herds. OBJECTIVES: To compare steroidal and non-steroidal anti-inflammatory drugs as adjunctive therapy in dairy calf pneumonia. METHODS: Forty calves less than six months of age diagnosed with calf pneumonia in dairy farms of Mashhad suburb were enrolled in this study based on the University of Wisconsin Calf Respiratory Scoring Chart. In this system, calves are scored based on factors such as nasal discharge, rectal temperature, cough, eye and ear staining. Calves should not have a history of any other disease. Moreover, factors such as age, sex, and severity of the disease were considered similar in distributing calves among different groups. These calves were divided into four treatment groups; all were treated with antibiotic florfenicol. The first group received dexamethasone, while dexaphenyl, phenylbutazone, distilled water were used in other groups. After 5 days, calves were examined and scored again and blood samples were taken. Complete blood count (CBC), fibrinogen, total protein, hapto-globulin and albumin measurements on blood samples before and after treatment were done. Repeated measurement ANOVA and Paired t-test were used for statistical analysis with the significance level of 0.05. RESULTS: The results showed that the degree of health, heart and respiratory rate, fibrinogen and total protein, Lymphocyte, N/L, TP-Fib/Fib ratio, MCV and MCHC significantly changed during the two sampling periods (p < /em>˂0.05), but there was no significant difference between the treatment groups (p < /em>˃0.05). Only the PCV factor and TP-Fib/Fib ratio was significant between groups (p < /em>˂0.05). CONCLUSIONS: Results indicate that in the treatment regimen of dairy calf pneumonia, the use of an anti-inflammatory drug, along with antibiotics and antibiotic treatment alone are not significantly different.