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7/29/2019 Legionella Infections Bhargav
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LEGIONELLA INFECTIONS
PRESENTOR : Dr.Bhargav
MODERATOR : Dr.Prof.M.Senthilvelan sir
1
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Introduction
There was a outbreak of pneumonia in
persons who attended a convocation of
American legion in Philadelphia.
There were around 200 cases and 20 deaths.
So there was a huge , expensive medical
investigation carried out and it was discovered
that legionella was the causative organism
from the cooling towers.
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organism
It is gram negative ,aerobic , fastidious ,
facultative intracellular organism
,coccobacillus , motile ,flagellated ,non
encapsulated.
There are around 50 species and 70 serotypes
Around 18 species will cause human
infections.
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organism
Most common among them are L.pneumophilia
,L.macdadei ,L.longbeachae.L.bozemanii ,L
.dumoffii.
Of all the species serotype 1 is most common
causing 70-90% of the infection
The incubation period on average 2 days for
pontiac fever and 7 days for legionnaires disease Commonly occurs in streams/lakes/cooling
towers/ geysers.
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organism
They grow more when it is protein substrate.
For culturing they need media containing ironand cystein
Buffered charcoal yeast extract is the commonmedium that is used.
It is closely related to the genus coxiella
causing Q fever. It is easily killed by formalin , glutaraldehyde ,
chlorine and ethyl alcohol.
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habitat
ubiquitous aquatic
Warm water-hot water springs
Cooling tower/mist machine/spa Water heater/swimming pool
Potable water plumbing/showers
The L.longbeachae which can grow in pottingsoil and soil as well as in water.
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biofilm
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Factors that increase colonisation
Presence of free living amoeba
Warm water
Rainfall Humidity
Sediment and scaling
The cooling towers are over estimated theydidnt satisfy the koch postulates.80% of
cooling towers showd their presence.
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Transmission
There is no person to person transmission
Aerosols
Aspiration Direct instillation
In hospital acquired cases
Micro apiration (GA) Nebulizers / Humidifiers
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pathogenesis
Through aerosol transmission they enter thelung there they attach to the epithelium.
Later they are engulfed by the alveolar
macrophages. They resist the lysosomic degradation by first
multiplying in ER.
Both cellular immunity and humoral immunityacts. However neutrophils and antibodiesseems to have no big role.
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pathogenesis
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pathogenesis
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Virulence factors
Type 4 pili
Flagella
Porin
LPS
MIP
Heat shock protein
Protein secretion system type 2 and 4
And many other enzymes
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terms
Legionellosisthe disease caused by legionella
are together called legionellosis
Legionnaires disease-pneumonia caused by
legionella is called legionnaires disease.
Pontiac fever-acute , febrile , self limited
disese caused by this organism.
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epidemiology
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Risk factors
Male gender
Cigarette smoking
Chronic heart disease /lung disease
Chronic kidney disease
Chemotheray
TNF-alfa inhibitor use
Corticosteroid use
Alcohol
Recent surgery in GA
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risk factors
Overnight travel
Recent plumbing work in the home
Whirlpool spas Hot water springs
Nebulization ,humidifiers , nasogastric tubes .
Near drowning
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Clinical features
Pontiac fever
It is acute , febrile , self limiting flu like illness.
The incubation period is from hours to 2 days.
Myalgia
Fatigue
Headache
Malaise
Diarrhea
Nausea
Abd pain
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continued
Fever occurs in 90% individuals(mostly with
chills)
Headache in 80%.
The secondary attack rates are high.
It is diagnosed by serology.
No treatment is usually necessary.
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Legionnaires disease
It is often included in the differential diagnosisof atypical pneumonia because it usuallyproduces non-productive cough.
It is more severe than other atypicalpneumonia
But the course and prognosis are similar to
streptococcal pneumonia. All the clinical features and radiological
findings are also similar
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Symptoms and signs
Fever usually with chills and rigors
Normally preceded by prodrome of
headache/malaise/myalgia.
Non productive cough usually
Dyspnoea
Some times blood streaked sputum Rarely chest pain
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Symptoms and signs
Diarrhea/abdominal pain
Confusion /altered sensorium
Temperature will be high >104 Relative bradycardia
Focal rales early
Consolidation later Pleural effusion
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Laboratory findings
Hyponatremia
Hypophosphatemia
Raised liver enzymes Haematuria
proteinuria
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Radiological findings
They can be present or absent at the time ofpresentation.
Patchy infiltrations
Consolidation Pleural effusion
In immunocompramised persons
Round nodular opacities Cavities -10%
Complete disappearance takes 1-4 months
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Extrapulmonary manifestations
Blood borne dissemination or direct
instillation
Most common site is heart- pericarditis,
myocarditis, prosthetic valve endocarditis
Others are brain , liver ,spleen , kidneys
There it forms microabscess
Arthritis, peritonitis, sinusitis can occur
Mostly in immunocompramised persons
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staining
Material obtained from sterile sites like lungtissue and pleural fluid
Presence of numerous leucocytes in absence
of organism is the usual picture If seen appear a small gram negative cocco-
bacilli
Direct fluroscence antibody testing is highlyspecific , rapid test but is less sensitive thanculture
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Antibody detection
Four fold rise in titre diagnostic
1:128 with circumstantial evidence can be
considered
Serolgy is useful in epidemiolgic studies
Limitation of its use is it requries 12 weeks for
the detection of antibody response.
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Urinary antigen
Rapid , inexpensive , easy to perform , highlysensitive and specific.
The antigen in urine will be present from 3
days to 2 months Even with treatment of antibiotics it is not
affected
It is available only for legionella serotype 1 Enzyme assays and immunochromatograhic
assay are also available
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culture
It requires 3-5 days
Buffered charcoal yeast extract media is used
It has to be pretreated with heat , acid andantibiotics to kill the other microbial flora
It is higly sensitive and specific
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Molecular methods
Direct fluroscence antibody stains are
available both monoclonal and polyclonal
PCR with DNA probes are highly sensitive and
specific than all other methods
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treatment
Beta-lactams and aminoglycosides are not
effective
The antibiotics which can attain high
intracellular concentration are effective like
macrolides, quinalones and tetracyclines.
Quinalones are preferred in transplant
patients as it have lesser interaction with
chemotherapeutic agents
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treatment
Clinical response takes 3-5 days
Total duration of therapy is 10-14 days in
immunocompetent persons and 3 weeks in
immunocompramised persons
Trimethoprim, imepenem and clindamycin
have both success and failures in studies
Combination of rifamin has shown failure in
some studies
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prognosis
Depends on
Underlying disease and its severity
Immune status
Timing of administration of antibiotc
Severity of pneumonia
10% mortality even in treated patients
80%mortality in immunocompramisedwithout treatment
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prophylaxis
No vaccine is available
Chemoprophylaxis with macrolides in
immunocompramised persons is considered
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prevention
Heat and Flush:
Heat hot water >160 oF
Flush through ALL fixtures at this temperature for >= 5 minutes.
Flow should be about the width of a pencil.
Hyperchlorination:
Add chlorine to the hot water system.
Flush chlorine through all fixtures until it is >=2.0 ppm free chlorine, and pHis between 7.0 and 8.0
Keep fixture closed for 2-24 hours, then flush thoroughly.
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prevention
1) Chlorine Injection
- Drawbacks: corrosive to pipes, dangerous chemicals
2) Chlorine Dioxide- Drawbacks: takes time, treatment failures have beenreported, dangerous chemicals, needs monitoring
3) Copper Silver Ionization System
- Drawbacks: Expensive, needs monitoring
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thankyou