Genetic evolution of Marek's disease virus in vaccinated poultry farms.

Autor: Yehia N; Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agricultural Research Center, Dokki, Giza 12618, Egypt., El-Sayed HS; Department of Poultry Diseases, Benha Provincial Laboratory, Animal Health Research Institute, Agricultural Research Center, Giza, Egypt., Omar SE; Department of Poultry Diseases, Benha Provincial Laboratory, Animal Health Research Institute, Agricultural Research Center, Giza, Egypt., Erfan A; Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agricultural Research Center, Dokki, Giza 12618, Egypt., Amer F; Reference Laboratory for Veterinary Quality Control on Poultry Production, Animal Health Research Institute, Agricultural Research Center, Dokki, Giza 12618, Egypt.
Jazyk: angličtina
Zdroj: Veterinary world [Vet World] 2021 May; Vol. 14 (5), pp. 1342-1353. Date of Electronic Publication: 2021 May 28.
DOI: 10.14202/vetworld.2021.1342-1353
Abstrakt: Background and Aim: The Marek's disease virus (MDV) is a neoplastic disease causing serious economic losses in poultry production. This study aimed to investigate MDV occurrence in poultry flocks in the Lower Egypt during the 2020 breakout and genetically characterized Meq , gL , and ICP4 genes in field strains of MDV.
Materials and Methods: Forty samples were collected from different breeds from eight Egyptian governorates in 2020. All flocks had received a bivalent vaccine (herpesvirus of turkey FC-126 + Rispens CVI988). However, weight loss, emaciation, reduced egg production, paralysis, and rough/raised feather follicles occurred. Samples were collected from feather follicles, liver, spleen, and nerve tissue for diagnosis by polymerase chain reaction. MDV genetic characterization was then performed by sequencing the Meq , gL, and ICP4 genes of five positive samples representing different governorates and breeds.
Results: A total of 28 samples were positive for MDV field strains, while two were related to MDV vaccinal strains. All samples tested negative for ALV (A, B, C, D, and J) and REV. Phylogenetic analysis of the Meq gene of sequenced samples revealed that all MDVs were related to the highly virulent European viruses (Gallid herpesvirus 2 ATE and PC12/30) with high amino acid (A.A.) identity 99.2-100%. Alternatively, there was low A.A. identity with the vaccine strains CVI988 and 3004 (up to 82.5%). These results indicate that further investigation of the efficacy of current Egyptian vaccines is required. The Egyptian strains also harbor a specific mutation, allowing clustering into two subgroups (A and B). By mutation analysis of the Meq gene, the Egyptian viruses in our study had R101K, P217A, and E263D mutations present in all Egyptian viruses. Furthermore, R176A and T180A mutations specific to our strains contributed to the high virulence of highly virulent strains. There were no mutations of the gL or ICP4 genes.
Conclusion: Further studies should evaluate the protection contributed by current vaccines used in Egypt.
(Copyright: © Yehia, et al.)
Databáze: MEDLINE
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