Leptospirosis, Flashcards

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1
Q

What is the prevalence rate of Leptospirosis?

A

10/100,000 prevalence rate

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2
Q

What is the seasonal peak of leptospirosis?

A

— seasonal with a peak incidence during the
rainy months of July to October

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3
Q

What is the etiology of Leptospirasos that causes pathology?

A

Leptospira interrogans
◦ Pathogenic strains

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4
Q

What is the nonpathogenic strain of Leptospirosis?

A

— Leptospira biflexa
◦ nonpathogenic strains

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5
Q

thin, coiled spirochetes (0.1 ×
6.0 to 20.0μm)
— hook at one or both pointed
ends

A

Leptospira

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6
Q

The motility of Leptospira sp is by means of

A

?— Motility by means of two
periplasmic flagella

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7
Q

What is the optimum growth of Leptospira?

A

— optimum growth at 28° C to
30° C

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8
Q

Leptospirasos is an obligate aerobes. T or F?

A

T

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9
Q

How is the sublclinal infection of Leptospirosis?

A

◦ mild influenza-like febrile illness

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10
Q

What is the severe systemic disease of Leptospirosis?

A

— severe systemic disease (Weil disease)

  • *◦ renal and hepatic failure**, extensive
  • *vasculitis, myocarditis, and death**
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11
Q

The pathogenesis of Leptospira is determined by?

A

— Determined by:

  • *1. Number of infecting organisms
    2. host’s immunologic defenses
    3. virulence of the infecting strain influence**
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12
Q

MOT of Leptospirosis?

A

penetrate intact mucous
membranes or skin through small
cuts or abrasions

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13
Q

◦ spread in the blood to all tissues, including
CNS

– multiply rapidly and damage the endothelium of
small blood vessels

– meningitis, hepatic and renal dysfunction,
hemorrhage

A

L. interrogans

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14
Q

Where is the early stage of Leptospirosis?

A

— Early Stges
◦ Blood, CSF

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15
Q

Late stage of Leptospirosis?

A

— later stages
◦ Urine

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16
Q

Clearance of Leptospirosis happens when?

A

Clearance
◦ When humoral activity develops

17
Q

2 type of host of Leptospirosis?

A

two types of hosts:
◦ reservoir hosts
– Rodents and small
mammals
◦ incidental hosts
– dogs, farm animals,
humans

18
Q

— asymptomatic infections

— colonize the renal tubules

— shed in urine in large numbers

— Streams, rivers, standing water, and moist soil can be contaminated with urine from infected animals

◦ organisms surviving for as long as 6 weeks

A

Reservoir hosts

19
Q

Most human infections of Leptospirosis

A

◦ Clinically inapparent

◦ detected only through the demonstration of specific antibodies

20
Q

Infection of Leptospirosis is introduced through

A

— Infection introduced through skin
abrasions or the conjunctiva

21
Q

What is the incubation period of Leptospirosis?

A

Incubation period 1-2 weeks

22
Q

What are the 2 phases of Leptospirosis?

A

— 2 phases:
◦ initial phase
◦ Severe disease

23
Q

— influenza-like illness
◦ fever and myalgia (muscle pain)
— Organisms isolated in CSF
— remit after 1 week, or the patient may
progress to the second phase

A

Initial phase

24
Q

What happens in the second phase of Leptospirosis?

A

Headache
— Myalgia
— Chills
— abdominal pain
— conjunctival suffusion
(i.e., reddening of the
eye)
— Can progress to:
◦ vascular collapse
◦ Thrombocytopenia
◦ Hemorrhage
◦ hepatic and renal
dysfunction

25
Q

acute febrile illness with headache, myalgia (particularly calf muscle) and prostration associated with any of the following symptoms/signs:

A

◦ Conjunctival suffusion

◦ Anuria or oliguria

◦ Jaundice

◦ Cough,

hemoptysis, and breathlessness

◦ Hemorrhages (intestine, lungs)

◦ Meningeal irritation

◦ Cardiac arryhthmia

◦ Skin rash

26
Q

The CNS Disease of Leptospirosis is

A

— viral aseptic meningitis
— course of the disease is generally
uncomplicated
— low mortality rate
— Negative CSF culture

27
Q

— Icteric form of generalized
disease
◦ 10% of all symptomatic infections
— 10% to 15% mortality
— Hepatic necrosis not seen
— most patients recover full renal function

A

Icteric disease, or Weil disease

28
Q

— Sudden onset of
◦ Headache
◦ Fever
◦ Myalgias
◦ diffuse rash

A

Congenital leptospirosis

29
Q

Laboratory Diagnosis of Leptospirosis

Microscopy ____________________

— Gram stain and silver stain ________

— Darkfield microscopy ◦ __________

◦ Yields nonspecific findings

— Fluorescein-labeled antibody ◦ _____________

A
  1. — cannot be seen by conventional light microscopy
  2. not reliable
  3. relatively insensitive
  4. used to stain leptospires

◦ Not available in most clinical laboratories

30
Q

Laboratory Diagnosis:LEptospirosis

Culture

—media:

— generation time: 6 to 16 hours

— 28° C to 30° C

— Most cultures positive within 2 weeks

A

Fletcher,

**EMJH [Ellinghausen- McCullough- Johnson-Harris], **

Tween 80-albumin

31
Q

Leptospirosis is present in the blood for present in blood or CSF

A

during the first 10 days of
infection
◦ several specimens should be
collected

32
Q

Leptospirosis is Present in urine after the ____________

A

first week and for as long as 3 months

Note : ◦ must be treated to neutralize the pH

◦ concentrated by centrifugation

— Detected by darkfield microscopy

33
Q

Laboratory Diagnosis: Leptospirosis

__________

— limited success

— nucleic acid amplification (e.g., PCR) more sensitive than culture — technique is not widely available at this time

A

Nucleic Acid–Based Tests

34
Q

Laboratory Diagnosis: Leptospirosis

Antibody Detection ______________

◦ reference method for all serologic tests

◦ measures the ability of the patient’s serum to agglutinate live leptospires

◦ serial dilutions of the patient’s serum are mixed with the test antigens and then examined microscopically for agglutination

◦ Agglutinins appear in the blood of untreated patients after 5 to 7 days of illness

A

— Microscopic agglutination test (MAT)

35
Q

Treatment, Prevention, and
Control of Leptospirosis?

A

— usually not fatal in the
absence of icteric
disease

— Treatment with
penicillin and
doxycycline
◦ Doxycycline for

prevention
— vaccination of livestock
and pets has proved
successful in reducing
incidence of disease
— Rodent control

36
Q
A