Lyme Disease Flashcards
What is Lyme disease ?
a bacterial (vector-born) disease caused by Borrelia species (Borrelia burgdoferi)
Basic characteristics (3)
GRAM NEGATIVE BACTERIA
motile
spiral shaped (Spirochete)
Transmission (3)
TRANSMITTED by bite of blacklegged tick (DEER TICK)
Tick is infected by Borrelia burgdorferi and RARELY by Borrelia mayonii
TRANSMISSION OCCURS after an infected tick has been attached for AT LEAST 24-36 hours (most transmission occurs after 36-48 hours)
Removing the tick (within 24 hours) after it is ATTACHED greatly reduces the chances of getting Lyme disease.
Geographic distribution of Borrelia species
B. burgdorferi
North America, Europe
B. mayonii
Upper Midwestern USA
B. afzelii AND B. garinii,
Europe, Asia
Lyme disease vectors
Ixodes scapularis - EASTERN and NORTH central regions of North America
Ixodes pacificus - WESTERN North America (eg, northern California and Oregon)
Ixodes persulcatus - Asia and Eastern Europe
Ixodes ricinus - Europe and Western Asia
Life Cycle
Blacklegged ticks have a 2 - 3 YEARS OF LIFE CYCLE
FOUR life stages: EGG, LARVA, NYMPH, and ADULT.
The LARVA and NYMPH each must take a blood meal to develop to another stage of their life (female need blood to produce eggs)
LARVA AND NYMPHAL TICKS might get infected with Borrelia burgdorferi when feeding on an infected wildlife host, usually a RODENT such as mice.
The bacteria are passed along to the next life stage.
Deer are important sources of blood for ticks and are important for tick ‘s survival and movement to new areas but are NOT INFECTED by Borrelia burgdorferi . Other mammals e.g., dogs, and sheep (Europe) can be host for Borrelia
Symptoms (MOST COMMON)
Lyme disease —> MULTIPHASE & MULTISYSTEM disease
1) Fever/chills. All tickborne diseases can cause fever.
2) Aches and pains (JOINT PAIN)
3) RASH —> Lyme disease, Southern tick associated rash illness (STAR), Rocky mountain spotted fever (RMSF), ehrlichiosis and tularemia can cause DISTINCTIVE rashes
4) Tick paralysis —> caused by a toxin in the saliva of an attached tick. (PARALYSIS MOVES UP THE BODY) also resembles Guillain-Barré syndrome or botulism. (patients gain movement if removed tick within 24 hours)
Clinical manifestations (3)
Early Localized Disease — STAGE 1
The bacteria have not yet spread throughout the body.
Early Disseminated Disease — STAGE 2
The bacteria have begun to spread throughout the body.
Late Disseminated Disease — STAGE 3
The bacteria have spread to distant sites such as the joints and nerves.
Types of rashes
Check the slides it’s better
Erythema migrans (EM) rash
Occurs in 70 to 80 PERCENT of infected persons
ALSO CALLED BULL’S EYE RASH
• Begins at the site of a tick bite after 3 to 30 days (average is about 7 days)
• Expands gradually over several days reaching up to 12 inches or more (30 cm) across
• May feel warm to the touch but is rarely itchy or painful
• May appear on any area of the body
• Does not always appear as a “classic” erythema migrans rash
Stage 2: Early disseminated Lyme disease
• MAY OCCUR weeks to months after the tick bite
• Numbness or pain in the distribution of a nerve
• Paralysis or weakness in the muscles of the face, especially a facial nerve palsy
• Meningitis, characterized by severe headache, stiff neck, fever
• Heart problems, such as skipped heartbeats, which can cause light headedness or fainting.
Stage 3: Late disseminated Lyme disease
OCCURS when treatment was either not successful or never started (usually occurring many months after the initial bite).
Usually associated with intermittent or persistent arthritis
Joint inflammation (arthritis), typically in the knees, occurs and may become chronic.
Abnormal nervous system sensation develops because of disease of peripheral nerves (peripheral neuropathy), and confusion.
Heart problems including inflammation of the heart muscle and an irregular beat may occur .
Paralysis or weakness in the muscles of the face, especially a facial nerve palsy.
Meningitis, characterized by severe headache, stiff neck, fever.
Cycle after transmission
• B. burgdorferi enters the skin at the site of the tick bite.
• After 3 to 32 days, the organisms migrate locally in the skin around the bite, spread via the lymphatics to cause regional adenopathy or disseminate in blood to organs or other skin sites.
• Initially, an inflammatory reaction (erythema migrans) occurs before significant antibody response to infection (serologic conversion).
It is invasive and persistent but NOT TOXIGENIC.
Tissue pathology appears to be primarily due to host inflammatory reactions
Attachment to host membranes
B. burgdorferi possesses:
P66 (outer membrane protein of B. burgdorferi) —> functions as porin protein and, ß3-intergin binding protein that binds to host integrins, proteoglycans and glycoproteins
BBK32 (Fibronectin binding protein of B. burgdorferi) and decorin binding protein facilitates dissemination of the bacteria on entry into the bloodstream, promotes serum resistance.
B. burgdorferi binds plasmin, a serine protease, capable of digesting many extracellular matrix components to disseminate from the site of inoculation.
Pathogenesis
Evasion of antibody-mediated killing
• By using borrelial surface proteins, including outer surface protein C (OspC), and flagellin, developed very early in infection.
• Antibodies against OspC can kill the spirochete.
Evasion of complement-mediated killing
• By using outer surface protein E (OspE)- related proteins (Erps), and complement regulator-acquiring surface proteins (CRASPs) that bind complement factor H, and complement factor H-like protein 1 of the mammalian host.