Assessment of the duration of maternal antibodies specific to the homologous peste des petits ruminant vaccine “Nigeria 75/1" in Djallonké lambs

The duration of maternal immunity was determined from 112 lambs born from vaccinated ewes with the homologous PPR vaccine “Nigeria 75/1" at day 90 and day 120 of pregnancy. Serum samples were collected from lambs starting from day 15 to day 150 after birth and analyzedusing the PPR specific competitive ELISA. At day 75 and day 90 after birth, 70% and 95% of these lambs respectively became negative. So it is recommended to vaccinate lambs against PPR in the interval from 75 to 90 days after birth

Diagnosis and surveillance of rinderpest using reverse transcription - PCR

PCR technique was used as an alternative method to detect evidence of rinderpest virus for diagnosis and in epidemiological surveys. Viral RNA was purified in 20 to 30 min using a commercial kit (RNaid (BIO 101). Primers used mapped in the nucleocapsid protein gene of rinderpest virus and gave specific and sensitive amplification from pathological samples. The size of the amplified fragment was 297 bp and the result was confirmed using internal non-radioactive probe SB1. The specificity of the PCRproducts was also confirmed by cleavage using restriction enzyme RsaI to give a major band of 200 bp

Comparison of two competitive ELISAs for the detection of specific peste-des-petits-ruminant antibodies in sheep and cattle populations

Peste-des-petits-ruminant (PPR) continues to be a major problem of small ruminants in Africa, the Middle East and Asia. The closely related paramyxovirus causing rinderpest (RP) has been largely eradicated by a global vaccination campaign. However, PPR screening of large populations has lacked a sufficiently reliable, fast and cheap screening test. This study compares two commercially available PPR antibodies ELISA kits using serum collected from experimental sheep and cattle populations with four different vaccination histories for RP and PPR. The aim was to estimate the levels of cross-reaction between antibodies to the two diseases for each kit and their test parameters in the different populations. There was considerable variation between kits and between the different vaccination groups. There was a clear problem of cross-reaction in both PPR kits with RP positive sera. However, in areas where RP has been eradicated and vaccination stopped both tests could be useful for screening small ruminants for PPR

Non-invasive genomics of respiratory pathogens infecting wild great apes using hybridisation capture

Human respiratory pathogens have repeatedly caused lethal outbreaks in wild great apes across Africa, leading to population declines. Nonetheless, our knowledge of potential genomic changes associated with pathogen introduction and spread at the human-great ape interface remains sparse. Here, we made use of target enrichment coupled with next generation sequencing to non-invasively investigate five outbreaks of human-introduced respiratory disease in wild chimpanzees living in Taï National Park, Ivory Coast. By retrieving 34 complete viral genomes and three distinct constellations of pneumococcal virulence factors, we provide genomic insights into these spillover events and describe a framework for non-invasive genomic surveillance in wildlife.Peer Reviewe

Peste des petits ruminants in large ruminants, camels and unusual hosts

Since its first report in 1942, peste-des-petits-ruminants virus (PPRV) has caused several epidemics in a wide range of susceptible hosts around the world. In the last 30 years, the evidence of natural and experimental infections and virus isolation were reported from novel but unusual hosts such as camel, cattle, buffalo, dogs, Asiatic lion and pigs. In addition, PPRV in a potential vector, biting midges (Culicoides imicola), has been reported. Either presented as clinical and/or subclinical infections, the presence of the virus in an extended range of susceptible hosts highlights the cross-species transmission and supports the hypothesis of an endemic circulation of PPRV among susceptible hosts. However, the potential role of large ruminants, camels and unusual hosts for PPRV epidemiology is still obscure. Therefore, there is a need for molecular and epidemiological investigations of the disease among usual and unusual hosts to achieve the goals of disease control and eradication programmes initiated by national and international organisations, such as the FAO and OIE. This review is the first to summarise the scattered data on PPR in large ruminants, camels and unusual hosts to obtain the global scientific communities' attention for further research on epidemiological aspects, not only in its native hosts, but also in large ruminants, camels and other unusual hosts