Evaluation of different diagnostic methods for diagnosis of Lumpy skin disease in cows

被引:30
作者
Awad, Walid S. [1 ]
Ibrahim, Adel K. [2 ]
Mahran, Khaled [2 ]
Fararh, Khaled M. [3 ]
Moniem, Mervet I. Abdel [4 ]
机构
[1] Cairo Univ, Fac Vet Med, Dept Med & Infect Dis, Giza, Egypt
[2] Cairo Univ, Fac Vet Med, Dept Clin Pathol, Giza, Egypt
[3] Banha Univ, Fac Vet Med, Dept Clin Pathol, Giza, Egypt
[4] Anim Hlth Res Inst, Dept Virol, Giza, Egypt
关键词
LSDV isolation; PCR; Dot blot hybridization; iELISA; SHEEP POXVIRUS IDENTIFICATION; BIOPSY SAMPLES; VIRUS; CATTLE; PCR; CAPRIPOXVIRUS;
D O I
10.1007/s11250-009-9486-5
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Viral isolation, polymerase chain reaction (PCR), dot blot hybridization (DBH), and indirect enzyme-linked immunosorbent assay (iELISA) were used for the diagnosis of lumpy skin disease in clinically infected, fevered, and apparently normal dairy cows. Lumpy skin disease virus (LSDV) was isolated from skin biopsies and blood samples collected from clinically infected cows in percentages of 72% and 20%, respectively. The virus recovered from blood samples collected from fevered cows in percentage of 33.3%. Both PCR and DBH detected viral DNA in 100% of skin biopsies collected from clinically infected cows whereas the detection rates in blood samples collected from clinically infected animals were 100% and 84% using PCR and DBH, respectively. Viral DNA was detected in blood samples collected from fevered cows using PCR and DBH in percentages of 77.8% and 66.6%, respectively. Only 19.1% of blood samples collected from in-contact cows was positive for both of PCR and DBH. Detection rates of antibodies against LSDV using iELISA in serum samples collected from clinically infected and fevered cows were 56% and 11.1%, respectively, whereas all in-contact cows had no antibodies against the virus.
引用
收藏
页码:777 / 783
页数:7
相关论文
共 27 条
[1]  
ALI AA, 1990, VET REC, V127, P549
[2]  
[Anonymous], 1989, Molecular Cloning: A Laboratory
[3]   Quantification of lumpy skin disease virus following experimental infection in cattle [J].
Babiuk, S. ;
Bowden, T. R. ;
Parkyn, G. ;
Dalman, B. ;
Manning, L. ;
Neufeld, J. ;
Embury-Hyatt, C. ;
Copps, J. ;
Boyle, D. B. .
TRANSBOUNDARY AND EMERGING DISEASES, 2008, 55 (07) :299-307
[4]  
Barnard B., 1994, Infectious diseases of livestock: with special reference to Southern Africa Vol, V1, P604
[5]   Detection of goat pox antibodies : Comparative efficacy of indirect ELISA and counterimmunoelectrophoresis [J].
Bhanuprakash, V. ;
Hosamani, M. ;
Juneja, Sominder ;
Kumar, Nitul ;
Singh, R. K. .
JOURNAL OF APPLIED ANIMAL RESEARCH, 2006, 30 (02) :177-180
[6]   Capripoxvirus tissue tropism and shedding: A quantitative study in experimentally infected sheep and goats [J].
Bowden, Timothy R. ;
Babiuk, Shawn L. ;
Parkyn, Geoff R. ;
Copps, John S. ;
Boyle, David B. .
VIROLOGY, 2008, 371 (02) :380-393
[7]   THE CLINICAL-RESPONSE OF CATTLE EXPERIMENTALLY INFECTED WITH LUMPY SKIN-DISEASE (NEETHLING) VIRUS [J].
CARN, VM ;
KITCHING, RP .
ARCHIVES OF VIROLOGY, 1995, 140 (03) :503-513
[8]  
Davies F. G., 1991, World Animal Review, V68, P37
[9]  
DAVIES FG, 1971, RES VET SCI, V12, P123
[10]  
HOLTKE HJ, 1995, CELL MOL BIOL, V41, P883