The purpose of this study was to develop a method to store viruses on filte
r paper without the need for special conditions for future use of the genet
ic material. Two non- enveloped viruses were used as models. Infectious bur
sal disease virus (IBDV), a double-stranded RNA virus that infects chickens
, belongs to the Birnaviridae family. Hemorrhagic enteritis virus (HEV), wi
th double-stranded DNA, belongs to the Adenoviridae family. Three different
solutions were found suitable for loading the virus. The viruses were stor
ed at room temperature or at 37 degrees C for periods of 5-30 days. Direct
reverse transcription-polymerase chain reaction (RT-PCR) (without previous
extraction of the RNA) was carried out on filter paper loaded with IBDV, an
d fragments of the expected size were detected. HEV DNA was extracted from
filter paper loaded with purified virus or crude tissue. PCR fragments were
found to be: of similar intensity to those of control virus that was kept
in a tube at - 20 degrees C. This method permits the storage and transport
of viruses from the field or from clinics to a regional laboratory or any l
aboratory elsewhere, without the need for prior treatment or special enviro
nmental conditions. (C) 1999 Elsevier Science B.V. All rights reserved.