Utility of automated real-time RT-PCR for the detection of foot-and-mouth disease virus excreted in milk

被引:28
作者
Reid, SM
Parida, S
King, DP
Hutchings, GH
Shaw, AE
Ferris, NP
Zhang, ZD
Hillerton, JE
Paton, DJ
机构
[1] Inst Anim Hlth, Pirbright Lab, Surrey GU24 0NF, England
[2] Inst Anim Hlth, Compton Lab, Newbury RG20 7NN, Berks, England
关键词
milk; milk components; foot-and-mouth disease virus; real-time RT-PCR; pasteurisation;
D O I
10.1051/vetres:2005040
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Foot-and-mouth disease virus ( FMDV) can be excreted in milk and thereby spread infection to susceptible animals in other holdings. The feasibility of using real-time reverse transcription polymerase chain reaction (rRT-PCR) as a diagnostic tool for detection of FMDV in milk was assessed by studying the excretion of virus from experimentally-infected cattle. Fore- and machine milk samples were collected over a 4-week period from two dairy cows infected with FMDV and from two in-contact cows held in the same pen. The whole, skim, cream and cellular debris components of the milks were tested by automated rRT-PCR and results compared to virus isolation ( VI) in cell culture. The onset of clinical signs of FMD in all four cows correlated with viraemia, and the presence of FMDV in other clinical samples. rRT-PCR results matched closely with VI in detecting FMDV in all milk components and generally coincided with, but did not consistently precede, the onset of clinical signs. rRT-PCR detected FMDV in milk up to 23 days post inoculation which was longer than VI. Furthermore, the detection limit of FMDV in milk was greater by rRT-PCR than VI and, in contrast to VI, rRT-PCR detected virus genome following heat treatment that simulated pasteurisation. rRT-PCR was also able to detect FMDV in preservative-treated milk. In conclusion, this study showed that automated rRT-PCR is quicker and more sensitive than VI and can be used to detect FMDV in whole milk as well as milk fractions from infected animals.
引用
收藏
页码:121 / 132
页数:12
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