The Carbon Monoxide Releasing Molecule CORM-2 Attenuates Pseudomonas aeruginosa Biofilm Formation

被引:48
作者
Murray, Thomas S. [1 ]
Okegbe, Chinweike [2 ]
Gao, Yuan
Kazmierczak, Barbara I.
Motterlini, Roberto [3 ]
Dietrich, Lars E. P. [2 ]
Bruscia, Emanuela M. [1 ]
机构
[1] Yale Univ, Sch Med, Dept Pediat, New Haven, CT 06510 USA
[2] Columbia Univ, Dept Biol Sci, New York, NY 10027 USA
[3] Univ Paris Est, INSERM, U955, Creteil, France
来源
PLOS ONE | 2012年 / 7卷 / 04期
基金
美国国家卫生研究院;
关键词
ANTIMICROBIAL ACTION; LIPOPOLYSACCHARIDE; RESPIRATION; INFECTIONS; TARGETS; OXYGEN;
D O I
10.1371/journal.pone.0035499
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Chronic infections resulting from biofilm formation are difficult to eradicate with current antimicrobial agents and consequently new therapies are needed. This work demonstrates that the carbon monoxide-releasing molecule CORM-2, previously shown to kill planktonic bacteria, also attenuates surface-associated growth of the Gram-negative pathogen Pseudomonas aeruginosa by both preventing biofilm maturation and killing bacteria within the established biofilm. CORM-2 treatment has an additive effect when combined with tobramycin, a drug commonly used to treat P. aeruginosa lung infections. CORM-2 inhibited biofilm formation and planktonic growth of the majority of clinical P. aeruginosa isolates tested, for both mucoid and non-mucoid strains. While CORM-2 treatment increased the production of reactive oxygen species by P. aeruginosa biofilms, this increase did not correlate with bacterial death. These data demonstrate that CO-RMs possess potential novel therapeutic properties against a subset of P. aeruginosa biofilm related infections.
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页数:11
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