Leptospira IgG ELISA

Leptospirosis (also known as Weil's syndrome) is probably the most widespread zoonosis in the world. It is caused by infection with spirochete bacteria of the genus Leptospira and affects humans as well as a broad spectrum of animal hosts. The incidence is significantly higher in warm climate countries than in temperate regions. The disease is seasonal, with peak incidence occurring in summer or fall in temperate regions, where temperature is the limiting factor in survival of leptospires, and during rainy seasons in warm climate regions, where rapid desiccation would otherwise prevent survival. Natural reservoirs for the pathogenic Leptospira interrogans include rodents as well as a large variety of domesticated mammals (e. g. pigs, cattle and dogs). Leptospires occupy the lumen of nephritic tubules in their natural host and are shed into the urine. Transmission can occur when humans are directly or indirectly exposed to the urine of infected animals or a urine-polluted environment. Leptospires gain entry into the human blood stream via cuts, skin abrasions or mucous membranes through contact with moist soil, vegetation, and contaminated waters; handling infected animal tissues; and ingestion of food and water. Leptospires are rarely transmitted from human to human. The incubation period is usually 5-14 days, with a range of 2-30 days. The spectrum of clinical symptoms is extremely wide. The vast majority of leptospiral infections are either subclinical or result in very mild illness and recover without any complications Clinical manifestations of leptospirosis range from mild influenza-like symptoms to severe life-threatening disease forms, characterized by jaundice, renal failure, bleeding and severe pulmonary hemorrhage. The clinical presentation of leptospirosis is biphasic, with the acute or septicemic phase lasting about a week, followed by the immune phase, characterized by antibody production and excretion of leptospires in the urine. Most of the complications of leptospirosis are associated with localization of leptospires within the tissues during the immune phase and thus occur during the second week of the illness. The classical syndrome of Weil’s disease represents only the most severe presentation. It is characterized by jaundice, renal failure, hemorrhage and myocarditis with arrhythmias. The presence of pathogen resp. infection may be identified by • Pathogen detection: dark-field microscopy, culture from blood, urine, cerebrospinal fluid or tissues • PCR • Serology: microscopic agglutination (MAT) test, ELISA.
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