| 7 Arthropod-borne
diseases
(other
than
malaria)
|
A
wide
range
of
diseases
are
transmitted
by
various
arthropod
vectors.
Many
are
of
great
significance
to
populations
residing
in
the
tropics
or
other
endemic
zones
but
are
of
little
risk
to
the
average
traveller,
although
isolated
cases
may
occur.
However,
cases
of
dengue
fever
imported
into
the
UK
are
increasing.
This
Chapter
includes
a
table
of
various
arthropod-borne
diseases,
some
information
about
dengue
and
the
three
immunisable
diseases
(Japanese
encephalitis,
tick-borne
encephailitis
and
yellow
fever)
and
information
on
physical
methods
of
protection.
| Disease
|
Type
of
|
Vector
|
Main
transmission
|
Vaccination
|
| |
organism
|
|
areas
|
available
in
|
| |
|
|
|
the
UK?
|
| Bartonellosis/
|
Bacterium |
Sandfly
|
Peru,
Ecuador,
and
Colombia
|
No |
| Oroya
fever
|
Bartonella
|
|
|
|
| |
bacilliformus
|
|
|
|
| Dengue |
Flavivirus
|
Mosquito
|
Most
tropics
and
subtropics
|
No |
| |
|
|
especially
Central
and
South
|
|
| |
|
|
America
(including
the
|
|
| |
|
|
Caribbean
and
Hawaii)
|
|
| |
|
|
SE
Asia,
S
Pacific,
and
|
|
| |
|
|
NE
Australia |
|
| Filariasis
|
Filariae
|
Mosquito
|
Sub-Saharan
Africa,
Egypt,
|
No |
| |
|
|
Asia,
W
Pacific
islands, |
|
| |
|
|
Central
America,
NE
coast
of |
|
| |
|
|
S
America
and
Caribbean |
|
| Japanese
|
Flavivirus |
Mosquito
|
Across
Asia
from
India
|
Yes |
| encephalitis
|
|
|
to
Korea,
Japan
and
SE
Asia
|
(unlicensed)
|
| |
|
|
(and
Pakistan);
Torres
Str
Is
|
|
| |
|
|
and
some
Pacific
Is
|
|
| Leishmaniasis
|
Parasite |
Sandfly
|
Tropics
and
subtropics
|
No |
| |
(Protozoa) |
|
(including
Mediterranean |
|
| |
Leishmania
|
|
areas)
|
|
| Lyme
|
Bacterium
|
Tick
|
Temperate
areas
of
Europe
|
No
(yes
in |
| |
(spirochete) |
|
and
Asia,
N/Central
and
|
USA
for
the
|
| |
Borrelia
|
|
Pacific
coast
of
N
America
|
USA
strain)
|
| |
burgdoferi
|
|
|
|
| Onchocerciasis
|
Filariae |
Black
fly
|
Across
C
Africa,
small
foci
in
|
No |
| (River
|
|
|
Yemen,
Americas
(S
Mexico,
|
|
| blindness)
|
|
|
Brazil,
Colombia,
Ecuador,
|
|
| |
|
|
Guatemala,
Venezuela) |
|
| |
|
|
|
|
| Plague
|
Bacterium
|
Rodent
|
Foci
in
S
America,
Western
|
No |
| |
Yersinia
pestis
|
flea |
USA,
N
Africa,
East
and
|
|
| |
|
|
Southern
Africa,Central |
|
| |
|
|
Asia,
India,
SE
Asia |
|
| Relapsing
|
Bacterium |
Body
and
|
Asia,
N
Africa,
Ethiopia
|
No |
| fever
|
(spirochete) |
head
louse
|
and
the
Sudan,
highland
|
|
| |
Borrelia
|
|
areas
of
C.
Africa
and
|
|
| |
recurrentis
|
|
S.
America
|
|
| |
7
Borrelia
Sp.
|
Tick |
Africa
including
North
and
|
|
| |
|
|
South
Middle
East,
Central |
|
| |
|
|
Asia,
India,
and
Spain.
Also
in
|
|
| |
|
|
S.
America;
sporadic
in |
|
| |
|
|
W.
Canada
and
W.
USA. |
|
| Rift
Valley
|
Phlebovirus |
Mosquito
|
Africa
including
Egypt,
|
No |
| fever
|
|
|
Somalia,
Mauritania,
Kenya
|
|
| Rocky
|
Rickettsia |
Tick
|
USA,
Canada,
Mexico |
No |
| Mountain
|
|
|
Panama,
Costa
Rica
and
|
|
| spotted
fever
|
|
|
Colombia
|
|
| Ross
River
|
Toga
virus |
Mosquito
|
Australia
(South,
Victoria,
|
No |
| fever
|
|
|
Western,
Coast
of
New
|
|
| |
|
|
South
Wales
and |
|
| |
|
|
Queensland)
and
South |
|
| |
|
|
Pacific |
|
| Sandfly
fever
|
Virus |
Sandfly
|
Subtropical
and
tropical
|
No |
| |
Sandfly
fever
|
|
areas
of
Europe,
Middle
|
|
| |
group
of
viruses
|
|
East,
Asia
and
Africa
|
|
| St
Louis
|
Flavivirus |
Mosquito
|
Americas |
No
|
| encephalitis
|
|
|
|
|
| Tick-borne
|
Flavivirus |
Tick
|
C.
and
eastern
Europe
and
|
Yes |
| encephalitis
|
|
|
across
former
USSR
to
Pacific
|
|
| Trypano-
|
Protozoa |
Tsetse
fly
|
East,
central
and
west
Africa
|
No |
| somiasis
|
(Trypanosome) |
|
|
|
| (African
|
2
main
forms
|
|
|
|
| sleeping |
in
different
|
|
|
|
| sickness) |
parts
of
Africa
|
|
Central
and
west
Africa
|
|
| |
T.
gambiense
|
|
Eastern
Africa
from
Ethiopia,
|
|
| |
T.
rhodesiense
|
|
south
to
Botswana
|
|
| Chagas'
|
Protozoa |
Reduviid
|
Americas
from
Mexico
to
|
No |
| (American
|
(Trypanosome) |
(cone
|
Argentina |
|
| Trypano-
|
|
nosed
|
|
|
| somiasis)
|
|
bug)
|
|
|
| |
|
|
|
|
| Tularaemia
|
Bacterium |
Mosquito
|
Parts
of
continental |
No |
| |
Francisella
|
Tick, |
Europe,
Russia,
|
|
| |
tularensis
|
Deerfly* |
China,
Japan,
USA.
|
|
| Typhus:
|
|
|
|
|
| Endemic
|
Rickettsiae
|
Rat
flea |
Temperate
areas
summer
|
No |
| |
(several
spp)
|
|
months
|
|
| Epidemic
|
|
Body
louse
|
Colder
months,
war/natural
|
|
| |
|
|
disaster,highland
areas |
|
| |
|
|
|
|
| Tick
(see
also
|
|
Tick
|
Africa
and
Indian |
|
| Rocky
|
|
|
subcontinent.
Also
|
|
| Mountain
|
|
|
Mediterranean
and
E.
Europe,
|
|
| spotted
fever)
|
|
|
Serbia
and
Australia
|
|
| |
|
|
|
|
| Scrub
|
|
Rodent
|
Asia,
South
Pacific
and
|
|
| |
|
mite
|
Australia |
|
| West
Nile
|
Flavivirus |
Mosquito
|
Africa,
Indian
subcontinent,
|
No |
| fever
|
|
|
Middle
East,
former
USSR,
|
|
| |
|
|
Europe,
one
outbreak
in
1999
|
|
| |
|
|
in
New
York |
|
| Yellow
fever
|
Flavivirus |
Mosquito
|
West,
Central
and
East
Africa,
|
Yes |
| |
|
|
Panama
and
Tropical
south |
|
| |
|
|
America
(see
maps
inside |
|
| |
|
|
back
cover) |
|
7.1 Dengue fever/Dengue haemorrhagic fever
Dengue fever (DF) and dengue haemorrhagic fever (DHF)
exist throughout most of the tropics and subtropics. There has
been a dramatic increase in transmission and cases in recent years
with epidemics in tropical South America, the Caribbean and SE
Asia and increased cases imported into the UK, from the Caribbean
and Thai islands especially.
The four dengue viruses (flaviviruses) are transmitted
to man by aedes mosquitoes. The disease may be subclinical or
non-specific or have a sudden onset of fever (one to five days),
severe headache, joint and muscle aches ('breakbone fever').
A transient early generalised rash may be replaced later by petechiae.
Nausea and vomiting may occur.
DF in travellers is usually self-limiting although
a return to complete health can sometimes be slow. Immunity is
to the type encountered but it is believed that infection with
a second type (usually within two years of the first) may result
in the more severe DHF which carries a high mortality (particularly
in local children) and has occurred in travellers.
There is no specific therapy. Prevention is by reduction
of mosquito bites during the day, especially just after dawn and
just before dusk (see 7.5).
No vaccine is currently available but several candidate
vaccines are under development.
7.2 Japanese encephalitis
Japanese encephalitis (JE) exists only in Asia, from
India (and a small area in Pakistan) eastwards across Thailand
and China to Korea and Japan and down through south east Asia.
It has recently reached the Torres Straight islands between Papua
New Guinea and northern Australia.
The flavivirus is transmitted by various species
of culicene mosquito from agricultural animals (often pigs) and
birds to man. The mosquitoes most commonly breed in rice fields.
The risk season corresponds with the hotter, wetter
seasons in the northern part of the endemic zone (usually May-October)
whilst it tends to be year round in Malaysia, Indonesia and the
Philippines.
The infection is asymptomatic in over 99 per cent
of cases. However, when encephalitis develops there is a 30 per
cent mortality rate and about 50 per cent of the survivors are
left with neurological sequelae.
The disease is extremely rare in travellers, the
risk estimated to be less than 0.1 per 100,000 in tourists and
business people. It is increased for those staying in rural, especially
agricultural, areas within the endemic zone and in the transmission
season. Vaccine should be considered for those who will be at
this increased risk for at least a month. Prevention for all travellers
to rural areas is by reducing the chance of being bitten by these
predominantly dusk to dawn biting mosquitoes (see 7.5).
Vaccine (see
also Immunisation
against Infectious Disease
and table in Chapter 8)
The unlicensed, inactivated, mouse brain derived
vaccine can be administered on a named doctor/named patient basis
to those considered at sufficient risk. Possible adverse events
include delayed allergic reactions and so the course should be
completed at least ten (and preferably 14) days before travel.
Vaccinees should be observed for 30 minutes after each dose. Those
with a history of urticaria or multiple allergies are considered
at higher risk of allergic reactions. Rare neurological reactions
also occur.
7.3 Yellow fever
Yellow fever exists within two endemic zones - a
belt across Africa and the tropical part of South America reaching
as far north as Panama (see maps inside back cover). The risks
within these zones will vary according to mosquito activity.
The flavivirus is transmitted by species of aedes
and haemagogus mosquitoes in a jungle cycle which includes non-human
primates (and occasional humans in the forest) and an urban cycle
involving humans.
The disease can be mild, flu-like or hepatitis-like
or a severe viral haemorrhagic fever with a 50 to 60 per cent
mortality in non-immune travellers.
Prevention is by reducing the chance of mosquito
bites from these day biting mosquitoes, especially after dawn
and late afternoon (see 7.5) and by vaccine.
Immunisation is advised for all travellers to endemic
zones unless travel is restricted to urban areas at high altitude
(whether or not it is a mandatory requirement for entry).
Immunisation is available only from designated centres
(see pages 3-4).
Vaccine (see
also Immunisation
against Infectious Disease
and table in Chapter 8)
The live attenuated 17D strain vaccine is highly
effective with a very low rate of serious adverse events.
An International Certificate of Vaccination against
yellow fever is required for entry to some countries (see 8.2.3).
7.4 Tick-borne encephalitis
Tick-borne encephalitis (TBE) exists in Scandinavia,
across Central and Eastern Europe and the Western part of the
former USSR. The flavivirus is transmitted by the vector tick
Ixodes ricinus.
A different tick Ixodes
persulcatus transmits
the closely related Russian spring summer encephalitis across
the former USSR, north of Mongolia to the Pacific coast and to
parts of China (far north east), Korea and Japan. The countries
with areas most affected by TBE are Austria, Belarus, Croatia,
Czech Republic, Estonia, Germany, Hungary, Latvia, Lithuania,
Poland, Russia, Slovakia and Ukraine.
Areas with lower prevalence or where sporadic cases
have been reported include Albania, Bulgaria, Denmark (Bornholm
Island), SW coast of Finland, France, Greece, Italy, Norway, Romania,
Serbia, the Baltic coast of Southern Sweden and Switzerland.
The infection is asymptomatic in 90 per cent of cases
especially in children. Those who develop flu-like symptoms may
recover but ten per cent of them suffer a relapse with encephalitis
with possible neurological sequelae or fatal outcome. The outlook
is worse with increasing age.
The risk is mainly to those who are working, walking
or camping in rural areas where ticks are prevalent. It is greatest
from April through to August and sometimes October. It can extend
outside those seasons in the warmer south of the area. The disease
is occasionally transmitted by eating or drinking unpasteurised
dairy products.
Prevention is by reduction of tick bites, avoidance
of consumption of unpasteurised dairy products and by vaccine.
The general measures to prevent ticks getting on to skin are described
below. Those in tick areas should check their skin for attached
ticks, which is easier to do with a partner. Ticks should be removed
as soon as possible with tweezers (or fingers covered by tissue
paper if no tweezers are available) as close to the skin attachment
as possible, by steady pulling without jerking or twisting. Only
one to two per cent of ticks are likely to be infected although
occasionally up to ten per cent are. Medical advice should be
sought locally as specific immunoglobulin may be available and
advised within 48 hours (manufacturers state 96 hours) of a tick
bite. However its efficacy has been questioned. Immunoglobulin
is unlicensed in the UK but can be obtained on a named doctor/named
patient basis where it is believed to be beneficial.
Vaccine (see
also Immunisation
against Infectious Disease
and table in Chapter 8)
Inactivated vaccines are available in the UK for
those considered at risk. Ideally immunisation should be completed
at least a month before travel. It is considered to be effective
against both strains of the disease. The specific immunoglobulin
may on occasion be considered for those at high risk and travelling
at short notice, although it is unlicensed in the UK.
Experience with TBE vaccine in the UK is limited.
Adverse reactions including tenderness and swelling at the injection
site with regional lymph gland swelling are reported, with some
more generalised malaise, limb aches and pyrexia in some cases.
Neuritis is rarely reported.
7.5 Physical methods of protection against
mosquito and tick-borne diseases
For the prevention of bites from night time (dusk-dawn)
biting mosquitoes see paragraph 6.4. For day time biting mosquitoes
this advice applies dawn to dusk. In practice this will often
include sleeping time.
Tick bites are reduced by preventing vegetation from
brushing against bare skin, which should therefore be covered
eg long trousers tucked into socks. Open sandals should not be
worn. DEET based repellents have some action against ticks and
can be used on skin or to spray clothing. Permethrin insecticide
spray can also be used on clothes. (See previous page for removal
of ticks).
|