Diagnostic evaluation of a real-time reverse transcriptase PCR assay for detection of classical swine fever virus

被引:36
作者
Risatti, G
Holinka, L
Lu, Z
Kutish, G
Callahan, JD
Nelson, WM
Tió, EB
Borca, MV
机构
[1] USDA ARS, Plum Isl Anim Dis Ctr, NAA, Greenport, NY 11944 USA
[2] Tetracore Inc, Gaithersburg, MD USA
[3] Lab Vet Cent LAVECEN, Santo Domingo, Dominican Rep
关键词
D O I
10.1128/JCM.43.1.468-471.2005
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
A fluorogenic-probe hydrolysis (TaqMan)-reverse transcriptase (RT) PCR for classical swine fever virus (CSFV) was evaluated for diagnostic sensitivity and specificity by using clinical samples obtained from the Dominican Republic, where the disease is enzootic. The sensitivity of this test, using nasal swab samples taken from both symptomatic and asymptomatic animals, exceeded the diagnostic sensitivity of virus isolation (100% versus 72.4%, respectively) with little loss of specificity (98.9% versus 100%, respectively). At the herd level, three of four infected farms were identified by virus isolation, while the CSFV real-time RT-PCR assay identified all four infected premises. This simple and accurate test permits rapid detection of CSFV in affected herds.
引用
收藏
页码:468 / 471
页数:4
相关论文
共 24 条
[1]   APPLICATION OF PEROXIDASE LABELED ANTIBODY-ASSAYS FOR DETECTION OF PORCINE IGG ANTIBODIES TO HOG-CHOLERA AND BOVINE VIRAL DIARRHEA VIRUSES [J].
AFSHAR, A ;
DULAC, GC ;
BOUFFARD, A .
JOURNAL OF VIROLOGICAL METHODS, 1989, 23 (03) :253-262
[2]   SPECIFIC SEQUENCE AMPLIFICATION OF BOVINE VIRUS DIARRHEA VIRUS (BVDV) AND HOG-CHOLERA VIRUS AND SEQUENCING OF BVDV NUCLEIC-ACID [J].
BOYE, M ;
KAMSTRUP, S ;
DALSGAARD, K .
VETERINARY MICROBIOLOGY, 1991, 29 (01) :1-13
[3]   Development and evaluation of a novel antigen capture assay for the detection of classical swine fever virus antigens [J].
Clavijo, A ;
Zhou, EM ;
Vydelingum, S ;
Heckert, R .
VETERINARY MICROBIOLOGY, 1998, 60 (2-4) :155-168
[4]   Laboratory decision-making during the classical swine fever epidemic of 1997-1998 in The Netherlands [J].
de Smit, AJ ;
Eblé, PL ;
de Kluijver, EP ;
Bloemraad, M ;
Bouma, A .
PREVENTIVE VETERINARY MEDICINE, 1999, 42 (3-4) :185-199
[5]  
DESMIT AJ, 2000, THESOIS U UTRECHT UT
[6]   THE DEVELOPMENT OF AN INTERNATIONAL REFERENCE PANEL OF MONOCLONAL-ANTIBODIES FOR THE DIFFERENTIATION OF HOG-CHOLERA VIRUS FROM OTHER PESTIVIRUSES [J].
EDWARDS, S ;
MOENNIG, V ;
WENSVOORT, G .
VETERINARY MICROBIOLOGY, 1991, 29 (02) :101-108
[7]   REVERSE-TRANSCRIPTASE PCR ASSAY FOR DETECTION OF HOG-CHOLERA VIRUS [J].
HARDING, M ;
LUTZEWALLACE, C ;
PRUDHOMME, I ;
ZHONG, XH ;
ROLA, J .
JOURNAL OF CLINICAL MICROBIOLOGY, 1994, 32 (10) :2600-2602
[8]  
HORZINEK MC, 1991, ARCH VIROL S, V3, P1
[9]   CAP3: A DNA sequence assembly program [J].
Huang, XQ ;
Madan, A .
GENOME RESEARCH, 1999, 9 (09) :868-877
[10]   PRESUMPTIVE DIAGNOSTIC DIFFERENTIATION OF HOG-CHOLERA VIRUS FROM BOVINE VIRAL DIARRHEA AND BORDER DISEASE VIRUSES BY USING A CDNA NESTED-AMPLIFICATION APPROACH [J].
KATZ, JB ;
RIDPATH, JF ;
BOLIN, SR .
JOURNAL OF CLINICAL MICROBIOLOGY, 1993, 31 (03) :565-568