TY - JOUR
T1 - Implementation and validation of a sensitive PCR detection method in the eradication campaign against Aleutian mink disease virus
AU - Jensen, Trine Hammer
AU - Christensen, Laurids Siig
AU - Chriél, Mariann
AU - Uttenthal, Åse
AU - Hammer, Anne Sofie
PY - 2011
Y1 - 2011
N2 - Aleutian mink disease virus (AMDV) is a severe progressive disease causing multiple different clinical
syndromes in mink. In Denmark, the disease is notifiable and under official control. The control
programme, based on serological screening, has confined successfully AMDV to the northern part of Denmark.
However, re-infections and new introductions of virus into farms require a confirmatory virological
test to verify the positive test results of single animals and ultimately to investigate disease transmission.
A one step PCR amplifying a 374-base fragment of the NS1 gene of AMDV was compared to the
counter-current immune electrophoresis (CIE) routinely used in the serological screening programme.
Mink organs (n = 299) obtained from 55 recently infected farms and 8 non-infected farms from 2008 to
2010 were tested by PCR, and the results were found to have a high correlation with the serological
status of the mink. The relative diagnostic sensitivity of the PCR was 94.7%, and the relative diagnostic
specificity was 97.9% when read in parallel with the CIE. PCR positive samples were sequenced and
phylogenetic analysis revealed high similarity within the analysed AMDV strains and to AMDV strains
described previously.
AB - Aleutian mink disease virus (AMDV) is a severe progressive disease causing multiple different clinical
syndromes in mink. In Denmark, the disease is notifiable and under official control. The control
programme, based on serological screening, has confined successfully AMDV to the northern part of Denmark.
However, re-infections and new introductions of virus into farms require a confirmatory virological
test to verify the positive test results of single animals and ultimately to investigate disease transmission.
A one step PCR amplifying a 374-base fragment of the NS1 gene of AMDV was compared to the
counter-current immune electrophoresis (CIE) routinely used in the serological screening programme.
Mink organs (n = 299) obtained from 55 recently infected farms and 8 non-infected farms from 2008 to
2010 were tested by PCR, and the results were found to have a high correlation with the serological
status of the mink. The relative diagnostic sensitivity of the PCR was 94.7%, and the relative diagnostic
specificity was 97.9% when read in parallel with the CIE. PCR positive samples were sequenced and
phylogenetic analysis revealed high similarity within the analysed AMDV strains and to AMDV strains
described previously.
U2 - 10.1016/j.jviromet.2010.10.004
DO - 10.1016/j.jviromet.2010.10.004
M3 - Journal article
SN - 0166-0934
VL - 171
SP - 81
EP - 85
JO - Journal of Virological Methods
JF - Journal of Virological Methods
IS - 1
ER -