Coinfection of Specific-Pathogen-Free Chickens with Marek's Disease Virus (MDV) and Chicken Infectious Anemia Virus: Effect of MDV Pathotype

A field Marek’s disease virus (MDV), named as BY strain, was firstly isolated from Tibetan chickens in Sichuan province, China, by method of co-cultivation of the lymphocytes with duck embryo fibroblasts (DEF). Analysis of the oncogenic genes showed that there were 2 copies of 132-bp repeated sequence in long terminal repeat of the BY strain, The nucleotide and amino acid sequence identities of Meq gene of BY strain with other prevalent MDV strains in China were 97.6-100.0% and 98.8-100.0%, respectively, and some point mutations assumed to be relevant to the oncogenecity of MDV also existed in the Meq gene of BY strain. The result of animal challenge test on specific-pathogen-free (SPF) chickens showed lymphomas may occur in a variety of organs as early as 18 days post challenge, and the rate of tumor occurrences and mortalities reached to 73.33% and 66.67% in HVT immunized chickens, respectively. In conclusion, an MDV strain charac-terized of acute oncogenicity was isolated from Tibetan chickens in China, though there were no obvious difference between the oncogenic genes of this strain and other virulent MDV strains isolated in China in recent years.

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Improving the potency of DNA vaccine against Chicken Anemia Virus (CAV) by fusing VP1 protein of CAV to Marek's Disease Virus (MDV) Type-1 VP22 protein

Virology Journal ◽

10.1186/1743-422x-8-119 ◽

2011 ◽

Vol 8 (1) ◽

pp. 119 ◽

Cited By ~ 15

Author(s):

Hassan Moeini ◽

Abdul Omar ◽

Raha Rahim ◽

Khatijah Yusoff

Keyword(s):

Disease Virus ◽

Dna Vaccine ◽

Marek's Disease Virus ◽

Marek's Disease ◽

Chicken Anemia Virus ◽

Marek’S Disease Virus ◽

Marek’S Disease ◽

Vp1 Protein ◽

Anemia Virus

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Isolation and identification of Marek’s disease virus (MDV) from feather follicle epithelium and internal organs of diseased chickens in Dakahlia Governorate, Egypt

Mansoura Veterinary Medical Journal ◽

10.35943/mvmj.2019.22.102 ◽

2019 ◽

Vol 20 (2) ◽

pp. 6-11

Author(s):

Aly El-Kenawy ◽

Mohamed El-Tholoth ◽

Emad A

Keyword(s):

Real Time ◽

Disease Virus ◽

Real Time Pcr ◽

Marek's Disease Virus ◽

Marek's Disease ◽

Marek’S Disease Virus ◽

Marek’S Disease ◽

Field Samples ◽

Feather Follicle ◽

Positive Results

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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