| VLA is the National Reference Laboratory
for rabies in the UK and the Laboratory was re-designated
as a Communicable Disease Surveillance and Response World
Health Organisation (WHO) Collaborating Centre for the characterisation
of rabies and rabies-related viruses in March 2003, and as
such is engaged on:
Research
- focussing on:
- improvements in diagnosis
- investigation of the pathogenesis of rabies and rabies-related
viruses in terrestrial mammals
- investigation of the molecular epidemiology of rabies
virus isolates collected from around the world
- investigation of epitope mapping and vaccine efficacy
- investigation of new therapeutic products for use in
post-exposure treatment regimes
Surveillance
In the UK, bats found dead are submitted and tested at VLA
under a programme of ‘passive surveillance’. This
work is undertaken in close collaboration with the UK Bat
Conservation Trust and between 1986 and 2002, only two out
of 3,213 bats tested have been confirmed positive.
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Microarray equipment detects the DNA
make-up of cells |
Pet Travel Scheme
(PETS)
The scheme permits dogs and cats to enter the UK from EU member
states and other specified countries without having to undergo
quarantine, providing specific conditions are met. One of
these conditions is for a blood sample to be tested by an
approved laboratory for the presence of rabies neutralising
antibodies. VLA has tested nearly 14,000 samples during the
year.
Rabies in the
UK
The UK is free from rabies with the last human death
from indigenous rabies (RABV; classical rabies virus) recorded
in 1902. Between 1977 and 2000, nine human rabies deaths occured
from infections acquired overseas; two additional human cases
in 2001 were imported from the Philippines and Nigeria.
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Daubenton’s bat (Myotis daubentonii) |
The first isolation of a lyssavirus from a bat in the UK
was from a Daubenton’s bat (Myotis daubentonii)
in Sussex in 1996. Daubenton’s bats are the third most
common species in the UK with a population estimated at 150,000.
The virus was subsequently characterised as a European bat
lyssavirus (EBLV) type-2a.
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Table Data
One per cent agarose gel showing the second round RT-PCR
for European bat lyssavirus type 2 nucleoprotein in organs
from the Lancashire Daubenton’s bat.
A summary of 1st- and 2nd-round PCR, with the results
of virus isolation, is also shown. ND - Not Done.
Click
here to open |
In September 2002, VLA reported a rabies-related virus in
another Daubenton’s bat in Lancashire using conventional
diagnostic tests on brain samples. Both the hemi-nested reverse
transcriptase polymerase chain reaction (RT-PCR) test and
ante-mortem saliva samples proved positive for rabies. A 400
base-pair region of the nucleoprotein gene was sequenced and
confirmed the presence of an EBLV type-2a.
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Map Data
Western Europe showing the approximate location of European
bat lyssavirus type 2 cases in bats and humans.
Click
here to open |
In November 2002, VLA reported the first indigenously acquired
case of EBLVtype-2a in a human from Scotland. A 55-year-old
bat conservationist was admitted to Ninewells Hospital Dundee,
Scotland with a rapidly progressive unexplained neurological
illness.He presented with a five day history of pain and paraesthesia
in the left arm followed by increasing weakness of his limbs
with evidence of evolving encephalitis.
He admitted to numerous exposures throughout 2002 involving
close handling of different species of bat and had been previously
bitten by bats on some occasions while not wearing gloves.
In September 2002, in Scotland, he was bitten on the ring
finger of his left hand. The bat associated with this biting
incident was considered to be a Daubenton’s bat. The
bat, however, was not retained for analysis and subsequently
no accurate information on the exact identification of the
species of bat has been possible. The source of infection
was almost certainly from the UK, as the victim had never
handled bats outside of Scotland except when he last travelled
abroad to Papua New Guinea during 1995/96.
On 24 November 2002, thirteen days after admission to hospital,
the patient died. Post-mortem diagnostic tests including the
fluorescent antibody test (FAT), RTCIT and RT-PCR on three
brain samples (cerebellum, medulla and hippocampus) were positive.
A mouse inoculation test was also performed. Clinical signs
of a rabies-like illness developed in five inoculated mice
between 13 and 17 days post-infection. Brain smears from each
infected animal were positive by the FAT and viable virus
was isolated.
This fatal incident is only the second confirmed case of
an EBLV type-2a infection in a human following exposure to
bats. The only previously recorded case of an EBLV type-2a
in a human patient was reported from Finland in 1985.
In order to understand the true prevalence of EBLVs in British
bats, an ‘active surveillance’ programme, jointly
funded by Defra and the Biotechnology and Biological Sciences
Research Council was initiated. Sampling of bats in Scotland,
funded by Scottish Natural Heritage, began in March 2003 and
future projects will be focussed in Lancashire and sampling
at some swarming sites will be carried out in South West England.
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