Brucella melitensis: Difference between revisions
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Brucella melitensis
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*[[Is treated by::Gentamicin]], [[Is treated by::streptomycin]], [[Is treated by::doxycycline]], [[Is treated by::TMP-SMX]] |
*[[Is treated by::Gentamicin]], [[Is treated by::streptomycin]], [[Is treated by::doxycycline]], [[Is treated by::TMP-SMX]] |
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== |
==Prevention== |
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===Lab Safety=== |
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*Assess risk and provide prophylaxis and monitoring per [https://www.cdc.gov/brucellosis/laboratories/risk-level.html CDC guidelines] |
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* |
*Assess risk |
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** |
**Minimal risk |
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***Manipulating routine specimen or enriched material in BSL2 with PPE |
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*** |
***Being present while someone manipulates a routine specimen in BSL2, or on an open bench without aerosol-generating procedures |
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*** |
***Manipulating or being present while someone manipulates enriched material in BSL2 |
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** |
**Low risk |
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*** |
***Being present more than 5 feet from someone manipulating enriched material on an open bench, without aerosol-generating procedures |
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** |
**High risk |
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*** |
***Manipulating a routine specimen resulting in contact with broken skin or mucous membranes |
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*** |
***Being present less than 5 feet from someone manipulating enriched material outside of a BSL2 |
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*** |
***Manipulating enriched material within a BSL2 without PPE |
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*** |
***Being present in the lab during an aerosol-generating procedure |
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* |
*Aerosol-generating procedures include centrifuging without sealed carriers, vortexing, sonicating, spillage/splashes |
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*Enriched material includes positive blood cultures, and reproductive clinical specimens (amniotic fluid, placental products) should be treated similarly |
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* |
*People with high-risk exposures should have post-exposure prophylaxis and follow-up |
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**PEP with [[doxycycline]] 100 mg PO bid plus [[rifampin]] 600 mg PO daily for 21 days |
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***Either can be replaced by [[TMP-SMX]] if contraindications exist, but should ensure two effect antibiotics are used |
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**Follow-up |
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***Daily fever checks and weekly symptom watch for 24 weeks after last known exposure |
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***Serial serology at 0, 6, 12, 18, and 24 weeks after last known exposure |
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{{DISPLAYTITLE:''Brucella melitensis''}} |
{{DISPLAYTITLE:''Brucella melitensis''}} |
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[[Category:Gram-negative coccobacilli]] |
[[Category:Gram-negative coccobacilli]] |
Revision as of 18:21, 12 September 2020
Background
- Causes brucellosis, also called Malta fever
Microbiology
- Facultative intracellular, Gram-negative coccobacillus
- Catalase positive, oxidase positive, nitrate positive, and urease positive
- Non-motile
- Risk group 3 organism
- When suspected, plates should be sealed and it should not be set up for mass spectrometry
Epidemiology
- Zoonotic transmission transmitted by ingesting contaminated food (such as unpasteurized milk products), direct contact with an infected animal, or inhalation of aerosols
Clinical Manifestations
Brucellosis
- Exposure to unpasteurized milk products or animals
- A common cause of fever without a focus in endemic countries
- Undulating fever
- Headache, arthralgia, night sweats, fatigue, anorexia
- Arthritis, spondylitis (especially sacroiliac and other large lower-extremity joints), osteomyelitis
- Hepatomegaly, splenomegaly, and lymphadenopathy
- Orchitis and epididymitis, prostatitis, and tubo-ovarian abscess
- Foul-smelling sweat
- Can have mild pancytopenia
Relapsed Brucellosis
- Occurs within six months of completing treatment in about 10% of patients
Diagnosis
- Culture
- May be isolated from blood culture, but only intermittent and is a fastidious organism
- Sensitivity is 50-70%
- Cultures should be held for 10 days
- Grows slowly on blood and chocolate agar; better on Brucella agar
- On gram stain, the small coccobacilli look like fine grains of sand
- May be isolated from blood culture, but only intermittent and is a fastidious organism
- Serology
- Acute and convalescent serology showing a fourfold rise in titres
- Serum agglutination test titres of 1:160 or greater in the right clinical context
- Cross-reacts with Francisella tularensis and Vibrio cholerae
Management
Prevention
Lab Safety
- Assess risk and provide prophylaxis and monitoring per CDC guidelines
- Assess risk
- Minimal risk
- Manipulating routine specimen or enriched material in BSL2 with PPE
- Being present while someone manipulates a routine specimen in BSL2, or on an open bench without aerosol-generating procedures
- Manipulating or being present while someone manipulates enriched material in BSL2
- Low risk
- Being present more than 5 feet from someone manipulating enriched material on an open bench, without aerosol-generating procedures
- High risk
- Manipulating a routine specimen resulting in contact with broken skin or mucous membranes
- Being present less than 5 feet from someone manipulating enriched material outside of a BSL2
- Manipulating enriched material within a BSL2 without PPE
- Being present in the lab during an aerosol-generating procedure
- Minimal risk
- Aerosol-generating procedures include centrifuging without sealed carriers, vortexing, sonicating, spillage/splashes
- Enriched material includes positive blood cultures, and reproductive clinical specimens (amniotic fluid, placental products) should be treated similarly
- People with high-risk exposures should have post-exposure prophylaxis and follow-up
- PEP with doxycycline 100 mg PO bid plus rifampin 600 mg PO daily for 21 days
- Either can be replaced by TMP-SMX if contraindications exist, but should ensure two effect antibiotics are used
- Follow-up
- Daily fever checks and weekly symptom watch for 24 weeks after last known exposure
- Serial serology at 0, 6, 12, 18, and 24 weeks after last known exposure
- PEP with doxycycline 100 mg PO bid plus rifampin 600 mg PO daily for 21 days