Mixed infection of peste-des-petits ruminants and Capripox in goats in south Kivu, Democratic Republic of Congo

Open Access Journal; Published online: 21 Dec 2017Objective: We aimed at determining the prevalence and characterizing the CaPV, determining the CaPV-PPRV coinfection prevalence and providing data about phylogenetic relationship between the fusion protein of PPRV and P32 gene of CaPV. Materials and methods: A total of 150 samples including animals swabs, tissues and blood were collected from unvaccinated goats in a PPR and/or Capripox outbreaks in South Kivu, Eastern of Democratic Republic of the Congo. Conventional PCR and reverse transcriptase (RT-PCR) were used respectively to amplify P32, RPO30, GPCR genes of Capripox virus and Fusion (F) protein of PPRV. Positive samples were sequenced for phylogenetic analysis. Results: Out of 150 tested animals, 64.7% (n=97/150) were PPRV positive, 52.7% (n=79/150) were Capripox positive and 38.7% (n=58/150) were positive for both PPRV and CaPV. The pairwise comparison of P32gene of CaPV and F gene of PPRV showed 99.75% of identity percentage among goatpox virus sequences, 96.95% among PPRV sequences and 47.91% between CaPV and PPRV sequences. Conclusion: The study has demonstrated high prevalence of CaP V-PPRV mixed infection in South Kivu. Lumpy skinvirus disease (LSVD) is a lineage circulating which has a genetic relationship between its P32gene and the Fgene of PPRV giving the challenge to differentiate the two diseases at the clinical farm level

Analysis of small ruminants’ pastoral management practices as risk factors of peste des petits ruminants (PPR) spread in Turkana District, Kenya

Peste des petits ruminants (PPR) is an emerging viral disease spreading throughout Kenya and East Africa causing major losses in the small stock. This study is an attempt to evaluate small stock management practices in Turkana pastoral system, Kenya as predictors of PPR outbreaks. Information on the social practices and the occurrence of PPR outbreaks was obtained by participatory techniques. The small stock management practices, evaluated as factors, in a previous study were simultaneously analyzed with seasons and administrative divisions as the independent risk factors for the presence or absence of PPR outbreaks in 142 Adakars (villages) as the dependent variable. Analyses were carried out for the years 2009 and 2010 combined as one data set and considered as longitudinal repeated data. In the analyses, the presence or absence of PPR outbreaks was the dependent variable. Data were further analyzed separately disaggregated by season where the presence or absence of PPR outbreaks in a season was considered as the dependent variable. All analyses utilized multivariable logistical regression analyses. In the longitudinal analysis, season was the only significant factor associated with PPR outbreak. Disaggregating the data by season revealed that certain seasonal-specific livestock management activities increased the risk of reporting PPR outbreaks: (1) sharing water sources leading to social aggregation of young stock in one point (Factor 3) (odds ratio (OR) = 2.0) in season 2 (wet season) of 2009; (2) sick dams left to nurse their young kids/lambs (Factor 7) (OR=1.62) in the same season in 2010. The finding of diverse risk factors in the same seasons across years suggests temporal heterogeneity in the distribution and occurrence of the determinants of PPR in the Turkana ecosystem. The study discusses the implications of these findings on disease control