scholarly journals Lumpy skin disease of cattle: epizootology, characterization of the pathogen, diagnosis (review)

2017 ◽  
Vol 31 ◽  
pp. 58-68
Author(s):  
L. M. Ishchenko ◽  
L. M. Muzykina ◽  
G. A. Kovalenko ◽  
I. V. Halka ◽  
N. V. Hudz ◽  
...  
Author(s):  
Zeinab Hedayati ◽  
Hamid Reza Varshovi ◽  
Ali Mohammadi ◽  
Mohammad Tabatabaei

Author(s):  
Jun Ma ◽  
Yaoxian Yuan ◽  
Jianwei Shao ◽  
Minghui Sun ◽  
Wei He ◽  
...  

2014 ◽  
Vol 109 ◽  
pp. 1-6 ◽  
Author(s):  
Eeva S.M. Tuppurainen ◽  
Caroline R. Pearson ◽  
Katarzyna Bachanek-Bankowska ◽  
Nick J. Knowles ◽  
Shadi Amareen ◽  
...  

2018 ◽  
Vol 163 (9) ◽  
pp. 2525-2529
Author(s):  
Umberto Molini ◽  
Gottlieb Aikukutu ◽  
Siegfried Khaiseb ◽  
Naindji N. Haindongo ◽  
Angela C. Lilungwe ◽  
...  

2020 ◽  
Vol 165 (11) ◽  
pp. 2675-2677
Author(s):  
Alexander Sprygin ◽  
Antoinette Van Schalkwyk ◽  
Irina Shumilova ◽  
Alexander Nesterov ◽  
Svetlana Kononova ◽  
...  

2021 ◽  
Vol 17 (1) ◽  
Author(s):  
Shukes Chandra Badhy ◽  
Mohammad Golam Azam Chowdhury ◽  
Tirumala Bharani Kumar Settypalli ◽  
Giovanni Cattoli ◽  
Charles Euloge Lamien ◽  
...  

Abstract Background Lumpy skin disease (LSD) is a contagious viral disease of cattle caused by lumpy skin disease virus (LSDV). LSD has recently spread in Asia following outbreaks in the Middle East and Europe. The disease emerged in Bangladesh in July 2019 in the Chattogram district, then rapidly spread throughout the entire country. We investigated six LSD outbreaks in Bangladesh to record the clinical signs and collect samples for diagnostic confirmation. Furthermore, we performed the molecular characterization of Bangladesh isolates, analyzing the full RPO30 and GPCR genes and the partial EEV glycoprotein gene. Results Clinical observations revealed common LSD clinical signs in the affected cattle. PCR and real-time PCR, showed the presence of the LSDV genome in samples from all six districts. Phylogenetic analysis and detailed inspection of multiple sequence alignments revealed that Bangladesh isolates differ from common LSDV field isolates encountered in Africa, the Middle East, and Europe, as well as newly emerged LSDV variants in Russia and China. Instead, they were closely related to LSDV KSGP-0240, LSDV NI2490, and LSDV Kenya. Conclusions These results show the importance of continuous monitoring and characterization of circulating strains and the need to continually refine the strategies for differentiating vaccine strains from field viruses.


2020 ◽  
Vol 13 (7) ◽  
pp. 1262-1268
Author(s):  
Ahmad M. Allam ◽  
Mohamed Karam Elbayoumy ◽  
Eman H. Abdel-Rahman ◽  
Ahmed G. Hegazi ◽  
Tarek Korany Farag

Background and Aim: Lumpy skin disease (LSD), an infectious disease of cattle, is characterized by raised nodules on the skin. Although the morbidity rate of LSD is low, it has a considerable fatality rate. Despite the annual mass vaccination of livestock with sheep pox vaccine (Veterinary Serum and Vaccine Research Institute, Egypt) enforced by Egyptian authorities, the LSD virus (LSDV) continues to circulate almost every summer. The present study aimed to discover the cause of cows naturally infected with LSDV circulating in Upper Egypt during the summer of 2018 using polymerase chain reaction (PCR) assay and to analyze their phylogenetics against reference genome sequences. Materials and Methods: We cultured LSDV in specific pathogen-free embryonated chicken eggs (SPF-ECE) and used conventional PCR to identify fusion and P32 genes, previously deposited in GenBank (MN694826, MN694827, and MN954664). Sequencing and phylogenetic analyses were performed on these two highly conserved viral genes. Results: LSDV infection of SPF-ECE resulted in characteristic white pock lesions. PCR products were identified on 1.5% agarose gel after electrophoresis at the expected positions for the fusion and P32 genes at 472 and 587 bp, respectively. Conclusion: The present study revealed that the two viral genes were identified from the Beni Suef and Sohag Governorates in all clinical cases and confirmed the circulation of LSDV in this outbreak. After sequencing, these genes were identical to those of the LSDV that had been identified and recorded in GenBank for the past 3 years.


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