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Published on: March 16, 2018
Adjunctive daptomycin attenuates brain damage and hearing loss more efficiently than rifampin in infant rat
Denis Grandgirard1, Melchior Burri, Philipp Agyeman
1Neuroinfection Laboratory, Institute for Infectious Diseases, University of Bern, Switzerland.
Abstract:
Exacerbation of cerebrospinal fluid (CSF) inflammation in response to bacteriolysis by beta-lactam antibiotics contributes to brain damage and neurological sequelae in bacterial meningitis. Daptomycin, a nonlytic antibiotic acting on Gram-positive bacteria, lessens inflammation and brain injury compared to ceftriaxone. With a view to a clinical application for pediatric bacterial meningitis, we investigated the effect of combining daptomycin or rifampin with ceftriaxone in an infant rat pneumococcal meningitis model. Eleven-day-old Wistar rats with pneumococcal meningitis were randomized to treatment starting at 18 h after infection with (i) ceftriaxone (100 mg/kg of body weight, subcutaneously [s.c.], twice a day [b.i.d.]), (ii) daptomycin (10 mg/kg, s.c., daily) followed 15 min later by ceftriaxone, or (iii) rifampin (20 mg/kg, intraperitoneally [i.p.], b.i.d.) followed 15 min later by ceftriaxone. CSF was sampled at 6 and 22 h after the initiation of therapy and was assessed for concentrations of defined chemokines and cytokines. Brain damage was quantified by histomorphometry at 40 h after infection and hearing loss was assessed at 3 weeks after infection. Daptomycin plus ceftriaxone versus ceftriaxone significantly (P < 0.04) lowered CSF concentrations of monocyte chemoattractant protein 1 (MCP-1), MIP-1α, and interleukin 6 (IL-6) at 6 h and MIP-1α, IL-6, and IL-10 at 22 h after initiation of therapy, led to significantly (P < 0.01) less apoptosis, and significantly (P < 0.01) improved hearing capacity. While rifampin plus ceftriaxone versus ceftriaxone also led to lower CSF inflammation (P < 0.02 for IL-6 at 6 h), it had no significant effect on apoptosis and hearing capacity. Adjuvant daptomycin could therefore offer added benefits for the treatment of pediatric pneumococcal meningitis.
Insights
Adding daptomycin to ceftriaxone treatment for pediatric pneumococcal meningitis significantly reduced cerebrospinal fluid inflammation and brain damage. This combination therapy also improved hearing outcomes in infant rats, suggesting daptomycin
Area of Science:
- Neuroscience
- Infectious Diseases
- Pharmacology
Background:
- Bacterial meningitis causes significant inflammation in cerebrospinal fluid (CSF), leading to brain damage.
- Beta-lactam antibiotics can exacerbate this inflammation through bacteriolysis, worsening neurological outcomes.
- Daptomycin, a nonlytic antibiotic, shows potential for reducing inflammation and injury compared to ceftriaxone.
Purpose of the Study:
- To investigate the efficacy of combining daptomycin or rifampin with ceftriaxone in a pediatric pneumococcal meningitis model.
- To evaluate the impact of these combination therapies on CSF inflammation, brain damage, and hearing loss.
Main Methods:
- An infant rat model of pneumococcal meningitis was used.
- Rats were treated with ceftriaxone alone, daptomycin plus ceftriaxone, or rifampin plus ceftriaxone.
- CSF was analyzed for cytokine and chemokine concentrations.
- Brain damage was assessed via histomorphometry, and hearing loss was evaluated.
Main Results:
- Daptomycin plus ceftriaxone significantly reduced CSF concentrations of MCP-1, MIP-1α, and IL-6 compared to ceftriaxone alone.
- This combination therapy also led to significantly less apoptosis and improved hearing capacity.
- Rifampin plus ceftriaxone showed some reduction in IL-6 but did not significantly impact apoptosis or hearing.
Conclusions:
- Adjuvant daptomycin offers significant benefits in treating pediatric pneumococcal meningitis by reducing inflammation and preventing brain injury.
- Combination therapy with daptomycin and ceftriaxone holds promise for improved clinical outcomes in pediatric bacterial meningitis.
- Daptomycin's nonlytic mechanism is advantageous in minimizing antibiotic-induced inflammation.
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