β-Lactam antibiotics trigger mouse TLR2/4- and human TLR2/5-dependent Jarisch-Herxheimer reaction in leptospirosis

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Abstract Leptospirosis is a neglected zoonotic disease causing ∼1 million cases and 60,000 deaths annually. Antibiotic therapy can trigger a detrimental inflammatory Jarisch-Herxheimer reaction (JHR). We investigated antibiotic effects in leptospirosis, using a mouse model of severe disease and human whole blood from healthy donors infected ex vivo with bioluminescent Leptospira interrogans . We tested the effect of amoxicillin and ceftriaxone, two bactericidal β-Lactams antibiotics and assessed bacterial survival, cytokines, pathophysiology and JHR mechanisms upon amoxicillin. β-lactams induced profound pro-inflammatory cytokine release. In mice, the inflammation was TLR2 and TLR4 dependent, accordingly to the TLR4 host-specificity of LPS recognition, and amoxicillin exacerbated disease severity within hours, notably worsening myocarditis. In human whole blood, this inflammation depended largely on TLR2 (lipoprotein receptor) and TLR5 (flagellin receptor). Interestingly, only stealthy virulent isolates of Leptospira interrogans, unlike some Leptospira species belonging to intermediate and non-virulent clades such as biffexa , induced in human whole blood a JHR-like effect, which was also observed with Borrelia burgdorferi . These findings demonstrate that host-specific TLR recognition of released spirochaetal components by antibiotic treatment drives JHR, evoking a cytokine storm and worsening outcomes.

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