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