Peste Des Petits Ruminants: An Update

Peste des petits ruminants (PPR) is a notifiable and reportable disease recognised by the Office Internationale Epizooties (OIE) and penned for eradication by 2030. It is an endemic and devastating disease of small ruminants in some countries of Africa, Asia, and the Middle East. The disease militates against small ruminant production and increased flock numbers in the region. Information and literature on the current review was especially obtained and compiled from CABI abstract data base, PubMed, Scopus, Elibrary USA and other online publications. This review highlights the viral structure, epidemiology, predisposing factors, clinical signs, pathology, immunoprophylaxis, diagnostic techniques and therapeutics of the disease with a view to generating increased scientific research interests on PPR. It is hoped that more robust scientific research breakthroughs could emerge particularly in the area of immunoprophylaxis, rapid penside diagnosis, and alternative therapeutics such as the use of probiotics. This will in no small measure boost small ruminant production, alleviate poverty and increase food security in countries endemic with the disease.

Progress in research on detection techniques for peste des petits ruminants virus / 中国生物制品学杂志

@#Peste des petits ruminants(PPR)is an acute and highly contagious disease caused by peste des petits ruminants virus(PPRV),which mainly infects goats and sheep with high morbidity and mortality. Because of its serious pathological damage and wide spread,PPR has caused huge economic losses to the aquaculture industry and international trade in various countries,so it is particularly important to establish a rapid and accurate detection method for the prevention and control of the disease. This paper reviews the progress in research on biological detection techniques for PPRV detection,such as routine RT-PCR,routine multiplex PCR,real-time fluorence quantitative PCR(RT-qPCR),pyrosequencing,nested PCR(nPCR),loop-mediated isothermal amplification(LAMP)and recombinase polymerase amplification(RPA),so as to provide bases and ideas for scientific detection and identification of PPRV.

Preparation of colloidal gold test strips for the detection of antibodies to peste des petits ruminants based on monoclonal antibodies to N protein / 生物工程学报

A simple, fast, and visual method for detecting antibodies against peste des petits ruminants virus (PPRV) using colloidal gold strips was developed. In this study, the pET-32a-N was transformed into Escherichia coli Rosetta (DE3) for expression. Hybridoma cell lines were generated by fusing SP2/0 myeloma cells with splenocytes from immunized mice with the expressed and purified N protein of PPRV. The PPRV N protein was labeled with colloidal gold particles as the gold-labeled antigen. The N protein served as the gold standard antigen and as the test (T) line-coated antigen, while the monoclonal antibody served as the quality control (C) line-coated antibody to assemble the colloidal gold immunochromatographic test strips for detecting antibodies against the N protein of PPRV. Hybridoma cell line designated as 1F1 was able to stably secrete the monoclonal antibody against the N protein of PPRV. The titer of 1F1 monoclonal antibody in ascites was 1:128 000 determined by indirect enzyme-linked immunosorbent assays (ELISA), and the immunoglobulin subtype of the monoclonal antibody was IgG1, with kappa chain. The obtained monoclonal antibody was able to specifically recognize the N protein of PPRV, as shown by Western blotting and indirect immunofluorescent assay (IFA). The developed colloidal gold test strip method was able to detect PPRV antibodies specifically, and there was no difference between different batches of the test strips. Testing of a total of 122 clinical sera showed that the compliance rate of the test strip with ELISA test was 97.6%.The test strip assay developed in this study has good specificity, reproducibility, and sensitivity, and it can be used for the rapid detection of PPRV antibodies.

Research progress of interaction between peste des petits ruminants virus and host cells / 中国生物制品学杂志

@#Peste des petits ruminants(PPR)is a highly contagious disease with high mortality which is caused by peste des petits ruminants virus(PPRV)infection and leads to enormous economic losses for sheep husbandry both at home and abroad. The knowledge of interactions between PPRV and host cells is the basis of understanding of the pathogenesis and the prerequisite of disease prevention and control. This paper reviews the studies on the activation of host innate immune response by PPRV infection,the immune evasion of PPRV mediated by viral protein products,and the induction of apoptosis,autophagy and inflammasome resistance to virus,which provides a reference for further discussion on the immune evasion of PPRV and the key nodes involved in the interaction between PPRV and the host,thus providing theoretical guidance for effective prevention and control of PPR transmission.

Comparative Efficacy of Different Chemotherapeutic Regimens in the Treatment of Peste des Petits Ruminants in West African Dwarf Goats / Eficacia comparativa de diferentes regímenes quimioterapéuticos en el tratamiento de la Peste des petits ruminants (PPR) en cabras enanas de África occidental

Abstract The comparative efficacy of different chemotherapeutic regimes in the treatment of natural clinical infection of Peste des petits ruminants (PPR) infection in West African Dwarf (WAD) goats were determined. Twenty WAD male goats divided into five groups, of four each were used. Group 1 was the combined therapy group treated with Acyclovir, Oxytetracycline and Ivermectin, Group 2 was treated with Acyclovir only, Group 3 was treated with Ivermectin only, Group 4 was treated with Oxytetracycline only and Group 5 was left untreated. Clinical signs such as nasal and ocular discharges, emaciation, anorexia, pyrexia, ulcerative oral lesions, respiratory distress and diarrhoea were observed in these goats during the period of their acclimatization. The prominent post-mortem lesion observed was discontinuous streaks of congestion (Zebra markings) in the mucosa of the colon and rectum. The physiologic parameters (temperature, pulse rate, heart rate, and respiratory rate) were taken daily. It was observed that there was a significant increase in the temperature above normal in the untreated group, suggesting pyrexia. It was also observed that the combined therapy group showed a smaller number of mortality and thus, had a better efficacy when compared to the other chemotherapeutic agents used singly.

Resumen Se determinó la eficacia comparativa de diferentes regímenes quimioterapéuticos en el tratamiento de la infección clínica natural con la Peste de los pequeños rumiantes (PPR) en cabras enanas de África occidental (WAD). Se usaron veinte cabras WAD machos, distribuidas en cinco grupos, de cuatro cabras cada uno. El grupo 1 fue el grupo de terapia combinada, tratado con aciclovir, oxitetraciclina e ivermectina. El grupo 2 fue tratado solo con aciclovir. El grupo 3 fue tratado con ivermectina solamente. El Grupo 4 fue tratado con oxitetraciclina y el grupo 5 no recibió tratamiento. Se observaron signos clínicos como secreciones nasales y oculares, emaciación, anorexia, pirexia, lesiones orales ulcerativas, dificultad respiratoria y diarrea en estas cabras durante su periodo de aclimatación. La lesión post-mórtem más notable que se observó fueron las manchas descontinuas de congestión (como las rayas de la cebra) en la mucosa del colon y del recto. Los parámetros fisiológicos (temperatura, frecuencia del pulso, ritmo cardiaco y frecuencia respiratoria) se midieron diariamente. Se observó que había un aumento significativo en la temperatura por encima de lo normal en el grupo sin tratamiento, lo que sugirió pirexia. También se observó que el grupo de terapia combinada mostró una cifra de mortalidad menor y, por ende, allí hubo una mejor eficacia en comparación con los otros agentes quimioterapéuticos usados solos.

Sample type is vital for diagnosing infection with peste des petits ruminants virus by reverse transcription PCR

Peste des petits ruminants (PPR) diagnosis from suspected samples from sheep and goats was carried out. Buffy coat, tissues, and oculo-nasal swabs were analyzed using nucleoprotein (NP3/NP4) and fusion protein (F1/F2) gene primers, respectively. Analysis of the sample types and primer set revealed that buffy coat are the best type of samples for PPR diagnosis and the use of two set of primers will increase the number of positives.

Cytokines Expression Profile and Kinetics of Peste des petits ruminants Virus Antigen and Antibody in Infected and Vaccinated Goats / 中国病毒学·英文版

The present study deals with the co-ordination of cytokine(IL-4 and IFN-γ) expression and kinetics of peste des petits ruminants(PPR) virus antigen and antibody in PPRV infected and vaccinated goats.The infected animals exhibited mixed cytokine(both TH1 and TH2) responses in the initial phase of the disease.The infected and dead goats had increased IFN-γ response before their death; while IL-4 remained at the base level.The cytokine expression in recovered animals was almost similar to that of vaccinated ones,where a unique biphasic response of IL-4 expression was observed with an up-regulation of IFN-γ on 7th days post vaccination(dpv).Analysis of PPR virus antigen and antibody kinetics in different components of blood from infected and vaccinated animals revealed that the PPR virus antigen load was highest in plasma followed by serum and blood of the infected animals,whereas vaccinated animals showed only marginal positivity on 9th dpv.The antibody titer was high in serum followed by plasma and blood in both vaccinated and infected animals.Therefore,it is inferred that the presence of antigen and antibody were significant with the expression of cytokine,and that a decreased response of IL-4 was noticed during intermediate phase of the disease i.e.,7 to 12th days post infection(dpi).This indicates the ability to mount a functional TH2 response after 14th dpi could be a critical determinant in deciding the survival of the PPR infected animal.