Introduction: Brucellosis is a neglected bacterial zoonosis with serious veterinary and public health importance throughout the world. A cross-sectional study on animal brucellosis was conducted aiming to estimate seroprevalence and molecular detection. Methods: Blood samples were collected from a total of 4274 individual animals (cattle, small ruminants and camel) from 241 herds/flocks for serology and PCR. Serum samples were tested using multispecies I-ELISA. Blood clots from seropositive animals were also tested for brucellosis via PCR. Additionally, 13 vaginal swab samples were collected from animals (2 from bovine and 11 from small ruminants) with recent abortion history for bacterial isolation and molecular detection. Results: The overall individual animal and herd level seroprevalence was 3.95% (169/4274) and 18.26% (44/241) respectively. The animal level seroprevalence at species level was 1.58% (47/2982), 8.89% (97/1091) and 12.44% (25/201) in bovine, small ruminants (sheep and goat) and camel, respectively. Herd level seroprevalence were 5.43% (10/184), 52.08% (25/48) and 100% (9/9) in bovine, small ruminant and camel, respectively. The animal level seroprevalence of bovine from intensive and extensive systems was 1.10% (31/2808) and 2.87% (5/174) respectively. Blood clots tested for brucellosis via PCR were negative by RT-PCR. Brucella species was isolated from 6/13 (46.15%) vaginal swab samples cultured on Brucella selective agar, and shown to be B. melitensis using Real-Time PCR. Conclusion: Overall, seropositivity for camels was higher than what has been reported previously. Also, there was a notable difference in this study in cattle seroprevalence when comparing extensive with intensive systems, with the extensive system having much greater seropositivity.

Background: Newcastle disease (ND) is a highly infectious poultry disease that causes major economic losses worldwide. The disease is caused by Newcastle Disease Virus (NDV) and early detection and identification of the viral strain is essential. Having knowledge of the NDV strain genotype that circulates in some regions would help in designing an effective vaccine to control the disease. In this regard, there is little information on NDV strain in chickens in mid Rift Valley and the central part of Ethiopia. Therefore, the purpose of this study was to detect and characterize NDV strain genotype from chickens in mid-Rift Valley and the central part of Ethiopia and test whether this NDV strain genotype matches the vaccine strain currently used in the study area. Methods: A total of 98 samples: 78 (tracheal and cloacal) swabs from chicken pools of five and 20 tissue samples were collected. To detect NDV strain, conserved region of the virus Matrix (M) gene was amplified by qRT-PCR. To characterize NDV strain genotypes, M-gene positive samples were specifically re-amplified by conventional PCR targeting the Fusion (F) gene region and sequenced by Sanger method. Results: 13.26% of tested samples were positive for NDV strain in the study area with statistically significant difference (P< 0.05) among the study sites. Further characterization of the F genes from NDV strain isolates by phylogenetic analysis indicated that one field isolate clustered with genotype VII whereas three of the isolates clustered to genotype I, II, and III. The isolate of the current NDV strain vaccine in use in the study area clustered with genotype II. Conclusion: The current study indicates the existence of different NDV strain genotype from that of the vaccine strain currently used. Even though large-scale characterization of several isolates is required at national level, the current study laid baseline information for the existence of variations between field NDV strain genotype and vaccine strain currently used against ND in the country.

Anthrax is a zoonotic disease characterized by rapid onset with usual fatal outcomes in livestock and wildlife. In Ethiopia, anthrax is a persistent disease; however, there are limited data on the isolation and molecular characterization of Bacillus anthracis strains. This study aimed to characterize B. anthracis isolated from animal anthrax outbreaks between 2019 and 2024, from different localities in Ethiopia. B. anthracis was identified using standard microbiology techniques and confirmed by real-time PCR. For the first time in Ethiopia, the genetic diversity of five Bacillus anthracis strains, isolated from dead cattle and goats, was investigated by Whole Genome Sequencing (WGS) and bioinformatics analyses. The five sequenced strains were compared to one Ethiopian B. anthracis genome and the other 29 B. anthracis genomes available in the global genetic databases to determine their phylogeny. The genomes of the strains were also analyzed to detect the presence of antimicrobial resistance and virulence genes. The whole genome SNP analysis showed that the Ethiopian B. anthracis strains were grouped in the A clade. Three strains (BA2, BA5, and BA6) belonged to the A.Br.034 subgroup (A.Br.005/006), and two strains (BA1 and BA4) belonged to the A.Br.161 (Heroin) clade of the Trans-Eurasian (TEA) group. The findings of this study will contribute to expanding the current understanding of the anthrax hotspots in Ethiopia, and the phylogenetic correlation and/or diversity of the circulating strains.

Background: Marek’s Disease (MD) is an economically devastating poultry disease that causes substantial livestock losses and drives up overall health management costs. There was no study conducted on isolation and molecular detection of Marek’s disease virus (MDV) in extensively managed local breed chickens in some parts of Central and Western Ethiopia. Methods: The present study was conducted from September 2021 to October 2022 with the aim of isolation and molecular detection of MDV suspected from outbreak cases in chickens in Central and Western Ethiopia. A total of 94 pooled samples were collected from clinically suspected chickens from four areas, namely, Mako, Guto Gida, Holeta, and Sebeta subcity. Samples were collected from chickens in both intensive and extensive production systems, but nonvaccinated birds against MDV were obtained only from the extensive system. Result: From the clinical samples tested based on quantitative real‐time PCR, 75 (79.78%; 75/94) tested positive for meq gene of the virus. Of these, 36.17% (34/94) of the positive samples were obtained from the feather (34/41) and the rest (43.62%; 41/94) were obtained from postmortem tissue (41/53) samples. From the overall prevalence of 79.78% (75/94), the highest score was recorded in Holeta town (95.65%), followed by Mako District (88.89%), Sebeta Subcity (62.5%), and Guto Gida District (57.89%). Though there are confounding factors such as vaccination status, significantly ( p = 0.04) higher real‐time PCR positive results were obtained in exotic breeds. From 10 pooled liver samples, all samples (100%) tested positive for the virus using real‐time PCR. Similarly, all examined organs showed complete positivity: kidney (10/10, 100%) and spleen (10/10, 100%). However, from six pooled samples of proventriculus samples, only one (1/6, 16.67%) sample was positive for the virus, whereas 34 (82.9%) pooled feather follicles from clinically sick chickens were positive for MDV1. From a total of 75 real‐time PCR positive samples inoculated into DF‐1 cells for virus isolation, 45 (60%) of them were able to show cytopathic effects (CPEs) on the cell line up to the third passage. The seven (40%) feather samples remained negative against the test until the third passage. Conclusion: This study provides critical insights into the isolation and molecular detection of MDV in chickens from Central and Western Ethiopia, highlighting its significant impact on poultry health and productivity. Detailed genetic characterization of the virus and differentiation of the vaccinal strain from the natural infection in exotic breeds are necessary to have effective prevention and control. Experimental studies are also needed to evaluate differences in susceptibility to MDV among local and exotic poultry breeds.

Background: Brucellosis is one of the most frequent contagious neglected bacterial diseases with serious veterinary and public health importance throughout the world. A cross-sectional study on animal brucellosis was conducted from October 2018 to July 2019 in southern and central Ethiopia with the objective of estimating seroprevalence and molecular detection. Blood samples were collected for serum extraction from a total of 4274 individual animals (cattle, small ruminants and camel) from 241 herds/flocks. Blood clots from seropositive animals were also tested for brucellosis via molecular techniques. Additionally, 13 vaginal swab samples were collected from animals with recent abortion history for bacterial isolation and molecular detection.Results: The extracted serum samples were tested using multispecies I-ELISA and the overall individual animal and herd level seroprevalence was 3.95% (169/4274) and 18.26% (44/241) respectively. The animal level seroprevalence at species level was 1.58%, 8.89%, 12.44% in bovine, small ruminants (sheep and goat) and camel, respectively. Herd level seroprevalence were 5.43%, 52.08%, 100% in bovine, small ruminant and camel, respectively. The animal and herd level seroprevalence of bovine from intensive and extensive systems was 1.1%, 2.87% and 9.2%, 50.00% respectively. Brucella species was isolated from 6/13 (46.15%) vaginal swab samples cultured on brucella selective agar, and shown to be B.melitensis using Real-Time PCR. All of the blood clots from seropositive animals were negative for the presence of Brucellaspp with PCR.Conclusions: In the regions sampled animals in all three categories – cattle, sheep/goats, and camels – mostly had low seroprevalence rates for brucellosis, without great differences from previous serosurveys done in Ethiopia. However, seropositivity for camels was higher than what has been reported previously. Also, there was a notable difference in this study in cattle seroprevalence when comparing extensive with intensive systems, with the extensive system being much higher.