Leptospirosis is a zoonosis found worldwide, but particularly in humid subtropical and tropical zones. It is caused by pathogenic bacteria of the Leptospira species of the spirochete family. It is estimated that there are over a million cases of leptospirosis worldwide each year, with 60,000 deaths. These figures place leptospirosis among the most dangerous bacterial zoonoses in the world. The disease affects the most disadvantaged populations, and also inflicts its burden on domestic and farm animals. To this day, however, leptospirosis remains a neglected disease, poorly understood because it has been little studied. Human leptospirosis initially presents as a febrile syndrome, with fever, headache, myalgia and joint pain. These symptoms are very similar to those observed in influenza, dengue fever and other acute febrile illnesses, making diagnosis very difficult. Delayed initiation of antibiotic therapy, a treatment recommended by the WHO, is associated with the development of severe forms of leptospirosis. Indeed, in 10% of cases, leptospirosis evolves into severe forms, which are still poorly described, but which result in haemorrhage, multivisceral failure (lungs, kidneys, liver) and a drastic increase in the case-fatality rate. In 2023, 152 cases of leptospirosis were reported in New Caledonia. Of these, 130 people (85%) were hospitalized and 4 deaths were recorded (2.6%). For patients suffering from leptospirosis, it is therefore important to be able to make the diagnosis quickly, ideally as soon as symptoms appear. It is also crucial to be able to monitor, or even prevent, the development of severe forms of the disease, to ensure optimal patient care.
The goal of this study is to identify diagnostic and prognostic biomarkers based on host response to human leptospirosis in New Caledonia. To achieve this goal, Individuals coming to the emergency department of the Centre Hospitalier Territorial de Nouvelle-Calédonie will be recruited either with suspected leptospirosis with signs and symptoms or healthy showing no infectious signs. For febrile patients with confirmed (group 1) or refuted (group 2) diagnosis of leptospirosis: * At D0: a 20-ml blood sample and a 5-ml urine sample * At D1, D3 and D15: a 20-ml blood sample For healthy patients (group 3): * At D0: a 20-ml blood sample and a 5-ml urine sample * At D15: a 20-ml blood sample. The analyses to be carried out are : * Host-pathogen sequencing, * Metagenomics, * Transcriptomics, * Metabolomics, * And cytokine assays to study the host immune response.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
DIAGNOSTIC
Masking
NONE
Enrollment
450
For febrile patients with confirmed (group 1) or refuted (group 2) diagnosis of leptospirosis: \- At D0, D1, D3 and D15 a 20-ml blood sample For healthy patients (group 3): \- At D0 and D15: a 20-ml blood sample
For all participants, a 5-ml urine sample at D0
Identify diagnostic and prognostic biomarkers based on host response to human leptospirosis in New Caledonia.
transcriptome study by sequencing host mRNA at different times, in the blood and urine of individuals suspected of having leptospirosis
Time frame: 4 years
Identify diagnostic and prognostic biomarkers based on host response to human leptospirosis in New Caledonia.
level of cytokines present at different times, in the blood and urine of individuals suspected of having leptospirosis
Time frame: 4 years
Identify diagnostic and prognostic biomarkers based on host response to human leptospirosis in New Caledonia.
identification of the Leptospira spp. serogroup by sequencing bacterial DNA or PCR at different times, in the blood and urine of individuals suspected of having leptospirosis
Time frame: 4 years
Develop and validate biomarkers that have already been identified for accurate diagnosis of leptospirosis of varying clinical severity.
Transcriptome study using host mRNA sequencing
Time frame: 4 years
Develop and validate biomarkers that have already been identified for accurate diagnosis of leptospirosis of varying clinical severity.
Level of cytokines or other markers previously identified as biomarkers of severity.
Time frame: 4 years
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