BACKGROUND: Cystic echinococosis (CE) is known to be one of the most important zoonotic diseases in different parts of Iran. Even though it causes major health problems, there is limited information regarding its transmission cycles and strain of this infection in eastern Iran. OBJECTIVES: The present study aimed to characterize the strain of Echinococcus granulosus cysts in the slaughtered sheep and goats in Birjand area using morphological and molecular criteria. METHODS: Isolates of E. granulosus were collected from sheep (30) and goats (30) from Birjand slaughterhouse and characterized employing both DNA (PCR-RFLP of ITS1) and morphological criteria (metacestode rostellar hook dimensions). In addition, the fragments of the genes coding for ITS-1 were sequenced. RESULTS: Among the two different identified strains/genotypes (sheep and camel), the sheep strain appeared to be the most common genotype of E. granulosus affecting sheep and goats. All of the 30 sheep samples and 20 out of 30 goat samples were infected with sheep strain. However, the camel genotype was only observed in the goats and 10 out of 30 goat isolates were infected with the camel genotype. The camel genotypes had RFLP patterns, which were different from the RFLP patterns of the rest of isolates (sheep strain). CONCLUSIONS: The results of this study revealed that the ‘sheep’ strain was the most prevalent strain in sheep and goats in this area. Moreover, the camel genotype (G6) was confirmed to trigger infection in the slaughtered goats of Birjand area.

BACKGROUND: Peste des petitis (PPR) is a highly contagious viral disease with high incidence and mortality rate, which is endemic in the Middle East, Southwest Asia, and Africa. This disease has been causing economic losses in sheep and goat flocks in these areas. Studies have shown that environmental and host risk factors can influence the severity of PPR infection. OBJECTIVES: We conducted the present study to investigate the prevalence of PPR in small ruminants population of Garmsar city and its suburbs. Furthermore, the effect of host factors, including animal species, gender, and age, and environmental factors, such as sampling season, geographical area, and sampling location, were evaluated. METHODS: Blood samples of 180 sheep and goats were taken in spring, summer, and autumn and after centrifugation, serum samples were isolated. We measured antibody response using competitive enzyme linked immunosorbent assay (C-ELISA). RESULTS: The apparent and true prevalence of contamination in small ruminants of Garmsar and its suburbs ware 24.44 % and 23.91 %, respectively. The results revealed non significant relationships between animal species (p < /em>= 0.08), gender (p < /em>= 0.14), and age (p < /em>= 0.98) with PPR serum prevalence. Meanwhile, there was a significant relationship between season (p < /em>= 0.03), geographical area (p < /em>= 0.0004), and sampling location (p < /em>= 0.0001). In addition, the odds ratio of PPRV infection in autumn was 2.62 (95% CI: 0.06 – 6.02; p < /em>< 0.05) times more than that of other season and in the south-eastern of Garmsar, it was 6.71 (95% CI: 3.01-17.60; p < /em>< 0.05) times more than that of other geographical regions. The odds ratio of PPRV infection in the Mahmood Abad village was 63.63 (95 % CI: 12.14 – 132.93; p < /em>< 0.05) times higher than that of other villages. CONCLUSIONS: According to the obtained findings, PPR was proven to be an endemic disease in Garmsar and its suburbs and the environmental risk factors have a greater impact on the seroprevalence of disease than host risk factors. Therefore, in order to control the disease in endemic areas, further attention should be paid to environmental risk factors and minimizing the risk of epidemics through vaccination at sensitive timescales and areas before high-risk environment changes.

The aim of the study was to determine how the spread of contagious agalactia in sheep and goats in the Odesa region depended on the age of the animals and the season.

Foot rot in small ruminants is highly contagious, causes severe lameness, and impairs fertility and wool and meat production. It is usually treated with parenteral antibiotics, with attendant antibiotic resistance risk, and with bactericidal footbaths, potentially harmful to humans and the environment. An alternative treatment in sheep is proposed based on repeated topical ozonated ointment application. Its effectiveness and safety were evaluated by estimation of acute-phase response, biochemical indicators of organic damage, and antioxidant/oxidant balance (AOB).

It is very important to monitor the infection of Mycoplasma ovipneumoniae as a potential threat to the sheep industry. Southern Xinjiang is a major sheep breeding base in China, however, there is no relevant information concerning the infection of the region’s ovine stock with this bacteria at present. This study aimed to address this knowledge gap.

Although ovine cysticercosis is not a zoonotic problem, it results in substantial economic losses due to the condemnation of infected tissues or entire carcasses. This study aimed to record preliminary data on the prevalence, and phylogenetic diversity of Cysticercus ovis isolates from slaughtered sheep in the province of Sulaymaniyah, Iraq.

Brachiaria decumbens is a highly productive tropical grass used for ruminant production. However, it can cause hepatogenous photosensitization, general ill-thrift, and deaths in ruminants due to the presence of steroidal saponins. This study determined the acute and chronic clinico-pathological responses of sheep to graded levels of B. decumbens diet. A total of 30 male crossbred Dorper sheep (six-month-old) used in the study were randomly divided into three treatment groups of 10 sheep each. Treatment 1 (T1), which served as the control group, was fed with Pennisetum purpureum and concentrates, whereas Treatments 2 (T2) and 3 (T3) were fed low (10%) and high (60%) levels of B. decumbens, respectively. The study period was divided into acute (7 days) and chronic (90 days) phases. The rectal temperature, respiratory rate, heart rate, and mucous membrane color were monitored throughout the experiment. At the end of each stage, five animals were selected from each treatment group and euthanized by slaughter to collect organs for gross pathology, organ morphometric and histopathological evaluations. The treated animals did not show significant changes (p>0.05) in rectal temperature, pulse, and respiration rates throughout the study period. However, the mucous membranes were noticeably becoming pale starting from day 60 to 90 in T3 and during the chronic phase (day 90) in T2. There was no lesion or morphometric change in any organ at postmortem examination. At histopathology, both T2 and T3 exhibited mild to moderate necrosis, hemorrhage, congestion, hydropic degeneration and edema (p<0.05) in the liver and brain. In summary, this study has established that both low and high levels of B. decumbens diets cause chronic brain and liver damages in the sheep model. This study can be used for future research on the effects of B. decumbens on grazing animals.

Although ovine cysticercosis is not a zoonotic problem, it results in substantial economic losses due to the condemnation of infected tissues or entire carcasses. This study aimed to record preliminary data on the prevalence, and phylogenetic diversity of Cysticercus ovis isolates from slaughtered sheep in the province of Sulaymaniyah, Iraq. From January to September 2020, 6, 411 slaughtered sheep were examined for C. ovis by routine meat inspection. The amplification and sequence analysis of the COX1 gene for up to 35 specimens of C. ovis was performed using conventional PCR. The overall prevalence rate was 1.3%, and the prevalence was significantly higher in older sheep (>1 year) than younger ones (<1 year) (P< 0.05). The cardiac muscle showed a higher tendency to carry C. ovis infection compared to other examined muscles. Sequence analysis of the COX1 gene revealed six haplotypes, and the level of pairwise nucleotide diversity between individual haplotypes was 1–2%. Five out of six of the Taenia ovis haplotypes recovered could have been recorded for the first time globally. Phylogenetic interpretation indicated that all the T. ovis haplotypes clustered in a single clade, and it also indicated an extremely close similarity to Iranian and New Zealand isolates. Globally, this report adds new data on C. ovis genetic diversity, which provide an extremely useful molecular background with regard to future preventive as well as control strategies.

Ovine interferon-tau (oIFN-τ) is a newly discovered type I interferon. This study used biochemical techniques to transform the oIFN-τ gene into Escherichia coli to obtain the mass and soluble expression of the recombinant protein. First, total RNA was extracted from fresh sheep embryonic tissues with TRIzol reagent and then used as a template to reverse transcribe and amplify the mature oIFN-τ gene with RT-PCR. The amplified product was next digested with the HindIII and XhoI restriction enzymes and inserted into the pET-32a(+) vector to construct the prokaryotic expression plasmid. The corrected in-frame recombinant plasmid, pET-32a(+)-oIFN-τ, was transformed into E. coli Rosetta (DE3) competent cells. After induction with isopropyl-beta-D-thiogalactopyranoside (IPTG), the recombinant protein was detected in bacteria. Finally, the bacteria were lysed by sonication, and the recombinant protein was purified by nickel affinity chromatography and DEAE anion exchange chromatography. The protein was confirmed to be oIFN-τ, which mainly existed in the soluble lysate fraction, as proven by SDS-PAGE and Western blot assays. Purified IFN-τ exists mostly in a soluble form, and its anti-vesicular stomatitis virus (VSV) activity reached 7.08×10(6)IU/mL.

Rhipicephalus bursa is a common tick parasite of small-to-medium size ungulates, principally in warm, temperate, and subtropical areas. Although common in livestock and showing a wide geographic distribution, its epidemiological role in tick-borne bacterial disease is barely known. This study addressed the knowledge gap and aimed to screen for the presence of Anaplasmataceae and spotted fever group (SFG) Rickettsia species in R. bursa ticks collected from domestic animals in Romania, Eastern Europe. A total of 64 pools of R. bursa ticks collected from small ungulates were tested by PCR for Anaplasmataceae DNA presence using group-specific primers. Specific testing was performed for Anaplasma marginale/A. centrale/A. ovis, A. platys, A. phagocytophilum, Ehrlichia canis, and SFG Rickettsia. The positive samples were purified and sequenced, and sequences analysis was used to identify the species and to confirm the PCR results. The only pathogen identified in this study was E. canis. The obtained sequences confirmed the PCR results. The presence of E. canis in R. bursa in Romania and in ticks from sheep was shown for the first time in this study. Based on these findings, it may be presumed that the E. canis DNA originated from ticks; however, the vectorial role of R. bursa (and other arthropod species) in the transmission of E. canis should be proved experimentally.