Haileleul Negussie

Assessment on major factors that cause skin rejection at Modjo export tannery, Ethiopia

A study was conducted from November 2009 to March 2010 with the objective of identifying the major causes of skin rejection on fresh, pickled, and wet blue skins at Modjo Mesaco Global tannery. A total of 401 fresh and 1,873 pickled and wet blue skins from the routine production system of the tannery were used. Overall, high prevalence of sheep ked (100%) followed by biting louse (64.4%), tick (50%), and sucking louse (45.8%) were observed on fresh sheep pelts, while, on fresh goat pelts, a high prevalence of sucking louse (54.5%), followed by tick (50%), and biting louse (35.5%) were observed. From the total of 90 rejected pickled and wet blue skins of sheep and goats, 98.8% were “ekek” and scratch, 85.6% sheep and goat pox, 74% poor substance, 73.3% heat, 72.2% scar, and 52.2% knife cut-in skins. Large number of skins rejections was recorded in large-sized skins (29.8%), and the lowest observed was in medium-sized skins (11.1%). There were highly statistically significant association (p < 0.05) between size and grades of shoat skins. Ekek and scratches together with sheep and goat pox were the common skin defects that hamper skin quality. However, there was no significant association (p > 0.05) between sheep and goat skins. Ekek and scratch caused high rejection of skin and entailed serious economic loss in terms of foreign exchange earning to Ethiopia. Therefore, the main causes of skin rejection and factors that cause downgrading of skin should be controlled.

Genetic characterisation of infectious bursal disease virus isolates in Ethiopia

Graphical abstract This paper describes a molecular characterisation of IBD circulating in commercial and breeding poultry farms in Ethiopia. Ethiopian vvIBDVs are clustered phylogenetically with the African IBDV genetic lineage, independent of the Asian/European genetic.

First confirmation of foot and mouth disease virus serotype SAT-1 in cattle and small ruminants in Ethiopia in 2007/08.

The study was conducted in three regional states of Ethiopia: Amhara, Oromia, and the Southern Nations Nationalities and people regional state from August 2007 to April 2008 with the objective of identifying the foot and mouth disease virus (FMDV) serotypes circulating in the region. Two serotypes were recorded from epithelial tissue and oesophageal–pharyngeal (OP) fluid that were taken from outbreaks in study regions of Ethiopia. Serotype O FMDV was identified in Girar Jarso, Yabello, and Ankesha Guagusa districts while SAT-1 was isolated in Surma and Maji districts from tissue samples and this was the first report of the FMDV serotype in Ethiopia. Similarly, the OP fluid samples were found positive for SAT-1 FMDV in Maji and Surma districts.

Dual infections of equine herpesvirus 1 and equine arteritis virus in equine respiratory mucosa explants.

Equine herpesvirus 1 (EHV-1) and equine arteritis virus (EAV) induce respiratory problems and abortion in horses and are considered as two serious threats to equine industry. Both EHV-1 and EAV misuse patrolling leukocytes in the upper respiratory tract to breach the basement membrane (BM) and to migrate to blood vessels. So far, the behavior and impact of a double infection in the respiratory mucosa of a horse are unknown. In the present study, the outcome of double infections with EHV-1 and the low virulent EAV strain 08P187 (superinfection with an interval of 12h or co-infection) were compared with single infections in fully susceptible RK-13 cells and equine upper respiratory mucosa explants. When RK-13 cells were inoculated with either EHV-1 or EAV 12h prior to the subsequent EAV or EHV-1 inoculation, the latter EAV or EHV-1 infection was clearly suppressed at 24hpi or 36hpi, respectively, without EHV-1 and EAV co-infecting the same RK-13 cells. After simultaneous infection with EHV-1 and EAV, higher numbers of EAV infected cells but similar numbers of EHV-1 infected cells were found compared to the single infections, with a low number of EHV-1 and EAV co-infected RK-13 cells at 48hpi and 72hpi. In the upper respiratory mucosa exposed to EAV 12h prior to EHV-1, the number and size of the EHV-1-induced plaques were similar to those of the EHV-1 single infected mucosa explants. In nasal and nasopharyngeal mucosae, EAV and EHV-1 pre-infections slightly reduced the number of EHV-1 and EAV infected leukocytes compared to the single infections and co-infection. In double EAV and EHV-1 infected explants, no co-infected leukocytes were detected. From these results, it can be concluded that EAV and EHV-1 are only slightly influencing each others infection and that they do not infect the same mucosal leukocytes.

Early events of canine herpesvirus 1 infections in canine respiratory and genital mucosae by the use of ex vivo models

Canine herpesvirus 1 (CaHV-1) causes a systemic disease in newborn puppies, kennel cough at all ages and genital lesions in adult dogs. The aim of the present study was to elucidate the viral behavior during the early stage of infection in respiratory and genital mucosae, the portals of entry for CaHV-1 by the use of ex vivo explants. CaHV-1 infected and replicated in respiratory and vaginal mucosae in a plaque wise manner. CaHV-1 started to penetrate the basement membrane (BM) only after 48 h post inoculation (hpi) in respiratory mucosal explants, but already after 24 hpi in vaginal explants. The plaque latitude and penetration depth increased over time and both were larger in the vaginal explants compared to the respiratory mucosal explants. The canine respiratory and genital mucosal explants were suitable to study the early pathogenesis of CaHV-1. CaHV-1 showed a better capacity to replicate and invade vaginal mucosa compared to respiratory mucosa, based on the latitude and penetration depth of the plaques of viral antigen positive cells.