Development of a novel real-time RT-PCR assay for quantitation of foot-and-mouth disease virus in diverse porcine tissues

被引:88
作者
Oleksiewicz, MB [1 ]
Donaldson, AI [1 ]
Alexandersen, S [1 ]
机构
[1] AFRC, Inst Anim Hlth, Pirbright Lab, Woking GU24 0NF, Surrey, England
关键词
FMDV; quantitation; TaqMan; RT-PCR; pigs; tissues; Ctmin; GAPDH; HPRT; beta actin;
D O I
10.1016/S0166-0934(00)00265-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Pigs are more difficult to immunise and more variable in their response to foot-and-mouth disease (FMD) than other livestock species. This has important consequences for FMD control during both prophylactic vaccination programmes in endemic situations and when emergency vaccination may be used as an adjunct to stamping out during outbreaks in countries normally free from the disease. The rapid and effective control of FMD in pigs is especially important in regions of high pig density since infected pigs have the potential to generate plumes of airborne virus and spread infection beyond the immediate control area. Increased knowledge of the kinetics of FMDV replication in pigs, especially in their respiratory tracts, could create opportunities for strategies to improve FMD vaccines for pigs. A fluorogenic TaqMan RT-PCR assay specific for the IRES (internal ribosome entry site) sequence of the O-1 Kaufbeuren/Lausanne strain of FMDV has been developed for this purpose. The assay had a sensitivity of 0.1 TCID50/ml, and a dynamic range of at least eight orders of magnitude. It was found that an established method of quantitation, relative to a housekeeping gene, exhibited two significant shortcomings when applied to a set of 16 anatomically highly diverse solid tissues: (i) tissue differences in housekeeping gene expression caused errors of up to 60-fold in estimated FMDV concentrations; and (ii) variability in total RNA yields caused unpredictable saturation of RT reactions, which in turn caused errors of up to 250-fold in the estimated FMDV concentration. A novel quantitation strategy, designated the C-t(min) method, was developed to overcome these problems. The C-t(min) method was based on the the RT-PCR examination of a dilution series of spectrophotometrically quantitated total RNA, spanning the optimum for the RT-PCR system used. The new method was influenced minimally by any tissue-specific RT-PCR inhibitors and was used to determine FMDV concentrations in tissues from four experimentally infected pigs. The results suggest that the lungs play a less important role in the replication of FMDV in pigs than was thought previously. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:23 / 35
页数:13
相关论文
共 13 条
[1]  
[Anonymous], 1969, REPORT COMMITTEE I 1
[2]   SUBTYPING OF EUROPEAN FOOT-AND-MOUTH-DISEASE VIRUS-STRAINS BY NUCLEOTIDE-SEQUENCE DETERMINATION [J].
BECK, E ;
STROHMAIER, K .
JOURNAL OF VIROLOGY, 1987, 61 (05) :1621-1629
[3]   DISTINCTIVE FEATURES OF FOOT-AND-MOUTH-DISEASE VIRUS, A MEMBER OF THE PICORNAVIRUS FAMILY - ASPECTS OF VIRUS PROTEIN-SYNTHESIS, PROTEIN PROCESSING AND STRUCTURE [J].
BELSHAM, GJ .
PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1993, 60 (03) :241-260
[4]   PATHOGENESIS OF FOOT-AND-MOUTH-DISEASE IN SWINE, STUDIED BY IN-SITU HYBRIDIZATION [J].
BROWN, CC ;
OLANDER, HJ ;
MEYER, RF .
JOURNAL OF COMPARATIVE PATHOLOGY, 1995, 113 (01) :51-58
[5]   INFECTIVITY ASSAY OF FOOT-AND-MOUTH DISEASE VIRUS IN PIGS [J].
BURROWS, R .
JOURNAL OF HYGIENE-CAMBRIDGE, 1966, 64 (04) :419-&
[6]   USE OF PREDICTION MODELS TO FORECAST AND ANALYZE AIRBORNE SPREAD DURING THE FOOT-AND-MOUTH-DISEASE OUTBREAKS IN BRITTANY, JERSEY AND THE ISLE OF WIGHT IN 1981 [J].
DONALDSON, AI ;
GLOSTER, J ;
HARVEY, LDJ ;
DEANS, DH .
VETERINARY RECORD, 1982, 110 (03) :53-57
[7]   Regulation of hypoxanthine phosphoribosyltransferase, glyceraldehyde-3-phosphate dehydrogenase and β-actin mRNA expression in porcine immune cells and tissues [J].
Foss, DL ;
Baarsch, MJ ;
Murtaugh, MP .
ANIMAL BIOTECHNOLOGY, 1998, 9 (01) :67-78
[8]   Quantitation of foot-and-mouth disease virus genomes in bovine tissue by competitive RT-PCR [J].
Niedbalski, W ;
Adam, KH ;
Marquardt, O .
JOURNAL OF VIROLOGICAL METHODS, 1998, 72 (02) :237-242
[9]   Emergency vaccination of pigs against foot-and-mouth disease: protection against disease and reduction in contact transmission [J].
Salt, JS ;
Barnett, PV ;
Dani, P ;
Williams, L .
VACCINE, 1998, 16 (07) :746-754
[10]   GROWTH OF FOOT-AND-MOUTH DISEASE VIRUS IN MONOLAYER CULTURES OF CALF THYROID CELLS [J].
SNOWDON, WA .
NATURE, 1966, 210 (5040) :1079-&