BACKGROUND: Peste des petits ruminants (PPR) is an acute and highly contagious viral disease of small ruminants that is characterized by high fever, ocular and nasal discharge, pneumonia, necrosis, ulceration of the mucous membranes and inflammation of the gastro-intestinal tract leading to severe diarrhea. OBJECTIVES: The aim of this study was to investigate the seroprevalence of peste des petits ruminants (PPR) virus infection in sheep and cattle in Ahvaz. METHODS: Blood samples were taken from 100 cattle and 100 sheep that were kept together from different parts of Ahvaz. Blood samples were also taken from 16 vaccinated sheep   against PPR for positive control. The sera were separated by centrifuge at 3000 ×g for 10 minutes and 3 mL of serum was harvested and stored at -20 °C until determination of antibody against PPR using VN method. RESULTS: The peste des petits ruminants (PPR) antibody seroprevalence was 23% in cattle and 58% in sheep and all the sheep samples collected for control were positive for PPR antibody. CONCLUSIONS: The present study indicates serological evidence for the natural transmission of PPRV from sheep to cattle under natural conditions and provides baseline information on prevalence of PPRV antibodies in cattle and sheep population in Ahvaz.

Fifty five milk samples were collected from dairy Friesian cows suffering from clinical mastitis in a farm at Quena Governorate. The samples were subjected to microbiological examination .The main isolated pathogenic bacteria were identified biochemically as Escherichia coli (36.3%), Staphylococcus aureus (23.6%) Streptococcus agalactiae (18.2%), Klebsiella pneumoniae (12.7%) and bacterial free samples (9.1%) . Sensitivity tests for the bacterial isolates revealed that the tested strains were sensitive to ciprofloxacin, nortril, gentamicin and lincospectin

The bronchopneumonia of calves represents a risk to national supply chain because it is an ecopathy and weakens the more intensive production systems. It is characterized by inflammatory changes in the bronchi, bronchioles, lung parenchyma, and pleura. It is a disease of multifactorial traits called Bovine Respiratory Disease (BRD). The association of infectious agents with host defense and management to which the animal is subjected leads to the emergence of major clinical manifestations of the disease. The clinical evolution of BRD can also have serious secondary changes such as pulmonary edema, sepsis, and pulmonary hypertension, or even be consequent to the involvement of other structures, such as in cases of myocarditis leading to congestive heart failure. Although this report refers to a non-experimental framework, the circumstances that caused the calf to be subjected to a protocol-specific respiratory assessment involving non-routine reviews has made it possible to associate circulatory and respiratory conditions, rarely considered in ruminant clinic. The focus of this report was pulmonary edema. Modern clinical vision requires of the veterinarian work with cost-benefit relation, so that the more accurate and the earlier the clinical diagnosis the less expensive the treatment.

Several factors can affect bovine mammary gland health and although bacterial mastitis is the most studied and reported cause, viral infections may also have negative effects on bovine udder health. Viral infections can indirectly damage the papillary duct of the teat, and induce or exacerbate signs of bovine mastitis due to viral-induced immunosuppressive effects that may lead to a greater susceptibility to bacterial mastitis and even intensify the severity of established bacterial infections. Some viruses (Bovine alphaherpesvirus 2, cowpox, pseudocowpox, foot-and-mouth disease, vesicular stomatitis and papillomavirus) affect the integrity of the udder skin, leading to teat lesions, favoring the entry of mastitis-causing pathogens. It is therefore possible that the association between mastitis and viruses is underestimated and may, for example, be associated with negative bacterial culture results. Few milk samples are tested for the presence of viruses, mainly because of the more laborious and expensive procedures required. Furthermore, samples for virus testing would require specific procedures in terms of collection, handling and storage. Thus, there is a knowledge gap in regard to the actual impact of viruses on bovine udder health. Despite the fact that serum anti-virus antibodies can be detected, there is not enough evidence to confirm or exclude the effect of viruses on udder health. However, any expectation of milk production from healthy animals should consider the possible impact of viral infections in mastitis development and not underestimate the importance of actions to diagnose and control the disease. Therefore, the purpose of this review is to describe the association of diagnosis and control of viral diseases and their effect on bovine udder health.

Prostaglandin F2α (PGF2α) determines luteolysis in cattle, and the ability to manipulate its endogenous synthesis is indispensible for large-scale animal breeding. Estradiol (E2) and progesterone (P4) modulate several molecular pathways in endometrial cells, including the synthesis of PGF2α; however, its specific mechanisms are still not totally known. This study investigated the production in vitro and possible modulation of endometrial PGF2α due to a local effect of endogenous E2 in the ipsilateral uterine horn (UH) containing the dominant follicle (DF) or from P4 in ipsilateral horn containing the corpus luteum (CL). The PGF2α stimulators oxytocin (OT) and phorbol 12,13-dibutyrate (PDBu) were incubated with endometrial explants, and PGF2α content was measured. For that, cycling cows were synchronized, the development of DF and CL was examined by ultrasonography and on the seventh day of the estrous cycle, endometrial explants were collected and cultured in medium supplemented with 10-6 M PDBu or 10-6 M OT or non-supplemented. Media samples were collected immediately after treatment and 60 min later. Radioimmunoassay showed that the PGF2α content of the UH ipsilateral to the DF was 49% less than that of the contralateral UH (8.22 ± 0.95 vs. 12.24 ± 0.95 pg/mL/mg tissue, respectively; P < 0.01). However, the PGF2α levels did not differ between the UHs as a function of the CL position (9.46 ± 0.95 vs. 11 ± 0.95 pg/mL/mg; P > 0.05). The cellular stimulators promoted an increase in PGF2α synthesis (P < 0.02), and the effects differed among the animals (P < 0.04). The PGF2a production was higher in the explants treated with PDBu rather than OT (13.68 ± 1.16 vs. 10.01 ± 1.16 pg/mL/mg tissue, respectively; P < 0.05). In conclusion, PGF2α synthesis is modulated by the presence of the DF (local E2) but not the CL (local P4), and both PDBu and OT stimulated PGF2a synthesis.

lumpy skin disease virus (LSDV) was isolated, from naturally infected cattle that have a history of previous vaccination with live attenuated sheep pox virus (SPV) vaccine. The virus was isolated on chorio-allantoic membranes (CAM) of embryonated chicken eggs (ECE) and Madin Darby Bovine Kidney Cells (MDBK) and identified by agar gel precipitation test (AGPT) and immunofluorescent antibody technique (IFA). Characteristic pock lesions and intracyptoplasmic flourescene granules are identified respectively. Molecular characterization using polymerase chain reaction (PCR) using specific primer for G-Protein Coupled Chemokine Receptor Gene of LSDV isolates specific amplified product 554 bp. Sequence analysis revealed tow new isolates of LSDV.

Health, religious, and commercial aspects justify the need for meat species identification. The lack of officially approved methods prompts the undertaking of research on validation of isoelectric focusing of proteins (IEF) for official purposes. Samples were prepared from pigs (Sus scrofa ferus domestica), cattle (Bos taurus), and poultry (Gallus gallus domesticus). Meat mixtures were made by blending 50%, 25%, 10%, 5%, 4%, 3%, 2%, 1%, 0.5%, or 0.2% meat of other species. Samples were examined on ultrathin polyacrylamide gels with pH 3–9 gradient. The results of the study confirmed the stable and reproducible pattern of meat protein bands. The detection limit of raw meat admixtures from pigs, cattle, and poultry mostly ranged from 2% down to 0.2% (0.2% for poultry). However, the IEF method can be used to detect the addition of pig meat to bovine meat in an amount higher than 3%. At the significant mixture level (i.e at least 5% addition of meat of another species) IEF proves itself with 100% specificity, sensitivity, and accuracy. The achieved detection limits provide a basis for recommending the IEF method for routine tests in laboratories detecting the species origin of meat.

Introduction: In the European Union, the use of thyreostatic drugs for fattening slaughter animals has been banned since 1981 under Council Directive 81/602/EEC. For protection of consumer health against unwanted residues and in compliance with Directive 96/23, each EU country must monitor thyreostats in samples of animal origin. This paper presents the results of research on thyreostatic residues carried out in Poland in 2011–2017. Material and Methods: The material for testing was urine (n = 3,491), drinking water (n = 127), and muscle samples (n = 349) officially collected by Veterinary Sanitary Inspectors in slaughterhouses and farms throughout the country in accordance with the national residue control plan. The samples were examined for the presence of tapazole, thiouracil, methylthiouracil, propylthiouracil, and phenylthiouracil using liquid chromatography tandem mass spectrometry through an accredited method. Results: In four bovine and three porcine urine samples, the permissible thiouracil concentration was exceeded. In one sample of porcine urine, methyl- and propylthiouracil were found. The presence of thiouracil and its derivatives in urine samples is most likely due to feeding animals diet containing cruciferous plants. Conclusions: The results of research indicate that thyreostats are not used for anabolic purposes in slaughter animals in Poland.

Introduction: The extremely high genetic variation and the continuously emerging variants of foot-and-mouth disease virus (FMDV) of Southern African Territory (SAT) serotypes including SAT1, SAT2, and SAT3 make it necessary to develop a new RT-PCR for general use for monitoring viruses based on the updated genome information. Material and Methods: A FMDV SAT-D8 one-step RT-PCR was established based on the 1D2A2B genes of the SAT serotype viruses with a multiplex primer set. FMDV A, O, C, and Asia 1 serotypes, other vesicular disease viruses, inactivated SAT viruses, and 125 bovine, ovine, caprine and porcine tissue samples collected from the Chinese mainland were included for evaluating the assay. Results: The new RT-PCR was proven to be specific without cross-reactions with Eurasian FMDV, swine vesicular disease virus (SVDV), Seneca valley virus (SVV), or other common viral pathogens of cattle, sheep, goat, and pig. An around 257 bp-sized amplicon clearly appeared when the inactivated SAT viruses were detected. However, all 125 samples collected from FMDV-susceptible animals from the Chinese mainland which has not known SAT epidemics showed negative results. Conclusions: A FMDV SAT-D8 one-step RT-PCR is a promising method for primary screening for FMDV SAT serotypes.

Objective: A significant number of animals enrolled at UVH regularly from surrounding villages for treating their sick animals, de-worming, vaccination purposes. Therefore, a study was done to define the occurrence of common diseases and disease conditions in cattle and goats at the Upazilla Veterinary Hospital, Debidwar under Comilla district. Materials and methods: Data on various diseases were collected from the record book of hospital during April 2016 to March 2017. The total number of animals were 889, among which cattle were 637 (71.65%) and goats were 252 (28.35%). The presumptive diagnosis was performed based on general examination, physical examination, and clinical examination of animals, and microscopic examination based on common laboratory techniques. Results: Based on clinical examinations, 14 different types of diseases and disease conditions were detected. In cattle (N=637; 71.65%), where FMD (14.44%, n=92), mastitis (6.59%, n=42), digestive disorders (19%, n=121), respiratory disorders (6.12%, n=39), parasitic infestations such as mixed infestation of both ecto- and endo-parasites (34.22%, n=218), acidosis (1.88%, n=12), myiasis (6.12%, n=39), corneal opacity (1.57%, n=10), protozoal diseases (1.26%, n=8), BQ (2.20%, n=14), milk fever (0.94%, n=6), reproductive disorders (4.87%, n=31) and others (0.75%, n=5) were detected. Age wise prevalence in young and adult were (38.62%, n=246) and (61.38%, n=391), respectively. Moreover, sex wise prevalence in male and female were (34.85%, n=222) and (65.15%, n=415) respectively. In goat, (N= 252; 28.35%) 11 different types of diseases and disease conditions such as PPR (12.30%, n=31), mastitis (2.38%, n=6), digestive disorders (19.84%, n=50), parasitic infestation (29.76%, n=75), respiratory disorders (15.08, n=38), myiasis (11.11%, n=28), corneal opacity (4.76%, n=12), acidosis (1.98%, n=5) protozoal diseases such as babesiosis, anaplasmosis (0.79%, n=2) and reproductive disorders (1.59%, n=4), correspondingly. Sex wise prevalence in male and female goat were (44.05%, n=111) and (55.95%, n=141), respectively. Conclusion: All the diseases and disease conditionswere recorded more or less frequently among all age group of cattle and goats though some of the specific diseases and disease conditionshad specific age and species susceptibility such as black quarter in young cattle and PPR in young goats, respectively. A comprehensive updated data with the total population record of that area and proper analysis is needed to identify the actual level of disease and disease conditions in UVH. [J Adv Vet Anim Res 2018; 5(2.000): 117-122]