TY - JOUR
T1 - Rescue of foot-and-mouth disease viruses that are pathogenic for cattle from preserved viral RNA samples
AU - Belsham, Graham
AU - Jamal, Syed Muhammad
AU - Tjørnehøj, Kirsten
AU - Bøtner, Anette
PY - 2011
Y1 - 2011
N2 - Background: Foot and mouth disease is an economically important disease of cloven-hoofed animals including cattle,
sheep and pigs. It is caused by a picornavirus, foot-and-mouth disease virus (FMDV), which has a positive sense RNA
genome which, when introduced into cells, can initiate virus replication.
Principal Findings: A system has been developed to rescue infectious FMDV from RNA preparations generated from clinical
samples obtained under experimental conditions and then applied to samples collected in the ‘‘field’’. Clinical samples from
suspect cases of foot-and-mouth disease (FMD) were obtained from within Pakistan and Afghanistan. The samples were
treated to preserve the RNA and then transported to National Veterinary Institute, Lindholm, Denmark. Following RNA
extraction, FMDV RNA was quantified by real-time RT-PCR and samples containing significant levels of FMDV RNA were
introduced into susceptible cells using electroporation. Progeny viruses were amplified in primary bovine thyroid cells and
characterized using antigen ELISA and also by RT-PCR plus sequencing. FMD viruses of three different serotypes and
multiple lineages have been successfully rescued from the RNA samples. Two of the rescued viruses (of serotype O and Asia
1) were inoculated into bull calves under high containment conditions. Acute clinical disease was observed in each case
which spread rapidly from the inoculated calves to in-contact animals. Thus the rescued viruses were highly pathogenic. The
availability of the rescued viruses enabled serotyping by antigen ELISA and facilitated genome sequencing.
Conclusions: The procedure described here should improve the characterization of FMDVs circulating in countries where
the disease is endemic and thus enhance disease control globally.
AB - Background: Foot and mouth disease is an economically important disease of cloven-hoofed animals including cattle,
sheep and pigs. It is caused by a picornavirus, foot-and-mouth disease virus (FMDV), which has a positive sense RNA
genome which, when introduced into cells, can initiate virus replication.
Principal Findings: A system has been developed to rescue infectious FMDV from RNA preparations generated from clinical
samples obtained under experimental conditions and then applied to samples collected in the ‘‘field’’. Clinical samples from
suspect cases of foot-and-mouth disease (FMD) were obtained from within Pakistan and Afghanistan. The samples were
treated to preserve the RNA and then transported to National Veterinary Institute, Lindholm, Denmark. Following RNA
extraction, FMDV RNA was quantified by real-time RT-PCR and samples containing significant levels of FMDV RNA were
introduced into susceptible cells using electroporation. Progeny viruses were amplified in primary bovine thyroid cells and
characterized using antigen ELISA and also by RT-PCR plus sequencing. FMD viruses of three different serotypes and
multiple lineages have been successfully rescued from the RNA samples. Two of the rescued viruses (of serotype O and Asia
1) were inoculated into bull calves under high containment conditions. Acute clinical disease was observed in each case
which spread rapidly from the inoculated calves to in-contact animals. Thus the rescued viruses were highly pathogenic. The
availability of the rescued viruses enabled serotyping by antigen ELISA and facilitated genome sequencing.
Conclusions: The procedure described here should improve the characterization of FMDVs circulating in countries where
the disease is endemic and thus enhance disease control globally.
U2 - 10.1371/journal.pone.0014621
DO - 10.1371/journal.pone.0014621
M3 - Journal article
SN - 1932-6203
VL - 6
SP - e14621
JO - P L o S One
JF - P L o S One
IS - 1
ER -