Using PCR for early diagnosis of bovine leukemia virus infection in some native cattle

被引:42
作者
Mohammadabadi, M. R. [1 ]
Soflaei, M. [2 ]
Mostafavi, H. [2 ]
Honarmand, M. [2 ]
机构
[1] Shahid Bahonar Univ, Dept Anim Sci, Kerman, Iran
[2] Kermans Jahad E Agr Educ Ctr, Inst Sci Appl Higher Educ Jahad E Agr, Dept Anim Sci, Kerman, Iran
关键词
Bovine leukemia virus; Leukosis; Cattle; PCR; BLV testing; Native Iranian and Russian breeds; POLYMERASE-CHAIN-REACTION; PROVIRAL DNA; PERSISTENT LYMPHOCYTOSIS; NESTED-PCR; CELL-LINE; BLV; CALVES; ANTIBODIES; ARGENTINA; LEUKOSIS;
D O I
10.4238/2011.October.27.2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Bovine leukemia virus (BLV), the causative agent of enzootic bovine leukosis, is an exogenous, B lymphotropic retrovirus belonging to the Retroviridae family that induces persistent lymphocytosis in cattle and sheep. PCR has proven to be particularly suitable for investigating herds of cattle with a very low incidence of BLV infection and for clarifying doubtful serological results obtained by immunodiffusion or ELISA. The native Iranian and Russian cattle have a series of valuable traits that discriminate them as unique breeds that are well able to compete with western analogues. However, their gene pools have not been analyzed with molecular markers, including detection of BLV by PCR. Two pairs of primers were used: gag1 and gag2, and pol1 and pol2, which encompass 347- and 599-bp fragments of the BLV gene, respectively. Sixty-five Iranian Sistani, 120 Yaroslavl, 50 Mongolian, and 35 Black Pied cows were investigated. Among these 270 animals, we obtained 42 positive and 15 doubtful results in the first PCR. The second PCR was very effective in increasing BLV test reliability data to support detection of BLV.
引用
收藏
页码:2658 / 2663
页数:6
相关论文
共 30 条
[1]  
AGRESTI A, 1993, AM J VET RES, V54, P373
[2]   Cytokine mRNA expression in B cells from bovine leukemia virus-infected cattle with persistent lymphocytosis [J].
Amills, M ;
Norimine, J ;
Olmstead, CA ;
Lewin, HA .
CYTOKINE, 2004, 28 (01) :25-28
[3]  
Amoril JG, 2009, BRAZ VET IMM, V128, P333
[4]   Establishment of a new bovine leukosis virus producing cell line [J].
Beier, D ;
Riebe, R ;
Blankenstein, P ;
Starick, E ;
Bondzio, A ;
Marquardt, O .
JOURNAL OF VIROLOGICAL METHODS, 2004, 121 (02) :239-246
[5]   MOLECULAR-CLONING AND SEQUENCING OF AN AUSTRALIAN ISOLATE OF PROVIRAL BOVINE LEUKEMIA-VIRUS DNA - COMPARISON WITH OTHER ISOLATES [J].
COULSTON, J ;
NAIF, H ;
BRANDON, R ;
KUMAR, S ;
KHAN, S ;
DANIEL, RCW ;
LAVIN, MF .
JOURNAL OF GENERAL VIROLOGY, 1990, 71 :1737-1746
[6]  
Czarnik U, 2000, B VET I PULAWY, V44, P143
[7]   MILK AND FAT YIELDS DECLINE IN BOVINE LEUKEMIA VIRUS-INFECTED HOLSTEIN CATTLE WITH PERSISTENT LYMPHOCYTOSIS [J].
DA, Y ;
SHANKS, RD ;
STEWART, JA ;
LEWIN, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) :6538-6541
[8]   Development of a PCR to diagnose BLV genome in frozen semen samples [J].
Dus Santos, Maria Jose ;
Trono, Karina ;
Lager, Irene ;
Wigdorovitz, Andres .
VETERINARY MICROBIOLOGY, 2007, 119 (01) :10-18
[9]   A FIELD-EVALUATION OF THE POLYMERASE CHAIN-REACTION PROCEDURE FOR THE DETECTION OF BOVINE LEUKEMIA-VIRUS PROVIRAL DNA IN CATTLE [J].
EAVES, FW ;
MOLLOY, JB ;
DIMMOCK, CK ;
EAVES, LE .
VETERINARY MICROBIOLOGY, 1994, 39 (3-4) :313-321
[10]  
FERRER JF, 1981, AM J VET RES, V42, P9