REVIEW OF PUBLIC HEALTH ADVICE ABOUT
TICKS
Citation: N S W Public Health
Bull 2004; 15(11–12) 212–215
Maria Torres
NSW Public Health Officer Training Program
NSW Department of Health
Victor Carey
Northern Sydney Public Health Unit
To make decisions about how to deal with ticks, the public,
clinicians and public health professionals require evidence-based,
unambiguous and practical information. This article provides
an introduction to ticks and a brief description of the review
of NSW Health’s public health advice about ticks.
BACKGROUND
Ticks are arthropods: that is, animals with an external skeleton
and jointed legs. Within this phylum they are arachnids, in
the subclass acari, closely related to mites. There are 2
main tick families: Ixodidae, or hard ticks, with over 700
species worldwide; and Argasidae, or soft ticks, with up to
185 species worldwide.[1]
In Australia there
are approximately 70 species of ticks, most of which are hard
ticks. The majority of these ticks are native, but some introduced
species are widely distributed. In New South Wales, from a
public health perspective, the mos t important is Ixodes
holocyclus, a native species also known as ‘paralysis
tick’. Like all ticks, I. holocyclus is sensitive to
desiccation (dehydration) and so a temperate climate with
relatively high levels of humidity is the best for tick survival.[2]
I. holocyclus is found from Queensland to Victoria,
mainly in humid bushland areas on the eastern seaboard along
a coastal band that, in parts, extends up to 70 km inland.
Encounters between I. holocyclus and humans are relatively
common, due to the fact that a large proportion of the human
population lives within the coastal band, and urban development
is increasingly encroaching into bushland.
Ticks are ectoparasites, which means they live and feed on
the outside of their hosts. The main hosts for I. holocyclus
are bandicoots, but the tick also attaches itself to other
animals including humans. The life cycle of the tick includes
4 stages of development: egg, larva, nymph and adult. During
their lifecycle, most species of hard ticks feed on the blood
of 3 different hosts, 1 each for the larva, nymph and adult
stages. Larvae and nymphs feed for several days and then drop
off the host to the ground where they moult into the next
stage. Adult females feed to obtain nutrients to develop eggs;
after feeding for several days they drop off the host and
lay thousands of eggs on the ground before dying. Adult male
ticks feed on hosts and on engorging adult female ticks. I.
holocyclus takes approximately 1 year to complete its
lifecycle. Larvae are most common in the autumn months, nymphs
are most common in winter, and adults are most common in spring,
but tick stages can overlap across the seasons. Figure
1 includes a graphic representation of the life
cycle of I. holocyclus.
From the ground, ticks climb to grasses or low bushes and
‘quest’ for a passing host. Once on the host they move upward
until they find a suitable place to attach. In humans this
is often a place where they will not be easily found such
as skin folds. Ticks use their conical lower lip (hypostome)
to penetrate the skin of the host. They then secrete a mixture
of substances, such as anticoagulants and prostaglandins,
to inhibit haemostasis, augment local blood flow and suppress
the inflammatory and immune response of the host, and thus
secure both attachment to and meals from the host.[2] In addition,
some ticks secrete a cement to further secure attachment.
I. holocyclus does not secrete cement but penetrates
the skin deeper than some of the other species of tick.
Clinical presentation and public health
importance
In addition to being itchy and sometimes painful, the bites
of I. holocyclus may be associated with other health
problems such as allergic reactions, tick paralysis and the
transmission of organisms that can cause infectious diseases.
Further, scratching at the site of the bite can lead to secondary
infection, and a foreign body granuloma may develop when parts
of the tick’s mouth are left in the host after incomplete
removal of the tick.[3]
Allergic reactions to tick bites
Allergic reactions to tick bites are caused by allergens
contained in the saliva of I. holocyclus. These allergens,
studied extensively by Gauci et al.,[4] are introduced into
the host from the time of the tick’s attachment. It has been
reported that all biting stages of I. holocyclus can
sensitise a host, which can later precipitate an allergic
reaction.[2,5] Anecdotal evidence suggests that most allergic
reactions follow bites by female adult ticks.
Allergic reactions range from mild local reactions to generalised
and sometimes severe reactions including anaphylaxis.[5,6]
Local reactions are the most common. They may last for weeks
and, depending on their severity, may require medical treatment.
Even though severe allergic reactions are rare, it is important
to be aware that they may occur shortly after a tick bite.[7]
Usually a history of worsening reactions to previous tick
bites precedes a severe systemic reaction,[2] and adrenaline
and resuscitation facilities may be needed to treat these
systemic reactions.[2,5] Individuals who have experienced
severe allergic reactions to tick bites should have access
to injectable adrenaline at all times.[2]
Tick paralysis
Tick paralysis in humans is a rare but potentially fatal
condition; young children are the most commonly affected.[8,9]
Tick paralysis is caused by neurotoxins contained in the saliva
of engorging female adult ticks. Symptoms start several days
after attachment of the tick, when the tick reaches a rapid
feeding phase accompanied by intense salivation, which coincides
with high production of toxins.[8 ]Initial symptoms of tick
paralysis include unsteady gait, weakness of limbs, and lethargy;
an ascending, flaccid and symmetrical paralysis progresses
over hours. In severe cases ventilatory failure may occur.
Tick paralysis, particularly in a child, should be treated
in intensive care where supportive management is usually sufficient.
In severe cases the use of an antitoxin may be necessary,[10]
but antitoxins should be used cautiously as they may cause
allergic reactions.[11 ]Removal of the tick is an important
step in the treatment of tick paralysis. However, an important
characteristic of paralysis caused by I. holocyclus
is that the condition may continue to deteriorate even after
the tick has been removed.[3,8,10 ]Recovery is often slow.
Tick-borne infectious diseases
After a few days of attachment, a tick infected with a pathogen
(whether a virus, bacteria or protozoa) may transmit the pathogen
to the host with its saliva and cause an infectious disease.
Spotted fevers are the main tick-borne infectious disease
in Australia. Even though they are not thought to be common
diseases, the real incidence of these and other tick-borne
infectious diseases in New South Wales is not known as the
conditions are not notifiable.
I. holocyclus is the main vector for human transmission
of Rickettsia australis, the bacterium that causes
one of the spotted fevers (Queensland tick typhus). The geographical
distribution of Queensland tick typhus is the same as that
of I. holocyclus. Nonspecific symptoms develop between
1 and 11 days after the tick bite and include fever, chills,
myalgia, arthralgia, headache and regional lymphadenopathy.
In up to 70 per cent of cases, a characteristic eschar (dry
scab) with a black necrotic centre and red areola is present
at the site of the bite.[11] A generalised maculopapular rash
(a rash that usually covers a large area, is red and has small
confluent bumps) may appear a few days after the onset of
the nonspecific symptoms. Clinical diagnosis is confirmed
by serology. Queensland tick typhus can be treated with doxycycline,
an antibiotic belonging to the class called tetracyclines.
Serious illness is rare.[3] If untreated, the fever usually
resolves in 1–2 weeks, but other symptoms may persist for
several months.[3]
Flinders Island spotted fever has a similar presentation
to Queensland tick typhus. It is caused by Rickettsia honei
and the main vector is the tick Ixodes cornuatus. Most
reported cases are from Flinders Island, mainland Tasmania
and Victoria.[3]
Lyme disease is caused by the bacterium Borrelia burgdorferi,
which is transmitted to humans by certain species of Ixodes
ticks. Symptoms of Lyme disease appear within days, weeks
or months of a tick bite and include early nonspecific symptoms
such as fever, headache, arthralgia and myalgia, which may
be accompanied by erythema migrans, a characteristic ‘bull’s-eye’
rash around the site of the tick bite. The nervous, cardiac
and musculoskeletal systems may be affected at later stages
of Lyme disease. Cases of patients with symptoms resembling
Lyme disease have been reported from eastern Australia since
1982,[12] but these cases have not been confirmed with serology.[3]
Hudson et al. postulate that the cause of the disease in Australia
is a spirochaete (a spirally-coiled rodlike bacterium) related
to B. burgdorferi.[13] However, a study that examined
over 12,000 ticks collected in coastal areas of New South
Wales failed to detect B. burgdorferi or any other
spirochaete.[14
]I. holocyclus, the logical candidate vector of the
pathogen in Australia, has been shown to be incapable of maintaining
or transmitting B. burgdorferi to humans.[15] The existence
of Lyme disease in Australia continues to be debated.
I. holocyclus is also a vector for Coxiella burnetti,
the agent responsible for Q fever. However, this disease is
mainly acquired through contact with infected farm and domestic
animals.
Other infectious diseases such as tick-borne arboviral infections,
babesiosis and ehrlichiosis are a burden in other parts of
the world because of their effect on both human and animal
health. The Australian Quarantine and Inspection Service ensures
that the species of ticks that are vectors for these diseases
are not introduced into Australia.
REVIEW OF PUBLIC HEALTH ADVICE ABOUT
TICKS, IN PARTICULAR ABOUT I. HOLOCYCLUS
In 2002, in response to public concern about ticks, the NSW
Department of Health published the brochure Tick Alert.
A review of the brochure, which is mainly about I. holocyclus,
was completed in March 2004. The review involved an initial
revision of the existing brochure by the Northern Sydney Public
Health Unit followed by consultation with relevant stakeholders.
These included infectious disease physicians, emergency medicine
clinicians, dermatologists, clinical toxicologists, immunologists,
entomologists, toxicologists, consumers, veterinarians, health
departments and other providers of information about ticks
to the public such as the NSW Poisons Information Centre and
St John Ambulance Australia.
There was general agreement that in addition to providing
information about health problems that may follow a tick bite,
one of the main messages of the brochure should be how to
prevent tick bites—just as prevention advice is provided about
other vectors of disease. To ground this advice, the brochure
includes information about the ecology of ticks, in particular
I. holocyclus, their lifecycle and habitat.
During the first round of consultation, many of the comments
received were about methods of tick removal. Most stakeholders
proposed 1 of 2 methods: mechanical removal of ticks or killing
the tick in situ prior to removal. One of the difficulties
faced at this point was that there is no clear evidence to
support or refute either method for the removal of I. holocyclus.
An evaluation of 5 methods commonly advocated for tick removal
concluded that mechanical removal by grasping the tick’s mouth-parts
close to the skin and pulling it off should be used for all
ticks unless research on a particular species suggested a
different approach.[16 ]This method is recommended in many
publications that refer to tick removal. However, proponents
of the method of killing the tick in situ pointed out that
certain characteristics of I. holocyclus (such as its
small size and its method of attachment by deep penetration
of the skin without deposit of cement) may require a different
method of removal. These proponents refer to advice provided
by Stone,[17] who postulated that the mechanical removal of
I. holocyclus may induce anaphylaxis as a result of
rapid dispersal of toxins and allergens away from the bite
site. Stone has suggested that I. holocyclus should
be killed in situ using an insect or tick repellent containing
pyrethrins or synthetic pyrethroids.[17]
A meeting of stakeholders was held in February 2004. Some
stakeholders provided comments in writing before the meeting
and these were used to inform the discussion. Consensus was
reached at the meeting to advise the public to remove ticks
as soon as they are found, using fine forceps (not ordinary
tweezers) or surgical scissors. There was agreement that there
was not enough evidence to suggest that killing the tick in
situ reduced an individual’s exposure to allergens. In addition,
participants discussed the danger of providing advice to the
public that recommended killing attached ticks with repellents,
as this advice may lead to the use of inappropriate products
on the skin.
There are several products and methods commonly used to treat
tick bites, including applying petroleum jelly, methylated
spirits or nail polish, and burning the tick with a hot match.
These methods were evaluated by Needham, who found that they
failed to cause ticks to detach.[16] Anecdotal accounts suggest
that sodium bicarbonate may be useful to calm the itchiness
associated with tick bites, but there is no evidence to support
this practice.
CONCLUSION
Even though the burden of disease attributable to tick-related
illness is perceived to be small, the incidence of tick-related
illnesses is unknown. Evidence is also lacking in relation
to methods of tick removal. Studies to answer these questions
would be useful.
The public health advice about ticks in New South Wales should
be reviewed regularly, particularly if new evidence relevant
to this advice becomes available.
| The revised public health information brochure Tick
Alert can be downloaded from the NSW Department of Health
website at www.health.nsw.gov.au.
|
REFERENCES
- Barker SC, Murrell A. Systematics and evaluation of ticks
with a list of valid genus and species names. Brisbane:
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- Sutherland SK. Ticks. Australian animal toxins.
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- Playford G, Whitby M. Tick-borne diseases in Australia.
Aust Fam Physician 1996; 25(12): 1841–5.
- Gauci M, Stone BF, Thong YH. Isolation and immunological
characterisation of allergens from salivary glands of the
Australian paralysis tick Ixodes holocyclus. Int
Arch Allergy Immunol 1988; 87(2): 208–12.
- Brown AFT, Hamilton DL. Tick bite anaphylaxis in Australia.
J Accid Emerg Med 1998; 15(2): 111–3.
- Gauci M, Loh RKS, Stone BF, Thong YH. Allergic reactions
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Clin Exp Allergy 1989; 19: 279–83.
- Kemp A. Tick bites. Med J Aust 1986; 144: 615.
- Grattan-Smith PJ, Morris JG, Johnston HM, Yiannikas C,
Malik R, Russell R, et al. Clinical and neurophysiological
features of tick paralysis. Brain 1997; 120: 102–13.
- Barber PA, Chambers ST, Parkin PJ. Australian paralysis
tick bite. N Z Med J 1994; 107(980): 252–3.
- Pearn J. The clinical features of tick bite. Med J
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- Storer E, Sheridan A, Warren L, Wayte J. Ticks in Australia.
Australas J Dermatol 2003; 44(2): 83–9.
- Stewart A, Glass J, Patel A, Watt G, Cripps A, Clancy
R. Lyme arthritis in the Hunter Valley. Med J Aust
1982; 1(3): 139.
- Hudson BJ, Barry RD, Shafren DR, Wills MC, Caves S, Lennox
VA. Does Lyme borreliosis exist in Australia? J Spirochetal
Tick-Borne Dis 1994; 1(2): 46–51.
- Russell RC, Doggett SL, Munro R, Ellis J, Avery D, Hunt
C, et al. Lyme disease: a search for a causative agent in
ticks in south-eastern Australia. Epidemiol Infect
1994; 112(2): 375–84.
- Piesman J, Stone BF. Vector competence of the Australian
paralysis tick, Ixodes holocyclus, for the Lyme disease
spirochete Borrelia burgdorferi. Int J Parasitol
1991; 21(1): 109–11.
- Needham GR. Evaluation of five popular methods for tick
removal. Pediatrics 1985; 75(6): 997–1002.
- Stone BF, Binnington KC, Gauci M, Aylward JH. Tick–host
interactions for Ixodes holocyclus: role, effects,
biosynthesis and nature of its toxic and allergenic oral
secretions. Exp Appl Acarol 1989; 7: 59–69.
Figure 1

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