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Apoptosis of chicken thymus lymphocytes induced by newcastle disease virus F48E8 in vivo

Lan Zhong-bao

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Abstract

Light microscope,transmission electron microscope,electrophoretic analysis of DNA fragmentation and terminal deoxynucleotidyl transfers(TdT) dUTP nick and labeling(TUNEL) were used to study the apoptosis of chicken thymus lymphocytes induced by Newcastle Disease Virus(NDV) F48E8 in vivo. The results showed that chicken thymus lymphocytes exhibited obvious apoptosis.Moreover the apoptotic index of infected group was significantly higher than that of the control group(P0.01).It suggested that NDVF48E8 can induce apoptosis of chicken thymus lymphocytes in vivo,which will lead to immunodepression and may be the most important pathogeny.

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What this paper is about

Light microscope,transmission electron microscope,electrophoretic analysis of DNA fragmentation and terminal deoxynucleotidyl transfers(TdT) dUTP nick and labeling(TUNEL) were used to study the apoptosis of chicken thymus lymphocytes induced by Newcastle Disease Virus(NDV) F48E8 in vivo. The results showed that chicken thymus lymphocytes exhibited obvious apoptosis.Moreover the apoptotic index of infected group was significantly higher than that of the control group(P0.01).It suggested that NDVF48E8 can induce apoptosis of chicken thymus lymphocytes in vivo,which will lead to immunodepression and may be the most important pathogeny.

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Available abstract

Light microscope,transmission electron microscope,electrophoretic analysis of DNA fragmentation and terminal deoxynucleotidyl transfers(TdT) dUTP nick and labeling(TUNEL) were used to study the apoptosis of chicken thymus lymphocytes induced by Newcastle Disease Virus(NDV) F48E8 in vivo. The results showed that chicken thymus lymphocytes exhibited obvious apoptosis.Moreover the apoptotic index of infected group was significantly higher than that of the control group(P0.01).It suggested that NDVF48E8 can induce apoptosis of chicken thymus lymphocytes in vivo,which will lead to immunodepression and may be the most important pathogeny.

Key concepts: TUNEL assay, Apoptosis, In vivo, Terminal deoxynucleotidyl transferase, Newcastle disease, DNA fragmentation, In Situ Nick-End Labeling, Virus

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