Orientia tsutsugamushi Is Highly Susceptible to the RNA Polymerase Switch Region Inhibitor Corallopyronin A In Vitro and In Vivo
Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by...
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Veröffentlicht in: | Antimicrobial agents and chemotherapy 2018-04, Vol.62 (4) |
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Sprache: | eng |
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Zusammenfassung: | Scrub typhus is a potentially lethal infection caused by the obligate intracellular bacterium
Reports on the emergence of doxycycline-resistant strains highlight the urgent need to develop novel antiinfectives against scrub typhus. Corallopyronin A (CorA) is a novel α-pyrone compound synthesized by the myxobacterium
that was characterized as a noncompetitive inhibitor of the switch region of the bacterial RNA polymerase (RNAP). We investigated the antimicrobial action of CorA against the human-pathogenic Karp strain of
and
The MIC of CorA against
was remarkably low (0.0078 μg/ml), 16-fold lower than that against
In the lethal intraperitoneal
mouse infection model, a minimum daily dose of 100 μg CorA protected 100% of infected mice. Two days of treatment were sufficient to confer protection. In contrast to BALB/c mice, SCID mice succumbed to the infection despite treatment with CorA or tetracycline, suggesting that antimicrobial treatment required synergistic action of the adaptive immune response. Similar to tetracycline, CorA did not prevent latent infection of
However, latency was not caused by acquisition of antimicrobial resistance, since
reisolated from latently infected BALB/c mice remained fully susceptible to CorA. No mutations were found in the CorA-binding regions of the β and β' RNAP subunit genes
and
Inhibition of the RNAP switch region of
by CorA is therefore a novel and highly potent target for antimicrobial therapy for scrub typhus. |
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ISSN: | 0066-4804 1098-6596 |
DOI: | 10.1128/AAC.01732-17 |