Selection for Resistance to Marek's Disease in Conjunction with Other Economic Traits in Chickens

1972 ◽  
Vol 16 (1) ◽  
pp. 2 ◽  
Author(s):  
G. W. Friars ◽  
J. R. Chambers ◽  
A. Kennedy ◽  
A. D. Smith
1972 ◽  
Vol 16 (1) ◽  
pp. 11 ◽  
Author(s):  
C. M. von Krosigk ◽  
C. F. McClary ◽  
E. Vielitz ◽  
D. V. Zander

1989 ◽  
Vol 68 (9) ◽  
pp. 1161-1167 ◽  
Author(s):  
U. KUHNLEIN ◽  
M. SABOUR ◽  
J.S. GAVORA ◽  
R.W. FAIRFULL ◽  
D.E. BERNON

1970 ◽  
Vol 50 (1) ◽  
pp. 69-81 ◽  
Author(s):  
J. R. MORRIS ◽  
A. E. FERGUSON ◽  
F. N. JEROME

Three thousand three hundred and thirty-five sire-pedigreed chicks from two commercial lines of Single Comb White Leghorns were inoculated with the Marek’s disease (MD) agent at one day of age and tested over a seven-week period for MD infection. Significant differences were observed between sexes and between lines with respect to MD mortality and total MD incidence. The females were more susceptible. Sire families in both lines showed heterogeneity in their ability to resist MD infection.A second experiment involving selection for resistance and for susceptibility to the disease was conducted on a population of University of Guelph Columbian Plymouth Rocks. Fully pedigreed chicks from this stock were inoculated and reared for 11 weeks while their full-sibs were reared separately to produce subsequent generations of selected families. Two successive generations of selection resulted in the formation of the resistant (R) and susceptible (S) lines. A random sample of the base population was propagated as a control population. Selection for MD resistance resulted in relatively greater progress than selection for MD susceptibility. After two generations of selection there was 12.5%, 54.1% and 61.9% MD mortality and 58.3%, 89.1% and 96.2% total MD incidence in the R, control and S lines, respectively. The more resistant the strain, the longer was the latent period before death. The variability between sexes and between half-sibs declined as MD mortality and total MD incidence approached high and low extremes. The results of the selection imposed showed progress despite the small population under test.


2009 ◽  
Vol 4 (3) ◽  
pp. e2-e2
Author(s):  
Celina Buscaglia ◽  
Priscilla H. O'Connell ◽  
Keith W. Jarosinski ◽  
Igal Pevzner ◽  
Karel A. Schat

2009 ◽  
Vol 53 (3) ◽  
pp. 336-340 ◽  
Author(s):  
Celina Buscaglia ◽  
Priscilla H. O'Connell ◽  
Keith W. Jarosinski ◽  
Igal Pevzner ◽  
Karel A. Schat

Author(s):  
Keyvan Nazerian

A herpes-like virus has been isolated from duck embryo fibroblast (DEF) cultures inoculated with blood from Marek's disease (MD) infected birds. Cultures which contained this virus produced MD in susceptible chickens while virus negative cultures and control cultures failed to do so. This and other circumstantial evidence including similarities in properties of the virus and the MD agent implicate this virus in the etiology of MD.Histochemical studies demonstrated the presence of DNA-staining intranuclear inclusion bodies in polykarocytes in infected cultures. Distinct nucleo-plasmic aggregates were also seen in sections of similar multinucleated cells examined with the electron microscope. These aggregates are probably the same as the inclusion bodies seen with the light microscope. Naked viral particles were observed in the nucleus of infected cells within or on the edges of the nucleoplasmic aggregates. These particles measured 95-100mμ, in diameter and rarely escaped into the cytoplasm or nuclear vesicles by budding through the nuclear membrane (Fig. 1). The enveloped particles (Fig. 2) formed in this manner measured 150-170mμ in diameter and always had a densely stained nucleoid. The virus in supernatant fluids consisted of naked capsids with 162 hollow, cylindrical capsomeres (Fig. 3). Enveloped particles were not seen in such preparations.


2019 ◽  
Vol 20 (2) ◽  
pp. 6-11
Author(s):  
Aly El-Kenawy ◽  
Mohamed El-Tholoth ◽  
Emad A

In the present study, a total of 16 samples including feather follicle epithelium, ovary, spleen and kidney (4 samples for each organ) were collected from diseased chicken flocks suspected to be infected with Marek’s disease virus (MDV) at Dakahlia Governorate, Egypt during the period from October 2016 to October 2017. Each sample was pooled randomly from three to five birds (90 to 360 days old). The isolation of the suspected virus from the collected samples was carried out via chorioallantoic membranes (CAMs) of 12 days old embryonated chicken eggs (ECEs). Three egg passages were carried out for each sample. Hyperimmune serum was prepared against standard MDV. MDV in both field and egg passaged samples (after 3rd passage) was identified by agar gel precipitation test (AGPT) and indirect fluorescence antibody test (IFAT). Molecular identification of virus was carried out by conventional polymerase chain reaction (PCR) and real- time PCR in four selected samples. The results revealed that 14 samples (87.5%) including 4 (100%) samples from feather follicle epithelium, ovary and kidney and 2 (50%) samples from spleen, showed positive results in virus isolation after 3rd passage. The positive results percentage by AGPT for field samples were 50% (8 out of 16 samples), while after the 3rd passage in ECEs were 37.5% (6 out of 16 samples) and the positive results percentage by IFAT for field samples were 62.5% (10 out of 16 samples), while after the 3rd passage in ECEs were 81.25 % (13 out of 16 samples). Viral nucleic acid was detected in all selected samples by conventional and real- time PCR. The results indicate that feather follicle epithelium is the best organ for MDV detection. IFAT is superior over AGPT in virus detection. Conventional and real - time PCR could be efficiently used for molecular detection of the virus.


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