In vitro Effects of Calcium, Magnesium, Mercury and Copper Ions on Neuraminidase of a Nigerian Newcastle Disease Virus Strains

2008 ◽  
Vol 7 (6) ◽  
pp. 565-569
Author(s):  
Sunday Blessing Oladele ◽  
King Akpofure Nelson Esi ◽  
Paul Abdu ◽  
Andrew Jonathan N
Keyword(s):  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Copper Ions ◽  
Calcium Magnesium ◽  
In Vitro Effects ◽  
Virus Strains

scholarly journals The in vitro effects of Newcastle disease virus on the metabolic and antibacterial functions of human neutrophils

Blood ◽  
1981 ◽  
Vol 58 (2) ◽  
pp. 221-227
Author(s):  
H Faden ◽  
J Humbert ◽  
J Lee ◽  
P Sutyla ◽  
PL Ogra
Keyword(s):  
Oxygen Consumption ◽  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Human Neutrophils ◽  
Myristate Acetate ◽  
Superoxide Generation ◽  
In Vitro Effects ◽  
Oil Red O

Live Newcastle disease virus (NDV) was used to investigate the in vitro effects of a viral infection on phagocytosis, chemiluminescence generation, superoxide production, oxygen consumption, NADPH-oxidase activity, and intracellular killing of bacteria by Ficoll-Hypaque separated human neutrophils. Phagocytosis of oil red O particles by NDV- treated PMN was inhibited by 50%. Chemiluminescence by PMN was inhibited 79% after zymosan stimulation and 86% after tetradeconyl phorbol acetate stimulation. Superoxide generation was inhibited by 68%. Oxygen consumption was inhibited in the presence of NDV by 37% after stimulation with phorbol myristate acetate, while membrane- associated NADPH-enzyme activity was decreased by 19%. The percent of surviving intracellular S. aureus was significantly elevated in NDV- treated PMN after 60 and 120 min of incubation. Purified bacterial neuraminidase markedly suppressed chemiluminescence, while neuraminic acid blocked the effects of the virus. These observations suggest that infections with myxoviruses may suppress a number of vital neutrophil functions. It appears that the effects may be partly mediated by the interaction of viral neuraminidase with the external neutrophil membrane.

scholarly journals The in vitro effects of Newcastle disease virus on the metabolic and antibacterial functions of human neutrophils

Blood ◽  
1981 ◽  
Vol 58 (2) ◽  
pp. 221-227 ◽  
Author(s):  
H Faden ◽  
J Humbert ◽  
J Lee ◽  
P Sutyla ◽  
PL Ogra
Keyword(s):  
Oxygen Consumption ◽  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Human Neutrophils ◽  
Myristate Acetate ◽  
Superoxide Generation ◽  
In Vitro Effects ◽  
Oil Red O

Abstract Live Newcastle disease virus (NDV) was used to investigate the in vitro effects of a viral infection on phagocytosis, chemiluminescence generation, superoxide production, oxygen consumption, NADPH-oxidase activity, and intracellular killing of bacteria by Ficoll-Hypaque separated human neutrophils. Phagocytosis of oil red O particles by NDV- treated PMN was inhibited by 50%. Chemiluminescence by PMN was inhibited 79% after zymosan stimulation and 86% after tetradeconyl phorbol acetate stimulation. Superoxide generation was inhibited by 68%. Oxygen consumption was inhibited in the presence of NDV by 37% after stimulation with phorbol myristate acetate, while membrane- associated NADPH-enzyme activity was decreased by 19%. The percent of surviving intracellular S. aureus was significantly elevated in NDV- treated PMN after 60 and 120 min of incubation. Purified bacterial neuraminidase markedly suppressed chemiluminescence, while neuraminic acid blocked the effects of the virus. These observations suggest that infections with myxoviruses may suppress a number of vital neutrophil functions. It appears that the effects may be partly mediated by the interaction of viral neuraminidase with the external neutrophil membrane.

Elevated Virulence of Newcastle Disease Virus Strains following Serial Passages in Kidney Cells in vitro

1989 ◽  
Vol 33 (2) ◽  
pp. 248 ◽  
Author(s):  
M. Slosaris ◽  
B. Levy ◽  
E. Katz ◽  
R. Levy ◽  
Z. Zakay-Rones
Keyword(s):  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Kidney Cells ◽  
Virus Strains

Transcription and translation of Newcastle disease virus mRNA's in vitro.

1978 ◽  
Vol 28 (1) ◽  
pp. 324-336 ◽  
Author(s):  
P L Collins ◽  
L E Hightower ◽  
L A Ball
Keyword(s):  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease

Comparative biology of two genetically closely related Newcastle disease virus strains with strongly contrasting pathogenicity

2021 ◽  
Vol 253 ◽  
pp. 108977
Author(s):  
Xi Chen ◽  
Siqi Chen ◽  
Haotian Chen ◽  
Jianxia Tian ◽  
Xueliang Zhao ◽  
...  
Keyword(s):  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Comparative Biology ◽  
Virus Strains

scholarly journals Role of the chicken oligoadenylate synthase-like gene during in vitro Newcastle disease virus infection

2021 ◽  
Vol 100 (5) ◽  
pp. 101067
Author(s):  
Ana Paula Del Vesco ◽  
Hyun Jun Jang ◽  
Melissa S. Monson ◽  
Susan J. Lamont
Keyword(s):  
Virus Infection ◽  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Newcastle Disease Virus Infection

scholarly journals Complete Genome Sequences of Two Newcastle Disease Virus Strains Isolated from a Wild Duck and a Pigeon in Russia

2016 ◽  
Vol 4 (6) ◽  
Author(s):  
Marsel R. Kabilov ◽  
Tatyana Y. Alikina ◽  
Kseniya S. Yurchenko ◽  
Alexandra V. Glushchenko ◽  
Konstantin V. Gunbin ◽  
...  
Keyword(s):  
Sequence Analysis ◽  
Newcastle Disease Virus ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Complete Genome ◽  
Comparative Sequence Analysis ◽  
Genome Sequences ◽  
Wild Duck ◽  
F Gene ◽  
Virus Strains

Here, we report the complete genome sequences of two Newcastle disease virus (NDV) isolates, Adygea/duck/12/2008, from a wild duck in Russia, and Altai/pigeon/777/2010, from a pigeon in Russia. Based on comparative sequence analysis of the F gene, these strains were classified as NDV class II, genotypes VIId and VIb/2, respectively.

scholarly journals Persistent Newcastle disease virus infection in bladder cancer cells is associated with putative pro-survival and anti-viral transcriptomic changes

BMC Cancer ◽  
2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Lee-Chin Chan ◽  
Jeevanathan Kalyanasundram ◽  
Sze-Wei Leong ◽  
Mas Jaffri Masarudin ◽  
Abhi Veerakumarasivam ◽  
...  
Keyword(s):  
Bladder Cancer ◽  
Newcastle Disease Virus ◽  
Cancer Cells ◽  
Disease Virus ◽  
Newcastle Disease ◽  
Persistent Infection ◽  
Signalling Pathways ◽  
Bladder Cancer Cells ◽  
Transcriptomic Changes

Abstract Background Newcastle disease virus (NDV) is an oncolytic virus with excellent selectivity against cancer cells, both in vitro and in vivo. Unfortunately, prolonged in vitro NDV infection results in the development of persistent infection in the cancer cells which are then able to resist NDV-mediated oncolysis. However, the mechanism of persistency of infection remains poorly understood. Methods In this study, we established persistently NDV-infected EJ28 bladder cancer cells, designated as EJ28P. Global transcriptomic analysis was subsequently carried out by microarray analysis. Differentially expressed genes (DEGs) between EJ28 and EJ28P cells identified by the edgeR program were further analysed by Gene Set Enrichment Analysis (GSEA) and Ingenuity Pathway Analysis (IPA) analyses. In addition, the microarray data were validated by RT-qPCR. Results Persistently NDV-infected EJ28 bladder cancer cells were successfully established and confirmed by flow cytometry. Microarray analysis identified a total of 368 genes as differentially expressed in EJ28P cells when compared to the non-infected EJ28 cells. GSEA revealed that the Wnt/β-catenin and KRAS signalling pathways were upregulated while the TGF-β signalling pathway was downregulated. Findings from this study suggest that the upregulation of genes that are associated with cell growth, pro-survival, and anti-apoptosis may explain the survivability of EJ28P cells and the development of persistent infection of NDV. Conclusions This study provides insights into the transcriptomic changes that occur and the specific signalling pathways that are potentially involved in the development and maintenance of NDV persistency of infection in bladder cancer cells. These findings warrant further investigation and is crucial towards the development of effective NDV oncolytic therapy against cancer.

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