Rapid detection of Peste des Petits Ruminants (PPR) virus antigen in Sudan by agar gel precipitation (AGPT) and haemagglutination (HA) Tests

2007 ◽  
Vol 40 (5) ◽  
pp. 363-368 ◽  
Author(s):  
Nussieba A. Osman ◽  
Mahasin E. A/Rahman ◽  
A. S. Ali ◽  
M. A. Fadol
1984 ◽  
Vol 93 (3) ◽  
pp. 579-586 ◽  
Author(s):  
T. U. Obi ◽  
D. Patrick

SummaryThe detectability of peste des petits ruminants (PPR) viral antigen in both ante-mortem secretions and necropsy samples from experimentally infected goats was investigated by both the agar gel precipitation test (AGPT) and counterimmunoelectrophoresis (CIE). Viral antigen was detected from 42·6% of the samples tested by the AGPT and 80–3% by CIE. The detection of viral antigen in a high proportion of the ocular and nasal secretions as well as the faeces and buccal scrapings, particularly from those collected within seven days of the onset of fever, by both techniques, would seem to obviate the need for lymph node biopsies or post-mortem samples in order to make a diagnosis of PPRV infection.


2019 ◽  
Vol 1 (17) ◽  
Author(s):  
F. S. Sumi ◽  
M. Nooruzzaman ◽  
M. M. Rahman ◽  
M. R. Islam ◽  
E. H. Chowdhury

Background: Emergence of exotic viral disease like peste des petits ruminants(PPR) possesses a great threat towards successful goat and sheep farming in Bangladesh. Implementation of effective control measures against PPR requires a proper and rapid diagnosis of the disease. Various diagnostic techniques are available for diagnosis of PPR in goats and sheep in Bangladesh. Among these, ELISA is an important technique to diagnose the disease as well as for seromonitoring. However, the ELISA kits that are being used in the country are mostly imported. This study was undertaken to develop an in-house indirect ELISA using local PPR virus isolate as an antigen.Methods: A local isolate of PPR virus (PPRV) was used as an antigen to develop an indirect ELISA kit. Standardization of the optimum antibody, conjugate and virus antigen concentration was performed using chequer-board titration with different dilutions of the reagents. Finally, the developed indirect ELISA kit was used in a pilot study to detect anti-PPRV antibodies in sheep sera samples.Results: A polyclonal antibody based indirect ELISA was developed successfully for the detection of PPRV antibodies. The developed ELISA could detect anti-PPRV antibody in sheep sera sample during our pilot field trial.Conclusions: After robust field validation, the indirect ELISA can be used to determine the antibody titer against PPRV in the field as to monitor the seroconversion after vaccination.


2019 ◽  
pp. 1
Author(s):  
Ashrafun Luna ◽  
Fardina Sumi ◽  
Jahan Begum ◽  
Md Rahman ◽  
Mohammad Islam ◽  
...  

2005 ◽  
Vol 28 (4) ◽  
pp. 287-296 ◽  
Author(s):  
K.K. Rajak ◽  
B.P. Sreenivasa ◽  
M. Hosamani ◽  
R.P. Singh ◽  
S.K. Singh ◽  
...  

Author(s):  
Kiran Aqil ◽  
Muti-ur-Rehman Khan ◽  
Asim Aslam ◽  
Aqeel Javeed ◽  
Rizwan Qayyum ◽  
...  

2012 ◽  
Vol 27 (4) ◽  
pp. 265-271 ◽  
Author(s):  
Arun Patel ◽  
Kaushal Kishor Rajak ◽  
Vinayagamurthy Balamurugan ◽  
Arnab Sen ◽  
Shashi Bhusan Sudhakar ◽  
...  

2021 ◽  
Vol 77 (05) ◽  
pp. 226-231
Author(s):  
WIESŁAW NIEDBALSKI ◽  
ANDRZEJ FITZNER ◽  
KRZYSZTOF BULENGER ◽  
ANDRZEJ KĘSY

Peste des petits ruminants (PPR) is a highly contagious and economically important, viral disease of small ruminants caused by the peste des petits ruminants virus (PPRV), which belongs to the genus Morbilivirus in the family Paramyxoviridae. PPR control is achieved mostly through vaccination and/or slaughter of susceptible animals coupled with clinical or laboratory-based diagnosis. Since clinical signs of PPR are not disease-specific and clinical diagnostics is not reliable, it should be confirmed by laboratory testing. Laboratory confirmation of clinical suspicions is made by detection of PPRV in blood, swabs or post-mortem tissues through classical virus isolation (VI), agar gel immunodiffusion (AGID)/agar gel precipitation test (AGPT), counter-immunoelectrophoresis (CIE), immunoperoxidase test (IPT) or enzyme-linked immunosorbent (ELISA) assays. However, these conventional methods have been superseded by more rapid, sensitive and accurate molecular diagnostic techniques based on the amplification of parts of either nucleocapsid (N) or fusion (F) protein gene, such as RT-PCR, real-time RT-PCR, reverse transcription loop-mediated isothermal amplification (RT-LAMP), reverse transcription recombinase polymerase amplification (RT-RPA) and Oxford nanopore MinION technology. Although these molecular diagnostic assays are accurate, rapid and sensitive, they have to be performed in laboratory settings, and samples must be transported under appropriate conditions from the field to the laboratory, which can delay the confirmation of PPRV infection. The recently developed immunochromatographic lateral flow device (IC-LFD) assay can be used in the field (“pen-side”) without the need for expensive equipment, so a well-established laboratory is not required. The control and eventual eradication of PPR is now one of the top priorities for the Food and Agriculture Organization (FAO) and the World Organization for Animal Health (OIE). In 2015, the international community agreed on a global strategy for PPR eradication, setting 2030 as a target date for elimination of the disease


1970 ◽  
Vol 13 (1) ◽  
pp. 48-52
Author(s):  
OZ Tenuche ◽  
BO Emikpe

There is dearth of information on the haematological changes associated with Mannheimia haemolytica vaccination in goats, hence this report which describes some haematological changes observed following vaccination with intranasal Recombinant Mannheimia haemolytica vaccine in goats naturally infected with peste des petits ruminants (PPR) virus. Twenty one (male, n=11; and female, n=10) goats were assigned to three vaccinated groups (A, B and D) with five goats per group (male: 3, female: 2), while the control group had 6 goats. Group A was vaccinated once intranasally, group B was vaccinated intranasally twice at one week interval and group D was vaccinated intranasally twice at two weeks interval . The control group (C) was not vaccinated. The vaccinated and control groups were challenged by comingling with pneumonic goats to simulate the field experience. PPR virus infection was later diagnosed in all the groups post vaccination. An average of four animals per treatment group in post-vaccination days were bled once weekly for six weeks (every week) to evaluate some haematological changes. The PCV values were within the normal range, while there was a decline in lymphocyte count at week 5, and a steady increase in neutrophil count in group A. In Group B, there was similar decline in lymphocyte count from the sixth week, while in groups C (Control) and D, the lymphocyte count declined at the 7th week, as the neutrophil counts increased. There were no significant changes in monocyte and eosinophil counts. The degree of changes in lymphocyte and neutrophil counts was mild in group B and marked in group D. This study revealed that intranasal vaccination of recombinant Mannheimia  haemolytica vaccine in the presence of PPR virus outbreak results in mild hematological derangement when the goats were vaccinated with  Mannheimia haemolytica bacterin at a week interval.Keywords: Goats, Haematology, Intranasal Recombinant Mannheimia haemolytica, Peste des Petits Ruminants, Vaccination


2006 ◽  
Vol 30 (1) ◽  
pp. 103-108 ◽  
Author(s):  
B. P. Sreenivasa ◽  
R. P. Singh ◽  
B. Mondal ◽  
P. Dhar ◽  
S. K. Bandyopadhyay

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