Abdul Sajid

Isolation, Characterization And Pathogenesis Of Capripox Virus - 2010

Goat pox is the most important pox diseases of livestock and it usually
causes huge economic losses. The economic losses occur in terms of mortality,
reduced productivity and lower quality of wool and leather. The clinical
manifestations of the disease include high temperature, lesions skin in the form of
macules, papules, vesicles, pustule and scabs on hairless areas of the body. The
disease is highly contagious having high morbidity and mortality in the infected
herds. The present study was conducted to document the prevalence of goat pox
disease in the different regions of Punjab. The study was based on clinical
manifestation of the disease in various collecting spots including slaughter houses,
cattle and hide markets and tanneries. The prevalence of goat pox at slaughter
houses in different regions was 9.93% in arid region followed by 8.69% and 7% in
southern and northern irrigated regions respectively. The prevalence of pox disease
in sheep was highest (8.54%) in the northern irrigated region, 7.69% and 6.62% in
arid and southern irrigated regions respectively.
The prevalence of pox recorded in the hide markets shows a trend of high
presence 7.29% in arid region followed by 6.22% and 3.84% in southern and
northern irrigated regions. Whereas in sheep the overall prevalence was 0.51 %,
4.44% and 1.66% in northern irrigated, arid and southern irrigated regions.

In tanneries the pox lesions were identified on the basis of method as
adopted in hide markets. The overall prevalence of pox in goat was 3.96%, 4.06%
and 4.09% while in sheep 9.58%, 2.41 % and 10% in northern irrigated, arid and
southern irrigated regions.
The overall prevalence of pox disease in goat was 5%, 5.79% and 5.34% in
Northern irrigated, arid and southern irrigated regions respectively. Where as in
sheep, pox was 3.133%, 4.11 % and 2.67% in Northern irrigated, arid and southern
irrigated regions respectively. The highest trend of incidence of disease was present
in the arid regions followed by southern and northern regions. The slaughter houses
shows high incidence of disease as compared to cattle and hide market and
tanneries. The result was significant (P<0.05) among the regions and samples
collecting spots.
A total of 100 samples consisting of 55 scabs and 45 skin tissues were
randomly selected from the different collecting spots of the three regions. The scabs
and skin tissue samples were processed on dehydrated minimum essential media
tor virus isolation. The virus was isolated on Vero cell line culture and its
characteristics were observed on the basis of specific cytopathic effects. All 55 scab
samples consisting 20 from cattle markets, 20 from slaughter house and 15 from
hide market and tannery were tested through cell culture. The cell culture positive
result for scabs was 60% cattle markets, 20% hide market and tannery and 40%
slaughter house.
All 45 skin tissue samples including 5 from cattle markets and tannery, 20
from hide market and 20 from slaughter house were subjected to virus isolation on
Vero cell line. The cell culture positive result for skin tissue samples was 100% cattle
markets, 30% hide market and tannery and 60% slaughter house. In this way the
total cell culture result for scabs and skin tissue samples from all areas become
41.82% and 51.11 % respectively.
The isolated virus was confirmed through peR. All the collected samples
were also analyzed through peR in order to compare the two techniques for disease
diagnosis. Out of 40 samples from slaughter houses 18 scabs and 15 tissues
sample were positive through peR with 82.5%. Out of 25 samples collected from
cattle markets consisting of 20 scabs and 5 skin tissues, 17 of scabs and 5 skin
tissues were positive with 92%.
Similarly a total of 35 samples out of which 15 were scabs and 20 were skin
tissues collected from hide markets and tanneries. The peR of 7 scabs and 14 skin
tissues was positive with 60%. In this way the total peR result for scabs and skin
tissue from all areas was 42% and 34% respectively.
In the 3rd study of the present project the isolated virus was inoculated in to
experimental animal to study the detail pathogenesis. The disease followed the
same pattern as in the natural outbreak. But however the routes of inoculation affect
the severity of the disease. During the study the diseased animals were periodically
slaughter at weekly interval after the appearance of 1 st clinical signs. The detailed
lesions were observed in different visceral organs and the tissues were collected
and preserved in 10% formalin. The tissues were processed for histopathology and
immunohistochemical examination. The IHC was successfully optimized for the
detection of viral antigen in the tissues of skin, lung and lymph nodes.



Department of Pathology
Phd. thesis

1372,T


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