acute zoonotic bacterial infection caused by pathogenic spirochetes of the genus Leptospira.
Aetiology
Causative Agent
- Genus: Leptospira
- Species: Leptospira interrogans (most common pathogenic species)
- Morphology:
- Thin, tightly coiled spirochete
- Aerobic
- Motile (hooked ends)

Reservoir Hosts
- Rodents (especially rats) – most important
- Dogs
- Cattle
- Pigs
- Wild mammals
Animals often carry leptospires in renal tubules and shed them in urine chronically.
Mode of Transmission
Entry through:
- Abraded skin
- Mucous membranes (eyes, nose, mouth)
Exposure to contaminated:
- Water
- Soil
- Food
No human-to-human transmission in most cases.
Pathophysiology
- Entry through skin/mucosa
- Hematogenous dissemination (leptospiremia)
- Endothelial damage → vasculitis
- Multiorgan involvement:
- Liver
- Kidneys
- Lungs
- CNS
Immune-mediated injury contributes in later phases.
Clinical presentation
Leptospirosis classically has a biphasic course:
Septicemic (Acute) Phase (First 5–7 days)
- Sudden onset of:
- High fever
- Chills
- Severe headache
- Myalgia (especially gastrocnemius and lumbar muscles)
- Conjunctival suffusion (characteristic)
- Nausea, vomiting
Immune Phase
- Occurs after brief improvement
- Antibody formation
- Organ involvement becomes evident
Clinical Forms
Anicteric Leptospirosis (Mild Form)
- Most common
- Flu-like illness
- Self-limited
Icteric Leptospirosis (Weil’s Disease)
Severe form, characterized by:
- Jaundice
- Acute kidney injury
- Hemorrhage
- Hypotension
- High mortality
Severe Complications
- Acute renal failure
- Hepatic dysfunction
- Pulmonary hemorrhage syndrome
- Aseptic meningitis
- Myocarditis
Investigations
Laboratory Findings
- Leukocytosis
- Thrombocytopenia
- Elevated liver enzymes (bilirubin disproportionately high)
- Elevated creatinine and urea
- Elevated CK
Specific Diagnostic Tests
Serology
- Microscopic Agglutination Test (MAT) – gold standard
- ELISA (IgM)
Molecular Tests
- PCR (early phase)
Culture
- Blood & CSF (early phase, within 10 days)
- Urine (late phase, after 7 days of onset)
- Slow-growing and rarely used clinically
Management
Mild Disease
- Doxycycline 100mg BID PO for 7 days → not safe for pregnancy or children
- Alternatives:
- Amoxicillin 500mg QID PO for 7 days
- Azithromycin 500mg QID PO for 7 days
Severe Disease
- IV Penicillin G 1.5 MU every 6 hours for 7 days
- Ceftriaxone 1g/24hr or cefotaxime 1g/6hr for 7 days (alternatives)
- Supportive care:
- Fluid and electrolyte management
- Dialysis for renal failure
- Ventilatory support if pulmonary hemorrhage