Detection of avian leukosis virus subgroup J in albumen of commercial and native fowl eggs using RT-PCR in Fars province of Iran

被引:0
作者
Rajabzadeh, M.
Dadras, H. [2 ]
Mohammadi, A. [1 ]
机构
[1] Shiraz Univ, Dept Pathobiol, Sch Vet Med, Shiraz, Iran
[2] Shiraz Univ, Dept Avian Med, Sch Vet Med, Shiraz, Iran
关键词
ALV-J; RT-PCR; Egg albumen; Fars province; Iran; POLYMERASE-CHAIN-REACTION; REVERSE TRANSCRIPTION; SEQUENCE; FLOCKS;
D O I
暂无
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
The subgroup J of ALV (ALV-J) has emerged as an important pathogen of meat-type chickens since 1989. This virus is responsible for economic losses due to both mortality and depressed performance in chickens. So, the objective of this study is the detection of ALV-J in the albumen of commercial and native fowl eggs using RT-PCR. Three hundred and seventy egg albumens were randomly selected from different farms of Fars province, Iran. These eggs were obtained from the flocks of two research centers on native fowl production (70 eggs), a broiler grandparent farm (60 eggs), three broiler breeder farms (180 eggs), and a commercial layer flock (60 eggs). RT-PCR was undertaken on isolated RNA from egg samples using a pair of ALV-J specific primers H5/H7 that produced a 545 basepair fragment. RT-PCR analyses detected ALV-J in 15 of 180 (8.33%) samples from three broiler breeders farms, 17 of 70 (24.28%) samples from flocks of two research centers of native fowls production, and none of the samples of commercial layer and broiler grandparent farms. Direct sequencing using primers specific for subgroup ALV-J verified the viral subgroup in the RT-PCR amplification products. This is the first report of the ALV-J in egg albumen in Iran which indicates the necessity to apply eradication programs for ALV-J in the poultry industry and native fowls in Iran.
引用
收藏
页码:1 / 7
页数:7
相关论文
共 24 条
[1]  
Abdel-Latif M. M., 2005, Journal of Animal and Veterinary Advances, V4, P407
[2]   SEQUENCE OF HOST-RANGE DETERMINANTS IN THE ENV GENE OF A FULL-LENGTH, INFECTIOUS PROVIRAL CLONE OF EXOGENOUS AVIAN-LEUKOSIS VIRUS HPRS-103 CONFIRMS THAT IT REPRESENTS A NEW SUBGROUP (DESIGNATED J) [J].
BAI, J ;
HOWES, K ;
PAYNE, LN ;
SKINNER, MA .
JOURNAL OF GENERAL VIROLOGY, 1995, 76 :181-187
[3]   Independent isolates of the emerging subgroup J avian leukosis virus derive from a common ancestor [J].
Benson, SJ ;
Ruis, BL ;
Garbers, AL ;
Fadly, AM ;
Conklin, KF .
JOURNAL OF VIROLOGY, 1998, 72 (12) :10301-10304
[4]  
Fadly A.M., 2003, DIS POULTRY, V11th, P465
[5]   Single and concurrent avian leukosis virus infections with avian leukosis virus-J and avian leukosis virus-A in Australian meat-type chickens [J].
Fenton, SP ;
Reddy, MR ;
Bagust, TJ .
AVIAN PATHOLOGY, 2005, 34 (01) :48-54
[6]  
Gingerich E, 2002, AVIAN DIS, V46, P745, DOI 10.1637/0005-2086(2002)046[0745:DOMLIB]2.0.CO
[7]  
2
[8]  
Hair-Bejo M., 2004, International Journal of Poultry Science, V3, P115
[9]   Nested polymerase chain reaction for detection of the avian leukosis virus causing so-called fowl glioma [J].
Hatai, H ;
Ochiai, K ;
Tomioka, Y ;
Toyoda, T ;
Hayashi, K ;
Anada, M ;
Kato, M ;
Toda, A ;
Ohashi, K ;
Ono, E ;
Kimura, T ;
Umemura, T .
AVIAN PATHOLOGY, 2005, 34 (06) :473-479
[10]   Development of quantitative competitive-reverse transcriptase-polymerase chain reaction for detection and quantitation of avian leukosis virus subgroup J [J].
Kim, Y ;
Brown, TP .
JOURNAL OF VETERINARY DIAGNOSTIC INVESTIGATION, 2004, 16 (03) :191-196