scholarly journals Current situation of Peste des petits ruminants (PPR) virus disease in some Egyptian Governorates in the period between years 2014 to 2019

2021 ◽  
Vol 1 (4) ◽  
pp. 35-48
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 ◽  
...  

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

2017 ◽  
Vol 28 (4) ◽  
pp. 306-314 ◽  
Author(s):  
G. R. Gowane ◽  
Najif Akram ◽  
L. L. L. Prince ◽  
Ved Prakash ◽  
Arun Kumar

2000 ◽  
Vol 74 (19) ◽  
pp. 9039-9047 ◽  
Author(s):  
Subash C. Das ◽  
Michael D. Baron ◽  
Thomas Barrett

ABSTRACT Rinderpest (RP) and peste-des-petits-ruminants (PPR) are two important diseases of domestic ruminants. To improve on currently available vaccines against PPR, we have created cDNA copies of the RP virus genome in which either the fusion (F) or hemagglutinin (H) gene, or both, was replaced with the corresponding gene from PPR virus. It was necessary to develop a modified rescue system in which the T7 RNA polymerase was provided by a recombinant fowlpox virus and the entire rescue procedure took place in Vero cells before we could obtain live virus from these chimeric constructs. No virus was recovered when only one of the glycoprotein genes was changed, but a chimeric virus containing both F and H genes from PPR virus was reproducibly rescued from cDNA, indicating that a virus-specific functional interaction takes place between the F and H proteins. The rescued virus expressing the PPR glycoproteins grew more slowly in tissue culture than either parental virus and formed abnormally large syncytia. Goats infected with the chimera showed no adverse reaction, as assessed by clinical signs, temperature, leukocyte count, virus isolation, and serology, and were protected from subsequent challenge with wild-type PPR virus.


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