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Objectives: This study was designed to detect Riemerella anatipestifer through polymerase chain reaction (PCR) from duck farming areas of the Mymensingh and Sylhet divisions and to determine the antibiogram profile of the PCR-positive isolates using the disc diffusion method. Materials and Methods: Fifty two samples were collected, comprising clinically sick (32 ducks) and dead ducks (20). PCR confirmation was accomplished, and consistent findings were observed, employing R. anatipestifer groEL (271-bp) gene as appropriate molecular markers. For further clarification, see R. anatipestifer specific PCR assay (546-bp) and gyrB-based PCR (162-bp) were also done. The disc diffusion method was followed for the antibiotic susceptibility test of the iso¬lates against commonly used antibiotics. Results: A total of 21 samples, 8 from clinically sick birds and 13 from dead birds, showed positive results in both conventional and molecular assays out of 52 samples. High occurrences were found in oropharyngeal swabs from sick ducks and the liver and heart from dead ducks. Antibiotic susceptibility testing revealed that the isolates were 100% resistant to penicillin G, cefradine, streptomycin, neomycin, gentamycin, meropenem, and erythromycin, but 100% sensitive to cotrimoxazole, florfenicol, and levofloxacin. Conclusion: For diverse duck-populated areas in Bangladesh, this study shows the severity of R. anatipestifer infection among ducks. [J Adv Vet Anim Res 2022; 9(4.000): 684-693]

Objective: Duck virus enteritis is a severe viral disease that kills ducks and swans worldwide. The clinical manifestations, gross pathology, molecular detection, and characterization of the duck virus enteritis virus (DVEV) in Australian black swans at a safari park in Bangladesh were described in this case report. Materials and Methods: On a safari park in Bangladesh, an Australian black swan flock exhibited clinical signs of anorexia, greenish watery diarrhea, increased thirst, partial paralysis, and death. Postmortem examinations of deceased swans revealed extensive pathological abnormalities in the trachea, liver, and spleen. To isolate DVEV, a viral inoculum produced from the liver and spleen of dead swans was implanted into 913-day-old embryonated duck eggs via the chorioallantoic membrane (CAM) route. DVEV was confirmed using a polymerase chain reaction (PCR) assay. Phylogenetic analysis was used to determine the genetic relationship between the DVEV isolates from Australian black swans, and 16 DVEV isolates previously described in the GenBank. Results: Hemorrhage was noted in the annular ring of the trachea, as well as an enlarged and hemorrhagic liver and spleen. The PCR assay amplified a 446-bp fragment of the DVEV DNA polymerase gene in the liver, spleen, and CAM homogenates. The phylogenetic analysis found that the DVEV isolates from swans were comparable to those from Bangladesh, India, Vietnam, China, Germany, the USA, and Egypt. Conclusion: According to the findings of this study, the DVEV was the cause of illness and mortality in an Australian black swan flock. [J Adv Vet Anim Res 2021; 8(4.000): 557-562]

Objective: This study is conducted to assess the seroprevalence and associated risk factors (e.g., age, sex, bio-security practices and management system) of Influenza A virus in swine population of Rangamati and Khagracchari Districts Materials and methods: Prevalence study Influenza A in swine population was conducted over a period of six months Rangamati and Khagracchari Districts between July to December 2013. 180 blood samples were collected from pigs, and the samples were tested for the detection of Influenza antibody using Indirect ELISA method. Results: Total numbers of samples were 180 and numbers of positive cases were 22.Then the overall seroprevalence between the aforesaid districts was found to be 12.22%. Results of the investigation revealed that the seroprevalence of influenza A was 15% in Rangamati district, 10% in Khagraccharidistrict . The highest seroprevalence was found in Rangamati district (15%) and the lowest seroprevalence was (10%) found in Khagracchari district. On the basis of sex, seroprevalence rate of influenza A was found 14.29% in male pigs and 976% in female pigs. Conclusion: The study confirms that influenza virus is circulating in the pig populations of hill tracts area of Bangladesh. Our study had a number of limitations. Veterinarians, researchers and health officials will get new information from this research which will be helpful for developing prevention strategy for combating against this disease. [J Adv Vet Anim Res 2018; 5(2.000): 204-210]

Objective: The study was undertaken with an objective to determine the seroprevalence of Peste des Petits Ruminants (PPR) in goats of different age groups. Materials and methods: A total of 606 goats (414 vaccinated and 192 unvaccinated) were randomly selected from Rajshahi, Sirajganj and Gazipur districts. The goats were categorized into different age gropus; (i) 0-6 months, (ii) 12-24 months, and (iii) >24 months. Blood samples were collected from the goats and sera were prepared. The sera were examined for the presence of antibodies against PPR virus (PPRV) by competitive enzyme linked immunosorbent assay (c-ELISA). Results: In the unvaccinated goats, overall seroprevalence was 8.70% (n=36/414). The highest seroprevalence was recorded in Rajshahi (28.57%; n=18/63) which was followed by Gazipur (16%; n=12/75) and Sirajganj (2.17%; n=6/276). The age-based overall seroprevalence in the unvaccinated samples from 0-6 months age group was 9.43% (n=15/159). Similarly, 12-24 and >24 months age groups of goats revealed the presence of 6% (n=9/150) and 11.43% (n=12/105) seroprevalence against PPRV. Of the vaccinated samples, overall 76.04% (n=146/192) were seropositive against PPRV. Within the age group of 0-6 months, vaccinated samples had the highest seroprevalence (80.25%; n=65/81) as compared to 12-24 (70.83%; n=34/48) and >24 months (74.60%; n=47/63) age groups of goats, respectively. Conclusion: The seroprevalence in the unvaccinated samples indicates that PPRV is circulating in Bangladesh which is inducing to produce natural antibody in goats. This study also states that the field level vaccination against PPRV could give protection to the goats. [J Adv Vet Anim Res 2016; 3(2.000): 127-133]