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Pneumonic pasteurellosis is the leading cause of recurrent morbidity and mortality in ruminant livestock in Ethiopia. Its control is mainly done using an annual vaccination with a monovalent whole broth culture of Pasteurella (P.) multocida. However, the multiplicity of the serotypes circulating in the field and the lack of cross-protective immunity hinder the effectiveness of the vaccination program warranting the development of a vaccine with better efficacy. To this effect, the identification, and characterization of the strains from different regions of the country is necessary. In this paper, Pasteurella organisms collected from camels, cattle, goats, and sheep with respiratory signs suggestive of pasteurellosis in the Afar, Tigray, and Benishangul Gumuz regional states were isolated, and characterized. From clinically pneumonic cases, 793 nasal swabs (286 goats, 276 sheep, 168 camels, and 63 cattle) were collected aseptically and cultured on Blood Agar. Bacteria pathogens were identified at the species level by biochemical tests. Culture positivity was 29.3% (243/793). The isolation frequencies of B. trehalosi, M. haemolytica, and P.multocida were 47.7% (116/243), 43.2% (105/243), and 9.1% (22/243), respectively. A higher isolation rate was observed in sheep (37.4%), and the lowest in cattle (6.2%). Mixed infection with B. trehalosi and M. haemolytica was observed in sheep, goats, and camels. Despite the higher frequencies of isolation of B. trehalosi and M. haemolytica from all host species, the vaccine currently being used in Ethiopia consists of only P. multocida biotypes A for sheep and goats and biotype B for cattle. Moreover, camels are not considered in the pasteurellosis vaccination program in the country. Therefore, the result of the study suggests the need to include B. trehalosi and M. haemolytica in the vaccine preparation as well as underlines the relevance of considering camels in the vaccination program. [ABSTRACT FROM AUTHOR]

The aim of the current study was to assess the major animal health problems and their impact on beef cattle production in Doba district of West Harerghe Zone, Ethiopia. The study area was purposively selected, and a simple random sampling method was used to selected households' fatteners from each kebele and interviewed using structured questionnaires. The present study showed that the overall prevalence of the diseases was internal and external parasite 93.3%, bloat 53.3%, black leg 71.1%, pasteurolosis 71.8%, wound 71.8%, FMD 22.2%, and anthrax 13.33% which affect fattening cattle, respectively, in the study area. All the respondents (100%) involved in the study were experienced with deworming of their animals to protect from parasites. But, only 46.7% and 42.2% of the respondents have accessed veterinary services with limited regularity and vaccination program, respectively, in the study area. Hence, the beef cattle fatting sector should be supported through considering alleviating the major disease affecting this sector and encouraging the farmers' indigenous knowledge practice with technology. [ABSTRACT FROM AUTHOR]

Background: Hepatitis E is an enteric and zoonotic disease caused by hepatitis E virus (HEV) that is mainly transmitted via the faecal-oral route through contaminated food or the environment. The virus is an emerging infectious agent causing acute human infection worldwide. A high seroprevalence of the disease was reported in pregnant women in Addis Ababa, Ethiopia, raising significant public health concern. The presence of HEV specific antibodies were also reported in dromedary camels in the country; however, the infectious virus and/or the viral genome have not been demonstrated to date in animal samples. Methods: To address this gap, a total of 95 faecal samples collected from both apparently healthy pigs of uncharacterised types (50 samples) in Burayu and Addis Ababa areas and camels (Camelus dromedarius, 45 samples) in west Hararghe were screened for the presence of HEV genome using universal primers in a fully nested reverse transcription polymerase chain reaction (nRT-PCR). The protocol is capable of detecting HEV in faecal samples from both pigs and camels. Results: The nRT-PCR detected HEV genes in six (12%) pig faecal samples and one camel sample (2.2%). Therefore, the results indicate that HEV is circulating in both pigs and camels in Ethiopia and these animals and their products could serve as a potential source of infection for humans. Conclusion: The detection of HEV in both animals could raise another concern regarding its public health importance as both animals' meat and camel milk are consumed in the country. Further studies to determine the prevalence and distribution of the virus in different animals and their products, water bodies, food chain, and vegetables are warranted, along with viral gene sequencing for detailed genetic characterisation of the isolates circulating in the country. This information is critically important to design and institute appropriate control and/or preventive measures. [ABSTRACT FROM AUTHOR]

Lumpy skin disease (LSD) is a viral disease caused by LSD virus and is one of the most economically significant transboundary and emerging diseases of cattle. LSD causes considerable economic losses due to emaciation, damage to hides, infertility, and loss of milk production. In Ethiopia, the disease is distributed almost in all regions and is regarded as one of the most economically important livestock diseases in the country. An outbreak investigation of the disease was monitored from October 2016 to April 2017 in southern pastoral areas of Bale Zone, Oromia, Ethiopia. In December 2016, LSD outbreak occurred in Sawena district of Bale Zone, from which necessary biopsy samples were collected from actively infected animals for the purpose of virus isolation, and characterization using different molecular techniques at National Animal Health and Diagnostic Investigation Center (NAHDIC) of Sebeta, Ethiopia. In addition, clinical examination of infected and in-contact animals was carried out together with a questionnaire survey. Based on the clinical manifestations, LSD was recorded in 18% (94/522) of examined cattle, whereas biopsy samples from 20 clinically positive animals were collected for further laboratory process. The morbidity rate was higher in animals less than two years 28.97% (31/107) than other ages and showed a statistically significant difference with P < 0.05. Female animals showed higher morbidity rate of 20.59% (76/369) than male animals (11.76%) (18/153) with a significant difference at P ≤ 0.003. Mortality rate and case fatality were also significantly higher in young animals than other age groups. Viruses were isolated from both skin biopsies and nasal swabs on Vero cell line. From both skin biopsies and nasal swabs, the virus DNA was identified by amplifying the 172 bp DNA fragment using real-time and conventional PCR. Providing adequate diagnostic facilities, establishing strategic policies for effective control and eradication and awareness creations for communities for early identification or reporting were recommendations made to minimize economic losses of the disease. [ABSTRACT FROM AUTHOR]