BORRELIOSIS (RELAPSING FEVER)
Etiology:
Borrelia recurrentis and Borrelia duttoni
Reservoir:
Relapsing fever is a vector borne disease that can be acquired
either by a louse or a tick. Relapsing fever, when acquired through a
louse, occurs in epidemics while those acquired through ticks are
sporadic. In case of louse-borne fever, the reservoir is the human while
the primary reservoir hosts for the tick-borne relapsing fevers are
rodents.
Vector and distribution:
The insect vector may be the soft ticks of the genus
Ornithodoros or the body louse (Pediculus humanus). The
louse-borne relapsing fevers are endemic only in parts of Africa and
South America while the tick-borne, in the Americas, Africa, Asia, and
Europe. The bacteria are transovarially passed to the next generation of
ticks. The louse-borne disease is called epidemic relapsing fever
because it can be rapidly disseminated under conditions of overcrowding
and poor personal hygiene, such as during wars and natural disasters.
The tick-borne relapsing fever is called endemic relapsing fever because
it occurs when humans are exposed to infected ticks.
Mode of infection:
The louse is infected by feeding on a patient during the febrile
stage. The spirochetes are not transmitted directly to man but when the
louse is crushed, they are released and enter abraded skin or bites.
Ticks acquire the spirochetes from rodents and humans are infected when
spirochetes in the tick's saliva or coxal fluid (excreta) enter the skin
as the tick bites. Congenital borreliosis has also been
reported.
Pathogenesis:
One tip of the spirochete attaches to the host cell and some
form of invasin apparently causes the host cell to release digestive
enzymes that enable the spirochete with its corkscrewing motility to
penetrate the host cell membrane. The relapsing fever borreliae use
antigenic variation as a mechanism to evade the host immune response and
this antigenic variation results in a disease characterized by recurrent
episodes of fever and spirochaetaemia. The fever, which is marked by
spirochetemia usually last for 3-5 days. As the body mounts a specific
immune response, the spirochetes are cleared from the peripheral blood
and the fever subsides. The patient may remain afebrile for few days to
few weeks. A new antigenic variant develops in this period that gives
rise to another episode of fever.
Clinical features:
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The incubation period ranges from 3 to 11 days
(mean, 6 days).
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The onset is sudden with chills, followed by high
fever, tachycardia, severe headache, vomiting, muscle and joint
pain, and often delirium.
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Late in the course of the fever, jaundice,
hepatomegaly, splenomegaly, myocarditis, and cardiac failure may
occur, especially in louse-borne disease.
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The spirochetes appear in the blood during the
febrile period and can be found in internal organs, especially the
spleen and brain.
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Hemorrhagic lesions may be seen in kidney and
intestine. Brain and meninges may also be involved.
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The duration of illness ranges from 4 to 10
days.
As the body mounts a specific humoral immune
response, borreliae disappear from peripheral blood. This results
in an afebrile period lasting few days to several weeks. An
antigenic variant of this spirochete multiplies resulting in
relapse. Relapse occurs with a sudden return of fever often
with, all the former symptoms and signs. Jaundice and arthralgia
are more common during relapse. The illness clears as before, but
2 to 10 similar febrile episodes may follow at intervals of 1 to 2
weeks. The episodes become progressively less severe, and recovery
eventually occurs as the patient develops immunity. Myocarditis
is the most common cause of death in fatal cases of relapsing
fever.
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Louse Borne RF
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Tick Borne RF
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Vector
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Pediculus humanus
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Ornithodorus spp
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Occurrence
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Epidemic
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Sporadic
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Transovarial transmission
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No
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Yes
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Severity
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Severe
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Mild
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Relapses
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Few
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Many
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Reservoir
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Humans
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Rodents
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Bacteria
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B. recurrentis
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B. duttoni
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Geography
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Africa and S. America
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Africa, Asia, America, Europe
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Laboratory Diagnosis:
Diagnosis is suggested by the recurrent fever and confirmed by the
appearance of spirochetes in the blood during a febrile
episode.
Specimen collected:
Blood, CSF, synovial fluid
Microscopy:
- Darkfield examination to look for actively motile spirochetes
- Wright's or Giemsa stained thick and thin blood smears
- Acridine orange stain (fluorescent stain) for examining blood or
tissue
Culture:
Not cultivable on routinely used culture media.
Animal Inoculation:
In tick-borne infection, intraperitoneal injection of the
patient's blood (1-2 ml) into a mouse or rat produces large numbers of
spirochetes in the animal's tail blood within 3 to 5
days.
The differential diagnosis includes malaria, dengue,
yellow fever, leptospirosis, typhus, influenza, and the enteric
fevers.
Treatment:
The commonly used antibiotics are Tetracycline, Doxycycline or
erythromycin. Therapy should be started early during fever or during the
afebrile stage, but should be avoided near the end of the episode
because of the danger of Jarisch-Herxheimer reaction, which is
characterised by abrupt chills, fever, headache, malaise, nausea and
vomiting.
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